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In vitro flow cytometry-based screening platform for cellulase engineering
Ultrahigh throughput screening (uHTS) plays an essential role in directed evolution for tailoring biocatalysts for industrial applications. Flow cytometry-based uHTS provides an efficient coverage of the generated protein sequence space by analysis of up to 10(7) events per hour. Cell-free enzyme pr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869107/ https://www.ncbi.nlm.nih.gov/pubmed/27184298 http://dx.doi.org/10.1038/srep26128 |
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author | Körfer, Georgette Pitzler, Christian Vojcic, Ljubica Martinez, Ronny Schwaneberg, Ulrich |
author_facet | Körfer, Georgette Pitzler, Christian Vojcic, Ljubica Martinez, Ronny Schwaneberg, Ulrich |
author_sort | Körfer, Georgette |
collection | PubMed |
description | Ultrahigh throughput screening (uHTS) plays an essential role in directed evolution for tailoring biocatalysts for industrial applications. Flow cytometry-based uHTS provides an efficient coverage of the generated protein sequence space by analysis of up to 10(7) events per hour. Cell-free enzyme production overcomes the challenge of diversity loss during the transformation of mutant libraries into expression hosts, enables directed evolution of toxic enzymes, and holds the promise to efficiently design enzymes of human or animal origin. The developed uHTS cell-free compartmentalization platform (InVitroFlow) is the first report in which a flow cytometry-based screened system has been combined with compartmentalized cell-free expression for directed cellulase enzyme evolution. InVitroFlow was validated by screening of a random cellulase mutant library employing a novel screening system (based on the substrate fluorescein-di-β-D-cellobioside), and yielded significantly improved cellulase variants (e.g. CelA2-H288F-M1 (N273D/H288F/N468S) with 13.3-fold increased specific activity (220.60 U/mg) compared to CelA2 wildtype: 16.57 U/mg). |
format | Online Article Text |
id | pubmed-4869107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48691072016-06-01 In vitro flow cytometry-based screening platform for cellulase engineering Körfer, Georgette Pitzler, Christian Vojcic, Ljubica Martinez, Ronny Schwaneberg, Ulrich Sci Rep Article Ultrahigh throughput screening (uHTS) plays an essential role in directed evolution for tailoring biocatalysts for industrial applications. Flow cytometry-based uHTS provides an efficient coverage of the generated protein sequence space by analysis of up to 10(7) events per hour. Cell-free enzyme production overcomes the challenge of diversity loss during the transformation of mutant libraries into expression hosts, enables directed evolution of toxic enzymes, and holds the promise to efficiently design enzymes of human or animal origin. The developed uHTS cell-free compartmentalization platform (InVitroFlow) is the first report in which a flow cytometry-based screened system has been combined with compartmentalized cell-free expression for directed cellulase enzyme evolution. InVitroFlow was validated by screening of a random cellulase mutant library employing a novel screening system (based on the substrate fluorescein-di-β-D-cellobioside), and yielded significantly improved cellulase variants (e.g. CelA2-H288F-M1 (N273D/H288F/N468S) with 13.3-fold increased specific activity (220.60 U/mg) compared to CelA2 wildtype: 16.57 U/mg). Nature Publishing Group 2016-05-17 /pmc/articles/PMC4869107/ /pubmed/27184298 http://dx.doi.org/10.1038/srep26128 Text en Copyright © 2016, Macmillan Publishers Limited 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 Körfer, Georgette Pitzler, Christian Vojcic, Ljubica Martinez, Ronny Schwaneberg, Ulrich In vitro flow cytometry-based screening platform for cellulase engineering |
title | In vitro flow cytometry-based screening platform for cellulase engineering |
title_full | In vitro flow cytometry-based screening platform for cellulase engineering |
title_fullStr | In vitro flow cytometry-based screening platform for cellulase engineering |
title_full_unstemmed | In vitro flow cytometry-based screening platform for cellulase engineering |
title_short | In vitro flow cytometry-based screening platform for cellulase engineering |
title_sort | in vitro flow cytometry-based screening platform for cellulase engineering |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869107/ https://www.ncbi.nlm.nih.gov/pubmed/27184298 http://dx.doi.org/10.1038/srep26128 |
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