Widely Distributed Bifunctional Bacterial Cytochrome P450 Enzymes Catalyze both Intramolecular C−C Bond Formation in <i>cyclo</i>‐<scp>l</scp>‐Tyr‐<scp>l</scp>‐Tyr and Its Coupling with Nucleobases
Jing Liu, Lauritz Harken, Yiling Yang, Xiulan Xie, Shu‐Ming Li
Abstract
Abstract Tailoring enzymes are important modification biocatalysts in natural product biosynthesis. We report herein six orthologous two‐gene clusters for mycocyclosin and guatyromycine biosynthesis. Expression of the cyclodipeptide synthase genes gymA 1 – gymA 6 in Escherichia coli resulted in the formation of cyclo ‐ l ‐Tyr‐ l ‐Tyr as the major product. Reconstruction of the biosynthetic pathways in Streptomyces albus and biochemical investigation proved that the cytochrome P450 enzymes GymB 1 –GymB 6 act as both intramolecular oxidases and intermolecular nucleobase transferases. They catalyze not only the oxidative C−C coupling within cyclo ‐ l ‐Tyr‐ l ‐Tyr, leading to mycocyclosin, but also its connection with guanine and hypoxanthine, and are thus responsible for the formation of tyrosine‐containing guatyromycines, instead of the reported tryptophan‐nucleobase adducts. Phylogenetic data suggest the presence of at least 47 GymB orthologues, indicating the occurrence of a widely distributed enzyme class.