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基于模式的基因组挖掘指导从海洋链霉菌中发现抗生素茚并吡咯A。

Pattern-based genome mining guides discovery of the antibiotic indanopyrrole A from a marine streptomycetef.

作者信息

Sweeney Douglas, Bogdanov Alexander, Chase Alexander B, Castro-Falcón Gabriel, Trinidad-Javier Alma, Dahesh Samira, Nizet Victor, Jensen Paul R

机构信息

Scripps Institution of Oceanography, University of California, San Diego, La Jolla, CA 92093, USA.

Department of Earth Sciences, Southern Methodist University, Dallas, TX 75275, USA.

出版信息

bioRxiv. 2024 Oct 29:2024.10.29.620887. doi: 10.1101/2024.10.29.620887.

Abstract

Terrestrial actinomycetes in the genus have long been recognized as prolific producers of small molecule natural products, including many clinically important antibiotics and cytotoxic agents. Although can also be isolated from marine environments, their potential for natural product biosynthesis remains underexplored. The MAR4 clade of largely marine-derived has been a rich source of novel halogenated natural products of diverse structural classes. To further explore the biosynthetic potential of this group, we applied pattern-based genome mining leading to the discovery of the first halogenated pyrroloketoindane natural products, indanopyrrole A () and B (), and the bioinformatic linkage of these compounds to an orphan biosynthetic gene cluster (BCG) in 20 MAR4 genomes. Indanopyrrole A displays potent broad-spectrum antibiotic activity against clinically relevant pathogens. A comparison of the putative indanopyrrole BGC with that of the related compound indanomycin provides new insights into the terminal cyclization and offloading mechanisms in pyrroloketoindane biosynthesis. Broader searches of public databases reveal the rarity of this BGC while also highlighting opportunities for discovering additional compounds in this uncommon class.

摘要

长期以来,该属的陆生放线菌一直被认为是小分子天然产物的丰富生产者,包括许多具有重要临床意义的抗生素和细胞毒性剂。虽然也可以从海洋环境中分离出该属,但它们在天然产物生物合成方面的潜力仍未得到充分探索。主要源自海洋的该属MAR4分支一直是各种结构类别的新型卤化天然产物的丰富来源。为了进一步探索该类群的生物合成潜力,我们应用基于模式的基因组挖掘方法,发现了首个卤化吡咯并酮茚天然产物茚并吡咯A()和B(),并通过生物信息学将这些化合物与20个MAR4基因组中的一个孤儿生物合成基因簇(BCG)联系起来。茚并吡咯A对临床相关病原体表现出强大的广谱抗生素活性。将假定的茚并吡咯生物合成基因簇与相关化合物茚霉素的基因簇进行比较,为吡咯并酮茚生物合成中的末端环化和卸载机制提供了新的见解。对公共数据库进行更广泛的搜索发现,该生物合成基因簇很罕见,同时也突出了发现这一不常见类别中其他化合物的机会。

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