Primers containing universal bases reduce multiple amoA gene specific DGGE band patterns when analysing the diversity of beta-ammonia oxidizers in the environment

被引:69
作者
Hornek, R
Pommerening-Röser, A
Koops, HP
Farnleitner, AH
Kreuzinger, N
Kirschner, A
Mach, RL
机构
[1] Tech Univ Vienna, Dept Chem & Biol Water, Inst Water Qual Resources & Waste Management, A-1040 Vienna, Austria
[2] Vienna Tech Univ, Working Grp Gene Technol, Inst Chem Engn, Vienna, Austria
[3] Univ Hamburg, Abt Mikrobiol, Biozentrum Klein Flottbek & Bot Garten, Hamburg, Germany
[4] Vienna Tech Univ, Dep Chem & Biol Water, Inst Water Qual Resources & Waste Management, Vienna, Austria
[5] Med Univ Vienna, Res Grp Microbiol, Ctr Anat & Cell Biol, A-1090 Vienna, Austria
基金
奥地利科学基金会;
关键词
ammonia oxidizing bacteria; amoA; DGGE inosine; soda pool; wastewater treatment plant;
D O I
10.1016/j.mimet.2005.11.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The gene encoding the active site of the ammonia monooxygenase (amoA) has been exploited as molecular marker for studying ammonia-oxidizing bacteria (AOB) diversity in the environment. Primers amplifying functional genes are often degenerated and therefore produce multiple band patterns, when analysed with the Denaturing gradient gel electrophoresis (DGGE) approach. To improve the DGGE band patterns we have designed new primer sets which contain inosine residues and are specific for the amoA gene. Primers were evaluated analysing pure AOB Cultures and two habitats (wastewater treatment plant, soda pools). We found that the application of inosine primers helped to reduce the apparent complexity of the DGGE band pattern. Comparison of sequences from environmental samples using either degenerated or inosine containing amoA primers retrieved both identical and additional sequences. Both primer sets seem to be limited in their ability to detect the presence of all AOB by DGGE analyses. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:147 / 155
页数:9
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