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Engineering E. coli for simultaneous glucose–xylose utilization during methyl ketone production

BACKGROUND: We previously developed an E. coli strain that overproduces medium-chain methyl ketones for potential use as diesel fuel blending agents or as flavors and fragrances. To date, the strain’s performance has been optimized during growth with glucose. However, lignocellulosic biomass hydroly...

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Autores principales: Wang, Xi, Goh, Ee-Been, Beller, Harry R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787283/
https://www.ncbi.nlm.nih.gov/pubmed/29374483
http://dx.doi.org/10.1186/s12934-018-0862-6
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author Wang, Xi
Goh, Ee-Been
Beller, Harry R.
author_facet Wang, Xi
Goh, Ee-Been
Beller, Harry R.
author_sort Wang, Xi
collection PubMed
description BACKGROUND: We previously developed an E. coli strain that overproduces medium-chain methyl ketones for potential use as diesel fuel blending agents or as flavors and fragrances. To date, the strain’s performance has been optimized during growth with glucose. However, lignocellulosic biomass hydrolysates also contain a substantial portion of hemicellulose-derived xylose, which is typically the second most abundant sugar after glucose. Commercialization of the methyl ketone-producing technology would benefit from the increased efficiency resulting from simultaneous, rather than the native sequential (diauxic), utilization of glucose and xylose. RESULTS: In this study, genetic manipulations were performed to alleviate carbon catabolite repression in our most efficient methyl ketone-producing strain. A strain engineered for constitutive expression of xylF and xylA (involved in xylose transport and metabolism) showed synchronized glucose and xylose consumption rates. However, this newly acquired capability came at the expense of methyl ketone titer, which decreased fivefold. Further efforts were made to improve methyl ketone production in this strain, and we found that two strategies were effective at enhancing methyl ketone titer: (1) chromosomal deletion of pgi (glucose-6-phosphate isomerase) to increase intracellular NADPH supply and (2) downregulation of CRP (cAMP receptor protein) expression by replacement of the native RBS with an RBS chosen based upon mutant library screening results. Combining these strategies resulted in the most favorable overall phenotypes for simultaneous glucose–xylose consumption without compromising methyl ketone titer at both 1 and 2% total sugar concentrations in shake flasks. CONCLUSIONS: This work demonstrated a strategy for engineering simultaneous utilization of C(6) and C(5) sugars in E. coli without sacrificing production of fatty acid-derived compounds. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-018-0862-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-57872832018-02-08 Engineering E. coli for simultaneous glucose–xylose utilization during methyl ketone production Wang, Xi Goh, Ee-Been Beller, Harry R. Microb Cell Fact Research BACKGROUND: We previously developed an E. coli strain that overproduces medium-chain methyl ketones for potential use as diesel fuel blending agents or as flavors and fragrances. To date, the strain’s performance has been optimized during growth with glucose. However, lignocellulosic biomass hydrolysates also contain a substantial portion of hemicellulose-derived xylose, which is typically the second most abundant sugar after glucose. Commercialization of the methyl ketone-producing technology would benefit from the increased efficiency resulting from simultaneous, rather than the native sequential (diauxic), utilization of glucose and xylose. RESULTS: In this study, genetic manipulations were performed to alleviate carbon catabolite repression in our most efficient methyl ketone-producing strain. A strain engineered for constitutive expression of xylF and xylA (involved in xylose transport and metabolism) showed synchronized glucose and xylose consumption rates. However, this newly acquired capability came at the expense of methyl ketone titer, which decreased fivefold. Further efforts were made to improve methyl ketone production in this strain, and we found that two strategies were effective at enhancing methyl ketone titer: (1) chromosomal deletion of pgi (glucose-6-phosphate isomerase) to increase intracellular NADPH supply and (2) downregulation of CRP (cAMP receptor protein) expression by replacement of the native RBS with an RBS chosen based upon mutant library screening results. Combining these strategies resulted in the most favorable overall phenotypes for simultaneous glucose–xylose consumption without compromising methyl ketone titer at both 1 and 2% total sugar concentrations in shake flasks. CONCLUSIONS: This work demonstrated a strategy for engineering simultaneous utilization of C(6) and C(5) sugars in E. coli without sacrificing production of fatty acid-derived compounds. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-018-0862-6) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-27 /pmc/articles/PMC5787283/ /pubmed/29374483 http://dx.doi.org/10.1186/s12934-018-0862-6 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
Wang, Xi
Goh, Ee-Been
Beller, Harry R.
Engineering E. coli for simultaneous glucose–xylose utilization during methyl ketone production
title Engineering E. coli for simultaneous glucose–xylose utilization during methyl ketone production
title_full Engineering E. coli for simultaneous glucose–xylose utilization during methyl ketone production
title_fullStr Engineering E. coli for simultaneous glucose–xylose utilization during methyl ketone production
title_full_unstemmed Engineering E. coli for simultaneous glucose–xylose utilization during methyl ketone production
title_short Engineering E. coli for simultaneous glucose–xylose utilization during methyl ketone production
title_sort engineering e. coli for simultaneous glucose–xylose utilization during methyl ketone production
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787283/
https://www.ncbi.nlm.nih.gov/pubmed/29374483
http://dx.doi.org/10.1186/s12934-018-0862-6
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