Improving Microbial Biogasoline Production in Escherichia coli Using Tolerance Engineering
Engineering microbial hosts for the production of fungible fuels requires mitigation of limitations posed on the production capacity. One such limitation arises from the inherent toxicity of solvent-like biofuel compounds to production strains, such as Escherichia coli. Here we show the importance o...
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sg-ntu-dr.10356-838572023-12-29T06:45:15Z Improving Microbial Biogasoline Production in Escherichia coli Using Tolerance Engineering Foo, Jee Loon Jensen, Heather M. Dahl, Robert H. George, Kevin Keasling, Jay D. Lee, Taek Soon Leong, Susanna Mukhopadhyay, Aindrila School of Chemical and Biomedical Engineering isopentenol biosynthesis Engineering microbial hosts for the production of fungible fuels requires mitigation of limitations posed on the production capacity. One such limitation arises from the inherent toxicity of solvent-like biofuel compounds to production strains, such as Escherichia coli. Here we show the importance of host engineering for the production of short-chain alcohols by studying the overexpression of genes upregulated in response to exogenous isopentenol. Using systems biology data, we selected 40 genes that were upregulated following isopentenol exposure and subsequently overexpressed them in E. coli. Overexpression of several of these candidates improved tolerance to exogenously added isopentenol. Genes conferring isopentenol tolerance phenotypes belonged to diverse functional groups, such as oxidative stress response (soxS, fpr, and nrdH), general stress response (metR, yqhD, and gidB), heat shock-related response (ibpA), and transport (mdlB). To determine if these genes could also improve isopentenol production, we coexpressed the tolerance-enhancing genes individually with an isopentenol production pathway. Our data show that expression of 6 of the 8 candidates improved the production of isopentenol in E. coli, with the methionine biosynthesis regulator MetR improving the titer for isopentenol production by 55%. Additionally, expression of MdlB, an ABC transporter, facilitated a 12% improvement in isopentenol production. To our knowledge, MdlB is the first example of a transporter that can be used to improve production of a short-chain alcohol and provides a valuable new avenue for host engineering in biogasoline production. NRF (Natl Research Foundation, S’pore) Published version 2016-02-23T03:18:35Z 2019-12-06T15:33:16Z 2016-02-23T03:18:35Z 2019-12-06T15:33:16Z 2014 Journal Article Foo, J. L., Jensen, H. M., Dahl, R. H., George, K., Keasling, J. D., Lee, T. S., et al. (2014). Improving Microbial Biogasoline Production in Escherichia coli Using Tolerance Engineering. mBio, 5(6), e01932-14. 2150-7511 https://hdl.handle.net/10356/83857 http://hdl.handle.net/10220/40040 10.1128/mBio.01932-14 25370492 en mBio © 2014 Foo et al. This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license, which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited. 9 p. application/pdf |
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isopentenol biosynthesis Foo, Jee Loon Jensen, Heather M. Dahl, Robert H. George, Kevin Keasling, Jay D. Lee, Taek Soon Leong, Susanna Mukhopadhyay, Aindrila Improving Microbial Biogasoline Production in Escherichia coli Using Tolerance Engineering |
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Engineering microbial hosts for the production of fungible fuels requires mitigation of limitations posed on the production capacity. One such limitation arises from the inherent toxicity of solvent-like biofuel compounds to production strains, such as Escherichia coli. Here we show the importance of host engineering for the production of short-chain alcohols by studying the overexpression of genes upregulated in response to exogenous isopentenol. Using systems biology data, we selected 40 genes that were upregulated following isopentenol exposure and subsequently overexpressed them in E. coli. Overexpression of several of these candidates improved tolerance to exogenously added isopentenol. Genes conferring isopentenol tolerance phenotypes belonged to diverse functional groups, such as oxidative stress response (soxS, fpr, and nrdH), general stress response (metR, yqhD, and gidB), heat shock-related response (ibpA), and transport (mdlB). To determine if these genes could also improve isopentenol production, we coexpressed the tolerance-enhancing genes individually with an isopentenol production pathway. Our data show that expression of 6 of the 8 candidates improved the production of isopentenol in E. coli, with the methionine biosynthesis regulator MetR improving the titer for isopentenol production by 55%. Additionally, expression of MdlB, an ABC transporter, facilitated a 12% improvement in isopentenol production. To our knowledge, MdlB is the first example of a transporter that can be used to improve production of a short-chain alcohol and provides a valuable new avenue for host engineering in biogasoline production. |
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School of Chemical and Biomedical Engineering |
author_facet |
School of Chemical and Biomedical Engineering Foo, Jee Loon Jensen, Heather M. Dahl, Robert H. George, Kevin Keasling, Jay D. Lee, Taek Soon Leong, Susanna Mukhopadhyay, Aindrila |
format |
Article |
author |
Foo, Jee Loon Jensen, Heather M. Dahl, Robert H. George, Kevin Keasling, Jay D. Lee, Taek Soon Leong, Susanna Mukhopadhyay, Aindrila |
author_sort |
Foo, Jee Loon |
title |
Improving Microbial Biogasoline Production in
Escherichia coli Using Tolerance Engineering |
title_short |
Improving Microbial Biogasoline Production in
Escherichia coli Using Tolerance Engineering |
title_full |
Improving Microbial Biogasoline Production in
Escherichia coli Using Tolerance Engineering |
title_fullStr |
Improving Microbial Biogasoline Production in
Escherichia coli Using Tolerance Engineering |
title_full_unstemmed |
Improving Microbial Biogasoline Production in
Escherichia coli Using Tolerance Engineering |
title_sort |
improving microbial biogasoline production in
escherichia coli using tolerance engineering |
publishDate |
2016 |
url |
https://hdl.handle.net/10356/83857 http://hdl.handle.net/10220/40040 |
_version_ |
1787136432360390656 |