Wei Wei, Isobe Kazuo, Nishizawa Tomoyasu, Zhu Lin, Shiratori Yutaka, Ohte Nobuhito, Koba Keisuke, Otsuka Shigeto, Senoo Keishi
Department of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan.
1] Department of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan [2] Department of Bioresource Science, College of Agriculture, Ibaraki University, Ibaraki, Japan.
ISME J. 2015 Sep;9(9):1954-65. doi: 10.1038/ismej.2015.9. Epub 2015 Mar 10.
Denitrification is an important process in the global nitrogen cycle. The genes encoding NirK and NirS (nirK and nirS), which catalyze the reduction of nitrite to nitric oxide, have been used as marker genes to study the ecological behavior of denitrifiers in environments. However, conventional polymerase chain reaction (PCR) primers can only detect a limited range of the phylogenetically diverse nirK and nirS. Thus, we developed new PCR primers covering the diverse nirK and nirS. Clone library and qPCR analysis using the primers showed that nirK and nirS in terrestrial environments are more phylogenetically diverse and 2-6 times more abundant than those revealed with the conventional primers. RNA- and culture-based analyses using a cropland soil also suggested that microorganisms with previously unconsidered nirK or nirS are responsible for denitrification in the soil. PCR techniques still have a greater capacity for the deep analysis of target genes than PCR-independent methods including metagenome analysis, although efforts are needed to minimize the PCR biases. The methodology and the insights obtained here should allow us to achieve a more precise understanding of the ecological behavior of denitrifiers and facilitate more precise estimate of denitrification in environments.
反硝化作用是全球氮循环中的一个重要过程。编码催化亚硝酸盐还原为一氧化氮的NirK和NirS(nirK和nirS)的基因,已被用作标记基因来研究环境中反硝化细菌的生态行为。然而,传统的聚合酶链反应(PCR)引物只能检测到系统发育上多样的nirK和nirS的有限范围。因此,我们开发了覆盖多种nirK和nirS的新PCR引物。使用这些引物进行的克隆文库和定量PCR分析表明,陆地环境中的nirK和nirS在系统发育上更加多样,且丰度比传统引物所揭示的高2至6倍。使用农田土壤进行的基于RNA和培养物的分析还表明,具有以前未被考虑的nirK或nirS的微生物在土壤反硝化作用中起作用。尽管需要努力尽量减少PCR偏差,但与包括宏基因组分析在内的非PCR方法相比,PCR技术在对靶基因进行深入分析方面仍具有更大的能力。这里获得的方法和见解应使我们能够更精确地了解反硝化细菌的生态行为,并有助于更精确地估计环境中的反硝化作用。