| Literature DB >> 29359944 |
Santosh Lamichhane1,2, Christian C Yde1,3, Henrik Max Jensen3, Wesley Morovic4, Ashley A Hibberd4, Arthur C Ouwehand5, Markku T Saarinen5, Sofia D Forssten5, Lars Wiebe6, Jørn Marcussen3, Kresten Bertelsen3,7, Sebastian Meier8, Jette F Young1, Hanne Christine Bertram1.
Abstract
The present study introduces a novel triple-phase (liquids, solids, and gases) approach, which employed uniformly labeled [U-13C] polydextrose (PDX) for the selective profiling of metabolites generated from dietary fiber fermentation in an in vitro colon simulator using human fecal inocula. Employing 13C NMR spectroscopy, [U-13C] PDX metabolism was observed from colonic digest samples. The major 13C-labeled metabolites generated were acetate, butyrate, propionate, and valerate. In addition to these short-chain fatty acids (SCFAs), 13C-labeled lactate, formate, succinate, and ethanol were detected in the colon simulator samples. Metabolite formation and PDX substrate degradation were examined comprehensively over time (24 and 48 h). Correlation analysis between 13C NMR spectra and gas production confirmed the anaerobic fermentation of PDX to SCFAs. In addition, 16S rRNA gene analysis showed that the level of Erysipelotrichaceae was influenced by PDX supplementation and Erysipelotrichaceae level was statistically correlated with SCFA formation. Overall, our study demonstrates a novel approach to link substrate fermentation and microbial function directly in a simulated colonic environment.Entities:
Keywords: 13C NMR; 13C-labeled metabolites; dietary fiber; gut microbiome
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Year: 2018 PMID: 29359944 DOI: 10.1021/acs.jproteome.7b00683
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 4.466