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Quorum Sensing Regulates the Production of Methanethiol in Vibrio harveyi.
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- Microorganisms, 2024, v. 12, n. 1, p. 35, doi. 10.3390/microorganisms12010035
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Deep-sea Bacteroidetes from the Mariana Trench specialize in hemicellulose and pectin degradation typically associated with terrestrial systems.
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- Microbiome, 2023, v. 11, n. 1, p. 1, doi. 10.1186/s40168-023-01618-7
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A new dimethylsulfoniopropionate lyase of the cupin superfamily in marine bacteria.
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- Environmental Microbiology, 2023, v. 25, n. 7, p. 1238, doi. 10.1111/1462-2920.16355
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Characterisation of a soil MINPP phytase with remarkable long-term stability and activity from Acinetobacter sp.
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- PLoS ONE, 2022, v. 17, n. 8, p. 1, doi. 10.1371/journal.pone.0272015
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Oceanospirillales containing the DMSP lyase DddD are key utilisers of carbon from DMSP in coastal seawater.
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- Microbiome, 2022, v. 10, n. 1, p. 1, doi. 10.1186/s40168-022-01304-0
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Insights into methionine S-methylation in diverse organisms.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30491-5
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Spatiotemporal distribution of bacterial dimethylsulfoniopropionate producing and catabolic genes in the Changjiang Estuary.
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- Environmental Microbiology, 2021, v. 23, n. 11, p. 7073, doi. 10.1111/1462-2920.15813
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Dimethylsulfoniopropionate Biosynthetic Bacteria in the Subseafloor Sediments of the South China Sea.
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- Frontiers in Microbiology, 2021, p. 1, doi. 10.3389/fmicb.2021.731524
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DiTing: A Pipeline to Infer and Compare Biogeochemical Pathways From Metagenomic and Metatranscriptomic Data.
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- Frontiers in Microbiology, 2021, v. 12, p. 1, doi. 10.3389/fmicb.2021.698286
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Improved sensitivity, accuracy and prediction provided by a high‐performance liquid chromatography screen for the isolation of phytase‐harbouring organisms from environmental samples.
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- Microbial Biotechnology, 2021, v. 14, n. 4, p. 1409, doi. 10.1111/1751-7915.13733
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A novel ATP dependent dimethylsulfoniopropionate lyase in bacteria that releases dimethyl sulfide and acryloyl-CoA.
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- eLife, 2021, p. 1, doi. 10.7554/eLife.64045
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Bacterial Dimethylsulfoniopropionate Biosynthesis in the East China Sea.
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- Microorganisms, 2021, v. 9, n. 3, p. 657, doi. 10.3390/microorganisms9030657
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Bacteria are important dimethylsulfoniopropionate producers in marine aphotic and high-pressure environments.
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- Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-18434-4
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Insights into the Vertical Stratification of Microbial Ecological Roles across the Deepest Seawater Column on Earth.
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- Microorganisms, 2020, v. 8, n. 9, p. 1309, doi. 10.3390/microorganisms8091309
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DMSP-Producing Bacteria Are More Abundant in the Surface Microlayer than Subsurface Seawater of the East China Sea.
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- Microbial Ecology, 2020, v. 80, n. 2, p. 350, doi. 10.1007/s00248-020-01507-8
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Novel insights into the Thaumarchaeota in the deepest oceans: their metabolism and potential adaptation mechanisms.
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- Microbiome, 2020, v. 8, n. 1, p. 1, doi. 10.1186/s40168-020-00849-2
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Metagenomic Insights Into the Cycling of Dimethylsulfoniopropionate and Related Molecules in the Eastern China Marginal Seas.
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- Frontiers in Microbiology, 2020, p. 1, doi. 10.3389/fmicb.2020.00157
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The Production and Fate of Volatile Organosulfur Compounds in Sulfidic and Ferruginous Sediment.
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- Journal of Geophysical Research. Biogeosciences, 2019, v. 124, n. 11, p. 3390, doi. 10.1029/2019JG005248
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Biogenic production of DMSP and its degradation to DMS—their roles in the global sulfur cycle.
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- SCIENCE CHINA Life Sciences, 2019, v. 62, n. 10, p. 1296, doi. 10.1007/s11427-018-9524-y
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Biosynthesis of CdS Quantum Dots Mediated by Volatile Sulfur Compounds Released by Antarctic Pseudomonas fragi.
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- Frontiers in Microbiology, 2019, p. 1, doi. 10.3389/fmicb.2019.01866
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Methanethiol and Dimethylsulfide Cycling in Stiffkey Saltmarsh.
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- Frontiers in Microbiology, 2019, p. N.PAG, doi. 10.3389/fmicb.2019.01040
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Proliferation of hydrocarbon-degrading microbes at the bottom of the Mariana Trench.
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- Microbiome, 2019, v. 7, n. 1, p. N.PAG, doi. 10.1186/s40168-019-0652-3
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Mechanistic insight into 3‐methylmercaptopropionate metabolism and kinetical regulation of demethylation pathway in marine dimethylsulfoniopropionate‐catabolizing bacteria.
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- Molecular Microbiology, 2019, v. 111, n. 4, p. 1057, doi. 10.1111/mmi.14211
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Mechanistic insight into acrylate metabolism and detoxification in marine dimethylsulfoniopropionate-catabolizing bacteria.
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- Molecular Microbiology, 2017, v. 105, n. 5, p. 674, doi. 10.1111/mmi.13727
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Recumbent Stepper Submaximal Test response is reliable in adults with and without stroke.
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- PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0172294
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Biochemical, Kinetic, and Spectroscopic Characterization of Ruegeria pomeroyi DddW—A Mononuclear Iron-Dependent DMSP Lyase.
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- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0127288
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Screening of Metagenomic and Genomic Libraries Reveals Three Classes of Bacterial Enzymes That Overcome the Toxicity of Acrylate.
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- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0097660
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Manganese uptake in marine bacteria; the novel MntX transporter is widespread in Roseobacters, Vibrios, Alteromonadales and the SAR11 and SAR116 clades.
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- ISME Journal: Multidisciplinary Journal of Microbial Ecology, 2013, v. 7, n. 3, p. 581, doi. 10.1038/ismej.2012.140
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Phylogenetic diversity of the dddP gene for dimethylsulfoniopropionate-dependent dimethyl sulfide synthesis in mangrove soils.
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- Canadian Journal of Microbiology, 2012, v. 58, n. 4, p. 523, doi. 10.1139/w2012-019
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The Ruegeria pomeroyi acuI Gene Has a Role in DMSP Catabolism and Resembles yhdH of E. coli and Other Bacteria in Conferring Resistance to Acrylate.
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- PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0035947
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DddW, a third DMSP lyase in a model Roseobacter marine bacterium, Ruegeria pomeroyi DSS-3.
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- ISME Journal: Multidisciplinary Journal of Microbial Ecology, 2012, v. 6, n. 1, p. 223, doi. 10.1038/ismej.2011.79
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Catabolism of dimethylsulphoniopropionate: microorganisms, enzymes and genes.
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- Nature Reviews Microbiology, 2011, v. 9, n. 12, p. 849, doi. 10.1038/nrmicro2653
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DddY, a periplasmic dimethylsulfoniopropionate lyase found in taxonomically diverse species of Proteobacteria.
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- ISME Journal: Multidisciplinary Journal of Microbial Ecology, 2011, v. 5, n. 7, p. 1191, doi. 10.1038/ismej.2010.203
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Heme binding to the second, lower-affinity site of the global iron regulator Irr from Rhizobium leguminosarum promotes oligomerization.
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- FEBS Journal, 2011, v. 278, n. 12, p. 2011, doi. 10.1111/j.1742-4658.2011.08117.x
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DddQ, a novel, cupin-containing, dimethylsulfoniopropionate lyase in marine roseobacters and in uncultured marine bacteria.
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- Environmental Microbiology, 2011, v. 13, n. 2, p. 427, doi. 10.1111/j.1462-2920.2010.02348.x
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Unusual Regulation of a Leaderless Operon Involved in the Catabolism of Dimethylsulfoniopropionate in Rhodobacter sphaeroides.
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- PLoS ONE, 2011, v. 6, n. 1, p. 1, doi. 10.1371/journal.pone.0015972
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Molecular dissection of bacterial acrylate catabolism – unexpected links with dimethylsulfoniopropionate catabolism and dimethyl sulfide production.
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- Environmental Microbiology, 2010, v. 12, n. 2, p. 327, doi. 10.1111/j.1462-2920.2009.02071.x
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Identification of genes for dimethyl sulfide production in bacteria in the gut of Atlantic Herring (Clupea harengus).
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- ISME Journal: Multidisciplinary Journal of Microbial Ecology, 2010, v. 4, n. 1, p. 144, doi. 10.1038/ismej.2009.93
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The opportunistic coral pathogen Aspergillus sydowii contains dddP and makes dimethyl sulfide from dimethylsulfoniopropionate.
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- ISME Journal: Multidisciplinary Journal of Microbial Ecology, 2010, v. 4, n. 1, p. 147, doi. 10.1038/ismej.2009.102
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Molecular diversity of bacterial production of the climate-changing gas, dimethyl sulphide, a molecule that impinges on local and global symbioses.
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- Journal of Experimental Botany, 2008, v. 59, n. 5, p. 1059, doi. 10.1093/jxb/erm264
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Computational Reconstruction of Iron- and Manganese-Responsive Transcriptional Networks in α-Proteobacteria.
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- PLoS Computational Biology, 2006, v. 2, n. 12, p. 1568, doi. 10.1371/journal.pcbi.0020163
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Proteomic analysis reveals the wide-ranging effects of the novel, iron-responsive regulator RirA in Rhizobium leguminosarum bv. viciae.
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- Molecular Genetics & Genomics, 2005, v. 273, n. 2, p. 197, doi. 10.1007/s00438-005-1127-8
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