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Structure and mechanism of oxalate transporter OxlT in an oxalate-degrading bacterium in the gut microbiota.
Jaunet-Lahary, Titouan; Shimamura, Tatsuro; Hayashi, Masahiro; Nomura, Norimichi; Hirasawa, Kouta; Shimizu, Tetsuya; Yamashita, Masao; Tsutsumi, Naotaka; Suehiro, Yuta; Kojima, Keiichi; Sudo, Yuki; Tamura, Takashi; Iwanari, Hiroko; Hamakubo, Takao; Iwata, So; Okazaki, Kei-Ichi; Hirai, Teruhisa; Yamashita, Atsuko.
Affiliation
  • Jaunet-Lahary T; Research Center for Computational Science, Institute for Molecular Science, National Institutes of Natural Sciences, Okazaki, 444-8585, Japan.
  • Shimamura T; Graduate School of Medicine, Kyoto University, Kyoto, 606-8501, Japan. t.shimamura@mfour.med.kyoto-u.ac.jp.
  • Hayashi M; Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, 700-8530, Japan.
  • Nomura N; Graduate School of Medicine, Kyoto University, Kyoto, 606-8501, Japan.
  • Hirasawa K; Graduate School of Medicine, Kyoto University, Kyoto, 606-8501, Japan.
  • Shimizu T; RIKEN SPring-8 Center, Sayo, 679-5148, Japan.
  • Yamashita M; RIKEN SPring-8 Center, Sayo, 679-5148, Japan.
  • Tsutsumi N; Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, 700-8530, Japan.
  • Suehiro Y; School of Pharmaceutical Sciences, Okayama University, Okayama, 700-8530, Japan.
  • Kojima K; School of Pharmaceutical Sciences, Okayama University, Okayama, 700-8530, Japan.
  • Sudo Y; Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, 700-8530, Japan.
  • Tamura T; Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, 700-8530, Japan.
  • Iwanari H; Graduate School of Environmental and Life Sciences, Okayama University, Okayama, 700-8530, Japan.
  • Hamakubo T; Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, 153-8904, Japan.
  • Iwata S; Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, 153-8904, Japan.
  • Okazaki KI; Graduate School of Medicine, Kyoto University, Kyoto, 606-8501, Japan.
  • Hirai T; Research Center for Computational Science, Institute for Molecular Science, National Institutes of Natural Sciences, Okazaki, 444-8585, Japan. keokazaki@ims.ac.jp.
  • Yamashita A; RIKEN SPring-8 Center, Sayo, 679-5148, Japan. teruhisahirai@gmail.com.
Nat Commun ; 14(1): 1730, 2023 04 03.
Article in En | MEDLINE | ID: mdl-37012268
ABSTRACT
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.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Oxalates / Gastrointestinal Microbiome Limits: Animals Language: En Year: 2023 Type: Article

Full text: 1 Database: MEDLINE Main subject: Oxalates / Gastrointestinal Microbiome Limits: Animals Language: En Year: 2023 Type: Article