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Robust and flexible platform for directed evolution of yeast genetic switches
A wide repertoire of genetic switches has accelerated prokaryotic synthetic biology, while eukaryotic synthetic biology has lagged in the model organism Saccharomyces cerevisiae. Eukaryotic genetic switches are larger and more complex than prokaryotic ones, complicating the rational design and evolu...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988172/ https://www.ncbi.nlm.nih.gov/pubmed/33758180 http://dx.doi.org/10.1038/s41467-021-22134-y |
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author | Tominaga, Masahiro Nozaki, Kenta Umeno, Daisuke Ishii, Jun Kondo, Akihiko |
author_facet | Tominaga, Masahiro Nozaki, Kenta Umeno, Daisuke Ishii, Jun Kondo, Akihiko |
author_sort | Tominaga, Masahiro |
collection | PubMed |
description | A wide repertoire of genetic switches has accelerated prokaryotic synthetic biology, while eukaryotic synthetic biology has lagged in the model organism Saccharomyces cerevisiae. Eukaryotic genetic switches are larger and more complex than prokaryotic ones, complicating the rational design and evolution of them. Here, we present a robust workflow for the creation and evolution of yeast genetic switches. The selector system was designed so that both ON- and OFF-state selection of genetic switches is completed solely by liquid handling, and it enabled parallel screen/selection of different motifs with different selection conditions. Because selection threshold of both ON- and OFF-state selection can be flexibly tuned, the desired selection conditions can be rapidly pinned down for individual directed evolution experiments without a prior knowledge either on the library population. The system’s utility was demonstrated using 20 independent directed evolution experiments, yielding genetic switches with elevated inducer sensitivities, inverted switching behaviours, sensory functions, and improved signal-to-noise ratio (>100-fold induction). The resulting yeast genetic switches were readily integrated, in a plug-and-play manner, into an AND-gated carotenoid biosynthesis pathway. |
format | Online Article Text |
id | pubmed-7988172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79881722021-04-16 Robust and flexible platform for directed evolution of yeast genetic switches Tominaga, Masahiro Nozaki, Kenta Umeno, Daisuke Ishii, Jun Kondo, Akihiko Nat Commun Article A wide repertoire of genetic switches has accelerated prokaryotic synthetic biology, while eukaryotic synthetic biology has lagged in the model organism Saccharomyces cerevisiae. Eukaryotic genetic switches are larger and more complex than prokaryotic ones, complicating the rational design and evolution of them. Here, we present a robust workflow for the creation and evolution of yeast genetic switches. The selector system was designed so that both ON- and OFF-state selection of genetic switches is completed solely by liquid handling, and it enabled parallel screen/selection of different motifs with different selection conditions. Because selection threshold of both ON- and OFF-state selection can be flexibly tuned, the desired selection conditions can be rapidly pinned down for individual directed evolution experiments without a prior knowledge either on the library population. The system’s utility was demonstrated using 20 independent directed evolution experiments, yielding genetic switches with elevated inducer sensitivities, inverted switching behaviours, sensory functions, and improved signal-to-noise ratio (>100-fold induction). The resulting yeast genetic switches were readily integrated, in a plug-and-play manner, into an AND-gated carotenoid biosynthesis pathway. Nature Publishing Group UK 2021-03-23 /pmc/articles/PMC7988172/ /pubmed/33758180 http://dx.doi.org/10.1038/s41467-021-22134-y Text en © The Author(s) 2021 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/. |
spellingShingle | Article Tominaga, Masahiro Nozaki, Kenta Umeno, Daisuke Ishii, Jun Kondo, Akihiko Robust and flexible platform for directed evolution of yeast genetic switches |
title | Robust and flexible platform for directed evolution of yeast genetic switches |
title_full | Robust and flexible platform for directed evolution of yeast genetic switches |
title_fullStr | Robust and flexible platform for directed evolution of yeast genetic switches |
title_full_unstemmed | Robust and flexible platform for directed evolution of yeast genetic switches |
title_short | Robust and flexible platform for directed evolution of yeast genetic switches |
title_sort | robust and flexible platform for directed evolution of yeast genetic switches |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988172/ https://www.ncbi.nlm.nih.gov/pubmed/33758180 http://dx.doi.org/10.1038/s41467-021-22134-y |
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