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  4. Differences in fine arabinoxylan structures govern microbial selection and competition among human gut microbiota
 
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Differences in fine arabinoxylan structures govern microbial selection and competition among human gut microbiota

Journal
Carbohydrate polymers
Journal Volume
316
Date Issued
2023-09-15
Author(s)
Yao, Tianming
Deemer, Dane G
MING-HSU CHEN  
Reuhs, Bradley L
Hamaker, Bruce R
Lindemann, Stephen R
DOI
10.1016/j.carbpol.2023.121039
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/632877
URL
https://api.elsevier.com/content/abstract/scopus_id/85161260358
Abstract
Dietary fibers are known to modulate microbiome composition, but it is unclear to what extent minor fiber structural differences impact community assembly, microbial division of labor, and organismal metabolic responses. To test the hypothesis that fine linkage variations afford different ecological niches for distinct communities and metabolism, we employed a 7-day in vitro sequential batch fecal fermentation with four fecal inocula and measured responses using an integrated multi-omics approach. Two sorghum arabinoxylans (SAXs) were fermented, with one (RSAX) having slightly more complex branch linkages than the other (WSAX). Although there were minor glycoysl linkage differences, consortia on RSAX retained much higher species diversity (42 members) than on WSAX (18-23 members) with distinct species-level genomes and metabolic outcomes (e.g., higher short chain fatty acid production from RSAX and more lactic acid produced from WSAX). The major SAX-selected members were from genera of Bacteroides and Bifidobacterium and family Lachnospiraceae. Carbohydrate active enzyme (CAZyme) genes in metagenomes revealed broad AX-related hydrolytic potentials among key members; however, CAZyme genes enriched in different consortia displayed various catabolic domain fusions with diverse accessory motifs that differ among the two SAX types. These results suggest that fine polysaccharide structure exerts deterministic selection effect for distinct fermenting consortia.
Subjects
CAZyme domains; Metabolomics; Metagenomics; Polysaccharide structure; Sequential passage fermentation
SDGs

[SDGs]SDG3

Type
journal article

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