|کد مقاله||کد نشریه||سال انتشار||مقاله انگلیسی||ترجمه فارسی||نسخه تمام متن|
|5515432||1400765||2017||7 صفحه PDF||ندارد||دانلود کنید|
â¢A method for specific detection of lipid peroxidation product MDA is described.â¢Senescence of tobacco leaves is not correlated with increased lipid peroxidation.â¢Stay-green phenotype of PSAG12::IPT tobacco is associated with increased MDA level.
The involvement of reactive oxygen species (ROS) in the progress of leaf senescence has long been suggested, but there are contrasting results to either support or deny the positive correlation between the senescence progression and the level of ROS-triggered lipid peroxidation. The inconsistency among reported results can partly be attributed to the poor specificity of the most commonly employed colorimetric assay and changes in the ratio of dry weight/fresh weight during leaf senescence. In this study we determined the end-product of lipid peroxidation malondialdehyde (MDA) by GS-MS, and analyzed its changes during senescence of tobacco leaves as calculated on dry weight basis. In leaves of the wild type plants the MDA level did not change during senescence. In the mutant PSAG12::IPT leaves stayed green because of the elevated synthesis of cytokinins, but the MDA level was much higher in comparison to WT when leaves of the same age were compared. These results clearly show that lipid peroxidation is not associated with leaf senescence, at least in tobacco. This GS-MS method can be used to judge the involvement of lipid peroxidation in senescence in other species.
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Journal: Plant Physiology and Biochemistry - Volume 118, September 2017, Pages 161-167