Research Article
In vitro fermentability of human milk oligosaccharides by several strains of bifidobacteria
Article first published online: 26 OCT 2007
DOI: 10.1002/mnfr.200700150
Copyright © 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Issue
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Molecular Nutrition & Food Research
Special Issue: Garlic
Volume 51, Issue 11, pages 1398–1405, November 2007
Additional Information
How to Cite
Ward, R. E., Niñonuevo, M., Mills, D. A., Lebrilla, C. B. and German, J. B. (2007), In vitro fermentability of human milk oligosaccharides by several strains of bifidobacteria. Mol. Nutr. Food Res., 51: 1398–1405. doi: 10.1002/mnfr.200700150
Publication History
- Issue published online: 26 OCT 2007
- Article first published online: 26 OCT 2007
- Manuscript Revised: 7 JUN 2007
- Manuscript Received: 19 APR 2007
Funded by
- NIHThe Training Program in Biomolecular Technology. Grant Number: T32GM08799
- California Dairy Foundation
- The CHARGE Study. Grant Number: P01 ES11269
- Abstract
- References
- Cited By
Keywords:
- Bifidobacteria;
- Fermentation;
- Milk;
- Oligosaccharide;
- Prebiotic
Abstract
This study was conducted to investigate the catabolism and fermentation of human milk oligosaccharides (HMO) by individual strains of bifidobacteria. Oligosaccharides were isolated from a pooled sample of human milk using solid-phase extraction, and then added to a growth medium as the sole source of fermentable carbohydrate. Of five strains of bifidobacteria tested (Bifidobacterium longum biovar infantis, Bifidobacterium bifidum, Bifidobacterium longum biovar longum, Bifidobacterium breve, and Bifidobacterium adolescentis), B. longum bv. infantis grew better, achieving triple the cell density then the other strains. B. bifidum did not reach a high cell density, yet generated free sialic acid, fucose and N-acetylglucosamine in the media, suggesting some capacity for HMO degradation. Thin layer chromatography profiles of spent fermentation broth suggests substantial degradation of oligosaccharides by B. longum bv. infantis, moderate degradation by B. bifidum and little degradation by other strains. While all strains were able to individually ferment two monosaccharide constituents of HMO, glucose and galactose, only B. longum bv. infantis and B. breve were able to ferment glucosamine, fucose and sialic acid. These results suggest that as a potential prebiotic, HMO may selectively promote the growth of certain bifidobacteria strains, and their catabolism may result in free monosaccharides in the colonic lumen.

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