The microcalorimetric bioassay for acute cellular toxicity is based on meta
bolic heat production from cultured cells. Microcalorimetry is a quantitati
ve, inexpensive, and versatile method for toxicology research. The biologic
al response to toxicants is the inhibition of the heat production rate in c
ells and toxicity is expressed as the concentration of toxicant that is 50%
effective in this inhibition (IC50). In this paper, the effect of Cd2+ on
Rhizopus nigricans growth was investigated at 25 degrees C. The relationshi
p between growth rate constants (k) and concentration of Cd2+ (C) shows a l
ogarithmic normal distribution, and described as k = 1.2742 X 10(61) exp[-1
.810 X 10(-3) (C + 283.0)(2)], and IC50 is 0.72 mu g/ml. These signals are
readily obtained by an LKB 2277-204 heat conduction microcalorimeter. (C) 2
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