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Activity of the photosynthetic apparatus and antioxidant enzymes in leaves of transgenic Solanum lycopersicum and Nicotiana tabacum plants, with FeSOD1 gene

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Abstract

Introduction of the FeSOD gene enhanced the stability of the photosynthetic apparatus of plants to the action of oxidative stress caused by UV irradiation. The expression of Arabidopsis thaliana FeSOD gene, targeting the enzyme in chloroplasts due to a signal sequence, leaded to significant changes in ultrastructure of cell subcompartments of tobacco and tomato leaves. The activity of superoxide dismutase in leaves of transgenic tomato plants exceeded the value of activity of this enzyme of control plants. Transgenic tobacco plants showed increasing in SOD activity compared with control non-transgenic tobacco. The activity of AP in the leaves of transgenic tobacco and tomato plants was similar with that of control non-transgenic plants, but activity of one accession of transgenic tomato, which is also characterized by high values of SOD activity, exceeded the value of control plant. Differences in ultrastructural organization of chloroplasts in the cells of transgenic and control tobacco and tomato plants have been manifested in a strong enlargement in the size of plastoglobuli. These distinctions were evident especially in the cells of the leaf parenchyma of transgenic tomato as well as transgenic tobacco. Also, a quantity of starch grains in the plastids of guard cells was increased. Chloroplasts in the cells of leaf parenchyma in transgenic plants contained less a starch grains than in wild-type plants.

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References

  1. Mittler, R., Oxidative Stress, Antioxidants and Stress Tolerance, Trends in Plant Sci., 2002, vol. 7, no. 9, pp. 405–410.

    Article  CAS  Google Scholar 

  2. Baranova, E.N. and Gulevich, A.A., Problems and Prospects of Genetic Engineering Approach in Addressing Issues of Plant Resistance to Salinity, Sel’skokhozyaistvennaya Biol., Ser. Bio., 2006, No. 1, pp. 39–56.

  3. Singla-Pareek, S.L., Pareek, A., and Sopory, S.K., Transgenic Plants for Dry and Saline Environments, Advances in Molecular Breeding Toward Drought and Salt Tolerant Crops, Springer, 2007, pp. 501–530.

  4. McKersie, B.D., Bowley, S.R., Harjanto, E., and Leprince, O., Water-Deficit tolerance and Field Performance of Transgenic Alfalfa Overexpressing Superoxide Dismutase, Plant Physiol., 1996, vol. 111, no. 4, pp. 1177–1181.

    CAS  PubMed  Google Scholar 

  5. Badawi, G.H., Yamauchi, Y., Shimada, E., Sasaki, R., Kawano, N., and Tanaka, K., Enhanced Tolerance to Salt Stress and Water Deficit by Overexpressing Superoxide Dismutase in Tobacco (Nicotiana tabacum) Chloroplasts, Plant Sci., vol. 166, no. 4, pp. 919–928.

  6. Roxas, V.P., Smith, R.K., Allen, Jr. Er.R., and Allen, R.D., Overexpression of Glutathione S-Transferase/Glutathioneperoxidase Enhances the Growth of Transgenic Tobacco Seedlings during Stress, Nature Biotechnol., 1997, vol. 15, pp. 988–991.

    Article  CAS  Google Scholar 

  7. Alscher, R.G., Erturk, N., and Heath, L.S., Role of Superoxide Dismutases (SODs) in Controlling Oxidative Stress in Plants, J. Exp. Bot., 2002, vol. 53, pp. 1331–1341.

    Article  CAS  PubMed  Google Scholar 

  8. Kliebenstein, D.J., Monde, R.A., and Last, R.L., Superoxide dismutase in Arabidopsis: an Eclectic Enzyme Family with Disparate Regulation and Protein Localization, Plant Physiol., 1998, vol. 118, pp. 637–650.

    Article  CAS  PubMed  Google Scholar 

  9. Myouga, F., Hosoda, Ch., Umezawa, T., Lizumi, H., Kuromori, T., Motohashi, R., Shono, Y., Nagata, N., Ikeuchi, M., and Shinozaki, K., A Heterocomplex of Iron Superoxide Dismutases Defends Chloroplast Nucleoids Against Oxidative Stress and is Essential for Chloroplast Development, Plant Cell, 2008, vol. 20, pp. 3148–3162.

    Article  CAS  PubMed  Google Scholar 

  10. Serenko, E.K., Ovchinnikov, V.N., Kurenina, L.V., Baranova, E.N., Gulevich, A.A., Maysuryan, A.N., and Kharchenko, P.N., Production of Transgenic Tomato Plants with the Gene for Fe-Dependent Superoxide Dismutase, Russ. J. Agr. Sci., 2009, vol. 35, no. 4, pp. 223–226.

    Article  Google Scholar 

  11. Kreslavsky, V.D., Fomina, I.R., Ivanov, A.A., Tatarinsev, N.P., Kosobryuhov, A.A., Biel, K.Ya., and Herbert, S.K., NaCl-Stimulated Fotoingibirovanie and Restoration of Photosynthetic Activity of the Mutant katG-Cyanobacterium Synechocystis sp. PCC 6803, Biophysics, 2010, No. 3, pp. 32–36.

  12. Giannopolitis, C.N. and Ries, S.K., Superoxide Dismutases Occurrence in Higher Plants, Plant Physiol., 1977, vol. 59, pp. 309–314.

    Article  CAS  PubMed  Google Scholar 

  13. Nakano, Y. and Asada, K., Hydrogen Peroxide Is Scavenged by Ascorbate-Specific Peroxidase in Spinach Chloroplasts, Plant Cell Physiol., 1981, vol. 22, pp. 867–880.

    CAS  Google Scholar 

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Correspondence to E. N. Baranova.

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Baranova, E.N., Serenko, E.K., Balachnina, T.I. et al. Activity of the photosynthetic apparatus and antioxidant enzymes in leaves of transgenic Solanum lycopersicum and Nicotiana tabacum plants, with FeSOD1 gene. Russ. Agricult. Sci. 36, 242–249 (2010). https://doi.org/10.3103/S1068367410040075

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  • DOI: https://doi.org/10.3103/S1068367410040075

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