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The comprehensive profile of fermentation products during in situ CO(2) recycling by Rubisco-based engineered Escherichia coli

BACKGROUND: In our previous study, the feasibility of Rubisco-based engineered E. coli (that contains heterologous phosphoribulokinase (PrkA) and Rubisco) for in situ CO(2) recycling during the fermentation of pentoses or hexoses was demonstrated. Nevertheless, it is perplexing to see that only roug...

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Autores principales: Yang, Cheng-Han, Liu, En-Jung, Chen, Yi-Ling, Ou-Yang, Fan-Yu, Li, Si-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4971712/
https://www.ncbi.nlm.nih.gov/pubmed/27485110
http://dx.doi.org/10.1186/s12934-016-0530-7
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author Yang, Cheng-Han
Liu, En-Jung
Chen, Yi-Ling
Ou-Yang, Fan-Yu
Li, Si-Yu
author_facet Yang, Cheng-Han
Liu, En-Jung
Chen, Yi-Ling
Ou-Yang, Fan-Yu
Li, Si-Yu
author_sort Yang, Cheng-Han
collection PubMed
description BACKGROUND: In our previous study, the feasibility of Rubisco-based engineered E. coli (that contains heterologous phosphoribulokinase (PrkA) and Rubisco) for in situ CO(2) recycling during the fermentation of pentoses or hexoses was demonstrated. Nevertheless, it is perplexing to see that only roughly 70 % of the carbon fed to the bacterial culture could be accounted for in the standard metabolic products. This low carbon recovery during fermentation occurred even though CO(2) emission was effectively reduced by Rubisco-based engineered pathway. RESULTS: In this study, the heterologous expression of form I Rubisco was found to enhance the accumulation of pyruvate in Escherichia coli MZLF [E. coli BL21(DE3) Δzwf, Δldh, Δfrd]. This may be attributed to the enhanced glycolytic reaction supported by the increased biomass and the ethanol/acetate ratio. Besides, it was found that the transcription of arcA (encodes the redox-dependent transcriptional activators ArcA that positively regulates the transcription of pyruvate formate-lyase) was down-regulated in the presence of Rubisco. The enhanced accumulation of pyruvate also occurs when PrkA is co-expressed with Rubisco in E. coli MZLF. Furthermore, E. coli containing Rubisco-based engineered pathway has a distinct profile of the fermentation products, indicating CO(2) was converted into fermentation products. By analyzing the ratio of total C-2 (2-carbon fermentation products) to total C-1 (1-carbon fermentation product) of MZLFB (MZLF containing Rubisco-based engineered pathway), it is estimated that 9 % of carbon is directed into Rubisco-based engineered pathway. CONCLUSIONS: Here, we report for the first time the complete profile of fermentation products using E. coli MZLF and its derived strains. It has been shown that the expression of Rubisco alone in MZLF enhances the accumulation of pyruvate. By including the contribution of pyruvate accumulation, the perplexing problem of low carbon recovery during fermentation by E. coli containing Rubisco-based engineered pathway has been solved. 9 % of glucose consumption is directed from glycolysis to Rubisco-based engineered pathway in MZLFB. The principle characteristics of mixotroph MZLFB are the high bacterial growth and the low CO(2) emission. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-016-0530-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-49717122016-08-04 The comprehensive profile of fermentation products during in situ CO(2) recycling by Rubisco-based engineered Escherichia coli Yang, Cheng-Han Liu, En-Jung Chen, Yi-Ling Ou-Yang, Fan-Yu Li, Si-Yu Microb Cell Fact Research BACKGROUND: In our previous study, the feasibility of Rubisco-based engineered E. coli (that contains heterologous phosphoribulokinase (PrkA) and Rubisco) for in situ CO(2) recycling during the fermentation of pentoses or hexoses was demonstrated. Nevertheless, it is perplexing to see that only roughly 70 % of the carbon fed to the bacterial culture could be accounted for in the standard metabolic products. This low carbon recovery during fermentation occurred even though CO(2) emission was effectively reduced by Rubisco-based engineered pathway. RESULTS: In this study, the heterologous expression of form I Rubisco was found to enhance the accumulation of pyruvate in Escherichia coli MZLF [E. coli BL21(DE3) Δzwf, Δldh, Δfrd]. This may be attributed to the enhanced glycolytic reaction supported by the increased biomass and the ethanol/acetate ratio. Besides, it was found that the transcription of arcA (encodes the redox-dependent transcriptional activators ArcA that positively regulates the transcription of pyruvate formate-lyase) was down-regulated in the presence of Rubisco. The enhanced accumulation of pyruvate also occurs when PrkA is co-expressed with Rubisco in E. coli MZLF. Furthermore, E. coli containing Rubisco-based engineered pathway has a distinct profile of the fermentation products, indicating CO(2) was converted into fermentation products. By analyzing the ratio of total C-2 (2-carbon fermentation products) to total C-1 (1-carbon fermentation product) of MZLFB (MZLF containing Rubisco-based engineered pathway), it is estimated that 9 % of carbon is directed into Rubisco-based engineered pathway. CONCLUSIONS: Here, we report for the first time the complete profile of fermentation products using E. coli MZLF and its derived strains. It has been shown that the expression of Rubisco alone in MZLF enhances the accumulation of pyruvate. By including the contribution of pyruvate accumulation, the perplexing problem of low carbon recovery during fermentation by E. coli containing Rubisco-based engineered pathway has been solved. 9 % of glucose consumption is directed from glycolysis to Rubisco-based engineered pathway in MZLFB. The principle characteristics of mixotroph MZLFB are the high bacterial growth and the low CO(2) emission. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-016-0530-7) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-02 /pmc/articles/PMC4971712/ /pubmed/27485110 http://dx.doi.org/10.1186/s12934-016-0530-7 Text en © The Author(s) 2016 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
Yang, Cheng-Han
Liu, En-Jung
Chen, Yi-Ling
Ou-Yang, Fan-Yu
Li, Si-Yu
The comprehensive profile of fermentation products during in situ CO(2) recycling by Rubisco-based engineered Escherichia coli
title The comprehensive profile of fermentation products during in situ CO(2) recycling by Rubisco-based engineered Escherichia coli
title_full The comprehensive profile of fermentation products during in situ CO(2) recycling by Rubisco-based engineered Escherichia coli
title_fullStr The comprehensive profile of fermentation products during in situ CO(2) recycling by Rubisco-based engineered Escherichia coli
title_full_unstemmed The comprehensive profile of fermentation products during in situ CO(2) recycling by Rubisco-based engineered Escherichia coli
title_short The comprehensive profile of fermentation products during in situ CO(2) recycling by Rubisco-based engineered Escherichia coli
title_sort comprehensive profile of fermentation products during in situ co(2) recycling by rubisco-based engineered escherichia coli
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4971712/
https://www.ncbi.nlm.nih.gov/pubmed/27485110
http://dx.doi.org/10.1186/s12934-016-0530-7
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