Aldol additions with mutant lipase: analysis by experiments and theoretical calculations

被引:56
作者
Branneby, C
Carlqvist, P
Hult, K
Brinck, T
Berglund, P [1 ]
机构
[1] AlbaNova Univ Ctr, Dept Biotechnol, Ctr Royal Inst Technol, KTH, SE-10691 Stockholm, Sweden
[2] Royal Inst Technol, KTH, Dept Chem, SE-10044 Stockholm, Sweden
关键词
oxyanion hole; reaction specificity; ab initio calculations; lipase; aldolase;
D O I
10.1016/j.molcatb.2004.08.005
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
A Ser 105Ala mutant of Candida antarctica lipase B has previously been shown to catalyze aldol additions. Quantum chemical calculations predicted a reaction rate similar to that of natural enzymes, whereas experiments showed a much lower reaction rate. Molecular dynamics simulations, presented here, show that the low reaction rate is a consequence of the low frequencies of near attack complexes in the enzyme. Equilibrium was also considered as a reason for the slow product formation, but could be excluded by performing a sequential reaction to push the reaction towards product formation. In this paper, further experimental results are also presented, highlighting the importance of the entire active site for catalysis. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:123 / 128
页数:6
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