Cholinesterase Inhibitors from an Endophytic Fungus Aspergillus niveus Fv-er401: Metabolomics, Isolation and Molecular Docking

Alzheimer's disease poses a global health concern with unmet demand requiring creative approaches to discover new medications. In this study, we investigated the chemical composition and the anticholinesterase activity of Aspergillus niveus Fv-er401 isolated from Foeniculum vulgare (Apiaceae) roots. Fifty-eight metabolites were identified using UHPLC-MS/MS analysis of the crude extract. The fungal extract showed acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) inhibitory effects with IC50 53.44 +/- 1.57 and 48.46 +/- 0.41 mu g/mL, respectively. Two known metabolites were isolated, terrequinone A and citrinin, showing moderate AChE and BuChE inhibitory activity using the Ellman's method (IC50 = 11.10 +/- 0.38 mu g/mL and 5.06 +/- 0.15 mu g/mL, respectively for AChE, and IC50 15.63 +/- 1.27 mu g/mL and 8.02 +/- 0.08 mu g/mL, respectively for BuChE). As evidenced by molecular docking, the isolated compounds and other structurally related metabolites identified by molecular networking had the required structural features for AChE and BuChE inhibition. Where varioxiranol G (-9.76 and -10.36 kcal/mol), penicitrinol B (-9.50 and -8.02 kcal/mol), dicitrinol A (-8.53 and -7.98 kcal/mol) and asterriquinone CT5 (-8.02 and -8.25 kcal/mol) showed better binding scores as AChE and BuChE inhibitors than the co-crystallized inhibitor (between -7.89 and 7.82 kcal/mol) making them promising candidates for the development of new drugs to treat Alzheimer's.

Automated summary

This study isolated a fungus named Aspergillus niveus Fv-er401 from the roots of Foeniculum vulgare (Apiaceae) and investigated its chemical composition and anticholinesterase activity. The results showed that the fungal extract had inhibitory effects on acetylcholinesterase and butyrylcholinesterase. Molecular docking experiments further demonstrated that some of the identified compounds exhibited promising activity as potential inhibitors of these enzymes.