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High throughput automated microbial bioreactor system used for clone selection and rapid scale‐down process optimization
High throughput automated fermentation systems have become a useful tool in early bioprocess development. In this study, we investigated a 24 x 15 mL single use microbioreactor system, ambr 15f, designed for microbial culture. We compared the fed‐batch growth and production capabilities of this syst...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836883/ https://www.ncbi.nlm.nih.gov/pubmed/28748655 http://dx.doi.org/10.1002/btpr.2534 |
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author | Velez‐Suberbie, M. Lourdes Betts, John P. J. Walker, Kelly L. Robinson, Colin Zoro, Barney Keshavarz‐Moore, Eli |
author_facet | Velez‐Suberbie, M. Lourdes Betts, John P. J. Walker, Kelly L. Robinson, Colin Zoro, Barney Keshavarz‐Moore, Eli |
author_sort | Velez‐Suberbie, M. Lourdes |
collection | PubMed |
description | High throughput automated fermentation systems have become a useful tool in early bioprocess development. In this study, we investigated a 24 x 15 mL single use microbioreactor system, ambr 15f, designed for microbial culture. We compared the fed‐batch growth and production capabilities of this system for two Escherichia coli strains, BL21 (DE3) and MC4100, and two industrially relevant molecules, hGH and scFv. In addition, different carbon sources were tested using bolus, linear or exponential feeding strategies, showing the capacity of the ambr 15f system to handle automated feeding. We used power per unit volume (P/V) as a scale criterion to compare the ambr 15f with 1 L stirred bioreactors which were previously scaled‐up to 20 L with a different biological system, thus showing a potential 1,300 fold scale comparability in terms of both growth and product yield. By exposing the cells grown in the ambr 15f system to a level of shear expected in an industrial centrifuge, we determined that the cells are as robust as those from a bench scale bioreactor. These results provide evidence that the ambr 15f system is an efficient high throughput microbial system that can be used for strain and molecule selection as well as rapid scale‐up. © 2017 The Authors Biotechnology Progress published by Wiley Periodicals, Inc. on behalf of American Institute of Chemical Engineers Biotechnol. Prog., 34:58–68, 2018 |
format | Online Article Text |
id | pubmed-5836883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58368832018-03-12 High throughput automated microbial bioreactor system used for clone selection and rapid scale‐down process optimization Velez‐Suberbie, M. Lourdes Betts, John P. J. Walker, Kelly L. Robinson, Colin Zoro, Barney Keshavarz‐Moore, Eli Biotechnol Prog RESEARCH ARTICLES High throughput automated fermentation systems have become a useful tool in early bioprocess development. In this study, we investigated a 24 x 15 mL single use microbioreactor system, ambr 15f, designed for microbial culture. We compared the fed‐batch growth and production capabilities of this system for two Escherichia coli strains, BL21 (DE3) and MC4100, and two industrially relevant molecules, hGH and scFv. In addition, different carbon sources were tested using bolus, linear or exponential feeding strategies, showing the capacity of the ambr 15f system to handle automated feeding. We used power per unit volume (P/V) as a scale criterion to compare the ambr 15f with 1 L stirred bioreactors which were previously scaled‐up to 20 L with a different biological system, thus showing a potential 1,300 fold scale comparability in terms of both growth and product yield. By exposing the cells grown in the ambr 15f system to a level of shear expected in an industrial centrifuge, we determined that the cells are as robust as those from a bench scale bioreactor. These results provide evidence that the ambr 15f system is an efficient high throughput microbial system that can be used for strain and molecule selection as well as rapid scale‐up. © 2017 The Authors Biotechnology Progress published by Wiley Periodicals, Inc. on behalf of American Institute of Chemical Engineers Biotechnol. Prog., 34:58–68, 2018 John Wiley and Sons Inc. 2017-08-10 2018 /pmc/articles/PMC5836883/ /pubmed/28748655 http://dx.doi.org/10.1002/btpr.2534 Text en © 2017 The Authors Biotechnology Progress published by Wiley Periodicals, Inc. on behalf of American Institute of Chemical Engineers This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RESEARCH ARTICLES Velez‐Suberbie, M. Lourdes Betts, John P. J. Walker, Kelly L. Robinson, Colin Zoro, Barney Keshavarz‐Moore, Eli High throughput automated microbial bioreactor system used for clone selection and rapid scale‐down process optimization |
title | High throughput automated microbial bioreactor system used for clone selection and rapid scale‐down process optimization |
title_full | High throughput automated microbial bioreactor system used for clone selection and rapid scale‐down process optimization |
title_fullStr | High throughput automated microbial bioreactor system used for clone selection and rapid scale‐down process optimization |
title_full_unstemmed | High throughput automated microbial bioreactor system used for clone selection and rapid scale‐down process optimization |
title_short | High throughput automated microbial bioreactor system used for clone selection and rapid scale‐down process optimization |
title_sort | high throughput automated microbial bioreactor system used for clone selection and rapid scale‐down process optimization |
topic | RESEARCH ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836883/ https://www.ncbi.nlm.nih.gov/pubmed/28748655 http://dx.doi.org/10.1002/btpr.2534 |
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