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Enzyme-catalyzed resolution of racemate using enzyme functionalized silica nanoparticles in the presence of surfactants

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dc.contributor.authorSong, Yoon Seok-
dc.contributor.authorLee, Hee Uk-
dc.contributor.authorLee, Jong Ho-
dc.contributor.authorPark, Chulhwan-
dc.contributor.authorKim, Seung Wook-
dc.date.accessioned2021-09-07T14:49:42Z-
dc.date.available2021-09-07T14:49:42Z-
dc.date.created2021-06-14-
dc.date.issued2011-03-
dc.identifier.issn1359-5113-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/113031-
dc.description.abstractThe enzyme-catalyzed resolution of racemic naproxen 2,2,2-trifluoroethyl thioester was performed by the immobilization of lipase on silica nanoparticles using a covalent bonding method. To increase the conversion and reaction rate of this resolution, we investigated the effect of non-ionic surfactants (M-SA 1025 and SM 20). The optimal reaction conditions such as temperature and loading amount of immobilized lipase were also determined. The addition of M-SA 1025 resulted in the increase in reaction rate (V-S), conversion (X-S) and enantioselectivity (E value) comparison with SM 20 and the control. The reaction performed in a mixture containing M-SA 1025 at 50 degrees C with 80 U/mL of immobilized lipase markedly improved the resolution of racemic naproxen 2,2,2-trifluoroethyl thioester compared to other conditions. (C) 2010 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER SCI LTD-
dc.subjectNAPROXEN 2,2,2-TRIFLUOROETHYL THIOESTER-
dc.subjectCANDIDA-RUGOSA LIPASE-
dc.subjectKINETIC RESOLUTION-
dc.subjectENANTIOSELECTIVE ESTERIFICATION-
dc.subjectHYDROLYSIS-
dc.subjectESTER-
dc.subjectOPTIMIZATION-
dc.subjectPERFORMANCE-
dc.subjectACID-
dc.titleEnzyme-catalyzed resolution of racemate using enzyme functionalized silica nanoparticles in the presence of surfactants-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Seung Wook-
dc.identifier.doi10.1016/j.procbio.2010.12.010-
dc.identifier.scopusid2-s2.0-79951511778-
dc.identifier.wosid000288419900033-
dc.identifier.bibliographicCitationPROCESS BIOCHEMISTRY, v.46, no.3, pp.817 - 820-
dc.relation.isPartOfPROCESS BIOCHEMISTRY-
dc.citation.titlePROCESS BIOCHEMISTRY-
dc.citation.volume46-
dc.citation.number3-
dc.citation.startPage817-
dc.citation.endPage820-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.subject.keywordPlusNAPROXEN 2,2,2-TRIFLUOROETHYL THIOESTER-
dc.subject.keywordPlusCANDIDA-RUGOSA LIPASE-
dc.subject.keywordPlusKINETIC RESOLUTION-
dc.subject.keywordPlusENANTIOSELECTIVE ESTERIFICATION-
dc.subject.keywordPlusHYDROLYSIS-
dc.subject.keywordPlusESTER-
dc.subject.keywordPlusOPTIMIZATION-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusACID-
dc.subject.keywordAuthorLipase-
dc.subject.keywordAuthorResolution-
dc.subject.keywordAuthorNaproxen-
dc.subject.keywordAuthorSurfactant-
dc.subject.keywordAuthorSilica nanoparticle-
dc.subject.keywordAuthorImmobilization-
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