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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...

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Autores principales: Merlo, Rosa, Del Prete, Sonia, Valenti, Anna, Mattossovich, Rosanna, Carginale, Vincenzo, Supuran, Claudiu T., Capasso, Clemente, Perugino, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
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.
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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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