Macronutrient deficiencies and differential antioxidant responses - Influence on the activity and expression of superoxide dismutase in maize

Plant Science

Volumn 166, Issue 3, 2004, Pages 687-694

  Tewari, Rajesh Kumar ^a   Kumar, Praveen ^a   Tewari, Neeraj ^a   Srivastava, Sugandha ^a,b   Sharma, Parma Nand ^a  

^a UNIVERSITY OF LUCKNOW   (India)

^b CSIR NATIONAL BOTANICAL RESEARCH INSTITUTE   (India)

Author keywords

Lipid peroxidation; Macronutrients deficiency stress; ROS; SOD; Zea mays

Indexed keywords

ANTIOXIDANTS; ENZYMES; HYDROGEN PEROXIDE; LIPIDS; OXIDATION;

MACRONUTRIENT DEFICIENCIES; OXIDATIVE STRESS;

PLANTS (BOTANY);

ZEA; ZEA MAYS;

EID: 1242300209     PISSN: 01689452     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plantsci.2003.11.004     Document Type: Article

References (63)

1. E.J. Hewitt, Essential nutrient elements for plants: requirement and interaction in plants, in: F.C. Steward, (Ed.), Plant Physiology, vol. III, Academic Press Inc., New York, USA, 1963, pp. 137-360.
2. Grossman A., Takahashi H. Macronutrient utilisation by photosynthetic eukaryotes and the fabric of interactions. Ann. Rev. Plant Physiol. Plant Mol. Biol. 52:2001;163-210.
3. Escoubas J.M., Lomas M., LaRoche J., Falkowski P.G. Light intensity regulation of cab gene transcription is signaled by a redox state of plastoquinone pool. Proc. Natl. Acad. Sci. U.S.A. 92:1995;10237-10241.
4. Vener A.V., Vankan P.J.M., Gal A., Andersson B., Ohad I. Activation-deactivation cycle of redox-controlled thylakoid protein phosphorylation: role of plastoquinol bound to the reduced cytochrome bf complex. J. Biol. Chem. 270:1995;25225-25232.
5. Alscher R.G., Donahue J.L., Cramer C.L. Reactive oxygen species and antioxidant: relationship in green cells. Physiol. Plant. 100:1997;224-233.
6. Foyer C.H., Lopez-Delgado H., Dat J.F., Scott I.M. Hydrogen peroxide and glutathione-associated mechanisms of acclamatory stress tolerance and signalling. Physiol. Plant. 100:1997;241-254.
7. Noctor G., Foyer C.H. Ascorbate and glutathione: keeping active oxygen under control. Ann. Rev. Plant Physiol. Plant Mol. Biol. 49:1998;249-279.
8. Grant J.J., Loake G.J. Role of reactive oxygen intermediates and cognate redox signaling in disease resistance. Plant Physiol. 124:2000;21-29.
9. Cuypers A., Vangronsveld J., Clijsters H. The redox status of plant cells (AsA and GSH) is sensitive to zinc imposed oxidative stress in roots and primary leaves of Phaseolus vulgaris. Plant Physiol. Biochem. 39:2001;657-664.
10. E. Cadenas, Mechanism of oxygen activation and reactive oxygen species detoxification, in: S. Ahmad, (Ed.), Oxidative Stress and Antioxidant Defences in Biology, Chapman and Hall, New York, 1995, pp. 1-61.
11. B. Halliwell, J.M.C. Gutteridge, Free Radicals in Biology and Medicine, Clarendon Press, Oxford, UK, 1989, pp. 164-165.
12. Martinez C.A., Loureiro M.E., Oliva M.A., Maestri M. Differential responses of superoxide dismutase in freezing resistant Solanum curtilobum and freezing sensitive Solanum tuberosum subjected to oxidative and water stress. Plant Sci. 160:2001;505-515.
13. Kaminaka H., Morita S., Tokumoto M., Masumura T., Tanaka K. Differential gene expressions of rice superoxide dismutase isoforms to oxidative and environmental stresses. Free Radic. Res. 31:1999;S219-225.
14. Logan B.N., Demming-Adams B., Rosenstiel T.N., Adams W.W. III Effect of nitrogen limitation on foliar antioxidants in relationship to other metabolic characteristics. Planta. 209:1999;213-220.
15. 2-scavenging enzymes and leaf chlorosis are enhanced magnesium and potassium-deficient leaves, but not in phosphorus-deficient leaves. J. Exp. Bot. 45:1994;1259-1266.
16. Juszczuk I., Malusà E., Rychter A.M. Oxidative stress during phosphate deficiency in roots of bean plants (Phaseolus vulgaris L.). J. Plant Physiol. 158:2001;1299-1305.
17. Malusà E., Laurenti E., Juszczuk I., Ferrari R.P., Rychter A.M. Free radical production in roots of Phaseolus vulgaris subjected to phosphate deficiency stress. Plant Physiol. Biochem. 40:2002;963-967.
18. Cakmak I., Marschner H. Magnesium deficiency and high light intensity enhance activities of superoxide dismutase, ascorbate peroxidase and glutathione reductase in bean leaves. Plant Physiol. 98:1992;1222-1227.
19. H. Marschner, Mineral Nutrition of Higher Plants, Academic Press Inc., London, 1995.
20. 2+ deficiency in the Mentha pulegium leaves. Plant Physiol. Biochem. 41:2003;35-40.
21. Paranhos A., Fernández-Tarrago J., Corchete P. Relationship between active oxygen species and cardenolide production in cell culture of Digitalis thapsi: effect of calcium restriction. New Phytol. 141:1999;51-60.
22. Schmitz-Eiberger M., Haefs R., Noga G. Calcium deficiency - influence on the antioxidative defense system in tomato plants. J. Plant Physiol. 159:2002;733-742.
23. E.J. Hewitt, Sand and Water Culture Methods Used in the Study of Plant Nutrition, Commonwealth Agricultural Bureaux, Farnham Royal Bucks, UK, 1966.
24. H.K. Lichtenthaler, Chlorophylls and carotenoids: Pigments of photosynthetic biomembranes, in: L. Packer, R. Douce (Eds.), Methods in Enzymology, vol. 148, Academic Press Inc., New York, USA, 1987, pp. 350-382.
25. Brennan T., Frenkel C. Involvement of hydrogen peroxide in regulation of senescence in pear. Plant Physiol. 59:1977;411-416.
26. Heath R.L., Packer L. Photoperoxidation in isolated chloroplast, I. Kinetics and stoichiometry of fatty acid peroxidation. Arch. Biochem. Biophys. 125:1968;180-198.
27. Lowry O.H., Rosebrough N.J., Farr A.L., Randall R.J. Protein measurement with Folin-phenol reagent. J. Biol. Chem. 193:1951;265-295.
28. Euler H.V., Josephson K. Uber Katalase I. Leibigs. Ann. 452:1927;158-187.
29. Bisht S.S., Sharma A., Chaturvedi K. Certain metabolic lesions of chromium toxicity in radish. Indian J. Agric. Biochem. 2:1989;109-115.
30. H. Luck, Peroxidase, in: H.U. Bergmeyer (Ed.), Methods of Enzymic Analysis, Academic Press Inc., New York, USA, 1963, pp. 895-897.
31. Nakano Y., Asada K. Hydrogen peroxide is scavenged by ascorbate specific peroxidase in spinach chloroplast. Plant Cell Physiol. 22:1981;867-880.
32. Giannopolitis C.N., Ries S.K. Superoxide dismutases. 1. Occurrence in higher plants. Plant Physiol. 59:1977;309-314.
33. Beauchamp C., Fridovich I. Superoxide dismutase: improved assays and assays applicable to acrylamide gels. Anal. Biochem. 44:1971;276-287.
34. R.D. Voss, Corn, in: W.F. Bennett (Ed.), Nutrient Deficiencies and Toxicities in Crop Plants, APS Press, St. Paul, MN, The American Phytopathological Society, 1993, pp. 11-14.
35. Pierce J. Determinants of substrate specificity and the role of metal in the reaction of ribulose bisphosphate carboxylase/oxygenase. Plant Physiol. 81:1986;943-945.
36. T.C. Hsiao, A. Läuchli, Role of potassium in plant-water relations, in: B. Tinker, A. Läuchli (Eds.), Advances in Plant Nutrition, vol. 2, Praeger Scientific, New York, USA, 1986, pp. 281-312.
37. Giordano M., Pezzoni V., Hell R. Strategies for the allocation of resources under sulfur limitation in the green alga Dunaliella salina. Plant Physiol. 124:2000;857-864.
38. Pieters A.J., Paul M.J., Lawlor D.W. Low sink demands limits photosynthesis under Pi deficiency. J. Exp. Bot. 52:2001;1083-1091.
39. Sauer J., Schreiber U., Schmid R., Völker U., Forchhammer K. Nitrogen starvation-induced chlorosis in Synechococcus PCC 7942, low-level photosynthesis as a mechanism of long-term survival. Plant Physiol. 126:2001;233-243.
40. Wardlaw I.A. The control of carbon partitioning in plants. New Phytol. 116:1990;341-381.
41. Rufty T.W., Huber S.C., Volk R.J. Alternations in leaf carbohydrate metabolism in response to nitrogen stress. Plant Physiol. 88:1988;725-730.
42. Cakmak I., Hengeler C., Marschner H. Partitioning of shoot and root dry matter and carbohydrates in bean plants suffering from phosphorus, potassium and magnesium deficiency. J. Exp. Bot. 45:1994;1245-1250.
43. Mollier A., Pellerin S. Maize root system growth and development as influenced by phosphorus deficiency. J. Exp. Bot. 50:1999;487-497.
44. Rufty T.W. Jr., Israel D.W., Volk R.J., Qui J., Sa T. Phosphate regulation of nitrate assimilation in soybean. J. Exp. Bot. 44:1993;879-891.
45. Trippi V.S., Gidrol X., Pradet A. Effect of oxidative stress caused by oxygen and hydrogen peroxide on energy metabolism and senescence in oat leaves. Plant Cell Physiol. 30:1989;157-162.
46. Casano L.M., Gómez L.D., Trippi V.S. Oxygen- and light-induced proteolysis in isolated oat chloroplast. Plant Cell Physiol. 31:1990;377-382.
47. J.E. Thompson, K.P. Pauls, L.S. Chia, S. Sridhara, Free radical-mediated changes in the organization of lipid bilayers, in: W.W. Thompson, J. Briand, M. Gibbs (Eds.), Biosynthesis and Function of Plant Lipids, American Society of Plant Physiologists, Rockville, MD, 1983, pp. 146-155.
48. Wise R.R., Naylor A.W. Chilling-enhanced photooxidation. The peroxidative destruction of lipids during chilling injury to photosynthesis and ultrastructure. Plant Physiol. 83:1987;272-277.
49. De Luca dOro G.M., Trippi V.S. Effect of stress conditions induced by temperature, water and rain on senescence development. Plant Cell Physiol. 28:1987;1389-1396.
50. Thompson J.E., Legge R.L., Barber R.J. The role of free radicals in senescence and wounding. New Phytol. 60:1987;333-340.
51. ChunHua L., LiangHua H., Lin Z., YongQuan C., ZhenFei G. Effect of N, P, K, Ca and Mg deficiency on nitrate accumulation, nitrate reductase and peroxidase activity in Chinese kale. J. South China Agric. Univ. 19:1998;55-58.
52. Raychaudhari S.S., Deng X.W. The role of superoxide dismutase in combating stress in higher plants. Bot. Rev. 66:2000;89-98.
53. Foyer C.H., Noctor G. Oxygen processing in photosynthesis: regulation and signalling. New Phytol. 146:2000;359-388.
54. Fodor J., Gullner G., Ádám A.L., Barna B., Kömives T., Király Z. Local and systemic responses of antioxidants to tobacco mosaic virus infection and salicylic acid in tobacco: role in systemic acquired resistance. Plant Physiol. 114:1997;1443-1451.
55. González A., Steffen K.L., Lynch J.P. Light and excess manganese: implications for oxidative stress in common bean. Plant Physiol. 118:1998;493-504.
56. Van Breusegem F., Slooten L., Stassart J.-M., Botterman J., Moens T., Montagu M.V., Inzé D. Effects of overproduction of tobacco MnSOD in maize chloroplast on foliar tolerance to cold and oxidative stress. J. Exp. Bot. 50:1999;71-78.
57. Bowler C., Van Montagu M., Inzé D. Superoxide dismutase and stress tolerance. Ann. Rev. Plant Physiol. Plant Mol. Biol. 43:1992;83-116.
58. G Allen R., Tresini M. Oxidative stress and gene regulation. Free Radic. Biol. Med. 28:2000;463-499.
59. Dinesh-Kumar S.P., Witham S., Choi D., Hehel R., Corr C., Baker B. Transposon tagging of tobacco mosaic virus resistance gene N: Its possible role in the TMV-N-mediated signal transduction pathway. Proc. Natl. Acad. Sci. U.S.A. 192:1995;4175-4180.
60. Baum J.A., Scandalios J.G. Multiple genes controlling superoxide dismutase expression in maize. J. Heredity. 73:1982;95-100.
61. Bowler C., Alliote T., De Loose M., Van Montagu M., Inzé D. The induction of manganese superoxide dismutase in response to stress in Nicotiana plumbaginifolia. EMBO J. 8:1989;31-38.
62. Mittler R., Zilinskas B.A. Molecular cloning and characterization of a gene encoding pea cytosolic ascorbate peroxidase. J. Biol. Chem. 267:1992;21802-21807.
63. Ievinsh G., Valcina A., Ozol D. Induction of ascorbate peroxidase-activity in stressed pine (Pinus sylvestris L.) needles - a putative role for ethylene. Plant Sci. 112:1995;167-173.