Document Type : Original Article

Authors

1 PhD student in Crop Ecology, Shahrood University

2 Faculty member of Shahrood University

Abstract

Introduction
Water shortage is one of the most important abiotic stresses which impose deleterious effect of growth and yield of crops including mung bean. Part of this effect comes from over production of reactive oxygen species (ROS) including OH·, O2·-, and H2O2. Crops try to scavenge these ROS using antioxidant enzymes like superoxide dismutase, guaiacol proxidase and catalase. This experiment was aimed to study the sensitivity of some traits of Mung Bean to water shortage and to see whether the activity of catalase, superoxide dismutase and guaiacol proxidase antioxidant enzymes is the same under different water shortage intensities or not.
 
Materials and methods
An experiment was conducted using pots with 5 kg capacity in which 5 seeds of mung bean were planted. The pots were put in an open filed to increase the possibility of generalizing the results to field results. At 4-leaf stage, 2 seedlings were removed, and left 3 ones. Treatment levels were control, weak water shortage [irrigation at 65% field capacity (FC)], moderate water shortage (irrigation at 50% FC), and severe water shortage (irrigation at 35% FC) which arranged as on completely randomized block design with 3 replications. At maturity stage, some attributes including biological yield, plant height, number of seed per pod, number of pod per plant, grain yield, and length of pod were measured. The sensitivity index of these attributes to water shortage was calculated using appropriate functions to test whether these attributed differ in terms of value of response to drought or not. For measuring the activity of 3 antioxidant enzymes, the plant samples were taken at flowering stage. Then the activity of catalase, superoxide dismutase, and guaiacol proxidase enzymes were measured as it has been presented in report of Havir and McHale (1987), Van Rossun et al. (1997), and Cavalcanti et al. (2004), respectively.
 
Results and discussion
Results indicated that all measured attributes were significantly affected by water shortage. It was found a low-sloped decreasing trend with increasing water shortage intensity in pod length. The value of plant height for plants experienced weak water shortage was statistically similar to those grown in no water shortage conditions (control). But it decreased sharply for plants treated with medium and severe water shortages. The sensitivity threshold of number of seed per pod was relatively high; because over the field capacities equal to 50% and greater than that, its quantity was similar to control. The sensitivity index of this attribute and number of pod per plant was 0.050182 and 0.038788, respectively. Considering the standard errors of these indices, the difference between number of seed per pod and number of pod per plant for quantitative response to water shortage is statistically negligible. The quantity of both biological yield (straw + grain) and grain yield appeared to be not changed in weak water shortage as compared to no water shortage conditions. Then after, they were negatively affected. Under severe water shortage condition, the percent of decrease in grain yield was higher than in biological yield. The sensitivity index of them was 0.120727 and 0.031512, respectively. The grain weight accumulation is dependent on current photosynthesis and non-structural carbohydrates stored in vegetative organs like stem before flowering. The activity of hydrolytic enzymes including alpha amylase is crucial. The higher decrease in grain yield than in biological yield may imply that the activity of these enzymes has also been negatively affected. Under weak and medium water shortage conditions it was found no change in activity of catalase as compared to control. But under severe water shortage condition, its activity was considerably (3 times) increased. The activity of superoxide dismutase was constant over control and weak water shortage situations; but it doubled under medium water shortage conditions. The guaiacol peroxidase activity did not respond to weak water shortage; subsequently, it showed an upward trend.
 
Conclusion
Grain yield and plant height were the most sensitive traits. Number of seed per pod, number of pod per plant and biological yield with statistically similar values of sensitivity were in 2nd order. The length of pod was the most tolerant trait as it tended to have the lowest sensitivity index. The increase in activity of superoxide dismutase was being witnessed in moderate water shortage. For catalase, it was true only for severe water shortage. The activity of guaiacol porxidase was statistically the same under control and weak water shortage conditions. But its activity increased proportionally with increasing water shortage intensity.

Keywords

Acar, O., Turkan, I., Zdemir, F.O., 2001. Superoxide dismutase and peroxidase activities in drought sensitive and resistant barley (Hordeum vulgare L.) varieties. Acta Physiologiae Plantarum. 3, 351–356.
Arora, A., Sairam, R.K., Srivastava, G.C., 2002. Oxidative stress and antioxidative system in plants. Current Science. 82, 1227–38.
Bor, M., Ozdemir, F., Turkan, I., 2003. The effect of salt stress on lipid peroxidation and antioxidants in leaves of sugar beet Beta vulgaris L. and wild beet Beta maritime L. Plant Science. 164, 77–84.
Castillo, F.J., 1996. Antioxidant protection in the inducible CAM plant Sedum album L. following the imposition of severe water stress and recovery. Oecologia. 107, 469-477.
Cavalcanti, F.R., Oliveira, J.T.A., Martins-Miranda, A.S., Viégas, R.A., Silveira, J.A.G., 2004. Superoxide dismutase, catalase and peroxidase activities do not confer protection against oxidative damage in salt-stressed cowpea leaves. New Phytologist. 163, 563– 571.
Cia, M.C., Guimaraes, A.C.R., Medici, L.O., Chabregas, S.M., Azevedo, R.A., 2012. Antioxidant responses to water deficit by drought-tolerant and -sensitive sugarcane varieties. Annals of Applied Biology. 161, 313–324.
Ehdaie, B., Alloush, G.A., Madore, M.A, Waines, J.G., 2006. Genotypic variation for stem reserves and mobilization in wheat: I. post anthesis changes in internode dry matter. Crop Sciences. 46, 735-746.
Foster, J.G., Hess, J.L., 1982. Oxygen effects on maize leaf superoxide dismutase and glutathione reductase. Phytochemistry. 21, 1527-1532.
Foyer, C.H., Noctor, G., 2000. Oxygen processing in photosynthesis: regulation and signaling. New Phytologist. 146, 359–388.
Gaspar, T., Penel, C., Hagege, D., Greppin H., 1991. Peroxidase in plant growth, differentiation and developmental processes. In: Lobarzewski, J., Greppin, H., Pennel, C., Gaspar, T. (eds.),  Biochemical, Molecular and Physiological Aspects of Plant Peroxidases.Lublin, Poland and Geneva, Switzerland, pp. 249–280.
Gelman, A., Hill, J., 2007. Data Analysis Using Regression and Multilevel/Hierarchical Models (1stEdition). Cambridge University Press.
Ghamsari, L., Keyhani, E., Golkhoo, S., 2007. Kinetics properties of guaiacol peroxidase activity in Crocus sativusL.corm during rooting. Iranian Biomedical Journal. 11, 137-146. [In Persian with English Summary].
Gratao, P.L., Polle, A., Lea, P.J., Azevedo, R.A., 2005. Making the life of heavy metal-stressed plants a little easier. Functional Plant Biology. 32, 481–494.
Guo, Z., Ou, W., Lu, S., Zhong, Q., 2006. Differential responses of antioxidative system to chilling and drought in four rice cultivars differing in sensitivity. Plant Physiology and Biochemistry. 44, 828–836.
Halliwell, B., Gutteridge, J.M.C., 1989. Free Radicals in Biology and Medicine. Oxford, Clarendon Press.
Havir, E.A., McHale, N.A., 1987. Biochemical and developmental characterization of multiple forms of catalase in tobacco leaves. Plant Physiology. 84, 450–455.
Hirt, H., Shinozaki, K., 2004. Plant Responses to Abiotic Stress. Springer, Vienna, Austria.
Khanna-Chopra, R., Selote, D.S., 2007. Acclimationto drought stress generates oxidative stress tolerance in drought-resistant than -susceptible wheat cultivar under field conditions. Environmental and Experimental Botany. 60, 276–283.
Klute, A., 1986. Water retention: laboratory methods. In: Black, C.A. (ed.), Methods of Soil Analysis. I. Physical and Mineralogical Methods. Madison, ASA, SSSA, pp. 635-662.
Manivannan, P., Abdul-Jaleel, C., Kishorekumar, A., Sankar, B., Somasundaram, R., Sridharan, R.,  Panneerselvam, R., 2007. Changes in antioxidant metabolism of Vigna unguiculata L. Walp. by propiconazole under water deficit stress. Colloids and Surfaces Biointerfaces. 57, 69–74.
Mittal, R., Dubey, R.S., 1991. Behaviour of peroxidases in rice: changes in enzyme activity and isoforms in relation to salt tolerance. Plant Physiology and Biochemistry. 29, 31– 40.
Mittova, V., Volokita, M., Guy, M., Tal, M., 2000. Activities of SOD and the ascorbate-glutathione cycle enzymes in subcellular compartments in leaves and roots of the cultivated tomato and its wild salt-tolerant relative Lycopersicon pennellii. Physiologia Plantarum. 110, 42–51.
Noctor, G., Veljovic-Jovanovic, S.D., Driscoll, S., Novitskaya, L., Foyer, C.H., 2002. Drought and oxidative load in wheat leaves. A predominant role for photorespiration? Annals of Botany. 89, 841–850.
Peltzer, D., Dreyer, E., Polle, A., 2002. Temperature dependencies of antioxidative enzymes in two contrasting species. Plant Physiology and Biochemistry. 40, 141–50.
Schulz, A.R., 1994. Enzyme Kinetics. Cambridge University Press, Cambridge.
Sreenivasulu, N., Grima, B., Wobus, U., Weschke, W., 2000. Differential response of antioxidant compounds to salinity stress in salt-tolerant and salt-sensitive seedlings of foxtail millet (Setaria italica). Physiologia Plantarum. 109, 435–442.
Tayefi-Nasrabadi, H., Dehghan, G., Daeihassani, B., Movafegi, A., Samadi, A., 2011. Some biochemical properties of guaiacol peroxidases as modified by salt stress in leaves of salt-tolerant and salt-sensitive safflower (Carthamus tinctorius L.) cultivars. African Journal of Biotechnology. 10, 751-763.
Villalobos, M.A., Bartels, D., Iturringa, G., 2004. Stress tolerance and glucose insensitive phenotypes in Arabidopsis over expressing the CpMYB10 transcription factor gene. Plant Physiology. 135, 309-324.
Van Rossun, M.W.P.C., Alberda, M., Van Der Plas, L.H.W., 1997. Role of oxidative damage in tulip bulb scale micropropagation. Plant Science. 130, 207–216.
Xu, P.L., Guo, Y.K., Bai, J.G., Shang, L., Wang, X.J., 2008. Effects of long-term chilling on ultrastructure and antioxidant activity in leaves of two cucumber cultivars under low light. Physiologia Plantarum. 132, 467–478.
Zhang, J., Kirkham, M.B., 1994. Drought-stress-induced changes in activities of superoxide dismutase, catalase, and peroxidase in wheat species. Plant Cell Physiology. 35, 785-791.