Light-Driven CO2 Reduction by Co-Cytochrome b 562

被引:12
|
作者
Alcala-Torano, Rafael [1 ]
Halloran, Nicholas [1 ]
Gwerder, Noah [1 ]
Sommer, Dayn J. [1 ]
Ghirlanda, Giovanna [1 ]
机构
[1] Arizona State Univ, Sch Mol Sci, Tempe, AZ 85281 USA
基金
美国国家科学基金会;
关键词
cobalt porphyrin; Carbon fixation; CO2; reduction; catalysis; protein design; proton reduction; CATALYZED ELECTROCHEMICAL REDUCTION; HYDROGEN EVOLUTION; CARBON-DIOXIDE; COBALT PORPHYRINS; DESIGN; WATER; EFFICIENT; IRON; COMPLEXES; B(562);
D O I
10.3389/fmolb.2021.609654
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
The current trend in atmospheric carbon dioxide concentrations is causing increasing concerns for its environmental impacts, and spurring the developments of sustainable methods to reduce CO2 to usable molecules. We report the light-driven CO2 reduction in water in mild conditions by artificial protein catalysts based on cytochrome b (562) and incorporating cobalt protoporphyrin IX as cofactor. Incorporation into the protein scaffolds enhances the intrinsic reactivity of the cobalt porphyrin toward proton reduction and CO generation. Mutations around the binding site modulate the activity of the enzyme, pointing to the possibility of further improving catalytic activity through rational design or directed evolution.
引用
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页数:8
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