Esterification of phenolic acids catalyzed by lipases immobilized in organogels

dc.contributor.authorZoumpanioti, M.en
dc.contributor.authorMerianou, E.en
dc.contributor.authorKarandreas, T.en
dc.contributor.authorStamatis, H.en
dc.contributor.authorXenakis, A.en
dc.date.accessioned2015-11-24T16:34:32Z
dc.date.available2015-11-24T16:34:32Z
dc.identifier.issn0141-5492-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/7815
dc.rightsDefault Licence-
dc.subjectbiocatalysisen
dc.subjectantioxidantsen
dc.subjecthydroxypropylmethyl celluloseen
dc.subjectenzymatic-synthesisen
dc.subjectferuloyl esteraseen
dc.subjectderivativesen
dc.subjecttransesterificationen
dc.subjectantioxidantsen
dc.subjectmediaen
dc.titleEsterification of phenolic acids catalyzed by lipases immobilized in organogelsen
heal.abstractLipases from Rhizomucor miehei and Candida antarctica B were immobilized in hydroxypropylmethyl cellulose organogels based on surfactant-free microemulsions consisting of n-hexane, 1-propanol and water. Both lipases kept their catalytic activity, catalyzing the esterification reactions of various phenolic acids including cinnamic acid derivatives. High reaction rates and yields (up to 94%) were obtained when lipase from C. antarctica was used. Kinetic studies have been performed and apparent kinetic constants were determined showing that ester synthesis catalyzed by immobilized lipases occurs via the Michaelis-Menten mechanism.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1007/s10529-010-0305-x-
heal.identifier.secondary<Go to ISI>://000281934700013-
heal.identifier.secondaryhttp://www.springerlink.com/content/hx2j664wh424271j/fulltext.pdf-
heal.journalNameBiotechnology Lettersen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2010-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών και Τεχνολογιών. Τμήμα Βιολογικών Εφαρμογών και Τεχνολογιώνel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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