Recombinant Escherichia coli JM109 (pZH3-5/pMT), harboring a manganese transport gene (mntA) and a metal-sequestering protein (metallothionein [MT]) gene, was cultivated to accumulate cadmium (Cd) in an aqueous phase. Isopropyl beta-D-thiogalactoside (IPTG)-induced cells showed rapid Cd2+ ion accumulation (90% of maximum accumulation in 15 min) and had an accumulation six times higher than that of the control. Under optimum conditions, i.e., pH 7, 37 degrees C and 0.5 (OD600), 1.5 mM IPTG induction resulted in the accumulation of 21.5 mu mol Cd/g dry cell. Storage at 37 degrees C for 24 h had no effect on the accumulation. Significantly, Cd was selectively accumulated in a solution containing an equal concentration of three other metals, resulting in more than 90% of the total accumulated metals being Cd. The accumulation of Cd was reduced by the presence of Mn" ion whereas no significant effect was observed with Cu2+, Zn2+ and Pb2+ ions. A chelator, EDTA, had no effect on the accumulation up to 100 mM. The bioaccumulation rate followed Michaelis-Menten kinetics (V-m=2.7 mu mol Cd2+/Min center dot g dry cell, K-m=0.67 mu M). The equilibrium isotherm showed a Langmuir isotherm. In the membrane reactor experiment, 1 mg/l Cd in an inlet solution decreased to 0.2 mg/l in the effluent, removing 80% of Cd, continuously. These results indicated the potentials of a genetically modified microorganism for the highly selective accumulation of Cd at a low concentration and the future application to the removal and recovery of Cd.