Skip to Main Content (Press Enter)

Logo CNR
  • ×
  • Home
  • Persone
  • Pubblicazioni
  • Strutture
  • Competenze

UNI-FIND
Logo CNR

|

UNI-FIND

cnr.it
  • ×
  • Home
  • Persone
  • Pubblicazioni
  • Strutture
  • Competenze
  1. Pubblicazioni

Sulfonamide inhibition studies of the gamma-carbonic anhydrase from the Antarctic bacterium Colwellia psychrerythraea

Articolo
Data di Pubblicazione:
2016
Abstract:
The Antarctic bacterium Colwellia psychrerythraea encodes for a gamma-class carbonic anhydrase (CA, EC 4.2.1.1), which was cloned, purified and characterized. The enzyme (CpsCA gamma) has a moderate catalytic activity for the physiologic reaction of CO2 hydration to bicarbonate and protons, with a k(cat) 6.0 x 10(5) s(-1) and a k(cat)/K-m of 4.7 x 10(6) M-1 s(-1). A series of sulfonamides and a sulfamate were investigated as inhibitors of the new enzyme. The best inhibitor was metanilamide (K-I of 83.5 nM) followed by indisulam, valdecoxib, celecoxib, sulthiame and hydrochlorothiazide (K(I)s ranging between 343 and 491 nM). Acetazolamide, methazolamide as well as other aromatic/heterocyclic derivatives showed inhibition constants between 502 and 7660 nM. The present study may shed some more light regarding the role that gamma-CAs play in the life cycle of psychrophilic bacteria as the Antarctic one investigated here, by allowing the identification of inhibitors which may be useful as pharmacologic tools. (C) 2016 Elsevier Ltd. All rights reserved.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
Carbonic anhydrase; Metalloenzymes; Inhibitors; Sulfonamide; Psychrophiles; Hydratase activity; Antarctic carbonic anhydrase; Cold adaptation; Cold enzymes
Elenco autori:
Carginale, Vincenzo; Capasso, Clemente
Autori di Ateneo:
CAPASSO CLEMENTE
CARGINALE VINCENZO
Link alla scheda completa:
https://iris.cnr.it/handle/20.500.14243/316603
Pubblicato in:
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Journal
  • Utilizzo dei cookie

Realizzato con VIVO | Designed by Cineca | 26.5.0.0 | Sorgente dati: PREPROD (Ribaltamento disabilitato)