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Confirmation of Vpr as a fibrinolytic enzyme present in extracellular proteins of Bacillus subtilis

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dc.contributor.authorKho, CW-
dc.contributor.authorPark, SG-
dc.contributor.authorCho, S-
dc.contributor.authorLee, DH-
dc.contributor.authorMyung, PK-
dc.contributor.authorPark, BC-
dc.date.available2019-05-30T08:33:22Z-
dc.date.issued2005-01-
dc.identifier.issn1046-5928-
dc.identifier.issn1096-0279-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/24689-
dc.description.abstractWe have previously reported a proteomic approach to detect fibrinolytic enzymes from the secreted proteins of Bacillis subtilis 168 and identified two extracellular fibrinolytic enzymes of Bacillus. namely, Vpr and WprA. In this study. to confirm the fibrinolytic activity of Vpr, we cloned the vpr gene and expressed it in Escherichia coli, where it is predominantly localized to inclusion bodies. After affinity purification and desalting steps, the expressed Vpr is auto-processed to an active form. Interestingly. after the desalting step, several additional bands with fibrinolytic activity were detected in zymography gel along with a mature form (68 kDa) of Vpr. MALDI-TOF analyses of these bands revealed that Vpr could exist in multiple forms. (C) 2004 Elsevier Inc. All rights reserved.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.titleConfirmation of Vpr as a fibrinolytic enzyme present in extracellular proteins of Bacillus subtilis-
dc.typeArticle-
dc.identifier.doi10.1016/j.pep.2004.08.008-
dc.identifier.bibliographicCitationPROTEIN EXPRESSION AND PURIFICATION, v.39, no.1, pp 1 - 7-
dc.description.isOpenAccessN-
dc.identifier.wosid000226153600001-
dc.identifier.scopusid2-s2.0-10644227920-
dc.citation.endPage7-
dc.citation.number1-
dc.citation.startPage1-
dc.citation.titlePROTEIN EXPRESSION AND PURIFICATION-
dc.citation.volume39-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordAuthorserine protease-
dc.subject.keywordAuthorVpr-
dc.subject.keywordAuthorzymography-
dc.subject.keywordAuthormass spectrometry-
dc.subject.keywordAuthorfibrinolytic enzymes-
dc.subject.keywordPlusSERINE PROTEASE-
dc.subject.keywordPlusZYMOGRAPHY-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusGELS-
dc.subject.keywordPlusBACILLUS-SUBTILIS-168-
dc.subject.keywordPlusMETALLOPROTEASE-
dc.subject.keywordPlusFORMS-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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