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Production of cinnamic and p-hydroxycinnamic acid from sugar mixtures with engineered Escherichia coli

BACKGROUND: The aromatic compounds cinnamic acid (CA) and p-hydroxycinnamic acid (pHCA) are used as flavoring agents as well as precursors of chemicals. These compounds are present in plants at low concentrations, therefore, complex purification processes are usually required to extract the product....

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Autores principales: Vargas-Tah, Alejandra, Martínez, Luz María, Hernández-Chávez, Georgina, Rocha, Mario, Martínez, Alfredo, Bolívar, Francisco, Gosset, Guillermo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4305220/
https://www.ncbi.nlm.nih.gov/pubmed/25592545
http://dx.doi.org/10.1186/s12934-014-0185-1
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author Vargas-Tah, Alejandra
Martínez, Luz María
Hernández-Chávez, Georgina
Rocha, Mario
Martínez, Alfredo
Bolívar, Francisco
Gosset, Guillermo
author_facet Vargas-Tah, Alejandra
Martínez, Luz María
Hernández-Chávez, Georgina
Rocha, Mario
Martínez, Alfredo
Bolívar, Francisco
Gosset, Guillermo
author_sort Vargas-Tah, Alejandra
collection PubMed
description BACKGROUND: The aromatic compounds cinnamic acid (CA) and p-hydroxycinnamic acid (pHCA) are used as flavoring agents as well as precursors of chemicals. These compounds are present in plants at low concentrations, therefore, complex purification processes are usually required to extract the product. An alternative production method for these aromatic acids is based on the use of microbial strains modified by metabolic engineering. These biotechnological processes are usually based on the use of simple sugars like glucose as a raw material. However, sustainable production processes should preferably be based on the use of waste material such as lignocellulosic hydrolysates. RESULTS: In this study, E. coli strains with active (W3110) and inactive phosphoenolpyruvate:sugar phosphotransferase system (PTS) (VH33) were engineered for CA and pHCA production by transforming them with plasmids expressing genes encoding phenylalanine/tyrosine ammonia lyase (PAL/TAL) enzymes from Rhodotorula glutinis or Arabidopsis thaliana as well as genes aroG(fbr) and tktA, encoding a feedback inhibition resistant version of 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase and transketolase, respectively. The generated strains were evaluated in cultures with glucose, xylose or arabinose, as well as a simulated lignocellulosic hydrolysate containing a mixture of these three sugars plus acetate. Production of CA was detected in strains expressing PAL/TAL from A. thaliana, whereas both CA and pHCA accumulated in strains expressing the enzyme from R. glutinis. These experiments identified arabinose and W3110 expressing PAL/TAL from A. thaliana, aroG(fbr) and tktA as the carbon source/strain combination resulting in the best CA specific productivity and titer. To improve pHCA production, a mutant with inactive pheA gene was generated, causing an 8-fold increase in the yield of this aromatic acid from the sugars in a simulated hydrolysate. CONCLUSIONS: In this study the quantitative contribution of active or inactive PTS as well as expression of PAL/TAL from R. glutinis or A. thaliana were determined for production performance of CA and pHCA when growing on carbon sources derived from lignocellulosic hydrolysates. These data will be a useful resource in efforts towards the development of sustainable technologies for the production of aromatic acids. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-014-0185-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-43052202015-01-25 Production of cinnamic and p-hydroxycinnamic acid from sugar mixtures with engineered Escherichia coli Vargas-Tah, Alejandra Martínez, Luz María Hernández-Chávez, Georgina Rocha, Mario Martínez, Alfredo Bolívar, Francisco Gosset, Guillermo Microb Cell Fact Research BACKGROUND: The aromatic compounds cinnamic acid (CA) and p-hydroxycinnamic acid (pHCA) are used as flavoring agents as well as precursors of chemicals. These compounds are present in plants at low concentrations, therefore, complex purification processes are usually required to extract the product. An alternative production method for these aromatic acids is based on the use of microbial strains modified by metabolic engineering. These biotechnological processes are usually based on the use of simple sugars like glucose as a raw material. However, sustainable production processes should preferably be based on the use of waste material such as lignocellulosic hydrolysates. RESULTS: In this study, E. coli strains with active (W3110) and inactive phosphoenolpyruvate:sugar phosphotransferase system (PTS) (VH33) were engineered for CA and pHCA production by transforming them with plasmids expressing genes encoding phenylalanine/tyrosine ammonia lyase (PAL/TAL) enzymes from Rhodotorula glutinis or Arabidopsis thaliana as well as genes aroG(fbr) and tktA, encoding a feedback inhibition resistant version of 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase and transketolase, respectively. The generated strains were evaluated in cultures with glucose, xylose or arabinose, as well as a simulated lignocellulosic hydrolysate containing a mixture of these three sugars plus acetate. Production of CA was detected in strains expressing PAL/TAL from A. thaliana, whereas both CA and pHCA accumulated in strains expressing the enzyme from R. glutinis. These experiments identified arabinose and W3110 expressing PAL/TAL from A. thaliana, aroG(fbr) and tktA as the carbon source/strain combination resulting in the best CA specific productivity and titer. To improve pHCA production, a mutant with inactive pheA gene was generated, causing an 8-fold increase in the yield of this aromatic acid from the sugars in a simulated hydrolysate. CONCLUSIONS: In this study the quantitative contribution of active or inactive PTS as well as expression of PAL/TAL from R. glutinis or A. thaliana were determined for production performance of CA and pHCA when growing on carbon sources derived from lignocellulosic hydrolysates. These data will be a useful resource in efforts towards the development of sustainable technologies for the production of aromatic acids. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-014-0185-1) contains supplementary material, which is available to authorized users. BioMed Central 2015-01-16 /pmc/articles/PMC4305220/ /pubmed/25592545 http://dx.doi.org/10.1186/s12934-014-0185-1 Text en © Vargas-Tah et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Vargas-Tah, Alejandra
Martínez, Luz María
Hernández-Chávez, Georgina
Rocha, Mario
Martínez, Alfredo
Bolívar, Francisco
Gosset, Guillermo
Production of cinnamic and p-hydroxycinnamic acid from sugar mixtures with engineered Escherichia coli
title Production of cinnamic and p-hydroxycinnamic acid from sugar mixtures with engineered Escherichia coli
title_full Production of cinnamic and p-hydroxycinnamic acid from sugar mixtures with engineered Escherichia coli
title_fullStr Production of cinnamic and p-hydroxycinnamic acid from sugar mixtures with engineered Escherichia coli
title_full_unstemmed Production of cinnamic and p-hydroxycinnamic acid from sugar mixtures with engineered Escherichia coli
title_short Production of cinnamic and p-hydroxycinnamic acid from sugar mixtures with engineered Escherichia coli
title_sort production of cinnamic and p-hydroxycinnamic acid from sugar mixtures with engineered escherichia coli
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4305220/
https://www.ncbi.nlm.nih.gov/pubmed/25592545
http://dx.doi.org/10.1186/s12934-014-0185-1
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