Exogenous spermidine alters in different way membrane permeability and lipid peroxidation in water stressed barley leaves

• Autorzy: Kubis J
• Języki publikacji: EN

Abstrakty

EN

In order to see whether polyamines will modify membrane functioning in the water stressed plants, barley (Hordeum vulgare) seedlings were treated with spermidine (Spd) prior to dehydration and then the stress-evoked changes in membrane permeability (i.e. in electrolyte leak age from leaves) and lipid peroxidation (indicated by modifications of the malondi -aldehyde (MDA) level, and of the lipoxygenase (LOX) activity) were fol lowed. The Spd treatement lowered in jury index in plants subjected to water deficit, al though it slightly in creased the stress-promoted LOX activity and in creased the MDA level in the studied leaves. Presented results confirm that spermidine stabi lizes plant membranes under water stress conditions. However, this effect does not seem to be asso ciated with the Spd-induced modifications in the lipid peroxidation activities.

Słowa kluczowe

EN

injury index; lipoxygenase; malondialdehyde; leaf; lipid peroxidation; water stress; dehydration; polyamine; stressed plant; barley; membrane permeability; Hordeum vulgare; plant

• Wydawca: -
• Czasopismo: Acta Physiologiae Plantarum
• Rocznik: 2006
• Tom: 28
• Numer: 1
• Opis fizyczny: p.27-33,fig.,ref.

Twórcy

autor

Kubis J

• August Cieszkowski Agricultural University, Wolynska 35, 60-637 Poznan, Poland

Bibliografia

• Bagni N., Torrigiani P. 1992. Polyamines: A new class of growth substances. – In Progress in Plant Growth Regulation (C.M. Karssen, L.C. van Loon and D. Vreugdenhil, eds). Pp.264-275. Kulver Academic Publishers, Dordrecht. ISBN 0-444-41576-3.
• Besford R.T., Richardson J.L., Campos A.F., Tiburcio A.F. 1993. Effect of polyamines in stabilization of molecular complexes of thylakoid membranes of osmotically stressed oat leaves. Planta 189: 201-206.
• Bigwood T., Read G. 1989. Pseudo malonaldehyde activity in the thiobarbituric acid test. Free Radic. Res. Commun. 6: 387-392.
• Biondi S., Scaramagli S., Capitani F., Altamura M.M., Torrigiani P. 2001. Methyl jasmonate upregulates biosynthetic gene expression, oxidation and conjugation of polyamines, and inhibits shoot formation in tobacco thin layers. J. Exp. Bot. 52: 231-242.
• Borrell A., Carbonell R., Farras R., Puig-Parellada P., Tiburcio A.F. 1997. Polyamines in hibit lipid peroxidation in senescing oat leaves. Physiol. Plant. 99: 385-390.
• Bors N., Langebartels C., Mitchel C., Sanderman H. 1989. Polyamines as radical scavengers and protectants against ozone damage. Phytochem. 28: 1589-1595.
• Bouchereau A., Aziz A., Larher F., Martin-Tanguy J. 1999. Polyamines and environmental chal lenges: recent development. Plant Science 140: 103-125.
• Bradford M.M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72: 248-254.
• Bratton D.L. 1994. Polyamine in hibition of transbilayer movements of plasma membrane phospholipids in the erythrocyte ghost. 1994. J. Biol. Chem. 269: 22517-22523.
• Brûggemann L.I., Pottosin I.I., Schõnknecht G. 1998. Cytoplasmic polyamines block the fast-activating vacuolar cation channels. Plant J. 16: 101-105.
• Chattopadhayay M.K., Tiwari B.S., Chattopadhayay G., Bose A., Sengupta D.N., Ghosh B. 2002. Protective role of exogenous polyamines on sa linity-stressed rice Oriza sativa) plants. Physiol. Plant. 116: 192-199.
• Creelman R.A., Mullet J.E. 1997. Biosynthesis and action of jasmonates in plants. Annu. Rev. Plant Physiol. Plant Mol. Biol. 48: 355-381.
• Dhindsa R.S., Matowe W. 1981. Drought tolerance in two mosses: correlated with enzymatic de fence against lipid peroxidation. J. Exp. Bot. 32: 79-91.
• Egert M., Tevini M. 2002. Influence of drought on some physiological parameters symptomatic for oxidative stress in leaves of chives (Alium schoenoprasum). Env. Exp. Bot. 48: 43-49.
• Flint H.Z., Boyce B.R., Brattie D.J. 1967. Index of injury – a use ful expression of freezing injury of plants tissues as determined by electric conductivity method. Can. J. Plant Sci. 47: 229-239.
• Galliard T. 1980. Degradation of acyllipids: hydrolytic and oxidative enzymes, - in Biochemistry of Plants. A Comprehensive Trea tise. (K. Stumpf, ed.), vol. 4, pp. 85-116, Ac a demic Press, New York.
• Galston A.W., Kaur-Sawhney R. 1995. Polyamines as endogenous growth regulators. – In Plant hor mones: Physiology, Biochemistry and Molecular Biology, 2nd Ed. (P.J. Davies, ed.), pp. 158-178. Kulver Academic Publishers, Dordrecht. ISBN 0-7923-2984-8.
• Gniazdowska-Skoczek H., Krzywanski Z. Kubis J. 1994. The influence of exogenous spermidine on polysomes and RNase activity in wheat leaves under water stress conditions. Acta Soc. Bot. Pol. 63: 25-28.
• Hildebrand D.F. 1989. Lipoxygenases. Plant Physiol. 76: 249-253.
• Kacperska A., Kubacka-Zebalska M. 1989. Formation of stress ethylene depends both on ACC syn thesis and on the activity of free radical-generating system. Physiol. Plant. 77: 231-237.
• Kakkar R.K., Sawhney V.K. 2002. Polyaminere -search in plants – a changing perspective. Physiol. Plant. 116: 281-292.
• Kikugawa K., Kojima T., Kosugi H. 1990. Major thiobarbituric acid-reactive substance of liver ho mogenate are alkadieanals. Free Radic. Res. Commun. 8: 107-113.
• Kubis J., Skoczek H., Krzywanski Z. 1991. Exogenous polyamines alter the activity of proteas es, Rnases and membrane permeability in wheat leaves under water stress conditions. Acta Physiol. Plant. 13: 139-146.
• Lester G.E., Stein E. 1993. Plasma membrane physicochemical changes during maturation and postharvest storage of muskmelon fruit. J. Am. Soc. Hort. Sci. 118: 223-227.
• Lester G.E. 2000. Polyamines and their cellular anti-senescence properties in honey dew musk melon fruit. Plant Science 160: 105-112.
• Porta H., Rocha-Sosa M. 2002. Plant Lipoxygenases. Physiological and molecular features. Plant Physiol. 130: 15-21.
• Roberts D.R., Dumdroff E.B., Thompson J.E. 1986. Exogenous polyamines alter membrane fluid ity in been leaves: a basic potential misinterpretation of their physiological role. Planta 167: 395-401.
• Rosahal S. 1996. Lipoxygenases in plants – their role in development and stress responses. Z. Naturforsch. 51C: 123-138
• Siedow J.N. 1991. Plant lipoxygenase: structure and function. Annu. Rev. Plant Physiol. Plant Mol. Biol. 42: 145-188.
• Slocum R.D., Kaur-Sawhney R., Galston A.W. 1984. The physiology and biochemistry of polyamines in higher plants. Arch. Biochem. Biophys. 235: 283-303.
• Smith T.A. 1985. Polyamines. Ann. Rev. Plant Physiol. 36: 117-143.
• Tassoni A., Antognoni F., Battistini M.L., Sanvido O., Bagni N. 1998. Characterization of spermidine binding to solubilized plasma membrane proteins from zucchini hypocotyls. Plant Physiol. 117: 971-077.
• Tassoni A., Napier R.M., Franceschetti M., Venis M.A., Bagni N. 2002. Spermidine-binding pro teins. Purification and expression analysis in maize. Plant Physiol. 128: 1303-1312.
• Thompson J.E., Legge R.L., Barber R.F. 1987. The role of free radicals in senescing and wounding. New Phytol. 105: 317-344.
• Tiburcio A.F., Kaur-Sawhney R., Galston A.W. 1990. Polyamine metabolism of plants, in: B.J. Miflin P.J. Lea (eds.), The Biochemistry of Plants, vol. 16, Academic Press, New York, pp. 283-325.
• Walters D., Cowley T., Mitchell A. 2002. Methyl jasmonate alters polyamine metabolism and induces systemic protection against powdery mildew infection in barley seedlings. J. Exp. Bot. 53: 747-756.
• Weatherley P.E. 1950. Studies in water relations of cotton plants. I. The field measurement of water deficits in leaves. New Phytol. 49: 81-97.