Journals / Journal of Agricultural Sciences / 2022 / Volume: 28 Issue: 4

Effects of Sequential Hydrogen Peroxide Applications on Salt Stress Tolerance in Bread Wheat Varieties

Elif Saadet Arıcan(TEKİRDAĞ NAMIK KEMAL ÜNİVERSİTESİ)0000-0003-2969-8724
Sefer Demirbaş(Tekirdağ Namık Kemal Üniversitesi)0000-0001-7201-3888
Pages
—
Publication Date
2022-10-17
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Biochemical results showed that the lowest H2O2 level was in NKÜ Lider variety and in -H2O2 and 1xH2O2 groups.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Salinity is affecting plant growth and development.
📊
Key Findings & Data:Low concentration of hydrogen peroxide (H2O2) has shown to be effective against various stress factors.
💡
Conclusion & Impact:Biochemical results showed that the lowest H2O2 level was in NKÜ Lider variety and in -H2O2 and 1xH2O2 groups.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Priming · Stress biomarkers · wheat cultivars

Abstract

Salinity is affecting plant growth and development. Low concentration of hydrogen peroxide (H2O2) has shown to be effective against various stress factors. In this study, effect of different H2O2 priming methods on growth, physiological and biochemical parameters in three wheat varieties (NKÜ Lider, Sultan-95, and Tosunbey) under salt stress were investigated. Salt stress (0 and 160 mM NaCl) was applied gradually to 100 μM H2O2 applied (-H2O2: negative control, no application; H2O2: positive control, 100 μM H2O2 applied; 1xH2O2: 100 μM H2O2 applied one year ago; 2xH2O2: 100 μM H2O2 applied second time after one year) wheat seedlings. Biochemical results showed that the lowest H2O2 level was in NKÜ Lider variety and in -H2O2 and 1xH2O2 groups. The lowest thiobarbituric acid reactive substances (TBARS) level was in Tosunbey variety and 2xH2O2 group. The highest superoxide dismutase (SOD) activity was in NKÜ Lider variety, all H2O2 pre-treatment caused an increase in SOD activity and 2xH2O2 pre-treatment caused the highest SOD activity. However, H2O2 and TBARS levels increased in all application groups except 2xH2O2 group, while the H2O2 amount increased and TBARS level decreased in 2xH2O2 group. MnSOD was not detected in any groups. CuZnSOD increased in all groups except 2xH2O2 groups under salt stress in Sultan-95 variety compared to FeSOD. H2O2 pre-treatment better tolerated salt stress, and second-applied H2O2 pre-treatment eliminated the stress and improved plant growth. In conclusion, it was determined that H2O2 re-pre-treatment to wheat seeds resulted in improvement of plant growth in tolerant varieties exposed to salt stress.

🔖

Cite This Article

Arıcan, E. S., Demirbaş, S. (2022). Effects of Sequential Hydrogen Peroxide Applications on Salt Stress Tolerance in Bread Wheat Varieties. Journal of Agricultural Sciences, Volume: 28 Issue: 4. https://doi.org/10.15832/ankutbd.896112

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (31)

  1. Ahanger M A & Agarwal R M (2017). Salinity stress induced alterations in antioxidant metabolism and nitrogen assimilation in wheat (Triticum aestivum L.) as influenced by potassium supplementation. Plant Physiology and Biochemistry 115: 449–460
  2. Ali Q, Daud M K, Haider M Z, Ali S, Rizwan M, Aslam N, Noman A, Iqbal N, Shahzad F, Deeba F, Ali I & Zhu S J (2017). Seed priming by sodium nitroprusside improves salt tolerance in wheat (Triticum aestivum L.) by enhancing physiological and biochemical parameters. Plant Physiology and Biochemistry 119: 50–58
  3. Arora D & Bhatla S C (2017). Melatonin and nitric oxide regulate sunflower seedling growth under salt stress accompanying differential expression of Cu/Zn SOD and Mn SOD. Free Radical Biology and Medicine, 106: 315–328
  4. Asensio A C, Gil-Monreal M, Pires L, Gogorcena Y, Aparicio-Tejo P M & Moran J F (2012). Two Fe-superoxide dismutase families respond differently to stress and senescence in legumes. Journal of Plant Physiology 169(13): 1253–1260
  5. Ashfaque F (2014). Exogenously applied H2O2 promotes proline accumulation, water relations, photosynthetic efficiency and growth of wheat (Triticum aestivum L.) under salt stress. Annual Research & Review in Biology 4(1): 105–120
  6. Ashraf M (2009). Biotechnological approach of improving plant salt tolerance using antioxidants as markers. In Biotechnology Advances 27(1): 84-93
  7. Ashraf M & Harris P J C (2004). Potential biochemical indicators of salinity tolerance in plants. Plant Science 166(1): 3–16
  8. Athar H ur R, Khan A & Ashraf M (2008). Exogenously applied ascorbic acid alleviates salt-induced oxidative stress in wheat. Environmental and Experimental Botany, 63(1–3): 224–231
  9. Baxter A, Mittler R & Suzuki N (2014). ROS as key players in plant stress signalling. Journal of Experimental Botany 65(5): 1229–1240
  10. Beauchamp C & Fridovich I (1971). Superoxide dismutase: Improved assays and an assay applicable to acrylamide gels. Analytical Biochemistry 44(1): 276–287
  11. Beauchamp C O & Fridovich I (1973). Isozymes of superoxide dismutase from wheat germ. BBA - Protein Structure 317(1): 50–64
  12. Bradford M M (1976). A rapid and sensitive method for the quantition of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry, 72: 248–254
  13. Bruce T J A, Matthes M C, Napier J A & Pickett J A (2007). Stressful “memories” of plants: Evidence and possible mechanisms. Plant Science 173(6): 603–608
  14. Demirbas S & Balkan A (2020). The effect of H2O2 pre-Treatment on Antioxidant Enzyme Activities of Triticale Under Salt Stress. JOTAF 8: 1169–1178
  15. Farooq S, Hussain M, Jabran K, Hassan W, Rizwan M S & Yasir T A (2017). Osmopriming with CaCl2 improves wheat (Triticum aestivum L.) production under water-limited environments. Environmental Science and Pollution Research 24(15): 13638–13649
  16. Giannipolities N & Ries S K (1977). Superoxide dismutase occurance in higher plants. Plant Physiology 59: 309–314
  17. He L H, Gao Z Q & Li R Z (2009). Pretreatment of seed with H2O2 enhances drought tolerance of wheat (Triticum aestivum L.) seedlings. African Journal of Biotechnology 8(22): 6151–6157
  18. He Y & Li Z (2018). Epigenetic Environmental memories in plants: establishment, maintenance, and reprogramming. Trends in Genetics 34(11): 856-866
  19. Jia M, Guan J, Zhai Z, Geng S, Zhang X, Mao L & Li A (2018). Wheat functional genomics in the era of next generation sequencing: An update. The Crop Journal, 6(1): 7–14
  20. Jisha K C, Vijayakumari K, Puthur J T (2013). Seed priming for abiotic stress tolerance: an overview. Acta Physiologie Plantarum 35: 1381-1396
  21. Madhava Rao K V & Sresty T V S (2000). Antioxidative parameters in the seedlings of pigeonpea (Cajanus cajan (L.) Millspaugh) in response to Zn and Ni stresses. Plant Science 157(1): 113–128
  22. Parida A K & Das A B (2005). Salt tolerance and salinity effects on plants: A review. Ecotoxicology and Environmental Safety 60(3): 324-349
  23. Radoglou K M & Jarvis P G (1990). Effects of CO2 enrichment on four poplar clones. I. growth and leaf anatomy. Annals of Botany 65(6): 617–626
  24. Savvides A, Ali S, Tester M & Fotopoulos V (2016). Chemical priming of plants against multiple abiotic stresses: mission possible? Trends in Plant Science 21(4): 329–340
  25. Saxena I, Srikanth S & Chen Z (2016). Cross talk between H2O2 and interacting signal molecules under plant stress response. Frontiers in Plant Science 7: 1–16
  26. Shi X & Ling H (2018). Current advances in genome sequencing of common wheat and its ancestral species. The Crop Journal 6(1): 15–21
  27. Smart R E & Bingham G E (1974). Rapid estimates of relative water content. Plant Physiology 53: 258–260
  28. Tabassum T, Farooq M, Ahmad R, Zohaib A & Wahid A (2017). Seed priming and transgenerational drought memory improves tolerance against salt stress in bread wheat. Plant Physiology and Biochemistry 118: 362–369
  29. Vitória A P, Lea P J & Azevedo R A (2001). Antioxidant enzymes responses to cadmium in radish tissues. Phytochemistry 57(5): 701–710
  30. Wani S H, Kumar V, Shriram V & Sah S K (2016). Phytohormones and their metabolic engineering for abiotic stress tolerance in crop plants. The Crop Journal 4(3): 162-176
  31. Jia M, Guan J, Zhai Z, Geng S, Zhang X, Mao L & Li A (2018). Wheat functional genomics in the era of next generation sequencing: An update. The Crop Journal, 6(1): 7–14