Botanisches Institut der Universität, 8000 München 19, West Germany.
Plant Physiol. 1976 Sep;58(3):288-91. doi: 10.1104/pp.58.3.288.
In vitro studies of dark (14)CO(2) fixation with isolated cell aggregates of Kalanchoë fedtschenkoi showed that malate synthesized after 20 sec is predominantly (85 to 92%) labeled at carbon 4, while after 20 min only 65 to 69% of the radioactivity was located in this position. The intramolecular labeling pattern of malate could not be changed by supplementing the cells with carboxylation reaction substrates such as ribulose diphosphate or phosphoenolpyruvate. The kinetic decline of label at carbon 4 of malate occurs independently of CO(2) fixation, since 4-(14)C-labeled aspartate fed to the cells gave rise to malate labeled 62% at carbon 4 after 20 min. Furthermore, the cells were capable of converting fed malate to fumarate. It is concluded that synthesis of malate during dark CO(2) fixation is accomplished by a single carboxylation step via phosphoenolpyruvate carboxylase and labeling patterns observed in malate are a consequence of the action of fumarase.
离体研究表明,fedtschenkoi 型长寿花细胞聚集体暗(14)CO2固定后,20 秒时合成的苹果酸,其碳 4 位主要(85%至 92%)被标记,而 20 分钟后只有 65%至 69%的放射性位于该位置。细胞补充羧化反应底物如二磷酸核酮糖或磷酸烯醇丙酮酸,不能改变苹果酸的分子内标记模式。苹果酸碳 4 位标记的动力学下降与 CO2 固定无关,因为向细胞中添加 4-(14)C 标记的天冬氨酸,20 分钟后生成的苹果酸有 62%标记在碳 4 位。此外,细胞能够将摄入的苹果酸转化为延胡索酸。因此,暗 CO2 固定期间苹果酸的合成是通过磷酸烯醇丙酮酸羧化酶的单一羧化步骤完成的,而在苹果酸中观察到的标记模式是延胡索酸酶作用的结果。