Assessing PCR Inhibition from Humic Substances

C. Matheson, Carli Gurney, N. Esau, Ryan Lehto
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引用次数: 121

Abstract

Inhibition remains the greatest methodological challenge in molecular analysis of buried biological remains. Inhibitory compounds associated with soil environments comprise primarily of humic acids and fulvic acids, collectively referred to as humic substances. We examined the sensitivity of 13 DNA polymerases to both humic acids (11ng-110� g) and fulvic acids (9.4ng-94� g) and the concentration at which successful amplification can be achieved. This research identified that all 13 DNA polymerases tested exhibited inhibition with varying concentrations of humic acids and that 5 out of the 13 DNA polymerase tested exhibited inhibition with varying concentrations of fulvic acid. The most tolerant DNA polymerase to inhibition due to the presence of humic and fulvic acids is pfu DNA polymerase followed by KlenTaq ® LA DNA polymerase and RealTaq DNA polymerase that were both only inhibited by 11� g and 110� g of humic acids. In addition, we present the use of size exclusion chromatography to remove small molecular weight humic substance, dramatically increasing the success of molecular analysis on material associated with burial. This research has implications to the fields of environmental microbiology, soil science, forensic science and archaeological science.
评估腐殖质对PCR的抑制作用
抑制仍然是埋藏生物遗骸分子分析中最大的方法学挑战。与土壤环境相关的抑制性化合物主要由腐植酸和黄腐酸组成,统称为腐植酸物质。我们检测了13种DNA聚合酶对腐植酸(11ng-110 μ g)和黄腐酸(9.4ng-94 μ g)的敏感性,以及成功扩增的浓度。本研究发现,所有13种DNA聚合酶都对不同浓度的腐植酸表现出抑制作用,13种DNA聚合酶中有5种对不同浓度的黄腐酸表现出抑制作用。腐植酸和黄腐酸对DNA聚合酶的抑制能力最强的是pfu DNA聚合酶,其次是KlenTaq®LA DNA聚合酶和RealTaq DNA聚合酶,它们都只被11 μ g和110 μ g的腐植酸抑制。此外,我们提出了使用粒径排除色谱法去除小分子量腐殖质,大大增加了分子分析的成功与埋藏有关的物质。本研究对环境微生物学、土壤学、法医学和考古学等领域具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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