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Changes in the activity of pro-/antioxidants in spring barley (Hordeum vulgare L.) seedlings under salt stress conditions upon seed treatment with chitosan-hydroxycinnamic acid conjugates

https://doi.org/10.29235/1029-8940-2026-71-3-204-218

Abstract

The effect of seed treatment with chitosan ferulic acid (Ch30-FA) or caffeic acid (Ch30-CA) conjugates on biometric parameters and pro-/antioxidant system activity in spring barley seedlings (Hordeum vulgare L.) was studied under optimal conditions, salt stress, and subsequent recovery. The Ch30-CA conjugate exerted a mild stress effect, triggering compensatory mechanisms that include activation of cellular repair processes and, likely, de novo enzyme synthesis. Treatment with chitosan–hydroxycinnamic acid conjugates, especially Ch30-CA, contributed to sustained high activity of antioxidant enzymes (SOD, POD, APX, GR) and low hydrogen peroxide accumulation in the roots and leaves of barley seedlings under salt stress and during the recovery period. This phenomenon resulted in enhanced adaptive response and accelerated growth of barley seedlings. Differences in the effects of the two conjugates on plants were observed. When applied during the transition from short-term salt stress to the post-stress period, the Ch30-FA conjugate reduced proline content in the leaves, whereas treatment with the Ch30-CA conjugate increased proline content. During the recovery period, POD and GR activities in the leaves increased under Ch30-CA treatment compared to salt stress, while they remained almost unchanged in leaves of plants treated with Ch30-FA.

About the Authors

I. A. Ovchinnikov
V. F. Kuprevich Institute of Experimental Botany of the National Academy of Sciences of Belarus
Belarus

Igor A. Ovchinnikov – Researcher, Postgraduate Student

27, Akademicheskaya Str., 220072, Minsk



J. N. Kalatskaja
V. F. Kuprevich Institute of Experimental Botany of the National Academy of Sciences of Belarus
Belarus

Joanna N. Kalatskaja – Ph. D. (Biol.), Associate Professor, Leading Researcher

27, Akademicheskaya Str., 220072, Minsk



V. V. Nikalaichuk
V. F. Kuprevich Institute of Experimental Botany of the National Academy of Sciences of Belarus
Belarus

Viktoria V. Nikalaichuk – Researcher, Postgraduate Student

27, Akademicheskaya Str., 220072, Minsk



K. S. Hileuskaya
V. F. Kuprevich Institute of Experimental Botany of the National Academy of Sciences of Belarus
Belarus

Kseniya S. Hileuskaya – Ph. D. (Chem.), Associate Professor, Leading Researcher

27, Akademicheskaya Str., 220072, Minsk



Е. Недведь
Институт экспериментальной ботаники имени В. Ф. Купревича Национальной академии наук Беларуси
Belarus


References

1. Global status of salt-affected soils. Main report. FAO. Rome, 2024. 240 p. Available at: https://openknowledge.fao.org/server/api/core/bitstreams/32d3b78b-d720-4f54-9163-70f55039dbb9/content (accessed 29.05.2026).

2. Demidchik V. Mechanisms of oxidative stress in plants: From classical chemistry to cell biology. Environmental and Experimental Botany, 2015, vol. 109, pp. 212–228. https://doi.org/10.1016/j.envexpbot.2014.06.021

3. Mittler R. Oxidative stress, antioxidants and stress tolerance. Trends in Plant Science, 2002, vol. 7, no. 9, pp. 405–410. https://doi.org/10.1016/s1360-1385(02)02312-9

4. Ahmad P., Sarwat M., Sharma S. Reactive oxygen species, antioxidants and signaling in plants. Journal of Plant Biology, 2008, vol. 51, no. 3, pp. 167–173. https://doi.org/10.1007/bf03030694

5. Hasanuzzaman M., Bhuyan M. H. M. B., Anee T. I., Parvin K., Nahar K., Al Mahmud J., Fujita M. Regulation of Ascorbate-Glutathione Pathway in Mitigating Oxidative Damage in Plants under Abiotic Stress. Antioxidants, 2019, vol. 8, no. 9, art. 384. https://doi.org/10.3390/antiox8090384

6. Popova E. V., Domnina N. S., Sokornova S. V., Kovalenko N. M., Tyuterev S. L. Inovel hybrid modulators of plant immune responses based on chitosan and bioactive anti-oxidants and pro-oxidants. Sel’skokhozyaistvennaya biologiya [Agricultural biology], 2021, vol. 56, no. 1, pp. 158–170 (in Russian).

7. Kumar M., Tak Y., Potkule J., Choyal P., Tomar M., Meena N. L., Kaur Ch. Phenolics as Plant Protective Companion Against Abiotic Stress. Plant Phenolics in Sustainable Agriculture. Vol. 1. Singapor, 2020, pp. 277–308. https://doi.org/10.1007/978-981-15-4890-1_12

8. Karimov O. Kh., Kolchina G. Yu., Teptereva G. A., Chetvertneva I. A., Karimov E. Kh., Badretdinov A. R. The reactivity of cinnamic acid derivatives as lignin precursors. Fine Tonkie khimicheskie tekhnologii = Chemical Technologies, 2020, vol. 15, no. 4, pp. 7–13 (in Russian).

9. Agatemor Ch., Ibsen K. N., Tanner E. E. L., Mitragotri S. Ionic liquids for addressing unmet needs in healthcare. Bioengineering and Translational Medicine, 2018, vol. 3, no. 1, pp. 7–25. https://doi.org/10.1002/btm2.10083

10. Rayanoothala P. S., Dweh T. J., Mahapatra S., Kayastha S. Unveiling the protective role of chitosan in plant defense: A comprehensive review with emphasis on abiotic stress management. Crop Design, 2024, vol. 3, no. 4, art. 100076. https://doi.org/10.1016/j.cropd.2024.100076

11. Je J.-Y., Kim S.-K. Reactive oxygen species scavenging activity of aminoderivatized chitosan with different degree of dea cetylation. Bioorganic and Medicinal Chemistry, 2006, vol. 14, no. 17, pp. 5989–5994. https://doi.org/10.1016/j.bmc.2006.05.016

12. Varlamov V. P., Il’’ina A. V., Shagdarova B. Ts., Lunkov A. P., Mysyakina I. S. Chitin/Chitosan and Its Derivatives: Fundamental Problems and Practical Approaches. Biochemistry Moscow, 2020, vol. 85, suppl. 1, pp. 154–176. https://doi.org/10.1134/S0006297920140084

13. Hileuskaya A. E., Nikalaichuk V. V., Kraskouski A. N., Hileuskaya K. S., Kulikouskaya V. I., Kalatskaja J. N., Nedved E. L., Vialichka N. I., Laman N. A. Chitosan–Hydroxycinnamic Acid Conjugates: Synthesis, Physicochemical Characteristics, and Estimation of Their Influence on Productivity and Quality of the Radish. Applied Biochemistry Microbiology, 2022, vol. 58, no. 2, pp. 175–185. https://doi.org/10.1134/S0003683822020065

14. Gerasimovich K. M., Rybinskaya E. I., Ovchinnikov I. A., Nedved’ E. L., Kalatskaya Zh. N., Gilevskaya K. S., Nikolaichuk V. V., Laman N. A. Influence of chitosan and hydroxycinnamic acids conjugates and nanoparticles on the growth of barley seedlings and proline contents under saline stress. Vestsi Natsyyanal’nai akademii navuk Belarusi. Seryya biyalagichnykh navuk = Proceedings of the National Academy of Sciences of Belarus. Biological series, 2022, vol. 67, no. 3, pp. 263–273 (in Russian).

15. Elovskaya N. A., Kalatskaya Zh. N., Laman N. A., Gilevskaya K. S., Kulikovskaya V. I., Nikolaichuk V. V. Effect of the hydroxycinnamic acids and their chitosan-based conjugates on the growth and biochemical parameters of microclone potato plants in vitro. Doklady Natsional’noi akademii nauk Belarusi = Doklady of the National Academy of Sciences of Belarus, 2022, vol. 66, no. 6, pp. 605–613 (in Russian).

16. Nedved E. L., Kalatskaja J. N., Ovchinnikov I. A., Rybinskaya E. I., Laman N. A., Kraskouski A. N., Nikalaichuk V. V., Hileuskaya K. S., Kulikouskaya V. I., Agabekov V. E. Growth Parameters and Antioxidant Activity in Cucumber Seedlings with the Application of Chitosan and Hydroxycinnamic Acids Conjugates under Salt Stress. Applied Biochemistry and Microbiology, 2022, vol. 58, no. 1, pp. 69–76. https://doi.org/10.1134/S0003683822010069

17. Ovchinnikov I. A., Kalatskaya Zh. N., Nikolaichuk V. V., Gilevskaya K. S., Morozova I. M. Effect of Chitosan–Hydroxycinnamic Acid Conjugates on the growth and development of cucumber plants (Cucumis sativus L.) under soil salinity conditions. Vestsi Natsyyanal’nai akademii navuk Belarusi. Seryya biyalagichnykh navuk = Proceedings of the National Academy of Sciences of Belarus. Biological series, 2025, vol. 70, no. 3, pp. 253–264 (in Russian).

18. Sudnik A. F., Laman N. A., Doroshchuk O. V., Kukanego L. B. Features of action of brassinosteroids as a part of insecticide-fungicide compositions on the growth of seedlings of rape (Brassica napus L.) in the conditions of low-temperature stress. Botanika (issledovaniya): sbornik nauchnykh trudov [Botany (research): collection of scientific papers]. Minsk, 2011, vol. 40, pp. 560–574 (in Russian).

19. Kumar G. N. M., Knowles N. R. Changes in Lipid Peroxidation and Lipolytic and Free-Radical Scavenging Enzyme Activities during Aging and Sprouting of Potato (Solanum tuberosum) Seed-Tubers. Plant Physiology, 1993, vol. 102, no. 1, pp. 115–124. https://doi.org/10.1104/pp.102.1.115

20. Bates L. S., Waldren R. P., Teare I. D. Rapid determination of free proline for water-stress studies. Plant and Soil, 1973, vol. 39, no. 1, pp. 205–207. https://doi.org/10.1007/bf00018060

21. Bellincampi D., Dipierro N., Salvi G., Cervone F., De Lorenzo G. Extracellular H2O2 Induced by Oligogalacturonides Is Not Involved in the Inhibition of the Auxin-Regulated rolB Gene Expression in Tobacco Leaf Explants. Plant Physiology, 2000, vol. 122, no. 4, pp. 1379–1385. https://doi.org/10.1104/pp.122.4.1379

22. Boyarkin A. N. Determination of peroxidase activity. Methods of biochemical study of plants. 3rd ed. Leningrad, 1987, pp. 41–43 (in Russian).

23. Giannopolitis C. N., Ries S. K. Superoxide Dismutases: I. Occurrence in Higher Plants. Plant Physiology, 1977, vol. 59, no. 2, pp. 309–314. https://doi.org/10.1104/pp.59.2.309

24. Nakano Y., Asada K. Hydrogen Peroxide is Scavenged by Ascorbate-specific Peroxidase in Spinach Chloroplasts. Plant and Cell Physiology, 1981, vol. 22, no. 5, pp. 867–880. https://doi.org/10.1093/oxfordjournals.pcp.a076232

25. Aono M., Kubo A., Saji H., Natori T., Tanaka K., Kondo N. Resistance to Active Oxygen Toxicity of Transgenic Nicotiana tabacum that Expresses the Gene for Glutathione Reductase from Escherichia coli. Plant and Cell Physiology, 1991, vol. 32, no. 5, pp. 691–697. https://doi.org/10.1093/oxfordjournals.pcp.a078132

26. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein–dye binding. Analytical Biochemistry, 1976, vol. 72, no. 1–2, pp. 248–254. https://doi.org/10.1016/0003-2697(76)90527-3

27. Kraskouski A., Nikalaichuk V., Kulikouskaya V., Hileuskaya K., Kalatskaja J., Nedved H., Laman N., Agabekov V. Synthesis and properties of hydrogel particles based on chitosan-ferulic acid conjugates. Soft Materials, 2021, vol. 19, no. 4, pp. 495–502. https://doi.org/10.1080/1539445x.2021.1877726

28. Nikalaichuk V., Hileuskaya K., Kraskouski A., Kulikouskaya V., Nedved H., Kalatskaja J., Rybinskaya E., Herasimovich K., Laman N., Agabekov V. Chitosan-hydroxycinnamic acid conjugates: Synthesis, photostability and phytotoxicity to seed germination of barley. Journal of Applied Polymer Science, 2021, vol. 139, no. 14, art. 51884. https://doi.org/10.1002/app.51884

29. Grantz S. A. Primer of Biostatistics. 7th ed. New York, McGraw-Hill Medical, 2011, 320 p.

30. Ayalew H., Liu H., Yan G. Identification and validation of root length QTLs for water stress resistance in hexaploid wheat (Titicum aestivum L.). Euphytica, 2017, vol. 213, art. 126. https://doi.org/10.1007/s10681-017-1914-4

31. Khalid M., Gul A., Amir R., Ali M., Afzal F., Quraishi U. M., Ahmed Z., Rasheed A. QTL mapping for seedling morphology under drought stress in wheat cross synthetic (W7984)/Opata. Plant Genetic Resources: Characterization and Utilization, 2018, vol. 16, no. 4, pp. 359–366. https://doi.org/10.1017/s1479262118000023

32. Trovato M., Mattioli R., Costantino P. Multiple roles of proline in plant stress tolerance and development. RENDICONTI LINCEI, 2008, vol. 19, pp. 325–346. https://doi.org/10.1007/s12210-008-0022-8

33. Ghosh U. K., Islam M. N., Siddiqui M. N., Cao X., Khan M. A. R. Proline, a multifaceted signalling molecule in plant responses to abiotic stress: understanding the physiological mechanisms. Plant Biology, 2021, vol. 24, no. 2, pp. 227–239. https://doi.org/10.1111/plb.13363

34. Garg N., Manchanda G. ROS generation in plants: Boon or bane? Plant Biosystems, 2009, vol. 143, no. 1, pp. 81–96. https://doi.org/10.1080/11263500802633626

35. Neill S., Desikan R., Hancock J. Hydrogen peroxide signalling. Current Opinion in Plant Biology, 2002, vol. 5, no. 5, pp. 388–395. https://doi.org/10.1016/s1369-5266(02)00282-0

36. Minibayeva F., Kolesnikov O., Chasov A., Beckett R. P., Lüthje S., Vylegzhanina N., Buck F., Böttger M. Woundinduced apoplastic peroxidase activities: their roles in the production and detoxification of reactive oxygen species. Plant, Cell and Environment, 2009, vol. 32, no. 5, pp. 497–508. https://doi.org/10.1111/j.1365-3040.2009.01944.x

37. Gill S. S., Tuteja N. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiology and Biochemistry, 2010, vol. 48, no. 12, pp. 909–930. https://doi.org/10.1016/j.plaphy.2010.08.016


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ISSN 1029-8940 (Print)
ISSN 2524-230X (Online)