Covalently immobilized lipase on a thermoresponsive polymer with an upper critical solution temperature as an efficient and recyclable asymmetric catalyst in aqueous media
Abstract
A thermoresponsive lipase catalyst with an upper critical solution temperature (UCST) of about 26 °C was exploited by covalent immobilization of an enzyme, Pseudomonas cepacia lipase (PSL), onto poly(acrylamide-co-acrylonitrile) via glutaraldehyde coupling. The experimental conditions for the PSL immobilization were optimized. The immobilized PSL was much more stable for wide ranges of temperature and pH than the free PSL. The material was also evaluated as an asymmetric catalyst in the kinetic resolution of racemic α-methylbenzyl butyrate at 55 °C in an aqueous medium and exhibited high catalytic performance and stability. Up to 50% conversion and 99.5% product enantiomeric excess were achieved, thus providing highly pure enantiomers. More importantly, this biocatalyst could be easily recovered by simple decantation for reuse based on temperature-induced precipitation. It showed good reusability and retained 80.5% of its original activity with a well reserved enantioselectivity in the 6th cycle. This work would shed light on the future development of new UCST-type enzyme catalysts.
Citation
Lou , L-L , Qu , H , Yu , W , Wang , B , Ouyang , L , Liu , S & Zhou , W 2018 , ' Covalently immobilized lipase on a thermoresponsive polymer with an upper critical solution temperature as an efficient and recyclable asymmetric catalyst in aqueous media ' , ChemCatChem , vol. 10 , no. 5 , pp. 1166-1172 . https://doi.org/10.1002/cctc.201701512
Publication
ChemCatChem
Status
Peer reviewed
ISSN
1867-3899Type
Journal article
Rights
© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. This work has been made available online in accordance with the publisher’s policies. This is the author created accepted version manuscript following peer review and as such may differ slightly from the final published version. The final published version of this work is available at https://doi.org/10.1002/cctc.201701512
Description
This work was financially supported by the National Natural Science Foundation of China (Grant No. 21203102), the Tianjin Municipal Natural Science Foundation (Grant No. 14JCQNJC06000), China Scholarship Council (Grant No. 201606200087), MOE (IRT13R30) and 111 Project (B12015).Collections
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