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fabH deletion increases DHA production in Escherichia coli expressing Pfa genes
BACKGROUND: Some marine bacteria, such as Moritella marina, produce the nutraceutical docosahexaenoic acid (DHA) thanks to a specific enzymatic complex called Pfa synthase. Escherichia coli heterologously expressing the pfa gene cluster from M. marina also produces DHA. The aim of this study was to...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992819/ https://www.ncbi.nlm.nih.gov/pubmed/29884177 http://dx.doi.org/10.1186/s12934-018-0928-5 |
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author | Giner-Robles, Laura Lázaro, Beatriz de la Cruz, Fernando Moncalián, Gabriel |
author_facet | Giner-Robles, Laura Lázaro, Beatriz de la Cruz, Fernando Moncalián, Gabriel |
author_sort | Giner-Robles, Laura |
collection | PubMed |
description | BACKGROUND: Some marine bacteria, such as Moritella marina, produce the nutraceutical docosahexaenoic acid (DHA) thanks to a specific enzymatic complex called Pfa synthase. Escherichia coli heterologously expressing the pfa gene cluster from M. marina also produces DHA. The aim of this study was to find genetic or metabolic conditions to increase DHA production in E. coli. RESULTS: First, we analysed the effect of the antibiotic cerulenin, showing that DHA production increased twofold. Then, we tested a series of single gene knockout mutations affecting fatty acid biosynthesis, in order to optimize the synthesis of DHA. The most effective mutant, fabH, showed a threefold increase compared to wild type strain. The combination of cerulenin inhibition and fabH deletion rendered a 6.5-fold improvement compared to control strain. Both strategies seem to have the same mechanism of action, in which fatty acid synthesis via the canonical pathway (fab pathway) is affected in its first catalytic step, which allows the substrates to be used by the heterologous pathway to synthesize DHA. CONCLUSIONS: DHA-producing E. coli strain that carries a fabH gene deletion boosts DHA production by tuning down the competing canonical biosynthesis pathway. Our approach can be used for optimization of DHA production in different organisms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-018-0928-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5992819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59928192018-07-05 fabH deletion increases DHA production in Escherichia coli expressing Pfa genes Giner-Robles, Laura Lázaro, Beatriz de la Cruz, Fernando Moncalián, Gabriel Microb Cell Fact Research BACKGROUND: Some marine bacteria, such as Moritella marina, produce the nutraceutical docosahexaenoic acid (DHA) thanks to a specific enzymatic complex called Pfa synthase. Escherichia coli heterologously expressing the pfa gene cluster from M. marina also produces DHA. The aim of this study was to find genetic or metabolic conditions to increase DHA production in E. coli. RESULTS: First, we analysed the effect of the antibiotic cerulenin, showing that DHA production increased twofold. Then, we tested a series of single gene knockout mutations affecting fatty acid biosynthesis, in order to optimize the synthesis of DHA. The most effective mutant, fabH, showed a threefold increase compared to wild type strain. The combination of cerulenin inhibition and fabH deletion rendered a 6.5-fold improvement compared to control strain. Both strategies seem to have the same mechanism of action, in which fatty acid synthesis via the canonical pathway (fab pathway) is affected in its first catalytic step, which allows the substrates to be used by the heterologous pathway to synthesize DHA. CONCLUSIONS: DHA-producing E. coli strain that carries a fabH gene deletion boosts DHA production by tuning down the competing canonical biosynthesis pathway. Our approach can be used for optimization of DHA production in different organisms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-018-0928-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-08 /pmc/articles/PMC5992819/ /pubmed/29884177 http://dx.doi.org/10.1186/s12934-018-0928-5 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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. |
spellingShingle | Research Giner-Robles, Laura Lázaro, Beatriz de la Cruz, Fernando Moncalián, Gabriel fabH deletion increases DHA production in Escherichia coli expressing Pfa genes |
title | fabH deletion increases DHA production in Escherichia coli expressing Pfa genes |
title_full | fabH deletion increases DHA production in Escherichia coli expressing Pfa genes |
title_fullStr | fabH deletion increases DHA production in Escherichia coli expressing Pfa genes |
title_full_unstemmed | fabH deletion increases DHA production in Escherichia coli expressing Pfa genes |
title_short | fabH deletion increases DHA production in Escherichia coli expressing Pfa genes |
title_sort | fabh deletion increases dha production in escherichia coli expressing pfa genes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992819/ https://www.ncbi.nlm.nih.gov/pubmed/29884177 http://dx.doi.org/10.1186/s12934-018-0928-5 |
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