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A rapid and sensitive fluorimetric β-galactosidase assay for coliform detection using chlorophenol red-β-D-galactopyranoside

机译:使用氯酚红-β-D-吡喃半乳糖苷进行大肠菌群检测的快速灵敏的荧光β-半乳糖苷酶测定

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摘要

We report on a new fluorimetric assay for β- galactosidase (β-gal) and faecal coliform bacteria that utilizes a long-wavelength dye, chlorophenol red-β-Dgalactopyranoside (CPRG), that has been widely used for colorimetric assays. The novel feature of this new assay is the unexpected development of a large fluorescence response from liberated chorophenol red (CPR) upon complexation with poly-L-arginine (pR) in solution. The binding of CPR to pR occurs through the sulphonate group of CPR, causing formation of a charge-transfer complex and up to a 70-fold increase in emission intensity. A major advantage of the assay is the ability to utilize excitation and emission wavelengths in the red end of the spectrum, which avoids common interferences obtained when using UV-absorbing dyes such as 4- methylumbelliferyl-β-D-galactopyranoside. We provide data on the utility of CPRG as a fluorimetric reporter for both β-gal and Escherichia coli ATCC 25922 and demonstrate optimized reaction conditions for rapid and sensitive detection of E. coli at a level of 1 colony-forming unit (cfu)/10 mL after 12 h of culture followed by a 1-h assay, which is below the regulatory limit for testing of recreational water.
机译:我们报告了一种新的荧光测定法,用于β-半乳糖苷酶(β-gal)和粪便大肠菌,该细菌利用长波长染料氯酚红-β-D-吡喃半乳糖苷(CPRG),该方法已被广泛用于比色测定。这项新测定法的新颖之处在于,与溶液中的聚L-精氨酸(pR)​​络合后,释放出的胆酚红(CPR)产生了巨大的荧光响应,这出乎意料。 CPR通过pPR的磺酸盐基团与pR结合,从而形成电荷转移复合物,并且发射强度最多增加70倍。该测定法的主要优点是能够利用光谱红色端的激发和发射波长,从而避免了在使用吸收紫外线的染料(如4-甲基伞形基-β-D-吡喃半乳糖苷)时产生的常见干扰。我们提供了有关CPRG用作β-gal和大肠杆菌ATCC 25922的荧光报告仪的实用数据,并展示了用于快速灵敏检测大肠杆菌的最佳反应条件(水平为1个菌落形成单位(cfu)/ 10)培养12 h后进行1 mL分析,然后进行1 h分析,该水平低于用于娱乐用水测试的标准限值。

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