Characterization of cadmium uptake in Lactobacillus plantarum and isolation of cadmium and manganese uptake mutants

Two different Cd2+ uptake systems were identified in Lactobacillus plantaru m. One is a high-affinity, high-velocity Mn2+ uptake system which also take s up Cd2+ and is induced by Mn2+ starvation. The calculated K-m and V-max a re 0.26 mu M and 3.6 mu mol g of dry cell(-1) min(-1), respectively. Unlike Mn2+ uptake, which is facilitated by citrate and related tricarboxylic aci ds, Cd2+ uptake is weakly inhibited by citrate. Cd2+ and Mn2+ are competiti ve inhibitors of each other, and the affinity of the system for Cd2+ is hig her than that for Mn2+. The other Cd2+ uptake system is expressed in Mn2+-s ufficient cells, and no K-m can be calculated for it because uptake is nons aturable. Mn2+ does not compete for transport through this system, nor does any other tested cation, i.e,, Zn2+, Cu2+, Co2+, Mg2+, Ca2+, Fe2+, or Ni2, Both systems require energy, since uncouplers completely inhibit their ac tivities. Two Mn2+-dependent L, plantarum mutants were isolated by chemical mutagenesis aod ampicillin Enrichment. They required more than 5,000 times as much Mn2+ for growth as the parental strain. Mn2+ starvation-induced Cd 2+ uptake in both mutants was less than 5% the wild-type rate. The low leve l of long-term Mn2+ or Cd2+ accumulation by the mutant strains also shows t hat the mutations eliminate the high-affinity Mn2+ and Cd2+ uptake system.