Journals / Türk Doğa ve Fen Dergisi / 2026 / Cilt: 14 Sayı: 3

Molecular Biological Effects of Gundelia tournefortii (Kenger Herb) Extract on Saccharomyces cerevisiae Cell Growth: Oxidative Stress and Protective Role

Pages
1–9
Publication Date
2025-09-26
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⚡ TL;DR(Too Long; Didn't Read)

Keywords: Gundelia tournefortii (Kenger plant), Hydrogen peroxide, Oxidative damage, Protein synthesis, Saccharomyces cerevisiae.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Gundelia tournefortii (Kenger plant) is traditionally used for liver diseases, diabetes, chest pain, heart failure, stomach pain, vitiligo, diarrhea, and bronchitis.
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Key Findings & Data:This project investigates whether Gundelia tournefortii has a protective role against hydrogen peroxide (H2O2)-induced oxidative damage in Saccharomyces cerevisiae.
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Conclusion & Impact:Keywords: Gundelia tournefortii (Kenger plant), Hydrogen peroxide, Oxidative damage, Protein synthesis, Saccharomyces cerevisiae.
🔬Design:Araştırma Makalesi
📍Scope:Comprehensive Sample
⚙️Variables:Gundelia tournefortii (Kenger plant) · Hydrogen peroxide · Oxidative damage

Abstract

Gundelia tournefortii (Kenger plant) is traditionally used for liver diseases, diabetes, chest pain, heart failure, stomach pain, vitiligo, diarrhea, and bronchitis. Additionally, it is known for its purgative, sedative, anti-inflammatory, antiparasitic, antiseptic, and antiemetic properties. This project investigates whether Gundelia tournefortii has a protective role against hydrogen peroxide (H2O2)-induced oxidative damage in Saccharomyces cerevisiae. In this study, four groups were established: Control group; H2O2 group (15 millimolar); G. tournefortii group (10%); G. tournefortii (10%) + H2O2 (15 millimolar) group. S. cerevisiae cultures were grown at 30°C for 1, 3, 5, and 24-hour intervals. Cell growth periods, lipid peroxidation malondialdehyde (MDA) analysis, glutathione (GSH) levels, and catalase activity (CAT) were measured using a spectrophotometer. The total protein concentration changes of S. cerevisiae cultures were determined by SDS-PAGE electrophoresis and calculated using the Bradford method. As a result, in the H2O2 group, MDA levels increased, while GSH levels and CAT activity decreased, indicating increased oxidative stress. In the G. tournefortii group, MDA levels decreased, while GSH levels and CAT activity increased, suggesting that this plant has a protective effect. Compared to the H2O2 group, the G. tournefortii + H2O2 group showed increased cell growth and protein concentration, indicating that this group provided stronger cellular defense against oxidative damage, significantly improving cellular functions. Keywords: Gundelia tournefortii (Kenger plant), Hydrogen peroxide, Oxidative damage, Protein synthesis, Saccharomyces cerevisiae.

Özet

Gundelia tournefortii (Kenger plant) is traditionally used for liver diseases, diabetes, chest pain, heart failure, stomach pain, vitiligo, diarrhea, and bronchitis. Additionally, it is known for its purgative, sedative, anti-inflammatory, antiparasitic, antiseptic, and antiemetic properties. This project investigates whether Gundelia tournefortii has a protective role against hydrogen peroxide (H2O2)-induced oxidative damage in Saccharomyces cerevisiae. In this study, four groups were established: Control group; H2O2 group (15 millimolar); G. tournefortii group (10%); G. tournefortii (10%) + H2O2 (15 millimolar) group. S. cerevisiae cultures were grown at 30°C for 1, 3, 5, and 24-hour intervals. Cell growth periods, lipid peroxidation malondialdehyde (MDA) analysis, glutathione (GSH) levels, and catalase activity (CAT) were measured using a spectrophotometer. The total protein concentration changes of S. cerevisiae cultures were determined by SDS-PAGE electrophoresis and calculated using the Bradford method. As a result, in the H2O2 group, MDA levels increased, while GSH levels and CAT activity decreased, indicating increased oxidative stress. In the G. tournefortii group, MDA levels decreased, while GSH levels and CAT activity increased, suggesting that this plant has a protective effect. Compared to the H2O2 group, the G. tournefortii + H2O2 group showed increased cell growth and protein concentration, indicating that this group provided stronger cellular defense against oxidative damage, significantly improving cellular functions.

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Cite This Article

Yılmaz, B., Fırat, H., Beyaz, S., Celayir, N., Aslan, A. (2025). Molecular Biological Effects of Gundelia tournefortii (Kenger Herb) Extract on Saccharomyces cerevisiae Cell Growth: Oxidative Stress and Protective Role. Türk Doğa ve Fen Dergisi, Cilt: 14 Sayı: 3, 1–9. https://doi.org/10.46810/tdfd.1675603

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References (27)

  1. Rakotondramasy-Rabesiaka, L., Havet, J.L., Porte, C., Fauduet, H. Solid–liquid extraction of protopine from Fumaria officinalis L.—analysis determination, kinetic reaction and model building. Separation and purification technology. 2007; 54(2), 253-261.
  2. Gezici, S., Sekeroglu, N. Comparative biological analyses on kenger and kenger coffee as novel functional food products. Journal of Food Science and Technology. 2021; 59(6), 2328–2338.
  3. Amer, J., Salhab, A., Jaradat, N., Abdallah, S., Aburas, H., Hattab, S., Ghanim, M., Alqub, M. Gundelia tournefortii inhibits hepatocellular carcinoma progression by lowering gene expression of the cell cycle and hepatocyte proliferation in immunodeficient mice. Biomedicine & Pharmacotherapy. 2022; 156, 113885.
  4. Mansi, K., Tabaza, Y., Aburjai, T. The iron chelating activity of Gundelia tournefortii in iron overloaded experimental rats. Journal of Ethnopharmacology. 2020; 263, 113114.
  5. Cheng, C.H., Ma, H.L., Liu, G.X., Deng, Y.Q., Feng, J., Jie, Y.K., Guo, Z.X. Oxidative stress, DNA damage, and cellular response in hydrogen peroxide-induced cell injury of mud crab (Scylla paramamosain). Fish & Shellfish Immunology. 2021; 114, 82-89.
  6. Bati, B., Celik, I., Vuran, N.E., Turan, A., Alkan, E.E., Zirek, A.K. Effects of Gundelia tournefortii L. on biochemical parameters, antioxidant activities and DNA damage in a rat model of experimental obesity. Brazilian Journal of Biology. 2021; 83, e251198.
  7. Ohkawa, H., Ohishi, N., Yagi, K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical Biochemistry. 1979; 95(2), 351-358.
  8. Gbaranor, K.B., Maakai, B., Olatunbosun, T.H., Ben, E.E., Otobo, B.M., Enebeli, K.S., Saronee, F., Etim, D.N., Ovili-Odili, B.Z, Daka, I.R. Effects of smoothies on oxidative stress markers following administration of monosodium glutamate in male wistar rats. Sch Int J Anat Physiol. 2024; 7(8), 129-134.
  9. Ellman, G.L. Tissue sulphydryl groups. Archives of biochemistry and biophysics. 1959; 195982(1), 70-77.
  10. Malayeri, A., Birgani, S.M., Basir, Z., Kalantar, H. Protective effects of diosmin on doxorubicin-induced testicular toxicity in rat. Naunyn-Schmiedeberg's Archives of Pharmacology. 2024; 397(10), 7881-7890.
  11. Aebi, H. Catalase in vitro. Methods in Enzymology. 1984; 105, 121-126.
  12. Kandemir, O., Kucukler, S., Comakli, S., Gur, C., İleriturk, M. Docetaxel-induced liver and kidney toxicity in rats can be alleviated by suppressing oxidative stress, endoplasmic reticulum stress, inflammation, apoptosis and autophagy signaling pathways after Silymarin treatment. Food and Chemical Toxicology. 2025; 196, 115202.
  13. Bradford MM. A rapid and sensitive methof for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding, Analytical Biochemistry. 1976; 72, 248–254.
  14. Nili‐Ahmadabadi, A., Abdpour, S., Omidifar, N., Hashemi, S.A., Mousavi, S.M., Ahmadabadi, M.N. Therapeutic potentials of N‐acetylcysteine immobilized polyrhodanine nanoparticles toward acetaminophen‐induced acute hepatotoxicity in rat. Chemical Biology & Drug Design. 2024; 103(1), e14430.
  15. Aslan, A. Protective effects of goji berry on oxidative damage induced by chromium (K₂Cr₂O₇) in Saccharomyces cerevisiae. Bitlis Eren University Journal of Science. 2021; 10, 784-795.
  16. Nergiz, M.A., Beyaz, S., Gok, O., Aslan, A. Evaluation of the antioxidative effects of Hibiscus sabdariffa l. extract on Saccharomyces cerevisiae with molecular biological and biochemical biomarkers. Journal of Applied Biological Sciences. 2024; 18(3), 342-354.
  17. LaemmLi, U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970; 227, 680–685.
  18. Beyaz, S. Investigation of antioxidant activities of Melissa officinalis and Lavandula angustifolia extracts against chromium induced oxidative damage in Saccharomyces cerevisiae with molecular biological and biochemical biomarkers. Progress in Nutrition. 2022; 24(3), 2-11.
  19. Yuksel, A., Celayir, D.N., Yenilmez Tunoglu, E.N., Tutar, L., Tutar, Y. Metabolite-induced apoptosis by Gundelia tournefortii in A549 lung cancer cells: A cytotoxic and gene expression study. Nutrients. 2025; 17(3), 374-388.
  20. Abu-Lafi, S., Rayan, B., Kadan, S., Abu-Lafi, M., Rayan, A. Anticancer activity and phytochemical composition of wild Gundelia tournefortii. Oncology Letters. 2019; 17(1), 713–717.
  21. Vázquez, J., Muñiz-Calvo, S., González, J. Melatonin reduces oxidative stress damage ınduced by hydrogen peroxide in Saccharomyces cerevisiae. Frontiers in Microbiology. 2017; 8, 1066.
  22. Hachem, S., Al Battal, M., Dakdouk, H., Natour, D.E., Borjac, J. Anti-inflammatory and antioxidant effects of Gundelia tournefortii aqueous extract on the liver and kidney of pcos mice. Journal of Evidence-Based Integrative Medicine. 2025; 30, 2515690X241304519.
  23. Karatas, F. Investigation of A, E, and C vitamins, malondialdehyde, and glutathione levels in kenger (Gundelia tournefortii) plant. Erzincan University Journal of Science and Technology. 2014; 7(2), 159-168.
  24. Beyaz, S., Dalkılıc, L.K., Gok, O., Aslan, A. The effect of black mulberry (Morus nigra L.) and cornelian cherry (Cornus mas L.) on some molecular biological and biochemical parameters against hydrogen peroxide-induced oxidative damage in Saccharomyces cerevisiae. Bitlis Eren University Journal of Science. 2020; 9(3), 1134-1144.
  25. Aslan, A. Cell culture development and the imaging of total protein product changing with SDS-PAGE in Saccharomyces cerevisiae. Progress in Nutrition. 2018; 20(1), 128-132.
  26. Aslan, A., Gok, O., Erman, O. The protective effect of kiwi fruit extract against to chromium effect on protein expression in Saccharomyces cerevisiae. Progress in Nutrition. 2017; 19(4), 472-476.
  27. Beyaz, S., Gok, O., Aslan, A., The therapeutic effects and antioxidant properties of epigallocatechin-3 gallate: A new review, International Journal of Secondary Metabolite. 2018; 9(2), 125-136.