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

Author

Listed:
  • Javier Abellon-Ruiz

    (Newcastle University)

  • Kalyanashis Jana

    (Constructor University)

  • Augustinas Silale

    (Newcastle University)

  • Andrew M. Frey

    (Newcastle University)

  • Arnaud Baslé

    (Newcastle University)

  • Matthias Trost

    (Newcastle University)

  • Ulrich Kleinekathöfer

    (Constructor University)

  • Bert Berg

    (Newcastle University)

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.

Suggested Citation

  • Javier Abellon-Ruiz & Kalyanashis Jana & Augustinas Silale & Andrew M. Frey & Arnaud Baslé & Matthias Trost & Ulrich Kleinekathöfer & Bert Berg, 2023. "BtuB TonB-dependent transporters and BtuG surface lipoproteins form stable complexes for vitamin B12 uptake in gut Bacteroides," Nature Communications, Nature, vol. 14(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-40427-2
    DOI: 10.1038/s41467-023-40427-2
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