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.

In our gut, oxalate-degrading bacteria absorb oxalate, a causative substance for kidney stone formation, and reduce our health risk. In this work, the authors report the structure of the oxalate transporter responsible for this process and how the protein works.

Details

Title
Structure and mechanism of oxalate transporter OxlT in an oxalate-degrading bacterium in the gut microbiota
Author
Jaunet-Lahary, Titouan 1   VIAFID ORCID Logo  ; Shimamura, Tatsuro 2   VIAFID ORCID Logo  ; Hayashi, Masahiro 3 ; Nomura, Norimichi 2   VIAFID ORCID Logo  ; Hirasawa, Kouta 2 ; Shimizu, Tetsuya 4 ; Yamashita, Masao 4 ; Tsutsumi, Naotaka 5   VIAFID ORCID Logo  ; Suehiro, Yuta 6   VIAFID ORCID Logo  ; Kojima, Keiichi 3   VIAFID ORCID Logo  ; Sudo, Yuki 3   VIAFID ORCID Logo  ; Tamura, Takashi 7   VIAFID ORCID Logo  ; Iwanari, Hiroko 8 ; Hamakubo, Takao 8   VIAFID ORCID Logo  ; Iwata, So 2 ; Okazaki, Kei-ichi 1   VIAFID ORCID Logo  ; Hirai, Teruhisa 4   VIAFID ORCID Logo  ; Yamashita, Atsuko 9   VIAFID ORCID Logo 

 National Institutes of Natural Sciences, Research Center for Computational Science, Institute for Molecular Science, Okazaki, Japan (GRID:grid.250358.9) (ISNI:0000 0000 9137 6732) 
 Kyoto University, Graduate School of Medicine, Kyoto, Japan (GRID:grid.258799.8) (ISNI:0000 0004 0372 2033) 
 Okayama University, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan (GRID:grid.261356.5) (ISNI:0000 0001 1302 4472) 
 RIKEN SPring-8 Center, Sayo, Japan (GRID:grid.472717.0) 
 Okayama University, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan (GRID:grid.261356.5) (ISNI:0000 0001 1302 4472); Okayama University, School of Pharmaceutical Sciences, Okayama, Japan (GRID:grid.261356.5) (ISNI:0000 0001 1302 4472) 
 Okayama University, School of Pharmaceutical Sciences, Okayama, Japan (GRID:grid.261356.5) (ISNI:0000 0001 1302 4472) 
 Okayama University, Graduate School of Environmental and Life Sciences, Okayama, Japan (GRID:grid.261356.5) (ISNI:0000 0001 1302 4472) 
 The University of Tokyo, Research Center for Advanced Science and Technology, Tokyo, Japan (GRID:grid.26999.3d) (ISNI:0000 0001 2151 536X) 
 Okayama University, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan (GRID:grid.261356.5) (ISNI:0000 0001 1302 4472); RIKEN SPring-8 Center, Sayo, Japan (GRID:grid.472717.0); Okayama University, School of Pharmaceutical Sciences, Okayama, Japan (GRID:grid.261356.5) (ISNI:0000 0001 1302 4472) 
Pages
1730
Publication year
2023
Publication date
2023
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2794409281
Copyright
© The Author(s) 2023. corrected publication 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.