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Lugdunomycin, an Angucycline-Derived Molecule with Unprecedented Chemical Architecture.


ABSTRACT: The angucyclines form the largest family of polycyclic aromatic polyketides, and have been studied extensively. Herein, we report the discovery of lugdunomycin, an angucycline-derived polyketide, produced by Streptomyces species QL37. Lugdunomycin has unique structural characteristics, including a heptacyclic ring system, a spiroatom, two all-carbon stereocenters, and a benzaza-[4,3,3]propellane motif. Considering the structural novelty, we propose that lugdunomycin represents a novel subclass of aromatic polyketides. Metabolomics, combined with MS-based molecular networking analysis of Streptomyces sp. QL37, elucidated 24 other rearranged and non-rearranged angucyclines, 11 of which were previously undescribed. A biosynthetic route for the lugdunomycin and limamycins is also proposed. This work demonstrates that revisiting well-known compound families and their producer strains still is a promising approach for drug discovery.

SUBMITTER: Wu C 

PROVIDER: S-EPMC6519343 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

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Lugdunomycin, an Angucycline-Derived Molecule with Unprecedented Chemical Architecture.

Wu Changsheng C   Wu Changsheng C   van der Heul Helga U HU   Melnik Alexey V AV   Lübben Jens J   Dorrestein Pieter C PC   Minnaard Adriaan J AJ   Choi Young Hae YH   van Wezel Gilles P GP  

Angewandte Chemie (International ed. in English) 20190129 9


The angucyclines form the largest family of polycyclic aromatic polyketides, and have been studied extensively. Herein, we report the discovery of lugdunomycin, an angucycline-derived polyketide, produced by Streptomyces species QL37. Lugdunomycin has unique structural characteristics, including a heptacyclic ring system, a spiroatom, two all-carbon stereocenters, and a benzaza-[4,3,3]propellane motif. Considering the structural novelty, we propose that lugdunomycin represents a novel subclass o  ...[more]

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