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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...

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Autores principales: Tominaga, Masahiro, Nozaki, Kenta, Umeno, Daisuke, Ishii, Jun, Kondo, Akihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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.
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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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