Litcius/Paper detail

Photoenzymatic Reductions Enabled by Direct Excitation of Flavin-Dependent “Ene”-Reductases

Braddock A. Sandoval, Phillip D. Clayman, Daniel G. Oblinsky, Seokjoon Oh, Yuji Nakano, Matthew J. Bird, Gregory D. Scholes, Todd K. Hyster

2020Journal of the American Chemical Society96 citationsDOIOpen Access PDF

Abstract

Non-natural photoenzymatic reactions reported to date have depended on the excitation of electron donor-acceptor complexes formed between substrates and cofactors within protein active sites to facilitate electron transfer. While this mechanism has unlocked new reactivity, it limits the types of substrates that can be involved in this area of catalysis. Here we demonstrate that direct excitation of flavin hydroquinone within "ene"-reductase active sites enables new substrates to participate in photoenzymatic reactions. We found that by using photoexcitation these enzymes gain the ability to reduce acrylamides through a single electron transfer mechanism.

Topics & Concepts

ChemistryPhotoexcitationFlavin groupElectron transferHydroquinoneReactivity (psychology)PhotochemistryExcitationCofactorCatalysisActive siteEne reactionElectron acceptorAcceptorStereochemistryCombinatorial chemistryEnzymeOrganic chemistryMedicineElectrical engineeringPathologyCondensed matter physicsAlternative medicinePhysicsEngineeringRadical Photochemical ReactionsSulfur Compounds in BiologyMicrobial Community Ecology and Physiology