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基因组挖掘揭示了粘细菌中的 III 型 PKS 产物中不常见的烷基吡喃酮。

Genome mining reveals uncommon alkylpyrones as type III PKS products from myxobacteria.

机构信息

Department Microbial Natural Products, Helmholtz-Institute for Pharmaceutical Research Saarland (HIPS), Helmholtz Centre for Infection Research (HZI), Campus E8.1, 66123, Saarbrücken, Germany.

Department of Pharmacy, Saarland University, Campus E8.1, 66123, Saarbrücken, Germany.

出版信息

J Ind Microbiol Biotechnol. 2019 Mar;46(3-4):319-334. doi: 10.1007/s10295-018-2105-6. Epub 2018 Dec 1.

Abstract

Type III polyketide synthases (PKSs) are comparatively small homodimeric enzymes affording natural products with diverse structures and functions. While type III PKS biosynthetic pathways have been studied thoroughly in plants, their counterparts from bacteria and fungi are to date scarcely characterized. This gap is exemplified by myxobacteria from which no type III PKS-derived small molecule has previously been isolated. In this study, we conducted a genomic survey of myxobacterial type III PKSs and report the identification of uncommon alkylpyrones as the products of type III PKS biosynthesis from the myxobacterial model strain Myxococcus xanthus DK1622 through a self-resistance-guided screening approach focusing on genes encoding pentapetide repeat proteins, proficient to confer resistance to topoisomerase inhibitors. Using promoter-induced gene expression in the native host as well as heterologous expression of biosynthetic type III PKS genes, sufficient amounts of material could be obtained for structural elucidation and bioactivity testing, revealing potent topoisomerase activity in vitro.

摘要

III 型聚酮合酶(PKSs)是相对较小的同二聚体酶,能够提供具有多种结构和功能的天然产物。虽然 III 型 PKS 生物合成途径在植物中已经得到了深入研究,但迄今为止,细菌和真菌中的相应途径几乎没有得到描述。粘细菌就是一个很好的例子,迄今为止尚未从这类细菌中分离到 III 型 PKS 衍生的小分子。在这项研究中,我们对粘细菌的 III 型 PKS 进行了基因组调查,并通过一种自我抗性导向的筛选方法,报告了 III 型 PKS 生物合成的罕见烷烃吡喃酮作为产物的鉴定,该方法的筛选重点是编码五肽重复蛋白的基因,这些基因能够赋予对拓扑异构酶抑制剂的抗性。通过在天然宿主中诱导启动子表达以及异源表达生物合成 III 型 PKS 基因,可以获得足够的物质进行结构阐明和生物活性测试,结果显示其具有很强的体外拓扑异构酶活性。

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