Activation studies of the α- and β-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae with amines and amino acids. (1st January 2018)
- Record Type:
- Journal Article
- Title:
- Activation studies of the α- and β-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae with amines and amino acids. (1st January 2018)
- Main Title:
- Activation studies of the α- and β-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae with amines and amino acids
- Authors:
- Angeli, Andrea
Del Prete, Sonia
Osman, Sameh M.
Alasmary, Fatmah A. S.
AlOthman, Zeid
Donald, William A.
Capasso, Clemente
Supuran, Claudiu T. - Abstract:
- Abstract: The α- and β-class carbonic anhydrases (CAs, EC 4.2.1.1) from the pathogenic bacterium Vibrio cholerae, VchCAα, and VchCAβ, were investigated for their activation with natural and non-natural amino acids and amines. The most effective VchCAα activators were L-tyrosine, histamine, serotonin, and 4-aminoethyl-morpholine, which had KA s in the range of 8.21–12.0 µM. The most effective VchCAβ activators were D-tyrosine, dopamine, serotonin, 2-pyridyl-methylamine, 2-aminoethylpyridine, and 2-aminoethylpiperazine, which had KA s in the submicromolar – low micromolar range (0.18–1.37 µM). The two bacterial enzymes had very different activation profiles with these compounds, between each other, and in comparison to the human isoforms hCA I and II. Some amines were selective activators of VchCAβ, including 2-pyridylmethylamine (KA of 180 nm for VchCAβ, and more than 20 µM for VchCAα and hCA I/II). The activation of CAs from bacteria, such as VchCAα/β has not been considered previously for possible biomedical applications. It would be of interest to study in more detail the extent that CA activators are implicated in the virulence and colonisation of the host by such pathogenic bacteria, which for Vibrio cholerae, is highly dependent on the bicarbonate concentration and pH in the surrounding tissue.
- Is Part Of:
- Journal of enzyme inhibition and medicinal chemistry. Volume 33:Number 1(2018)
- Journal:
- Journal of enzyme inhibition and medicinal chemistry
- Issue:
- Volume 33:Number 1(2018)
- Issue Display:
- Volume 33, Issue 1 (2018)
- Year:
- 2018
- Volume:
- 33
- Issue:
- 1
- Issue Sort Value:
- 2018-0033-0001-0000
- Page Start:
- 227
- Page End:
- 233
- Publication Date:
- 2018-01-01
- Subjects:
- Carbonic anhydrase -- metalloenzymes -- pathogens -- activators -- Vibrio cholerae
Enzyme inhibitors -- Periodicals
Enzyme Inhibitors -- periodicals
Biochemistry -- periodicals
572.7 - Journal URLs:
- http://informahealthcare.com/loi/enz ↗
http://informahealthcare.com ↗ - DOI:
- 10.1080/14756366.2017.1412316 ↗
- Languages:
- English
- ISSNs:
- 1475-6366
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4979.465000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11946.xml