AFRICAN JOURNAL OF BIOTECHNOLOGY · 2006 · 10 citations · 14 references
Life SciencesBiochemistryMicrobiologyEnvironmental ChemistryEnzymologyWater TreatmentEnzyme AssaysEnzyme CharacterizationEnzyme KineticsEnzyme ScreeningWater ChemistryChemical InterferenceEnvironmental Effects On Enzyme FunctionEnzymatic AssaysEnzyme ActivityEnzymesInterferencePh Effects On Enzyme ActivityPh Effects On Enzymes
A study of the activity of Escherichia coli -D-glucuronidase (GUS) in polluted stagnant and running water samples was performed with an objective of assessing the viability of a direct marker enzyme assay as a suitable alternative to membrane filtration for the indication of faecal pollution in water intended for drinking purposes. The effects of temperature, pH and the presence of different ions on enzyme activity were investigated. GUS exhibited optimal activity at 40oC over a broad pH range (5-9). In general, CO3 2- (as Na2CO3), Cl- (NaCl) and NO3 - (KNO3) increased GUS activity, while ferric chloride (FeCl3), OCl- (as NaOCl) and ferulic acid were inhibitory. However, the enzymatic response to these effectors differed with the source of the sample. Therefore, when these compounds are present in water intended for drinking purposes they can either exaggerate or give false negatives with regards to GUS activity. Environmental GUS properties are different from those of the commercially available (and pure) E. coli GUS. This helps to explain difficulties encountered in applying laboratory methods (developed through seeding of pure water samples with pure enzymes and cultures) to environmental analyses.
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Active Site Residues of Human β-Glucuronidase
Md. Rafiqul Islam, Shunji Tomatsu, Gul N. Shah et al. · Journal of Biological Chemistry · 1999 · 80 citations · Full text