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Directed evolution of Escherichia coli with lower-than-natural plasmid mutation rates
Unwanted evolution of designed DNA sequences limits metabolic and genome engineering efforts. Engineered functions that are burdensome to host cells and slow their replication are rapidly inactivated by mutations, and unplanned mutations with unpredictable effects often accumulate alongside designed...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158703/ https://www.ncbi.nlm.nih.gov/pubmed/30137492 http://dx.doi.org/10.1093/nar/gky751 |
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author | Deatherage, Daniel E Leon, Dacia Rodriguez, Álvaro E Omar, Salma K Barrick, Jeffrey E |
author_facet | Deatherage, Daniel E Leon, Dacia Rodriguez, Álvaro E Omar, Salma K Barrick, Jeffrey E |
author_sort | Deatherage, Daniel E |
collection | PubMed |
description | Unwanted evolution of designed DNA sequences limits metabolic and genome engineering efforts. Engineered functions that are burdensome to host cells and slow their replication are rapidly inactivated by mutations, and unplanned mutations with unpredictable effects often accumulate alongside designed changes in large-scale genome editing projects. We developed a directed evolution strategy, Periodic Reselection for Evolutionarily Reliable Variants (PResERV), to discover mutations that prolong the function of a burdensome DNA sequence in an engineered organism. Here, we used PResERV to isolate Escherichia coli cells that replicate ColE1-type plasmids with higher fidelity. We found mutations in DNA polymerase I and in RNase E that reduce plasmid mutation rates by 6- to 30-fold. The PResERV method implicitly selects to maintain the growth rate of host cells, and high plasmid copy numbers and gene expression levels are maintained in some of the evolved E. coli strains, indicating that it is possible to improve the genetic stability of cellular chassis without encountering trade-offs in other desirable performance characteristics. Utilizing these new antimutator E. coli and applying PResERV to other organisms in the future promises to prevent evolutionary failures and unpredictability to provide a more stable genetic foundation for synthetic biology. |
format | Online Article Text |
id | pubmed-6158703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61587032018-10-02 Directed evolution of Escherichia coli with lower-than-natural plasmid mutation rates Deatherage, Daniel E Leon, Dacia Rodriguez, Álvaro E Omar, Salma K Barrick, Jeffrey E Nucleic Acids Res Synthetic Biology and Bioengineering Unwanted evolution of designed DNA sequences limits metabolic and genome engineering efforts. Engineered functions that are burdensome to host cells and slow their replication are rapidly inactivated by mutations, and unplanned mutations with unpredictable effects often accumulate alongside designed changes in large-scale genome editing projects. We developed a directed evolution strategy, Periodic Reselection for Evolutionarily Reliable Variants (PResERV), to discover mutations that prolong the function of a burdensome DNA sequence in an engineered organism. Here, we used PResERV to isolate Escherichia coli cells that replicate ColE1-type plasmids with higher fidelity. We found mutations in DNA polymerase I and in RNase E that reduce plasmid mutation rates by 6- to 30-fold. The PResERV method implicitly selects to maintain the growth rate of host cells, and high plasmid copy numbers and gene expression levels are maintained in some of the evolved E. coli strains, indicating that it is possible to improve the genetic stability of cellular chassis without encountering trade-offs in other desirable performance characteristics. Utilizing these new antimutator E. coli and applying PResERV to other organisms in the future promises to prevent evolutionary failures and unpredictability to provide a more stable genetic foundation for synthetic biology. Oxford University Press 2018-09-28 2018-08-22 /pmc/articles/PMC6158703/ /pubmed/30137492 http://dx.doi.org/10.1093/nar/gky751 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Synthetic Biology and Bioengineering Deatherage, Daniel E Leon, Dacia Rodriguez, Álvaro E Omar, Salma K Barrick, Jeffrey E Directed evolution of Escherichia coli with lower-than-natural plasmid mutation rates |
title | Directed evolution of Escherichia coli with lower-than-natural plasmid mutation rates |
title_full | Directed evolution of Escherichia coli with lower-than-natural plasmid mutation rates |
title_fullStr | Directed evolution of Escherichia coli with lower-than-natural plasmid mutation rates |
title_full_unstemmed | Directed evolution of Escherichia coli with lower-than-natural plasmid mutation rates |
title_short | Directed evolution of Escherichia coli with lower-than-natural plasmid mutation rates |
title_sort | directed evolution of escherichia coli with lower-than-natural plasmid mutation rates |
topic | Synthetic Biology and Bioengineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158703/ https://www.ncbi.nlm.nih.gov/pubmed/30137492 http://dx.doi.org/10.1093/nar/gky751 |
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