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CO(2)-elevated cell-free protein synthesis

Gases are the vital nutrition of all organisms as the precursor of metabolism pathways. As a potential biological process, protein synthesis is inevitably regulated by gas transport and utilization. However, the effect of carbon dioxide (CO(2)) present in many metabolic pathways on protein synthesis...

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Autores principales: Lin, Xiaomei, Zhou, Caijin, Wang, Ting, Huang, Xiaoting, Chen, Junxin, Li, Zhixia, Zhang, Jisong, Lu, Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136254/
https://www.ncbi.nlm.nih.gov/pubmed/35664930
http://dx.doi.org/10.1016/j.synbio.2022.05.002
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author Lin, Xiaomei
Zhou, Caijin
Wang, Ting
Huang, Xiaoting
Chen, Junxin
Li, Zhixia
Zhang, Jisong
Lu, Yuan
author_facet Lin, Xiaomei
Zhou, Caijin
Wang, Ting
Huang, Xiaoting
Chen, Junxin
Li, Zhixia
Zhang, Jisong
Lu, Yuan
author_sort Lin, Xiaomei
collection PubMed
description Gases are the vital nutrition of all organisms as the precursor of metabolism pathways. As a potential biological process, protein synthesis is inevitably regulated by gas transport and utilization. However, the effect of carbon dioxide (CO(2)) present in many metabolic pathways on protein synthesis has not been studied well. In this work, carbon dioxide combined with oxygen was employed for cell-free protein synthesis (CFPS) in the tube-in-tube reactor with precise control of gas concentration. In this in vitro system, gases could directly affect the protein synthesis process without transmembrane transport. Varied concentrations of carbon dioxide (0–1%) and constant oxygen concentration (21%) were employed for CFPS to assess the effects. The cell-free reactions with 0.3% CO(2) and 21% O(2) showed the highest protein yields. The combined effect of CO(2) and O(2) also resulted in relatively high protein expression under high oxygen conditions (0.3% CO(2) and 100% O(2)). Moreover, metabolomics assays were performed to gain insight into metabolic changes, which showed that CO(2) slightly improved energy metabolism and redox balance. In particular, the extra supplied CO(2) activated the decarboxylating reactions and removed toxic metabolites to recover the protein synthesis activity. The exploration of CO(2) on protein synthesis could provide guiding implications for basic studies and biomanufacturing.
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spelling pubmed-91362542022-06-04 CO(2)-elevated cell-free protein synthesis Lin, Xiaomei Zhou, Caijin Wang, Ting Huang, Xiaoting Chen, Junxin Li, Zhixia Zhang, Jisong Lu, Yuan Synth Syst Biotechnol Short Communication Gases are the vital nutrition of all organisms as the precursor of metabolism pathways. As a potential biological process, protein synthesis is inevitably regulated by gas transport and utilization. However, the effect of carbon dioxide (CO(2)) present in many metabolic pathways on protein synthesis has not been studied well. In this work, carbon dioxide combined with oxygen was employed for cell-free protein synthesis (CFPS) in the tube-in-tube reactor with precise control of gas concentration. In this in vitro system, gases could directly affect the protein synthesis process without transmembrane transport. Varied concentrations of carbon dioxide (0–1%) and constant oxygen concentration (21%) were employed for CFPS to assess the effects. The cell-free reactions with 0.3% CO(2) and 21% O(2) showed the highest protein yields. The combined effect of CO(2) and O(2) also resulted in relatively high protein expression under high oxygen conditions (0.3% CO(2) and 100% O(2)). Moreover, metabolomics assays were performed to gain insight into metabolic changes, which showed that CO(2) slightly improved energy metabolism and redox balance. In particular, the extra supplied CO(2) activated the decarboxylating reactions and removed toxic metabolites to recover the protein synthesis activity. The exploration of CO(2) on protein synthesis could provide guiding implications for basic studies and biomanufacturing. KeAi Publishing 2022-05-20 /pmc/articles/PMC9136254/ /pubmed/35664930 http://dx.doi.org/10.1016/j.synbio.2022.05.002 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Short Communication
Lin, Xiaomei
Zhou, Caijin
Wang, Ting
Huang, Xiaoting
Chen, Junxin
Li, Zhixia
Zhang, Jisong
Lu, Yuan
CO(2)-elevated cell-free protein synthesis
title CO(2)-elevated cell-free protein synthesis
title_full CO(2)-elevated cell-free protein synthesis
title_fullStr CO(2)-elevated cell-free protein synthesis
title_full_unstemmed CO(2)-elevated cell-free protein synthesis
title_short CO(2)-elevated cell-free protein synthesis
title_sort co(2)-elevated cell-free protein synthesis
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136254/
https://www.ncbi.nlm.nih.gov/pubmed/35664930
http://dx.doi.org/10.1016/j.synbio.2022.05.002
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