Influence of sodium chloride on the dehydroascorbate reductase activity in Arabidopsis thaliana catalase 2 knokout mutant
Abstract
Aim. To better understand the mechanisms of abiotic stress resistance in plants, it is important to clarify the role of individual antioxidant enzymes from the same multiproteinic family in the response to stress. It is known that the loss of some isoforms of antioxidant enzymes can be compensated by activation of other enzymes. However, the functional interaction of the ascorbate-glutathione cycle enzymes with catalase under salt stress still remains unexplored. Respectively, we determined the activity of DHAR in knock-out mutants of Arabidopsis thaliana under salt stress. Methods. The DHAR activity was determined in the knock-out line cat2 and in wild-type (WT) Arabidopsis plants after various regimes of treatment with sodium chloride. Results. After treatment with 200 mM sodium chloride in the dark, activation of DHAR was found after 8 hours in WT plants and after 4 hours in the knock-out line cat2. However stress treatment under illumination resulted in significant increase in DHAR activity after 8 hours in both studied lines. In this case, DHAR activity in cat2 was lower than in WT, whereas in non-treated plants or upon stress treatment in the dark no difference between the tested lines was detected. Conclusions. The obtained data indicate that under salt stress conditions, changes in the DHAR activity are included into functional rearrangements of the antioxidant system in cat2 line, which compensate the loss of activity of CAT2 isoenzyme.
Keywords: dehydroascorbate reductase, antioxidants, reactive oxygen species (ROS), salt stress, Arabidopsis thaliana
References
Golldack D., Li C., Mohan H., Probst N. Tolerance to drought and salt stress in plants: Unraveling the signaling networks. Frontiers in Plant Science. 2014. Vol. 5(151). P. 1 –10. doi: 10.3389/fpls.2014.00151.
Mhamdi A., Queval G., Chaouch S., Vanderauwera S., Van Breusegem F., Noctor G. Catalase function in plants: a focus on Arabidopsis mutants as stress-mimic models. Journal of Experimental Botany. 2010. Vol. 61(15). P. 4197–4220. doi: 10.1093/jxb/erq282.
Gill S. S., Tuteja N. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiology and Biochemistry. 2010. Vol. 48(12). P. 909–930. doi: 10.1016/j.plaphy.2010.08.016.
Gallie D. R. The role of L-ascorbic acid recycling in responding to environmental stress and in promoting plant growth. Journal of Experimental Botany. 2013. Vol. 64(2). P. 433–443. doi: 10.1093/jxb/ers330.
Noshi M., Yamada H., Hatanaka R., Tanabe N., Tamoi M., Shigeoka S. Arabidopsis dehydroascorbate reductase 1 and 2 modulate redox states of ascorbateglutathione cycle in the cytosol in response to photooxidative stress. Bioscience, Biotechnology, and Biochemistry. 2016. Vol. 1. P. 1 –11. doi: 10.1080/09168451.2016.1256759.
Yin L., Wang S., Eltayeb A. E., Uddin M. I., Yamamoto Y., Tsuji W., Takeuchi Y., Tanaka K. Overexpression of dehydroascorbate reductase, but not monodehydroascorbate reductase, confers tolerance to aluminum stress in transgenic tobacco. Planta. 2010. Vol. 231. P. 609–621. doi: 10.1007/s00425-009-1075-3.
Wang Z., Xiao Y., Chen W., Tang K., Zhang L. Increased vitamin C content accompanied by an enhanced recycling pathway confers oxidative stress tolerance in Arabidopsis. Journal of Integrative Plant Biology. 2010. Vol. 52. P. 400–409. doi: 10.1111/j.1744-7909.2010.00921.x.
Zhang Y., Li Z., Peng Y., Wang X., Peng D., Li Y., He X., Zhang H., Ma X., Huang L., Yan Y. Clones of Fe-SOD, MDHAR, DHAR genes from white clover and gene expression analysis of ROS-scavenging enzymes during abiotic stress and hormone treatments. Molecules. 2015. Vol. 20. P. 20939–20954. doi: 10.3390/molecules201119741.
Kim Y. S., Kim I. S., Shin S. Y., Park T. H., Park H. M., Kim Y. H., Lee G. S., Kang H. G., Lee S. H., Yoon H. S. Overexpression of dehydroascorbate reductase confers enhanced tolerance to salt stress in rice plants (Oryza sativa L. japonica). Journal of Agronomy and Crop Science. 2014. P. 1–13. doi: 10.1111/jac.12078
Hossain M. A., Asada K. Purification of dehydroascorbate reductase from spinach and its characterization as a thiol enzyme. Plant and Cell Physiology. 1984. Vol. 25(1). P. 85–92. doi: 10.1093/oxfordjournals.pcp.a076700
Bradford M. M. A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry. 1976. Vol. 72. P. 248–254. doi: 10.1016/0003-2697(76)90527-3
Budhzak V. V. Biometrics. Chernivtsi: Ruta, 2013. 326 p. ISBN 978-966-423-312-2
Gupta B., Huang B. Mechanism of salinity tolerance in plants: physiological, biochemical, and molecular characterization. International Journal of Genomics. 2014. Vol. 14. P. 1 –18. doi: 10.1155/2014/70159d
Abbaspour H. Effect of salt stress on lipid peroxidation, antioxidative enzymes, and proline accumulation in pistachio plants. Journal of Medicinal Plants Research. 2012. Vol. 6(3). P. 526–529.
Das K., Roychoundhury A. Reactive oxygen species (ROS) and response of antioxidants as ROSscavengers during environmental stress in plants. Frontiers in Environmental Science. 2014. Vol. 2. P. 1–13. doi: 10.3389/fenvs.2014.00053
Agarwal P. K., Shukla P. S., Gupta K., Jha B. Bioengineering for salinity tolerance in plants: state of the art. Molecular Biotechnology. 2013. Vol. 54. P. 102–123. doi: 10.1007/s12033-012-9538-3
Sazzad M., Dietz K-J. Tuning of redox regulatory mechanisms, reactive oxygen species and redox homeostasis under salinity stress. Frontiers in Plant Science. 2016. Vol. 7(548). P. 1 –15. doi:10.3389/fpls.2016.00548
Didenko N. O., Buzduga I. M., Volkov R. A., Panchuk I. I. Activity of ascorbate and guaiacol peroxidases in Arabidopsis thaliana cat2 knockout mutants under salt stress. The Bulletin of Vavilov Society of Geneticists and Breeders of Ukraine. 2015. Vol. 13(1). P. 34–38.
Didenko N. A., Buzduga I. N., Volkov R. A., Panchuk I. I. The influence of acute salt stress on lipid peroxidation in Arabidopsis thaliana. Scientific Bulletin Chişinău. 2015. Vol. 22. P. 16–20.
Noshi M., Hatanaka R., Tanabe N., Terai Y., Maruta T., Shigeoka S. Redox regulation of ascorbate and glutathione by a chloroplastic dehydroascorbate reductase is required for high-light stress tolerance in Arabidopsis. Bioscience, Biotechnology, and Biochemistry. 2015. Vol. 1. P. 1 –7. doi: 10.1080/09168451.2015.1135042
Rahman A., Hossain M. S., Mahmud J. A., NaharK., Hasanuzzaman M., Fujita M. Manganese-induced salt stress tolerance in rice seedlings: regulation of ion homeostasis, antioxidant defense and glyoxalase systems. Physiology and Molecular Biology of Plants. 2016. Vol. 22(3). P. 291–306. doi: 10.1007/s12298-016-0371-1
Sofo A., Scopa A., Nuzzaci M., Vitti A. Ascorbate peroxidase and catalase activities and their genetic regulation in plants subjected to drought and salinity stresses. International Journal of Molecular Sciences. 2015. Vol. 16(6). P. 13561–13578. doi:10.3390/ijms160613561
Buzduga I. M., Volkov R. A., Panchuk I. I. Metabolic compensation for Arabidopsis thaliana mutants with loss of catalase activity. Cytology and Genetics. 2018. Vol. 52(1). P. 41–51. doi: 10.3103/S0095452718010036
Queval G., Issakidis-Bourguet E., Hoeberichts F. A., Vandorpe M., Gakiere B., Vanacker H., Miginiac-Maslow M., Van Breusegem F., Noctor G. Conditional oxidative stress responses in the Arabidopsis photorespiratory mutant cat2 demonstrate that redox state is a key modulator of daylength-dependent gene expression, and define photoperiod as a crucial factor in the regulation of H2O2-induced cell death. The Plant Journal. 2007. Vol. 52(4). P. 640–657. doi: 10.1111/j.1365-313X.2007.03263.x
Gao X., Yuan H. M., Hu Y. Q., Li J., Lu Y. T. Mutation of Arabidopsis CATALASE2 results in hyponastic leaves by changes of auxin levels. Plant, Cell and Environment. 2014. Vol. 37(1). P. 175–188. doi: 10.1111/pce.12144
Sudan J., Negi B., Arora S. Oxidative stress induced expression of monodehydroascorbate reductase gene in Eleusine coracana. Physiology and Molecular Biology of Plants. 2015. Vol. 21(4). P. 551–558. doi: 10.1007/s12298-015-0327-x
Balsera M., Schuermann P., Buchanan B. Redox regulation in chloroplasts. In: Chloroplasts. Current research and future trends. Eds. H. Kirchhoff. Caister Academic Press, 2016. 290 p. ISBN: 978-1-910190-47-0