1983
DOI: 10.1007/bf02535784
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Effects of triarimol and tridemorph on sterol biosynthesis inSaprolegnia ferax

Abstract: The effects of two fungicides, triarimol and tridemorph, on sterol biosynthesis inSaprolegnia ferax were examined. Cultures grown in the presence of triarimol accumulated lanosterol. Tridemorph‐treated cultures accumulated Δ8‐sterols including zymosterol, fecosterol and stigmasta‐8‐24(28)‐dienol. The latter is a new sterol. A proposed scheme is given for sterol biosynthesis inS. ferax showing points of inhibition of triarimol and tridemorph. Results point to the intermediacy of lanosterol but not cycloartenol … Show more

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Cited by 26 publications
(12 citation statements)
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“…Similar lanosterol accumulation was observed in S. ferax that had been treated with triarimol, a CYP51-inhibiting pyrimidine fungicide (36), and accumulation of eburicol was observed in fungi treated with azole antifungals (69)(70)(71). Malachite green-treated Saprolegnia had unaltered sterol profiles, indicating that the mode of action of malachite green was different from that of azole antifungals, with no inhibition of CYP51 function.…”
mentioning
confidence: 54%
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“…Similar lanosterol accumulation was observed in S. ferax that had been treated with triarimol, a CYP51-inhibiting pyrimidine fungicide (36), and accumulation of eburicol was observed in fungi treated with azole antifungals (69)(70)(71). Malachite green-treated Saprolegnia had unaltered sterol profiles, indicating that the mode of action of malachite green was different from that of azole antifungals, with no inhibition of CYP51 function.…”
mentioning
confidence: 54%
“…However, the recent discovery of a sterol metabolism pathway in the oomycete Aphanomyces euteiches (a legume root pathogen) (35), including a CYP51 gene, led us to investigate whether such a pathway was also present in S. parasitica. Previous investigations into the sterol profile of Saprolegnia were limited to S. ferax (36,37).…”
mentioning
confidence: 99%
“…One would expect, if this were the case, that the relative amount of lanosterol would decrease in the presence of these inhibitors, with little or no effect on the absolute amount of cycloartenol and 24-methylenecycloartenol. This same strategy was attempted by Berg in an examination of sterol biosynthesis in Saprolegnja ferax [21). Depending on the biological controls, the total amount of these cyclopropyl sterols could be increased in the presence of the inhibitors.…”
Section: Cycloartenol Is Further Metabolized In Plants Tomentioning
confidence: 98%
“…There are reports of a wide variety of pentacyclic triterpenols of the B':A'-Neogammacerane (hopane) (12) and A'-Neogammacerane (13) families [18][19][20][21]. To determine the exact identity of E would have required a fair amount of effort: it constitutes only about one percent of the triterpenol mixture from latex and can only be separated from the others by HPLC.…”
mentioning
confidence: 99%
“…Amphotericin B binds lowing scenario is proposed. Saprolegnia zoospores ergosterol in fungal cell membranes, causlng a rapld become embedded in catfish mucus, encyst, and are leakage of potassium which inhibits a variety of meta- dCatfish were subjected to a drop In water temperature and exposed to Saprolegnia (CF1) zoospores hCatfish were subjected to drop in water temperature but not exposed to Saprolegnia ( bolic processes (Tilton & McGinnis 1987); the Saprolegnia also have sterols in the cell membrane (Berg et al 1983). Although the use of amphotericin B with catfish is not foreseen, agents with similar actions should be investigated for their potential in the treatment of this disease.…”
mentioning
confidence: 99%