Nakano M M, Hoffmann T, Zhu Y, Jahn D
Department of Biochemistry and Molecular Biology, Louisiana State University Medical Center, Shreveport, Louisiana 71130-3932, USA mnakano @bmb.ogi.edu
J Bacteriol. 1998 Oct;180(20):5344-50. doi: 10.1128/JB.180.20.5344-5350.1998.
The nitrate and nitrite reductases of Bacillus subtilis have two different physiological functions. Under conditions of nitrogen limitation, these enzymes catalyze the reduction of nitrate via nitrite to ammonia for the anabolic incorporation of nitrogen into biomolecules. They also function catabolically in anaerobic respiration, which involves the use of nitrate and nitrite as terminal electron acceptors. Two distinct nitrate reductases, encoded by narGHI and nasBC, function in anabolic and catabolic nitrogen metabolism, respectively. However, as reported herein, a single NADH-dependent, soluble nitrite reductase encoded by the nasDE genes is required for both catabolic and anabolic processes. The nasDE genes, together with nasBC (encoding assimilatory nitrate reductase) and nasF (required for nitrite reductase siroheme cofactor formation), constitute the nas operon. Data presented show that transcription of nasDEF is driven not only by the previously characterized nas operon promoter but also from an internal promoter residing between the nasC and nasD genes. Transcription from both promoters is activated by nitrogen limitation during aerobic growth by the nitrogen regulator, TnrA. However, under conditions of oxygen limitation, nasDEF expression and nitrite reductase activity were significantly induced. Anaerobic induction of nasDEF required the ResDE two-component regulatory system and the presence of nitrite, indicating partial coregulation of NasDEF with the respiratory nitrate reductase NarGHI during nitrate respiration.
枯草芽孢杆菌的硝酸盐还原酶和亚硝酸盐还原酶具有两种不同的生理功能。在氮限制条件下,这些酶催化硝酸盐经亚硝酸盐还原为氨,以便将氮合成代谢性地掺入生物分子中。它们在无氧呼吸的分解代谢中也发挥作用,无氧呼吸涉及利用硝酸盐和亚硝酸盐作为末端电子受体。由narGHI和nasBC编码的两种不同的硝酸盐还原酶分别在合成代谢和分解代谢的氮代谢中发挥作用。然而,如本文所报道的,由nasDE基因编码的单一依赖NADH的可溶性亚硝酸盐还原酶在分解代谢和合成代谢过程中都是必需的。nasDE基因与nasBC(编码同化硝酸盐还原酶)和nasF(亚硝酸盐还原酶西罗血红素辅因子形成所必需的)共同构成nas操纵子。所呈现的数据表明,nasDEF的转录不仅由先前鉴定的nas操纵子启动子驱动,还由位于nasC和nasD基因之间的内部启动子驱动。在需氧生长期间,通过氮调节因子TnrA,氮限制可激活这两个启动子的转录。然而,在氧限制条件下,nasDEF的表达和亚硝酸盐还原酶活性被显著诱导。nasDEF的厌氧诱导需要ResDE双组分调节系统和亚硝酸盐 的存在,这表明在硝酸盐呼吸过程中,NasDEF与呼吸硝酸盐还原酶NarGHI存在部分共调节。