posted on 2015-10-14, 00:00authored byMuhammad
Abdul Mojid Mondol, Musrat Zahan Surovy, M. Tofazzal Islam, Anja Schüffler, Hartmut Laatsch
The cytotoxicity of the extract obtained
from Myrothecium
roridum M10 and a characteristic 1H signal
at δH ∼8 led to the assumption that verrucarin/roridin-type
compounds were present. Upscaling on rice medium led to the isolation
of four new metabolites: verrucarins Y (1) and Z (6) (macrocyclic trichothecenes), bilain D (12) (a diketopiperazine derivative), and hamavellone C (14) (an unusual cyclopropyl diketone). In addition, nine known trichothecenes
[verrucarin A (3), 16-hydroxyverrucarin A (5), verrucarin B (7), 16-hydroxyverrucarin B (8), verrucarin J (2), verrucarin X (4),
roridin A (9), roridin L-2 (10), and trichoverritone
(11)] and a bicyclic lactone [myrotheciumone A (15)] were identified. Their structures and configurations
were determined by spectroscopic methods, published data, Mosher’s
method, and considering biosyntheses. Some trichothecenes showed motility
inhibition followed by lysis of the zoospores against devastating Phytophthora nicotianae within 5 min. Compounds 2, 3, 7, and 9 also
exhibited potent activities against Candida albicans and Mucor miehei.