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Mosses are one of the earliest land plants that diverged from fresh-water green algae. They are considered to have acquired a higher capacity for thermal energy dissipation to cope with dynamically changing solar irradiance by utilizing both the "algal-type" light-harvesting complex stress-related (LHCSR)-dependent and the "plant-type" PsbS-dependent mechanisms. It is hypothesized that the formation of photosystem (PS) I and II megacomplex is another mechanism to protect photosynthetic machinery from strong irradiance. Herein, we describe the analysis of the PSI-PSII megacomplex from the model moss, Physcomitrella patens, which was resolved using large-pore clear-native polyacrylamide gel electrophoresis (lpCN-PAGE). The similarity in the migration distance of the Physcomitrella PSI-PSII megacomplex to the Arabidopsis megacomplex shown during lpCN-PAGE suggested that the Physcomitrella PSI-PSII and Arabidopsis megacomplexes have similar structures. Time-resolved chlorophyll fluorescence measurements show that excitation energy was rapidly and efficiently transferred from PSII to PSI, providing evidence of an ordered association of the two photosystems. We also found that LHCSR and PsbS co-migrated with the Physcomitrella PSI-PSII megacomplex. The megacomplex showed pH-dependent chlorophyll fluorescence quenching, which may have been induced by LHCSR and/or PsbS proteins with the collaboration of zeaxanthin. We discuss the mechanism that regulates the energy distribution balance between two photosystems in Physcomitrella.
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http://dx.doi.org/10.1007/s10265-019-01138-2 | DOI Listing |
Plant Physiol
April 2024
School of Mathematics and Science, Institute for Chemistry and Biology of the Marine Environment (ICBM), Carl von Ossietzky Universität Oldenburg, 26129 Oldenburg, Germany.
Marine photosynthetic (micro)organisms drive multiple biogeochemical cycles and display a large diversity. Among them, the bloom-forming, free-living dinoflagellate Prorocentrum cordatum CCMP 1329 (formerly P. minimum) stands out with its distinct cell biological features.
View Article and Find Full Text PDFBiochim Biophys Acta Bioenerg
January 2024
Division of Environmental Photobiology, National Institute for Basic Biology, Okazaki, Japan; Basic Biology Program, The Graduate University for Advanced Studies, SOKENDAI, Okazaki, Japan.
Various megacomplexes in which Photosystem I and Photosystem II are physically bound (PSI-PSII m.c.) have been found in many organisms.
View Article and Find Full Text PDFBiochim Biophys Acta Bioenerg
November 2023
Division of Environmental Photobiology, National Institute for Basic Biology, Okazaki, Japan; Department of Basic Biology, School of Life Science, The Graduate University for Advanced Studies, Okazaki, Japan.
Plant Cell Physiol
August 2023
Division of Applied Life Sciences, Graduate School of Agriculture, Kyoto University, Kitashirakawa Oiwake-cho, Sakyo-ku, Kyoto, 606-8502 Japan.
Plant Cell Physiol
August 2023
Division of Environmental Photobiology, National Institute for Basic Biology, 38 Nishigonaka, Myodaiji Okazaki, Aichi, 444-8585 Japan.
In green plants, photosystem I (PSI) and photosystem II (PSII) bind to their respective light-harvesting complexes (LHCI and LHCII) to form the PSI-LHCI supercomplex and the PSII-LHCII supercomplex, respectively. These supercomplexes further form megacomplexes, like PSI-PSII and PSII-PSII in Arabidopsis (Arabidopsis thaliana) and spinach to modulate their light-harvesting properties, but not in the green alga Chlamydomonas reinhardtii. Here, we fractionated and characterized the stable rice PSI-PSII megacomplex.
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