Nitric Oxide in Plants. Группа авторов

Чтение книги онлайн.

Читать онлайн книгу Nitric Oxide in Plants - Группа авторов страница 22

Nitric Oxide in Plants - Группа авторов

Скачать книгу

K+ absorption, thus sustaining the optimal ratio of K+/Na+, is essential to endure salt stress (Amini and Ehsanpour 2005; Ahmad et al. 2016; Shams et al. 2019).

      During periods of biological strain in plants, the production of signaling molecules (NO, H2S, and CO) has been observed. There are several reports indicating that NO prompts the development of an essential osmolyte like proline in wheat (Wang et al. 2019), cabbage, and rye grass (Lou et al. 2015) by enhancing the expression of P5C5and down regulating the proDH genes. It has been suggested that NO enhances the accumulation of osmolytes, e.g. proline and glycine betaine, in tomato during cadmium stress when applied externally. Additionally, NO application confines the uptake of Cd and boosts the buildup of nutrients in various portions of tomato plants (Ahmad et al. 2018). The activities of SOD, catalase, ascorbate peroxidase, glutathione reductase, monodehydroascorbate reductase, dehydroascorbate reductase (antioxidant enzymes), and other enzymatic activities of the ascorbate–glutathione cycle are also improved by the application of nitric oxide (Kaya et al. 2020a).

      Water deficiency is one of the leading reasons for low agri-productivity and addition of NO has been shown to have an ameliorating effect during water stress in wheat. It has been proposed that SNP applied to wheat seedlings under polyethylene glycol-induced drought stress led to enhanced plantlet growth and high relative water contents and lessened the oxidative destruction to the seedlings under stress (Tian and Lei 2006). In this case, whether NO is protective or toxic to plants was found to be concentration dependent. A low concentration (0.2 mM) inhibits the loss of water, lowers the content of H2O2, and leads to higher antioxidative enzyme activity, which supports the wheat seedling growth, while high concentrations (2 mM) of SNP have the opposite effect.

      2.7 Conclusions

      Many studies have stated that NO has a presence and role in plant growth, development, and defense responses. It is widely recognized that NO is a second messenger and key regulator in plants, and at low concentrations, it acts as a signal to induce or stabilize the expression of many antioxidative enzymes such as SOD, CAT, etc. It also reacts with ROS, acting as a chain breaker, and exhibits antioxidant properties. It also reacts with lipid alkoxyl and peroxyl radicals and stops the proliferation of radical-mediated oxidation of lipids. Thus, NO helps plants to survive under stressful conditions, but its role is mainly concentration dependent.

      References

      1 Abedi, S., Iranbakhsh, A., Ardebili, Z.O. et al. (2021). Nitric oxide and selenium nanoparticles confer changes in growth, metabolism, antioxidant machinery, gene expression, and flowering in chicory (Cichorium intybus L.): potential benefits and risk assessment. Environmental Science and Pollution Research 28: 3136–3148.

      2 Ahmad, A., Khan, W.U., Shah, A.A. et al. (2021). Synergistic effects of nitric oxide and silicon on promoting plant growth, oxidative stress tolerance and reduction of arsenic uptake in Brassica juncea. Chemosphere 262: 128384.

      3 Ahmad, P., Abdel Latef, A.A., Hashem, A. et al. (2016). Nitric oxide mitigates salt stress by regulating levels of osmolytes and antioxidant enzymes in chickpea. Frontiers in Plant Science 7: 347.

      4 Ahmad, P., Ahanger, M.A., Alyemeni, M.N. et al. (2018). Exogenous application of nitric oxide modulates osmolyte metabolism, antioxidants, enzymes of ascorbate-glutathione cycle and promotes growth under cadmium stress in tomato. Protoplasma 255: 79–93.

      5 Amini, F. and Ehsanpour, A.A. (2005). Soluble proteins, proline, carbohydrates and Na+/K+ changes in two tomato (Lycopersicon esculentum Mill.) cultivars under in vitro salt stress. American Journal of Biochemistry and Biotechnology 1: 204–208.

      6 Arc, E., Galland, M., Godin, B. et al. (2013). Nitric oxide implication in the control of seed dormancy and germination. Frontiers in Plant Science 4: 346.

      7 Astier, J., Gross, I., and Durner, J. (2018). Nitric oxide production in plants: an update. Journal of Experimental Botany 69: 3401–3411.

      8 Bajguz, A. (2014). Nitric oxide: role in plants under abiotic stress. In: Physiological Mechanisms and Adaptation Strategies in Plants under Changing Environment (eds. P. Ahmad and M.R. Wani), 137–159. London: Springer.

      9 Bartha-Dima, B., Kolbert, Z., and Erdei, L. (2005). Nitric oxide production induced by heavy metals in Brassica juncea L. Czern. and Pisum sativum L. Acta Biologica Szegediensis 49: 9–12.

      10 Bashir, K., Matsui, A., Rasheed, S. et al. (2019). Recent advances in the characterization of plant transcriptomes in response to drought, salinity, heat, and cold stress. F1000 Research 8: 658.

      11 Besson-Bard, A., Pugin, A., and Wendehenne, D. (2008). New insights into nitric oxide signaling in plants. Annual Review of Plant Biology 59: 21–39.

      12 Bethke, P.C., Badger, M.R., and Jones, R.L. (2004). Apoplastic synthesis of nitric oxide by plant tissues. The Plant Cell 16: 332–341.

      13 Bethke, P.C., Libourel, I.G., and Jones, R.L. (2006). Nitric oxide reduces seed dormancy in Arabidopsis. Journal of Experimental Botany 57: 517–526.

      14 Brouquisse, R. (2019). Multifaceted roles of nitric oxide in plants. Journal of Experimental Botany 70: 4319–4322.

      15 Butler, A.R., Flitney, F.W., and Williams, D.L.H. (1995). NO, nitrosonium ions, nitroxide ions, nitrosothiols and iron-nitrosyls in biology: a chemist’s perspective. Trends in Pharmacological Sciences 16: 18–22.

      16 Chamizo-Ampudia, A., Sanz-Luque, E., Llamas, A. et al. (2017). Nitrate reductase regulates plant nitric oxide homeostasis. Trends in Plant Science 22: 163–174.

      17 Chen, Z.H., Wang, Y., Wang, J.W. et al. (2016). Nitrate reductase mutation alters potassium nutrition as well as nitric oxide-mediated control of guard cell ion channels in Arabidopsis. The New Phytologist 209: 1456–1469.

      18 Corpas, F.J., González-Gordo, S., Cañas, A. et al. (2019). Nitric oxide and hydrogen sulfide in plants: which comes first? Journal of Experimental Botany 70: 4391–4404.

      19 Courtois, C., Besson, A., Dahan, J. et al. (2008). Nitric oxide signalling in plants: interplays with Ca2+ and protein kinases. Journal of Experimental Botany 59: 155–163.

      20 Delledonne, M. (2005). NO news is good news for plants. Current Opinion in Plant Biology 8: 390–396.

      21 Del Río, L.A., Corpas, F.J., and Barroso, J.B. (2004).Nitric oxide and nitric oxide synthase activity in plants. Phytochemistry 65: 783–792.

      22 Falak, N., Imran, Q.M., Hussain, A. et al. (2021). Transcription factors as the “blitzkrieg” of plant defense: a pragmatic view of nitric oxide’s role in gene regulation. International Journal of Molecular Sciences 22: 522.

      23 Fatima, A., Husain, T., Suhel, M. et al. (2021). Implication of nitric oxide under salinity stress: the possible interaction with other signaling molecules. Journal of Plant Growth Regulation. https://doi.org/10.1007/s00344-020-10255-5.

      24 Gao, Z., Wang, Y., Chen, G. et al. (2019). The indica nitrate reductase gene OsNR2 allele enhances rice yield potential and nitrogen use efficiency. Nature Communications 10: 1–10.

      25 Gong, Z., Xiong, L., Shi, H. et al. (2020). Plant abiotic stress response and nutrient use efficiency. Science China Life Sciences 63: 635–674.

      26 González-Moscoso, M., González-García, Y., Martínez-Villegas, N.V. et al. (2021). Nitric oxide modified growth, nutrient uptake and the antioxidant defense

Скачать книгу