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Esterification of phenolic acids catalyzed by lipases immobilized in organogels

Identifieur interne : 000088 ( Main/Exploration ); précédent : 000087; suivant : 000089

Esterification of phenolic acids catalyzed by lipases immobilized in organogels

Auteurs : M. Zoumpanioti [Grèce] ; E. Merianou [Grèce] ; T. Karandreas [Grèce] ; H. Stamatis [Grèce] ; A. Xenakis [Grèce]

Source :

RBID : Hal:hal-00594822

English descriptors

Abstract

Lipases from and 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 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.

Url:
DOI: 10.1007/s10529-010-0305-x


Affiliations:


Links toward previous steps (curation, corpus...)


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