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Systematic strategies for developing phage resistant Escherichia coli strains
Phages are regarded as powerful antagonists of bacteria, especially in industrial fermentation processes involving bacteria. While bacteria have developed various defense mechanisms, most of which are effective against a narrow range of phages and consequently exert limited protection from phage inf...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9345386/ https://www.ncbi.nlm.nih.gov/pubmed/35918338 http://dx.doi.org/10.1038/s41467-022-31934-9 |
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author | Zou, Xuan Xiao, Xiaohong Mo, Ziran Ge, Yashi Jiang, Xing Huang, Ruolin Li, Mengxue Deng, Zixin Chen, Shi Wang, Lianrong Lee, Sang Yup |
author_facet | Zou, Xuan Xiao, Xiaohong Mo, Ziran Ge, Yashi Jiang, Xing Huang, Ruolin Li, Mengxue Deng, Zixin Chen, Shi Wang, Lianrong Lee, Sang Yup |
author_sort | Zou, Xuan |
collection | PubMed |
description | Phages are regarded as powerful antagonists of bacteria, especially in industrial fermentation processes involving bacteria. While bacteria have developed various defense mechanisms, most of which are effective against a narrow range of phages and consequently exert limited protection from phage infection. Here, we report a strategy for developing phage-resistant Escherichia coli strains through the simultaneous genomic integration of a DNA phosphorothioation-based Ssp defense module and mutations of components essential for the phage life cycle. The engineered E. coli strains show strong resistance against diverse phages tested without affecting cell growth. Additionally, the resultant engineered phage-resistant strains maintain the capabilities of producing example recombinant proteins, D-amino acid oxidase and coronavirus-encoded nonstructural protein nsp8, even under high levels of phage cocktail challenge. The strategy reported here will be useful for developing engineered E. coli strains with improved phage resistance for various industrial fermentation processes for producing recombinant proteins and chemicals of interest. |
format | Online Article Text |
id | pubmed-9345386 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93453862022-08-03 Systematic strategies for developing phage resistant Escherichia coli strains Zou, Xuan Xiao, Xiaohong Mo, Ziran Ge, Yashi Jiang, Xing Huang, Ruolin Li, Mengxue Deng, Zixin Chen, Shi Wang, Lianrong Lee, Sang Yup Nat Commun Article Phages are regarded as powerful antagonists of bacteria, especially in industrial fermentation processes involving bacteria. While bacteria have developed various defense mechanisms, most of which are effective against a narrow range of phages and consequently exert limited protection from phage infection. Here, we report a strategy for developing phage-resistant Escherichia coli strains through the simultaneous genomic integration of a DNA phosphorothioation-based Ssp defense module and mutations of components essential for the phage life cycle. The engineered E. coli strains show strong resistance against diverse phages tested without affecting cell growth. Additionally, the resultant engineered phage-resistant strains maintain the capabilities of producing example recombinant proteins, D-amino acid oxidase and coronavirus-encoded nonstructural protein nsp8, even under high levels of phage cocktail challenge. The strategy reported here will be useful for developing engineered E. coli strains with improved phage resistance for various industrial fermentation processes for producing recombinant proteins and chemicals of interest. Nature Publishing Group UK 2022-08-02 /pmc/articles/PMC9345386/ /pubmed/35918338 http://dx.doi.org/10.1038/s41467-022-31934-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zou, Xuan Xiao, Xiaohong Mo, Ziran Ge, Yashi Jiang, Xing Huang, Ruolin Li, Mengxue Deng, Zixin Chen, Shi Wang, Lianrong Lee, Sang Yup Systematic strategies for developing phage resistant Escherichia coli strains |
title | Systematic strategies for developing phage resistant Escherichia coli strains |
title_full | Systematic strategies for developing phage resistant Escherichia coli strains |
title_fullStr | Systematic strategies for developing phage resistant Escherichia coli strains |
title_full_unstemmed | Systematic strategies for developing phage resistant Escherichia coli strains |
title_short | Systematic strategies for developing phage resistant Escherichia coli strains |
title_sort | systematic strategies for developing phage resistant escherichia coli strains |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9345386/ https://www.ncbi.nlm.nih.gov/pubmed/35918338 http://dx.doi.org/10.1038/s41467-022-31934-9 |
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