Cargando…
Antibiotic free selection for the high level biosynthesis of a silk-elastin-like protein
Silk-elastin-like proteins (SELPs) are a family of genetically engineered recombinant protein polymers exhibiting mechanical and biological properties suited for a wide range of applications in the biomedicine and materials fields. They are being explored as the next generation of biomaterials but l...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5159808/ https://www.ncbi.nlm.nih.gov/pubmed/27982135 http://dx.doi.org/10.1038/srep39329 |
_version_ | 1782481823185502208 |
---|---|
author | Barroca, Mário Rodrigues, Paulo Sobral, Rómulo Costa, M. Manuela R. Chaves, Susana R. Machado, Raul Casal, Margarida Collins, Tony |
author_facet | Barroca, Mário Rodrigues, Paulo Sobral, Rómulo Costa, M. Manuela R. Chaves, Susana R. Machado, Raul Casal, Margarida Collins, Tony |
author_sort | Barroca, Mário |
collection | PubMed |
description | Silk-elastin-like proteins (SELPs) are a family of genetically engineered recombinant protein polymers exhibiting mechanical and biological properties suited for a wide range of applications in the biomedicine and materials fields. They are being explored as the next generation of biomaterials but low productivities and use of antibiotics during production undermine their economic viability and safety. We have developed an industrially relevant, scalable, fed-batch process for the high level production of a novel SELP in E. coli in which the commonly used antibiotic selection marker of the expression vector is exchanged for a post segregational suicide system, the separate-component-stabilisation system (SCS). SCS significantly augments SELP productivity but also enhances the product safety profile and reduces process costs by eliminating the use of antibiotics. Plasmid content increased following induction but no significant differences in plasmid levels were discerned when using SCS or the antibiotic selection markers under the controlled fed-batch conditions employed. It is suggested that the absence of competing plasmid-free cells improves host cell viability and enables increased productivity with SCS. With the process developed, 12.8 g L(−1) purified SELP was obtained, this is the highest SELP productivity reported to date and clearly demonstrates the commercial viability of these promising polymers. |
format | Online Article Text |
id | pubmed-5159808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51598082016-12-21 Antibiotic free selection for the high level biosynthesis of a silk-elastin-like protein Barroca, Mário Rodrigues, Paulo Sobral, Rómulo Costa, M. Manuela R. Chaves, Susana R. Machado, Raul Casal, Margarida Collins, Tony Sci Rep Article Silk-elastin-like proteins (SELPs) are a family of genetically engineered recombinant protein polymers exhibiting mechanical and biological properties suited for a wide range of applications in the biomedicine and materials fields. They are being explored as the next generation of biomaterials but low productivities and use of antibiotics during production undermine their economic viability and safety. We have developed an industrially relevant, scalable, fed-batch process for the high level production of a novel SELP in E. coli in which the commonly used antibiotic selection marker of the expression vector is exchanged for a post segregational suicide system, the separate-component-stabilisation system (SCS). SCS significantly augments SELP productivity but also enhances the product safety profile and reduces process costs by eliminating the use of antibiotics. Plasmid content increased following induction but no significant differences in plasmid levels were discerned when using SCS or the antibiotic selection markers under the controlled fed-batch conditions employed. It is suggested that the absence of competing plasmid-free cells improves host cell viability and enables increased productivity with SCS. With the process developed, 12.8 g L(−1) purified SELP was obtained, this is the highest SELP productivity reported to date and clearly demonstrates the commercial viability of these promising polymers. Nature Publishing Group 2016-12-16 /pmc/articles/PMC5159808/ /pubmed/27982135 http://dx.doi.org/10.1038/srep39329 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Barroca, Mário Rodrigues, Paulo Sobral, Rómulo Costa, M. Manuela R. Chaves, Susana R. Machado, Raul Casal, Margarida Collins, Tony Antibiotic free selection for the high level biosynthesis of a silk-elastin-like protein |
title | Antibiotic free selection for the high level biosynthesis of a silk-elastin-like protein |
title_full | Antibiotic free selection for the high level biosynthesis of a silk-elastin-like protein |
title_fullStr | Antibiotic free selection for the high level biosynthesis of a silk-elastin-like protein |
title_full_unstemmed | Antibiotic free selection for the high level biosynthesis of a silk-elastin-like protein |
title_short | Antibiotic free selection for the high level biosynthesis of a silk-elastin-like protein |
title_sort | antibiotic free selection for the high level biosynthesis of a silk-elastin-like protein |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5159808/ https://www.ncbi.nlm.nih.gov/pubmed/27982135 http://dx.doi.org/10.1038/srep39329 |
work_keys_str_mv | AT barrocamario antibioticfreeselectionforthehighlevelbiosynthesisofasilkelastinlikeprotein AT rodriguespaulo antibioticfreeselectionforthehighlevelbiosynthesisofasilkelastinlikeprotein AT sobralromulo antibioticfreeselectionforthehighlevelbiosynthesisofasilkelastinlikeprotein AT costammanuelar antibioticfreeselectionforthehighlevelbiosynthesisofasilkelastinlikeprotein AT chavessusanar antibioticfreeselectionforthehighlevelbiosynthesisofasilkelastinlikeprotein AT machadoraul antibioticfreeselectionforthehighlevelbiosynthesisofasilkelastinlikeprotein AT casalmargarida antibioticfreeselectionforthehighlevelbiosynthesisofasilkelastinlikeprotein AT collinstony antibioticfreeselectionforthehighlevelbiosynthesisofasilkelastinlikeprotein |