Phenotypic engineering by reprogramming gene transcription using novel artificial transcription factors in Escherichia coli

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dc.contributor.authorLee, Ju-Youngko
dc.contributor.authorSung, Bong-Hyunko
dc.contributor.authorYu, Byung-Joko
dc.contributor.authorLee, Jun-Hyoungko
dc.contributor.authorLee, Sang-Heeko
dc.contributor.authorKim, Mi-Sunko
dc.contributor.authorKoob, Michael D.ko
dc.contributor.authorKim, Sun-Changko
dc.date.accessioned2013-03-07T14:36:00Z-
dc.date.available2013-03-07T14:36:00Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2008-09-
dc.identifier.citationNUCLEIC ACIDS RESEARCH, v.36, no.16-
dc.identifier.issn0305-1048-
dc.identifier.urihttp://hdl.handle.net/10203/90411-
dc.description.abstractNow that many genomes have been sequenced and the products of newly identified genes have been annotated, the next goal is to engineer the desired phenotypes in organisms of interest. For the phenotypic engineering of microorganisms, we have developed novel artificial transcription factors (ATFs) capable of reprogramming innate gene expression circuits in Escherichia coli. These ATFs are composed of zinc finger (ZF) DNA-binding proteins, with distinct specificities, fused to an E. coli cyclic AMP receptor protein (CRP). By randomly assembling 40 different types of ZFs, we have constructed more than 6.4 x 10(4) ATFs that consist of 3 ZF DNA-binding domains and a CRP effector domain. Using these ATFs, we induced various phenotypic changes in E. coli and selected for industrially important traits, such as resistance to heat shock, osmotic pressure and cold shock. Genes associated with the heat-shock resistance phenotype were then characterized. These results and the general applicability of this platform clearly indicate that novel ATFs are powerful tools for the phenotypic engineering of microorganisms and can facilitate microbial functional genomic studies.-
dc.languageEnglish-
dc.publisherOXFORD UNIV PRESS-
dc.titlePhenotypic engineering by reprogramming gene transcription using novel artificial transcription factors in Escherichia coli-
dc.typeArticle-
dc.identifier.wosid000259205600004-
dc.identifier.scopusid2-s2.0-52649115929-
dc.type.rimsART-
dc.citation.volume36-
dc.citation.issue16-
dc.citation.publicationnameNUCLEIC ACIDS RESEARCH-
dc.identifier.doi10.1093/nar/gkn449-
dc.contributor.localauthorLee, Ju-Young-
dc.contributor.localauthorKim, Sun-Chang-
dc.contributor.nonIdAuthorKim, Mi-Sun-
dc.contributor.nonIdAuthorKoob, Michael D.-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusZINC-FINGER PROTEINS-
dc.subject.keywordPlusACTIVATOR PROTEIN-
dc.subject.keywordPlusRECEPTOR PROTEIN-
dc.subject.keywordPlusLOW-TEMPERATURE-
dc.subject.keywordPlusDRUG DISCOVERY-
dc.subject.keywordPlusBIOSYNTHESIS-
dc.subject.keywordPlusLIBRARIES-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusOSMOTOLERANCE-
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