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Azoreductase activity of dye-decolorizing bacteria isolated from the human gut microbiota

The gut microbiota enriches the human gene pool and contributes to xenobiotic metabolism. Microbial azoreductases modulate the reduction of azo-bonds, activating produgs and azo polymer-coated dosage forms, or degrading food additives. Here, we aimed to screen the healthy human gut microbiota for fo...

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Autores principales: Zahran, Sara A., Ali-Tammam, Marwa, Hashem, Abdelgawad M., Aziz, Ramy K., Ali, Amal E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6445285/
https://www.ncbi.nlm.nih.gov/pubmed/30940826
http://dx.doi.org/10.1038/s41598-019-41894-8
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author Zahran, Sara A.
Ali-Tammam, Marwa
Hashem, Abdelgawad M.
Aziz, Ramy K.
Ali, Amal E.
author_facet Zahran, Sara A.
Ali-Tammam, Marwa
Hashem, Abdelgawad M.
Aziz, Ramy K.
Ali, Amal E.
author_sort Zahran, Sara A.
collection PubMed
description The gut microbiota enriches the human gene pool and contributes to xenobiotic metabolism. Microbial azoreductases modulate the reduction of azo-bonds, activating produgs and azo polymer-coated dosage forms, or degrading food additives. Here, we aimed to screen the healthy human gut microbiota for food colorant-reducing activity and to characterize factors modulating it. Four representative isolates from screened fecal samples were identified as E. coli (AZO-Ec), E. faecalis (AZO-Ef), E. avium (AZO-Ev) and B. cereus (AZO-Bc). Both AZO-Ef and AZO-Ev decolorized amaranth aerobically and microaerophilically while AZO-Ec and AZO-Bc had higher aerobic reduction rates. The isolates varied in their activities against different dyes, and the azo-reduction activity mostly followed zero-order reaction kinetics, with a few exceptions. Additionally, the isolates had different pH dependence, e.g., AZO-Ec was not affected by pH variation while AZO-Bc exhibited variable degradation kinetics at different pH levels. Cell-free extracts showed NADH-dependent enzymatic activities 14–19 times higher than extracellular fractions. FMN did not affect the reducing activity of AZO-Ef cell-free extract, whereas AZO-Ec, AZO-Ev and AZO-Bc had significantly higher reduction rates in its presence (P values = 0.02, 0.0001 and 0.02, respectively). Using Degenerate primers allowed the amplification of azoreductase genes, whose sequences were 98–99% similar to genes encoding FMN-dependent-NADH azoreductases.
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spelling pubmed-64452852019-04-05 Azoreductase activity of dye-decolorizing bacteria isolated from the human gut microbiota Zahran, Sara A. Ali-Tammam, Marwa Hashem, Abdelgawad M. Aziz, Ramy K. Ali, Amal E. Sci Rep Article The gut microbiota enriches the human gene pool and contributes to xenobiotic metabolism. Microbial azoreductases modulate the reduction of azo-bonds, activating produgs and azo polymer-coated dosage forms, or degrading food additives. Here, we aimed to screen the healthy human gut microbiota for food colorant-reducing activity and to characterize factors modulating it. Four representative isolates from screened fecal samples were identified as E. coli (AZO-Ec), E. faecalis (AZO-Ef), E. avium (AZO-Ev) and B. cereus (AZO-Bc). Both AZO-Ef and AZO-Ev decolorized amaranth aerobically and microaerophilically while AZO-Ec and AZO-Bc had higher aerobic reduction rates. The isolates varied in their activities against different dyes, and the azo-reduction activity mostly followed zero-order reaction kinetics, with a few exceptions. Additionally, the isolates had different pH dependence, e.g., AZO-Ec was not affected by pH variation while AZO-Bc exhibited variable degradation kinetics at different pH levels. Cell-free extracts showed NADH-dependent enzymatic activities 14–19 times higher than extracellular fractions. FMN did not affect the reducing activity of AZO-Ef cell-free extract, whereas AZO-Ec, AZO-Ev and AZO-Bc had significantly higher reduction rates in its presence (P values = 0.02, 0.0001 and 0.02, respectively). Using Degenerate primers allowed the amplification of azoreductase genes, whose sequences were 98–99% similar to genes encoding FMN-dependent-NADH azoreductases. Nature Publishing Group UK 2019-04-02 /pmc/articles/PMC6445285/ /pubmed/30940826 http://dx.doi.org/10.1038/s41598-019-41894-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zahran, Sara A.
Ali-Tammam, Marwa
Hashem, Abdelgawad M.
Aziz, Ramy K.
Ali, Amal E.
Azoreductase activity of dye-decolorizing bacteria isolated from the human gut microbiota
title Azoreductase activity of dye-decolorizing bacteria isolated from the human gut microbiota
title_full Azoreductase activity of dye-decolorizing bacteria isolated from the human gut microbiota
title_fullStr Azoreductase activity of dye-decolorizing bacteria isolated from the human gut microbiota
title_full_unstemmed Azoreductase activity of dye-decolorizing bacteria isolated from the human gut microbiota
title_short Azoreductase activity of dye-decolorizing bacteria isolated from the human gut microbiota
title_sort azoreductase activity of dye-decolorizing bacteria isolated from the human gut microbiota
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6445285/
https://www.ncbi.nlm.nih.gov/pubmed/30940826
http://dx.doi.org/10.1038/s41598-019-41894-8
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