De novo design of non-coordinating indolones as potential inhibitors for lanosterol 14-α-demethylase (CYP51).

The development of antifungal drugs that inhibit lanosterol 14-α-demethylase (CYP51) via non-covalent ligand interactions is a strategy that is gaining importance. A series of novel tetraindol-4-one derivatives with 1- and 2-(2,4-substituted phenyl) side chains were designed and synthesized based on the structure of CYP51 and fluconazole. The antifungal activities of these derivatives against eight human pathogenic filamentous fungi and yeast strains were evaluated in vitro by measuring the minimal inhibitory concentrations.

Biosorption of Mercury (II) from Aqueous Solutions onto Fungal Biomass.

The biosorption of mercury (II) on 14 fungal biomasses, Aspergillus flavus I-V, Aspergillus fumigatus I-II, Helminthosporium sp., Cladosporium sp., Mucor rouxii mutant, M.

Partial purification and biochemical characterization of a soluble alpha-glucosidase II-like activity from Candida albicans.

A soluble alpha-glucosidase was partially purified from Candida albicans cells by a three-step procedure consisting of size-exclusion, ion-exchange and adsorption chromatographies. After the last step, enzyme was enriched about 8.7-fold with a yield of 13% over the starting material and analysis of the purified preparation revealed two major polypeptides of 36 and 47 kDa.