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DC Field | Value | Language |
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dc.citation.startPage | 129814 | - |
dc.citation.title | BIORESOURCE TECHNOLOGY | - |
dc.citation.volume | 389 | - |
dc.contributor.author | Islam, Tayyab | - |
dc.contributor.author | Nguyen-Vo, Thuan Phu | - |
dc.contributor.author | Cho, Seunghyun | - |
dc.contributor.author | Lee, Junhak | - |
dc.contributor.author | Gaur, Vivek Kumar | - |
dc.contributor.author | Park, Sunghoon | - |
dc.date.accessioned | 2023-12-20T15:35:12Z | - |
dc.date.available | 2023-12-20T15:35:12Z | - |
dc.date.created | 2023-12-06 | - |
dc.date.issued | 2023-12 | - |
dc.description.abstract | 1,3-Butanediol (1,3-BDO) finds versatile applications in the cosmetic, chemical, and food industries. This study focuses on the metabolic engineering of Escherichia coli K12 to achieve efficient production of 1,3-BDO from glucose via acetoacetyl-CoA, 3-hydroxybutyryl-CoA, and 3-hydroxybutyraldehyde. The accumulation of an intermediary metabolite (pyruvate) and a byproduct (3-hydroxybutyric acid) was reduced by disruption of the negative transcription factor (PdhR) for pyruvate dehydrogenase complex (PDHc) and employing an efficient alcohol dehydrogenase (YjgB), respectively. Additionally, to improve NADPH availability, carbon flux was redirected from the Embden-Meyerhof-Parnas (EMP) pathway to the Entner-Doudoroff (ED) pathway. One resulting strain achieved a record-high titer of 790 mM (similar to 71.1 g/L) with a yield of 0.65 mol/mol for optically pure (R)-1,3-BDO, with an enantiomeric excess (e.e.) value of 98.5 %. These findings are useful in the commercial production of 1,3-BDO and provide valuable insights into the development of an efficient cell factory for other acetyl-CoA derivatives. | - |
dc.identifier.bibliographicCitation | BIORESOURCE TECHNOLOGY, v.389, pp.129814 | - |
dc.identifier.doi | 10.1016/j.biortech.2023.129814 | - |
dc.identifier.issn | 0960-8524 | - |
dc.identifier.scopusid | 2-s2.0-85173157355 | - |
dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/66678 | - |
dc.identifier.wosid | 001096968400001 | - |
dc.language | 영어 | - |
dc.publisher | ELSEVIER SCI LTD | - |
dc.title | Metabolic engineering of Escherichia coli for enhanced production of 1,3-butanediol from glucose | - |
dc.type | Article | - |
dc.description.isOpenAccess | FALSE | - |
dc.relation.journalWebOfScienceCategory | Agricultural Engineering; Biotechnology & Applied Microbiology; Energy & Fuels | - |
dc.relation.journalResearchArea | Agriculture; Biotechnology & Applied Microbiology; Energy & Fuels | - |
dc.type.docType | Article | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordAuthor | (R)-1,3-BDO | - |
dc.subject.keywordAuthor | Metabolic engineering | - |
dc.subject.keywordAuthor | E. coli | - |
dc.subject.keywordAuthor | Enantiomeric excess | - |
dc.subject.keywordPlus | PYRUVATE-DEHYDROGENASE COMPLEX | - |
dc.subject.keywordPlus | PHOSPHOGLUCOSE ISOMERASE | - |
dc.subject.keywordPlus | (R)-1,3-BUTANEDIOL PRODUCTION | - |
dc.subject.keywordPlus | GLUCOSE-6-PHOSPHATE-DEHYDROGENASE | - |
dc.subject.keywordPlus | SYSTEM | - |
dc.subject.keywordPlus | GENE | - |
dc.subject.keywordPlus | UDHA | - |
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