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Architecture of symbiotic dinoflagellate photosystem I–light-harvesting supercomplex in Symbiodinium

Author

Listed:
  • Long-Sheng Zhao

    (Ocean University of China
    Shandong University
    Laoshan Laboratory)

  • Ning Wang

    (Ocean University of China)

  • Kang Li

    (Laoshan Laboratory)

  • Chun-Yang Li

    (Ocean University of China
    Laoshan Laboratory)

  • Jian-Ping Guo

    (Huazhong Agricultural University)

  • Fei-Yu He

    (Shandong University)

  • Gui-Ming Liu

    (Beijing Academy of Agriculture and Forestry Sciences)

  • Xiu-Lan Chen

    (Shandong University
    Laoshan Laboratory)

  • Jun Gao

    (Huazhong Agricultural University)

  • Lu-Ning Liu

    (Ocean University of China
    University of Liverpool)

  • Yu-Zhong Zhang

    (Ocean University of China
    Shandong University
    Laoshan Laboratory)

Abstract

Symbiodinium are the photosynthetic endosymbionts for corals and play a vital role in supplying their coral hosts with photosynthetic products, forming the nutritional foundation for high-yield coral reef ecosystems. Here, we determine the cryo-electron microscopy structure of Symbiodinium photosystem I (PSI) supercomplex with a PSI core composed of 13 subunits including 2 previously unidentified subunits, PsaT and PsaU, as well as 13 peridinin-Chl a/c-binding light-harvesting antenna proteins (AcpPCIs). The PSI–AcpPCI supercomplex exhibits distinctive structural features compared to their red lineage counterparts, including extended termini of PsaD/E/I/J/L/M/R and AcpPCI-1/3/5/7/8/11 subunits, conformational changes in the surface loops of PsaA and PsaB subunits, facilitating the association between the PSI core and peripheral antennae. Structural analysis and computational calculation of excitation energy transfer rates unravel specific pigment networks in Symbiodinium PSI–AcpPCI for efficient excitation energy transfer. Overall, this study provides a structural basis for deciphering the mechanisms governing light harvesting and energy transfer in Symbiodinium PSI–AcpPCI supercomplexes adapted to their symbiotic ecosystem, as well as insights into the evolutionary diversity of PSI–LHCI among various photosynthetic organisms.

Suggested Citation

  • Long-Sheng Zhao & Ning Wang & Kang Li & Chun-Yang Li & Jian-Ping Guo & Fei-Yu He & Gui-Ming Liu & Xiu-Lan Chen & Jun Gao & Lu-Ning Liu & Yu-Zhong Zhang, 2024. "Architecture of symbiotic dinoflagellate photosystem I–light-harvesting supercomplex in Symbiodinium," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-46791-x
    DOI: 10.1038/s41467-024-46791-x
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    1. Ryo Nagao & Koji Kato & Kentaro Ifuku & Takehiro Suzuki & Minoru Kumazawa & Ikuo Uchiyama & Yasuhiro Kashino & Naoshi Dohmae & Seiji Akimoto & Jian-Ren Shen & Naoyuki Miyazaki & Fusamichi Akita, 2020. "Structural basis for assembly and function of a diatom photosystem I-light-harvesting supercomplex," Nature Communications, Nature, vol. 11(1), pages 1-12, December.
    2. Jürgen F. H. Strassert & Iker Irisarri & Tom A. Williams & Fabien Burki, 2021. "A molecular timescale for eukaryote evolution with implications for the origin of red algal-derived plastids," Nature Communications, Nature, vol. 12(1), pages 1-13, December.
    3. Jürgen F. H. Strassert & Iker Irisarri & Tom A. Williams & Fabien Burki, 2021. "Author Correction: A molecular timescale for eukaryote evolution with implications for the origin of red algal-derived plastids," Nature Communications, Nature, vol. 12(1), pages 1-2, December.
    4. Xin You & Xing Zhang & Jing Cheng & Yanan Xiao & Jianfei Ma & Shan Sun & Xinzheng Zhang & Hong-Wei Wang & Sen-Fang Sui, 2023. "In situ structure of the red algal phycobilisome–PSII–PSI–LHC megacomplex," Nature, Nature, vol. 616(7955), pages 199-206, April.
    5. Caizhe Xu & Xiong Pi & Yawen Huang & Guangye Han & Xiaobo Chen & Xiaochun Qin & Guoqiang Huang & Songhao Zhao & Yanyan Yang & Tingyun Kuang & Wenda Wang & Sen-Fang Sui & Jian-Ren Shen, 2020. "Structural basis for energy transfer in a huge diatom PSI-FCPI supercomplex," Nature Communications, Nature, vol. 11(1), pages 1-12, December.
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