An efficient plasmid vector for constitutive high-level expression of foreign genes in Escherichia coli = 대장균에서 외래유전자를 항시 고발현 시키기 위한 발현 벡터

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dc.contributor.authorJeong Woo Seo-
dc.contributor.authorWon-Kyung Hong-
dc.contributor.authorD Rairakhwada-
dc.contributor.authorPil-Soo Seo-
dc.contributor.authorMin-Ho Choi-
dc.contributor.authorK B Song-
dc.contributor.authorSang Ki Rhee-
dc.contributor.authorChul Ho Kim-
dc.date.accessioned2017-04-19T09:13:46Z-
dc.date.available2017-04-19T09:13:46Z-
dc.date.issued2009-
dc.identifier.issn0141-5492-
dc.identifier.uri10.1007/s10529-009-9941-4ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/8951-
dc.description.abstractThe levansucrase gene (lsrA) from Rahnella aquatilis was strongly expressed in a constitutive manner in Escherichia coli when cloned into a pBluescript KS-based pRL1CP plasmid vector. The native promoter upstream of lsrA and the lacZ promoter cooperatively enhanced the expression of lsrA to a level that was comparable to that of the T7 promoter, which is used in commercial pET expression vector system. A putative rho-independent transcription termination signal downstream of lsrA was crucial for gene expression. This plasmid vector also proved to be applicable for efficient expression of other foreign genes in E. coli.-
dc.publisherSpringer-
dc.titleAn efficient plasmid vector for constitutive high-level expression of foreign genes in Escherichia coli = 대장균에서 외래유전자를 항시 고발현 시키기 위한 발현 벡터-
dc.title.alternativeAn efficient plasmid vector for constitutive high-level expression of foreign genes in Escherichia coli-
dc.typeArticle-
dc.citation.titleBiotechnology Letters-
dc.citation.number6-
dc.citation.endPage881-
dc.citation.startPage877-
dc.citation.volume31-
dc.contributor.affiliatedAuthorJeong Woo Seo-
dc.contributor.affiliatedAuthorWon-Kyung Hong-
dc.contributor.affiliatedAuthorMin-Ho Choi-
dc.contributor.affiliatedAuthorSang Ki Rhee-
dc.contributor.affiliatedAuthorChul Ho Kim-
dc.contributor.alternativeName서정우-
dc.contributor.alternativeName홍원경-
dc.contributor.alternativeNameRairakhwada-
dc.contributor.alternativeName서필수-
dc.contributor.alternativeName최민호-
dc.contributor.alternativeName송기방-
dc.contributor.alternativeName이상기-
dc.contributor.alternativeName김철호-
dc.identifier.bibliographicCitationBiotechnology Letters, vol. 31, no. 6, pp. 877-881-
dc.identifier.doi10.1007/s10529-009-9941-4-
dc.subject.keywordescherichia coli-
dc.subject.keywordgene expression-
dc.subject.keywordlevansucrase gene-
dc.subject.keywordpromoter-
dc.subject.keywordrahnella aquatilis-
dc.subject.localEscherichia coli.-
dc.subject.localescherichia coli-
dc.subject.localEscherichia Coli-
dc.subject.localEscherichia coli-
dc.subject.localE.coli-
dc.subject.localescherichia coil-
dc.subject.localE. coli-
dc.subject.localE. Coli-
dc.subject.localGene Expression-
dc.subject.localGene expression-
dc.subject.localgene expression-
dc.subject.locallevansucrase gene-
dc.subject.locallevansucrase gene (lsrA)-
dc.subject.localPromoter-
dc.subject.localpromoter-
dc.subject.localPromoters-
dc.subject.localRahnella aquatilis-
dc.subject.localrahnella aquatilis-
dc.description.journalClassY-
Appears in Collections:
Jeonbuk Branch Institute > Microbial Biotechnology Research Center > 1. Journal Articles
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