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Carbonic Anhydrase from Porphyromonas Gingivalis as a Drug Target

Periodontitis originates from a microbial synergy causing the development of a mouth microbial imbalance (dysbiosis), consisting of a microbial community composed of anaerobic bacteria. Most studies concerning the treatment of periodontitis have primarily take into account the Gram-negative bacteriu...

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Autores principales: Supuran, Claudiu T., Capasso, Clemente
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617987/
https://www.ncbi.nlm.nih.gov/pubmed/28714894
http://dx.doi.org/10.3390/pathogens6030030
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author Supuran, Claudiu T.
Capasso, Clemente
author_facet Supuran, Claudiu T.
Capasso, Clemente
author_sort Supuran, Claudiu T.
collection PubMed
description Periodontitis originates from a microbial synergy causing the development of a mouth microbial imbalance (dysbiosis), consisting of a microbial community composed of anaerobic bacteria. Most studies concerning the treatment of periodontitis have primarily take into account the Gram-negative bacterium Porphyromonas gingivalis, because it is a prominent component of the oral microbiome and a successful colonizer of the oral epithelium. Here, we focus our attention on the study of the carbonic anhydrases (CAs, EC 4.2.1.1) encoded in the genome of this pathogen as a possible drug target. Carbonic anhydrases are a superfamily of metalloenzymes, which catalyze the simple but physiologically crucial reaction of carbon dioxide hydration to bicarbonate and protons. Bacterial CAs have attracted significant attention for affecting the survival, invasion, and pathogenicity of many microorganisms. The P. gingivalis genome encodes for two CAs belonging to β-CA (PgiCAβ) and γ-CA (PgiCAγ) families. These two enzymes were cloned, heterologously expressed in Escherichia coli, and purified to homogeneity. Moreover, they were subject to extensive inhibition studies using the classical CA inhibitors (sulfonamides and anions) with the aim of identifying selective inhibitors of PgiCAβ and PgiCAγ to be used as pharmacological tools for P. gingivalis eradication.
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spelling pubmed-56179872017-09-30 Carbonic Anhydrase from Porphyromonas Gingivalis as a Drug Target Supuran, Claudiu T. Capasso, Clemente Pathogens Review Periodontitis originates from a microbial synergy causing the development of a mouth microbial imbalance (dysbiosis), consisting of a microbial community composed of anaerobic bacteria. Most studies concerning the treatment of periodontitis have primarily take into account the Gram-negative bacterium Porphyromonas gingivalis, because it is a prominent component of the oral microbiome and a successful colonizer of the oral epithelium. Here, we focus our attention on the study of the carbonic anhydrases (CAs, EC 4.2.1.1) encoded in the genome of this pathogen as a possible drug target. Carbonic anhydrases are a superfamily of metalloenzymes, which catalyze the simple but physiologically crucial reaction of carbon dioxide hydration to bicarbonate and protons. Bacterial CAs have attracted significant attention for affecting the survival, invasion, and pathogenicity of many microorganisms. The P. gingivalis genome encodes for two CAs belonging to β-CA (PgiCAβ) and γ-CA (PgiCAγ) families. These two enzymes were cloned, heterologously expressed in Escherichia coli, and purified to homogeneity. Moreover, they were subject to extensive inhibition studies using the classical CA inhibitors (sulfonamides and anions) with the aim of identifying selective inhibitors of PgiCAβ and PgiCAγ to be used as pharmacological tools for P. gingivalis eradication. MDPI 2017-07-15 /pmc/articles/PMC5617987/ /pubmed/28714894 http://dx.doi.org/10.3390/pathogens6030030 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Supuran, Claudiu T.
Capasso, Clemente
Carbonic Anhydrase from Porphyromonas Gingivalis as a Drug Target
title Carbonic Anhydrase from Porphyromonas Gingivalis as a Drug Target
title_full Carbonic Anhydrase from Porphyromonas Gingivalis as a Drug Target
title_fullStr Carbonic Anhydrase from Porphyromonas Gingivalis as a Drug Target
title_full_unstemmed Carbonic Anhydrase from Porphyromonas Gingivalis as a Drug Target
title_short Carbonic Anhydrase from Porphyromonas Gingivalis as a Drug Target
title_sort carbonic anhydrase from porphyromonas gingivalis as a drug target
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617987/
https://www.ncbi.nlm.nih.gov/pubmed/28714894
http://dx.doi.org/10.3390/pathogens6030030
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