Institut für Botanik der Technischen Hochschule, Schnittspahnstrasse 3-5, D-6100, Darmstadt, Federal Republic of Germany.
Planta. 1984 Feb;160(2):121-8. doi: 10.1007/BF00392860.
In the Crassulacean acid metabolism (CAM) plants Kalanchoë tubiflora and Sedum morganianum a shift in the pathways occurs by which external CO2 enters the metabolism during the initial light period (phase II of the diurnal CAM cycle). At the beginning of phase II, CO2 is fixed mainly by the C4 pathway; during late phase II, however, it is fixed mainly via the C3 pathway. The C3 pathway contributes to the phosphoenolpyruvate-carboxylase-mediated CO2 fixation by the provision of three-carbon skeletons. Since the shift in the carbon-flow pathway is delayed after a CO2-free night when malic-acid accumulation in the vacuoles is prevented, it is very likely that the amount of malic acid in the vacuole is integrated in the mechanism which controls CAM during the initial light period. A light-on signal at the beginning of phase II is not required to bring about the shifts in the carbon-flow pathways, as is shown by the reaction of plants to a prolonged dark period. A model of carbon flow during phase II is proposed.
在景天酸代谢(CAM)植物长寿花和落地生根中,通过一种途径的转变,外部 CO2 在初始光照期(昼夜 CAM 循环的第二期)进入代谢。在第二期的开始,CO2 主要通过 C4 途径固定;然而,在第二期的后期,它主要通过 C3 途径固定。C3 途径通过提供三碳骨架为磷酸烯醇丙酮酸羧化酶介导的 CO2 固定做出贡献。由于在 CO2 被阻止积累到液泡中的苹果酸的无 CO2 的夜晚之后,碳流途径的转变被延迟,因此很可能液泡中苹果酸的量被整合到控制初始光照期 CAM 的机制中。正如植物对延长的黑暗期的反应所表明的那样,在第二期的开始时不需要光照信号来引起碳流途径的转变。提出了第二期碳流的模型。