Research Article
BibTex RIS Cite

Year 2025, Volume: 4 Issue: 1, 1 - 10, 13.07.2025

Abstract

References

  • 1. Zohary, D., Hopf, M., & Weiss, E. Domestication of Plants in the Old World: The origin and spread of domesticated plants in Southwest Asia, Europe, and the Mediterranean Basin. Oxford University Press. 2012.
  • 2. Ortiz R, Sayre KD, Govaerts B, Gupta R, Subbarao GV, Ban T, Reynolds M. Climate change: can wheat beat the heat?. Agriculture, Ecosystems & Environment. 2008;126(1-2):46-58.
  • 3. Singh R, Upadhyay AK, Chandra P, Singh DP. Sodium chloride incites reactive oxygen species in green algae Chlorococcum humicola and Chlorella vulgaris: implication on lipid synthesis, mineral nutrients, and antioxidant system. Bioresource technology. 2018;270:489-497.
  • 4. Hidalgo A, Brandolini, A. Nutritional properties of einkorn wheat (Triticum monococcum L.). Journal of the Science of Food and Agriculture. 2014;94(4), 601-612.
  • 5. Turfan N, Sarıyıldız T, Mutlu E. Variation in Chemical Constituents of Siyez Wheat (Triticum monococcum L.) in Response to Some Abiotic Stress Factors. Turkish Journal of Agriculture-Food Science and Technology. 2019;7(4), 598-605.
  • 6. Ilhan S, Ozdemir F, Bor M. Contribution of trehalose biosynthetic pathway to drought stress tolerance of Capparis ovata Desf. Plant Biology. 2015;17(2):402-407.
  • 7. Vijayakumar M, Vijayakumar R, Stephen R. In vitro propagation of Bacopa monnieri L.-a multipurpose medicinal plant. Indian Journal of Science and Technology. 2010;3(7):782-787.
  • 8. Kim DH, Gopal J, Sivanesan I. Nanomaterials in plant tissue culture: the disclosed and undisclosed. RSC advances. 2017;7(58):36492-36505.
  • 9. Yu H, Luo D, Li SFY, Qu M, Liu D, He Y, Cheng F. Interpretable machine learning-accelerated seed treatment using nanomaterials for environmental stress alleviation. Nanoscale. 2023; 15(32), 13437-13449.
  • 10. Zhou P, Adeel M, Shakoor N, Guo M, Hao Y, Azeem I, Rui Y. Application of nanoparticles alleviates heavy metals stress and promotes plant growth: An overview. Nanomaterials. 2020; 11(1), 26.
  • 11. Mazhar MW, Ishtiaq M, Maqbool M, Akram R. Seed priming with Calcium oxide nanoparticles improves germination, biomass, antioxidant defence, and yield traits of canola plants under drought stress. South African Journal of Botany. 2022;151, 889-899.
  • 12. Finkelstein R. Abscisic acid synthesis and response. The Arabidopsis book/American society of plant biologistsPlant Biologists. 2013 ;11, e0166.
  • 13. Tuteja N. Abscisic acid and abiotic stress signaling. Plant signaling & behavior. 2007;2(3), 135-138.
  • 14. Sah SK, Reddy KR, Li J. Abscisic acid and abiotic stress tolerance in crop plants. Frontiers in plant sciencePlant Science. 2016;7, 571.
  • 15. Vahdati K, Bayat S, Ebrahimzadeh H, Jariteh M, Mirmasoumi M. Effect of exogenous ABA on somatic embryo maturation and germination in Persian walnut (Juglans regia L.). Plant Cell, Tissue and Organ Culture. 2008; 93, 163-171.
  • 16. Purohit SD, Singhvi A. Micropropagation of Achras sapota through enhanced axillary branching. Scientia Horticulturae. 1998;76(3-4):219-229.
  • 17. Rai MK, Shekhawat NS, Harish, Gupta AK, Phulwaria M, Ram K, Jaiswal U. The role of abscisic acid in plant tissue culture: a review of recent progress. Plant Cell, Tissue and Organ Culture (PCTOC). 2011;106:179-190.
  • 18. Murashige T, Skoog F.A A A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiologia plantarum. 1962;15(3).
  • 19. Sayir F, Sehitogullan A, Demir H. Serum prolidase activity, total oxidant/antioxidant, and nitric oxide levels in patients with esophageal squamous cell carcinoma. Türk Gogus Kalp Damar Cerrahisi Derg. 2019; 27:206–211.
  • 20. Blois MS. Antioxidant determinations by the use of a stable free radical. Nature. 1958;181(4617), 1199-1200.
  • 21. Apak R, Güçlü K, Demirata B, Özyürek M, Çelik SE, Bektaşoğlu B, Özyurt D. Comparative evaluation of various total antioxidant capacity assays applied to phenolic compounds with the CUPRAC assay. Molecules. 2007;12(7):1496-1547.
  • 22. Flurkey WH. Polyphenoloxidase in higher plants: immunological detection and analysis of in vitro translation products. Plant physiology. 1986;81(2), 614-618.
  • 23. Nadaroğlu H, Demir Y, Demir N. Antioxidant and radical scavenging properties of Iris germanica. Pharmaceutical Chemistry Journal. 2007;41(8), 409-415.
  • 24. Jiang M, Zhang J. Water stress‐induced abscisic acid accumulation triggers the increased generation of reactive oxygen species and up‐regulates the activities of antioxidant enzymes in maize leaves. Journal of experimental botanyExperimental Botany. 2002; 53(379), 2401-2410.
  • 25. Taşğın E, Nadaroğlu H, Adıgüzel A, Baltacı MÖ, Sönmez Z. Soya bitkisindeki glutatyon redüktaz aktivitesi ve mrna seviyesinin kuraklık stresinde salisilik asit ile değişimleri. Akademik Platform Mühendislik ve Fen Bilimleri Dergisi.2017;5(2), 48-52.
  • 26. Ertuş MM, Yazıcılar B. CaO nanoparticle enhances the seedling growth of Onobrycis viciifolia under drought stress via mannitol use. Biologia. 2023;78(4):1119-1127.
  • 27. Kudla J, Batistič O, Hashimoto K. Calcium signals: the lead currency of plant information processing. The Plant Cell. 2010;22(3):541-563.
  • 28. B Bursal E, Aras A, Doğru M, Kılıç Ö. Phenolic content, antioxidant potentials of Saponaria prostrata endemic plant. International Journal of Life Sciences and Biotechnology. 2021;5(1):1-8.
  • 29. Karakavuk E. Determination of antioxidant capacity and phenolic content of Tunceli garlic extracts (allium Allium Ttuncelianum) by different solvents. Eurasian Journal of Food Science and Technology. 2021;5(2):205-212.
  • 30. Wang S, Li F, Wang G, Li H, Li X, Cao X, Wang J. Polyphenol oxidase gene editing changed the flavonoid composition and browning process of litchi (Litchi chinensis Sonn.) callus. Gene. 2025 ;936:149130.
  • 31. Sharma R, Kaur R. Insights into fluoride-induced oxidative stress and antioxidant defences in plants. Acta physiologiae plantarum. 2018;40(10):181.

Triticum monococcum callus of ecotypes applying ABA and CaO exhibit improved antioxidant enzyme activities

Year 2025, Volume: 4 Issue: 1, 1 - 10, 13.07.2025

Abstract

CaO (Ca2+) nanoparticles (NPs) are important macromolecules that act as signal transducers in the growth and survival processes of plants. In this report, the responses of two different (Incedere and Kurekdere) Triticum monococcum landraces to various antioxidant and physiological processes were analyzed under tissue culture conditions. Two Triticum monococcum landraces were cultivated in the presence of 1 and 10 mM mannitol, consisting of 0.5 ppm and 1.5 ppm Ca2+ nanoparticles. The influences of CaO NPs, total oxidant levels, DPPH free radical removal activity, cupra, PPO and glutathione reductase activities were determined for in vitro calli and ABA-induced. CaO significantly enchanced the activation of growth factors in the two tested landraces. Synergistic applications of NPs affected shootings more than either application alone. TOS, DPPH, cuprac, PPO, and GR were found to be significant with Ca2+ NP application and demonstrated a high level associated with the tolerance degrees of the varieties. When the results of the total antioxidant test were analyzed, It was detected that oxidant levels decreased significantly when CaO NPs were treated at increasing concentrations. While the antioxidant capacity of CaO NPs was limited at low concentrations (10-30 µg/mL) in the first 7 days, a highly promote was detected at higher concentrations (50 µg/mL). The activity increased in the second week and the antioxidant effect continued especially in the 30 and 50 µg/mL groups. While a significant increase was observed in the results of wheat samples treated with CaO NPs in the 1st week, it was seen that the increase in copper ion reducing activity became more balanced in the 2nd week. This trend shows that CaO NPs activate phenolic metabolism in short-term applications, but in the long term, cellular regulation mechanisms come into play and balance the enzyme activity. The 2nd week data show that GR activity reached a plateau level in certain dose groups; It is shown that GR activity in the 50 µg/mL group did not change compared to the 1st week (p > 0.05), but a slight decrease was observed in the 10 and 30 µg/mL applications (p < 0.05). ABA and CaO NP were observed to have a positive effect on wheat development.

References

  • 1. Zohary, D., Hopf, M., & Weiss, E. Domestication of Plants in the Old World: The origin and spread of domesticated plants in Southwest Asia, Europe, and the Mediterranean Basin. Oxford University Press. 2012.
  • 2. Ortiz R, Sayre KD, Govaerts B, Gupta R, Subbarao GV, Ban T, Reynolds M. Climate change: can wheat beat the heat?. Agriculture, Ecosystems & Environment. 2008;126(1-2):46-58.
  • 3. Singh R, Upadhyay AK, Chandra P, Singh DP. Sodium chloride incites reactive oxygen species in green algae Chlorococcum humicola and Chlorella vulgaris: implication on lipid synthesis, mineral nutrients, and antioxidant system. Bioresource technology. 2018;270:489-497.
  • 4. Hidalgo A, Brandolini, A. Nutritional properties of einkorn wheat (Triticum monococcum L.). Journal of the Science of Food and Agriculture. 2014;94(4), 601-612.
  • 5. Turfan N, Sarıyıldız T, Mutlu E. Variation in Chemical Constituents of Siyez Wheat (Triticum monococcum L.) in Response to Some Abiotic Stress Factors. Turkish Journal of Agriculture-Food Science and Technology. 2019;7(4), 598-605.
  • 6. Ilhan S, Ozdemir F, Bor M. Contribution of trehalose biosynthetic pathway to drought stress tolerance of Capparis ovata Desf. Plant Biology. 2015;17(2):402-407.
  • 7. Vijayakumar M, Vijayakumar R, Stephen R. In vitro propagation of Bacopa monnieri L.-a multipurpose medicinal plant. Indian Journal of Science and Technology. 2010;3(7):782-787.
  • 8. Kim DH, Gopal J, Sivanesan I. Nanomaterials in plant tissue culture: the disclosed and undisclosed. RSC advances. 2017;7(58):36492-36505.
  • 9. Yu H, Luo D, Li SFY, Qu M, Liu D, He Y, Cheng F. Interpretable machine learning-accelerated seed treatment using nanomaterials for environmental stress alleviation. Nanoscale. 2023; 15(32), 13437-13449.
  • 10. Zhou P, Adeel M, Shakoor N, Guo M, Hao Y, Azeem I, Rui Y. Application of nanoparticles alleviates heavy metals stress and promotes plant growth: An overview. Nanomaterials. 2020; 11(1), 26.
  • 11. Mazhar MW, Ishtiaq M, Maqbool M, Akram R. Seed priming with Calcium oxide nanoparticles improves germination, biomass, antioxidant defence, and yield traits of canola plants under drought stress. South African Journal of Botany. 2022;151, 889-899.
  • 12. Finkelstein R. Abscisic acid synthesis and response. The Arabidopsis book/American society of plant biologistsPlant Biologists. 2013 ;11, e0166.
  • 13. Tuteja N. Abscisic acid and abiotic stress signaling. Plant signaling & behavior. 2007;2(3), 135-138.
  • 14. Sah SK, Reddy KR, Li J. Abscisic acid and abiotic stress tolerance in crop plants. Frontiers in plant sciencePlant Science. 2016;7, 571.
  • 15. Vahdati K, Bayat S, Ebrahimzadeh H, Jariteh M, Mirmasoumi M. Effect of exogenous ABA on somatic embryo maturation and germination in Persian walnut (Juglans regia L.). Plant Cell, Tissue and Organ Culture. 2008; 93, 163-171.
  • 16. Purohit SD, Singhvi A. Micropropagation of Achras sapota through enhanced axillary branching. Scientia Horticulturae. 1998;76(3-4):219-229.
  • 17. Rai MK, Shekhawat NS, Harish, Gupta AK, Phulwaria M, Ram K, Jaiswal U. The role of abscisic acid in plant tissue culture: a review of recent progress. Plant Cell, Tissue and Organ Culture (PCTOC). 2011;106:179-190.
  • 18. Murashige T, Skoog F.A A A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiologia plantarum. 1962;15(3).
  • 19. Sayir F, Sehitogullan A, Demir H. Serum prolidase activity, total oxidant/antioxidant, and nitric oxide levels in patients with esophageal squamous cell carcinoma. Türk Gogus Kalp Damar Cerrahisi Derg. 2019; 27:206–211.
  • 20. Blois MS. Antioxidant determinations by the use of a stable free radical. Nature. 1958;181(4617), 1199-1200.
  • 21. Apak R, Güçlü K, Demirata B, Özyürek M, Çelik SE, Bektaşoğlu B, Özyurt D. Comparative evaluation of various total antioxidant capacity assays applied to phenolic compounds with the CUPRAC assay. Molecules. 2007;12(7):1496-1547.
  • 22. Flurkey WH. Polyphenoloxidase in higher plants: immunological detection and analysis of in vitro translation products. Plant physiology. 1986;81(2), 614-618.
  • 23. Nadaroğlu H, Demir Y, Demir N. Antioxidant and radical scavenging properties of Iris germanica. Pharmaceutical Chemistry Journal. 2007;41(8), 409-415.
  • 24. Jiang M, Zhang J. Water stress‐induced abscisic acid accumulation triggers the increased generation of reactive oxygen species and up‐regulates the activities of antioxidant enzymes in maize leaves. Journal of experimental botanyExperimental Botany. 2002; 53(379), 2401-2410.
  • 25. Taşğın E, Nadaroğlu H, Adıgüzel A, Baltacı MÖ, Sönmez Z. Soya bitkisindeki glutatyon redüktaz aktivitesi ve mrna seviyesinin kuraklık stresinde salisilik asit ile değişimleri. Akademik Platform Mühendislik ve Fen Bilimleri Dergisi.2017;5(2), 48-52.
  • 26. Ertuş MM, Yazıcılar B. CaO nanoparticle enhances the seedling growth of Onobrycis viciifolia under drought stress via mannitol use. Biologia. 2023;78(4):1119-1127.
  • 27. Kudla J, Batistič O, Hashimoto K. Calcium signals: the lead currency of plant information processing. The Plant Cell. 2010;22(3):541-563.
  • 28. B Bursal E, Aras A, Doğru M, Kılıç Ö. Phenolic content, antioxidant potentials of Saponaria prostrata endemic plant. International Journal of Life Sciences and Biotechnology. 2021;5(1):1-8.
  • 29. Karakavuk E. Determination of antioxidant capacity and phenolic content of Tunceli garlic extracts (allium Allium Ttuncelianum) by different solvents. Eurasian Journal of Food Science and Technology. 2021;5(2):205-212.
  • 30. Wang S, Li F, Wang G, Li H, Li X, Cao X, Wang J. Polyphenol oxidase gene editing changed the flavonoid composition and browning process of litchi (Litchi chinensis Sonn.) callus. Gene. 2025 ;936:149130.
  • 31. Sharma R, Kaur R. Insights into fluoride-induced oxidative stress and antioxidant defences in plants. Acta physiologiae plantarum. 2018;40(10):181.
There are 31 citations in total.

Details

Primary Language English
Subjects Plant Cell and Molecular Biology, Biochemistry and Cell Biology (Other)
Journal Section Research Article[En]
Authors

Bahar Halis 0009-0002-1503-2323

Oğuzhan Ertüfekçi 0009-0006-3538-2354

Büşra Yazıcılar 0000-0001-8806-0291

Merve Şimşek Geyik 0000-0002-4088-183X

Ayşe Üstün Başkut 0000-0002-4723-052X

Hayrunnisa Nadaroğlu 0000-0002-0536-4212

Early Pub Date July 21, 2025
Publication Date July 13, 2025
Submission Date March 27, 2025
Acceptance Date July 1, 2025
Published in Issue Year 2025 Volume: 4 Issue: 1

Cite

APA Halis, B., Ertüfekçi, O., Yazıcılar, B., … Şimşek Geyik, M. (2025). Triticum monococcum callus of ecotypes applying ABA and CaO exhibit improved antioxidant enzyme activities. Eurasian Journal of Molecular and Biochemical Sciences, 4(1), 1-10.