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NaCl and CuSO 4 treatments trigger distinct oxidative defence mechanisms in Nicotiana plumbaginifolia L.
Author(s) -
SAVOURÉ A.,
THORIN D.,
DAVEY M.,
HUA XUEJUN,
MAURO S.,
VAN MONTAGU M.,
INZÉ D.,
VERBRUGGEN N.
Publication year - 1999
Publication title -
plant, cell and environment
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.646
H-Index - 200
eISSN - 1365-3040
pISSN - 0140-7791
DOI - 10.1046/j.1365-3040.1999.00404.x
Subject(s) - superoxide dismutase , antioxidant , chemistry , biochemistry , catalase , peroxidase , oxidative stress , osmolyte , proline , glutathione reductase , glutathione , photoinhibition , peroxynitrite , photosynthesis , superoxide , glutathione peroxidase , enzyme , photosystem ii , amino acid
To gain better insights into the generation of oxidative stress by NaCl stress, we compared the effects of toxic, sublethal concentrations of NaCl (150 m M ) with those of CuSO 4 (100 μ M ) on the antioxidant defence responses of Nicotiana plumbaginifolia L. plants grown in hydroponic culture. Short‐ and long‐term adaptive responses were investigated as well as the effects of root cutting to allow rapid absorption of ions. Our results show that photosynthesis is already affected after 12 h of both treatments and that photoinhibition is induced. Furthermore, the two treatments showed distinct patterns of induction of the genes of the antioxidant systems. Principally, NaCl stimulated catalase activity through activation of the Cat2 and Cat3 genes, whereas with CuSO 4 , transcript levels, protein levels, and enzymatic activities of glutathione peroxidase, ascorbate peroxidase, and superoxide dismutase were differentially induced. The antioxidants ascorbate and glutathione were found to be largely oxidized after 12 h, suggesting an inability of the recycling process to cope with the stress. In addition, both NaCl and CuSO 4 treatments stimulated the accumulation of the osmolyte proline. Therefore, we conclude that the uptake and accumulation of different types of ions lead to the generation of distinct antioxidant responses in N. plumbaginifolia .