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High throughput mutagenesis and screening for yeast engineering

The eukaryotic yeast Saccharomyces cerevisiae is a model host utilized for whole cell biocatalytic conversions, protein evolution, and scientific inquiries into the pathogenesis of human disease. Over the past decade, the scale and pace of such studies has drastically increased alongside the advent...

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Autores principales: Holland, Kendreze, Blazeck, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9793380/
https://www.ncbi.nlm.nih.gov/pubmed/36575525
http://dx.doi.org/10.1186/s13036-022-00315-7
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author Holland, Kendreze
Blazeck, John
author_facet Holland, Kendreze
Blazeck, John
author_sort Holland, Kendreze
collection PubMed
description The eukaryotic yeast Saccharomyces cerevisiae is a model host utilized for whole cell biocatalytic conversions, protein evolution, and scientific inquiries into the pathogenesis of human disease. Over the past decade, the scale and pace of such studies has drastically increased alongside the advent of novel tools for both genome-wide studies and targeted genetic mutagenesis. In this review, we will detail past and present (e.g., CRISPR/Cas) genome-scale screening platforms, typically employed in the context of growth-based selections for improved whole cell phenotype or for mechanistic interrogations. We will further highlight recent advances that enable the rapid and often continuous evolution of biomolecules with improved function. Additionally, we will detail the corresponding advances in high throughput selection and screening strategies that are essential for assessing or isolating cellular and protein improvements. Finally, we will describe how future developments can continue to advance yeast high throughput engineering.
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spelling pubmed-97933802022-12-27 High throughput mutagenesis and screening for yeast engineering Holland, Kendreze Blazeck, John J Biol Eng Review The eukaryotic yeast Saccharomyces cerevisiae is a model host utilized for whole cell biocatalytic conversions, protein evolution, and scientific inquiries into the pathogenesis of human disease. Over the past decade, the scale and pace of such studies has drastically increased alongside the advent of novel tools for both genome-wide studies and targeted genetic mutagenesis. In this review, we will detail past and present (e.g., CRISPR/Cas) genome-scale screening platforms, typically employed in the context of growth-based selections for improved whole cell phenotype or for mechanistic interrogations. We will further highlight recent advances that enable the rapid and often continuous evolution of biomolecules with improved function. Additionally, we will detail the corresponding advances in high throughput selection and screening strategies that are essential for assessing or isolating cellular and protein improvements. Finally, we will describe how future developments can continue to advance yeast high throughput engineering. BioMed Central 2022-12-27 /pmc/articles/PMC9793380/ /pubmed/36575525 http://dx.doi.org/10.1186/s13036-022-00315-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Holland, Kendreze
Blazeck, John
High throughput mutagenesis and screening for yeast engineering
title High throughput mutagenesis and screening for yeast engineering
title_full High throughput mutagenesis and screening for yeast engineering
title_fullStr High throughput mutagenesis and screening for yeast engineering
title_full_unstemmed High throughput mutagenesis and screening for yeast engineering
title_short High throughput mutagenesis and screening for yeast engineering
title_sort high throughput mutagenesis and screening for yeast engineering
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9793380/
https://www.ncbi.nlm.nih.gov/pubmed/36575525
http://dx.doi.org/10.1186/s13036-022-00315-7
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