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Protein over-expression in Escherichia coli triggers adaptation analogous to antimicrobial resistance
BACKGROUND: The E. coli pET system is the most widely used protein over-expression system worldwide. It relies on the assumption that all cells produce target protein and it is generally believed that integral membrane protein (IMP) over-expression is more toxic than their soluble counterparts. RESU...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7798265/ https://www.ncbi.nlm.nih.gov/pubmed/33430875 http://dx.doi.org/10.1186/s12934-020-01462-6 |
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author | James, Jack Yarnall, Benjamin Koranteng, Andy Gibson, Jane Rahman, Tahmina Doyle, Declan A. |
author_facet | James, Jack Yarnall, Benjamin Koranteng, Andy Gibson, Jane Rahman, Tahmina Doyle, Declan A. |
author_sort | James, Jack |
collection | PubMed |
description | BACKGROUND: The E. coli pET system is the most widely used protein over-expression system worldwide. It relies on the assumption that all cells produce target protein and it is generally believed that integral membrane protein (IMP) over-expression is more toxic than their soluble counterparts. RESULTS: Using GFP-tagged proteins, high level over-expression of either soluble or IMP targets results in > 99.9% cell loss with survival rate of only < 0.03%. Selective pressure generates three phenotypes: large green, large white and small colony variants. As a result, in overnight cultures, ~ 50% of the overall cell mass produces no protein. Genome sequencing of the phenotypes revealed genomic mutations that causes either the loss of T7 RNAP activity or its transcriptional downregulation. The over-expression process is bactericidal and is observed for both soluble and membrane proteins. CONCLUSIONS: We demonstrate that it is the act of high-level over-expression of exogenous proteins in E. coli that sets in motion a chain of events leading to > 99.9% cell death. These results redefine our understanding of protein over-production and link it to the adaptive survival response seen in the development of antimicrobial resistance. |
format | Online Article Text |
id | pubmed-7798265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77982652021-01-11 Protein over-expression in Escherichia coli triggers adaptation analogous to antimicrobial resistance James, Jack Yarnall, Benjamin Koranteng, Andy Gibson, Jane Rahman, Tahmina Doyle, Declan A. Microb Cell Fact Research BACKGROUND: The E. coli pET system is the most widely used protein over-expression system worldwide. It relies on the assumption that all cells produce target protein and it is generally believed that integral membrane protein (IMP) over-expression is more toxic than their soluble counterparts. RESULTS: Using GFP-tagged proteins, high level over-expression of either soluble or IMP targets results in > 99.9% cell loss with survival rate of only < 0.03%. Selective pressure generates three phenotypes: large green, large white and small colony variants. As a result, in overnight cultures, ~ 50% of the overall cell mass produces no protein. Genome sequencing of the phenotypes revealed genomic mutations that causes either the loss of T7 RNAP activity or its transcriptional downregulation. The over-expression process is bactericidal and is observed for both soluble and membrane proteins. CONCLUSIONS: We demonstrate that it is the act of high-level over-expression of exogenous proteins in E. coli that sets in motion a chain of events leading to > 99.9% cell death. These results redefine our understanding of protein over-production and link it to the adaptive survival response seen in the development of antimicrobial resistance. BioMed Central 2021-01-11 /pmc/articles/PMC7798265/ /pubmed/33430875 http://dx.doi.org/10.1186/s12934-020-01462-6 Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research James, Jack Yarnall, Benjamin Koranteng, Andy Gibson, Jane Rahman, Tahmina Doyle, Declan A. Protein over-expression in Escherichia coli triggers adaptation analogous to antimicrobial resistance |
title | Protein over-expression in Escherichia coli triggers adaptation analogous to antimicrobial resistance |
title_full | Protein over-expression in Escherichia coli triggers adaptation analogous to antimicrobial resistance |
title_fullStr | Protein over-expression in Escherichia coli triggers adaptation analogous to antimicrobial resistance |
title_full_unstemmed | Protein over-expression in Escherichia coli triggers adaptation analogous to antimicrobial resistance |
title_short | Protein over-expression in Escherichia coli triggers adaptation analogous to antimicrobial resistance |
title_sort | protein over-expression in escherichia coli triggers adaptation analogous to antimicrobial resistance |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7798265/ https://www.ncbi.nlm.nih.gov/pubmed/33430875 http://dx.doi.org/10.1186/s12934-020-01462-6 |
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