A Comprehensive Evaluation of PCR Primers to Amplify the nifH Gene of Nitrogenase

被引:278
作者
Gaby, John Christian [1 ]
Buckley, Daniel H. [1 ]
机构
[1] Cornell Univ, Dept Crop & Soil Sci, Ithaca, NY 14853 USA
来源
PLOS ONE | 2012年 / 7卷 / 07期
基金
美国国家科学基金会;
关键词
COMMUNITY STRUCTURE; PHYLOGENETIC DIVERSITY; BACTERIAL DIVERSITY; FIXATION GENES; SOIL; AMPLIFICATION; BIODIVERSITY; ASSEMBLAGES; RHIZOSPHERE; DIAZOTROPHS;
D O I
10.1371/journal.pone.0042149
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页数:12
相关论文
共 60 条
[1]   Detection of nifH Sequences in sugarcane (Saccharum officinarum L.) and pineapple (Ananas comosus [L.] Merr.) [J].
Ando, S ;
Goto, M ;
Meunchang, S ;
Thongra-ar, P ;
Fujiwara, T ;
Hayashi, H ;
Yoneyama, T .
SOIL SCIENCE AND PLANT NUTRITION, 2005, 51 (02) :303-308
[2]   In silico evaluation of molecular probes for detection and identification of Ralstonia solanacearum and Clavibacter michiganensis subsp sepedonicus [J].
Arahal, DR ;
Llop, P ;
Alons, MP ;
López, MM .
SYSTEMATIC AND APPLIED MICROBIOLOGY, 2004, 27 (05) :581-591
[3]  
Bagwell CE, 1998, APPL ENVIRON MICROB, V64, P4276
[4]   New evidence for nitrogen fixation within the Italian white truffle Tuber magnatum [J].
Barbieri, Elena ;
Ceccaroli, Paola ;
Saltarelli, Roberta ;
Guidi, Chiara ;
Potenza, Lucia ;
Basaglia, Marina ;
Fontana, Federico ;
Baldan, Enrico ;
Casella, Sergio ;
Ryahi, Ouafae ;
Zambonelli, Alessandra ;
Stocchi, Vilberto .
FUNGAL BIOLOGY, 2010, 114 (11-12) :936-942
[5]   Regionalized GC content of template DNA as a predictor of PCR success [J].
Benita, Y ;
Oosting, RS ;
Lok, MC ;
Wise, MJ ;
Humphery-Smith, I .
NUCLEIC ACIDS RESEARCH, 2003, 31 (16)
[6]   The elimination of primer-dimer accumulation in PCR [J].
Brownie, J ;
Shawcross, S ;
Theaker, J ;
Whitcombe, D ;
Ferrie, R ;
Newton, C ;
Little, S .
NUCLEIC ACIDS RESEARCH, 1997, 25 (16) :3235-3241
[7]   Quantification of the detrimental effect of a single primer-template mismatch by real-time PCR using the 16S rRNA gene as an example [J].
Bru, D. ;
Martin-Laurent, F. ;
Philippot, L. .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2008, 74 (05) :1660-1663
[8]   New molecular screening tools for analysis of free-living diazotrophs in soil [J].
Bürgmann, H ;
Widmer, F ;
Von Sigler, W ;
Zeyer, J .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (01) :240-247
[9]   β-Rhizobia from Mimosa pigra, a newly discovered invasive plant in Taiwan [J].
Chen, WM ;
James, EK ;
Chou, JH ;
Sheu, SY ;
Yang, SZ ;
Sprent, JI .
NEW PHYTOLOGIST, 2005, 168 (03) :661-675
[10]   CLONING, DNA-SEQUENCING, AND CHARACTERIZATION OF A NIFD-HOMOLOGOUS GENE FROM THE ARCHAEON METHANOSARCINA-BARKERI-227 WHICH RESEMBLES NIFD1 FROM THE EUBACTERIUM CLOSTRIDIUM-PASTEURIANUM [J].
CHIEN, YT ;
ZINDER, SH .
JOURNAL OF BACTERIOLOGY, 1994, 176 (21) :6590-6598