Neelabh, Neha Nidhi Tirkey, Karuna Karuna
In-silico and in-vitro studies on fungal chitinase as a target enzyme for antifungal activity of closantel
Číslo: 5/2017/2018
Periodikum: Journal of Microbiology, Biotechnology and Food Sciences
DOI: 10.15414/jmbfs.2018.7.5.449-453
Klíčová slova: Closantel; Antifungal; In-silico; Chitinase; Minimum inhibitory concentration
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The current work deals with closantel, a veterinary drug targeting chitinase, which is utilized as a therapeutic option against helminths. The fact that chitin is an important constituent of the cell wall of the fungi also and it undergoes regular degradation and remodelling through an enzyme called fungal chitinase motivated the authors to test the efficacy of closantel against fungal chitinase. In the present study Cryptococcus neoformans has been used as a model organism against which the antifungal activity of closantel has been tested.
In-silico studies carried out using PatchDock and FireDock predicted the global energy (binding energy)involved in docking closantel on chitinase as -47.58 Kcal/mol. Further, the results obtained through the in-silico studies were validated by the minimum inhibitory concentration assay (MIC). It was observed that 736 (±7.024) µg/ml of closantel can inhibit the cryptococcal growth by 80% (MIC80).