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Efficient Synthesis of Food-Derived Antioxidant L-Ergothioneine by Engineered Corynebacterium glutamicum

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dc.contributor.authorKim, Minhye-
dc.contributor.authorJeong, Da Woon-
dc.contributor.authorOh, Jun Won-
dc.contributor.authorJeong, Hyun Jin-
dc.contributor.authorKo, Young Jin-
dc.contributor.authorPark, Sung Eun-
dc.contributor.authorHan, Sung Ok-
dc.date.accessioned2022-04-01T15:40:22Z-
dc.date.available2022-04-01T15:40:22Z-
dc.date.created2022-04-01-
dc.date.issued2022-02-09-
dc.identifier.issn0021-8561-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/139375-
dc.description.abstractL-Ergothioneine (EGT) is a strong antioxidant used in industry, and it is commonly extracted from mushrooms; however, its production is limited. As an alternative, we developed metabolically engineered Corynebacterium glutamicum with reinforced sulfur assimilation and pentose phosphate pathways, which led to the accumulation of 45.0 and 63.2 mg/L EGT, respectively. Additionally, the overexpression of cysEKR resulted in further promoted EGT production in ET4 (66.5 mg/L) and ET7 (85.0 mg/L). Based on this result, we developed the strain ET11, in which all sulfur assimilatory, PP, and L-cysteine synthetic pathways were reinforced, and it synthesized 264.4 mg/L EGT. This study presents the first strategy for EGT synthesis that does not require precursor addition in C. glutamicum, and the production time was shortened. In addition, the synthesized EGT showed high radical scavenging activity (70.7%), thus confirming its antioxidant function. Consequently, this study showed the possibility of EGT commercialization by overcoming the limitations of industrial processes.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.subjectL-HISTIDINE-
dc.subjectBIOSYNTHESIS-
dc.subjectEXPRESSION-
dc.subjectGENES-
dc.titleEfficient Synthesis of Food-Derived Antioxidant L-Ergothioneine by Engineered Corynebacterium glutamicum-
dc.typeArticle-
dc.contributor.affiliatedAuthorHan, Sung Ok-
dc.identifier.doi10.1021/acs.jafc.1c07541-
dc.identifier.scopusid2-s2.0-85124073990-
dc.identifier.wosid000762960100012-
dc.identifier.bibliographicCitationJOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, v.70, no.5, pp.1516 - 1524-
dc.relation.isPartOfJOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY-
dc.citation.titleJOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY-
dc.citation.volume70-
dc.citation.number5-
dc.citation.startPage1516-
dc.citation.endPage1524-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaAgriculture-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaFood Science & Technology-
dc.relation.journalWebOfScienceCategoryAgriculture, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Applied-
dc.relation.journalWebOfScienceCategoryFood Science & Technology-
dc.subject.keywordPlusL-HISTIDINE-
dc.subject.keywordPlusBIOSYNTHESIS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusGENES-
dc.subject.keywordAuthorl-ergothioneine-
dc.subject.keywordAuthorpentose phosphate pathway-
dc.subject.keywordAuthorsulfur assimilation-
dc.subject.keywordAuthorl-cysteine pathway-
dc.subject.keywordAuthorl-ergothioneine synthetic pathway-
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