Biocatalysis in Organic Chemistry and Biotechnology: Past, Present, and Future

被引:608
作者
Reetz, Manfred T. [1 ,2 ]
机构
[1] Univ Marburg, Dept Chem, D-35032 Marburg, Germany
[2] Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
关键词
SITE-SATURATION MUTAGENESIS; BAEYER-VILLIGER MONOOXYGENASES; CANDIDA-ANTARCTICA LIPASE; ENZYMATIC TOTAL-SYNTHESIS; GENETIC SELECTION SYSTEM; DIRECTED EVOLUTION; LABORATORY EVOLUTION; AMINO-ACID; EPOXIDE HYDROLASE; IN-VITRO;
D O I
10.1021/ja405051f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Enzymes as catalysts in synthetic organic chemistry gained importance in the latter half of the 20th century, but nevertheless suffered from two major limitations. First, many enzymes were not accessible in large enough quantities for practical applications. The advent of recombinant DNA technology changed this dramatically in the late 1970s. Second, many enzymes showed a narrow substrate scope, often poor stereo- and/or regioselectivity and/or insufficient stability under operating conditions. With the development of directed evolution beginning in the 1990s and continuing to the present day, all of these problems can be addressed and generally solved. The present Perspective focuses on these and other developments which have popularized enzymes as part of the toolkit of synthetic organic chemists and biotechnologists. Included is a discussion of the scope and limitation of cascade reactions using enzyme mixtures in vitro and of metabolic engineering of pathways in cells as factories for the production of simple compounds such as biofuels and complex natural products. Future trends and problems are also highlighted, as is the discussion concerning biocatalysis versus nonbiological catalysis in synthetic organic chemistry. This Perspective does not constitute a comprehensive review, and therefore the author apologizes to those researchers whose work is not specifically treated here.
引用
收藏
页码:12480 / 12496
页数:17
相关论文
共 228 条
[41]   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
[42]   Enzymatic total synthesis of enterocin polyketides [J].
Cheng, Qian ;
Xiang, Longkuan ;
Izumikawa, Miho ;
Meluzzi, Dario ;
Moore, Bradley S. .
NATURE CHEMICAL BIOLOGY, 2007, 3 (09) :557-558
[43]  
Church G., 2012, REGENESIS HOW SYNTHE
[44]   Olefin Cyclopropanation via Carbene Transfer Catalyzed by Engineered Cytochrome P450 Enzymes [J].
Coelho, Pedro S. ;
Brustad, Eric M. ;
Kannan, Arvind ;
Arnold, Frances H. .
SCIENCE, 2013, 339 (6117) :307-310
[45]   Hydroxynitrile Lyases: Insights into Biochemistry, Discovery, and Engineering [J].
Dadashipour, Mohammad ;
Asano, Yasuhisa .
ACS CATALYSIS, 2011, 1 (09) :1121-1149
[46]   Recent Developments in the Application of Baeyer-Villiger Monooxygenases as Biocatalysts [J].
de Gonzalo, Gonzalo ;
Mihovilovic, Marko D. ;
Fraaije, Marco W. .
CHEMBIOCHEM, 2010, 11 (16) :2208-2231
[47]   Creating lactose phosphorylase enzymes by directed evolution of cellobiose phosphorylase [J].
De Groeve, Manu R. M. ;
De Baere, Miet ;
Hoflack, Lieve ;
Desmet, Tom ;
Vandamme, Erick J. ;
Soetaert, Wim .
PROTEIN ENGINEERING DESIGN & SELECTION, 2009, 22 (07) :393-399
[48]   Biocatalytic reductions: From lab curiosity to "first choice" [J].
De Wildeman, Stefaan M. A. ;
Sonke, Theo ;
Schoemaker, Hants E. ;
May, Oliver .
ACCOUNTS OF CHEMICAL RESEARCH, 2007, 40 (12) :1260-1266
[49]   Improving the diastereoselectivity of penicillin G acylase for ampicillin synthesis from racemic substrates [J].
Deaguero, Andria L. ;
Blum, Janna K. ;
Bommarius, Andreas S. .
PROTEIN ENGINEERING DESIGN & SELECTION, 2012, 25 (03) :135-144
[50]  
Denault M, 2007, METH MOL B, V352, P127