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本文引用的文献

1
Comparative analysis of environmental DNA extraction and purification methods from different humic acid-rich soils.不同富腐殖酸土壤环境DNA提取与纯化方法的比较分析
J Appl Microbiol. 2007 Jan;102(1):265-73. doi: 10.1111/j.1365-2672.2006.03052.x.
2
Statistical methods for characterizing diversity of microbial communities by analysis of terminal restriction fragment length polymorphisms of 16S rRNA genes.通过分析16S rRNA基因的末端限制性片段长度多态性来表征微生物群落多样性的统计方法。
Environ Microbiol. 2006 May;8(5):929-38. doi: 10.1111/j.1462-2920.2005.00959.x.
3
Removal of humic substances from soil DNA using aluminium sulfate.使用硫酸铝从土壤DNA中去除腐殖质物质。
J Microbiol Methods. 2006 Aug;66(2):217-22. doi: 10.1016/j.mimet.2005.11.010. Epub 2005 Dec 27.
4
Application of a new PCR primer for terminal restriction fragment length polymorphism analysis of the bacterial communities in plant roots.一种用于植物根际细菌群落末端限制性片段长度多态性分析的新型PCR引物的应用。
J Microbiol Methods. 2004 Oct;59(1):81-9. doi: 10.1016/j.mimet.2004.06.005.
5
DNA isolation from soil samples for cloning in different hosts.从土壤样本中提取DNA以在不同宿主中进行克隆。
Appl Microbiol Biotechnol. 2004 Jun;64(5):665-70. doi: 10.1007/s00253-003-1528-8. Epub 2004 Feb 3.
6
Removal of PCR inhibitors from soil DNA by chemical flocculation.通过化学絮凝去除土壤DNA中的PCR抑制剂。
J Microbiol Methods. 2003 Mar;52(3):389-93. doi: 10.1016/s0167-7012(02)00210-5.
7
PRIMROSE: a computer program for generating and estimating the phylogenetic range of 16S rRNA oligonucleotide probes and primers in conjunction with the RDP-II database.报春花:一种与RDP-II数据库结合使用,用于生成和估计16S rRNA寡核苷酸探针及引物系统发育范围的计算机程序。
Nucleic Acids Res. 2002 Aug 1;30(15):3481-9. doi: 10.1093/nar/gkf450.
8
PCR-SSCP comparison of 16S rDNA sequence diversity in soil DNA obtained using different isolation and purification methods.使用不同提取和纯化方法获得的土壤DNA中16S rDNA序列多样性的PCR-SSCP比较
FEMS Microbiol Ecol. 2001 Jul;36(2-3):139-151. doi: 10.1111/j.1574-6941.2001.tb00834.x.
9
DNA extraction from soils: old bias for new microbial diversity analysis methods.从土壤中提取DNA:新的微生物多样性分析方法存在的旧有偏差
Appl Environ Microbiol. 2001 May;67(5):2354-9. doi: 10.1128/AEM.67.5.2354-2359.2001.
10
A strategy for optimizing quality and quantity of DNA extracted from soil.一种优化从土壤中提取DNA的质量和数量的策略。
J Microbiol Methods. 2001 May;45(1):7-20. doi: 10.1016/s0167-7012(01)00213-5.

在具有广泛不同特征的土壤中测试的土壤DNA纯化创新方法。

Innovative methods for soil DNA purification tested in soils with widely differing characteristics.

作者信息

Sagova-Mareckova Marketa, Cermak Ladislav, Novotna Jitka, Plhackova Kamila, Forstova Jana, Kopecky Jan

机构信息

Crop Research Institute v.v.i., Drnovska 507, CZ-161 06 Prague 6, Czech Republic.

出版信息

Appl Environ Microbiol. 2008 May;74(9):2902-7. doi: 10.1128/AEM.02161-07. Epub 2008 Mar 14.

DOI:10.1128/AEM.02161-07
PMID:18344341
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2394906/
Abstract

Seven methods of soil DNA extraction and purification were tested in a set of 14 soils differing in bedrock, texture, pH, salinity, moisture, organic matter content, and vegetation cover. The methods introduced in this study included pretreatment of soil with CaCO(3) or purification of extracted DNA by CaCl(2). The performance of innovated methods was compared to that of the commercial kit Mo Bio PowerSoil and the phenol-chloroform-based method of D. N. Miller, J. E. Bryant, E. L. Madsen, and W. C. Ghiorse (Appl. Environ. Microbiol. 65:4715-4724, 1999). This study demonstrated significant differences between the tested methods in terms of DNA yield, PCR performance, and recovered bacterial diversity. The differences in DNA yields were correlated to vegetation cover, soil pH, and clay content. The differences in PCR performances were correlated to vegetation cover and soil pH. The innovative methods improved PCR performance in our set of soils, in particular for forest acidic soils. PCR was successful in 95% of cases by the method using CaCl(2) purification and in 93% of cases by the method based on CaCO(3) pretreatment, but only in 79% by Mo Bio PowerSoil, for our range of soils. Also, the innovative methods recovered a higher percentage of actinomycete diversity from a subset of three soils. Recommendations include the assessment of soil characteristics prior to selecting the optimal protocol for soil DNA extraction and purification.

摘要

在一组14种土壤中测试了七种土壤DNA提取和纯化方法,这些土壤在基岩、质地、pH值、盐度、湿度、有机质含量和植被覆盖方面存在差异。本研究中引入的方法包括用CaCO₃对土壤进行预处理或用CaCl₂对提取的DNA进行纯化。将创新方法的性能与商业试剂盒Mo Bio PowerSoil以及D. N. Miller、J. E. Bryant、E. L. Madsen和W. C. Ghiorse基于苯酚-氯仿的方法(《应用与环境微生物学》65:4715 - 4724,1999年)进行了比较。本研究表明,在DNA产量、PCR性能和恢复的细菌多样性方面,测试方法之间存在显著差异。DNA产量的差异与植被覆盖、土壤pH值和粘土含量相关。PCR性能的差异与植被覆盖和土壤pH值相关。创新方法在我们的土壤组中提高了PCR性能,特别是对于森林酸性土壤。对于我们的一系列土壤,使用CaCl₂纯化的方法在95%的情况下PCR成功,基于CaCO₃预处理的方法在93%的情况下成功,但Mo Bio PowerSoil仅在79%的情况下成功。此外,创新方法从三种土壤的子集中恢复了更高比例的放线菌多样性。建议包括在选择土壤DNA提取和纯化的最佳方案之前评估土壤特性。