| Literature DB >> 29779666 |
Abstract
Flavoenzymes often function as oxygenases and have been extensively studied for many decades. Commonly, oxygenation reactions are mediated by a transient C4a-peroxyflavin formed from reaction of reduced flavin with O2. EncM, however, employs a previously unrecognized flavin-oxygenating species, the flavin-N5-oxide, which is key to a complex oxidative Favorskii-type rearrangement and cyclization cascade in the biosynthesis of the bacterial polyketide antibiotic enterocin produced by the marine bacterium Streptomyces maritimus. Here, the methodology and key experiments are described that led to the discovery of this novel flavin redox species and granted insight into one of the most astounding single-enzyme-catalyzed reaction cascades in natural product biosynthesis.Entities:
Keywords: FAD; Flavin cofactor; Flavin-N5-oxide; Flavoenzyme; Monooxygenase; Polyketides; Redox tailoring
Mesh:
Substances:
Year: 2018 PMID: 29779666 DOI: 10.1016/bs.mie.2018.01.036
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600