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2010 | 32 | 3 |

Tytuł artykułu

Osmolytes and metal ions accumulation, oxidative stress and antioxidant enzymes activity as determinants of salinity stress tolerance in maize genotypes

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Effect of soil salinity was studied in two maize (Zea mays L.) genotypes, DTP-w-c 9 (comparatively tolerant) and Prabhat (susceptible) under control and three levels of salinity at vegetative and anthesis stages during summer– rainy season. Salinity stress decreased relative water content (RWC), chlorophyll (Chl) and carotenoid (Car) contents, membrane stability index (MSI), potassium (K⁺) and calcium (Ca²⁺) contents, and increased the rate of superoxide radical (O₂⁻) production, contents of hydrogen peroxide (H₂O₂), thiobarbituric acid reactive substances (TBARS) (measure of lipid peroxidation), proline, glycine-betaine, total soluble sugars, sodium (Na⁺), and Na⁺/K⁺ and Na⁺/Ca²⁺ ratios in both the genotypes. Activities of superoxide dismutase (SOD), ascorbate peroxidase (APX), catalase (CAT) and glutathione reductase (GR) increased up to S2 salinity level in both the genotypes, and up to highest salinity level (S3) in DTP-w-c 9 at the two stages. Salinity-induced decrease in RWC, Chl, Car, MSI, K⁺ and Ca²⁺ was significantly greater in Prabhat, which also recorded higher Na⁺ content and Na⁺/K⁺ and Na⁺/Ca²⁺ ratios than DTP-w-c 9. DTP-w-c 9 recorded higher contents of proline, glycine-betaine, total soluble sugars, K⁺, Ca²⁺, activity of SOD, APX, CAT, GR, and comparatively lower O₂⁻, H₂O₂ and TBARS contents compared to Prabhat. Results show that salinity tolerance of DTP-w-c 9, as manifested by less decrease in RWC, Chl, Car and MSI, is associated with maintenance of adequate levels of K⁺ and Ca²⁺, greater contents of osmolytes, higher antioxidant enzymes activity, and lower O₂⁻, H₂O₂, TBARS and Na⁺ contents than Prabhat.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

32

Numer

3

Opis fizyczny

p.477-486,fig.,ref.

Twórcy

autor
  • Division of Plant Physiology, Indian Agricultural Research Institute, New Delhi 110012, India
  • Department of Genetics and Microbiology, Faculty of Science, Charles University, Vinicˇna´ 5, 12843 Prague 2, Czech Republic
autor
  • Division of Plant Physiology, Indian Agricultural Research Institute, New Delhi 110012, India
autor
  • Division of Plant Physiology, Indian Agricultural Research Institute, New Delhi 110012, India

Bibliografia

  • Abd el Samad HM (1993) Counteraction of NaCl and CaCl₂ or KCl on pigment, saccharide and mineral contents in wheat. Biol Plant 35:555–560
  • Aebi H (1984) Catalase in vitro. Methods Enzymol 105:121–126
  • Agarwal S, Sairam RK, Srivastava GC, Tyagi A, Meena RC (2005) Role of ABA, salicylic acid, calcium and hydrogen peroxide on antioxidant enzymes induction in wheat seedlings. Plant Sci 169:559–570
  • Arnon DI (1949) Copper enzymes in isolated chloroplasts. Polyphenol oxidase in Beta vulgaris. Plant Physiol 24:1–15
  • Asada K (1992) Ascorbate peroxidase—a hydrogen peroxide scavenging enzyme in plants. Physiol Plant 85:235–241
  • Asada K, Takahashi M (1987) Production and scavenging of active oxygen in photosynthesis. In: Kyde DJ, Osmond CB, Arntzen CJ (eds) Photoinhibition. Elsevier, Amsterdam, pp 227–287
  • Bates LS, Waldran RP, Teare ID (1973) Rapid determination of free proline for water stress studies. Plant Soil 39:205–208
  • Bhattacharjee S, Mukherjee AK (1996) Ethylene evolution and membrane lipid peroxidation as indicators of salt injury in leaf tissues of Amaranthus lividus seedlings. Indian J Exp Biol 34:279–281
  • Bohnert HJ, Jensen RG (1996) Strategies for engineering water stress tolerance in plants. Trends Biotechnol 14:89–97
  • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of proteins utilizing the principle of protein dye binding. Anal Biochem 72:248–254
  • Brennan T, Frenkel C (1977) Involvement of hydrogen peroxide in the regulation of senescence in pear. Plant Physiol 59:411–416
  • Brown AD, Simpson JR (1972) Water relations of sugar tolerant yeasts: the role of intracellular polyols. J Gen Microbiol 72:589–591
  • Chaitanya KSK, Naithani SC (1994) Role of superoxide, lipid peroxidation and superoxide dismutase in membrane perturbation during loss of viability in seeds of Shorea robusta Gaertnf. New Phytol 126:623–627
  • Cushman JC, Meyers G, Michalowski CB, Schmitt JM, Bohnert HJ (1989) Salt stress leads to differential expression of two isogenes of phosphoenol pyruvate carboxylase during crassulacean acid metabolism induction in the common ice plant. Plant Cell 1:715–725
  • Davies KJA (1987) Protein damage and degradation by oxygen radicals. I. General aspects. J Biol Chem 262:9895–9901
  • Dhindsa RS, Plumb-Dhindsa P, Throne TA (1981) Leaf senescence: correlated with increased levels of membrane permeability and lipid peroxidation and decreased levels of superoxide dismutase and catalase. J Exp Bot 32:93–101
  • Epstein E, Norlyn JD, Rush DW, Kingsburg RW, Kelley DB, Cunningham GA, Wrona AF (1980) Saline culture of crops: a genetic approach. Science 210:399–404
  • Fridovich I (1986) Biological effects of superoxide radical. Arch Biochem Biophys 247:1–11
  • Gadallah MAA (1999) Effect of proline and glycine betaine on Vicia faba responses to salt stress. Biol Plant 42:247–249
  • Greenway H, Munns R (1980) Mechanism of salt tolerance in non halophytes. Ann Rev Plant Physiol 31:149–190
  • Greive CM, Grattan SR (1983) Rapid assay for determination of water soluble quaternary-amino compounds. Plant Soil 70:303–307
  • Gueta-Dahan Y, Yaniv Z, Zilinskas BA, Ben-Hayyim G (1997) Salt and oxidative stress: similar and specific responses and their relation to salt tolerance in citrus. Planta 203:460–469
  • Heath RL, Packer L (1968) Photoperoxidation in isolated chloroplast. I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189–198
  • Hernandez JA, Francisco J, Corpas FJ, Gomez GM, del Rio LA, Sevilla F (1993) Salt induced oxidative stresses mediated by activated oxygen species in pea leaf mitochondria. Physiol Plant 89:103–110
  • Hernandez JA, Olmos E, Corpas FJ, Sevilla F, Del Rio LA (1995) Salt induced oxidative stress in chloroplasts of pea plants. Plant Sci 105:151–167
  • Hernandez JA, Jimenez A, Mullineaux P, Sevilla F (2000) Tolerance of (Pisum sativum) to long term salt stress is associated with induction of antioxidant defences. Plant Cell Biol 23:853–862
  • Hiscox JD, Isrealstam GF (1979) A method for the extraction of chlorophyll from leaf tissue without maceration. Can J Bot 57:1332–1334
  • Imlay JA, Linn S (1988) DNA damage and oxygen radical toxicity. Science 240:1302–1309
  • Joshi YC, Quadar A, Rana RS (1979) Differential sodium and potassium accumulation related to sodicity tolerance in wheat. Indian J Plant Physiol 22:226–230
  • Knox JP, Dodge AO (1985) Singlet oxygen and plants. Phytochemistry 24:889–896
  • Lutts S, Kinet JN, Bouharmont J (1996) Effects of various salts and of mannitol on ion and proline accumulation in relation to osmotic adjustment in rice (Oryza sativa L.) callus culture. J Plant Physiol 149:186–195
  • Melakeselam L, Zhou WJ (1999) Effects of freezing and heat stresses on antioxidant enzymes activities, lipid peroxidation and membrane deterioration in rape. J Zhejiang Univ 25:43–49
  • Moustafa AH, Shabassy AI, Gohar AI, Abd-El-Naim EN, Rahman AA, Elshal ME (1966) Growth and cationic accumulation by wheat and barley, as influenced by various levels of exchangeable sodium. Agric Res Rev Cairo 44:1–17
  • Naik GR, Joshi GV (1983) Ineffectual role of proline metabolism in salt stressed sugarcane leaves. Proc Indian Acad Sci 92:265
  • Nakano Y, Asada K (1981) Hydrogen peroxide is scavenged by ascorbate specific peroxidase in spinach chloroplasts. Plant Cell Physiol 22:867–880
  • Olmos E, Hellin E (1996) Cellular adaptation from a salt tolerant cell line of Pisum sativum. J Plant Physiol 148:727–734
  • Poonia SR, Virmani SM, Bhumbla DR (1972) Effect of ESP (exchangeable sodium percentage) of soil on the yield, chemical composition and uptake of applied calcium by wheat. J Indian Soc Soil Sci 20:183–185
  • Rao MV, Paliyath G, Ormrod DP, Murr DP (1997) Watkins CB Influence of salicylic acid on H₂O₂ production, oxidative stress and H₂O₂ metabolizing enzymes. Plant Physiol 115:137–149
  • Rhodes D (1987) Metabolic responses to stress. In: Stumpf PK, Priess J (eds) The biochemistry of plants, vol 12. Academic Press, San Deigo, CA, pp 201–241
  • Sairam RK, Deshmukh PS, Shukla DS (1997) Tolerance to drought and temperature stress in relation to increased antioxidant enzyme activity in wheat. J Agron Crop Sci 178:171–177
  • Sairam RK, Veerabhadra Rao K, Srivastava GC (2002) Differential response of wheat genotypes to long term salinity stress in relation to oxidative stress, antioxidant activity and osmolyte concentration. Plant Sci 163:1037–1046
  • Sairam RK, Srivastava GC, Agarwal S, Meena RC (2005) Differences in antioxidant activity in response to salinity stress in tolerant and susceptible wheat genotypes. Biol Plant 49:85–91
  • Salin ML (1988) Toxic oxygen species and protective systems of the chloroplast. Physiol Plant 72:681–689
  • Serrano R, Gaxiola R (1994) Microbial models and salt stress tolerance in plants. Crit Rev Plant Sci 13:121–138
  • Smirnoff N, Cumbes QT (1989) Hydroxyl radicals scavenging activity of compatible isolates. Phytochemistry 28:1057–1060
  • Smith IK, Vierheller TL, Throne CA (1988) Assay of glutathione reductase in crude tissue homogeneous using 5,5'-dithiobis (2-nitrobenzoic acid). Anal Biochem 175:408–413
  • Srivastava TP, Gupta SC, Lal P, Muralia PN, Kumar A (1988) Effect of salt stress on physiological and biochemical parameters of wheat. Ann Arid Zone 27:197–204
  • Stewart GR, Lee JA (1974) The role of proline accumulation in halophytes. Planta 120:279–289
  • Storey R, Wyn-Jones RG (1975) Betaine and choline levels in plants and their relationship to NaCl stress. Plant Sci Lett 4:161–168
  • Tandon HLS (1995) Estimation of sodium and potassium. Methods of analysis of soils, plants, water and fertilizers. FDCO, New Delhi, pp 62–63
  • Wan L, Hu WY, Xie FD, Zou HD (1995) Effect of NaCl stress and exogenous free radicals on oxygen and membrane lipid peroxidation of isolated wheat leaves. Plant Physiol Commun 31:26–29
  • Weatherley PE (1950) Studies in water relations of cotton plants. I. The field measurement of water deficit in leaves. New Phytol 49:81–87
  • Wyn-Jones RG, Storey R (1981) Betains. In: Paleg LG, Aspinall O (eds) Physiology and biochemistry of drought tolerance. Academic Press, Sydney, pp 171–204
  • Yemm EW, Willis AJ (1954) The estimation of carbohydrates in plant extracts by anthrone. Biochem J 57:508–514
  • Yeo RR, Flowers TJ (1983) Varietal differences in the toxicity of sodium ions in rice leaves. Physiol Plant 59:189–195
  • Ying HC, Chen YM, Huang CY, Chen YM (1995) Role of glutathione reductase and related enzymes in salt tolerant mechanism of soybean plants grown under salt stress conditions. Taiwania 40:21–34
  • Yu Z, Rengel Q (1999) Drought and salinity differentially influence activities of superoxide dismutase in narrow leafed lupines. Plant Sci 141:1–11

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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