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ID 65543
フルテキストURL
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著者
Jaunet-Lahary, Titouan Research Center for Computational Science, Institute for Molecular Science, National Institutes of Natural Sciences
Shimamura, Tatsuro Graduate School of Medicine, Kyoto University
Hayashi, Masahiro Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Nomura, Norimichi Graduate School of Medicine, Kyoto University
Hirasawa, Kouta Graduate School of Medicine, Kyoto University
Shimizu, Tetsuya RIKEN SPring-8 Center
Yamashita, Masao RIKEN SPring-8 Center
Tsutsumi, Naotaka Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Suehiro, Yuta School of Pharmaceutical Sciences, Okayama University
Kojima, Keiichi Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University ORCID Kaken ID researchmap
Sudo, Yuki Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University ORCID Kaken ID researchmap
Tamura, Takashi Graduate School of Environmental and Life Sciences, Okayama University ORCID Kaken ID publons researchmap
Iwanari, Hiroko Research Center for Advanced Science and Technology, The University of Tokyo
Hamakubo, Takao Research Center for Advanced Science and Technology, The University of Tokyo
Iwata, So Graduate School of Medicine, Kyoto University
Okazaki, Kei-Ichi Research Center for Computational Science, Institute for Molecular Science, National Institutes of Natural Sciences
Hirai, Teruhisa RIKEN SPring-8 Center
Yamashita, Atsuko Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University ORCID Kaken ID publons researchmap
抄録
An oxalate-degrading bacterium in the gut microbiota absorbs food-derived oxalate to use this as a carbon and energy source, thereby reducing the risk of kidney stone formation in host animals. The bacterial oxalate transporter OxlT selectively uptakes oxalate from the gut to bacterial cells with a strict discrimination from other nutrient carboxylates. Here, we present crystal structures of oxalate-bound and ligand-free OxlT in two distinct conformations, occluded and outward-facing states. The ligand-binding pocket contains basic residues that form salt bridges with oxalate while preventing the conformational switch to the occluded state without an acidic substrate. The occluded pocket can accommodate oxalate but not larger dicarboxylates, such as metabolic intermediates. The permeation pathways from the pocket are completely blocked by extensive interdomain interactions, which can be opened solely by a flip of a single side chain neighbouring the substrate. This study shows the structural basis underlying metabolic interactions enabling favourable symbiosis.
備考
The version of record of this article, first published in Nature Communications, is available online at Publisher’s website: http://dx.doi.org/10.1038/s41467-023-36883-5
発行日
2023-04-03
出版物タイトル
Nature Communications
14巻
1号
出版者
Nature Portfolio
開始ページ
1730
ISSN
2041-1723
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© The Author(s) 2023
論文のバージョン
publisher
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.1038/s41467-023-36883-5
ライセンス
http://creativecommons.org/licenses/by/4.0/
Citation
Jaunet-Lahary, T., Shimamura, T., Hayashi, M. et al. Structure and mechanism of oxalate transporter OxlT in an oxalate-degrading bacterium in the gut microbiota. Nat Commun 14, 1730 (2023). https://doi.org/10.1038/s41467-023-36883-5
助成機関名
Japan Society for the Promotion of Science
Japan Agency for Medical Research and Development
助成番号
JP20H03195
JP18H02415
JP26440086
JP20am0101079