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dc.contributorFacultad de Ciencias Biologicas y Ambientaleses_ES
dc.contributor.authorRodríguez García, Antonio 
dc.contributor.authorCombes, Patricia
dc.contributor.authorPérez Redondo, Rosario
dc.contributor.authorSmith, Matthew C. A.
dc.contributor.authorSmith, Margaret C. M.
dc.contributor.otherMicrobiologiaes_ES
dc.date2005-05-01
dc.date.accessioned2024-01-23T10:04:46Z
dc.date.available2024-01-23T10:04:46Z
dc.identifier.citationRodríguez-García, A., Combes, P., Pérez-Redondo, R., Smith, M. C. A., & Smith, M. C. M. (2005). Natural and synthetic tetracycline-inducible promoters for use in the antibiotic-producing bacteria Streptomyces. Nucleic Acids Research, 33(9), Article e87. https://doi.org/10.1093/NAR/GNI086es_ES
dc.identifier.issn0305-1048
dc.identifier.otherhttps://academic.oup.com/nar/article/33/9/e87/2401590es_ES
dc.identifier.urihttps://hdl.handle.net/10612/17725
dc.description.abstract[EN] Bacteria in the genus Streptomyces are major producers of antibiotics and other pharmacologically active compounds. Genetic and physiological manipulations of these bacteria are important for new drug discovery and production development. An essential part of any ‘genetic toolkit’ is the availability of regulatable promoters. We have adapted the tetracycline (Tc) repressor/operator (TetR/ tetO ) regulatable system from transposon Tn 10 for use in Streptomyces . The synthetic Tc controllable promoter (tcp), tcp830 , was active in a wide range of Streptomyces species, and varying levels of induction were observed after the addition of 1–100 ng/ml of anhydrotetracycline (aTc). Streptomyces coelicolor contained an innate Tc-controllable promoter regulated by a TetR homologue (SCO0253). Both natural and synthetic promoters were active and inducible throughout growth. Using the luxAB genes expressing luciferase as a reporter system, we showed that induction factors of up to 270 could be obtained for tcp830 . The effect of inducers on the growth of S.coelicolor was determined; addition of aTc at concentrations where induction is optimal, i.e. 0.1–1 μg/ml, ranged from no effect on growth rate to a small increase in the lag period compared with cultures with no induceres_ES
dc.languageenges_ES
dc.publisherOxford University Presses_ES
dc.subjectBiotecnologíaes_ES
dc.subject.otherInducible promoteres_ES
dc.subject.otherStreptomyceses_ES
dc.subject.otherTetracycline operatores_ES
dc.subject.otherTetRes_ES
dc.subject.otherSynthetic promoteres_ES
dc.subject.otherAnhydrotetracyclinees_ES
dc.subject.otherLuciferase reporteres_ES
dc.titleNatural and synthetic tetracycline-inducible promoters for use in the antibiotic-producing bacteria Streptomyceses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doi10.1093/nar/gni086
dc.description.peerreviewedSIes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/BBSRC/Investigating Gene Function 1999-2005/IGF12436/UK/A concerted approach to global mutational analysis of gene function in Streptomyces coelicolores_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn1362-4962
dc.journal.titleNucleic Acids Researches_ES
dc.volume.number33es_ES
dc.issue.number9es_ES
dc.page.initial87es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.unesco2415.01 Biología Molecular de Microorganismoses_ES
dc.description.projectThe authors acknowledge gifts of plasmids and strains from Prof. Leadlay, Prof. Hillen, Prof. Bujard, Dr Herron and Dr Paget. The authors thank Dr Sumby, Dr Ding and Wael Hussein for the construction of several plasmids and vectors. The authors also thank Prof. Williams for the use of Lucy. This work was funded by the BBSRC. Funding to pay the Open Access publication charges for this article was provided by JISCes_ES


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