Jain Roshan, Shapleigh James P
Department of Microbiology, Wing Hall, Cornell University, Ithaca, NY 14853-8101, USA1.
Microbiology (Reading). 2001 Sep;147(Pt 9):2505-2515. doi: 10.1099/00221287-147-9-2505.
Sequencing of the region flanking nirK, the gene encoding the copper-containing nitrite reductase in Rhodobacter sphaeroides 2.4.3, has identified two genes whose products could potentially be involved in nitrite reductase expression and activity. One of the genes has been designated nirV. Putative nirV orthologues are found in other denitrifiers, where they are also located downstream of the structural gene for nitrite reductase. The nirV in 2.4.3 is apparently cotranscribed with nirK. Inactivation of nirV had no effect on cell growth, or on nitrite reductase expression or activity. Downstream of nirV and divergently transcribed is a gene, designated ppaZ, encoding a protein with significant similarity to pseudoazurins from other denitrifiers. However, three of the four residues required for binding of the type I copper centre are not conserved in the deduced sequence of the protein in 2.4.3. ppaZ is expressed only when oxygen becomes limiting. ppaZ expression is dependent on both FnrL and NnrR, and a putative binding site for these proteins has been identified. Expression of ppaZ is also dependent on the two-component PrrB/PrrA system. Inactivation of ppaZ had no significant effect on cell growth or on nitrite reductase expression or activity. Expression of a maltose-binding protein-PpaZ fusion indicated that the protein could not bind copper. Examination of the genome of the related bacterium R. sphaeroides 2.4.1 revealed that it encodes ppaZ but not nirV and evidence is presented suggesting that a common ancestor of 2.4.3 and 2.4.1 had both nitrite and nitric oxide reductase activity but as the strains diverged 2.4.1 lost nirK and nirV, making it incapable of nitrite reduction.
对球形红细菌2.4.3中编码含铜亚硝酸还原酶的nirK基因侧翼区域进行测序,已鉴定出两个基因,其产物可能参与亚硝酸还原酶的表达和活性调控。其中一个基因被命名为nirV。在其他反硝化细菌中也发现了推定的nirV直系同源物,它们同样位于亚硝酸还原酶结构基因的下游。2.4.3中的nirV显然与nirK共转录。nirV失活对细胞生长、亚硝酸还原酶的表达或活性均无影响。nirV下游且转录方向相反的是一个名为ppaZ的基因,它编码一种与其他反硝化细菌的假天青蛋白具有显著相似性的蛋白质。然而,在2.4.3中该蛋白质的推导序列中,I型铜中心结合所需的四个残基中有三个并不保守。ppaZ仅在氧气变得有限时表达。ppaZ的表达依赖于FnrL和NnrR,并且已鉴定出这些蛋白质的一个推定结合位点。ppaZ的表达还依赖于双组分PrrB/PrrA系统。ppaZ失活对细胞生长、亚硝酸还原酶的表达或活性均无显著影响。麦芽糖结合蛋白-PpaZ融合蛋白的表达表明该蛋白质不能结合铜。对相关细菌球形红细菌2.4.1的基因组进行检测发现,它编码ppaZ但不编码nirV,并且有证据表明2.4.3和2.4.1的共同祖先同时具有亚硝酸和一氧化氮还原酶活性,但随着菌株分化,2.4.1失去了nirK和nirV,使其无法进行亚硝酸盐还原。