Aerobic biodegradation of the chelating agent EDTA by a mixed bacteria
l culture was investigated. Bacterial growth and degradation of the su
bstrate required the presence of sufficient metal ions in the culture
fluid. Uncomplexed EDTA interacted negatively with the cell walls of t
he bacteria and completely inhibited bacterial growth, whereas Mg(II)/
Ca(II)-EDTA was degraded up to an initial concentration of 4.7 g/l. Th
erefore, concentrations of metal ions must be stoichiometric to that o
f EDTA or higher. Specific degradation rates ranged between 120 mg EDT
A g(-1) (cell dry weight) h(-1) and 285 mg EDTA g(-1) h(-1). In contra
st, complexes with high thermodynamic stability constants such as Fe(I
II)-EDTA remained as inert compounds in the solution. Specific growth
rates of the mixed culture were found to vary between 0.03 h(-1) and 0
.07 h(-1), which could be explained by population dynamics within the
synergistic mixed community. Growth was significantly accelerated by t
he addition of vitamins.