Arai H, Igarashi Y, Kodama T
Department of Agricultural Chemistry, University of Tokyo, Japan.
Biosci Biotechnol Biochem. 1994 Jul;58(7):1286-91. doi: 10.1271/bbb.58.1286.
In the denitrification gene cluster from Pseudomonas aeruginosa, an operon encoding three open reading frames (nirQ, ORF2, ORF3) was upstream of the structural gene for nitrite reductase (nirS) as a divergent transcriptional organization. A nucleotide-binding protein encoded by nirQ was 76% identical to the Pseudomonas stutzeri nirQ gene product, which was shown to be necessary for activating nitrite and nitric oxide reductases. The gene product of ORF2 was homologous to subunit III of cytochrome oxidases. The nirQ gene was transcribed under denitrifying conditions. The intergenic region of nirS and nirQ has only one binding motif for ANR, a regulatory protein for anaerobic gene expression correspond to FNR in E. coli. Complementation analyses showed that the transcription of both nirS and nirQ completely depended on ANR.
在铜绿假单胞菌的反硝化基因簇中,一个编码三个开放阅读框(nirQ、ORF2、ORF3)的操纵子位于亚硝酸盐还原酶(nirS)结构基因的上游,呈反向转录组织形式。nirQ编码的一种核苷酸结合蛋白与施氏假单胞菌的nirQ基因产物有76%的同一性,已证明该产物对激活亚硝酸盐和一氧化氮还原酶是必需的。ORF2的基因产物与细胞色素氧化酶的亚基III同源。nirQ基因在反硝化条件下转录。nirS和nirQ的基因间区域只有一个用于ANR的结合基序,ANR是一种厌氧基因表达的调节蛋白,相当于大肠杆菌中的FNR。互补分析表明,nirS和nirQ的转录完全依赖于ANR。