Enantioselective hydrolysis of (R,S)-naproxen methyl ester using two-step acetone-treated Candida rugosa lipase = 2단계 아세톤 침전법으로부터 얻어진 Candida rugosa lipase를 이용한 (R,S)-Naproxen methyl ester의 광학선택성 수화반응

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Title
Enantioselective hydrolysis of (R,S)-naproxen methyl ester using two-step acetone-treated Candida rugosa lipase = 2단계 아세톤 침전법으로부터 얻어진 Candida rugosa lipase를 이용한 (R,S)-Naproxen methyl ester의 광학선택성 수화반응
Author(s)
Eun Gyo Lee; Soon Ja Choi; Bong Hyun Chung
Bibliographic Citation
Korean Journal of (Applied) Microbiology & Biotechnology, vol. 28, no. 4, pp. 223-227
Publication Year
2000
Abstract
A novel two-step acetone treatment method was developed to enhance the enantioselectivity of Candida rugosa lipase (CRL) toward the hydrolysis of racemic naproxen methyl ester. The acetone-treated CRL was considerably more enantioselective than the crude CRL, yielding an enantiomeric excess of 98-100%. The crude and acetone-treated CRLs were subjected to anion exchange chromatography, and their chromatography profiles were compared. In consequence, both chromatography profiles were found to be almost identical, resulting in two separate lipase peaks (lipase A and B). The lipase B, which is known to be less enantioselective, was treated with acetone using a two-step treatment method. The enantioselectivity of acetone-treated lipase B was dramatically increased, yielding an enantiomeric excess of 99 %.
Keyword
Candida rugosa lipase (CRL)(S)-naproxen(R,S)-naproxen methyl estertwo-step acetone treatment
ISSN
0257-2389
Publisher
Korea Soc-Assoc-Inst
DOI
http://dx.doi.org/10.1016/S0032-9592(01)00213-8
Type
Article
Appears in Collections:
Division of Bio Technology Innovation > BioProcess Engineering Center > 1. Journal Articles
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