PHOTOPROTECTIIVE STRATEGIES OF UNICELULAR RED ALGA RHODELLA VIOLACEA DURING ACCLIMATION TO STRONG LIGHT
Аннотация
Red algae contain in their photosynthetic machinery water-soluble antenna complexes - phycobilisomes (PBSs) attached to thylakoid membranes to transfer excitation energy to photosystems. Strong light absorbed by the PBSs triggers a fast formation of transthylakoid ΔpH that follows the non-photochemical quenching of chlorophyll (Chl) fluorescence. The ΔpH build-up seems to be essential for photoprotecting the photosynthetic apparatus in the absence of xanthophyll cycle common to higher plants. However, the photoprotective mechanisms of red algae are not studied in details yet.
We present here our research of the Chl fluorescence quenching in unicellular red algae Rhodella violacea and its correlation with the ΔpH gradient being formed. The relation of this phenomenon to photoprotection of photosystem 2 (PS 2) in the normal and high light-acclimated Rhodella cells is also examined.
Under the photoinhibitory conditions (white light of 2000-3000 μE/m2s), the ΔpH-dependent Chl fluorescence quenching was found to delay the kinetics of PS 2 photoinhibition. The uncouplers like nigericin and NH4Cl are known to break down ΔpH gradient, lead to the dissipation of Chl fluorescence quenching followed by enhancing the PS 2 photoinhibition rate. The same effect showed far-red (FR) light consuming transthylakoid ΔpH. ATPase inhibitor, DCCD, having no impact on ΔpH didn’t influence PS 2 photoinhibition as well this implies the photoprotection to be fulfilled by the proton gradient rather than by ATP synthesis.
Long-term acclimation of Rhodella cells to higher irradiances (500-1000 μE/m2s) results in a partial loss of the periphery phycoerythrin-containing subunits by PBSs. The light-acclimated cultures display a higher resistance to the photoinhibitory light than the non-acclimated ones. This could be explained by diminishing the energy transfer from the reduced PBSs to PS 2 as well as light screening by the secondary carotenoids synthesized during light exposure.
Data on low-temperature (77K) fluorescence allow to evaluate the molecular mechanisms of light-induced Chl fluorescence suppression in Rhodella cells and its recovery in darkness.
Литература
Anderson, J.M., Park, Y.-I., Chow, W.S. Photoinactivation and photoprotection of photosystem II in nature. Physiol. Plant. 1997; 100: 214-223.
Aro, E.-M., Virgin, I., Andersson, B. Photoinhibition of photosystem II. Inactivation, protein damage and turnover. Biochim. Biophys. Acta. 1993; 1143: 113-134.
Barber, J., Andersson, B. Too much of a good thing: light can be bad for photosynthesis. Trends Biochem. Sci. 1992; 17: 61-66.
Bernard, C., Etienne, A.L., Thomas, J.C. Synthesis and binding of phycoerythrin and its associated linkers to the phycobilisome in Rhodella violacea (Rhodophyta): compared effects of high light and translation inhibitors. J Phycol. 1996; 32: 265–271.
Chekanov, K., Schastnaya, E., Neverov, K., et al. Non-photochemical quenching in the cells of the carotenogenic chlorophyte Haematococcus lacustris under favorable condition and under stress. Biochim Biophys Acta Gen Subj. 2019; 1863:1429–1442.
Choudhury, N.K., Aslam, M., Huffaker, R.C. Photochemical activities in wheat chloroplasts incubated under irradiation and possible protection by zeaxanthin. Photosynthetica. 1994; 30: 397-405.
Critchley, C., Russell, A.W. Photoinhibition of photosynthesis in vivo: the role of protein turnover in photosystem II. Physiol. Plant. 1994; 92: 188-196.
Delphin, E., Duval, J.C., Etienne, A.-L., et al. State transitions or pH dependent quenching of photosystem 2 fluorescence in red algae. Biochemistry. 1996; 35: 9435-9445.
Delphin, E., Duval, J.C., Etienne, A.-L., et al. pH-dependent photosystem 2 fluorescence quenching induced by saturating, multiturnover pulses in red algae. Plant Physiol. 1998; 118: 103-113.
Demmig-Adams, B. Carotenoids and photoprotection in plants: a role for the xanthophyll zeaxanthin. Biochim. biophys. Acta. 1990; 1020: 1-24.
Demmig-Adams, B., Adams, W.W., III. Photoprotection and other responses of plants to high light stress. Annu. Rev. Plant Physiol. Plant Mol. Biol. 1997; 43: 599-626.
Gantt, E. Phycobilisomes. Annu Rev Plant Physiol. 1981; 32: 327-347.
Horton, P., Ruban, A.V., Young, A.J. Regulation of the structure and function of the lightharvesting complexes of photosystem II by the xanthophyll cycle. In: Frank, H.A., Young, A.J., Britton, G., Cogdell, R.J. (eds.): The Photochemistry of Carotenoids. Kluwer Academic Publ., Dordrecht. 1999; 8: 271-291.
Koller, K.P., Wehrmeyer, W., Schneider, H. Isolation and characterization of disc-shaped phycobilisomes from the red alga Rhodella violacea. Arch. Microbiol. 1977; 112: 61-67.
Krause, G.H., Weis, E. Chlorophyll fluorescence and photosynthesis: the basics. Annu. Rev. Plant Physiol. Plant Mol. Biol. 1991; 42: 313-349.
Mishra, N.P., Francke, C., van Gorkom, H.J., et al. Destructive role of singlet oxygen during aerobic illumination of the Photosystem II core complex. Biochim. Biophys. Acta 1994; 1186: 81-90.
Muller, P., Li, X.-P., Niyogi, K.K. Nonphotochemical quenching. A response to excess light energy. Plant Physiol. 2001;125: 1558-1566.
Neverov, K.V., Krasnovsky ,A.A. Jr., Zabelin, A.A., et al. Low-temperature (77 K) phosphorescence of triplet chlorophyll in isolated reaction centers of Photosystem II. Photosynthesis Research. 2015; 125: 43-49.
Ort, D.R., Yocum, C.F. Electron transport and energy transduction in photosynthesis: an overview. In: Ort, D.R., Yocum, C.F. (eds.): Oxygenic Photosynthesis: The Light Reactions. Kluwer Academic Publishers, Dordrecht.1996; P. 1-9.
Ritz, M., Neverov, K.V., Etienne, A.-L. pHdependent fluorescence quenching and its photoprotective role in the unicellular red alga Rhodella violacea. Photosynthetica. 1999; 37: 267-280.
Ritz, M., Thomas, J.-C., Spilar, A., et al. Kinetics of photoacclimation in response to a shift to high light of the red alga Rhodella violacea adapted to low irradiance. Plant Physiol. 2000; 123: 1415-1425.
Satoh, K, Murata, N, Asada, K, et al. Molecular mechanism for relaxation of and protection from light stress. In: Satoh, K., Murata. N. (eds.): Stress Responses of Photosynthetic Organisms. Elsevier Science Publishing, Amsterdam. 1998; P. 37-52.
Siefermann-Harms, D. The light-harvesting and protective functions of carotenoids in photosynthetic membranes. Physiol. Plant. 1987; 69: 561-568.
Solovchenko, A.E., Neverov, K.V. Carotenogenic response in photosynthetic organisms: a colorful story. Photosynthesis Research. 2017; 133 (13): 31-47.
Strizh, I.G., Neverov, K.V. Photoinhibition of photosystem II in vitro: spectral and kinetic analyses. Russian Journal of Plant Physiol. 2007; 54: 439–449.
Young, A.J., Philip, D., Frank, H.A., et al. The xanthophyll cycle and carotenoid mediated dissipation of excess excitation energy in photosynthesis. Pure Appl. Chem. 1997; 69: 2125-2130.
Zabelin, A.A., Neverov, K.V., Krasnovsky,
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