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Cited 16 time in webofscience Cited 21 time in scopus
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dc.contributor.authorSanghak Cha-
dc.contributor.authorHyun Gyu Lim-
dc.contributor.authorSeokmu Kwon-
dc.contributor.authorDong-hwan Kim-
dc.contributor.authorChae Won Kang-
dc.contributor.authorGyoo Yeol Jung-
dc.date.accessioned2021-06-01T02:01:13Z-
dc.date.available2021-06-01T02:01:13Z-
dc.date.created2021-03-07-
dc.date.issued2021-03-
dc.identifier.issn1096-7176-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/105147-
dc.description.abstractCarbon monoxide (CO) is a promising carbon source for producing value-added biochemicals via microbial fermentation. However, its microbial conversion has been challenging because of difficulties in genetic engineering of CO-utilizing microorganisms and, more importantly, maintaining CO consumption which is negatively affected by the toxicity of CO and accumulated byproducts. To overcome these issues, we devised mutualistic microbial consortia, co-culturing Eubacterium limosum and genetically engineered Escherichia coli for the production of 3-hydroxypropionic acid (3-HP) and itaconic acid (ITA). During the co-culture, E. limosum assimilated CO and produced acetate, a toxic by-product, while E. coli utilized acetate as a sole carbon source. We found that this mutualistic interaction dramatically stabilized and improved CO consumption of E. limosum compared to monoculture. Consequently, the improved CO consumption allowed successful production of 3-HP and ITA from CO. This study is the first demonstration of value-added biochemical production from CO using a microbial consortium. Moreover, it suggests that synthetic mutualistic microbial consortium can serve as a powerful platform for the valorization of CO.-
dc.languageEnglish-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.relation.isPartOfMETABOLIC ENGINEERING-
dc.titleDesign of mutualistic microbial consortia for stable conversion of carbon monoxide to value-added chemicals-
dc.typeArticle-
dc.identifier.doi10.1016/j.ymben.2021.02.001-
dc.type.rimsART-
dc.identifier.bibliographicCitationMETABOLIC ENGINEERING, v.64, pp.146 - 153-
dc.identifier.wosid000631887200004-
dc.citation.endPage153-
dc.citation.startPage146-
dc.citation.titleMETABOLIC ENGINEERING-
dc.citation.volume64-
dc.contributor.affiliatedAuthorSanghak Cha-
dc.contributor.affiliatedAuthorDong-hwan Kim-
dc.contributor.affiliatedAuthorChae Won Kang-
dc.contributor.affiliatedAuthorGyoo Yeol Jung-
dc.identifier.scopusid2-s2.0-85100654719-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.type.docTypeArticle-
dc.subject.keywordAuthorMicrobial consortia-
dc.subject.keywordAuthorCarbon monoxide-
dc.subject.keywordAuthorFermentation stability-
dc.subject.keywordAuthor3-Hydroxypropionic acid-
dc.subject.keywordAuthorItaconic acid-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-

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