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Towards scalable production of a collagen-like protein from Streptococcus pyogenes for biomedical applications

BACKGROUND: Collagen has proved valuable as biomedical materials for a range of clinical applications, particularly in wound healing. It is normally produced from animal sources, such as from bovines, but concerns have emerged over transmission of diseases. Recombinant collagens would be preferable,...

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Autores principales: Peng, Yong Y, Howell, Linda, Stoichevska, Violet, Werkmeister, Jerome A, Dumsday, Geoff J, Ramshaw, John A M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3539881/
https://www.ncbi.nlm.nih.gov/pubmed/23126526
http://dx.doi.org/10.1186/1475-2859-11-146
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author Peng, Yong Y
Howell, Linda
Stoichevska, Violet
Werkmeister, Jerome A
Dumsday, Geoff J
Ramshaw, John A M
author_facet Peng, Yong Y
Howell, Linda
Stoichevska, Violet
Werkmeister, Jerome A
Dumsday, Geoff J
Ramshaw, John A M
author_sort Peng, Yong Y
collection PubMed
description BACKGROUND: Collagen has proved valuable as biomedical materials for a range of clinical applications, particularly in wound healing. It is normally produced from animal sources, such as from bovines, but concerns have emerged over transmission of diseases. Recombinant collagens would be preferable, but are difficult to produce. Recently, studies have shown that ‘collagens’ from bacteria, including Streptococcus pyogenes, can be produced in the laboratory as recombinant products, and that these are biocompatible. In the present study we have established that examples of bacterial collagens can be produced in a bioreactor with high yields providing proof of manufacture of this important group of proteins. RESULTS: Production trials in shake flask cultures gave low yields of recombinant product, < 1 g/L. Increased yields, of around 1 g/L, were obtained when the shake flask process was transferred to a stirred tank bioreactor, and the yield was further enhanced to around 10 g/L by implementation of a high cell density fed-batch process and the use of suitably formulated fully defined media. Similar yields were obtained with 2 different constructs, one containing an introduced heparin binding domain. The best yields, of up to 19 g/L were obtained using this high cell density strategy, with an extended 24 h production time. CONCLUSIONS: These data have shown that recombinant bacterial collagen from S. pyogenes, can be produced in sufficient yield by a scalable microbial production process to give commercially acceptable yields for broad use in biomedical applications.
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spelling pubmed-35398812013-01-10 Towards scalable production of a collagen-like protein from Streptococcus pyogenes for biomedical applications Peng, Yong Y Howell, Linda Stoichevska, Violet Werkmeister, Jerome A Dumsday, Geoff J Ramshaw, John A M Microb Cell Fact Research BACKGROUND: Collagen has proved valuable as biomedical materials for a range of clinical applications, particularly in wound healing. It is normally produced from animal sources, such as from bovines, but concerns have emerged over transmission of diseases. Recombinant collagens would be preferable, but are difficult to produce. Recently, studies have shown that ‘collagens’ from bacteria, including Streptococcus pyogenes, can be produced in the laboratory as recombinant products, and that these are biocompatible. In the present study we have established that examples of bacterial collagens can be produced in a bioreactor with high yields providing proof of manufacture of this important group of proteins. RESULTS: Production trials in shake flask cultures gave low yields of recombinant product, < 1 g/L. Increased yields, of around 1 g/L, were obtained when the shake flask process was transferred to a stirred tank bioreactor, and the yield was further enhanced to around 10 g/L by implementation of a high cell density fed-batch process and the use of suitably formulated fully defined media. Similar yields were obtained with 2 different constructs, one containing an introduced heparin binding domain. The best yields, of up to 19 g/L were obtained using this high cell density strategy, with an extended 24 h production time. CONCLUSIONS: These data have shown that recombinant bacterial collagen from S. pyogenes, can be produced in sufficient yield by a scalable microbial production process to give commercially acceptable yields for broad use in biomedical applications. BioMed Central 2012-11-05 /pmc/articles/PMC3539881/ /pubmed/23126526 http://dx.doi.org/10.1186/1475-2859-11-146 Text en Copyright ©2012 Peng et al.; 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 Research
Peng, Yong Y
Howell, Linda
Stoichevska, Violet
Werkmeister, Jerome A
Dumsday, Geoff J
Ramshaw, John A M
Towards scalable production of a collagen-like protein from Streptococcus pyogenes for biomedical applications
title Towards scalable production of a collagen-like protein from Streptococcus pyogenes for biomedical applications
title_full Towards scalable production of a collagen-like protein from Streptococcus pyogenes for biomedical applications
title_fullStr Towards scalable production of a collagen-like protein from Streptococcus pyogenes for biomedical applications
title_full_unstemmed Towards scalable production of a collagen-like protein from Streptococcus pyogenes for biomedical applications
title_short Towards scalable production of a collagen-like protein from Streptococcus pyogenes for biomedical applications
title_sort towards scalable production of a collagen-like protein from streptococcus pyogenes for biomedical applications
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3539881/
https://www.ncbi.nlm.nih.gov/pubmed/23126526
http://dx.doi.org/10.1186/1475-2859-11-146
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