Department of Plant Physiology, Institute of Plant Biology, University of Wrocław, Kanonia 6/8, 50-328, Wrocław, Poland.
J Plant Res. 2012 Mar;125(2):291-300. doi: 10.1007/s10265-011-0438-6. Epub 2011 Jun 3.
The effect of low temperature (LT, 10°C) on modification of plasma membrane (PM) H(+)-ATPase (EC 3.6.3.14) activity in cucumber roots was studied. Plants were grown under LT for 3 or 6 days. Some of the plants after 3 days exposure to LT were transferred to control conditions for another 3 days (post-cold, PC). The activity of PM-H(+)-ATPase was decreased in plants treated for 3 days with LT. However, the activity of PM-H(+)-ATPase was higher in plants treated with LT for a longer time and in PC plants as well. Estimation of transcript levels of cucumber PM-H(+)-ATPase in roots indicates that the action of LT involves the gene expression level. The level of PM-H(+)-ATPase mRNA was markedly decreased in roots exposed to LT for 3 days. Moreover, the increased H(+)-ATPase activity in PM isolated from plants treated for 6 days with LT and from PC plants was positively correlated with higher levels of CsHA transcripts. Western blot analysis with an anti-phosphothreonine antibody showed that modification of the activity of PM-H(+)-ATPase under LT stress did not result from phosphorylation/dephosphorylation of the enzyme protein. However, the stimulation of PM-H(+)-ATPase activity in the case of PC plants could partially have emanated from increased activity of PM NAD(P)H oxidoreductase. In addition, modification of the transcript level of proton pump genes could have resulted from the action of H(2)O(2). In PC plants, an increase in H(2)O(2) level was observed. Moreover, treatment of plants with H(2)O(2) induced expression of PM H(+)-ATPase genes.
研究了低温(10°C)对黄瓜根系质膜 H(+)-ATP 酶(EC 3.6.3.14)活性修饰的影响。植物在低温下生长 3 或 6 天。一些植物在低温暴露 3 天后被转移到对照条件下再培养 3 天(冷后,PC)。用 LT 处理 3 天的植物中 PM-H(+)-ATP 酶的活性降低。然而,用 LT 处理时间更长的植物以及 PC 植物中的 PM-H(+)-ATP 酶活性更高。根中黄瓜 PM-H(+)-ATP 酶的转录水平表明,LT 的作用涉及基因表达水平。在 LT 暴露 3 天的根中,PM-H(+)-ATP 酶的 mRNA 水平明显降低。此外,用 LT 处理 6 天的植物和 PC 植物分离的 PM 中 H(+)-ATP 酶活性的增加与较高水平的 CsHA 转录物呈正相关。用抗磷酸苏氨酸抗体进行的 Western blot 分析表明,LT 应激下 PM-H(+)-ATP 酶活性的修饰不是由于酶蛋白的磷酸化/去磷酸化。然而,PC 植物中 PM-H(+)-ATP 酶活性的刺激可能部分来自 PM NAD(P)H 氧化还原酶活性的增加。此外,质子泵基因转录水平的修饰可能是由于 H(2)O(2)的作用。在 PC 植物中,观察到 H(2)O(2)水平的增加。此外,用 H(2)O(2)处理植物诱导了 PM H(+)-ATP 酶基因的表达。