The microbial degradation of two recalcitrant pharmaceutical compounds, carbamazepine (CBZ) and diatrizoate (DTZ), was studied in laboratory batch experiments. We used a defined mixed microbial culture comprising four distinct microbial species that were previously known to have high decomposition capacity toward recalcitrant substances. Biological decomposition in liquid phase cultures for either CBZ or DTZ, or in a combination of the two, was conducted for 12 days. DTZ and CBZ were degraded by 43.2% and 60%, respectively from an initial concentration of 100 µg L(-1). When degradation was assessed using a mixture of the two compounds, the initial degradation rates of CBZ and DTZ were lower than those observed in the single-compound study. However, the final cumulative removal efficiency was very similar. The extent of dissolved organic carbon (DOC) removal was correlated with the degradation of the pharmaceuticals.

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This study was conducted to biologically convert methane into methanol. Methane contained in biogas was bio-catalytically oxidized by methane monooxygenase (MMO) of methanotrophs, while methanol conversion was observed by inhibiting methanol dehydrogenase (MDH) using MDH activity inhibitors such as phosphate, NaCl, NH4Cl, and EDTA. The degree of methane oxidation by methanotrophs was the most highly accomplished as 0.56 mmol for the condition at 35℃ and pH 7 under 0.4 (v/v%) of biogas (CH4 50%, CO2 50%) / Air ratio. By the inhibition of 40 mM of phosphate, 50 mM of NaCl, 40 mM of NH4Cl and 150 µm of EDTA, methane oxidation rate could achieve more than 80% regardless of type of inhibitors. In the meantime, addition of 40 mM of phosphate, 100 mM of NaCl, 40 mM of NH4Cl and 50 µm of EDTA each led to generating the highest amount of methanol, i.e, 0.71, 0.60, 0.66, and 0.66 mmol when 1.3, 0.67, 0.74, and 1.3 mmol of methane was each concurrently consumed. At that time, methanol conversion rate was 54.7, 89.9, 89.6, and 47.8% respectively, and maximum methanol production rate was 7.4 µmol/mg․h. From this, it was decided that the methanol production could be maximized as 89.9% when MDH activity was specifically inhibited into the typical level of 35% for the inhibitor of concern.

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