Upregulation of Chloroplast Antioxidant System to Alleviate Salt Dependent Oxidative System in Rice Varieties

Автор: Lins S., Yusuf A.

Журнал: Журнал стресс-физиологии и биохимии @jspb

Статья в выпуске: 3 т.16, 2020 года.

Бесплатный доступ

The chloroplast antioxidant system in pokkali (vytilla-2), kaipad (ezhome-1) and upland (koduvelliyan) rice varieties showed upregulation of enzymatic and non- enzymatic antioxidants under salt stress. The levels of hydrogen peroxide (H2O2), malondialdehyde (MDA) with respect to the lipid peroxidation of thylakoid membrane, non-enzymatic antioxidants like ascorbate (AsA), glutathione (GSH) content, enzymatic antioxidants- superoxide dismutase (SOD) and ascorbate-glutathione cycle enzymes viz, ascorbate peroxidase (APX), glutathione reductase (GR), monodehydroascorbate reductase (MDHAR) and dehydroascorbate reductase (DHAR) were quantified using the isolated chloroplast fraction on the 7,14 and 21 days of NaCl treatment. Chlorophyll in the NaCl treated plants decreased concomitantly with an increase in NaCl concentration. The H2O2 content and lipid peroxidation, proportionate to MDA content and the enzymatic antioxidants of the chloroplast fraction upregulated during NaCl treatment. The specific activity of the chloroplast antioxidant and ascorbate-glutathione cycle enzymes (SOD, APX, GR, MDHAR and DHAR) showed salt dependant upregulation consistently with NaCl application. Salinity induced oxidative stress alleviation by the antioxidant system in the chloroplasts of these varieties indicate the effective cooperation between antioxidant and ascorbate-glutathione cycle enzymes and holds a vital role in combating the ROS generation, thus protecting the chloroplast in the aerobic environment.

Еще

Antioxidant enzymes, Ascorbate-glutathione cycle, Chloroplast, Salt tolerant rice

Короткий адрес: https://sciup.org/143173842

IDR: 143173842

Список литературы Upregulation of Chloroplast Antioxidant System to Alleviate Salt Dependent Oxidative System in Rice Varieties

  • Abdeljawad, S. M., Zaqoot, H. A., Aish, A. M. (2016) Evaluation of Small and Large Scale Reverse Osmosis Desalination Plants Performance in the Gaza Strip During 2013. Nature Environment and Pollution Technology, 15(2), 693.
  • Akram, M., Malik, M.A., Ashraf, M.Y., Saleem, M. F. and Hussain, M. (2007) Competitive seedling growth and K+/Na+ ratio in different maize (Zea mays l.) Hybrids under salinity stress. Pak. J. Bot. 39(7), 2553-2563.
  • Anjum, S.A., Xie, X.Y., Wang, L.C., Saleem, M.F., Man, C., Lei, W. (2011) Morphological, physiological and biochemical responses of plants to drought stress. African Journal of Agricultural Research, 6(9), 2026-2032.
  • Arnon, D.I. (1949) Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant physiology, 24(1), 1.
  • Asada, K. (1999) The water-water cycle in chloroplasts: scavenging of active oxygens and dissipation of excess photons. Annual review of plant biology, 50(1), 601-639.
  • Baier M., Dietz K-J. (2005) Chloroplasts as source and target of cellular redox regulation: a discussion on chloroplast redox signals in the context of plant physiology. Journal of Experimental Botany, 56 (416), 1449–1462.
  • Bienert, G.P., Schjoerring J. K.,Jahn T.P. (2006) Membrane transport of hydrogen peroxide. Biochimica et Biophysica Acta (BBA) – Biomembranes, 1758(8), 994-1003.
  • Bose, J., Rodrigo-Moreno, A., Shabala, S. (2014) ROS homeostasis in halophytes in the context of salinity stress tolerance. J. Exp. Bot. 65, 1241–1257.
  • Candan, N., Tarhan, L. (2003) Changes in chlorophyllcarotenoid contents, antioxidant enzyme activities and lipid peroxidation levels in Zn-stressed Mentha pulegium. Turkish Journal of Chemistry, 27: 21-30.
  • Chao, Y.Y., Hong, C.Y., Kao, C.H. (2010) The decline in ascorbic acid content is as-sociated with cadmium toxicity of rice seedlings. Plant Physiol. Biochem, 48, 374–381.
  • Chawla, S., Naraghi, M., Davoudi, A. (2013) Effect of twist and porosity on the electrical conductivity of carbon nanofiber yarns. Nanotechnology, 24(25), 255708.
  • Chang, L., Sun, H., Yang, H., Wang, X., Su, Z., Chen, F., Wei, W. (2017) Over-expression of dehydroascorbate reductase enhances oxidative stress tolerance in tobacco. Electronic Journal of Biotechnology, 25, 1-8.
  • Chen, J. X., Wang, X. F. (2002) Guide to plant physiological experiments. Guange hou: South China University of Technology Press, pp.123-127.
  • Covello, P. S., Chang, A., Dumbroff, E. B., Thompson, J. E. (1989) Inhibition of photosystem II precedes thylakoid membrane lipid peroxidation in bisulfitetreated leaves of Phaseolus vulgaris. Plant physiology, 90(4), 1492-1497.
  • Cui, J., Jiang, N., Zhou, X., Hou, X., Yang, G., Meng, J., Luan, Y. (2018) Tomato MYB49 enhances resistance to Phytophthora infestation and tolerance to water deficit and salt stress. Planta, 248(6), 1487-1503.
  • Foyer, C. H., Noctor, G. (2003) Redox sensing and signalling associated with reactive oxygen in chloroplasts, peroxisomes and mitochondria. Physiologia plantarum, 119(3), 355-364.
  • Giannopolitis, C.N., Reis, S.K. (1977) Superoxide dismutases: II. Purification and quantitative relationship with water soluble protein in seedlings. Plant Physiol, 59: 315–318.
  • Gill, S.S., Tuteja, N. (2010) Reactive oxygen species and antioxi-dant machinery in abiotic stress tolerance in crop plants. Plant Physiology and Biochemistry, 48, 909–930.
  • Gomez J.M.. Hernandez J.A.,Jimenez A., del Rio L.,A., Sevilla F. (1999) Differential responses of antioxidant system of chloroplast and mitochondria to long- term NaCl stress on pea plants. Free Radicals Research, 31, 11-18.
  • Hanin, M., Ebel, C., Ngom, M., Laplaze, L., Masmoudi, K. (2016) New insights on plant salt tolerance mechanisms and their potential use for breeding. Frontiers in Plant Science, 7, 1787.
  • Hasegawa, P.M., Bressan, R.A., Zhu, J. K., Bohnert, H.J. (2000) Plant cellular and molecular responses to high salinity. Annual review of plant biology, 51(1), 463-499.
  • Hassan, M., Mansoor, S. (2014) Oxidative stress and antioxidant defense mechanism in mung bean seedlings after lead and cadmium treatments. Turkish Journal of Agriculture and Forestry, 38(1), 55-61.
  • Hervera, A., De Virgiliis, F., Palmisano, I., Zhou, L., Tantardini, E., Kong, G., Kapustin, A. N. (2018) Reactive oxygen species regulate axonal regeneration through the release of exosomal NADPH oxidase 2 complexes into injured axons. Nature cell biology, 20(3), 307.
  • Hoque, M.A., Banu, M.N., Nakamura, Y., Shimoishi, Y., Murata, Y. (2008) Proline and glycinebetaine enhance antioxidant and methylglyoxal detoxification systems and reduce NaCl-induced damage in cultured tobacco cells. Plant Physiol., 165: 813–882.
  • Hossain, Z., Mustafa, G., Komatsu, S. (2015) Plant responses to nanoparticle stress. Int. J. Mol. Sci., 16, 26644–26653.
  • Hossain, M.A., Nakano, Y., Asada, K. (1984) Monodehydroascorbate reductase in spinach chloroplasts and its participation in regeneration of ascorbate for scavenging hydrogen peroxide. Plant Cell Physiol., 25: 385-395.
  • Kohan-Baghkheirati, E., Bagherieh-Najjar, M., Abdolzadeh, A., Geisler-Lee, J. (2018) Altered DREB1A Gene Expression in Arabidopsis thaliana Leads to Change in Root Growth, Antioxidant Enzymes Activity, and Response to Salinity but Not to Cold. Journal of Genetic Resources, 4(2), 90-104.
  • Lee, Y. P., Kim, S.H., Bang, J.W., Lee, H.S., Kwak, S.S., Kwon, S.Y. (2007) Enhanced tolerance to oxidative stress in transgenic tobacco plants expressing three antioxidant enzymes in chloroplasts. Plant cell reports, 26(5), 591-598.
  • Lowry, Ο.Η., Rosebrough, Ν.J., Farr, A.L., Randall, R.J. (1951) Protein measurement with the folin phenol reagent. J. Biol. Chem, 193, 265-275.
  • Mittler, R. (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Science, 7, 405–410.
  • Mittler, R., Vanderauwera, S., Suzuki, N., Miller, G.A.D., Tognetti, V.B., Vandepoele, K., Van Breusegem, F. (2011) ROS signaling: the new wave?. Trends in plant science, 16(6), 300-309.
  • Mittova, V., Tal, M., Volokita, M., Guy, M. (2002) Salt stress induces up‐regulation of an efficient chloroplast antioxidant system in the salt‐tolerant wild tomato species Lycopersicon pennellii but not in the cultivated species. Physiologia Plantarum, 115(3), 393-400.
  • Munns, R., James, R. A., Gilliham, M., Flowers, T. J., Colmer, T.D. (2016) Tissue tolerance: an essential but elusive trait for salt-tolerant crops. Functional Plant Biology, 43(12), 1103- 1113.
  • Nakano, Y., Asada, K. (1981) Hydrogen peroxide is scavenged by ascobate-specific peroxidase in spinach chloroplasts. Plant Cell Physiol., 22: 867–880.
  • Poór, P., Borbély, P., Czékus, Z., Takács, Z., Ördög, A., Popović, B., Tari, I. (2019) Comparison of changes in water status and photosynthetic parameters in wild type and abscisic aciddeficient sitiens mutant of tomato (Solanum lycopersicum cv. Rheinlands Ruhm) exposed to sublethal and lethal salt stress. Journal of plant physiology, 232, 130-140.
  • Qadir, M., Quillérou, E., Nangia, V., Murtaza, G., Singh, M., Thomas, R. J., Noble, A. D. (2014) Economics of salt‐induced land degradation and restoration. In Natural Resources Forum. 38(4), pp. 282-295.
  • Rao, S.P., Mishra, B., Gupta, S.R., Rathore, A. (2008) Reproductive stage tolerance to salinity and alkalinity stresses in rice genotypes. Plant Breeding, 127: 256–261.
  • Rossatto, T., do Amaral, M. N., Benitez, L. C., Vighi, I. L., Braga, E. J. B., de Magalhaes Júnior, A. M., da Silva Pinto, L. (2017) Gene expression and activity of antioxidant enzymes in rice plants, cv. BRS AG, under saline stress. Physiology and Molecular Biology of Plants, 23(4), 865-875.
  • Singh, A.K. (2018) The physiology of salt tolerance in four genotypes of chickpea during germination. Smith, I. K., Vierheller, T.L., Thorne, C. A. (1989) Properties and functions of glutathione reductase in plants. Physiologia Plantarum, 77(3), 449-456.
  • Srivastava, S. K., Beutler, E. (1968) Accurate measurement of oxidized glutathione content of human, rabbit, and rat red blood cells and tissues. Analytical biochemistry, 25, 70-76.
  • Steffens, B., Steffen-Heins, A., Sauter, M. (2013) Reactive oxygen species mediate growth and death in submerged plants. Front. Plant Sci., 4: 179.
  • Stewart, R. R., Bewley, J. D. (1980) Lipid peroxidation associated with accelerated aging of soybean axes. Plant physiology, 65(2), 245-248.
  • Suzuki, N., Miller, G., Sejima, H., Harper, J., Mittler, R. (2012) Enhanced seed production under prolonged heat stress conditions in Arabidopsis thaliana plants deficient in cytosolic ascorbate peroxidase 2. Journal of experimental botany. 64(1), 253-263.
  • Teixeira, F. K., Menezes-Benavente, L., Galvão, V. C., Margis, R., Margis-Pinheiro, M. (2006) Rice ascorbate peroxidase gene family encodes functionally diverse isoforms localized in different subcellular compartments. Planta, 224(2), 300.
  • Toivonen, P. M. (2004) Postharvest storage procedures and oxidative stress. Hort. Science. 39(5), 938-942.
  • Velikova, V., Yordanov, I. and Edreva, A.(2000) Oxidative Stress and Some Antioxidant Systems in Acid RainTreated Bean Plants: Protective Role of Exogenous Polyamines. Plant Science. 151, 59-66.
  • Vranová, E., Inzé, D., Van Breusegem, F. (2002) Signal transduction during oxidative stress. Journal of experimental botany, 53(372), 1227-1236.
  • Wang, G. P., Zhang, X. Y., Li, F., Luo, Y., Wang, W. (2010) Overaccumulation of glycine betaine enhances tolerance to drought and heat stress in wheat leaves in the protection of photosynthesis. Photosynthetica. 48(1), 117-126.
  • Wood, P. M., Bhagavan, H. N., Crane, F. L. (1966) Requirement for plastoquinone A in the Hill reaction of isolated chloroplasts. Plant physiology, 41(4), 633-640.
  • Yousuf, P. Y., Hakeem, K. U. R., Chandna, R., Ahmad, P. (2012) Role of glutathione reductase in plant abiotic stress. In Abiotic Stress Responses in Plants. Springer, New York, NY. pp. 149-158.
  • Zhao, Y., Truhlar, D. G. (2006) A new local density functional for main-group thermochemistry, transition metal bonding, thermochemical kinetics, and noncovalent interactions. The Journal of chemical physics, 125(19), 194101.
Еще
Статья научная