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Enriching plant microbiota for a metagenomic library construction

机译:丰富植物微生物群以构建宏基因组文库

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摘要

Plant microbiota (the microorganisms that live in any associations with plant tissues) represents a rather unexplored area of metagenomic research compared with soils and oceans. Constructing a metagenomic library for plant microbiota is technically challenging. Using all the biomass without pre-enrichment could lead to vast proportions of the host plant DNA in the metagenomic library, doubtless obliterating the microbial contribution. Therefore, the first and essential step is to enrich for the constituent microorganisms from plant tissues. Here, a strong enrichment for plant microbiota was achieved by coupling SDS (sodium dodecyl sulfate) with NaCl, creating a predominantly microbial metagenomic library that contains 88% bacterial inserts. 16S rDNA sequence analysis revealed that the metagenomic DNA of enrichments originates from very diverse microorganisms. At least 74 distinct ribotypes (at a 97% threshold) from seven different bacterial phyla were identified and mainly distributed among Actinobacteria and Proteobacteria. Additionally, a simplified version of Amplified Ribosomal DNA Restriction Analysis (ARDRA) was developed for a quick and efficient assessment of the enriching procedures. This work opens further insight into the great biotechnical potential of plant microbiota, holding more potential for drug discovery through a metagenomic strategy, and paving the way for recovery and biochemical characterization of functional gene repertoire from plant microbiota.
机译:与土壤和海洋相比,植物微生物群(与植物组织有任何联系的微生物)是宏基因组学研究中一个尚未开发的领域。构建用于植物微生物群的宏基因组库在技术上具有挑战性。使用所有生物质而不进行预富集会导致宏基因组文库中的宿主植物DNA占很大比例,这无疑会消除微生物的贡献。因此,第一步也是必不可少的步骤是从植物组织中富集组成微生物。在这里,通过将SDS(十二烷基硫酸钠)与NaCl偶联而获得了对植物微生物群的强力富集,从而创建了一个主要的微生物宏基因组库,其中包含88%的细菌插入片段。 16S rDNA序列分析表明,富集的宏基因组DNA源自非常多样的微生物。从七个不同细菌门中至少鉴定出74种不同的核糖型(以97%为阈值),并且主要分布在放线菌和变形杆菌中。此外,还开发了简化版的核糖体DNA限制性酶切分析(ARDRA),以快速,有效地评估富集程序。这项工作为植物微生物的巨大生物技术潜力打开了进一步的视野,通过宏基因组学策略为药物发现提供了更大的潜力,并为从植物微生物中恢复功能基因库和进行生化表征铺平了道路。

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