Institut de Recherche en Biologie Végétale, Université de Montréal, 4101 Sherbrooke est, Montréal, Qc, H1X 2B2, Canada.
Planta. 2019 May;249(5):1319-1336. doi: 10.1007/s00425-019-03088-4. Epub 2019 Jan 9.
Futile cycling between free sugars and hexose phosphates occurring under phosphate deficiency could be involved in the maintenance of a threshold level of free cellular phosphate to preserve respiratory metabolism. We studied the metabolic response of potato cell cultures growing in Pi sufficient (2.5 mM, +Pi) or deficient (125 µM, -Pi) conditions. Under Pi deficiency, cellular growth was severely affected, however -Pi cells were able to maintain a low but steady level of free Pi. We surveyed the activities of 33 primary metabolic enzymes during the course of a 12 days Pi deficiency period. Our results show that many of these enzymes had higher specific activity in -Pi cells. Among these, we found typical markers of Pi deficiency such as phosphoenolpyruvate phosphatase and phosphoenolpyruvate carboxylase as well as enzymes involved in the biosynthesis of organic acids. Intriguingly, several ATP-consuming enzymes such as hexokinase (HK) and phosphofructokinase also displayed increased activity in -Pi condition. For HK, this was associated with an increase in the steady state of a specific HK polypeptide. Quantification of glycolytic intermediates showed a pronounced decrease in phosphate esters under Pi deficiency. Adenylate levels also decreased in -Pi cells, but the Adenylate Energy Charge was not affected by the treatment. To investigate the significance of HK induction under low Pi, [U-C]-glucose tracer studies were conducted. We found in vivo evidence of futile cycling between pools of hexose phosphates and free sugars under Pi deficiency. Our study suggests that the futile cycling between hexose phosphates and free sugars which is active under +Pi conditions is sustained under Pi deficiency. The possibility that this process represents a metabolic adaptation to Pi deficiency is discussed with respect to Pi homeostasis in Pi-deficient conditions.
在缺磷条件下,游离糖和己糖磷酸之间的无效循环可能参与维持游离细胞磷酸盐的阈值水平,以维持呼吸代谢。我们研究了在磷充足(2.5 mM,+Pi)或缺乏(125 μM,-Pi)条件下生长的马铃薯细胞培养物的代谢反应。在缺磷条件下,细胞生长受到严重影响,但 -Pi 细胞能够维持低但稳定的游离 Pi 水平。我们在 12 天的缺磷期间调查了 33 种主要代谢酶的活性。我们的结果表明,这些酶中的许多在 -Pi 细胞中的比活性更高。其中,我们发现了典型的缺磷标志物,如磷酸烯醇丙酮酸磷酸酶和磷酸烯醇丙酮酸羧激酶,以及参与有机酸生物合成的酶。有趣的是,几种消耗 ATP 的酶,如己糖激酶(HK)和磷酸果糖激酶,在 -Pi 条件下也显示出较高的活性。对于 HK,这与特定 HK 多肽的稳态增加有关。糖酵解中间产物的定量分析表明,缺磷条件下磷酸盐酯明显减少。腺嘌呤核苷酸水平在 -Pi 细胞中也降低,但处理对腺苷酸能荷没有影响。为了研究低磷条件下 HK 诱导的意义,进行了 [U-C]-葡萄糖示踪研究。我们发现体内证据表明,在缺磷条件下,己糖磷酸和游离糖之间存在无效循环。我们的研究表明,在 +Pi 条件下活跃的己糖磷酸和游离糖之间的无效循环在缺磷条件下得以维持。讨论了这个过程代表对缺磷条件下磷稳态的代谢适应的可能性。