YOU ARE NOW CONNECTED TO THE TOXLINE (1981 FORWARD, NON-ROYALTY) FILE. ==ERGOSTEROL== 3 AUTHOR Axelsson BO AUTHOR Saraf A AUTHOR Larsson L TITLE Determination of ergosterol in organic dust by gas chromatography-mass spectrometry. SOURCE J Chromatogr B Biomed Appl; VOL 666, ISS 1, 1995, P77-84 ABSTRACT A gas chromatographic-mass spectrometric method was developed for the determination of ergosterol in organic dust. Samples were hydrolyzed under alkaline conditions, and the hydrolysate was extracted, purified on a silica-gel column, and subjected to derivatization. The limit of detection of the trimethylsilyl ether derivative of ergosterol was approximately 10 pg and that of the tert.-butyldimethylsilyl ether derivative was approximately 20 pg (injected amounts). House dust contained 6-45 micrograms ergosterol/g and air from a pig barn contained 0.2-0.3 ng ergosterol/liter. The proposed method can be used as a complement or alternative to microscopy and culturing for measuring fungal biomass in air-borne organic dust. 11 AUTHOR Muller HM AUTHOR Schwadorf K TITLE [Ergosterol as a measure for fungal growth in feed. 2. Ergosterol content of mixed feed components and mixed feed] SOURCE Arch Tierernahr; VOL 40, ISS 4, 1990, P385-95 ABSTRACT Ergosterol was determined as a chemical indicator of fungal biomass in commodities which were used for the production of mixed feeds. It was found in all samples of each of the following components (content in mg/kg DM): Wheat (2.6 +/- 1.0), low grade wheat flour (fibre less than or equal to 3.5%) (17.3 +/- 9.1), wheat semolina bran (fibre less than or equal to 10%) (29.4 +/- 16.8), wheat bran (35.2 +/- 9.4), grain corn (1.0 +/- 0.6), corn gluten feed (7.8 +/- 3.0), corn gluten (10.3 +/- 5.0), maize germ meal (8.0 +/- 2.0), barley (3.1 +/- 1.1), malt sprouts (40.6 +/- 15.9), broad beans (0.6 +/- 0.3), peas (summer varieties, white flowering) (2.2 +/- 1.0), soya flakes (2.2 +/- 0.9), soya meal (1.1 +/- 0.7), sunflower meal (5.0 +/- 2.4), copra meal/expeller (9.1 +/- 1.6), palm kernel meal (12.6 +/- 11.0), rapeseed meal (2.6 +/- 0.8), linseed meal (3.2 +/- 1.6), manioc meal (8.3 +/- 2.7), beet pulp, dried (1.6 +/- 0.3), beet pulp with molasses (2.2 +/- 0.9), alfalfa meal (37.8 +/- 10.4), grass meal (62.4 +/- 37.0). Ergosterol was not found in molasses, citrus pulp, carcass meal, meat-and-bone-meal, skim milk powder, whey powder, fish meal (2 of 3 samples), mineral components, vitamin mixtures and other additives. Differences in ergosterol contents are discussed. With four mixed feeds it was demonstrated that the ergosterol content determined chemically in the mixture is in good accordance with the value calculated from the ergosterol content of the components and their percentage in the mixture. 1 AUTHOR Barrett-Bee K AUTHOR Dixon G TITLE Ergosterol biosynthesis inhibition: a target for antifungal agents. SOURCE Acta Biochim Pol; VOL 42, ISS 4, 1995, P465-79 (REF: 71) ABSTRACT The isoprenoid sterols play a crucial role in the viability of all fungi; those unable to synthesise ergosterol because of inhibition, growth conditions or mutation must take it up from the environment. A range of compound types have been discovered which interfere with the biosynthetic pathway from acetate to ergosterol and these compounds have antifungal actions. Inhibition of several of the steps has yielded agents which have been used with great success as medical and agrochemical agents. The most important biosynthetic steps that have been exploited are inhibition of squalene epoxidase, (the allylamines and tolnaftate) C14 demethylation (the azoles), delta 7,8 isomerase and delta 14 reductase which are inhibited by the morpholines. Recent research has shown that inhibition of C24 methyltransferase and C4 demethylation also yield antifungal agents. Combination studies demonstrate that synergy between agents of different types can be measured. Fungicidal effects were observed when a combination of two fungistatic agents was used. 2 AUTHOR De Luca C AUTHOR Passi S AUTHOR Fabbri AA AUTHOR Fanelli C TITLE Ergosterol oxidation may be considered a signal for fungal growth and aflatoxin production in Aspergillus parasiticus. SOURCE Food Addit Contam; VOL 12, ISS 3, 1995, P445-50 ABSTRACT The addition of compounds able to peroxidize cell lipids (carbon tetrachloride (CCl4), cumene hydroperoxide (CUH), or linoleic acid hydroperoxide (LAH)) to 5-day-old Czapek-Dox Medium cultures of Aspergillus parasiticus induces a significant reduction of the tri-unsaturated ergosterol (ERG) levels in fungal microsomes and mitochondria, whereas the concentrations of the di-unsaturated linoleic acid (LA; C18:2 n-6) are unaffected. Aflatoxin (AFT) output follows ERG reduction and is associated with both a renewal of fungal growth and a slow increase of ERG concentration in subcellular membranes. We suggest that, by analogy with the regulatory role played on cell proliferation and metabolism by polyunsaturated fatty acid by-products (eicosanoids) in mammalian membranes, by-products of ERG oxidation may be considered triggers sufficient to induce both further fungal growth and AFT biosynthesis. 1 AUTHOR Barug D AUTHOR Bastiaanse HB AUTHOR van Rossum JM AUTHOR Kerkenaar A TITLE Action of lombazole, and inhibitor of fungal ergosterol biosynthesis, on Staphylococcus epidermidis. SOURCE Antimicrob Agents Chemother; VOL 30, ISS 2, 1986, P238-44 ABSTRACT Lombazole had no effect on respiration at any tested concentration and had little effect on the K+ permeability of Staphylococcus epidermidis. Of the major metabolic processes investigated in this bacterium, only de novo synthesis of the cell envelope was inhibited by lombazole well in advance of an effect on growth. The time course of inhibition indicated that lombazole exerted its primary effect via inhibition of lipid synthesis; other induced changes, such as reduced synthesis of lipoteichoic acid and cell wall components, were considered to be secondary effects. Although the precise site of action in S. epidermidis has to be established, the absence of alterations in lipid patterns after treatment with lombazole suggests the toxicant may affect an essential step in lipid biosynthesis. In Candida albicans, lombazole inhibited the sterol C-14 demethylation step in the ergosterol biosynthesis pathway. 1 AUTHOR Johnston G TITLE The study of interactive effects of pollutants: a biomarker approach. SOURCE Sci Total Environ; VOL 171, ISS 1-3, 1995, P205-12 (REF: 18) ABSTRACT Biochemical biomarkers, such as inhibition of serum butyryl cholinesterase (BuChE) and brain acetyl cholinesterase (AChE), have been useful in studies of interactive effects of pesticides in birds. Examples of interactions due to increased activation or decreased detoxication are reviewed. Studies have shown that hybrid red-legged partridges (Alectoris rufa cross) pretreated with the inducing ergosterol biosynthesis inhibiting (EBI) fungicide, prochloraz, were more sensitive to the toxic effects of the organophosphorous (OP) insecticide, malathion, than controls. A dose of 90 mg/kg prochloraz produced greater inhibition at 1, 4 and 24 h following oral administration of 50 mg/kg malathion, compared to corn oil controls. Pigeons (Columba livia) given 180 or 90 mg/kg prochloraz showed greater inhibition of BuChE activity following malathion administration than did control birds. Starlings (Stumus vulgaris), however, appeared not to be induced by 180 or 300 mg/kg prochloraz, and no difference in BuChE activity following dosing with malathion was apparent in comparison with controls. Other EBIs and OP combinations have been investigated in the partridge. Birds pretreated with prochloraz showed a trend towards greater inhibition of serum BuChE activity at most time points following dosing with the OPs dimethoate and chlorpyriphos. Birds pretreated with the EBI penconazole showed significantly greater inhibition of serum BuChE activity at 1, 4 and 24 h after malathion administration than did controls. The mechanism of increased activation of malathion due to induction of cytochrome P-450 by prochloraz is reviewed. In the case of interactions due to inhibition of detoxication, inhibition of brain AChE activity was a useful biochemical biomarker.(ABSTRACT TRUNCATED AT 250 WORDS) 1 AUTHOR JOSEPH-HORNE T AUTHOR HOLLOMON D AUTHOR LOEFFLER R ST AUTHOR KELLY SL TITLE Altered P450 activity associated with direct selection for fungal azole resistance. SOURCE FEBS LETTERS; 374 (2). 1995. 174-178. ABSTRACT BIOSIS COPYRIGHT: BIOL ABS. Azole antifungals inhibit CYP51A1-mediated sterol 14alpha-demethylation and the mechanism(s) of resistance to such compounds in Ustilago maydis were examined. The inhibition of growth was correlated with the accumulation of the substrate, 24-methylene-24,25-dihydrolanosterol (eburicol), and depletion of ergosterol. Mutants overcoming the effect of azole antifungal treatment exhibited a unique phenotype with leaky CYP51A1 activity which was resistant to inhibition. The results demonstrate that alterations at the level of inhibitor binding to the target site can produce azole resistance. Similar changes may account for fungal azole resistance phenomena in agriculture, and also in medicine where resistance has become a problem in immunocompromised patients suffering from AIDS.