Enzyme-Based Electrobiotechnological Synthesis

被引:9
|
作者
Schmitz, Lisa Marie [1 ]
Rosenthal, Katrin [1 ]
Luetz, Stephan [1 ]
机构
[1] TU Dortmund Univ, Dept Biochem & Chem Engn, Dortmund, Germany
来源
BIOELECTROSYNTHESIS | 2019年 / 167卷
关键词
Cofactor regeneration; Electrochemistry; Electron mediator; Enzyme catalysis; Oxidoreductases; Reactor design; Rhodium complex; AMINO-ACID OXIDASE; INDIRECT ELECTROCHEMICAL REGENERATION; TRANSITION-METAL-COMPLEXES; ELECTROENZYMATIC SYNTHESIS; MEMBRANE REACTOR; COFACTOR REGENERATION; ELECTRON-TRANSFER; NICOTINAMIDE COFACTORS; ALCOHOL-DEHYDROGENASE; GLUCOSE-DEHYDROGENASE;
D O I
10.1007/10_2017_33
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
Oxidoreductases are enzymes with a high potential for organic synthesis, as their selectivity often exceeds comparable chemical syntheses. The biochemical cofactors of these enzymes need regeneration during synthesis. Several regeneration methods are available but the electrochemical approach offers an efficient and quasi mass-free method for providing the required redox equivalents. Electron transfer systems involving direct regeneration of natural and artificial cofactors, indirect electrochemical regeneration via a mediator, and indirect electroenzymatic cofactor regeneration via enzyme and mediator have been investigated. This chapter gives an overview of electroenzymatic syntheses with oxidoreductases, structured by the enzyme subclass and their usage of cofactors for electron relay. Particular attention is given to the productivity of electroenzymatic biotransformation processes. Because most electroenzymatic syntheses suffer from low productivity, we discuss reaction engineering concepts to overcome the main limiting factors, with a focus on media conductivity optimization, approaches to prevent enzyme inactivation, and the application of advanced cell designs. [GRAPHICS] .
引用
收藏
页码:87 / 134
页数:48
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