Comparison of the extracellular proteomes of Escherichia coli B and K-12 strains during high cell density cultivation

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dc.contributor.authorXia, XXko
dc.contributor.authorHan, MJko
dc.contributor.authorLee, SangYupko
dc.contributor.authorYoo, JSko
dc.date.accessioned2010-11-16T06:06:30Z-
dc.date.available2010-11-16T06:06:30Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2008-05-
dc.identifier.citationPROTEOMICS, v.8, no.10, pp.2089 - 2103-
dc.identifier.issn1615-9853-
dc.identifier.urihttp://hdl.handle.net/10203/20033-
dc.description.abstractEscherichia coli BL21 (DE3) and W3110 strains, belonging to the family B and K-12, respectively, have been most widely employed for recombinant protein production. During the excretory production of recombinant proteins by high cell density cultivation (HCDC) of these strains, other native E. coli proteins were also released. Thus, we analyzed the extracellular proteomes of E. coli BL21 (DE3) and W3110 during HCDC. E. coli BL21 (DE3) released more than twice the amount of protein compared with W3110 during HCDC. A total of 204 protein spots including 83 nonredundant proteins were unambiguously identified by 2-DE and MS. Of these, 32 proteins were conserved in the two strains, while 20 and 33 strain-specific proteins were identified for E. coli BL21 (DE3) and W3110, respectively. More than 70% of identified proteins were found to be of periplasmic origin. The outer membrane proteins, OmpA and OmpF, were most abundant. Two strains showed much different patterns in their released proteins. Also, cell density-dependent variations in the released proteins were observed in both strains. These findings summarized as reference proteome maps will be useful for studying protein release in further detail, and provide new strategies for enhanced excretory production of recombinant proteins.-
dc.description.sponsorshipThis work was supported by the Korean Systems Biology Research Grant (M10309020000-03B5002-00000) of the Ministry of Science and Technology. Further supports by LG Chem Chair Professorship, IBM SUR Program, Microsoft, and by the KOSEF through the Center for Ultramicrochemical Process Systems are appreciated.en
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleComparison of the extracellular proteomes of Escherichia coli B and K-12 strains during high cell density cultivation-
dc.typeArticle-
dc.identifier.wosid000256293300016-
dc.identifier.scopusid2-s2.0-44649118664-
dc.type.rimsART-
dc.citation.volume8-
dc.citation.issue10-
dc.citation.beginningpage2089-
dc.citation.endingpage2103-
dc.citation.publicationnamePROTEOMICS-
dc.identifier.doi10.1002/pmic.200700826-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorLee, SangYup-
dc.contributor.nonIdAuthorXia, XX-
dc.contributor.nonIdAuthorHan, MJ-
dc.contributor.nonIdAuthorYoo, JS-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorEscherichia coli-
dc.subject.keywordAuthorextracellular proteome-
dc.subject.keywordAuthorhigh cell density cultivation-
dc.subject.keywordPlusGENERAL SECRETORY PATHWAY-
dc.subject.keywordPlusGRAM-NEGATIVE BACTERIA-
dc.subject.keywordPlusOUTER-MEMBRANE-
dc.subject.keywordPlusBACILLUS-SUBTILIS-
dc.subject.keywordPlusGLUCOSE-UTILIZATION-
dc.subject.keywordPlusPROTEIN SECRETION-
dc.subject.keywordPlusSIGNAL PEPTIDES-
dc.subject.keywordPlusCULTURE-
dc.subject.keywordPlusRECOMBINANT-
dc.subject.keywordPlusSTRESS-
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