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Characterization of an Entner–Doudoroff pathway-activated Escherichia coli

BACKGROUND: Escherichia coli have both the Embden–Meyerhof–Parnas pathway (EMPP) and Entner–Doudoroff pathway (EDP) for glucose breakdown, while the EDP primarily remains inactive for glucose metabolism. However, EDP is a more favorable route than EMPP for the production of certain products. RESULTS...

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Autores principales: Kim, Ye Eun, Cho, Kyung Hyun, Bang, Ina, Kim, Chang Hee, Ryu, Young Shin, Kim, Yuchan, Choi, Eun Mi, Nong, Linh Khanh, Kim, Donghyuk, Lee, Sung Kuk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9648032/
https://www.ncbi.nlm.nih.gov/pubmed/36352474
http://dx.doi.org/10.1186/s13068-022-02219-6
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author Kim, Ye Eun
Cho, Kyung Hyun
Bang, Ina
Kim, Chang Hee
Ryu, Young Shin
Kim, Yuchan
Choi, Eun Mi
Nong, Linh Khanh
Kim, Donghyuk
Lee, Sung Kuk
author_facet Kim, Ye Eun
Cho, Kyung Hyun
Bang, Ina
Kim, Chang Hee
Ryu, Young Shin
Kim, Yuchan
Choi, Eun Mi
Nong, Linh Khanh
Kim, Donghyuk
Lee, Sung Kuk
author_sort Kim, Ye Eun
collection PubMed
description BACKGROUND: Escherichia coli have both the Embden–Meyerhof–Parnas pathway (EMPP) and Entner–Doudoroff pathway (EDP) for glucose breakdown, while the EDP primarily remains inactive for glucose metabolism. However, EDP is a more favorable route than EMPP for the production of certain products. RESULTS: EDP was activated by deleting the pfkAB genes in conjunction with subsequent adaptive laboratory evolution (ALE). The evolved strains acquired mutations in transcriptional regulatory genes for glycolytic process (crp, galR, and gntR) and in glycolysis-related genes (gnd, ptsG, and talB). The genotypic, transcriptomic and phenotypic analyses of those mutations deepen our understanding of their beneficial effects on cellulosic biomass bio-conversion. On top of these scientific understandings, we further engineered the strain to produce higher level of lycopene and 3-hydroxypropionic acid. CONCLUSIONS: These results indicate that the E. coli strain has innate capability to use EDP in lieu of EMPP for glucose metabolism, and this versatility can be harnessed to further engineer E. coli for specific biotechnological applications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13068-022-02219-6.
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spelling pubmed-96480322022-11-15 Characterization of an Entner–Doudoroff pathway-activated Escherichia coli Kim, Ye Eun Cho, Kyung Hyun Bang, Ina Kim, Chang Hee Ryu, Young Shin Kim, Yuchan Choi, Eun Mi Nong, Linh Khanh Kim, Donghyuk Lee, Sung Kuk Biotechnol Biofuels Bioprod Research BACKGROUND: Escherichia coli have both the Embden–Meyerhof–Parnas pathway (EMPP) and Entner–Doudoroff pathway (EDP) for glucose breakdown, while the EDP primarily remains inactive for glucose metabolism. However, EDP is a more favorable route than EMPP for the production of certain products. RESULTS: EDP was activated by deleting the pfkAB genes in conjunction with subsequent adaptive laboratory evolution (ALE). The evolved strains acquired mutations in transcriptional regulatory genes for glycolytic process (crp, galR, and gntR) and in glycolysis-related genes (gnd, ptsG, and talB). The genotypic, transcriptomic and phenotypic analyses of those mutations deepen our understanding of their beneficial effects on cellulosic biomass bio-conversion. On top of these scientific understandings, we further engineered the strain to produce higher level of lycopene and 3-hydroxypropionic acid. CONCLUSIONS: These results indicate that the E. coli strain has innate capability to use EDP in lieu of EMPP for glucose metabolism, and this versatility can be harnessed to further engineer E. coli for specific biotechnological applications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13068-022-02219-6. BioMed Central 2022-11-09 /pmc/articles/PMC9648032/ /pubmed/36352474 http://dx.doi.org/10.1186/s13068-022-02219-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Kim, Ye Eun
Cho, Kyung Hyun
Bang, Ina
Kim, Chang Hee
Ryu, Young Shin
Kim, Yuchan
Choi, Eun Mi
Nong, Linh Khanh
Kim, Donghyuk
Lee, Sung Kuk
Characterization of an Entner–Doudoroff pathway-activated Escherichia coli
title Characterization of an Entner–Doudoroff pathway-activated Escherichia coli
title_full Characterization of an Entner–Doudoroff pathway-activated Escherichia coli
title_fullStr Characterization of an Entner–Doudoroff pathway-activated Escherichia coli
title_full_unstemmed Characterization of an Entner–Doudoroff pathway-activated Escherichia coli
title_short Characterization of an Entner–Doudoroff pathway-activated Escherichia coli
title_sort characterization of an entner–doudoroff pathway-activated escherichia coli
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9648032/
https://www.ncbi.nlm.nih.gov/pubmed/36352474
http://dx.doi.org/10.1186/s13068-022-02219-6
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