Abstract
Nitraria tangutorum Bobr., a typical desert halophyte, plays an important ecological role because of its superior tolerance to severe drought and high salinity. Very little is known about the physiological adaptative mechanism of this species to environmental stresses. The aim of this study was to investigate the changes of antioxidant enzyme activities and the regulatory mechanism of ascorbate peroxidase (APX) activity in the calli from Nitraria tangutorum Bobr. after treatment with different NaCl concentrations. The activities of superoxide dismutase (SOD) and catalase (CAT) significantly increased in the calli treated with NaCl, while the peroxidase activity decreased. APX activity was also elevated significantly in response to NaCl, but the increase was partly abolished by H2O2 scavenger dimethylthiourea (DMTU). Furthermore, the excitatory effect of salinity on APX could be alleviated by the addition of exogenous CAT and nicotinamide adenine dinucleotide phosphate (NADPH) oxidase inhibitor diphenylene iodonium, indicating that the modulation of the APX activity in Nitraria tangutorum Bobr. calli might be associated with NADPH oxidase-dependent H2O2 generation. Measurement and analysis using fluorescent dye 2′,7′-dichlorodihydrofluorescein diacetate showed the increase of H2O2 content in salinity-treated calli. The investigation of NADPH-dependent O −2 production in plasma membrane (PM) vesicles isolated from Nitraria tangutorum Bobr. calli revealed that salinity treatment stimulated NADPH oxidase activity. In conclusion, these results suggest that the higher activities of antioxidant enzymes play an important role in the salt tolerance of Nitraria tangutorum Bobr. calli and that the extracellular production of H2O2, depending on the excitation of PM NADPH oxidase, is responsible for enhancing the APX activity in Nitraria tangutorum Bobr. calli under salinity stress.
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Abbreviations
- APX:
-
Ascorbate peroxidase
- ASA:
-
Ascorbate
- CAT:
-
Catalase
- DMTU:
-
Dimethylthiourea
- DPI:
-
Diphenylene iodonium
- DTT:
-
1,4-dithiothreitol
- EDTA:
-
Ethylenediaminetetraacetic acid
- FW:
-
Fresh weight
- H2DCF-DA:
-
2′,7′-dichlorodihydrofluorescein diacetate
- H2O2 :
-
Hydrogen peroxide
- LSCM:
-
Laser scanning confocal microscope
- MS:
-
Murashige and Skoog
- NADPH:
-
Nicotinamide adenine dinucleotide phosphate
- NBT:
-
Nitroblue tetrazolium
- PBS:
-
Phosphate-buffered saline
- PM:
-
Plasma membrane
- PMSF:
-
Phenylmethanesulfonyl fluoride
- POD:
-
Peroxidase
- PVP:
-
Polyvinylpyrrolidone
- ROS:
-
Reactive oxygen species
- SOD:
-
Superoxide dismutase
- Tris:
-
Tris-(hydroxymethyl) amino methane
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Acknowledgements
This work is financially supported by the National Natural Science Foundation of China (grant no. 30960064) and the National Science Foundation for Distinguished Young Scholars of China (grant no. 30625008).
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Yang, Y., Shi, R., Wei, X. et al. Effect of salinity on antioxidant enzymes in calli of the halophyte Nitraria tangutorum Bobr.. Plant Cell Tiss Organ Cult 102, 387–395 (2010). https://doi.org/10.1007/s11240-010-9745-1
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DOI: https://doi.org/10.1007/s11240-010-9745-1