Abstract
Resting cell batch kinetic studies were performed to evaluate the alcohol-dependent cometabolic degradation of chlorinated aliphatic hydrocarbons (CAHs) and 1,4-dioxane (1,4-D) by Rhodococcus rhodochrous strain ATCC 21198. This strain grew on diverse alcohols, organic acids, esters, and other organic compounds. Only growth on 2-butanol resulted in labeling of monooxygenase enzymes and the ability to oxidize propylene, the cylic ether 1,4-D, and its close structural analog tetrahydrofuran. In single compound rate tests, 2-butanol-grown cells exhibited faster degradation rates for less chlorinated compounds. The rates of degradation are ranked as follows from high to low: vinyl chloride > cis-dichloroethene (cis-DCE) >1,1-dichoroethane >1,1-dichoroethene (1,1-DCE) >1,4-D > 1,1,1-trichoroethane (1,1,1-TCA) >1,1,2-trichoroethene. All rates were significantly lower than isobutane-grown cells. 2-Butanol-grown cells exhibited a lag period before cometabolic degradation of most CAHs, including cis-DCE; however, production of cis-1,2-dichloro-1,2-epoxyethane (cis-DCE epoxide) was detected with no lag. Cells grown on 1-butanol, 2-butanol, or 2-ethyl-1-butanol also cometabolically degraded 1,4-D and various CAHs. However, compared to cells grown on 1-butanol or 2-ethyl-1-butanol, cells grown on 2-butanol had a larger transformation capacity and faster degradation rates and were able to fully degrade (>99% removal) a mixture of 1,4-D, cis-DCE, and 1,1,1-TCA. With CAH mixtures, alcohol-grown cells degraded cis-DCE faster than both 1,1,1-TCA and 1,4-D. sec-Butyl-acetate (sBA) was demonstrated as a potential slow-release substrate that hydrolyzes to yield 2-butanol and acetate. Cells grown on this ester degraded a mixture of 1,1,1-TCA and 1,4-D at rates faster than 2-butanol-grown cells. The cometabolic transformation of 1,1,1-TCA and 1,4-D was also observed in reactors where growth occurred with sBA as the growth substrate.
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