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The in vivo effects of CrCl
3 on an ergosterol-producing
33 erg
+ strain of the eukaryotic yeast
Candida albicans, and on its ergosterol-deficient
erg
−2
mutant, were studied by using electron paramagnetic resonance spectroscopy. A 5-doxylstearic acid spin probe was applied to label the membranes. The absence of ergosterol, an increased accumulation of Δ
8 sterols, a decreased fatty acid chainlength and a lower proportion of unsaturated fatty acids of the
erg
−2
mutant resulted in a higher membrane rigidity and an increased sensitivity to Cr(III) than those of the parental
33 erg
+ strain. Cr(III) significantly increased the fluidity of the spin labelled membranes, this being more pronounced for the
erg
−2
mutant. The break in the slopes measured for the
erg
−2
mutant was decreased (ΔAT∼4°C) from 17 to 13°C. Cr(III) treatment for 10 h caused a loss of metabolites adsorbing at 260 nm: this loss was 40% for
33 erg
+ and 60% for
erg
−2
. This decriptification process might be the main cause of growth inhibition and cell killing by the impermeable Cr(III) ions.