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从一种蜘蛛传播的真菌中挖掘共生体,揭示了针对细胞毒素苯并内酯的未开发生物合成途径。

Mining Symbionts of a Spider-Transmitted Fungus Illuminates Uncharted Biosynthetic Pathways to Cytotoxic Benzolactones.

机构信息

Department of Biomolecular Chemistry, Leibniz Institute for Natural Product Chemistry and Infection Biology (HKI), Beutenbergstr. 11a, 07745, Jena, Germany.

Department of Microbiology and Immunology, Doherty Institute, 792 Elizabeth Street, Melbourne, 3000, Australia.

出版信息

Angew Chem Int Ed Engl. 2020 May 11;59(20):7766-7771. doi: 10.1002/anie.201916007. Epub 2020 Mar 18.

Abstract

A spider-transmitted fungus (Rhizopus microsporus) that was isolated from necrotic human tissue was found to harbor endofungal bacteria (Burkholderia sp.). Metabolic profiling of the symbionts revealed a complex of cytotoxic agents (necroximes). Their structures were characterized as oxime-substituted benzolactone enamides with a peptidic side chain. The potently cytotoxic necroximes are also formed in symbiosis with the fungal host and could have contributed to the necrosis. Genome sequencing and computational analyses revealed a novel modular PKS/NRPS assembly line equipped with several non-canonical domains. Based on gene-deletion mutants, we propose a biosynthetic model for bacterial benzolactones. We identified specific traits that serve as genetic handles to find related salicylate macrolide pathways (lobatamide, oximidine, apicularen) in various other bacterial genera. Knowledge of the biosynthetic pathway enables biosynthetic engineering and genome-mining approaches.

摘要

从坏死的人体组织中分离出的一种由蜘蛛传播的真菌(Rhizopus microsporus)中发现了内生真菌(Burkholderia sp.)。对共生体的代谢组学分析揭示了一系列细胞毒素(necroximes)。它们的结构被表征为肟取代的苯并内酯烯酰胺,具有肽侧链。与真菌宿主共生时也会形成具有强烈细胞毒性的 necroximes,这可能导致了坏死。基因组测序和计算分析揭示了一种新型的模块化 PKS/NRPS 装配线,配备了几个非典型结构域。基于基因缺失突变体,我们提出了细菌苯并内酯的生物合成模型。我们确定了特定的特征,这些特征可作为遗传控制手段,在其他各种细菌属中找到相关的水杨酸内酯途径(lobatamide、oximidine、apicularen)。对生物合成途径的了解可实现生物合成工程和基因组挖掘方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6bc/7318616/6a3ed93cd501/ANIE-59-7766-g001.jpg

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