Implication of substrate-assisted catalysis on improving lipase activity or enantioselectivity in organic solvents

被引:26
作者
Tsai, Shau-Wei [1 ]
Chen, Chun-Chi
Yang, Hung-Shien
Ng, I-Son
Chen, Teh-Liang
机构
[1] Chang Gung Univ, Inst Biochem & Biomed Engn, Tao Yuan 33302, Taiwan
[2] Natl Cheng Kung Univ, Dept Chem Engn, Tainan 70101, Taiwan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2006年 / 1764卷 / 08期
关键词
lipases; substrate-assisted catalysis; proton transfer; acylation step; hydrolysis resolution;
D O I
10.1016/j.bbapap.2006.07.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In comparison with the biocatalyst engineering and medium engineering approaches, very few examples have been reported on using the substrate engineering approach such as substrate-assisted catalysis (SAC) for naturally occurring or engineered lipases and serine proteases to improve the enzyme activity and enantioselectivity. By employing lipase-catalyzed hydrolysis of (R,S)-naproxen esters in water-saturated isooctane as the model system, we demonstrate the proton shuttle device to the leaving alcohol of the substrate as a new means of SAC to effectively improve the lipase activity or enantioselectivity. The result cannot only provide a strong evidence for the rate-limiting proton transfer for the bond-breaking of tetrahedron intermediate of the acylation step, but also sheds light for performing the hydrolysis, transesterification or aminolysis in organic solvents for the ester substrate that originally lipases cannot catalyze, but now can after introducing the device. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1424 / 1428
页数:5
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