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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...

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Detalles Bibliográficos
Autores principales: Deatherage, Daniel E, Leon, Dacia, Rodriguez, Álvaro E, Omar, Salma K, Barrick, Jeffrey E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
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.
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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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