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Induction of cryptic metabolites of the endophytic fungus Trichocladium sp. through OSMAC and co-cultivation
Authors:Nam Michael Tran-Cong,Attila Má  ndi,Tibor Kurtá  n,Werner E. G. Mü  ller,Rainer Kalscheuer,Wenhan Lin,Zhen Liu,Peter Proksch
Affiliation:Institute of Pharmaceutical Biology and Biotechnology, Heinrich Heine University Düsseldorf, Universitätsstrasse 1, 40225 Düsseldorf Germany.; Department of Organic Chemistry, University of Debrecen, P. O. Box 400 H-4002 Debrecen Hungary ; Institute of Physiological Chemistry, Universitätsmedizin der Johannes Gutenberg-Universität Mainz, 55128 Mainz Germany ; State Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing 100191 China
Abstract:The endophytic fungus Trichocladium sp. isolated from roots of Houttuynia cordata was cultured on solid rice medium, yielding a new amidepsine derivative (1) and a new reduced spiro azaphilone derivative (3) together with eight known compounds (4–11). Co-cultivation of Trichocladium sp. with Bacillus subtilis resulted in induction of a further new compound (2) and a 10-fold increase of 11 compared to the axenic fungal culture. Moreover, when the fungus was cultivated on peas instead of rice, a new sesquiterpene derivative (13) and two known compounds (12 and 14) were obtained. Addition of 2% tryptophan to rice medium led to the isolation of a new bismacrolactone (15). The structures of the new compounds were elucidated by HRESIMS, 1D and 2D NMR as well as by comparison with the literature. A combination of TDDFT-ECD, TDDFT-SOR, DFT-VCD and DFT-NMR calculations were applied to determine the absolute and relative configurations of 13 and 15. Compounds 7, 11 and 15 exhibited strong cytotoxicity against the L5178Y mouse lymphoma cell line with IC50 values of 0.3, 0.5 and 0.2 μM, respectively.

The endophytic fungus Trichocladium sp. isolated from roots of Houttuynia cordata yielded fifteen compounds including five new ones through OSMAC and co-cultivation approaches.
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