Influence of different levels of ammonium concentrations on cell growth, RNA and protein production by Candida albicans.

Candida albicans starved cells were incubated in minimal synthetic liquid media containing different concentrations of ammonium sulphate (0.00, 0.02, 0.05, 0.10, 0.03, 0.50 g/L). Culture growth was monitored by measuring daily the optical density and by evaluating RNA and protein cellular content after 48 and 96 hours from the inoculum. The environmental availability of ammonium ion influenced the biomass production, that was maximum when its concentration was 0.10 and 0.30 g/L. In addition, an effect on cell duplication time was observed, this was particularly evident when the (NH4)2SO4 concentration was 0.10 g/L. The protein content increased in relation to the increase of ammonium ion availability, with a peak in correspondence to 0.30 g/L and a drop when the greatest concentrations were employed. RNA production was inversely proportional in respect to protein production. The optimal range of ammonium sulphate concentration for C. albicans growth was 0.10-0.30 g/L; over these concentrations there was an inhibitory effect. The rate of the protein and RNA syntheses seems to indicate the growth phase and the nitrogen nutritional conditions of the cultures, respectively.

[Behavior of Candida albicans during a period of nutritional deprivation. Preliminary results]. / Comportamento di Candida albicans durante un periodo di carenza nutrizionale. Risultati preliminari.

Cells of Candida albicans, after 24 hours of growth in YM, were starved, alternatively, in citrate buffer, physiological solution, MMS deprived of glucose or ammonium sulphate. The eventual growth was monitored by determining the absorbance at 675 nm. Simultaneously, the cell morphology was also controlled. In a second series of experiments, the C. albicans cells taken from YM were starved for 72 hours in one of the mediums as stated above, and then reinoculated in MMS liquid without, alternatively, glucose or ammonium sulphate. Again the eventual growth was monitored as in the above method. The achieved results indicate the presence of a reserve of nitrogen, which can be utilized when a source of C is given to the cell. We therefore discuss the apparent lack of glucidic reserve and we propose a method for the consumption of nitrogen reserve. The aim of the work is to define how to obtain cells that contain the smallest amount possible of endogenous reserve.