Cloning, sequencing and expression of the amylase isozyme gene from Pseudomonas sp KFCC 10818

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dc.contributor.authorKim, ESko
dc.contributor.authorNa, HKko
dc.contributor.authorJhon, DYko
dc.contributor.authorYoo, Ook-Joonko
dc.contributor.authorChun, SBko
dc.contributor.authorWui, ISko
dc.date.accessioned2013-03-03T06:28:23Z-
dc.date.available2013-03-03T06:28:23Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1996-02-
dc.identifier.citationBIOTECHNOLOGY LETTERS, v.18, no.2, pp.169 - 174-
dc.identifier.issn0141-5492-
dc.identifier.urihttp://hdl.handle.net/10203/77634-
dc.description.abstractA gene coding for amylase was cloned and sequenced from an alkalophilic Pseudomonas sp. KFCC 10818. The coding region for the amylase precursor contained 1,692 nucleotides. The presumed Shine-Dalgarno sequence, AAGG, was located at 8 nucleotides upstream from the ATG initiation codon. The precursor protein had a putative signal peptide of 25 amino acid residues at its amino terminus. The Pseudomonas amylase had four highly conserved regions as other cr-amylases. The amylase expressed from E. coli harboring the Pseudomonas gene produced maltose and maltotriose from soluble starch.-
dc.languageEnglish-
dc.publisherCHAPMAN HALL LTD-
dc.subjectNUCLEOTIDE-SEQUENCE-
dc.subjectFORMING AMYLASE-
dc.titleCloning, sequencing and expression of the amylase isozyme gene from Pseudomonas sp KFCC 10818-
dc.typeArticle-
dc.identifier.wosidA1996TV58100011-
dc.identifier.scopusid2-s2.0-0030063288-
dc.type.rimsART-
dc.citation.volume18-
dc.citation.issue2-
dc.citation.beginningpage169-
dc.citation.endingpage174-
dc.citation.publicationnameBIOTECHNOLOGY LETTERS-
dc.identifier.doi10.1007/BF00128674-
dc.contributor.localauthorYoo, Ook-Joon-
dc.contributor.nonIdAuthorKim, ES-
dc.contributor.nonIdAuthorNa, HK-
dc.contributor.nonIdAuthorJhon, DY-
dc.contributor.nonIdAuthorChun, SB-
dc.contributor.nonIdAuthorWui, IS-
dc.type.journalArticleArticle-
dc.subject.keywordPlusNUCLEOTIDE-SEQUENCE-
dc.subject.keywordPlusFORMING AMYLASE-
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