Discovery of Human Gut Bacteria Responsible for Biotransformation and Structural Diversification of Oat Steroidal Saponins

Abstract Oat steroidal saponins undergo biotransformation by the gut microbiota, yet the bacteria involved and the structural diversity of the resulting metabolites remain incompletely characterized. Incubation of avenacoside B (AVE-B), a major oat steroidal saponin, with fecal microbiota from six human donors revealed marked interindividual variation in avenacoside E (AVE-E) production. Five bacterial species capable of AVE-B metabolism were isolated, with Bacteroides uniformis SS-F-0001 exhibiting the broadest metabolic profile. Quantitative PCR and carbohydrate-active enzyme profiling suggested that abundance alone did not explain conversion capacity. Comparative 1D and 2D NMR analysis of isolated AVE-E and its isomer revealed diagnostic C-22 and C-25 chemical-shift differences and H2-26 → C-22 HMBC correlations, supporting an isonuatigenin-type isomer with a six-membered F ring. These findings identify bacterial contributors to oat saponin metabolism and reveal structural diversity involving both deglycosylation and aglycone ring rearrangement, providing a basis for investigating the mechanisms and biological consequences of microbial saponin metabolism.

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Publication Details

Journal
Journal of Agricultural and Food Chemistry
Published
2026-11-10
DOI
https://doi.org/10.1021/acs.jafc.6c14250
Primary Topic
Steroid Chemistry and Biochemistry
Type
article
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article

Discovery of Human Gut Bacteria Responsible for Biotransformation and Structural Diversification of Oat Steroidal Saponins

Fatemeh Taktaz, Shengmin Sang, Salar Hafez Ghoran, Shuwei Zhang et al.
Journal of Agricultural and Food Chemistry
Steroid Chemistry and Biochemistry
article

Discovery of Human Gut Bacteria Responsible for Biotransformation and Structural Diversification of Oat Steroidal Saponins

Fatemeh Taktaz, Shengmin Sang, Salar Hafez Ghoran, Shuwei Zhang, Pengpeng Zhou, Juanjuan Hu
article en

Abstract

Abstract Oat steroidal saponins undergo biotransformation by the gut microbiota, yet the bacteria involved and the structural diversity of the resulting metabolites remain incompletely characterized. Incubation of avenacoside B (AVE-B), a major oat steroidal saponin, with fecal microbiota from six human donors revealed marked interindividual variation in avenacoside E (AVE-E) production. Five bacterial species capable of AVE-B metabolism were isolated, with Bacteroides uniformis SS-F-0001 exhibiting the broadest metabolic profile. Quantitative PCR and carbohydrate-active enzyme profiling suggested that abundance alone did not explain conversion capacity. Comparative 1D and 2D NMR analysis of isolated AVE-E and its isomer revealed diagnostic C-22 and C-25 chemical-shift differences and H2-26 → C-22 HMBC correlations, supporting an isonuatigenin-type isomer with a six-membered F ring. These findings identify bacterial contributors to oat saponin metabolism and reveal structural diversity involving both deglycosylation and aglycone ring rearrangement, providing a basis for investigating the mechanisms and biological consequences of microbial saponin metabolism.

Journal of Agricultural and Food Chemistry
North Carolina Agricultural and Technical State University (US)
Steroid Chemistry and Biochemistry
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