Please use this identifier to cite or link to this item:
doi:10.22028/D291-38818
Title: | High-efficiency production of 5-hydroxyectoine using metabolically engineered Corynebacterium glutamicum |
Author(s): | Jungmann, Lukas Hoffmann, Sarah Lisa Lang, Caroline De Agazio, Raphaela Becker, Judith Kohlstedt, Michael Wittmann, Christoph |
Language: | English |
Title: | Microbial Cell Factories |
Volume: | 21 |
Issue: | 1 |
Publisher/Platform: | BMC |
Year of Publication: | 2022 |
Free key words: | Corynebacterium glutamicum Extremolyte Ectoine 5-Hydroxyectoine Ectoine hydroxylase Biotransformation Intracellular metabolite Proline Trehalose High-value product |
DDC notations: | 500 Science |
Publikation type: | Journal Article |
Abstract: | 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 fagship, 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 ectDPST 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 ectABCopt, was successfully achieved without intermediate purifcation. Conclusions: C. glutamicum is a well-known and industrially proven host, allowing the synthesis of commercial products with granted GRAS status, a great beneft 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. |
DOI of the first publication: | 10.1186/s12934-022-02003-z |
URL of the first publication: | https://doi.org/10.1186/s12934-022-02003-z |
Link to this record: | urn:nbn:de:bsz:291--ds-388181 hdl:20.500.11880/35002 http://dx.doi.org/10.22028/D291-38818 |
ISSN: | 1475-2859 |
Date of registration: | 24-Jan-2023 |
Description of the related object: | Supplementary Information |
Related object: | https://static-content.springer.com/esm/art%3A10.1186%2Fs12934-022-02003-z/MediaObjects/12934_2022_2003_MOESM1_ESM.docx |
Faculty: | NT - Naturwissenschaftlich- Technische Fakultät |
Department: | NT - Biowissenschaften |
Professorship: | NT - Prof. Dr. Christoph Wittmann |
Collections: | SciDok - Der Wissenschaftsserver der Universität des Saarlandes |
Files for this record:
File | Description | Size | Format | |
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s12934-022-02003-z.pdf | 4,42 MB | Adobe PDF | View/Open |
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