Directed evolution of enzyme catalysts

被引:271
作者
Kuchner, O
Arnold, FH
机构
[1] Div. of Chem. and Chem. Eng. 210-41, California Institute of Technology, Pasadena
关键词
D O I
10.1016/S0167-7799(97)01138-4
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
Directed enzyme evolution has emerged in the past few years as a powerful alternative to rational approaches for engineering biocatalysts. Prerequisites for successful directed evolution are functional expression in a suitable microbial host, a rapid screen for the desired feature(s) and a well-thought-out working strategy for navigating protein landscapes. The rapidly growing body of literature on enzyme evolution in vitro includes techniques for creating and searching combinatorial enzyme libraries, as well as several successful examples of different evolutionary strategies being used.
引用
收藏
页码:523 / 530
页数:8
相关论文
共 51 条
[1]   Fitness spectrum among random mutants on Mt Fuji-type fitness landscape [J].
Aita, T ;
Husimi, Y .
JOURNAL OF THEORETICAL BIOLOGY, 1996, 182 (04) :469-485
[2]   Directed evolution: Creating biocatalysts for the future [J].
Arnold, FH .
CHEMICAL ENGINEERING SCIENCE, 1996, 51 (23) :5091-5102
[3]   FROM ADENYLATE-CYCLASE TO GUANYLATE-CYCLASE - MUTATIONAL ANALYSIS OF A CHANGE IN SUBSTRATE-SPECIFICITY [J].
BEUVE, A ;
DANCHIN, A .
JOURNAL OF MOLECULAR BIOLOGY, 1992, 225 (04) :933-938
[4]   Creation of drug-specific herpes simplex virus type 1 thymidine kinase mutants for gene therapy [J].
Black, ME ;
Newcomb, TG ;
Wilson, HMP ;
Loeb, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (08) :3525-3529
[5]  
BRYAN P N, 1986, Proteins Structure Function and Genetics, V1, P326
[6]  
CADWELL RC, 1994, MUTAGENIC PCR
[7]   TUNING THE ACTIVITY OF AN ENZYME FOR UNUSUAL ENVIRONMENTS - SEQUENTIAL RANDOM MUTAGENESIS OF SUBTILISIN-E FOR CATALYSIS IN DIMETHYLFORMAMIDE [J].
CHEN, KQ ;
ARNOLD, FH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (12) :5618-5622
[8]   Molecular evolution of an arsenate detoxification pathway DNA shuffling [J].
Crameri, A ;
Dawes, G ;
Rodriguez, E ;
Silver, S ;
Stemmer, WPC .
NATURE BIOTECHNOLOGY, 1997, 15 (05) :436-438
[9]   CONTEXT DEPENDENCE OF PHENOTYPE PREDICTION AND DIVERSITY IN COMBINATORIAL MUTAGENESIS [J].
DELAGRAVE, S ;
GOLDMAN, ER ;
YOUVAN, DC .
PROTEIN ENGINEERING, 1995, 8 (03) :237-242
[10]   A SIMPLE AND EFFICIENT PROCEDURE FOR SATURATION MUTAGENESIS USING MIXED OLIGODEOXYNUCLEOTIDES [J].
DERBYSHIRE, KM ;
SALVO, JJ ;
GRINDLEY, NDF .
GENE, 1986, 46 (2-3) :145-152