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Improving squalene production by enhancing the NADPH/NADP(+) ratio, modifying the isoprenoid-feeding module and blocking the menaquinone pathway in Escherichia coli

BACKGROUND: Squalene is currently used widely in the food, cosmetics, and medicine industries. It could also replace petroleum as a raw material for fuels. Microbial fermentation processes for squalene production have been emerging over recent years. In this study, to study the squalene-producing po...

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Autores principales: Xu, Wen, Yao, Jia, Liu, Lijun, Ma, Xi, Li, Wei, Sun, Xiaojing, Wang, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437923/
https://www.ncbi.nlm.nih.gov/pubmed/30962822
http://dx.doi.org/10.1186/s13068-019-1415-x
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author Xu, Wen
Yao, Jia
Liu, Lijun
Ma, Xi
Li, Wei
Sun, Xiaojing
Wang, Yang
author_facet Xu, Wen
Yao, Jia
Liu, Lijun
Ma, Xi
Li, Wei
Sun, Xiaojing
Wang, Yang
author_sort Xu, Wen
collection PubMed
description BACKGROUND: Squalene is currently used widely in the food, cosmetics, and medicine industries. It could also replace petroleum as a raw material for fuels. Microbial fermentation processes for squalene production have been emerging over recent years. In this study, to study the squalene-producing potential of Escherichia coli (E. coli), we employed several increasing strategies for systematic metabolic engineering. These include the expression of human truncated squalene synthase, the overexpression of rate-limiting enzymes in isoprenoid pathway, the modification of isoprenoid-feeding module and the blocking of menaquinone pathway. RESULTS: Herein, human truncated squalene synthase was engineered in Escherichia coli to create a squalene-producing bacterial strain. To increase squalene yield, we employed several metabolic engineering strategies. A fivefold squalene titer increase was achieved by expressing rate-limiting enzymes (IDI, DXS, and FPS) involved in the isoprenoid pathway. Pyridine nucleotide transhydrogenase (UdhA) was then expressed to improve the cellular NADPH/NADP(+) ratio, resulting in a 59% increase in squalene titer. The Embden–Meyerhof pathway (EMP) was replaced with the Entner–Doudoroff pathway (EDP) and pentose phosphate pathway (PPP) to feed the isoprenoid pathway, along with the overexpression of zwf and pgl genes which encode rate-limiting enzymes in the EDP and PPP, leading to a 104% squalene content increase. Based on the blocking of menaquinone pathway, a further 17.7% increase in squalene content was achieved. Squalene content reached a final 28.5 mg/g DCW and 52.1 mg/L. CONCLUSIONS: This study provided novel strategies for improving squalene yield and demonstrated the potential of producing squalene by E. coli. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-019-1415-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-64379232019-04-08 Improving squalene production by enhancing the NADPH/NADP(+) ratio, modifying the isoprenoid-feeding module and blocking the menaquinone pathway in Escherichia coli Xu, Wen Yao, Jia Liu, Lijun Ma, Xi Li, Wei Sun, Xiaojing Wang, Yang Biotechnol Biofuels Research BACKGROUND: Squalene is currently used widely in the food, cosmetics, and medicine industries. It could also replace petroleum as a raw material for fuels. Microbial fermentation processes for squalene production have been emerging over recent years. In this study, to study the squalene-producing potential of Escherichia coli (E. coli), we employed several increasing strategies for systematic metabolic engineering. These include the expression of human truncated squalene synthase, the overexpression of rate-limiting enzymes in isoprenoid pathway, the modification of isoprenoid-feeding module and the blocking of menaquinone pathway. RESULTS: Herein, human truncated squalene synthase was engineered in Escherichia coli to create a squalene-producing bacterial strain. To increase squalene yield, we employed several metabolic engineering strategies. A fivefold squalene titer increase was achieved by expressing rate-limiting enzymes (IDI, DXS, and FPS) involved in the isoprenoid pathway. Pyridine nucleotide transhydrogenase (UdhA) was then expressed to improve the cellular NADPH/NADP(+) ratio, resulting in a 59% increase in squalene titer. The Embden–Meyerhof pathway (EMP) was replaced with the Entner–Doudoroff pathway (EDP) and pentose phosphate pathway (PPP) to feed the isoprenoid pathway, along with the overexpression of zwf and pgl genes which encode rate-limiting enzymes in the EDP and PPP, leading to a 104% squalene content increase. Based on the blocking of menaquinone pathway, a further 17.7% increase in squalene content was achieved. Squalene content reached a final 28.5 mg/g DCW and 52.1 mg/L. CONCLUSIONS: This study provided novel strategies for improving squalene yield and demonstrated the potential of producing squalene by E. coli. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-019-1415-x) contains supplementary material, which is available to authorized users. BioMed Central 2019-03-28 /pmc/articles/PMC6437923/ /pubmed/30962822 http://dx.doi.org/10.1186/s13068-019-1415-x Text en © The Author(s) 2019 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
Xu, Wen
Yao, Jia
Liu, Lijun
Ma, Xi
Li, Wei
Sun, Xiaojing
Wang, Yang
Improving squalene production by enhancing the NADPH/NADP(+) ratio, modifying the isoprenoid-feeding module and blocking the menaquinone pathway in Escherichia coli
title Improving squalene production by enhancing the NADPH/NADP(+) ratio, modifying the isoprenoid-feeding module and blocking the menaquinone pathway in Escherichia coli
title_full Improving squalene production by enhancing the NADPH/NADP(+) ratio, modifying the isoprenoid-feeding module and blocking the menaquinone pathway in Escherichia coli
title_fullStr Improving squalene production by enhancing the NADPH/NADP(+) ratio, modifying the isoprenoid-feeding module and blocking the menaquinone pathway in Escherichia coli
title_full_unstemmed Improving squalene production by enhancing the NADPH/NADP(+) ratio, modifying the isoprenoid-feeding module and blocking the menaquinone pathway in Escherichia coli
title_short Improving squalene production by enhancing the NADPH/NADP(+) ratio, modifying the isoprenoid-feeding module and blocking the menaquinone pathway in Escherichia coli
title_sort improving squalene production by enhancing the nadph/nadp(+) ratio, modifying the isoprenoid-feeding module and blocking the menaquinone pathway in escherichia coli
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437923/
https://www.ncbi.nlm.nih.gov/pubmed/30962822
http://dx.doi.org/10.1186/s13068-019-1415-x
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