Due to the low environmental concentrations
and substance-specific
behavior of trace organic chemicals (TOrCs), general mechanistic insights
can hardly be gained from biotransformation studies with individual
substances. In this study, we aimed to identify prevalent enzymatic
reactions under different redox and substrate conditions in a well-defined
laboratory-scale column system. Biotransformation of chemicals in
the first column, which was characterized by a relatively high biomass
and rapid depletion of dissolved oxygen, was initiated by frequent
and fast reactions such as the oxidation of alcohols or amide hydrolysis.
Slower reactions, e.g., the initial dealkylation of primary and secondary
amines, were inefficient in the first column and benefited from oxic
and carbon-limited conditions prevalent in the second column system
after reaeration. Moreover, several compound-specific reactions such
as the cleavage of C–Cl and C–O bonds through substitution
with glutathione occurred only under carbon-limited conditions. The
link between system-specific TOrC removal and suggested initial reactions
from the literature can serve as a starting point for a suspect screening
of relevant enzymes for the biotransformation of TOrCs based on metagenomic
or metatranscriptomic data. Complementary batch experiments with media
from the columns confirmed the observed removal under carbon-rich
conditions but revealed a limited reproducibility of microbial degradation
under oligotrophic conditions.