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- W2974583809 endingPage "868" @default.
- W2974583809 startingPage "868" @default.
- W2974583809 abstract "The asymmetric reduction of enoates, imines and ketones are among the most important reactions in biocatalysis. These reactions are routinely conducted using enzymes that use nicotinamide cofactors as reductants. The deazaflavin cofactor F420 also has electrochemical properties that make it suitable as an alternative to nicotinamide cofactors for use in asymmetric reduction reactions. However, cofactor F420-dependent enzymes remain under-explored as a resource for biocatalysis. This review considers the cofactor F420-dependent enzyme families with the greatest potential for the discovery of new biocatalysts: the flavin/deazaflavin-dependent oxidoreductases (FDORs) and the luciferase-like hydride transferases (LLHTs). The characterized F420-dependent reductions that have the potential for adaptation for biocatalysis are discussed, and the enzymes best suited for use in the reduction of oxidized cofactor F420 to allow cofactor recycling in situ are considered. Further discussed are the recent advances in the production of cofactor F420 and its functional analog FO-5′-phosphate, which remains an impediment to the adoption of this family of enzymes for industrial biocatalytic processes. Finally, the prospects for the use of this cofactor and dependent enzymes as a resource for industrial biocatalysis are discussed." @default.
- W2974583809 created "2019-09-26" @default.
- W2974583809 creator A5012067250 @default.
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- W2974583809 creator A5070023486 @default.
- W2974583809 creator A5072057568 @default.
- W2974583809 date "2019-10-20" @default.
- W2974583809 modified "2023-10-17" @default.
- W2974583809 title "Cofactor F420-Dependent Enzymes: An Under-Explored Resource for Asymmetric Redox Biocatalysis" @default.
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- W2974583809 doi "https://doi.org/10.3390/catal9100868" @default.
- W2974583809 hasPublicationYear "2019" @default.
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