Degradation of Cross-Linked and Non-Cross-Linked Arabinoxylans by the Intestinal Microbiota in Children
Male
2. Zero hunger
0301 basic medicine
Coumaric Acids
Colon
Molecular Sequence Data
Prevotella
Starch
Sequence Analysis, DNA
DNA, Ribosomal
Bacteria, Anaerobic
Feces
03 medical and health sciences
Cross-Linking Reagents
Child, Preschool
RNA, Ribosomal, 16S
Fermentation
Dietary Carbohydrates
Bacteroides
Humans
Female
Anaerobiosis
Porphyromonas
DOI:
10.1128/aem.69.11.6354-6360.2003
Publication Date:
2003-11-06T13:42:33Z
AUTHORS (6)
ABSTRACT
ABSTRACT
In humans, nonstarch polysaccharides (NSP), such as arabinoxylans (AX), are not digested in the upper gut and provide fermentable carbon sources for bacteria growing in the large bowel. Despite the ubiquity of AX in nature, the microbiologic and physiologic consequences of AX digestion in the gut are poorly understood. In this study, we investigated the breakdown of ferulic acid-cross-linked AX (AXF) and non-cross-linked AX in children's intestinal microbiotas, using starch as a readily fermentable polysaccharide for comparative purposes. The experiments were performed using pH-controlled fermentation vessels under anaerobic conditions. The results demonstrated that there was variation in the metabolism of these polysaccharides by colonic microbiotas. AX was always degraded more slowly than starch, while ferulic acid cross-linking reduced the rate of AX fermentation, as shown by fermentation product measurements. Starch digestion was associated with significant acetate and butyrate production, whereas AX breakdown resulted in increased propionate formation. In general, the presence of fermentable carbohydrate significantly increased the total anaerobe counts and eubacterial rRNA concentrations (
P
< 0.01), while non-cross-linked AX digestion was principally associated with increased viable counts of
Bacteroides fragilis
group organisms, which was supported by increases in
Bacteroides
-
Porphyromonas
-
Prevotella
group rRNA (
P
< 0.01). Starch was considerably more bifidogenic than AX in these fermentations. In conclusion, in this study we found that the effects of AX and AXF on the microbial ecology and metabolism of intestinal microbiotas are similar in children and adults.
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