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High-efficiency production of 5-hydroxyectoine using metabolically engineered Corynebacterium glutamicum
BACKGROUND: Extremolytes enable microbes to withstand even the most extreme conditions in nature. Due to their unique protective properties, the small organic molecules, more and more, become high-value active ingredients for the cosmetics and the pharmaceutical industries. While ectoine, the indust...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798599/ https://www.ncbi.nlm.nih.gov/pubmed/36578077 http://dx.doi.org/10.1186/s12934-022-02003-z |
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author | Jungmann, Lukas Hoffmann, Sarah Lisa Lang, Caroline De Agazio, Raphaela Becker, Judith Kohlstedt, Michael Wittmann, Christoph |
author_facet | Jungmann, Lukas Hoffmann, Sarah Lisa Lang, Caroline De Agazio, Raphaela Becker, Judith Kohlstedt, Michael Wittmann, Christoph |
author_sort | Jungmann, Lukas |
collection | PubMed |
description | BACKGROUND: Extremolytes enable microbes to withstand even the most extreme conditions in nature. Due to their unique protective properties, the small organic molecules, more and more, become high-value active ingredients for the cosmetics and the pharmaceutical industries. While ectoine, the industrial extremolyte flagship, has been successfully commercialized before, an economically viable route to its highly interesting derivative 5-hydroxyectoine (hydroxyectoine) is not existing. RESULTS: Here, we demonstrate high-level hydroxyectoine production, using metabolically engineered strains of C. glutamicum that express a codon-optimized, heterologous ectD gene, encoding for ectoine hydroxylase, to convert supplemented ectoine in the presence of sucrose as growth substrate into the desired derivative. Fourteen out of sixteen codon-optimized ectD variants from phylogenetically diverse bacterial and archaeal donors enabled hydroxyectoine production, showing the strategy to work almost regardless of the origin of the gene. The genes from Pseudomonas stutzeri (PST) and Mycobacterium smegmatis (MSM) worked best and enabled hydroxyectoine production up to 97% yield. Metabolic analyses revealed high enrichment of the ectoines inside the cells, which, inter alia, reduced the synthesis of other compatible solutes, including proline and trehalose. After further optimization, C. glutamicum Ptuf ectD(PST) achieved a titre of 74 g L(−1) hydroxyectoine at 70% selectivity within 12 h, using a simple batch process. In a two-step procedure, hydroxyectoine production from ectoine, previously synthesized fermentatively with C. glutamicum ectABC(opt), was successfully achieved without intermediate purification. CONCLUSIONS: C. glutamicum is a well-known and industrially proven host, allowing the synthesis of commercial products with granted GRAS status, a great benefit for a safe production of hydroxyectoine as active ingredient for cosmetic and pharmaceutical applications. Because ectoine is already available at commercial scale, its use as precursor appears straightforward. In the future, two-step processes might provide hydroxyectoine de novo from sugar. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-022-02003-z. |
format | Online Article Text |
id | pubmed-9798599 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97985992022-12-30 High-efficiency production of 5-hydroxyectoine using metabolically engineered Corynebacterium glutamicum Jungmann, Lukas Hoffmann, Sarah Lisa Lang, Caroline De Agazio, Raphaela Becker, Judith Kohlstedt, Michael Wittmann, Christoph Microb Cell Fact Research BACKGROUND: Extremolytes enable microbes to withstand even the most extreme conditions in nature. Due to their unique protective properties, the small organic molecules, more and more, become high-value active ingredients for the cosmetics and the pharmaceutical industries. While ectoine, the industrial extremolyte flagship, has been successfully commercialized before, an economically viable route to its highly interesting derivative 5-hydroxyectoine (hydroxyectoine) is not existing. RESULTS: Here, we demonstrate high-level hydroxyectoine production, using metabolically engineered strains of C. glutamicum that express a codon-optimized, heterologous ectD gene, encoding for ectoine hydroxylase, to convert supplemented ectoine in the presence of sucrose as growth substrate into the desired derivative. Fourteen out of sixteen codon-optimized ectD variants from phylogenetically diverse bacterial and archaeal donors enabled hydroxyectoine production, showing the strategy to work almost regardless of the origin of the gene. The genes from Pseudomonas stutzeri (PST) and Mycobacterium smegmatis (MSM) worked best and enabled hydroxyectoine production up to 97% yield. Metabolic analyses revealed high enrichment of the ectoines inside the cells, which, inter alia, reduced the synthesis of other compatible solutes, including proline and trehalose. After further optimization, C. glutamicum Ptuf ectD(PST) achieved a titre of 74 g L(−1) hydroxyectoine at 70% selectivity within 12 h, using a simple batch process. In a two-step procedure, hydroxyectoine production from ectoine, previously synthesized fermentatively with C. glutamicum ectABC(opt), was successfully achieved without intermediate purification. CONCLUSIONS: C. glutamicum is a well-known and industrially proven host, allowing the synthesis of commercial products with granted GRAS status, a great benefit for a safe production of hydroxyectoine as active ingredient for cosmetic and pharmaceutical applications. Because ectoine is already available at commercial scale, its use as precursor appears straightforward. In the future, two-step processes might provide hydroxyectoine de novo from sugar. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-022-02003-z. BioMed Central 2022-12-28 /pmc/articles/PMC9798599/ /pubmed/36578077 http://dx.doi.org/10.1186/s12934-022-02003-z 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 | Research Jungmann, Lukas Hoffmann, Sarah Lisa Lang, Caroline De Agazio, Raphaela Becker, Judith Kohlstedt, Michael Wittmann, Christoph High-efficiency production of 5-hydroxyectoine using metabolically engineered Corynebacterium glutamicum |
title | High-efficiency production of 5-hydroxyectoine using metabolically engineered Corynebacterium glutamicum |
title_full | High-efficiency production of 5-hydroxyectoine using metabolically engineered Corynebacterium glutamicum |
title_fullStr | High-efficiency production of 5-hydroxyectoine using metabolically engineered Corynebacterium glutamicum |
title_full_unstemmed | High-efficiency production of 5-hydroxyectoine using metabolically engineered Corynebacterium glutamicum |
title_short | High-efficiency production of 5-hydroxyectoine using metabolically engineered Corynebacterium glutamicum |
title_sort | high-efficiency production of 5-hydroxyectoine using metabolically engineered corynebacterium glutamicum |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798599/ https://www.ncbi.nlm.nih.gov/pubmed/36578077 http://dx.doi.org/10.1186/s12934-022-02003-z |
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