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Engineering of Saccharomyces cerevisiae for anthranilate and methyl anthranilate production
BACKGROUND: Anthranilate is a platform chemical used by the industry in the synthesis of a broad range of high-value products, such as dyes, perfumes and pharmaceutical compounds. Currently anthranilate is produced via chemical synthesis from non-renewable resources. Biological synthesis would allow...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7860014/ https://www.ncbi.nlm.nih.gov/pubmed/33536025 http://dx.doi.org/10.1186/s12934-021-01532-3 |
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author | Kuivanen, Joosu Kannisto, Matti Mojzita, Dominik Rischer, Heiko Toivari, Mervi Jäntti, Jussi |
author_facet | Kuivanen, Joosu Kannisto, Matti Mojzita, Dominik Rischer, Heiko Toivari, Mervi Jäntti, Jussi |
author_sort | Kuivanen, Joosu |
collection | PubMed |
description | BACKGROUND: Anthranilate is a platform chemical used by the industry in the synthesis of a broad range of high-value products, such as dyes, perfumes and pharmaceutical compounds. Currently anthranilate is produced via chemical synthesis from non-renewable resources. Biological synthesis would allow the use of renewable carbon sources and avoid accumulation of toxic by-products. Microorganisms produce anthranilate as an intermediate in the tryptophan biosynthetic pathway. Several prokaryotic microorganisms have been engineered to overproduce anthranilate but attempts to engineer eukaryotic microorganisms for anthranilate production are scarce. RESULTS: We subjected Saccharomyces cerevisiae, a widely used eukaryotic production host organism, to metabolic engineering for anthranilate production. A single gene knockout was sufficient to trigger anthranilate accumulation both in minimal and SCD media and the titer could be further improved by subsequent genomic alterations. The effects of the modifications on anthranilate production depended heavily on the growth medium used. By growing an engineered strain in SCD medium an anthranilate titer of 567.9 mg l(−1) was obtained, which is the highest reported with an eukaryotic microorganism. Furthermore, the anthranilate biosynthetic pathway was extended by expression of anthranilic acid methyltransferase 1 from Medicago truncatula. When cultivated in YPD medium, this pathway extension enabled production of the grape flavor compound methyl anthranilate in S. cerevisiae at 414 mg l(−1). CONCLUSIONS: In this study we have engineered metabolism of S. cerevisiae for improved anthranilate production. The resulting strains may serve as a basis for development of efficient production host organisms for anthranilate-derived compounds. In order to demonstrate suitability of the engineered S. cerevisiae strains for production of such compounds, we successfully extended the anthranilate biosynthesis pathway to synthesis of methyl anthranilate. |
format | Online Article Text |
id | pubmed-7860014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78600142021-02-04 Engineering of Saccharomyces cerevisiae for anthranilate and methyl anthranilate production Kuivanen, Joosu Kannisto, Matti Mojzita, Dominik Rischer, Heiko Toivari, Mervi Jäntti, Jussi Microb Cell Fact Research BACKGROUND: Anthranilate is a platform chemical used by the industry in the synthesis of a broad range of high-value products, such as dyes, perfumes and pharmaceutical compounds. Currently anthranilate is produced via chemical synthesis from non-renewable resources. Biological synthesis would allow the use of renewable carbon sources and avoid accumulation of toxic by-products. Microorganisms produce anthranilate as an intermediate in the tryptophan biosynthetic pathway. Several prokaryotic microorganisms have been engineered to overproduce anthranilate but attempts to engineer eukaryotic microorganisms for anthranilate production are scarce. RESULTS: We subjected Saccharomyces cerevisiae, a widely used eukaryotic production host organism, to metabolic engineering for anthranilate production. A single gene knockout was sufficient to trigger anthranilate accumulation both in minimal and SCD media and the titer could be further improved by subsequent genomic alterations. The effects of the modifications on anthranilate production depended heavily on the growth medium used. By growing an engineered strain in SCD medium an anthranilate titer of 567.9 mg l(−1) was obtained, which is the highest reported with an eukaryotic microorganism. Furthermore, the anthranilate biosynthetic pathway was extended by expression of anthranilic acid methyltransferase 1 from Medicago truncatula. When cultivated in YPD medium, this pathway extension enabled production of the grape flavor compound methyl anthranilate in S. cerevisiae at 414 mg l(−1). CONCLUSIONS: In this study we have engineered metabolism of S. cerevisiae for improved anthranilate production. The resulting strains may serve as a basis for development of efficient production host organisms for anthranilate-derived compounds. In order to demonstrate suitability of the engineered S. cerevisiae strains for production of such compounds, we successfully extended the anthranilate biosynthesis pathway to synthesis of methyl anthranilate. BioMed Central 2021-02-03 /pmc/articles/PMC7860014/ /pubmed/33536025 http://dx.doi.org/10.1186/s12934-021-01532-3 Text en © The Author(s) 2021 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/. 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 in a credit line to the data. |
spellingShingle | Research Kuivanen, Joosu Kannisto, Matti Mojzita, Dominik Rischer, Heiko Toivari, Mervi Jäntti, Jussi Engineering of Saccharomyces cerevisiae for anthranilate and methyl anthranilate production |
title | Engineering of Saccharomyces cerevisiae for anthranilate and methyl anthranilate production |
title_full | Engineering of Saccharomyces cerevisiae for anthranilate and methyl anthranilate production |
title_fullStr | Engineering of Saccharomyces cerevisiae for anthranilate and methyl anthranilate production |
title_full_unstemmed | Engineering of Saccharomyces cerevisiae for anthranilate and methyl anthranilate production |
title_short | Engineering of Saccharomyces cerevisiae for anthranilate and methyl anthranilate production |
title_sort | engineering of saccharomyces cerevisiae for anthranilate and methyl anthranilate production |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7860014/ https://www.ncbi.nlm.nih.gov/pubmed/33536025 http://dx.doi.org/10.1186/s12934-021-01532-3 |
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