TY - JOUR
T1 - Isolation of the elusive supercomplex that drives cyclic electron flow in photosynthesis
AU - Iwai, Masakazu
AU - Takizawa, Kenji
AU - Tokutsu, Ryutaro
AU - Okamuro, Akira
AU - Takahashi, Yuichiro
AU - Minagawa, Jun
N1 - Funding Information:
Acknowledgements We thank S. Ozawa and M. Kuwano for technical help with MS/MS analysis, D. Kramer for valuable discussions, T. Shikanai, D. Leister and T. Hase for providing antibodies, and K. Redding for providing the PSI-His mutant. This study was supported by the Research Fellowship for Young Scientists from the Japan Society for the Promotion of Science (M.I., R.T.), Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology (Y.T., 18GS0318; J.M.,18GS0318, 2120006309, 2157003109), the Strategic International Cooperative Program by Japan Science and Technology Agency (J.M.), and a Research Grant in the Natural Sciences by the Mitsubishi Foundation (J.M.).
PY - 2010/4/22
Y1 - 2010/4/22
N2 - Photosynthetic light reactions establish electron flow in the chloroplasts thylakoid membranes, leading to the production of the ATP and NADPH that participate in carbon fixation. Two modes of electron flow existlinear electron flow (LEF) from water to NADP + via photosystem (PS) II and PSI in series and cyclic electron flow (CEF) around PSI (ref. 2). Although CEF is essential for satisfying the varying demand for ATP, the exact molecule(s) and operational site are as yet unclear. In the green alga Chlamydomonas reinhardtii, the electron flow shifts from LEF to CEF on preferential excitation of PSII (ref. 3), which is brought about by an energy balancing mechanism between PSII and PSI (state transitions). Here, we isolated a protein supercomplex composed of PSI with its own light-harvesting complex (LHCI), the PSII light-harvesting complex (LHCII), the cytochrome b6f complex (Cyt bf), ferredoxin (Fd)-NADPH oxidoreductase (FNR), and the integral membrane protein PGRL1 (ref. 5) from C. reinhardtii cells under PSII-favouring conditions. Spectroscopic analyses indicated that on illumination, reducing equivalents from downstream of PSI were transferred to Cyt bf, whereas oxidised PSI was re-reduced by reducing equivalents from Cyt bf, indicating that this supercomplex is engaged in CEF (Supplementary Fig. 1). Thus, formation and dissociation of the PSI-LHCI-LHCII-FNR-Cyt bf-PGRL1 supercomplex not only controlled the energy balance of the two photosystems, but also switched the mode of photosynthetic electron flow.
AB - Photosynthetic light reactions establish electron flow in the chloroplasts thylakoid membranes, leading to the production of the ATP and NADPH that participate in carbon fixation. Two modes of electron flow existlinear electron flow (LEF) from water to NADP + via photosystem (PS) II and PSI in series and cyclic electron flow (CEF) around PSI (ref. 2). Although CEF is essential for satisfying the varying demand for ATP, the exact molecule(s) and operational site are as yet unclear. In the green alga Chlamydomonas reinhardtii, the electron flow shifts from LEF to CEF on preferential excitation of PSII (ref. 3), which is brought about by an energy balancing mechanism between PSII and PSI (state transitions). Here, we isolated a protein supercomplex composed of PSI with its own light-harvesting complex (LHCI), the PSII light-harvesting complex (LHCII), the cytochrome b6f complex (Cyt bf), ferredoxin (Fd)-NADPH oxidoreductase (FNR), and the integral membrane protein PGRL1 (ref. 5) from C. reinhardtii cells under PSII-favouring conditions. Spectroscopic analyses indicated that on illumination, reducing equivalents from downstream of PSI were transferred to Cyt bf, whereas oxidised PSI was re-reduced by reducing equivalents from Cyt bf, indicating that this supercomplex is engaged in CEF (Supplementary Fig. 1). Thus, formation and dissociation of the PSI-LHCI-LHCII-FNR-Cyt bf-PGRL1 supercomplex not only controlled the energy balance of the two photosystems, but also switched the mode of photosynthetic electron flow.
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U2 - 10.1038/nature08885
DO - 10.1038/nature08885
M3 - Article
C2 - 20364124
AN - SCOPUS:77951622488
SN - 0028-0836
VL - 464
SP - 1210
EP - 1213
JO - Nature
JF - Nature
IS - 7292
ER -