Lipase-catalyzed esterification of rutin and naringin with fatty acids of medium carbon chain (Journal article)
Kontogianni, A./ Skouridou, V./ Sereti, V./ Stamatis, H./ Kolisis, F. N.
Flavonoids rutin and naringin were acylated with fatty acids of medium carbon chain (with 8-12 carbon atoms on their molecule) in a reaction catalyzed by immobilized lipase from Candida antarctica (Novozyme) in various solvent systems. The reaction parameters affecting the acylation rate and the conversion of the enzymatic process, such as the nature of the organic solvent and acyl donor used, the water activity (aw) of the system, as well as the kinetic of the reaction have been investigated. In all cases studied, only flavonoid monoester is identified as the product, which indicates that this lipase-catalyzed esterification is regioselective. The enzymatic acylation of flavonoids seems to follow Michaelis-Menten kinetics.
|Institution and School/Department of submitter:||Πανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών και Τεχνολογιών. Τμήμα Βιολογικών Εφαρμογών και Τεχνολογιών|
|Keywords:||Water activity,Monoester,Acylation rate|
|Appears in Collections:||Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά)|
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|stamatis-2003-Lipasecatalyzed esterification of rutin and naringin with fatty acids of medium carbon.pdf||114.44 kB||Adobe PDF||View/Open Request a copy|
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