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Carbon assimilation and metabolism in potato leaves deficient in plastidial phosphoglucomutase

机译:缺乏质体性磷酸葡萄糖变位酶的马铃薯叶片碳同化和代谢

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We have previously described the generation of transgenic potato (Solanum tuberosum L. cv. Desiree) lines expressing the S. tuberosum plastidial phosphoglucomutase (StpPGM) gene in the antisense orientation under the control of the 35S promoter and characterised heterotrophic metabolism in these lines [E. Tauberger et al. (2000) Plant J 23:43–53]. The aim of the current work was to examine the role of plastidial phosphoglucomutase (pPGM, EC 5.4.2.2) in photosynthetic carbon partitioning. Here we characterise the metabolism of leaves of the same lines and show that reducing the activity of this enzyme has profound effects on carbon partitioning, characterised by a strong (up to 50%) reduction in the rate of starch accumulation accompanied by a minor reduction in the rate of sucrose accumulation. Gas-exchange and 14CO2-feeding experiments revealed that the transgenic lines exhibited a decreased rate of photosynthesis and a corresponding reduced assimilation of radiolabel into starch, even in lines exhibiting only a minor decrease in pPGM activity. In illuminated leaves, decreasing the amount of pPGM resulted in decreased amounts of triose-phosphates, hexose-phosphates and inorganic phosphate without changes in the level of 3-phosphoglycerate. Most importantly, the deduced ratio of phosphoesters to inorganic phosphate increased, indicating the likelihood that photosynthesis was phosphate-limited in these lines. Determination of a more complete metabolic profile of leaf material from these lines revealed a large number of changes in the levels of amino and organic acids, consistent with an inhibition of triose-phosphate export from the chloroplast, but little change in the energy status of the transformants. We discuss the implications of these changes with respect to both consequences of inhibiting starch synthesis and of inhibiting photosynthesis, and conclude that a high activity of pPGM is required both to prevent phosphate limitation of photosynthesis and for co-ordination of plastidially and cytosolically compartmented photosynthetic metabolism.
机译:先前我们已经描述了在35S启动子控制下以反义方向表达结核分枝杆菌质体磷酸葡萄糖变位酶(StpPGM)基因的转基因马铃薯(Solanum tuberosum L. cv。Desiree)系的生成,并表征了这些系中的异养代谢[E 。陶伯格等。 (2000)Plant J 23:43-53]。当前工作的目的是研究质体磷酸葡糖变位酶(pPGM,EC 5.4.2.2)在光合碳分配中的作用。在这里,我们表征了相同品系的叶片的新陈代谢,并表明降低这种酶的活性对碳分配具有深远的影响,其特征是淀粉积累速率显着降低(最多50%),而淀粉的积累略有降低。蔗糖积累的速率。气体交换和14 CO2 饲喂实验表明,转基因品系的光合作用速率降低,放射性标记与淀粉的同化程度也相应降低,即使品系中pPGM活性仅略有降低。在光照的叶片中,减少pPGM的量会导致磷酸三磷酸酯,磷酸己糖和无机磷酸酯的含量降低,而3-磷酸甘油酸酯的含量却没有变化。最重要的是,磷酸酯与无机磷酸酯的推导比例增加,表明在这些品系中光合作用受到磷酸酯限制的可能性。从这些品系确定叶片材料更完整的代谢谱表明,氨基酸和有机酸水平发生了许多变化,这与抑制叶绿体中的磷酸三糖输出有关,但其能量状态变化很小。转化子。我们讨论了这些变化对于抑制淀粉合成和抑制光合作用的影响,并得出结论,pPGM的高活性既需要防止磷限制光合作用,又需要协调质体和细胞质分隔的光合作用代谢。

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