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Characterization of a Glutamate Decarboxylase (GAD) from Enterococcus avium M5 Isolated from Jeotgal, a Korean Fermented Seafood

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dc.contributor.authorLee, Kang Wook-
dc.contributor.authorShim, Jae Min-
dc.contributor.authorYao, Zhuang-
dc.contributor.authorKim, Jeong A.-
dc.contributor.authorKim, Hyun-Jin-
dc.contributor.authorKim, Jeong Hwan-
dc.date.accessioned2022-12-26T18:35:49Z-
dc.date.available2022-12-26T18:35:49Z-
dc.date.issued2017-07-
dc.identifier.issn1017-7825-
dc.identifier.issn1738-8872-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/13651-
dc.description.abstractTo develop starters for the production of functional foods or materials, lactic acid bacteria producing gamma-aminobutyric acid (GABA) were screened from jeotgals, Korean fermented seafoods. One isolate producing a high amount of GABA from monosodium L-glutamate (MSG) was identified as Enterococcus avium by 16S rRNA gene sequencing. E. avium M5 produced 18.47 +/- 1.26 mg/ml GABA when incubated for 48 h at 37 degrees C in MRS broth with MSG (3% (w/v)). A gadB gene encoding glutamate decarboxylase (GAD) was cloned and overexpressed in E. coli BL21 (DE3) using the pET26b (+) expression vector. Recombinant GAD was purified through a Ni-NTA column and the size was estimated to be 53 kDa by SDS-PAGE. Maximum GAD activity was observed at pH 4.5 and 55 degrees C and the activity was dependent on pyridoxal 5'-phosphate. The K-m and V-max values of GAD were 3.26 +/- 0.21 mM and 0.0120 +/- 0.0001 mM/min, respectively, when MSG was used as a substrate. Enterococcus avium M5 secretes a lot of GABA when grown on MRS with MSG, and the strain is useful for the production of fermented foods containing a high amount of GABA.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherKOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY-
dc.titleCharacterization of a Glutamate Decarboxylase (GAD) from Enterococcus avium M5 Isolated from Jeotgal, a Korean Fermented Seafood-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.4014/jmb.1701.01058-
dc.identifier.scopusid2-s2.0-85026478374-
dc.identifier.wosid000408232100002-
dc.identifier.bibliographicCitationJOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, v.27, no.7, pp 1216 - 1222-
dc.citation.titleJOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY-
dc.citation.volume27-
dc.citation.number7-
dc.citation.startPage1216-
dc.citation.endPage1222-
dc.type.docTypeArticle-
dc.identifier.kciidART002246478-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaMicrobiology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryMicrobiology-
dc.subject.keywordPlusGAMMA-AMINOBUTYRIC-ACID-
dc.subject.keywordPlusLACTOBACILLUS-BREVIS-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusGABA-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusCLONING-
dc.subject.keywordPlusBACTERIUM-
dc.subject.keywordAuthorGamma-aminobutyric acid-
dc.subject.keywordAuthorglutamate decarboxylase-
dc.subject.keywordAuthorgad gene cloning-
dc.subject.keywordAuthorEnterococcus avium-
dc.subject.keywordAuthorjeotgal-
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