Response of embryo axes of germinating seeds of yellow lupine to Fusarium oxysporum

Plant Physiology and Biochemistry

Volumn 42, Issue 6, 2004, Pages 493-499

  Morkunas, Iwona ^a   Bednarski, Waldemar ^b   Kozłowska, Monika ^a  

^a POZNA UNIVERSITY OF LIFE SCIENCES   (Poland)

^b INSTITUTE OF MOLECULAR PHYSICS   (Poland)

Author keywords

2,2 Azino bis (3 ethylbenz thiazoline) 6 sulfonic acid; ABTS; CAT; catalase; electron paramagnetic resonance; EPR; Free radicals; Fusarium oxysporum; Germinating seeds; Hydrogen peroxide; Lipid peroxidation; Lupinus luteus; Oxidative stress

Indexed keywords

CATALASE; HYDROGEN PEROXIDE; SUPEROXIDE DISMUTASE;

ARTICLE; ELECTRON SPIN RESONANCE; FUSARIUM; GERMINATION; GROWTH, DEVELOPMENT AND AGING; LIPID PEROXIDATION; LUPIN; METABOLISM; MICROBIOLOGY; PATHOGENICITY; PHYSIOLOGY; PLANT DISEASE; PLANT SEED;

CATALASE; ELECTRON SPIN RESONANCE SPECTROSCOPY; FUSARIUM; GERMINATION; HYDROGEN PEROXIDE; LIPID PEROXIDATION; LUPINUS; PLANT DISEASES; SEEDS; SUPEROXIDE DISMUTASE;

FELIS CATUS; FUNGI; FUSARIUM; FUSARIUM OXYSPORUM; FUSARIUM SP.; LUPINUS; LUPINUS LUTEUS;

EID: 3142649185     PISSN: 09819428     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plaphy.2004.05.007     Document Type: Article

References (39)

1. Agrios G.N. How plants defend themselves against pathogens. Plant Pathology. 1997;93-114 Academic Press, San Diego
2. Ascough P.B. Electron spin resonance in chemistry. 1967;Methuen and Co. Ltd. London
3. Atherton N.M., Hendry G.A.F., Möbius K., Rohrer M., Törring J.T. A free radical ubiquitously associated with senescence in plants: evidence for a quinine. Free Radical Res. Commun. 19:1993;297-301
4. Baker C.J., Orlandi E.W. Active oxygen species in plant pathogenesis. Annu. Rev. Phytopathol. 33:1995;299-321
5. Bartling D., Radzio R., Steiner U., Weiler E.W. A glutathione-S- transferase with glutathione-peroxidase-activity from Arabidopsis thaliana-molecular cloning and functional characterization. Eur. J. Biochem. 216:1993;579-586
6. Beauchamp C.H., Fridovich I. Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Anal. Biochem. 44:1971;276-287
7. 2 Bestimmung Verfahren mit 2.2-Azino-di-(3-äthylbenzthiazolin)-6-sulfonat (ABTS). Bergmeyer H.U. Methoden der Enzymatischen Analyse. 1974;1257-1258 Verlag Chemie, Weinheim
8. Bolwell G.P., Wojtaszek P. Mechanisms for the generation of reactive oxygen species in plant defence: a broad perspective. Physiol. Mol. Plant Pathol. 51:1997;347-366
9. Bradford M. A rapid and sensitive method for quantitation of microgram quantities of protein using the principle of protein-dye binding. Anal. Biochem. 72:1976;248-254
10. Conklin P.L., Williams E.H., Last R.L. Environmental stress sensitivity of an ascorbic acid-deficient Arabidopsis mutant. Proc. Natl. Acad. Sci. USA. 93:1996;9970-9974
11. Cook R.J. Fusarium: Diseases, Biology and Taxonomy. 1981;The Pennsylvania State University Press, Park and London
12. Deighton N., Muckenschnabel I., Goodman B.A., Williamson B. Lipid peroxidation and the oxidative burst associated with infection of Capsicum annum by Botrytis cinerea. Plant J. 20:(4):1999;485-492
13. Dhindsa R., Matowe W. Drought tolerance in two mosses: correlated with enzymatic defence against lipid peroxidation. J. Exp. Bot. 32:1981;79-91
14. Dhindsa R.S., Plumb-Dhindsa F., Thorpe T.A. Leaf senescence: correlated with increased levels of membrane permeability and lipid peroxidation, and decrease levels of superoxide dismutase and catalase. J. Exp. Bot. 32:1981;93-101
15. Gil-ad N.L., Mayer A.M. Evidence for rapid breakdown of hydrogen peroxide by Botrytis cinerea. FEMS Microbiol. Lett. 176:1999;455-461
16. Guan L.M., Scandalios J.G. Hydrogen peroxide-mediated catalase gene expression in response to wounding. Free Radical Biol. Med. 28:2000;1182-1190
17. Hamond-Kosacke E., Jonatan D., Jones G. Resistance gene-dependent plant defense responses. Plant Cell. 8:1996;1773-1791
18. Hückelhooven R., Kogel K.H. Reactive oxygen intermediates in plant-microbe interactions: Who is who in powdery mildew resistance. Planta. 216:2003;891-902
19. Janero D.R. Malondialdehyde and thiobarbituric acid reactivity as diagnostic indices of lipid peroxidation and peroxidative tissue injury. Free Radical Biol. Med. 9:1990;515-540
20. Kombrink E., Somssich I.E. Defense responses of plants to pathogens. Callow J.A. Advances in Botanical Research 21. 1995;1-34 Academic Press, New York
21. Kvaratskhelia M., Winkel C., Naldrett M.T., Thorneley R.N.F. A novel high activity cationic ascorbate peroxidase from tea (Camellia sinensis): a class III peroxidase with unusual substrate specificity. J. Plant Physiol. 154:1999;273-282
22. Lamb C., Dixon R.A. The oxidative burst in plant disease resistance. Annu. Rev. Plant Physiol. Plant Mol. Biol. 48:1997;251-275
23. 2 from the oxidative burst orchestrates the plant hypersensitive disease response. Cell. 79:1994;583-593
24. Low P.S., Merida J.R. The oxidative burst in plant defense: function and signal transduction. Physiol. Plant. 96:1996;533-542
25. Loprasert S., Vattanaviboon P., Praituan W., Chamnongpol S., Mongkolsuk S. Regulation of the oxidative stress protective enzymes, catalase and superoxide dismutase in Xanthomona. Gene. 179:1996;33-37
26. Lu H., Higgins V.J. The effect of hydrogen peroxide on the viability of tomato cells and of the fungal pathogen Cladosporium fulvum. Physiol. Mol. Plant Pathol. 54:1999;131-143
27. Malolepsza U., Urbanek H. The oxidants and antioxidant enzymes in tomato leaves treated with o-hydroxyethylorutin and infected with Botrytis cinerea. Eur. J. Plant Pathol. 106:2000;657-665
28. Mayer A.M., Staples R.C., Gil-ad N.L. Mechanisms of survival of necrotrophic fungal plant pathogens in hosts expressing the hypersensitive response. Phytochemistry. 58:2001;33-41
29. Mehdy M.C. Active oxygen species in plant defense against pathogens. Plant Physiol. 105:1994;467-472
30. Morkunas I., Kozlowska M., Bednarski W. Generation of free radicals at seed germination stage of yellow lupin infected with Fusarium oxysporum under carbohydrate stress. J. Appl. Genet. 43A:2002;27-34
31. Morkunas I., Garnczarska M., Bednarski W., Ratajczak W., Waplak S. Metabolic and ultrastructural responses of lupine embryo axes to sugar starvation. J. Plant Physiol. 160:2003;311-319
32. Muckenschnabel I., Williamson B., Goodman B.A., Lyon G.D., Stewart D., Deighton N. Markers for oxidative stress associated with soft rots in French beans (Phaseolus vulgaris) infected by Botrytis cinerea. Planta. 212:2001;376-381
33. Muckenschnabel I., Goodman B.A., Williamson B., Lyon G.D., Deighton N. Infection of leaves of Arabidopsis thaliana by Botrytis cinerea: changes in ascorbic acid, free radicals and lipid peroxidation products. J. Exp. Bot. 367:2002;207-214
34. Ogawa K., Kanematsu S., Asada K. Intra- and extra-cellular localization of "cytosolic" CuZn-superoxide dismutase in spinach leaf and hypocotyls. Plant Cell Physiol. 37:1996;790-799
35. Polidoros A.N., Scandalios J.G. Role of hydrogen peroxide and different classes of antioxidants in the regulation of catalase and glutathione S-transferase gene expression in maize (Zea mays L.). Physiol. Plant. 106:1999;112-120
36. Schopfer P., Plachy C., Frahry G. Release of reactive oxygen intermediates (superoxide radicals, hydrogen peroxide, and hydroxyl radicals) and peroxidase in germinating radish seeds controlled by light, gibberellin, and abscisic acid. Plant Physiol. 125:2001;1591-1602
37. Smith M.T., Van Staden J. Infochemicals: the seed-fungus-root continuum. Environ. Exp. Bot. 35:(2):1995;113-123
38. Srobarova A., Pavlov A. The resistance of wheat to Fusarium culmorum and its metabolites: a survey. J. Appl. Genet. 43A:2002;193-196
39. Sutherland M.W. The generation of oxygen radicals during host plant responses to infections. Physiol. Mol. Plant Pathol. 39:1991;79-93