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Transcriptomic and proteomic changes associated with cobalamin-dependent propionate production by the rumen bacterium Xylanibacter ruminicola

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posted on 2024-10-31, 19:53 authored by Sam Mahoney-KurpeSam Mahoney-Kurpe, Nik PalevichNik Palevich, Dragana Gagic, Patrick J. Biggs, Peter ReidPeter Reid, Ianina Altshuler, Phillip Pope, Graeme AttwoodGraeme Attwood, Christina MoonChristina Moon

Xylanibacter ruminicola is an abundant rumen bacterium that produces propionate in a cobalamin (vitamin B12)-dependent manner via the succinate pathway. However, the extent to which this occurs across ruminal Xylanibacter and closely related bacteria, and the effect of cobalamin supplementation on the expression of propionate pathway genes and enzymes has yet to be investigated. To assess this, we screened 14 strains and found that almost all strains produced propionate when supplemented with cobalamin. X. ruminicola KHP1 was selected for further study, including complete genome sequencing, and comparative transcriptomics and proteomics of KHP1 cultures grown with and without supplemented cobalamin. The complete KHP1 genome was searched for cobalamin-binding riboswitches and four were predicted, though none were closely located to any of the succinate pathway genes, which were dispersed at numerous genomic loci. Cobalamin supplementation led to the differential expression of 17.5% of genes, including genes encoding the cobalamin-dependent methylmalonyl-CoA mutase and some methylmalonyl-CoA decarboxylase subunits, but most propionate biosynthesis pathway genes were not differentially expressed. The effect of cobalamin supplementation on the KHP1 proteome was much less pronounced, with the only differentially abundant propionate pathway enzyme being methylmalonyl-CoA mutase, which had greater abundance when supplemented with cobalamin. Our results demonstrate that cobalamin supplementation does not result in induction of the entire propionate biosynthesis pathway, but consistently increased expression of methylmalonyl-CoA mutase at transcriptome and proteome levels. The magnitude of the differential expression of propionate pathway genes observed was minor compared to that of genes proximate to predicted cobalamin riboswitches.

Funding

Ministry of Business, Innovation and Employment (MBIE) C10X1702

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Rights statement

Copyright © 2024 Mahoney-Kurpe et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

Publication date

2024-10-29

Project number

  • PRJ0646310

Language

  • English

Does this contain Māori information or data?

  • No

Publisher

American Society for Microbiology

Journal title

mSystems

ISSN

2379-5077

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