Department of Biology, Queen's University, Kingston, Ontario, Canada, K7L 3N6.
Plant Physiol. 1982 Feb;69(2):508-13. doi: 10.1104/pp.69.2.508.
Protoplasts were isolated from the leaves of nitrate-cultured wheat (Triticum aestivum L. var. Frederick) seedlings. When incubated in the dark, protoplasts accumulated nitrite under anaerobic, but not under aerobic, conditions. The assimilation of [(15)N]nitrite by protoplasts was strictly light-dependent, and no loss of nitrite from the assay medium was observed under dark aerobic conditions. Therefore, the absence of nitrite accumulation under dark aerobic conditions was the result of an O(2) inhibition of nitrate reduction and not a stimulation of nitrite reduction. In the presence of antimycin A, protoplasts accumulated nitrite under dark aerobic conditions. The oxygen inhibition of nitrate reduction was apparently due to a competition between nitrate reduction and dark respiration for cytoplasmic-reducing equivalents.Oxygen control of nitrate reduction was not observed in the light, since protoplasts assimilated [(15)N]nitrate to amino-N under light aerobic conditions. It has been proposed that the increase of the ATP-to-ADP ratio in the light inhibits dark respiration and allows nitrate reduction to occur under aerobic conditions. To test this hypothesis, protoplast N and C assimilation was assayed in the presence of nigericin, an uncoupler of photophosphorylation. The dark to light increase of the protoplast energy charge was not observed in the presence of nigericin, and CO(2) fixation was completely inhibited by the uncoupler. In contrast, rates of in vivo nitrate reduction (N(2) and air) and nitrite reduction were relatively unaffected by nigericin, and light-driven nitrate assimilation was inhibited by only 20%. Nigericin had no effect on the dark-to-light increase of protoplast NADH and NADPH levels. It is proposed that the light-induced increase of cytoplasmic-reducing equivalents suppresses the competition between nitrate reduction and dark respiration and allows nitrate reduction to occur under aerobic conditions. Dark-to-light changes of the ATP-to-ADP ratio apparently are not critical to the regulation of nitrate reduction.
从硝酸盐培养的小麦(Triticum aestivum L. var. Frederick)幼苗叶片中分离原生质体。在黑暗中孵育时,原生质体在厌氧条件下但不在有氧条件下积累亚硝酸盐。原生质体对[(15)N]亚硝酸盐的同化严格依赖于光,并且在黑暗有氧条件下观察到测定介质中没有亚硝酸盐损失。因此,黑暗有氧条件下亚硝酸盐积累的缺乏是由于 O(2)抑制硝酸盐还原而不是刺激亚硝酸盐还原的结果。在抗霉素 A 的存在下,原生质体在黑暗有氧条件下积累亚硝酸盐。硝酸盐还原的氧抑制显然是由于硝酸盐还原和暗呼吸之间对细胞质还原当量的竞争。在光下未观察到硝酸盐还原的氧控制,因为原生质体在光有氧条件下将[(15)N]硝酸盐同化到氨基酸-N。已经提出,在光下 ATP 与 ADP 比值的增加抑制暗呼吸并允许硝酸盐还原在有氧条件下发生。为了检验这一假设,在存在解偶联剂 Nigericin 的情况下测定了原生质体的 N 和 C 同化。在 Nigericin 的存在下,没有观察到原生质体能量电荷从黑暗到光的增加,并且该解偶联剂完全抑制了 CO(2)固定。相比之下,体内硝酸盐还原(N(2)和空气)和亚硝酸盐还原的速率相对不受 Nigericin 的影响,并且光驱动的硝酸盐同化仅被抑制 20%。Nigericin 对原生质体 NADH 和 NADPH 水平从黑暗到光的增加没有影响。据推测,细胞质还原当量的光诱导增加抑制了硝酸盐还原和暗呼吸之间的竞争,并允许硝酸盐还原在有氧条件下发生。ATP 与 ADP 比值从黑暗到光的变化显然对硝酸盐还原的调节不是关键的。