Giacomucci L, Purdy K J, Zanardini E, Polo A, Cappitelli F
Dipartimento di Scienze per gli Alimenti, la Nutrizione e l'Ambiente, Università degli Studi di Milano, Milan, Italy.
J Mol Microbiol Biotechnol. 2012;22(6):345-51. doi: 10.1159/000345768. Epub 2012 Dec 28.
Dissimilatory nitrate reduction to ammonia (DNRA) is the process in which nitrate is reduced, via nitrite, to ammonia. Bacteria known to carry out DNRA mainly originate from wastewater treatment plants, where DNRA is a relevant process. The ability to carry out DNRA is phylogenetically widespread, and the gene nrfA, encoding for the key enzyme of the second step of the pathway, could be used as a marker for this process. In this study we developed a new primer pair specific for nrfA in the genus Desulfovibrio. The specificity of the primer pair was tested on DNA from thirteen species of Desulfovibrio and DNA from two wastewater samples. PCR amplifications yielded products of the expected size (850 bp), and sequences obtained from Desulfovibrio strains and environmental sample clone libraries matched the Desulfovibrio nrfA gene. Nevertheless, we found nrfA gene sequences in the environmental samples that are not present in the databases. The new primer set can be used to obtain more sequences of the nrfA gene and improve our knowledge of the DNRA pathway in this genus, e.g. with the aim to improve the wastewater treatment process.
异化硝酸盐还原为氨(DNRA)是指硝酸盐通过亚硝酸盐还原为氨的过程。已知能够进行DNRA的细菌主要源自污水处理厂,在那里DNRA是一个相关过程。进行DNRA的能力在系统发育上广泛存在,编码该途径第二步关键酶的nrfA基因可作为此过程的标志物。在本研究中,我们开发了一对针对脱硫弧菌属中nrfA的新引物对。该引物对的特异性在来自13种脱硫弧菌的DNA和两个废水样品的DNA上进行了测试。PCR扩增产生了预期大小(850 bp)的产物,从脱硫弧菌菌株和环境样品克隆文库获得的序列与脱硫弧菌nrfA基因匹配。然而,我们在环境样品中发现了数据库中不存在的nrfA基因序列。新引物组可用于获得更多nrfA基因的序列,并增进我们对该属中DNRA途径的了解,例如旨在改进废水处理过程。