Ameliorative effect by calcium on NaCl salinity stress related to reactive oxygen species metabolism in Amaranthus tricolor L
Abstract
Soil salinity affects plant growth and development by way of osmotic imbalance which induces oxidative damage in plant tissues. Oxidative stress is caused by increased production of Active Oxygen Species (AOS), such as O2−, •OH, H2O2 and 1O2 these lead to lipid peroxidation, enzyme inactivation and oxidative damage to DNA. Plants have antioxidant defense systems to protect against the production and action of the AOSs. Plants with high level of antioxidants, either constitutive or induced, have been reported to produce greater resistance to this oxidative damage in plant cells. AOS synthesis and its scavenging were investigated in the control, different concentrations of NaCl and NaCl + CaCl2 stressed Amaranthus tricolor L. and Phaseolus vulgaris L.. AOS such as superoxide anion and H2O2 content showed a steady increase in the plants of all NaCl treated media compared to control. When the salinized media were supplemented with CaCl2 the AOS level drastically decreased compared to the corresponding plants grown on salt alone. Similarly, the activity of antioxidant enzymes such as superoxide dismutase, ascorbate peroxidase, catalase and glutathione reductase under salt stress were higher in NaCl + CaCl2 supplemented media than the plants on the salinized media alone. This suggested that the alleviation effect of calcium under saline condition was through modulation of the enzyme complexes that accelerate the rate of antioxidant enzymes biosynthesis under salt stress. Similarly, the level of lipid peroxidation was found to be lower in plants of all NaCl + CaCl2 media than control
References
Bowler C Fluhr R. 2000. The role of calcium and activated oxygens as signals for controlling crosstolerance. Trends Plant Sci., 5:241-246.
Chappelle EW, Kim MS and McMurtrey JE. 1992. Ratio analysis of reflectance spectra (RARS): an algorithm for the remote estimation of the concentrations of chlorophyll a, chlorophyll b and carotenoids in soybean leaves. Remote Sens. Environ., 39:239-247.
Demidchik V, Bowen HC, Maathuis FJM, Shabala SN, Tester MA, Davies JM. 2002a. Arabidopsis thaliana root non-selective cation channels mediate calcium uptake and are involved in growth. Plant J 32:799-808.
Elphick CH, Sanders D, Maathuis FJM. 2001. Critical role of divalent cations and Na+ efflux in Arabidopsis thaliana salt tolerance. Plant Cell Environ., 24:733-740.
Gallati H and Pracht I. 1985. Horseradish peroxidase: kinetic studies and optimization of peroxidase activity determination using the substrates H2O2 and 3,3',5,5'-tetramethylbenzidine. J. Clin. Chem. Clin. Biochem., 23:453-460.
Girija C, Smith BN, and Swamy PM. 2002. Interactive effects of sodium chloride and calcium chloride on the accumulation of proline and glycinebetaine in peanut (Arachis hypogaea L.). Environ. Exp. Bot., 47:1-10.
Halfter U, Ishitani M, Zhu JK. 2000. The Arabidopsis SOS2 protein kinase physically interacts with and is activated by the calciumbinding protein SOS3. Proc Natl Acad Sci USA. 97:3735-3740.
Heath RL, Packer L. 1968. Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189-98.
Ishitani M, Liu JP, Halfter U, Kim CS, Shi WM, Zhu JK. 2000. SOS3 function in plant salt tolerance requires N-myristoylation and calcium binding. Plant Cell 12:1667-1677.
Jaleel CA, Ashok kishorekumar, Paramasivam Manivannan, Beemarao Sankar, Muthiah Gomathinayagam, Rajaram Panneerselvam. 2008. Salt stress mitigation by calcium chloride in Phyllanthus amarus Acta Bot. Croat., 67(1):53-62.
Jaleel CA, Gopi R, Manivannan P, Panneerselvam R. 2007b. Antioxidative potentials as a protective mechanism in Catharanthus roseus (L.) G. Don. plants under salinity stress. Tur. J. Bot., 31:245-251.
Jiang M, Zhang J. 2002. A. Involvement of plasma membrane NADPH oxidase in abscisic acid - and water stress-induced antioxidant defense in leaves of maize seedlings. Planta 215:1022-1030.
Michaela Schmitz-Eiberger, Roland Haefs, Georg Noga. 2002. Calcium deficiency – Influence on the antioxidative defense system in tomato plants J. Plant Physiol., 159:733-742.
Pei ZM, Murata Y, Benning G., Thomine S, Klusener B, Allen G J, Grill E, Schroeder JI. 2000. Calcium channels activated by hydrogen peroxide mediate abscisic acid signalling in guard cells. Nature 406:731-734.
Price AH, Taylor A, Ripley SJ, Griffiths A, Trewavas AJ and Knight MR. 1994. Oxidative signals in tobacco increase cytosolic calcium. Plant Cell 6:1301-1310.
Rengel Z. 1992. The role of calcium in salt toxicity. Plant Cell Environ., 15:625-632.
Romano LA, Miedema H, Assmann SM. 1998. Ca2+ -permeable, outwardly-rectifying K+ channels in mesophyll cells of Arabidopsis thaliana. Plant Cell Physiol., 39:1133-1144.
Shabala S, Demidchik V, Shabala L, Cuin TA, Smith SJ, Miller AJ, Davies JM, Newman IA. 2006. Extracellular Ca2+ Ameliorates NaClInduced K1 Loss from Arabidopsis Root and Leaf Cells by Controlling Plasma Membrane K+Permeable Channels Plant Physiology, August 141:1653-1665.
Shabala S, Newman I. 2000. Salinity effects on the activity of plasma membrane H+ and Ca2+ transporters in bean leaf mesophyll: masking role of the cell wall. Ann Bot (Lond) 85:681-686.
Shabala SN, Newman IA, Morris J. 1997. Oscillations in H+ and Ca2+ ion fluxes around the elongation region of corn roots and effects of external pH. Plant Physiol., 113:111-118.
Sko´rzyn ska-Polit E, Tukendorf A, Selstam E, Baszyn ski T. 1998. Calcium modifies Cd effect on runner bean plants Environmental and Experimental Botany 40:275-286.
Suntres ZE. 2002. Role of antioxidants in paraquat toxicity. Toxicology 180:65-77.
Vaidyanathan H, Sivakumar P, Chakrabarty R and Thomas G. 2003. Scavenging of reactive oxygen species in NaCl-stressed rice (Oryza sativa L.)-differential response in salt-tolerant and sensitive varieties. Plant Sci. 165:1411-1418.
White PJ, Broadley MR. 2003. Calcium in plants. Ann Bot (Lond) 92:487-511.
Yanagida M, Matsumoto H and Usui K. 1999. Responses of antioxidative systems to oxyfluorfen and their role in herbicidal tolerance of plants. J.Weed Sci. Tech., 44:67-76.