Effects of salt stress on antioxidant and ascorbate glutathione cycle enzyme activities in Pokkali rice varieties – Vytilla 1-9

Authors

  • Lins Simon Inter University Centre for Plant Biotechnology, Department of Botany, University of Calicut, Kerala 673 635, India
  • Akkara Yusuf Inter University Centre for Plant Biotechnology, Department of Botany, University of Calicut, Kerala 673 635, India http://orcid.org/0000-0002-1931-5278

DOI:

https://doi.org/10.14719/pst.2020.7.3.701

Keywords:

Antioxidant enzymes, Pokkali rice, Ascorbate- glutathione cycle, Rice, Salt tolerance

Abstract

The enzymatic and non-enzymatic antioxidant levels in the released salt tolerant Pokkali, (vytilla, VTL 1-9) varieties were studied under different NaCl concentrations (0-150 mM NaCl). The specific activity of superoxide dismutase (SOD), catalase (CAT) and ascorbate-glutathione cycle enzymes and non-enzymatic antioxidants like superoxide (O2-), hydrogen peroxide (H2O2), malondialdehyde (MDA), glutathione (GSH) and ascorbic acid (AsA) was determined in plants exposed to salt stress. IR-28 was used as positive control and the VTL varieties were used as negative control. The H2O2 and superoxide (O2-) contents were higher in IR-28 at all the applied concentrations of NaCl. The VTL varieties without salt treatment did not evoke any response substantiating the role of salt priming in antioxidant signalling. The MDA contents were higher in the positive and negative control. MDA content was reduced in the NaCl treated VTL varieties. In the positive and negative control varieties, the quantity of ascorbate and glutathione contents were lesser and upregulated in salt treated VTL varieties. Highest H2O2 content was observed in 150 mM NaCl treatment. The H2O2 contents decreased with the increase in all concentrations of NaCl and lowest H2O2 contents was observed in VTL-1 and highest in VTL-2 and VTL-8 treated with 150 mM NaCl. Superoxide contents varied in all the nine varieties depending on the salt concentration. The SOD levels in all the varieties showed a positive correlation with the superoxide and H2O2 content. Lesser quantities of SOD, CAT and the ascorbate - glutathione cycle enzymes were expressed in the positive and negative control. The increased NaCl concentration (25-150 mM) upregulated antioxidant and ascorbate-glutathione cycle enzymes in the VTL varieties. The APX activity was lower in the control and salt treated plants. The GR activity increased linearly in all the varieties with respect to salt concentrations. The MDHAR and DHAR activities showed marginally linear increase, with all concentrations of NaCl. The APX activity was similar or lower to MDHAR activity while DHAR activity was similar to MDHAR activity. The results of the present study reveals the higher levels of enzymatic and non-enzymatic antioxidants under salt stress reflect the salt tolerance potential of pokkali varieties mediated by the up regulation of ROS scavenging enzymes.

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Author Biographies

Lins Simon, Inter University Centre for Plant Biotechnology, Department of Botany, University of Calicut, Kerala 673 635, India

Lins Simon, a postgraduate in Botany from Bharathiar University, Tamil Nadu, India, is currently pursuing PhD in Botany from Interuniversity Centre for Plant Biotechnology, Department of Botany, University of Calicut. His research interests cover several aspects across plant biochemistry, plant physiology and plant biotechnology.

Akkara Yusuf, Inter University Centre for Plant Biotechnology, Department of Botany, University of Calicut, Kerala 673 635, India

Dr. A. Yusuf, a postgraduate in Botany from University of Calicut, Kerala, India, awarded PhD in Plant Biotechnology from Jai NarainVyas University, Jodhpur, India on Micropropagation and somatic cell genetics of some trees of arid regions. He published 30 International papers and presented research papers in various National and International conferences, isolated and published more than 150 gene sequences. He secured VATAT International fellowship from Govt. of Israel for post-doctoral research. He has completed 2 major research projects funded by UGC and KSCSTE. He ispresently working as Assistant Professor at Department of Botany, University of Calicut.

References

1. Song T, Zhang Q, Wang H, Han J, Xu Z, Yan S, Zhu Z. OsJMJ703, a rice histone demethylase gene, plays key roles in plant development and responds to drought stress. Plant Physiology and Biochemistry. 2018;132:183-88. https://doi.org/10.1016/j.plaphy.2018.09.007

2. Jayan PR, Sathyanathan N. Overview of farming practices in the water-logged areas of Kerala, India. International Journal of Agricultural and Biological Engineering. 2010;3(4),28-43. https://doi.org/10.3965/j.issn.1934-6344.2010.04.018-03

3. Del Rio LA, Corpas FJ, Sandaliyo LM, Palma JM, Gomez M, Borroso JB. Reactive oxygen species, antioxidant systems and nitric oxide in peroxisomes. J Exp Bot. 2002;53(372):1255-72. https://doi.org/10.1093/jexbot/53.372.1255

4. Levine A. Oxidative stress as a regulator of environmental response in plants In: Lerner H.R. (editor). Plant Responses to Environmental Stresses from Phytohormones to Genome reorganisation. Marcel Dekker Inc., New York, NY. 1999;247-64. https://doi.org/10.1201/9780203743157-11

5. Asada K. Radical production and scavenging in chloroplasts. In: Baker N.R. (editor) Photosynthesis and Environment. Kluwer Academic Publisher, Dordrecht, The Netherlands. 1996;123-50. https://doi.org/10.1007/0-306-48135-9_5

6. Yu Q, Rengel Z. Drought and salinity differentially influence activites of superoxide dismutase in narrow leafed lupins. Plant Sci. 1999;142:1-11. https://doi.org/10.1016/S0168-9452(98)00246-5

7. Smirnoff N. The role of active oxygen in response of plants to water deficit and desiccation. New Phytol. 1993;125:27-58. https://doi.org/10.1111/j.1469-8137.1993.tb03863.x

8. Prasard TK, Anderson MD, Martin BA, Stewart CR. Evidence for chilling –induced oxidative stress in maize seedlings and a regulatory role for hydrogen peroxide. Plant Cell. 1994;6:65-74. https://doi.org/10.1105/tpc.6.1.65

9. Bowler C, Van Montagu M, Inze D. Superoxide dismutase and stress tolerance. Annu Rev Plant Physiol. Plant Mol Biol. 1992;43:83-116. https://doi.org/10.1146/annurev.pp.43.060192.000503

10. Foyer CH, Noctor G. Oxygen processing in photosynthesis: Regulation and signalling. New Phytol. 2000;146:359-388. https://doi.org/10.1046/j.1469-8137.2000.00667.x

11. Rossatto T, do Amaral MN, Benitez LC, Vighi IL, Braga EJB, de MagalhaesJúnior A M, da Silva Pinto L.Gene expression and activity of antioxidant enzymes in rice plants, cv. BRS AG, under saline stress. Physiology and Molecular Biology of Plants. 2017;23(4):865-75. https://doi.org/10.1007/s12298-017-0467-2

12. Guo WL, Chen RG, Gong ZH, Yin YX,Ahmed SS, He YM. Exogenous abscisic acid increases antioxidant enzymes and related gene expression in pepper (Capsicum annuum) leaves subjected to chilling stress. Genet. Mol. Res. 2012;11(4):4063-80. http://dx.doi.org/10.4238/2012.September.10.5

13. Mittova V, Tal M, Volokita M, Guy M. Up regulation of the leaf mitochondrial and peroxisomal antioxidant systems in response to salt-induced oxidative stress in the wild salt-tolerant tomato species Lycopersicon pennellii. Plant cell and Environ. 2003;26:845-56. https://doi.org/10.1046/j.1365-3040.2003.01016.x

14. Kaur N, Dhawan M, Sharma I, Pati PK. Interdependency of Reactive Oxygen Species generating and scavenging system in salt sensitive and salt tolerant cultivars of rice. BMC Plant Biology. 2016;16:131. https://doi.org/10.1186/s12870-016-0824-2

15. Li C, Bai T, Maa F, Hana M. Hypoxia tolerance and adaptation of anaerobic respiration to hypoxia stress in two Malus species. SciHortic. 2010;124:274–79. https://doi.org/10.1016/j.scienta.2009.12.029

16. Velikova V, Yordanov I, Edreva A. Oxidative stress and some antioxidant systems in acid rain-treated bean plants. Plant Sci. 2000;151:59–66. https://doi.org/10.1016/S0168-9452(99)00197-1

17. Stewart RR, Bewley JD. Lipid peroxidation associated with accelerated aging of soybean axes. Plant Physiology. 1980;65(2):245-48. https://doi.org/10.1104/pp.65.2.245

18. Chen JX, Wang XF. Guide to plant physiological experiments. Guangehou: South China University of Technology Press. 2002;pp.123-27.

19. Srivastava SK, Beutler E. Accurate measurement of oxidized glutathione content of human, rabbit and rat red blood cells and tissues. Analytical Biochemistry. 1968;25,70-76. https://doi.org/10.1016/0003-2697(68)90082-1

20. Giannopolitis CN, Ries KS. Superoxide Dismutases II. Purification and quantitative relationship with water-soluble protein in seedlings. Plant Physiol. 1977;59(2):315–18. https://doi.org/10.1104/pp.59.2.315

21. Aebi H. Catalase. In: Bergmeies H (editor), Methods of enzyme analysis. ChemieWenhein, Verlag. 1983; 273–77.

22. Nakano Y, Asada K. Hydrogen peroxide is scavenged by ascorbate specific peroxidase in spinach chloroplasts. Plant Cell Physiol. 1981;22:867–80. https://doi.org/10.1093/oxfordjournals.pcp.a076232

23. Smith IK, Vierheller TL, Thorne CA. Assay of glutathione reductase in crude tissue homogenates using 5, 5' dithiobis (2- nitrobenzoic acid). Ann Biochem. 1988;175:408–13. https://doi.org/10.1016/0003-2697(88)90564-7

24. Hossain NA, Asada K. Purification of dehydro ascorbate reductase from spinach and its characterization as a thiol enzyme. Plant and Cell Physiol. 1984;25:85–92. https://doi.org/10.1093/oxfordjournals.pcp.a076700

25. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951;193:265–75.

26. Shabala S, Wua H, Bose J. Salt stress sensing and early signalling events inplant roots: Current knowledge and hypothesis. Plant Sci. 2015;241:109–19. https://doi.org/10.1016/j.plantsci.2015.10.003

27. Chawla S, Jain S, Jain V. Salinity induced oxidative stress and antioxidant system in salt tolerant and salt sensitive cultivars of rice (Oryza sativa L.) J Plant Biochem Biotechnol. 2013;22(1):27- 34. https://doi.org/10.1007/s13562-012-0107-4

28. Gill SS, Tutej N. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol Biochem. 2000;48:909-30. https://doi.org/10.1016/j.plaphy.2010.08.016

29. Wang Y, Li X, Li J, Bao Q, Zhang F, Tulaxi G. Wang Z. Salt-induced hydrogen peroxide is involved in modulation of antioxidant enzymes in cotton. The Crop Journal. 2016;4:490-98. https://doi.org/10.1016/j.cj.2016.03.005

30. Jalali P, Navabpour S, Yamchi A, Soltanloo H, Bagherikia S. Differential responses of antioxidant system and expression profile of some genes of two rice genotypes in response to salinity stress. Biologia. 2019;1-9. https://doi.org/10.2478/s11756-019-00393-x

31. Salwa AO, Mona GD, Salman SR. Comparative study between the physiological role of hydrogen peroxide and salicylic acid in alleviating the harmful effect of low temperature on tomato plants grown under sand ponic culture. Sci Agric. 2015;9:49–59. https://doi.org/10.15192/PSCP.SA.2015.1.9.4959

32. Sofo A, Scopa A, Nuzzaci M, Vitti A. Ascorbate peroxidase and CAT activities and their genetic regulation in plants subjected to drought and salinity stresses. Int J Mol Sci. 2015;16:13561–78. https://doi.org/10.3390/ijms160613561

33. Davey MW, Stals E, Panis B, Keulemans J, Swennen RL. High-throughput determination of malondialdehyde in plant tissues. Anal Biochem. 2005;347:201–07. https://doi.org/10.1016/j.ab.2005.09.041

34. Bor M, Ozdemir F, Turkan TO. The effects of salt stress on lipid peroxidise and antioxidants in leaves of sugar beet, Beta vulgaris L. and wild beet Beta maritime L. Plant Science. 2003;164(1):77-84. https://doi.org/10.1016/S0168-9452(02)00338-2

35. Mallick S, Sinam G, Sinha S. Study on arsenate tolerant and sensitive cultivars of Zea mays L.: differential detoxification mechanism and effect on nutrients status. Ecotoxicology and Environmental Safety. 2011;74(5),1316-24. https://doi.org/10.1016/j.ecoenv.2011.02.012

36. Scandalios JG. Molecular genetics of superoxide dismutase in plants In: Scandalios JG (editor) Oxidative Stress and Molecular Biology of Antioxidant Defences (Cold Spring Harbor Laboratory Press, New York). 1997; pp.527-68.

37. Corpas F, Gomez JM, Hernandez JA, Del-Rio JA. Metabolism of activated oxygen in leaf peroxisomes from two Pisum sativum L. cultivars with different sensitivity to sodium chloride. J Plant Physiol. 1993;141:160–65. https://doi.org/10.1016/S0176-1617(11)80753-4

38. Noctor G, Foyer C. Ascorbate and Glutathione: Keeping active oxygen under control. Annual Review of Plant Physiology and Plant Mol Biol. 1998;49:249-79. https://doi.org/10.1146/annurev.arplant.49.1.249

39. Hasanuzzaman M, Nahar K, Anee TI, Fujita M. Glutathione in plants: biosynthesis and physiological role in environmental stress tolerance Physiol Mol Biol Plants. 2017;23:249-68. https://doi.org/10.1007/s12298-017-0422-2

40. Li J, Hu L, Zhang L, Pan X, Hu X. Exogenous spermidine is enhancing tomato tolerance to salinity–alkalinity stress by regulating chloroplast antioxidant system and chlorophyll metabolism. BMC Plant Biology. 2015;15(1):303. https://doi.org/10.1186/s12870-015-0699-7

41. Mittova V, Guy M, Tal M, Volokita M. Response of the cultivated tomato and its wild salt tolerant relative Lycopersicon pennelli to salt dependant oxidative stress: Increased activities of antioxidant enzymes in root plastids. Free Rad. Res. 2002;36(2):195-202. https://doi.org/10.1080/10715760290006402

42. Bleau G, Giasson C, Burnette I. Measurement of Hydrogen peroxide in biological samples containing high levels of ascorbic acid. Ann Biochem. 1998;263:13-17. https://doi.org/10.1006/abio.1998.2801

43. El-Shabrawi H, Kumar B, Kaul T, Reddy MK, Singla-Pareek SL, Sopory SK. Redox homeostasis, antioxidant defense and methylglyoxal detoxification as markers for salt tolerance in Pokkali rice. Protoplasma. 2010;245:85–96. https://doi.org/10.1007/s00709-010-0144-6

Published

01-07-2020

How to Cite

1.
Simon L, Yusuf A. Effects of salt stress on antioxidant and ascorbate glutathione cycle enzyme activities in Pokkali rice varieties – Vytilla 1-9. Plant Sci. Today [Internet]. 2020 Jul. 1 [cited 2024 May 10];7(3):341-8. Available from: https://horizonepublishing.com/journals/index.php/PST/article/view/701

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Research Articles