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A novel toolbox for E. coli lysis monitoring
The bacterium Escherichia coli is a well-studied recombinant host organism with a plethora of applications in biotechnology. Highly valuable biopharmaceuticals, such as antibody fragments and growth factors, are currently being produced in E. coli. However, the high metabolic burden during recombina...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5233743/ https://www.ncbi.nlm.nih.gov/pubmed/27590321 http://dx.doi.org/10.1007/s00216-016-9907-z |
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author | Rajamanickam, Vignesh Wurm, David Slouka, Christoph Herwig, Christoph Spadiut, Oliver |
author_facet | Rajamanickam, Vignesh Wurm, David Slouka, Christoph Herwig, Christoph Spadiut, Oliver |
author_sort | Rajamanickam, Vignesh |
collection | PubMed |
description | The bacterium Escherichia coli is a well-studied recombinant host organism with a plethora of applications in biotechnology. Highly valuable biopharmaceuticals, such as antibody fragments and growth factors, are currently being produced in E. coli. However, the high metabolic burden during recombinant protein production can lead to cell death, consequent lysis, and undesired product loss. Thus, fast and precise analyzers to monitor E. coli bioprocesses and to retrieve key process information, such as the optimal time point of harvest, are needed. However, such reliable monitoring tools are still scarce to date. In this study, we cultivated an E. coli strain producing a recombinant single-chain antibody fragment in the cytoplasm. In bioreactor cultivations, we purposely triggered cell lysis by pH ramps. We developed a novel toolbox using UV chromatograms as fingerprints and chemometric techniques to monitor these lysis events and used flow cytometry (FCM) as reference method to quantify viability offline. Summarizing, we were able to show that a novel toolbox comprising HPLC chromatogram fingerprinting and data science tools allowed the identification of E. coli lysis in a fast and reliable manner. We are convinced that this toolbox will not only facilitate E. coli bioprocess monitoring but will also allow enhanced process control in the future. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00216-016-9907-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5233743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-52337432017-01-25 A novel toolbox for E. coli lysis monitoring Rajamanickam, Vignesh Wurm, David Slouka, Christoph Herwig, Christoph Spadiut, Oliver Anal Bioanal Chem Rapid Communication The bacterium Escherichia coli is a well-studied recombinant host organism with a plethora of applications in biotechnology. Highly valuable biopharmaceuticals, such as antibody fragments and growth factors, are currently being produced in E. coli. However, the high metabolic burden during recombinant protein production can lead to cell death, consequent lysis, and undesired product loss. Thus, fast and precise analyzers to monitor E. coli bioprocesses and to retrieve key process information, such as the optimal time point of harvest, are needed. However, such reliable monitoring tools are still scarce to date. In this study, we cultivated an E. coli strain producing a recombinant single-chain antibody fragment in the cytoplasm. In bioreactor cultivations, we purposely triggered cell lysis by pH ramps. We developed a novel toolbox using UV chromatograms as fingerprints and chemometric techniques to monitor these lysis events and used flow cytometry (FCM) as reference method to quantify viability offline. Summarizing, we were able to show that a novel toolbox comprising HPLC chromatogram fingerprinting and data science tools allowed the identification of E. coli lysis in a fast and reliable manner. We are convinced that this toolbox will not only facilitate E. coli bioprocess monitoring but will also allow enhanced process control in the future. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00216-016-9907-z) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-09-02 2017 /pmc/articles/PMC5233743/ /pubmed/27590321 http://dx.doi.org/10.1007/s00216-016-9907-z Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Rapid Communication Rajamanickam, Vignesh Wurm, David Slouka, Christoph Herwig, Christoph Spadiut, Oliver A novel toolbox for E. coli lysis monitoring |
title | A novel toolbox for E. coli lysis monitoring |
title_full | A novel toolbox for E. coli lysis monitoring |
title_fullStr | A novel toolbox for E. coli lysis monitoring |
title_full_unstemmed | A novel toolbox for E. coli lysis monitoring |
title_short | A novel toolbox for E. coli lysis monitoring |
title_sort | novel toolbox for e. coli lysis monitoring |
topic | Rapid Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5233743/ https://www.ncbi.nlm.nih.gov/pubmed/27590321 http://dx.doi.org/10.1007/s00216-016-9907-z |
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