Plant Soil Environ., 2026, 72(7):438-454

Foliar proline alleviates drought stress in peppermint via consistent growth and essential oil benefits, with stress-dependent regulation of ion balance and abscisic acidOriginal Paper

Abeer H. Elhakem ORCID...1, Amira Hassan2
1 Department of Biology, College of Sciences and Humanities, Prince Sattam Bin Abdulaziz University, Al-Kharj, Saudi Arabia
2 Materials Engineering, German University in Cairo, New Cairo, Egypt

This study examined whether exogenous proline (Pro, 10 mmol/L, foliar) uniformly alleviates drought stress in peppermint (Mentha × piperita L.) or whether its benefit intensifies with increasing stress severity. Plants were grown under four water field capacity (WFC) levels (95, 75, 50, 25%), with or without Pro, in a 4 × 2 factorial randomised design. Two-way ANOVA (Levene’s test confirmed homogeneous variance) partitioned each variable into WFC and Pro main effects and their interaction, followed by Tukey’s HSD (P < 0.05). Water deficit reduced growth and relative water content, increased osmolytes, disrupted ionic homeostasis (higher Na+ and Na+/K+; lower K+, Ca2+, Mg2+), activated antioxidant defences, and altered hormone levels (higher abscisic acid (ABA); lower indole-3-acetic acid (IAA), gibberellic acid (GA3)). Pro significantly improved growth, water status, most osmolytes, antioxidants, IAA, GA3, and essential oil (EO) yield, with no significant WFC × Pro interaction detected for these variables, providing no statistically detectable evidence that the magnitude of the effect differed among WFC levels. Pro’s effect on Na+, the Na+/K+ ratio, and ABA instead showed a significant WFC × Pro interaction (P = 0.040, 0.046, 0.001), intensifying under severe deficit. EO yield showed a biphasic response, rising at 75% and 50% WFC and falling at 25%, with Pro further increasing yield and menthol content. Pro thus acts mainly as a consistent protectant with no detected WFC × Pro interaction, alongside a distinct, stress-dependent role in ion and ABA regulation under severe drought.

Keywords: compatible solutes; phytochemical modulation; monoterpene profile; irrigation regime; metabolic reprogramming; nutrient partitioning

Received: May 24, 2026; Revised: July 17, 2026; Accepted: July 20, 2026; Published: July 23, 2026  Show citation

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Elhakem AH, Hassan A. Foliar proline alleviates drought stress in peppermint via consistent growth and essential oil benefits, with stress-dependent regulation of ion balance and abscisic acid. Plant, Soil and Environment. 2026;72(7):438-454.
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References

  1. Adams R.P. (2007): Identification of Essential Oil Components by Gas Chromatography/Mass Spectrometry. 4th Edition. Carol Stream, Allured Publishing Corporation. ISBN-13: 978-1-932633-21-4
  2. Aebi H. (1984): Catalase in vitro. Methods in Enzymology, 105: 121-126. Go to original source...
  3. Araniti F., Prinsi B., Cocetta G., Negrini N., Nocito F.F., Espen L. (2024): Impact of cyclic-mild-drought stress on the metabolism of Mentha spicata L.: a strategy to improve quality traits. Industrial Crops and Products, 210: 118129. Go to original source...
  4. Beyer W.F., Fridovich I. (1987): Assaying for superoxide dismutase activity: some large consequences of minor changes in conditions. Analytical Biochemistry, 161: 559-566. Go to original source...
  5. Bhatt G., Tiwari A.K., Venkatesha K.T., Upadhyay R.K., Chauhan A., Verma R.S., Singh V.R., Padalia R.C. (2020): Harvest and post-harvest studies on Mentha arvensis var. CIM-Kranti for quality essential oil production in winter and summer cropping seasons. Journal of Medicinal and Aromatic Plant Sciences, 42: 114-120. Go to original source...
  6. Bistgani Z.E., Barker A.V., Hashemi M. (2024): Physiology of medicinal and aromatic plants under drought stress. The Crop Journal, 12: 330-339. Go to original source...
  7. Bradford M.M. (1976): A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry, 72: 248-254. Go to original source... Go to PubMed...
  8. Cottenie A., Verloo M., Kiekens L., Velghe G., Camerlynck R. (1982): Chemical Analysis of Plant and Soil. Laboratory of Analytical and Agrochemistry. Ghent, State University of Ghent.
  9. Dere S., Günes T., Sivaci R. (1998): Spectrophotometric determination of chlorophyll-A, B and total carotenoid contents of some algae species using different solvents. Turkish Journal of Botany, 22: 13-17.
  10. Elhakem A.H. (2025): Exogenous proline enhances salt tolerance in wheat: regulating osmolytes, hormonal balance, antioxidant de-fense, and yield performance. Plant, Soil and Environment, 71: 278-292. Go to original source...
  11. Ellman G.L. (1959): Tissue sulfhydryl groups. Archives of Biochemistry and Biophysics, 82: 70-77. Go to original source... Go to PubMed...
  12. Formica V., Romano D., Verdeguer M., Zingale S., Leoni F., Carlesi S., Barberi P., Guarnaccia P. (2026): Mild abiotic stresses improve essential oils yield and composition of Mediterranean medicinal and aromatic plants with minimal impact on plant growth: a sys-tematic literature review. Italian Journal of Agronomy, 21: 100079. Go to original source...
  13. Foyer C.H., Halliwell B. (1976): The presence of glutathione and glutathione reductase in chloroplasts: a proposed role in ascorbic acid metabolism. Planta, 133: 21-25. Go to original source... Go to PubMed...
  14. Haghpanah M., Hashemipetroudi S., Arzani A., Araniti F. (2024): Drought tolerance in plants: physiological and molecular responses. Plants, 13: 2962. Go to original source... Go to PubMed...
  15. Huang S., Jin S. (2025): Enhancing drought tolerance in horticultural plants through plant hormones: a strategic coping mechanism. Frontiers in Plant Science, 15: 1502438. Go to original source... Go to PubMed...
  16. Jackson M.L. (1973): Soil Chemical Analysis. New Delhi, Prentice Hall of India.
  17. Jangpangi D., Patni B., Chandola V., Chandra S. (2025): Medicinal plants in a changing climate: understanding the links between environmental stress and secondary metabolite synthesis. Frontiers in Plant Science, 16: 1587337. Go to original source... Go to PubMed...
  18. Khan P., Abdelbacki A.M.M., Albaqami M., Jan R., Kim K.-M. (2025): Proline promotes drought tolerance in maize. Biology, 14: 41. Go to original source...
  19. Lee M.R., Kim C.S., Park T., Choi Y.S., Lee K.H. (2018): Optimization of the ninhydrin reaction and development of a multiwell plate-based high-throughput proline detection assay. Analytical Biochemistry, 556: 57-62. Go to original source... Go to PubMed...
  20. Lowry O.H., Rosebrough N.J., Farr A.L., Randall R.J. (1951): Protein measurement with the Folin phenol reagent. Journal of Biological Chemistry, 193: 265-275. Go to original source...
  21. Mukherjee S.P., Choudhuri M.A. (1983): Implications of water stress-induced changes in the levels of endogenous ascorbic acid and hydrogen peroxide in Vigna seedlings. Physiologia Plantarum, 58: 166-170. Go to original source...
  22. Müller M., Munné-Bosch S. (2011): Rapid and sensitive hormonal profiling of complex plant samples by liquid chromatography cou-pled to electrospray ionization tandem mass spectrometry. Plant Methods, 7: 37. Go to original source... Go to PubMed...
  23. Nakano Y., Asada K. (1981): Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant and Cell Physiology, 22: 867-880. Go to original source...
  24. Ozhuner E. (2025): Plant growth-promoting rhizobacteria enhance essential oil production and antioxidant activity of Mentha piperi-ta under water deficit stress. Agricultural Water Management, 321: 109936. Go to original source...
  25. Padalia R.C., Verma R.S., Chauhan A., Sundaresan V., Chanotiya C.S. (2013): Essential oil composition of sixteen elite cultivars of Mentha from western Himalayan region, India. Maejo International Journal of Science and Technology, 7: 83-93.
  26. Pecka J., Kraus K., Zelený M., Hniličková H. (2025): Exogenous proline modulates physiological responses and induces stress memory in wheat under repeated and delayed drought stress. Agronomy, 15: 1370. Go to original source...
  27. Renzetti M., Funck D., Trovato M. (2025): Proline and ROS: a unified mechanism in plant development and stress response? Plants, 14: 2. Go to original source... Go to PubMed...
  28. Schonfeld M.A., Johnson R.C., Carver B.F., Mornhinweg D.W. (1988): Water relations in winter wheat as drought resistance indica-tors. Crop Science, 28: 526-531. Go to original source...
  29. Shahhoseini R., Farhadi N., Angourani H.R. (2025): Metabolic activities, biochemical, and physiological processes in Mentha pulegium L. induced by drought stress and application of 5-aminolevulinic acid. BMC Plant Biology, 25: 1410. Go to original source... Go to PubMed...
  30. Singh S., Thakur A., Dulta K., Sharma A.J., Kumar N., Dwivedi S., Choudhury M.D., Verma K., Singh N. (2025): Effects of exogenous proline treatment on antioxidant and biochemical parameters in Lepidium sativum L. plants cultivated in a water-stressed condi-tion. Plant Science Today, 12: 2. Go to original source...
  31. Wolf B. (1982): A comprehensive system of leaf analysis and its use for diagnosing crop nutrient status. Communications in Soil Sci-ence and Plant Analysis, 13: 1035-1059. Go to original source...
  32. Yoshida S., Forno D.A., Cock J.H., Gomez K.A. (1976): Laboratory Manual for Physiological Studies of Rice. 3rd Edition. Los Baños, International Rice Research Institute. ISBN: 971-104-035-2

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