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Microbial factories for recombinant pharmaceuticals
Most of the hosts used to produce the 151 recombinant pharmaceuticals so far approved for human use by the Food and Drug Administration (FDA) and/or by the European Medicines Agency (EMEA) are microbial cells, either bacteria or yeast. This fact indicates that despite the diverse bottlenecks and obs...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2669800/ https://www.ncbi.nlm.nih.gov/pubmed/19317892 http://dx.doi.org/10.1186/1475-2859-8-17 |
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author | Ferrer-Miralles, Neus Domingo-Espín, Joan Corchero, José Luis Vázquez, Esther Villaverde, Antonio |
author_facet | Ferrer-Miralles, Neus Domingo-Espín, Joan Corchero, José Luis Vázquez, Esther Villaverde, Antonio |
author_sort | Ferrer-Miralles, Neus |
collection | PubMed |
description | Most of the hosts used to produce the 151 recombinant pharmaceuticals so far approved for human use by the Food and Drug Administration (FDA) and/or by the European Medicines Agency (EMEA) are microbial cells, either bacteria or yeast. This fact indicates that despite the diverse bottlenecks and obstacles that microbial systems pose to the efficient production of functional mammalian proteins, namely lack or unconventional post-translational modifications, proteolytic instability, poor solubility and activation of cell stress responses, among others, they represent convenient and powerful tools for recombinant protein production. The entering into the market of a progressively increasing number of protein drugs produced in non-microbial systems has not impaired the development of products obtained in microbial cells, proving the robustness of the microbial set of cellular systems (so far Escherichia coli and Saccharomyces cerevisae) developed for protein drug production. We summarize here the nature, properties and applications of all those pharmaceuticals and the relevant features of the current and potential producing hosts, in a comparative way. |
format | Text |
id | pubmed-2669800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26698002009-04-17 Microbial factories for recombinant pharmaceuticals Ferrer-Miralles, Neus Domingo-Espín, Joan Corchero, José Luis Vázquez, Esther Villaverde, Antonio Microb Cell Fact Review Most of the hosts used to produce the 151 recombinant pharmaceuticals so far approved for human use by the Food and Drug Administration (FDA) and/or by the European Medicines Agency (EMEA) are microbial cells, either bacteria or yeast. This fact indicates that despite the diverse bottlenecks and obstacles that microbial systems pose to the efficient production of functional mammalian proteins, namely lack or unconventional post-translational modifications, proteolytic instability, poor solubility and activation of cell stress responses, among others, they represent convenient and powerful tools for recombinant protein production. The entering into the market of a progressively increasing number of protein drugs produced in non-microbial systems has not impaired the development of products obtained in microbial cells, proving the robustness of the microbial set of cellular systems (so far Escherichia coli and Saccharomyces cerevisae) developed for protein drug production. We summarize here the nature, properties and applications of all those pharmaceuticals and the relevant features of the current and potential producing hosts, in a comparative way. BioMed Central 2009-03-24 /pmc/articles/PMC2669800/ /pubmed/19317892 http://dx.doi.org/10.1186/1475-2859-8-17 Text en Copyright © 2009 Ferrer-Miralles 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 | Review Ferrer-Miralles, Neus Domingo-Espín, Joan Corchero, José Luis Vázquez, Esther Villaverde, Antonio Microbial factories for recombinant pharmaceuticals |
title | Microbial factories for recombinant pharmaceuticals |
title_full | Microbial factories for recombinant pharmaceuticals |
title_fullStr | Microbial factories for recombinant pharmaceuticals |
title_full_unstemmed | Microbial factories for recombinant pharmaceuticals |
title_short | Microbial factories for recombinant pharmaceuticals |
title_sort | microbial factories for recombinant pharmaceuticals |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2669800/ https://www.ncbi.nlm.nih.gov/pubmed/19317892 http://dx.doi.org/10.1186/1475-2859-8-17 |
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