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Targeting Polyphosphate Kinases in the Fight against Pseudomonas aeruginosa

Polyphosphate (polyP) is a universally conserved molecule that plays critical roles in managing bacterial stress responses, in addition to biofilm formation and virulence. The enzymes that make polyphosphate molecules are called polyphosphate kinases (PPKs). Since these enzymes are not conserved in...

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Detalles Bibliográficos
Autores principales: Baijal, Kanchi, Downey, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406150/
https://www.ncbi.nlm.nih.gov/pubmed/34340551
http://dx.doi.org/10.1128/mBio.01477-21
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author Baijal, Kanchi
Downey, Michael
author_facet Baijal, Kanchi
Downey, Michael
author_sort Baijal, Kanchi
collection PubMed
description Polyphosphate (polyP) is a universally conserved molecule that plays critical roles in managing bacterial stress responses, in addition to biofilm formation and virulence. The enzymes that make polyphosphate molecules are called polyphosphate kinases (PPKs). Since these enzymes are not conserved in higher eukaryotes, PPKs make excellent therapeutic targets. In a recent paper in mBio, Neville and colleagues described gallein, a commercially available G-protein antagonist, as a novel dual-specificity inhibitor against two families of PPK enzymes in Pseudomonas aeruginosa. In this commentary, we discuss the impact of this discovery, outline potential challenges of implementing gallein use in the clinic, and describe how gallein will serve as a fantastic new tool to further fundamental PPK and polyP research in bacteria.
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spelling pubmed-84061502021-09-09 Targeting Polyphosphate Kinases in the Fight against Pseudomonas aeruginosa Baijal, Kanchi Downey, Michael mBio Commentary Polyphosphate (polyP) is a universally conserved molecule that plays critical roles in managing bacterial stress responses, in addition to biofilm formation and virulence. The enzymes that make polyphosphate molecules are called polyphosphate kinases (PPKs). Since these enzymes are not conserved in higher eukaryotes, PPKs make excellent therapeutic targets. In a recent paper in mBio, Neville and colleagues described gallein, a commercially available G-protein antagonist, as a novel dual-specificity inhibitor against two families of PPK enzymes in Pseudomonas aeruginosa. In this commentary, we discuss the impact of this discovery, outline potential challenges of implementing gallein use in the clinic, and describe how gallein will serve as a fantastic new tool to further fundamental PPK and polyP research in bacteria. American Society for Microbiology 2021-08-03 /pmc/articles/PMC8406150/ /pubmed/34340551 http://dx.doi.org/10.1128/mBio.01477-21 Text en Copyright © 2021 Baijal and Downey. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Commentary
Baijal, Kanchi
Downey, Michael
Targeting Polyphosphate Kinases in the Fight against Pseudomonas aeruginosa
title Targeting Polyphosphate Kinases in the Fight against Pseudomonas aeruginosa
title_full Targeting Polyphosphate Kinases in the Fight against Pseudomonas aeruginosa
title_fullStr Targeting Polyphosphate Kinases in the Fight against Pseudomonas aeruginosa
title_full_unstemmed Targeting Polyphosphate Kinases in the Fight against Pseudomonas aeruginosa
title_short Targeting Polyphosphate Kinases in the Fight against Pseudomonas aeruginosa
title_sort targeting polyphosphate kinases in the fight against pseudomonas aeruginosa
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8406150/
https://www.ncbi.nlm.nih.gov/pubmed/34340551
http://dx.doi.org/10.1128/mBio.01477-21
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