Enhanced stress-tolerance of transgenic tobacco plants expressing a human dehydroascorbate reductase gene
To analyze the physiological role of dehydroascorbate reductase (DHAR, EC 1.8.5.1) catalyzing the reduction of DHA to ascorbate in environmental stress adaptation, T 1 transgenic tobacco ( Nicotiana tabacum cv. Xanthi) plants expressing a human DHAR gene in chloroplasts were biochemically characteri...
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Published in | Journal of plant physiology Vol. 160; no. 4; pp. 347 - 353 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Jena
Elsevier GmbH
01.04.2003
Elsevier Elsevier Science Ltd |
Subjects | |
Online Access | Get full text |
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Summary: | To analyze the physiological role of dehydroascorbate reductase (DHAR, EC 1.8.5.1) catalyzing the reduction of DHA to ascorbate in environmental stress adaptation, T
1 transgenic tobacco (
Nicotiana tabacum cv. Xanthi) plants expressing a human DHAR gene in chloroplasts were biochemically characterized and tested for responses to various stresses. Fully expanded leaves of transgenic plants had about 2.29 times higher DHAR activity (units/g fresh wt) than non-transgenic (NT) plants. Interestingly, transgenic plants also showed a 1.43 times higher glutathione reductase activity than NT plants. As a result, the ratio of AsA/DHA was changed from 0.21 to 0.48, even though total ascorbate content was not significantly changed. When tobacco leaf discs were subjected to methyl viologen (MV) at 5 μmol/L and hydrogen peroxide (H
2O
2) at 200 mmol/L, transgenic plants showed about a 40 percnt; and 25 percnt; reduction in membrane damage relative to NT plants, respectively. Furthermore, transgenic seedlings showed enhanced tolerance to low temperature (15 °C) and NaCl (100 mmol/L) compared to NT plants. These results suggest that a human derived DHAR properly works for the protection against oxidative stress in plants. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0176-1617 1618-1328 |
DOI: | 10.1078/0176-1617-00926 |