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Research Articles

Vol. 12 No. sp4 (2025): Recent Advances in Agriculture by Young Minds - III

Seed priming with silicon dioxide and potassium nitrate alleviates the ill effects of water stress in chilli (Capsicum annuum L.) by suppressing reactive oxygen species (ROS) accumulation and improving antioxidant defence systems

DOI
https://doi.org/10.14719/pst.5814
Submitted
14 October 2024
Published
15-10-2025 — Updated on 24-10-2025
Versions

Abstract

Deficit soil moisture is one of the most critical limiting factors affecting crop growth and overall productivity. Because of its low membrane integrity, high stomatal conductance and increased transpiring leaf surface, the essential solanaceous crop chilli is highly vulnerable to drought. One crucial stress management technique for combating water stress is seed priming. Chilli seeds were subjected to different priming agents 2.5 % potassium nitrate (KNO3), 3 % silicon dioxide (SiO2) and unprimed seeds with distilled water for 24 hours. Prior to the flowering stage, the crop was subjected to moisture stress by withholding irrigation in both greenhouse and field conditions. Results of both experiments revealed that seed priming with 2.5 % KNO3, resulted in enhanced physiological traits like relative water content, specific leaf area, total chlorophyll and biochemical traits like malonaldehyde, H2O2, trehalose, α-amylase activity, superoxide dismutase, total soluble sugars and total soluble protein, followed by quality traits like capsaicin, vitamin C and yield traits viz., plant height, number of flowers plant-1, number of fruits plant-1 and fruit yield plant-1, whereas 3 % SiO2 primed seeds recorded significantly higher values for total proline content and cell membrane stability index compared to unprimed seeds. Seeds primed with 3 % SiO2 recorded early flowering, whereas seeds primed with 2.5 % KNO3 recorded the first fruiting stage. The results showed that seeds with 3% SiO2 can be recommended for seed formation in cases of water shortage and seeds primed with 2.5 % KNO3 demonstrated high antioxidant levels and the maximum capacity to absorb water.

References

  1. 1. Bhattacharyya R, Baruah U, Bhattacharyya RK. Quint essential chillies of northeast India. Int J Food Nutri and Dietetics. 2018;6(3): http://dx.doi.org/10.21088/ijfnd.2322.0775.6318.1
  2. 2. Abdalla A, Sadak MS, Elhamid AE, Ezo M. Amelioration of drought stress reduced effects by exogenous application of L-Phenylalanine on (Moringa oleifera). Egyptian J Chem. 2022;65(8):523–32. https://doi.org/10.21608/ejchem.2022.109253.4978
  3. 3. Kopta T, Sekara A, Pokluda R, Ferby V, Caruso G. Screening of chilli pepper genotypes as a source of capsaicinoids and antioxidants under conditions of simulated drought stress. Plants. 2020;9(3):364. https://doi.org/10.3390/plants9030364
  4. 4. Kaya MD, Okcu G, Atak M, Cikili Y, Kolsarici O. Seed treatments to overcome salt and drought stress during germination in sunflower (Helianthus annuus L.). European J Agron. 2006;24(4):291–95. https://doi.org/10.1016/j.eja.2005.08.001
  5. 5. Costa LD, Gianquinto G. Water stress and water table depth influence yield, water use efficiency and nitrogen recovery in bell pepper: lysimeter studies. Australian J Agri Res. 2002;53:201–10. https://doi.org/10.1071/AR00133
  6. 6. Estrada-Campuzano G, Miralles DJ, Slafer GA. Genotypic variability and response to water stress of pre-and post-anthesis phases in triticale. European J Agron. 2008;28(3):171–77. https://doi.org/10.1016/j.eja.2007.07.005
  7. 7. Lestari P, Syukur M, Trikoesoemaningtyas T, Widiyono W. Morpho-physiological-based selection criteria for chili (Capsicum annuum) under drought stress during vegetative to generative phase. Biodivers J Biological Diversity. 2023;24(4):https://doi.org/10.13057/biodiv/d240445
  8. 8. Heydecker W, Gibbins B. The 'priming' of seeds. Acta Hortic. 1978;83:213–15. https://doi.org/10.17660/ActaHortic.1978.83.29
  9. 9. Nawaz A, Amjad M, Khan SM, Ahmed AT, Ahmed T, Iqbal Q, Iqbal J. Tomato seed invigoration with cytokinins. J Animal Plant Sci. 2012;22(4):121–28.
  10. 10. Ellouzi H, Oueslati S, Hessini K, Rabhi M, Abdelly C. Seed-priming with H2O2 alleviates subsequent salt stress by preventing ROS production and amplifying antioxidant defense in cauliflower seeds and seedlings. Scientia Horticulturae. 2021;288:110360. https://doi.org/10.1016/j.scienta.2021.110360
  11. 11. Mcdonald MB. Seed priming. In: Black M, Bewley JD, editors. Seed technology and its biological basis, Sheffield Academic Press, Sheffield, UK; 2000. 287–325
  12. 12. Raheem S, Khan J, Gurmani AR, Waqas M, Hamayun M, Khan AL, et al. Seed priming with Gibberellic Acid (GA3) in sponge-gourd modulated high salinity stress. Pakhtunkhwa J Life Sci. 2014;2(1):75–86.
  13. 13. Dhal P, Sahu G, Dhal A, Mohanty S, Dash SK. Priming of vegetable seeds: a review. Pharm Innov J. 2022;11(2):519–25.
  14. 14. Zheng M, Tao Y, Hussain S, Jiang Q, Peng S, Huang J, et al. Seed priming in dry direct-seeded rice: consequences for emergence, seedling growth and associated metabolic events under drought stress. Plant Growth Regul. 2016;78:167–78. https://doi.org/10.1007/s10725-015-0083-5
  15. 15. Ali LG, Nulit R, Ibrahim MH, Yien CYS. Efficacy of KNO3 , SiO2 and SA priming for improving emergence, seedling growth and antioxidant enzymes of rice (Oryza sativa L.) under drought. Sci Rep. 2021;11(1):3864. https://doi.org/10.1038/s41598-021-83434-3
  16. 16. Kabilan M, Balakumbahan R, Nageswari K, Santha S. Effect of seed treatments on seed germination and seedling parameters in the F2 generation of mundu chilli (Capsicum annum L.). J Applied Natural Sci. 2022;4:53–57. https://doi.org/10.31018/jans.v14iSI.3565
  17. 17. Kerala Agricultural University. Package of practices. Kerala:KAU; 2016
  18. 18. Turner NC. Techniques and experimental approaches for the measurement of plant water status. Plant Soil. 1981;58(3):339–66. https://doi.org/10.1007/BF02180062
  19. 19. Sairam RK. Effect of moisture stress on physiological activities of two contrasting wheat genotypes. Indian J Exp Bio. 1994;32:594–97.
  20. 20. Heath RL, Packer L. Photoperoxidation in isolated chloroplasts: I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophy; 1968. 125(1):189–98. https://doi.org/10.1016/0003-9861(68)90654-1
  21. 21. Velikova V, Yordanov I, Edreva A. Oxidative stress and some antioxidant systems in acid rain-treated bean plants – the protective role of exogenous polyamines. Plant Sci. 2000;151(1):59–66. https://doi.org/10.1016/S0168-9452(99)00197-1
  22. 22. Bates LS, Waldren RP, Teare ID. Rapid determination of free proline for water-stress studies. Plant Soil. 1973;39(1):205–07. https://doi.org/10.1007/BF00018060
  23. 23. Dhindsa RS, Dhindsa PP, Thorpe TA. Leaf senescence correlated with increased levels of membrane permeability and lipid peroxidation and decreased levels of superoxide dismutase and catalase. J Exp Bot. 1980;32:93–101. https://doi.org/10.1093/jxb/32.1.93
  24. 24. Giannopolitis CN, Ries SK. Superoxide dismutase occurrence in higher plants. Plant Physiol Rep. 1977;59:309–14. https://doi.org/10.1104/pp.59.2.309
  25. 25. Li ZG, Luo LJ, Zhu LP. Involvement of trehalose in hydrogen sulfide donor sodium hydrosulfide-induced the acquisition of heat tolerance in maize (Zea mays L.) seedlings. Bot Stud. 2014;55:1–9. https://doi.org/10.1186/1999-3110-55-20
  26. 26. Thayumanavan B, Sadasivam S. Physiochemical basis for the preferential uses of certain rice varieties. Plant Foods Hum Nutr. 1984;34:253–59. https://doi.org/10.1007/BF01126554
  27. 27. Hedge JE, Hofreiter BT. Carbohydrates. In: Whistler RL, Miller JNB, editors. Methods in carbohydrate chemistry. Academic Press, New York; 1962. p. 17‒22
  28. 28. Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding. Anal Biochem. 1976;72:248–54. https://doi.org/10.1016/0003-2697(76)90527-3
  29. 29. Kumari R, Ashraf S, Bagri GK, Khatik SK, Bagri DK, Bagdi DL. Extraction and estimation of chlorophyll content of seed treated lentil crop using DMSO and acetone. J Pharmacog Phytochem. 2018;7(3):249–50.
  30. 30. Mathew AG, Nambudiri ES, Ananthakrishna SM, Krishnamurthy N, Lewis YS. An improved method for estimation of capsaicinin capsicum oleoresin. Lab Pract. 197;20:856–58.
  31. 31. Harris, LJ, Ray SN. Determination of plasma ascorbic acid by 2, 6-dichlorophenol indophenol titration. Lancet. 1935;1:462. https://doi.org/10.1016/S0140-6736(00)57120-7
  32. 32. Gopinath PP, Parsad R, Joseph B, Adarsh VS. GrapesAgri1: Collection of shiny apps for data analysis in agriculture. J Open Source Software. 2021;6(63):34–37. https://doi.org/10.21105/joss.03437
  33. 33. Ahluwalia O, Singh PC, Bhatia R. A review on drought stress in plants: Implications, mitigation and the role of plant growth promoting rhizobacteria. Res Environ Sustain. 2021;5:100032. https://doi.org/10.1016/j.resenv.2021.100032
  34. 34. Sirisuntornlak N, Ghafoori S, Datta A, Arirob W. Seed priming and soil incorporation with silicon influence growth and yield of maize under water-deficit stress. Arch Agron Soil Sci. 2018;1–11. https://doi.org/10.1080/03650340.2018.1492713
  35. 35. Rao DSN, Naidu T, Rani YA. Change in photosynthetic rate, RWC, SCMR, dry matter production and yield of mung bean due to foliar nutrition under receding soil moisture condition. Advances Life Sci. 2016;5(19):3849.
  36. 36. Alam S, Aubert M, Avila S, Balland C, Bautista JE, Bershady MA, et al. Completed SDSS-IV extended Baryon oscillation spectroscopic survey: cosmological implications from two decades of spectroscopic surveys at the apache point observatory. Physic Rev D. 2021;103(8):083533. https://doi.org/10.1103/PhysRevD.103.083533
  37. 37. Anwar A, Xianchang YU, Yansu LI. Seed priming as a promising technique to improve growth, chlorophyll, photosynthesis and nutrient contents in cucumber seedlings. Notulae Botanicae Horti Agrobotanici Cluj-Napoca. 2020;48(1):116–27. https://doi.org/10.15835/nbha48111806
  38. 38. Langeroodi ARS, Noora R. Seed priming improves the germination and field performance of soybean under drought stress. J Animal Plant Sci. 2017;27(5):1611–20.
  39. 39. Bukhari SABH, Lalarukh I, Amjad SF, Mansoora N, Naz M, Naeem M, et al. Drought stress alleviation by potassium-nitrate-containing chitosan/montmorillonite microparticles confers changes in (Spinacia oleracea L.). Sustain. 2021;13(17):9903. https://doi.org/10.3390/su13179903
  40. 40. Younas HS, Abid M, Ashraf M, Shaaban M. Seed priming with silicon and chitosan for alleviating water stress effects in maize (Zea mays L.) by improving antioxidant enzyme activities, water status and photosynthesis. J Plant Nutri. 2022;45(15):2263–76. https://doi.org/10.1080/01904167.2022.2046070
  41. 41. Wenli S, Shahrajabian MH, Huang Q. Soybean seeds treated with single walled carbon nanotubes (SwCNTs) showed enhanced drought tolerance during germination. Int J Adv Biol Biomed Res. 2020;8:9–16. https://doi.org/10.33945/SAMI/IJABBR.2020.1.2
  42. 42. Parveen A, Liu W, Hussain S, Asghar J, Perveen S, Xiong Y. Silicon priming regulates morpho-physiological growth and oxidative metabolism in maize under drought stress. Plants. 2019; 8(10):431. https://doi.org/10.3390/plants8100431
  43. 43. Madhavi V, Madhavi G, Reddy A. A scrupulous overview on controlled release fertilizers. Agric Allied Sci. 2016;5:26–33.
  44. 44. Penna S, Teixeira da Silva JA, Anant BV. Plant abiotic stress, sugars and transgenics: a perspective. Flori Ornament Plant Biotech: Adv Topical Issues. 2006;3:86–93.
  45. 45. Farooq M, Hussain M, Nawaz AL, Dong-Jin A, Salem S, Siddique KHM. Seed priming improves chilling tolerance in chickpea by modulating germination metabolism, trehalose accumulation and carbon assimilation. Plant Physiol Biochem. 2017;11:274–83. https://doi.org/10.1016/j.plaphy.2016.12.012
  46. 46. Altaf MA, Shahid R, Ren MX, Naz S, Altaf MM, Khan LU, et al. Melatonin improves drought stress tolerance of tomato by modulating plant growth, root architecture, photosynthesis and antioxidant defense system. Antioxidants. 2022;11(2):309. https://doi.org/10.3390/antiox11020309
  47. 47. Mahmood T, Rana RM, Ahmar S, Saeed S, Gulzar A, Khan MA, et al. Effect of drought stress on capsaicin and antioxidant contents in pepper genotypes at reproductive stage. Plants. 2021; 10(7):1286. https://doi.org/10.3390/plants10071286
  48. 48. Rohitha K, Beena R, Jayalekshmy VG, Nivedhitha MS, Vijayakumar A, Gopinath PP. Changes in water stress indicators and antioxidant systems in chilli by chemical seed priming under water stress condition. Vegetos. 2023;37:1489–1502. https://doi.org/10.1007/s42535-023-00695-1
  49. 49. Rehman MM, Liu J, Nijabat A, Alsudays IM, Saleh MA, Alamer KH, et al. Seed priming with potassium nitrate alleviates the high temperature stress by modulating growth and antioxidant potential in carrot seeds and seedlings. BMC Plant Biol. 2024;24:606. https://doi.org/10.1186/s12870-024-05414-9
  50. 50. Chakma R, Saekong P, Biswas A, Ullah H, Datta A. Growth, fruit yield, quality and water productivity of grape tomato as affected by seed priming and soil application of silicon under drought stress. Agric Water Manag. 2021;256:107055. https://doi.org/10.1016/j.agwat.2021.107055

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