Production of aromatic D-amino acids from α-keto acids and ammonia by coupling of four enzyme reactions

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dc.contributor.authorHee Sung Bae-
dc.contributor.authorSeung Goo Lee-
dc.contributor.authorSeung Pyo Hong-
dc.contributor.authorMi Sun Kwak-
dc.contributor.authorN Esaki-
dc.contributor.authorK Soda-
dc.contributor.authorMoon Hee Sung-
dc.date.accessioned2017-04-19T08:55:54Z-
dc.date.available2017-04-19T08:55:54Z-
dc.date.issued1999-
dc.identifier.issn1381-1177-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/4650-
dc.description.abstractA multi-enzyme system composed of glutamate racemase, thermostable D- amino acid aminotransferase, glutamate dehydrogenase and formate dehydrogenase was employed for the production of aromatic D-amino acids, D- phenylalanine and D-tyrosine, from the corresponding α-keto acids, phenylpyruvate and hydroxyphenylpyruvate, respectively. The optimal concentration of ammonium formate for the production of these D-amino acids was found in the range of 0.25-1.0 M. The optimal concentration of α-keto acid was determined to be 50 mM, above which the productivity greatly decreased. To keep the concentration of α-keto acid around this concentration, α-keto acid was intermittently fed into the multi-enzyme system during the production period. By running the multi-enzyme system for 35 h, 48 gl-1 of D-phenylalanine and 60 gl-1 of D-tyrosine were produced with 100% of optical purity from the equimolar amounts of phenylpyruvate and hydroxyphenylpyruvate, respectively. The production levels of both aromatic D-amino acids were demonstrated to be dependent on the stability of glutamate racemase.-
dc.publisherElsevier-
dc.titleProduction of aromatic D-amino acids from α-keto acids and ammonia by coupling of four enzyme reactions-
dc.title.alternativeProduction of aromatic D-amino acids from α-keto acids and ammonia by coupling of four enzyme reactions-
dc.typeArticle-
dc.citation.titleJournal of Molecular Catalysis B: Enzymatic-
dc.citation.number0-
dc.citation.endPage247-
dc.citation.startPage241-
dc.citation.volume6-
dc.contributor.affiliatedAuthorHee Sung Bae-
dc.contributor.affiliatedAuthorSeung Goo Lee-
dc.contributor.affiliatedAuthorSeung Pyo Hong-
dc.contributor.affiliatedAuthorMi Sun Kwak-
dc.contributor.affiliatedAuthorMoon Hee Sung-
dc.contributor.alternativeName배희성-
dc.contributor.alternativeName이승구-
dc.contributor.alternativeName홍승표-
dc.contributor.alternativeName곽미선-
dc.contributor.alternativeNameEsaki-
dc.contributor.alternativeNameSoda-
dc.contributor.alternativeName성문희-
dc.identifier.bibliographicCitationJournal of Molecular Catalysis B: Enzymatic, vol. 6, pp. 241-247-
dc.identifier.doi10.1016/S1381-1177(98)00073-3-
dc.subject.keywordAromatic D-amino acid-
dc.subject.keywordD-Amino acid aminotransferase-
dc.subject.keywordGlutamate racemase-
dc.subject.keywordα-Keto acid-
dc.subject.keywordMulti-enzyme system-
dc.subject.localAromatic D-amino acid-
dc.subject.localD-Amino acid aminotransferase-
dc.subject.localD-amino acid aminotransferase-
dc.subject.localGlutamate racemase-
dc.subject.localα-Keto acid-
dc.subject.localMulti-enzyme system-
dc.description.journalClassN-
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