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Engineering Escherichia coli to grow constitutively on D-xylose using the carbon-efficient Weimberg pathway

Bio-production of fuels and chemicals from lignocellulosic C5 sugars usually requires the use of the pentose phosphate pathway (PPP) to produce pyruvate. Unfortunately, the oxidation of pyruvate to acetyl-coenzyme A results in the loss of 33 % of the carbon as CO(2), to the detriment of sustainabili...

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Autores principales: Rossoni, Luca, Carr, Reuben, Baxter, Scott, Cortis, Roxann, Thorpe, Thomas, Eastham, Graham, Stephens, Gill
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882109/
https://www.ncbi.nlm.nih.gov/pubmed/29458683
http://dx.doi.org/10.1099/mic.0.000611
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author Rossoni, Luca
Carr, Reuben
Baxter, Scott
Cortis, Roxann
Thorpe, Thomas
Eastham, Graham
Stephens, Gill
author_facet Rossoni, Luca
Carr, Reuben
Baxter, Scott
Cortis, Roxann
Thorpe, Thomas
Eastham, Graham
Stephens, Gill
author_sort Rossoni, Luca
collection PubMed
description Bio-production of fuels and chemicals from lignocellulosic C5 sugars usually requires the use of the pentose phosphate pathway (PPP) to produce pyruvate. Unfortunately, the oxidation of pyruvate to acetyl-coenzyme A results in the loss of 33 % of the carbon as CO(2), to the detriment of sustainability and process economics. To improve atom efficiency, we engineered Escherichia coli to utilize d-xylose constitutively using the Weimberg pathway, to allow direct production of 2-oxoglutarate without CO(2) loss. After confirming enzyme expression in vitro, the pathway expression was optimized in vivo using a combinatorial approach, by screening a range of constitutive promoters whilst systematically varying the gene order. A PPP-deficient (ΔxylAB), 2-oxoglutarate auxotroph (Δicd) was used as the host strain, so that growth on d-xylose depended on the expression of the Weimberg pathway, and variants expressing Caulobacter crescentus xylXAB could be selected on minimal agar plates. The strains were isolated and high-throughput measurement of the growth rates on d-xylose was used to identify the fastest growing variant. This strain contained the pL promoter, with C. crescentus xylA at the first position in the synthetic operon, and grew at 42 % of the rate on d-xylose compared to wild-type E. coli using the PPP. Remarkably, the biomass yield was improved by 53.5 % compared with the wild-type upon restoration of icd activity. Therefore, the strain grows efficiently and constitutively on d-xylose, and offers great potential for use as a new host strain to engineer carbon-efficient production of fuels and chemicals via the Weimberg pathway.
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spelling pubmed-58821092018-04-05 Engineering Escherichia coli to grow constitutively on D-xylose using the carbon-efficient Weimberg pathway Rossoni, Luca Carr, Reuben Baxter, Scott Cortis, Roxann Thorpe, Thomas Eastham, Graham Stephens, Gill Microbiology (Reading) Biotechnology Bio-production of fuels and chemicals from lignocellulosic C5 sugars usually requires the use of the pentose phosphate pathway (PPP) to produce pyruvate. Unfortunately, the oxidation of pyruvate to acetyl-coenzyme A results in the loss of 33 % of the carbon as CO(2), to the detriment of sustainability and process economics. To improve atom efficiency, we engineered Escherichia coli to utilize d-xylose constitutively using the Weimberg pathway, to allow direct production of 2-oxoglutarate without CO(2) loss. After confirming enzyme expression in vitro, the pathway expression was optimized in vivo using a combinatorial approach, by screening a range of constitutive promoters whilst systematically varying the gene order. A PPP-deficient (ΔxylAB), 2-oxoglutarate auxotroph (Δicd) was used as the host strain, so that growth on d-xylose depended on the expression of the Weimberg pathway, and variants expressing Caulobacter crescentus xylXAB could be selected on minimal agar plates. The strains were isolated and high-throughput measurement of the growth rates on d-xylose was used to identify the fastest growing variant. This strain contained the pL promoter, with C. crescentus xylA at the first position in the synthetic operon, and grew at 42 % of the rate on d-xylose compared to wild-type E. coli using the PPP. Remarkably, the biomass yield was improved by 53.5 % compared with the wild-type upon restoration of icd activity. Therefore, the strain grows efficiently and constitutively on d-xylose, and offers great potential for use as a new host strain to engineer carbon-efficient production of fuels and chemicals via the Weimberg pathway. Microbiology Society 2018-03 2018-02-05 /pmc/articles/PMC5882109/ /pubmed/29458683 http://dx.doi.org/10.1099/mic.0.000611 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of theCreative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Biotechnology
Rossoni, Luca
Carr, Reuben
Baxter, Scott
Cortis, Roxann
Thorpe, Thomas
Eastham, Graham
Stephens, Gill
Engineering Escherichia coli to grow constitutively on D-xylose using the carbon-efficient Weimberg pathway
title Engineering Escherichia coli to grow constitutively on D-xylose using the carbon-efficient Weimberg pathway
title_full Engineering Escherichia coli to grow constitutively on D-xylose using the carbon-efficient Weimberg pathway
title_fullStr Engineering Escherichia coli to grow constitutively on D-xylose using the carbon-efficient Weimberg pathway
title_full_unstemmed Engineering Escherichia coli to grow constitutively on D-xylose using the carbon-efficient Weimberg pathway
title_short Engineering Escherichia coli to grow constitutively on D-xylose using the carbon-efficient Weimberg pathway
title_sort engineering escherichia coli to grow constitutively on d-xylose using the carbon-efficient weimberg pathway
topic Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882109/
https://www.ncbi.nlm.nih.gov/pubmed/29458683
http://dx.doi.org/10.1099/mic.0.000611
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