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从宏基因组中挖掘出未培养微生物群落中多样化的抗生素生物合成基因。

Mining metagenomes reveals diverse antibiotic biosynthetic genes in uncultured microbial communities.

机构信息

Microbiology Department, Faculty of Science, Ain Shams University, Cairo, 11566, Egypt.

Medical Microbiology and Immunology Department, Faculty of Medicine, Suez Canal University, Ismailia, 41111, Egypt.

出版信息

Braz J Microbiol. 2023 Jun;54(2):983-995. doi: 10.1007/s42770-023-00953-z. Epub 2023 Mar 28.

Abstract

Pathogens resistant to antimicrobials form a significant threat to public health worldwide. Tackling multidrug-resistant pathogens via screening metagenomic libraries has become a common approach for the discovery of new antibiotics from uncultured microorganisms. This study focuses on capturing nonribosomal peptide synthase (NRPS) gene clusters implicated in the synthesis of many natural compounds of industrial relevance. A NRPS PCR assay was used to screen 2976 Escherichia coli clones in a soil metagenomic library to target NRPS genes. DNA extracts from 4 clones were sequenced and subjected to bioinformatic analysis to identify NRPS domains, their phylogeny, and substrate specificity.Successfully, 17 NRPS-positive hits with a biosynthetic potential were identified. DNA sequencing and BLAST analysis confirmed that NRPS protein sequences shared similarities with members of the genus Delftia in the Proteobacteria taxonomic position. Multiple alignment and phylogenetic analysis demonstrated that clones no. 15cd35 and 15cd37 shared low bootstrap values (54%) and were distantly far from close phylogenetic neighbors. Additionally, NRPS domain substrate specificity has no hits with the known ones; hence, they are more likely to use different substrates to produce new diverse antimicrobials. Further analysis confirmed that the NRPS hits resemble several transposon elements from other bacterial taxa, confirming its diversity. We confirmed that the analyses of the soil metagenomic library revealed a diverse set of NRPS related to the genus Delftia. An in-depth understanding of those positive NRPS hits is a crucial step for genetic manipulation of NRPS, shedding light on alternative novel antimicrobial compounds that can be used in drug discovery and hence supports the pharmaceutical sector.

摘要

对抗微生物的病原体对全球公共卫生构成重大威胁。通过筛选宏基因组文库来应对多药耐药病原体已成为从未培养微生物中发现新抗生素的常用方法。本研究专注于捕获涉及许多具有工业相关性天然化合物合成的非核糖体肽合酶 (NRPS) 基因簇。使用 NRPS PCR 测定法筛选土壤宏基因组文库中的 2976 个大肠杆菌克隆,以针对 NRPS 基因。对 4 个克隆的 DNA 提取物进行测序,并进行生物信息学分析以鉴定 NRPS 结构域、它们的系统发育和底物特异性。成功鉴定出 17 个具有生物合成潜力的 NRPS 阳性命中。DNA 测序和 BLAST 分析证实,NRPS 蛋白序列与变形菌门的代尔夫特菌属成员具有相似性。多重比对和系统发育分析表明,克隆 15cd35 和 15cd37 具有较低的自举值(54%),并且与密切的近缘种相距甚远。此外,NRPS 结构域底物特异性与已知的没有命中;因此,它们更有可能使用不同的底物来产生新的多样化的抗生素。进一步的分析证实,NRPS 命中与来自其他细菌类群的几种转座子元件相似,证实了其多样性。我们证实,对土壤宏基因组文库的分析揭示了与代尔夫特菌属相关的一系列多样化的 NRPS。对这些阳性 NRPS 命中的深入了解是对 NRPS 进行遗传操作的关键步骤,为发现可用于药物发现的替代新型抗菌化合物提供了线索,从而为制药行业提供了支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c502/10235377/6a516df393f9/42770_2023_953_Fig1_HTML.jpg

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