Repurposing Iron‐ and 2‐Oxoglutarate‐Dependent Oxygenases to Catalyze Olefin Hydration

Author:

Wang Bingnan1ORCID,Lu Yong1ORCID,Cha Lide2,Chen Tzu‐Yu2,Palacios Philip M.3,Li Liping1,Guo Yisong3ORCID,Chang Wei‐chen2ORCID,Chen Chuo1ORCID

Affiliation:

1. Department of Biochemistry UT Southwestern Medical Center 5323 Harry Hines Boulevard Dallas TX 75390 USA

2. Department of Chemistry NC State University 2620 Yarbrough Drive Raleigh NC 27695 USA

3. Department of Chemistry Carnegie Mellon University 4400 Fifth Avenue Pittsburgh PA 15213 USA

Abstract

AbstractMononuclear nonheme iron(II) and 2‐oxoglutarate (Fe/2OG)‐dependent oxygenases and halogenases are known to catalyze a diverse set of oxidative reactions, including hydroxylation, halogenation, epoxidation, and desaturation in primary metabolism and natural product maturation. However, their use in abiotic transformations has mainly been limited to C−H oxidation. Herein, we show that various enzymes of this family, when reconstituted with Fe(II) or Fe(III), can catalyze Mukaiyama hydration—a redox neutral transformation. Distinct from the native reactions of the Fe/2OG enzymes, wherein oxygen atom transfer (OAT) catalyzed by an iron‐oxo species is involved, this nonnative transformation proceeds through a hydrogen atom transfer (HAT) pathway in a 2OG‐independent manner. Additionally, in contrast to conventional inorganic catalysts, wherein a dinuclear iron species is responsible for HAT, the Fe/2OG enzymes exploit a mononuclear iron center to support this reaction. Collectively, our work demonstrates that Fe/2OG enzymes have utility in catalysis beyond the current scope of catalytic oxidation.

Funder

National Institute of General Medical Sciences

Division of Chemistry

Publisher

Wiley

Subject

General Medicine

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