Kang, Suk Woo Antoney, James Lupton, David W. Speight, Robert Scott, Colin Jackson, Colin J. 2024-01-19T10:04:46Z 2024-01-19T10:04:46Z 2023-01-13 2023-02 0006-2960 https://pubs.kist.re.kr/handle/201004/114061 The stereoselective reduction of alkenes conjugated to electron-withdrawing groups by ene-reductases has been extensively applied to the commercial preparation of fine chemicals. Although several different enzyme families are known to possess ene-reductase activity, the old yellow enzyme (OYE) family has been the most thoroughly investigated. Recently, it was shown that a subset of ene-reductases belonging to the flavin/ deazaflavin oxidoreductase (FDOR) superfamily exhibit enantio-selectivity that is generally complementary to that seen in the OYE family. These enzymes belong to one of several FDOR subgroups that use the unusual deazaflavin cofactor F420. Here, we explore several enzymes of the FDOR-A subgroup, characterizing their substrate range and enantioselectivity with 20 different com-pounds, identifying enzymes (MSMEG_2027 and MSMEG_2850) that could reduce a wide range of compounds stereoselectively. For example, MSMEG_2027 catalyzed the complete conversion of both isomers of citral to (R)-citronellal with 99% ee, while MSMEG_2850 catalyzed complete conversion of ketoisophorone to (S)-levodione with 99% ee. Protein crystallography combined with computational docking has allowed the observed stereoselectivity to be mechanistically rationalized for two enzymes. These findings add further support for the FDOR and OYE families of ene-reductases displaying general stereocomplementarity to each other and highlight their potential value in asymmetric ene-reduction. English American Chemical Society Asymmetric Ene-Reduction of α,β-Unsaturated Compounds by F420-Dependent Oxidoreductases A Enzymes from Mycobacterium smegmatis Article 10.1021/acs.biochem.2c00557 1 Biochemistry, v.62, no.3, pp.873 - 891 Biochemistry 62 3 873 891 N scie scopus 000893148800001 2-s2.0-85143488904 Biochemistry & Molecular Biology Biochemistry & Molecular Biology Article PENTAERYTHRITOL TETRANITRATE REDUCTASE DEAZAFLAVIN-DEPENDENT NITROREDUCTASE BIOREDUCTION TUBERCULOSIS REFINEMENT ACTIVATION COENZYME SPECTRA PROTEIN FAMILY