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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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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. |
format | Online Article Text |
id | pubmed-5617987 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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