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dc.contributorFacultad de Ciencias Biologicas y Ambientaleses_ES
dc.contributor.authorThomas, Louise
dc.contributor.authorHodgson, David A.
dc.contributor.authorWentzel, Alexander
dc.contributor.authorNieselt, Kay
dc.contributor.authorEllingsen, Trond E.
dc.contributor.authorMoore, Jonathan
dc.contributor.authorMorrissey, Edward R.
dc.contributor.authorLegaie, Roxane
dc.contributor.authorWohlleben, Wolfgang
dc.contributor.authorRodríguez García, Antonio 
dc.contributor.authorMartín Martín, Juan Francisco 
dc.contributor.authorBurroughs, Nigel J.
dc.contributor.authorWellington, Elizabeth M.H.
dc.contributor.authorSmith, Margaret C. M.
dc.contributor.otherMicrobiologiaes_ES
dc.date2012-02-01
dc.date.accessioned2024-01-31T09:08:52Z
dc.date.available2024-01-31T09:08:52Z
dc.identifier.citationThomas, L., Hodgson, D. A., Wentzel, A., Nieselt, K., Ellingsen, T. E., Moore, J., Morrissey, E. R., Legaie, R., Wohlleben, W., Rodríguez-García, A., Martín, J. F., Burroughs, N. J., Wellington, E. M. H., & Smith, M. C. M. (2012). Metabolic switches and adaptations deduced from the proteomes of Streptomyces coelicolor wild type and phoP mutant grown in batch culture Molecular and Cellular Proteomics, 11(2), Article eM111.013797. https://doi.org/10.1074/MCP.M111.013797es_ES
dc.identifier.issn1535-9476
dc.identifier.otherhttps://www.sciencedirect.com/science/article/pii/S1535947620305314es_ES
dc.identifier.urihttps://hdl.handle.net/10612/17940
dc.description.abstract[EN] Bacteria in the genus Streptomyces are soil-dwelling oligotrophs and important producers of secondary metabolites. Previously, we showed that global messenger RNA expression was subject to a series of metabolic and regulatory switches during the lifetime of a fermentor batch culture of Streptomyces coelicolor M145. Here we analyze the proteome from eight time points from the same fermentor culture and, because phosphate availability is an important regulator of secondary metabolite production, compare this to the proteome of a similar time course from an S. coelicolor mutant, INB201 (ΔphoP), defective in the control of phosphate utilization. The proteomes provide a detailed view of enzymes involved in central carbon and nitrogen metabolism. Trends in protein expression over the time courses were deduced from a protein abundance index, which also revealed the importance of stress pathway proteins in both cultures. As expected, the ΔphoP mutant was deficient in expression of PhoP-dependent genes, and several putatively compensatory metabolic and regulatory pathways for phosphate scavenging were detected. Notably there is a succession of switches that coordinately induce the production of enzymes for five different secondary metabolite biosynthesis pathways over the course of the batch cultureses_ES
dc.languageenges_ES
dc.publisherAmerican Society for Biochemistry and Molecular Biologyes_ES
dc.publisherElsevieres_ES
dc.subjectBiologíaes_ES
dc.subjectBiotecnologíaes_ES
dc.subject.otherMetabolic switches_ES
dc.subject.otherPhosphate regulationes_ES
dc.subject.otherPhoR-PhoPes_ES
dc.subject.otherStreptomyces coelicolores_ES
dc.subject.otherProteomicses_ES
dc.subject.otherAntibotics biosynthesis regulationes_ES
dc.titleMetabolic switches and adaptations deduced from the proteomes of Streptomyces coelicolor wild type and phoP mutant grown in batch culturees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doi10.1074/mcp.M111.013797
dc.description.peerreviewedSIes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/BBSRC/BB/F003439/1es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EU//GEN2006-27745-E/SYSes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/RCN//181840/130es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/235447/EUes_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.journal.titleMolecular & Cellular Proteomicses_ES
dc.volume.number11es_ES
dc.issue.number2es_ES
dc.page.initialM111.013797es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.unesco2415.01 Biología Molecular de Microorganismoses_ES
dc.subject.unesco2414.02 Fisiología Bacterianaes_ES
dc.description.projectThis work was funded by Biotechnology and Biological Sciences Research Council Grant BB/F003439/1, ERA-NET SysMO Project GEN2006-27745-E/SYS Grant P-UK-01-11-3i, and Research Council of Norway Project 181840/I30. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.es_ES


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