Esterification of phenolic acids catalyzed by lipases immobilized in organogels
Identifieur interne : 000088 ( Main/Exploration ); précédent : 000087; suivant : 000089Esterification 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 :
- Biotechnology Letters [ 0141-5492 ] ; 2010-05-21.
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:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">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.</div>
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