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A new mercury‐accumulating Mucor hiemalis strain EH8 from cold sulfidic spring water biofilms
Here, we report about a unique aquatic fungus Mucor hiemalis EH8 that can remove toxic ionic mercury from water by intracellular accumulation and reduction into elemental mercury (Hg(0)). EH8 was isolated from a microbial biofilm grown in sulfidic‐reducing spring water sourced at a Marching's s...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5061714/ https://www.ncbi.nlm.nih.gov/pubmed/27177603 http://dx.doi.org/10.1002/mbo3.368 |
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author | Hoque, Enamul Fritscher, Johannes |
author_facet | Hoque, Enamul Fritscher, Johannes |
author_sort | Hoque, Enamul |
collection | PubMed |
description | Here, we report about a unique aquatic fungus Mucor hiemalis EH8 that can remove toxic ionic mercury from water by intracellular accumulation and reduction into elemental mercury (Hg(0)). EH8 was isolated from a microbial biofilm grown in sulfidic‐reducing spring water sourced at a Marching's site located downhill from hop cultivation areas with a history of mercury use. A thorough biodiversity survey and mercury‐removal function analyses were undertaken in an area of about 200 km(2) in Bavaria (Germany) to find the key biofilm and microbe for mercury removal. After a systematic search using metal removal assays we identified Marching spring's biofilm out of 18 different sulfidic springs' biofilms as the only one that was capable of removing ionic Hg from water. EH8 was selected, due to its molecular biological identification as the key microorganism of this biofilm with the capability of mercury removal, and cultivated as a pure culture on solid and in liquid media to produce germinating sporangiospores. They removed 99% of mercury from water within 10–48 h after initial exposure to Hg(II). Scanning electron microscopy demonstrated occurrence of intracellular mercury in germinating sporangiospores exposed to mercury. Not only associated with intracellular components, but mercury was also found to be released and deposited as metallic‐shiny nanospheres. Electron‐dispersive x‐ray analysis of such a nanosphere confirmed presence of mercury by the HgM(α) peak at 2.195 keV. Thus, a first aquatic eukaryotic microbe has been found that is able to grow even at low temperature under sulfur‐reducing conditions with promising performance in mercury removal to safeguard our environment from mercury pollution. |
format | Online Article Text |
id | pubmed-5061714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50617142016-10-24 A new mercury‐accumulating Mucor hiemalis strain EH8 from cold sulfidic spring water biofilms Hoque, Enamul Fritscher, Johannes Microbiologyopen Original Research Here, we report about a unique aquatic fungus Mucor hiemalis EH8 that can remove toxic ionic mercury from water by intracellular accumulation and reduction into elemental mercury (Hg(0)). EH8 was isolated from a microbial biofilm grown in sulfidic‐reducing spring water sourced at a Marching's site located downhill from hop cultivation areas with a history of mercury use. A thorough biodiversity survey and mercury‐removal function analyses were undertaken in an area of about 200 km(2) in Bavaria (Germany) to find the key biofilm and microbe for mercury removal. After a systematic search using metal removal assays we identified Marching spring's biofilm out of 18 different sulfidic springs' biofilms as the only one that was capable of removing ionic Hg from water. EH8 was selected, due to its molecular biological identification as the key microorganism of this biofilm with the capability of mercury removal, and cultivated as a pure culture on solid and in liquid media to produce germinating sporangiospores. They removed 99% of mercury from water within 10–48 h after initial exposure to Hg(II). Scanning electron microscopy demonstrated occurrence of intracellular mercury in germinating sporangiospores exposed to mercury. Not only associated with intracellular components, but mercury was also found to be released and deposited as metallic‐shiny nanospheres. Electron‐dispersive x‐ray analysis of such a nanosphere confirmed presence of mercury by the HgM(α) peak at 2.195 keV. Thus, a first aquatic eukaryotic microbe has been found that is able to grow even at low temperature under sulfur‐reducing conditions with promising performance in mercury removal to safeguard our environment from mercury pollution. John Wiley and Sons Inc. 2016-05-13 /pmc/articles/PMC5061714/ /pubmed/27177603 http://dx.doi.org/10.1002/mbo3.368 Text en © 2016 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Hoque, Enamul Fritscher, Johannes A new mercury‐accumulating Mucor hiemalis strain EH8 from cold sulfidic spring water biofilms |
title | A new mercury‐accumulating Mucor hiemalis strain EH8 from cold sulfidic spring water biofilms |
title_full | A new mercury‐accumulating Mucor hiemalis strain EH8 from cold sulfidic spring water biofilms |
title_fullStr | A new mercury‐accumulating Mucor hiemalis strain EH8 from cold sulfidic spring water biofilms |
title_full_unstemmed | A new mercury‐accumulating Mucor hiemalis strain EH8 from cold sulfidic spring water biofilms |
title_short | A new mercury‐accumulating Mucor hiemalis strain EH8 from cold sulfidic spring water biofilms |
title_sort | new mercury‐accumulating mucor hiemalis strain eh8 from cold sulfidic spring water biofilms |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5061714/ https://www.ncbi.nlm.nih.gov/pubmed/27177603 http://dx.doi.org/10.1002/mbo3.368 |
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