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NA PP . 1997. The biodegradation of benzothiazoles by pure and mixed microbial cultures derived from activated sludge has been studied. The degradation of 2-aminobenzothiazole (ABT) by both pure and mixed bacterial cultures has been demonstrated for the first time. ABT is degraded to give high yields of ammonia and sulphate (87 and 100 %, respectively of the theoretical yield). We also report for the first time the isolation of a pure bacterial culture PA, thought to be a strain of Rhodococcus, capable of growing on benzothiazole (BTH) itself as a sole carbon, nitrogen and energy source. Evidence is presented to suggest that this organism degrades BTH via the meta-cleavage pathway. The Rhodococcus PA degrades BTH but only releases a small proportion (5%) of the sulphur as sulphate. Mixed cultures containing this organism released ca 100% of the sulphur as sulphate, suggesting that other members of the consortium catalyse conversion of a sulphur-containing intermediate to sulphate. 2-Mercaptobenzothiazole (MBT) could not act as a growth substrate for any of the cultures studied but some could cause biotransformation of MBT to some extent. Attempts to obtain cultures degrading ABT and BTH from polluted river water were unsuccessful.

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The direct cytotoxicity of mebendazole (MBZ) was investigated by using cell lines derived from human, mouse and rat liver. It was demonstrated that Chang liver cells (derived from human liver) were more sensitive to the cytotoxic effects of MBZ than the other two cell lines. Longer incubation of the cells with MBZ resulted in stronger toxicity, and the cytotoxicity was dependent on the MBZ concentration above a certain threshold value (0.25-0.50 mg/l in a 42-h culture). Inhibition of the proliferation of Chang liver cells by MBZ was detected at a concentration of 0.008 mg/l, a lower concentration than that having a cytotoxic effect. The other two cell lines were less sensitive to the inhibitory effect of MBZ. Proliferation of human mononuclear cells following stimulation by phytohemagglutinin (PHA) was inhibited by MBZ, and this inhibition was more extensive than that of cells stimulated with whole formalin-treated Pseudomonas aeruginosa. It is suggested that dividing cells may be more sensitive to MBZ cytotoxicity. This anti-proliferative effect may be related to its clinically known side effects, such as hepatotoxicity and bone marrow suppression.

We evaluated the usefulness of a Nested PCR method for detecting Legionella pneumophila. This method resulted in L. pneumophila specific detection as far as we evaluated. The first and second step PCR achieved the sensitivity as small as 10 pg and 10 fg of the target DNA, respectively. In the detection from Legionella seeded sputa, the method could detect 0.1 cfu/ml of the bacteria, and it took about 12 hours to detect the target DNA. We demonstrated that the Nested PCR method was superior in sensitivity and rapidity for isolation of the bacteria to the conventional using low pH treatment and selective media for Legionella.