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Subcellular localization and stress responses of superoxide dismutase isoforms from leaves in the C3‐CAM intermediate halophyte Mesembryanthemum crystallinum L

Miszalski, Z. ; Ślesak, I. ; Niewiadomska, E. ; Baczek‐Kwinta, R. ; Lüttge, U. ; Ratajczak, R.

Plant, cell and environment, 1998-02, Vol.21 (2), p.169-179 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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  • Título:
    Subcellular localization and stress responses of superoxide dismutase isoforms from leaves in the C3‐CAM intermediate halophyte Mesembryanthemum crystallinum L
  • Autor: Miszalski, Z. ; Ślesak, I. ; Niewiadomska, E. ; Baczek‐Kwinta, R. ; Lüttge, U. ; Ratajczak, R.
  • Assuntos: Biological and medical sciences ; C3‐photosynthesis ; CAM ; Enzymes ; Fundamental and applied biological sciences. Psychology ; Mesembryanthemum crystallinum L ; Metabolism ; oxidative stress ; Plant physiology and development ; salt stress ; SOD ; Water and solutes. Absorption, translocation and permeability
  • É parte de: Plant, cell and environment, 1998-02, Vol.21 (2), p.169-179
  • Descrição: BSA, bovine serum albumin
CAM, Crassulacean acid metabolism
DTT, dithiothreitol
EDTA, ethylenediaminetetraacetic acid
FPLCfast protein liquid chromatography
HEPES, N‐(2‐hydroxyethyl)piperazine‐Ń‐(ethanesulphonic acid)
ME, β‐mercaptoethanol
NBT, nitro blue tetrazolium
PAGE, polyacrylamide gel electrophoresis
SDS, sodium dodecyl sulphate
SDS‐PAGE, sodium dodecyl sulphate polyacrylamide gel electrophoresis
Rubisco, ribulose‐1,5‐bisphosphate carboxylase/oxygenase (EC 4.1.1.39)
SOD, superoxide dismutase (EC 1.15.1.1)
TEMED, N,N,Ń,Ń‐tetramethylethylenediamine
Tris, Tris (hydroxymethyl) aminomethane
Tricine, N‐Tris(hydroxymethyl)methylglycine

Treatment of Mesembryanthemum crystallinum for several days with 0·4 kmol m–3 NaCl in the root medium, in parallel to an increase of the cell sap osmolarity enhances activity of important antioxidative enzymes, such as superoxide dismutases (SODs). M. crystallinum is equipped with three SOD isoforms. These isoforms were identified as Mn‐, Fe‐, and Cu/Zn‐SODs, respectively. Mn‐SOD was found in the mitochondrial fraction, Fe‐SOD in the chloroplast fraction, and Cu/Zn‐SOD is probably localized in the cytosol. The Fe‐SOD found in M. crystallinum is the first iron‐containing SOD enzyme to be characterized in the plant family Aizoaceae. Salt treatment increases the activity of this isoform earlier than the other SODs. Molecular masses of SOD isoforms were determined as 82, 48 and 34 kDa for Mn‐, Fe‐, Cu/Zn‐SODs, respectively. Native Mn‐SOD seems to be a tetramer, while Fe‐SOD and Cu/Zn‐SOD are dimers. All SOD isoforms show high thermal stability. Mn‐SOD is active even after short heating at 90 °C and Fe‐SOD at 70 °C. Moreover, high concentrations of β‐mercaptoethanol used as a reducing agent did not destroy the function of all isoforms. With the salinity treatment in M. crystallinum, Crassulacean acid metabolism (CAM) is induced. Build‐up of large stationary O2 concentrations in the leaf air spaces is associated with the photosynthetic CO2 reduction behind closed stomata in phase III of CAM. This illustrates why M. crystallinum may require higher antioxidative activities under NaCl stress and also explains earlier findings that CAM plants are more resistant than C3 plants to environmental stress as imposed by, for example, SO2 and O3.
  • Editor: Oxford, UK: Blackwell Publishing Ltd
  • Idioma: Inglês
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