Centro de Biología Molecular Severo Ochoa, Universidad Autónoma de Madrid-Consejo Superior de Investigaciones Científicas, Madrid, Spain.
J Bacteriol. 2014 Apr;196(7):1350-8. doi: 10.1128/JB.01042-13. Epub 2014 Jan 17.
Respiratory reduction of nitrate and nitrite is encoded in Thermus thermophilus by the respective transferable gene clusters. Nitrate is reduced by a heterotetrameric nitrate reductase (Nar) encoded along transporters and regulatory signal transduction systems within the nitrate respiration conjugative element (NCE). The nitrite respiration cluster (nic) encodes homologues of nitrite reductase (Nir) and nitric oxide reductase (Nor). The expression and role of the nirSJM genes in nitrite respiration were analyzed. The three genes are expressed from two promoters, one (nirSp) producing a tricistronic mRNA under aerobic and anaerobic conditions and the other (nirJp) producing a bicistronic mRNA only under conditions of anoxia plus a nitrogen oxide. As for its nitrite reductase homologues, NirS is expressed in the periplasm, has a covalently bound heme c, and conserves the heme d1 binding pocket. NirJ is a cytoplasmic protein likely required for heme d1 synthesis and NirS maturation. NirM is a soluble periplasmic homologue of cytochrome c552. Mutants defective in nirS show normal anaerobic growth with nitrite and nitrate, supporting the existence of an alternative Nir in the cells. Gene knockout analysis of different candidate genes did not allow us to identify this alternative Nir protein but revealed the requirement for Nar in NirS-dependent and NirS-independent nitrite reduction. As the likely role for Nar in the process is in electron transport through its additional cytochrome c periplasmic subunit (NarC), we concluded all the Nir activity takes place in the periplasm by parallel pathways.
硝酸盐和亚硝酸盐的呼吸还原作用在嗜热栖热菌中由各自可转移的基因簇编码。硝酸盐由异源四聚体硝酸盐还原酶 (Nar) 还原,Nar 与硝酸盐呼吸共轭元件 (NCE) 中的转运蛋白和调节信号转导系统一起编码。亚硝酸盐呼吸簇 (nic) 编码亚硝酸盐还原酶 (Nir) 和一氧化氮还原酶 (Nor) 的同源物。分析了 nirSJM 基因在亚硝酸盐呼吸中的表达和作用。这三个基因由两个启动子表达,一个(nirSp)在有氧和无氧条件下产生一个三顺反子 mRNA,另一个(nirJp)仅在缺氧加氮氧化物条件下产生一个双顺反子 mRNA。作为其亚硝酸盐还原酶同源物,NirS 在周质中表达,具有共价结合的血红素 c,并保守血红素 d1 结合口袋。NirJ 是一种细胞质蛋白,可能需要用于血红素 d1 合成和 NirS 成熟。NirM 是细胞色素 c552 的可溶性周质同源物。在 nirS 缺陷突变体中,硝酸盐和亚硝酸盐的正常厌氧生长表明细胞中存在替代的 Nir。对不同候选基因的基因敲除分析不允许我们鉴定这种替代的 Nir 蛋白,但揭示了 Nar 在 NirS 依赖和 NirS 独立的亚硝酸盐还原中的必要性。由于 Nar 在该过程中的可能作用是通过其额外的细胞色素 c 周质亚基 (NarC) 进行电子传递,因此我们得出结论,所有的 Nir 活性都通过平行途径发生在周质中。