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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, 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)...

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Autores principales: Ishii, Asako, Shan, Jianyu, Sheng, Xin, Kim, Eunchul, Watanabe, Akimasa, Yokono, Makio, Noda, Chiyo, Song, Chihong, Murata, Kazuyoshi, Liu, Zhenfeng, Minagawa, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10097422/
https://www.ncbi.nlm.nih.gov/pubmed/36951548
http://dx.doi.org/10.7554/eLife.84488
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author Ishii, Asako
Shan, Jianyu
Sheng, Xin
Kim, Eunchul
Watanabe, Akimasa
Yokono, Makio
Noda, Chiyo
Song, Chihong
Murata, Kazuyoshi
Liu, Zhenfeng
Minagawa, Jun
author_facet Ishii, Asako
Shan, Jianyu
Sheng, Xin
Kim, Eunchul
Watanabe, Akimasa
Yokono, Makio
Noda, Chiyo
Song, Chihong
Murata, Kazuyoshi
Liu, Zhenfeng
Minagawa, Jun
author_sort Ishii, Asako
collection PubMed
description 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.
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spelling pubmed-100974222023-04-13 The photosystem I supercomplex from a primordial green alga Ostreococcus tauri harbors three light-harvesting complex trimers Ishii, Asako Shan, Jianyu Sheng, Xin Kim, Eunchul Watanabe, Akimasa Yokono, Makio Noda, Chiyo Song, Chihong Murata, Kazuyoshi Liu, Zhenfeng Minagawa, Jun eLife Plant Biology 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. eLife Sciences Publications, Ltd 2023-03-23 /pmc/articles/PMC10097422/ /pubmed/36951548 http://dx.doi.org/10.7554/eLife.84488 Text en © 2023, Ishii, Shan et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Plant Biology
Ishii, Asako
Shan, Jianyu
Sheng, Xin
Kim, Eunchul
Watanabe, Akimasa
Yokono, Makio
Noda, Chiyo
Song, Chihong
Murata, Kazuyoshi
Liu, Zhenfeng
Minagawa, Jun
The photosystem I supercomplex from a primordial green alga Ostreococcus tauri harbors three light-harvesting complex trimers
title The photosystem I supercomplex from a primordial green alga Ostreococcus tauri harbors three light-harvesting complex trimers
title_full The photosystem I supercomplex from a primordial green alga Ostreococcus tauri harbors three light-harvesting complex trimers
title_fullStr The photosystem I supercomplex from a primordial green alga Ostreococcus tauri harbors three light-harvesting complex trimers
title_full_unstemmed The photosystem I supercomplex from a primordial green alga Ostreococcus tauri harbors three light-harvesting complex trimers
title_short The photosystem I supercomplex from a primordial green alga Ostreococcus tauri harbors three light-harvesting complex trimers
title_sort photosystem i supercomplex from a primordial green alga ostreococcus tauri harbors three light-harvesting complex trimers
topic Plant Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10097422/
https://www.ncbi.nlm.nih.gov/pubmed/36951548
http://dx.doi.org/10.7554/eLife.84488
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