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Cited 19 time in webofscience Cited 23 time in scopus
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dc.contributor.authorKim, YH-
dc.contributor.authorLee, I-
dc.contributor.authorChoi, SH-
dc.contributor.authorLee, OK-
dc.contributor.authorShim, J-
dc.contributor.authorLee, J-
dc.contributor.authorKim, J-
dc.contributor.authorLee, EY-
dc.date.accessioned2016-03-31T08:12:59Z-
dc.date.available2016-03-31T08:12:59Z-
dc.date.created2014-03-06-
dc.date.issued2013-05-
dc.identifier.issn1381-1177-
dc.identifier.other2013-OAK-0000029259-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/14815-
dc.description.abstractWe developed magnetically-separable and highly-stable biocatalyst system of Mugil cephalus epoxide hydrolase (McEH) for enantioselective hydrolysis of racemic epoxides. McEH protein was adsorbed and cross-linked into mesoporous silica with bottle-neck mesopores, which effectively prevented the leaching of cross-linked McEH in a larger mesocellular pores. This ship-in-a-bottle approach allows for highly loaded and stable McEH system. For example, free McEH showed only 7.5% of initial activity under shaking condition at 80 h while ship-in-a-bottled McEH retained 79.5% of initial activity in the same condition. Stable McEH in magnetically-separable mesoporous silica could achieve the yield of 45% for the preparation of enantiopure (S)-styrene oxide with 98%ee. The magnetic nanoparticles pre-incorporated in mesoporous silica enabled an easy recovery of immobilized McEH for repetitive batch resolutions of racemic styrene oxide, allowing for more than 50% of the initial activity was retained after seven recycled uses. (C) 2012 Elsevier B.V. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.relation.isPartOfJOURNAL OF MOLECULAR CATALYSIS B: ENZYMATIC-
dc.subjectEpoxide hydrolase-
dc.subjectMugil cephalus-
dc.subjectNanoscale enzyme reactor-
dc.subjectMesoporous silica-
dc.subjectEnzyme immobilization-
dc.subjectMUGIL-CEPHALUS-
dc.subjectIMMOBILIZATION-
dc.subjectSTABILIZATION-
dc.subjectNANOPARTICLES-
dc.subjectIMPROVEMENT-
dc.subjectCATALYSIS-
dc.subjectENZYMES-
dc.subjectSYSTEM-
dc.titleEnhanced stability and reusability of marine epoxide hydrolase using ship-in-a-bottle approach with magnetically-separable mesoporous silica-
dc.typeArticle-
dc.contributor.college화학공학과-
dc.identifier.doi10.1016/J.MOLCATB.2012.12.012-
dc.author.googleKim, YH-
dc.author.googleLee, I-
dc.author.googleChoi, SH-
dc.author.googleLee, OK-
dc.author.googleShim, J-
dc.author.googleLee, J-
dc.author.googleKim, J-
dc.author.googleLee, EY-
dc.relation.volume89-
dc.relation.startpage48-
dc.relation.lastpage51-
dc.contributor.id10138815-
dc.relation.journalJOURNAL OF MOLECULAR CATALYSIS B: ENZYMATIC-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationJOURNAL OF MOLECULAR CATALYSIS B: ENZYMATIC, v.89, pp.48 - 51-
dc.identifier.wosid000315552300008-
dc.date.tcdate2019-01-01-
dc.citation.endPage51-
dc.citation.startPage48-
dc.citation.titleJOURNAL OF MOLECULAR CATALYSIS B: ENZYMATIC-
dc.citation.volume89-
dc.contributor.affiliatedAuthorLee, J-
dc.identifier.scopusid2-s2.0-84873045563-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc11-
dc.type.docTypeArticle-
dc.subject.keywordPlusIMMOBILIZATION-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusIMPROVEMENT-
dc.subject.keywordPlusCATALYSIS-
dc.subject.keywordPlusENZYMES-
dc.subject.keywordAuthorEpoxide hydrolase-
dc.subject.keywordAuthorMugil cephalus-
dc.subject.keywordAuthorNanoscale enzyme reactor-
dc.subject.keywordAuthorMesoporous silica-
dc.subject.keywordAuthorEnzyme immobilization-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-

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