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BtuB TonB-dependent transporters and BtuG surface lipoproteins form stable complexes for vitamin B12 uptake in gut Bacteroides

  • Javier Abellon-Ruiz
  • , Kalyanashis Jana
  • , Augustinas Silale
  • , Andrew M Frey
  • , Arnaud Baslé
  • , Matthias Trost
  • , Ulrich Kleinekathöfer
  • , Bert van den Berg
  • Newcastle University
  • Constructor University

Research output: Contribution to journal › Article › peer-review

Abstract

Vitamin B12 (cobalamin) is required for most human gut microbes, many of which are dependent on scavenging to obtain this vitamin. Since bacterial densities in the gut are extremely high, competition for this keystone micronutrient is severe. Contrasting with Enterobacteria, members of the dominant genus Bacteroides often encode several BtuB vitamin B12 outer membrane transporters together with a conserved array of surface-exposed B12-binding lipoproteins. Here we show that the BtuB transporters from Bacteroides thetaiotaomicron form stable, pedal bin-like complexes with surface-exposed BtuG lipoprotein lids, which bind B12 with high affinities. Closing of the BtuG lid following B12 capture causes destabilisation of the bound B12 by a conserved BtuB extracellular loop, causing translocation of the vitamin to BtuB and subsequent transport. We propose that TonB-dependent, lipoprotein-assisted small molecule uptake is a general feature of Bacteroides spp. that is important for the success of this genus in colonising the human gut.

Original languageEnglish
Pages (from-to)4714
JournalNature Communications
Volume14
Issue number1
DOIs
Publication statusPublished - 5 Aug 2023

Keywords

  • Humans
  • Vitamin B 12/metabolism
  • Bacteroides/genetics
  • Bacterial Outer Membrane Proteins/metabolism
  • Membrane Transport Proteins/metabolism
  • Vitamins/metabolism
  • Lipoproteins/metabolism
  • Escherichia coli Proteins/metabolism

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