TY - JOUR
T1 - Toxicity and genotoxicity enhancement during polycyclic aromatic hydrocarbons' biodegradation
AU - Belkin, Shimshon
AU - Stieber, Michael
AU - Tiehm, Andreas
AU - Frimmel, F. H.
AU - Abeliovich, Aharon
AU - Werner, Peter
AU - Ulitzur, Shimon
PY - 1994/11
Y1 - 1994/11
N2 - Several laboratory column percolators were operated in order to study the bioremediation potential of polycyclic aromatic hydrocarbons (PAH)‐contaminated soils. The columns contained either soil artificially amended with specific PAH mixtures or contaminated soil from a site in Karlsruhe, Germany. In all cases, biodegradative processes led to the elimination of the original contaminants. This, however, was accompanied by a marked increase in genotoxic activity of the column effluents as determined by the MutatoxTM assay. Genotoxicity was practically abolished, however, when a surfactant was added to the percolating fluids. While in some cases the changes in genotoxicity were paralleled by toxicity (MicrotoxTM) data, in others the trend was opposite. It is concluded that when degradation is incomplete, the potential exists for toxicity and genotoxicity enhancement, with the latter hazard not always predictable by short‐term toxicity assays. Routine genotoxicity monitoring is thus advocated for bioremediation projects; the MutatoxTM assay appears to be a convenient tool for this purpose. © 1994 by John Wiley & Sons, Inc..
AB - Several laboratory column percolators were operated in order to study the bioremediation potential of polycyclic aromatic hydrocarbons (PAH)‐contaminated soils. The columns contained either soil artificially amended with specific PAH mixtures or contaminated soil from a site in Karlsruhe, Germany. In all cases, biodegradative processes led to the elimination of the original contaminants. This, however, was accompanied by a marked increase in genotoxic activity of the column effluents as determined by the MutatoxTM assay. Genotoxicity was practically abolished, however, when a surfactant was added to the percolating fluids. While in some cases the changes in genotoxicity were paralleled by toxicity (MicrotoxTM) data, in others the trend was opposite. It is concluded that when degradation is incomplete, the potential exists for toxicity and genotoxicity enhancement, with the latter hazard not always predictable by short‐term toxicity assays. Routine genotoxicity monitoring is thus advocated for bioremediation projects; the MutatoxTM assay appears to be a convenient tool for this purpose. © 1994 by John Wiley & Sons, Inc..
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U2 - 10.1002/tox.2530090409
DO - 10.1002/tox.2530090409
M3 - Article
AN - SCOPUS:0028044201
SN - 1053-4725
VL - 9
SP - 303
EP - 309
JO - Environmental Toxicology and Water Quality
JF - Environmental Toxicology and Water Quality
IS - 4
ER -