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Characterization of Capsicum annuum Recombinant alpha- and beta-Tubulin

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dc.contributor.authorKoo, Bon-Sung-
dc.contributor.authorJang, Myung-Hyun-
dc.contributor.authorPark, Haechul-
dc.contributor.authorKalme, Satish-
dc.contributor.authorPark, Hey-Yeon-
dc.contributor.authorHan, Jin-Wook-
dc.contributor.authorYeo, Yun-Soo-
dc.contributor.authorYoon, Sang-Hong-
dc.contributor.authorKim, Soo-Jin-
dc.contributor.authorLee, Chang-Muk-
dc.contributor.authorYoon, Moon-Young-
dc.date.accessioned2022-12-20T19:20:04Z-
dc.date.available2022-12-20T19:20:04Z-
dc.date.issued2010-01-
dc.identifier.issn0273-2289-
dc.identifier.issn1559-0291-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/175591-
dc.description.abstractThere are several conditions which might modulate polymerization to produce polymers having normal lattice structure. In the absence of 1 mM MgCl2 the assembly was reduced by 36% in Capsicum annuum tubulin (CAnm tubulin). There was no significant difference in the final assembly formation in the presence of 5% to 10% glycerol. However, nucleation rate was slow and apparent study state was achieved lately in the presence of 10% glycerol. Taxol at 100 mu M concentration increased 23% tubulin assembly. One millimolar CaCl2, >= 1% dimethyl sulfoxide (DMSO) and physiologically low temperature reduced CAnm tubulin assembly. A value of 0.089 mg/ml was obtained as critical concentration for polymerization. Benomyl significantly reduced the number of cysteine residues accessible to 5,5'-dithiobis-(2-nitrobenzoic acid); there were 4.77 +/- 0.21 and 3.49 +/- 0.35 residues accessible per tubulin dimer in the presence of 50 and 100 mu M benomyl respectively.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherHumana Press, Inc.-
dc.titleCharacterization of Capsicum annuum Recombinant alpha- and beta-Tubulin-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1007/s12010-008-8489-4-
dc.identifier.scopusid2-s2.0-73649098829-
dc.identifier.wosid000273159200012-
dc.identifier.bibliographicCitationApplied Biochemistry and Biotechnology, v.160, no.1, pp 122 - 128-
dc.citation.titleApplied Biochemistry and Biotechnology-
dc.citation.volume160-
dc.citation.number1-
dc.citation.startPage122-
dc.citation.endPage128-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.subject.keywordPlusASSEMBLY IN-VITRO-
dc.subject.keywordPlusCOLCHICINE-BINDING-
dc.subject.keywordPlusBOVINE BRAIN-
dc.subject.keywordPlusSACCHAROMYCES-CEREVISIAE-
dc.subject.keywordPlusDIMETHYL-SULFOXIDE-
dc.subject.keywordPlusDISULFIDE BONDS-
dc.subject.keywordPlusPLANT TUBULIN-
dc.subject.keywordPlusPOLYMERIZATION-
dc.subject.keywordPlusPURIFICATION-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordAuthorBenomyl-
dc.subject.keywordAuthorCapsicum annuum-
dc.subject.keywordAuthorPolymerization-
dc.subject.keywordAuthorSulfhydryl group-
dc.subject.keywordAuthorTaxol-
dc.identifier.urlhttps://link.springer.com/article/10.1007/s12010-008-8489-4-
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