Literature DB >> 23414807

Anion inhibition studies of the α-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae.

Daniela Vullo1, Semra Isik, Sonia Del Prete, Viviana De Luca, Vincenzo Carginale, Andrea Scozzafava, Claudiu T Supuran, Clemente Capasso.   

Abstract

An α-carbonic anhydrase (CA, EC 4.2.1.1) has been recently cloned and characterized in the human pathogenic bacterium Vibrio cholerae, denominated VchCA (Del Prete et al. J. Med. Chem.2012, 55, 10742). This enzyme shows a good catalytic activity for the CO2 hydration reaction, comparable to that of the human (h) isoform hCA I. Many inorganic anions and several small molecules were investigated as VchCA inhibitors. Inorganic anions such as cyanate, cyanide, hydrogen sulfide, hydrogen sulfite, and trithiocarbonate were effective VchCA inhibitors with inhibition constants in the range of 33-88μM. Other effective inhibitors were diethyldithiocarbamate, sulfamide, sulfamate, phenylboronic acid and phenylarsonic acid, with KIs of 7-43μM. Halides (bromide, iodide), bicarbonate and carbonate were much less effective VchCA inhibitors, with KIs in the range of 4.64-28.0mM. The resistance of VchCA to bicarbonate inhibition may represent an evolutionary adaptation of this enzyme to living in an environment rich in this ion, such as the gastrointestinal tract, as bicarbonate is a virulence enhancer of this bacterium.
Copyright © 2013 Elsevier Ltd. All rights reserved.

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Year:  2013        PMID: 23414807     DOI: 10.1016/j.bmcl.2013.01.084

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  6 in total

1.  Activity and anion inhibition studies of the α-carbonic anhydrase from Thiomicrospira crunogena XCL-2 Gammaproteobacterium.

Authors:  Brian P Mahon; Natalia A Díaz-Torres; Melissa A Pinard; Chingkuang Tu; David N Silverman; Kathleen M Scott; Robert McKenna
Journal:  Bioorg Med Chem Lett       Date:  2015-05-06       Impact factor: 2.823

Review 2.  Carbonic Anhydrase from Porphyromonas Gingivalis as a Drug Target.

Authors:  Claudiu T Supuran; Clemente Capasso
Journal:  Pathogens       Date:  2017-07-15

3.  Activation studies of the α- and β-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae with amines and amino acids.

Authors:  Andrea Angeli; Sonia Del Prete; Sameh M Osman; Fatmah A S Alasmary; Zeid AlOthman; William A Donald; Clemente Capasso; Claudiu T Supuran
Journal:  J Enzyme Inhib Med Chem       Date:  2018-12       Impact factor: 5.051

4.  Phaeodactylum tricornutum as a model organism for testing the membrane penetrability of sulphonamide carbonic anhydrase inhibitors.

Authors:  Alessandra Rogato; Sonia Del Prete; Alessio Nocentini; Vincenzo Carginale; Claudiu T Supuran; Clemente Capasso
Journal:  J Enzyme Inhib Med Chem       Date:  2019-12       Impact factor: 5.051

5.  Inhibition of α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae with aromatic sulphonamides and clinically licenced drugs - a joint docking/molecular dynamics study.

Authors:  Alessandro Bonardi; Alessio Nocentini; Sameh Mohamed Osman; Fatmah Ali Alasmary; Tahani Mazyad Almutairi; Dalal Saied Abdullah; Paola Gratteri; Claudiu T Supuran
Journal:  J Enzyme Inhib Med Chem       Date:  2021-12       Impact factor: 5.051

6.  Pyrazolo[4,3-c]pyridine Sulfonamides as Carbonic Anhydrase Inhibitors: Synthesis, Biological and In Silico Studies.

Authors:  Andrea Angeli; Victor Kartsev; Anthi Petrou; Boris Lichitsky; Andrey Komogortsev; Mariana Pinteala; Athina Geronikaki; Claudiu T Supuran
Journal:  Pharmaceuticals (Basel)       Date:  2022-03-07
  6 in total

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