Interactive effect of nitric oxide and brassinosteroids on photosynthesis and the antioxidant system of Lycopersicon esculentum

Russian Journal of Plant Physiology

Volumn 57, Issue 2, 2010, Pages 212-221

  Hayat, Sh ^a   Yadav, S ^a   Ali, B ^b   Ahmad, A ^c  

^a ALIGARH MUSLIM UNIVERSITY   (India)

^b Government College for Women   (India)

^c HIGHER COLLEGE OF TECHNOLOGY   (Oman)

Author keywords

Antioxidants; Growth; Lipid peroxidation; Lycopersicon esculentum; Photosynthesis

Indexed keywords

LYCOPERSICON ESCULENTUM;

EID: 77952014907     PISSN: 10214437     EISSN: None     Source Type: Journal    
DOI: 10.1134/S1021443710020081     Document Type: Article

References (30)

1. Leshem, Y. Y., Nitric Oxide in Plants: Occurrence, Function and Use, Dordrecht: Kluwer, 2000.
2. Guo, F., Okamoto, M., and Crawford, N. M., Identification of a Plant Nitric Oxide Synthase Gene Involved in Hormonal Signaling, Science, 2003, vol. 302, pp. 100-103.
3. Neill, S. J., Desikan, R., and Hancock, J. T., Nitric Oxide Signaling in Plants, New Phytol., 2003, vol. 159, pp. 11-35.
4. Arasimowicz, M. and Floryszak-Wieczorek, J., Nitric Oxide as a Bioactive Signaling Molecule in Plant Stress Responses, Plant Sci., 2007, vol. 172, pp. 876-887.
5. Stoehr, C. and Ulrich, W. R., Generation and Possible Roles of NO in Plant Roots and Their Apoplastic Space, J. Exp. Bot., 2002, vol. 53, pp. 2293-2303.
6. Kramlinch, J. C. and Linak, W. P., Nitrous Oxide Behavior in the Atmosphere and in Combustion and Industrial Systems, Prog. Energy Combus. Sci., 1994, vol. 20, pp. 149-202.
7. Sasse, J. M., Physiological Actions of Brassinosteroids: An Update, J. Plant Growth Regul., 2003, vol. 22, pp. 276-288.
8. Ali, B., Hayat, S., and Ahmad, A., 28-Homobrassinolide Ameliorates the Saline Stress in Chickpea (Cicer arietinum L.), Environ. Exp. Bot., 2007, vol. 59, pp. 217-223.
9. Hasan, S. A., Hayat, S., Ali, B., and Ahmad, A., 28-Homobrassinolide Protects Chickpea (Cicer arietinum) from Cadmium Toxicity by Stimulating Antioxidants, Environ. Pollut., 2008, vol. 151, pp. 60-66.
10. Lichtenthaler, H. K., Chlorophylls and Carotenoids: Pigments of Photosynthetic Biomembranes, Methods Enzymol., 1987, vol. 148, pp. 350-382.
11. Hodges, M. D., DeLong, J. M., Forney, C. F., and Prange, R. K., Improving the Thiobarbituric Acid Reactive Substances Assay for Lipid Peroxidation in Plant Tissues Containing Anthocyanin and Other Interfering Compounds, Planta, 1999, vol. 207, pp. 604-611.
12. Terasaki, S., Sakurai, N., Yamamoto, R., Wada, N., and Nevins, D. J., Changes in Cell Wall Polysaccharides of Kiwifruit and the Viscoelastic Properties Detected by Laser Doppler Method, J. Jap. Soc. Hortic. Sci., 2001, vol. 70, pp. 572-580.
13. Zhang, M., An, L., Feng, H., Chen, T., Chen, K., Liu, Y., Tang, H., Chang, J., and Wang, X., The Cascade Mechanisms of Nitric Oxide as a Second Messenger of Ultraviolet-B in Inhibiting Mesocotyl Elongations, Photochem. Photobiol., 2003, vol. 77, pp. 219-225.
14. Beligni, M. V. and Lamattina, L., Nitric Oxide Stimulates Seed Germination and De-Etiolation and Inhibits Hypocotyls Elongation, Three Light Inducible Responses in Plants, Planta, 2000, vol. 210, pp. 215-221.
15. Felner, M., Recent Progress in Brassinosteroid Research: Hormone Perception and Signal Transduction, Brassinosteroids: Bioactivity and Crop Productivity, Hayat, S. and Ahmad, A., Eds., Dordrecht: Kluwer, 2003, pp. 69-86.
16. Cosgrove, D., Relaxation in a High Stress Environment: The Molecular Basis of Extensible Cell Walls and Enlargement, Plant Cell, 1997, vol. 9, pp. 1031-1041.
17. Ali, B., Hayat, S., Hasan, S. A., and Ahmad, A., Effect of Root Applied 28-Homobrassinolide on the Performance of Lycopersicon esculentum, Sci. Hortic., 2006, vol. 110, pp. 267-273.
18. Garcia-Mata, C. and Lamattina, L., Nitric Oxide Induces Stomatal Closure and Enhances the Adaptive Plant Responses against Drought Stress, Plant Physiol., 2001, vol. 126, pp. 1196-1204.
19. Tiwari, A., Kumar, P., Singh, S., and Ansari, S. A., Carbonic Anhydrase in Relation to Higher Plants, Photosynthetica, 2005, vol. 43, pp. 1-9.
20. Yu, J. Q., Huang, L. F., Hu, W. H., Zhou, Y. H., Mao, W. H., Ye, S. F., and Nogues, S., A Role of Brassinosteroids in the Regulation of Photosynthesis in Cucumis sativus, J. Exp. Bot., 2004, vol. 55, pp. 1135-1143.
21. Beligni, M. V. and Lamattina, L., Nitric Oxide Counteracts Cytotoxic Processes Mediated by Reactive Oxygen Species in Plant Tissue, Planta, 1999, vol. 208, pp. 337-344.
22. Campbell, H. W., Nitrate Reductase Structure, Function and Regulation. Bridging the Gap between Biochemistry and Physiology, Annu. Rev. Plant Physiol. Plant Mol. Biol., 1999, vol. 50, pp. 277-303.
23. Kulaeva, O. N., Burakhanova, E. A., Fedina, A. B., Khokhlova, V. A., Bokebayeva, G. A., Vorbrodt, H. M., and Adam, G., Effect of Brassinosteroid on Protein Synthesis and Plant Cell Ultrastructure under Stress Condition, ACS Symp., Ser. 474, Brassinosteroids: Chemistry, Bioactivity and Applications, Cutler, H. G., Yokata, T., and Adam, G., Eds., Washington: Am. Chem. Soc., 1999, pp. 141-155.
24. Dawson, T. M., Nitric Oxide, PARP and Other Perpetrators Relevant to Stroke and Neurodegeneration, Progress in Brain Research, 1998, http://www. pas-teur. fr/conf/nitricabstracts. html.
25. Kehrer, J., Free Radicals as Mediators of Tissue Injury and Diseases, Crit. Rev. Toxicol., 1993, vol. 23, pp. 21-48.
26. Kanner, J., Harel, S., and Granit, R., Nitric Oxide as an Antioxidant, Arch. Biochem. Biophys., 1991, vol. 289, pp. 130-136.
27. Joshi, M. S., Ponthier, J. L., and Lancaster, J. R., Cellular Antioxidant and Prooxidant Actions of Nitric Oxide, Free Radic. Biol. Med., 1999, vol. 27, pp. 1357-1366.
28. Lamattina, L., Garcia-Mata, C., Graziano, M., and Pagnussat, G., Nitric Oxide: The Versatility of an Extensive Signal Molecule, Annu. Rev. Plant Biol., 2003, vol. 54, pp. 109-136.
29. Halliwell, B. and Gutteridge, J. M. C., Free Radicals in Biology and Medicine, London: Oxford Univ. Press, 1999.
30. Cao, S., Xu, Q., Cao, Y., Qian, K., An, K., Zhu, Y., Binzeng, H., Zhao, H., and Kuai, B., Loss of Function Mutations in Det2 Gene Lead to an Enhanced Resistance to Oxidative Stress in Arabidopsis, Physiol. Plant., 2005, vol. 123, pp. 57-66.