Optimized hybrid nanospheres immobilizing Rhizomucor miehei lipase for chiral biotransformation
Autor: | F. Verri, Urbano Díaz, Girolamo Giordano, Anastasia Macario, A. Corma |
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Rok vydání: | 2016 |
Předmět: |
Heterogeneous hybrid biocatalysts
(R S)-ibuprofen Rhizomucor miehei Bioengineering 010402 general chemistry Heterogeneous catalysis 01 natural sciences Applied Microbiology and Biotechnology Biochemistry Catalysis Rhizomucor miehei lipase QUIMICA ORGANICA Organic chemistry Lipase Biotransformation biology 010405 organic chemistry Chemistry Enantioselective synthesis biology.organism_classification 0104 chemical sciences Liposome Solvent Yield (chemistry) biology.protein Enantiomer |
Zdroj: | RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia instname |
ISSN: | 1359-5113 2009-0005 |
Popis: | [EN] In this study, the immobilization of Rhizomucor miehei lipase into hybrid nanospheres containing a liposomal core was reported. Organic internal liposomal enzyme phase was protected by inorganic silica matrix, obtained with and without surfactant, that stabilizes the internal organic phase and isolates and protects the bioactive molecules. The optimized heterogeneous catalyst thus prepared was used for enantioselective esterification of (R,S)-ibuprofen. The influence of several catalytic parameters on the activity of hybrid nanospheres (type of solvent, nature of the alcohol, reaction temperature, etc.,) was investigated. The heterogeneous biocatalysts best performed at 37 degrees C, using isooctane as solvent and 1-propanol as alcohol (with ester yield ranging between 78 and 93%). High activity and stability (up to nine reaction cycles) of enzyme-immobilized hybrid nanospheres, with respect to the free form, were observed. R. miehei lipase, both in its free and immobilized forms, reacts only with the S(+) enantiomer of (R,S)-ibuprofen, in all the tested reaction conditions. (C) 2015 Elsevier Ltd. All rights reserved. The authors thank the financial support from Consolider-Ingenio MULTICAT CSD2009-00050, MAT2014-52085-C2-1-P, and Severo Ochoa Excellence Program SEV-2012-0267. |
Databáze: | OpenAIRE |
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