Lin J T, Stewart V
Section of Biochemistry, Molecular and Cell Biology, Cornell University, Ithaca, New York 14853, USA.
Adv Microb Physiol. 1998;39:1-30, 379. doi: 10.1016/s0065-2911(08)60014-4.
Nitrate is a significant nitrogen source for plants and microorganisms. Recent molecular genetic analyses of representative bacterial species have revealed structural and regulatory genes responsible for the nitrate-assimilation phenotype. Together with results from physiological and biochemical studies, this information has unveiled fundamental aspects of bacterial nitrate assimilation and provides the foundation for further investigations. Well-studied genera are: the cyanobacteria, including the unicellular Synechococcus and the filamentous Anabaena; the gamma-proteobacteria Klebsiella and Azotobacter; and a Gram-positive bacterium, Bacillus. Nitrate uptake in most of these groups seems to involve a periplasmic binding protein-dependent system that presumably is energized by ATP hydrolysis (ATP-binding cassette transporters). However, Bacillus may, like fungi and plants, utilize electrogenic uptake through a representative of the major facilitator superfamily of transport proteins. Nitrate reductase contains both molybdenum cofactor and an iron-sulfur cluster. Electron donors for the enzymes from cyanobacteria and Azotobacter are ferredoxin and flavodoxin, respectively, whereas the Klebsiella and Bacillus enzymes apparently accept electrons from a specific NAD(P)H-reducing subunit. These subunits share sequence similarity with the reductase components of bacterial aromatic ring-hydroxylating dehydrogenases such as toluene dioxygenase. Nitrite reductase contains sirohaem and an iron-sulfur cluster. The enzymes from cyanobacteria and plants use ferredoxin as the electron donor, whereas the larger enzymes from other bacteria and fungi contain FAD and NAD(P)H binding sites. Nevertheless, the two forms of nitrite reductase share recognizable sequence and structural similarity. Synthesis of nitrate assimilation enzymes and uptake systems is controlled by nitrogen limitation in all bacteria examined, but the relevant regulatory proteins exhibit considerable structural and mechanistic diversity in different bacterial groups. A second level of control, pathway-specific induction by nitrate and nitrite in Klebsiella, involves transcription antitermination. Several issues await further experimentation, including the mechanism and energetics of nitrate uptake, the pathway(s) for nitrite uptake, the nature of electron flow during nitrate reduction, and the action of transcriptional regulatory circuits. Fundamental knowledge of nitrate assimilation physiology should also enhance the study of nitrate metabolism in soil, water and other natural environments, a challenging topic of considerable interest and importance.
硝酸盐是植物和微生物的重要氮源。近期对代表性细菌物种的分子遗传学分析揭示了负责硝酸盐同化表型的结构基因和调控基因。结合生理生化研究结果,这些信息揭示了细菌硝酸盐同化的基本方面,并为进一步研究奠定了基础。研究充分的属包括:蓝细菌,如单细胞的聚球藻属和丝状的鱼腥藻属;γ-变形菌纲的克雷伯氏菌属和固氮菌属;以及革兰氏阳性菌芽孢杆菌属。这些菌群中的大多数硝酸盐摄取似乎涉及一种依赖周质结合蛋白的系统,推测该系统由ATP水解供能(ATP结合盒转运蛋白)。然而,芽孢杆菌属可能像真菌和植物一样,通过主要转运蛋白超家族的一种代表蛋白利用电致摄取。硝酸还原酶同时含有钼辅因子和铁硫簇。蓝细菌和固氮菌属的该酶的电子供体分别是铁氧化还原蛋白和黄素氧化还原蛋白,而克雷伯氏菌属和芽孢杆菌属的酶显然从特定的NAD(P)H还原亚基接受电子。这些亚基与细菌芳香环羟基化脱氢酶(如甲苯双加氧酶)的还原酶组分具有序列相似性。亚硝酸还原酶含有西罗血红素和铁硫簇。蓝细菌和植物的该酶以铁氧化还原蛋白作为电子供体,而其他细菌和真菌的较大型酶含有FAD和NAD(P)H结合位点。尽管如此,两种形式的亚硝酸还原酶具有可识别的序列和结构相似性。在所有检测的细菌中,硝酸盐同化酶和摄取系统的合成受氮限制控制,但不同细菌群体中的相关调控蛋白在结构和机制上表现出相当大的多样性。克雷伯氏菌属中由硝酸盐和亚硝酸盐进行的途径特异性诱导这一二级控制涉及转录抗终止。还有几个问题有待进一步实验研究,包括硝酸盐摄取的机制和能量学、亚硝酸盐摄取途径、硝酸盐还原过程中的电子流性质以及转录调控回路的作用。硝酸盐同化生理学的基础知识也应加强对土壤、水和其他自然环境中硝酸盐代谢的研究,这是一个极具挑战性且相当有趣和重要的课题。