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UV-B radiation induces biphasic burst of hydrogen peroxide in mesophyll Chlorella vulgaris

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Abstract

The fluctuations of hydrogen peroxide and total hydroperoxides were followed up at different time points in UV-B-irradiated cell suspension cultures of the green microalga Chlorella vulgaris. A biphasic burst of hydrogen peroxide was recorded, while cell viability was strongly reduced. This pattern is similar to the two wave oxidative burst in plants expressing hypersensitive response to pathogens and PCD and implies the occurrence of a PCD-like response in UV-B-exposed unicellular green algae.

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Abbreviations

EPR:

electron paramagnetic resonance

PAR:

4-(2-pyridylazo)resorcinol

PCD:

programmed cell death

TCA:

trichloroacetic acid

TTC:

triphenyl tetrazolium chloride

References

  1. Smith, R.C., Prezelin, B.B., Baker, K.S., Bidigare, R.R., Boucher, N.P., Coley, T., Karentz, D., MacIntyre, S., Matlick, H.A., Menzies, D., Ondrusek, M., Wan, Z., and Waters, K.J., Ozone depletion: ultraviolet radiation and phytoplankton biology in Antarctic waters, Science, 1992, vol. 255, pp. 952–959.

    Article  CAS  PubMed  Google Scholar 

  2. Halliwell, B. and Gutteridge, J.M.C., Free Radicals in Biology and Medicine, Oxford: Oxford University Press, 2007.

    Google Scholar 

  3. Prado, F.E., Rosa, M., Prado, C., Podazza, G., Interdonato, R., Gonzales, H., and Hilal, M. UV-B radiation, its effects and defense mechanisms in terrestrial plants, Environmental Adaptations and Stress Tolerance in Plants in the Era of Climate Change, Ahmad P., and Prasad M.N.V., Eds., New York: Springer, 2012, pp. 57–83.

    Chapter  Google Scholar 

  4. Gadjev, I., Stone, J.M., and Gechev, T.S., Programmed cell death in plants: new insights into redox regulation and the role of hydrogen peroxide, Int. Rev. Cell Mol. Biol., 2008, vol. 270, pp. 87–143.

    Article  CAS  PubMed  Google Scholar 

  5. Matilla-Vázquez, M.A., and Matilla, A.J., Role of H2O2 as signaling molecule in plants, Environmental Adaptations and Stress Tolerance in Plants in the Era of Climate Change, Ahmad, P. and Prasad, M.N.V., Eds., New York, Dordrecht: Springer, 2012, pp. 361–380.

    Chapter  Google Scholar 

  6. He, R., Druri, G.E., Rotari, V.I., Gordon, A., Willer, M., Farzaneh, T., Woltering, E.J., and Gallois, P., Metacaspase-8 modulates programmed cell death induced by ultraviolet light and H2O2 in Arabidopsis, J. Biol. Chem., 2008, vol. 283, pp. 774–783.

    Article  CAS  PubMed  Google Scholar 

  7. Gao, C., **ng, D., Li, L., and Zhang, L., Implication of reactive oxygen species and mitochondrial dysfunction in the early stages of plant programmed cell death induced by ultraviolet-C overexposure, Planta, 2008, vol. 227, pp. 755–767.

    Article  CAS  PubMed  Google Scholar 

  8. He, Y.Y. and Häder, D.P., Reactive oxygen species and UV-B: effect on cyanobacteria, Photochem. Photobiol. Sci., 2002, vol. 1, pp. 729–736.

    Article  CAS  PubMed  Google Scholar 

  9. Shiu, C.T. and Lee, T.M., Ultraviolet-B-induced oxidative stress and responses of the ascorbate-glutathione cycle in a marine macroalga Ulva fasciata, J. Exp. Bot., 2005, vol. 56, pp. 2851–2865.

    Article  CAS  PubMed  Google Scholar 

  10. Malanga, B. and Puntarulo, S., Oxidative stress and antioxidant content in Chlorella vulgaris after exposure to ultraviolet-B radiation, Physiol. Plant., 1995, vol. 94, pp. 672–679.

    Article  CAS  Google Scholar 

  11. Malanga, G., Calmanovici, G., and Puntarulo, S., Oxidative damage to chloroplasts from chlorella vulgaris exposed to ultraviolet-b radiation, Physiol. Plant., 1997, vol. 101, pp. 455–462.

    Article  CAS  Google Scholar 

  12. Estevez, M.S., Malanga, G., and Puntarulo, S., UV-B effects on Antarctic Chlorella sp. cells, J. Photochem. Photobiol., Ser. B: Biol., 2001, vol. 62, pp. 19–25.

    Article  CAS  Google Scholar 

  13. Chen, L., Deng, L., DePhilippis, R., Tian, W., Wu, H., and Wang, J., UV-B resistance as a criterion for the selection of desert microalgae to be utilized for inoculating desert soils, J. Appl. Phycol., 2013, vol. 25, pp. 1009–1015.

    Article  CAS  Google Scholar 

  14. Edreva, A., Pouneva, I., and Gesheva, E., Biphasic burst of hydrogen peroxide in UV-B-irradiated green alga Chlorella vulgaris, C. R. Acad. Bulg. Sci., 2010, vol. 63, pp. 1315–1320.

    CAS  Google Scholar 

  15. Georgiev, G., Dilov, H., and Avramova, S., Millieu nutritif tamponé et méthode de culture intensive des microalgues vertes, Hydrobiology (Bulgaria), 1978, vol. 7, pp. 14–23.

    CAS  Google Scholar 

  16. Patterson, B.D., MacRae, E.A., and Ferguson, I.B., Estimation of hydrogen peroxide in plant extracts using titanium (IV), Anal. Biochem., 1984, vol. 139, pp. 487–492.

    Article  CAS  PubMed  Google Scholar 

  17. Wolff, S.P., Ferrous ion oxidation in presence of ferric ion indicator xylenol orange for measurement of hydroperoxides, Methods Enzymol., 1994, vol. 233, pp. 182–189.

    Article  CAS  Google Scholar 

  18. Steponkus, P.L. and Lanphear, F.O., Refinement of the triphenyl tetrazolium chloride method of determining cold injury, Plant Physiol., 1967, vol. 42, pp. 1423–1426.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  19. Edreva, A., Generation and scavenging of reactive oxygen species in chloroplasts: a submolecular approach, Agr. Ecosyst. Environ., 2005, vol. 106, pp. 119–133.

    Article  CAS  Google Scholar 

  20. Malanga, G., Kozak, R.G., and Puntarulo, S., N-acetylcysteine-dependent protection against UV-B damage in two photosynthetic organisms, Plant Sci., 1999, vol. 141, pp. 129–137.

    Article  CAS  Google Scholar 

  21. Kováčik, J., Klejdus, B., and Bačkor, M., Physiological responses of Scenedesmus quadricauda (Clorophyceae) to UV-A and UV-C light, Photochem. Photobiol., 2010, vol. 86, pp. 612–616.

    Article  PubMed  Google Scholar 

  22. Darehshouri, A. and Lütz-Meindl, U., H2O2 localization in the green alga Micrasterias after salt and osmotic stress by TEM-coupled electron energy loss spectroscopy, Protoplasma, 2010, vol. 239, pp. 49–56.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  23. He, Y.Y. and Häder, D.P., Involvement of reactive oxygen species in UV-B damage to the cyanobacterium Anabaena sp., J. Photochem. Photobiol., Ser. B: Biol., 2002, vol. 66, pp. 73–80.

    Article  CAS  Google Scholar 

  24. Lamb, C. and Dixon, R.A., The oxidative burst in plant disease resistance, Annu. Rev. Plant Physiol. Plant Mol. Biol., 1997, vol. 48, pp. 251–275.

    Article  CAS  PubMed  Google Scholar 

  25. Mahalingam, R., Jambunathan, N., Gunjan, S.K., Faustin, E., Weng, H., and Ayoubi, P., Analysis of oxidative signalling induced by ozone in Arabidopsis thaliana, Plant Cell Environ., 2006, vol. 29, pp. 1357–1371.

    Article  CAS  PubMed  Google Scholar 

  26. Pellegrini, E., Trivellini, A., Campanella, A., Francini, A., Lorenzini, G., Nali, C., and Vernieri, P., Signalling molecules and cell death in Melissa officinalis plants exposed to ozone, Plant Cell Rep., 2013, vol. 32, pp. 1965–1980.

    Article  CAS  PubMed  Google Scholar 

  27. Kreslavski, V.D., Lyubimov, V.Yu., Shirshikova, G.N., Shmarev, A.N., Kosobryukhov, A.A., Schmitt, F.-J., Friedrich, Th., and Allakhverdiev, S.I., Preillumination of lettuce seedlings with red light enhances the resistance of photosynthetic apparatus to UV-A, J. Photochem. Photobiol., Ser. B: Biol., 2013, vol. 122, pp. 1–6.

    Article  CAS  Google Scholar 

  28. Moharicar, S., D’Souza, J.S., Kulkarni, A.B., and Rao, B.J., Apoptotic-like cell death pathway is induced in unicellular chlorophyte Chlamidomonas reinhardtii (chlorophyceae) cells following UV irradiation: detection and functional analyses, J. Phycol., 2006, vol. 42, pp. 423–433.

    Article  Google Scholar 

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Correspondence to A. M. Edreva.

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Edreva, A.M., Pouneva, I.D. & Gesheva, E.Z. UV-B radiation induces biphasic burst of hydrogen peroxide in mesophyll Chlorella vulgaris . Russ J Plant Physiol 62, 219–223 (2015). https://doi.org/10.1134/S1021443715010069

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