Hayakawa T, Hopkins L, Peat LJ, Yamaya T, Tobin AK
Laboratory of Plant Cell Biochemistry, Graduate School of Agricultural Science, Tohoku University, 1-1 Tsutsumidori-Amamiyamachi, Aoba-ku, Sendai 981-8555, Japan (T.H., T. Y.).
Plant Physiol. 1999 Feb;119(2):409-16. doi: 10.1104/pp.119.2.409.
The quantitative analysis with immunogold-electron microscopy using a single-affinity-purified anti-NADH-glutamate synthase (GOGAT) immunoglobulin G (IgG) as the primary antibody showed that the NADH-GOGAT protein was present in various forms of plastids in the cells of the epidermis and exodermis, in the cortex parenchyma, and in the vascular parenchyma of root tips (<10 mm) of rice (Oryza sativa) seedlings supplied with 1 mM NH4+ for 24 h. The values of the mean immunolabeling density of plastids were almost equal among these different cell types in the roots. However, the number of plastids per individual cell type was not identical, and some parts of the cells in the epidermis and exodermis contained large numbers of plastids that were heavily immunolabeled. Although there was an indication of labeling in the mitochondria using the single-affinity-purified anti-NADH-GOGAT IgG, this was not confirmed when a twice-affinity-purified IgG was used, indicating an exclusively plastidial location of the NADH-GOGAT protein in rice roots. These results, together with previous work from our laboratory (K. Ishiyama, T. Hayakawa, and T. Yamaya [1998] Planta 204: 288-294), suggest that the assimilation of exogeneously supplied NH4+ ions is primarily via the cytosolic glutamine synthetase/plastidial NADH-GOGAT cycle in specific regions of the epidermis and exodermis in rice roots. We also discuss the role of the NADH-GOGAT protein in vascular parenchyma cells.
使用单亲和纯化的抗NADH-谷氨酸合酶(GOGAT)免疫球蛋白G(IgG)作为一抗的免疫金电子显微镜定量分析表明,在供应1 mM NH4+ 24小时的水稻(Oryza sativa)幼苗根尖(<10 mm)的表皮和外皮层细胞、皮层薄壁组织以及维管束薄壁组织的各种质体形式中均存在NADH-GOGAT蛋白。根中这些不同细胞类型的质体平均免疫标记密度值几乎相等。然而,每种细胞类型中的质体数量并不相同,表皮和外皮层细胞的某些部分含有大量免疫标记强烈的质体。尽管使用单亲和纯化的抗NADH-GOGAT IgG时线粒体中有标记迹象,但使用双亲和纯化的IgG时未得到证实,这表明水稻根中NADH-GOGAT蛋白仅位于质体中。这些结果与我们实验室之前的工作(K. Ishiyama、T. Hayakawa和T. Yamaya [1998] Planta 204: 288 - 294)一起表明,外源供应的NH4+离子的同化主要通过水稻根表皮和外皮层特定区域的胞质谷氨酰胺合成酶/质体NADH-GOGAT循环进行。我们还讨论了NADH-GOGAT蛋白在维管束薄壁组织细胞中的作用。