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全面评估聚合酶链反应引物扩增固氮酶 nifH 基因。

A comprehensive evaluation of PCR primers to amplify the nifH gene of nitrogenase.

机构信息

Department of Crop and Soil Sciences, Cornell University, Ithaca, New York, United States of America.

出版信息

PLoS One. 2012;7(7):e42149. doi: 10.1371/journal.pone.0042149. Epub 2012 Jul 25.

Abstract

The nifH gene is the most widely sequenced marker gene used to identify nitrogen-fixing Bacteria and Archaea. Numerous PCR primers have been designed to amplify nifH, but a comprehensive evaluation of nifH PCR primers has not been performed. We performed an in silico analysis of the specificity and coverage of 51 universal and 35 group-specific nifH primers by using an aligned database of 23,847 nifH sequences. We found that there are 15 universal nifH primers that target 90% or more of nitrogen fixers, but that there are also 23 nifH primers that target less than 50% of nifH sequences. The nifH primers we evaluated vary in their phylogenetic bias and their ability to recover sequences from commonly sampled environments. In addition, many of these primers will amplify genes that do not mediate nitrogen fixation, and thus it would be advisable for researchers to screen their sequencing results for the presence of non-target genes before analysis. Universal primers that performed well in silico were tested empirically with soil samples and with genomic DNA from a phylogenetically diverse set of nitrogen-fixing strains. This analysis will be of great utility to those engaged in molecular analysis of nifH genes from isolates and environmental samples.

摘要

nifH 基因是用于鉴定固氮细菌和古菌的最广泛测序的标记基因。已经设计了许多 PCR 引物来扩增 nifH,但尚未对 nifH PCR 引物进行全面评估。我们使用经过比对的 23847 个 nifH 序列数据库,对 51 个通用和 35 个组特异性 nifH 引物的特异性和覆盖范围进行了计算机分析。我们发现有 15 个通用 nifH 引物可以靶向 90%或更多的固氮生物,但也有 23 个 nifH 引物只能靶向不到 50%的 nifH 序列。我们评估的 nifH 引物在系统发育偏倚和从常见采样环境中恢复序列的能力方面存在差异。此外,这些引物中的许多都会扩增不介导固氮的基因,因此研究人员在分析之前,最好先筛选测序结果中是否存在非目标基因。我们通过土壤样本和来自具有多样化系统发育的固氮菌株的基因组 DNA 对计算机分析中表现良好的通用引物进行了实证测试。这项分析对于从事从分离物和环境样本中分析 nifH 基因的分子分析的人员非常有用。

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