Skip to main navigation menu Skip to main content Skip to site footer

Research Articles

Early Access

Identification of the responsiveness of some enzymes of the antioxidant system of the biotechnological cotton variety to salt stress

DOI
https://doi.org/10.14719/pst.9921
Submitted
9 June 2025
Published
10-10-2025
Versions

Abstract

In this article, we studied the responsiveness of the antioxidant system of the biotechnological cotton variety to salt stress. We compared the reaction of two salt-resistant cotton varieties to elevated concentrations of sodium chloride (NaCl) and sodium sulfate (Na2SO4). To obtain more complete information about the resistance of the biotechnological variety to salt stress, we analyzed the activity of certain enzymes in the antioxidant system as well as the level of malondialdehyde (MDA). Plants respond to salt stress through the highly regulated protective enzymes such as MDA and superoxide dismutase (SOD), which enhance their ability to neutralize reactive oxygen species (ROS). Such abiotic stressors disrupt the ionic and osmotic balance of the cells. In this study, the activity of the antioxidant system of cotton (MDA and SOD) was determined in the leaves of seedlings grown in the laboratory under saline conditions. The stress resistance of plants and the accumulation of antioxidant enzymes in cotton have been thoroughly investigated in various experiments. The plant material used in this study was the Porloq-4 cotton variety, developed through individual selection of lines obtained by crossing the RNAi Coker-312 line with the commercial Namangan-77 variety. The object of this study was the modified Porloq-4 cotton genotype, while the parental Coker-312 genotype served as the control. Findings indicate that Porloq-4 and Coker-312 cotton varieties respond differently to stress induced by NaCl and Na2SO4 and their combination, with Porloq-4 exhibited a more active and responsive antioxidant enzyme system.

References

  1. 1. Yu Z, Duan X, Luo L, Dai S, Ding Z, Xia G. How plant hormones mediate salt stress responses. Trends Plant Sci. 2020;25(11):1117–30. https://doi.org/10.1016/j.tplants.2020.06.008
  2. 2. Verma V, Ravindran P, Kumar PP. Plant hormone-mediated regulation of stress responses. BMC Plant Biol. 2016;16:86. https://doi.org/10.1186/s12870-016-0771-y
  3. 3. Ku YS, Sintaha M, Cheung MY, Lam HM. Plant hormone signaling crosstalks between biotic and abiotic stress responses. Int J Mol Sci. 2018;19(10):3206. https://doi.org/10.3390/ijms19103206
  4. 4. Isayenkov SV, Maathuis FJM. Plant salinity stress: Many unanswered questions remain. Front Plant Sci. 2019;10:80. https://doi.org/10.3389/fpls.2019.00080
  5. 5. Ji X, Tang J, Zhang J. Effects of salt stress on the morphology, growth and physiological parameters of Juglans microcarpa L. seedlings. Plants (Basel). 2022;11(18):2381. https://doi.org/10.3390/plants11182381
  6. 6. Hannachi S, Steppe K, Eloudi M, Mechi L, Bahrini I, Van Labeke MC. Salt stress induced changes in photosynthesis and metabolic profiles of one tolerant ('Bonica') and one sensitive ('Black Beauty') eggplant cultivars (Solanum melongena L.). Plants (Basel). 2022;11(5):590. https://doi.org/10.3390/plants11050590
  7. 7. Rafaliarivony S, Ranarijaona HLT, Rasoafalimanana M, Radanielina T, Wissuwa M. Evaluation of salinity tolerance of lowland rice genotypes at the reproductive stage. Afr J Agric Res. 2022;18(1):16–24. https://doi.org/10.5897/AJAR2022.16229
  8. 8. Balasubramaniam T, Shen G, Esmaeili N, Zhang H. Plants' response mechanisms to salinity stress. Plants (Basel). 2023;12(12):2253. https://doi.org/10.3390/plants12122253
  9. 9. Rakhmatova NR, Imamkhodzhaeva AS, Buriev ZT. Monitoring proline and salicylic acid accumulation in the leaves of a biotechnological cotton variety under salt stress. Niva Povolzhya. 2024;3(71):1001. https://doi.org/10.36461/NP.2024.71.3.006
  10. 10. Rakhmatova N, Imamkhodjayeva A, Uzbekov V, Ubaydullaeva K, Zuparova D. Comparative analysis of the content of salicylic acid in biotechnological cotton genotypes under some kinds of abiotic stress. Sci Horiz. 2023;26(1):43-51. https://doi.org/10.48077/scihor.26(1).2023.43-51
  11. 11. Heath RL, Packer L. Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys. 1968;125(1):189–98. https://doi.org/10.1016/0003-9861(68)90654-1
  12. 12. Leonowicz G, Trzebuniak KF, Zimak-Piekarczyk P, Ślesak I, Mysliwa-Kurdziel B. The activity of superoxide dismutases (SODs) at the early stages of wheat deetiolation. PLoS One. 2018;13(3):e0194678. https://doi.org/10.1371/journal.pone.0194678
  13. 13. Reich M, Aghajanzadeh T, Stuiver CEE, Koralewska A, De Kok LJ. Impact of sulfate salinity on the uptake and metabolism of sulfur in Chinese cabbage. In: De Kok LJ, Rennenberg H, editors. Molecular Physiology and Ecophysiology of Sulfur. Cham: Springer; 2015. p. 227–38. https://doi.org/10.1007/978-3-319-20137-5_25
  14. 14. Abogadallah GM. Antioxidative defense under salt stress. Plant Signal Behav. 2010;5(4):369–74. https://doi.org/10.4161/psb.5.4.10873
  15. 15. Sharif I, Aleem S, Farooq J, Rizwan M, Younas A, Sarwar G, Chohan SM. Salinity stress in cotton: Effects, mechanism of tolerance and its management strategies. Physiol Mol Biol Plants. 2019;25(4):807–20. https://doi.org/10.1007/s12298-019-00676-2
  16. 16. Saleh B. Effect of salt stress on growth and chlorophyll content of some cultivated cotton varieties grown in Syria. Commun Soil Sci Plant Anal. 2012;43(15):1976–83. https://doi.org/10.1080/00103624.2012.693229
  17. 17. Zhao G, Song Y, Wang Q, Yao D, Li D, Qin W, et al. Gossypium hirsutum salt tolerance is enhanced by overexpression of G. arboreum JAZ1. Front Bioeng Biotechnol. 2020;8:157. https://doi.org/10.3389/fbioe.2020.00157
  18. 18. Harinasut P, Tsutsui K, Takabe T, Nomura M, Takabe T, Kishitani S. Exogenous glycinebetaine accumulation and increased salt-tolerance in rice seedlings. Biosci Biotechnol Biochem. 1996;60(2):366–68. https://doi.org/10.1271/bbb.60.366
  19. 19. Kohli SK, Khanna K, Bhardwaj R, Abd Allah EF, Ahmad P, Corpas FJ. Assessment of subcellular ROS and NO metabolism in higher plants: Multifunctional signaling molecules. Antioxidants (Basel). 2019;8(12):641. https://doi.org/10.3390/antiox8120641

Downloads

Download data is not yet available.