首页> 外文期刊>Polish Journal of Microbiology >Effect of DNA Extraction Methods on the Apparent Structure of Yak Rumen Microbial Communities as Revealed by 16S rDNA Sequencing
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Effect of DNA Extraction Methods on the Apparent Structure of Yak Rumen Microbial Communities as Revealed by 16S rDNA Sequencing

机译:DNA提取方法对Ya牛瘤胃微生物群落表观结构的影响(如16S rDNA测序所示)

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To more efficiently identify the microbial community of the yak rumen, the standardization of DNA extraction is key to ensure fidelity while studying environmental microbial communities. In this study, we systematically compared the efficiency of several extraction methods based on DNA yield, purity, and 16S rDNA sequencing to determine the optimal DNA extraction methods whose DNA products reflect complete bacterial communities. The results indicate that method 6 (hexadecyltrimethylammomium bromide-lysozyme-physical lysis by bead beating) is recommended for the DNA isolation of the rumen microbial community due to its high yield, operational taxonomic unit, bacterial diversity, and excellent cell-breaking capability. The results also indicate that the bead-beating step is necessary to effectively break down the cell walls of all of the microbes, especially Gram-positive bacteria. Another aim of this study was to preliminarily analyze the bacterial community via 16S rDNA sequencing. The microbial community spanned approximately 21 phyla, 35 classes, 75 families, and 112 genera. A comparative analysis showed some variations in the microbial community between yaks and cattle that may be attributed to diet and environmental differences. Interestingly, numerous uncultured or unclassified bacteria were found in yak rumen, suggesting that further research is required to determine the specific functional and ecological roles of these bacteria in yak rumen. In summary, the investigation of the optimal DNA extraction methods and the preliminary evaluation of the bacterial community composition of yak rumen support further identification of the specificity of the rumen microbial community in yak and the discovery of distinct gene resources.
机译:为了更有效地识别牛瘤胃的微生物群落,DNA提取的标准化是确保研究环境微生物群落保真度的关键。在这项研究中,我们系统地比较了基于DNA产量,纯度和16S rDNA测序的几种提取方法的效率,以确定其DNA产物反映完整细菌群落的最佳DNA提取方法。结果表明,由于瘤胃微生物群落的高产率,可操作的生物分类单位,细菌多样性和优异的细胞破碎能力,因此建议使用方法6(通过珠击法进行十六烷基三甲基溴化铵-溶菌酶的物理裂解)进行瘤胃微生物群落的DNA分离。结果还表明,敲珠步骤对于有效分解所有微生物(尤其是革兰氏阳性细菌)的细胞壁是必需的。这项研究的另一个目的是通过16S rDNA测序初步分析细菌群落。微生物群落跨越大约21个门,35个类,75个科和112属。一项比较分析表明,牛和牛之间的微生物群落有些差异,这可能归因于饮食和环境差异。有趣的是,在牛瘤胃中发现了许多未经培养或未分类的细菌,这表明需要进一步研究以确定这些细菌在牛瘤胃中的特定功能和生态作用。总之,对the牛瘤胃最佳DNA提取方法的研究和细菌群落组成的初步评估有助于进一步鉴定identification牛瘤胃微生物群落的特异性和发现独特的基因资源。

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