Literature DB >> 29779666

Preparation and Characterization of the Favorskiiase Flavoprotein EncM and Its Distinctive Flavin-N5-Oxide Cofactor.

Robin Teufel1.   

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.
© 2018 Elsevier Inc. All rights reserved.

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


  2 in total

1.  Aminoperoxide adducts expand the catalytic repertoire of flavin monooxygenases.

Authors:  Arne Matthews; Raspudin Saleem-Batcha; Jacob N Sanders; Frederick Stull; K N Houk; Robin Teufel
Journal:  Nat Chem Biol       Date:  2020-02-17       Impact factor: 15.040

2.  Three Rings to Rule Them All: How Versatile Flavoenzymes Orchestrate the Structural Diversification of Natural Products.

Authors:  Marina Toplak; Robin Teufel
Journal:  Biochemistry       Date:  2021-12-28       Impact factor: 3.162

  2 in total

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