Skip to main content
Log in

Differential response of antioxidative enzymes to various abiotic stresses in Pennisetum glaucum seedlings

  • Research Papers
  • Published:
Russian Journal of Plant Physiology Aims and scope Submit manuscript

Abstract

Antioxidative enzyme activities and their isozyme patterns under water-deficit, salinity, high and low temperature stresses were studied in the seedlings of Pennisetum glaucum (L.) R.Br. It was observed that under water-deficit stress glutathione reductase (GR) was the key enzyme while in case of high temperature stress, GR along with catalase played a major role. Superoxide dismutase was found to be the main enzyme under low temperature stress. Co-ordinated higher expression of all the antioxidative enzymes was observed under salt stress. This study revealed the operation of different enzymatic antioxidative mechanisms under various abiotic stresses that will aid in understanding the metabolic basis of stress tolerance in pearl millet.

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

Abbreviations

AOX:

antioxidative

APX:

ascorbate peroxidase

CAT:

catalase

GPX:

guaiacol peroxidase

GR:

glutathione reductase

SOD:

superoxide dismutase

References

  1. Hassanuzzaman, M., Hossain, M.A., Teixeira da Silva, J.A., and Fujita, M., Plant response and tolerance to abiotic oxidative stress: antioxidant defense is a key factor, in Crop Stress and Its Management: Perspectives and Strategies, Venkateswarlu, B., Shanker, A.K., Shanker, C., and Maheswari, M., Eds., Dordrecht, Heidelberg, New York: Springer, 2012, pp. 261–316. doi 10.1007/978-94-007-2220-0_8

    Chapter  Google Scholar 

  2. El-baky, A., Hanaa, H., Amal, M.A., and Hussei, M.M., Influence of salinity on lipid peroxidation, antioxidant enzymes and electrophoretic patterns of proteins and isozymes in leaves of some onion cultivars, Asian J. Plant Sci., 2003, vol. 2, pp. 633–638.

    Google Scholar 

  3. Lata, C., Jha, S., Dixit, V., Sreenivaasulu, N., and Prasad, M., Differential antioxidative responses to dehydration-induced oxidative stress in core set of foxtail millet cultivars [Setaria italica (L.)], Protoplasma, 2011, vol. 248, pp. 817–828. doi 10.1007/s00709-010-0257-y

    Article  CAS  PubMed  Google Scholar 

  4. Mukhopadhyay, R., Reddy, P.S., Pallela, R., Chakra Reddy, N., Venkateswara Rao, J., Hash, C.T., and Kavi Kishor, P.B., Differential responses of proline, ion accumulation and antioxidative enzyme activities in pearl millet [Pennisetum glaucum (L.) R. Br.] lines differing in salt sensitivity, J. Plant Biol., 2007, vol. 34, pp. 185–192.

    CAS  Google Scholar 

  5. Bidinger, F.R. and Hash, C.T., Pearl millet, physiology and biotechnology, in Integration for Plant Breeding, Nguyen, H.T. and Blum, A., Eds., New York: Marcel Dekker, 2003, pp. 225–270.

    Google Scholar 

  6. Barrs, H.D. and Weatherly, P.E., Are-examination of the relative turgidity technique for estimating water deficits in leaves, Aust. J. Biol. Sci., 1962, vol. 24, pp. 519–570.

    Google Scholar 

  7. Bates, L.S., Waldren, R.P., and Teare, I.D., Rapid determination of free proline for water stress studies, Plant Soil, 1973, vol. 39, pp. 205–207. doi 10.1007/BF00018060

    Article  CAS  Google Scholar 

  8. Arnon, D.I., Copper enzymes in isolated chloroplasts, polyphenoloxidase in Beta vulgaris, Plant Physiol., 1949, vol. 24, pp.1–15. doi org/10.1104/pp.24.1.1

    CAS  PubMed  Google Scholar 

  9. Sairam, R.K., Effect of moisture stress on physiological activities of two contrasting wheat genotypes, Indian J. Exp. Biol., 1994, vol. 32, pp. 584–593.

    Google Scholar 

  10. Heath, R.L. and Packer, L., Photo peroxidation in isolated chloroplasts: I. Kinetics and stoichiometry of fatty acid peroxidation, Arch. Biochem. Biophys., 1968, vol. 125, pp. 189–198. doi 10.1016/0003-9861(68)90654-1

    Article  CAS  PubMed  Google Scholar 

  11. Dhindsa, R.S., Dhindsa, P.P., and Throne, T.A., Leaf senescence: correlated with increased levels of membrane permeability and lipid peroxidation and decreased levels of superoxide dismutase and catalase, J. Exp. Bot., 1981, vol. 32, pp. 93–101. doi 10.1093/jxb/32.1.93

    Article  CAS  Google Scholar 

  12. Claiborne, A., Catalase activity, in CRC Handbook of Methods for Oxygen Radical Research, Greenwald, R.A., Ed., Boca Raton: CRC, 1985, pp. 283–284.

    Google Scholar 

  13. Smith, I.K., Vierheller, T.L., and Thorne, C.A., Assay of glutathione reductase in crude tissue homogenates using 5,5-dithio(2-nitobenzoic acid), Anal. Biochem., 1988, vol. 175, pp. 408–413. doi 10.1016/0003-2697(88)90564-7

    Article  CAS  PubMed  Google Scholar 

  14. Nakano, Y. and Asada, K., Hydrogen peroxide is scavenged by ascorbate specific peroxides in spinach chloroplasts, Plant Cell Physiol., 1981, vol. 22, pp. 867–880.

    CAS  Google Scholar 

  15. Chance, B. and Machly, A.C., Assay of catalase and peroxidases, Methods Enzymol., 1955, vol. 2, pp. 764–775. doi 10.1016/S0076-6879(55)02300-8

    Article  Google Scholar 

  16. Laemmli, U.K., Cleavage of structural proteins during the assembly of the head of bacteriophage T4, Nature, 1970, vol. 227, pp. 680–685.

    Article  CAS  PubMed  Google Scholar 

  17. Beauchamp, C.O. and Fridovich, I., Superoxide dismutase: improved assays and an assay applicable to acrylamide gels, Anal. Biochem., 1971, vol. 44, pp. 276–287. doi 10.1016/0003-2697(71)90370-8

    Article  CAS  PubMed  Google Scholar 

  18. Mittler, R. and Zilinskas, B.A., Regulation of pea cytosolic ascorbate peroxidase and other antioxidant enzymes during the progression of drought stress and following recovery from drought, Plant J., 1994, vol. 5, pp. 397–405. doi 10.1111/j.1365-313X.1994.00397.x

    Article  CAS  PubMed  Google Scholar 

  19. Rao, M.V., Paliyath, G., and Ormrod, D.P., Ultraviolet-B-and ozone-induced biochemical changes in antioxidant enzymes of Arabidopsis thaliana, Plant Physiol., 1996, vol. 110, pp. 125–136.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Birecka, H. and Garraway, M.O., Corn leaf isoperoxidase reaction to mechanical injury and infection with Helminthosporium maydis, Plant Physiol., 1975, vol. 61, pp. 561–566.

    Article  Google Scholar 

  21. Snedecor, G.W. and Cochran, W.G., Statistical Methods, New Delhi: IBH, 1967. doi 10.1177/001316446902900247

    Google Scholar 

  22. Sairam, R.K., Rao, K., and Srivastava, G.C., Differential response of wheat genotypes to long term salinity stress in relation to oxidative stress, antioxidant activity and osmolyte concentration, Plant Sci., 2002, vol. 163, pp.1037–1046. doi 10.1016/S0168-9452(02)00278-9

    CAS  Google Scholar 

  23. Vijayalakshmi, T., Varalaxmi, Y., Jainender, S., Yadav, S.K., Vanaja, M., Jyothilakshmi, N., and Maheswari, M., Physiological and biochemical basis of water-deficit stress tolerance in pearl millet hybrid and parents, Am. J. Plant Sci., 2012, vol. 3, pp. 1730–1740. doi 10.4236/ajps.2012.312211

    Article  CAS  Google Scholar 

  24. Houmani, H., Rodríguez-Ruiz, M., Palma, J.M., Chedly, A., and Francisco, J.C., Modulation of superoxide dismutase (SOD) isozymes by organ development and high long-term salinity in the halophyte Cakile maritima, Protoplasma, 2016, vol. 253, pp. 885–894. doi 10.1007/s00709-015-0850-1

    Article  CAS  PubMed  Google Scholar 

  25. Wang, C., Wen, D., Sun, A., Han, X., Zhang, J., Wang, Z., and Yin, Y., Differential activity and expression of antioxidant enzymes and alteration in osmolyte accumulation under high temperature stress in wheat seedlings, J. Cereal Sci., 2014, vol. 60, pp. 653–659. doi 10.1016/j.jcs.2014.05.004

    Article  CAS  Google Scholar 

  26. Xu, J., Yang, J., Duan, X., Jiang, Y., and Zhang, P., Increased expression of native cytosolic Cu/Zn superoxide dismutase and ascorbate peroxidase improves tolerance to oxidative and chilling stress in cassava (Manihot esculenta Crantz), BMC Plant Biol., 2014, vol. 14, p. 208. doi 10.1186/s12870-014-02

    Article  PubMed  PubMed Central  Google Scholar 

  27. Sharma, P., Jha, A.B., Dubey, R.S., and Pessarakli, M., Reactive oxygen species, oxidative damage and antioxidative defense mechanism in plants under stressful conditions, J. Bot., 2012, pp. 1–26. doi 10.1155/2012/217037.08-4

    Google Scholar 

  28. Liu, X., Hua, X., Guo, J., Qi, D., Wang, L., Liu, Z., Jin, S., and Chen, G., Enhanced tolerance to drought stress in transgenic tobacco plants overexpressing VTE1 for increased tocopherol production from Arabidopsis thaliana, Biotechnol. Lett., 2008, vol. 30, pp. 1275–1280. doi 200810.1007/s10529-008-9672-y

    Article  CAS  PubMed  Google Scholar 

  29. Heidari, M., Antioxidant activity and osmolyte concentration of sorghum (Sorghum bicolor) and wheat (Triticum aestivum) genotypes under salinity stress, Asian J. Plant Sci., 2009, vol. 8, pp. 240–244.

    Article  CAS  Google Scholar 

  30. Ghosh, N., Adak, M.K., and Ghosh, P.D., Sen Gupta, D.N., and Mandal, C., Differential response of two rice varieties to salt stress, Plant Biotechnol. Rep., 2011, vol. 5, pp. 89–103.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to M. Maheswari.

Additional information

The article is published in the original.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Vijaya Lakshmi, T., Varalaxmi, Y., Yadav, S.K. et al. Differential response of antioxidative enzymes to various abiotic stresses in Pennisetum glaucum seedlings. Russ J Plant Physiol 64, 889–898 (2017). https://doi.org/10.1134/S1021443717060061

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S1021443717060061

Keywords

Navigation