Role of reactive oxygen and nitrogen species in the induction of heat resistance of wheat plantlets by exogenous hydrogen sulfide
DOI:
https://doi.org/10.15407/dopovidi2019.03.089Keywords:
heat resistance, hydrogen peroxide, hydrogen sulfide, nitric oxide, signal mediators, Triticum aestivumAbstract
The influence of sodium hydrosulfide (NaHS) as a donor of hydrogen sulfide (H2S) on the heat resistance of wheat plantlets and the possible participation of H2O2 and NO as mediators in the realization of stress protective effects of H2S have been studied. The treatment of plantlets with NaHS increases their survival after the damaging heating. During the first four hours after the beginning of the influence of the H2S donor, an increase in the content of H2O2 and NO in roots is registered. The treatments of plantlets with antioxidant dimethyl thiourea (DMTU), NADPH oxidase inhibitor imidazole, and antagonists of nitric oxide remove the stress protective effect of the H2S donor. At the same time, antagonists of NO only partially inhibit an increase in the content of H2O2 in roots at the NaHS treatment, and DMTU and imidazole almost completely level an increase in the NO content caused by the H2S donor. The results indicate the importance of the preliminary accumulation of H2O2 for an increase of the NO content at the influence of hydrogen sulfide and the participation of both mediators in the realization of its stress protective effects.
Downloads
References
Hancock, J. T. (2018). Hydrogen sulfide and environmental stresses. Environ. Exp. Bot. doi: https://doi.org/10.1016/j.envexpbot.2018.08.034
Hancock, J. T. & Whiteman, M. (2014). Hydrogen sulfide and cell signaling: Team player or referee? Plant Physiol. Biochem., 78, pp. 37-42. doi: https://doi.org/10.1016/j.plaphy.2014.02.012
Aroca, A., Gotor, C. & Luis, C. (2018). Romero hydrogen sulfide signaling in plants: emerging roles of protein persulfidation. Front. Plant Sci., 9, 1369. doi: https://doi.org/10.3389/fpls.2018.01369
Wang, Y., Li, L., Cui, W., Xu, S., Shen, W. & Wang, R. (2012). Hydrogen sulfide enhances alfalfa (Medicago sativa) tolerance against salinity during seed germination by nitric oxide pathway. Plant Soil., 351, No. 12, pp. 107-119. doi: https://doi.org/10.1007/s1110401109362
Singh, V. P., Singh, S., Kumar, J. & Prasad, S. M. (2015). Hydrogen sulfide alleviates toxic effects of arsenate in pea seedlings through upregulation of the ascorbateglutathione cycle: possible involvement of nitric oxide. J. Plant Physiol., 181, pp. 20-29. doi: https://doi.org/10.1016/j.jplph.2015.03.015
Li, Z. G., Yang, S. Z., Long, W. B., Yang, G. X. & Shen, Z. Z. (2013). Hydrogen sulphide may be a novel downstream signal molecule in nitric oxideinduced heat tolerance of maize (Zea mays L.) seedlings. Plant Cell Environ., 36, No. 8. pp. 1564-1572. doi: https://doi.org/10.1111/pce.12092
Kolupaev, Yu. E., Firsova, E. N., Yastreb, T. O. & Lugovaya, A. A. (2017). The participation of calcium ions and reactive oxygen species in the induction of antioxidant enzymes and heat resistance in plant cells by hydrogen sulfide donor. Appl. Biochem. Microbiol., 53, No. 5, pp. 573-579. doi: https://doi.org/10.1134/S0003683817050088
Karpets, Yu. V., Kolupaev, Yu. E. & Vayner, A. A. (2015). Functional interaction between nitric oxide and hydrogen peroxide during formation of wheat seedling induced heat resistance. Russ. J. Plant Physiol., 62, No. 1, pp. 65-70. doi: https://doi.org/10.1134/S1021443714060090
Sagisaka, S. (1976). The occurrence of peroxide in a perennial plant, Populus gelrica. Plant Physiol., 57, No. 2, pp. 308-309. doi: https://doi.org/10.1104/pp.57.2.308
Karpets, Yu. V., Kolupaev, Yu. E., Yastreb, T. O. & Oboznyi, A. I. (2015). Effects of NOstatus modification, heat hardening, and hydrogen peroxide on the activity of antioxidant enzymes in wheat seedlings. Russ. J. Plant Physiol., 62, No. 3, pp. 292-298. doi: https://doi.org/10.1134/S1021443715030097
Saddhe, A. A., Malvankar, M. R., Karle, S. B. & Kumar, K. (2018). Reactive nitrogen species: paradigms of cellular signaling and regulation of salt stress in plants. Environ. Exp. Bot., doi: https://doi.org/10.1016/j.envexpbot.2018.11.010
daSilva, C. J. & Modolo, L. V. (2018). Hydrogen sulfide: a new endogenous player in an old mechanism of plant tolerance to high salinity. Acta Bot. Bras., 32, No. 1, pp. 150-160. doi: https://doi.org/10.1590/010233062017abb0229
Flores, T., Todd, C. D., TovarMendez, A., Dhanoa, P. K., CorreaAragunde, N., Hoyos, M. E., Brownfield, D. M., Mullen, R. T., Lamattina, L. & Polacco, J. C. (2008). Arginasenegative mutants of Arabidopsis exhibit increased nitric oxide signaling in root development. Plant Physiol., 147, pp. 1936-1946. doi: https://doi.org/10.1104/pp.108.121459
Karpets, Y. V., Kolupaev, Yu. E., Lugovaya, A. A., Shvidenko, N. V. & Yastreb, T. O. (2018). Effects of nitrate and Larginine on content of nitric oxide and activities of antioxidant enzymes in roots of wheat seedlings and their heat resistance. Russ. J. Plant Physiol., 65, No. 6, pp. 908-915. doi: https://doi.org/10.1134/S1021443718050096
Xu, M. J., Dong, J. F. & Zhang, X. B. (2008). Signal interaction between nitric oxide and hydrogen peroxide in heat shock induced hypericin production of Hypericum perforatum suspension cells. Sci. China. Ser. C: Life Sci., 51, pp. 676-686. doi: https://doi.org/10.1007/s1142700800958
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2024 Reports of the National Academy of Sciences of Ukraine
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
