Induction of Secondary Metabolites from the Marine-Derived Fungus Aspergillus versicolor through Co-cultivation with Bacillus subtilis

Author:

Abdel-Wahab Nada12,Scharf Sebastian1,Özkaya Ferhat1,Kurtán Tibor3,Mándi Attila3,Fouad Mostafa2,Kamel Mohamed24,Müller Werner5,Kalscheuer Rainer1,Lin Wenhan6,Daletos Georgios1,Ebrahim Weaam17,Liu Zhen1,Proksch Peter1

Affiliation:

1. Institut für Pharmazeutische Biologie und Biotechnologie, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany

2. Department of Pharmacognosy, Faculty of Pharmacy, Minia University, Minia, Egypt

3. Department of Organic Chemistry, University of Debrecen, Debrecen, Hungary

4. Department of Pharmacognosy, Faculty of Pharmacy, Deraya University, New Minia, Egypt

5. Institut für Physiologische Chemie, Universitätsmedizin der Johannes-Gutenberg-Universität Mainz, Mainz, Germany

6. State Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing, China

7. Department of Pharmacognosy, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt

Abstract

AbstractA new cyclic pentapeptide, cotteslosin C (1), a new aflaquinolone, 22-epi-aflaquinolone B (3), and two new anthraquinones (9 and 10), along with thirty known compounds (2, 4 – 8, 11 – 34) were isolated from a co-culture of the sponge-associated fungus Aspergillus versicolor with Bacillus subtilis. The new metabolites were only detected in the co-culture extract, but not when the fungus was grown under axenic conditions. Furthermore, the co-culture extract exhibited an enhanced accumulation of the known constituents versicolorin B (14), averufin (16), and sterigmatocyctin (19) by factors of 1.5, 2.0, and 4.7, respectively, compared to the axenic fungal culture. The structures of the isolated compounds were elucidated on the basis of 1D and 2D NMR spectra and mass spectrometry as well as by comparison with literature data. The absolute configuration of compounds 3, 9, and 10 was determined by ECD (electronic circular dichroism) analysis aided by TDDFT-ECD (time-dependent density functional theory electronic circular dichroism) calculations. Compounds 15, 18 – 21, and 26 exhibited strong to moderate cytotoxic activity against the mouse lymphoma cell line L5178Y, with IC50 values ranging from 2.0 to 21.2 µM, while compounds 14, 16, 31, 32, and 33 displayed moderate inhibitory activities against several gram-positive bacteria, with MIC values ranging from 12.5 to 50 µM.

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry

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