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An AGT-based protein-tag system for the labelling and surface immobilization of enzymes on E. coli outer membrane
The use of natural systems, such as outer membrane protein A (OmpA), phosphoporin E (PhoE), ice nucleation protein (INP), etc., has been proved very useful for the surface exposure of proteins on the outer membrane of Gram-negative bacteria. These strategies have the clear advantage of unifying in a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6366409/ https://www.ncbi.nlm.nih.gov/pubmed/30724623 http://dx.doi.org/10.1080/14756366.2018.1559161 |
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author | Merlo, Rosa Del Prete, Sonia Valenti, Anna Mattossovich, Rosanna Carginale, Vincenzo Supuran, Claudiu T. Capasso, Clemente Perugino, Giuseppe |
author_facet | Merlo, Rosa Del Prete, Sonia Valenti, Anna Mattossovich, Rosanna Carginale, Vincenzo Supuran, Claudiu T. Capasso, Clemente Perugino, Giuseppe |
author_sort | Merlo, Rosa |
collection | PubMed |
description | The use of natural systems, such as outer membrane protein A (OmpA), phosphoporin E (PhoE), ice nucleation protein (INP), etc., has been proved very useful for the surface exposure of proteins on the outer membrane of Gram-negative bacteria. These strategies have the clear advantage of unifying in a one-step the production, the purification and the in vivo immobilisation of proteins/biocatalysts onto a specific biological support. Here, we introduce the novel Anchoring-and-Self-Labelling-protein-tag (ASL(tag)), which allows the in vivo immobilisation of enzymes on E. coli surface and the labelling of the neosynthesised proteins with the engineered alkylguanine-DNA-alkyl-transferase (H(5)) from Sulfolobus solfataricus. Our results demonstrated that this tag enhanced the overexpression of thermostable enzymes, such as the carbonic anhydrase (SspCA) from Sulfurihydrogenibium yellowstonense and the β-glycoside hydrolase (SsβGly) from S. solfataricus, without affecting their folding and catalytic activity, proposing a new tool for the improvement in the utilisation of biocatalysts of biotechnological interest. |
format | Online Article Text |
id | pubmed-6366409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-63664092019-02-15 An AGT-based protein-tag system for the labelling and surface immobilization of enzymes on E. coli outer membrane Merlo, Rosa Del Prete, Sonia Valenti, Anna Mattossovich, Rosanna Carginale, Vincenzo Supuran, Claudiu T. Capasso, Clemente Perugino, Giuseppe J Enzyme Inhib Med Chem Research Paper The use of natural systems, such as outer membrane protein A (OmpA), phosphoporin E (PhoE), ice nucleation protein (INP), etc., has been proved very useful for the surface exposure of proteins on the outer membrane of Gram-negative bacteria. These strategies have the clear advantage of unifying in a one-step the production, the purification and the in vivo immobilisation of proteins/biocatalysts onto a specific biological support. Here, we introduce the novel Anchoring-and-Self-Labelling-protein-tag (ASL(tag)), which allows the in vivo immobilisation of enzymes on E. coli surface and the labelling of the neosynthesised proteins with the engineered alkylguanine-DNA-alkyl-transferase (H(5)) from Sulfolobus solfataricus. Our results demonstrated that this tag enhanced the overexpression of thermostable enzymes, such as the carbonic anhydrase (SspCA) from Sulfurihydrogenibium yellowstonense and the β-glycoside hydrolase (SsβGly) from S. solfataricus, without affecting their folding and catalytic activity, proposing a new tool for the improvement in the utilisation of biocatalysts of biotechnological interest. Taylor & Francis 2019-02-06 /pmc/articles/PMC6366409/ /pubmed/30724623 http://dx.doi.org/10.1080/14756366.2018.1559161 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Merlo, Rosa Del Prete, Sonia Valenti, Anna Mattossovich, Rosanna Carginale, Vincenzo Supuran, Claudiu T. Capasso, Clemente Perugino, Giuseppe An AGT-based protein-tag system for the labelling and surface immobilization of enzymes on E. coli outer membrane |
title | An AGT-based protein-tag system for the labelling and surface immobilization of enzymes on E. coli outer membrane |
title_full | An AGT-based protein-tag system for the labelling and surface immobilization of enzymes on E. coli outer membrane |
title_fullStr | An AGT-based protein-tag system for the labelling and surface immobilization of enzymes on E. coli outer membrane |
title_full_unstemmed | An AGT-based protein-tag system for the labelling and surface immobilization of enzymes on E. coli outer membrane |
title_short | An AGT-based protein-tag system for the labelling and surface immobilization of enzymes on E. coli outer membrane |
title_sort | agt-based protein-tag system for the labelling and surface immobilization of enzymes on e. coli outer membrane |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6366409/ https://www.ncbi.nlm.nih.gov/pubmed/30724623 http://dx.doi.org/10.1080/14756366.2018.1559161 |
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