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Modulation of oxidative stress responsive enzymes by excess cobalt
- Source :
- Plant Science. 162:381-388
- Publication Year :
- 2002
- Publisher :
- Elsevier BV, 2002.
-
Abstract
- Excess concentration of cobalt in the growth medium produced visual symptoms of toxicity that intensified with increasing level and duration of metal supply. The tissue concentration of cobalt increased with increasing level of supply. Decreased concentrations of chlorophylls and carotenoids and an increased carotenoids/chlorophyll ratio along with a marked increase in the activities of anti-oxidative enzymes, viz. superoxide dismutase (SOD), ascorbate peroxidase (APOD) and nonspecific peroxidase (POD) suggest strong induction of oxidative stress due to excess cobalt in the growth medium. Decrease in the activity of catalase (CAT)—an iron enzyme, may suggest interference of excess cobalt in iron metabolism of plants, particularly above a 50 μM supply. Decrease in hydrogen peroxide with an increase in cobalt supply has been attributed to increased activities of POD and APOD. Increase in dry matter yield of plants supplied 50 μM cobalt and the decrease in lipid peroxidation with increasing cobalt supply in the range 50–200 μM is suggested as a result from depletion of functional iron as phosphate and/or in ferritin. Appearance of the metal specific toxicity is the likely result of damages predominantly due to enhanced reactive oxygen species (ROS) generation at higher, 300–400 μM, cobalt supplies.
- Subjects :
- inorganic chemicals
chemistry.chemical_classification
Reactive oxygen species
chemistry.chemical_element
Plant Science
General Medicine
Biology
medicine.disease_cause
Superoxide dismutase
Lipid peroxidation
chemistry.chemical_compound
L-ascorbate peroxidase
chemistry
Biochemistry
Catalase
Genetics
biology.protein
medicine
Food science
Agronomy and Crop Science
Cobalt
Oxidative stress
Peroxidase
Subjects
Details
- ISSN :
- 01689452
- Volume :
- 162
- Database :
- OpenAIRE
- Journal :
- Plant Science
- Accession number :
- edsair.doi...........13129e0df87ef0e19bfa8e34adee9b41