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Microbial Glycosylation of Daidzein, Genistein and Biochanin A: Two New Glucosides of Biochanin A
Biotransformation of daidzein, genistein and biochanin A by three selected filamentous fungi was investigated. As a result of biotransformations, six glycosylation products were obtained. Fungus Beauveria bassiana converted all tested isoflavones to 4″-O-methyl-7-O-glucosyl derivatives, whereas Absi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155839/ https://www.ncbi.nlm.nih.gov/pubmed/28054950 http://dx.doi.org/10.3390/molecules22010081 |
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author | Sordon, Sandra Popłoński, Jarosław Tronina, Tomasz Huszcza, Ewa |
author_facet | Sordon, Sandra Popłoński, Jarosław Tronina, Tomasz Huszcza, Ewa |
author_sort | Sordon, Sandra |
collection | PubMed |
description | Biotransformation of daidzein, genistein and biochanin A by three selected filamentous fungi was investigated. As a result of biotransformations, six glycosylation products were obtained. Fungus Beauveria bassiana converted all tested isoflavones to 4″-O-methyl-7-O-glucosyl derivatives, whereas Absidia coerulea and Absidia glauca were able to transform genistein and biochanin A to genistin and sissotrin, respectively. In the culture of Absidia coerulea, in addition to the sissotrin, the product of glucosylation at position 5 was formed. Two of the obtained compounds have not been published so far: 4″-O-methyl-7-O-glucosyl biochanin A and 5-O-glucosyl biochanin A (isosissotrin). Biotransformation products were obtained with 22%–40% isolated yield. |
format | Online Article Text |
id | pubmed-6155839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61558392018-11-13 Microbial Glycosylation of Daidzein, Genistein and Biochanin A: Two New Glucosides of Biochanin A Sordon, Sandra Popłoński, Jarosław Tronina, Tomasz Huszcza, Ewa Molecules Article Biotransformation of daidzein, genistein and biochanin A by three selected filamentous fungi was investigated. As a result of biotransformations, six glycosylation products were obtained. Fungus Beauveria bassiana converted all tested isoflavones to 4″-O-methyl-7-O-glucosyl derivatives, whereas Absidia coerulea and Absidia glauca were able to transform genistein and biochanin A to genistin and sissotrin, respectively. In the culture of Absidia coerulea, in addition to the sissotrin, the product of glucosylation at position 5 was formed. Two of the obtained compounds have not been published so far: 4″-O-methyl-7-O-glucosyl biochanin A and 5-O-glucosyl biochanin A (isosissotrin). Biotransformation products were obtained with 22%–40% isolated yield. MDPI 2017-01-03 /pmc/articles/PMC6155839/ /pubmed/28054950 http://dx.doi.org/10.3390/molecules22010081 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sordon, Sandra Popłoński, Jarosław Tronina, Tomasz Huszcza, Ewa Microbial Glycosylation of Daidzein, Genistein and Biochanin A: Two New Glucosides of Biochanin A |
title | Microbial Glycosylation of Daidzein, Genistein and Biochanin A: Two New Glucosides of Biochanin A |
title_full | Microbial Glycosylation of Daidzein, Genistein and Biochanin A: Two New Glucosides of Biochanin A |
title_fullStr | Microbial Glycosylation of Daidzein, Genistein and Biochanin A: Two New Glucosides of Biochanin A |
title_full_unstemmed | Microbial Glycosylation of Daidzein, Genistein and Biochanin A: Two New Glucosides of Biochanin A |
title_short | Microbial Glycosylation of Daidzein, Genistein and Biochanin A: Two New Glucosides of Biochanin A |
title_sort | microbial glycosylation of daidzein, genistein and biochanin a: two new glucosides of biochanin a |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155839/ https://www.ncbi.nlm.nih.gov/pubmed/28054950 http://dx.doi.org/10.3390/molecules22010081 |
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