Light-driven catalysis with engineered enzymes and biomimetic systems

被引:28
|
作者
Edwards, Emily H. [1 ]
Bren, Kara L. [1 ]
机构
[1] Univ Rochester, Dept Chem, RC Box 270216, Rochester, NY 14627 USA
基金
美国国家科学基金会;
关键词
biocatalysis; photocatalysis; C-H activation; small-molecule activation; artificial photosynthesis; PHOTOCATALYTIC WATER OXIDATION; NICKEL-SUBSTITUTED RUBREDOXIN; HOMOGENEOUS CO2 REDUCTION; OUTER COORDINATION SPHERE; COUPLED ELECTRON-TRANSFER; P450; BM3; ENZYMES; C-H BONDS; HYDROGEN-PRODUCTION; ARTIFICIAL PHOTOSYNTHESIS; PHOTOSYSTEM-I;
D O I
10.1002/bab.1976
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
Efforts to drive catalytic reactions with light, inspired by natural processes like photosynthesis, have a long history and have seen significant recent growth. Successfully engineering systems using biomolecular and bioinspired catalysts to carry out light-driven chemical reactions capitalizes on advantages offered from the fields of biocatalysis and photocatalysis. In particular, driving reactions under mild conditions and in water, in which enzymes are operative, using sunlight as a renewable energy source yield environmentally friendly systems. Furthermore, using enzymes and bioinspired systems can take advantage of the high efficiency and specificity of biocatalysts. There are many challenges to overcome to fully capitalize on the potential of light-driven biocatalysis. In this mini-review, we discuss examples of enzymes and engineered biomolecular catalysts that are activated via electron transfer from a photosensitizer in a photocatalytic system. We place an emphasis on selected forefront chemical reactions of high interest, including C-H oxidation, proton reduction, water oxidation, CO(2)reduction, and N(2)reduction.
引用
收藏
页码:463 / 483
页数:21
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