4.4 Article

Divulging the anti-acetylcholinesterase activity of Colletotrichum lentis strain KU1 extract as sustainable AChE active site inhibitors

Journal

ARCHIVES OF MICROBIOLOGY
Volume 204, Issue 12, Pages -

Publisher

SPRINGER
DOI: 10.1007/s00203-022-03288-9

Keywords

Acetylcholinesterase inhibitor; Endophytic fungi; Colletotrichum lentis strain KU1; In silico

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This study focuses on screening endophytic fungi for the production of active acetylcholinesterase inhibitors. Three isolates were found to inhibit AChE inhibitory activity and were identified as 9-hexadecen-1-ol and erucamide. Computational studies revealed that these compounds have significant activity in inhibiting AD.
Alzheimer's disease (AD), also called senile dementia is a neurodegenerative disease seen commonly in the elderly and is characterised by the formation of beta-amyloid plaques and neurofibrillary tangles (NFT). Though a complete understanding of the disease is lacking, recent studies showed the role of the enzyme acetylcholinesterase (AChE) in pathogenesis. Finding new lead compounds from natural sources has always been a quest for researchers. Endophytic fungi are a set of microbes that reside within plants without causing any harm. This study focuses on screening endophytes for the production of active acetylcholinesterase inhibitors. Five endophytic fungi were isolated from Catharanthus roseus and screened for AChE inhibitory activity. Three isolates were found to inhibit AChE inhibitory activity and were distinguished based on molecular and microscopic methods. The mycelial extract was taken for the bioassay-guided column chromatography and TLC was performed on the active fraction. The GC-MS and NMR analysis identified the active compounds in the extract as 9-hexadecen-1-ol and erucamide. Molecular docking studies revealed that the compounds are thermodynamically feasible and have significant glide scores. Computational studies revealed that the hydroxyl group of 9-hexadecen-1-ol forms a hydrogen bond with Ser 293 in the active site of AChE, whereas the active site interactions were predominantly hydrophobic in the case of erucamide and are reflected in AChE inhibition assays.

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