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Cell-free protein synthesis energized by slowly-metabolized maltodextrin

BACKGROUND: Cell-free protein synthesis (CFPS) is a rapid and high throughput technology for obtaining proteins from their genes. The primary energy source ATP is regenerated from the secondary energy source through substrate phosphorylation in CFPS. RESULTS: Distinct from common secondary energy so...

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Detalles Bibliográficos
Autores principales: Wang, Yiran, Zhang, Y-H Percival
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716334/
https://www.ncbi.nlm.nih.gov/pubmed/19558718
http://dx.doi.org/10.1186/1472-6750-9-58
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author Wang, Yiran
Zhang, Y-H Percival
author_facet Wang, Yiran
Zhang, Y-H Percival
author_sort Wang, Yiran
collection PubMed
description BACKGROUND: Cell-free protein synthesis (CFPS) is a rapid and high throughput technology for obtaining proteins from their genes. The primary energy source ATP is regenerated from the secondary energy source through substrate phosphorylation in CFPS. RESULTS: Distinct from common secondary energy sources (e.g., phosphoenolpyruvate – PEP, glucose-6-phosphate), maltodextrin was used for energizing CFPS through substrate phosphorylation and the glycolytic pathway because (i) maltodextrin can be slowly catabolized by maltodextrin phosphorylase for continuous ATP regeneration, (ii) maltodextrin phosphorylation can recycle one phosphate per reaction for glucose-1-phosphate generation, and (iii) the maltodextrin chain-shortening reaction can produce one ATP per glucose equivalent more than glucose can. Three model proteins, esterase 2 from Alicyclobacillus acidocaldarius, green fluorescent protein, and xylose reductase from Neurospora crassa were synthesized for demonstration. CONCLUSION: Slowly-metabolized maltodextrin as a low-cost secondary energy compound for CFPS produced higher levels of proteins than PEP, glucose, and glucose-6-phospahte. The enhancement of protein synthesis was largely attributed to better-controlled phosphate levels (recycling of inorganic phosphate) and a more homeostatic reaction environment.
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spelling pubmed-27163342009-07-28 Cell-free protein synthesis energized by slowly-metabolized maltodextrin Wang, Yiran Zhang, Y-H Percival BMC Biotechnol Methodology Article BACKGROUND: Cell-free protein synthesis (CFPS) is a rapid and high throughput technology for obtaining proteins from their genes. The primary energy source ATP is regenerated from the secondary energy source through substrate phosphorylation in CFPS. RESULTS: Distinct from common secondary energy sources (e.g., phosphoenolpyruvate – PEP, glucose-6-phosphate), maltodextrin was used for energizing CFPS through substrate phosphorylation and the glycolytic pathway because (i) maltodextrin can be slowly catabolized by maltodextrin phosphorylase for continuous ATP regeneration, (ii) maltodextrin phosphorylation can recycle one phosphate per reaction for glucose-1-phosphate generation, and (iii) the maltodextrin chain-shortening reaction can produce one ATP per glucose equivalent more than glucose can. Three model proteins, esterase 2 from Alicyclobacillus acidocaldarius, green fluorescent protein, and xylose reductase from Neurospora crassa were synthesized for demonstration. CONCLUSION: Slowly-metabolized maltodextrin as a low-cost secondary energy compound for CFPS produced higher levels of proteins than PEP, glucose, and glucose-6-phospahte. The enhancement of protein synthesis was largely attributed to better-controlled phosphate levels (recycling of inorganic phosphate) and a more homeostatic reaction environment. BioMed Central 2009-06-28 /pmc/articles/PMC2716334/ /pubmed/19558718 http://dx.doi.org/10.1186/1472-6750-9-58 Text en Copyright © 2009 Wang and Zhang; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology Article
Wang, Yiran
Zhang, Y-H Percival
Cell-free protein synthesis energized by slowly-metabolized maltodextrin
title Cell-free protein synthesis energized by slowly-metabolized maltodextrin
title_full Cell-free protein synthesis energized by slowly-metabolized maltodextrin
title_fullStr Cell-free protein synthesis energized by slowly-metabolized maltodextrin
title_full_unstemmed Cell-free protein synthesis energized by slowly-metabolized maltodextrin
title_short Cell-free protein synthesis energized by slowly-metabolized maltodextrin
title_sort cell-free protein synthesis energized by slowly-metabolized maltodextrin
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716334/
https://www.ncbi.nlm.nih.gov/pubmed/19558718
http://dx.doi.org/10.1186/1472-6750-9-58
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