Anion inhibition profiles of α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae

2016 ◽  
Vol 24 (16) ◽  
pp. 3413-3417 ◽  
Author(s):  
Sonia Del Prete ◽  
Daniela Vullo ◽  
Viviana De Luca ◽  
Vincenzo Carginale ◽  
Pietro di Fonzo ◽  
...  
2020 ◽  
Vol 11 (11) ◽  
pp. 2277-2284
Author(s):  
Alessandro Bonardi ◽  
Alessio Nocentini ◽  
Roberta Cadoni ◽  
Sonia del Prete ◽  
Pascal Dumy ◽  
...  

2017 ◽  
Vol 75 ◽  
pp. 170-172 ◽  
Author(s):  
Andrea Angeli ◽  
Ghulam Abbas ◽  
Sonia Del Prete ◽  
Fabrizio Carta ◽  
Clemente Capasso ◽  
...  

2017 ◽  
Vol 33 (1) ◽  
pp. 227-233 ◽  
Author(s):  
Andrea Angeli ◽  
Sonia Del Prete ◽  
Sameh M. Osman ◽  
Fatmah A. S. Alasmary ◽  
Zeid AlOthman ◽  
...  

2016 ◽  
Vol 26 (8) ◽  
pp. 1941-1946 ◽  
Author(s):  
Sonia Del Prete ◽  
Daniela Vullo ◽  
Viviana De Luca ◽  
Vincenzo Carginale ◽  
Sameh M. Osman ◽  
...  

2020 ◽  
Vol 21 (9) ◽  
pp. 3131
Author(s):  
Kübra Demir-Yazıcı ◽  
Özlen Güzel-Akdemir ◽  
Andrea Angeli ◽  
Claudiu T. Supuran ◽  
Atilla Akdemir

Due to the increasing resistance of currently used antimicrobial drugs, there is an urgent problem for the treatment of cholera disease, selective inhibition of the α-class carbonic anhydrases (CA, EC 4.2.1.1) from the pathogenic bacterium Vibrio cholerae (VcCA) presents an alternative therapeutic target. In this study, a series of hydrazone derivatives, carrying the 2-(hydrazinocarbonyl)-3-phenyl-1H-indole-5-sulfonamide scaffold, have been evaluated as inhibitors of the VcCA with molecular modeling studies. The results suggest that these compounds may bind to the active site of VcCA. To verify this, VcCA enzyme inhibition studies were performed and as predicted most of the tested compounds displayed potent inhibitory activities against VcCA with three compounds showing KI values lower than 30 nM. In addition, all these compounds showed selectivity for VcCA and the off-targets hCA I and II.


2020 ◽  
Vol 11 (11) ◽  
pp. 2294-2299
Author(s):  
Francesca Mancuso ◽  
Laura De Luca ◽  
Andrea Angeli ◽  
Emanuela Berrino ◽  
Sonia Del Prete ◽  
...  

2018 ◽  
Vol 77 ◽  
pp. 1-5 ◽  
Author(s):  
Andrea Angeli ◽  
Sonia Del Prete ◽  
William A. Donald ◽  
Clemente Capasso ◽  
Claudiu T. Supuran

1998 ◽  
Vol 180 (19) ◽  
pp. 5256-5259 ◽  
Author(s):  
Karl E. Klose ◽  
Veronica Novik ◽  
John J. Mekalanos

ABSTRACT In the pathogenic bacterium Vibrio cholerae, the alternate sigma factor ς54 is required for expression of multiple sets of genes, including an unidentified gene(s) necessary for enhanced colonization within the host. To identify ς54-dependent transcriptional activators involved in colonization, PCR was performed with V. choleraechromosomal DNA and degenerate primers, revealing six novel and distinct coding sequences with homology to ς54-dependent activators. One sequence had high homology to the luxO gene of V. harveyi, which in that organism is involved in quorum sensing. Phenotypes of V. cholerae strains containing mutations in each of the six putative ς54-dependent activator genes identified one as a probable ntrChomologue. None of the mutant strains exhibited a defect in the ability to colonize infant mice, suggesting the presence of additional ς54-dependent activators not identified by this technique.


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