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Validating DNA Extraction Protocols for Bentonite Clay

机译:验证膨润土的DNA提取方案

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Bentonite clay is an integral component of the engineered barrier system of deep geological repositories (DGRs) that are planned for the long-term storage of high-level radioactive waste. Although nucleic acid extraction and analysis can provide powerful qualitative and quantitative data reflecting the presence, abundance, and functional potential of microorganisms within DGR materials, extraction of microbial DNA from bentonite clay is challenging due to the low biomass and adsorption of nucleic acids to the charged clay matrix. In this study, we used quantitative PCR, gel fingerprinting, and high-throughput sequencing of 16S rRNA gene amplicons to assess DNA extraction efficiency from natural MX-80 bentonite and the same material “spiked” with Escherichia coli genomic DNA. Extraction protocols were tested without additives and with casein and phosphate as blocking agents. Although we demonstrate improved DNA recovery by blocking agents at relatively high DNA spiking concentrations, at relatively low spiking concentrations, we detected a high proportion of contaminant nucleic acids from blocking agents that masked sample-specific microbial profile data. Because bacterial genomic DNA associated with casein preparations was insufficiently removed by UV treatment, casein is not recommended as an additive for DNA extractions from low-biomass samples. Instead, we recommend a kit-based extraction protocol for bentonite clay without additional blocking agents, as tested here and validated with multiple MX-80 bentonite samples, ensuring relatively high DNA recoveries with minimal contamination. IMPORTANCE Extraction of microbial DNA from MX-80 bentonite is challenging due to low biomass and adsorption of nucleic acid molecules to the charged clay matrix. Blocking agents improve DNA recovery, but their impact on microbial community profiles from low-biomass samples has not been characterized well. In this study, we evaluated the effect of casein and phosphate as blocking agents for quantitative recovery of nucleic acids from MX-80 bentonite. Our data justify a simplified framework for analyzing microbial community DNA associated with swelling MX-80 bentonite samples within the context of a deep geological repository for used nuclear fuel. This study is among the first to demonstrate successful extraction of DNA from Wyoming MX-80 bentonite.
机译:膨润土是深层地质处置库(DGR)工程屏障系统的组成部分,该系统计划用于长期储存高放射性废物。尽管核酸提取和分析可以提供强大的定性和定量数据,以反映DGR材料中微生物的存在,丰度和功能潜力,但是由于膨松土中微生物的低生物量和核酸对带电物质的吸附,从膨润土中提取微生物DNA仍然具有挑战性。粘土基质。在这项研究中,我们使用了16S rRNA基因扩增子的定量PCR,凝胶指纹图谱和高通量测序来评估从天然MX-80膨润土和“掺入”了大肠杆菌基因组DNA的相同材料中提取DNA的效率。在没有添加剂的情况下测试了提取方案,并以酪蛋白和磷酸盐作为封闭剂。尽管我们证明了通过在较高DNA掺入浓度下使用封闭剂来提高DNA的回收率,但是在较低掺入浓度下,我们从封闭了样品特异性微生物谱数据的封闭剂中检测到了高比例的污染核酸。由于与酪蛋白制剂相关的细菌基因组DNA无法通过紫外线处理充分去除,因此不建议将酪蛋白用作从低生物量样品中提取DNA的添加剂。取而代之的是,我们建议使用基于试剂盒的膨润土粘土提取方案,而无需使用其他封闭剂,如本文所述,并已通过多个MX-80膨润土样品进行了验证,以确保相对较高的DNA回收率并将污染降至最低。重要信息由于生物量低以及核酸分子对带电粘土基质的吸附,从MX-80膨润土中提取微生物DNA具有挑战性。封闭剂可提高DNA的回收率,但其对低生物量样品对微生物群落特征的影响尚未得到很好的表征。在这项研究中,我们评估了酪蛋白和磷酸盐作为封闭剂从MX-80膨润土中定量回收核酸的效果。我们的数据为简化的框架提供了理由,该框架用于在使用过的核燃料的深层地质库中分析与膨胀的MX-80膨润土样品相关的微生物群落DNA。该研究是首次证明成功从怀俄明州MX-80膨润土中提取DNA的研究之一。

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