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• W4289766494 abstract "Abstract Fungal infections are more predominant in agricultural and clinical fields. Aspergillosis caused by Aspergillus fumigatus leads to respiratory failure in patients along with various illnesses. Due to the limitation of antifungal therapy and antifungal drugs, there is an emergence to develop efficient antifungal compounds (AFCs) from natural sources to cure and prevent fungal infections. The present study deals with the investigation of the mechanism of the active compounds from Aspergillus giganteus against aspergillosis. Primarily, the bioavailability and toxicological properties of antifungal proteins such as, sarcin, thionin, chitinase and their derivatives have proved the efficiency of pharmacokinetic properties of selected compounds. Molecular interactions of selected compounds from A. giganteus with the virulence proteins of A. fumigatus (UDP-N-acetylglucosamine pyrophosphorylase, N-myristoyl transferase and Chitinase) have exhibited a good glide score and druggable nature of the AFCs. The antagonistic potential of AFCs on the pathogen was confirmed by SEM analysis where the shrunken and damaged spores of AFCs treated pathogen were observed. The integrity of A. fumigatus cell membrane and nuclear membrane treated with AFCs were analyzed by determining the release of cellular materials. The effective concentration of AFCs was found to be 250 µg/ml (P&lt;0.0001). The GC-MS profiling has revealed the volatile bioactive metabolites present in A. giganteus. Further, interaction studies might provide more information on the synergism activity with the non-volatile metabolites which leads to the development of novel drugs for the treatment of aspergillosis." @default.
• W4289766494 created "2022-08-04" @default.
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• W4289766494 date "2022-09-01" @default.
• W4289766494 modified "2023-10-01" @default.
• W4289766494 title "Pharmacokinetic profile of sarcin and thionin from <i>Aspergillus giganteus</i> and <i>in vitro</i> validation against human fungal pathogen" @default.
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• W4289766494 doi "https://doi.org/10.1042/bsr20220229" @default.
• W4289766494 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35924795" @default.
• W4289766494 hasPublicationYear "2022" @default.
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