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Microbial Transformations of 7-Hydroxyflavanone

Microbial transformations of racemic 7-hydroxyflavanone using strains of genus Aspergillus (A. niger KB, A. niger 13/5, A. ochraceus 456) and the species Penicillium chermesinum 113 were studied. The products of O-methylation, O-methylation along with hydroxylation at C-3′ and C-4′, reduction of the...

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Detalles Bibliográficos
Autores principales: Kostrzewa-Susłow, Edyta, Janeczko, Tomasz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific World Journal 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3361144/
https://www.ncbi.nlm.nih.gov/pubmed/22654578
http://dx.doi.org/10.1100/2012/254929
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author Kostrzewa-Susłow, Edyta
Janeczko, Tomasz
author_facet Kostrzewa-Susłow, Edyta
Janeczko, Tomasz
author_sort Kostrzewa-Susłow, Edyta
collection PubMed
description Microbial transformations of racemic 7-hydroxyflavanone using strains of genus Aspergillus (A. niger KB, A. niger 13/5, A. ochraceus 456) and the species Penicillium chermesinum 113 were studied. The products of O-methylation, O-methylation along with hydroxylation at C-3′ and C-4′, reduction of the carbonyl group, reduction of the carbonyl group along with hydroxylation at C-5, and dehydrogenation of C-2 and C-3 were obtained. Most of the products (with the exception of the O-methylation one) have stronger antioxidant properties than the initial substrate.
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spelling pubmed-33611442012-05-31 Microbial Transformations of 7-Hydroxyflavanone Kostrzewa-Susłow, Edyta Janeczko, Tomasz ScientificWorldJournal Research Article Microbial transformations of racemic 7-hydroxyflavanone using strains of genus Aspergillus (A. niger KB, A. niger 13/5, A. ochraceus 456) and the species Penicillium chermesinum 113 were studied. The products of O-methylation, O-methylation along with hydroxylation at C-3′ and C-4′, reduction of the carbonyl group, reduction of the carbonyl group along with hydroxylation at C-5, and dehydrogenation of C-2 and C-3 were obtained. Most of the products (with the exception of the O-methylation one) have stronger antioxidant properties than the initial substrate. The Scientific World Journal 2012-04-30 /pmc/articles/PMC3361144/ /pubmed/22654578 http://dx.doi.org/10.1100/2012/254929 Text en Copyright © 2012 E. Kostrzewa-Susłow and T. Janeczko. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kostrzewa-Susłow, Edyta
Janeczko, Tomasz
Microbial Transformations of 7-Hydroxyflavanone
title Microbial Transformations of 7-Hydroxyflavanone
title_full Microbial Transformations of 7-Hydroxyflavanone
title_fullStr Microbial Transformations of 7-Hydroxyflavanone
title_full_unstemmed Microbial Transformations of 7-Hydroxyflavanone
title_short Microbial Transformations of 7-Hydroxyflavanone
title_sort microbial transformations of 7-hydroxyflavanone
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3361144/
https://www.ncbi.nlm.nih.gov/pubmed/22654578
http://dx.doi.org/10.1100/2012/254929
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