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Metabolic engineering for high yield synthesis of astaxanthin in Xanthophyllomyces dendrorhous
Astaxanthin is a carotenoid with a number of assets useful for the food, cosmetic and pharmaceutical industries. Nowadays, it is mainly produced by chemical synthesis. However, the process leads to an enantiomeric mixture where the biologically assimilable forms (3R, 3′R or 3S, 3′S) are a minority....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8420053/ https://www.ncbi.nlm.nih.gov/pubmed/34488760 http://dx.doi.org/10.1186/s12934-021-01664-6 |
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author | Torres-Haro, Alejandro Verdín, Jorge Kirchmayr, Manuel R. Arellano-Plaza, Melchor |
author_facet | Torres-Haro, Alejandro Verdín, Jorge Kirchmayr, Manuel R. Arellano-Plaza, Melchor |
author_sort | Torres-Haro, Alejandro |
collection | PubMed |
description | Astaxanthin is a carotenoid with a number of assets useful for the food, cosmetic and pharmaceutical industries. Nowadays, it is mainly produced by chemical synthesis. However, the process leads to an enantiomeric mixture where the biologically assimilable forms (3R, 3′R or 3S, 3′S) are a minority. Microbial production of (3R, 3′R) astaxanthin by Xanthophyllomyces dendrorhous is an appealing alternative due to its fast growth rate and easy large-scale production. In order to increase X. dendrorhous astaxanthin yields, random mutant strains able to produce from 6 to 10 mg/g dry mass have been generated; nevertheless, they often are unstable. On the other hand, site-directed mutant strains have also been obtained, but they increase only the yield of non-astaxanthin carotenoids. In this review, we insightfully analyze the metabolic carbon flow converging in astaxanthin biosynthesis and, by integrating the biological features of X. dendrorhous with available metabolic, genomic, transcriptomic, and proteomic data, as well as the knowledge gained with random and site-directed mutants that lead to increased carotenoids yield, we propose new metabolic engineering targets to increase astaxanthin biosynthesis. |
format | Online Article Text |
id | pubmed-8420053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84200532021-09-09 Metabolic engineering for high yield synthesis of astaxanthin in Xanthophyllomyces dendrorhous Torres-Haro, Alejandro Verdín, Jorge Kirchmayr, Manuel R. Arellano-Plaza, Melchor Microb Cell Fact Review Astaxanthin is a carotenoid with a number of assets useful for the food, cosmetic and pharmaceutical industries. Nowadays, it is mainly produced by chemical synthesis. However, the process leads to an enantiomeric mixture where the biologically assimilable forms (3R, 3′R or 3S, 3′S) are a minority. Microbial production of (3R, 3′R) astaxanthin by Xanthophyllomyces dendrorhous is an appealing alternative due to its fast growth rate and easy large-scale production. In order to increase X. dendrorhous astaxanthin yields, random mutant strains able to produce from 6 to 10 mg/g dry mass have been generated; nevertheless, they often are unstable. On the other hand, site-directed mutant strains have also been obtained, but they increase only the yield of non-astaxanthin carotenoids. In this review, we insightfully analyze the metabolic carbon flow converging in astaxanthin biosynthesis and, by integrating the biological features of X. dendrorhous with available metabolic, genomic, transcriptomic, and proteomic data, as well as the knowledge gained with random and site-directed mutants that lead to increased carotenoids yield, we propose new metabolic engineering targets to increase astaxanthin biosynthesis. BioMed Central 2021-09-06 /pmc/articles/PMC8420053/ /pubmed/34488760 http://dx.doi.org/10.1186/s12934-021-01664-6 Text en © The Author(s) 2021 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 Torres-Haro, Alejandro Verdín, Jorge Kirchmayr, Manuel R. Arellano-Plaza, Melchor Metabolic engineering for high yield synthesis of astaxanthin in Xanthophyllomyces dendrorhous |
title | Metabolic engineering for high yield synthesis of astaxanthin in Xanthophyllomyces dendrorhous |
title_full | Metabolic engineering for high yield synthesis of astaxanthin in Xanthophyllomyces dendrorhous |
title_fullStr | Metabolic engineering for high yield synthesis of astaxanthin in Xanthophyllomyces dendrorhous |
title_full_unstemmed | Metabolic engineering for high yield synthesis of astaxanthin in Xanthophyllomyces dendrorhous |
title_short | Metabolic engineering for high yield synthesis of astaxanthin in Xanthophyllomyces dendrorhous |
title_sort | metabolic engineering for high yield synthesis of astaxanthin in xanthophyllomyces dendrorhous |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8420053/ https://www.ncbi.nlm.nih.gov/pubmed/34488760 http://dx.doi.org/10.1186/s12934-021-01664-6 |
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