Department of Biomolecular Chemistry, Leibniz Institute for Natural Product Research and Infection Biology, HKI, Beutenbergstr. 11a, 07745, Jena, Germany.
Department for Evolutionary Ecology, Institute of Organismic and Molecular Evolution, Johannes Gutenberg University Mainz, Hanns-Dieter-Hüsch-Weg 15, 55128, Mainz, Germany.
Angew Chem Int Ed Engl. 2020 Dec 14;59(51):23122-23126. doi: 10.1002/anie.202005711. Epub 2020 Oct 15.
Genome mining of one of the protective symbionts (Burkholderia gladioli) of the invasive beetle Lagria villosa revealed a cryptic gene cluster that codes for the biosynthesis of a novel antifungal polyketide with a glutarimide pharmacophore. Targeted gene inactivation, metabolic profiling, and bioassays led to the discovery of the gladiofungins as previously-overlooked components of the antimicrobial armory of the beetle symbiont, which are highly active against the entomopathogenic fungus Purpureocillium lilacinum. By mutational analyses, isotope labeling, and computational analyses of the modular polyketide synthase, we found that the rare butenolide moiety of gladiofungins derives from an unprecedented polyketide chain termination reaction involving a glycerol-derived C3 building block. The key role of an A-factor synthase (AfsA)-like offloading domain was corroborated by CRISPR-Cas-mediated gene editing, which facilitated precise excision within a PKS domain.
从入侵甲虫 Lagria villosa 的一种保护共生菌(黄单胞菌属 gladioli)中进行基因组挖掘,揭示了一个隐藏的基因簇,该基因簇编码一种新型抗真菌聚酮化合物,具有戊二酰亚胺药效团。靶向基因失活、代谢谱分析和生物测定导致发现了 gladiofungins,这是甲虫共生菌抗菌武器库中以前被忽视的成分,对昆虫病原真菌 Purpureocillium lilacinum 具有高度活性。通过突变分析、同位素标记和模块化聚酮合酶的计算分析,我们发现 gladiofungins 中罕见的丁烯内酯部分源自涉及甘油衍生的 C3 构建块的前所未有的聚酮链终止反应。CRISPR-Cas 介导的基因编辑证实了 A 因子合酶 (AfsA)-样卸载结构域的关键作用,该结构域有助于在 PKS 结构域内进行精确切除。