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Microbial Conjugation Studies of Licochalcones and Xanthohumol

Microbial conjugation studies of licochalcones (1–4) and xanthohumol (5) were performed by using the fungi Mucor hiemalis and Absidia coerulea. As a result, one new glucosylated metabolite was produced by M. hiemalis whereas four new and three known sulfated metabolites were obtained by transformati...

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Autores principales: Han, Fubo, Xiao, Yina, Lee, Ik-Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268106/
https://www.ncbi.nlm.nih.gov/pubmed/34206985
http://dx.doi.org/10.3390/ijms22136893
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author Han, Fubo
Xiao, Yina
Lee, Ik-Soo
author_facet Han, Fubo
Xiao, Yina
Lee, Ik-Soo
author_sort Han, Fubo
collection PubMed
description Microbial conjugation studies of licochalcones (1–4) and xanthohumol (5) were performed by using the fungi Mucor hiemalis and Absidia coerulea. As a result, one new glucosylated metabolite was produced by M. hiemalis whereas four new and three known sulfated metabolites were obtained by transformation with A. coerulea. Chemical structures of all the metabolites were elucidated on the basis of 1D-, 2D-NMR and mass spectroscopic data analyses. These results could contribute to a better understanding of the metabolic fates of licochalcones and xanthohumol in mammalian systems. Although licochalcone A 4′-sulfate (7) showed less cytotoxic activity against human cancer cell lines compared to its substrate licochalcone A, its activity was fairly retained with the IC(50) values in the range of 27.35–43.07 μM.
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spelling pubmed-82681062021-07-10 Microbial Conjugation Studies of Licochalcones and Xanthohumol Han, Fubo Xiao, Yina Lee, Ik-Soo Int J Mol Sci Article Microbial conjugation studies of licochalcones (1–4) and xanthohumol (5) were performed by using the fungi Mucor hiemalis and Absidia coerulea. As a result, one new glucosylated metabolite was produced by M. hiemalis whereas four new and three known sulfated metabolites were obtained by transformation with A. coerulea. Chemical structures of all the metabolites were elucidated on the basis of 1D-, 2D-NMR and mass spectroscopic data analyses. These results could contribute to a better understanding of the metabolic fates of licochalcones and xanthohumol in mammalian systems. Although licochalcone A 4′-sulfate (7) showed less cytotoxic activity against human cancer cell lines compared to its substrate licochalcone A, its activity was fairly retained with the IC(50) values in the range of 27.35–43.07 μM. MDPI 2021-06-26 /pmc/articles/PMC8268106/ /pubmed/34206985 http://dx.doi.org/10.3390/ijms22136893 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Han, Fubo
Xiao, Yina
Lee, Ik-Soo
Microbial Conjugation Studies of Licochalcones and Xanthohumol
title Microbial Conjugation Studies of Licochalcones and Xanthohumol
title_full Microbial Conjugation Studies of Licochalcones and Xanthohumol
title_fullStr Microbial Conjugation Studies of Licochalcones and Xanthohumol
title_full_unstemmed Microbial Conjugation Studies of Licochalcones and Xanthohumol
title_short Microbial Conjugation Studies of Licochalcones and Xanthohumol
title_sort microbial conjugation studies of licochalcones and xanthohumol
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268106/
https://www.ncbi.nlm.nih.gov/pubmed/34206985
http://dx.doi.org/10.3390/ijms22136893
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