Structure and Biochemistry of the LH1–RC Photocomplex from the Halophilic Purple Bacterium, <i>Rhodothalassium salexigens</i>
<i>Rhodothalassium (Rts.) salexigens</i> is a moderately halophilic purple nonsulfur bacterium whose unique cell wall composition and phylogeny are distinct from those of all other purple phototrophs. Here we present a cryo-EM structure and biochemical analysis of the light-harvesting 1-reaction center (LH1-RC) complex from <i>Rts. salexigens</i> at 2.29 Å resolution. The LH1 complex forms a closed ring structure with 16 αβ-polypeptides surrounding the RC and contains 16 phosphatidylglycerols regularly positioned between the β-polypeptides. Extensive interactions were observed between the C-terminal domains of LH1 α-and β-polypeptides and between the regularly arranged phosphatidylglycerols and β-polypeptides, supporting the hypothesis that LH1 C-terminal interactions define the post-translational truncation sites of αβ-polypeptides in phototrophic purple bacteria. Multiple insertions were identified in the membrane-extruded RC cytochrome- and H-subunits of <i>Rts. salexigens</i>. Insertions in the periplasm-exposed cytochrome subunit contain high proportions of Gly, Asp, and Glu, contributing to an overall negatively charged surface of this subunit. The cytoplasm-exposed H-subunit contained an unusually long 57-residue insert rich in Pro and Ala that was invisible in the cryo-EM density map, indicating its highly flexible nature. The extensive Pro-Ala repetitive motifs in this insertion points to a regulatory role in assemblies of the RC and LH1-RC complexes. The structural features of <i>Rts. salexigens</i> LH1-RC are also discussed in relation to differences in the physiological environment between the periplasmic and cytoplasmic sides of membranes in halophiles, necessary for maintaining cellular activities under the high ionic strength conditions of hypersaline environments.
Authors
- Endang R. Purba (ORCID: https://orcid.org/0000-0001-6037-4504)
- Shinichi Takaichi (ORCID: https://orcid.org/0000-0002-1621-9141)
- Bruno M. Humbel (ORCID: https://orcid.org/0000-0002-7095-1368)
- Yukihiro Kimura (ORCID: https://orcid.org/0000-0003-3747-0367)
- Akira Mizoguchi (ORCID: https://orcid.org/0000-0002-7492-2791)
- Kazutoshi Tani (ORCID: https://orcid.org/0000-0003-4835-154X)
- Masaki Inami
- Malgorzata Hall
- Michael T. Madigan (ORCID: https://orcid.org/0000-0002-7785-4026)
- Toshiaki Mochizuki (ORCID: https://orcid.org/0000-0001-6401-5605)
- Ryo Matsushita (ORCID: https://orcid.org/0000-0003-4333-7167)
- Zheng‐Yu Wang‐Otomo
- Shinji Takenaka (ORCID: https://orcid.org/0000-0002-7189-5927)
- T. Ooya
- Ryo Kanno
- Kazuki Inada
- Long-Jiang Yu
Institutions
- Tokyo University of Agriculture (JP)
- Okinawa Institute of Science and Technology Graduate University (JP)
- University of Tsukuba (JP)
- Mie University (JP)
- Chinese Academy of Sciences (CN)
- Juntendo University (JP)
- Quantum (Australia) (AU)
- Joint Center for Artificial Photosynthesis (US)
- Life Science Center for Survival Dynamics, Tsukuba Advanced Research Alliance (TARA)
- Ibaraki University (JP)
- Kobe University (JP)
Publication Details
- Journal
- Biochemistry
- Published
- 2025-06-24
- DOI
- https://doi.org/10.1021/acs.biochem.5c00181
- Citations
- 1
- Primary Topic
- Photosynthetic Processes and Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.81
Funders
- National Aeronautics and Space Administration
- Japan Agency for Medical Research and Development
- Cabinet Office, Government of Japan
- Okinawa Institute of Science and Technology Graduate University
- University of Tsukuba
- Japan Society for the Promotion of Science
- National Key Research and Development Program of China