with the collaboration of Iranian Scientific Association for Landscape (ISAL)

Effect of Putrescine Foliar Application on Growth and Physiological Characteristics of Echium amoenum Seedlings Under Salinity Conditions

Document Type : Research Article

Authors

Department of Plant Production, Faculty of Agriculture, University of Torbat Heydarieh, Torbat Heydarieh, Iran

Abstract
Introduction
Polyamines are a group of low molecular weight organic compounds with two or more amine groups that are present in almost all living organisms. Polyamines are organic compounds that play a crucial role in various physiological processes in plants, particularly in response to stress. Research has demonstrated that these compounds-primarily putrescine, spermidine, and spermine-are involved in cellular functions such as growth regulation, cell division, and differentiation. Their role in stress responses is complex and varies significantly depending on the plant species and the specific type of stress encountered. The level of polyamines in plants increases under stress conditions, and this increase of polyamines from the plant against salinity by removing free radicals, stabilizing membrane and cell structure, creating cation and anion balance, regulating it protects ion channels. The foliar application of putrescine can significantly improve various physiological traits in plants subjected to salinity stress. By enhancing growth, photosynthetic efficiency, osmotic adjustment and oxidative stress tolerance, putrescine acts as a valuable tool for improving plant resilience under challenging environmental conditions. Echium amoenum is an annual plant of Boraginaceae family and is considered as one of the important medicinal plants in traditional medicine. Blue-violet petals of E. amoenum are used in Iranian traditional medicine as a painkiller, relaxant, invigorator, anti-inflammatory and pain reliever. To investigate the impact of putrescine on the morpho-physiological characteristics of Echium amoenum seedlings under salinity stress, a greenhouse experiment was conducted.
 
Materials and Methods
The experimental design was factorial, incorporating two factors: the application of putrescine and salinity stress induced by sodium chloride. This was organized as a completely randomized design. The first factor involved two levels of putrescine (0 and 1.5 mM), while the second factor included three levels of salinity stress (1600, 4000, and 8000 dS.m-1). Seeds were purchased from Pakaan Seed Company in Isfahan. Selecting high-quality seeds suitable for the growing conditions is crucial for successful plant growth. After soaking, the seeds were transferred to small pots containing a mixture of three parts peat moss and one part perlite. This mixture enhances aeration and moisture retention in the soil, creating an optimal environment for root development. One week after transplanting the seedlings to the main pots, a foliar application of putrescine was performed. Putrescine is a polyamine compound that can enhance plant growth and resilience against stress. This application was repeated every two weeks. One week after the first application of putrescine, salinity stress was introduced. To prevent shock to the plants, the salinity treatment was gradually applied in three stages. This gradual approach helps the plants acclimate to the new conditions. To prevent salt buildup in the soil, leaching with regular water was conducted every two weeks.
 
Results and Discussion
The results indicated that both the individual effects of salinity and putrescine, as well as their interaction, significantly influenced shoot fresh weight, root fresh weight, root length, and the overall dry weight of the Iranian borage plants. The application of putrescine enhanced the levels of proline and potassium in the leaves, which mitigated the detrimental effects of salinity stress on the Iranian borage plants. Furthermore, foliar spraying of putrescine increased chlorophyll content, thereby promoting photosynthesis and improving plant growth under saline conditions. Comparative analysis of the average data revealed that the highest dry weight of Iranian borage seedlings (0.6 g), relative leaf water content (85%), chlorophyll a (4 mg.g-1), and chlorophyll b (1.2 mg.g-1) were achieved with the combination of putrescine and salinity at 1.6 mm.m-1. The results underscore the potential of putrescine as a practical strategy for enhancing the growth and resilience of Iranian borage plants under salinity stress. By improving growth parameters such as shoot and root weights, root length, and overall dry weight, as well as enhancing physiological traits like proline and potassium levels, putrescine plays a crucial role in mitigating the adverse effects of salinity.
 
Conclusion
The foliar application of putrescine at 1.5 mM presents a valuable and practical strategy for managing salinity stress in Iranian borage seedling production. By enhancing photosynthetic pigments and antioxidant properties, putrescine helps the plant maintain its physiological functions and resilience under stress. This approach not only supports the growth and health of Iranian borage but also has implications for improving the quality and yield of its medicinal properties.

Keywords

Subjects

©2024 The author(s). This is an open access article distributed under Creative Commons Attribution 4.0 International License (CC BY 4.0).

  1. Abdel Rahman, R., Gomaa, S. E., Abdelsalam, N., El-Din, H., El-Wakil, M. F., Khaled, A. S., & Hassan, H. M. )2013). Effect of sodium chloride on tropane alkaloids accumulation and proline content in Datura metel and stramonium callus cultures. Journal of Advances in Medical and Biomedical Research, 1(2), 197-210.
  2. Ahanger, M. A., Qin, C., Maodong, Q., Dong, X. X., Ahmad, P., Abd Allah, E. F., & Zhang, L. (2019). Spermine application alleviates salinity induced growth and photosynthetic inhibition in Solanum lycopersicum by modulating osmolyte and secondary metabolite accumulation and differentially regulating antioxidant metabolism. Plant Physiology Biochemistry, 144, 1-13. https://doi.org/10.1016/j.plaphy.2019.09.021
  3. Alcazar, R., Marco, F., Cuevas, J. C., Patron, M., Ferrando, A., Carrasco, P., Tiburcio, A. F., & Altabella, T. (2006). Involvement of polyamines in plant response to abiotic stress. BiotechnologyLetters, 28, 1867-1876. https://doi.org/10.1016/B978-0-12-818204-8.00021-7.
  4. Alizadeh-Salteh, S., Najjarzadeh, S., Panahandeh, J., & Eghlima, G. (2024). The effect of foliar application of salicylic acid and putrescine on essential oil yield and composition of peppermint (Mentha piperita). Plant Productions, 47(1), 147-160. https://doi.org/10.22055/ppd.2024.45206.2129
  5. Amini, F., & Ehsanpour, A. A. (2005). Soluble proteins, proline, carbohydrates and Na/K changes in two tomato (Lycopersicon esculentum) cultivars under in vitro salt stress. African Journal of Biotechnology, 2(5), 133-135.
  6. Arnon, A. N. (1967). Method of extraction of chlorophyll in the plants. Agronomy Journal, 23(1), 112-121.
  7. Azizi, H., Gafari, S., Ghods, R., Shojaeii, A., Salmanian, M., & Ghafarzadeh, J. (2018). A review study on pharmacological activities, chemical constituents, and traditional uses of Echium amoenum. Pharmacognosy Reviews, 12(24), 208-217. https://doi.org/10.4103/phrev.phrev_13_18
  8. Bates, L. S., Walderen, R. D., & Taere, I. D. (1973). Rapid determination of free proline for water stress studies. Plant and Soil, 39, 205-207. https://doi.org/10.1007/BF00018060.
  9. Barrs, H. D., & Weatherley, P. E. (1962). A re-examination of the relative turgidity technique for estimating water deficits in leaves. Australian Journal of Biological Sciences, 15(3), 413-428.
  10. Chattopadhayay, M. K., Tiwari, B. S., Chattopadhyay, G., Bose, A., Sengupta, D. N., & Ghosh, B. (2002) Protective role of exogenous polyamines on salinity stressed rice (Oryza sativa) plants. Acta Facultatis Rerum Naturalium Universitatis Comenianae, Physiologia Plantarum, 116, 192-9.
  11. Evans, P. T., & Malmberg, R. L. (1989) Do polyamines have roles in plant development? Annual Review of Plant
  12. Physiology and Molecular Biology, 40, 235-241.
  13. Fahmideh, L., Mazarie, A., & Pahlavan, P. (2025). Investigation of relative expression of TaMYB73 gene in some native barley of Sistan region under drought stress. Journal of Plant Research (Iranian Journal of Biology), 37(4), 469-485.(in Persian with English abstract).
  14. Farsari, S. (2020). Morphophysiological and biochemical response of basil cultivar Keshkeni Luveluo under salinity stress and super absorbent polymers application. Journal of Plant Research (Iranian Journal of Biology), 33(4), 982-996. (in Persian with English abstract). https://dorl.net/dor/1001.1.23832592.1399.33.4.19.5.
  15. Farooq, M., Wahid, A., & Lee, D. J. (2009). Exogenously applied polyamines increase drought tolerance of rice by improving leaf water status, photosynthesis and membrane properties. Acta Physiologiae Plantarum, 31, 937-945. https://doi.org/10.1007/s11738-009-0307-2
  16. Golestani, M. (2020). Salt stress effect on some agronomical and physiological traits in Thymus daenensis Daenensis ecotypes. Journal of Plant Process and Function, 9(38), 459-477. http://jispp.iut.ac.ir/article-1-1361-fa.html
  17. Jouyban, Z. (2012). The effects of salt stress on plant growth. Technical Journal of Engineering and Applied Sciences, 2(1), 7-10. http://jispp.iut.ac.ir/article-1-1361-fa.html.
  18. Kamiab, F. (2016). Effects of different polyamines on vase life, ethylene production and some physiological traits of carnation (Dianthus caryophyllus Red Corsa). Journal of Crops Improvement, 18(2), 275-288. https://doi.org/10.22059/jci.2016.56619.
  19. Ilektra, S., & Michael, M. (2012). Interaction of proline, sugars and anthocyanins during photosynthetic acclimation of Arabidopsis thaliana to drought stress. Plant Physiology, 169, 577-585. https://doi.org/10.1016/j.jplph.2011.12.015. Epub 2012 Feb 2.
  20. Jalili Marandi, R. (2010). Physiology of Environmental Stresses and Mechanisms of Resistance in Horticultural Plants. Urmia: Jahad Publications Urmia, Urmia, Iran 637.
  21. Mahgoub, M. H., El-Aziz, N. G. A., & Mazhar, A. M. A. (2011). Response of Dahlia pinnata plant to foliar spray with putrescine and thiamine on growth, flowering and photosynthetic pigments. American-Eurasian Journal of Agricultural & Environmental Sciences, 10(5), 769-775. https://www.idosi.org/aejaes/jaes10(5)/9.
  22. Mahros, K. M., Badawy, E. M., Mahgoub, M. H., Habib, A. M., & El-Sayed, I. M. (2011). Effect of putrescine and uniconazole treatments on flower characters and photosynthetic pigments of (Chrysanthemum indicum) plant. Journal of South American Earth Sciences, 7, 399-408.
  23. Makkizadeh Tafti, M., Tavakol Afshari, R., Majnoon Hosseini, N., & Naghdi Badi, H. A. (2008). Evaluation of salinity tolerance and absorption of salt by borage (Borago officinalis). Iranian Journal of Medicinal and Aromatic Plants Research, 24(3), 253-262.(in Persian with English abstract).
  24. Mortazavi, S. H., Arghavani, M., Hassanpour Asil, M., & Kheiri, A. (2021). Effect of polyamines onmorphophysiological characteristics of Dutch iris (Iris hollandica 'Blue Magic') cut flower. Iranian Journal of Horticultural Science, 52(2), 269-280. (in Persian with English abstract) https://doi.org/10.22059/ijhs.2020.287494.1701.
  25. Munns, R., James, R. A., & Lauchli, A. (2006) Approaches to increasing the salt tolerance of wheat and other cereals. Journal Experimental Botany, 57, 1025-1043. http://dx.doi.org/1093/jxb/erj100.Epub 2006 Mar 1.
  26. Murray, M. B., Cape, J. N., & Fowler, D. (1989). Quantification of frost damage in plant tissues by rates of electrolyte leakage. New phytologist, 113(3), 307-311.
  27. Niakan, M., Rezapour Mahjoob, S., & Ghorbanli, M. (2015). Effect of exogenous putrescine on growth, photosynthesis and alkaloid compounds of datura (Datura stramonium) in response to salinity stress under hydroponic conditions. Journal of Soil and Plant Interactions-Isfahan University of Technology, 6(1), 111-123. https://doi.org/10.18869/acadpub.ejgcst.6.1.111
  28. Orabi, S. A., Salman, S. R., & Shalaby, M. A. (2010). Increasing resistance to oxidative damage in cucumber (Cucumis sativus) plants by exogenous application of salicylic acid and paclobutrazol. World Journal of Agricultural Sciences, 6(3), 252-259.
  29. Rubinowska, K., Pogroszewska, E., & Michalek, W. (2012). The effect of polyamines on physiological parameters of post - harvest quality of cut stems of Rosa ‘Red Berlin’. Acta Scientiarum Polonorum Hortorum Cultus, 11, 81-93.
  30. Roychoudhury, A., Basu, S., & Sengupta, D. N. (2011). Amelioration of salinity stress by exogenously applied spermidine or spermine in three varieties of Indica rice differing in their level of salt tolerance. Journal of Plant Physiology, 168(4), 317-328. https://doi.org/1016/j.jplph.2010.07.009. Epub 2010 Aug 21.
  31. Saffari, M., Oveisi, M., & Zarghami, R. (2015). Investigation of the effect of putrescia polyamine on some traits of Thymus vulgaris in conditions of water shortage. Agriculture Research, 12(4), 279-289.
  32. Safavi, M., Mohammadzadeh, M., & Vojodimehrabani, L. (2024). The effects of biochar on the growth and some physiological characteristics of Artemisia dracunculus under salinity stress. Plant Productions, 47(2), 229-244. https://doi.org/10.22055/ppd.2024.47046.2173.
  33. Santiago, M., Diego, H., Sauchez, A. G., Alponso, V., & Oscar A. R. (2004). Effect of polyamines on growth and salinity resistance of two rice cultivars. Biology Planta, 54, 199-201.
  34. Shahraki, H., Mahdi Nezhad, N., & Fakheri, B. A. (2021). The effect of synthesis nanosilver by plant extract on morphological and antioxidant properties of artichoke (Cynara scolymus) under salinity stress. Plant Productions, 44(1), 103-114. https://doi.org/10.22055/ppd.2020.29011.1746.
  35. Shu, S., Yuan, L., Guo, S. R., Sun, J., & Liu, C. J. (2012). Effects of exogenous spermidine on photosynthesis, xanthophyll cycle and endogenous polyamines in cucumber seedlings exposed to salinity. African Journal of Biotechnology, 11, 6064-6074. https://doi.org/10.5897/AJB11.1354. https://doi.org/10.5897/AJB11.1354
  36. Stahl, W., & Sies, H. (2005). Bioactivity and protective effects of natural carotenoids. Biochimica Biophysica Acta, 1740, 101-107. https://doi.org/10.1016/j.bbadis.2004.12.006
  37. Tang, W., & Newton, J. R. (2005). Polyamines reduced salt induced oxidative damage by increasing the activities of antioxidant enzymes and decreasing lipid peroxidation in Virginia pine. Plant Growth Regulation, 46, 31-43. https://doi.org/10.1007/s10725-005-6395-0

 

Send comment about this article
Enter Name.
Enter a valid email address.
Enter a vaid affiliation.
Enter comments (At leaset 10 words)
CAPTCHA Image
Enter Security Code Correctly.

  • Receive Date 09 February 2025
  • Revise Date 10 June 2025
  • Accept Date 11 June 2025
  • First Publish Date 17 June 2025