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2013 | 35 | 03 |
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Hydrogen peroxide is involved in the regulation of rice (Oryza sativa L.) tolerance to salt stress

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Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
In the present study, we investigated the salt tolerance mechanism of two rice cultivars (Zhenghan-2 and Yujing-6), which show different tolerance to drought and disease. NaCl induced higher extent of lipid peroxide and ion leakage in Yujing-6 roots than those in Zhenghan-2 roots. H2O2 accumulation in Zhenghan-2 roots was lower than that in Yujing-6 roots under salt stress. Comparatively, NaCl treatment did not increase O2 - contents in both rice roots, however, O2 - level in Yujing-6 roots was higher than that in Zhenghan-2 roots under both control and salt stress conditions. Ascorbate peroxidases (APX) activity increased more significantly in Zhenghan-2 roots than that in Yujing-6 roots. The activity of catalase (CAT), peroxidase (POD), superoxide dismutase (SOD), and glucose- 6-phosphate dehydrogenase (G6PDH) was similarly enhanced in both rice roots under salt stress; however, they showed higher levels in Zhenghan-2 roots than in Yujing-6 roots. Exogenous H2O2 could enhance APX, CAT, POD, SOD and G6PDH activities in a concentration-dependent manner in both rice roots. Diphenylene iodonium (DPI), a plasma membrane (PM) NADPH oxidase inhibitor, which counteracted the NaCl-induced H2O2 accumulation, markedly decreased the activity of above enzymes. Moreover, ion leakage increased dramatically in Zhenghan-2 roots and reached to the similar level of Yujing-6 roots under NaCl+DPI treatment. Taken together, H2O2, which is mainly generated from PM NADPH oxidase, is involved in Zhenghan-2 rice tolerance to salt stress by enhancing the cellular antioxidant level.
Słowa kluczowe
Wydawca
-
Rocznik
Tom
35
Numer
03
Opis fizyczny
p.891-900,fig.,ref.
Twórcy
autor
  • Key Laboratory of Cell Activities and Stress Adaptations, Ministry of Education, School of Life Sciences, Lanzhou University, Lanzhou 730000, People’s Republic of China
autor
  • Key Laboratory of Cell Activities and Stress Adaptations, Ministry of Education, School of Life Sciences, Lanzhou University, Lanzhou 730000, People’s Republic of China
autor
  • Key Laboratory of Cell Activities and Stress Adaptations, Ministry of Education, School of Life Sciences, Lanzhou University, Lanzhou 730000, People’s Republic of China
autor
  • Key Laboratory of Cell Activities and Stress Adaptations, Ministry of Education, School of Life Sciences, Lanzhou University, Lanzhou 730000, People’s Republic of China
autor
  • Key Laboratory of Cell Activities and Stress Adaptations, Ministry of Education, School of Life Sciences, Lanzhou University, Lanzhou 730000, People’s Republic of China
autor
  • Key Laboratory of Cell Activities and Stress Adaptations, Ministry of Education, School of Life Sciences, Lanzhou University, Lanzhou 730000, People’s Republic of China
autor
  • Key Laboratory of Cell Activities and Stress Adaptations, Ministry of Education, School of Life Sciences, Lanzhou University, Lanzhou 730000, People’s Republic of China
Bibliografia
  • Apel K, Hirt H (2004) Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu Rev Plant Biol 55:373–399
  • Bartosz G (1997) Oxidative stress in plants. Acta Physiol Plant 19:47–64
  • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254
  • Bright J, Desikan R, Hancock JT, Weir IS, Neill SJ (2006) ABAinduced NO generation and stomatal closure in Arabidopsis are dependent on H2O2 synthesis. Plant J 45:113–122
  • Davletova S, Rizhsky L, liang H, Shengqiang Z, Oliver DJ, Coutu J et al (2005) Cytosolic ascorbate peroxidase 1 is a central component of the reactive oxygen gene network of Arabidopsis. Plant Cell 17:268–281
  • Durner J, Klessing DF (1996) Salicylic acid is a modulator of tobacco and mammalian catalases. J Biol Chem 271:28492–28502
  • Dutilleul C, Garmier M, Noctor G, Mathieu C, Che´trit P, Foyer CH, de Paepe R (2003) Leaf mitochondria modulate whole cell redox homeostasis, set antioxidant capacity, and determine stress resistance through altered signaling and diurnal regulation. Plant Cell 15:1212–1226
  • Elstner EF, Heupel A (1976) Inhibition of nitrite formation from hydroxylammonium chloride: a simple assay for superoxide dismutase. Anal Biochem 70:616–620
  • Esposito S, Carfagna S, Massaro G, Vona V, Di MRV (2001) Glucose-6-phosphate dehydrogenase in barley roots: kinetic properties and localization of the isoforms. Planta 212:627–634
  • Foyer CH, Halliwell B (1976) The presence of glutathione and glutathione reductase in chloroplasts: a proposed role in ascorbic acid metabolism. Planta 133:21–25
  • Foyer CH, Noctor G (2000) Oxygen processing in photosynthesis: regulation and signalling. New Phytol 146:359–388
  • Foyer CH, Noctor G (2005a) Redox homeostasis and antioxidant signaling: a metabolic interface between stress perception and physiological responses. Plant Cell 17:1866–1875
  • Foyer CH, Noctor G (2005b) Oxidant and antioxidant signaling in plants: a re-evaluation of the concept of oxidative stress in a physiological context. Plant, Cell Environ 28:1056–1071
  • Fridovich I (1986) Biological effects of the superoxide radical. Arch Biochem Biophys 247:1–11
  • Fridovich I, Beauchamp C (1971) Superoxide dismutase improved assays and an assay applicable to acrylamide gels. Anal Biochem 44:276–287
  • Gong M, Chen B, Li ZG, Guo LH (2001) Heat-shock-induced cross adaptation to heat, chilling, drought and salt stress in maize seedlings and involvement of H202. J Plant Physiol 158:125–1130
  • Hammerschmidt R, Nuckles EM, Kuc J (1982) Association of enhanced peroxidase activity with induced systemic resistance of cucumber to colletotrchum lagenarium. Physiol Plant Pathol 20:73–82
  • Hasegawa PM, Bressan RA, Zhu JK, Bohnert HJ (2000) Plant cellular and molecular responses to high salinity. Annu Rev Plant Physiol Plant Mol Biol 51:463–499
  • Heath RL, Packer L (1968) Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189–198
  • Herna´ndez JA, Olmos E, Corpas FJ, Sevilla F, del Rı´o LA (1995) Salt-induced oxidative stress in chloroplasts of pea plants. Plant Sci 105:151–167
  • Herna´ndez JA, Ferrer MA, Jime´nez A, Barcelo´ AR, Sevilla F (2001) Antioxidant systems and O2-/H2O2 production in the apoplast of pea leaves. Its relation with salt-induced necrotic lesions in minor veins. Plant Physiol 127:817–831
  • Heyser JW, Nabors MW (1981) Osmotic adjustment of cultured tobacco cells (Nicotiana tabacum var. Samsun) grown on sodium chloride. Plant Physiol 67:720–727
  • Huang CH, He WL, Guo JK, Chang XX, Su PX, Zhang LX (2005) Increased sensitivity to salt stress in an ascorbate-deficient Arabidopsis mutant. J Exp Bot 56:3041–3049
  • Li JS, Chen GC, Wang XM, Zhang YL, Jia HL, Bi YR (2010) Glucose-6-phosphate dehydrogenase-dependent hydrogen peroxide production is involved in the regulation of plasma membrane H+-ATPase and Na+/H? antiporter protein in salt-stressed callus from Carex moorcroftii. Physiol Plant 141(3):239–250
  • Li JS, Wang XM, Zhang YL, Jia HL, Bi YR (2011) cGMP regulates hydrogen peroxide accumulation in calcium-dependent salt resistance pathway in Arabidopsis thaliana roots. Planta 234(4):709–722
  • Liu YG, Wu RR, Wan Q, Xie GQ, Bi YR (2007) Glucose-6-phosphate dehydrogenase plays a pivotal role in nitric oxideinvolved defense against oxidative stress under salt stress in red kidney bean roots. Plant Cell Physiol 48:511–522
  • Marino D, Gonzalez EM, Frendo P, Puppo A, Arrese-Igor C (2007) NADPH recycling systems in oxidative stressed pea nodules: a key role for the NADP+-dependent isocitrate dehydrogenase. Planta 225:413–421
  • Mittler R, Vanderauwera S, Gollery M, Van Breusegem F (2004) The reactive oxygen gene network of plants. Trends Plant Sci 9:490–498
  • Nakano Y, Asada K (1981) Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiol 22:867–880
  • Neill SJ, Desikan R, Clarke A, Hurst RD, Hancock JT (2002) Hydrogen peroxide and nitric oxide as signaling molecules in plants. J Exp Bot 53:1237–1242
  • Noctor G, Foyer CH (1998) Ascorbate and glutathione: keeping active oxygen under control. Annu Rev Plant Physiol Plant Mol Biol 49:249–279
  • Noctor G, Arisi A-CM, Jouanin L, Kunert K-J, Rennenberg H, Foyer CH (1998) Glutathione: biosynthesis, metabolism and relationship to stress tolerance explored in transformed plants. J Exp Bot 49:623–647
  • Pandolfi PP, Sonati F, Riv RI, Mason P, Grosveld F, Luzzatto L (1995) Targeted disruption of the housekeeping gene encoding glucose 6-phosphate dehydrogenase (G6PD): G6PD is dispensable for pentose synthesis but essential for defense against oxidative stress. EMBO J 14:5209–5215
  • Pastori GM, Foyer H (2002) Common components, networks and pathways of cross-tolerance to stress. The central role of ‘redox’ and abscisic acid-mediated controls. Plant Physiol 129:460–468
  • Polidoros A, Scandalios J (1999) Role of hydrogen peroxide and different classes of antioxidants in the regulation of catalase and glutathione-S-transferase gene expression in maize (Zea mays L.). Physiol Plant 106:112–120
  • Pugin A, Frachisse JM, Tavernier E, Bligny R, Gout E, Douce R, Guern J (1997) Early events induced by the elicitor cryptogein in tobacco cells: involvement of a plasma membrane NADPH oxidase and activation of glycolysis and the pentose phosphate pathway. Plant Cell 9:2077–2091
  • Sairam RK, Srivastava GC (2002) Changes in antioxidant activity in subcellular fraction of tolerant and susceptible wheat genotypes in response to long term salt stress. Plant Sci 162:897–904
  • Salvemini F, Franze A, Iervolino A, Filosa S, Salzano S, Ursini MV (1999) Enhanced glutathione levels and oxidoresistance mediated by Increased glucose-6-phosphate dehydrogenase expression. J Biol Chem 274:2750–2757
  • Scandalios JG (1993) Oxygen stress and superoxide dismutases. Plant Physiol 101:7–12
  • Shang QM, Li XF, Zhang ZG (2007) Molecular mechanisms of cross adaptation in plants. Acta Bot Boreal-Occident Sin 27(9):1921–1928
  • Simon-Plas F, Elmayan T, Blein JP (2002) The plasma membrane oxidase NtrbohD is responsible for AOS production in elicited tobacco cells. Plant J 31:137–147
  • Tian WN, Braunstein LD, Pang J, Stuhlmeier KM, Xi QC, Tian X, Stanton RC (1998) Importance of glucose-6-phosphate dehydrogenase activity for cell growth. J Biol Chem 273:10609–10617
  • Ursini MV, Parrella A, Rosa G, Salzano S, Martini G (1997) Enhanced expression of glucose-6-phosphate dehydrogenase in human cells sustaining oxidative stress. Biochem J 323:801–806
  • Veljovic-Jovanovic SD, Noctor G, Foyer CH (2002) Are leaf hydrogen peroxide concentrations commonly overestimated? The potential influence of artefactual interference by tissue phenolics and ascorbate. Plant Physiol Biochem 40:501–507
  • Vittoria L, Maria CP, Laura DG (2009) Different involvement of the mitochondrial, plastidial and cytosolic ascorbate-glutathione redox enzymes in heat shock responses. Physiol Plant 135:296–306
  • Wang SX, Yin HQ, Tang BJ, Wang YT, Chen SF (2003a) Zhenghan-2: a new variety of rice with high yield and the tolerance to drought stress. China Seed Industry 10:64
  • Wang SX, Yin HQ, Tang BJ, Wang YT, Huang L (2003b) The selection of Zhenghan-2, a new variety of rice with high yield and the tolerance to drought stress. Crops 5:51–52
  • Wang XM, Ma YY, Huang CH, Wan Q, Li N, Bi YR (2008a) Glucose-6-phosphate dehydrogenase plays a central role in modulating reduced glutathione levels in reed callus under salt stress. Planta 227:611–623
  • Wang XM, Ma YY, Huang CH, Li JS, Wan Q, Bi YR (2008b) Involvement of glucose-6-phosphate dehydrogenase in reduced glutathione maintenance and hydrogen peroxide signal under salt stress. Plant Signal Behav 3(6):394–395
  • Wang HH, Liang XL, Huang JJ, Zhang DK, Lu HX, Liu ZJ, Bi YR (2010) Involvement of ethylene and hydrogen peroxide in induction of alternative respiratory pathway in salt-treated Arabidopsis calluses. Plant Cell Physiol 51:1754–1765
  • Yang YL, Zhang F, He WL, Wang XM, Zhang LX (2003) Ironmediated inhibition of H+-ATPase in plasma membrane vesicles isolated from wheat roots. Cell Mol Life Sci 60:1249–1257
  • Yu LJ, Lan WZ, Chen C, Yang Y (2004) Glutathione levels control glucose-6-phosphate dehydrogenase activity during elicitorinduced oxidative stress in cell suspension cultures of Taxus chinensis. Plant Sci 167:329–335
  • Zhang F, Guo JK, Yang YL, He WL, Zhang LX (2004) Changes in the pattern of antioxidant enzymes in wheat exposed to water deficit and rewatering. Acta Physiol Plant 26:345–352
  • Zhang ZY, Wang HH, Wang XM, Bi YR (2011) Nitric oxide enhances aluminum tolerance by affecting cell wall polysaccharides in rice roots. Plant Cell Rep 30(9):1701–1711
  • Zhao LQ, Zhang F, Guo JK, Yang YL, Li BB, Zhang LX (2004) Nitric oxide functions as a signal in salt resistance in the calli from two ecotypes of reed. Plant Physiol 134:849–857
  • Zhao L, He JX, Wang XM, Zhang LX (2008) Nitric oxide protects against polyethylene glycol-induced oxidative damage in two ecotypes of reed suspension cultures. J Plant Physiol 165:182–191
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