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Comparison of Metagenomic DNA Extraction Methods for Soil Sediments of High Elevation Puga Hot Spring in Ladakh, India to Explore Bacterial Diversity

机译:拉达赫,印度拉达克高海拔水泉土壤沉积物的比较探讨细菌多样性

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Extraction of good-quality metagenomic DNA from extreme environments is quite challenging, particularly from high elevation hot spring sediments. Low microbial load, high humic acid content and other contaminants complicate the process of extraction of metagenomic DNA from hot spring sediments. In the present study, efficacy of five manual DNA extraction protocols with modifications has been evaluated for metagenomic DNA extraction from boron-sulfur rich high elevation Puga hot spring sediments. Best suited protocol was identified based on the cell lysis efficiency, DNA yield, humic acid content, PCR reproducibility and representation of bacterial diversity. Quantity as well as quality of crude metagenomic DNA differed remarkably between various protocols used and were not pure enough to give PCR amplification using 16S rRNA bacterial and archaeal primers. Crude metagenomic DNA extracted using five different DNA extraction protocols was purified using spin column based purification method. Even after purification, only three protocols C, D and E yielded metagenomic DNA that could be amplified using both archaeal and bacterial primers. To evaluate the degree of microbial diversity represented by protocols C, D and E, phylogenetic genes amplified were subjected to amplified ribosomal DNA restriction analysis (ARDRA) and denaturing gradient gel electrophoresis analysis (DGGE) analysis. ARDRA banding pattern of amplicons generated for all the three extraction protocols, i.e., C, D and E were found to be similar. DGGE of protocol E derived amplicons resulted in the similar number of dominant bands but a greater number of non-dominant bands, i.e., the highest microbial diversity in comparison to protocols C and D, respectively. In the present study, protocol E developed from Yeates et al. protocol has been found to be best in terms of DNA yield, DNA purity and bacterial diversity depiction associated with boron-sulfur rich sediment of high elevation hot springs.
机译:从极端环境中提取优质的偏心组织DNA是非常具有挑战性的,特别是从高海拔温泉沉积物。低微生物载荷,高腐殖酸含量和其他污染物使来自热弹簧沉积物提取的偏见性DNA的过程复杂化。在本研究中,已经评估了五种手动DNA提取方案的疗效,用于从硼 - 硫的高升高的高升高的高泉水温泉沉积物进行偏心组织DNA提取。基于细胞裂解效率,DNA产量,腐殖酸含量,PCR再现性和细菌多样性的表示来鉴定最佳方案。数量以及原油均衡质量DNA的质量显着不同,在所用的各种方案之间具有显着性,并且不足以足够纯,以使用16S rRNA细菌和古末端引物给予PCR扩增。利用基于旋柱的纯化方法纯化使用五种不同的DNA提取方案提取的粗组织DNA。甚至在纯化后,只有三种方案C,D和E产生的偏见DNA可以使用古物和细菌引物扩增。为了评估方案C,D和E所示的微生物分量的程度,对扩增的核糖体DNA限制性分析(ARDRA)进行扩增的系统发育基因和变性梯度凝胶电泳分析(DGGE)分析。发现针对所有三种提取方案,即C,D和E产生的扩增子的ARDRA系形图案类似。协议e导出的扩增子的DGGE导致相似数量的显性频带,但与协议C和D相比,分别与协议C和D相比的最高微生物分集。在本研究中,由Yeates等人开发的协议E.已经发现协议是最好的,即与高升高温泉的硼硫磺沉积物相关的DNA产率,DNA纯度和细菌分集描述。

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