Electrocatalytic NAD(P)H regeneration for biosynthesis

被引:15
|
作者
Li, Yaoxuan [1 ]
Liu, Guanhua [1 ]
Kong, Weixi [1 ]
Zhang, Suoqing [2 ]
Bao, Yuemei [3 ]
Zhao, Hao [1 ]
Wang, Lihui [1 ]
Zhou, Liya [1 ]
Jiang, Yanjun [1 ]
机构
[1] Hebei Univ Technol, Sch Chem Engn & Technol, Natl Local Joint Engn Lab Energy Conservat Chem Pr, Tianjin 300401, Peoples R China
[2] North China Pharmaceut Grp Corp, Shijiazhuang 050015, Peoples R China
[3] Tianjin Food Res Inst, Tianjin 301609, Peoples R China
基金
中国国家自然科学基金;
关键词
Biosynthesis; Cofactor regeneration; Bioelectrocatalysis; NAD(P)H; Electron mediator; DIRECT ELECTROCHEMICAL REGENERATION; CATALYZED ELECTRON-TRANSFER; NADH REGENERATION; ENZYMATIC REDUCTION; CO2; REDUCTION; NICOTINAMIDE COFACTORS; CHIRAL ALCOHOLS; CARBON-DIOXIDE; AMINO-ACIDS; FORMATE;
D O I
10.1016/j.gce.2023.02.001
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The highly efficient chemoselectivity, stereoselectivity, and regioselectivity render enzyme catalysis an ideal pathway for the synthesis of various chemicals in broad applications. While the cofactor of an enzyme is necessary but expensive, the conversed state of the cofactor is not beneficial for the positive direction of the reaction. Cofactor regeneration using electrochemical methods has the advantages of simple operation, low cost, easy process monitoring, and easy product separation, and the electrical energy is green and sustainable. Therefore, bioelectrocatalysis has great potential in synthesis by combining electrochemical cofactor regeneration with enzymatic catalysis. In this review, we detail the mechanism of cofactor regeneration and categorize the common electron mediators and enzymes used in cofactor regeneration. The reaction type and the recent progress are summarized in electrochemically coupled enzymatic catalysis. The main challenges of such electroenzymatic catalysis are pointed out and future developments in this field are foreseen.
引用
收藏
页码:1 / 15
页数:15
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