P. Jitnuyanont et al., Bioaugmentation of butane-utilizing microorganisms to promote cometabolismof 1,1,1-trichloroethane in groundwater microcosms, BIODEGRADAT, 12(1), 2001, pp. 11-22
The transformation of 1,1,1-trichloroethane (1,1,1-TCA) in ioaugmented and
non-augmented microcosms was evaluated. The microcosms contained roundwater
and aquifer materials from a test site at Moffett Field, Sunnyvale, CA. Th
e initial inoculum for bioaugmentation was a butane-utilizing enrichment fr
om the subsurface of the Hanford DOE site. The non-augmented microcosm requ
ired 80 days of incubation before butane-utilization was observed while the
augmented microcosms required 3 days. Initially the augmented microcosms w
ere effective in transforming 1,1,1-TCA, but their transformation ability d
ecreased after prolonged incubation. The non-augmented microcosms initially
showed limited 1,1,1-TCA transformation but improved with time. After 440
days, both the non-augmented and augmented microcosms had similar transform
ation yields (0.04 mg 1,1,1-TCA/mg butane) and had similar microbial compos
ition (DNA fingerprints). Subsequent microcosms, when bioaugmented with a H
anford enrichment that was repeatedly grown in 100% mineral media, did not
effectively grow or transform 1,1,1-TCA under groundwater nutrient conditio
ns. Microcosm tests to study the effect of mineral media on transformation
ability were performed with the Hanford enrichment. Microcosms with 50% min
eral media in groundwater most effectively utilized butane and transformed
1,1,1-TCA, while microcosms with groundwater only and microcosms with 5% mi
neral media in groundwater lost their 1,1,1-TCA transformation ability. DNA
fingerprinting indicated shifts in the microbial composition with the diff
erent mineral media combinations. Successful bioaugmentation was achieved b
y enriching butane-utilizers from Moffett Field microcosms that were effect
ive in groundwater with no mineral media added. The results suggest that su
ccessful in-situ bioaugmentation might be achieved through the addition of
enriched cultures that perform well under subsurface nutrient conditions.