Diverse polyketides and alkaloids from Penicillium sp. KHMM: structural elucidation, biological and molecular docking studies

Author:

Hamed Abdelaaty12,Ismail Mohamed13,El-Metwally Mohammad M.4,Frese Marcel1,Ibrahim Tarek M.A.2,El-Haddad Atef F.2,Sewald Norbert1,Shaaban Mohamed15ORCID

Affiliation:

1. Organic and Bioorganic Chemistry, Department of Chemistry , Bielefeld University , Universitätsstraße 25 , D-33501 Bielefeld , Germany

2. Chemistry Department, Faculty of Science , Al-Azhar University , Nasr City-Cairo 11884 , Egypt

3. Microbiology Department, Faculty of Science , Helwan University , Helwan-Cairo , Egypt

4. Botany and Microbiology Department, Faculty of Science , Damanhour University , Damanhour , Egypt

5. Chemistry of Natural Compounds Department, Pharmaceutical and Drug Industries Research Division , National Research Centre , El-Behoos St. 33 , Dokki-Cairo 12622 , Egypt

Abstract

Abstract As a continuation of our earlier research concerning the investigation of microbial bioactive secondary metabolites from the terrestrial Penicillium sp.KH Link 1809 isolate KHMM, the fungus was re-cultivated on a large scale to explore its bioactive compounds intensively. Fifteen compounds, including seven alkaloids (1–7), one sesquiterpene (8), an acetylenic system (9), two sterols, and sphengolipid, were identified. Their structures were established on the bases of extensive one- and two-dimensional nuclear magnetic resonance and mass measurements, and by comparison with literature data. The antimicrobial activity of the fungal extract and the corresponding compounds were studied using a panel of pathogenic microorganisms, and their in vitro cytotoxicity against the human cervix carcinoma cell line (KB-3-1) was reported as well. The molecular docking of the isolated compounds showed promising affinities for the alkaloidal compounds 46 towards α, β tubulins.

Publisher

Walter de Gruyter GmbH

Subject

General Biochemistry, Genetics and Molecular Biology

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