Concurrent Linear Deracemization of Secondary Benzylic Alcohols via Simultaneous Photocatalysis and Whole-cell Biocatalysis

Photobiocatalysis enables remarkable synthetic transformations by combining the exquisite stereoselectivity of enzymes with the mild generation of high-energy intermediates by photocatalysis, but practical applications remain limited due to enzyme photodamage. The deracemization of secondary alcohols is a key model reaction for photobiocatalytic protocols due to the importance of the enantioenriched products. However, current strategies rely on the temporal separation of catalytic cycles to circumvent incompatibilities, precluding photobiocatalytic transformations that require the <i>in situ</i> generation of reactive intermediates. We report a single-step concurrent linear deracemization protocol by combining a water-soluble photocatalyst (sodium anthraquinone-2-sulfonate) with a promiscuous alcohol dehydrogenase (<i>Geotrichum candidum</i> acetophenone reductase) encapsulated in lyophilized microbial whole cells. Insights into enzyme selectivity and system dynamics from molecular docking and kinetic modeling guided the optimization of the multicomponent system. Our approach represents a modular and generalizable strategy for developing photobiocatalytic cascades operating under mutually compatible conditions, wherein spatial separation mitigates photodamage and enables simultaneous dual catalytic turnover.

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Journal
ACS Catalysis
Published
2025-08-18
DOI
https://doi.org/10.1021/acscatal.5c04974
Primary Topic
Innovative Microfluidic and Catalytic Techniques Innovation
Type
article
Field-Weighted Citation Impact
0.00

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article

Concurrent Linear Deracemization of Secondary Benzylic Alcohols via Simultaneous Photocatalysis and Whole-cell Biocatalysis

Stephen Wallace, Craig P. Johnston, W. WONG
ACS Catalysis
Innovative Microfluidic and Catalytic Techniques Innovation
article

Concurrent Linear Deracemization of Secondary Benzylic Alcohols via Simultaneous Photocatalysis and Whole-cell Biocatalysis

Stephen Wallace, Craig P. Johnston, W. WONG
article en

Abstract

Photobiocatalysis enables remarkable synthetic transformations by combining the exquisite stereoselectivity of enzymes with the mild generation of high-energy intermediates by photocatalysis, but practical applications remain limited due to enzyme photodamage. The deracemization of secondary alcohols is a key model reaction for photobiocatalytic protocols due to the importance of the enantioenriched products. However, current strategies rely on the temporal separation of catalytic cycles to circumvent incompatibilities, precluding photobiocatalytic transformations that require the <i>in situ</i> generation of reactive intermediates. We report a single-step concurrent linear deracemization protocol by combining a water-soluble photocatalyst (sodium anthraquinone-2-sulfonate) with a promiscuous alcohol dehydrogenase (<i>Geotrichum candidum</i> acetophenone reductase) encapsulated in lyophilized microbial whole cells. Insights into enzyme selectivity and system dynamics from molecular docking and kinetic modeling guided the optimization of the multicomponent system. Our approach represents a modular and generalizable strategy for developing photobiocatalytic cascades operating under mutually compatible conditions, wherein spatial separation mitigates photodamage and enables simultaneous dual catalytic turnover.

ACS CatalysisVol. 15(17)
University of St Andrews (GB), Quantitative BioSciences (US), University of Edinburgh (GB)
UK Research and Innovation, Royal Society, Directorate for Biological Sciences, Biotechnology and Biological Sciences Research Council
Openalex Percentile: Top 80%
Innovative Microfluidic and Catalytic Techniques Innovation
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