Regenerable copper anode for the Cu(I)-mediated reduction of FAD in the electroenzymatic styrene epoxidation reaction
Autor: | Robert Adongo Amongre, George T. Gassner |
---|---|
Rok vydání: | 2020 |
Předmět: |
Inorganic chemistry
Biophysics Flavoprotein 02 engineering and technology Flavin group Electrochemistry 01 natural sciences Redox Catalysis Styrene chemistry.chemical_compound Styrene oxide Flavin reductase Physical and Theoretical Chemistry Electrodes biology 010401 analytical chemistry General Medicine 021001 nanoscience & nanotechnology 0104 chemical sciences Enzymes Kinetics chemistry biology.protein Flavin-Adenine Dinucleotide Potentiometry Epoxy Compounds 0210 nano-technology Oxidation-Reduction Copper |
Zdroj: | Bioelectrochemistry (Amsterdam, Netherlands). 137 |
ISSN: | 1878-562X |
Popis: | Styrene monooxygenase (SMO) is a two-component flavoenzyme composed of NADH-dependent flavin reductase (SMOB) and FAD-specific styrene epoxidase (NSMOA) components. The enantioselective styrene epoxidation reaction catalyzed by this enzyme can be streamlined for chemosynthetic applications by substituting NADH and the reductase with an electrode to supply the epoxidase with reducing equivalents required for catalysis. Slow kinetics of adsorption and desorption of FAD from the electrode surface and unproductive side reactions of the reduced flavin with oxygen limit the efficiency of direct electroenzymatic catalysis. In the present work we develop a miniature spectroelectrochemical cell equipped with a copper electrode for the anodic synthesis of Cu(I) chelates of EDTA, glutamate, and citrate as FAD-reducing agents, and a platinum electrode for the electrolytic generation of oxygen. Copper oxidized in the flavin reduction reaction can be reclaimed subsequently as copper metal at the electrode surface. About 80% transformation of styrene is achieved in a single cell cycle of reduction and oxygenation at pH 7 and 25 °C in good agreement with that predicted by numerical simulation. When the cell is operated in two successive cycles, styrene oxide can be synthesized with an electroenzymatic epoxidation activity of 663U/g in 94% yield. This approach to electroenzymatic catalysis shows promise for the quantitative transformation of styrene to styrene oxide and may be applied more generally to other flavoprotein monooxygenases. |
Databáze: | OpenAIRE |
Externí odkaz: |