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Nine-day-old seedlings of two wheat cultivars (Misr1 and Sakha93) were treated with NaCl at 75, 150 and 225 mM for 15 days with or without the presence of 10 mM CaCl₂. All concentrations of NaCl led to significant decreases in fresh and dry weights of only Sakha93; however, Misr1 seemed to be affected only at the highest concentration. Nonetheless, growth parameters of both cultivars under normal conditions were most likely similar. On the other hand, lipid peroxides (as MDA) and H₂O₂ were greatly accumulated particularly in Sakha93; significant increases were detected in Misr1 treated only at 225 mM. Also, all concentrations of NaCl decreased GSH content in Sakha93; nevertheless, there were no great differences among both cultivars under normal conditions. On the other hand, the activities of the enzymatic antioxidants, GR, GST, CAT and POD were unaffected in Misr1 by all concentrations but inhibited in Sakha93. AOX responded differently to NaCl, there were decreases in Misr1 by 75 and 225 mM and in Sakha93 by 75 and 150 mM. However, the application of CaCl₂ alleviated the impacts of NaCl; there was a retraction in growth reduction in Misr1 to reach most likely those of the control. In addition, the accumulated MDA and H₂O₂ were greatly counterbalanced. On the contrary, the decreased GSH contents seemed unrecovered in Sakha93 in spite of the alleviations in magnitudes. Moreover, there were recoveries in the activities of GR and POD in Sakha93; nevertheless, GST and CAT activities remained significantly inhibited. These findings suggest that Misr1 is a more tolerant cultivar to NaCl than Sakha93. Moreover, the results reveal that ROS scavenging is efficient and became more inducible in the less susceptible than in the more susceptible cultivar. The response of AOX appeared to coincide with antioxidants so that the damage which was inflicted by NaCl can be ameliorated by overexpression of antioxidants especially with the presence of CaCl₂.
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p.2103-2112,fig.,ref.
Twórcy
autor
- Botany Department, Faculty Science, Damietta University, 34517 Damietta, Egypt
autor
- Botany Department, Faculty Science, Damietta University, 34517 Damietta, Egypt
autor
- Botany Department, Faculty Science, Damietta University, 34517 Damietta, Egypt
autor
- Botany Department, Faculty Science, Damietta University, 34517 Damietta, Egypt
autor
- Botany Department, Faculty Science, Damietta University, 34517 Damietta, Egypt
Bibliografia
- Abo-Kassem EEM (2007) Effects of salinity: calcium interaction on growth and nucleic acid metabolism in five species of Chenopodiaceae. Turk J Bot 31:125–134
- Aebi H (1984) Catalase in vitro. Method Enzymol 105:121–126
- Amirsadeghi S, Robson CA, Vanlerberghe GC (2007) The role of the mitochondrion in plant responses to biotic stress. Physiol Plant 129:253–266
- Anderson JV, Davis DG (2004) Abiotic stress alters transcript profiles and activity of glutathione S-transferase, glutathione peroxidase, and glutathione reductase in Euphorbia esula. Physiol Plant 120:421–433
- Anderson MP, Gronwalds JW (1991) Atrazine resistance in velvetleaf (Abutilon theophrasti) biotype due to enhanced glutathione S-transferase activity. Plant Physiol 96:107–109
- Aravind P, Prasad MN (2005) Modulation of cadmium-induced oxidative stress in Ceratophyllum demersum by zinc involves ascorbate–glutathione cycle and glutathione metabolism. Plant Physiol Biochem 43:107–116
- Barakat NA (2011) Ameliorative effects of Ca²⁺ on the growth, metabolism, cationic status and cell wall degrading enzymes of induced salinity stress Vicia faba L. J Stress Physiol Biochem 7:369–386
- 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 72:154–248
- Buege JA, Aust SD (1972) Microsomal lipid peroxidation. Method Enzymol. 52:302–310
- Cachorro P, Ortiz A, Cerda A (1993) Effects of saline stress and calcium on lipid composition in bean roots. Phytochemistry 32:1131–1136
- Chance B, Maehly AC (1955) Assay of catalase and peroxidases. Method Enzymol 2:764–775
- Clifton R, Millar AH, Whelan J (2006) Alternative oxidases in Arabidopsis: a comparative analysis of differential expression in the gene family provides new insights into function of nonphosphorylating bypasses. Biochim Biophys Acta 1757:730–741
- Cramer G, Lauchli RA, Polito VS (1985) Displacement of Ca²⁺ by Na⁺ form the plasmalemma of root cells. A primary response to salt stress? Plant Physiol 79:207–211
- Dixon DP, Edwards R, Robinson NJ, Fordham-Skelton AP, Cole DJ (1995) Spectrum of herbicide reactive glutathione transferases in maize. Brighton Crop Prot. conference, Weeds, UK, pp 255–260
- Escobar MA, Geisler DA, Rasmusson AG (2006) Reorganization of the alternative pathways of the Arabidopsis respiratory chain by nitrogen supply: opposing effects of ammonium and nitrate. Plant J 45:775–788
- Fiorani F, Umbach AL, Siedow JN (2005) The alternative oxidase of plant mitochondria is involved in the acclimation of shoot growth at low temperature. A study of Arabidopsis AOX1a transgenic plants. Plant Physiol 139:1795–1805
- Fu A, Liu H, Yu F, Kambakam S, Luan S, Rodermel S (2012) Alternative oxidases (AOX1a and AOX2) can functionally substitute for plastid terminal oxidase in Arabidopsis chloroplasts. Plant Cell 24:159–1579
- Gobinathan P, Sankar B, Murali PV, Panneerselvam R (2009) Interactive effects of calcium chloride on salinity-induced oxidative stress in Pennisetum typoidies. Bot Res Int 2:143–148
- Hassan NM, Nemat Alla MM (2005) Oxidative stress in herbicide-treated broad bean and maize plants. Acta Physiol Plant 27:429–438
- Hassan NM, Serag MS, El-Feky FM, Nemat Alla MM (2008) In vitro selection of mung bean and tomato for improving tolerance to NaCl. Ann Appl Biol 152:319–330
- Juszczuk IM, Rychter AM (2003) Alternative oxidase in higher plants. Acta Biochim Pol 50:1257–1271
- Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7:405–410
- Moradi F, Ismail AM (2007) Responses of photosynthesis, chlorophyll fluorescence and ROS-scavenging systems to salt stress during seedling and reproductive stages in rice. Ann Bot 99:1161–1173
- Murgia I, Tarantino D, Vannini C, Bracale M, Carravieri S, Soave C (2004) Arabidopsis thaliana plants overexpressing thylakoidal ascorbate peroxidase show increased resistance to paraquat-induced photooxidative stress and to nitric oxide-induced cell death. Plant J 38:940–953
- Nemat Alla MM (1995) Glutathione regulation of glutathione S-transferase and peroxidase activity in herbicide-treated Zea mays. Plant Physiol Biochem 33:185–192
- Nemat Alla MM, Hassan NM (1998) Efficacy of exogenous GA3 and herbicide safeners in protection of Zea mays from metolachlor toxicity. Plant Physiol Biochem 36:809–815
- Nemat Alla MM, Hassan NM (2006) Changes of antioxidants levels in two maize lines following atrazine treatments. Plant Physiol Biochem 44:202–210
- Nemat Alla MM, Hassan NM (2007) Changes of antioxidants and GSH-associated enzymes in isoproturon-treated maize. Acta Physiol Plant 29:247–258
- Nemat Alla MM, Hassan NM (2012) A possible role for C4 photosynthetic enzymes in tolerance of Zea mays to NaCl. Protoplasma 249:1109–1117
- Nemat Alla MM, Hassan NM, El-Bastawisy ZM (2008a) Changes in antioxidants and kinetics of glutathione-S-transferase of maize in response to isoproturon treatment. Plant Biosyst 142:5–16
- Nemat Alla MM, Badawi AM, Hassan NM, El-Bastawisy ZM, Badran EG (2008b) Herbicide tolerance in maize is related increased levels of glutathione and glutathione-associated enzymes. Acta Physiol Plant 30:371–379
- Nemat Alla MM, Khedr AA, Serag MM, Abu-Alnaga AZ, Nada RM (2012) Regulation of metabolomics in Atriplex halimus growth under salt and drought stress. Plant Growth Regul 67:281–304
- Okuda T, Masuda Y, Yamanaka A, Sagisaka S (1991) Abrupt increase in the level of hydrogen peroxide in leaves of winter wheat is caused by cold treatment. Plant Physiol 97:1265–1267
- Parida A, Das AB (2005) Salt tolerance and salinity effects on plants. Ecotox Environ Saf 60:324–349
- Pietrobon DF, Virgilio O, Pozzea T (1990) Structural and functional aspects of calcium homeostasis in eukaryotic cells. Eur J Biochem 193:559–622
- Sanders D, Brownlee C, Harper JF (1999) Communicating with calcium. Plant Cell 11:691–706
- Shu MY, Fan MQ (2000) Effect of osmotic stress and calcium on membrane-lipid peroxidation and the activity of defense enzymes in fir seedling. For Res 4:391–396
- Sieger SM, Kristensen BK, Robson CA, Amirsadeghi S, Eng EW, Abdel-Mesih A, Moller IM, Vanlerberghe GC (2005) The role of alternative oxidase in modulating carbon use efficiency and growth during macronutrient stress in tobacco cells. J Exp Bot 56:1499–1515
- Smith IK, Vierheller TL, Thorne CA (1988) Assay of glutathione reductase in crude tissue homogenates using 5,5-dithiobis-(2-nitrobenzoic acid). Anal Biochem 175:408–413
- Tuteja N (2007) Mechanisms of high salinity tolerance in plants. Method Enzymol 428:419–438
- Vanlerberghe GC, McIntosh L (1996) Signals regulating the expression of the nuclear gene encoding alternative oxidase of plant mitochondria. Plant Physiol 111:589–595
- Wagner AM, Wagner MJ (1995) Changes in mitochondrial respiratory chain components of petunia cells during culture in the presence of antimycin A. Plant Physiol 115:617–622
- Yang GP, Gao AL, Jiang JH (1993) The relation of calcium to cell permeability in water stressed soybean hypocotyls. Plant Physiol Commun 29:179–181
- Yang F, Liang ZW, Wang ZC, Chen Y (2008) Relationship between diurnal changes of net photosynthetic rate and influencing factors in rice under saline sodic stress. Rice Sci 15:119–124
- Yasar F, Ellialtioglu S, Yildiz K (2008) Effect of salt stress on antioxidant defense systems, lipid peroxidation, and chlorophyll content in green bean. Russ J Plant Physiol 55:782–786
- Yip JY, Vanlerberghe GC (2001) Mitochondrial alternative oxidase acts to dampen the generation of active oxygen species during a period of rapid respiration induced to support a high rate of nutrient uptake. Physiol Plant 112:327–333
- Zhu JK (2003) Regulation of ion homeostasis under salt stress. Curr Opin Plant Biol 6:441–445
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Bibliografia
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