Semiartificial Photoelectrochemistry for CO2-Mediated Enantioselective Organic Synthesis.
Photoelectrochemical (PEC) cells are under intensive development for the synthesis of solar fuels, but CO2 reduction typically only results in simple building blocks such as HCOO-. Here, we demonstrate that CO2-converting PEC cells can drive integrated enzymatic domino catalysis to produce chiral organic molecules by using CO2/HCOO- as a sustainable redox couple. First, we establish a semiartificial electrode consisting of three enzymes co-immobilized on a high surface area electrode based on carbon felt covered by a mesoporous indium tin oxide (ITO) coating. When applying a mild cathodic potential (-0.25 V vs the reversible hydrogen electrode (RHE)), CO2 is reduced to HCOO- using a W-formate dehydrogenase (FDHNvH) from Nitratidesulfovibrio vulgaris Hildenborough, which then enables the reduction of NAD+ to NADH by an NAD+-cofactor-dependent formate dehydrogenase from Candida boidinii (FDHCB). Subsequently, an alcohol dehydrogenase (ADH) uses NADH generated from CO2/HCOO- cycling to reduce acetophenone to chiral 1-phenylethanol in good enantiomeric excess (93%) and conversion yields (38%). Depending on the specific ADH (ADHS or ADHR), either (S)- or (R)-1-phenylethanol can be synthesized at pH 6 and 20 °C. To illustrate solar energy utilization, we integrate the three nanoconfined enzymes with a PEC platform based on an integrated organic semiconductor photocathode to allow for enantioselective synthesis (at +0.8 V vs RHE) based on a solar fuel device. This proof-of-principle demonstration shows that concepts and devices from artificial photosynthesis can be readily translated to precise and sustainable biocatalysis, including the production of chiral organic molecules using light.
Publication Details
- Journal
- Apollo (University of Cambridge)
- Published
- 2025-04-04
- DOI
- https://doi.org/10.17863/cam.117221
- Primary Topic
- Enzyme Catalysis and Immobilization
- Type
- article
- Field-Weighted Citation Impact
- 0.00