Talaropeptins A and B, Tripeptides with an <i>N</i>-<i>trans</i>-Cinnamoyl Moiety from the Marine-Derived Fungus <i>Talaromyces purpureogenus</i> CX11
Chengzeng Zhou, Xun Cao, Yichao Ge, Xiaodan Wu, Zunjing Zhang, Yihan Ma, Jeroen S. Dickschat, Bin Wu
Abstract
We report the discovery of talaropeptins A (1) and B (2), tripeptides with an unusual 5/6/5 heterocyclic scaffold and an N-trans-cinnamoyl moiety, which were identified from the marine-derived fungus Talaromyces purpureogenus CX11. A bioinformatic analysis of the genome of T. purpureogenus CX11 and gene inactivation revealed that the biosynthesis of talaropeptins involves a nonribosomal peptide synthase gene cluster. Their chemical structures were elucidated using a combination of 1D and 2D NMR spectroscopy and mass spectrometry. The absolute configurations of 1 and 2 were established by electronic circular dichroism calculations and Marfey’s method. The plausible biosynthesis of 1 and 2 is also proposed on the basis of gene deletion, substrate feeding, and heterologous expression. Compounds 1 and 2 showed moderate antifungal activity against phytopathogenic fungus Fusarium oxysporum with MIC values of 12.5 and 25 μg/mL, respectively.