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dc.contributorFacultad de Ciencias Biologicas y Ambientaleses_ES
dc.contributor.authorApel, Alexander Kristian
dc.contributor.authorSola Landa, Alberto
dc.contributor.authorRodríguez García, Antonio 
dc.contributor.authorMartín Martín, Juan Francisco 
dc.contributor.otherMicrobiologiaes_ES
dc.date2007-10-01
dc.date.accessioned2024-01-29T13:20:04Z
dc.date.available2024-01-29T13:20:04Z
dc.identifier.citationApel, A. K., Sola-Landa, A., Rodríguez-García, A., & Martín, J. F. (2007). Phosphate control of phoA, phoC and phoD gene expression in Streptomyces coelicolor reveals significant differences in binding of PhoP to their promoter regions. Microbiology, 153(10), 3527-3537. https://doi.org/10.1099/MIC.0.2007/007070-0es_ES
dc.identifier.issn1350-0872
dc.identifier.otherhttps://www.microbiologyresearch.org/content/journal/micro/10.1099/mic.0.2007/007070-0es_ES
dc.identifier.urihttps://hdl.handle.net/10612/17887
dc.description.abstract[EN] Three putative alkaline phosphatase genes, phoA, phoC and phoD, were identified in the genome of Streptomyces coelicolor by homology with the amino acid sequence obtained from the PhoA protein of Streptomyces griseus. PhoA and PhoC correspond to broad-spectrum alkaline phosphatases whereas PhoD is similar to a Ca2+-dependent phospholipase D of Streptomyces chromofuscus. The phoA and phoD genes were efficiently expressed in R5 medium under phosphate-limited conditions, as shown by studies using the xylE reporter gene, whereas phoC was poorly transcribed under the same conditions. Expression of phoA was clearly PhoP-dependent since it was not transcribed in the S. coelicolor ΔphoP mutant and was strongly activated under low phosphate concentrations. Similarly, expression of phoD was PhoP-dependent and highly sensitive to phosphate availability. By contrast, expression of phoC was not PhoP-dependent. Electrophoretic mobility shift assays showed that PhoP binds to the phoA and phoD promoters, but not to that of phoC. Footprinting studies with GST-PhoP revealed the presence of a PHO box (two direct 11 nt repeats) in the phoA promoter and two PHO boxes in the promoter of phoD. The transcription start points of the three promoters were identified by primer extension. The transcription start point of phoD coincides with the G of its translation start codon, indicating that this gene is transcribed as a leaderless mRNA. The deduced -10 and -35 regions of phoD (but not those of phoA) overlapped with the PHO boxes in this promoter, suggesting that an excess of PhoP interferes with binding of the RNA polymerase to this promoter. In summary, the three promoters showed clear differences in the modulation of their expression by PhoPes_ES
dc.languageenges_ES
dc.publisherMicrobiology Societyes_ES
dc.subjectBiologíaes_ES
dc.subject.otherPhosphate regulationes_ES
dc.subject.otherStreptomyceses_ES
dc.subject.otherAlkaline phosphatasees_ES
dc.subject.otherphoAes_ES
dc.subject.otherphoCes_ES
dc.subject.otherphoDes_ES
dc.subject.otherEMSAes_ES
dc.titlePhosphate control of phoA, phoC and phoD gene expression in Streptomyces coelicolor reveals significant differences in binding of PhoP to their promoter regionses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doi10.1099/mic.0.2007/007070-0
dc.description.peerreviewedSIes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MICYT//BIO2003-01489/ESes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EU//LSHM-CT-2004-005224/ACTINOGENes_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn1465-2080
dc.journal.titleMicrobiologyes_ES
dc.volume.number153es_ES
dc.issue.number10es_ES
dc.page.initial3527es_ES
dc.page.final3537es_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 supported by grants of the CICYT (BIO2003-01489), Madrid (Spain) and the European Union (Project ACTINOGEN, LSHM-CT-2004-005224) Brussels. A. K. Apel received a F.P.U. fellowship of the Ministry of Education and Science. We thank J. Merino, B. Martín, B. Aguado and A. Casenave for their excellent technical assistance.es_ES


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