The addition of Ca (as CaCl(2)) in optimal concentrations (0.75 to 2.0 mM) to a fermentation medium with a trace contaminating concentration of Ca (0.025 mM) led to the rapid production of higher concentrations of ethanol by Saccharomyces cerevisiae, Saccharomyces bayanus, and Kluyveromyces marxianus. The positive effect of calcium supplementation (0.75 mM) on alcoholic fermentation by S. bayanus was explained by the increase in its ethanol tolerance. The ethanol inhibition of growth and fermentation followed the equation mu(xi) = mu(oi) [1 - (X/X(mi))], where mu(oi) and mu(xi) are, respectively, the specific growth (i = g) and fermentation (i = f) rates in the absence or presence of a concentration (X) of added ethanol, and X(mi) is the maximal concentration of ethanol which allows growth or fermentation. The toxic power is given by n(i). In Ca - supplemented medium (0.75 mM), n(g) = 0.42 for growth and n(f) = 0.43 for fermentation compared with 0.52 and 0.55, respectively, in unsupplemented medium; for both media, X(mg) = 10% (vol/vol) and X(mf) = 13% (vol/vol). For lethal concentrations of ethanol, the specific death rates were minimal for cells that were grown and incubated with ethanol in medium with an optimal concentration of Ca, maximal for cells grown and incubated with ethanol in unsupplemented medium, and intermediate for cells grown in unsupplemented medium and incubated with ethanol in calcium-supplemented medium. The effect of Ca on the acidification curve of energized cells in the presence of ethanol was found to be closely associated with its protective effect on growth, fermentation, and viability.
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Nabais et al. (1988) studied this question.