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Activity of photosynthetic membranes in Fusarium oxysporum-infected cucumber (Сucumis sativus L.) plants under different proportions of blue LED illumination

https://doi.org/10.29235/1029-8940-2025-70-2-95-107

Abstract

The effect of LED illumination with different proportions of blue light (BL, 20 and 60 %) and different durations on the functionality of photosystems (PS) in healthy and infected with the fungus Fusarium oxysporum (Fus. oxy.) cucumber leaves was studied. Long-term exposure (25 days) to a light regime with a high share of BL, 60 % and subsequent infection with Fus. oxy., suppressed the functional activity of PSII relative to white light (WL), which was reflected in a significant decrease in the maximum fluorescence of temporarily closed PSII reaction centers (Fm), the effective quantum yield of photochemical reactions (Fv/Fm), the maximum quantum efficiency of PSII (Y(II)), as well as in changes to the nature of the redistribution of absorbed light energy. This resulted in a decline in the intensity of photochemical conversion (qP), the number of open PSII reaction centers (qL) and the rate of electron transport through PSII (ETR(II)). During a 7-day exposure of plants to different light conditions, the main changes in PSII parameters were observed only in infected leaves formed in the BL, 60 %.

Growing on WL and BL, 20 % only slightly changed the contribution of the electron flow on the donor and acceptor sides of PSI in infected cucumber leaves, without affecting the level of P700 oxidation and the quantum yield of photochemical reactions. Infection of plants grown for a long time on BL, 60 % caused a 10-fold decrease in the quantum yield of photochemical reactions of PSI and a significant increase in non-photochemical energy dissipation on the donor and acceptor sides of PSI. The stress effect of the pathogen also enhanced the suppressive effect of BL, 60 % at short exposure, which was reflected in a significant decrease of such parameters as the quantum yield of PSI (Y(I)) and the efficiency of electron transfer in the electron transport chain of PSI (ETR(I)).

The results obtained can be used as a methodological basis for the development of energy-saving LED light sources optimized for growing cucumber plants in closed soil, as well as for monitoring the degree of infection of plants in the early stages of Fusarium infection.

About the Authors

I. N. Domanskaya
Institute of Biophysics and Cell Engineering of the National Academy of Sciences of Belarus
Belarus

Irina N. Domanskaya – Ph. D. (Biol.), Аssociate Рrofessor, Senior Researcher

27, Akademicheskaya Str., 220072, Minsk



Ya. N. Artemchuk
Institute of Biophysics and Cell Engineering of the National Academy of Sciences of Belarus
Belarus

Yana N. Artemchuk – Junior Researcher

27, Akademicheskaya Str., 220072, Minsk



S. S. Gordienko
Institute of Biophysics and Cell Engineering of the National Academy of Sciences of Belarus
Belarus

Sofya S. Gordienko – Junior Researcher

27, Akademicheskaya Str., 220072, Minsk



O. V. Molchan
Institute of Experimental Botany named after V. F. Kuprevich of the National Academy of Sciences of Belarus
Belarus

Olga V. Molchan – Ph. D. (Biol.), Аssociate Рrofessor, Head of the Laboratory

27, Akademicheskaya Str., 220072, Minsk



L. F. Kabashnikova
Institute of Biophysics and Cell Engineering of the National Academy of Sciences of Belarus
Belarus

Lyudmila F. Kabashnikova – Corresponding Member, D. Sc. (Biol.), Assistant Professor, Head of the Laboratory

27, Akademicheskaya Str., 220072, Minsk



References

1. Casal J. J. Phytochromes, cryptochromes, phototropin: photoreceptor interactions in plants. Photochemistry and Photobiology, 2007, vol. 71, no. 1, pp. 1–11. https://doi.org/10.1562/0031-8655(2000)0710001pcppii2.0.co2

2. Voitsekhovskaja O. V. Phytochromes and other (Photo)Receptors of information in plants. Russian Journal of Plant Phy siology, 2019, vol. 66, pp. 351–364. https://doi.org/10.1134/s1021443719030154

3. D’Amico-Damiao V., Carvalho R. F. Cryptochrome-related abiotic stress responses in plants. Frontiers in Plant Science, 2018, vol. 9, art. 1897. https://doi.org/10.3389/fpls.2018.01897

4. Banerjee R., Batschauer A. Plant blue-light receptors. Planta, 2005, vol. 220, pp. 498–502. https://doi.org/10.1007/s00425-004-1418-z

5. Khudyakova A. Yu., Kreslavskii V. D., Shmarev A. N., Shirshikova G. N., Lyubimov V. Yu., Kosobryukhov A. A. The effect of cryptochrome 1 and 2 deficiency on photosynthetic activity and pro-antioxidant balance in leaves of Arabidopsis thaliana plants under the action of UV-B1. Fiziologiya rastenii [Plant Physiology], 2022, vol. 69, no. 2, pp. 207–215 (in Russian).

6. Kleine T., Kindgren P., Benedict C., Hendrickson L., Strand A. Genome-wide gene expression analysis reveals a critical role for cryptochrome1 in the response of Arabidopsis to high irradiance. Plant Physiology, 2007, vol. 144, no. 3, pp. 1391–1406.

7. Lin C., Todo T. The cryptochromes. Genome biology, 2005, vol. 6, no. 5, art. 220. https://doi.org/10.1186/gb-2005-6-5-220

8. Khudyakova A. Yu., Kreslavski V. D., Shmarev A. N., Lyubimov V. Yu., Shirshikova G. N., Pashkovskiy P. P., Kuzne- tsov V. V., Suleyman I. AllakhverdievImpact of UV-B radiation on the photosystem II activity, pro-/antioxidant balance and expression of light-activated genes in Arabidopsis thaliana hy4 mutants grown under light of different spectral composition. Journal of Photo chemistry and Photobiology B: Biology, 2019, vol. 194, pp. 14–20.

9. Sowden R. G., Watson S. J., Jarvis P. The role of chloroplasts in plant pathology. Essays in Biochemistry, 2018, vol. 62, no. 1, pp. 21–39. https://doi.org/10.1042/ebc20170020

10. Jones J. D. G., Dangl J. L. The plant immune system. Nature, 2006, vol. 444, pp. 323–332. https://doi.org/10.1038/nature05286

11. Bethke P. C., Jones R. L. Cell death of barley aleurone protoplasts is mediated by reactive oxygen species. The Plant Journal, 2001, vol. 25, no. 1, pp. 19–29. https://doi.org/10.1046/j.1365-313x.2001.00930.x

12. Hu G., Yalpani H., Briggs S. P., Johal G. S. A porphyrin pathway impairment is responsible for the phenotype of a dominant disease lesion mimic mutant of maize. The Plant Cell, 1998, vol. 10, no. 7, pp. 1095–1105. https://doi.org/10.2307/3870714

13. Brodersen P., Petersen M., Pike H. M., Olszak B., Skov S., Ødum N., Jørgensen L. B., Brown R. E., Mundy J. Knockout of Arabidopsis accelerated-cell-death11 encoding a sphingosine transfer protein causes activation of programmed cell death and defense. Genes and development, 2002, vol. 16, no. 4, pp. 490–502. https://doi.org/10.1101/gad.218202

14. Lorrain S., Lin B., Auriac M. C., Kroj T., Saindrenan P., Nicole M., Balagué C., Roby D. Vascular associated death1, a novel GRAM domain–containing protein, is a regulator of cell death and defense responses in vascular tissues. The Plant Cell, 2004, vol. 16, no. 8, pp. 2217–2232. https://doi.org/10.1105/tpc.104.022038

15. Asai T., Stone J. M., Heard J. E., Kovtun Y., Yorgey P., Sheen J., Ausubel F. M. Fumonisin B1-induced cell death in Arabidopsis protoplasts requires jasmonate-, ethylene-, and salicylate-dependent signaling pathways. The Plant Cell, 2000, vol. 12, no. 10, pp. 1823–1835. https://doi.org/10.2307/3871195

16. Liu Y., Ren D., Pike S., Pallardy S., Gassmann W., Zhang S. Chloroplast‐generated reactive oxygen species are involved in hypersensitive response‐like cell death mediated by a mitogen‐activated protein kinase cascade. The Plant Journal, 2007, vol. 51, no. 6, pp. 941–954. https://doi.org/10.1111/j.1365-313x.2007.03191.x

17. De Lucca A. J., Carter‐Wientjes C., Williams K. A., Bhatnagar D. Blue light (470 nm) effectively inhibits bacterial and fungal growth. Letters in applied microbiology, 2012, vol. 55, no. 6, pp. 460–466. https://doi.org/10.1111/lam.12002

18. Wu L., Yang H. Q. Cryptochrome 1 is implicated in promoting R protein-mediated plant resistance to Pseudomonas syringae in Arabidopsis. Molecular plant, 2010, vol. 3, no. 3, pp. 539–548. https://doi.org/10.1093/mp/ssp107

19. Krause G. H., Weis E. Chlorophyll fluorescence and photosynthesis: the basics. Annual Review of Plant Physiology and Plant Molecular Biology, 1991, vol. 42, no. 1, pp. 313–349. https://doi.org/10.1146/annurev.pp.42.060191.001525

20. Kramer D. M., Johnson G., Kiirats O., Edwards G. E. New flux parameters for the determination of QA redox state and excitation fluxes. Photosynthesis Reseach, 2004, vol. 79, pp. 209–218. https://doi.org/10.1023/b:pres.0000015391.99477.0d

21. Makarenko M. S., Kozel N. V., Usatov A. V., Gorbachenko O. F., Averina N. G. A state of PS1 and PSII ptotochemistry of sunflower yellow-green plastome mutant. OnLine Journal of Biological Sciences, 2016, vol. 16, no. 4, pp. 193–198. https://doi.org/10.3844/ojbsci.2016.193.198

22. Kreslavskii V. D., Khristin M. S. Aftereffect of heat shock on fluorescence induction and low-temperature fluorescence spectra of wheat leaves. Biofizika [Biophysics], 2003, vol. 48, no. 5, pp. 865–872 (in Russian).

23. Dual-PAM-100. Measuring System for Simultaneous Assessment of P700 and Chlorophyll Fluorescence: Instrument Description and Instructions for Users. 2nd ed. 2009. Available at: https://www.htsperu.com.pe/download/Manual-de-Dual-PAM100.7WDGupiZObTOUCgT71xZ97gSK4ZzWFXY.pdf (accessed 09.02.2025).

24. Rokitskii P. F. Biological statistics. Minsk, Vysheishaya shkola Publ., 1973. 320 p. (in Russian).

25. Briggs W. R., Christie J. M. Phototropins 1 and 2 versatile plant blue-light receptors. Trends in Plant Science, 2002, vol. 7, no. 5, pp. 204–210. https://doi.org/10.1016/s1360-1385(02)02245-8

26. Goltsev V. N., Kalaji H. M., Paunov M., Bąba W., Horaczek T., Mojski J., Kociel H., Allakhverdiev S. I. Variable chlorophyll fluorescence and its use for assessing physiological condition of plant photosynthetic apparatus. Russian Journal of Plant Physiology, 2016, vol. 63, no. 6, pp. 869–893. https://doi.org/10.1134/S1021443716050058

27. Baker N. R. Chlorophyll fluorescence: a probe of photosynthesis in vivo. Annual Review of Plant Biology, 2008, vol. 59, pp. 89–113. https://doi.org/10.1146/annurev.arplant.59.032607.092759

28. Gervais T., Creelman A., Li X.-Q., Bizimungu B., De Koeyer D., Dahal K. Potato Response to Drought Stress: Physiological and Growth Basis. Frontiers in Plant Science, 2021, vol. 12, art. 698060. https://doi.org/10.3389/fpls.2021.698060

29. Comadira G., Rasool B., Karpinska B., Morris J., Verrall S. V., Hedley P. E., Foyer C. H., Hancock R. D. Nitrogen deficiency in barley (Hordeum vulgare) seedlings induces molecular and metabolic adjustments that trigger aphid resistance. Journal of Expe- rimental Botany, 2015, vol. 66, no. 12, pp. 3639–3655. https://doi.org/10.1093/jxb/erv276

30. Akhter M. S., Noreen S., Mahmood S., Athar H. R., Ashraf M., Alsahli A. A., Ahmad P. Influence of salinity stress on PSII in barley (Hordeum vulgare L.) genotypes, probed by chlorophyll-a fluorescence. Journal of King Saud University – Science, 2021, vol. 33, no. 1, art. 101239. https://doi.org/10.1016/j.jksus.2020.101239

31. Huang W., Zhang S. B., Cao K. F. Stimulation of cyclic electron flow during recovery after chilling-induced photoinhibition of PSII. Plant Cell Physiology, 2010, vol. 51, no. 11, pp. 1922–1928. https://doi.org/10.1093/pcp/pcq144

32. Zhang R., Sharkey T. D. Photosynthetic electron transport and proton flux under moderate heat stress. Photosynthesis research, 2009, vol. 100, pp. 29–43. https://doi.org/10.1007/s11120-009-9420-8

33. Sun Y., Frankenberg C., Wood J. D., Schimel D. S., Jung M., Guanter L., Drewry D. T., Verma M., Porcar-Castell A., Griffis T. J., Gu L., Magney T. S., Köhler P., Evans B., Yuen K. OCO-2 advances photosynthesis observation from space via solar-induced chlorophyll fluorescence. Science, 2017, vol. 358, no. 6360, art. eaam5747. https://doi.org/10.1126/science.aam5747

34. Wada S., Takagi D., Miyake Ch., Makino A., Suzuki Yu. Responses of the photosynthetic electron transport reactions stimulate the oxidation of the reaction center chlorophyll of photosystem I, P700, under drought and high temperatures in rice. International Journal of Molecular Sciences. 2019, vol. 20, no. 9, p. 2068. https://doi.org/10.3390/ijms20092068

35. Pshibytko N. L. Assessment of P700 Redox State of Tomato Plants Under Conjugated Influence of Elevated Tempera ture and Fusarium Oxysporum Infection by the Method of Differential Absorption Photometry Using Technology of Saturating Light Pulse. Zhurnal prikladnoi spektroskopii [Journal of Applied Spectroscopy], 2024, vol. 91, no. 1, pp. 56–64 (in Russian).


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ISSN 1029-8940 (Print)
ISSN 2524-230X (Online)