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A novel bi-directional promoter system allows tunable recombinant protein production in Pichia pastoris

BACKGROUND: The methylotrophic yeast Pichia pastoris is a well-studied host organism for recombinant protein production, which is usually regulated either by a constitutive promoter (e.g. promoter of glyceraldehyde-3-phosphate dehydrogenase; P(GAP)) or an inducible promoter (e.g. promoter of alcohol...

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Autores principales: Rajamanickam, Vignesh, Metzger, Karl, Schmid, Christian, Spadiut, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598003/
https://www.ncbi.nlm.nih.gov/pubmed/28903770
http://dx.doi.org/10.1186/s12934-017-0768-8
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author Rajamanickam, Vignesh
Metzger, Karl
Schmid, Christian
Spadiut, Oliver
author_facet Rajamanickam, Vignesh
Metzger, Karl
Schmid, Christian
Spadiut, Oliver
author_sort Rajamanickam, Vignesh
collection PubMed
description BACKGROUND: The methylotrophic yeast Pichia pastoris is a well-studied host organism for recombinant protein production, which is usually regulated either by a constitutive promoter (e.g. promoter of glyceraldehyde-3-phosphate dehydrogenase; P(GAP)) or an inducible promoter (e.g. promoter of alcohol oxidase 1; P(AOX1)). Both promoter systems have several advantages and disadvantages; with one of the main disadvantages being their lack of tunability. Various novel promoter systems, which are either inducible or de-repressed, allowing higher degrees of freedom, have been reported. Recently, bi-directional promoter systems in P. pastoris with two promoter systems regulating recombinant expression of one or more genes were developed. In this study, we introduce a novel bi-directional promoter system combining a modified catalase promoter system (P(DC); derepressible and inducible) and the traditional P(AOX1), allowing tunable recombinant protein production. RESULTS: We characterized a recombinant P. pastoris strain, carrying the novel bi-directional promoter system, during growth and production in three dynamic bioreactor cultivations. We cloned the model enzyme cellobiohydralase downstream of either promoter and applied different feeding strategies to determine the physiological boundaries of the strain. We succeeded in demonstrating tunability of recombinant protein production solely in response to the different feeding strategies and identified a mixed feed regime allowing highest productivity. CONCLUSION: In this feasibility study, we present the first controlled bioreactor experiments with a recombinant P. pastoris strain carrying a novel bi-directional promotor combination of a catalase promoter variant (P(DC)) and the traditional P(AOX1). We demonstrated that this bi-directional promoter system allows tunable recombinant protein expression only in response to the available C-sources. This bi-directional promoter system offers a high degree of freedom for bioprocess design and development, making bi-directional promoters in P. pastoris highly attractive for recombinant protein production.
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spelling pubmed-55980032017-09-18 A novel bi-directional promoter system allows tunable recombinant protein production in Pichia pastoris Rajamanickam, Vignesh Metzger, Karl Schmid, Christian Spadiut, Oliver Microb Cell Fact Technical Notes BACKGROUND: The methylotrophic yeast Pichia pastoris is a well-studied host organism for recombinant protein production, which is usually regulated either by a constitutive promoter (e.g. promoter of glyceraldehyde-3-phosphate dehydrogenase; P(GAP)) or an inducible promoter (e.g. promoter of alcohol oxidase 1; P(AOX1)). Both promoter systems have several advantages and disadvantages; with one of the main disadvantages being their lack of tunability. Various novel promoter systems, which are either inducible or de-repressed, allowing higher degrees of freedom, have been reported. Recently, bi-directional promoter systems in P. pastoris with two promoter systems regulating recombinant expression of one or more genes were developed. In this study, we introduce a novel bi-directional promoter system combining a modified catalase promoter system (P(DC); derepressible and inducible) and the traditional P(AOX1), allowing tunable recombinant protein production. RESULTS: We characterized a recombinant P. pastoris strain, carrying the novel bi-directional promoter system, during growth and production in three dynamic bioreactor cultivations. We cloned the model enzyme cellobiohydralase downstream of either promoter and applied different feeding strategies to determine the physiological boundaries of the strain. We succeeded in demonstrating tunability of recombinant protein production solely in response to the different feeding strategies and identified a mixed feed regime allowing highest productivity. CONCLUSION: In this feasibility study, we present the first controlled bioreactor experiments with a recombinant P. pastoris strain carrying a novel bi-directional promotor combination of a catalase promoter variant (P(DC)) and the traditional P(AOX1). We demonstrated that this bi-directional promoter system allows tunable recombinant protein expression only in response to the available C-sources. This bi-directional promoter system offers a high degree of freedom for bioprocess design and development, making bi-directional promoters in P. pastoris highly attractive for recombinant protein production. BioMed Central 2017-09-13 /pmc/articles/PMC5598003/ /pubmed/28903770 http://dx.doi.org/10.1186/s12934-017-0768-8 Text en © The Author(s) 2017 Open AccessThis 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Technical Notes
Rajamanickam, Vignesh
Metzger, Karl
Schmid, Christian
Spadiut, Oliver
A novel bi-directional promoter system allows tunable recombinant protein production in Pichia pastoris
title A novel bi-directional promoter system allows tunable recombinant protein production in Pichia pastoris
title_full A novel bi-directional promoter system allows tunable recombinant protein production in Pichia pastoris
title_fullStr A novel bi-directional promoter system allows tunable recombinant protein production in Pichia pastoris
title_full_unstemmed A novel bi-directional promoter system allows tunable recombinant protein production in Pichia pastoris
title_short A novel bi-directional promoter system allows tunable recombinant protein production in Pichia pastoris
title_sort novel bi-directional promoter system allows tunable recombinant protein production in pichia pastoris
topic Technical Notes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598003/
https://www.ncbi.nlm.nih.gov/pubmed/28903770
http://dx.doi.org/10.1186/s12934-017-0768-8
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