2 research outputs found
Mineralization of the Common Groundwater Pollutant 2,6-Dichlorobenzamide (BAM) and its Metabolite 2,6-Dichlorobenzoic Acid (2,6-DCBA) in Sand Filter Units of Drinking Water Treatment Plants
The
intrinsic capacity to mineralize the groundwater pollutant
2,6-dichlorobenzamide (BAM) and its metabolite 2,6-dichlorobenzoic
acid (2,6-DCBA) was evaluated in samples from sand filters (SFs) of
drinking water treatment plants (DWTPs). Whereas BAM mineralization
occurred rarely and only in SFs exposed to BAM, 2,6-DCBA mineralization
was common in SFs, including those treating uncontaminated water.
Nevertheless, SFs treating BAM contaminated water showed the highest
2,6-DCBA mineralization rates. For comparison, 2,6-DCBA and BAM mineralization
were determined in various topsoil samples. As in SF samples, BAM
mineralization was rare, whereas 2,6-DCBA mineralization capacity
appeared widespread, with high mineralization rates found especially
in forest soils. Multivariate analysis showed that in both SF and
soil samples, high 2,6-DCBA mineralization correlated with high organic
carbon content. Adding a 2,6-DCBA degradation deficient mutant of
the BAM mineralizing <i>Aminobacter</i> sp. MSH1 confirmed
that 2,6-DCBA produced from BAM is rapidly mineralized by the endogenous
microbial community in SFs showing intrinsic 2,6-DCBA mineralization.
This study demonstrates that (i) 2,6-DCBA mineralization is widely
established in SFs of DWTPs, allowing the mineralization of 2,6-DCBA
produced during BAM degradation and (ii) the first metabolic step
in BAM mineralization is rare in microbial communities, rather than
its further degradation beyond 2,6-DCBA
Biocarriers Improve Bioaugmentation Efficiency of a Rapid Sand Filter for the Treatment of 2,6-Dichlorobenzamide-Contaminated Drinking Water
Aminobacter sp. MSH1 immobilized
in an alginate matrix in porous stones was tested in a pilot system
as an alternative inoculation strategy to the use of free suspended
cells for biological removal of micropollutant concentrations of 2,6-dichlorobenzamide
(BAM) in drinking water treatment plants (DWTPs). BAM removal rates
and MSH1 cell numbers were recorded during operation and assessed
with specific BAM degradation rates obtained in lab conditions using
either freshly grown cells or starved cells to explain reactor performance.
Both reactors inoculated with either suspended or immobilized cells
showed immediate BAM removal under the threshold of 0.1 μg/L,
but the duration of sufficient BAM removal was 2-fold (44 days) longer
for immobilized cells. The longer sufficient BAM removal in case of
immobilized cells compared to suspended cells was mainly explained
by a lower initial loss of MSH1 cells at operational start due to
volume replacement and shear. Overall loss of activity in the reactors
though was due to starvation, and final removal rates did not differ
between reactors inoculated with immobilized and suspended cells.
Management of assimilable organic carbon, in addition to cell immobilization,
appears crucial for guaranteeing long-term BAM degradation activity
of MSH1 in DWTP units