Heylen Kim, Gevers Dirk, Vanparys Bram, Wittebolle Lieven, Geets Joke, Boon Nico, De Vos Paul
Laboratory of Microbiology, Department of Biochemistry, Physiology and Microbiology, Ghent University, K. L. Ledeganckstraat 35, B-9000 Gent, Belgium.
Environ Microbiol. 2006 Nov;8(11):2012-21. doi: 10.1111/j.1462-2920.2006.01081.x.
Gene sequence analysis of nirS and nirK, both encoding nitrite reductases, was performed on cultivated denitrifiers to assess their incidence in different bacterial taxa and their taxonomical value. Almost half of the 227 investigated denitrifying strains did not render an nir amplicon with any of five previously described primers. NirK and nirS were found to be prevalent in Alphaproteobacteria and Betaproteobacteria, respectively, nirK was detected in the Firmicutes and Bacteroidetes and nirS and nirK with equal frequency in the Gammaproteobacteria. These observations deviated from the hitherto reported incidence of nir genes in bacterial taxa. NirS gene phylogeny was congruent with the 16S rRNA gene phylogeny on family or genus level, although some strains did group within clusters of other bacterial classes. Phylogenetic nirK gene sequence analysis was incongruent with the 16S rRNA gene phylogeny. NirK sequences were also found to be significantly more similar to nirK sequences from the same habitat than to nirK sequences retrieved from highly related taxa. This study supports the hypothesis that horizontal gene transfer events of denitrification genes have occurred and underlines that denitrification genes should not be linked with organism diversity of denitrifiers in cultivation-independent studies.
对培养的反硝化菌进行了编码亚硝酸还原酶的nirS和nirK基因序列分析,以评估它们在不同细菌类群中的发生率及其分类学价值。在227株被研究的反硝化菌株中,近一半未能用之前描述的五种引物中的任何一种扩增出nir扩增子。发现nirK和nirS分别在α-变形菌纲和β-变形菌纲中普遍存在,在厚壁菌门和拟杆菌门中检测到nirK,在γ-变形菌纲中nirS和nirK的出现频率相同。这些观察结果与迄今报道的细菌类群中nir基因的发生率有所不同。在科或属水平上,nirS基因系统发育与16S rRNA基因系统发育一致,尽管一些菌株确实聚集在其他细菌类别的簇中。nirK基因序列的系统发育分析与16S rRNA基因系统发育不一致。还发现,nirK序列与来自相同栖息地的nirK序列的相似性显著高于与从高度相关类群中检索到的nirK序列的相似性。本研究支持反硝化基因发生水平基因转移事件的假设,并强调在不依赖培养的研究中,反硝化基因不应与反硝化菌的生物多样性相关联。