Fìzìol. rosl. genet. 2025, vol. 57, no. 4, 308-315, doi: https://doi.org/10.15407/frg2025.04.308

Effect of Na-ascorbate in the protection of PSII activity under conditions of simultaneous action of Co2+ and photoinhibition

Ganiyeva R.A., Atakishiyeva S.A., Dadashova S.B.

  • Institute of Botany, Ministry of Science and Education of the Republic of Azerbaijan 99 A. Abbaszade St., Baku AZ1004, Azerbaijan

In nature, a plant organism is exposed to many stress factors that negatively affect the photosynthetic apparatus and especially PSII, which is most vulnerable to stress. Determination of the site of toxic action of stress factors in the electron transport chain (ETC) of PSII was the aim of this work. The functional state of the of PSII ETC in the leaves of wheat seedlings subjected to the complex toxic effect of Co2+ and photoinhibition was determined based on various characteristics of delayed chlorophyll a fluorescence (ms DF Chl a). The effect of Co2+ was expressed in a sharp decrease in the characteristic value of ms DF Chl a of the PSII reaction center (RC) and in a weaker blocking of the donor side characterizing the state of the Mn4O5Ca cluster and Yz. Reactive oxygen species (ROS) generated in the process of photoinhibition also blocked to a greater extent the acceptor side of the PSII ETC. With an increase in the adaptation time, a significant decrease in activity on the donor side of the ETC of PSII was observed. The combined effect of both factors had little effect on the change in fluorescent chara­cteristics, which remained almost at the level of Co2+ action. It was shown that the adaptive capabilities of photochemical reactions occurring in the PSII ETC under combined stress are stimulated by the low-molecular antioxidant Na-ascorbate. Restoration by Na-ascorbate of the processes suppressed by the simultaneous action of photoinhibition and Co2+ occurs during the induction period of the ms DF Chl a, and is apparently expressed as a result of effective neutralization of the formed ROS. This indicates that the mechanism leading to a change in the character of the induction pattern of the ms DF Chl a as a result of the action of both factors has a single nature. The stress resistance of the photosynthetic apparatus increases due to an increase in the activity of antioxidant enzymes or the effectiveness of low-molecular antioxidants. As a result, the photosynthetic apparatus switches to the adaptive program, which ensures an increase in its stress resistance. It is assumed that Na-ascorbate plays a decisive role in protecting chloroplasts from oxidative stress by quenching O2– and *OH1.

Keywords: Triticum aestivum L., PSII, ETC, Со2+, photoinhibition, ROS, Na-ascorbate

Fìzìol. rosl. genet.
2025, vol. 57, no. 4, 308-315

Full text and supplemented materials

Free full text: PDF  

References

1. Ahmad, P., Sarwat, M. & Sharma, S. (2008). Reactive oxygen species, antioxidants and signaling in plants. J. Plant Biol., 51, pp. 167-173. https://doi.org/10.1007/BF03030694

2. Sharma, A., Kumar, V., Shahzad, B., Ramakrishnan, M., Singh Sidhu, G.P., Bali, A.Sh., Handa, N., Kapoor, Dh., Yadav, P., Khanna, K., Bakshi, P., Rehman, A., Kohli, S. K., Khan, E.A., Parihar, R. D., Yuan, H., Thukral, A.K., Bhardwaj, R. & Zheng, B. (2020). Photosynthetic response of plants under different abiotic stresses: A review. J. Plant Growth Regul., 39, pp. 509-531. https://doi.org/10.1007/s00344-019-10018-x

3. Breusegem, F.V. & Dat, J.F. (2006). Reactive oxygen species in plant cell death. Plant Physiol., 141, (2), pp. 384-390. https://doi.org/10.1104/pp.106.078295

4. Barber, J. (2003). Photosystem II: the engine of life. Q. Rev. Biophys., 36(1), pp. 71-89. https://doi.org/10.1017/S0033583502003839

5. Foyer, Ch.H. & Noctor, G. (2005). Redox homeostasis and antioxidant signaling: a metabolic interface between stress perception and physiological responses. Plant Cell, 17(7), pp. 1866-1875. https://doi.org/10.1105/tpc.105.033589

6. Polle, A. (2001). Dissecting the superoxide dismutase-ascorbate-glutathione-pathway in chloroplasts by metabolic modeling. Computer simulations as a step towards flux analysis. Plant Physiol., 126, (1), pp. 445-462. https://doi.org/10.1104/pp.126.1.445

7. Sabehat, A., Weiss, D. & Lurie, S. (1998). Heat-shock proteins and cross-tolerance in plants. Physiol. Plant., 103(3), pp. 437-441. https://doi.org/10.1034/j.1399-3054.1998.1030317.x

8. Andersson, B. & Barber, J. (1996). Mechanisms of photodamage and protein degradation during photoinhibition of photosystem II. In N.R. Baker (Ed.), Photosynthesis and the Environment (pp. 101-121). UK: Springer Dordrecht. https://doi.org/10.1007/0-306-48135-9

9. Biswal, B. (2005). Photosynthetic response of green plants to environmental stress: Inhibition of photosynthesis and adaptational of photosynthesis and adaptational mechanisms. In M. Pessarakli (Ed.), Photosynthesis (pp. 739-749). USA: CRC Press Taylor & Francis Group. https://doi.org/10.1201/9781420027877.ch38

10. Biswal, B., Joshi, P.N., Raval, M.K. & Biswal, U.C. (2011). Photosyntesis, a global sensor of environmental stress in green plants: Stress signaling and adaptation. Current Sci., 101(1), pp. 47-56.

11. Jafarova, J., Ganieva, R., Mammadova, L., Agalarov, R. & Gasanov, R. (2021). Structural and functional dependence of PSII activity under oxidative stress. Fiziol. rast. genet., 53(5), pp. 435-443. https://doi.org/10.15407/frg2021.05.435

12. Ganieva, R.A., Kurbanova, I.M. & Dadashova, S.B. (2000). Chlorophyll fluorescence and polypeptide composition of thylakoids upon exposure of wheat sprouts to NaCl and polyethyleneglycol. Physiol. biochem. cultivat. plants, 32(4), pp. 273-278 [in Russian].

13. Gaziyev, A., Aliyeva, S., Kurbanova, I., Ganiyeva, R., Bayramova, S. & Gasanov, R. (2011). Molecular operation of metals into the function and state of photosystem II. Metallomics, 3(12), pp. 1362-1367. https://doi.org/10.1039/c1mt00100k

14. Kтpper, H., ћetlHk, I., Spiller, M., Kтpper, F.C. & Pr«лil, O. (2002). Heavy metal-induced inhibition of photosynthesis: targets of in vivo heavy metal chlorophyll formation. J. Phycol., 38(3), pp. 429-441. https://doi.org/10.1046/j.1529-8817.2002.01148.x

15. Tyystj¬rvi, E. (2008). Photoinhibition of photosystem II and photodamage of the oxygen evolving manganese cluster. Coordinat. Chem. Rev., 252(3-4), pp. 361-376. https://doi.org/10.1016/j.ccr.2007.08.021

16. Vass, I. (2012). Molecular mechanisms of photodamage in the Photosystem II complex. Biochim. Biophys. Acta-Bioenergetics, 1817(1), pp. 209-217. https://doi.org/10.1016/j.bbabio.2011.04.014

17. Chan, T., Shimizu, Y., PospHлil, P., Nijo, N., Fujiwara, A., Taninaka, Y., Ishikawa, T., Hori, H., Nanba, D., Imai, A., Morita, N., Yoshioka-Nishimura, M., Izumi, Y., Yamamoto, Y., Kobayashi, H., Mizusawa, N., Wada, H. & Yamamoto, Y. (2012). Quality control of photosystem II: lipid peroxidation accelerates photoinhibition under excessive illumination. Plos One, 7(12), e52100. https://doi.org/10.1371/journal.pone.0052100

18. Jafarova, J., Bayramova, S. & Ganiyeva, R. (2012). The role of ascorbate in protection of FSII from photooxidative stress in cucumber (Cucumis sativus L.) leaves. X International scientific-metodical conference «Introduction of nontraditional and rare plants», pp. 215-220 [in Russian].

19. Nijs, D., Kelley, P.M. (1991). Vitamins C and E donate single hydrogen atoms in vivo. FEBS Lett., 284(2), pp. 147-151. https://doi.org/10.1016/0014-5793(91)80672-P

20. Rubin, A.B., Krendeleva, T.Y., Venediktov, P.S. & Matorin, D.N. (1984) Primary processes of photosynthesis and photosynthetic productivity. Agricult. Biol., 6, pp. 81-92.

21. Goltsev, V., Zaharieva, I., Chernev, P. & Strasser, R.J. (2009). Delayed chlorophyll fluorescence as a monitor for physiological state of photosynthetic apparatus. Biotechnol. Biotechnol. Equip., 23(1), pp. 452-457. https://doi.org/10.1080/13102818.2009.10818461

22. Gasanov, R.A., Aliyeva, S., Arao, S., Ismailova, A., Katsuta, N., Kitade, H., Yamada, Sh., Kawamori, A. & Mamedov, F. (2007). Comparative study of the water oxidizing reactions and the millisecond delayed chlorophyll fluorescence in photosystem II at different pH. J. Photochem. Photobiol., B: Biology, 86(2), pp. 160-164. https://doi.org/10.1016/j.jphotobiol.2006.08.008

23. Mahmudov, Z.M., Abdullayev, Kh.D. & Gasanov, R.A. (2005). Photoinhibition in vivo of photosystem II reactions during development of the photosystems of wheat seedlings. Photosynth. Res., 84(1-3), pp. 9-14. https://doi.org/10.1007/s11120-005-0897-5

24. Gasanov, R.A., Aliyeva, S.A. & Mamedov, F. (2015). Delayed fluorescence in a millisecond range - a probe for the donor side-induced photoinhibition of photosystem II. In S. Itoh, P. Mohanty, K.N. Guruprasad (Ed.), Photosynthesis: Basics to applications (pp. 101-107). New Delhi, India: I.K. International Publishing House Pvt. Ltd.

25. Kurbanova, I.M., Ganiyeva, R.A., Dadashova, S.B., Bayramova, S.A. & Gasanov, R.A. (2010). The state of chlorophyll-protein complexes of RC FS II and LHC under action of Cd2+ and Co2+ on wheat seedlings. Actual problems of bioecol., pp. 168-172 [in Russian].

26. Naz, H., Akram, N.A. & Ashraf, M. (2016). Impact of ascorbic acid on growth and some physiological attributes of cucumber (Cucumis sativus) plants under water-deficit conditions. Pak. J. Bot., 48(3), pp. 877-883.

27. Akram, N.A., Shafiq, F. & Ashraf, M. (2017). Ascorbic acid - a potential oxidant scavenger and its role in plant development and abiotic stress tolerance. Front. Plant Sci., 8, pp. 613. https://doi.org/10.3389/fpls.2017.00613

28. Xiao, M., Li, Z., Zhu, L., Wang, J., Zhang, B., Zheng, F., Zhao, B., Zhang, H., Wang, Y. & Zhang, Zh. (2021). The multiple roles of ascorbate in the abiotic stress response of plants: Antioxidant, Cofactor, and Regulator. Front. Plant Sci., 12, p. 598173.