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Identification of the lactic acid bacteria in Kimchi according to initial and over-ripened fermentation using PCR and 16S rRNA gene sequence analysis

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dc.contributor.authorPark, Jung-Min-
dc.contributor.authorShin, Jin-Ho-
dc.contributor.authorLee, Dan-Won-
dc.contributor.authorSong, Jae-Chul-
dc.contributor.authorSuh, Hyung-Joo-
dc.contributor.authorChang, Un-Jae-
dc.contributor.authorKim, Jin-Man-
dc.date.accessioned2021-09-08T04:04:14Z-
dc.date.available2021-09-08T04:04:14Z-
dc.date.created2021-06-11-
dc.date.issued2010-04-
dc.identifier.issn1226-7708-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/116679-
dc.description.abstractThis paper aimed to identify the lactic acid bacteria species involved in kimchi fermentation at different fermentation periods by using culture-independent 16S rRNA gene clone libraries, and develop polymerase chain reaction for the detection of lactic acid bacteria (LAB). We investigated 6 commercially produced kimchi samples, including kimchi at an initial stage of fermentation and kimchi that was fermented to an over-ripened stage. The results of our study show that the analysis with cultureindependent 16S rRNA gene clone libraries could successfully identify 134 clones, 11 species, including Weissella, Lactobacillus, Pediococcus, and Leuconostoc from the 6 commercial kimchi samples. Weisella koreensis and Lactobacillus brevis were the predominant LAB in the initial stage of kimchi fermentation at 4A degrees C (pH 4.96-5.27 and acidity 0.81-0.88), and Leuconostoc gelidum and Lactobacillus sakei subsp. sakei may play an important role in kimchi fermentation at the over-ripened stage (pH 3.61-3.91 and acidity 1.70-1.79).-
dc.languageEnglish-
dc.language.isoen-
dc.publisherKOREAN SOCIETY FOOD SCIENCE & TECHNOLOGY-KOSFOST-
dc.subjectSP-NOV.-
dc.subjectPHYLOGENETIC ANALYSIS-
dc.subjectLEUCONOSTOC-GELIDUM-
dc.subjectWEISSELLA-
dc.subjectBLAST-
dc.subjectFOOD-
dc.titleIdentification of the lactic acid bacteria in Kimchi according to initial and over-ripened fermentation using PCR and 16S rRNA gene sequence analysis-
dc.typeArticle-
dc.contributor.affiliatedAuthorSuh, Hyung-Joo-
dc.identifier.doi10.1007/s10068-010-0075-1-
dc.identifier.scopusid2-s2.0-79953278905-
dc.identifier.wosid000277239600035-
dc.identifier.bibliographicCitationFOOD SCIENCE AND BIOTECHNOLOGY, v.19, no.2, pp.541 - 546-
dc.relation.isPartOfFOOD SCIENCE AND BIOTECHNOLOGY-
dc.citation.titleFOOD SCIENCE AND BIOTECHNOLOGY-
dc.citation.volume19-
dc.citation.number2-
dc.citation.startPage541-
dc.citation.endPage546-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART001441086-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaFood Science & Technology-
dc.relation.journalWebOfScienceCategoryFood Science & Technology-
dc.subject.keywordPlusSP-NOV.-
dc.subject.keywordPlusPHYLOGENETIC ANALYSIS-
dc.subject.keywordPlusLEUCONOSTOC-GELIDUM-
dc.subject.keywordPlusWEISSELLA-
dc.subject.keywordPlusBLAST-
dc.subject.keywordPlusFOOD-
dc.subject.keywordAuthorkimchi-
dc.subject.keywordAuthor16S rRNA sequence analysis-
dc.subject.keywordAuthorlactic acid bacteria-
dc.subject.keywordAuthorpolymerase chain reaction-
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보건과학대학 (바이오시스템의과학부)
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