Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/119350
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dc.contributor.authorMartín Rodríguez, Alberto Jonatanen_US
dc.contributor.authorHigdon, Shawn M.en_US
dc.contributor.authorThorell, Kaisaen_US
dc.contributor.authorTellgren-Roth, Christianen_US
dc.contributor.authorSjöling, Åsaen_US
dc.contributor.authorGalperin, Michael Y.en_US
dc.contributor.authorKrell, Tinoen_US
dc.contributor.authorRömling, Uteen_US
dc.contributor.editorKovács, Ákos T.-
dc.date.accessioned2022-11-24T12:20:51Z-
dc.date.available2022-11-24T12:20:51Z-
dc.date.issued2022en_US
dc.identifier.issn2379-5077en_US
dc.identifier.urihttp://hdl.handle.net/10553/119350-
dc.description.abstractShewanella spp. play important ecological and biogeochemical roles, due in part to their versatile metabolism and swift integration of stimuli. While Shewanella spp. are primarily considered environmental microbes, Shewanella algae is increasingly recognized as an occasional human pathogen. S. algae shares the broad metabolic and respiratory repertoire of Shewanella spp. and thrives in similar ecological niches. In S. algae, nitrate and dimethyl sulfoxide (DMSO) respiration promote biofilm formation strain specifically, with potential implication of taxis and cyclic diguanosine monophosphate (c-di-GMP) signaling. Signal transduction systems in S. algae have not been investigated. To fill these knowledge gaps, we provide here an inventory of the c-di-GMP turnover proteome and chemosensory networks of the type strain S. algae CECT 5071 and compare them with those of 41 whole-genome-sequenced clinical and environmental S. algae isolates. Besides comparative analysis of genetic content and identification of laterally transferred genes, the occurrence and topology of c-di-GMP turnover proteins and chemoreceptors were analyzed. We found S. algae strains to encode 61 to 67 c-di-GMP turnover proteins and 28 to 31 chemoreceptors, placing S. algae near the top in terms of these signaling capacities per Mbp of genome. Most c-di-GMP turnover proteins were predicted to be catalytically active; we describe in them six novel N-terminal sensory domains that appear to control their catalytic activity. Overall, our work defines the c-di-GMP and chemosensory signal transduction pathways in S. algae, contributing to a better understanding of its ecophysiology and establishing S. algae as an auspicious model for the analysis of metabolic and signaling pathways within the genus Shewanella.en_US
dc.languageengen_US
dc.relation.ispartofmSystemsen_US
dc.sourcemSystems [ISSN 2379-5077], v. 7 (2): e01518-21, (Abril 2022)en_US
dc.subject32 Ciencias médicasen_US
dc.subject320102 Genética clínicaen_US
dc.subject.otherc-di-GMPen_US
dc.subject.otherChemotaxisen_US
dc.subject.otherSensingen_US
dc.subject.otherShewanellaen_US
dc.subject.otherSignal transductionen_US
dc.subject.otherWhole-genome sequencingen_US
dc.titleComparative Genomics of Cyclic di-GMP Metabolism and Chemosensory Pathways in Shewanella algae Strains: Novel Bacterial Sensory Domains and Functional Insights into Lifestyle Regulationen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1128/msystems.01518-21en_US
dc.identifier.pmid35311563-
dc.identifier.scopus2-s2.0-85129075931-
dc.contributor.orcid#NODATA#-
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dc.identifier.issue2-
dc.identifier.pmcidPMC9040814-
dc.relation.volume7en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.identifier.external118350390-
dc.description.numberofpages26en_US
dc.utils.revisionen_US
dc.contributor.wosstandardKovács, Ákos T.-
dc.contributor.wosstandardKovács, Ákos T.-
dc.contributor.wosstandardKovács, Ákos T.-
dc.contributor.wosstandardKovács, Ákos T.-
dc.contributor.wosstandardKovács, Ákos T.-
dc.contributor.wosstandardKovács, Ákos T.-
dc.contributor.wosstandardKovács, Ákos T.-
dc.date.coverdateAbril 2022en_US
dc.identifier.ulpgcNoen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr1,691
dc.description.jcr6,4
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
dc.description.miaricds10,2
item.fulltextCon texto completo-
item.grantfulltextopen-
crisitem.author.deptGIR Investigación Básica y Aplicada en Ciencias de la Salud-
crisitem.author.deptDepartamento de Ciencias Clínicas-
crisitem.author.orcid0000-0003-2422-129X-
crisitem.author.parentorgDepartamento de Ciencias Clínicas-
crisitem.author.fullNameMartín Rodríguez, Alberto Jonatan-
Colección:Artículos
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