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A novel system for stable, high-level expression from the T7 promoter
BACKGROUND: The most widespread, efficient prokaryotic protein-producing system is one where the T7 phage polymerase recognizes the T7 phage promoter (T7 p/p system). Unfortunately, in this system, target protein expression gradually declines and is often undetectable following 3 to 5 subcultures. A...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3512507/ https://www.ncbi.nlm.nih.gov/pubmed/22897977 http://dx.doi.org/10.1186/1475-2859-11-109 |
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author | Kesik-Brodacka, Malgorzata Romanik, Agnieszka Mikiewicz-Sygula, Diana Plucienniczak, Grazyna Plucienniczak, Andrzej |
author_facet | Kesik-Brodacka, Malgorzata Romanik, Agnieszka Mikiewicz-Sygula, Diana Plucienniczak, Grazyna Plucienniczak, Andrzej |
author_sort | Kesik-Brodacka, Malgorzata |
collection | PubMed |
description | BACKGROUND: The most widespread, efficient prokaryotic protein-producing system is one where the T7 phage polymerase recognizes the T7 phage promoter (T7 p/p system). Unfortunately, in this system, target protein expression gradually declines and is often undetectable following 3 to 5 subcultures. Although a number of studies have attempted to stabilize the expression levels of the T7 p/p system, none has resolved the problem adequately and thus precludes the use of this system for the production of recombinant proteins on a large scale. RESULTS: We created an expression cassette enabling stable, high-level expression in the T7p/p system. The cassette was tested with two different vector backbones and two target proteins. In all experiments, the expression system using the new cassette exhibited high and stable protein expression levels when compared to the traditional system. CONCLUSIONS: Herein, we describe a universal expression cassette that enables high-level, stable target protein expression in T7 RNA polymerase-based expression systems. We also present the successful use of this cassette as a novel expression platform and demonstrate its ability to overcome the main deficiency of the T7 p/p system. Thus, we provide a method for using the T7 p/p system on an industrial scale. |
format | Online Article Text |
id | pubmed-3512507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35125072012-12-04 A novel system for stable, high-level expression from the T7 promoter Kesik-Brodacka, Malgorzata Romanik, Agnieszka Mikiewicz-Sygula, Diana Plucienniczak, Grazyna Plucienniczak, Andrzej Microb Cell Fact Research BACKGROUND: The most widespread, efficient prokaryotic protein-producing system is one where the T7 phage polymerase recognizes the T7 phage promoter (T7 p/p system). Unfortunately, in this system, target protein expression gradually declines and is often undetectable following 3 to 5 subcultures. Although a number of studies have attempted to stabilize the expression levels of the T7 p/p system, none has resolved the problem adequately and thus precludes the use of this system for the production of recombinant proteins on a large scale. RESULTS: We created an expression cassette enabling stable, high-level expression in the T7p/p system. The cassette was tested with two different vector backbones and two target proteins. In all experiments, the expression system using the new cassette exhibited high and stable protein expression levels when compared to the traditional system. CONCLUSIONS: Herein, we describe a universal expression cassette that enables high-level, stable target protein expression in T7 RNA polymerase-based expression systems. We also present the successful use of this cassette as a novel expression platform and demonstrate its ability to overcome the main deficiency of the T7 p/p system. Thus, we provide a method for using the T7 p/p system on an industrial scale. BioMed Central 2012-08-16 /pmc/articles/PMC3512507/ /pubmed/22897977 http://dx.doi.org/10.1186/1475-2859-11-109 Text en Copyright ©2012 Kesik-Brodacka et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Kesik-Brodacka, Malgorzata Romanik, Agnieszka Mikiewicz-Sygula, Diana Plucienniczak, Grazyna Plucienniczak, Andrzej A novel system for stable, high-level expression from the T7 promoter |
title | A novel system for stable, high-level expression from the T7 promoter |
title_full | A novel system for stable, high-level expression from the T7 promoter |
title_fullStr | A novel system for stable, high-level expression from the T7 promoter |
title_full_unstemmed | A novel system for stable, high-level expression from the T7 promoter |
title_short | A novel system for stable, high-level expression from the T7 promoter |
title_sort | novel system for stable, high-level expression from the t7 promoter |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3512507/ https://www.ncbi.nlm.nih.gov/pubmed/22897977 http://dx.doi.org/10.1186/1475-2859-11-109 |
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