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The Microbiota Is Essential for the Generation of Black Tea Theaflavins-Derived Metabolites
BACKGROUND: Theaflavins including theaflavin (TF), theaflavin-3-gallate (TF3G), theaflavin-3′-gallate (TF3′G), and theaflavin-3,3′-digallate (TFDG), are the most important bioactive polyphenols in black tea. Because of their poor systemic bioavailability, it is still unclear how these compounds can...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515489/ https://www.ncbi.nlm.nih.gov/pubmed/23227227 http://dx.doi.org/10.1371/journal.pone.0051001 |
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author | Chen, Huadong Hayek, Saeed Rivera Guzman, Javier Gillitt, Nicholas D. Ibrahim, Salam A. Jobin, Christian Sang, Shengmin |
author_facet | Chen, Huadong Hayek, Saeed Rivera Guzman, Javier Gillitt, Nicholas D. Ibrahim, Salam A. Jobin, Christian Sang, Shengmin |
author_sort | Chen, Huadong |
collection | PubMed |
description | BACKGROUND: Theaflavins including theaflavin (TF), theaflavin-3-gallate (TF3G), theaflavin-3′-gallate (TF3′G), and theaflavin-3,3′-digallate (TFDG), are the most important bioactive polyphenols in black tea. Because of their poor systemic bioavailability, it is still unclear how these compounds can exert their biological functions. The objective of this study is to identify the microbial metabolites of theaflavins in mice and in humans. METHODS AND FINDINGS: In the present study, we gavaged specific pathogen free (SPF) mice and germ free (GF) mice with 200 mg/kg TFDG and identified TF, TF3G, TF3′G, and gallic acid as the major fecal metabolites of TFDG in SPF mice. These metabolites were absent in TFDG- gavaged GF mice. The microbial bioconversion of TFDG, TF3G, and TF3′G was also investigated in vitro using fecal slurries collected from three healthy human subjects. Our results indicate that TFDG is metabolized to TF, TF3G, TF3′G, gallic acid, and pyrogallol by human microbiota. Moreover, both TF3G and TF3′G are metabolized to TF, gallic acid, and pyrogallol by human microbiota. Importantly, we observed interindividual differences on the metabolism rate of gallic acid to pyrogallol among the three human subjects. In addition, we demonstrated that Lactobacillus plantarum 299v and Bacillus subtilis have the capacity to metabolize TFDG. CONCLUSIONS: The microbiota is important for the metabolism of theaflavins in both mice and humans. The in vivo functional impact of microbiota-generated theaflavins-derived metabolites is worthwhile of further study. |
format | Online Article Text |
id | pubmed-3515489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35154892012-12-07 The Microbiota Is Essential for the Generation of Black Tea Theaflavins-Derived Metabolites Chen, Huadong Hayek, Saeed Rivera Guzman, Javier Gillitt, Nicholas D. Ibrahim, Salam A. Jobin, Christian Sang, Shengmin PLoS One Research Article BACKGROUND: Theaflavins including theaflavin (TF), theaflavin-3-gallate (TF3G), theaflavin-3′-gallate (TF3′G), and theaflavin-3,3′-digallate (TFDG), are the most important bioactive polyphenols in black tea. Because of their poor systemic bioavailability, it is still unclear how these compounds can exert their biological functions. The objective of this study is to identify the microbial metabolites of theaflavins in mice and in humans. METHODS AND FINDINGS: In the present study, we gavaged specific pathogen free (SPF) mice and germ free (GF) mice with 200 mg/kg TFDG and identified TF, TF3G, TF3′G, and gallic acid as the major fecal metabolites of TFDG in SPF mice. These metabolites were absent in TFDG- gavaged GF mice. The microbial bioconversion of TFDG, TF3G, and TF3′G was also investigated in vitro using fecal slurries collected from three healthy human subjects. Our results indicate that TFDG is metabolized to TF, TF3G, TF3′G, gallic acid, and pyrogallol by human microbiota. Moreover, both TF3G and TF3′G are metabolized to TF, gallic acid, and pyrogallol by human microbiota. Importantly, we observed interindividual differences on the metabolism rate of gallic acid to pyrogallol among the three human subjects. In addition, we demonstrated that Lactobacillus plantarum 299v and Bacillus subtilis have the capacity to metabolize TFDG. CONCLUSIONS: The microbiota is important for the metabolism of theaflavins in both mice and humans. The in vivo functional impact of microbiota-generated theaflavins-derived metabolites is worthwhile of further study. Public Library of Science 2012-12-05 /pmc/articles/PMC3515489/ /pubmed/23227227 http://dx.doi.org/10.1371/journal.pone.0051001 Text en © 2012 Chen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Chen, Huadong Hayek, Saeed Rivera Guzman, Javier Gillitt, Nicholas D. Ibrahim, Salam A. Jobin, Christian Sang, Shengmin The Microbiota Is Essential for the Generation of Black Tea Theaflavins-Derived Metabolites |
title | The Microbiota Is Essential for the Generation of Black Tea Theaflavins-Derived Metabolites |
title_full | The Microbiota Is Essential for the Generation of Black Tea Theaflavins-Derived Metabolites |
title_fullStr | The Microbiota Is Essential for the Generation of Black Tea Theaflavins-Derived Metabolites |
title_full_unstemmed | The Microbiota Is Essential for the Generation of Black Tea Theaflavins-Derived Metabolites |
title_short | The Microbiota Is Essential for the Generation of Black Tea Theaflavins-Derived Metabolites |
title_sort | microbiota is essential for the generation of black tea theaflavins-derived metabolites |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515489/ https://www.ncbi.nlm.nih.gov/pubmed/23227227 http://dx.doi.org/10.1371/journal.pone.0051001 |
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