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应用乙二胺四乙酸螯合过量金属离子以改善从尾矿中回收下游DNA,用于嗜酸真菌群落的长读长扩增子测序。

Applying EDTA in Chelating Excess Metal Ions to Improve Downstream DNA Recovery from Mine Tailings for Long-Read Amplicon Sequencing of Acidophilic Fungi Communities.

作者信息

Nkuna Rosina, Ijoma Grace N, Matambo Tonderayi S

机构信息

Institute for the Development of Energy for African Sustainability, University of South Africa, Christiaan De Wet/Pioneer Dr. P.O. Box X6, Florida 1710, South Africa.

出版信息

J Fungi (Basel). 2022 Apr 20;8(5):419. doi: 10.3390/jof8050419.

Abstract

The hostile environment of mine tailings contains unique microbial life capable of bioleaching. The metagenomic analysis of such an environment provides an in-depth understanding of the microbial life and its potential, especially in biomining operations. However, DNA recovery from samples collected in those environments is challenging due to the presence of metal ions that interfere with the DNA analysis. A varied concentration of EDTA (4-13 µg/µL) to chelate the metal ions of enriched tailing samples prior to DNA extraction was performed. The results show that 9 µg/µL of EDTA was effective in most samples. However, the increasing concentration of EDTA negatively affected the DNA recovery. The sequencing of the successfully extracted DNA revealed a diverse range of fungal genera, some of which have not been previously reported in tailing or bioleaching applications. The dominant genera include , , , , and ; their traits were determined using the FungalTraits database. This study demonstrates the need to include a preliminary metal-chelating step using EDTA before DNA extractions for samples collected from metal-rich environments. It further showed the need for optimization but provided a benchmark range, particularly for tailings. However, we caution that a further EDTA removal step from the extracted DNA should be included to avoid its interferences in downstream applications.

摘要

尾矿的恶劣环境中存在能够进行生物浸出的独特微生物群落。对这种环境进行宏基因组分析可以深入了解微生物群落及其潜力,特别是在生物采矿作业方面。然而,从这些环境中采集的样本中回收DNA具有挑战性,因为存在干扰DNA分析的金属离子。在DNA提取之前,使用不同浓度的EDTA(4-13µg/µL)螯合富集尾矿样本中的金属离子。结果表明,9µg/µL的EDTA对大多数样本有效。然而,EDTA浓度的增加对DNA回收产生了负面影响。对成功提取的DNA进行测序,发现了多种真菌属,其中一些在尾矿或生物浸出应用中以前未曾报道过。优势属包括 、 、 、 和 ;利用FungalTraits数据库确定了它们的特性。本研究表明,对于从富含金属的环境中采集的样本,在DNA提取之前需要使用EDTA进行初步的金属螯合步骤。它进一步表明需要进行优化,但提供了一个基准范围,特别是对于尾矿。然而,我们提醒,应包括从提取的DNA中进一步去除EDTA的步骤,以避免其对下游应用的干扰。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e343/9143545/d97f2143eb90/jof-08-00419-g001.jpg

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