Bio-Activity and Dereplication-Based Discovery of Ophiobolins and Other Fungal Secondary Metabolites Targeting Leukemia Cells

Molecules

Tanja Thorskov Bladt²  Claudia Dürr³  Peter Boldsen Knudsen²  Sara Kildgaard²  Jens Christian Frisvad²  Charlotte Held Gotfredsen¹  Martina Seiffert³ 

[1]Department of Chemistry, Technical University of Denmark, Kemitorvet, Building 201, Kgs. Lyngby DK-2800, Denmark

[2] E-Mail:

[3]Department of Systems Biology, Technical University of Denmark, Søltofts Plads, Building 221, Kgs. Lyngby DK-2800, Denmark

[4] E-Mails:

[5]German Cancer Research Center, Molecular Genetics, Im Neuenheimer Feld 280, Heidelberg D-69120, Germany

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关键词: natural products;    ophiobolin U;    dereplication;    explorative solid phase extraction (E-SPE);    filamentous fungi;    cytotoxic;    cancer;    leukemia;   

DOI  :  10.3390/molecules181214629

来源: mdpi

【 摘 要 】

The purpose of this study was to identify and characterize fungal natural products (NPs) with in vitro bioactivity towards leukemia cells. We based our screening on a combined analytical and bio-guided approach of LC-DAD-HRMS dereplication, explorative solid-phase extraction (E-SPE), and a co-culture platform of CLL and stromal cells. A total of 289 fungal extracts were screened and we tracked the activity to single compounds in seven of the most active extracts. The novel ophiobolin U was isolated together with the known ophiobolins C, H, K as well as 6-epiophiobolins G, K and N from three fungal strains in the Aspergillus section Usti. Ophiobolins A, B, C and K displayed bioactivity towards leukemia cells with induction of apoptosis at nanomolar concentrations. The remaining ophiobolins were mainly inactive or only slightly active at micromolar concentrations. Dereplication of those ophiobolin derivatives possessing different activity in combination with structural analysis allowed a correlation of the chemical structure and conformation with the extent of bioactivity, identifying the hydroxy group at C3 and an aldehyde at C21, as well as the A/B-cis ring structure, as indispensible for the strong activity of the ophiobolins. The known compounds penicillic acid, viridicatumtoxin, calbistrin A, brefeldin A, emestrin A, and neosolaniol monoacetate were identified from the extracts and also found generally cytotoxic.

【 授权许可】

CC BY   
© 2013 by the authors; licensee MDPI, Basel, Switzerland.