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Differential antioxidative responses of ascorbate-glutathione cycle enzymes and metabolites to chromium stress in green gram ( Vigna radiata L. wilczek) leaves

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TLDR
It is demonstrated that Cr-induced oxidative stress is an important component of the plant’s reaction to toxic levels of Cr and that increased enzyme activities would be responsible for the removal of H2O2.
Abstract
Chromium-induced antioxidative responses of ascorbate-glutathione cycle enzymes and metabolites in green gram(Vigna radiata L. Wilczek) leaves were investigated in both dose and time-dependent manners. Rapid uptake of Cr was observed immediately after the start of treatment. Significant reduction was observed in leaf biomass under 300 µM Cr-treatment. Treatment with 300 µM Cr increases the content of hydrogen peroxide and Superoxide dismytase activity upto initial 96 h, and then gradually declined to the basal level. Ascorbate peroxidase and guaiacol peroxidase activities were low in 300 µM Cr-treated leaves during the first 96 h, but significantly increased therefore, suggesting that increased enzyme activities would be responsible for the removal of H2O2. Catalase activities were always suppressed under Cr stress. Contents of reduced ascorbate and dehydroascorbate were significantly decreased under 300 uM Cr-treatment. The reduced glutathione content decreased at early stages of Cr-treatment. However, it was restored to the normal level as in controls thereafter. In contrast, the glutathione disulphide content showed a progressive increase during the initial hours of Cr-treatment. The non-protein thiol content was shown to increase during the first several hours, but it declines at later stages. The present results demonstrate that Cr-induced oxidative stress is an important component of the plant’s reaction to toxic levels of Cr.

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Reactive Oxygen Species in Plants: Their Generation, Signal Transduction, and Scavenging Mechanisms

TL;DR: The generation, origin, and role of ROS in signal transduction and cell death, and the removal of ROS by antioxidative defense systems in plants during various developmental pathways are described.
Journal ArticleDOI

Uncommon heavy metals, metalloids and their plant toxicity: a review

TL;DR: In this article, the phytotoxicity of rare heavy metals and metalloids such as tellurium, germanium, gallium, scandium, gold, platinum group metals (palladium, platinum and rhodium), technetium, tungsten, uranium, thorium, and rare earth elements yttrium and lanthanum are reviewed.
Journal ArticleDOI

2,4-dichlorophenoxyacetic acid-induced leaf senescence in mung bean (Vigna radiata L. Wilczek) and senescence inhibition by co-treatment with silver nanoparticles.

TL;DR: It is suggested that increased oxidative stress and H(2)O(2)) led to senescence in mung bean leaves and significantly induced antioxidative enzymes are not sufficient to protect mungbean cells from 2,4-D-induced harmful ROS.
Journal ArticleDOI

Cobalt-induced oxidative stress causes growth inhibition associated with enhanced lipid peroxidation and activates antioxidant responses in Indian mustard ( Brassica juncea L.) leaves

TL;DR: It is suggested that excess Co reduces seedling growth by inducing oxidative stress related to lipid peroxidation and overproduction of O2·− and H2O2.
References
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Journal Article

Protein Measurement with the Folin Phenol Reagent

TL;DR: Procedures are described for measuring protein in solution or after precipitation with acids or other agents, and for the determination of as little as 0.2 gamma of protein.
Journal ArticleDOI

Tissue sulfhydryl groups

TL;DR: A water-soluble (at pH 8) aromatic disulfide [5,5′-dithiobis(2-nitrobenzoic acid] has been synthesized and shown to be useful for determination of sulfhydryl groups.
Book ChapterDOI

Catalase in vitro

Hugo Aebi
TL;DR: In this article, the catalytic activity of catalase has been investigated using ultraviolet (UV) spectrophotometry and Titrimetric methods, which is suitable for comparative studies for large series of measurements.
Journal ArticleDOI

Superoxide dismutase: Improved assays and an assay applicable to acrylamide gels☆

TL;DR: The staining procedure for localizing superoxide dismutase on polyacrylamide electrophoretograms has been applied to extracts obtained from a variety of sources and could thus be assayed either in crude extracts or in purified protein fractions.
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