Light‐Controlled Biocatalysis by Unspecific Peroxygenases with Genetically Encoded Photosensitizers

Author:

Püllmann Pascal12ORCID,Homann Dominik13,Karl Tobias A.4ORCID,König Burkhard4ORCID,Weissenborn Martin J.13ORCID

Affiliation:

1. Research Group Bioorganic Chemistry Leibniz Institute for Plant Biochemistry Weinberg 3 06120 Halle (Saale) Germany

2. Present address: Molecular Design and Engineering Bayer AG Aprather Weg 18 A 42113 Wuppertal Germany

3. Institute of Chemistry Martin-Luther-University Halle-Wittenberg Weinbergweg 22 06120 Halle (Saale) Germany

4. Institute for Organic Chemistry University of Regensburg Universitätstr. 31 93053 Regensburg Germany

Abstract

AbstractFungal unspecific peroxygenases (UPOs) have gained substantial attention for their versatile oxyfunctionalization chemistry paired with impressive catalytic capabilities. A major drawback, however, remains their sensitivity towards their co‐substrate hydrogen peroxide, necessitating the use of smart in situ hydrogen peroxide generation methods to enable efficient catalysis setups. Herein, we introduce flavin‐containing protein photosensitizers as a new general tool for light‐controlled in situ hydrogen peroxide production. By genetically fusing flavin binding fluorescent proteins and UPOs, we have created two virtually self‐sufficient photo‐enzymes (PhotUPO). Subsequent testing of a versatile substrate panel with the two divergent PhotUPOs revealed two stereoselective conversions. The catalytic performance of the fusion protein was optimized through enzyme and substrate loading variation, enabling up to 24300 turnover numbers (TONs) for the sulfoxidation of methyl phenyl sulfide. The PhotUPO concept was upscaled to a 100 mg substrate preparative scale, enabling the extraction of enantiomerically pure alcohol products.

Funder

Deutsche Bundesstiftung Umwelt

Friedrich-Ebert-Stiftung

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

General Chemistry,Catalysis

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