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Other p-substituted phenols such as 4-chlorophenol 4-CP were also degraded by strain S rRNA gene sequences, strain LZ-1 was identified as a Stenotrophomonas sp. Based on the results of phenotypic features and phylogenetic similarity of 16 LZ-1, and both PNP and 4-CP were degraded via the hydroquinone pathway.
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These properties made it potentially useful for the biotreatment of high concentrations of PNP. The effects of pH and temperature were similar to the case of PNP.
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However, strain LZ-1 could not degrade ortho- or meta-substituted phenols.
Generally, strain LZ-1 showed substrate specificity for p-substituted phenols such as 4-halophenols, as mentioned in previous reports Westerberg et al. Resting-cell assay Resting-cell assays were also conducted as described elsewhere Rappert et al.
In contrast, no decrease of PNP was observed in noninduced controls. The results revealed that the enzyme systems catalyzing their degradation were inducible and identical.
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The peaks were both identified as HQ based on mass spectral properties. The samples drawn overnight did not show any intermediate, indicating the complete degradation of substrates.
Degradation was inhibited in water conditions pH 4.
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Potential metabolites were added separately to induced resting-cells or cell-free extracts.
After 30 min, the reaction mixture showed no significant absorbance in the UV region of the spectrum.
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No depletion of 4-nitrocatechol or 4-chlorocatechol was observed. Under aerobic conditions, cell-free extracts of strain LZ-1 showed oxidation activities catalyzing the stoichiometric release of nitrite ions from PNP or chloride ions from 4-CP.
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S 1, indicating that crime LZ-1 was imposed to genus Stenotrophomonas.
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Cytochrome c, acriflavin and picric acid 50 mM, known oxygenase inhibitors, could inhibit the hydroxylation.