Improved biocatalysts by directed evolution and rational protein design

被引:339
作者
Bornscheuer, UT
Pohl, M
机构
[1] Ernst Moritz Arndt Univ Greifswald, Inst Chem & Biochem, Dept Tech Chem & Biotechnol, D-17487 Greifswald, Germany
[2] MPB Cologne GmbH, D-51063 Cologne, Germany
关键词
D O I
10.1016/S1367-5931(00)00182-4
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
The efficient application of biocatalysts requires the; availability of suitable: enzymes with high activity and stability under process conditions, desired substrate selectivity and high enantioselectivity. However, wild-type enzymes: often need to be optimized La fulfill these requirements. Two: rather contradictory tools can be used on a, molecular level to create tailor-made bio-catalysts: directed evolution and rational protein design.
引用
收藏
页码:137 / 143
页数:7
相关论文
共 70 条
[1]   Further improvement of the thermal stability of a partially stabilized Bacillus subtilis 3-isopropylmalate dehydrogenase variant by random and site-directed mutagenesis [J].
Akanuma, S ;
Yamagishi, A ;
Tanaka, N ;
Oshima, T .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 260 (02) :499-504
[2]   RETRACTED: Directed evolution of new catalytic activity using the α/β-barrel scaffold (Retracted article. See vol 417, pg 468, 2002) [J].
Altamirano, MM ;
Blackburn, JM ;
Aguayo, C ;
Fersht, AR .
NATURE, 2000, 403 (6770) :617-622
[3]   Combinatorial and computational challenges for biocatalyst design [J].
Arnold, FH .
NATURE, 2001, 409 (6817) :253-257
[4]   Directed evolution of biocatalysts [J].
Arnold, FH ;
Volkov, AA .
CURRENT OPINION IN CHEMICAL BIOLOGY, 1999, 3 (01) :54-59
[5]  
Bornscheuer U.T., 2000, ENZYMES LIPID MODIFI
[6]   Directed evolution of an esterase: Screening of enzyme libraries based on pH-Indicators and a growth assay [J].
Bornscheuer, UT ;
Altenbuchner, J ;
Meyer, HH .
BIOORGANIC & MEDICINAL CHEMISTRY, 1999, 7 (10) :2169-2173
[7]  
Bornscheuer UT, 2006, HYDROLASES IN ORGANIC SYNTHESIS: REGIO- AND STEREOSELECTIVE BIOTRANSFORMATIONS, 2ND EDITION, P1
[8]  
Bornscheuer UT, 1998, ANGEW CHEM INT EDIT, V37, P3105, DOI 10.1002/(SICI)1521-3773(19981204)37:22<3105::AID-ANIE3105>3.0.CO
[9]  
2-#
[10]   Site-directed mutagenesis of residues 164, 170, 171, 179, 220, 237 and 242 in PER-1 β-lactamase hydrolysing expanded-spectrum cephalosporins [J].
Bouthors, AT ;
Delettré, J ;
Mugnier, P ;
Jarlier, V ;
Sougakoff, W .
PROTEIN ENGINEERING, 1999, 12 (04) :313-318