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High-quality metagenomic DNA from marine sediment samples for genomic studies through a preprocessing approach

机译:来自海洋沉积物样品的高质量宏基因组DNA通过预处理方法进行基因组研究

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摘要

Recent advances in culture-independent studies of microbes had proved to be more reliable and efficient than the conventional ones. The isolation of good quality and quantity of total community DNA are one of the major hurdles in this endeavour. Shearing of DNA during the extraction process and the co-extraction of inhibitory compounds reduce the quality of the isolated nucleic acids making it unsuitable for the construction of large insert metagenomic libraries. In the present study, a multi-level filtration step was brought in which efficiently isolated total bacterial DNA from three different environment samples. The preprocessing method could efficiently improve the 260/230 ratio of the isolated DNA by 2.3–45 % and decreased the protein contamination by 22.5–34.5 % on saltpan and arctic sediment samples, respectively. The more significant part of the experiment was that the DNA obtained was of high quality with minimal shearing making it most suitable for the construction of large insert genomic libraries. PCR amplification of 16S rRNA gene confirmed that the filtration method was effective in the isolation of high-quality DNA.
机译:事实证明,与培养无关的微生物研究的最新进展比常规研究更可靠,更有效。高质量和高质量的总社区DNA的分离是这一努力的主要障碍之一。提取过程中DNA的剪切和抑制性化合物的共提取降低了分离核酸的质量,使其不适合构建大型插入宏基因组文库。在本研究中,提出了一个多级过滤步骤,该步骤可从三个不同的环境样品中有效分离出总细菌DNA。预处理方法可以有效地将分离出的DNA的260/230比提高2.3–45%,并在盐底和北极沉积物样品上分别减少22.5–34.5%的蛋白质污染。实验最重要的部分是获得的DNA质量高,剪切力极小,使其最适合构建大型插入基因组文库。对16S rRNA基因进行PCR扩增证实,该过滤方法可有效分离高质量的DNA。

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