The photosystem I supercomplex from a primordial green alga Ostreococcus tauri harbors three light-harvesting complex trimers
As a ubiquitous picophytoplankton in the ocean and an early-branching green alga, is a model prasinophyte species for studying the functional evolution of the light-harvesting systems in photosynthesis. Here, we report the structure and function of the photosystem I (PSI) supercomplex in low light c...
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Abstract | As a ubiquitous picophytoplankton in the ocean and an early-branching green alga,
is a model prasinophyte species for studying the functional evolution of the light-harvesting systems in photosynthesis. Here, we report the structure and function of the
photosystem I (PSI) supercomplex in low light conditions, where it expands its photon-absorbing capacity by assembling with the light-harvesting complexes I (LHCI) and a prasinophyte-specific light-harvesting complex (Lhcp). The architecture of the supercomplex exhibits hybrid features of the plant-type and the green algal-type PSI supercomplexes, consisting of a PSI core, an Lhca1-Lhca4-Lhca2-Lhca3 belt attached on one side and an Lhca5-Lhca6 heterodimer associated on the other side between PsaG and PsaH. Interestingly, nine Lhcp subunits, including one Lhcp1 monomer with a phosphorylated amino-terminal threonine and eight Lhcp2 monomers, oligomerize into three trimers and associate with PSI on the third side between Lhca6 and PsaK. The Lhcp1 phosphorylation and the light-harvesting capacity of PSI were subjected to reversible photoacclimation, suggesting that the formation of
PSI-LHCI-Lhcp supercomplex is likely due to a phosphorylation-dependent mechanism induced by changes in light intensity. Notably, this supercomplex did not exhibit far-red peaks in the 77 K fluorescence spectra, which is possibly due to the weak coupling of the chlorophyll
603-
609 pair in
Lhca1-4. |
---|---|
AbstractList | As a ubiquitous picophytoplankton in the ocean and an early-branching green alga,
Ostreococcus tauri
is a model prasinophyte species for studying the functional evolution of the light-harvesting systems in photosynthesis. Here, we report the structure and function of the
O. tauri
photosystem I (PSI) supercomplex in low light conditions, where it expands its photon-absorbing capacity by assembling with the light-harvesting complexes I (LHCI) and a prasinophyte-specific light-harvesting complex (Lhcp). The architecture of the supercomplex exhibits hybrid features of the plant-type and the green algal-type PSI supercomplexes, consisting of a PSI core, an Lhca1-Lhca4-Lhca2-Lhca3 belt attached on one side and an Lhca5-Lhca6 heterodimer associated on the other side between PsaG and PsaH. Interestingly, nine Lhcp subunits, including one Lhcp1 monomer with a phosphorylated amino-terminal threonine and eight Lhcp2 monomers, oligomerize into three trimers and associate with PSI on the third side between Lhca6 and PsaK. The Lhcp1 phosphorylation and the light-harvesting capacity of PSI were subjected to reversible photoacclimation, suggesting that the formation of
Ot
PSI-LHCI-Lhcp supercomplex is likely due to a phosphorylation-dependent mechanism induced by changes in light intensity. Notably, this supercomplex did not exhibit far-red peaks in the 77 K fluorescence spectra, which is possibly due to the weak coupling of the chlorophyll
a
603-
a
609 pair in
Ot
Lhca1-4. As a ubiquitous picophytoplankton in the ocean and an early-branching green alga, Ostreococcus tauri is a model prasinophyte species for studying the functional evolution of the light-harvesting systems in photosynthesis. Here, we report the structure and function of the O. tauri photosystem I (PSI) supercomplex in low light conditions, where it expands its photon-absorbing capacity by assembling with the light-harvesting complexes I (LHCI) and a prasinophyte-specific light-harvesting complex (Lhcp). The architecture of the supercomplex exhibits hybrid features of the plant-type and the green algal-type PSI supercomplexes, consisting of a PSI core, an Lhca1-Lhca4-Lhca2-Lhca3 belt attached on one side and an Lhca5-Lhca6 heterodimer associated on the other side between PsaG and PsaH. Interestingly, nine Lhcp subunits, including one Lhcp1 monomer with a phosphorylated amino-terminal threonine and eight Lhcp2 monomers, oligomerize into three trimers and associate with PSI on the third side between Lhca6 and PsaK. The Lhcp1 phosphorylation and the light-harvesting capacity of PSI were subjected to reversible photoacclimation, suggesting that the formation of OtPSI-LHCI-Lhcp supercomplex is likely due to a phosphorylation-dependent mechanism induced by changes in light intensity. Notably, this supercomplex did not exhibit far-red peaks in the 77 K fluorescence spectra, which is possibly due to the weak coupling of the chlorophyll a603-a609 pair in OtLhca1-4. As a ubiquitous picophytoplankton in the ocean and an early-branching green alga, is a model prasinophyte species for studying the functional evolution of the light-harvesting systems in photosynthesis. Here, we report the structure and function of the photosystem I (PSI) supercomplex in low light conditions, where it expands its photon-absorbing capacity by assembling with the light-harvesting complexes I (LHCI) and a prasinophyte-specific light-harvesting complex (Lhcp). The architecture of the supercomplex exhibits hybrid features of the plant-type and the green algal-type PSI supercomplexes, consisting of a PSI core, an Lhca1-Lhca4-Lhca2-Lhca3 belt attached on one side and an Lhca5-Lhca6 heterodimer associated on the other side between PsaG and PsaH. Interestingly, nine Lhcp subunits, including one Lhcp1 monomer with a phosphorylated amino-terminal threonine and eight Lhcp2 monomers, oligomerize into three trimers and associate with PSI on the third side between Lhca6 and PsaK. The Lhcp1 phosphorylation and the light-harvesting capacity of PSI were subjected to reversible photoacclimation, suggesting that the formation of PSI-LHCI-Lhcp supercomplex is likely due to a phosphorylation-dependent mechanism induced by changes in light intensity. Notably, this supercomplex did not exhibit far-red peaks in the 77 K fluorescence spectra, which is possibly due to the weak coupling of the chlorophyll 603- 609 pair in Lhca1-4. |
Author | Sheng, Xin Murata, Kazuyoshi Liu, Zhenfeng Watanabe, Akimasa Song, Chihong Yokono, Makio Noda, Chiyo Minagawa, Jun Shan, Jianyu Ishii, Asako Kim, Eunchul |
Author_xml | – sequence: 1 givenname: Asako surname: Ishii fullname: Ishii, Asako organization: Division of Environmental Photobiology, National Institute for Basic Biology, Okazaki, Japan – sequence: 2 givenname: Jianyu surname: Shan fullname: Shan, Jianyu organization: College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China – sequence: 3 givenname: Xin surname: Sheng fullname: Sheng, Xin organization: National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China – sequence: 4 givenname: Eunchul surname: Kim fullname: Kim, Eunchul organization: Department of Basic Biology, School of Life Science, the Graduate University for Advanced Studies, Okazaki, Japan – sequence: 5 givenname: Akimasa orcidid: 0000-0001-6068-1328 surname: Watanabe fullname: Watanabe, Akimasa organization: Department of Basic Biology, School of Life Science, the Graduate University for Advanced Studies, Okazaki, Japan – sequence: 6 givenname: Makio surname: Yokono fullname: Yokono, Makio organization: Department of Basic Biology, School of Life Science, the Graduate University for Advanced Studies, Okazaki, Japan – sequence: 7 givenname: Chiyo surname: Noda fullname: Noda, Chiyo organization: Division of Environmental Photobiology, National Institute for Basic Biology, Okazaki, Japan – sequence: 8 givenname: Chihong surname: Song fullname: Song, Chihong organization: Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural Sciences, Okazaki, Japan – sequence: 9 givenname: Kazuyoshi orcidid: 0000-0001-9446-3652 surname: Murata fullname: Murata, Kazuyoshi organization: Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural Sciences, Okazaki, Japan – sequence: 10 givenname: Zhenfeng orcidid: 0000-0001-5502-9474 surname: Liu fullname: Liu, Zhenfeng organization: College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China – sequence: 11 givenname: Jun orcidid: 0000-0002-3028-3203 surname: Minagawa fullname: Minagawa, Jun organization: Department of Basic Biology, School of Life Science, the Graduate University for Advanced Studies, Okazaki, Japan |
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CitedBy_id | crossref_primary_10_1016_j_bbabio_2023_148995 crossref_primary_10_1038_s41467_024_46791_x crossref_primary_10_1073_pnas_2315476121 crossref_primary_10_1016_j_molp_2023_12_016 crossref_primary_10_3390_ijms25052765 |
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Keywords | computational biology light-harvesting complex systems biology prasinophyte Ostreococcus tauri photosystem I plant biology phosphorylation state transitions |
Language | English |
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is a model prasinophyte species for studying the functional evolution of the... As a ubiquitous picophytoplankton in the ocean and an early-branching green alga, Ostreococcus tauri is a model prasinophyte species for studying the... As a ubiquitous picophytoplankton in the ocean and an early-branching green alga, Ostreococcus tauri is a model prasinophyte species for studying the... |
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SubjectTerms | Chlorophyll Chlorophyta - metabolism Computational and Systems Biology light-harvesting complex Light-Harvesting Protein Complexes - chemistry Light-Harvesting Protein Complexes - metabolism Ostreococcus tauri phosphorylation Photosynthesis photosystem I Photosystem I Protein Complex - chemistry Plant Biology prasinophyte state transitions |
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Title | The photosystem I supercomplex from a primordial green alga Ostreococcus tauri harbors three light-harvesting complex trimers |
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