| Literature DB >> 26206556 |
Sheng Huang1, Jioji Tabudravu2, Somayah S Elsayed2, Jeanne Travert2, Doe Peace2, Ming Him Tong2, Kwaku Kyeremeh3, Sharon M Kelly4, Laurent Trembleau2, Rainer Ebel2, Marcel Jaspars2, Yi Yu5, Hai Deng6.
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.Entities:
Keywords: biosynthesis; legonmycins; multifunctional enzymes; non-ribosomal peptide synthetases; pyrrolizidine alkaloids
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Year: 2015 PMID: 26206556 DOI: 10.1002/anie.201502902
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336