Thermal stability changes of photosynthesis during osmotic and salt stress in wheat varieties cultivated in Central Europe and Mediterranean North Africa
Jazyk angličtina Země Česko Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
40766740
PubMed Central
PMC12319942
DOI
10.32615/ps.2025.019
PII: PS63165
Knihovny.cz E-zdroje
- Klíčová slova
- chlorophyll fluorescence, osmotic stress, photosynthesis, salt stress, thermal tolerance, wheat,
- MeSH
- fotosyntéza * fyziologie MeSH
- fotosystém II (proteinový komplex) metabolismus MeSH
- osmotický tlak * MeSH
- pšenice * fyziologie účinky léků MeSH
- solný stres * MeSH
- teplota MeSH
- Publikační typ
- časopisecké články MeSH
- Geografické názvy
- Evropa MeSH
- Středomoří MeSH
- Názvy látek
- fotosystém II (proteinový komplex) MeSH
The thermal stability of photosynthetic apparatus under osmotic/salt stress was examined in wheat cultivars grown under different climatic conditions. The thermostability of nonstressed plants did not differ significantly from each other and it was not improved by osmotic treatment in the absence of light. In contrast, the salt stress resulted in better thermostability. This was also manifested in the temperature dependence of maximal quantum yield of PSII photochemistry. The temperature dependence of steady-state fluorescence and other photosynthetic parameters indicated a moderate reduction in thermal sensitivity of photosynthesis in well-watered plants which was further enhanced by osmotic, but even more by salt treatment. It seems likely that the osmotic stress-induced thermal stability increase of PSII occurs only in energized thylakoids. The temperature dependence of quantum yield of regulated energy dissipation seems to suggest that the secondary effects of lumen pH might have a role in the protective mechanisms concerning these stresses, but salt stress can also affect thermal stability in other ways as well.
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Allakhverdiev S.I., Kreslavski V.D., Klimov V.V. et al. : Heat stress: an overview of molecular responses in photosynthesis. – Photosynth. Res PubMed DOI
Asada K.: Production and scavenging of reactive oxygen species in chloroplasts and their functions. – Plant Physiol. 141: 391-396, 2006. 10.1104/pp.106.082040 PubMed DOI PMC
Ashraf M., Harris P.J.C.: Photosynthesis under stressful environments: an overview. – Photosynthetica 51: 163-190, 2013. 10.1007/s11099-013-0021-6 DOI
Atta K., Mondal S., Gorai S. et al. : Impacts of salinity stress on crop plants: improving salt tolerance through genetic and molecular dissection. – Front. Plant Sci. 14: 1241736, 2023. 10.3389/fpls.2023.1241736 PubMed DOI PMC
Bellasio C.: Quantifying photosynthetic restrictions. – Photosynth. Res. 163: 19, 2025. 10.1007/s11120-024-01129-y PubMed DOI PMC
Berry J.A., Björkman O.: Photosynthetic response and adaptation to temperature in higher plants. – Annu. Rev. Plant Physiol. 31: 491-543, 1980. 10.1146/annurev.pp.31.060180.002423 DOI
Centritto M., Loreto F., Chartzoulakis K.: The use of low [CO DOI
Chauhan J., Prathibha M.D., Singh P. et al. : Plant photosynthesis under abiotic stresses: damages, adaptive, and signaling mechanisms. – Plant Stress 10: 100296, 2023. 10.1016/j.stress.2023.100296 DOI
Chaves M.M., Flexas J., Pinheiro C.: Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. – Ann. Bot.-London 103: 551-560, 2009. 10.1093/aob/mcn125 PubMed DOI PMC
Chen H.-X., Li W.-J., An S.-Z., Gao X.-Y.: Characterization of PSII photochemistry and thermostability in salt-treated PubMed DOI
Chen T.H.H., Murata N.: Glycinebetaine: an effective protectant against abiotic stress in plants. – Trends Plant Sci. 13: 499-505, 2008. 10.1016/j.tplants.2008.06.007 PubMed DOI
Clifford S.C., Arndt S.K., Corlett J.E. et al. : The role of solute accumulation, osmotic adjustment and changes in cell wall elasticity in drought tolerance in DOI
Coast O., Posch B.C., Rognoni B.G.: Wheat photosystem II heat tolerance: evidence for genotype-by-environment interactions. – Plant J. 111: 1368-1382, 2022. 10.1111/tpj.15894 PubMed DOI
Darkó É., Janda T., Majláth I. et al. : Salt stress response of wheat–barley addition lines carrying chromosomes from the winter barley “Manas”. – Euphytica 203: 491-504, 2015. 10.1007/s10681-014-1245-7 DOI
Dau H.: New trends in photobiology: Short-term adaptation of plants to changing light intensities and its relation to Photosystem II photochemistry and fluorescence emission. – J. Photoch. Photobio. B 26: 3-27, 1994. 10.1016/1011-1344(94)85032-1 DOI
Demmig B., Winter K., Krüger A., Czygan F.C.: Zeaxanthin and the heat dissipation of excess light energy in PubMed DOI PMC
Demmig-Adams B.: Carotenoids and photoprotection in plants: a role for the xanthophyll zeaxanthin. – BBA-Bioenergetics 1020: 1-24, 1990. 10.1016/0005-2728(90)90088-L DOI
Demmig-Adams B., Stewart J.J., López-Pozo M. et al. : Zeaxanthin, a molecule for photoprotection in many different environments. – Molecules 25: 5825, 2020. 10.3390/molecules25245825 PubMed DOI PMC
dos Santos T.B., Ribas A.F., de Souza S.G.H. et al. : Physiological responses to drought, salinity, and heat stress in plants: a review. – Stresses 2: 113-135, 2022. 10.3390/stresses2010009 DOI
Dulai S., Molnár I., Lehoczki E.: Effects of growth temperatures of 5 and 25°C on long-term responses of photosystem II to heat stress in atrazine-resistant and susceptible biotypes of DOI
Dulai S., Molnár I., Szopkó D. et al. : Wheat– PubMed DOI
Dulai S., Molnár I., Prónay J. et al. : Effects of drought on thermal stability of photosynthetic apparatus in bread wheat and
Dulai S., Molnár I., Prónay J. et al. : Effects of drought on photosynthetic parameters and heat stability of PSII in wheat and in
El Sabagh A., Islam M.S., Skalicky M. et al. : Salinity stress in wheat ( DOI
Guo Q., Liu L., Barkla B.J.: Membrane lipid remodeling in response to salinity. – Int. J. Mol. Sci PubMed DOI PMC
Flexas J., Bota J., Galmés J. et al. : Keeping a positive carbon balance under adverse conditions: responses of photosynthesis and respiration to water stress. – Physiol. Plantarum 127: 343-352, 2006. 10.1111/j.1399-3054.2006.00621.x DOI
Flexas J., Bota J., Loreto F. et al. : Diffusive and metabolic limitations to photosynthesis under drought and salinity in C PubMed DOI
Havaux M.: Stress tolerance of photosystem II PubMed DOI PMC
Havaux M., Tardy F.: Temperature-dependent adjustment of the thermal stability of photosystem II DOI
Havaux M., Tardy F., Ravenel J. et al. : Thylakoid membrane stability to heat stress studied by flash spectroscopic measurements of the electrochromic shift in intact potato leaves: influence of the xanthophyll content. – Plant Cell Environ. 19: 1359-1368, 1996. 10.1111/j.1365-3040.1996.tb00014.x DOI
Hemker F., Zielasek F., Jahns P.: Combined high light and salt stress enhances accumulation of PsbS and zeaxanthin in PubMed DOI
Hill R., Ulstrup K.E., Ralph P.J.: Temperature induced changes in thylakoid membrane thermostability of cultured, freshly isolated, and expelled zooxanthellae from scleractinian corals. – B. Mar. Sci. 85: 223-244, 2009. https://www.ingentaconnect.com/content/umrsmas/bullmar/2009/00000085/00000003/art00003
Horton P., Ruban A.V., Rees D. et al. : Control of the light-harvesting function of chloroplast membranes by aggregation of the LHCII chlorophyll–protein complex. – FEBS Lett. 292: 1-4, 1991. 10.1016/0014-5793(91)80819-O PubMed DOI
Jahns P., Holzwarth A.R.: The role of the xanthophyll cycle and of lutein in photoprotection of photosystem II. – BBA-Bioenergetics 1817: 182-193, 2012. 10.1016/j.bbabio.2011.04.012 PubMed DOI
Jat M., Ray M., Ahmad M.A., Prakash P.: Unravelling the photosynthetic dynamics and fluorescence parameters under ameliorative effects of 24-epibrassinolide in wheat ( PubMed DOI PMC
Jiang Z., van Zanten M., Sasidharan R.: Mechanisms of plant acclimation to multiple abiotic stresses. – Commun. Biol. 8: 655, 2025. 10.1038/s42003-025-08077-w PubMed DOI PMC
Kalaji H.M., Govindjee, Bosa K. et al. : Effects of salt stress on photosystem II efficiency and CO DOI
Kaur G., Sanwal S.K., Kumar A. et al. : Role of osmolytes dynamics in plant metabolism to cope with salinity induced osmotic stress. – Discov. Agric. 2: 59, 2024. 10.1007/s44279-024-00070-x DOI
Khristin M.S., Smolova T.N., Kreslavski V.D.: Thermal stress, aggregation of chlorophyll–protein complexes, and light-dependent recovery of PSII activity in wheat seedlings. – Russ. J. Plant Physiol. 68: 867-872, 2021. 10.1134/S1021443721050071 DOI
Kiss A.Z., Ruban A.V., Horton P.: The PsbS protein controls the organization of the photosystem II antenna in higher plant thylakoid membranes. – J. Biol. Chem. 283: 3972-3978, 2008. 10.1074/jbc.M707410200 PubMed DOI
Klughammer C., Schreiber U.: Complementary PS II quantum yields calculated from simple fluorescence parameters measured by PAM fluorometry and the Saturation Pulse method. – PAM Appl. Notes 1: 27-35, 2008. https://www.walz.com/files/downloads/pan/PAN078007.pdf
Kouřil R., Lazár D., Ilík P. et al. : High-temperature induced chlorophyll fluorescence rise in plants at 40–50°C: experimental and theoretical approach. – Photosynth. Res. 81: 49-66, 2004. 10.1023/B:PRES.0000028391.70533.eb PubMed DOI
Ladjal M., Epron D., Ducrey M.: Effects of drought preconditioning on thermotolerance of photosystem II and susceptibility of photosynthesis to heat stress in cedar seedlings. –Tree Physiol. 20: 1235-1241, 2000. 10.1093/treephys/20.18.1235 PubMed DOI
Lavaud J., Kroth P.: In diatoms, the transthylakoid proton gradient regulates the photoprotective non-photochemical fluorescence quenching beyond its control on the xanthophyll cycle. – Plant Cell Physiol. 47: 1010-1016, 2006. 10.1093/pcp/pcj058 PubMed DOI
Lawlor D.W., Cornic G.: Photosynthetic carbon assimilation and associated metabolism in relation to water deficits in higher plants. – Plant Cell Environ. 25: 275-294, 2002. 10.1046/j.0016-8025.2001.00814.x PubMed DOI
Lazár D., Ilík P.: High-temperature induced chlorophyll fluorescence changes in barley leaves: comparison of the critical temperatures determined from fluorescence induction and from fluorescence temperature curve. – Plant Sci. 124: 159-164, 1997. 10.1016/S0168-9452(97)04602-5 DOI
Lazár D., Ilík P., Nauš J.: An appearance of K-peak in fluorescence induction depends on the acclimation of barley leaves to higher temperatures. – J. Lumin. 72-74: 595-596, 1997. 10.1016/S0022-2313(96)00293-1 DOI
Lu C., Li L., Liu X. et al. : Salt stress inhibits photosynthesis and destroys chloroplast structure by downregulating chloroplast development-related genes in PubMed DOI PMC
Lu C., Zhang J.: Effects of water stress on PSII photochemistry and its thermostability in wheat plants. – J. Exp. Bot. 50: 1199-1206, 1999. 10.1093/jxb/50.336.1199 DOI
Mathur S., Mehta P., Jajoo A.: Effects of dual stress (high salt and high temperature) on the photochemical efficiency of wheat leaves ( PubMed DOI PMC
Medrano H., Escalona J.M., Cifre J. et al. : A ten-year study on physiology of two Spanish grapevine cultivars under field conditions: effects of water availability from leaf photosynthesis to grape yield and quality. – Funct. Plant Biol. 30: 607-619, 2003. 10.1071/FP02110 PubMed DOI
Mitchell D., Schönbeck L., Shah S., Santiago L.S.: Leaf drought and heat tolerance are integrated across three temperate biome types. – Sci. Rep.-UK 15: 12201, 2025. 10.1038/s41598-025-95623-5 PubMed DOI PMC
Molnár I., Gáspár L., Sárvári É. et al. : Physiological and morphological responses to water stress in PubMed DOI
Molnár I., Csízi K., Dulai S. et al. : Light dependence of thermostability of photosynthetic apparatus. – In: Garab G. (ed.): Photosynthesis: Mechanisms and Effects. Pp. 2241-2244. Springer, Dordrecht: 1998. 10.1007/978-94-011-3953-3_524 DOI
Moloi M.J., Tóth C., Hafeez A., Tóth B.: Insights into the photosynthetic efficiency and chloroplast ultrastructure of heat-stressed edamame cultivars during the reproductive stages. – Agronomy 15: 301, 2025. 10.3390/agronomy15020301 DOI
Mondal S., Singh R.P., Crossa J. et al. : Earliness in wheat: a key to adaptation under terminal and continual high temperature stress in South Asia. – Field Crop. Res. 151: 19-26, 2013. 10.1016/j.fcr.2013.06.015 DOI
Munns R.: Comparative physiology of salt and water stress. – Plant Cell Environ. 25: 239-250, 2002. 10.1046/j.0016-8025.2001.00808.x PubMed DOI
Munns R., Tester M.: Mechanisms of salinity tolerance. – Annu. Rev. Plant Biol. 59: 651-681, 2008. 10.1146/annurev.arplant.59.032607.092911 PubMed DOI
Murata N., Mohanty P.S., Hayashi H., Papageorgiou G.C.: Glycinebetaine stabilizes the association of extrinsic proteins with the photosynthetic oxygen-evolving complex. – FEBS Lett. 296: 187-189, 1992. 10.1016/0014-5793(92)80376-R PubMed DOI
Müller P., Li X.-P., Niyogi K.K.: Non-photochemical quenching: a response to excess light energy. – Plant Physiol. 125: 1558-1566, 2001. 10.1104/pp.125.4.1558 PubMed DOI PMC
Nagy Z., Galiba G.: Drought and salt tolerance are not necessarily linked: a study on wheat varieties differing in drought resistance under consecutive water and salinity stresses. – J. Plant Physiol DOI
Nash D., Miyao M., Murata N.: Heat inactivation of oxygen evolution in photosystem II particles and its acceleration by chloride depletion and exogenous manganese. – BBA-Bioenergetics 807: 127-133, 1985. 10.1016/0005-2728(85)90115-X DOI
Nauš J., Kuropatwa R., Klinkovský T. et al. : Heat injury of barley leaves detected by the chlorophyll fluorescence temperature curve. – BBA-Bioenergetics 1101: 359-362, 1992. 10.1016/0005-2728(92)90093-H DOI
Ozturk M., Unal B.T., García-Caparrós P. et al. : Osmoregulation and its actions during the drought stress in plants. – Physiol. Plantarum 172: 1321-1335, 2021. 10.1111/ppl.13297 PubMed DOI
Pshybytko N.L., Kruk J., Kabashnikova L.F., Strzalka K. et al. : Function of plastoquinone in heat stress reactions of plants. – BBA-Bioenergetics 1777: 1393-1399, 2008. 10.1016/j.bbabio.2008.08.005 PubMed DOI
Raison J.K., Roberts J.K.M., Berry J.A.: Correlation between the thermal stability of chloroplast (thylakoid) membranes and the composition and fluidity of their polar lipids upon acclimation of the higher plant, DOI
Ramakers L.A.I., Harbinson J., Wientjes E., van Amerongen H.: Unravelling the different components of nonphotochemical quenching using a novel analytical pipeline. – New Phytol. 245: 625-636, 2025. 10.1111/nph.20271 PubMed DOI PMC
Rehman S., Yang J., Zhang J. et al. : Salt stress in wheat: a physiological and genetic perspective. – Plant Stress 16: 100832, 2025. 10.1016/j.stress.2025.100832 DOI
Ribeiro R.V., Santos M.G., Machado E.C., Oliveira R.F.: Photochemical heat-shock response in common bean leaves as affected by previous water deficit. – Russ. J. Plant Physiol. 55: 350-358, 2008. 10.1134/S1021443708030102 DOI
Schreiber U., Berry J.A.: Heat-induced changes of chlorophyll fluorescence in intact leaves correlated with damage of the photosynthetic apparatus. – Planta 136: 233-238, 1977. 10.1007/BF00385990 PubMed DOI
Schreiber U., Bilger W.: Rapid assessment of stress effects on plant leaves by chlorophyll fluorescence measurements. – In: Tenhunen J.D., Cararino F.M., Lange O.L., Oechel W.D. (ed.): Plant Response to Stress. NATO ASI Series. Vol. 15. Pp. 27-53. Springer, Berlin-Heidelberg: 1987. 10.1007/978-3-642-70868-8_2 DOI
Shanker A.K., Amirineni S., Bhanu D. et al. : High-resolution dissection of photosystem II electron transport reveals differential response to water deficit and heat stress in isolation and combination in pearl millet [ PubMed DOI PMC
Sharkey T.D.: Effects of moderate heat stress on photosynthesis: importance of thylakoid reactions, rubisco deactivation, reactive oxygen species, and thermotolerance provided by isoprene. – Plant Cell Environ. 28: 269-277, 2005. 10.1111/j.1365-3040.2005.01324.x DOI
Shu S., Yuan Y., Chen J. et al. : The role of putrescine in the regulation of proteins and fatty acids of thylakoid membranes under salt stress. – Sci. Rep.-UK 5: 14390, 2015. 10.1038/srep14390 PubMed DOI PMC
Smirnoff N.: The role of active oxygen in response of plants to water deficit and desiccation. – New Phytol. 125: 27-58, 1993. 10.1111/j.1469-8137.1993.tb03863.x PubMed DOI
Stefanov M.A., Rashkov G.D., Borisova P.B., Apostolova E.L.: Changes in photosystem II complex and physiological activities in pea and maize plants in response to salt stress. – Plants-Basel 13: 1025, 2024. 10.3390/plants13071025 PubMed DOI PMC
Sun Y., Wang Q., Xiao H., Cheng J.: Low light facilitates cyclic electron flows around PSI to assist PSII against high temperature stress. – Plants-Basel 11: 3537, 2022. 10.3390/plants11243537 PubMed DOI PMC
Suzuki N., Rivero R.M., Shulaev V. et al. : Abiotic and biotic stress combinations. – New Phytol. 203: 32-43, 2014. 10.1111/nph.12797 PubMed DOI
Szopkó D., Darkó É., Molnár I. et al. : Photosynthetic responses of a wheat (Asakaze)–barley (Manas) 7H addition line to salt stress. – Photosynthetica 55: 317-328, 2017. 10.1007/s11099-016-0241-7 DOI
Szopkó D., Dulai S.: Environmental factors affecting the heat stability of the photosynthetic apparatus. – Acta Biol. Plant. Agr. 6: 90-107, 2018. 10.21406/abpa.2018.6.90 DOI
Tang Y., Wen X., Lu Q. et al. : Heat stress induces an aggregation of the light-harvesting complex of photosystem II in spinach plants. – Plant Physiol. 143: 629-638, 2007. 10.1104/pp.106.090712 PubMed DOI PMC
Tardy F., Havaux M.: Thylakoid membrane fluidity and thermostability during the operation of the xanthophyll cycle in higher-plant chloroplasts. – BBA-Biomembranes 1330: 179-193, 1997. 10.1016/S0005-2736(97)00168-5 PubMed DOI
Tóth S., Puthur J.T., Nagy V., Garab G.: Experimental evidence for ascorbate-dependent electron transport in leaves with inactive oxygen-evolving complexes. – Plant Physiol. 149: 1568-1578, 2009. 10.1104/pp.108.132621 PubMed DOI PMC
Tóth S., Schansker G., Garab G., Strasser R.J.: Photosynthetic electron transport activity in heat-treated barley leaves: the role of internal alternative electron donors to photosystem II. – BBA-Bioenergetics 1767: 295-305, 2007. 10.1016/j.bbabio.2007.02.019 PubMed DOI
Touchette B.W., Schmitt S.R., Moody J.W.G.: Enhanced thermotolerance of photosystem II by elevated pore-water salinity in the coastal marsh graminoid DOI
Urban L., Aarrouf J., Bidel L.P.R.: Assessing the effects of water deficit on photosynthesis using parameters derived from measurements of leaf gas exchange and of chlorophyll PubMed DOI PMC
Vani B., Saradhi P., Mohanty P.: Alteration in chloroplast structure and thylakoid membrane composition due to DOI
Vineeth T.V., Krishna G.K., Pandesha P.H. et al. : Photosynthetic machinery under salinity stress: trepidations and adaptive mechanisms. – Photosynthetica 61: 73-93, 2023. 10.32615/ps.2023.002 PubMed DOI PMC
Wang G.P., Li F., Zhang J. et al. : Overaccumulation of glycine betaine enhances tolerance of the photosynthetic apparatus to drought and heat stress in wheat. – Photosynthetica 48: 30-41, 2010. 10.1007/s11099-010-0006-7 DOI
Wang Q.-L., Chen J.-H., He N.-Y., Guo F.-Q.: Metabolic reprogramming in chloroplasts under heat stress in plants. – Int. J. Mol. Sci. 19: 849, 2018. 10.3390/ijms19030849 PubMed DOI PMC
Wang X., Chen Z., Sui N.: Sensitivity and responses of chloroplasts to salt stress in plants. – Front. Plant Sci. 15: 1374086, 2024. 10.3389/fpls.2024.1374086 PubMed DOI PMC
Wen X., Qiu N., Lu Q., Lu C.: Enhanced thermotolerance of photosystem II in salt-adapted plants of the halophyte PubMed DOI
Yamane Y., Kashino Y., Koike H., Satoh K.: Increases in the fluorescence F DOI
Yan K., Chen P., Shao H. et al. : Responses of photosynthesis and photosystem II to higher temperature and salt stress in sorghum. – J. Agron. Crop Sci. 198: 218-225, 2012. 10.1111/j.1439-037X.2011.00498.x DOI
Yang X., Lu M., Wang Y. et al. : Response mechanism of plants to drought stress. – Horticulturae 7: 50, 2021. 10.3390/horticulturae7030050 DOI
Yang Z., Li J.-L., Liu L.-N. et al. : Photosynthetic regulation under salt stress and salt-tolerance mechanism of sweet sorghum. – Front. Plant Sci. 10: 1722, 2020. 10.3389/fpls.2019.01722 PubMed DOI PMC
Zahra N., Hafeez M.B., Ghaffar A. et al. : Plant photosynthesis under heat stress: effects and management. – Environ. Exp. Bot. 206: 105178, 2023. 10.1016/j.envexpbot.2022.105178 DOI