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Metabolic engineering of Escherichia coli for high-specificity production of isoprenol and prenol as next generation of biofuels

BACKGROUND: The isopentenols, including isoprenol and prenol, are excellent alternative fuels. However, they are not compounds largely accumulated in natural organism. The need for the next generation of biofuels with better physical and chemical properties impels us to develop biosynthetic routes f...

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Autores principales: Zheng, Yanning, Liu, Qiang, Li, Lingling, Qin, Wen, Yang, Jianming, Zhang, Haibo, Jiang, Xinglin, Cheng, Tao, Liu, Wei, Xu, Xin, Xian, Mo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654967/
https://www.ncbi.nlm.nih.gov/pubmed/23618128
http://dx.doi.org/10.1186/1754-6834-6-57
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author Zheng, Yanning
Liu, Qiang
Li, Lingling
Qin, Wen
Yang, Jianming
Zhang, Haibo
Jiang, Xinglin
Cheng, Tao
Liu, Wei
Xu, Xin
Xian, Mo
author_facet Zheng, Yanning
Liu, Qiang
Li, Lingling
Qin, Wen
Yang, Jianming
Zhang, Haibo
Jiang, Xinglin
Cheng, Tao
Liu, Wei
Xu, Xin
Xian, Mo
author_sort Zheng, Yanning
collection PubMed
description BACKGROUND: The isopentenols, including isoprenol and prenol, are excellent alternative fuels. However, they are not compounds largely accumulated in natural organism. The need for the next generation of biofuels with better physical and chemical properties impels us to develop biosynthetic routes for the production of isoprenol and prenol from renewable sugar. In this study, we use the heterogenous mevalonate-dependent (MVA) isoprenoid pathway for the synthesis of isopentenyl pyrophosphate (IPP) and dimethylallyl pyrophosphate (DMAPP) intermediates, and then convert IPP and DMAPP to isoprenol and prenol, respectively. RESULTS: A mevalonate titer of 1.7 g/L was obtained by constructing an efficient MVA upper pathway in engineered E. coli. Different phosphatases and pyrophosphatases were investigated for their abilities in hydrolyzing the IPP and DMAPP. Consequently, ADP-ribose pyrophosphatase was found to be an efficient IPP and DMAPP hydrolase. Moreover, ADP-ribose pyrophosphatase from Bacillus subtilis (BsNudF) exhibited a equivalent substrate specificity towards IPP and DMAPP, while ADP-ribose pyrophosphatase from E. coli (EcNudF) presented a high substrate preference for DMAPP. Without the expression of any phosphatases or pyrophosphatases, a background level of isopentenols was synthesized. When the endogenous pyrophosphatase genes (EcNudF and yggV) that were capable of enhancing the hydrolyzation of the IPP and DMAPP were knocked out, the background level of isopentenols was still obtained. Maybe the synthesized IPP and DMAPP were hydrolyzed by some unknown hydrolases of E. coli. Finally, 1.3 g/L single isoprenol was obtained by blocking the conversion of IPP to DMAPP and employing the BsNudF, and 0.2 g/L ~80% prenol was produced by employing the EcNudF. A maximal yield of 12% was achieved in both isoprenol and prenol producing strains. CONCLUSIONS: To the best of our knowledge, this is the first successful report on high-specificity production of isoprenol and prenol by microbial fermentation. Over 1.3 g/L isoprenol achieved in shake-flask experiments represents a quite encouraging titer of higher alcohols. In addition, the substrate specificities of ADP-ribose pyrophosphatases were determined and successfully applied for the high-specificity synthesis of isoprenol and prenol. Altogether, this work presents a promising strategy for high-specificity production of two excellent biofuels, isoprenol and prenol.
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spelling pubmed-36549672013-05-16 Metabolic engineering of Escherichia coli for high-specificity production of isoprenol and prenol as next generation of biofuels Zheng, Yanning Liu, Qiang Li, Lingling Qin, Wen Yang, Jianming Zhang, Haibo Jiang, Xinglin Cheng, Tao Liu, Wei Xu, Xin Xian, Mo Biotechnol Biofuels Research BACKGROUND: The isopentenols, including isoprenol and prenol, are excellent alternative fuels. However, they are not compounds largely accumulated in natural organism. The need for the next generation of biofuels with better physical and chemical properties impels us to develop biosynthetic routes for the production of isoprenol and prenol from renewable sugar. In this study, we use the heterogenous mevalonate-dependent (MVA) isoprenoid pathway for the synthesis of isopentenyl pyrophosphate (IPP) and dimethylallyl pyrophosphate (DMAPP) intermediates, and then convert IPP and DMAPP to isoprenol and prenol, respectively. RESULTS: A mevalonate titer of 1.7 g/L was obtained by constructing an efficient MVA upper pathway in engineered E. coli. Different phosphatases and pyrophosphatases were investigated for their abilities in hydrolyzing the IPP and DMAPP. Consequently, ADP-ribose pyrophosphatase was found to be an efficient IPP and DMAPP hydrolase. Moreover, ADP-ribose pyrophosphatase from Bacillus subtilis (BsNudF) exhibited a equivalent substrate specificity towards IPP and DMAPP, while ADP-ribose pyrophosphatase from E. coli (EcNudF) presented a high substrate preference for DMAPP. Without the expression of any phosphatases or pyrophosphatases, a background level of isopentenols was synthesized. When the endogenous pyrophosphatase genes (EcNudF and yggV) that were capable of enhancing the hydrolyzation of the IPP and DMAPP were knocked out, the background level of isopentenols was still obtained. Maybe the synthesized IPP and DMAPP were hydrolyzed by some unknown hydrolases of E. coli. Finally, 1.3 g/L single isoprenol was obtained by blocking the conversion of IPP to DMAPP and employing the BsNudF, and 0.2 g/L ~80% prenol was produced by employing the EcNudF. A maximal yield of 12% was achieved in both isoprenol and prenol producing strains. CONCLUSIONS: To the best of our knowledge, this is the first successful report on high-specificity production of isoprenol and prenol by microbial fermentation. Over 1.3 g/L isoprenol achieved in shake-flask experiments represents a quite encouraging titer of higher alcohols. In addition, the substrate specificities of ADP-ribose pyrophosphatases were determined and successfully applied for the high-specificity synthesis of isoprenol and prenol. Altogether, this work presents a promising strategy for high-specificity production of two excellent biofuels, isoprenol and prenol. BioMed Central 2013-04-24 /pmc/articles/PMC3654967/ /pubmed/23618128 http://dx.doi.org/10.1186/1754-6834-6-57 Text en Copyright © 2013 Zheng 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 cited.
spellingShingle Research
Zheng, Yanning
Liu, Qiang
Li, Lingling
Qin, Wen
Yang, Jianming
Zhang, Haibo
Jiang, Xinglin
Cheng, Tao
Liu, Wei
Xu, Xin
Xian, Mo
Metabolic engineering of Escherichia coli for high-specificity production of isoprenol and prenol as next generation of biofuels
title Metabolic engineering of Escherichia coli for high-specificity production of isoprenol and prenol as next generation of biofuels
title_full Metabolic engineering of Escherichia coli for high-specificity production of isoprenol and prenol as next generation of biofuels
title_fullStr Metabolic engineering of Escherichia coli for high-specificity production of isoprenol and prenol as next generation of biofuels
title_full_unstemmed Metabolic engineering of Escherichia coli for high-specificity production of isoprenol and prenol as next generation of biofuels
title_short Metabolic engineering of Escherichia coli for high-specificity production of isoprenol and prenol as next generation of biofuels
title_sort metabolic engineering of escherichia coli for high-specificity production of isoprenol and prenol as next generation of biofuels
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654967/
https://www.ncbi.nlm.nih.gov/pubmed/23618128
http://dx.doi.org/10.1186/1754-6834-6-57
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