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Evolutionary engineering improves tolerance for medium-chain alcohols in Saccharomyces cerevisiae
BACKGROUND: Yeast-based chemical production is an environmentally friendly alternative to petroleum-based production or processes that involve harsh chemicals. However, many potential alcohol biofuels, such as n-butanol, isobutanol and n-hexanol, are toxic to production organisms, lowering the effic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880003/ https://www.ncbi.nlm.nih.gov/pubmed/29619086 http://dx.doi.org/10.1186/s13068-018-1089-9 |
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author | Davis López, Stephanie A. Griffith, Douglas Andrew Choi, Brian Cate, Jamie H. D. Tullman-Ercek, Danielle |
author_facet | Davis López, Stephanie A. Griffith, Douglas Andrew Choi, Brian Cate, Jamie H. D. Tullman-Ercek, Danielle |
author_sort | Davis López, Stephanie A. |
collection | PubMed |
description | BACKGROUND: Yeast-based chemical production is an environmentally friendly alternative to petroleum-based production or processes that involve harsh chemicals. However, many potential alcohol biofuels, such as n-butanol, isobutanol and n-hexanol, are toxic to production organisms, lowering the efficiency and cost-effectiveness of these processes. We set out to improve the tolerance of Saccharomyces cerevisiae toward these alcohols. RESULTS: We evolved the laboratory strain of S. cerevisiae BY4741 to be more tolerant toward n-hexanol and show that the mutations which confer tolerance occur in proteins of the translation initiation complex. We found that n-hexanol inhibits initiation of translation and evolved mutations in the α subunit of eIF2 and the γ subunit of its guanine exchange factor eIF2B rescue this inhibition. We further demonstrate that translation initiation is affected by other alcohols such as n-pentanol and n-heptanol, and that mutations in the eIF2 and eIF2B complexes greatly improve tolerance to these medium-chain alcohols. CONCLUSIONS: We successfully generated S. cerevisiae strains that have improved tolerance toward medium-chain alcohols and have demonstrated that the causative mutations overcome inhibition of translation initiation by these alcohols. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1089-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5880003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58800032018-04-04 Evolutionary engineering improves tolerance for medium-chain alcohols in Saccharomyces cerevisiae Davis López, Stephanie A. Griffith, Douglas Andrew Choi, Brian Cate, Jamie H. D. Tullman-Ercek, Danielle Biotechnol Biofuels Research BACKGROUND: Yeast-based chemical production is an environmentally friendly alternative to petroleum-based production or processes that involve harsh chemicals. However, many potential alcohol biofuels, such as n-butanol, isobutanol and n-hexanol, are toxic to production organisms, lowering the efficiency and cost-effectiveness of these processes. We set out to improve the tolerance of Saccharomyces cerevisiae toward these alcohols. RESULTS: We evolved the laboratory strain of S. cerevisiae BY4741 to be more tolerant toward n-hexanol and show that the mutations which confer tolerance occur in proteins of the translation initiation complex. We found that n-hexanol inhibits initiation of translation and evolved mutations in the α subunit of eIF2 and the γ subunit of its guanine exchange factor eIF2B rescue this inhibition. We further demonstrate that translation initiation is affected by other alcohols such as n-pentanol and n-heptanol, and that mutations in the eIF2 and eIF2B complexes greatly improve tolerance to these medium-chain alcohols. CONCLUSIONS: We successfully generated S. cerevisiae strains that have improved tolerance toward medium-chain alcohols and have demonstrated that the causative mutations overcome inhibition of translation initiation by these alcohols. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1089-9) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-02 /pmc/articles/PMC5880003/ /pubmed/29619086 http://dx.doi.org/10.1186/s13068-018-1089-9 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Davis López, Stephanie A. Griffith, Douglas Andrew Choi, Brian Cate, Jamie H. D. Tullman-Ercek, Danielle Evolutionary engineering improves tolerance for medium-chain alcohols in Saccharomyces cerevisiae |
title | Evolutionary engineering improves tolerance for medium-chain alcohols in Saccharomyces cerevisiae |
title_full | Evolutionary engineering improves tolerance for medium-chain alcohols in Saccharomyces cerevisiae |
title_fullStr | Evolutionary engineering improves tolerance for medium-chain alcohols in Saccharomyces cerevisiae |
title_full_unstemmed | Evolutionary engineering improves tolerance for medium-chain alcohols in Saccharomyces cerevisiae |
title_short | Evolutionary engineering improves tolerance for medium-chain alcohols in Saccharomyces cerevisiae |
title_sort | evolutionary engineering improves tolerance for medium-chain alcohols in saccharomyces cerevisiae |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880003/ https://www.ncbi.nlm.nih.gov/pubmed/29619086 http://dx.doi.org/10.1186/s13068-018-1089-9 |
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