Published January 1, 2014
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Improving catalytic hydrolysis reaction efficiency of sol-gel-encapsulated Candida rugosa lipase with magnetic beta-cyclodextrin nanoparticles
- 1. Selcuk Univ, Dept Chem, TR-42075 Konya, Turkey
- 2. Kirklareli Univ, Dept Chem, TR-39000 Kirklareli, Turkey
Description
A silica-based p-cyclodextrin was immobilized on magnetic nanoparticles to obtain a macrocyclic compound with magnetic property. Then, the beta-cyclodextrin-grafted magnetic nanoparticles were encapsulated with Candida rugosa lipase in sol-gel matrices using alkoxysilane precursors. The catalytic activity of the encapsulated lipases was evaluated with model reactions, i.e., the hydrolysis of p-nitro-phenylpalmitate (p-NPP) and the enantioselective hydrolysis of rasemic Naproxen methyl ester that was studied in an aqueous buffer solution/isooctane reaction system. The results indicate that the cyclodextrin-based, encapsulated lipase particularly exhibited high conversion and enantioselectivity behavior compared to the sol-gel free lipase. It was also observed that excellent enantioselectivity (E=399) was obtained for the encapsulated lipase with magnetic beta-cyclodextrin that has an ee value of S-Naproxen acid of about 98%. (C) 2013 Elsevier B.V. All rights reserved.
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