Department of Biochemistry, The Connecticut Agricultural Experiment Station, Box 1106, 123 Huntington Street, New Haven, Connecticut 06504.
Plant Physiol. 1978 Nov;62(5):690-2. doi: 10.1104/pp.62.5.690.
Net photosynthetic (14)CO(2) fixation by isolated maize (Zea mays) bundle sheath strands was stimulated 20 to 35% by the inclusion of l-glutamate or l-aspartate in the reaction mixture. Maximal stimulation occurred at a 7.5 mm concentration of either amino acid. Since the photosynthetic rate and the glutamate-dependent stimulation in the rate were equally sensitive to a photosynthetic electron transport inhibitor, 3-(p-chlorophenyl)-1,1-dimethylurea, it was concluded that glutamate did not stimulate CO(2) fixation by supplying needed NADPH (NADH) through glutamate dehydrogenase. Treatment of the bundle sheath strands with glutamate inhibited glycolate synthesis by 59%. Photorespiration in this tissue, measured as the O(2) inhibition of CO(2) fixation (the Warburg effect), was inhibited by treatment with glutamate. The stimulation in net photosynthetic CO(2) fixation probably results from the decrease in photorespiratory CO(2) loss. This metabolic regulation of the rate of glycolate synthesis and photorespiration observed with isolated bundle sheath strands could account for the inability to detect rapid photorespiration in the mature intact maize leaf.
用离体玉米(Zea mays)束鞘丝进行的净光合(14)CO2 固定,在反应混合物中加入 l-谷氨酸或 l-天冬氨酸可刺激 20%至 35%。两种氨基酸的最大刺激浓度均为 7.5mm。由于光合速率和谷氨酸依赖的速率刺激对光合电子传递抑制剂 3-(对氯苯基)-1,1-二甲基脲同样敏感,因此可以得出结论,谷氨酸不是通过谷氨酸脱氢酶提供所需的 NADPH(NADH)来刺激 CO2 固定的。用谷氨酸处理束鞘丝可使甘氨酸合成抑制 59%。用光呼吸作为 O2 抑制 CO2 固定(Warburg 效应)来测量,该组织中的光呼吸被谷氨酸处理抑制。净光合 CO2 固定的刺激可能是由于光呼吸 CO2 损失减少所致。用离体束鞘丝观察到的这种甘氨酸合成和光呼吸速率的代谢调节,可以解释在成熟完整的玉米叶片中无法检测到快速光呼吸的原因。