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    <title>Recent sio_cmbc_rw items</title>
    <link>https://escholarship.org/uc/sio_cmbc_rw/rss</link>
    <description>Recent eScholarship items from Other Recent Work</description>
    <pubDate>Tue, 15 Sep 2026 09:00:43 +0000</pubDate>
    <item>
      <title>Carboxyhemoglobin and depletion of blood oxygen in sleeping elephant seals</title>
      <link>https://escholarship.org/uc/item/2cj1v6m0</link>
      <description>An exceptionally large blood O2 store underlies the remarkable dive performance of elephant seals. However, elevated carboxyhemoglobin (COHb) concentrations in these seals complicate estimations of blood O2 content and O2 depletion rates, and may also affect monitoring of brain oxygenation in seals with new non-invasive near-infrared (NIR) recorders. Using hemoximetry analyses of blood samples during sleep apneas of juvenile northern elephant seals (Mirounga angustirostris), we constructed in vivo Hill plot equations and O2–Hb dissociation curves (ODCs). We found: (a) COHb and methemoglobin (both of which do not bind O2 and increase hemoglobin (Hb) affinity for O2) comprised 8% of Hb, (b) an in vivo P50 (partial pressure of O2 at 50% Hb saturation, an index of O2 affinity of Hb) of 27.1&amp;nbsp;mm Hg that was Hg 3.4&amp;nbsp;mm Hg less than that previously determined with an in vitro laboratory approach, and (c) when the in vivo and in vitro Hill plot equations were applied to arterial,...</description>
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      <pubDate>Fri, 11 Sep 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Ponganis, PJ</name>
      </author>
      <author>
        <name>McDonald, BI</name>
      </author>
      <author>
        <name>Williams, CL</name>
        <uri>https://orcid.org/0000-0002-3977-2900</uri>
      </author>
      <author>
        <name>Meir, JU</name>
      </author>
      <author>
        <name>Brown, CV</name>
      </author>
      <author>
        <name>Patrician, A</name>
      </author>
      <author>
        <name>Tremblay, JC</name>
      </author>
      <author>
        <name>Hindle, AG</name>
      </author>
      <author>
        <name>Pallin, LJ</name>
      </author>
      <author>
        <name>Kendall-Bar, JM</name>
        <uri>https://orcid.org/0000-0003-4758-1386</uri>
      </author>
      <author>
        <name>McKnight, JC</name>
      </author>
      <author>
        <name>Costa, DP</name>
        <uri>https://orcid.org/0000-0002-0334-3899</uri>
      </author>
      <author>
        <name>Williams, TM</name>
      </author>
      <author>
        <name>Ainslie, PN</name>
      </author>
    </item>
    <item>
      <title>A sorghum pangenome reference improves global crop trait discovery</title>
      <link>https://escholarship.org/uc/item/69b358rz</link>
      <description>Although the green revolution adapted a handful of crops to homogeneous and high-input industrialized agriculture, much of the global population still relies on the local production of variable crop cultivars by low-input smallholder farms. This diversity of unhomogenized crops1, like that of the grain and bioenergy crop sorghum2, 3, 4–5, offers raw materials for genetic gain and cultivar improvement. However, breeding efforts can be constrained by highly specialized traits and breeding targets6. Here, to bridge this diversity, we constructed a 33-member pangenome reference and a diversity panel across 1,984 cultivars and landraces. We leveraged these resources to explore the complex interplay among historical contingency, ongoing adaptation and previously uncharacterized structural diversity. Specifically, our analyses conclusively demonstrated multiple nested and deeply diverged structural variants in the domestication gene SHATTERING1, which distinguish the previously established...</description>
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      <pubDate>Mon, 31 Aug 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Morris, Geoffrey P</name>
      </author>
      <author>
        <name>Harder, Avril M</name>
      </author>
      <author>
        <name>Healey, Adam L</name>
      </author>
      <author>
        <name>McLaughlin, Chloee M</name>
      </author>
      <author>
        <name>Rifkin, Joanna L</name>
      </author>
      <author>
        <name>Cruet-Burgos, Clara</name>
      </author>
      <author>
        <name>Jenkins, Jerry W</name>
      </author>
      <author>
        <name>Shu, Shengqiang</name>
      </author>
      <author>
        <name>Spiekerman, John J</name>
      </author>
      <author>
        <name>VanGessel, Carl J</name>
      </author>
      <author>
        <name>Agnew, Erica</name>
      </author>
      <author>
        <name>Audebert, Alain</name>
      </author>
      <author>
        <name>Barry, Kerrie</name>
        <uri>https://orcid.org/0000-0002-8999-6785</uri>
      </author>
      <author>
        <name>Baxter, Ivan</name>
      </author>
      <author>
        <name>Beurier, Gregory</name>
      </author>
      <author>
        <name>Boston, Lori Beth</name>
      </author>
      <author>
        <name>Boyles, Richard E</name>
      </author>
      <author>
        <name>Brady, Siobhan M</name>
        <uri>https://orcid.org/0000-0001-9424-8055</uri>
      </author>
      <author>
        <name>Bunting, Victoria</name>
      </author>
      <author>
        <name>Chaparro, Jacqueline M</name>
      </author>
      <author>
        <name>Courtney, Chaney</name>
      </author>
      <author>
        <name>Dembele, Joseph Sékou B</name>
      </author>
      <author>
        <name>Deshpande, Santosh</name>
      </author>
      <author>
        <name>Diatta, Cyril</name>
      </author>
      <author>
        <name>Eck, Nathaniel</name>
      </author>
      <author>
        <name>Eveland, Andrea L</name>
      </author>
      <author>
        <name>Faye, Jacques M</name>
      </author>
      <author>
        <name>Flowers, Dave</name>
      </author>
      <author>
        <name>Fonceka, Daniel</name>
      </author>
      <author>
        <name>Gano, Boubacar</name>
      </author>
      <author>
        <name>de Gracia Coquerel, Marie</name>
      </author>
      <author>
        <name>Goodstein, David</name>
      </author>
      <author>
        <name>Grimwood, Jane</name>
      </author>
      <author>
        <name>Hudson, Matthew E</name>
      </author>
      <author>
        <name>Kholova, Jana</name>
      </author>
      <author>
        <name>Johnson, Katherine</name>
      </author>
      <author>
        <name>Johnson, Kristen K</name>
      </author>
      <author>
        <name>Kawa, Dorota</name>
      </author>
      <author>
        <name>Kouressy, Mamoutou</name>
      </author>
      <author>
        <name>Kresovich, Stephen</name>
      </author>
      <author>
        <name>Lee, Scott</name>
      </author>
      <author>
        <name>Lemaux, Peggy G</name>
      </author>
      <author>
        <name>Lowery, Robert</name>
      </author>
      <author>
        <name>Luquet, Delphine</name>
      </author>
      <author>
        <name>Maina, Fanna</name>
      </author>
      <author>
        <name>Mamidi, Sujan</name>
      </author>
      <author>
        <name>McKay, John K</name>
      </author>
      <author>
        <name>Michael, Todd P</name>
        <uri>https://orcid.org/0000-0001-6272-2875</uri>
      </author>
      <author>
        <name>Mindaye, Taye T</name>
      </author>
      <author>
        <name>Mullet, John</name>
      </author>
      <author>
        <name>Ozersky, Philip</name>
      </author>
      <author>
        <name>Plott, Christopher</name>
      </author>
      <author>
        <name>Prenni, Jessica E</name>
      </author>
      <author>
        <name>Pressoir, Gael</name>
      </author>
      <author>
        <name>Rami, Jean-François</name>
      </author>
      <author>
        <name>Rife, Trevor W</name>
      </author>
      <author>
        <name>Saxton, Jocelyn</name>
      </author>
      <author>
        <name>Sine, Bassirou</name>
      </author>
      <author>
        <name>Sreedasyam, Avinash</name>
      </author>
      <author>
        <name>Talag, Jayson</name>
      </author>
      <author>
        <name>Teme, Niaba</name>
      </author>
      <author>
        <name>Tuinstra, Mitchell R</name>
      </author>
      <author>
        <name>Vadez, Vincent</name>
      </author>
      <author>
        <name>Vogel, John P</name>
        <uri>https://orcid.org/0000-0003-1786-2689</uri>
      </author>
      <author>
        <name>Walstead, Rachel</name>
      </author>
      <author>
        <name>Wang, Jianan</name>
      </author>
      <author>
        <name>Webber, Jenell</name>
      </author>
      <author>
        <name>Williams, Melissa</name>
      </author>
      <author>
        <name>Xu, Yuxing</name>
      </author>
      <author>
        <name>Mockler, Todd C</name>
      </author>
      <author>
        <name>Lasky, Jesse R</name>
      </author>
      <author>
        <name>Rice, Brian R</name>
      </author>
      <author>
        <name>Schmutz, Jeremy</name>
      </author>
      <author>
        <name>Shakoor, Nadia</name>
      </author>
      <author>
        <name>Lovell, John T</name>
      </author>
    </item>
    <item>
      <title>STREAMS guidelines: standards for technical reporting in environmental and host-associated microbiome studies</title>
      <link>https://escholarship.org/uc/item/0nt0t4k2</link>
      <description>The interdisciplinary nature of microbiome research, coupled with the generation of complex multi-omics data, makes knowledge sharing challenging. The Strengthening the Organization and Reporting of Microbiome Studies (STORMS) guidelines provide a checklist for the reporting of study information, experimental design and analytical methods within a scientific manuscript on human microbiome research. Here, in this Consensus Statement, we present the standards for technical reporting in environmental and host-associated microbiome studies (STREAMS) guidelines. The guidelines expand on STORMS and include 67 items to support the reporting and review of environmental (for example, terrestrial, aquatic, atmospheric and engineered), synthetic and non-human host-associated microbiome studies in a standardized and machine-actionable manner. Based on input from 248 researchers spanning 28 countries, we provide detailed guidance, including comparisons with STORMS, and case studies that demonstrate...</description>
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      <pubDate>Wed, 6 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kelliher, Julia M</name>
      </author>
      <author>
        <name>Mirzayi, Chloe</name>
      </author>
      <author>
        <name>Bordenstein, Sarah R</name>
      </author>
      <author>
        <name>Oliver, Aaron</name>
        <uri>https://orcid.org/0000-0002-0410-8284</uri>
      </author>
      <author>
        <name>Kellogg, Christina A</name>
      </author>
      <author>
        <name>Hatcher, Eneida L</name>
      </author>
      <author>
        <name>Berg, Maureen</name>
      </author>
      <author>
        <name>Baldrian, Petr</name>
      </author>
      <author>
        <name>Aljumaah, Mashael</name>
      </author>
      <author>
        <name>Miller, Cassandra Maria Luz</name>
      </author>
      <author>
        <name>Mungall, Christopher</name>
      </author>
      <author>
        <name>Novak, Vlastimil</name>
        <uri>https://orcid.org/0000-0001-7890-4593</uri>
      </author>
      <author>
        <name>Palucki, Alexis</name>
      </author>
      <author>
        <name>Smith, Ethan</name>
      </author>
      <author>
        <name>Tabassum, Nazifa</name>
      </author>
      <author>
        <name>Bonito, Gregory</name>
      </author>
      <author>
        <name>Brister, J Rodney</name>
      </author>
      <author>
        <name>Chain, Patrick SG</name>
      </author>
      <author>
        <name>Chen, Mingfei</name>
      </author>
      <author>
        <name>Degregori, Samuel</name>
      </author>
      <author>
        <name>Dundore-Arias, Jose Pablo</name>
      </author>
      <author>
        <name>Emerson, Joanne B</name>
        <uri>https://orcid.org/0000-0001-9983-5566</uri>
      </author>
      <author>
        <name>Moreira C. Fernandes, Vanessa</name>
      </author>
      <author>
        <name>Flores, Roberto</name>
      </author>
      <author>
        <name>Gonzalez, Antonio</name>
      </author>
      <author>
        <name>Hansen, Zoe A</name>
      </author>
      <author>
        <name>Jackson, Scott A</name>
      </author>
      <author>
        <name>Moustafa, Ahmed M</name>
      </author>
      <author>
        <name>Northen, Trent R</name>
        <uri>https://orcid.org/0000-0001-8404-3259</uri>
      </author>
      <author>
        <name>Pariente, Nonia</name>
      </author>
      <author>
        <name>Pett-Ridge, Jennifer</name>
      </author>
      <author>
        <name>Record, Sydne</name>
      </author>
      <author>
        <name>Reji, Linta</name>
      </author>
      <author>
        <name>Reysenbach, Anna-Louise</name>
      </author>
      <author>
        <name>Rich, Virginia I</name>
      </author>
      <author>
        <name>Richardson, Lorna</name>
      </author>
      <author>
        <name>Roux, Simon</name>
        <uri>https://orcid.org/0000-0002-5831-5895</uri>
      </author>
      <author>
        <name>Schriml, Lynn M</name>
      </author>
      <author>
        <name>Shabman, Reed S</name>
      </author>
      <author>
        <name>Sierra, Maria A</name>
      </author>
      <author>
        <name>Sullivan, Matthew B</name>
      </author>
      <author>
        <name>Sundaramurthy, Punithavathi</name>
      </author>
      <author>
        <name>Thibault, Katherine M</name>
      </author>
      <author>
        <name>Thompson, Luke R</name>
      </author>
      <author>
        <name>Tighe, Scott</name>
      </author>
      <author>
        <name>Vereen, Ethell</name>
      </author>
      <author>
        <name>Eloe-Fadrosh, Emiley A</name>
        <uri>https://orcid.org/0000-0002-8162-1276</uri>
      </author>
    </item>
    <item>
      <title>Correction: A microbial survey of the International Space Station (ISS)</title>
      <link>https://escholarship.org/uc/item/3ht0p7jb</link>
      <description>[This corrects the article DOI: 10.7717/peerj.4029.].</description>
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      <pubDate>Tue, 21 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Lang, Jenna M</name>
      </author>
      <author>
        <name>Coil, David A</name>
        <uri>https://orcid.org/0000-0001-6049-8240</uri>
      </author>
      <author>
        <name>Neches, Russell Y</name>
        <uri>https://orcid.org/0000-0002-2055-8381</uri>
      </author>
      <author>
        <name>Brown, Wendy E</name>
      </author>
      <author>
        <name>Cavalier, Darlene</name>
      </author>
      <author>
        <name>Severance, Mark</name>
      </author>
      <author>
        <name>Hampton-Marcell, Jarrad T</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
      <author>
        <name>Eisen, Jonathan A</name>
        <uri>https://orcid.org/0000-0002-0159-2197</uri>
      </author>
    </item>
    <item>
      <title>Green genes from blue greens: challenges and solutions to unlocking the potential of cyanobacteria in drug discovery</title>
      <link>https://escholarship.org/uc/item/0pr7f7ks</link>
      <description>Cyanobacteria are prolific producers of biologically active compounds that are important in influencing ecology, behavior of interacting organisms, and as leads in drug discovery efforts. Here we discuss the challenges faced by all natural product researchers, especially those that focus on cyanobacteria, and then describe progress that has been made in these areas. We also propose some solutions, paths forward, and thoughts for consideration on these challenges.</description>
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      <pubDate>Tue, 9 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Philmus, Benjamin</name>
      </author>
      <author>
        <name>Avalon, Nicole E</name>
      </author>
      <author>
        <name>Ding, Yousong</name>
      </author>
      <author>
        <name>Doering, Drew T</name>
      </author>
      <author>
        <name>Eustáquio, Alessandra S</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
        <uri>https://orcid.org/0000-0003-1403-4458</uri>
      </author>
      <author>
        <name>Luesch, Hendrik</name>
      </author>
      <author>
        <name>Orjala, Jimmy</name>
      </author>
      <author>
        <name>Sutherland, Shaz</name>
      </author>
      <author>
        <name>Taton, Arnaud</name>
      </author>
      <author>
        <name>Udwary, Daniel</name>
        <uri>https://orcid.org/0000-0002-3491-0198</uri>
      </author>
    </item>
    <item>
      <title>Osmolyte chemical diversity in Lingulaulax polyedra red tides: a critical overlooked factor to respiratory irritations?</title>
      <link>https://escholarship.org/uc/item/0x39m3qh</link>
      <description>The detrimental effects on human health sometimes observed during blooms of Lingulaulax polyedra have been formerly attributed to the yessotoxin analogs this species produces. In this paper we show that natural concentrations of yessotoxin analogs present in seawater and sea spray aerosols during an unprecedented L. polyedra bloom in 2020 in Southern California did not induce inflammation in mammal macrophage cells, questioning the role played by yessotoxin in causing respiratory irritations. This bloom was associated with unprecedented levels of particulate dimethylsulfoniopropionate (2.74 ± 1.63 to 10.11 ± 1.39 µM), gonyol and several new structural analogs ofgonyol . We profiled the metabolic content of dinoflagellate cells and recorded increasing amounts of quaternary amines of the betaine family (carnitine, actinin, ectoine) as the bloom progressed. Being precursors of sulfur and nitrogenous small volatile compounds, we hypothesize that, in addition to their recognized role...</description>
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      <pubDate>Thu, 4 Dec 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Eva, Ternon</name>
      </author>
      <author>
        <name>Evgenia, Glukhov</name>
      </author>
      <author>
        <name>Vallet, Marine</name>
      </author>
      <author>
        <name>Julie, Dinasquet</name>
      </author>
      <author>
        <name>Melissa, Carter L</name>
      </author>
      <author>
        <name>Lena, Gerwick</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
      </author>
      <author>
        <name>Clarissa, Anderson</name>
      </author>
    </item>
    <item>
      <title>Extremophile hotspots linked to containerized industrial waste dumping in a deep-sea basin</title>
      <link>https://escholarship.org/uc/item/4nm729gv</link>
      <description>Decaying barrels on the seafloor linked to DDT contamination have raised concerns about the public health implications of decades old industrial waste dumped off the coast of Los Angeles. To explore their contents, we collected sediment cores perpendicular to five deep-sea barrels. The concentration of DDT and its breakdown products were highly elevated relative to control sites yet did not vary with distance from the barrels, suggesting that they were not associated with the contamination. Sediment cores collected through white halos surrounding three barrels were enriched in calcite and had elevated pH. The associated microbial communities were low diversity and dominated by alkalophilic bacteria with metagenome-assembled genomes adapted to high pH. A solid concretion sampled between a white halo and barrel was composed of brucite, a magnesium hydroxide mineral that forms at high pH. Based on these findings, we postulate that leakage of containerized alkaline waste triggered...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4nm729gv</guid>
      <pubDate>Thu, 20 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Gutleben, Johanna</name>
      </author>
      <author>
        <name>Podell, Sheila</name>
      </author>
      <author>
        <name>Mizell, Kira</name>
      </author>
      <author>
        <name>Sweeney, Douglas</name>
      </author>
      <author>
        <name>Neira, Carlos</name>
      </author>
      <author>
        <name>Levin, Lisa A</name>
        <uri>https://orcid.org/0000-0002-2858-8622</uri>
      </author>
      <author>
        <name>Jensen, Paul R</name>
      </author>
    </item>
    <item>
      <title>Population Genomics Reveals Panmixia in Pacific Sardine (Sardinops sagax) of the North Pacific</title>
      <link>https://escholarship.org/uc/item/32r273j1</link>
      <description>The spatial structure and dynamics of populations are important considerations when defining management units in organisms that are harvested as natural resources. In the Eastern Pacific, Pacific Sardine range from Chile to Alaska, the northernmost state of the United States (U.S.), and once supported an expansive and productive fishery. Along its North American range, it is hypothesized to comprise three subpopulations: a northern and southern subpopulation, which primarily occur off the coast of the U.S. and Baja California, Mexico (M.X.), respectively, and a third in the Gulf of California, M.X. We used low coverage whole genome sequencing to generate genotype likelihoods for millions of SNPs in 317 individuals collected from the Gulf of California, M.X., to Oregon, U.S., to assess population structure in Pacific Sardine. Differentiation across the genome was driven by variation at several putative chromosomal inversions ranging in size from ~21 MB to 0.89 MB, although none...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/32r273j1</guid>
      <pubDate>Fri, 12 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Longo, Gary C</name>
      </author>
      <author>
        <name>D′Amelio, Katie</name>
      </author>
      <author>
        <name>Larson, Wes</name>
      </author>
      <author>
        <name>Enciso, Concepción Enciso</name>
      </author>
      <author>
        <name>Torre, Jorge</name>
      </author>
      <author>
        <name>Minich, Jeremiah J</name>
      </author>
      <author>
        <name>Michael, Todd P</name>
        <uri>https://orcid.org/0000-0001-6272-2875</uri>
      </author>
      <author>
        <name>Craig, Matthew T</name>
      </author>
    </item>
    <item>
      <title>Cyanobacteria Join the Kahalalide Conversation: Genome and Metabolite Evidence for Structurally Related Peptides</title>
      <link>https://escholarship.org/uc/item/36v4d69t</link>
      <description>Kahalalide F is a cyclic depsipeptide with notable anticancer properties, initially discovered from the green alga &lt;i&gt;Bryopsis&lt;/i&gt; sp. and its molluscan predator &lt;i&gt;Elysia rufescens&lt;/i&gt;. Recent studies have pinpointed a bacterial endosymbiont of the green alga, &lt;i&gt;Candidatus&lt;/i&gt; Endobryopsis kahalalidefaciens, as the true producer of kahalalide F. In the present work, we characterize a closely related kahalalide F analog, kahalalide Z&lt;sub&gt;5&lt;/sub&gt;, from the marine cyanobacterium &lt;i&gt;Limnoraphis&lt;/i&gt; sp. collected in the Las Perlas Islands, Panama, and propose the structures of several related compounds by detailed MS analysis. To uncover novel metabolites and prioritize them for targeted isolation from this organism, we employed a robust metabolomics strategy combining LC-MS/MS with SMART NMR and DeepSAT, artificial intelligence platforms trained to infer chemical structures from &lt;sup&gt;1&lt;/sup&gt;H-&lt;sup&gt;13&lt;/sup&gt;C HSQC NMR data. This integrated approach annotated a compound with structural...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/36v4d69t</guid>
      <pubDate>Thu, 28 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Ryu, Byeol</name>
        <uri>https://orcid.org/0000-0002-3405-2875</uri>
      </author>
      <author>
        <name>Avalon, Nicole E</name>
      </author>
      <author>
        <name>Cuau, Marine</name>
      </author>
      <author>
        <name>Almaliti, Jehad</name>
      </author>
      <author>
        <name>Din, M Omar</name>
      </author>
      <author>
        <name>Brennan, Caitriona</name>
      </author>
      <author>
        <name>Glukhov, Evgenia</name>
      </author>
      <author>
        <name>Knight, Rob</name>
      </author>
      <author>
        <name>Gerwick, Lena</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
        <uri>https://orcid.org/0000-0003-1403-4458</uri>
      </author>
    </item>
    <item>
      <title>Metagenomic Identification of Brominated Indole Biosynthetic Machinery from Cyanobacteria</title>
      <link>https://escholarship.org/uc/item/6kx2k27j</link>
      <description>Halogenated indole natural products have been isolated from a variety of organisms, including plants, marine algae, marine invertebrates, and bacteria. Aquatic cyanobacteria, in particular, are rich producers of brominated indoles, but their cognate biosynthetic enzymes have only been successfully linked in a limited number of natural products, such as the eagle-killing toxin aetokthonotoxin (AETX). The biosynthetic pathway for AETX involves five enzymes, two of which were previously undescribed due to incomplete annotations as hypothetical proteins. Our recent elucidation of AETX biosynthesis established functions of the two previously unknown proteins as enzymes responsible for tryptophan halogenation (AetF) and nitrile synthesis (AetD). Given their sequence novelty, we queried metagenomic data sets for these two enzymes and identified two new cyanobacterial haloindole biosynthetic gene clusters (BGCs) from marine sediment in Moorea, French Polynesia, and soil-derived samples...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6kx2k27j</guid>
      <pubDate>Mon, 14 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Adak, Sanjoy</name>
      </author>
      <author>
        <name>Chase, Alexander B</name>
      </author>
      <author>
        <name>Skrip, Anna E</name>
      </author>
      <author>
        <name>Moore, Bradley S</name>
      </author>
      <author>
        <name>Lukowski, April L</name>
        <uri>https://orcid.org/0000-0003-4865-0910</uri>
      </author>
    </item>
    <item>
      <title>Promiscuity in Nature Extends to Central Protein Biosynthetic Machinery</title>
      <link>https://escholarship.org/uc/item/2cc4k1zt</link>
      <description>Thioesters, rather than oxo-esters, can be tolerated and processed during translation to incorporate unnatural monomers.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2cc4k1zt</guid>
      <pubDate>Mon, 14 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lukowski, April L</name>
        <uri>https://orcid.org/0000-0003-4865-0910</uri>
      </author>
    </item>
    <item>
      <title>Microbiome data management in action workshop: Atlanta, GA, USA, June 12–13, 2024</title>
      <link>https://escholarship.org/uc/item/5tz1m4qf</link>
      <description>Microbiome research is revolutionizing human and environmental health, but the value and reuse of microbiome data are significantly hampered by the limited development and adoption of data standards. While several ongoing efforts are aimed at improving microbiome data management, significant gaps still remain in terms of defining and promoting adoption of consensus standards for these datasets. The Strengthening the Organization and Reporting of Microbiome Studies (STORMS) guidelines for human microbiome research have been endorsed and successfully utilized by many research organizations, publishers, and funding agencies, and have been recognized as a consensus community standard. No equivalent effort has occurred for environmental, synthetic, and non-human host-associated microbiomes. To address this growing need within the microbiome research community, we convened the Microbiome Data Management in Action Workshop (June 12–13, 2024, in Atlanta, GA, USA), to bring together key...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5tz1m4qf</guid>
      <pubDate>Mon, 23 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kelliher, Julia M</name>
      </author>
      <author>
        <name>Aljumaah, Mashael</name>
      </author>
      <author>
        <name>Bordenstein, Sarah R</name>
      </author>
      <author>
        <name>Brister, J Rodney</name>
      </author>
      <author>
        <name>Chain, Patrick SG</name>
      </author>
      <author>
        <name>Dundore-Arias, Jose Pablo</name>
      </author>
      <author>
        <name>Emerson, Joanne B</name>
        <uri>https://orcid.org/0000-0001-9983-5566</uri>
      </author>
      <author>
        <name>Fernandes, Vanessa Moreira C</name>
      </author>
      <author>
        <name>Flores, Roberto</name>
      </author>
      <author>
        <name>Gonzalez, Antonio</name>
      </author>
      <author>
        <name>Hansen, Zoe A</name>
      </author>
      <author>
        <name>Hatcher, Eneida L</name>
      </author>
      <author>
        <name>Jackson, Scott A</name>
      </author>
      <author>
        <name>Kellogg, Christina A</name>
      </author>
      <author>
        <name>Madupu, Ramana</name>
      </author>
      <author>
        <name>Miller, Cassandra Maria Luz</name>
      </author>
      <author>
        <name>Mirzayi, Chloe</name>
      </author>
      <author>
        <name>Moustafa, Ahmed M</name>
      </author>
      <author>
        <name>Mungall, Christopher</name>
      </author>
      <author>
        <name>Oliver, Aaron</name>
        <uri>https://orcid.org/0000-0002-0410-8284</uri>
      </author>
      <author>
        <name>Pariente, Nonia</name>
      </author>
      <author>
        <name>Pett-Ridge, Jennifer</name>
      </author>
      <author>
        <name>Record, Sydne</name>
      </author>
      <author>
        <name>Reji, Linta</name>
      </author>
      <author>
        <name>Reysenbach, Anna-Louise</name>
      </author>
      <author>
        <name>Rich, Virginia I</name>
      </author>
      <author>
        <name>Richardson, Lorna</name>
      </author>
      <author>
        <name>Schriml, Lynn M</name>
      </author>
      <author>
        <name>Shabman, Reed S</name>
      </author>
      <author>
        <name>Sierra, Maria A</name>
      </author>
      <author>
        <name>Sullivan, Matthew B</name>
      </author>
      <author>
        <name>Sundaramurthy, Punithavathi</name>
      </author>
      <author>
        <name>Thibault, Katherine M</name>
      </author>
      <author>
        <name>Thompson, Luke R</name>
      </author>
      <author>
        <name>Tighe, Scott</name>
      </author>
      <author>
        <name>Vereen, Ethell</name>
      </author>
      <author>
        <name>Eloe-Fadrosh, Emiley A</name>
        <uri>https://orcid.org/0000-0002-8162-1276</uri>
      </author>
    </item>
    <item>
      <title>From Tryptophan to Toxin: Nature’s Convergent Biosynthetic Strategy to Aetokthonotoxin</title>
      <link>https://escholarship.org/uc/item/9kw4z90p</link>
      <description>Aetokthonotoxin (AETX) is a cyanobacterial neurotoxin that causes vacuolar myelinopathy, a neurological disease that is particularly deadly to bald eagles in the United States. The recently characterized AETX is structurally unique among cyanotoxins and is composed of a pentabrominated biindole nitrile. Herein we report the discovery of an efficient, five-enzyme biosynthetic pathway that the freshwater cyanobacterium &lt;i&gt;Aetokthonos hydrillicola&lt;/i&gt; uses to convert two molecules of tryptophan to AETX. We demonstrate that the biosynthetic pathway follows a convergent route in which two functionalized indole monomers are assembled and then reunited by biaryl coupling catalyzed by the cytochrome P450 AetB. Our results revealed enzymes with novel biochemical functions, including the single-component flavin-dependent tryptophan halogenase AetF and the iron-dependent nitrile synthase AetD.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9kw4z90p</guid>
      <pubDate>Thu, 22 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Adak, Sanjoy</name>
      </author>
      <author>
        <name>Lukowski, April L</name>
        <uri>https://orcid.org/0000-0003-4865-0910</uri>
      </author>
      <author>
        <name>Schäfer, Rebecca JB</name>
      </author>
      <author>
        <name>Moore, Bradley S</name>
      </author>
    </item>
    <item>
      <title>A modular plasmid toolkit applied in marine bacteria reveals functional insights during bacteria-stimulated metamorphosis</title>
      <link>https://escholarship.org/uc/item/8qp1z8mk</link>
      <description>A conspicuous roadblock to studying marine bacteria for fundamental research and biotechnology is a lack of modular synthetic biology tools for their genetic manipulation. Here, we applied, and generated new parts for, a modular plasmid toolkit to study marine bacteria in the context of symbioses and host-microbe interactions. To demonstrate the utility of this plasmid system, we genetically manipulated the marine bacterium &lt;i&gt;Pseudoalteromonas luteoviolacea&lt;/i&gt;, which stimulates the metamorphosis of the model tubeworm, &lt;i&gt;Hydroides elegans&lt;/i&gt;. Using these tools, we quantified constitutive and native promoter expression, developed reporter strains that enable the imaging of host-bacteria interactions, and used CRISPR interference (CRISPRi) to knock down a secondary metabolite and a host-associated gene. We demonstrate the broader utility of this modular system for testing the genetic tractability of marine bacteria that are known to be associated with diverse host-microbe symbioses....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8qp1z8mk</guid>
      <pubDate>Thu, 22 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Alker, Amanda T</name>
      </author>
      <author>
        <name>Farrell, Morgan V</name>
      </author>
      <author>
        <name>Aspiras, Alpher E</name>
      </author>
      <author>
        <name>Dunbar, Tiffany L</name>
      </author>
      <author>
        <name>Fedoriouk, Andriy</name>
      </author>
      <author>
        <name>Jones, Jeffrey E</name>
      </author>
      <author>
        <name>Mikhail, Sama R</name>
      </author>
      <author>
        <name>Salcedo, Gabriella Y</name>
      </author>
      <author>
        <name>Moore, Bradley S</name>
      </author>
      <author>
        <name>Shikuma, Nicholas J</name>
      </author>
    </item>
    <item>
      <title>Chromosome-Level Genome Assembly and Annotation of Corallium rubrum: A Mediterranean Coral Threatened by Overharvesting and Climate Change</title>
      <link>https://escholarship.org/uc/item/73d22793</link>
      <description>Reference genomes are key resources in biodiversity conservation. Yet, sequencing efforts are not evenly distributed across the tree of life raising concerns over our ability to enlighten conservation with genomic data. Good-quality reference genomes remain scarce in octocorals while these species are highly relevant targets for conservation. Here, we present the first annotated reference genome in the red coral, Corallium rubrum (Linnaeus, 1758), a habitat-forming octocoral from the Mediterranean and neighboring Atlantic, impacted by overharvesting and anthropogenic warming-induced mass mortality events. Combining long reads from Oxford Nanopore Technologies (ONT), Illumina paired-end reads for improving the base accuracy of the ONT-based genome assembly, and Arima Hi-C contact data to place the sequences into chromosomes, we assembled a genome of 532 Mb (20 chromosomes, 309 scaffolds) with contig and scaffold N50 of 1.6 and 18.5 Mb, respectively. Fifty percent of the sequence...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/73d22793</guid>
      <pubDate>Thu, 22 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Ledoux, Jean-Baptiste</name>
      </author>
      <author>
        <name>Gomez-Garrido, Jessica</name>
      </author>
      <author>
        <name>Cruz, Fernando</name>
      </author>
      <author>
        <name>Ferreira, Francisco Camara</name>
      </author>
      <author>
        <name>Matos, Ana</name>
      </author>
      <author>
        <name>Sarropoulou, Xenia</name>
      </author>
      <author>
        <name>Ramirez-Calero, Sandra</name>
      </author>
      <author>
        <name>Aurelle, Didier</name>
      </author>
      <author>
        <name>Lopez-Sendino, Paula</name>
      </author>
      <author>
        <name>Grayson, Natalie E</name>
      </author>
      <author>
        <name>Moore, Bradley S</name>
      </author>
      <author>
        <name>Antunes, Agostinho</name>
      </author>
      <author>
        <name>Aguilera, Laura</name>
      </author>
      <author>
        <name>Gut, Marta</name>
      </author>
      <author>
        <name>Salces-Ortiz, Judit</name>
      </author>
      <author>
        <name>Fernández, Rosa</name>
      </author>
      <author>
        <name>Linares, Cristina</name>
      </author>
      <author>
        <name>Garrabou, Joaquim</name>
      </author>
      <author>
        <name>Alioto, Tyler</name>
      </author>
    </item>
    <item>
      <title>Harnessing ortho-Quinone Methides in Natural Product Biosynthesis and Biocatalysis</title>
      <link>https://escholarship.org/uc/item/6q92q256</link>
      <description>The implementation of &lt;i&gt;ortho&lt;/i&gt;-quinone methide (&lt;i&gt;o&lt;/i&gt;-QM) intermediates in complex molecule assembly represents a remarkably efficient strategy designed by Nature and utilized by synthetic chemists. &lt;i&gt;o&lt;/i&gt;-QMs have been taken advantage of in biomimetic syntheses for decades, yet relatively few examples of &lt;i&gt;o-&lt;/i&gt;QM-generating enzymes in natural product biosynthetic pathways have been reported. The biosynthetic enzymes that have been discovered thus far exhibit tremendous potential for biocatalytic applications, enabling the selective production of desirable compounds that are otherwise intractable or inherently difficult to achieve by traditional synthetic methods. Characterization of this biosynthetic machinery has the potential to shine a light on new enzymes capable of similar chemistry on diverse substrates, thus expanding our knowledge of Nature's catalytic repertoire. The presently known &lt;i&gt;o&lt;/i&gt;-QM-generating enzymes include flavin-dependent oxidases, hetero-Diels-Alderases,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6q92q256</guid>
      <pubDate>Thu, 22 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Purdy, Trevor N</name>
      </author>
      <author>
        <name>Moore, Bradley S</name>
      </author>
      <author>
        <name>Lukowski, April L</name>
        <uri>https://orcid.org/0000-0003-4865-0910</uri>
      </author>
    </item>
    <item>
      <title>Single-Enzyme Conversion of Tryptophan to Skatole and Cyanide Expands the Mechanistic Competence of Diiron Oxidases</title>
      <link>https://escholarship.org/uc/item/64n754hb</link>
      <description>Skatole is a pungent heterocyclic compound derived from the essential amino acid l-tryptophan by bacteria in the mammalian digestive tract. The four-step anaerobic conversion of tryptophan to skatole is well-established; though, to date, no aerobic counterpart has been reported. Herein, we report the discovery of the oxygen-dependent skatole synthase SktA that single-handedly converts 5-bromo-l-tryptophan to 5-bromoskatole, obviating the need for a multienzyme process. SktA is part of a three-gene biosynthetic gene cluster (BGC) in the cyanobacterium &lt;i&gt;Nostoc punctiforme&lt;/i&gt; NIES-2108 and functions as a nonheme diiron enzyme belonging to the heme oxygenase-like domain-containing oxidase (HDO) superfamily. Our detailed biochemical analyses revealed cyanide and bicarbonate as biosynthetic coproducts, while stopped-flow experiments showed the hallmark formation of a substrate-triggered peroxo Fe&lt;sub&gt;2&lt;/sub&gt;(III) intermediate. Overall, this work unravels an alternative pathway for...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/64n754hb</guid>
      <pubDate>Thu, 22 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Adak, Sanjoy</name>
      </author>
      <author>
        <name>Calderone, Logan A</name>
      </author>
      <author>
        <name>Krueger, August</name>
      </author>
      <author>
        <name>Pandelia, Maria-Eirini</name>
      </author>
      <author>
        <name>Moore, Bradley S</name>
      </author>
    </item>
    <item>
      <title>A biosynthetic pathway to aromatic amines that uses glycyl-tRNA as nitrogen donor</title>
      <link>https://escholarship.org/uc/item/5v01x3kg</link>
      <description>Aromatic amines in nature are typically installed with Glu or Gln as the nitrogen donor. Here we report a pathway that features glycyl-tRNA instead. During the biosynthesis of pyrroloiminoquinone-type natural products such as ammosamides, peptide-aminoacyl tRNA ligases append amino acids to the C-terminus of a ribosomally synthesized peptide. First, AmmBCTrp$${\mathrm{Amm}}{{{\mathrm{B}}}}_{{{\mathrm{C}}}}^{{{{\mathrm{Trp}}}}}$$ adds Trp in a Trp-tRNA-dependent reaction and the flavoprotein AmmC1 then carries out three hydroxylations of the indole ring of Trp. After oxidation to the corresponding ortho-hydroxy para-quinone, AmmBDGly$${\mathrm{Amm}}{{{\mathrm{B}}}}_{{{\mathrm{D}}}}^{{{{\mathrm{Gly}}}}}$$ attaches Gly to the indole ring in a Gly-tRNA dependent fashion. Subsequent decarboxylation and hydrolysis results in an amino-substituted indole. Similar transformations are catalysed by orthologous enzymes from Bacillus halodurans. This pathway features three previously unknown...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5v01x3kg</guid>
      <pubDate>Thu, 22 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Daniels, Page N</name>
      </author>
      <author>
        <name>Lee, Hyunji</name>
      </author>
      <author>
        <name>Splain, Rebecca A</name>
      </author>
      <author>
        <name>Ting, Chi P</name>
      </author>
      <author>
        <name>Zhu, Lingyang</name>
      </author>
      <author>
        <name>Zhao, Xiling</name>
      </author>
      <author>
        <name>Moore, Bradley S</name>
      </author>
      <author>
        <name>van der Donk, Wilfred A</name>
      </author>
    </item>
    <item>
      <title>Identification of Isonitrile‐Containing Natural Products in Complex Biological Matrices through Ligation with Chlorooximes</title>
      <link>https://escholarship.org/uc/item/54r195h3</link>
      <description>Isonitrile-containing natural products have garnered attention for their manifold bioactivities but are difficult to detect and isolate due to the chemical lability of the isonitrile functional group. Here, we used the isonitrile-chlorooxime ligation (INC) in a reactivity-based screening (RBS) protocol for the detection and isolation of alkaloid and terpene isonitriles in the cyanobacterium Fischerella ambigua and a marine sponge of the order Bubarida, respectively. A trifunctional probe bearing a chlorooxime moiety, a UV active aromatic moiety, and a bromine label facilitated the chemoselective reaction with isonitriles, UV-Vis spectroscopic detection, and mass spectrometric analysis. The INC-based RBS allowed for the detection, isolation, and structural elucidation of isonitriles in microgram quantities.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/54r195h3</guid>
      <pubDate>Thu, 22 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Schäfer, Rebecca JB</name>
      </author>
      <author>
        <name>Wilson, Kayla</name>
      </author>
      <author>
        <name>Biedermann, Maurice</name>
      </author>
      <author>
        <name>Moore, Bradley S</name>
      </author>
      <author>
        <name>Sieber, Simon</name>
      </author>
      <author>
        <name>Wennemers, Helma</name>
      </author>
    </item>
    <item>
      <title>Linking bacterial tetrabromopyrrole biosynthesis to coral metamorphosis</title>
      <link>https://escholarship.org/uc/item/4mn9v582</link>
      <description>An important factor dictating coral fitness is the quality of bacteria associated with corals and coral reefs. One way that bacteria benefit corals is by stimulating the larval to juvenile life cycle transition of settlement and metamorphosis. Tetrabromopyrrole (TBP) is a small molecule produced by bacteria that stimulates metamorphosis with and without attachment in a range of coral species. A standing debate remains, however, about whether TBP biosynthesis from live Pseudoalteromonas bacteria is the primary stimulant of coral metamorphosis. In this study, we create a Pseudoalteromonas sp. PS5 mutant lacking the TBP brominase gene, bmp2. Using this mutant, we confirm that the bmp2 gene is critical for TBP biosynthesis in Pseudoalteromonas sp. PS5. Mutation of this gene ablates the bacterium's ability in live cultures to stimulate the metamorphosis of the stony coral Porites astreoides. We further demonstrate that expression of TBP biosynthesis genes is strongest in stationary...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4mn9v582</guid>
      <pubDate>Thu, 22 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Alker, Amanda T</name>
      </author>
      <author>
        <name>Farrell, Morgan V</name>
      </author>
      <author>
        <name>Demko, Alyssa M</name>
      </author>
      <author>
        <name>Purdy, Trevor N</name>
      </author>
      <author>
        <name>Adak, Sanjoy</name>
      </author>
      <author>
        <name>Moore, Bradley S</name>
      </author>
      <author>
        <name>Sneed, Jennifer M</name>
      </author>
      <author>
        <name>Paul, Valerie J</name>
      </author>
      <author>
        <name>Shikuma, Nicholas J</name>
      </author>
    </item>
    <item>
      <title>Methods for the discovery and characterization of octocoral terpene cyclases</title>
      <link>https://escholarship.org/uc/item/3z70t67n</link>
      <description>Octocorals are the most prolific source of terpenoids in the marine environment, with more than 4000 different compounds known from the phylum to date. However, the biochemical and genetic origin of their production remained elusive until recent studies showed that octocorals encode genes responsible for the biosynthesis of terpenoids in their own chromosomal DNA rather than from microbial symbionts as originally proposed. The identified coral genes include those encoding a new group of class I terpene cyclases (TCs) clustered among other candidate classes of tailoring enzymes. Phylogenetic analyses established octocoral TCs as a monophyletic clade, distinct from TCs of plants, bacteria, and other organisms. The newly discovered group of TCs appears to be ubiquitous in octocorals and is evolutionarily ancient. Given the recent discovery of octocoral terpenoid biochemistry and only limited genomic data presently available, there is substantial potential for discovering new biosynthetic...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3z70t67n</guid>
      <pubDate>Thu, 22 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Burkhardt, Immo</name>
        <uri>https://orcid.org/0000-0001-9515-4042</uri>
      </author>
      <author>
        <name>Dürr, Lara</name>
      </author>
      <author>
        <name>Grayson, Natalie E</name>
      </author>
      <author>
        <name>Moore, Bradley S</name>
      </author>
    </item>
    <item>
      <title>Soil depth determines the microbial communities in Sorghum bicolor fields within a uniform regional environment</title>
      <link>https://escholarship.org/uc/item/3m74w1kn</link>
      <description>&lt;i&gt;Sorghum bicolor,&lt;/i&gt; an important global crop, adapted to thrive in hotter and drier conditions than maize or rice, has deep roots that interact with a stratified soil microbiome that plays a crucial role in plant health, growth, and carbon storage. Microbiome studies on agricultural soils, particularly fields growing &lt;i&gt;S. bicolor&lt;/i&gt;, have been mostly limited to surface soils (&amp;lt;30 cm). Here we investigated the abiotic factors of soil properties, field location, depth, and the biotic factors of sorghum type across 38 genotypes of the soil microbiome. Utilizing 16S rRNA gene amplicon sequencing, our analysis reveals significant changes in microbial composition and decreasing diversity at increasing soil depths within &lt;i&gt;S. bicolor&lt;/i&gt; fields, regardless of genotype or field, with microbial richness and diversity declining to a minimum at the 60-90 cm layer and increasing beyond the 90 cm depth. Notably, specific microbial families, such as Thermogemmatisporaceae and an unclassified...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3m74w1kn</guid>
      <pubDate>Thu, 22 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Murray, Emily R</name>
      </author>
      <author>
        <name>Minich, Jeremiah J</name>
      </author>
      <author>
        <name>Saxton, Jocelyn</name>
      </author>
      <author>
        <name>de Gracia, Marie</name>
      </author>
      <author>
        <name>Eck, Nathaniel</name>
      </author>
      <author>
        <name>Allsing, Nicholas</name>
      </author>
      <author>
        <name>Kitony, Justine</name>
      </author>
      <author>
        <name>Patel-Jhawar, Kavi</name>
      </author>
      <author>
        <name>Allen, Eric E</name>
        <uri>https://orcid.org/0000-0002-1229-8794</uri>
      </author>
      <author>
        <name>Michael, Todd P</name>
        <uri>https://orcid.org/0000-0001-6272-2875</uri>
      </author>
      <author>
        <name>Shakoor, Nadia</name>
      </author>
    </item>
    <item>
      <title>Genetic examination of the marine bacterium Pseudoalteromonas luteoviolacea and effects of its metamorphosis‐inducing factors</title>
      <link>https://escholarship.org/uc/item/10m29501</link>
      <description>Pseudoalteromonas luteoviolacea is a globally distributed marine bacterium that stimulates the metamorphosis of marine animal larvae, an important bacteria-animal interaction that can promote the recruitment of animals to benthic ecosystems. Recently, different P. luteoviolacea isolates have been shown to produce two stimulatory factors that can induce tubeworm and coral metamorphosis; Metamorphosis-Associated Contractile structures (MACs) and tetrabromopyrrole (TBP) respectively. However, it remains unclear what proportion of P. luteoviolacea isolates possess the genes encoding MACs, and what phenotypic effect MACs and TBP have on other larval species. Here, we show that 9 of 19 sequenced P. luteoviolacea genomes genetically encode both MACs and TBP. While P. luteoviolacea biofilms producing MACs stimulate the metamorphosis of the tubeworm Hydroides elegans, TBP biosynthesis genes had no effect under the conditions tested. Although MACs are lethal to larvae of the cnidarian Hydractinia...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/10m29501</guid>
      <pubDate>Thu, 22 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Alker, Amanda T</name>
      </author>
      <author>
        <name>Delherbe, Nathalie</name>
      </author>
      <author>
        <name>Purdy, Trevor N</name>
      </author>
      <author>
        <name>Moore, Bradley S</name>
      </author>
      <author>
        <name>Shikuma, Nicholas J</name>
      </author>
    </item>
    <item>
      <title>Engineering the green algae Chlamydomonas incerta for recombinant protein production</title>
      <link>https://escholarship.org/uc/item/72z4c06z</link>
      <description>Chlamydomonas incerta, a genetically close relative of the model green alga Chlamydomonas reinhardtii, shows significant potential as a host for recombinant protein expression. Because of the close genetic relationship between C. incerta and C. reinhardtii, this species offers an additional reference point for advancing our understanding of photosynthetic organisms, and also provides a potential new candidate for biotechnological applications. This study investigates C. incerta's capacity to express three recombinant proteins: the fluorescent protein mCherry, the hemicellulose-degrading enzyme xylanase, and the plastic-degrading enzyme PHL7. We have also examined the capacity to target protein expression to various cellular compartments in this alga, including the cytosol, secretory pathway, cytoplasmic membrane, and cell wall. When compared directly with C. reinhardtii, C. incerta exhibited a distinct but notable capacity for recombinant protein production. Cellular transformation...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/72z4c06z</guid>
      <pubDate>Sat, 26 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kang, Kalisa</name>
      </author>
      <author>
        <name>do Espirito Santo, Évellin</name>
      </author>
      <author>
        <name>Diaz, Crisandra Jade</name>
      </author>
      <author>
        <name>Oliver, Aaron</name>
        <uri>https://orcid.org/0000-0002-0410-8284</uri>
      </author>
      <author>
        <name>Saxton, Lisa</name>
      </author>
      <author>
        <name>May, Lauren</name>
      </author>
      <author>
        <name>Mayfield, Stephen</name>
        <uri>https://orcid.org/0000-0001-7642-9047</uri>
      </author>
      <author>
        <name>Molino, João Vitor Dutra</name>
      </author>
    </item>
    <item>
      <title>Atmospheric methane consumption in arid ecosystems acts as a reverse chimney and is accelerated by plant-methanotroph biomes</title>
      <link>https://escholarship.org/uc/item/438906r8</link>
      <description>Drylands cover one-third of the Earth's surface and are one of the largest terrestrial sinks for methane. Understanding the structure-function interplay between members of arid biomes can provide critical insights into mechanisms of resilience toward anthropogenic and climate-change-driven environmental stressors-water scarcity, heatwaves, and increased atmospheric greenhouse gases. This study integrates in situ measurements with culture-independent and enrichment-based investigations of methane-consuming microbiomes inhabiting soil in the Anza-Borrego Desert, a model arid ecosystem in Southern California, United States. The atmospheric methane consumption ranged between 2.26 and 12.73&amp;nbsp;μmol&amp;nbsp;m2&amp;nbsp;h-1, peaking during the daytime at vegetated sites. Metagenomic studies revealed similar soil-microbiome compositions at vegetated and unvegetated sites, with Methylocaldum being the major methanotrophic clade. Eighty-four metagenome-assembled genomes were recovered, six represented...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/438906r8</guid>
      <pubDate>Mon, 14 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Delherbe, Nathalie A</name>
      </author>
      <author>
        <name>Gomez, Oscar</name>
      </author>
      <author>
        <name>Plominsky, Alvaro M</name>
      </author>
      <author>
        <name>Oliver, Aaron</name>
        <uri>https://orcid.org/0000-0002-0410-8284</uri>
      </author>
      <author>
        <name>Manzanera, Maximino</name>
      </author>
      <author>
        <name>Kalyuzhnaya, Marina G</name>
      </author>
    </item>
    <item>
      <title>Isolation and Biosynthesis of Hyellamide, a Glycosylated N‑Acyltyrosine Derivative, from the Cyanobacterium Hyella patelloides LEGE 07179</title>
      <link>https://escholarship.org/uc/item/75r2h2ww</link>
      <description>Recent analyses of genome data indicate that members of the cyanobacterial order Pleurocapsales show tremendous potential for natural product discovery. However, only a few compounds have been reported from this order. Here, we report the isolation of hyellamide (&lt;b&gt;1&lt;/b&gt;), a glycosylated N-acyl tyrosine-derived eneamide, from the pleurocapsalean cyanobacterium &lt;i&gt;Hyella patelloides&lt;/i&gt; LEGE 07179. The putative biosynthetic gene cluster for &lt;b&gt;1&lt;/b&gt; was identified in the genome of the producing organism and a biosynthetic proposal is presented. This work sheds light on the chemistry of the Pleurocapsales and expands the chemical repertoire of cyanobacterial natural products to include N-acyl tyrosine-derived molecules.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/75r2h2ww</guid>
      <pubDate>Sat, 12 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Brito, Ângela</name>
      </author>
      <author>
        <name>Martins, Teresa</name>
      </author>
      <author>
        <name>Freitas, Sara</name>
      </author>
      <author>
        <name>Branco, Raquel Castelo</name>
      </author>
      <author>
        <name>Rego, Adriana</name>
      </author>
      <author>
        <name>Vasconcelos, Vitor M</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
        <uri>https://orcid.org/0000-0003-1403-4458</uri>
      </author>
      <author>
        <name>Tamagnini, Paula</name>
      </author>
      <author>
        <name>Leão, Pedro N</name>
      </author>
    </item>
    <item>
      <title>Activation of Cytosolic Cathepsin B Activity in the Brain by Traumatic Brain Injury and Inhibition by the Neutral pH Selective Inhibitor Probe Z‑Arg-Lys-AOMK</title>
      <link>https://escholarship.org/uc/item/39x597n8</link>
      <description>Cathepsin B has been shown to contribute to deficits in traumatic brain injury (TBI), an important risk factor for Alzheimer's disease (AD). Cathepsin B is elevated in TBI and AD patients, as well as in animal models of these conditions. Knockout of the cathepsin B gene results in amelioration of TBI-induced motor dysfunction and improvement of AD memory deficit in mice. The mechanism of cathepsin B pathogenesis in these brain disorders has been hypothesized to involve its translocation to the cytosol from its normal lysosomal location. This study, therefore, evaluated brain cytosolic cathepsin B activity in the controlled cortical impact (CCI) mouse model of TBI. CCI-TBI resulted in motor deficits demonstrated by the rotarod assay, brain tissue lesions, and disorganization of the hippocampus. Significantly, CCI-TBI increased cytosolic cathepsin B activity in the brain cortex in the ipsilateral brain hemisphere that received the CCI-TBI injury, with a concomitant decrease in the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/39x597n8</guid>
      <pubDate>Sat, 12 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Podvin, Sonia</name>
      </author>
      <author>
        <name>Florio, Jazmin</name>
      </author>
      <author>
        <name>Spencer, Brian</name>
      </author>
      <author>
        <name>Mante, Michael</name>
      </author>
      <author>
        <name>Guzman, Estefani</name>
      </author>
      <author>
        <name>Arias, Carlos</name>
      </author>
      <author>
        <name>Mosier, Charles</name>
      </author>
      <author>
        <name>Phan, Von V</name>
      </author>
      <author>
        <name>Yoon, Michael C</name>
        <uri>https://orcid.org/0000-0002-2900-5257</uri>
      </author>
      <author>
        <name>Almaliti, Jehad</name>
      </author>
      <author>
        <name>O’Donoghue, Anthony J</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
        <uri>https://orcid.org/0000-0003-1403-4458</uri>
      </author>
      <author>
        <name>Rissman, Robert A</name>
      </author>
      <author>
        <name>Hook, Vivian</name>
      </author>
    </item>
    <item>
      <title>Structure Elucidation, Biosynthetic Gene Cluster Distribution, and Biological Activities of Ketomemicin Analogs in Salinispora</title>
      <link>https://escholarship.org/uc/item/2198z0n3</link>
      <description>Pseudopeptides are attractive agents for protease inhibition due to their structural similarities to the natural substrates of these enzymes, as well as their enhanced stability and resistance to enzymatic degradation. We report three new ketomemicin pseudopeptides (&lt;b&gt;1&lt;/b&gt;-&lt;b&gt;3&lt;/b&gt;) from extracts of the marine actinomycete &lt;i&gt;Salinispora pacifica&lt;/i&gt; strain CNY-498. Their constitution and relative configuration were elucidated using NMR, mass spectrometry, and quantum chemical calculations. Using GNPS molecular networking and publicly available &lt;i&gt;Salinispora&lt;/i&gt; LCMS datasets, five additional ketomemicin analogs (&lt;b&gt;4&lt;/b&gt;-&lt;b&gt;8&lt;/b&gt;) were identified with ketomemicin production detected broadly across &lt;i&gt;Salinispora&lt;/i&gt; species. The ketomemicin biosynthetic gene cluster (&lt;i&gt;ktm&lt;/i&gt;) is highly conserved in &lt;i&gt;Salinispora&lt;/i&gt;, occurring in 79 of 118 public genome sequences, including eight of the nine named species. Outside &lt;i&gt;Salinispora&lt;/i&gt;, &lt;i&gt;ktm&lt;/i&gt; homologs were detected in...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2198z0n3</guid>
      <pubDate>Fri, 11 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Castro-Falcón, Gabriel</name>
      </author>
      <author>
        <name>Guillén-Matus, Dulce G</name>
      </author>
      <author>
        <name>Da Silva, Elany Barbosa</name>
      </author>
      <author>
        <name>Guo, Wentao</name>
      </author>
      <author>
        <name>Ross, Alicia</name>
      </author>
      <author>
        <name>Serafim, Mateus Sá Magalhães</name>
      </author>
      <author>
        <name>Fernandes, Thaís Helena Maciel</name>
      </author>
      <author>
        <name>Tantillo, Dean J</name>
        <uri>https://orcid.org/0000-0002-2992-8844</uri>
      </author>
      <author>
        <name>O’Donoghue, Anthony J</name>
      </author>
      <author>
        <name>Jensen, Paul R</name>
      </author>
    </item>
    <item>
      <title>Synthesis and Performance of l‑Tryptophanamide and (S)‑1-(Naphthalen-2′-yl)ethanamine-Based Marfey-Type Derivatives for Amino Acid Configurational Analysis: Diastereomeric Resolutions Directed by π–Cation Bonding</title>
      <link>https://escholarship.org/uc/item/32x6223r</link>
      <description>The configurational analysis of amino acids (AAs) in natural product peptides, often containing nonproteinogenic AAs, is mostly carried out by the venerable Marfey's method using a chiral derivatizing agent (CDA) 1-fluoro-2,4-dinitrophenyl-5-l-alaninamide (l-FDAA)─Marfey's reagent─which undergoes &lt;i&gt;S&lt;/i&gt;&lt;sub&gt;N&lt;/sub&gt;Ar reaction of the 1° amino group. The resulting AA-DAA derivatives are mostly well-separated by reversed-phase HPLC, but some DAA derivatives resist resolution. Here, we report the synthesis and characterization of two CDAs: l-FDTA (&lt;b&gt;4&lt;/b&gt;) in which the l-alanine-derived auxiliary is replaced by l-tryptophanamide and (&lt;i&gt;S&lt;/i&gt;)-FDNE (&lt;b&gt;3&lt;/b&gt;) where the auxiliary is &lt;i&gt;S&lt;/i&gt;-(6-methoxynaphth-2-yl)-1-ethylamine. Side-by-side comparisons of the two reagents were carried out by AA derivatization and reversed-phase HPLC analysis with variables such as organic solvent, additives, and the ionic strength of the mobile phase. l-DTA derivatives of l- and d-AAs were found...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/32x6223r</guid>
      <pubDate>Wed, 2 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Salib, Mariam N</name>
      </author>
      <author>
        <name>Molinski, Tadeusz F</name>
        <uri>https://orcid.org/0000-0003-1935-2535</uri>
      </author>
    </item>
    <item>
      <title>Objectively measured moderate-to-vigorous physical activity does not attenuate prospective weight gain among african-origin adults spanning the epidemiological transition</title>
      <link>https://escholarship.org/uc/item/1qh03794</link>
      <description>Traditional obesity-related public health messaging often includes physical activity (PA) recommendations. However, at the population level, the data are conflicting, especially when comparing different self-reported vs. measured techniques across different settings and populations. We measured the association between moderate-to-vigorous intensity PA (MVPA) and prospective weight change across five African-origin populations and the extent to which MVPA attenuated weight change over time. At baseline, 2,500 adults (median age: 37y) were recruited into the Modelling the Epidemiologic Transition Study (METS), from Ghana, South Africa, Jamaica, Seychelles, and US. 2000 participants were followed up 8 years later, with 851 participants having complete 7-day accelerometry to measure MVPA at both time points. Generalised estimating equations were used to explore the longitudinal association between weight and MVPA adjusted for several confounders. The obesity prevalence at baseline...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1qh03794</guid>
      <pubDate>Wed, 2 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Davies, Jessica C</name>
      </author>
      <author>
        <name>Choo-Kang, Candice</name>
      </author>
      <author>
        <name>Soepnel, Larske</name>
      </author>
      <author>
        <name>Geffen, Hayli</name>
      </author>
      <author>
        <name>Africa, Chad</name>
      </author>
      <author>
        <name>Mtintsilana, Asanda</name>
      </author>
      <author>
        <name>Bovet, Pascal</name>
      </author>
      <author>
        <name>Viswanathan, Bharathi</name>
      </author>
      <author>
        <name>Bedu-Addo, Kweku</name>
      </author>
      <author>
        <name>Plange-Rhule, Jacob</name>
      </author>
      <author>
        <name>Boateng, Prince Oti</name>
      </author>
      <author>
        <name>Apusiga, Kingsley</name>
      </author>
      <author>
        <name>Dei, Oscar Akunor</name>
      </author>
      <author>
        <name>Forrester, Terrence E</name>
      </author>
      <author>
        <name>Williams, Marie</name>
      </author>
      <author>
        <name>Lambert, Estelle V</name>
      </author>
      <author>
        <name>Rae, Dale E</name>
      </author>
      <author>
        <name>Sinyanya, Nandipha</name>
      </author>
      <author>
        <name>Layden, Brian T</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
      <author>
        <name>Ecklu-Mensah, Gertrude</name>
      </author>
      <author>
        <name>Joyce, Cara</name>
      </author>
      <author>
        <name>Luke, Amy</name>
      </author>
      <author>
        <name>Dugas, Lara R</name>
      </author>
    </item>
    <item>
      <title>Fatuamide A, a Hybrid PKS/NRPS Metallophore from a Leptolyngbya sp. Marine Cyanobacterium Collected in American Samoa</title>
      <link>https://escholarship.org/uc/item/0bb8k7kn</link>
      <description>A structurally novel metabolite, fatuamide A (&lt;b&gt;1&lt;/b&gt;), was discovered from a laboratory cultured strain of the marine cyanobacterium &lt;i&gt;Leptolyngbya&lt;/i&gt; sp., collected from Faga'itua Bay, American Samoa. A bioassay-guided approach using NCI-H460 human lung cancer cells directed the isolation of fatuamide A, which was obtained from the most cytotoxic fraction. The planar structure of fatuamide A was elucidated by integrated NMR and MS/MS analysis, and a combination of bioinformatic and computational approaches was used to deduce the absolute configuration at its eight stereocenters. A putative hybrid PKS/NRPS biosynthetic gene cluster responsible for fatuamide A production was identified from the sequenced genomic DNA of the cultured cyanobacterium. The biosynthetic gene cluster possessed elements that suggested fatuamide A binds metals, and this metallophore property was demonstrated by native metabolomics and indicated a preference for binding copper. The producing strain was...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0bb8k7kn</guid>
      <pubDate>Tue, 1 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Alexander, Kelsey L</name>
      </author>
      <author>
        <name>Naman, C Benjamin</name>
      </author>
      <author>
        <name>Iwasaki, Arihiro</name>
      </author>
      <author>
        <name>Mangoni, Alfonso</name>
      </author>
      <author>
        <name>Leao, Tiago</name>
      </author>
      <author>
        <name>Reher, Raphael</name>
      </author>
      <author>
        <name>Petras, Daniel</name>
      </author>
      <author>
        <name>Kim, Hyunwoo</name>
      </author>
      <author>
        <name>Ternon, Eva</name>
      </author>
      <author>
        <name>Caro-Diaz, Eduardo JE</name>
      </author>
      <author>
        <name>Glukhov, Evgenia</name>
      </author>
      <author>
        <name>Mitrevska, Jana A</name>
      </author>
      <author>
        <name>Avalon, Nicole E</name>
      </author>
      <author>
        <name>Duggan, Brendan M</name>
        <uri>https://orcid.org/0000-0002-7034-8374</uri>
      </author>
      <author>
        <name>Gerwick, Lena</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
        <uri>https://orcid.org/0000-0003-1403-4458</uri>
      </author>
    </item>
    <item>
      <title>Petrosamine Revisited. Experimental and Computational Investigation of Solvatochromism, Tautomerism and Free Energy Landscapes of a Pyridoacridinium Quaternary Salt</title>
      <link>https://escholarship.org/uc/item/9g39392r</link>
      <description>Petrosamine (&lt;b&gt;1&lt;/b&gt;)-a colored pyridoacridine alkaloid from the Belizean sponge, &lt;i&gt;Petrosia&lt;/i&gt; sp., that is also a potent inhibitor of acetylcholine esterase (AChE)-was investigated by spectroscopic and computational methods. Analysis of the petrosamine-free energy landscapes, p&lt;i&gt;K&lt;/i&gt;&lt;sub&gt;a&lt;/sub&gt; and tautomerism, revealed an accurate electronic depiction of the molecular structure of &lt;b&gt;1&lt;/b&gt; as the di-keto form, with a net charge of &lt;i&gt;q&lt;/i&gt; = +1, rather than a dication (&lt;i&gt;q&lt;/i&gt; = +2) under ambient conditions of isolation-purification. The pronounced solvatochromism (UV-vis) reported for &lt;b&gt;1&lt;/b&gt;, and related analogs were investigated in detail and is best explained by charge delocalization and stabilization of the ground state (HOMO) of &lt;b&gt;1&lt;/b&gt; rather than an equilibrium of competing tautomers. Refinement of the molecular structure &lt;b&gt;1&lt;/b&gt; by QM methods complements published computational docking studies to define the contact points in the enzyme active site that may...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9g39392r</guid>
      <pubDate>Tue, 18 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Gartshore, Christopher J</name>
      </author>
      <author>
        <name>Wang, Xiao</name>
      </author>
      <author>
        <name>Su, Yongxuan</name>
      </author>
      <author>
        <name>Molinski, Tadeusz F</name>
        <uri>https://orcid.org/0000-0003-1935-2535</uri>
      </author>
    </item>
    <item>
      <title>Chapter 18 The gut microbiome in personalized precision medicine</title>
      <link>https://escholarship.org/uc/item/4dg906ch</link>
      <description>Chapter 18 The gut microbiome in personalized precision medicine</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4dg906ch</guid>
      <pubDate>Mon, 17 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Buschmann, Mary M</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
      </author>
    </item>
    <item>
      <title>Ultra‐high resolution band‐selective HSQC for nanomole‐scale identification of chlorine‐substituted 13C in natural products drug discovery</title>
      <link>https://escholarship.org/uc/item/0f7462j4</link>
      <description>Ultra-high resolution band-selective HSQC (bsHSQC) has been employed for detection of &lt;sup&gt;35&lt;/sup&gt; Cl-&lt;sup&gt;37&lt;/sup&gt; Cl isotope shifted &lt;sup&gt;13&lt;/sup&gt; C NMR signals for assignment of regioisomerism in bromo-chloro natural products. Optimum pulse sequence and instrumental parameters for maximization of detection of the isotope shifts were explored. The chlorine isotope shifts (Δδ) were detected within crosspeaks and were shown to vary with hybridization of &lt;sup&gt;13&lt;/sup&gt; C, substitution of &lt;sup&gt;13&lt;/sup&gt; C, presence of β-chloro substituents, and their relative configuration. Deconvolution of Cl-substituted CH bsHSQC crosspeaks may provide other useful information, including a potentially MS-independent method for quantitating &lt;sup&gt;37&lt;/sup&gt; Cl/&lt;sup&gt;35&lt;/sup&gt; C isotopic fractionation during the biosynthesis of halogenated natural products. Copyright © 2016 John Wiley &amp;amp; Sons, Ltd.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0f7462j4</guid>
      <pubDate>Fri, 14 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Wang, Xiao</name>
      </author>
      <author>
        <name>Duggan, Brendan M</name>
        <uri>https://orcid.org/0000-0002-7034-8374</uri>
      </author>
      <author>
        <name>Molinski, Tadeusz F</name>
        <uri>https://orcid.org/0000-0003-1935-2535</uri>
      </author>
    </item>
    <item>
      <title>Perspective: Current Scientific Evidence and Research Strategies in the Role of Almonds in Cardiometabolic Health</title>
      <link>https://escholarship.org/uc/item/8t83c79f</link>
      <description>Almonds are consumed by individuals around the world. Because almonds are rich in protein, unsaturated fatty acids, and fiber, a significant amount of research has been conducted on their role in affecting various cardiometabolic endpoints (body weight, blood pressure, blood cholesterol levels, and glycemic response). The most current meta-analyses on almond consumption and various health-related endpoints suggest that almond consumption does not result in weight gain and results in small reductions in LDL cholesterol and diastolic blood pressure, as well as improved glycemic responses in certain populations (i.e. Asian Indians). A number of research gaps on almond consumption and cardiometabolic health were identified that should be addressed to further understand their role in the various cardiometabolic endpoints, including the mechanisms of action interactions with the microbiome with regular consumption and their role as part of a healthy dietary pattern for both individuals...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8t83c79f</guid>
      <pubDate>Tue, 18 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Trumbo, Paula R</name>
      </author>
      <author>
        <name>Ard, Jamy</name>
      </author>
      <author>
        <name>Bellisle, France</name>
      </author>
      <author>
        <name>Drewnowski, Adam</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
      <author>
        <name>Kleinman, Ronald</name>
      </author>
      <author>
        <name>Misra, Anoop</name>
      </author>
      <author>
        <name>Sievenpiper, John</name>
      </author>
      <author>
        <name>Tahiri, Maha</name>
      </author>
      <author>
        <name>Watson, Karol E</name>
      </author>
      <author>
        <name>Hill, James</name>
      </author>
    </item>
    <item>
      <title>Giant polyketide synthase enzymes in the biosynthesis of giant marine polyether toxins</title>
      <link>https://escholarship.org/uc/item/7c36g97g</link>
      <description>&lt;i&gt;Prymnesium parvum&lt;/i&gt; are harmful haptophyte algae that cause massive environmental fish kills. Their polyketide polyether toxins, the prymnesins, are among the largest nonpolymeric compounds in nature and have biosynthetic origins that have remained enigmatic for more than 40 years. In this work, we report the "PKZILLAs," massive &lt;i&gt;P. parvum&lt;/i&gt; polyketide synthase (PKS) genes that have evaded previous detection. PKZILLA-1 and -2 encode giant protein products of 4.7 and 3.2 megadaltons that have 140 and 99 enzyme domains. Their predicted polyene product matches the proposed pre-prymnesin precursor of the 90-carbon-backbone A-type prymnesins. We further characterize the variant PKZILLA-B1, which is responsible for the shorter B-type analog prymnesin-B1, from &lt;i&gt;P. parvum&lt;/i&gt; RCC3426 and thus establish a general model of haptophyte polyether biosynthetic logic. This work expands expectations of genetic and enzymatic size limits in biology.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7c36g97g</guid>
      <pubDate>Mon, 17 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Fallon, Timothy R</name>
        <uri>https://orcid.org/0000-0002-3048-7679</uri>
      </author>
      <author>
        <name>Shende, Vikram V</name>
        <uri>https://orcid.org/0000-0001-8396-6297</uri>
      </author>
      <author>
        <name>Wierzbicki, Igor H</name>
      </author>
      <author>
        <name>Pendleton, Amanda L</name>
      </author>
      <author>
        <name>Watervoort, Nathan F</name>
      </author>
      <author>
        <name>Auber, Robert P</name>
      </author>
      <author>
        <name>Gonzalez, David J</name>
      </author>
      <author>
        <name>Wisecaver, Jennifer H</name>
      </author>
      <author>
        <name>Moore, Bradley S</name>
        <uri>https://orcid.org/0000-0002-4652-1253</uri>
      </author>
    </item>
    <item>
      <title>The Paradox of Antimalarial Terpenoid Isonitrile Biosynthesis Explained. Proposal of Cyanoformate as an NC Delivery Vector</title>
      <link>https://escholarship.org/uc/item/45q2d13k</link>
      <description>Marine sponge diterpenoid isonitriles are exceptional nitrogenous natural products that exhibit antiplasmodial activity. Their biosynthesis presents a biosynthetic puzzle: how do the elements of NC engage terpenyl carbocations in isoprenoid secondary metabolism, and what is the biosynthetic precursor of the NC group? Cyanoformic acid (NC-COOH, &lt;b&gt;B1&lt;/b&gt;) is proposed as a plausible delivery vehicle of NC that resolves a paradox in the commonly held proposition that an inorganic cyanide anion, CN&lt;sup&gt;-&lt;/sup&gt;, terminates terpenoid isonitrile (TI) biosynthesis. DFT calculations of NC-COOH and its conjugate base, cyanoformate, NC-COO&lt;sup&gt;-&lt;/sup&gt; (&lt;b&gt;B2&lt;/b&gt;), support high nucleophilicity at N and explain bond-forming constitutionality: attack at N and formation of an isonitrile over its nitrile isomer. TI biogenesis is compared to the cyanoformamide-containing ceratamines that arise from oxidation of a terminal &lt;i&gt;N&lt;/i&gt;-Gly amide precursor. A unifying model links C-NC vs C-CN bond formation...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/45q2d13k</guid>
      <pubDate>Mon, 17 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Molinski, Tadeusz F</name>
        <uri>https://orcid.org/0000-0003-1935-2535</uri>
      </author>
    </item>
    <item>
      <title>Temporal and Spatial Dynamics of Synechococcus Clade II and Other Microbes in the Eutrophic Subtropical San Diego Bay</title>
      <link>https://escholarship.org/uc/item/0qv0q1qj</link>
      <description>The diversity of the marine cyanobacterium Synechococcus can be broadly separated into clades, with clade II typically present in warm oligotrophic water, and clades I and IV found in cooler coastal water. We found amplicon sequence variants (ASVs) belonging to clade II in the nutrient-replete waters of San Diego Bay (SDB). Using the 16S rRNA gene, 18S rRNA gene and internal transcribed spacer region sequencing, we analysed multiple locations in SDB monthly for over a year, with additional samples dating back to 2015. Synechococcus community composition differed from the nearby coast into SDB in terms of dominant clade and ASVs. Specific clade II ASVs became relatively more abundant towards the back of the bay and showed seasonality, with higher relative abundance in the warm months. Select ASVs group phylogenetically and show similar seasonal and spatial distribution patterns, indicating these ASVs have adapted to SDB. Isolates matching clade II ASVs from SDB show pigment composition...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0qv0q1qj</guid>
      <pubDate>Fri, 14 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Harding, Katie J</name>
      </author>
      <author>
        <name>Nagarkar, Maitreyi</name>
      </author>
      <author>
        <name>Wang, Maggie</name>
      </author>
      <author>
        <name>Ramsing, Kailey</name>
      </author>
      <author>
        <name>Anidjar, Niv</name>
      </author>
      <author>
        <name>Giddings, Sarah</name>
      </author>
      <author>
        <name>Brahamsha, Bianca</name>
      </author>
      <author>
        <name>Palenik, Brian</name>
      </author>
    </item>
    <item>
      <title>Where do the pathogens that cause surgical site infections come from?</title>
      <link>https://escholarship.org/uc/item/3pn280cm</link>
      <description>A study from Long &lt;i&gt;et al.&lt;/i&gt; shows that many pathogens that cause surgical site infections during spine surgery come from the patient's own microbiome, suggesting a paradigm shift in the understanding of surgical site infections that questions the effectiveness of current enhanced sterility and antibiotic protocols.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3pn280cm</guid>
      <pubDate>Tue, 21 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
      <author>
        <name>Alverdy, John</name>
      </author>
    </item>
    <item>
      <title>Modulating the human gut microbiome and health markers through kombucha consumption: a controlled clinical study</title>
      <link>https://escholarship.org/uc/item/3bc9455b</link>
      <description>Fermented foods are becoming more popular due to their purported links to metabolic health and the gut microbiome. However, direct clinical evidence for the health claims is lacking. Here, we describe an eight-week clinical trial that explored the effects of a four-week kombucha supplement in healthy individuals consuming a Western diet, randomized into the kombucha (n = 16) or control (n = 8) group. We collected longitudinal stool and blood samples to profile the human microbiome and inflammation markers. We did not observe significant changes in either biochemical parameters or levels of circulating markers of inflammation across the entire cohort. However, paired analysis between baseline and end of intervention time points within kombucha or control groups revealed increases in fasting insulin and in HOMA-IR in the kombucha group whereas reductions in HDL cholesterol were associated with the control group. Shotgun metagenomic analysis revealed the relative abundance of Weizmannia,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3bc9455b</guid>
      <pubDate>Fri, 17 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Ecklu-Mensah, Gertrude</name>
      </author>
      <author>
        <name>Miller, Rachel</name>
      </author>
      <author>
        <name>Maseng, Maria Gjerstad</name>
      </author>
      <author>
        <name>Hawes, Vienna</name>
      </author>
      <author>
        <name>Hinz, Denise</name>
      </author>
      <author>
        <name>Kim, Cheryl</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
    </item>
    <item>
      <title>Biosynthesis of Haloterpenoids in Red Algae via Microbial-like Type I Terpene Synthases</title>
      <link>https://escholarship.org/uc/item/4329527s</link>
      <description>Red algae or seaweeds produce highly distinctive halogenated terpenoid compounds, including the pentabromochlorinated monoterpene halomon that was once heralded as a promising anticancer agent. The first dedicated step in the biosynthesis of these natural product molecules is expected to be catalyzed by terpene synthase (TS) enzymes. Recent work has demonstrated an emerging class of type I TSs in red algal terpene biosynthesis. However, only one such enzyme from a notoriously haloterpenoid-producing red alga (&lt;i&gt;Laurencia pacifica&lt;/i&gt;) has been functionally characterized and the product structure is not related to halogenated terpenoids. Herein, we report 10 new type I TSs from the red algae &lt;i&gt;Portieria hornemannii&lt;/i&gt;, &lt;i&gt;Plocamium pacificum&lt;/i&gt;, &lt;i&gt;L. pacifica&lt;/i&gt;, and &lt;i&gt;Laurencia subopposita&lt;/i&gt; that produce a diversity of halogenated mono- and sesquiterpenes. We used a combination of genome sequencing, terpenoid metabolomics, &lt;i&gt;in vitro&lt;/i&gt; biochemistry, and bioinformatics...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4329527s</guid>
      <pubDate>Wed, 15 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Steele, Taylor S</name>
      </author>
      <author>
        <name>Burkhardt, Immo</name>
        <uri>https://orcid.org/0000-0001-9515-4042</uri>
      </author>
      <author>
        <name>Moore, Malia L</name>
      </author>
      <author>
        <name>de Rond, Tristan</name>
      </author>
      <author>
        <name>Bone, Hannah K</name>
      </author>
      <author>
        <name>Barry, Kerrie</name>
        <uri>https://orcid.org/0000-0002-8999-6785</uri>
      </author>
      <author>
        <name>Bunting, Victoria Mae</name>
      </author>
      <author>
        <name>Grimwood, Jane</name>
      </author>
      <author>
        <name>Handley, Lori H</name>
      </author>
      <author>
        <name>Rajasekar, Shanmugam</name>
      </author>
      <author>
        <name>Talag, Jayson</name>
      </author>
      <author>
        <name>Michael, Todd P</name>
      </author>
      <author>
        <name>Moore, Bradley S</name>
        <uri>https://orcid.org/0000-0002-4652-1253</uri>
      </author>
    </item>
    <item>
      <title>MIBiG 4.0: advancing biosynthetic gene cluster curation through global collaboration</title>
      <link>https://escholarship.org/uc/item/33w736t3</link>
      <description>Specialized or secondary metabolites are small molecules of biological origin, often showing potent biological activities with applications in agriculture, engineering and medicine. Usually, the biosynthesis of these natural products is governed by sets of co-regulated and physically clustered genes known as biosynthetic gene clusters (BGCs). To share information about BGCs in a standardized and machine-readable way, the Minimum Information about a Biosynthetic Gene cluster (MIBiG) data standard and repository was initiated in 2015. Since its conception, MIBiG has been regularly updated to expand data coverage and remain up to date with innovations in natural product research. Here, we describe MIBiG version 4.0, an extensive update to the data repository and the underlying data standard. In a massive community annotation effort, 267 contributors performed 8304 edits, creating 557 new entries and modifying 590 existing entries, resulting in a new total of 3059 curated entries...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/33w736t3</guid>
      <pubDate>Wed, 15 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zdouc, Mitja M</name>
      </author>
      <author>
        <name>Blin, Kai</name>
      </author>
      <author>
        <name>Louwen, Nico LL</name>
      </author>
      <author>
        <name>Navarro, Jorge</name>
      </author>
      <author>
        <name>Loureiro, Catarina</name>
      </author>
      <author>
        <name>Bader, Chantal D</name>
      </author>
      <author>
        <name>Bailey, Constance B</name>
      </author>
      <author>
        <name>Barra, Lena</name>
      </author>
      <author>
        <name>Booth, Thomas J</name>
      </author>
      <author>
        <name>Bozhüyük, Kenan AJ</name>
      </author>
      <author>
        <name>Cediel-Becerra, José DD</name>
      </author>
      <author>
        <name>Charlop-Powers, Zachary</name>
      </author>
      <author>
        <name>Chevrette, Marc G</name>
      </author>
      <author>
        <name>Chooi, Yit Heng</name>
      </author>
      <author>
        <name>D’Agostino, Paul M</name>
      </author>
      <author>
        <name>de Rond, Tristan</name>
      </author>
      <author>
        <name>Del Pup, Elena</name>
      </author>
      <author>
        <name>Duncan, Katherine R</name>
      </author>
      <author>
        <name>Gu, Wenjia</name>
      </author>
      <author>
        <name>Hanif, Novriyandi</name>
      </author>
      <author>
        <name>Helfrich, Eric JN</name>
      </author>
      <author>
        <name>Jenner, Matthew</name>
      </author>
      <author>
        <name>Katsuyama, Yohei</name>
      </author>
      <author>
        <name>Korenskaia, Aleksandra</name>
      </author>
      <author>
        <name>Krug, Daniel</name>
      </author>
      <author>
        <name>Libis, Vincent</name>
      </author>
      <author>
        <name>Lund, George A</name>
      </author>
      <author>
        <name>Mantri, Shrikant</name>
      </author>
      <author>
        <name>Morgan, Kalindi D</name>
      </author>
      <author>
        <name>Owen, Charlotte</name>
      </author>
      <author>
        <name>Phan, Chin-Soon</name>
      </author>
      <author>
        <name>Philmus, Benjamin</name>
      </author>
      <author>
        <name>Reitz, Zachary L</name>
      </author>
      <author>
        <name>Robinson, Serina L</name>
      </author>
      <author>
        <name>Singh, Kumar Saurabh</name>
      </author>
      <author>
        <name>Teufel, Robin</name>
      </author>
      <author>
        <name>Tong, Yaojun</name>
      </author>
      <author>
        <name>Tugizimana, Fidele</name>
      </author>
      <author>
        <name>Ulanova, Dana</name>
      </author>
      <author>
        <name>Winter, Jaclyn M</name>
      </author>
      <author>
        <name>Aguilar, César</name>
      </author>
      <author>
        <name>Akiyama, Daniel Y</name>
      </author>
      <author>
        <name>Al-Salihi, Suhad AA</name>
      </author>
      <author>
        <name>Alanjary, Mohammad</name>
      </author>
      <author>
        <name>Alberti, Fabrizio</name>
      </author>
      <author>
        <name>Aleti, Gajender</name>
      </author>
      <author>
        <name>Alharthi, Shumukh A</name>
      </author>
      <author>
        <name>Rojo, Mariela Y Arias</name>
      </author>
      <author>
        <name>Arishi, Amr A</name>
      </author>
      <author>
        <name>Augustijn, Hannah E</name>
      </author>
      <author>
        <name>Avalon, Nicole E</name>
      </author>
      <author>
        <name>Avelar-Rivas, J Abraham</name>
      </author>
      <author>
        <name>Axt, Kyle K</name>
      </author>
      <author>
        <name>Barbieri, Hellen B</name>
      </author>
      <author>
        <name>Barbosa, Julio Cesar J</name>
      </author>
      <author>
        <name>Segato, Lucas Gabriel Barboza</name>
      </author>
      <author>
        <name>Barrett, Susanna E</name>
      </author>
      <author>
        <name>Baunach, Martin</name>
      </author>
      <author>
        <name>Beemelmanns, Christine</name>
      </author>
      <author>
        <name>Beqaj, Dardan</name>
      </author>
      <author>
        <name>Berger, Tim</name>
      </author>
      <author>
        <name>Bernaldo-Agüero, Jordan</name>
      </author>
      <author>
        <name>Bettenbühl, Sandra M</name>
      </author>
      <author>
        <name>Bielinski, Vincent A</name>
      </author>
      <author>
        <name>Biermann, Friederike</name>
      </author>
      <author>
        <name>Borges, Ricardo M</name>
      </author>
      <author>
        <name>Borriss, Rainer</name>
      </author>
      <author>
        <name>Breitenbach, Milena</name>
      </author>
      <author>
        <name>Bretscher, Kevin M</name>
      </author>
      <author>
        <name>Brigham, Michael W</name>
      </author>
      <author>
        <name>Buedenbender, Larissa</name>
      </author>
      <author>
        <name>Bulcock, Brodie W</name>
      </author>
      <author>
        <name>Cano-Prieto, Carolina</name>
      </author>
      <author>
        <name>Capela, João</name>
      </author>
      <author>
        <name>Carrion, Victor J</name>
      </author>
      <author>
        <name>Carter, Riley S</name>
      </author>
      <author>
        <name>Castelo-Branco, Raquel</name>
      </author>
      <author>
        <name>Castro-Falcón, Gabriel</name>
      </author>
      <author>
        <name>Chagas, Fernanda O</name>
      </author>
      <author>
        <name>Charria-Girón, Esteban</name>
      </author>
      <author>
        <name>Chaudhri, Ayesha Ahmed</name>
      </author>
      <author>
        <name>Chaudhry, Vasvi</name>
      </author>
      <author>
        <name>Choi, Hyukjae</name>
      </author>
      <author>
        <name>Choi, Yukyung</name>
      </author>
      <author>
        <name>Choupannejad, Roya</name>
      </author>
      <author>
        <name>Chromy, Jakub</name>
      </author>
      <author>
        <name>Donahey, Melinda S Chue</name>
      </author>
      <author>
        <name>Collemare, Jérôme</name>
      </author>
      <author>
        <name>Connolly, Jack A</name>
      </author>
      <author>
        <name>Creamer, Kaitlin E</name>
        <uri>https://orcid.org/0000-0002-0666-2107</uri>
      </author>
      <author>
        <name>Crüsemann, Max</name>
      </author>
      <author>
        <name>Cruz, Andres Arredondo</name>
      </author>
      <author>
        <name>Cumsille, Andres</name>
      </author>
      <author>
        <name>Dallery, Jean-Felix</name>
      </author>
      <author>
        <name>Damas-Ramos, Luis Caleb</name>
      </author>
      <author>
        <name>Damiani, Tito</name>
      </author>
      <author>
        <name>de Kruijff, Martinus</name>
      </author>
      <author>
        <name>Martín, Belén Delgado</name>
      </author>
      <author>
        <name>Della Sala, Gerardo</name>
      </author>
      <author>
        <name>Dillen, Jelle</name>
      </author>
    </item>
    <item>
      <title>Caged luciferins enable rapid multicomponent bioluminescence imaging</title>
      <link>https://escholarship.org/uc/item/6ff8w98z</link>
      <description>Bioluminescence is a sensitive technique for imaging biological features over time. Historically, though, the modality has been challenging to employ for multiplexed tracking due to a lack of resolvable luciferase-luciferin pairs. Recent years have seen the development of numerous orthogonal probes for multi-parameter imaging. While successful, generating such tools often requires complex syntheses and lengthy enzyme evolution campaigns. This work showcases an alternative strategy for multiplexed bioluminescence that takes advantage of already-orthogonal caged luciferins and established uncaging enzymes. These probes generate unique bioluminescent signals that can be distinguished via a linear unmixing algorithm. Caged luciferins enabled two- and three-component imaging on the minutes time scale. We further showed that the tools can be used in conjunction with endogenous enzymes for multiplexed studies. Collectively, this approach lowers the barrier to multicomponent bioluminescence...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6ff8w98z</guid>
      <pubDate>Sat, 4 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Navarro, Mariana X</name>
      </author>
      <author>
        <name>Brennan, Caroline K</name>
      </author>
      <author>
        <name>Love, Anna C</name>
        <uri>https://orcid.org/0000-0001-5657-2858</uri>
      </author>
      <author>
        <name>Prescher, Jennifer A</name>
        <uri>https://orcid.org/0000-0002-9250-4702</uri>
      </author>
    </item>
    <item>
      <title>Two decades of three-dimensional movement data from adult female northern elephant seals</title>
      <link>https://escholarship.org/uc/item/16n1r4g2</link>
      <description>Northern elephant seals (Mirounga angustirostris) have been integral to the development and progress of biologging technology and movement data analysis, which continue to improve our understanding of this and other species. Adult female elephant seals at Año Nuevo Reserve and other colonies along the west coast of North America were tracked annually from 2004 to 2020, resulting in a total of 653 instrument deployments. This paper outlines the compilation and curation process of these high-resolution diving and location data, now accessible in two Dryad repositories. The code used for data processing alongside the corresponding workflow is available through GitHub and Zenodo. This data set represents 3,844,927 dives and 596,815 locations collected from 475 individual seals with 178 repeat samplings over 17 years. We anticipate that these data will stimulate further analysis and investigation into elephant seal biology and aid in developing new analytical approaches for large marine...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/16n1r4g2</guid>
      <pubDate>Sat, 4 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Costa, Daniel P</name>
        <uri>https://orcid.org/0000-0002-0334-3899</uri>
      </author>
      <author>
        <name>Holser, Rachel R</name>
        <uri>https://orcid.org/0000-0002-8668-3839</uri>
      </author>
      <author>
        <name>Keates, Theresa R</name>
      </author>
      <author>
        <name>Adachi, Taiki</name>
      </author>
      <author>
        <name>Beltran, Roxanne S</name>
      </author>
      <author>
        <name>Champagne, Cory D</name>
      </author>
      <author>
        <name>Crocker, Daniel E</name>
      </author>
      <author>
        <name>Favilla, Arina B</name>
      </author>
      <author>
        <name>Fowler, Melinda A</name>
      </author>
      <author>
        <name>Gallo-Reynoso, Juan Pablo</name>
      </author>
      <author>
        <name>Goetsch, Chandra</name>
      </author>
      <author>
        <name>Hassrick, Jason L</name>
      </author>
      <author>
        <name>Hückstädt, Luis A</name>
      </author>
      <author>
        <name>Kendall-Bar, Jessica M</name>
        <uri>https://orcid.org/0000-0003-4758-1386</uri>
      </author>
      <author>
        <name>Kienle, Sarah S</name>
      </author>
      <author>
        <name>Kuhn, Carey E</name>
      </author>
      <author>
        <name>Maresh, Jennifer L</name>
      </author>
      <author>
        <name>Maxwell, Sara M</name>
      </author>
      <author>
        <name>McDonald, Birgitte I</name>
      </author>
      <author>
        <name>McHuron, Elizabeth A</name>
      </author>
      <author>
        <name>Morris, Patricia A</name>
      </author>
      <author>
        <name>Naito, Yasuhiko</name>
      </author>
      <author>
        <name>Pallin, Logan J</name>
      </author>
      <author>
        <name>Peterson, Sarah H</name>
      </author>
      <author>
        <name>Robinson, Patrick W</name>
        <uri>https://orcid.org/0000-0003-3957-8347</uri>
      </author>
      <author>
        <name>Simmons, Samantha E</name>
      </author>
      <author>
        <name>Takahashi, Akinori</name>
      </author>
      <author>
        <name>Teuschel, Nicole M</name>
      </author>
      <author>
        <name>Tift, Michael S</name>
      </author>
      <author>
        <name>Tremblay, Yann</name>
      </author>
      <author>
        <name>Villegas-Amtmann, Stella</name>
      </author>
      <author>
        <name>Yoda, Ken</name>
      </author>
    </item>
    <item>
      <title>Early patterning of ABCB, ABCC, and ABCG transporters establishes unique territories of small molecule transport in embryonic mesoderm and endoderm</title>
      <link>https://escholarship.org/uc/item/94m6j17z</link>
      <description>Directed intercellular movement of diverse small molecules, including metabolites, signal molecules and xenobiotics, is a key feature of multicellularity. Networks of small molecule transporters (SMTs), including several ATP Binding Cassette (ABC) transporters, are central to this process. While small molecule transporters are well described in differentiated organs, little is known about their patterns of expression in early embryogenesis. Here we report the pattern of ABC-type SMT expression and activity during the early development of sea urchins. Of the six major ABCs in this embryo (ABCB1, -B4, -C1, -C4, -C5 and -G2), three expression patterns were observed: 1) ABCB1 and ABCC1 are first expressed ubiquitously, and then become enriched in endoderm and ectoderm-derived structures. 2) ABCC4 and ABCC5 are restricted to a ring of mesoderm in the blastula and ABCC4 is later expressed in the coelomic pouches, the embryonic niche of the primordial germ cells. 3) ABCB4 and ABCG2 are...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/94m6j17z</guid>
      <pubDate>Fri, 3 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Schrankel, Catherine S</name>
      </author>
      <author>
        <name>Hamdoun, Amro</name>
      </author>
    </item>
    <item>
      <title>A single diiron enzyme catalyses the oxidative rearrangement of tryptophan to indole nitrile</title>
      <link>https://escholarship.org/uc/item/7pv0q496</link>
      <description>Nitriles are uncommon in nature and are typically constructed from oximes through the oxidative decarboxylation of amino acid substrates or from the derivatization of carboxylic acids. Here we report a third nitrile biosynthesis strategy featuring the cyanobacterial nitrile synthase AetD. During the biosynthesis of the eagle-killing neurotoxin, aetokthonotoxin, AetD transforms the 2-aminopropionate portion of 5,7-dibromo-l-tryptophan to a nitrile. Employing a combination of structural, biochemical and biophysical techniques, we characterized AetD as a non-haem diiron enzyme that belongs to the emerging haem-oxygenase-like dimetal oxidase superfamily. High-resolution crystal structures of AetD together with the identification of catalytically relevant products provide mechanistic insights into how AetD affords this unique transformation, which we propose proceeds via an aziridine intermediate. Our work presents a unique template for nitrile biogenesis and portrays a substrate binding...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7pv0q496</guid>
      <pubDate>Mon, 9 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Adak, Sanjoy</name>
      </author>
      <author>
        <name>Ye, Naike</name>
      </author>
      <author>
        <name>Calderone, Logan A</name>
      </author>
      <author>
        <name>Duan, Meng</name>
      </author>
      <author>
        <name>Lubeck, Wilson</name>
      </author>
      <author>
        <name>Schäfer, Rebecca JB</name>
      </author>
      <author>
        <name>Lukowski, April L</name>
        <uri>https://orcid.org/0000-0003-4865-0910</uri>
      </author>
      <author>
        <name>Houk, KN</name>
      </author>
      <author>
        <name>Pandelia, Maria-Eirini</name>
      </author>
      <author>
        <name>Drennan, Catherine L</name>
      </author>
      <author>
        <name>Moore, Bradley S</name>
        <uri>https://orcid.org/0000-0002-4652-1253</uri>
      </author>
    </item>
    <item>
      <title>Single dish gradient screening of small molecule localization</title>
      <link>https://escholarship.org/uc/item/0j89p8m3</link>
      <description>Understanding trafficking in cells and tissues is one of the most critical steps in exploring the mechanisms and modes of action (MOAs) of a small molecule. Typically, deciphering the role of concentration presents one of the most difficult challenges associated with this task. Herein, we present a practical solution to this problem by developing concentration gradients within single dishes of cells. We demonstrate the method by evaluating fluorescently-labelled probes developed from two classes of natural products that have been identified as potential anti-cancer leads by STORM super-resolution microscopy.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0j89p8m3</guid>
      <pubDate>Fri, 6 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Beuzer, Paolo</name>
      </author>
      <author>
        <name>Axelrod, Joshua</name>
      </author>
      <author>
        <name>Trzoss, Lynnie</name>
      </author>
      <author>
        <name>Fenical, Willam</name>
        <uri>https://orcid.org/0000-0002-8955-1735</uri>
      </author>
      <author>
        <name>Dasari, Ramesh</name>
      </author>
      <author>
        <name>Evidente, Antonio</name>
      </author>
      <author>
        <name>Kornienko, Alexander</name>
      </author>
      <author>
        <name>Cang, Hu</name>
      </author>
      <author>
        <name>La Clair, James J</name>
        <uri>https://orcid.org/0000-0001-6500-4107</uri>
      </author>
    </item>
    <item>
      <title>Gut and oral microbial compositional differences in women with breast cancer, women with ductal carcinoma in situ, and healthy women</title>
      <link>https://escholarship.org/uc/item/9sv9w98w</link>
      <description>This study characterized and compared the fecal and oral microbiota from women with early-stage breast cancer (BC), women with ductal carcinoma &lt;i&gt;in situ&lt;/i&gt; (DCIS), and healthy women. Fecal and oral samples were collected from newly diagnosed patients prior to any therapy and characterized using 16S rRNA sequencing. Measures of gut microbial alpha diversity were significantly lower in the BC vs healthy cohort. Beta diversity differed significantly between the BC or DCIS and healthy groups, and several differentially abundant taxa were identified. Clustering (non-negative matrix factorization) of the gut microbiota identified five bacterial guilds dominated by &lt;i&gt;Prevotella&lt;/i&gt;, Enterobacteriaceae, &lt;i&gt;Akkermansia&lt;/i&gt;, Clostridiales, or &lt;i&gt;Bacteroides&lt;/i&gt;. The &lt;i&gt;Bacteroides&lt;/i&gt; and Enterobacteriaceae guilds were significantly more abundant in the BC cohort compared to healthy controls, whereas the Clostridiales guild was more abundant in the healthy group. Finally, prediction...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9sv9w98w</guid>
      <pubDate>Thu, 5 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>McCune, Emma</name>
      </author>
      <author>
        <name>Sharma, Anukriti</name>
      </author>
      <author>
        <name>Johnson, Breanna</name>
      </author>
      <author>
        <name>O'Meara, Tess</name>
      </author>
      <author>
        <name>Theiner, Sarah</name>
      </author>
      <author>
        <name>Campos, Maribel</name>
      </author>
      <author>
        <name>Heditsian, Diane</name>
      </author>
      <author>
        <name>Brain, Susie</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
      <author>
        <name>Esserman, Laura</name>
      </author>
      <author>
        <name>Campbell, Michael J</name>
      </author>
    </item>
    <item>
      <title>Identification of hidden N4-like viruses and their interactions with hosts</title>
      <link>https://escholarship.org/uc/item/6868q7sk</link>
      <description>IMPORTANCE: The findings of this study are significant, as N4-like viruses represent a unique viral lineage with a distinct replication mechanism and a conserved core genome. This work has resulted in a comprehensive global map of the entire N4-like viral lineage, including information on their distribution in different biomes, evolutionary divergence, genomic diversity, and the potential for viral-mediated host metabolic reprogramming. As such, this work significantly contributes to our understanding of the ecological function and viral-host interactions of bacteriophages.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6868q7sk</guid>
      <pubDate>Thu, 5 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Zheng, Kaiyang</name>
      </author>
      <author>
        <name>Liang, Yantao</name>
      </author>
      <author>
        <name>Paez-Espino, David</name>
      </author>
      <author>
        <name>Zou, Xiao</name>
      </author>
      <author>
        <name>Gao, Chen</name>
      </author>
      <author>
        <name>Shao, Hongbing</name>
      </author>
      <author>
        <name>Sung, Yeong Yik</name>
      </author>
      <author>
        <name>Mok, Wen Jye</name>
      </author>
      <author>
        <name>Wong, Li Lian</name>
      </author>
      <author>
        <name>Zhang, Yu-Zhong</name>
      </author>
      <author>
        <name>Tian, Jiwei</name>
      </author>
      <author>
        <name>Chen, Feng</name>
      </author>
      <author>
        <name>Jiao, Nianzhi</name>
      </author>
      <author>
        <name>Suttle, Curtis A</name>
      </author>
      <author>
        <name>He, Jianfeng</name>
      </author>
      <author>
        <name>McMinn, Andrew</name>
      </author>
      <author>
        <name>Wang, Min</name>
      </author>
    </item>
    <item>
      <title>Microbial solutions must be deployed against climate catastrophe</title>
      <link>https://escholarship.org/uc/item/60x4b52x</link>
      <description>This paper is a call to action. By publishing concurrently across journals like an emergency bulletin, we are not merely making a plea for awareness about climate change. Instead, we are demanding immediate, tangible steps that harness the power of microbiology and the expertise of researchers and policymakers to safeguard the planet for future generations.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/60x4b52x</guid>
      <pubDate>Mon, 2 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Peixoto, Raquel</name>
      </author>
      <author>
        <name>Voolstra, Christian R</name>
      </author>
      <author>
        <name>Stein, Lisa Y</name>
      </author>
      <author>
        <name>Hugenholtz, Philip</name>
      </author>
      <author>
        <name>Salles, Joana Falcao</name>
      </author>
      <author>
        <name>Amin, Shady A</name>
      </author>
      <author>
        <name>Häggblom, Max</name>
      </author>
      <author>
        <name>Gregory, Ann</name>
      </author>
      <author>
        <name>Makhalanyane, Thulani P</name>
      </author>
      <author>
        <name>Wang, Fengping</name>
      </author>
      <author>
        <name>Agbodjato, Nadège Adoukè</name>
      </author>
      <author>
        <name>Wang, Yinzhao</name>
      </author>
      <author>
        <name>Jiao, Nianzhi</name>
      </author>
      <author>
        <name>Lennon, Jay T</name>
      </author>
      <author>
        <name>Ventosa, Antonio</name>
      </author>
      <author>
        <name>Bavoil, Patrik M</name>
      </author>
      <author>
        <name>Miller, Virginia</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
    </item>
    <item>
      <title>Microbial solutions must be deployed against climate catastrophe</title>
      <link>https://escholarship.org/uc/item/2br3t67x</link>
      <description>Injecting H2 in deep underground to store this energy carrier will produce artificial subsurface lithoautotrophic microbial ecosystems that modify the taxonomic diversity of indigenous microbial communities and their metabolic activities.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2br3t67x</guid>
      <pubDate>Mon, 2 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Peixoto, Raquel</name>
      </author>
      <author>
        <name>Voolstra, Christian R</name>
      </author>
      <author>
        <name>Stein, Lisa Y</name>
      </author>
      <author>
        <name>Hugenholtz, Philip</name>
      </author>
      <author>
        <name>Salles, Joana Falcao</name>
      </author>
      <author>
        <name>Amin, Shady A</name>
      </author>
      <author>
        <name>Häggblom, Max</name>
      </author>
      <author>
        <name>Gregory, Ann</name>
      </author>
      <author>
        <name>Makhalanyane, Thulani P</name>
      </author>
      <author>
        <name>Wang, Fengping</name>
      </author>
      <author>
        <name>Agbodjato, Nadège Adoukè</name>
      </author>
      <author>
        <name>Wang, Yinzhao</name>
      </author>
      <author>
        <name>Jiao, Nianzhi</name>
      </author>
      <author>
        <name>Lennon, Jay T</name>
      </author>
      <author>
        <name>Ventosa, Antonio</name>
      </author>
      <author>
        <name>Bavoil, Patrik M</name>
      </author>
      <author>
        <name>Miller, Virginia</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
    </item>
    <item>
      <title>Evaluating Antimalarial Proteasome Inhibitors for Efficacy in Babesia Blood Stage Cultures</title>
      <link>https://escholarship.org/uc/item/47p077j7</link>
      <description>Tick-transmitted &lt;i&gt;Babesia&lt;/i&gt; are a major global veterinary threat and an emerging risk to humans. Unlike their &lt;i&gt;Plasmodium&lt;/i&gt; relatives, these erythrocyte-infecting Apicomplexa have been largely overlooked and lack specific treatment. Selective targeting of the &lt;i&gt;Babesia&lt;/i&gt; proteasome holds promise for drug development. In this study, we screened a library of peptide epoxyketone inhibitors derived from the marine natural product carmaphycin B for their activity against &lt;i&gt;Babesia&lt;/i&gt;. Several of these compounds showed activity against both the asexual and sexual blood stages of &lt;i&gt;Plasmodium falciparum&lt;/i&gt;. These compounds inactivate β5 proteasome subunit activity in the lysates of &lt;i&gt;Babesia divergens&lt;/i&gt; and &lt;i&gt;Babesia microti&lt;/i&gt; in the low nanomolar range. Several compounds were tested with the purified &lt;i&gt;B. divergens&lt;/i&gt; proteasome and showed IC&lt;sub&gt;50&lt;/sub&gt; values comparable to carfilzomib, an approved anticancer proteasome inhibitor. They also inhibited &lt;i&gt;B. divergens&lt;/i&gt;...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/47p077j7</guid>
      <pubDate>Fri, 22 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Robbertse, Luïse</name>
      </author>
      <author>
        <name>Fajtová, Pavla</name>
      </author>
      <author>
        <name>Šnebergerová, Pavla</name>
      </author>
      <author>
        <name>Jalovecká, Marie</name>
      </author>
      <author>
        <name>Levytska, Viktoriya</name>
      </author>
      <author>
        <name>da Silva, Elany Barbosa</name>
      </author>
      <author>
        <name>Sharma, Vandna</name>
      </author>
      <author>
        <name>Pachl, Petr</name>
      </author>
      <author>
        <name>Almaliti, Jehad</name>
      </author>
      <author>
        <name>Al-Hindy, Momen</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
        <uri>https://orcid.org/0000-0003-1403-4458</uri>
      </author>
      <author>
        <name>Bouřa, Evžen</name>
      </author>
      <author>
        <name>O’Donoghue, Anthony J</name>
      </author>
      <author>
        <name>Sojka, Daniel</name>
      </author>
    </item>
    <item>
      <title>Microbial solutions must be deployed against climate catastrophe</title>
      <link>https://escholarship.org/uc/item/75s604xq</link>
      <description>This paper is a call to action. By publishing concurrently across journals like an emergency bulletin, we are not merely making a plea for awareness about climate change. Instead, we are demanding immediate, tangible steps that harness the power of microbiology and the expertise of researchers and policymakers to safeguard the planet for future generations.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/75s604xq</guid>
      <pubDate>Mon, 18 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Peixoto, Raquel</name>
      </author>
      <author>
        <name>Voolstra, Christian R</name>
      </author>
      <author>
        <name>Stein, Lisa Y</name>
      </author>
      <author>
        <name>Hugenholtz, Philip</name>
      </author>
      <author>
        <name>Salles, Joana Falcao</name>
      </author>
      <author>
        <name>Amin, Shady A</name>
      </author>
      <author>
        <name>Häggblom, Max</name>
      </author>
      <author>
        <name>Gregory, Ann</name>
      </author>
      <author>
        <name>Makhalanyane, Thulani P</name>
      </author>
      <author>
        <name>Wang, Fengping</name>
      </author>
      <author>
        <name>Agbodjato, Nadège Adoukè</name>
      </author>
      <author>
        <name>Wang, Yinzhao</name>
      </author>
      <author>
        <name>Jiao, Nianzhi</name>
      </author>
      <author>
        <name>Lennon, Jay T</name>
      </author>
      <author>
        <name>Ventosa, Antonio</name>
      </author>
      <author>
        <name>Bavoil, Patrik M</name>
      </author>
      <author>
        <name>Miller, Virginia</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
    </item>
    <item>
      <title>Microbial solutions must be deployed against climate catastrophe</title>
      <link>https://escholarship.org/uc/item/6jf8f9j1</link>
      <description>This paper is a call to action. By publishing concurrently across journals like an emergency bulletin, we are not merely making a plea for awareness about climate change. Instead, we are demanding immediate, tangible steps that harness the power of microbiology and the expertise of researchers and policymakers to safeguard the planet for future generations.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6jf8f9j1</guid>
      <pubDate>Mon, 18 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Peixoto, Raquel</name>
      </author>
      <author>
        <name>Voolstra, Christian R</name>
      </author>
      <author>
        <name>Stein, Lisa Y</name>
      </author>
      <author>
        <name>Hugenholtz, Philip</name>
      </author>
      <author>
        <name>Salles, Joana Falcao</name>
      </author>
      <author>
        <name>Amin, Shady A</name>
      </author>
      <author>
        <name>Häggblom, Max</name>
      </author>
      <author>
        <name>Gregory, Ann</name>
      </author>
      <author>
        <name>Makhalanyane, Thulani P</name>
      </author>
      <author>
        <name>Wang, Fengping</name>
      </author>
      <author>
        <name>Agbodjato, Nadège Adoukè</name>
      </author>
      <author>
        <name>Wang, Yinzhao</name>
      </author>
      <author>
        <name>Jiao, Nianzhi</name>
      </author>
      <author>
        <name>Lennon, Jay T</name>
      </author>
      <author>
        <name>Ventosa, Antonio</name>
      </author>
      <author>
        <name>Bavoil, Patrik M</name>
      </author>
      <author>
        <name>Miller, Virginia</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
    </item>
    <item>
      <title>Microbial solutions must be deployed against climate catastrophe</title>
      <link>https://escholarship.org/uc/item/6720c689</link>
      <description>This paper is a call to action. By publishing concurrently across journals like an emergency bulletin, we are not merely making a plea for awareness about climate change. Instead, we are demanding immediate, tangible steps that harness the power of microbiology and the expertise of researchers and policymakers to safeguard the planet for future generations.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6720c689</guid>
      <pubDate>Mon, 18 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Peixoto, Raquel</name>
      </author>
      <author>
        <name>Voolstra, Christian R</name>
      </author>
      <author>
        <name>Stein, Lisa Y</name>
      </author>
      <author>
        <name>Hugenholtz, Philip</name>
      </author>
      <author>
        <name>Salles, Joana Falcao</name>
      </author>
      <author>
        <name>Amin, Shady A</name>
      </author>
      <author>
        <name>Häggblom, Max</name>
      </author>
      <author>
        <name>Gregory, Ann</name>
      </author>
      <author>
        <name>Makhalanyane, Thulani P</name>
      </author>
      <author>
        <name>Wang, Fengping</name>
      </author>
      <author>
        <name>Agbodjato, Nadège Adoukè</name>
      </author>
      <author>
        <name>Wang, Yinzhao</name>
      </author>
      <author>
        <name>Jiao, Nianzhi</name>
      </author>
      <author>
        <name>Lennon, Jay T</name>
      </author>
      <author>
        <name>Ventosa, Antonio</name>
      </author>
      <author>
        <name>Bavoil, Patrik M</name>
      </author>
      <author>
        <name>Miller, Virginia</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
    </item>
    <item>
      <title>The adult shell matrix protein repertoire of the marine snail Crepidula is dominated by conserved genes that are also expressed in larvae</title>
      <link>https://escholarship.org/uc/item/32p4m55k</link>
      <description>Mollusca is a morphologically diverse phylum, exhibiting an immense variety of calcium carbonate structures. Proteomic studies of adult shells often report high levels of rapidly-evolving, ‘novel’ shell matrix proteins (SMPs), which are hypothesized to drive shell diversification. However, relatively little is known about the phylogenetic distribution of SMPs, or about the function of individual SMPs in shell construction. To understand how SMPs contribute to shell diversification a thorough characterization of SMPs is required. Here, we build tools and a foundational understanding of SMPs in the marine gastropod species Crepidula fornicata and Crepidula atrasolea because they are genetically-enabled mollusc model organisms. First, we established a staging system of shell development in C. atrasolea for the first time. Next, we leveraged previous findings in C. fornicata combined with phylogenomic analyses of 95 metazoan species to determine the evolutionary lineage of its adult...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/32p4m55k</guid>
      <pubDate>Mon, 11 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Lopez-Anido, Rebecca N</name>
      </author>
      <author>
        <name>Batzel, Grant O</name>
      </author>
      <author>
        <name>Ramirez, Gabriela</name>
      </author>
      <author>
        <name>Wang, Yiqun</name>
      </author>
      <author>
        <name>Neal, Stephanie</name>
      </author>
      <author>
        <name>Lesoway, Maryna P</name>
      </author>
      <author>
        <name>Goodheart, Jessica A</name>
      </author>
      <author>
        <name>Lyons, Deirdre C</name>
      </author>
    </item>
    <item>
      <title>Structural elucidation of recombinant Trichomonas vaginalis 20S proteasome bound to covalent inhibitors</title>
      <link>https://escholarship.org/uc/item/44c8k2c1</link>
      <description>The proteasome is a proteolytic enzyme complex essential for protein homeostasis in mammalian cells and protozoan parasites like Trichomonas vaginalis (Tv), the cause of the most common, non-viral sexually transmitted disease. Tv and other protozoan 20S proteasomes have been validated as druggable targets for antimicrobials. However, low yields and purity of the native proteasome have hindered studies of the Tv 20S proteasome (Tv20S). We address this challenge by creating a recombinant protozoan proteasome by expressing all seven α and seven β subunits of Tv20S alongside the Ump-1 chaperone in insect cells. The recombinant Tv20S displays biochemical equivalence to its native counterpart, confirmed by various assays. Notably, the marizomib (MZB) inhibits all catalytic subunits of Tv20S, while the peptide inhibitor carmaphycin-17 (CP-17) specifically targets β2 and β5. Cryo-electron microscopy (cryo-EM) unveils the structures of Tv20S bound to MZB and CP-17 at 2.8 Å. These findings...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/44c8k2c1</guid>
      <pubDate>Sat, 9 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Silhan, Jan</name>
      </author>
      <author>
        <name>Fajtova, Pavla</name>
      </author>
      <author>
        <name>Bartosova, Jitka</name>
      </author>
      <author>
        <name>Hurysz, Brianna M</name>
      </author>
      <author>
        <name>Almaliti, Jehad</name>
      </author>
      <author>
        <name>Miyamoto, Yukiko</name>
      </author>
      <author>
        <name>Eckmann, Lars</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
        <uri>https://orcid.org/0000-0003-1403-4458</uri>
      </author>
      <author>
        <name>O’Donoghue, Anthony J</name>
      </author>
      <author>
        <name>Boura, Evzen</name>
      </author>
    </item>
    <item>
      <title>Molecular forecasting of domoic acid during a pervasive toxic diatom bloom</title>
      <link>https://escholarship.org/uc/item/1q46843w</link>
      <description>In 2015, the largest recorded harmful algal bloom (HAB) occurred in the Northeast Pacific, causing nearly 100 million dollars in damages to fisheries and killing many protected marine mammals. Dominated by the toxic diatom &lt;i&gt;Pseudo-nitzschia australis&lt;/i&gt;, this bloom produced high levels of the neurotoxin domoic acid (DA). Through molecular and transcriptional characterization of 52 near-weekly phytoplankton net-tow samples collected at a bloom hotspot in Monterey Bay, California, we identified active transcription of known DA biosynthesis (&lt;i&gt;dab&lt;/i&gt;) genes from the three identified toxigenic species, including &lt;i&gt;P. australis&lt;/i&gt; as the primary origin of toxicity. Elevated expression of silicon transporters (&lt;i&gt;sit1&lt;/i&gt;) during the bloom supports the previously hypothesized role of dissolved silica (Si) exhaustion in contributing to bloom physiology and toxicity. We find that coexpression of the &lt;i&gt;dabA&lt;/i&gt; and &lt;i&gt;sit1&lt;/i&gt; genes serves as a robust predictor of DA one week in...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1q46843w</guid>
      <pubDate>Fri, 8 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Brunson, John K</name>
      </author>
      <author>
        <name>Thukral, Monica</name>
      </author>
      <author>
        <name>Ryan, John P</name>
      </author>
      <author>
        <name>Anderson, Clarissa R</name>
      </author>
      <author>
        <name>Kolody, Bethany C</name>
      </author>
      <author>
        <name>James, Chase C</name>
      </author>
      <author>
        <name>Chavez, Francisco P</name>
      </author>
      <author>
        <name>Leaw, Chui Pin</name>
      </author>
      <author>
        <name>Rabines, Ariel J</name>
      </author>
      <author>
        <name>Venepally, Pratap</name>
      </author>
      <author>
        <name>Fussy, Zoltan</name>
      </author>
      <author>
        <name>Zheng, Hong</name>
      </author>
      <author>
        <name>Kudela, Raphael M</name>
        <uri>https://orcid.org/0000-0002-8640-1205</uri>
      </author>
      <author>
        <name>Smith, G Jason</name>
      </author>
      <author>
        <name>Moore, Bradley S</name>
        <uri>https://orcid.org/0000-0002-4652-1253</uri>
      </author>
      <author>
        <name>Allen, Andrew E</name>
        <uri>https://orcid.org/0000-0001-5911-6081</uri>
      </author>
    </item>
    <item>
      <title>Host-associated microbes mitigate the negative impacts of aquatic pollution</title>
      <link>https://escholarship.org/uc/item/0237c9m0</link>
      <description>Pollution can negatively impact aquatic ecosystems, aquaculture operations, and recreational water quality. Many aquatic microbes can sequester or degrade pollutants and have been utilized for bioremediation. While planktonic and benthic microbes are well-studied, host-associated microbes likely play an important role in mitigating the negative impacts of aquatic pollution and represent an unrealized source of microbial potential. For example, aquatic organisms that thrive in highly polluted environments or concentrate pollutants may have microbiomes adapted to these selective pressures. Understanding microbe-pollutant interactions in sensitive and valuable species could help protect human well-being and improve ecosystem resilience. Investigating these interactions using appropriate experimental systems and overcoming methodological challenges will present novel opportunities to protect and improve aquatic systems. In this perspective, we review examples of how microbes could...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0237c9m0</guid>
      <pubDate>Sat, 2 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Diner, Rachel E</name>
      </author>
      <author>
        <name>Allard, Sarah M</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
    </item>
    <item>
      <title>Enhancing Human Health and Wellbeing through Sustainably and Equitably Unlocking a Healthy Ocean’s Potential</title>
      <link>https://escholarship.org/uc/item/44q520d5</link>
      <description>A healthy ocean is essential for human health, and yet the links between the ocean and human health are often overlooked. By providing new medicines, technologies, energy, foods, recreation, and inspiration, the ocean has the potential to enhance human health and wellbeing. However, climate change, pollution, biodiversity loss, and inequity threaten both ocean and human health. Sustainable realisation of the ocean's health benefits will require overcoming these challenges through equitable partnerships, enforcement of laws and treaties, robust monitoring, and use of metrics that assess both the ocean's natural capital and human wellbeing. Achieving this will require an explicit focus on human rights, equity, sustainability, and social justice. In addition to highlighting the potential unique role of the healthcare sector, we offer science-based recommendations to protect both ocean health and human health, and we highlight the unique potential of the healthcare sector tolead this...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/44q520d5</guid>
      <pubDate>Mon, 30 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Fleming, Lora E</name>
      </author>
      <author>
        <name>Landrigan, Philip J</name>
      </author>
      <author>
        <name>Ashford, Oliver S</name>
      </author>
      <author>
        <name>Whitman, Ella M</name>
      </author>
      <author>
        <name>Swift, Amy</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
        <uri>https://orcid.org/0000-0003-1403-4458</uri>
      </author>
      <author>
        <name>Heymans, Johanna J</name>
      </author>
      <author>
        <name>Hicks, Christina C</name>
      </author>
      <author>
        <name>Morrissey, Karyn</name>
      </author>
      <author>
        <name>White, Mathew P</name>
      </author>
      <author>
        <name>Alcantara-Creencia, Lota</name>
      </author>
      <author>
        <name>Alexander, Karen A</name>
      </author>
      <author>
        <name>Astell-Burt, Thomas</name>
      </author>
      <author>
        <name>Berlinck, Roberto GS</name>
      </author>
      <author>
        <name>Cohen, Philippa J</name>
      </author>
      <author>
        <name>Hixson, Richard</name>
      </author>
      <author>
        <name>Islam, Mohammad Mahmudul</name>
      </author>
      <author>
        <name>Iwasaki, Arihiro</name>
      </author>
      <author>
        <name>Praptiwi, Radisti A</name>
      </author>
      <author>
        <name>Raps, Hervé</name>
      </author>
      <author>
        <name>Remy, Jan Yves</name>
      </author>
      <author>
        <name>Sowman, Georgina</name>
      </author>
      <author>
        <name>Ternon, Eva</name>
      </author>
      <author>
        <name>Thiele, Torsten</name>
      </author>
      <author>
        <name>Thilsted, Shakuntala H</name>
      </author>
      <author>
        <name>Uku, Jacqueline</name>
      </author>
      <author>
        <name>Ockenden, Stephanie</name>
      </author>
      <author>
        <name>Kumar, Pushpam</name>
      </author>
    </item>
    <item>
      <title>Light-gated integrator for highlighting kinase activity in living cells</title>
      <link>https://escholarship.org/uc/item/3862836p</link>
      <description>Protein kinases are key signaling nodes that regulate fundamental biological and disease processes. Illuminating kinase signaling from multiple angles can provide deeper insights into disease mechanisms and improve therapeutic targeting. While fluorescent biosensors are powerful tools for visualizing live-cell kinase activity dynamics in real time, new molecular tools are needed that enable recording of transient signaling activities for post hoc analysis and targeted manipulation. Here, we develop a light-gated kinase activity coupled transcriptional integrator (KINACT) that converts dynamic kinase signals into “permanent” fluorescent marks. KINACT enables robust monitoring of kinase activity across scales, accurately recording subcellular PKA activity, highlighting PKA activity distribution in 3D cultures, and identifying PKA activators and inhibitors in high-throughput screens. We further leverage the ability of KINACT to drive signaling effector expression to allow feedback...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3862836p</guid>
      <pubDate>Tue, 24 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Lin, Wei</name>
      </author>
      <author>
        <name>Phatarphekar, Abhishek</name>
      </author>
      <author>
        <name>Zhong, Yanghao</name>
      </author>
      <author>
        <name>Liu, Longwei</name>
      </author>
      <author>
        <name>Kwon, Hyung-Bae</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
        <uri>https://orcid.org/0000-0003-1403-4458</uri>
      </author>
      <author>
        <name>Wang, Yingxiao</name>
      </author>
      <author>
        <name>Mehta, Sohum</name>
        <uri>https://orcid.org/0000-0003-4764-8579</uri>
      </author>
      <author>
        <name>Zhang, Jin</name>
      </author>
    </item>
    <item>
      <title>Solitary humpback whales manufacture bubble-nets as tools to increase prey intake</title>
      <link>https://escholarship.org/uc/item/0mf625bb</link>
      <description>Several animal species use tools for foraging; however, very few manufacture and/or modify those tools. Humpback whales, which manufacture bubble-net tools while foraging, are among these rare species. Using animal-borne tag and unoccupied aerial system technologies, we examine bubble-nets manufactured by solitary humpback whales (&lt;i&gt;Megaptera novaeangliae&lt;/i&gt;) in Southeast Alaska while feeding on krill. We demonstrate that the nets consist of internally tangential rings and suggest that whales actively control the number of rings in a net, net size and depth and the horizontal spacing between neighbouring bubbles. We argue that whales regulate these net structural elements to increase per-lunge prey intake by, on average, sevenfold. We measured breath rate and swimming and lunge kinematics to show that the resulting increase in prey density does not increase energetic expenditure. Our results provide a novel insight into how bubble-net tools manufactured by solitary foraging...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0mf625bb</guid>
      <pubDate>Mon, 16 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Szabo, A</name>
      </author>
      <author>
        <name>Bejder, L</name>
      </author>
      <author>
        <name>Warick, H</name>
      </author>
      <author>
        <name>van Aswegen, M</name>
      </author>
      <author>
        <name>Friedlaender, AS</name>
        <uri>https://orcid.org/0000-0002-0851-0211</uri>
      </author>
      <author>
        <name>Goldbogen, J</name>
      </author>
      <author>
        <name>Kendall-Bar, JM</name>
        <uri>https://orcid.org/0000-0003-4758-1386</uri>
      </author>
      <author>
        <name>Leunissen, EM</name>
      </author>
      <author>
        <name>Angot, M</name>
      </author>
      <author>
        <name>Gough, WT</name>
      </author>
    </item>
    <item>
      <title>Metabolite diversity among representatives of divergent Prochlorococcus ecotypes</title>
      <link>https://escholarship.org/uc/item/6sb5n0pr</link>
      <description>IMPORTANCE: Approximately half of the annual carbon fixation on Earth occurs in the surface ocean through the photosynthetic activities of phytoplankton such as the ubiquitous picocyanobacterium &lt;i&gt;Prochlorococcus&lt;/i&gt;. Ecologically distinct subpopulations (or ecotypes) of &lt;i&gt;Prochlorococcus&lt;/i&gt; are central conduits of organic substrates into the ocean microbiome, thus playing important roles in surface ocean production. We measured the chemical profile of three cultured ecotype strains, observing striking differences among them that have implications for the likely chemical impact of &lt;i&gt;Prochlorococcus&lt;/i&gt; subpopulations on their surroundings in the wild. Subpopulations differ in abundance along gradients of temperature, light, and nutrient concentrations, suggesting that these chemical differences could affect carbon cycling in different ocean strata and should be considered in models of &lt;i&gt;Prochlorococcus&lt;/i&gt; physiology and marine carbon dynamics.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6sb5n0pr</guid>
      <pubDate>Tue, 10 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Kujawinski, Elizabeth B</name>
      </author>
      <author>
        <name>Braakman, Rogier</name>
      </author>
      <author>
        <name>Longnecker, Krista</name>
      </author>
      <author>
        <name>Becker, Jamie W</name>
      </author>
      <author>
        <name>Chisholm, Sallie W</name>
      </author>
      <author>
        <name>Dooley, Keven</name>
      </author>
      <author>
        <name>Soule, Melissa C Kido</name>
      </author>
      <author>
        <name>Swarr, Gretchen J</name>
      </author>
      <author>
        <name>Halloran, Kathryn</name>
      </author>
    </item>
    <item>
      <title>Extreme genome diversity and cryptic speciation in a harmful algal-bloom-forming eukaryote</title>
      <link>https://escholarship.org/uc/item/8d20x3c3</link>
      <description>Harmful algal blooms of the toxic haptophyte Prymnesium parvum are a recurrent problem in many inland and estuarine waters around the world. Strains of P.&amp;nbsp;parvum vary in the toxins they produce and in other physiological traits associated with harmful algal blooms, but the genetic basis for this variation is unknown. To investigate genome diversity in this morphospecies, we generated genome assemblies for 15 phylogenetically and geographically diverse strains of P.&amp;nbsp;parvum, including Hi-C guided, near-chromosome-level assemblies for two strains. Comparative analysis revealed considerable DNA content variation between strains, ranging from 115 to 845 Mbp. Strains included haploids, diploids, and polyploids, but not all differences in DNA content were due to variation in genome copy number. Haploid genome size between strains of different chemotypes differed by as much as 243 Mbp. Syntenic and phylogenetic analyses indicate that UTEX 2797, a common laboratory strain from...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8d20x3c3</guid>
      <pubDate>Fri, 30 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Wisecaver, Jennifer H</name>
      </author>
      <author>
        <name>Auber, Robert P</name>
      </author>
      <author>
        <name>Pendleton, Amanda L</name>
      </author>
      <author>
        <name>Watervoort, Nathan F</name>
      </author>
      <author>
        <name>Fallon, Timothy R</name>
        <uri>https://orcid.org/0000-0002-3048-7679</uri>
      </author>
      <author>
        <name>Riedling, Olivia L</name>
      </author>
      <author>
        <name>Manning, Schonna R</name>
      </author>
      <author>
        <name>Moore, Bradley S</name>
      </author>
      <author>
        <name>Driscoll, William W</name>
      </author>
    </item>
    <item>
      <title>Integrative analysis of multimodal mass spectrometry data in MZmine 3</title>
      <link>https://escholarship.org/uc/item/6tx1g53v</link>
      <description>Integrative analysis of multimodal mass spectrometry data in MZmine 3</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6tx1g53v</guid>
      <pubDate>Thu, 29 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Schmid, Robin</name>
      </author>
      <author>
        <name>Heuckeroth, Steffen</name>
      </author>
      <author>
        <name>Korf, Ansgar</name>
      </author>
      <author>
        <name>Smirnov, Aleksandr</name>
      </author>
      <author>
        <name>Myers, Owen</name>
      </author>
      <author>
        <name>Dyrlund, Thomas S</name>
      </author>
      <author>
        <name>Bushuiev, Roman</name>
      </author>
      <author>
        <name>Murray, Kevin J</name>
      </author>
      <author>
        <name>Hoffmann, Nils</name>
      </author>
      <author>
        <name>Lu, Miaoshan</name>
      </author>
      <author>
        <name>Sarvepalli, Abinesh</name>
      </author>
      <author>
        <name>Zhang, Zheng</name>
      </author>
      <author>
        <name>Fleischauer, Markus</name>
      </author>
      <author>
        <name>Dührkop, Kai</name>
      </author>
      <author>
        <name>Wesner, Mark</name>
      </author>
      <author>
        <name>Hoogstra, Shawn J</name>
      </author>
      <author>
        <name>Rudt, Edward</name>
      </author>
      <author>
        <name>Mokshyna, Olena</name>
      </author>
      <author>
        <name>Brungs, Corinna</name>
      </author>
      <author>
        <name>Ponomarov, Kirill</name>
      </author>
      <author>
        <name>Mutabdžija, Lana</name>
      </author>
      <author>
        <name>Damiani, Tito</name>
      </author>
      <author>
        <name>Pudney, Chris J</name>
      </author>
      <author>
        <name>Earll, Mark</name>
      </author>
      <author>
        <name>Helmer, Patrick O</name>
      </author>
      <author>
        <name>Fallon, Timothy R</name>
        <uri>https://orcid.org/0000-0002-3048-7679</uri>
      </author>
      <author>
        <name>Schulze, Tobias</name>
      </author>
      <author>
        <name>Rivas-Ubach, Albert</name>
      </author>
      <author>
        <name>Bilbao, Aivett</name>
      </author>
      <author>
        <name>Richter, Henning</name>
      </author>
      <author>
        <name>Nothias, Louis-Félix</name>
      </author>
      <author>
        <name>Wang, Mingxun</name>
        <uri>https://orcid.org/0000-0001-7647-6097</uri>
      </author>
      <author>
        <name>Orešič, Matej</name>
      </author>
      <author>
        <name>Weng, Jing-Ke</name>
      </author>
      <author>
        <name>Böcker, Sebastian</name>
      </author>
      <author>
        <name>Jeibmann, Astrid</name>
      </author>
      <author>
        <name>Hayen, Heiko</name>
      </author>
      <author>
        <name>Karst, Uwe</name>
      </author>
      <author>
        <name>Dorrestein, Pieter C</name>
      </author>
      <author>
        <name>Petras, Daniel</name>
      </author>
      <author>
        <name>Du, Xiuxia</name>
      </author>
      <author>
        <name>Pluskal, Tomáš</name>
      </author>
    </item>
    <item>
      <title>transXpress: a Snakemake pipeline for streamlined de novo transcriptome assembly and annotation</title>
      <link>https://escholarship.org/uc/item/40m1r17j</link>
      <description>BackgroundRNA-seq followed by de novo transcriptome assembly has been a transformative technique in biological research of non-model organisms, but the computational processing of RNA-seq data entails many different software tools. The complexity of these de novo transcriptomics workflows therefore presents a major barrier for researchers to adopt best-practice methods and up-to-date versions of software.ResultsHere we present a streamlined and universal de novo transcriptome assembly and annotation pipeline, transXpress, implemented in Snakemake. transXpress supports two popular assembly programs, Trinity and rnaSPAdes, and allows parallel execution on heterogeneous cluster computing hardware.ConclusionstransXpress simplifies the use of best-practice methods and up-to-date software for de novo transcriptome assembly, and produces standardized output files that can be mined using SequenceServer to facilitate rapid discovery of new genes and proteins in non-model organisms.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/40m1r17j</guid>
      <pubDate>Thu, 29 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Fallon, Timothy R</name>
        <uri>https://orcid.org/0000-0002-3048-7679</uri>
      </author>
      <author>
        <name>Čalounová, Tereza</name>
      </author>
      <author>
        <name>Mokrejš, Martin</name>
      </author>
      <author>
        <name>Weng, Jing-Ke</name>
      </author>
      <author>
        <name>Pluskal, Tomáš</name>
      </author>
    </item>
    <item>
      <title>Sixteen diverse laboratory mouse reference genomes define strain-specific haplotypes and novel functional loci</title>
      <link>https://escholarship.org/uc/item/3hm825m5</link>
      <description>We report full-length draft de novo genome assemblies for 16 widely used inbred mouse strains and find extensive strain-specific haplotype variation. We identify and characterize 2,567 regions on the current mouse reference genome exhibiting the greatest sequence diversity. These regions are enriched for genes involved in pathogen defence and immunity and exhibit enrichment of transposable elements and signatures of recent retrotransposition events. Combinations of alleles and genes unique to an individual strain are commonly observed at these loci, reflecting distinct strain phenotypes. We used these genomes to improve the mouse reference genome, resulting in the completion of 10 new gene structures. Also, 62 new coding loci were added to the reference genome annotation. These genomes identified a large, previously unannotated, gene (Efcab3-like) encoding 5,874 amino acids. Mutant Efcab3-like mice display anomalies in multiple brain regions, suggesting a possible role for this...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3hm825m5</guid>
      <pubDate>Thu, 29 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Lilue, Jingtao</name>
      </author>
      <author>
        <name>Doran, Anthony G</name>
      </author>
      <author>
        <name>Fiddes, Ian T</name>
      </author>
      <author>
        <name>Abrudan, Monica</name>
      </author>
      <author>
        <name>Armstrong, Joel</name>
      </author>
      <author>
        <name>Bennett, Ruth</name>
      </author>
      <author>
        <name>Chow, William</name>
      </author>
      <author>
        <name>Collins, Joanna</name>
      </author>
      <author>
        <name>Collins, Stephan</name>
      </author>
      <author>
        <name>Czechanski, Anne</name>
      </author>
      <author>
        <name>Danecek, Petr</name>
      </author>
      <author>
        <name>Diekhans, Mark</name>
      </author>
      <author>
        <name>Dolle, Dirk-Dominik</name>
      </author>
      <author>
        <name>Dunn, Matt</name>
      </author>
      <author>
        <name>Durbin, Richard</name>
      </author>
      <author>
        <name>Earl, Dent</name>
      </author>
      <author>
        <name>Ferguson-Smith, Anne</name>
      </author>
      <author>
        <name>Flicek, Paul</name>
      </author>
      <author>
        <name>Flint, Jonathan</name>
        <uri>https://orcid.org/0000-0002-9427-4429</uri>
      </author>
      <author>
        <name>Frankish, Adam</name>
      </author>
      <author>
        <name>Fu, Beiyuan</name>
      </author>
      <author>
        <name>Gerstein, Mark</name>
      </author>
      <author>
        <name>Gilbert, James</name>
        <uri>https://orcid.org/0000-0002-7733-2033</uri>
      </author>
      <author>
        <name>Goodstadt, Leo</name>
      </author>
      <author>
        <name>Harrow, Jennifer</name>
      </author>
      <author>
        <name>Howe, Kerstin</name>
      </author>
      <author>
        <name>Ibarra-Soria, Ximena</name>
      </author>
      <author>
        <name>Kolmogorov, Mikhail</name>
      </author>
      <author>
        <name>Lelliott, Chris J</name>
      </author>
      <author>
        <name>Logan, Darren W</name>
      </author>
      <author>
        <name>Loveland, Jane</name>
      </author>
      <author>
        <name>Mathews, Clayton E</name>
      </author>
      <author>
        <name>Mott, Richard</name>
      </author>
      <author>
        <name>Muir, Paul</name>
      </author>
      <author>
        <name>Nachtweide, Stefanie</name>
      </author>
      <author>
        <name>Navarro, Fabio CP</name>
      </author>
      <author>
        <name>Odom, Duncan T</name>
      </author>
      <author>
        <name>Park, Naomi</name>
      </author>
      <author>
        <name>Pelan, Sarah</name>
      </author>
      <author>
        <name>Pham, Son K</name>
      </author>
      <author>
        <name>Quail, Mike</name>
      </author>
      <author>
        <name>Reinholdt, Laura</name>
      </author>
      <author>
        <name>Romoth, Lars</name>
      </author>
      <author>
        <name>Shirley, Lesley</name>
      </author>
      <author>
        <name>Sisu, Cristina</name>
      </author>
      <author>
        <name>Sjoberg-Herrera, Marcela</name>
      </author>
      <author>
        <name>Stanke, Mario</name>
      </author>
      <author>
        <name>Steward, Charles</name>
      </author>
      <author>
        <name>Thomas, Mark</name>
      </author>
      <author>
        <name>Threadgold, Glen</name>
      </author>
      <author>
        <name>Thybert, David</name>
      </author>
      <author>
        <name>Torrance, James</name>
      </author>
      <author>
        <name>Wong, Kim</name>
      </author>
      <author>
        <name>Wood, Jonathan</name>
      </author>
      <author>
        <name>Yalcin, Binnaz</name>
      </author>
      <author>
        <name>Yang, Fengtang</name>
      </author>
      <author>
        <name>Adams, David J</name>
      </author>
      <author>
        <name>Paten, Benedict</name>
      </author>
      <author>
        <name>Keane, Thomas M</name>
      </author>
    </item>
    <item>
      <title>Empirical Chiroptical Analyses of Vicinal Bromochloro Natural Products by van’t Hoff’s Principle of Optical Superposition: Assignment of the C‑16 Configurations of Callophycols A and B</title>
      <link>https://escholarship.org/uc/item/9d1047px</link>
      <description>A simple empirical method is described that allows the assignment of absolute configurations of natural products containing chiral vicinal bromochloro (VBC) units, including the bromochloro substituted isoprenyl units present in the structures of antiproliferative halomon (&lt;b&gt;1a&lt;/b&gt;) and its halogen-swapped isomer &lt;i&gt;iso&lt;/i&gt;-halomon (&lt;b&gt;1b&lt;/b&gt;) from the red alga, &lt;i&gt;Portieria hornemannii&lt;/i&gt;, and callophycols A (&lt;b&gt;3&lt;/b&gt;) and B (&lt;b&gt;4&lt;/b&gt;) from &lt;i&gt;Callophycus serratus&lt;/i&gt;. The relative configurations of &lt;b&gt;3&lt;/b&gt; and &lt;b&gt;4&lt;/b&gt;, published in 2007, were incomplete: C-16 was left unassigned. It is now shown that the additivity of molar rotations, [&lt;i&gt;M&lt;/i&gt;]&lt;sub&gt;D&lt;/sub&gt; (herein, abbreviated [&lt;i&gt;M&lt;/i&gt;])─a consequence of van't Hoff's principle of optical superposition─could be used to deconvolute rotatory contributions, designated as [&lt;i&gt;M&lt;/i&gt;&lt;sub&gt;X&lt;/sub&gt;] and [&lt;i&gt;M&lt;/i&gt;&lt;sub&gt;Y&lt;/sub&gt;] of the two remotely spaced chiral substructures within &lt;b&gt;3&lt;/b&gt; and &lt;b&gt;4&lt;/b&gt; using simple arithmetic. Input...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9d1047px</guid>
      <pubDate>Sat, 3 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Molinski, Tadeusz F</name>
        <uri>https://orcid.org/0000-0003-1935-2535</uri>
      </author>
    </item>
    <item>
      <title>The Metabolome of a Cyanobacterial Bloom Visualized by MS/MS-Based Molecular Networking Reveals New Neurotoxic Smenamide Analogs (C, D, and E)</title>
      <link>https://escholarship.org/uc/item/5p06d9hf</link>
      <description>Members of the cyanobacterial genus &lt;i&gt;Trichodesmium&lt;/i&gt; are well known for their substantial impact on nitrogen influx in ocean ecosystems and the enormous surface blooms they form in tropical and subtropical locations. However, the secondary metabolite composition of these complex environmental bloom events is not well known, nor the possibility of the production of potent toxins that have been observed in other bloom-forming marine and freshwater cyanobacteria species. In the present work, we aimed to characterize the metabolome of a &lt;i&gt;Trichodesmium&lt;/i&gt; bloom utilizing MS/MS-based molecular networking. Furthermore, we integrated cytotoxicity assays in order to identify and ultimately isolate potential cyanotoxins from the bloom. These efforts led to the isolation and identification of several members of the smenamide family, including three new smenamide analogs (&lt;b&gt;1-3&lt;/b&gt;) as well as the previously reported smenothiazole A-hybrid polyketide-peptide compounds. Two of these...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5p06d9hf</guid>
      <pubDate>Fri, 2 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Via, Christopher W</name>
      </author>
      <author>
        <name>Glukhov, Evgenia</name>
      </author>
      <author>
        <name>Costa, Samuel</name>
      </author>
      <author>
        <name>Zimba, Paul V</name>
      </author>
      <author>
        <name>Moeller, Peter DR</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
      </author>
      <author>
        <name>Bertin, Matthew J</name>
      </author>
    </item>
    <item>
      <title>Comparative genomics uncovers the prolific and distinctive metabolic potential of the cyanobacterial genus Moorea</title>
      <link>https://escholarship.org/uc/item/5nh2r1n1</link>
      <description>Cyanobacteria are major sources of oxygen, nitrogen, and carbon in nature. In addition to the importance of their primary metabolism, some cyanobacteria are prolific producers of unique and bioactive secondary metabolites. Chemical investigations of the cyanobacterial genus &lt;i&gt;Moorea&lt;/i&gt; have resulted in the isolation of over 190 compounds in the last two decades. However, preliminary genomic analysis has suggested that genome-guided approaches can enable the discovery of novel compounds from even well-studied &lt;i&gt;Moorea&lt;/i&gt; strains, highlighting the importance of obtaining complete genomes. We report a complete genome of a filamentous tropical marine cyanobacterium, &lt;i&gt;Moorea producens&lt;/i&gt; PAL, which reveals that about one-fifth of its genome is devoted to production of secondary metabolites, an impressive four times the cyanobacterial average. Moreover, possession of the complete PAL genome has allowed improvement to the assembly of three other &lt;i&gt;Moorea&lt;/i&gt; draft genomes. Comparative...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5nh2r1n1</guid>
      <pubDate>Fri, 2 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Leao, Tiago</name>
      </author>
      <author>
        <name>Castelão, Guilherme</name>
      </author>
      <author>
        <name>Korobeynikov, Anton</name>
      </author>
      <author>
        <name>Monroe, Emily A</name>
      </author>
      <author>
        <name>Podell, Sheila</name>
      </author>
      <author>
        <name>Glukhov, Evgenia</name>
      </author>
      <author>
        <name>Allen, Eric E</name>
        <uri>https://orcid.org/0000-0002-1229-8794</uri>
      </author>
      <author>
        <name>Gerwick, William H</name>
      </author>
      <author>
        <name>Gerwick, Lena</name>
      </author>
    </item>
    <item>
      <title>Applying a Chemogeographic Strategy for Natural Product Discovery from the Marine Cyanobacterium Moorena bouillonii</title>
      <link>https://escholarship.org/uc/item/32r1z3vp</link>
      <description>The tropical marine cyanobacterium &lt;i&gt;Moorena bouillonii&lt;/i&gt; occupies a large geographic range across the Indian and Western Tropical Pacific Oceans and is a prolific producer of structurally unique and biologically active natural products. An ensemble of computational approaches, including the creation of the ORCA (Objective Relational Comparative Analysis) pipeline for flexible MS&lt;sup&gt;1&lt;/sup&gt; feature detection and multivariate analyses, were used to analyze various &lt;i&gt;M. bouillonii&lt;/i&gt; samples. The observed chemogeographic patterns suggested the production of regionally specific natural products by &lt;i&gt;M. bouillonii&lt;/i&gt;. Analyzing the drivers of these chemogeographic patterns allowed for the identification, targeted isolation, and structure elucidation of a regionally specific natural product, doscadenamide A (&lt;b&gt;1&lt;/b&gt;). Analyses of MS&lt;sup&gt;2&lt;/sup&gt; fragmentation patterns further revealed this natural product to be part of an extensive family of herein annotated, proposed natural...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/32r1z3vp</guid>
      <pubDate>Fri, 2 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Leber, Christopher A</name>
      </author>
      <author>
        <name>Naman, C Benjamin</name>
      </author>
      <author>
        <name>Keller, Lena</name>
      </author>
      <author>
        <name>Almaliti, Jehad</name>
      </author>
      <author>
        <name>Caro-Diaz, Eduardo JE</name>
      </author>
      <author>
        <name>Glukhov, Evgenia</name>
      </author>
      <author>
        <name>Joseph, Valsamma</name>
      </author>
      <author>
        <name>Sajeevan, TP</name>
      </author>
      <author>
        <name>Reyes, Andres Joshua</name>
      </author>
      <author>
        <name>Biggs, Jason S</name>
      </author>
      <author>
        <name>Li, Te</name>
      </author>
      <author>
        <name>Yuan, Ye</name>
      </author>
      <author>
        <name>He, Shan</name>
      </author>
      <author>
        <name>Yan, Xiaojun</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
      </author>
    </item>
    <item>
      <title>Discovery of Novel Tyrosinase Inhibitors From Marine Cyanobacteria</title>
      <link>https://escholarship.org/uc/item/2k3760dp</link>
      <description>Tyrosinase, an important oxidase involved in the primary immune response in humans, can sometimes become problematic as it can catalyze undesirable oxidation reactions. Therefore, for decades there has been a strong pharmaceutical interest in the discovery of novel inhibitors of this enzyme. Recent studies have also indicated that tyrosinase inhibitors can potentially be used in the treatment of melanoma cancer. Over the years, many new tyrosinase inhibitors have been discovered from various natural sources; however, marine natural products (MNPs) have contributed only a small number of promising candidates. Therefore, in this study we focused on the discovery of new MNP tyrosinase inhibitors of marine cyanobacterial and algal origins. A colorimetric tyrosinase inhibitory assay was used to screen over 4,500 marine extracts against mushroom tyrosinase (&lt;i&gt;A. bisporus&lt;/i&gt;). Our results revealed that scytonemin monomer (ScyM), a pure compound from our compound library and also the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2k3760dp</guid>
      <pubDate>Fri, 2 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>He, Yifan</name>
      </author>
      <author>
        <name>Suyama, Takashi L</name>
      </author>
      <author>
        <name>Kim, Hyunwoo</name>
      </author>
      <author>
        <name>Glukhov, Evgenia</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
      </author>
    </item>
    <item>
      <title>Leptochelins A–C, Cytotoxic Metallophores Produced by Geographically Dispersed Leptothoe Strains of Marine Cyanobacteria</title>
      <link>https://escholarship.org/uc/item/88j9f90p</link>
      <description>Metals are important cofactors in the metabolic processes of cyanobacteria, including photosynthesis, cellular respiration, DNA replication, and the biosynthesis of primary and secondary metabolites. In adaptation to the marine environment, cyanobacteria use metallophores to acquire trace metals when necessary as well as to reduce potential toxicity from excessive metal concentrations. Leptochelins A-C were identified as structurally novel metallophores from three geographically dispersed cyanobacteria of the genus &lt;i&gt;Leptothoe&lt;/i&gt;. Determination of the complex structures of these metabolites presented numerous challenges, but they were ultimately solved using integrated data from NMR, mass spectrometry and deductions from the biosynthetic gene cluster. The leptochelins are comprised of halogenated linear NRPS-PKS hybrid products with multiple heterocycles that have potential for hexadentate and tetradentate coordination with metal ions. The genomes of the three leptochelin producers...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/88j9f90p</guid>
      <pubDate>Mon, 29 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Avalon, Nicole E</name>
      </author>
      <author>
        <name>Reis, Mariana A</name>
      </author>
      <author>
        <name>Thornburg, Christopher C</name>
      </author>
      <author>
        <name>Williamson, R Thomas</name>
      </author>
      <author>
        <name>Petras, Daniel</name>
      </author>
      <author>
        <name>Aron, Allegra T</name>
      </author>
      <author>
        <name>Neuhaus, George F</name>
      </author>
      <author>
        <name>Al-Hindy, Momen</name>
      </author>
      <author>
        <name>Mitrevska, Jana</name>
      </author>
      <author>
        <name>Ferreira, Leonor</name>
      </author>
      <author>
        <name>Morais, João</name>
      </author>
      <author>
        <name>Abiead, Yasin El</name>
      </author>
      <author>
        <name>Glukhov, Evgenia</name>
      </author>
      <author>
        <name>Alexander, Kelsey L</name>
      </author>
      <author>
        <name>Vulpanovici, F Alexandra</name>
      </author>
      <author>
        <name>Bertin, Matthew J</name>
      </author>
      <author>
        <name>Whitner, Syrena</name>
      </author>
      <author>
        <name>Choi, Hyukjae</name>
      </author>
      <author>
        <name>Spengler, Gabriella</name>
      </author>
      <author>
        <name>Blinov, Kirill</name>
      </author>
      <author>
        <name>Almohammadi, Ameen M</name>
      </author>
      <author>
        <name>Shaala, Lamiaa A</name>
      </author>
      <author>
        <name>Kew, William R</name>
      </author>
      <author>
        <name>Paša-Tolić, Ljiljana</name>
      </author>
      <author>
        <name>Youssef, Diaa TA</name>
      </author>
      <author>
        <name>Dorrestein, Pieter C</name>
      </author>
      <author>
        <name>Vasconcelos, Vitor</name>
      </author>
      <author>
        <name>Gerwick, Lena</name>
      </author>
      <author>
        <name>McPhail, Kerry L</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
        <uri>https://orcid.org/0000-0003-1403-4458</uri>
      </author>
    </item>
    <item>
      <title>The Kavaratamides: Discovery of Linear Lipodepsipeptides from the Marine Cyanobacterium Moorena bouillonii Using a Comparative Chemogeographic Analysis</title>
      <link>https://escholarship.org/uc/item/9gz138t2</link>
      <description>Kavaratamide A (&lt;b&gt;1&lt;/b&gt;), a new linear lipodepsipeptide possessing an unusual isopropyl-&lt;i&gt;O&lt;/i&gt;-methylpyrrolinone moiety, was discovered from the tropical marine filamentous cyanobacterium &lt;i&gt;Moorena bouillonii&lt;/i&gt; collected from Kavaratti, India. A comparative chemogeographic analysis of &lt;i&gt;M&lt;/i&gt;. &lt;i&gt;bouillonii&lt;/i&gt; collected from six different geographical regions led to the prioritized isolation of this metabolite from India as distinctive among our data sets. AI-based structure annotation tools, including SMART 2.1 and DeepSAT, accelerated the structure elucidation by providing useful structural clues, and the full planar structure was elucidated based on comprehensive HRMS, MS/MS fragmentation, and NMR data interpretation. Subsequently, the absolute configuration of &lt;b&gt;1&lt;/b&gt; was determined using advanced Marfey's analysis, modified Mosher's ester derivatization, and chiral-phase HPLC. The structures of kavaratamides B (&lt;b&gt;2&lt;/b&gt;) and C (&lt;b&gt;3&lt;/b&gt;) are proposed based on a detailed...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9gz138t2</guid>
      <pubDate>Fri, 19 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Ryu, Byeol</name>
        <uri>https://orcid.org/0000-0002-3405-2875</uri>
      </author>
      <author>
        <name>Glukhov, Evgenia</name>
      </author>
      <author>
        <name>Teixeira, Thaiz R</name>
      </author>
      <author>
        <name>Caffrey, Conor R</name>
      </author>
      <author>
        <name>Madiyan, Saranya</name>
      </author>
      <author>
        <name>Joseph, Valsamma</name>
      </author>
      <author>
        <name>Avalon, Nicole E</name>
      </author>
      <author>
        <name>Leber, Christopher A</name>
      </author>
      <author>
        <name>Naman, C Benjamin</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
        <uri>https://orcid.org/0000-0003-1403-4458</uri>
      </author>
    </item>
    <item>
      <title>The Termite Fungal Cultivar Termitomyces Combines Diverse Enzymes and Oxidative Reactions for Plant Biomass Conversion</title>
      <link>https://escholarship.org/uc/item/56d6h4xd</link>
      <description>Macrotermitine termites have domesticated fungi in the genus &lt;i&gt;Termitomyces&lt;/i&gt; as their primary food source using predigested plant biomass. To access the full nutritional value of lignin-enriched plant biomass, the termite-fungus symbiosis requires the depolymerization of this complex phenolic polymer. While most previous work suggests that lignocellulose degradation is accomplished predominantly by the fungal cultivar, our current understanding of the underlying biomolecular mechanisms remains rudimentary. Here, we provide conclusive omics and activity-based evidence that &lt;i&gt;Termitomyces&lt;/i&gt; employs not only a broad array of carbohydrate-active enzymes (CAZymes) but also a restricted set of oxidizing enzymes (manganese peroxidase, dye decolorization peroxidase, an unspecific peroxygenase, laccases, and aryl-alcohol oxidases) and Fenton chemistry for biomass degradation. We propose for the first time that &lt;i&gt;Termitomyces&lt;/i&gt; induces hydroquinone-mediated Fenton chemistry (Fe&lt;sup&gt;2+&lt;/sup&gt;...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/56d6h4xd</guid>
      <pubDate>Fri, 19 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Schalk, Felix</name>
      </author>
      <author>
        <name>Gostinčar, Cene</name>
      </author>
      <author>
        <name>Kreuzenbeck, Nina B</name>
      </author>
      <author>
        <name>Conlon, Benjamin H</name>
      </author>
      <author>
        <name>Sommerwerk, Elisabeth</name>
      </author>
      <author>
        <name>Rabe, Patrick</name>
      </author>
      <author>
        <name>Burkhardt, Immo</name>
        <uri>https://orcid.org/0000-0001-9515-4042</uri>
      </author>
      <author>
        <name>Krüger, Thomas</name>
      </author>
      <author>
        <name>Kniemeyer, Olaf</name>
      </author>
      <author>
        <name>Brakhage, Axel A</name>
      </author>
      <author>
        <name>Gunde-Cimerman, Nina</name>
      </author>
      <author>
        <name>de Beer, Z Wilhelm</name>
      </author>
      <author>
        <name>Dickschat, Jeroen S</name>
      </author>
      <author>
        <name>Poulsen, Michael</name>
      </author>
      <author>
        <name>Beemelmanns, Christine</name>
      </author>
    </item>
    <item>
      <title>Isolation, (bio)synthetic studies and evaluation of antimicrobial properties of drimenol-type sesquiterpenes of Termitomyces fungi</title>
      <link>https://escholarship.org/uc/item/13w1k9s9</link>
      <description>Macrotermitinae termites have farmed fungi in the genus Termitomyces as a food source for millions of years. However, the biochemical mechanisms orchestrating this mutualistic relationship are largely unknown. To deduce fungal signals and ecological patterns that relate to the stability of this symbiosis, we explored the volatile organic compound (VOC) repertoire of Termitomyces from Macrotermes natalensis colonies. Results show that mushrooms emit a VOC pattern that differs from mycelium grown in fungal gardens and laboratory cultures. The abundance of sesquiterpenoids from mushrooms allowed targeted isolation of five drimane sesquiterpenes from plate cultivations. The total synthesis of one of these, drimenol, and related drimanes assisted in structural and comparative analysis of volatile organic compounds (VOCs) and antimicrobial activity testing. Enzyme candidates putatively involved in terpene biosynthesis were heterologously expressed and while these were not involved in...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/13w1k9s9</guid>
      <pubDate>Fri, 19 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Kreuzenbeck, Nina B</name>
      </author>
      <author>
        <name>Dhiman, Seema</name>
      </author>
      <author>
        <name>Roman, Dávid</name>
      </author>
      <author>
        <name>Burkhardt, Immo</name>
        <uri>https://orcid.org/0000-0001-9515-4042</uri>
      </author>
      <author>
        <name>Conlon, Benjamin H</name>
      </author>
      <author>
        <name>Fricke, Janis</name>
      </author>
      <author>
        <name>Guo, Huijuan</name>
      </author>
      <author>
        <name>Blume, Janis</name>
      </author>
      <author>
        <name>Görls, Helmar</name>
      </author>
      <author>
        <name>Poulsen, Michael</name>
      </author>
      <author>
        <name>Dickschat, Jeroen S</name>
      </author>
      <author>
        <name>Köllner, Tobias G</name>
      </author>
      <author>
        <name>Arndt, Hans-Dieter</name>
      </author>
      <author>
        <name>Beemelmanns, Christine</name>
      </author>
    </item>
    <item>
      <title>Metagenome-assembled genome of withering syndrome causative agent, “Candidatus Xenohaliotis californiensis,“ from endangered white abalone (Haliotis sorenseni)</title>
      <link>https://escholarship.org/uc/item/8m41f4f9</link>
      <description>The genome of "&lt;i&gt;Candidatus&lt;/i&gt; Xenohaliotis californiensis" was assembled from shotgun metagenomic sequencing of experimentally infected white abalone. Ninety-one percent genome completeness was achieved with low contamination. Sequencing this genome provides the opportunity to track pathogen evolution over time, conduct gene expression experiments, and study dynamics between this pathogen and its phage.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8m41f4f9</guid>
      <pubDate>Thu, 18 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Kunselman, Emily</name>
      </author>
      <author>
        <name>Allard, Sarah</name>
      </author>
      <author>
        <name>Burge, Colleen</name>
      </author>
      <author>
        <name>Marshman, Blythe</name>
      </author>
      <author>
        <name>Frederick, Alyssa</name>
      </author>
      <author>
        <name>Gilbert, Jack</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
    </item>
    <item>
      <title>Small molecule in situ resin capture provides a compound first approach to natural product discovery</title>
      <link>https://escholarship.org/uc/item/2m47v7ft</link>
      <description>Culture-based microbial natural product discovery strategies fail to realize the extraordinary biosynthetic potential detected across earth’s microbiomes. Here we introduce Small Molecule In situ Resin Capture (SMIRC), a culture-independent method to obtain natural products directly from the environments in which they are produced. We use SMIRC to capture numerous compounds including two new carbon skeletons that were characterized using NMR and contain structural features that are, to the best of our knowledge, unprecedented among natural products. Applications across diverse marine habitats reveal biome-specific metabolomic signatures and levels of chemical diversity in concordance with sequence-based predictions. Expanded deployments, in situ cultivation, and metagenomics facilitate compound discovery, enhance yields, and link compounds to candidate producing organisms, although microbial community complexity creates challenges for the later. This compound-first approach to...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2m47v7ft</guid>
      <pubDate>Sat, 6 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Bogdanov, Alexander</name>
      </author>
      <author>
        <name>Salib, Mariam N</name>
      </author>
      <author>
        <name>Chase, Alexander B</name>
      </author>
      <author>
        <name>Hammerlindl, Heinz</name>
      </author>
      <author>
        <name>Muskat, Mitchell N</name>
      </author>
      <author>
        <name>Luedtke, Stephanie</name>
      </author>
      <author>
        <name>da Silva, Elany Barbosa</name>
      </author>
      <author>
        <name>O’Donoghue, Anthony J</name>
      </author>
      <author>
        <name>Wu, Lani F</name>
      </author>
      <author>
        <name>Altschuler, Steven J</name>
        <uri>https://orcid.org/0000-0001-9142-0796</uri>
      </author>
      <author>
        <name>Molinski, Tadeusz F</name>
        <uri>https://orcid.org/0000-0003-1935-2535</uri>
      </author>
      <author>
        <name>Jensen, Paul R</name>
      </author>
    </item>
    <item>
      <title>Nature-Inspired Gallinamides Are Potent Antischistosomal Agents: Inhibition of the Cathepsin B1 Protease Target and Binding Mode Analysis</title>
      <link>https://escholarship.org/uc/item/29t9q2g4</link>
      <description>Schistosomiasis, caused by a parasitic blood fluke of the genus &lt;i&gt;Schistosoma,&lt;/i&gt; is a global health problem for which new chemotherapeutic options are needed. We explored the scaffold of gallinamide A, a natural peptidic metabolite of marine cyanobacteria that has previously been shown to inhibit cathepsin L-type proteases. We screened a library of 19 synthetic gallinamide A analogs and identified nanomolar inhibitors of the cathepsin B-type protease SmCB1, which is a drug target for the treatment of schistosomiasis mansoni. Against cultured &lt;i&gt;S. mansoni&lt;/i&gt; schistosomula and adult worms, many of the gallinamides generated a range of deleterious phenotypic responses. Imaging with a fluorescent-activity-based probe derived from gallinamide A demonstrated that SmCB1 is the primary target for gallinamides in the parasite. Furthermore, we solved the high-resolution crystal structures of SmCB1 in complex with gallinamide A and its two analogs and describe the acrylamide covalent...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/29t9q2g4</guid>
      <pubDate>Sat, 6 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Spiwoková, Petra</name>
      </author>
      <author>
        <name>Horn, Martin</name>
      </author>
      <author>
        <name>Fanfrlík, Jindřich</name>
      </author>
      <author>
        <name>Jílková, Adéla</name>
      </author>
      <author>
        <name>Fajtová, Pavla</name>
      </author>
      <author>
        <name>Leontovyč, Adrian</name>
      </author>
      <author>
        <name>Houštecká, Radka</name>
      </author>
      <author>
        <name>Bieliková, Lucia</name>
      </author>
      <author>
        <name>Brynda, Jiří</name>
      </author>
      <author>
        <name>Chanová, Marta</name>
      </author>
      <author>
        <name>Mertlíková-Kaiserová, Helena</name>
      </author>
      <author>
        <name>Caro-Diaz, Eduardo JE</name>
      </author>
      <author>
        <name>Almaliti, Jehad</name>
      </author>
      <author>
        <name>El-Sakkary, Nelly</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
        <uri>https://orcid.org/0000-0003-1403-4458</uri>
      </author>
      <author>
        <name>Caffrey, Conor R</name>
      </author>
      <author>
        <name>Mareš, Michael</name>
      </author>
    </item>
    <item>
      <title>A concept for international societally relevant microbiology education and microbiology knowledge promulgation in society</title>
      <link>https://escholarship.org/uc/item/0wg940fd</link>
      <description>EXECUTIVE SUMMARY: Microbes are all pervasive in their distribution and influence on the functioning and well-being of humans, life in general and the planet. Microbially-based technologies contribute hugely to the supply of important goods and services we depend upon, such as the provision of food, medicines and clean water. They also offer mechanisms and strategies to mitigate and solve a wide range of problems and crises facing humanity at all levels, including those encapsulated in the sustainable development goals (SDGs) formulated by the United Nations. For example, microbial technologies can contribute in multiple ways to decarbonisation and hence confronting global warming, provide sanitation and clean water to the billions of people&amp;nbsp;lacking them, improve soil fertility and hence food production and develop vaccines and other medicines to reduce and in some cases eliminate deadly infections. They are the foundation of biotechnology, an increasingly important and growing...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0wg940fd</guid>
      <pubDate>Wed, 12 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Timmis, Kenneth</name>
      </author>
      <author>
        <name>Hallsworth, John E</name>
      </author>
      <author>
        <name>McGenity, Terry J</name>
      </author>
      <author>
        <name>Armstrong, Rachel</name>
      </author>
      <author>
        <name>Colom, María Francisca</name>
      </author>
      <author>
        <name>Karahan, Zeynep Ceren</name>
      </author>
      <author>
        <name>Chavarría, Max</name>
      </author>
      <author>
        <name>Bernal, Patricia</name>
      </author>
      <author>
        <name>Boyd, Eric S</name>
      </author>
      <author>
        <name>Ramos, Juan Luis</name>
      </author>
      <author>
        <name>Kaltenpoth, Martin</name>
      </author>
      <author>
        <name>Pruzzo, Carla</name>
      </author>
      <author>
        <name>Clarke, Gerard</name>
      </author>
      <author>
        <name>López‐Garcia, Purificación</name>
      </author>
      <author>
        <name>Yakimov, Michail M</name>
      </author>
      <author>
        <name>Perlmutter, Jessamyn</name>
      </author>
      <author>
        <name>Greening, Chris</name>
      </author>
      <author>
        <name>Eloe‐Fadrosh, Emiley</name>
      </author>
      <author>
        <name>Verstraete, Willy</name>
      </author>
      <author>
        <name>Nunes, Olga C</name>
      </author>
      <author>
        <name>Kotsyurbenko, Oleg</name>
      </author>
      <author>
        <name>Nikel, Pablo Iván</name>
      </author>
      <author>
        <name>Scavone, Paola</name>
      </author>
      <author>
        <name>Häggblom, Max M</name>
      </author>
      <author>
        <name>Lavigne, Rob</name>
      </author>
      <author>
        <name>Le Roux, Frédérique</name>
      </author>
      <author>
        <name>Timmis, James K</name>
      </author>
      <author>
        <name>Parro, Victor</name>
      </author>
      <author>
        <name>Michán, Carmen</name>
      </author>
      <author>
        <name>García, José Luis</name>
      </author>
      <author>
        <name>Casadevall, Arturo</name>
      </author>
      <author>
        <name>Payne, Shelley M</name>
      </author>
      <author>
        <name>Frey, Joachim</name>
      </author>
      <author>
        <name>Koren, Omry</name>
      </author>
      <author>
        <name>Prosser, James I</name>
      </author>
      <author>
        <name>Lahti, Leo</name>
      </author>
      <author>
        <name>Lal, Rup</name>
      </author>
      <author>
        <name>Anand, Shailly</name>
      </author>
      <author>
        <name>Sood, Utkarsh</name>
      </author>
      <author>
        <name>Offre, Pierre</name>
      </author>
      <author>
        <name>Bryce, Casey C</name>
      </author>
      <author>
        <name>Mswaka, Allen Y</name>
      </author>
      <author>
        <name>Jores, Jörg</name>
      </author>
      <author>
        <name>Kaçar, Betül</name>
      </author>
      <author>
        <name>Blank, Lars Mathias</name>
      </author>
      <author>
        <name>Maaßen, Nicole</name>
      </author>
      <author>
        <name>Pope, Phillip B</name>
      </author>
      <author>
        <name>Banciu, Horia L</name>
      </author>
      <author>
        <name>Armitage, Judith</name>
      </author>
      <author>
        <name>Lee, Sang Yup</name>
      </author>
      <author>
        <name>Wang, Fengping</name>
      </author>
      <author>
        <name>Makhalanyane, Thulani P</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
      <author>
        <name>Wood, Thomas K</name>
      </author>
      <author>
        <name>Vasiljevic, Branka</name>
      </author>
      <author>
        <name>Soberón, Mario</name>
      </author>
      <author>
        <name>Udaondo, Zulema</name>
      </author>
      <author>
        <name>Rojo, Fernando</name>
      </author>
      <author>
        <name>Tamang, Jyoti Prakash</name>
      </author>
      <author>
        <name>Giraud, Tatiana</name>
      </author>
      <author>
        <name>Ropars, Jeanne</name>
      </author>
      <author>
        <name>Ezeji, Thaddeus</name>
      </author>
      <author>
        <name>Müller, Volker</name>
      </author>
      <author>
        <name>Danbara, Hirofume</name>
      </author>
      <author>
        <name>Averhoff, Beate</name>
      </author>
      <author>
        <name>Sessitsch, Angela</name>
      </author>
      <author>
        <name>Partida‐Martínez, Laila Pamela</name>
      </author>
      <author>
        <name>Huang, Wei</name>
      </author>
      <author>
        <name>Molin, Søren</name>
      </author>
      <author>
        <name>Junier, Pilar</name>
      </author>
      <author>
        <name>Amils, Ricardo</name>
      </author>
      <author>
        <name>Wu, Xiao‐Lei</name>
      </author>
      <author>
        <name>Ron, Eliora</name>
      </author>
      <author>
        <name>Erten, Huseyin</name>
      </author>
      <author>
        <name>de Martinis, Elaine Cristina Pereira</name>
      </author>
      <author>
        <name>Rapoport, Alexander</name>
      </author>
      <author>
        <name>Öpik, Maarja</name>
      </author>
      <author>
        <name>Pokatong, W Donald R</name>
      </author>
      <author>
        <name>Stairs, Courtney</name>
      </author>
      <author>
        <name>Amoozegar, Mohammad Ali</name>
      </author>
      <author>
        <name>Serna, Jéssica Gil</name>
      </author>
    </item>
    <item>
      <title>Unveiling a CAAX Protease‐Like Protein Involved in Didemnin Drug Maturation and Secretion</title>
      <link>https://escholarship.org/uc/item/5d582590</link>
      <description>The assembly line biosynthesis of the powerful anticancer-antiviral didemnin cyclic peptides is proposed to follow a prodrug release mechanism in Tristella bacteria. This strategy commences with the formation of N-terminal prodrug scaffolds and culminates in their cleavage during the cellular export of the mature products. In this study, a comprehensive exploration of the genetic and biochemical aspects of the enzymes responsible for both the assembly and cleavage of the acylated peptide prodrug scaffolds is provided. This process involves the assembly of N-acyl-polyglutamine moieties orchestrated by the nonribosomal peptide synthetase DidA and the cleavage of these components at the post-assembly stage by DidK, a transmembrane CAAX hydrolase homolog. The findings not only shed light on the complex prodrug mechanism that underlies the synthesis and secretion of didemnin compounds but also offer novel insights into the expanded role of CAAX hydrolases in microbes. Furthermore,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5d582590</guid>
      <pubDate>Tue, 4 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Zou, Xiaolin</name>
      </author>
      <author>
        <name>Hui, Zhen</name>
      </author>
      <author>
        <name>Shepherd, Robert A</name>
      </author>
      <author>
        <name>Zhao, Shuaiqiang</name>
      </author>
      <author>
        <name>Wu, Yanfei</name>
      </author>
      <author>
        <name>Shen, Zhuanglin</name>
      </author>
      <author>
        <name>Pang, Cuiping</name>
      </author>
      <author>
        <name>Zhou, Shipeng</name>
      </author>
      <author>
        <name>Yu, Zehai</name>
      </author>
      <author>
        <name>Zhou, Jiahai</name>
      </author>
      <author>
        <name>Moore, Bradley S</name>
      </author>
      <author>
        <name>Sanchez, Laura M</name>
        <uri>https://orcid.org/0000-0001-9223-7977</uri>
      </author>
      <author>
        <name>Tang, Xiaoyu</name>
      </author>
    </item>
    <item>
      <title>Enrichable consortia of microbial symbionts degrade macroalgal polysaccharides in Kyphosus fish</title>
      <link>https://escholarship.org/uc/item/0f55z6gq</link>
      <description>Coastal herbivorous fishes consume macroalgae, which is then degraded by microbes along their digestive tract. However, there is scarce genomic information about the microbiota that perform this degradation. This study explores the potential of &lt;i&gt;Kyphosus&lt;/i&gt; gastrointestinal microbial symbionts to collaboratively degrade and ferment polysaccharides from red, green, and brown macroalgae through &lt;i&gt;in silico&lt;/i&gt; study of carbohydrate-active enzyme and sulfatase sequences. Recovery of metagenome-assembled genomes (MAGs) from previously described &lt;i&gt;Kyphosus&lt;/i&gt; gut metagenomes and newly sequenced bioreactor enrichments reveals differences in enzymatic capabilities between the major microbial taxa in &lt;i&gt;Kyphosus&lt;/i&gt; guts. The most versatile of the recovered MAGs were from the &lt;i&gt;Bacteroidota&lt;/i&gt; phylum, whose MAGs house enzyme collections able to decompose a variety of algal polysaccharides. Unique enzymes and predicted degradative capacities of genomes from the &lt;i&gt;Bacillota&lt;/i&gt;...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0f55z6gq</guid>
      <pubDate>Mon, 27 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Oliver, Aaron</name>
        <uri>https://orcid.org/0000-0002-0410-8284</uri>
      </author>
      <author>
        <name>Podell, Sheila</name>
      </author>
      <author>
        <name>Kelly, Linda Wegley</name>
      </author>
      <author>
        <name>Sparagon, Wesley J</name>
      </author>
      <author>
        <name>Plominsky, Alvaro M</name>
      </author>
      <author>
        <name>Nelson, Robert S</name>
      </author>
      <author>
        <name>Laurens, Lieve ML</name>
      </author>
      <author>
        <name>Augyte, Simona</name>
      </author>
      <author>
        <name>Sims, Neil A</name>
      </author>
      <author>
        <name>Nelson, Craig E</name>
      </author>
      <author>
        <name>Allen, Eric E</name>
        <uri>https://orcid.org/0000-0002-1229-8794</uri>
      </author>
    </item>
    <item>
      <title>AI is a viable alternative to high throughput screening: a 318-target study</title>
      <link>https://escholarship.org/uc/item/61v3z0qq</link>
      <description>High throughput screening (HTS) is routinely used to identify bioactive small molecules. This requires physical compounds, which limits coverage of accessible chemical space. Computational approaches combined with vast on-demand chemical libraries can access far greater chemical space, provided that the predictive accuracy is sufficient to identify useful molecules. Through the largest and most diverse virtual HTS campaign reported to date, comprising 318 individual projects, we demonstrate that our AtomNet® convolutional neural network successfully finds novel hits across every major therapeutic area and protein class. We address historical limitations of computational screening by demonstrating success for target proteins without known binders, high-quality X-ray crystal structures, or manual cherry-picking of compounds. We show that the molecules selected by the AtomNet® model are novel drug-like scaffolds rather than minor modifications to known bioactive compounds. Our empirical...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/61v3z0qq</guid>
      <pubDate>Wed, 22 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Wallach, Izhar</name>
      </author>
      <author>
        <name>Bernard, Denzil</name>
      </author>
      <author>
        <name>Nguyen, Kong</name>
      </author>
      <author>
        <name>Ho, Gregory</name>
      </author>
      <author>
        <name>Morrison, Adrian</name>
      </author>
      <author>
        <name>Stecula, Adrian</name>
      </author>
      <author>
        <name>Rosnik, Andreana</name>
      </author>
      <author>
        <name>O’Sullivan, Ann Marie</name>
      </author>
      <author>
        <name>Davtyan, Aram</name>
      </author>
      <author>
        <name>Samudio, Ben</name>
      </author>
      <author>
        <name>Thomas, Bill</name>
      </author>
      <author>
        <name>Worley, Brad</name>
      </author>
      <author>
        <name>Butler, Brittany</name>
      </author>
      <author>
        <name>Laggner, Christian</name>
      </author>
      <author>
        <name>Thayer, Desiree</name>
      </author>
      <author>
        <name>Moharreri, Ehsan</name>
      </author>
      <author>
        <name>Friedland, Greg</name>
      </author>
      <author>
        <name>Truong, Ha</name>
      </author>
      <author>
        <name>van den Bedem, Henry</name>
      </author>
      <author>
        <name>Ng, Ho Leung</name>
      </author>
      <author>
        <name>Stafford, Kate</name>
      </author>
      <author>
        <name>Sarangapani, Krishna</name>
      </author>
      <author>
        <name>Giesler, Kyle</name>
      </author>
      <author>
        <name>Ngo, Lien</name>
      </author>
      <author>
        <name>Mysinger, Michael</name>
      </author>
      <author>
        <name>Ahmed, Mostafa</name>
      </author>
      <author>
        <name>Anthis, Nicholas J</name>
      </author>
      <author>
        <name>Henriksen, Niel</name>
      </author>
      <author>
        <name>Gniewek, Pawel</name>
      </author>
      <author>
        <name>Eckert, Sam</name>
      </author>
      <author>
        <name>de Oliveira, Saulo</name>
      </author>
      <author>
        <name>Suterwala, Shabbir</name>
      </author>
      <author>
        <name>PrasadPrasad, Srimukh Veccham Krishna</name>
      </author>
      <author>
        <name>Shek, Stefani</name>
      </author>
      <author>
        <name>Contreras, Stephanie</name>
      </author>
      <author>
        <name>Hare, Stephanie</name>
      </author>
      <author>
        <name>Palazzo, Teresa</name>
      </author>
      <author>
        <name>O’Brien, Terrence E</name>
      </author>
      <author>
        <name>Van Grack, Tessa</name>
      </author>
      <author>
        <name>Williams, Tiffany</name>
      </author>
      <author>
        <name>Chern, Ting-Rong</name>
      </author>
      <author>
        <name>Kenyon, Victor</name>
      </author>
      <author>
        <name>Lee, Andreia H</name>
      </author>
      <author>
        <name>Cann, Andrew B</name>
      </author>
      <author>
        <name>Bergman, Bastiaan</name>
      </author>
      <author>
        <name>Anderson, Brandon M</name>
      </author>
      <author>
        <name>Cox, Bryan D</name>
      </author>
      <author>
        <name>Warrington, Jeffrey M</name>
      </author>
      <author>
        <name>Sorenson, Jon M</name>
      </author>
      <author>
        <name>Goldenberg, Joshua M</name>
      </author>
      <author>
        <name>Young, Matthew A</name>
      </author>
      <author>
        <name>DeHaan, Nicholas</name>
      </author>
      <author>
        <name>Pemberton, Ryan P</name>
      </author>
      <author>
        <name>Schroedl, Stefan</name>
      </author>
      <author>
        <name>Abramyan, Tigran M</name>
      </author>
      <author>
        <name>Gupta, Tushita</name>
      </author>
      <author>
        <name>Mysore, Venkatesh</name>
      </author>
      <author>
        <name>Presser, Adam G</name>
      </author>
      <author>
        <name>Ferrando, Adolfo A</name>
      </author>
      <author>
        <name>Andricopulo, Adriano D</name>
      </author>
      <author>
        <name>Ghosh, Agnidipta</name>
      </author>
      <author>
        <name>Ayachi, Aicha Gharbi</name>
      </author>
      <author>
        <name>Mushtaq, Aisha</name>
      </author>
      <author>
        <name>Shaqra, Ala M</name>
      </author>
      <author>
        <name>Toh, Alan Kie Leong</name>
      </author>
      <author>
        <name>Smrcka, Alan V</name>
      </author>
      <author>
        <name>Ciccia, Alberto</name>
      </author>
      <author>
        <name>de Oliveira, Aldo Sena</name>
      </author>
      <author>
        <name>Sverzhinsky, Aleksandr</name>
      </author>
      <author>
        <name>de Sousa, Alessandra Mara</name>
      </author>
      <author>
        <name>Agoulnik, Alexander I</name>
      </author>
      <author>
        <name>Kushnir, Alexander</name>
      </author>
      <author>
        <name>Freiberg, Alexander N</name>
      </author>
      <author>
        <name>Statsyuk, Alexander V</name>
      </author>
      <author>
        <name>Gingras, Alexandre R</name>
      </author>
      <author>
        <name>Degterev, Alexei</name>
      </author>
      <author>
        <name>Tomilov, Alexey</name>
      </author>
      <author>
        <name>Vrielink, Alice</name>
      </author>
      <author>
        <name>Garaeva, Alisa A</name>
      </author>
      <author>
        <name>Bryant-Friedrich, Amanda</name>
      </author>
      <author>
        <name>Caflisch, Amedeo</name>
      </author>
      <author>
        <name>Patel, Amit K</name>
      </author>
      <author>
        <name>Rangarajan, Amith Vikram</name>
      </author>
      <author>
        <name>Matheeussen, An</name>
      </author>
      <author>
        <name>Battistoni, Andrea</name>
      </author>
      <author>
        <name>Caporali, Andrea</name>
      </author>
      <author>
        <name>Chini, Andrea</name>
      </author>
      <author>
        <name>Ilari, Andrea</name>
      </author>
      <author>
        <name>Mattevi, Andrea</name>
      </author>
      <author>
        <name>Foote, Andrea Talbot</name>
      </author>
      <author>
        <name>Trabocchi, Andrea</name>
      </author>
      <author>
        <name>Stahl, Andreas</name>
      </author>
      <author>
        <name>Herr, Andrew B</name>
      </author>
      <author>
        <name>Berti, Andrew</name>
      </author>
      <author>
        <name>Freywald, Andrew</name>
      </author>
      <author>
        <name>Reidenbach, Andrew G</name>
      </author>
      <author>
        <name>Lam, Andrew</name>
      </author>
      <author>
        <name>Cuddihy, Andrew R</name>
      </author>
      <author>
        <name>White, Andrew</name>
      </author>
      <author>
        <name>Taglialatela, Angelo</name>
      </author>
    </item>
    <item>
      <title>Optimization of cancer immunotherapy on the basis of programmed death ligand‐1 distribution and function</title>
      <link>https://escholarship.org/uc/item/7gc267fv</link>
      <description>Programmed cell death protein-1 (PD-1)/programmed death ligand-1 (PD-L1) immune checkpoint blockade as a breakthrough in cancer immunotherapy has shown unprecedented positive outcomes in the clinic. However, the overall effectiveness of PD-L1 antibody is less than expected. An increasing number of studies have demonstrated that PD-L1 is widely distributed and expressed not only on the cell membrane but also on the inside of the cells as well as on the extracellular vesicles secreted by tumour cells. Both endogenous and exogenous PD-L1 play significant roles in influencing the therapeutic effect of anti-tumour immunity. Herein, we mainly focused on the distribution and function of PD-L1 and further summarized the potential targeted therapeutic strategies. More importantly, in addition to taking the overall expression abundance of PD-L1 as a predictive indicator for selecting corresponding PD-1/PD-L1 monoclonal antibodies (mAbs), we also proposed that personalized combination therapies...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7gc267fv</guid>
      <pubDate>Tue, 21 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Zou, Wei</name>
      </author>
      <author>
        <name>Luo, Xin</name>
      </author>
      <author>
        <name>Gao, Mengyuan</name>
      </author>
      <author>
        <name>Yu, Chang</name>
      </author>
      <author>
        <name>Wan, Xueting</name>
      </author>
      <author>
        <name>Yu, Suyun</name>
      </author>
      <author>
        <name>Wu, Yuanyuan</name>
      </author>
      <author>
        <name>Wang, Aiyun</name>
      </author>
      <author>
        <name>Fenical, William</name>
        <uri>https://orcid.org/0000-0002-8955-1735</uri>
      </author>
      <author>
        <name>Wei, Zhonghong</name>
      </author>
      <author>
        <name>Zhao, Yang</name>
      </author>
      <author>
        <name>Lu, Yin</name>
      </author>
    </item>
    <item>
      <title>Molecular Dynamics Simulations Guide Chimeragenesis and Engineered Control of Chemoselectivity in Diketopiperazine Dimerases</title>
      <link>https://escholarship.org/uc/item/95f898zz</link>
      <description>In the biosynthesis of the tryptophan-linked dimeric diketopiperazines (DKPs), cytochromes P450 selectively couple DKP monomers to generate a variety of intricate and isomeric frameworks. To determine the molecular basis for selectivity of these biocatalysts we obtained a high-resolution crystal structure of selective Csp&lt;sup&gt;2&lt;/sup&gt; -N bond forming dimerase, AspB. Overlay of the AspB structure onto C-C and C-N bond forming homolog NzeB revealed no significant structural variance to explain their divergent chemoselectivities. Molecular dynamics (MD) simulations identified a region of NzeB with increased conformational flexibility relative to AspB, and interchange of this region along with a single active site mutation led to a variant that catalyzes exclusive C-N bond formation. MD simulations also suggest that intermolecular C-C or C-N bond formation results from a change in mechanism, supported experimentally through use of a substrate mimic.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/95f898zz</guid>
      <pubDate>Mon, 13 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Shende, Vikram V</name>
        <uri>https://orcid.org/0000-0001-8396-6297</uri>
      </author>
      <author>
        <name>Harris, Natalia R</name>
      </author>
      <author>
        <name>Sanders, Jacob N</name>
      </author>
      <author>
        <name>Newmister, Sean A</name>
      </author>
      <author>
        <name>Khatri, Yogan</name>
      </author>
      <author>
        <name>Movassaghi, Mohammad</name>
      </author>
      <author>
        <name>Houk, Kendall N</name>
      </author>
      <author>
        <name>Sherman, David H</name>
      </author>
    </item>
    <item>
      <title>Harnessing the power within: engineering the microbiome for enhanced gynecologic health</title>
      <link>https://escholarship.org/uc/item/9np4t85v</link>
      <description>Abstract: Although numerous studies have demonstrated the impact of microbiome manipulation on human health, research on the microbiome's influence on female health remains relatively limited despite substantial disease burden. In light of this, we present a selected review of clinical trials and preclinical studies targeting both the vaginal and gut microbiomes for the prevention or treatment of various gynecologic conditions. Specifically, we explore studies that leverage microbiota transplants, probiotics, prebiotics, diet modifications, and engineered microbial strains. A healthy vaginal microbiome for females of reproductive age consists of lactic acid-producing bacteria predominantly of the Lactobacillus genus, which serves as a protective barrier against pathogens and maintains a balanced ecosystem. The gut microbiota's production of short-chain fatty acids, metabolism of primary bile acids, and modulation of sex steroid levels have significant implications for the interplay...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9np4t85v</guid>
      <pubDate>Mon, 6 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Brennan, Caitriona</name>
        <uri>https://orcid.org/0000-0003-3943-6701</uri>
      </author>
      <author>
        <name>Chan, Kristina</name>
      </author>
      <author>
        <name>Kumar, Tanya</name>
      </author>
      <author>
        <name>Maissy, Erica</name>
      </author>
      <author>
        <name>Brubaker, Linda</name>
      </author>
      <author>
        <name>Dothard, Marisol I</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0002-7733-2033</uri>
      </author>
      <author>
        <name>Gilbert, Katharine E</name>
      </author>
      <author>
        <name>Lewis, Amanda L</name>
      </author>
      <author>
        <name>Thackray, Varykina G</name>
      </author>
      <author>
        <name>Zarrinpar, Amir</name>
        <uri>https://orcid.org/0000-0001-6423-5982</uri>
      </author>
      <author>
        <name>Knight, Rob</name>
        <uri>https://orcid.org/0000-0002-0975-9019</uri>
      </author>
    </item>
    <item>
      <title>Inflammatory Dietary Potential Is Associated with Vitamin Depletion and Gut Microbial Dysbiosis in Early Pregnancy</title>
      <link>https://escholarship.org/uc/item/8wz6218r</link>
      <description>Pregnancy alters many physiological systems, including the maternal gut microbiota. Diet is a key regulator of this system and can alter the host immune system to promote inflammation. Multiple perinatal disorders have been associated with inflammation, maternal metabolic alterations, and gut microbial dysbiosis, including gestational diabetes mellitus, pre-eclampsia, preterm birth, and mood disorders. However, the effects of high-inflammatory diets on the gut microbiota during pregnancy have yet to be fully explored. We aimed to address this gap using a system-based approach to characterize associations among dietary inflammatory potential, a measure of diet quality, and the gut microbiome during pregnancy. Forty-seven pregnant persons were recruited prior to 16 weeks of gestation. Participants completed a food frequency questionnaire (FFQ) and provided fecal samples. Dietary inflammatory potential was assessed using the Dietary Inflammatory Index (DII) from the FFQ data. Fecal...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8wz6218r</guid>
      <pubDate>Tue, 30 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Alvernaz, Suzanne A</name>
      </author>
      <author>
        <name>Wenzel, Elizabeth S</name>
      </author>
      <author>
        <name>Nagelli, Unnathi</name>
      </author>
      <author>
        <name>Pezley, Lacey B</name>
      </author>
      <author>
        <name>LaBomascus, Bazil</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
      <author>
        <name>Maki, Pauline M</name>
      </author>
      <author>
        <name>Tussing-Humphreys, Lisa</name>
      </author>
      <author>
        <name>Bernabé, Beatriz Peñalver</name>
      </author>
    </item>
    <item>
      <title>Searching for Small Molecules with an Atomic Sort</title>
      <link>https://escholarship.org/uc/item/1q05m9m2</link>
      <description>Abstract: 
The discovery of biologically active small molecules requires sifting through large amounts of data to identify unique or unusual arrangements of atoms. Here, we develop, test and evaluate an atom‐based sort to identify novel features of secondary metabolites and demonstrate its use to evaluate novelty in marine microbial and sponge extracts. This study outlines an important ongoing advance towards the translation of autonomous systems to identify, and ultimately elucidate, atomic novelty within a complex mixture of small molecules.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1q05m9m2</guid>
      <pubDate>Thu, 25 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Duggan, Brendan M</name>
        <uri>https://orcid.org/0000-0002-7034-8374</uri>
      </author>
      <author>
        <name>Cullum, Reiko</name>
      </author>
      <author>
        <name>Fenical, William</name>
        <uri>https://orcid.org/0000-0002-8955-1735</uri>
      </author>
      <author>
        <name>Amador, Luis A</name>
      </author>
      <author>
        <name>Rodríguez, Abimael D</name>
      </author>
      <author>
        <name>La Clair, James J</name>
      </author>
    </item>
    <item>
      <title>Strong selective effects of mitochondrial DNA on the nuclear genome</title>
      <link>https://escholarship.org/uc/item/3zw0j9jj</link>
      <description>Oxidative phosphorylation, the primary source of cellular energy in eukaryotes, requires gene products encoded in both the nuclear and mitochondrial genomes. As a result, functional integration between the genomes is essential for efficient adenosine triphosphate (ATP) generation. Although within populations this integration is presumably maintained by coevolution, the importance of mitonuclear coevolution in key biological processes such as speciation and mitochondrial disease has been questioned. In this study, we crossed populations of the intertidal copepod &lt;i&gt;Tigriopus californicus&lt;/i&gt; to disrupt putatively coevolved mitonuclear genotypes in reciprocal F&lt;sub&gt;2&lt;/sub&gt; hybrids. We utilized interindividual variation in developmental rate among these hybrids as a proxy for fitness to assess the strength of selection imposed on the nuclear genome by alternate mitochondrial genotypes. Developmental rate varied among hybrid individuals, and in vitro ATP synthesis rates of mitochondria...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3zw0j9jj</guid>
      <pubDate>Sun, 7 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Healy, Timothy M</name>
      </author>
      <author>
        <name>Burton, Ronald S</name>
        <uri>https://orcid.org/0000-0002-6995-5329</uri>
      </author>
    </item>
    <item>
      <title>Silhouette showcards confirm altered obesity-associated body image perception in international cohort study of African-origin populations</title>
      <link>https://escholarship.org/uc/item/40t0j425</link>
      <description>OBJECTIVES: Given the increasing prevalence of obesity and need for effective interventions, there is a growing interest in understanding how an individual's body image can inform obesity prevention and management. This study's objective was to examine the use of silhouette showcards to measure body size perception compared with measured body mass index, and assess body size dissatisfaction, in three different African-origin populations spanning the epidemiological transition. An ancillary objective was to investigate associations between body size perception and dissatisfaction with diabetes and hypertension.
SETTING: Research visits were completed in local research clinics in respective countries.
PARTICIPANTS: Seven hundred and fifty-one African-origin participants from the USA and the Republic of Seychelles (both high-income countries), and Ghana (low/middle-income country).
PRIMARY AND SECONDARY OUTCOME MEASURES: Silhouette showcards were used to measure perceived body size...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/40t0j425</guid>
      <pubDate>Fri, 5 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Choo-Kang, Candice</name>
      </author>
      <author>
        <name>Reese, Tyler O</name>
      </author>
      <author>
        <name>Micklesfield, Lisa K</name>
      </author>
      <author>
        <name>Bovet, Pascal</name>
      </author>
      <author>
        <name>Bedu-Addo, Kweku</name>
      </author>
      <author>
        <name>Forrester, Terrence</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
      <author>
        <name>Goedecke, Julia H</name>
      </author>
      <author>
        <name>Plange-Rhule, Jacob</name>
      </author>
      <author>
        <name>Lambert, Estelle V</name>
      </author>
      <author>
        <name>Layden, Brian T</name>
      </author>
      <author>
        <name>Rae, Dale E</name>
      </author>
      <author>
        <name>Viswanathan, Bharathi</name>
      </author>
      <author>
        <name>Luke, Amy</name>
      </author>
      <author>
        <name>Dugas, Lara</name>
      </author>
    </item>
    <item>
      <title>Bacterial diversity and chemical ecology of natural product–producing bacteria from Great Salt Lake sediment</title>
      <link>https://escholarship.org/uc/item/6s6771rp</link>
      <description>Great Salt Lake (GSL), located northwest of Salt Lake City, UT, is the largest terminal lake in the USA. While the average salinity of seawater is ~3.3%, the salinity in GSL ranges between 5% and 28%. In addition to being a hypersaline environment, GSL also contains toxic concentrations of heavy metals, such as arsenic, mercury, and lead. The extreme environment of GSL makes it an intriguing subject of study, both for its unique microbiome and its potential to harbor novel natural product-producing bacteria, which could be used as resources for the discovery of biologically active compounds. Though work has been done to survey and catalog bacteria found in GSL, the Lake's microbiome is largely unexplored, and little to no work has been done to characterize the natural product potential of GSL microbes. Here, we investigate the bacterial diversity of two important regions within GSL, describe the first genomic characterization of Actinomycetota isolated from GSL sediment, including...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6s6771rp</guid>
      <pubDate>Sat, 30 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Horvath, Elijah R Bring</name>
      </author>
      <author>
        <name>Brazelton, William J</name>
      </author>
      <author>
        <name>Kim, Min Cheol</name>
      </author>
      <author>
        <name>Cullum, Reiko</name>
      </author>
      <author>
        <name>Mulvey, Matthew A</name>
      </author>
      <author>
        <name>Fenical, William</name>
        <uri>https://orcid.org/0000-0002-8955-1735</uri>
      </author>
      <author>
        <name>Winter, Jaclyn M</name>
      </author>
    </item>
    <item>
      <title>Structure and Biosynthesis of Hectoramide B, a Linear Depsipeptide from Marine Cyanobacterium Moorena producens JHB Discovered via Coculture with Candida albicans</title>
      <link>https://escholarship.org/uc/item/9qp2375s</link>
      <description>The tropical marine cyanobacterium &lt;i&gt;Moorena producens&lt;/i&gt; JHB is a prolific source of secondary metabolites with potential biomedical utility. Previous studies on this strain led to the discovery of several novel compounds such as hectochlorins and jamaicamides. However, bioinformatic analyses of its genome indicate the presence of numerous cryptic biosynthetic gene clusters that have yet to be characterized. To potentially stimulate the production of novel compounds from this strain, it was cocultured with &lt;i&gt;Candida albicans&lt;/i&gt;. From this experiment, we observed the increased production of a new compound that we characterize here as hectoramide B. Bioinformatic analysis of the &lt;i&gt;M. producens&lt;/i&gt; JHB genome enabled the identification of a putative biosynthetic gene cluster responsible for hectoramide B biosynthesis. This work demonstrates that coculture competition experiments can be a valuable method to facilitate the discovery of novel natural products from cyanobacteria.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9qp2375s</guid>
      <pubDate>Fri, 29 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Ngo, Thuan-Ethan</name>
      </author>
      <author>
        <name>Ecker, Andrew</name>
      </author>
      <author>
        <name>Ryu, Byeol</name>
        <uri>https://orcid.org/0000-0002-3405-2875</uri>
      </author>
      <author>
        <name>Guild, Aurora</name>
      </author>
      <author>
        <name>Remmel, Ariana</name>
      </author>
      <author>
        <name>Boudreau, Paul D</name>
      </author>
      <author>
        <name>Alexander, Kelsey L</name>
      </author>
      <author>
        <name>Naman, C Benjamin</name>
      </author>
      <author>
        <name>Glukhov, Evgenia</name>
      </author>
      <author>
        <name>Avalon, Nicole E</name>
      </author>
      <author>
        <name>Shende, Vikram V</name>
        <uri>https://orcid.org/0000-0001-8396-6297</uri>
      </author>
      <author>
        <name>Thomas, Lamar</name>
      </author>
      <author>
        <name>Dahesh, Samira</name>
      </author>
      <author>
        <name>Nizet, Victor</name>
      </author>
      <author>
        <name>Gerwick, Lena</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
        <uri>https://orcid.org/0000-0003-1403-4458</uri>
      </author>
    </item>
    <item>
      <title>PECAN Predicts Patterns of Cancer Cell Cytostatic Activity of Natural Products Using Deep Learning</title>
      <link>https://escholarship.org/uc/item/7gr9853s</link>
      <description>Many machine learning techniques are used as drug discovery tools with the intent to speed characterization by determining relationships between compound structure and biological function. However, particularly in anticancer drug discovery, these models often make only binary decisions about the biological activity for a narrow scope of drug targets. We present a feed-forward neural network, PECAN (Prediction Engine for the Cytostatic Activity of Natural product-like compounds), that simultaneously classifies the potential antiproliferative activity of compounds against 59 cancer cell lines. It predicts the activity to be one of six categories, indicating not only if activity is present but the degree of activity. Using an independent subset of NCI data as a test set, we show that PECAN can reach 60.1% accuracy in a six-way classification and present further evidence that it classifies based on useful structural features of compounds using a "within-one" measure that reaches 93.0%...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7gr9853s</guid>
      <pubDate>Fri, 29 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Gahl, Martha</name>
      </author>
      <author>
        <name>Kim, Hyun Woo</name>
      </author>
      <author>
        <name>Glukhov, Evgenia</name>
      </author>
      <author>
        <name>Gerwick, William H</name>
      </author>
      <author>
        <name>Cottrell, Garrison W</name>
        <uri>https://orcid.org/0000-0001-7538-1715</uri>
      </author>
    </item>
    <item>
      <title>Synthesis of π‐Conjugated Chiral Aza/Boracyclophanes with a meta and para Substitution</title>
      <link>https://escholarship.org/uc/item/4731n94d</link>
      <description>We herein describe the synthesis of a new class of axially chiral aza/boracyclophanes (BDN1, BXN1, BDB1 and BXB1) using binaphthyls as chiral building blocks and the main-group (B/N) chemistry with tunable electronic effects. All macrocycles substituted with triarylamine donors or triarylborane acceptors are strongly luminescent. These macrocycles showed two distinct meta and para π-conjugation pathways, leading to the formation of quasi figure-of-eight and square-shaped conformations. Interestingly, comparison of such structural models revealed that the former type of macrocycles BXN1 and BXB1 gave higher racemization barriers relative to the other ones. The results reported here may provide a new approach to engineer the optical stability of π-conjugated chiral macrocycles by controlling π-substitution patterns. The ring constraints induced by macrocyclization were also demonstrated to contribute to the configurational persistence as compared with the open-chain analogues p-BTT...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4731n94d</guid>
      <pubDate>Thu, 21 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Kai</name>
      </author>
      <author>
        <name>Hao, Mengyao</name>
      </author>
      <author>
        <name>Jin, Tianyun</name>
      </author>
      <author>
        <name>Shi, Yafei</name>
      </author>
      <author>
        <name>Tian, Guoqing</name>
      </author>
      <author>
        <name>Li, Chenglong</name>
      </author>
      <author>
        <name>Ma, Hongwei</name>
      </author>
      <author>
        <name>Zhang, Niu</name>
      </author>
      <author>
        <name>Li, Quansong</name>
      </author>
      <author>
        <name>Chen, Pangkuan</name>
      </author>
    </item>
    <item>
      <title>Polycationic Open‐Shell Cyclophanes: Synthesis of Electron‐Rich Chiral Macrocycles, and Redox‐Dependent Electronic States</title>
      <link>https://escholarship.org/uc/item/2247j6mg</link>
      <description>π‐Conjugated chiral nanorings with intriguing electronic structures and chiroptical properties have attracted considerable interests in synthetic chemistry and materials science. We present the design principles to access new chiral macrocycles (1 and 2) that are essentially built on the key components of main‐group electron‐donating carbazolyl moieties or the π‐expanded aza[7]helicenes. Both macrocycles show the unique molecular conformations with a (quasi) figure‐of‐eight topology as a result of the conjugation patterns of 2,2’,7,7’‐spirobifluorenyl in 1 and triarylamine‐coupled aza[7]helicene‐based building blocks in 2. This electronic nature of redox‐active, carbazole‐rich backbones enabled these macrocycles to be readily oxidized chemically and electrochemically, leading to the sequential production of a series of positively charged polycationic open‐shell cyclophanes. Their redox‐dependent electronic states of the resulting multispin polyradicals have been characterized...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2247j6mg</guid>
      <pubDate>Thu, 21 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Shi, Yafei</name>
      </author>
      <author>
        <name>Li, Chenglong</name>
      </author>
      <author>
        <name>Di, Jiaqi</name>
      </author>
      <author>
        <name>Xue, Yuting</name>
      </author>
      <author>
        <name>Jia, Yawei</name>
      </author>
      <author>
        <name>Duan, Jiaxian</name>
      </author>
      <author>
        <name>Hu, Xiaoyu</name>
      </author>
      <author>
        <name>Tian, Yu</name>
      </author>
      <author>
        <name>Li, Yanqiu</name>
      </author>
      <author>
        <name>Sun, Cuiping</name>
      </author>
      <author>
        <name>Zhang, Niu</name>
      </author>
      <author>
        <name>Xiong, Yan</name>
      </author>
      <author>
        <name>Jin, Tianyun</name>
      </author>
      <author>
        <name>Chen, Pangkuan</name>
      </author>
    </item>
    <item>
      <title>Polycationic Open‐Shell Cyclophanes: Synthesis of Electron‐Rich Chiral Macrocycles, and Redox‐Dependent Electronic States</title>
      <link>https://escholarship.org/uc/item/14q3j0k6</link>
      <description>π-Conjugated chiral nanorings with intriguing electronic structures and chiroptical properties have attracted considerable interests in synthetic chemistry and materials science. We present the design principles to access new chiral macrocycles (1 and 2) that are essentially built on the key components of main-group electron-donating carbazolyl moieties or the π-expanded aza[7]helicenes. Both macrocycles show the unique molecular conformations with a (quasi) figure-of-eight topology as a result of the conjugation patterns of 2,2',7,7'-spirobifluorenyl in 1 and triarylamine-coupled aza[7]helicene-based building blocks in 2. This electronic nature of redox-active, carbazole-rich backbones enabled these macrocycles to be readily oxidized chemically and electrochemically, leading to the sequential production of a series of positively charged polycationic open-shell cyclophanes. Their redox-dependent electronic states of the resulting multispin polyradicals have been characterized...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/14q3j0k6</guid>
      <pubDate>Thu, 21 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Shi, Yafei</name>
      </author>
      <author>
        <name>Li, Chenglong</name>
      </author>
      <author>
        <name>Di, Jiaqi</name>
      </author>
      <author>
        <name>Xue, Yuting</name>
      </author>
      <author>
        <name>Jia, Yawei</name>
      </author>
      <author>
        <name>Duan, Jiaxian</name>
      </author>
      <author>
        <name>Hu, Xiaoyu</name>
      </author>
      <author>
        <name>Tian, Yu</name>
      </author>
      <author>
        <name>Li, Yanqiu</name>
      </author>
      <author>
        <name>Sun, Cuiping</name>
      </author>
      <author>
        <name>Zhang, Niu</name>
      </author>
      <author>
        <name>Xiong, Yan</name>
      </author>
      <author>
        <name>Jin, Tianyun</name>
      </author>
      <author>
        <name>Chen, Pangkuan</name>
      </author>
    </item>
    <item>
      <title>Development of Potent and Highly Selective Epoxyketone‐Based Plasmodium Proteasome Inhibitors</title>
      <link>https://escholarship.org/uc/item/6x99c667</link>
      <description>Here, we present remarkable epoxyketone-based proteasome inhibitors with low nanomolar in vitro potency for blood-stage Plasmodium falciparum and low cytotoxicity for human cells. Our best compound has more than 2,000-fold greater selectivity for erythrocytic-stage P. falciparum over HepG2 and H460 cells, which is largely driven by the accommodation of the parasite proteasome for a D-amino acid in the P3 position and the preference for a difluorobenzyl group in the P1 position. We isolated the proteasome from P. falciparum cell extracts and determined that the best compound is 171-fold more potent at inhibiting the β5 subunit of P. falciparum proteasome when compared to the same subunit of the human constitutive proteasome. These compounds also significantly reduce parasitemia in a P. berghei mouse infection model and prolong survival of animals by an average of 6 days. The current epoxyketone inhibitors are ideal starting compounds for orally bioavailable anti-malarial drugs.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6x99c667</guid>
      <pubDate>Tue, 12 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Almaliti, Jehad</name>
      </author>
      <author>
        <name>Fajtová, Pavla</name>
      </author>
      <author>
        <name>Calla, Jaeson</name>
      </author>
      <author>
        <name>LaMonte, Gregory M</name>
      </author>
      <author>
        <name>Feng, Mudong</name>
      </author>
      <author>
        <name>Rocamora, Frances</name>
      </author>
      <author>
        <name>Ottilie, Sabine</name>
      </author>
      <author>
        <name>Glukhov, Evgenia</name>
      </author>
      <author>
        <name>Boura, Evzen</name>
      </author>
      <author>
        <name>Suhandynata, Raymond T</name>
        <uri>https://orcid.org/0000-0002-4767-7639</uri>
      </author>
      <author>
        <name>Momper, Jeremiah D</name>
      </author>
      <author>
        <name>Gilson, Michael K</name>
      </author>
      <author>
        <name>Winzeler, Elizabeth A</name>
        <uri>https://orcid.org/0000-0002-4049-2113</uri>
      </author>
      <author>
        <name>Gerwick, William H</name>
        <uri>https://orcid.org/0000-0003-1403-4458</uri>
      </author>
      <author>
        <name>O'Donoghue, Anthony J</name>
      </author>
    </item>
    <item>
      <title>Biocontrol in built environments to reduce pathogen exposure and infection risk</title>
      <link>https://escholarship.org/uc/item/94f3m7w2</link>
      <description>The microbiome of the built environment comprises bacterial, archaeal, fungal, and viral communities associated with human-made structures. Even though most of these microbes are benign, antibiotic-resistant pathogens can colonize and emerge indoors, creating infection risk through surface transmission or inhalation. Several studies have catalogued the microbial composition and ecology in different built environment types. These have informed in vitro studies that seek to replicate the physicochemical features that promote pathogenic survival and transmission, ultimately facilitating the development and validation of intervention techniques used to reduce pathogen accumulation. Such interventions include using Bacillus-based cleaning products on surfaces or integrating bacilli into printable materials. Though this work is in its infancy, early research suggests the potential to use microbial biocontrol to reduce hospital- and home-acquired multidrug-resistant infections. Although...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/94f3m7w2</guid>
      <pubDate>Wed, 6 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Gottel, Neil R</name>
      </author>
      <author>
        <name>Hill, Megan S</name>
      </author>
      <author>
        <name>Neal, Maxwell J</name>
        <uri>https://orcid.org/0009-0009-6284-3656</uri>
      </author>
      <author>
        <name>Allard, Sarah M</name>
        <uri>https://orcid.org/0000-0001-7626-0472</uri>
      </author>
      <author>
        <name>Zengler, Karsten</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
    </item>
    <item>
      <title>Sodium oligomannate alters gut microbiota, reduces cerebral amyloidosis and reactive microglia in a sex-specific manner</title>
      <link>https://escholarship.org/uc/item/7mr5s3s5</link>
      <description>It has recently become well-established that there is a connection between Alzheimer’s disease pathology and gut microbiome dysbiosis. We have previously demonstrated that antibiotic-mediated gut microbiota perturbations lead to attenuation of Aβ deposition, phosphorylated tau accumulation, and disease-associated glial cell phenotypes in a sex-dependent manner. In this regard, we were intrigued by the finding that a marine-derived oligosaccharide, GV-971, was reported to alter gut microbiota and reduce Aβ amyloidosis in the 5XFAD mouse model that were treated at a point when Aβ burden was near plateau levels.&amp;nbsp;Utilizing comparable methodologies, but with distinct technical and temporal features, we now report on the impact of GV-971 on gut microbiota, Aβ amyloidosis and microglial phenotypes in the APPPS1-21 model, studies performed at the University of Chicago, and independently in the 5X FAD model, studies performed at Washington University, St. Louis.Methods To comprehensively...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7mr5s3s5</guid>
      <pubDate>Sat, 2 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Bosch, Megan E</name>
      </author>
      <author>
        <name>Dodiya, Hemraj B</name>
      </author>
      <author>
        <name>Michalkiewicz, Julia</name>
      </author>
      <author>
        <name>Lee, Choonghee</name>
      </author>
      <author>
        <name>Shaik, Shabana M</name>
      </author>
      <author>
        <name>Weigle, Ian Q</name>
      </author>
      <author>
        <name>Zhang, Can</name>
      </author>
      <author>
        <name>Osborn, Jack</name>
      </author>
      <author>
        <name>Nambiar, Aishwarya</name>
      </author>
      <author>
        <name>Patel, Priyam</name>
      </author>
      <author>
        <name>Parhizkar, Samira</name>
      </author>
      <author>
        <name>Zhang, Xiaoqiong</name>
      </author>
      <author>
        <name>Laury, Marie L</name>
      </author>
      <author>
        <name>Mondal, Prasenjit</name>
      </author>
      <author>
        <name>Gomm, Ashley</name>
      </author>
      <author>
        <name>Schipma, Matthew John</name>
      </author>
      <author>
        <name>Mallah, Dania</name>
      </author>
      <author>
        <name>Butovsky, Oleg</name>
      </author>
      <author>
        <name>Chang, Eugene B</name>
      </author>
      <author>
        <name>Tanzi, Rudolph E</name>
      </author>
      <author>
        <name>Gilbert, Jack A</name>
        <uri>https://orcid.org/0000-0001-7920-7001</uri>
      </author>
      <author>
        <name>Holtzman, David M</name>
      </author>
      <author>
        <name>Sisodia, Sangram S</name>
      </author>
    </item>
    <item>
      <title>Red-Shifted Coumarin Luciferins for Improved Bioluminescence Imaging</title>
      <link>https://escholarship.org/uc/item/3907d94k</link>
      <description>Multicomponent bioluminescence imaging &lt;i&gt;in vivo&lt;/i&gt; requires an expanded collection of tissue-penetrant probes. Toward this end, we generated a new class of near-infrared (NIR) emitting coumarin luciferin analogues (CouLuc-3s). The scaffolds were easily accessed from commercially available dyes. Complementary mutant luciferases for the CouLuc-3 analogues were also identified. The brightest probes enabled sensitive imaging &lt;i&gt;in vivo&lt;/i&gt;. The CouLuc-3 scaffolds are also orthogonal to popular bioluminescent reporters and can be used for multicomponent imaging applications. Collectively, this work showcases a new set of bioluminescent tools that can be readily implemented for multiplexed imaging in a variety of biological settings.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3907d94k</guid>
      <pubDate>Fri, 1 Mar 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Love, Anna C</name>
        <uri>https://orcid.org/0000-0001-5657-2858</uri>
      </author>
      <author>
        <name>Caldwell, Donald R</name>
      </author>
      <author>
        <name>Kolbaba-Kartchner, Bethany</name>
      </author>
      <author>
        <name>Townsend, Katherine M</name>
      </author>
      <author>
        <name>Halbers, Lila P</name>
      </author>
      <author>
        <name>Yao, Zi</name>
      </author>
      <author>
        <name>Brennan, Caroline K</name>
      </author>
      <author>
        <name>Ivanic, Joseph</name>
      </author>
      <author>
        <name>Hadjian, Tanya</name>
      </author>
      <author>
        <name>Mills, Jeremy H</name>
      </author>
      <author>
        <name>Schnermann, Martin J</name>
      </author>
      <author>
        <name>Prescher, Jennifer A</name>
        <uri>https://orcid.org/0000-0002-9250-4702</uri>
      </author>
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