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A simple technique for suppressor detection inEscherichia coli
To study the viability of agyrA S83 stop mutation found in anEscherichia coli J53 ciprofloxacin-resistant strain (J53 CipR27), a pBR322 derivative was constructed with a TAG mutation in thebla gene knocking out ampicillin resistance. Ampicillin resistance was restored, suggesting that the strain con...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7207127/ https://www.ncbi.nlm.nih.gov/pubmed/27682418 http://dx.doi.org/10.1093/femsle/fnw228 |
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author | Vinué, Laura Hooper, David C. |
author_facet | Vinué, Laura Hooper, David C. |
author_sort | Vinué, Laura |
collection | PubMed |
description | To study the viability of agyrA S83 stop mutation found in anEscherichia coli J53 ciprofloxacin-resistant strain (J53 CipR27), a pBR322 derivative was constructed with a TAG mutation in thebla gene knocking out ampicillin resistance. Ampicillin resistance was restored, suggesting that the strain contains tRNA suppressor activity able to suppress the UAG codongyrA and allow viability. The method was applied to 22 unique clinicalE. coli isolates, and all were found to have low-level suppressor activity. |
format | Online Article Text |
id | pubmed-7207127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-72071272020-05-13 A simple technique for suppressor detection inEscherichia coli Vinué, Laura Hooper, David C. FEMS Microbiol Lett Letter to the Editor To study the viability of agyrA S83 stop mutation found in anEscherichia coli J53 ciprofloxacin-resistant strain (J53 CipR27), a pBR322 derivative was constructed with a TAG mutation in thebla gene knocking out ampicillin resistance. Ampicillin resistance was restored, suggesting that the strain contains tRNA suppressor activity able to suppress the UAG codongyrA and allow viability. The method was applied to 22 unique clinicalE. coli isolates, and all were found to have low-level suppressor activity. Oxford University Press 2016-09-27 2016-10-01 /pmc/articles/PMC7207127/ /pubmed/27682418 http://dx.doi.org/10.1093/femsle/fnw228 Text en © FEMS 2016. All rights reserved. For permissions, please e-mail:journals.permissions@oup.com http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Letter to the Editor Vinué, Laura Hooper, David C. A simple technique for suppressor detection inEscherichia coli |
title | A simple technique for suppressor detection inEscherichia coli |
title_full | A simple technique for suppressor detection inEscherichia coli |
title_fullStr | A simple technique for suppressor detection inEscherichia coli |
title_full_unstemmed | A simple technique for suppressor detection inEscherichia coli |
title_short | A simple technique for suppressor detection inEscherichia coli |
title_sort | simple technique for suppressor detection inescherichia coli |
topic | Letter to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7207127/ https://www.ncbi.nlm.nih.gov/pubmed/27682418 http://dx.doi.org/10.1093/femsle/fnw228 |
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