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Development of a RAPD-PCR method for identification of Bacillus species isolated from Cheonggukjang

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dc.contributor.authorKwon, Gun-Hee-
dc.contributor.authorLee, Hwang-A-
dc.contributor.authorPark, Jae-Young-
dc.contributor.authorKim, Jong Sang-
dc.contributor.authorLim, Jinkyu-
dc.contributor.authorPark, Cheon-Seok-
dc.contributor.authorKwon, Dae Young-
dc.contributor.authorKim, Yong-Suk-
dc.contributor.authorKim, Jeong Hwan-
dc.date.accessioned2022-12-27T05:19:46Z-
dc.date.available2022-12-27T05:19:46Z-
dc.date.issued2009-02-28-
dc.identifier.issn0168-1605-
dc.identifier.issn1879-3460-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/26388-
dc.description.abstractA RAPD-PCR (Randomly Amplified Polymorphic DNA-PCR) method was developed for rapid identification of Bacillus species. especially B. subtilis, B. licheniformis, and B. amyloliquefaciens, the most frequently isolated organisms from fermented soy foods such as Cheonggukjang. a Korean traditional food. A RAPD-PCR using a 10-mer (S-30) produced species specific bands reproducibly. All B. subtilis strains tested produced common bands of 0.5 and 0.88 kb in size. All B. amyloliquefociens strains generated 1.1 and 1.5 kb bands together with 0.5 kb fragment whereas B. licheniformis strains produced 1.25, 1.70, and 1.9 kb bands with an occasional 0.5 kb band. Using the RAPD-PCR protocol, six bacilli strains isolated from Cheonggukjang were identified to the species level, which was difficult by 16S rRNA gene and recA gene sequencing for some isolates. The 0.5 kb fragment. the major band for B. subtilis strains, was an internal part of a ytcP gene encoding a hypothetical ABC-type transporter. A B. subtilis species specific primer pair was designed based on ytcP sequences and PCR using the primer pair produced a 0.46 kb fragment only from B. subtilis strains. (C) 2008 Elsevier B.V. All rights reserved.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER-
dc.titleDevelopment of a RAPD-PCR method for identification of Bacillus species isolated from Cheonggukjang-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.ijfoodmicro.2008.12.013-
dc.identifier.scopusid2-s2.0-59349105256-
dc.identifier.wosid000264048200010-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, v.129, no.3, pp 282 - 287-
dc.citation.titleINTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY-
dc.citation.volume129-
dc.citation.number3-
dc.citation.startPage282-
dc.citation.endPage287-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaFood Science & Technology-
dc.relation.journalResearchAreaMicrobiology-
dc.relation.journalWebOfScienceCategoryFood Science & Technology-
dc.relation.journalWebOfScienceCategoryMicrobiology-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusCLONING-
dc.subject.keywordPlusASSAY-
dc.subject.keywordPlusFOOD-
dc.subject.keywordAuthorBacillus subtilis-
dc.subject.keywordAuthorBacillus licheniformis-
dc.subject.keywordAuthorBacillus amyloliquefaciens-
dc.subject.keywordAuthorCheonggukjang-
dc.subject.keywordAuthorRAPD-PCR-
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