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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Scientific World Journal
2012
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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. |
format | Online Article Text |
id | pubmed-3361144 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Scientific World Journal |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT kostrzewasusłowedyta microbialtransformationsof7hydroxyflavanone AT janeczkotomasz microbialtransformationsof7hydroxyflavanone |