Zhang Feng, Wang Yuping, Yang Yingli, Wu Hao, Wang Di, Liu Jianquan
Gansu Key Laboratory of Crop Genetic & Germplasm Enhancement, College of Life Sciences and Technology, Gansu Agricultural University, Lanzhou 730070, China.
Plant Cell Environ. 2007 Jul;30(7):775-85. doi: 10.1111/j.1365-3040.2007.01667.x.
Nitric oxide (NO) and hydrogen peroxide (H2O2) function as signalling molecules in plants under abiotic and biotic stresses. Calluses from Populus euphratica, which show salt tolerance, were used to study the interaction of NO and H2O2 in plant adaptation to salt resistance. The nitric oxide synthase (NOS) activity was identified in the calluses, and this activity was induced under 150 mM NaCl treatment. Under 150 mM NaCl treatment, the sodium (Na) percentage decreased, but the potassium (K) percentage and the K/Na ratio increased in P. euphratica calluses. Application of glucose/glucose oxidase (G/GO, a H2O2 donor) and sodium nitroprusside (SNP, a NO donor) revealed that both H2O2 and NO resulted in increased K/Na ratio in a concentration-dependent manner. Diphenylene iodonium (DPI, an NADPH oxidase inhibitor) counteracted H2O2 and NO effect by increasing the Na percentage, decreasing the K percentage and K/Na ratio. NG-monomethyl-L-Arg monoacetate (NMMA, an NO synthase inhibitor) and 2-phenyl-4,4,5,5-tetramethyl-imidazoline-1-oxyl-3-oxyde (PTIO, a specific NO scavenger) only reversed NO effect, but did not block H2O2 effect. The increased activity of plasma membrane (PM) H+ -ATPase caused by salt stress was reversed by treatment with DPI and NMMA. Exogenous H2O2 increased the activity of PM H+ -ATPase, but the effect could not be diminished by NMMA and PTIO. The NO-induced increase of PM H+ -ATPase can be reversed by NMMA and PTIO, but not by DPI. Western blot analysis demonstrated that NO and H2O2 stimulated the expression of PM H+ -ATPase in P. euphratica calluses. These results indicate that NO and H2O2 served as intermediate molecules in inducing salt resistance in the calluses from P. euphratica under slat stress by increasing the K/Na ratio, which was dependent on the increased PM H+ -ATPase activity.
一氧化氮(NO)和过氧化氢(H₂O₂)在植物应对非生物和生物胁迫时作为信号分子发挥作用。以具有耐盐性的胡杨愈伤组织为材料,研究NO与H₂O₂在植物耐盐适应性中的相互作用。在愈伤组织中鉴定出一氧化氮合酶(NOS)活性,且该活性在150 mM NaCl处理下被诱导。在150 mM NaCl处理下,胡杨愈伤组织中的钠(Na)百分比降低,但钾(K)百分比和K/Na比值升高。施用葡萄糖/葡萄糖氧化酶(G/GO,一种H₂O₂供体)和硝普钠(SNP,一种NO供体)表明,H₂O₂和NO均以浓度依赖的方式导致K/Na比值升高。二亚苯基碘鎓(DPI,一种NADPH氧化酶抑制剂)通过增加Na百分比、降低K百分比和K/Na比值来抵消H₂O₂和NO的作用。NG-甲基-L-精氨酸单乙酸酯(NMMA,一种NO合酶抑制剂)和2-苯基-4,4,5,5-四甲基-咪唑啉-1-氧基-3-氧化物(PTIO,一种特异性NO清除剂)仅逆转NO的作用,但不阻断H₂O₂的作用。盐胁迫引起的质膜(PM)H⁺-ATP酶活性增加通过DPI和NMMA处理得以逆转。外源H₂O₂增加了PM H⁺-ATP酶的活性,但NMMA和PTIO不能减弱该作用。NO诱导的PM H⁺-ATP酶增加可被NMMA和PTIO逆转,但不能被DPI逆转。蛋白质免疫印迹分析表明,NO和H₂O₂刺激了胡杨愈伤组织中PM H⁺-ATP酶的表达。这些结果表明,在盐胁迫下,NO和H₂O₂通过增加K/Na比值,作为诱导胡杨愈伤组织耐盐性的中间分子,这依赖于PM H⁺-ATP酶活性的增加。