Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining 810008, China School of Life Sciences, Lanzhou University, Lanzhou 730000, China.
Physiol Plant. 2011 Mar;141(3):239-50. doi: 10.1111/j.1399-3054.2010.01429.x. Epub 2010 Dec 12.
Glucose-6-phosphate dehydrogenase (G6PDH) is important for the activation of plant resistance to environmental stresses, and ion homeostasis is the physiological foundation for living cells. In this study, we investigated G6PDH roles in modulating ion homeostasis under salt stress in Carex moorcroftii callus. G6PDH activity increased to its maximum in 100 mM NaCl treatment and decreased with further increased NaCl concentrations. K+/Na+ ratio in 100 mM NaCl treatment did not exhibit significant difference compared with the control; however, in 300 mM NaCl treatment, it decreased. Low-concentration NaCl (100 mM) stimulated plasma membrane (PM) H+-ATPase and NADPH oxidase activities as well as Na+/H+ antiporter protein expression, whereas high-concentration NaCl (300 mM) decreased their activity and expression. When G6PDH activity and expression were reduced by glycerol treatments, PM H+-ATPase and NADPH oxidase activities, Na+/H+ antiporter protein level and K+/Na+ ratio dramatically decreased. Simultaneously, NaCl-induced hydrogen peroxide (H₂O₂) accumulation was abolished. Exogenous application of H₂O₂ increased G6PDH, PM H+-ATPase and NADPH oxidase activities, Na+/H+ antiporter protein expression and K+/Na+ ratio in the control and glycerol treatments. Diphenylene iodonium (DPI), the NADPH oxidase inhibitor, which counteracted NaCl-induced H₂O₂ accumulation, decreased G6PDH, PM H+-ATPase and NADPH oxidase activities, Na+/H+ antiporter protein level and K+/Na+ ratio. Western blot result showed that G6PDH expression was stimulated by NaCl and H₂O₂, and blocked by DPI. Taken together, G6PDH is involved in H₂O₂ accumulation under salt stress. H₂O₂, as a signal, upregulated PM H+-ATPase activity and Na+/H+ antiporter protein level, which subsequently resulted in the enhanced K+/Na+ ratio. G6PDH played a central role in the process.
葡萄糖-6-磷酸脱氢酶(G6PDH)对植物抵抗环境胁迫的激活很重要,而离子稳态是活细胞的生理基础。在这项研究中,我们研究了 G6PDH 在调节盐胁迫下藓毛荸荠愈伤组织中的离子稳态中的作用。在 100mM NaCl 处理下,G6PDH 活性增加到最大值,随着 NaCl 浓度的进一步增加而降低。在 300mM NaCl 处理下,K+/Na+ 比值与对照相比没有显著差异;然而,在 300mM NaCl 处理下,它降低了。低浓度 NaCl(100mM)刺激质膜(PM)H+-ATPase 和 NADPH 氧化酶活性以及 Na+/H+ 反向转运蛋白表达,而高浓度 NaCl(300mM)降低了它们的活性和表达。当 G6PDH 活性和表达被甘油处理降低时,PM H+-ATPase 和 NADPH 氧化酶活性、Na+/H+ 反向转运蛋白水平和 K+/Na+ 比值显著降低。同时,NaCl 诱导的过氧化氢(H₂O₂)积累被消除。外源应用 H₂O₂增加了对照和甘油处理中的 G6PDH、PM H+-ATPase 和 NADPH 氧化酶活性、Na+/H+ 反向转运蛋白表达和 K+/Na+ 比值。二苯基碘(DPI),NADPH 氧化酶抑制剂,抵消了 NaCl 诱导的 H₂O₂ 积累,降低了 G6PDH、PM H+-ATPase 和 NADPH 氧化酶活性、Na+/H+ 反向转运蛋白水平和 K+/Na+ 比值。Western blot 结果表明,G6PDH 表达受 NaCl 和 H₂O₂ 的刺激,被 DPI 阻断。综上所述,G6PDH 参与了盐胁迫下 H₂O₂ 的积累。H₂O₂ 作为一种信号,上调 PM H+-ATPase 活性和 Na+/H+ 反向转运蛋白水平,从而增强 K+/Na+ 比值。G6PDH 在这个过程中起着核心作用。