Integrative genome-scale metabolic analysis of Vibrio vulnificus for drug targeting and discovery

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dc.contributor.authorKim, Hyun Ukko
dc.contributor.authorKim, Soo-Youngko
dc.contributor.authorJeong, Hae-Youngko
dc.contributor.authorKim, Tae-Yongko
dc.contributor.authorKim, Jae-Jongko
dc.contributor.authorChoy, Hyon-Eko
dc.contributor.authorYi, Kyu-Yangko
dc.contributor.authorRhee, Joon-Haengko
dc.contributor.authorLee, Sang-Yupko
dc.date.accessioned2013-03-11T03:20:52Z-
dc.date.available2013-03-11T03:20:52Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2011-01-
dc.identifier.citationMOLECULAR SYSTEMS BIOLOGY, v.7, pp.1 - 11-
dc.identifier.issn1744-4292-
dc.identifier.urihttp://hdl.handle.net/10203/98132-
dc.description.abstractAlthough the genomes of many microbial pathogens have been studied to help identify effective drug targets and novel drugs, such efforts have not yet reached full fruition. In this study, we report a systems biological approach that efficiently utilizes genomic information for drug targeting and discovery, and apply this approach to the opportunistic pathogen Vibrio vulnificus CMCP6. First, we partially re-sequenced and fully re-annotated the V. vulnificus CMCP6 genome, and accordingly reconstructed its genome-scale metabolic network, VvuMBEL943. The validated network model was employed to systematically predict drug targets using the concept of metabolite essentiality, along with additional filtering criteria. Target genes encoding enzymes that interact with the five essential metabolites finally selected were experimentally validated. These five essential metabolites are critical to the survival of the cell, and hence were used to guide the cost-effective selection of chemical analogs, which were then screened for antimicrobial activity in a whole-cell assay. This approach is expected to help fill the existing gap between genomics and drug discovery. Molecular Systems Biology 7: 460; published online 18 January 2011; doi:10.1038/msb.2010.115-
dc.languageEnglish-
dc.publisherNATURE PUBLISHING GROUP-
dc.titleIntegrative genome-scale metabolic analysis of Vibrio vulnificus for drug targeting and discovery-
dc.typeArticle-
dc.identifier.wosid000287095100005-
dc.identifier.scopusid2-s2.0-78751556862-
dc.type.rimsART-
dc.citation.volume7-
dc.citation.beginningpage1-
dc.citation.endingpage11-
dc.citation.publicationnameMOLECULAR SYSTEMS BIOLOGY-
dc.identifier.doi10.1038/msb.2010.115-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorKim, Hyun Uk-
dc.contributor.localauthorLee, Sang-Yup-
dc.contributor.nonIdAuthorKim, Soo-Young-
dc.contributor.nonIdAuthorJeong, Hae-Young-
dc.contributor.nonIdAuthorKim, Jae-Jong-
dc.contributor.nonIdAuthorChoy, Hyon-E-
dc.contributor.nonIdAuthorYi, Kyu-Yang-
dc.contributor.nonIdAuthorRhee, Joon-Haeng-
dc.description.isOpenAccessY-
dc.type.journalArticleArticle-
dc.subject.keywordAuthordrug discovery-
dc.subject.keywordAuthordrug targeting-
dc.subject.keywordAuthorgenome analysis-
dc.subject.keywordAuthormetabolic network-
dc.subject.keywordAuthorVibrio vulnificus-
dc.subject.keywordPlusESCHERICHIA-COLI-
dc.subject.keywordPlus6-HYDROXYMETHYL-7,8-DIHYDROPTERIN PYROPHOSPHOKINASE-
dc.subject.keywordPlusDIHYDROPTEROATE SYNTHASE-
dc.subject.keywordPlusANTIBACTERIAL DISCOVERY-
dc.subject.keywordPlusANTIBIOTIC-RESISTANCE-
dc.subject.keywordPlusFLUX ANALYSIS-
dc.subject.keywordPlusRECONSTRUCTION-
dc.subject.keywordPlusPATHOGEN-
dc.subject.keywordPlusNETWORK-
dc.subject.keywordPlusIDENTIFICATION-
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