4.7 Article

Regenerable copper anode for the Cu(I)-mediated reduction of FAD in the electroenzymatic styrene epoxidation reaction

Journal

BIOELECTROCHEMISTRY
Volume 137, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.bioelechem.2020.107679

Keywords

Styrene; Monooxygenase; Flavoprotein; Biocatalysis; Electrochemistry; Copper

Funding

  1. NIH [MBRS-RISE R25-GM059289]

Ask authors/readers for more resources

The study introduced an electroenzymatic method for epoxidation of styrene, utilizing a copper electrode for FAD reduction and a platinum electrode for oxygen generation, achieving a high conversion rate. This approach shows promise for other flavoprotein monooxygenases and may lead to advancements in quantitative transformation of styrene to styrene oxide.
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 degrees 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. Published by Elsevier B.V.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available