Abstract
A human intestinal bacterium, Eubacterium (E.) sp. strain SDG-2, was tested for its ability to metabolize various (3R)- and (3S)-flavan-3-ols and their 3-O-gallates. This bacterium cleaved the C-ring of (3R)- and (3S)flavan-3-ols to give 1,3-diphenylpropan-2-ol derivatives, but not their 3-O-gallates. Furthermore, E. sp. strain SDG-2 had the ability of p-dehydroxylation in the B-ring of (3R)-flavan-3-ols, such as (-)-catechin, (-)-epicatechin, (-)-gallocatechin and (-)-epigallocatechin, but not of (3S)-flavan-3-ols, such as (+)-catechin and (+)-epicatechin.
Author supplied keywords
Cite
CITATION STYLE
Wang, L. Q., Meselhy, M. R., Li, Y., Nakamura, N., Min, B. S., Qin, G. W., & Hattori, M. (2001). The heterocyclic ring fission and dehydroxylation of catechins and related compounds by Eubacterium sp. strain SDG-2, a human intestinal bacterium. Chemical and Pharmaceutical Bulletin, 49(12), 1640–1643. https://doi.org/10.1248/cpb.49.1640
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.