Westby C A, Enderlin C S, Steinberg N A, Joseph C M, Meeks J C
J Bacteriol. 1987 Sep;169(9):4211-4. doi: 10.1128/jb.169.9.4211-4214.1987.
The specific activities of glutamine synthetase (GS) and glutamate synthase (GOGAT) were 4.2- and 2.2-fold higher, respectively, in cells of Azospirillum brasilense grown with N2 than with 43 mM NH4+ as the source of nitrogen. Conversely, the specific activity of glutamate dehydrogenase (GDH) was 2.7-fold higher in 43 mM NH4+-grown cells than in N2-grown cells. These results indicate that NH4+ could be assimilated and that glutamate could be formed by either the GS-GOGAT or GDH pathway or both, depending on the cellular concentration of NH4+. The routes of in vivo synthesis of glutamate were identified by using 13N as a metabolic tracer. The products of assimilation of 13NH4+ were, in order of decreasing radioactivity, glutamine, glutamate, and alanine. The formation of [13N]glutamine and [13N]glutamate by NH4+-grown cells was inhibited in the additional presence of methionine sulfoximine (an inhibitor of GS) and diazooxonorleucine (an inhibitor of GOGAT). Incorporation of 13N into glutamine, glutamate, and alanine decreased in parallel in the presence of carrier NH4+. These results imply that the GS-GOGAT pathway is the primary route of NH4+ assimilation by A. brasilense grown with excess or limiting nitrogen and that GDH has, at best, a minor role in the synthesis of glutamate.
与以43 mM NH₄⁺作为氮源培养的巴西固氮螺菌细胞相比,以N₂培养的巴西固氮螺菌细胞中谷氨酰胺合成酶(GS)和谷氨酸合酶(GOGAT)的比活性分别高4.2倍和2.2倍。相反,在以43 mM NH₄⁺培养的细胞中,谷氨酸脱氢酶(GDH)的比活性比以N₂培养的细胞高2.7倍。这些结果表明,NH₄⁺可以被同化,并且谷氨酸可以通过GS-GOGAT途径或GDH途径或两者形成,这取决于细胞内NH₄⁺的浓度。通过使用¹³N作为代谢示踪剂确定了体内谷氨酸的合成途径。¹³NH₄⁺同化产物的放射性从高到低依次为谷氨酰胺、谷氨酸和丙氨酸。在甲硫氨酸亚砜亚胺(GS的抑制剂)和重氮氧代正亮氨酸(GOGAT的抑制剂)存在的情况下,以NH₄⁺培养的细胞中[¹³N]谷氨酰胺和[¹³N]谷氨酸的形成受到抑制。在存在载体NH₄⁺的情况下,¹³N掺入谷氨酰胺、谷氨酸和丙氨酸的量平行下降。这些结果表明,GS-GOGAT途径是过量或限量氮培养的巴西固氮螺菌同化NH₄⁺的主要途径,并且GDH在谷氨酸合成中充其量只起次要作用。