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Production of free monounsaturated fatty acids by metabolically engineered Escherichia coli

BACKGROUND: Monounsaturated fatty acids (MUFAs) are the best components for biodiesel when considering the low temperature fluidity and oxidative stability. However, biodiesel derived from vegetable oils or microbial lipids always consists of significant amounts of polyunsaturated and saturated fatt...

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Autores principales: Cao, Yujin, Liu, Wei, Xu, Xin, Zhang, Haibo, Wang, Jiming, Xian, Mo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021618/
https://www.ncbi.nlm.nih.gov/pubmed/24716602
http://dx.doi.org/10.1186/1754-6834-7-59
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author Cao, Yujin
Liu, Wei
Xu, Xin
Zhang, Haibo
Wang, Jiming
Xian, Mo
author_facet Cao, Yujin
Liu, Wei
Xu, Xin
Zhang, Haibo
Wang, Jiming
Xian, Mo
author_sort Cao, Yujin
collection PubMed
description BACKGROUND: Monounsaturated fatty acids (MUFAs) are the best components for biodiesel when considering the low temperature fluidity and oxidative stability. However, biodiesel derived from vegetable oils or microbial lipids always consists of significant amounts of polyunsaturated and saturated fatty acids (SFAs) alkyl esters, which hampers its practical applications. Therefore, the fatty acid composition should be modified to increase MUFA contents as well as enhancing oil and lipid production. RESULTS: The model microorganism Escherichia coli was engineered to produce free MUFAs. The fatty acyl-ACP thioesterase (AtFatA) and fatty acid desaturase (SSI2) from Arabidopsis thaliana were heterologously expressed in E. coli BL21 star(DE3) to specifically release free unsaturated fatty acids (UFAs) and convert SFAs to UFAs. In addition, the endogenous fadD gene (encoding acyl-CoA synthetase) was disrupted to block fatty acid catabolism while the native acetyl-CoA carboxylase (ACCase) was overexpressed to increase the malonyl coenzyme A (malonyl-CoA) pool and boost fatty acid biosynthesis. The finally engineered strain BL21ΔfadD/pE-AtFatAssi2&pA-acc produced 82.6 mg/L free fatty acids (FFAs) under shake-flask conditions and FFAs yield on glucose reached about 3.3% of the theoretical yield. Two types of MUFAs, palmitoleate (16:1Δ9) and cis-vaccenate (18:1Δ11) made up more than 75% of the FFA profiles. Fed-batch fermentation of this strain further enhanced FFAs production to a titer of 1.27 g/L without affecting fatty acid compositions. CONCLUSIONS: This study demonstrated the possibility to regulate fatty acid composition by using metabolic engineering approaches. FFAs produced by the recombinant E. coli strain consisted of high-level MUFAs and biodiesel manufactured from these fatty acids would be more suitable for current diesel engines.
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spelling pubmed-40216182014-05-28 Production of free monounsaturated fatty acids by metabolically engineered Escherichia coli Cao, Yujin Liu, Wei Xu, Xin Zhang, Haibo Wang, Jiming Xian, Mo Biotechnol Biofuels Research BACKGROUND: Monounsaturated fatty acids (MUFAs) are the best components for biodiesel when considering the low temperature fluidity and oxidative stability. However, biodiesel derived from vegetable oils or microbial lipids always consists of significant amounts of polyunsaturated and saturated fatty acids (SFAs) alkyl esters, which hampers its practical applications. Therefore, the fatty acid composition should be modified to increase MUFA contents as well as enhancing oil and lipid production. RESULTS: The model microorganism Escherichia coli was engineered to produce free MUFAs. The fatty acyl-ACP thioesterase (AtFatA) and fatty acid desaturase (SSI2) from Arabidopsis thaliana were heterologously expressed in E. coli BL21 star(DE3) to specifically release free unsaturated fatty acids (UFAs) and convert SFAs to UFAs. In addition, the endogenous fadD gene (encoding acyl-CoA synthetase) was disrupted to block fatty acid catabolism while the native acetyl-CoA carboxylase (ACCase) was overexpressed to increase the malonyl coenzyme A (malonyl-CoA) pool and boost fatty acid biosynthesis. The finally engineered strain BL21ΔfadD/pE-AtFatAssi2&pA-acc produced 82.6 mg/L free fatty acids (FFAs) under shake-flask conditions and FFAs yield on glucose reached about 3.3% of the theoretical yield. Two types of MUFAs, palmitoleate (16:1Δ9) and cis-vaccenate (18:1Δ11) made up more than 75% of the FFA profiles. Fed-batch fermentation of this strain further enhanced FFAs production to a titer of 1.27 g/L without affecting fatty acid compositions. CONCLUSIONS: This study demonstrated the possibility to regulate fatty acid composition by using metabolic engineering approaches. FFAs produced by the recombinant E. coli strain consisted of high-level MUFAs and biodiesel manufactured from these fatty acids would be more suitable for current diesel engines. BioMed Central 2014-04-10 /pmc/articles/PMC4021618/ /pubmed/24716602 http://dx.doi.org/10.1186/1754-6834-7-59 Text en Copyright © 2014 Cao et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research
Cao, Yujin
Liu, Wei
Xu, Xin
Zhang, Haibo
Wang, Jiming
Xian, Mo
Production of free monounsaturated fatty acids by metabolically engineered Escherichia coli
title Production of free monounsaturated fatty acids by metabolically engineered Escherichia coli
title_full Production of free monounsaturated fatty acids by metabolically engineered Escherichia coli
title_fullStr Production of free monounsaturated fatty acids by metabolically engineered Escherichia coli
title_full_unstemmed Production of free monounsaturated fatty acids by metabolically engineered Escherichia coli
title_short Production of free monounsaturated fatty acids by metabolically engineered Escherichia coli
title_sort production of free monounsaturated fatty acids by metabolically engineered escherichia coli
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021618/
https://www.ncbi.nlm.nih.gov/pubmed/24716602
http://dx.doi.org/10.1186/1754-6834-7-59
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