Skip to main content
Log in

Behaviour of antioxidant defense system in the adaptive response to salt stress in Helianthus annuus L. cells

  • Published:
Plant Growth Regulation Aims and scope Submit manuscript

Abstract

A relationship between the antioxidant defense system and salt tolerance in two types of sunflower calli differing in salt sensitivity was studied. No reduction in growth occurred in the NaCl-salt-adapted cell line (T) when grown on 175 mM NaCl but growth of the salt-stressed cell line (S) was reduced by 83%. Lipid peroxidation and protein oxidation increased during acute stress of salt stressed cells at 14 and 28 d of the experiment, while salt-adapted calli (T) remained similar to non-shocked (C) values. The antioxidant defense system of callus adapted to growth under NaCl responded differently to 175 mM of salt compared with the corresponding controls under shock treatment. Salt-adapted and salt-stressed calli showed a similar pattern in GSH content at day 14 but at day 28 in S calli, GSH content was increased 100% over the non-shocked calli, while T calli returned to the initial values. In the salt-stressed calli, a general decrease in all the antioxidant enzymes studied (except for glutathione reductase and dehydroascorbate reductase activities) was observed at day 28. Except for catalase, the antioxidant enzymes were elevated constitutively in adapted calli as compared to stressed cells, when both were grown in the absence of NaCl (time 0), and remained unaltered until 28 d after the beginning of the experiment. These results suggest the involvement of an enzymatic antioxidant defense system in the adaptive response to salt stress in Helianthus annuus L. cells.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Ahmad S. 1995. Oxidative Stress and Antioxidant Defenses in Biology. Chapman & Hall., New York.

    Google Scholar 

  • Anderson M.E. 1985. Determination of glutathione and glutathione disulfide in biological samples. Meth. Enzymol. 113: 548–554.

    Google Scholar 

  • Becana M., Aparico-Tejo P., Irigoyen J.J. and Sanchez-Diaz M. 1986. Some enzymes of hydrogen peroxide metabolism in leaves and root nodules of Medicago sativa. Plant Physiol. 82: 1169–1171.

    Google Scholar 

  • Bellaire B.A., Carmody J., Braud J., Gosset D.R., Banks S.W., Cran Lucas M. et al. 2000. Involvement of abscisic acid-dependent and independent pathways in the upregulation of antioxidant enzyme activity during NaCl stress in cotton callus tissue. Free Rad. Res. 33: 531–545.

    Google Scholar 

  • Benavides M.P., Marconi P.L., Gallego S.M., Comba M.E. and Tomaro M.L. 2000. Relationship between antioxidant defence systems and salt tolerance in Solanum tuberosum. Aus. J. Plant Physiol. 27: 273–278.

    Google Scholar 

  • Chance B., Sies H. and Boveris A. 1979. Hydroperoxide metabolism in mammalian organs. Physiol. Rev. 59: 527–605.

    Google Scholar 

  • Comba M.E., Benavides M.P. and Tomaro M.L. 1998. Effect of salt stress on antioxidant defence system in soybean root nodules. Aus. J. Plant Physiol. 25: 665–671.

    Google Scholar 

  • Gallego S.M., Benavides M.P. and Tomaro M.L. 1996. Effect of heavy metal ion excess on sunflower leaves: evidence for involvement of oxidative stress. Plant Sci. 121: 151–159.

    Google Scholar 

  • Giannopolitis C.N. and Ries S.K. 1977. Superoxide Dismutase, I. Occurrence in higher plants. Plant Physiol. 59: 309–314.

    Google Scholar 

  • Gosset D.R., Baris S.W., Millhollon E.P. and Cran Lucas M. 1996. Antioxidant response to NaCl stress in a control and an NaCltolerant cotton cell line grown in the presence of paraquat, buthionine sulfoximine, and exogenous glutathione. Plant Physiol. 112: 803–809.

    Google Scholar 

  • Gueta-Dahan Y., Yaniv Z., Zilinskas B.A. and Ben-Hayyim G. 1997. Salt and oxidative stress: similar and specific responses and their relation to salt tolerance in Citrus. Planta 203: 460–469.

    Google Scholar 

  • Heath R.L. and Packer L. 1968. Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Arch. Biochem. Biophys. 125: 189–198.

    Google Scholar 

  • Hernadez J.A., Jimenez A., Mullineaux P. and Sevilla F. 2000. Tolerance of pea (Pisum sativum L.) to long-term salt stress is associated with induction of antioxidant defences. Plant Cell. Environm. 23: 853–862.

    Google Scholar 

  • Hernandez J.A., Corpas F.J., Gomez M., del Rio L.A. and Sevilla F. 1993. Salt-induced oxidative stress mediated by activated oxygen species en pea leaf mitochondria. Physiol. Plantarum 89: 103–110.

    Google Scholar 

  • Hernandez J.A., Olmos E., Corpas F.J., Sevilla F. and del Rio L.A. 1995. Salt-induced oxidative stress in chloroplast of pea plants. Plant Sci. 105: 151–167.

    Google Scholar 

  • Levine R.L., Garland D., Oliver C.N., Amici A., Climent I., Lenz A.G. et al. 1990. Determination of carbonyl content in oxidatively modified protein. Meth. Enzymol. 186: 464–478.

    Google Scholar 

  • Lopez F., Vansuyt G., Casse-Delbart F. and Fourcroy P. 1996. Ascorbate peroxidase activity, not the mRNA level, is enhanced in salt-stress Raphanus sativus plants. Physiol. Plantarum 97: 13–20.

    Google Scholar 

  • Munns R. 1993. Physiological processes limiting plant growth in saline soils: some dogmas and hypothesis. Plant Cell Environ. 16: 15–24.

    Google Scholar 

  • Murashige T. and Skoog F. 1962. A revised medium for rapid growth and bioassays with tobacco tissue culture. Physiol. Plantarum 15: 473–497.

    Google Scholar 

  • Nakano Y. and Asada K. 1981. Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplast. Plant Cell Physiol. 22: 867–880.

    Google Scholar 

  • Noctor G. and Foyer C.H. 1998. Ascorbate and glutathione: Keeping active oxygen under control. Ann. Rev. Plant Physiol. Plant Mol. Biol. 49: 249–279.

    Google Scholar 

  • Scandalio L.M., Dalurzo H.C., Gómez M., Romero-Puertas M.C. and del Río L.A. 2001. Cadmium-induced changes in the growth and oxidative metabolism of pea plants. J. Exp. Bot. 52: 2115–2126.

    Google Scholar 

  • Schaedle M. and Bassham J.A. 1977. Chloroplast glutathione reductase. Plant Physiol. 59: 1011–1012.

    Google Scholar 

  • Schupp R. and Rennenberg H. 1988. Diurnal changes in the glutathione content of spruce needles (Picea abies L.). Plant Sci. 57: 113–117.

    Google Scholar 

  • Screenivasulu N., Grimm B., Wobus U. and Weschke W. 2000. Differential response of antioxidant compounds to salinity stress in salt-tolerant and salt-sensitive seedling of foxtail millet (Setaria italica). Physiol. Plantarum 109: 435–442.

    Google Scholar 

  • Singha S. and Choudhuri M.A. 1990. Effect of salinity (NaCl) stress on H2O2 metabolism in Vigna and Oryza seedlings. Biochem. Physiol. Pflanz 186: 69–74.

    Google Scholar 

  • Smirnoff N. 1998. Plant resistance to environmental stress. Cur. Opin. Biotech. 9: 214–219.

    Google Scholar 

  • Tsugane K., Kobayashi K., Niwa Y., Ohba Y., Wada K. and Kobayashi H. 1999. A recessive Arabidopsis mutant that grows photoautotrophically under salt stress shows enhance active oxygen detoxification. Plant Cell 7: 1195–1206.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Davenport, S.B., Gallego, S.M., Benavides, M.P. et al. Behaviour of antioxidant defense system in the adaptive response to salt stress in Helianthus annuus L. cells. Plant Growth Regulation 40, 81–88 (2003). https://doi.org/10.1023/A:1023060211546

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1023060211546

Navigation