Bru D, Sarr A, Philippot L
INRA, University of Burgundy, Soil and Environmental Microbiology, CMSE, 17 rue Sully, BP 86510, 21065 Dijon Cedex, France.
Appl Environ Microbiol. 2007 Sep;73(18):5971-4. doi: 10.1128/AEM.00643-07. Epub 2007 Jul 13.
Dissimilatory nitrate reduction is catalyzed by a membrane-bound and a periplasmic nitrate reductase. We set up a real-time PCR assay to quantify these two enzymes, using the narG and napA genes, encoding the catalytic subunits of the two types of nitrate reductases, as molecular markers. The narG and napA gene copy numbers in DNA extracted from 18 different environments showed high variations, with most numbers ranging from 2 x 10(2) to 6.8 x 10(4) copies per ng of DNA. This study provides evidence that, in soil samples, the number of proteobacteria carrying the napA gene is often as high as that of proteobacteria carrying the narG gene. The high correlation observed between narG and napA gene copy numbers in soils suggests that the ecological roles of the corresponding enzymes might be linked.
异化硝酸盐还原由一种膜结合型和一种周质硝酸盐还原酶催化。我们建立了一种实时PCR测定法,以使用narG和napA基因(编码这两种类型硝酸盐还原酶的催化亚基)作为分子标记来定量这两种酶。从18种不同环境中提取的DNA中的narG和napA基因拷贝数显示出高度变化,大多数数量范围为每纳克DNA 2×10²至6.8×10⁴个拷贝。这项研究提供了证据,表明在土壤样品中,携带napA基因的变形菌数量通常与携带narG基因的变形菌数量一样高。在土壤中观察到的narG和napA基因拷贝数之间的高度相关性表明,相应酶的生态作用可能是相关联的。