Abstract
Oxidative stress causes damage to proteins, lipids and nucleic acids, and thereby compromises cell viability. Some of the oxidative stress markers in an eukaryotic model organism, fission yeast Schizosaccharomyces pombe, were evaluated in this study. Intracellular oxidation, protein carbonyls, lipid peroxidation and reduced glutathione (GSH) levels were investigated in H2O2-treated and non-treated control cells. It was observed that increased H2O2 concentration proportionally lowered the cell number and increased the intracellular oxidation, lipid peroxidation and protein carbonyl levels in S. pombe. A dose-dependent decrease in GSH level was also detected. The fission yeast S. pombe is best known for its contribution to understanding of eukaryotic cell cycle control. S. pombe displays a different physiology from Saccharomyces cerevisiae in several ways and is thus probably more closely related to higher eukaryotes. The purpose of this study was to provide some data about the effects of hydrogen peroxide on the proteins and lipids in the fission yeast. The data obtained here is expected to constitute a basis for the further studies on redox balance and related processes in yeast and mammalian cells.
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Abbreviations
- DCFH:
-
2,7-dichlorofluorescein
- DCFH-DA:
-
2,7-dichlorofluorescein diacetate
- GSH:
-
glutathione
- MDA:
-
malondialdehyde
- ROS:
-
reactive oxygen species
- TBARS:
-
thiobarbituric acid reactive substances
References
Aust S.D. 1994. Thiobarbituric acid assay reactants. Methods Toxicol. 1B: 367–374.
Bass D.A., Parce J.W., Dechatelet L.R., Szejda P., Seeds M.C. & Thomas M. 1983. Flow cytometric studies of oxidative product formation by neutrophils: a graded response to membrane stimulation. J. Immunol. 130: 1910–1917.
Beutler E. 1975. Red Cell Metabolism. A Manual of Biochemical Methods, 2nd ed., Grune & Stratton, New York, 160 pp.
Cabiscol E., Piulats E., Echave P., Hierrero E. & Ros J. 2000. Oxidative stress promotes specific protein damage in Saccharomyces cerevisiae. J. Biol. Chem. 275: 27393–27398.
Cabiscol E. & Ros J. 2006. Oxidative damage to proteins: structural modifications and consequences in cell function, pp. 399–471. In: Dalle-Donne I., Scaloni A. & Butterfield D.A. (eds), Redox Proteomics: From Protein Modifications to Cellular Dysfunction and Disease, John Wiley & Sons, Inc., Hoboken.
Costa V.M., Amorim M.A., Quintanilha A. & Modoras-Ferreria P. 2002. Hydrogen peroxide-induced carbonylation of key metabolic enzymes in Saccharomyces cerevisiae: the involvement of the oxidative stress response regulators Yap1 and Skn7. Free Radic. Biol. Med. 33: 1507–1515.
Dalle-Donne I., Adlini G., Carini M., Colombo R., Rossi, R. & Milzani A. 2006. Protein carbonylation, cellular dysfunction, and disease progression. J. Cell Mol. Med. 10: 389–406.
Davies M.J., Fu S., Wang H. & Dean R.T. 1999. Stable markers of oxidant damage to proteins and their application in study of human disease. Free Radic. Biol. Med. 27: 1151–1161.
Grant C.M., MacIver F.H. & Dawes I.W. 1996. Glutathione is an essential metabolite required for resistance to oxidative stress in the yeast Saccharomyces cerevisiae. Curr. Genet. 29: 511–515.
Grant C.M., Perrone G. & Dawes, I.W. 1998. Glutathione and catalase provide overlapping defenses for protection against hydrogen peroxide in the yeast Saccharomyces cerevisiae. Biochem. Biophys. Res. Commun. 253: 893–898.
Halliwell B. & Gutteridge M.C.J. 1998. Free Radicals in Biology and Medicine, 3rd ed., Oxford University Press, London, 980 pp.
Inai Y. & Nishikimi M. 2002. Increased degradation of oxidised proteins in yeast defective in 26 S proteasome assembly. Arch. Biochem. Biophys. 404: 279–284.
Izawa S., Inoue Y. & Kimura A. 1995. Oxidative stress response in yeast: effect of glutathione on adaptation to hydrogen peroxide stress in Saccharomyces cerevisiae. FEBS Lett. 368: 73–76.
Lee J., Spector D., Godon C., Labarre J. & Toledano M.B. 1999. A new antioxidant with alkyl hydroperoxide defense properties in yeast. J. Biol. Chem.274: 4537–4544.
Nasim A., Young P. & Johnson B. F. 1989. Molecular Biology of the Fission Yeast, Academic Press, San Diego, 488 pp.
Okai Y., Okai H.K., Machida K., Nakamura H., Nakayama K., Fujita K., Tanaka T., Otani S. & Taniguchi M. 2000. Protective effect of antioxidants against para-nonylphenol-induced inhibition of cell growth in Saccharomyces cerevisiae. FEMS Microbiol. Lett. 185: 65–70.
Penninckx M. 2000. A short review on the role of glutathione in response of yeasts to nutritional, environmental, and oxidative stresses. Enzyme Microb. Technol. 26: 737–742.
Waterborg, J.H. 2002. The Lowry Method for Protein Quantitaion, pp. 7–9. In: Walker J.M. (ed.) The Protein Protocols Handbook, Humana Press, Totowa, New Jersey.
Wang J.F., Jerrels T.R. & Spitzer J.J. 1996. Decreased production of reactive oxygen intermediates is an early event during in vitro apoptosis of rat thymocytes. Free Radic. Biol. Med. 20: 533–542.
Yanagida M. 2002. The model unicellular eukaryote, Schizosaccharomyces pombe. Genome Biol. 3: 1–4.
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Pekmez, M., Arda, N., Hamad, İ. et al. Hydrogen peroxide-induced oxidative damages in Schizosaccharomyces pombe . Biologia 63, 151–155 (2008). https://doi.org/10.2478/s11756-008-0040-0
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DOI: https://doi.org/10.2478/s11756-008-0040-0