New Reactions and Products Resulting from Alternative Interactions between the P450 Enzyme and Redox Partners

• Published in: Journal of the American Chemical Society Vol. 136; no. 9; pp. 3640 - 3646
• Main Authors: Zhang, Wei, Liu, Yi, Yan, Jinyong, Cao, Shaona, Bai, Fali, Yang, Ying, Huang, Shaohua, Yao, Lishan, Anzai, Yojiro, Kato, Fumio, Podust, Larissa M, Sherman, David H, Li, Shengying
• Format: Journal Article
• Language: English
• Published: WASHINGTON American Chemical Society 05.03.2014; Amer Chemical Soc
• Subjects: Bacterial Proteins - chemistry; Bacterial Proteins - metabolism; Catalytic activity; Catalytic Domain; Chemistry; Chemistry, Multidisciplinary; Cytochrome P-450 Enzyme System - chemistry; Cytochrome P-450 Enzyme System - metabolism; Cytochromes P450; Enzymes; Epoxidation; Hydroxylation; Macrolides - metabolism; Models, Molecular; Oxidation-Reduction; Physical Sciences; Protein Binding; Proteins; Reductases; Rhodococcus; Science & Technology; ORGANIZATION; GENE; ACTIVE-SITE; MYCINAMICIN; BIOSYNTHESIS; HYDROXYLATION; MACROLIDE ANTIBIOTICS; CYTOCHROME B; IDENTIFICATION; EPOXIDATION
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja4130302

Cytochrome P450 enzymes are capable of catalyzing a great variety of synthetically useful reactions such as selective C–H functionalization. Surrogate redox partners are widely used for reconstitution of P450 activity based on the assumption that the choice of these auxiliary proteins or their mode of action does not affect the type and selectivity of reactions catalyzed by P450s. Herein, we present an exceptional example to challenge this postulate. MycG, a multifunctional biosynthetic P450 monooxygenase responsible for hydroxylation and epoxidation of 16-membered ring macrolide mycinamicins, is shown to catalyze the unnatural N-demethylation(s) of a range of mycinamicin substrates when partnered with the free Rhodococcus reductase domain RhFRED or the engineered Rhodococcus-spinach hybrid reductase RhFRED-Fdx. By contrast, MycG fused with the RhFRED or RhFRED-Fdx reductase domain mediates only physiological oxidations. This finding highlights the larger potential role of variant redox partner protein–protein interactions in modulating the catalytic activity of P450 enzymes.