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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...

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Autores principales: Cheng, Hsieh-Ting-Yang, Lo, Shou-Chen, Huang, Chieh-Chen, Ho, Tsung-Yi, Yang, Ya-Tang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2019
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.
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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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