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The dehydrogenase‐mediated recycling of NADPH is a key antioxidant system against salt‐induced oxidative stress in olive plants
Open accessAbstract
NADPH is an important molecule in the redox balance of the cell. In this paper, using olive tissue cultures as a model of the function of the NADPH‐generating dehydrogenases in the mechanism of oxidative stress induced by severe salinity conditions was studied. When olive (Olea europaea) plants were grown with 200 m m NaCl, a 40% reduction in leaf fresh weight was produced. The content of non‐enzymatic antioxidants such as ascorbate and glutathione was diminished between 20% to 39%, whereas the H 2 O 2 content was increased threefold. In contrast, the analysis of the activity and protein contents of the main antioxidative enzymes showed a significant increase of catalase, superoxide dismutase and glutathione reductase. Overall, these changes strongly suggests that NaCl induces oxidative stress in olive plants. On the other hand, while the content of glucose‐6‐phosphate was increased almost eightfold in leaves of plants grown under salt stress, the content of NAD(P)H (reduced and oxided forms) did not show significant variations. Under salt stress conditions, the activity and protein contents of the main NADPH‐recycling enzymes, glucose‐6‐phosphate dehydrogenase (G6PDH), isocitrate dehydrogenase (ICDH), malic enzyme (ME) and ferrodoxin‐NADP reductase (FNR) showed an enhancement of 30–50%. In leaves of olive plants grown with 200 m m NaCl, analysis of G6PDH by immunocytochemistry and confocal laser scanning microscopy showed a general increase of this protein in epidermis, palisade and spongy mesophyll cells. These results indicate that in olive plants, salinity causes reactive oxygen species (ROS)‐mediated oxidative stress, and plants respond to this situation by inducing different antioxidative enzymes, especially the NADPH‐producing dehydrogenases in order to recycle NADPH necessary for the protection against oxidative damages. These NADP‐dehydrogenases appear to be key antioxidative enzymes in olive plants under salt stress conditions.
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Cites
Superoxide dismutase: Improved assays and an assay applicable to acrylamide gels
Beauchamp, C., & Fridovich, I. (1971) · Analytical Biochemistry · doi:10.1016/0003-2697(71)90370-8 · Cited by 12,892
Hernández, J. A., Jiménez, A., Mullineaux, P., & Sevilia, F. (2000) · Plant, Cell & Environment · doi:10.1046/j.1365-3040.2000.00602.x · Cited by 837
Cited by
Redox Regulation in Photosynthetic Organisms: Signaling, Acclimation, and Practical Implications
Foyer, C. H., & Noctor, G. (2009) · Antioxidants & Redox Signaling · doi:10.1089/ars.2008.2177 · Cited by 1,431
Noctor, G., Mhamdi, A., & Foyer, C. H. (2016) · Plant, Cell & Environment · doi:10.1111/pce.12726 · Cited by 406
Talhaoui, N., Taamalli, A., Gómez-Caravaca, A. M., Fernández-Gutiérrez, A., & Segura-Carretero, A. (2015) · Food Research International · doi:10.1016/j.foodres.2015.09.011 · Cited by 338
ROS Generation in Peroxisomes and its Role in Cell Signaling
del Río, L. A., & López-Huertas, E. (2016) · Plant and Cell Physiology · doi:10.1093/pcp/pcw076 · Cited by 331
Self-citationHossain, M. S., & Dietz, K.-J. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00548 · Cited by 323
Metadata
- Authors
- VALDERRAMA, R., CORPAS, F. J., CARRERAS, A., GÓMEZ‐RODRÍGUEZ, M. V., CHAKI, M., PEDRAJAS, J. R., FERNÁNDEZ‐OCAÑA, A., DEL RÍO, L. A., & BARROSO, J. B.
- Venue
- Plant, Cell & Environment
- Publisher
- Wiley
- Published
- 2006-05-16
- Volume
- 29
- Issue
- 7
- Pages
- 1449-1459
- ISSN
- 0140-7791 (ISSN-L)
- 1365-3040
- OpenAlex
- W2022524895
- Cited by
- 248
- References
- 2
- FWCI
- 13.55
- Type
- journal article
- Language
- en
- Open access
- bronze
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- The paper
- VALDERRAMA, R., CORPAS, F. J., CARRERAS, A., GÓMEZ‐RODRÍGUEZ, M. V., CHAKI, M., PEDRAJAS, J. R., FERNÁNDEZ‐OCAÑA, A., DEL RÍO, L. A., & BARROSO, J. B. (2006). The dehydrogenase‐mediated recycling of NADPH is a key antioxidant system against salt‐induced oxidative stress in olive plants. Plant, Cell & Environment. https://doi.org/10.1111/j.1365-3040.2006.01530.x
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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