Combinatorial biocatalysis: a natural approach to drug discovery

被引:76
作者
Michels, PC [1 ]
Khmelnitsky, YL
Dordick, JS
Clark, DS
机构
[1] EnzyMed Inc, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Chem & Biochem Engn, Iowa City, IA 52242 USA
[3] Univ Calif Berkeley, Dept Chem Engn, Berkeley, CA 94720 USA
关键词
D O I
10.1016/S0167-7799(98)01190-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Nature's most potent molecules are produced by enzyme-catalysed reactions, coupled with the natural selection of those products that possess optimal biological activity. Combinatorial biocatalysis harnesses the natural diversity of enzymatic reactions for the iterative synthesis of organic libraries. Iterative reactions can be performed using isolated enzymes or whole cells, in natural and unnatural environments, and on substrates in solution or on a solid phase. Combinatorial biocatalysis is a powerful addition to the expanding array of combinatorial methods for the generation and optimization of lead compounds in drug discovery and development.
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页码:210 / 215
页数:6
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