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Detailed profiling of carbon fixation of in silico synthetic autotrophy with reductive tricarboxylic acid cycle and Calvin-Benson-Bassham cycle in Esherichia coli using hydrogen as an energy source
Carbon fixation is the main route of inorganic carbon in the form of CO(2) into the biosphere. In nature, RuBisCO is the most abundant protein that photosynthetic organisms use to fix CO(2) from the atmosphere through the Calvin-Benson-Bassham (CBB) cycle. However, the CBB cycle is limited by its lo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
KeAi Publishing
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6739492/ https://www.ncbi.nlm.nih.gov/pubmed/31528741 http://dx.doi.org/10.1016/j.synbio.2019.08.003 |
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author | Cheng, Hsieh-Ting-Yang Lo, Shou-Chen Huang, Chieh-Chen Ho, Tsung-Yi Yang, Ya-Tang |
author_facet | Cheng, Hsieh-Ting-Yang Lo, Shou-Chen Huang, Chieh-Chen Ho, Tsung-Yi Yang, Ya-Tang |
author_sort | Cheng, Hsieh-Ting-Yang |
collection | PubMed |
description | Carbon fixation is the main route of inorganic carbon in the form of CO(2) into the biosphere. In nature, RuBisCO is the most abundant protein that photosynthetic organisms use to fix CO(2) from the atmosphere through the Calvin-Benson-Bassham (CBB) cycle. However, the CBB cycle is limited by its low catalytic rate and low energy efficiency. In this work, we attempt to integrate the reductive tricarboxylic acid and CBB cycles in silico to further improve carbon fixation capacity. Key heterologous enzymes, mostly carboxylating enzymes, are inserted into the Esherichia coli core metabolic network to assimilate CO(2) into biomass using hydrogen as energy source. Overall, such a strain shows enhanced growth yield with simultaneous running of dual carbon fixation cycles. Our key results include the following. (i) We identified two main growth states: carbon-limited and hydrogen-limited; (ii) we identified a hierarchy of carbon fixation usage when hydrogen supply is limited; and (iii) we identified the alternative sub-optimal growth mode while performing genetic perturbation. The results and modeling approach can guide bioengineering projects toward optimal production using such a strain as a microbial cell factory. |
format | Online Article Text |
id | pubmed-6739492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | KeAi Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-67394922019-09-16 Detailed profiling of carbon fixation of in silico synthetic autotrophy with reductive tricarboxylic acid cycle and Calvin-Benson-Bassham cycle in Esherichia coli using hydrogen as an energy source Cheng, Hsieh-Ting-Yang Lo, Shou-Chen Huang, Chieh-Chen Ho, Tsung-Yi Yang, Ya-Tang Synth Syst Biotechnol Article Carbon fixation is the main route of inorganic carbon in the form of CO(2) into the biosphere. In nature, RuBisCO is the most abundant protein that photosynthetic organisms use to fix CO(2) from the atmosphere through the Calvin-Benson-Bassham (CBB) cycle. However, the CBB cycle is limited by its low catalytic rate and low energy efficiency. In this work, we attempt to integrate the reductive tricarboxylic acid and CBB cycles in silico to further improve carbon fixation capacity. Key heterologous enzymes, mostly carboxylating enzymes, are inserted into the Esherichia coli core metabolic network to assimilate CO(2) into biomass using hydrogen as energy source. Overall, such a strain shows enhanced growth yield with simultaneous running of dual carbon fixation cycles. Our key results include the following. (i) We identified two main growth states: carbon-limited and hydrogen-limited; (ii) we identified a hierarchy of carbon fixation usage when hydrogen supply is limited; and (iii) we identified the alternative sub-optimal growth mode while performing genetic perturbation. The results and modeling approach can guide bioengineering projects toward optimal production using such a strain as a microbial cell factory. KeAi Publishing 2019-09-10 /pmc/articles/PMC6739492/ /pubmed/31528741 http://dx.doi.org/10.1016/j.synbio.2019.08.003 Text en © 2019 Production and hosting by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Cheng, Hsieh-Ting-Yang Lo, Shou-Chen Huang, Chieh-Chen Ho, Tsung-Yi Yang, Ya-Tang Detailed profiling of carbon fixation of in silico synthetic autotrophy with reductive tricarboxylic acid cycle and Calvin-Benson-Bassham cycle in Esherichia coli using hydrogen as an energy source |
title | Detailed profiling of carbon fixation of in silico synthetic autotrophy with reductive tricarboxylic acid cycle and Calvin-Benson-Bassham cycle in Esherichia coli using hydrogen as an energy source |
title_full | Detailed profiling of carbon fixation of in silico synthetic autotrophy with reductive tricarboxylic acid cycle and Calvin-Benson-Bassham cycle in Esherichia coli using hydrogen as an energy source |
title_fullStr | Detailed profiling of carbon fixation of in silico synthetic autotrophy with reductive tricarboxylic acid cycle and Calvin-Benson-Bassham cycle in Esherichia coli using hydrogen as an energy source |
title_full_unstemmed | Detailed profiling of carbon fixation of in silico synthetic autotrophy with reductive tricarboxylic acid cycle and Calvin-Benson-Bassham cycle in Esherichia coli using hydrogen as an energy source |
title_short | Detailed profiling of carbon fixation of in silico synthetic autotrophy with reductive tricarboxylic acid cycle and Calvin-Benson-Bassham cycle in Esherichia coli using hydrogen as an energy source |
title_sort | detailed profiling of carbon fixation of in silico synthetic autotrophy with reductive tricarboxylic acid cycle and calvin-benson-bassham cycle in esherichia coli using hydrogen as an energy source |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6739492/ https://www.ncbi.nlm.nih.gov/pubmed/31528741 http://dx.doi.org/10.1016/j.synbio.2019.08.003 |
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