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Biosensor-guided rapid screening for improved recombinant protein secretion in Pichia pastoris

Pichia pastoris (Komagataella phaffii) is widely used for industrial production of heterologous proteins due to high secretory capabilities but selection of highly productive engineered strains remains a limiting step. Despite availability of a comprehensive molecular toolbox for construct design an...

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Autores principales: Navone, Laura, Moffitt, Kaylee, Behrendorff, James, Sadowski, Pawel, Hartley, Carol, Speight, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155391/
https://www.ncbi.nlm.nih.gov/pubmed/37138331
http://dx.doi.org/10.1186/s12934-023-02089-z
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author Navone, Laura
Moffitt, Kaylee
Behrendorff, James
Sadowski, Pawel
Hartley, Carol
Speight, Robert
author_facet Navone, Laura
Moffitt, Kaylee
Behrendorff, James
Sadowski, Pawel
Hartley, Carol
Speight, Robert
author_sort Navone, Laura
collection PubMed
description Pichia pastoris (Komagataella phaffii) is widely used for industrial production of heterologous proteins due to high secretory capabilities but selection of highly productive engineered strains remains a limiting step. Despite availability of a comprehensive molecular toolbox for construct design and gene integration, there is high clonal variability among transformants due to frequent multi-copy and off-target random integration. Therefore, functional screening of several hundreds of transformant clones is essential to identify the best protein production strains. Screening methods are commonly based on deep-well plate cultures with analysis by immunoblotting or enzyme activity assays of post-induction samples, and each heterologous protein produced may require development of bespoke assays with multiple sample processing steps. In this work, we developed a generic system based on a P. pastoris strain that uses a protein-based biosensor to identify highly productive protein secretion clones from a heterogeneous set of transformants. The biosensor uses a split green fluorescent protein where the large GFP fragment (GFP1-10) is fused to a sequence-specific protease from Tobacco Etch Virus (TEV) and is targeted to the endoplasmic reticulum. Recombinant proteins targeted for secretion are tagged with the small fragment of the split GFP (GFP11). Recombinant protein production can be measured by monitoring GFP fluorescence, which is dependent on interaction between the large and small GFP fragments. The reconstituted GFP is cleaved from the target protein by TEV protease, allowing for secretion of the untagged protein of interest and intracellular retention of the mature GFP. We demonstrate this technology with four recombinant proteins (phytase, laccase, β-casein and β-lactoglobulin) and show that the biosensor directly reports protein production levels that correlate with traditional assays. Our results confirm that the split GFP biosensor can be used for facile, generic, and rapid screening of P. pastoris clones to identify those with the highest production levels. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-023-02089-z.
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spelling pubmed-101553912023-05-04 Biosensor-guided rapid screening for improved recombinant protein secretion in Pichia pastoris Navone, Laura Moffitt, Kaylee Behrendorff, James Sadowski, Pawel Hartley, Carol Speight, Robert Microb Cell Fact Research Pichia pastoris (Komagataella phaffii) is widely used for industrial production of heterologous proteins due to high secretory capabilities but selection of highly productive engineered strains remains a limiting step. Despite availability of a comprehensive molecular toolbox for construct design and gene integration, there is high clonal variability among transformants due to frequent multi-copy and off-target random integration. Therefore, functional screening of several hundreds of transformant clones is essential to identify the best protein production strains. Screening methods are commonly based on deep-well plate cultures with analysis by immunoblotting or enzyme activity assays of post-induction samples, and each heterologous protein produced may require development of bespoke assays with multiple sample processing steps. In this work, we developed a generic system based on a P. pastoris strain that uses a protein-based biosensor to identify highly productive protein secretion clones from a heterogeneous set of transformants. The biosensor uses a split green fluorescent protein where the large GFP fragment (GFP1-10) is fused to a sequence-specific protease from Tobacco Etch Virus (TEV) and is targeted to the endoplasmic reticulum. Recombinant proteins targeted for secretion are tagged with the small fragment of the split GFP (GFP11). Recombinant protein production can be measured by monitoring GFP fluorescence, which is dependent on interaction between the large and small GFP fragments. The reconstituted GFP is cleaved from the target protein by TEV protease, allowing for secretion of the untagged protein of interest and intracellular retention of the mature GFP. We demonstrate this technology with four recombinant proteins (phytase, laccase, β-casein and β-lactoglobulin) and show that the biosensor directly reports protein production levels that correlate with traditional assays. Our results confirm that the split GFP biosensor can be used for facile, generic, and rapid screening of P. pastoris clones to identify those with the highest production levels. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-023-02089-z. BioMed Central 2023-05-03 /pmc/articles/PMC10155391/ /pubmed/37138331 http://dx.doi.org/10.1186/s12934-023-02089-z Text en © The Author(s) 2023 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/) . 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
Navone, Laura
Moffitt, Kaylee
Behrendorff, James
Sadowski, Pawel
Hartley, Carol
Speight, Robert
Biosensor-guided rapid screening for improved recombinant protein secretion in Pichia pastoris
title Biosensor-guided rapid screening for improved recombinant protein secretion in Pichia pastoris
title_full Biosensor-guided rapid screening for improved recombinant protein secretion in Pichia pastoris
title_fullStr Biosensor-guided rapid screening for improved recombinant protein secretion in Pichia pastoris
title_full_unstemmed Biosensor-guided rapid screening for improved recombinant protein secretion in Pichia pastoris
title_short Biosensor-guided rapid screening for improved recombinant protein secretion in Pichia pastoris
title_sort biosensor-guided rapid screening for improved recombinant protein secretion in pichia pastoris
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155391/
https://www.ncbi.nlm.nih.gov/pubmed/37138331
http://dx.doi.org/10.1186/s12934-023-02089-z
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