Discovery of a Single Monooxygenase that Catalyzes Carbamate Formation and Ring Contraction in the Biosynthesis of the Legonmycins

Huang, Sheng, Tabudravu, Jioji orcid iconORCID: 0000-0002-6930-6572, Elsayed, Somayah S., Travert, Jeanne, Peace, Doe, Tong, Ming Him, Kyeremeh, Kwaku, Kelly, Sharon M., Trembleau, Laurent et al (2015) Discovery of a Single Monooxygenase that Catalyzes Carbamate Formation and Ring Contraction in the Biosynthesis of the Legonmycins. Angewandte Chemie International Edition, 54 (43). pp. 12697-12701. ISSN 1433-7851

[thumbnail of Version of Record] PDF (Version of Record) - Published Version
Restricted to Repository staff only
Available under License Creative Commons Attribution Non-commercial No Derivatives.

2MB

Official URL: https://doi.org/10.1002/anie.201502902

Abstract

Pyrrolizidine alkaloids (PAs) are a group of natural products with important biological activities. The discovery and characterization of the multifunctional FAD-dependent enzyme LgnC is now described. The enzyme is shown to convert indolizidine intermediates into pyrrolizidines through an unusual ring expansion/contraction mechanism, and catalyze the biosynthesis of new bacterial PAs, the so-called legonmycins. By genome-driven analysis, heterologous expression, and gene inactivation, the legonmycins were also shown to originate from non-ribosomal peptide synthetases (NRPSs). The biosynthetic origin of bacterial PAs has thus been disclosed for the first time.


Repository Staff Only: item control page