The Institute of Low Temperature Science, Hokkaido University, Sapporo, Japan.
Plant Physiol. 1974 Oct;54(4):544-9. doi: 10.1104/pp.54.4.544.
Activities of glucose 6-phosphate, 6-phosphogluconate, and isocitrate dehydrogenases, together with intermediate levels of the glycolytic pathway and the pentose phosphate cycle, were measured throughout a year in the living bark of poplar (Populus gelrica). Shoots, immediately after budding (early May), contained very high levels of the three enzyme activities, which fell gradually by early or mid-July to a level, roughly equivalent to budding (May) or growing (July) 2-year-old twigs. In September, the former two dehydrogenase activities of the new shoots and 2-year-old twigs began to rise, while the latter activity started to decrease. The rise of the two dehydrogenase activities continued until late November (or early December). The high level of the two dehydrogenase activities lasted until early in April of the following year and then the decrease in the activities began prior to the onset of budding, reaching a low, basal level in early May. The profile of changes in the two dehydrogenase activities appeared to coincide with the increase and decrease of soluble proteins.Normal concentrations of total hexose phosphates in the glycolytic pathway plus 6-phosphogluconate were found to be 288 to 895 mumoles/kilogram dry weight. During the metabolism transition (September and April), a transient and striking increase of 6-phosphogluconate was observed. In September, 6-phosphogluconate reached a level on the order of 10(-4)m and was 4 times that of fructose 6-phosphate. The increase in 6-phosphogluconate coincided with the increase in the glucose 6-phosphate dehydrogenase activity. Coincidentally, with the change of 6-phosphogluconate level, a large deviation of the in vivo ratio of fructose 6-phosphate to glucose 6-phosphate from the known equilibrium constant was observed, showing the relation of pentose phosphate cycle enzyme activity to the control of glycolysis. The ratio of glucose 6-phosphate to glucose 1-phosphate deviated from that predicted. These ratios fluctuated throughout the year and were affected by the growth phases. The levels of pentose phosphate cycle metabolites, except for 6-phosphogluconate, in the bark were extremely low.The level of inorganic phosphate in the living bark throughout the year was dependent upon the growth phases, suggesting the presence of a regulatory mechanism to maintain inorganic phosphate at a given level as the growth phase changed.Sugar phosphate levels of popular twigs or potato tubers (Solanum tuberosum) remained constant after they were stored for 2 weeks at low temperatures, whereas in sweet potato roots (Ipomoea batatas), the level rose to about 9-fold of the control, indicating the presence of a strict regulatory system for the synthesis and catabolism of sugar phosphate in the former two.
在杨树(Populus gelrica)活体树皮中,全年测定了葡萄糖 6-磷酸、6-磷酸葡萄糖酸和异柠檬酸脱氢酶的活性,以及糖酵解途径和戊糖磷酸循环的中间水平。芽刚萌出(五月初)的枝条含有非常高的三种酶活性,到 7 月初或中旬,酶活性逐渐下降到与芽出(5 月)或生长(7 月)的 2 年生小枝相当的水平。9 月,新梢和 2 年生小枝的前两种脱氢酶活性开始上升,而后者开始下降。两种脱氢酶活性的上升一直持续到 11 月底(或 12 月初)。两种脱氢酶活性的高水平一直持续到次年 4 月初,然后在芽出之前开始下降,到 5 月初达到低基础水平。两种脱氢酶活性变化的情况似乎与可溶性蛋白的增加和减少相吻合。糖酵解途径和 6-磷酸葡萄糖酸的总己糖磷酸盐的正常浓度为 288 至 895 微摩尔/千克干重。在代谢转换期(9 月和 4 月),观察到 6-磷酸葡萄糖酸的短暂而显著增加。9 月,6-磷酸葡萄糖酸达到 10(-4)m 的水平,是果糖 6-磷酸的 4 倍。6-磷酸葡萄糖酸的增加与葡萄糖 6-磷酸脱氢酶活性的增加相吻合。巧合的是,随着 6-磷酸葡萄糖酸水平的变化,观察到果糖 6-磷酸与葡萄糖 6-磷酸的体内比从已知的平衡常数显著偏离,表明戊糖磷酸循环酶活性与糖酵解的控制有关。葡萄糖 6-磷酸与葡萄糖 1-磷酸的比值偏离了预测值。这些比值全年波动,并受生长阶段的影响。树皮中戊糖磷酸循环代谢物的水平,除 6-磷酸葡萄糖酸外,都非常低。全年活体树皮中的无机磷酸盐水平取决于生长阶段,表明存在一种调节机制,以在生长阶段变化时将无机磷酸盐维持在给定水平。在低温下储存 2 周后,杨树小枝或土豆块茎(Solanum tuberosum)的糖磷酸盐水平保持不变,而在番薯根(Ipomoea batatas)中,水平上升到对照的约 9 倍,表明前两者的糖磷酸盐合成和分解代谢存在严格的调节系统。