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Characterizing an engineered carotenoid-producing yeast as an anti-stress chassis for building cell factories
BACKGROUND: A microorganism engineered for non-native tasks may suffer stresses it never met before. Therefore, we examined whether a Kluyveromyces marxianus strain engineered with a carotenoid biosynthesis pathway can serve as an anti-stress chassis for building cell factories. RESULTS: Carotenoids...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737703/ https://www.ncbi.nlm.nih.gov/pubmed/31506091 http://dx.doi.org/10.1186/s12934-019-1205-y |
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author | Liu, Hsien-Lin Chang, Jui-Jen Thia, Caroline Lin, Yu-Ju Lo, Shou-Chen Huang, Chieh-Chen Li, Wen-Hsiung |
author_facet | Liu, Hsien-Lin Chang, Jui-Jen Thia, Caroline Lin, Yu-Ju Lo, Shou-Chen Huang, Chieh-Chen Li, Wen-Hsiung |
author_sort | Liu, Hsien-Lin |
collection | PubMed |
description | BACKGROUND: A microorganism engineered for non-native tasks may suffer stresses it never met before. Therefore, we examined whether a Kluyveromyces marxianus strain engineered with a carotenoid biosynthesis pathway can serve as an anti-stress chassis for building cell factories. RESULTS: Carotenoids, a family of antioxidants, are valuable natural products with high commercial potential. We showed that the free radical removal ability of carotenoids can confer the engineered host with a higher tolerance to ethanol, so that it can produce more bio-ethanol than the wild type. Moreover, we found that this engineered strain has improved tolerance to other toxic effects including furfurals, heavy metals such as arsenate (biomass contaminant) and isobutanol (end product). Furthermore, the enhanced ethanol tolerance of the host can be applied to bioconversion of a natural medicine that needs to use ethanol as the delivery solvent of hydrophobic precursors. The result suggested that the engineered yeast showed enhanced tolerance to ethanol-dissolved hydrophobic 10-deacetylbaccatin III, which is considered a sustainable precursor for paclitaxel (taxol) bioconversion. CONCLUSIONS: The stress tolerances of the engineered yeast strain showed tolerance to several toxins, so it may serve as a chassis for cell factories to produce target products, and the co-production of carotenoids may make the biorefinary more cost-effective. |
format | Online Article Text |
id | pubmed-6737703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67377032019-09-16 Characterizing an engineered carotenoid-producing yeast as an anti-stress chassis for building cell factories Liu, Hsien-Lin Chang, Jui-Jen Thia, Caroline Lin, Yu-Ju Lo, Shou-Chen Huang, Chieh-Chen Li, Wen-Hsiung Microb Cell Fact Research BACKGROUND: A microorganism engineered for non-native tasks may suffer stresses it never met before. Therefore, we examined whether a Kluyveromyces marxianus strain engineered with a carotenoid biosynthesis pathway can serve as an anti-stress chassis for building cell factories. RESULTS: Carotenoids, a family of antioxidants, are valuable natural products with high commercial potential. We showed that the free radical removal ability of carotenoids can confer the engineered host with a higher tolerance to ethanol, so that it can produce more bio-ethanol than the wild type. Moreover, we found that this engineered strain has improved tolerance to other toxic effects including furfurals, heavy metals such as arsenate (biomass contaminant) and isobutanol (end product). Furthermore, the enhanced ethanol tolerance of the host can be applied to bioconversion of a natural medicine that needs to use ethanol as the delivery solvent of hydrophobic precursors. The result suggested that the engineered yeast showed enhanced tolerance to ethanol-dissolved hydrophobic 10-deacetylbaccatin III, which is considered a sustainable precursor for paclitaxel (taxol) bioconversion. CONCLUSIONS: The stress tolerances of the engineered yeast strain showed tolerance to several toxins, so it may serve as a chassis for cell factories to produce target products, and the co-production of carotenoids may make the biorefinary more cost-effective. BioMed Central 2019-09-10 /pmc/articles/PMC6737703/ /pubmed/31506091 http://dx.doi.org/10.1186/s12934-019-1205-y Text en © The Author(s) 2019 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 Liu, Hsien-Lin Chang, Jui-Jen Thia, Caroline Lin, Yu-Ju Lo, Shou-Chen Huang, Chieh-Chen Li, Wen-Hsiung Characterizing an engineered carotenoid-producing yeast as an anti-stress chassis for building cell factories |
title | Characterizing an engineered carotenoid-producing yeast as an anti-stress chassis for building cell factories |
title_full | Characterizing an engineered carotenoid-producing yeast as an anti-stress chassis for building cell factories |
title_fullStr | Characterizing an engineered carotenoid-producing yeast as an anti-stress chassis for building cell factories |
title_full_unstemmed | Characterizing an engineered carotenoid-producing yeast as an anti-stress chassis for building cell factories |
title_short | Characterizing an engineered carotenoid-producing yeast as an anti-stress chassis for building cell factories |
title_sort | characterizing an engineered carotenoid-producing yeast as an anti-stress chassis for building cell factories |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6737703/ https://www.ncbi.nlm.nih.gov/pubmed/31506091 http://dx.doi.org/10.1186/s12934-019-1205-y |
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