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Ozone detoxification in the mesophyll cell wall during a simulated oxidative burst
1Institute of Molecular and Cell Biology, University of Tartu, Estonia. hei@ut.ee
Free Radical Research
|February 29, 2000
Summary
Superoxide radical (O2*-) generation during oxidative bursts is ineffective in reducing ozone (O3) in plant cell walls. High hydrogen peroxide (H2O2) generation rates do not significantly contribute to O3 detoxification.
Area of Science:
- Plant Physiology
- Biochemistry
- Environmental Science
Background:
- Ozone (O3) is a phytotoxic air pollutant causing oxidative stress in plants.
- Plant cell walls possess antioxidant systems to detoxify reactive oxygen species (ROS).
- Oxidative bursts can generate superoxide radicals (O2*-) and hydrogen peroxide (H2O2).
Purpose of the Study:
- To assess the role of superoxide radical (O2*-) in ozone (O3) reduction within mesophyll cell walls.
- To compare O3 reduction pathways involving O2*- with those involving hydrogen peroxide (H2O2) and ascorbate.
- To evaluate the effectiveness of O2*- generation during oxidative bursts in detoxifying O3.
Main Methods:
- Computational modeling of O3 reduction reactions in plant cell walls.
- Comparison of O3 flow through O2*- dependent and H2O2-forming reaction sequences.
- Inclusion of direct O3 reaction with ascorbate and O2*- disproportionation/reduction.
- Simulations based on experimental exposure of Phaseolus vulgaris leaves to O3.
Main Results:
- O3 reduction via reaction with O2*- accounted for only 25-44% of O3 detoxified by direct ascorbate reaction.
- Over 99% of O2*- was converted to H2O2 through spontaneous disproportionation (pH 5) or ascorbate reduction (pH 7).
- Calculated steady-state H2O2 concentrations (40-80 microM) were primarily scavenged by peroxidase.
- Postulated H2O2 generation rates were excessively high for significant O3 reduction.
Conclusions:
- Superoxide radical (O2*-) generation during oxidative bursts is inefficient for detoxifying ozone (O3) in plant cell walls.
- The calculated H2O2 generation rates were too high to be effectively utilized for O3 reduction.
- Superoxide dismutase induction in the cell wall under O3 exposure warrants further investigation.