Ethylenediaminetetraacetate (EDTA), an industrially
important chelating agent, forms very stable complexes
with di- and trivalent metal ions, and in both wastewater
and natural waters it is normally present in the metal-associated form. Therefore, the influence of EDTA speciation
on its utilization by the EDTA-degrading bacterial strain
DSM 9103 was investigated. EDTA-grown cells harvested
from the exponential phase of a batch culture were
incubated with 1 mM of various EDTA species and the
EDTA concentration in the assay was monitored as a function
of time. Uncomplexed EDTA as well as complexes with
low stability constants (MgEDTA2-, CaEDTA2-, and MnEDTA2-,
stability constant < 1016) were found to be readily
degraded to completion at a constant rate. For more
stable EDTA chelates (i.e. chelates of Co2+, Cu2+, Zn2+,
and Pb2+) the data suggest that these complexes were not
used directly by the cells but that they had to dissociate
prior to degradation. The rate of this dissociation step possibly
determined the microbial degradation of these complexes.
CdEDTA2- and Fe(III)EDTA- were not degraded within
48 h. In case of CdEDTA2- the toxicity of freed Cd2+ ions
most likely prevented a significant degradation of the complex,
whereas in case of Fe(III)EDTA- a combination of metal
or complex toxicity and the very slow dissociation of the
complex might explain the absence of degradation.
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