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A host-vector toolbox for improved secretory protein overproduction in Bacillus subtilis
ABSTRACT: Target proteins in biotechnological applications are highly diverse. Therefore, versatile flexible expression systems for their functional overproduction are required. In order to find the right heterologous gene expression strategy, suitable host-vector systems, which combine different ge...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9329435/ https://www.ncbi.nlm.nih.gov/pubmed/35802157 http://dx.doi.org/10.1007/s00253-022-12062-2 |
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author | Krüger, Anna Welsch, Norma Dürwald, Alexandra Brundiek, Henrike Wardenga, Rainer Piascheck, Henning Mengers, Hendrik G. Krabbe, Jana Beyer, Sandra Kabisch, Johannes F. Popper, Lutz Hübel, Tanno Antranikian, Garabed Schweder, Thomas |
author_facet | Krüger, Anna Welsch, Norma Dürwald, Alexandra Brundiek, Henrike Wardenga, Rainer Piascheck, Henning Mengers, Hendrik G. Krabbe, Jana Beyer, Sandra Kabisch, Johannes F. Popper, Lutz Hübel, Tanno Antranikian, Garabed Schweder, Thomas |
author_sort | Krüger, Anna |
collection | PubMed |
description | ABSTRACT: Target proteins in biotechnological applications are highly diverse. Therefore, versatile flexible expression systems for their functional overproduction are required. In order to find the right heterologous gene expression strategy, suitable host-vector systems, which combine different genetic circuits, are useful. In this study, we designed a novel Bacillus subtilis expression toolbox, which allows the overproduction and secretion of potentially toxic enzymes. This toolbox comprises a set of 60 expression vectors, which combine two promoter variants, four strong secretion signals, a translation-enhancing downstream box, and three plasmid backbones. This B. subtilis toolbox is based on a tailor-made, clean deletion mutant strain, which is protease and sporulation deficient and exhibits reduced autolysis and secondary metabolism. The appropriateness of this alternative expression platform was tested for the overproduction of two difficult-to-produce eukaryotic model proteins. These included the sulfhydryl oxidase Sox from Saccharomyces cerevisiae, which forms reactive hydrogen peroxide and undesired cross-linking of functional proteins, and the human interleukin-1β, a pro-inflammatory cytokine. For the best performing Sox and interleukin, overproducing and secreting variants of these new B. subtilis toolbox fermentation strategies were developed and tested. This study demonstrates the suitability of the prokaryotic B. subtilis host-vector system for the extracellular production of two eukaryotic proteins with biotechnological relevance. KEY POINTS: • Construction of a versatile Bacillus subtilis gene expression toolbox. • Verification of the toolbox by the secretory overproduction of two difficult-to-express proteins. • Fermentation strategy for an acetoin-controlled overproduction of heterologous proteins. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-022-12062-2. |
format | Online Article Text |
id | pubmed-9329435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-93294352022-07-29 A host-vector toolbox for improved secretory protein overproduction in Bacillus subtilis Krüger, Anna Welsch, Norma Dürwald, Alexandra Brundiek, Henrike Wardenga, Rainer Piascheck, Henning Mengers, Hendrik G. Krabbe, Jana Beyer, Sandra Kabisch, Johannes F. Popper, Lutz Hübel, Tanno Antranikian, Garabed Schweder, Thomas Appl Microbiol Biotechnol Applied Genetics and Molecular Biotechnology ABSTRACT: Target proteins in biotechnological applications are highly diverse. Therefore, versatile flexible expression systems for their functional overproduction are required. In order to find the right heterologous gene expression strategy, suitable host-vector systems, which combine different genetic circuits, are useful. In this study, we designed a novel Bacillus subtilis expression toolbox, which allows the overproduction and secretion of potentially toxic enzymes. This toolbox comprises a set of 60 expression vectors, which combine two promoter variants, four strong secretion signals, a translation-enhancing downstream box, and three plasmid backbones. This B. subtilis toolbox is based on a tailor-made, clean deletion mutant strain, which is protease and sporulation deficient and exhibits reduced autolysis and secondary metabolism. The appropriateness of this alternative expression platform was tested for the overproduction of two difficult-to-produce eukaryotic model proteins. These included the sulfhydryl oxidase Sox from Saccharomyces cerevisiae, which forms reactive hydrogen peroxide and undesired cross-linking of functional proteins, and the human interleukin-1β, a pro-inflammatory cytokine. For the best performing Sox and interleukin, overproducing and secreting variants of these new B. subtilis toolbox fermentation strategies were developed and tested. This study demonstrates the suitability of the prokaryotic B. subtilis host-vector system for the extracellular production of two eukaryotic proteins with biotechnological relevance. KEY POINTS: • Construction of a versatile Bacillus subtilis gene expression toolbox. • Verification of the toolbox by the secretory overproduction of two difficult-to-express proteins. • Fermentation strategy for an acetoin-controlled overproduction of heterologous proteins. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-022-12062-2. Springer Berlin Heidelberg 2022-07-08 2022 /pmc/articles/PMC9329435/ /pubmed/35802157 http://dx.doi.org/10.1007/s00253-022-12062-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . |
spellingShingle | Applied Genetics and Molecular Biotechnology Krüger, Anna Welsch, Norma Dürwald, Alexandra Brundiek, Henrike Wardenga, Rainer Piascheck, Henning Mengers, Hendrik G. Krabbe, Jana Beyer, Sandra Kabisch, Johannes F. Popper, Lutz Hübel, Tanno Antranikian, Garabed Schweder, Thomas A host-vector toolbox for improved secretory protein overproduction in Bacillus subtilis |
title | A host-vector toolbox for improved secretory protein overproduction in Bacillus subtilis |
title_full | A host-vector toolbox for improved secretory protein overproduction in Bacillus subtilis |
title_fullStr | A host-vector toolbox for improved secretory protein overproduction in Bacillus subtilis |
title_full_unstemmed | A host-vector toolbox for improved secretory protein overproduction in Bacillus subtilis |
title_short | A host-vector toolbox for improved secretory protein overproduction in Bacillus subtilis |
title_sort | host-vector toolbox for improved secretory protein overproduction in bacillus subtilis |
topic | Applied Genetics and Molecular Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9329435/ https://www.ncbi.nlm.nih.gov/pubmed/35802157 http://dx.doi.org/10.1007/s00253-022-12062-2 |
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