完整後設資料紀錄
DC 欄位語言
dc.contributor.authorKu, Jason T.en_US
dc.contributor.authorChen, Arvin Y.en_US
dc.contributor.authorLan, Ethan I.en_US
dc.date.accessioned2020-07-01T05:22:05Z-
dc.date.available2020-07-01T05:22:05Z-
dc.date.issued2020-04-01en_US
dc.identifier.urihttp://dx.doi.org/10.3390/metabo10040166en_US
dc.identifier.urihttp://hdl.handle.net/11536/154501-
dc.description.abstractAcetyl-CoA is a key metabolite precursor for the biosynthesis of lipids, polyketides, isoprenoids, amino acids, and numerous other bioproducts which are used in various industries. Metabolic engineering efforts aim to increase carbon flux towards acetyl-CoA in order to achieve higher productivities of its downstream products. In this review, we summarize the strategies that have been implemented for increasing acetyl-CoA flux and concentration, and discuss their effects. Furthermore, recent works have developed synthetic acetyl-CoA biosynthesis routes that achieve higher stoichiometric yield of acetyl-CoA from glycolytic substrates.en_US
dc.language.isoen_USen_US
dc.subjectacetyl-CoAen_US
dc.subjectmetabolic bypassen_US
dc.subjectpyruvate dehydrogenaseen_US
dc.subjectcoenzyme Aen_US
dc.titleMetabolic Engineering Design Strategies for Increasing Acetyl-CoA Fluxen_US
dc.typeArticleen_US
dc.identifier.doi10.3390/metabo10040166en_US
dc.identifier.journalMETABOLITESen_US
dc.citation.volume10en_US
dc.citation.issue4en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.department分子醫學與生物工程研究所zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.contributor.departmentInstitute of Molecular Medicine and Bioengineeringen_US
dc.identifier.wosnumberWOS:000533907300026en_US
dc.citation.woscount0en_US
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