Abstract
The objective of this study was to determine the development of the antioxidant enzymes induced by drought stress in white clover (Trifolium repens L.) leaves. Water stress was imposed during 28 d by decreasing the daily irrigation. Leaf water potential (Φw) gradually decreased from −0.46 to −2.33 MPa. For the first 7 d, dry mass (DM), H2O2 and lipid peroxidation were not significantly affected by water deficit. From 14 d of treatment, water stress decreased dry mass and increased content of reactive oxygen species (O2 ·− and H2O2) and oxidative stress (malondialdehyde content). The ascorbate peroxidase (APOD) was activated most rapidly, already during the first week of water stress, but then its activity slowly decreased. Activation of superoxide dismutase (SOD) and catalase (CAT) by water deficit continued during the 14 d (Φw ≥ −1.65 MPa) and then their activities remain on the similar level. The activity of guaiacol-peroxidase (GPOD) increased mostly under progressive water stress and was correlated with increase in lipid peroxidation and growth restriction.
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Abbreviations
- APOD:
-
ascorbate peroxidase
- CAT:
-
catalase
- DM:
-
dry mass
- GPOD:
-
guaiacol peroxidase
- MDA:
-
malondialdehyde
- NBT:
-
nitroblue tetrazolium
- ROS:
-
reactive oxygen species
- RWC:
-
relative water content
- SOD:
-
superoxide dismutase
- TEMED:
-
N,N,Ń,Ń-tetramethylethylenediamine
- TBA:
-
thiobarbituric acid
- TCA:
-
trichloroacetic acid
- ε:
-
coefficient of absorbance
- Φw :
-
leaf water potential
References
Asada, K.: Ascorbate peroxidase — a hydrogen peroxide scavenging enzyme in plant. — Physiol. Plant. 85:235–241, 1992.
Beauchamp, C., Fridovich, I.: Superoxide dismutase: improved assays and assay applicable to acrylamide gels. — Anal. Biochem. 44:276–287, 1971.
Bradford, M.M.: A rapid sensitive method for the quantification of microgram quantities of protein utilizing the principle of proteins-dye binding. — Anal. Biochem. 72:248–254, 1976.
Cakmak, I., Horst, J.H.: Effects of aluminum on lipid peroxidation, superoxide dismutase, catalase, and peroxidase activities in root tips of soybean (Glycine max). — Physiol. Plant. 83:463–468, 1991.
Caruso, C., Chilosi, G., Caporale, C., Leonardi, L., Bertini, L., Magro, P., Buonocore, V.: Induction of pathogenesis-related proteins in germinating wheat seeds infected with Fusarium culmorum. — Plant. Sci. 140:107–120, 1999.
Cavalcanti, F.R., Oliveira, J.T.A., Martins-Miranda, A.S., Viégas, R.A., Silvira, J.A.G.: Superoxide dismutase, catalase and peroxidase activities do not confer protection against oxidative damage in salt-stressed cowpea leaves. — New Phytol. 163:563–571, 2004.
Chazen, O, Neumann, P.M.: Hydraulic signals from roots and rapid cell-wall hardening in growing maize (Zea mays L.) leaves are primary responses to polyethylene glycol-induced water deficits. — Plant Physiol. 104:1385–1392, 1994.
Chen, G., Asada, K.: Ascorbate peroxidase in tea leaves: Occurrence of two isozymes and the differences in their enzymatic and molecular properties. — Plant Cell Physiol. 30:987–998, 1989.
Chen, Y.A., Shin, J.W., Liu, Z.H.: Effect of light on peroxidase and lignin synthesis in mungbean hypocotyls. — Plant Physiol. Biochem. 40:33–39, 2002.
Costa França, M.G., Thi, A.T.P., Pimntel, C., Pereyra Rossiello, R.O., Zuily-Fodil, Y., Laffray, D.: Differences in growth and water relations among Phaseolus vulgaris cultivars in response to induced drought stress. — Environ. exp. Bot. 43:227–237, 2000.
Foyer, C.H., Lopez-Delgado, H., Dat, J.F., Scott, I.M.: Hydrogen peroxide- and glutathione-associated mechanisms of acclamatory stress tolerance and signaling. — Physiol. Plant. 100:241–254, 1997.
Foyer, C.H., Noctor, G.: Oxygen processing in photosynthesis: regulation and signaling. — New Phytol. 146:359–388, 2000.
Foyer, C.H., Noctor, G.: Redox sensing and signaling associated with reactive oxygen in chloroplasts, peroxisomes and mitochondria. — Physiol. Plant. 119:355–364, 2003.
Foyer, C.H., Valadier, M.H., Andre, M., Becker, T.W.: Drought-induced effects on nitrate reductase activity and mRNA and on the coordination of nitrogen and carbon metabolism in maize leaves. — Plant Physiol. 117:283–292, 1998.
Giannopolities, C.H., Ries, S.K.: Superoxide dismutase. I. Occurrence in higher plant. — Plant Physiol. 59:309–314, 1977.
Jiang, Y., Huang, B.: Drought and heat stress injury to two cool-season turfgrasses in relation to antioxidant metabolism and lipid peroxidation. — Crop Sci. 41:436–442, 2001.
Jung, S.: Variation in antioxidant metabolism of young and mature leaves of Arabidopsis thaliana subjected to drought. — Plant Sci. 166:459–466, 2004.
Kim, T.H., Lee, B.R., Jung, W.J., Kim, K.Y., Avice, J.C., Ourry, A.: De novo protein synthesis in relation to ammonia and proline accumulation in water stressed white clover. — Funct. Plant Biol. 31:847–855, 2004.
Lee, T.M., Lin, Y.H.: Changes in soluble and cell wall-bound peroxidase activities with growth in anoxia-treated rice (Oryza sativa L.) coleoptiles and roots. — Plant Sci. 106:1–7, 1995.
Lin, C.C., Kao, C.H.: Cell wall peroxidase activity, hydrogen peroxidase level and NaCl-inhibited root growth of rice seedling. — Plant Soil 230:135–143, 2001.
Lin, C.L., Kao, C.H.: Osmotic stress-induced changes in cell wall peroxidase activity and hydrogen peroxide level in roots of rice seedlings. — Plant Growth Regul, 37:177–184, 2002.
Mishra, N.P., Mishra, R.K., Singhal, G.S.: Changes in the activities of antioxidant enzymes during exposure of intact wheat leaves of strong visible light at different temperature in the presence of protein synthesis inhibitors. — Plant Physiol. 102:903–910, 1993.
Peltzer, D., Dreyer, E., Polle, A.: Differential temperature dependencies of antioxidative enzymes in two contrasting species: Fagus sylvatica and Coleus blumei. — Plant Physiol. Biochem. 40:141–150, 2002.
Rao, M.V., Paliyath, G., Ormrod, D.P.: Ultraviolet-B- and ozone-induced biochemical changes in antioxidant enzymes of Arabidopsis thaliana. — Plant Physiol. 110:125–136, 1996.
Selote, D.S., Bharti, S., Khanna-Chopra, R.: Drought acclimation reduces O2 ·− accumulation and lipid peroxidation in wheat seedlings. — Biochem. biophys. Res. Commun. 314:724–729, 2004.
Silva, H.A.S., Romeiro, R.S., Macagnan, D., Halfeld-Vieira, B.A., Pereira, M.C.B., Mounteer, A.: Rhizobacterial induction of systemic resistance in tomato plants: nonspecific protection a decrease in enzyme activities. — Biol. Control 29:288–295, 2004.
Sivritepe, N., Erturk, U., Yerlikaya, C., Turkan, I., Bor, M., Ozdemir, F.: Response of cherry rootstock to water stress induced in vitro. — Biol. Plant. 52:573–576, 2008.
Smirnoff, N.: The role of active oxygen in the response of plants to water deficit and desiccation. — New Phytol. 125:27–58, 1993.
Vaidyanathan, H., Sivakumar, P., Chakrabarty, R., Thomas, G.: 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, 2003.
Wang, A.G., Luo, G.H.: Quantitative relation between the reaction of hydroxylamine and superoxide anion radicals in plants. — Plant Physiol. Commun. 6:55–57, 1990.
Woodbury, W., Spencer, A.K., Stahmann, M.A.: Improved procedure using ferricyanide for detecting catalase isozymes. — Anal. Biochem. 44:301–305, 1971.
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Acknowledgements: This work was supported by the Technology Development Program for Agriculture and Forestry, Ministry of Agriculture and Forestry, Republic of Korea, through the Environmental-Friendly Agriculture Research Center at Chonnam National University.
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Lee, B.R., Li, L.S., Jung, W.J. et al. Water deficit-induced oxidative stress and the activation of antioxidant enzymes in white clover leaves. Biol Plant 53, 505–510 (2009). https://doi.org/10.1007/s10535-009-0091-2
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DOI: https://doi.org/10.1007/s10535-009-0091-2