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Electrochemical transformations catalyzed by cytochrome P450s and peroxidases

Journal

CHEMICAL SOCIETY REVIEWS
Volume 52, Issue 15, Pages 5135-5171

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d3cs00461a

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Cytochrome P450s (Cyt P450s) and peroxidases are enzymes with iron heme cofactors used as biocatalysts in chemical syntheses. By incorporating them into thin films on electrodes, these enzymes can accept electrons and catalyze organic transformations in a cost-effective way. This paper reviews the electrochemical reactions catalyzed by Cyt P450s and peroxidases, including C-H activation, S-oxidation, epoxidation, N-hydroxylation, and oxidative N- and O-dealkylation. Design aspects of these bioelectrocatalytic reactions are discussed, as well as challenges and future perspectives of these systems.
Cytochrome P450s (Cyt P450s) and peroxidases are enzymes featuring iron heme cofactors that have wide applicability as biocatalysts in chemical syntheses. Cyt P450s are a family of monooxygenases that oxidize fatty acids, steroids, and xenobiotics, synthesize hormones, and convert drugs and other chemicals to metabolites. Peroxidases are involved in breaking down hydrogen peroxide and can oxidize organic compounds during this process. Both heme-containing enzymes utilize active Fe-IV (sic)O intermediates to oxidize reactants. By incorporating these enzymes in stable thin films on electrodes, Cyt P450s and peroxidases can accept electrons from an electrode, albeit by different mechanisms, and catalyze organic transformations in a feasible and cost-effective way. This is an advantageous approach, often called bioelectrocatalysis, compared to their biological pathways in solution that require expensive biochemical reductants such as NADPH or additional enzymes to recycle NADPH for Cyt P450s. Bioelectrocatalysis also serves as an ex situ platform to investigate metabolism of drugs and bio-relevant chemicals. In this paper we review biocatalytic electrochemical reactions using Cyt P450s including C-H activation, S-oxidation, epoxidation, N-hydroxylation, and oxidative N-, and O-dealkylation; as well as reactions catalyzed by peroxidases including synthetically important oxidations of organic compounds. Design aspects of these bioelectrocatalytic reactions are presented and discussed, including enzyme film formation on electrodes, temperature, pH, solvents, and activation of the enzymes. Finally, we discuss challenges and future perspective of these two important bioelectrocatalytic systems.

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