Chemomimetic Biocatalysis: Exploiting the Synthetic Potential of Cofactor-Dependent Enzymes To Create New Catalysts

被引:124
作者
Prier, Christopher K. [1 ]
Arnold, Frances H. [1 ]
机构
[1] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
基金
美国国家科学基金会;
关键词
CARBONIC-ANHYDRASE II; BIOTIN-AVIDIN TECHNOLOGY; MICHAEL-TYPE ADDITIONS; ARTIFICIAL METALLOENZYMES; THIAMIN DIPHOSPHATE; DIRECTED EVOLUTION; ACTIVE-SITE; BENZOYLFORMATE DECARBOXYLASE; ENANTIOSELECTIVE REDUCTION; METALLOPEPTIDE CATALYSTS;
D O I
10.1021/jacs.5b09348
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Despite the astonishing breadth of enzymes in nature, no enzymes are known for many of the valuable catalytic transformations discovered by chemists. Recent work in enzyme design and evolution, however, gives us good reason to think that this will change. We describe a chemomimetic biocatalysis approach that draws from small-molecule catalysis and synthetic chemistry, enzymology, and molecular evolution to discover or create enzymes with non-natural reactivities. We illustrate how cofactor-dependent enzymes can be exploited to promote reactions first established with related chemical catalysts. The cofactors can be biological, or they can be non-biological to further expand catalytic possibilities. The ability of enzymes to amplify and precisely control the reactivity of their cofactors together with the ability to optimize non-natural reactivity by directed evolution promises to yield exceptional catalysts for challenging transformations that have no biological counterparts.
引用
收藏
页码:13992 / 14006
页数:15
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