Fischer Marco, Falke Dörte, Pawlik Tony, Sawers R Gary
Institute of Biology/Microbiology, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany.
Institute of Biology/Microbiology, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany
J Bacteriol. 2014 Dec;196(23):4152-62. doi: 10.1128/JB.02202-14. Epub 2014 Sep 15.
Several members of the obligately aerobic genus Streptomyces are able to reduce nitrate, catalyzed by Nar-type respiratory nitrate reductases. A unique feature of Streptomyces coelicolor A3(2) compared with other streptomycetes is that it synthesizes three nonredundant Nar enzymes. In this study, we show that Nar2 is the main Nar enzyme active in mycelium and could characterize the conditions governing its synthesis. Nar2 was present at low levels in aerobically cultivated mycelium, but synthesis was induced when cultures were grown under oxygen limitation. Growth in the presence of high oxygen concentrations prevented the induction of Nar2 synthesis. Equally, an abrupt shift from aerobiosis to anaerobiosis did not result in the immediate induction of Nar2 synthesis. This suggests that the synthesis of Nar2 is induced during a hypoxic downshift, probably to allow maintenance of a proton gradient during the transition to anaerobiosis. Although no Nar2 could be detected in freshly harvested mature spores, synthesis of the enzyme could be induced after long-term (several days) incubation of these resting spores under anaerobic conditions. Induction of Nar2 synthesis in spores was linked to transcriptional control. Nar2 activity in whole mycelium was strictly dependent on the presence of a putative nitrate transporter, NarK2. The oxygen-dependent inhibition of nitrate reduction by Nar2 was mediated by NarK2-dependent nitrate:nitrite antiport. This antiport mechanism likely prevents the accumulation of toxic nitrite in the cytoplasm. A deletion of the narK2 gene had no effect on Nar1-dependent nitrate reduction in resting spores. Together, our results indicate redox-dependent transcriptional and posttranslational control of nitrate reduction by Nar2.
专性需氧的链霉菌属的几个成员能够在Nar型呼吸硝酸盐还原酶的催化下还原硝酸盐。与其他链霉菌相比,天蓝色链霉菌A3(2)的一个独特特征是它能合成三种非冗余的Nar酶。在本研究中,我们表明Nar2是菌丝体中主要的有活性的Nar酶,并能够描述其合成的调控条件。Nar2在需氧培养的菌丝体中含量较低,但当培养物在氧气限制条件下生长时,其合成会被诱导。在高氧浓度下生长会阻止Nar2合成的诱导。同样,从需氧状态突然转变为厌氧状态并不会立即诱导Nar2的合成。这表明Nar2的合成是在低氧转变过程中被诱导的,可能是为了在向厌氧状态转变期间维持质子梯度。虽然在刚收获的成熟孢子中检测不到Nar2,但在这些静止孢子在厌氧条件下长期(数天)培养后,该酶的合成可以被诱导。孢子中Nar2合成的诱导与转录控制有关。整个菌丝体中Nar2的活性严格依赖于一种假定的硝酸盐转运蛋白NarK2的存在。Nar2对硝酸盐还原的氧依赖性抑制是由NarK2依赖性硝酸盐:亚硝酸盐反向转运介导的。这种反向转运机制可能防止有毒亚硝酸盐在细胞质中积累。narK2基因的缺失对静止孢子中Nar1依赖性硝酸盐还原没有影响。总之,我们的结果表明Nar2对硝酸盐还原存在氧化还原依赖性的转录和翻译后控制。