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Application of rapid enzyme assay techniques for monitoring of microbial water quality

机译:快速酶分析技术在微生物水质监测中的应用

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Rapid enzyme assay techniques based on direct measurement Of P-D-galactosidase (GALase). or beta-D-glucuroniclase (GLUase) activity without selective cultivation are used for rapid estimation of the level of coliform bacteria and Escherichia coli in water samples. Reported detection limits using fluorogenic substrates correspond to culturable target bacteria concentrations that can be appropriate within present guidelines for recreational waters. The rapidity, that is detection within one hour, compromises the specificity of the assay; enzyme activity contributions from other than target bacteria need to be considered, particularly at low levels of target bacteria. Enzyme activities are more persistent than the culturability of target bacteria to environmental and disinfection stress, thus water samples may express enzyme activities of both culturable and viable non-culturable cells.
机译:基于直接测量P-D-半乳糖苷酶(GALase)的快速酶法测定技术。无需选择性培养的或β-D-葡萄糖醛酸酶(GLUase)活性可用于快速估算水样中的大肠菌和大肠杆菌水平。报告的使用荧光底物的检测限对应于可培养目标细菌的浓度,该浓度在现行娱乐水准则中可能适当。快速性(即在一小时内检测到)损害了测定的特异性。需要考虑来自目标细菌以外的酶活性的贡献,特别是在目标细菌水平较低时。酶的活性比目标细菌对环境和消毒压力的可培养性更具持久性,因此水样可表达可培养和不可培养的细胞的酶活性。

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