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Manganese‐oxidizing bacteria mediate the degradation of 17α‐ethinylestradiol
Manganese (II) and manganese‐oxidizing bacteria were used as an efficient biological system for the degradation of the xenoestrogen 17α‐ethinylestradiol (EE2) at trace concentrations. Mn(2+)‐derived higher oxidation states of Mn (Mn(3+), Mn(4+)) by Mn(2+)‐oxidizing bacteria mediate the oxidative cle...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815292/ https://www.ncbi.nlm.nih.gov/pubmed/21261871 http://dx.doi.org/10.1111/j.1751-7915.2008.00051.x |
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author | Sabirova, Julia S. Cloetens, L. F. F. Vanhaecke, L. Forrez, I. Verstraete, Willy Boon, N. |
author_facet | Sabirova, Julia S. Cloetens, L. F. F. Vanhaecke, L. Forrez, I. Verstraete, Willy Boon, N. |
author_sort | Sabirova, Julia S. |
collection | PubMed |
description | Manganese (II) and manganese‐oxidizing bacteria were used as an efficient biological system for the degradation of the xenoestrogen 17α‐ethinylestradiol (EE2) at trace concentrations. Mn(2+)‐derived higher oxidation states of Mn (Mn(3+), Mn(4+)) by Mn(2+)‐oxidizing bacteria mediate the oxidative cleavage of the polycyclic target compound EE2. The presence of manganese (II) was found to be essential for the degradation of EE2 by Leptothrix discophora, Pseudomonas putida MB1, P. putida MB6 and P. putida MB29. Mn(2+)‐dependent degradation of EE2 was found to be a slow process, which requires multi‐fold excess of Mn(2+) and occurs in the late stationary phase of growth, implying a chemical process taking place. EE2‐derived degradation products were shown to no longer exhibit undesirable estrogenic activity. |
format | Online Article Text |
id | pubmed-3815292 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38152922014-02-12 Manganese‐oxidizing bacteria mediate the degradation of 17α‐ethinylestradiol Sabirova, Julia S. Cloetens, L. F. F. Vanhaecke, L. Forrez, I. Verstraete, Willy Boon, N. Microb Biotechnol Research Articles Manganese (II) and manganese‐oxidizing bacteria were used as an efficient biological system for the degradation of the xenoestrogen 17α‐ethinylestradiol (EE2) at trace concentrations. Mn(2+)‐derived higher oxidation states of Mn (Mn(3+), Mn(4+)) by Mn(2+)‐oxidizing bacteria mediate the oxidative cleavage of the polycyclic target compound EE2. The presence of manganese (II) was found to be essential for the degradation of EE2 by Leptothrix discophora, Pseudomonas putida MB1, P. putida MB6 and P. putida MB29. Mn(2+)‐dependent degradation of EE2 was found to be a slow process, which requires multi‐fold excess of Mn(2+) and occurs in the late stationary phase of growth, implying a chemical process taking place. EE2‐derived degradation products were shown to no longer exhibit undesirable estrogenic activity. Blackwell Publishing Ltd 2008-11 2008-10-14 /pmc/articles/PMC3815292/ /pubmed/21261871 http://dx.doi.org/10.1111/j.1751-7915.2008.00051.x Text en © 2008 The Authors. Journal compilation © 2008 Society for Applied Microbiology and Blackwell Publishing Ltd |
spellingShingle | Research Articles Sabirova, Julia S. Cloetens, L. F. F. Vanhaecke, L. Forrez, I. Verstraete, Willy Boon, N. Manganese‐oxidizing bacteria mediate the degradation of 17α‐ethinylestradiol |
title | Manganese‐oxidizing bacteria mediate the degradation of 17α‐ethinylestradiol |
title_full | Manganese‐oxidizing bacteria mediate the degradation of 17α‐ethinylestradiol |
title_fullStr | Manganese‐oxidizing bacteria mediate the degradation of 17α‐ethinylestradiol |
title_full_unstemmed | Manganese‐oxidizing bacteria mediate the degradation of 17α‐ethinylestradiol |
title_short | Manganese‐oxidizing bacteria mediate the degradation of 17α‐ethinylestradiol |
title_sort | manganese‐oxidizing bacteria mediate the degradation of 17α‐ethinylestradiol |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815292/ https://www.ncbi.nlm.nih.gov/pubmed/21261871 http://dx.doi.org/10.1111/j.1751-7915.2008.00051.x |
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