Relay Oxidation with Engineered P450 BM3 and Aldo-Keto Reductase: Chemoenzymatic Synthesis of Erythrina Alkaloids

Direct selective C–H oxidation poses a significant challenge in natural product synthesis. Enzymes serve as enabling catalysts to precisely control the transformation with high chemo-, regio-, and stereoselectivity. In this study, we report the screening and engineering of a P450 BM3 variant capable of selective hydroxylation in the tricyclic core of erythrina alkaloids with high diastereoselectivity. To further address the enantioselectivity to construct the chiral α-tertiary amine, an enzymatic kinetic resolution by relay oxidation with engineered P450 BM3 and aldo-keto reductase was successfully implemented, utilizing a highly enantioselective aldo-keto reductase, resulting in the chiral intermediate, which has been successfully applied to the synthesis of 3-demethoxyerythratidinone. The selectivity modulation not only deepens our understanding of enzyme-catalyzed non-natural chemical transformations but also inaugurates an alternative synthetic route for bioactive molecules.

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Publication Details

Journal
ACS Catalysis
Published
2026-03-14
DOI
https://doi.org/10.1021/acscatal.6c00910
Primary Topic
Bioactive natural compounds
Type
article
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article

Relay Oxidation with Engineered P450 BM3 and Aldo-Keto Reductase: Chemoenzymatic Synthesis of Erythrina Alkaloids

Longxing Wang, Lingyong Wang, Min Shi, Huilei Yu et al.
ACS Catalysis
Bioactive natural compounds
article

Relay Oxidation with Engineered P450 BM3 and Aldo-Keto Reductase: Chemoenzymatic Synthesis of Erythrina Alkaloids

Longxing Wang, Lingyong Wang, Min Shi, Huilei Yu, Ran Hong, Lili Zhu
article en

Abstract

Direct selective C–H oxidation poses a significant challenge in natural product synthesis. Enzymes serve as enabling catalysts to precisely control the transformation with high chemo-, regio-, and stereoselectivity. In this study, we report the screening and engineering of a P450 BM3 variant capable of selective hydroxylation in the tricyclic core of erythrina alkaloids with high diastereoselectivity. To further address the enantioselectivity to construct the chiral α-tertiary amine, an enzymatic kinetic resolution by relay oxidation with engineered P450 BM3 and aldo-keto reductase was successfully implemented, utilizing a highly enantioselective aldo-keto reductase, resulting in the chiral intermediate, which has been successfully applied to the synthesis of 3-demethoxyerythratidinone. The selectivity modulation not only deepens our understanding of enzyme-catalyzed non-natural chemical transformations but also inaugurates an alternative synthetic route for bioactive molecules.

ACS Catalysis
East China University of Science and Technology (CN), Chinese Academy of Sciences (CN), Shanghai Institute of Organic Chemistry (CN)
Openalex Percentile: Top 22%
Bioactive natural compounds
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