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Construction of a Modular Arsenic-Resistance Operon in E. coli and the Production of Arsenic Nanoparticles
Arsenic is a widespread contaminant of both land and water around the world. Current methods of decontamination such as phytoremediation and chemical adsorbents can be resource and time intensive, and may not be suitable for some areas such as remote communities where cost and transportation are maj...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4611968/ https://www.ncbi.nlm.nih.gov/pubmed/26539432 http://dx.doi.org/10.3389/fbioe.2015.00160 |
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author | Edmundson, Matthew Charles Horsfall, Louise |
author_facet | Edmundson, Matthew Charles Horsfall, Louise |
author_sort | Edmundson, Matthew Charles |
collection | PubMed |
description | Arsenic is a widespread contaminant of both land and water around the world. Current methods of decontamination such as phytoremediation and chemical adsorbents can be resource and time intensive, and may not be suitable for some areas such as remote communities where cost and transportation are major issues. Bacterial decontamination, with strict controls preventing environmental release, may offer a cost-effective alternative or provide a financial incentive when used in combination with other remediation techniques. In this study, we have produced Escherichia coli strains containing arsenic-resistance genes from a number of sources, overexpressing them and testing their effects on arsenic resistance. While the lab E. coli strain JM109 (the “wild-type”) is resistant up to 20 mM sodium arsenate, the strain containing our plasmid pEC20 is resistant up to 80 mM. When combined with our construct pArsRBCC arsenic-containing nanoparticles were observed at the cell surface; the elements of pEC20 and pArsRBCC were therefore combined in a modular construct, pArs, in order to evaluate the roles and synergistic effects of the components of the original plasmids in arsenic resistance and nanoparticle formation. We have also investigated introducing the lac operator in order to more tightly control expression from pArs. We demonstrate that our strains are able to reduce toxic forms of arsenic into stable, insoluble metallic As(0), providing one way to remove arsenate contamination, and which may also be of benefit for other heavy metals. |
format | Online Article Text |
id | pubmed-4611968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-46119682015-11-04 Construction of a Modular Arsenic-Resistance Operon in E. coli and the Production of Arsenic Nanoparticles Edmundson, Matthew Charles Horsfall, Louise Front Bioeng Biotechnol Bioengineering and Biotechnology Arsenic is a widespread contaminant of both land and water around the world. Current methods of decontamination such as phytoremediation and chemical adsorbents can be resource and time intensive, and may not be suitable for some areas such as remote communities where cost and transportation are major issues. Bacterial decontamination, with strict controls preventing environmental release, may offer a cost-effective alternative or provide a financial incentive when used in combination with other remediation techniques. In this study, we have produced Escherichia coli strains containing arsenic-resistance genes from a number of sources, overexpressing them and testing their effects on arsenic resistance. While the lab E. coli strain JM109 (the “wild-type”) is resistant up to 20 mM sodium arsenate, the strain containing our plasmid pEC20 is resistant up to 80 mM. When combined with our construct pArsRBCC arsenic-containing nanoparticles were observed at the cell surface; the elements of pEC20 and pArsRBCC were therefore combined in a modular construct, pArs, in order to evaluate the roles and synergistic effects of the components of the original plasmids in arsenic resistance and nanoparticle formation. We have also investigated introducing the lac operator in order to more tightly control expression from pArs. We demonstrate that our strains are able to reduce toxic forms of arsenic into stable, insoluble metallic As(0), providing one way to remove arsenate contamination, and which may also be of benefit for other heavy metals. Frontiers Media S.A. 2015-10-20 /pmc/articles/PMC4611968/ /pubmed/26539432 http://dx.doi.org/10.3389/fbioe.2015.00160 Text en Copyright © 2015 Edmundson and Horsfall. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Edmundson, Matthew Charles Horsfall, Louise Construction of a Modular Arsenic-Resistance Operon in E. coli and the Production of Arsenic Nanoparticles |
title | Construction of a Modular Arsenic-Resistance Operon in E. coli and the Production of Arsenic Nanoparticles |
title_full | Construction of a Modular Arsenic-Resistance Operon in E. coli and the Production of Arsenic Nanoparticles |
title_fullStr | Construction of a Modular Arsenic-Resistance Operon in E. coli and the Production of Arsenic Nanoparticles |
title_full_unstemmed | Construction of a Modular Arsenic-Resistance Operon in E. coli and the Production of Arsenic Nanoparticles |
title_short | Construction of a Modular Arsenic-Resistance Operon in E. coli and the Production of Arsenic Nanoparticles |
title_sort | construction of a modular arsenic-resistance operon in e. coli and the production of arsenic nanoparticles |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4611968/ https://www.ncbi.nlm.nih.gov/pubmed/26539432 http://dx.doi.org/10.3389/fbioe.2015.00160 |
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