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腐殖酸对SYBR Green I定量DNA的影响机制及其对土壤和水生沉积物分析的影响

Mechanisms underlying the impact of humic acids on DNA quantification by SYBR Green I and consequences for the analysis of soils and aquatic sediments.

作者信息

Zipper Hubert, Buta Christiane, Lämmle Katrin, Brunner Herwig, Bernhagen Jürgen, Vitzthum Frank

机构信息

Laboratory of Biochemistry, Chair for Interfacial Engineering, University of Stuttgart and Fraunhofer IGB, Nobelstrasse 12, D-70569 Stuttgart, Germany.

出版信息

Nucleic Acids Res. 2003 Apr 1;31(7):e39. doi: 10.1093/nar/gng039.

Abstract

DNA quantification of soils and sediments is useful for the investigation of microbial communities and for the acquisition of their genomes that are exploited for the production of natural products. However, in such samples DNA quantification is impaired by humic acids (HA). Due to its lack of specificity and sensitivity, UV spectrophotometry cannot be applied. Consequently, fluorimetric assays applying Hoechst (H) 33258 or PicoGreen (PG) are used. Here, we investigated the SYBR Green I (SG) assay, which was also affected by HA, but was found to be 25- and 1.7-fold more sensitive compared to the H 33258 and PG assays, respectively. Spectrophotometric, fluorimetric and quenching studies as well as gel mobility shift assays suggested that the effect of HA on the SG assay was based on an inner filter effect, collisional quenching and binding of SG to HA. As to the latter finding, the standard 6250-fold dilution of the SG reagent was optimised to a 2000-fold dilution. Although the sensitivity of the optimised SG assay was reduced by a factor of 1.3, the interfering effect of HA could be reduced up to 22-fold. A significant reduction of HA interferences by lowering the pH of the assay was not observed. Finally, the performance of the modified SG assay and the corresponding evaluation methods were verified by the determination of DNA recoveries and concentrations of standards and environmental samples in comparison to the PG assay.

摘要

土壤和沉积物的DNA定量分析对于微生物群落的研究以及获取用于天然产物生产的微生物基因组非常有用。然而,在这类样品中,腐殖酸(HA)会干扰DNA定量分析。由于缺乏特异性和灵敏度,紫外分光光度法无法应用。因此,采用了应用Hoechst(H)33258或PicoGreen(PG)的荧光测定法。在此,我们研究了SYBR Green I(SG)测定法,该方法也受到HA的影响,但分别比H 33258和PG测定法灵敏25倍和1.7倍。分光光度法、荧光测定法和猝灭研究以及凝胶迁移率变动分析表明,HA对SG测定法的影响基于内滤效应、碰撞猝灭以及SG与HA的结合。关于后一个发现,将SG试剂的标准6250倍稀释优化为2000倍稀释。尽管优化后的SG测定法的灵敏度降低了1.3倍,但HA的干扰效应可降低多达22倍。未观察到通过降低测定法的pH值可显著减少HA干扰。最后,通过与PG测定法比较,测定DNA回收率以及标准品和环境样品的浓度,验证了改良的SG测定法的性能及相应的评估方法。

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