Transport of Mn 2+ was repressed in Candida utilis cells grown in continuous culture in high-Mn 2÷ (100 /IM Mn 2÷) medium as compared to cells grown in basic (0.45 # M Mn 2 ÷) and low-Mn 2 + (< 0.05 #M Mn 2+) media. In contrast, no repression of Cu 2+ uptake occurred in high-Cu2÷-grown (25/tM Cu 2÷) cells as compared to cells grown in basic medium (0.54/LM Cu2÷). Cu2÷-limited cells did not hyperaccumulate Cu 2÷ and there was not significant difference in initial uptake rates for all 3 Cu 2÷ conditions. Mn 2÷ uptake appears to be regulated by a mechanism sensitive to the external Mn 2÷ concentration, whereas Cu 2+ transport is not governed in this way by the external Cu 2+.
INTRODUCTIONMn 2+ and Cu 2+ are both required in trace amounts by yeasts [1] although Cu 2+ at higher concentrations exerts a number of toxic effects [2].Regulation of internal solute levels in the presence of high external ion concentrations is an important feature of cellular metabolism. There are a number of strategies by which micro-organisms may maintain homeostasis of cellular metal ions and these include energy-driven metal efflux systems [3,4], a tonoplast transport system to regulate cytosolic and vacuolar divalent cation concentrations [5] and the presence of metal-binding proteins [6] and polyphosphates [7].While many studies of metal ion transport in yeasts have been reported [8], few have considered the control of these transport systems. Such regulation may markedly affect cellular metal levels, particularly during exposure of cells to toxic external concentrations of metal ions.Studies of Mn 2+ uptake in bacteria [9,10] and' Mg 2+ uptake [11] have demonstrated repression of transport following growth in media containing high concentrations of Mn 2+ and Mg 2+, respectively. Cells of C. utilis grown in continuous culture under conditions of Zn 2 + limitation possessed the capacity to hyperaccumulate Zn 2+ far in excess of the level attained in Zn2+-supplemented medium [12], indicating derepression of the uptake mechanism under these conditions. Whilst a number of other authors have found it impossible to create Mn2+-deficient conditions as cells are capable of growth in media containing Mn 2+ present as trace impurities of medium constituents [3], it is however possible to prepare 0378-1097/86/$03.50