Enzyme stabilization -: recent experimental progress

被引:306
|
作者
O'Fágáin, C [1 ]
机构
[1] Dublin City Univ, Sch Biotechnol, Dublin 9, Ireland
[2] Dublin City Univ, Natl Ctr Sensors Res, Dublin 9, Ireland
关键词
enzyme stabilization; inactivation model; protein engineering; directed evolution; chemical modification; stabilizing additives;
D O I
10.1016/S0141-0229(03)00160-1
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
This article surveys the enzyme stabilization literature since 1997, focusing on protein engineering and chemical modification. Within protein engineering, directed evolution strategies have yielded notable successes. Polypeptide chain extension, manipulation of chimeric proteins and rational design have also led to stability gains. Chemical modification, as manifested in crosslinked enzyme crystals (CLECs), covalent attachment of polymers and surface modification, remains useful. Inactivation models, stabilizing additives and organic solvents also receive mention. Since extremophilic proteins have received much attention elsewhere, recent reviews are merely indicated. Immobilized proteins are not considered; neither is the computational design or prediction of protein stability. Case studies focus on enzymes used, or potentially useful, in industrial processes or in biosensors. Examples include peroxidases, phospholipase, cellulase, phytase, luciferase, bacterial proteases, alpha-amylase and glucose isomerase (GI), among others. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:137 / 149
页数:13
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