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Formation of Phosphoglycosides in Caenorhabditis elegans: A Novel Biotransformation Pathway
BACKGROUND: Caenorhabditis elegans (C. elegans) has become a widely used model to explore the effect of food constituents on health as well as on life-span extension. The results imply that besides essential nutrients several flavonoids are able to impact the aging process. What is less investigated...
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/PMC3474776/ https://www.ncbi.nlm.nih.gov/pubmed/23082135 http://dx.doi.org/10.1371/journal.pone.0046914 |
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author | Soukup, Sebastian T. Spanier, Britta Grünz, Gregor Bunzel, Diana Daniel, Hannelore Kulling, Sabine E. |
author_facet | Soukup, Sebastian T. Spanier, Britta Grünz, Gregor Bunzel, Diana Daniel, Hannelore Kulling, Sabine E. |
author_sort | Soukup, Sebastian T. |
collection | PubMed |
description | BACKGROUND: Caenorhabditis elegans (C. elegans) has become a widely used model to explore the effect of food constituents on health as well as on life-span extension. The results imply that besides essential nutrients several flavonoids are able to impact the aging process. What is less investigated is the bioavailability and biotransformation of these compounds in C. elegans. In the present study, we focused on the soy isoflavone genistein and its metabolism in the nematode as a basis for assessing whether this model system mimics the mammalian condition. PRINCIPAL FINDINGS: C. elegans was exposed to 100 µM genistein for 48 hours. The worm homogenate was extracted and analyzed by liquid chromatography (LC). 11 metabolites of genistein were detected and characterized using LC electrospray ionization mass spectrometry. All genistein metabolites formed by C. elegans were found to be sugar conjugates, primarily genistein-O-glucosides. The dominant metabolite was identified as genistein-7-O-phosphoglucoside. Further interesting metabolites include two genistein-di-O-glycosides, a genistein-O-disaccharide as well as a genistein-O-phosphodisaccharide. CONCLUSIONS/SIGNIFICANCE: Our study provides evidence for a novel biotransformation pathway in C. elegans leading to conjugative metabolites which are not known for mammals. The metabolism of genistein in mammals and in C. elegans differs widely which may greatly impact the bioactivity. These differences need to be appropriately taken into consideration when C. elegans is used as a model to assess possible health or aging effects. |
format | Online Article Text |
id | pubmed-3474776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34747762012-10-18 Formation of Phosphoglycosides in Caenorhabditis elegans: A Novel Biotransformation Pathway Soukup, Sebastian T. Spanier, Britta Grünz, Gregor Bunzel, Diana Daniel, Hannelore Kulling, Sabine E. PLoS One Research Article BACKGROUND: Caenorhabditis elegans (C. elegans) has become a widely used model to explore the effect of food constituents on health as well as on life-span extension. The results imply that besides essential nutrients several flavonoids are able to impact the aging process. What is less investigated is the bioavailability and biotransformation of these compounds in C. elegans. In the present study, we focused on the soy isoflavone genistein and its metabolism in the nematode as a basis for assessing whether this model system mimics the mammalian condition. PRINCIPAL FINDINGS: C. elegans was exposed to 100 µM genistein for 48 hours. The worm homogenate was extracted and analyzed by liquid chromatography (LC). 11 metabolites of genistein were detected and characterized using LC electrospray ionization mass spectrometry. All genistein metabolites formed by C. elegans were found to be sugar conjugates, primarily genistein-O-glucosides. The dominant metabolite was identified as genistein-7-O-phosphoglucoside. Further interesting metabolites include two genistein-di-O-glycosides, a genistein-O-disaccharide as well as a genistein-O-phosphodisaccharide. CONCLUSIONS/SIGNIFICANCE: Our study provides evidence for a novel biotransformation pathway in C. elegans leading to conjugative metabolites which are not known for mammals. The metabolism of genistein in mammals and in C. elegans differs widely which may greatly impact the bioactivity. These differences need to be appropriately taken into consideration when C. elegans is used as a model to assess possible health or aging effects. Public Library of Science 2012-10-17 /pmc/articles/PMC3474776/ /pubmed/23082135 http://dx.doi.org/10.1371/journal.pone.0046914 Text en © 2012 Soukup 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 Soukup, Sebastian T. Spanier, Britta Grünz, Gregor Bunzel, Diana Daniel, Hannelore Kulling, Sabine E. Formation of Phosphoglycosides in Caenorhabditis elegans: A Novel Biotransformation Pathway |
title | Formation of Phosphoglycosides in Caenorhabditis elegans: A Novel Biotransformation Pathway |
title_full | Formation of Phosphoglycosides in Caenorhabditis elegans: A Novel Biotransformation Pathway |
title_fullStr | Formation of Phosphoglycosides in Caenorhabditis elegans: A Novel Biotransformation Pathway |
title_full_unstemmed | Formation of Phosphoglycosides in Caenorhabditis elegans: A Novel Biotransformation Pathway |
title_short | Formation of Phosphoglycosides in Caenorhabditis elegans: A Novel Biotransformation Pathway |
title_sort | formation of phosphoglycosides in caenorhabditis elegans: a novel biotransformation pathway |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3474776/ https://www.ncbi.nlm.nih.gov/pubmed/23082135 http://dx.doi.org/10.1371/journal.pone.0046914 |
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