Evidence for Naturally Produced Beauvericins Containing -Methyl-Tyrosine in Fungi.

Beauvericin is a depsipeptide mycotoxin. The production of several beauvericin analogues has previously been shown among various genera among fungi. This includes so-called beauvenniatins, in which one or more -methyl-phenylalanine residues is exchanged with other amino acids. In addition, a range of "unnatural" beauvericins has been prepared by a precursor addition to growth medium. Our aim was to get insight into the natural production of beauvericin analogues among different fungi, such as and spp. In addition to beauvericin, we tentatively identified six earlier described analogues in the extracts; these were beauvericin A and/or its structural isomer beauvericin F, beauvericin C, beauvericin J, beauvericin D, and beauvenniatin A. Other analogues contained at least one additional oxygen atom. We show that the additional oxygen atom(s) were due to the presence of one to three -methyl-tyrosine moieties in the depsipeptide molecules by using different liquid chromatography⁻mass spectrometry-based approaches. In addition, we also tentatively identified a beauvenniatin that contained -methyl-leucine, which we named beauvenniatin L. This compound has not been reported before. Our data show that -methyl-tyrosine containing beauvericins may be among the major naturally produced analogues in certain fungal strains.