Production of 5-aminovaleric acid in recombinant Corynebacterium glutamicum strains from a Miscanthus hydrolysate solution prepared by a newly developed Miscanthus hydrolysis process

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dc.contributor.authorJoo, Jeong Chanko
dc.contributor.authorOh, Young Hoonko
dc.contributor.authorYu, Ju Hyunko
dc.contributor.authorHyun, Sung Minko
dc.contributor.authorKhang, Tae Ukko
dc.contributor.authorKang, Kyoung Heeko
dc.contributor.authorSong, Bong Keunko
dc.contributor.authorPark, Kyungmoonko
dc.contributor.authorOh, Min-Kyuko
dc.contributor.authorLee, Sang Yupko
dc.contributor.authorPark, Si Jaeko
dc.date.accessioned2017-11-08T05:04:05Z-
dc.date.available2017-11-08T05:04:05Z-
dc.date.created2017-10-30-
dc.date.created2017-10-30-
dc.date.created2017-10-30-
dc.date.created2017-10-30-
dc.date.issued2017-12-
dc.identifier.citationBIORESOURCE TECHNOLOGY, v.245, pp.1692 - 1700-
dc.identifier.issn0960-8524-
dc.identifier.urihttp://hdl.handle.net/10203/226814-
dc.description.abstractThis study examined nine expired industrial Corynebacterium glutamicum strains with high lysine producing capability for enhanced production of 5-AVA. C. glutamicum KCTC 1857 exhibiting the highest lysine production was transformed with either original Pseudomonas putida davBA genes, encoding the 5-AVA biosynthesis pathway, or C. glutamicum codon-optimized davBA genes. C. glutamicum KCTC 1857 expressing the original genes had superior cell viability and 5-AVA production capability compared to the other strain. This strain produced 39.93 g/L of 5-AVA, which is the highest titer reported to date in fed-batch fermentation from glucose. Indeed, Miscanthus hydrolysate solution prepared from a novel process, comprising pretreatment, hydrolysis, purification, and concentration, was used as feedstock for 5-AVA production. A total of 12.51 g/L 5-AVA was produced from the Miscanthus hydrolysate; this value is 34.7% higher than that obtained from glucose in batch fermentation.-
dc.languageEnglish-
dc.publisherELSEVIER SCI LTD-
dc.titleProduction of 5-aminovaleric acid in recombinant Corynebacterium glutamicum strains from a Miscanthus hydrolysate solution prepared by a newly developed Miscanthus hydrolysis process-
dc.typeArticle-
dc.identifier.wosid000413038300048-
dc.identifier.scopusid2-s2.0-85020107107-
dc.type.rimsART-
dc.citation.volume245-
dc.citation.beginningpage1692-
dc.citation.endingpage1700-
dc.citation.publicationnameBIORESOURCE TECHNOLOGY-
dc.identifier.doi10.1016/j.biortech.2017.05.131-
dc.contributor.localauthorLee, Sang Yup-
dc.contributor.nonIdAuthorJoo, Jeong Chan-
dc.contributor.nonIdAuthorOh, Young Hoon-
dc.contributor.nonIdAuthorYu, Ju Hyun-
dc.contributor.nonIdAuthorHyun, Sung Min-
dc.contributor.nonIdAuthorKhang, Tae Uk-
dc.contributor.nonIdAuthorKang, Kyoung Hee-
dc.contributor.nonIdAuthorSong, Bong Keun-
dc.contributor.nonIdAuthorPark, Kyungmoon-
dc.contributor.nonIdAuthorOh, Min-Kyu-
dc.contributor.nonIdAuthorPark, Si Jae-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorCorynebacterium glutamicum-
dc.subject.keywordAuthorMetabolic engineering-
dc.subject.keywordAuthor5-Aminovaleric acid-
dc.subject.keywordAuthorMiscanthus-
dc.subject.keywordAuthorPretreatment-
dc.subject.keywordPlusSUBSEQUENT ENZYMATIC-HYDROLYSIS-
dc.subject.keywordPlusHIGH-LEVEL CONVERSION-
dc.subject.keywordPlusESCHERICHIA-COLI-
dc.subject.keywordPlusL-LYSINE-
dc.subject.keywordPlusCHEMICALS-
dc.subject.keywordPlusBIOMASS-
dc.subject.keywordPlusHYDROTHERMOLYSIS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusCADAVERINE-
dc.subject.keywordPlusGLUTARATE-
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CBE-Journal Papers(저널논문)
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