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First time β-farnesene production by the versatile bacterium Cupriavidus necator

BACKGROUND: Terpenes are remarkably diverse natural structures, which can be formed via two different pathways leading to two common intermediates. Among those, sesquiterpenes represent a variety of industrially relevant products. One important industrially produced product is β-farnesene as a precu...

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Autores principales: Milker, Sofia, Holtmann, Dirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8074451/
https://www.ncbi.nlm.nih.gov/pubmed/33902586
http://dx.doi.org/10.1186/s12934-021-01562-x
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author Milker, Sofia
Holtmann, Dirk
author_facet Milker, Sofia
Holtmann, Dirk
author_sort Milker, Sofia
collection PubMed
description BACKGROUND: Terpenes are remarkably diverse natural structures, which can be formed via two different pathways leading to two common intermediates. Among those, sesquiterpenes represent a variety of industrially relevant products. One important industrially produced product is β-farnesene as a precursor for a jet fuel additive. So far, microbial terpene production has been mostly limited to known production hosts, which are only able to grow on heterotrophic substrates. RESULTS: In this paper, we for the first time describe β-farnesene production by the versatile bacterial host Cupriavidus necator on fructose, which is known to grow hetero- and autotrophically and even in bioelectrochemical systems. We were able to show a growth-dependent production of β-farnesene by expressing the β-farnesene synthase from Artemisia annua in C. necator H16 PHB(-)4. Additionally, we performed a scale-up in a parallel reactor system with production titers of 26.3 ± 1.3 µM β-farnesene with a fed-batch process. CONCLUSIONS: The β-farnesene production titers reported in this paper are not in the same range as titers published with known heterotrophic producers E. coli or S. cerevisiae. However, this proof-of-principle study with C. necator as production host opens new synthesis routes toward a sustainable economy and leaves room for further optimizations, which have been already performed with the known production strains. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-021-01562-x.
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spelling pubmed-80744512021-04-26 First time β-farnesene production by the versatile bacterium Cupriavidus necator Milker, Sofia Holtmann, Dirk Microb Cell Fact Research BACKGROUND: Terpenes are remarkably diverse natural structures, which can be formed via two different pathways leading to two common intermediates. Among those, sesquiterpenes represent a variety of industrially relevant products. One important industrially produced product is β-farnesene as a precursor for a jet fuel additive. So far, microbial terpene production has been mostly limited to known production hosts, which are only able to grow on heterotrophic substrates. RESULTS: In this paper, we for the first time describe β-farnesene production by the versatile bacterial host Cupriavidus necator on fructose, which is known to grow hetero- and autotrophically and even in bioelectrochemical systems. We were able to show a growth-dependent production of β-farnesene by expressing the β-farnesene synthase from Artemisia annua in C. necator H16 PHB(-)4. Additionally, we performed a scale-up in a parallel reactor system with production titers of 26.3 ± 1.3 µM β-farnesene with a fed-batch process. CONCLUSIONS: The β-farnesene production titers reported in this paper are not in the same range as titers published with known heterotrophic producers E. coli or S. cerevisiae. However, this proof-of-principle study with C. necator as production host opens new synthesis routes toward a sustainable economy and leaves room for further optimizations, which have been already performed with the known production strains. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-021-01562-x. BioMed Central 2021-04-26 /pmc/articles/PMC8074451/ /pubmed/33902586 http://dx.doi.org/10.1186/s12934-021-01562-x 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 Research
Milker, Sofia
Holtmann, Dirk
First time β-farnesene production by the versatile bacterium Cupriavidus necator
title First time β-farnesene production by the versatile bacterium Cupriavidus necator
title_full First time β-farnesene production by the versatile bacterium Cupriavidus necator
title_fullStr First time β-farnesene production by the versatile bacterium Cupriavidus necator
title_full_unstemmed First time β-farnesene production by the versatile bacterium Cupriavidus necator
title_short First time β-farnesene production by the versatile bacterium Cupriavidus necator
title_sort first time β-farnesene production by the versatile bacterium cupriavidus necator
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8074451/
https://www.ncbi.nlm.nih.gov/pubmed/33902586
http://dx.doi.org/10.1186/s12934-021-01562-x
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