Id. Brodowsky et Eh. Oliw, BIOSYNTHESIS OF 8R-HYDROPEROXYLINOLEIC ACID BY THE FUNGUS LAETISARIA-ARVALIS, Biochimica et biophysica acta, 1168(1), 1993, pp. 68-72
8-Hydroxylinoleic acid is known to be a fungicidal metabolite formed b
y the fungus Laetisaria arvalis (Bowers, W.S. et al. (1986) Science 23
2, 105-106). In the present report, the mechanism of formation of 8-hy
droxylinoleic acid was investigated. L. arvalis metabolized [C-14]lino
leic acid to 8-hydroperoxylinoleic acid and 8-hydroxylinoleic acid as
major metabolites. The identification is based on the reduction of the
hydroperoxide to an alcohol with stannous chloride and gas chromatogr
aphy-mass spectrometry. The absolute configuration of the hydroxyl was
determined to be R by ozonolysis of the (-)-menthoxycarbonyl derivati
ve of 8-hydroxylinoleic acid. Linoleic acid 8 R-dioxygenase activity w
as present in the 100 000 X g supernatant of the cell lysate. In summa
ry, the 8R-linoleic acid dioxygenase of L. arvalis shows many similari
ties with the 8R-dioxygenase recently described in the fungus Gaeumann
omyces graminis.