Physiological responses of Salvinia natans L. to aluminium stress and its interaction with putrescine

Автор: Mandal C., Ghosh N., Dey N., Adak M.K.

Журнал: Журнал стресс-физиологии и биохимии @jspb

Статья в выпуске: 4 т.9, 2013 года.

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Salvinia natans L. a water fern is displayed with some of its physiological attributes in response to aluminium (Al) stress in aqua culture as well as its interaction with externally applied putrescine (put). At the tissue level the Al deposition is prominent and mostly distributed in the intracellular spaces as well as cellular interfaces. The accumulation of Al and its induced oxidative damages are also revealed through Evan’s blue staining. In both the cases dose dependent responses of Al induced oxidative damages and its mitigation with Put was the resultant. Under non enzymatic antioxidation pathways, anthocyanin and flavonoids were the two phenolics over expressed as a function of Al and ameliorated with Put application. The property of root membranes was changed with an up regulation of H +/ATPase activity which was moderated by Put.The peroxidase activity particularly those were restricted to the wall bound also showed variability according to Al doses as revealed through in gel staining. From these studies of Al accumulation and its concomitant changes in physiological attributes in Salvinia plants, the species could be selected as a potential hyper accumulator of Al. The role of Put in Al accumulation as well as its moderation has been discussed with reference to physiological activities.

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Aluminium toxicity, antioxidative enzymes, putrescine, reactive oxygen species, salvinia sp

Короткий адрес: https://sciup.org/14323798

IDR: 14323798

Список литературы Physiological responses of Salvinia natans L. to aluminium stress and its interaction with putrescine

  • Achary, V.M.M., Jena, S., Panda, K. and Panda, B. (2007) Aluminium induced oxidative stress and DNA damage in root cells of Allium cepa L. Ecotoxicolo. Environment. Safety., 70, 300-310
  • Almagro, L., Ros, L.V.G., Belchi-Navarro, S., Bru, R., Barcelo, A.R. and Pedreno, M.A. (2009) Class III peroxidases in plant defence reactions. J. Experiment. Bot., 60, 377-390
  • Annalisa, T., Richard, M., Napier, M., Franceschetti, M.A.V. and Nello, B. (2002) Spermidine-binding proteins. Purification and expression analysis in maize. Plant. Physiol., 128, 1303-1312
  • Asthir, B., Koundal, A. and Bains N.S. (2009) Kinetic and thermodynamic behaviour of wall-bound peroxidase from wheat leaves infected with stripe rust. Plant. Growth. Regul., 59, 117-124
  • Baker, C.J. and Mock, N.M. (1994) An improved method for monitoring cell deathin cell suspension and leaf disc assays using evan’s blue. Plant. Cell. Tissue. Organ. Cult., 39, 7-12
  • Boscolo, P.R., Menossi, M. and Jorge, R.A. (2003) Aluminum-induced oxidative stress in maize. Phytochemistry., 62, 181-189
  • Bradford, M.M. (1976) Rapid and sensitive method for quantitation of micro gram quantities of protein utilizing the principle of protein-binding dye. Ann. Biochem., 72, 248-254
  • Damanik, R.I., Mahmood, M., Ismail, M.R., Ahmad, S. and Zain, A.M. (2010) Responses of antioxidative enzymes in Malaysian rice (Oryza sativa L.) cultivars under submergence condition. Acta. Physiol. Plant., 32, 739-747
  • Dhir, B., Sharmila, P., PardhaSaradhi, P. and Nasim, S.A. (2009) Physiological and antioxidant responses of Salvinia natans exposed to chromium-rich waste water. Ecotoxicol. Environment. Safety., 72, 1790-1797
  • Eryılmaz, F. (2006) The relationships between salt stress and anthocyanin content in higher plants. Biotechnol. Equip., 20, 47-52
  • Exley, C. (2004) The pro-oxidant activity of aluminum. Free. Radic. Biol. Med., 36, 380-387
  • Farooq, M., Wahid, A., Kobayashi, N., Fujita, D. and Basra, S.M.A. (2009) Plant drought stress: effects, mechanisms and management. Agron. Sustain. Dev., 29, 185-212
  • Ghosh, N., Adak, M.K., Ghosh, P.D., Gupta, S., SenGupta, D.N. and Mandal, C. (2011) Differential responses of two rice varieties to salt stress. Plant. Biotechnol. Rep., 5, 89-103
  • Giannakoula, C.N. and Ries, S.K. (2010) Superoxide dismutase. Plant. Physiol., 59, 309-314
  • Gifford, E.M. and Foster, AS (1989) Morphology and evolution of vascular plants. W.H., Freeman and Company, New York
  • Hu, Y., Ge, Y., Zang, C., Zu, T. and Cheng, W. (2009) Cd toxicity and translocation in rice seedlings are reduced by hydrogen peroxide treatments. Plant. Growth. Regul., 5, 51-61
  • Janicka-Russak, M., Kaba1a, K., Burzynski, M. and K1obus, G. (2008) Response of plasma membrane H+/ATPase to heavy metal stress in Cucumis sativus roots. J. Experiment. Bot., 59, 3721-3728
  • Kabała, K. and Janicka-Russak, M. (2011) Differential regulation of vacuolar H+/ATPase and H+/PPase in Cucumis sativus roots by zinc and nickel. Plant. Sci., 180, 531-9
  • Koizumi, Y., Hara, Y., Yazaki, Y., Sakano, K. and Ishizawa, K. (2011) Involvement of plasma membrane H+-ATPase in anoxic elongation of stems in pondweed (Potamogeton distinctus) turions. New. Phytologist., 190, 421-430
  • Korenkov, V., Hirschi, K., Crutchfield, J.D. and Wagner, G.J. (2007) Enhancing tonoplast Cd/H antiporter activity increases Cd, Zn and Mn tolerance, and impacts root/shoot Cd partitioning in Nicotiana tabacum L. Planta., 226, 1379-1387
  • Kramer, U. (2010) Metal Hyperaccumulation in Plants. Annual. Review. Plant. Biology., 6, 517-534
  • Larue, C., Korboulewsky, N., Wang, R. and Mevy, J.P. (2010) Depollution potential of three macrophytes: exudated, wall-bound and intracellular peroxidase activities plus intracellular phenol concentrations. Bioresou. Technol., 101, 7951-7957
  • Liu, J., Yu, B.J. and Liu, Y.L. (2006) Effects of spermidine and spermine levels on salt tolerance associated with tonoplast H+/ATPase and H+/PPase activities in barley roots. Plant. Growth. Regul., 49, 119-126
  • Liu, J.H., Inove, H., Moriguchi, T. (2008) Salt stress mediated changes in free polyamine titers and expression of genes responsible for polyamine biosynthesis of apple in vitro shoots. Environ. Exp. Bot. 62, 28-35
  • Mandal, C., Ghosh, N., Maiti, S., Das, K., Gupta, S., Dey, N. and Adak, M.K. (2013) Antioxidative responses of Salvinia (Salvinia natans Linn.) to aluminium stress and it’s modulation by polyamine. Physiol. Mol. Biol. Plants. 19, 91-103
  • Mariale, S., Sanchez, D.H., Guirado, V.A. and Riiz, O.A. (2004) Spermine accumulation under salt stress. J. Plant. Physiol. 161, 35-4
  • Mika, A. and Luthje, S. (2003) Properties of guaiacol peroxidase isolated from corn root plasma membranes. Plant. Physiol. 132, 1489-1498
  • Mohamed, A.A. and Aly, A.A. (2008) Alteration of some secondary metabolites and enzymes activity by using exogenous antioxidant compound in onion plants grown under seawater salt stress. American. Eurasian. J. Sci. 3, 139-146
  • Murashige, T. and Skoog, F. (1962) A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol. Plant. 15, 473-497
  • Nakano, Y. and Asada, K. (1981) Hydrogen peroxide is scavenged by ascorbate specific peroxidase in spinach chloroplasts. Plant. Cell. Physiol. 22, 867-880
  • Peter, W., Gloria, M.P., Alba, L.C., Jorge, E.M. and Idupulapati, M.R. (2001) The High Level of Aluminum Resistance in Signalgrass Is Not Associated with Known Mechanisms of External Aluminum Detoxification in Root Apices. Plant. Physiology. 125, 1473-1484
  • Roy, P., Niyogi, K., SenGupta, D.N. and Ghosh, B. (2005) Spermidine treatment to rice seedlings recovers salinity stress-induced damage of plasma membrane and PM-bound H+/ATPase in salt-tolerant and salt-sensitive rice cultivars. Plant. Sci. 168, 583-591
  • Roychoudhury, A. and Pradhan, S. (2011) Role of Potentially Important Microbes in Bioremediation. Science. Culture. 77, 324-330
  • Sakihama, Y., Cohen, M.F., Grace, S.C. and Yamasaki, H. (2007) Plant phenolic antioxidant and prooxidant activities:phenolics-induced oxidative damage mediated by metals in plants. Toxicology. 177, 67-80
  • Saroop, S., Chanda, S.V. and Singh, Y.D. (2002) Changes in soluble and ionically bound peroxidase activities during brassica juncea seed development. Bulg. J. Plant. Physiol. 28, 26-34
  • Skinner, K., Wright, N. and Porter-Goff, E. (2007) Mercury uptake and accumulation by four aquatic plants. Environmental. Pollution. 145, 234-237
  • Sonia, S. (2012) Aluminium Toxicity Targets in Plants. J. Botany DOI: 10.1155/2012/219462
  • Tang, W. and Newton, R.J. (2005) Polyamine reduces salt induced oxidative damage by increasing the activity of antioxidant enzyme and decreasing lipid peroxidation. Plant. Growth. Regul. 46, 31-43
  • Xu, Q.S., Ji, W.D., Yang, H.Y., Wang, H.X., Xu, Y., Zhao, J. and Shi, G.X. (2009) Cadmium accumulation and phytotoxicity in an aquatic fern, Salvinia natans (Linn.). Acta. Ecologica. Sinica 29, 3019-3027
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