A comparison of cycloartenol and lanosterol biosynthesis and metabolism by the Oomycetes

Tipo de material: Texto

TextoSeries ; Cellular and Molecular Life Science, 42(5), p.556-558, 1986Trabajos contenidos:

Nes, W.D
Le, P.H
Berg, L.R
Patterson, G.W
Kerwin, J.L

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Resumen: Representative members in each of the four orders of Oomycetes (Phytophthora cactorum, Peronosporales; Lagenidium callineetes, L.giganteum, Lagenidiales; Saprolegnia ferax, Saprolegniales; Apodaehylella completa, Leptomitales)have been examined for their ability to synthesize and polycyclize squalene-oxide (SO)to a tetracyclic product and to differentiate between cycloartenol and lanosterol metabolism to sterols. P. eactorum and L. giganteum failed to synthesize or metabolize SO, cycloartenol or lanosterol. While the other three fungi synthesized sterols via SO and lanosterol, a minor metabolism of added cycloartenol to the 4,4-desmethyl-14e-methylcyclosteroid dehydropollinastanol was observed.

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Representative members in each of the four orders of Oomycetes (Phytophthora cactorum, Peronosporales; Lagenidium callineetes, L.giganteum, Lagenidiales; Saprolegnia ferax, Saprolegniales; Apodaehylella completa, Leptomitales)have been examined for their ability to synthesize and polycyclize squalene-oxide (SO)to a tetracyclic product and to differentiate between cycloartenol and lanosterol metabolism to sterols. P. eactorum and L. giganteum failed to synthesize or metabolize SO, cycloartenol or lanosterol. While the other three fungi synthesized sterols via SO and lanosterol, a minor metabolism of added cycloartenol to the 4,4-desmethyl-14e-methylcyclosteroid dehydropollinastanol was observed.

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