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C4 Photosynthesis: Light-dependent CO2 Fixation by Mesophyll Cells Protoplasts and Protoplast Extracts of Digitaria sanguinalis

机译:C4光合作用:洋地黄的叶肉细胞原生质体和原生质体提取物对光的CO2固定作用

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摘要

Mesophyll cells, protoplasts, and protoplast extracts of Digitaria sanguinalis were used for comparative studies of light-dependent CO2 fixation. CO2 fixation was low without the addition of organic substrates. Pyruvate, oxaloacetate, and 3-phosphoglycerate induced relatively low rates (10 to 90 μmoles/mg chlorophyll·hr) of CO2 fixation when added separately. However, a highly synergistic relationship was found between pyruvate + oxaloacetate and pyruvate + 3-phosphoglycerate for inducing light-dependent CO2 fixation in the mesophyll preparations. Highest rates of CO2 fixation were obtained with protoplast extracts. Pyruvate, in combination with oxaloacetate or 3-phosphoglycerate induced light-dependent rates from 150 to 380 μmoles of CO2 fixed/mg chlorophyll·hr which are equivalent to or exceed reported rates of whole leaf photosynthesis in C4 species. Concentrations of various substrates required to give half-maximum velocities of CO2 fixation were determined, with the protoplast extracts generally saturating at the lowest substrate concentrations. Chloroplasts separated from protoplast extracts showed little capacity for CO2 fixation. The results suggest that CO2 fixation in C4 mesophyll cells is dependent on chloroplasts and extrachloroplastic phosphoenolpyruvate carboxylase.The stimulation of pyruvate-induced CO2 fixation by oxaloacetate and 3-phosphoglycerate is thought to be due to induction of noncyclic electron transport which generates ATP for the conversion of pyruvate to phosphoenolpyruvate by pyruvate Pi dikinase. The primary products of the substrate-induced CO2 fixation were oxaloacetate and malate, which provides further evidence for carbon fixation through the β-carboxylation pathway. High rates of light-dependent CO2 fixation with a significant percentage of 14C fixed into malate suggest an efficient operation of both photosystems I and II.The substrate inductions are discussed with respect to the proposed role of the mesophyll cell in C4 photosynthesis, and schemes suggesting the stoichiometry of energy requirements for photosynthetic carbon metabolism in C4 mesophyll cells are presented.
机译:Digitaria sanguinalis的叶肉细胞,原生质体和原生质体提取物用于光依赖性CO2固定的比较研究。不添加有机底物,二氧化碳固定率低。单独添加时,丙酮酸,草酰乙酸和3-磷酸甘油酸诱导较低的CO2固定速率(10至90μmoles/ mg叶绿素·小时)。然而,发现在丙酮酸+草酰乙酸盐和丙酮酸+ 3-磷酸甘油酸之间存在高度协同的关系,以诱导叶肉制品中光依赖性CO 2固定。用原生质体提取物获得最高的二氧化碳固定率。丙酮酸与草酰乙酸或3-磷酸甘油酸酯的结合引起的光依赖速率为150至380μmolCO2固定/ mg叶绿素·小时,等于或超过了C4物种全叶光合作用的速率。确定了给出一半最大CO2固定速度所需的各种底物的浓度,原生质体提取物通常在最低底物浓度下达到饱和。从原生质体提取物中分离出的叶绿体几乎没有固定二氧化碳的能力。结果表明,C4叶肉细胞中的CO2固定取决于叶绿体和叶绿体磷酸烯醇丙酮酸羧化酶。草酰乙酸和3-磷酸甘油酸酯对丙酮酸诱导的CO2固定的刺激被认为是由于非循环电子转运的诱导,该转运产生ATP进行转化丙酮酸Pi二激酶将丙酮酸转化为磷酸烯醇丙酮酸。底物诱导的CO2固定的主要产物是草酰乙酸和苹果酸,这为通过β-羧化途径进行碳固定提供了进一步的证据。高比例的光依赖性CO2固定以及大量的 14 C固定在苹果酸中表明光系统I和II均有效运行。讨论了底物诱导与叶肉的拟议作用提出了在C4光合作用中的细胞,以及提出了建议在C4叶肉细胞中进行光合作用碳代谢所需能量的化学计量的方案。

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