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From frozen cell bank to product assay: high-throughput strain characterisation for autonomous Design-Build-Test-Learn cycles
BACKGROUND: Modern genome editing enables rapid construction of genetic variants, which are further developed in Design-Build-Test-Learn cycles. To operate such cycles in high throughput, fully automated screening, including cultivation and analytics, is crucial in the Test phase. Here, we present t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349472/ https://www.ncbi.nlm.nih.gov/pubmed/37452397 http://dx.doi.org/10.1186/s12934-023-02140-z |
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author | Helleckes, Laura M. Puchta, Debora Czech, Hannah Morschett, Holger Geinitz, Bertram Wiechert, Wolfgang Oldiges, Marco |
author_facet | Helleckes, Laura M. Puchta, Debora Czech, Hannah Morschett, Holger Geinitz, Bertram Wiechert, Wolfgang Oldiges, Marco |
author_sort | Helleckes, Laura M. |
collection | PubMed |
description | BACKGROUND: Modern genome editing enables rapid construction of genetic variants, which are further developed in Design-Build-Test-Learn cycles. To operate such cycles in high throughput, fully automated screening, including cultivation and analytics, is crucial in the Test phase. Here, we present the required steps to meet these demands, resulting in an automated microbioreactor platform that facilitates autonomous phenotyping from cryo culture to product assay. RESULTS: First, an automated deep freezer was integrated into the robotic platform to provide working cell banks at all times. A mobile cart allows flexible docking of the freezer to multiple platforms. Next, precultures were integrated within the microtiter plate for cultivation, resulting in highly reproducible main cultures as demonstrated for Corynebacterium glutamicum. To avoid manual exchange of microtiter plates after cultivation, two clean-in-place strategies were established and validated, resulting in restored sterile conditions within two hours. Combined with the previous steps, these changes enable a flexible start of experiments and greatly increase the walk-away time. CONCLUSIONS: Overall, this work demonstrates the capability of our microbioreactor platform to perform autonomous, consecutive cultivation and phenotyping experiments. As highlighted in a case study of cutinase-secreting strains of C. glutamicum, the new procedure allows for flexible experimentation without human interaction while maintaining high reproducibility in early-stage screening processes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-023-02140-z. |
format | Online Article Text |
id | pubmed-10349472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103494722023-07-16 From frozen cell bank to product assay: high-throughput strain characterisation for autonomous Design-Build-Test-Learn cycles Helleckes, Laura M. Puchta, Debora Czech, Hannah Morschett, Holger Geinitz, Bertram Wiechert, Wolfgang Oldiges, Marco Microb Cell Fact Research BACKGROUND: Modern genome editing enables rapid construction of genetic variants, which are further developed in Design-Build-Test-Learn cycles. To operate such cycles in high throughput, fully automated screening, including cultivation and analytics, is crucial in the Test phase. Here, we present the required steps to meet these demands, resulting in an automated microbioreactor platform that facilitates autonomous phenotyping from cryo culture to product assay. RESULTS: First, an automated deep freezer was integrated into the robotic platform to provide working cell banks at all times. A mobile cart allows flexible docking of the freezer to multiple platforms. Next, precultures were integrated within the microtiter plate for cultivation, resulting in highly reproducible main cultures as demonstrated for Corynebacterium glutamicum. To avoid manual exchange of microtiter plates after cultivation, two clean-in-place strategies were established and validated, resulting in restored sterile conditions within two hours. Combined with the previous steps, these changes enable a flexible start of experiments and greatly increase the walk-away time. CONCLUSIONS: Overall, this work demonstrates the capability of our microbioreactor platform to perform autonomous, consecutive cultivation and phenotyping experiments. As highlighted in a case study of cutinase-secreting strains of C. glutamicum, the new procedure allows for flexible experimentation without human interaction while maintaining high reproducibility in early-stage screening processes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-023-02140-z. BioMed Central 2023-07-14 /pmc/articles/PMC10349472/ /pubmed/37452397 http://dx.doi.org/10.1186/s12934-023-02140-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Helleckes, Laura M. Puchta, Debora Czech, Hannah Morschett, Holger Geinitz, Bertram Wiechert, Wolfgang Oldiges, Marco From frozen cell bank to product assay: high-throughput strain characterisation for autonomous Design-Build-Test-Learn cycles |
title | From frozen cell bank to product assay: high-throughput strain characterisation for autonomous Design-Build-Test-Learn cycles |
title_full | From frozen cell bank to product assay: high-throughput strain characterisation for autonomous Design-Build-Test-Learn cycles |
title_fullStr | From frozen cell bank to product assay: high-throughput strain characterisation for autonomous Design-Build-Test-Learn cycles |
title_full_unstemmed | From frozen cell bank to product assay: high-throughput strain characterisation for autonomous Design-Build-Test-Learn cycles |
title_short | From frozen cell bank to product assay: high-throughput strain characterisation for autonomous Design-Build-Test-Learn cycles |
title_sort | from frozen cell bank to product assay: high-throughput strain characterisation for autonomous design-build-test-learn cycles |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349472/ https://www.ncbi.nlm.nih.gov/pubmed/37452397 http://dx.doi.org/10.1186/s12934-023-02140-z |
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