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首页> 外文期刊>Journal of Microbiological Methods >Analytical limits of four beta-glucuronidase and beta-galactosidase-based commercial culture methods used to detect Escherichia coli and total coliforms
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Analytical limits of four beta-glucuronidase and beta-galactosidase-based commercial culture methods used to detect Escherichia coli and total coliforms

机译:用于检测大肠杆菌和大肠菌群的四种基于β-葡萄糖醛酸苷酶和β-半乳糖苷酶的商业培养方法的分析极限

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Colilerte((R)) (Colilert), Readycult((R)) Coliforms 100 (Readycult), Chromocult((R)) Coliform agar ES (Chromocult), and MI agar (MI) are beta-galactosidase and p-glucuronidase-based commercial culture methods used to assess water quality. Their analytical performance, in terms of their respective ability to detect different strains of Escherichia coli and total coliforms, had never been systematically compared with pure cultures. Here, their ability to detect P-glucuronidase production from E. coli isolates was evaluated by using 74 E. coli strains of different geographic origins and serotypes encountered in fecal and environmental settings. Their ability to detect beta-galactosidase production was studied by testing the 74 E. coli strains as well as 33 reference and environmental non-E. coli total coliform strains. Chromocult. Ml, Readycult, and Colilert detected beta-glucuronidase production from respectively 79.9, 79.9, 81.1, and 51.4% of the 74 E. coli strains tested. These 4 methods detected beta-galactosidase production from respectively 85.1, 73.8, 84.1, and 84.1% of the total coliform strains tested. The results of the present study suggest that Colilert is the weakest method tested to detect beta-glucuronidase production and MI the weakest to detect P-galactosidase production. Furthermore, the high level of false-negative results for E. coli recognition obtained by all four methods suggests that they may not be appropriate for identification of presumptive E. coli strains.
机译:Colilerte(Colilert),ReadycultColiforms100(Readycult),Chromocult Coliform琼脂ES(Chromocult)和MI琼脂(MI)是β-半乳糖苷酶和p-葡萄糖醛酸苷酶-。基础的商业养殖方法,用于评估水质。就其分别检测不同菌株大肠埃希菌和大肠菌群的能力而言,其分析性能从未与纯培养物进行系统比较。在这里,通过使用粪便和环境中遇到的74种不同地理起源和血清型的大肠杆菌菌株,评估了它们从大肠杆菌分离物中检测P-葡萄糖醛酸苷酶产生的能力。通过测试74株大肠杆菌以及33例参比和环境非大肠杆菌,研究了它们检测β-半乳糖苷酶产生的能力。大肠菌群变色。 M1,Readycult和Colilert从所测试的74株大肠杆菌中分别检出79.9%,79.9%,81.1%和51.4%的β-葡萄糖醛酸酶。这4种方法分别检测了测试的大肠菌群中85.1%,73.8%,84.1%和84.1%的β-半乳糖苷酶产量。本研究的结果表明,Collilert是检测β-葡糖醛酸糖苷酶产生的最弱方法,而MI是检测P-半乳糖苷酶产生的最弱方法。此外,通过所有四种方法获得的高水平假阴性大肠杆菌识别阴性结果表明它们可能不适合鉴定推测的大肠杆菌菌株。

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