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首页> 外文期刊>Applied and Environmental Microbiology >Distribution of uidA gene sequences in Escherichia coli isolates in water sources and comparison with the expression of beta-glucuronidase activity in 4-methylumbelliferyl-beta-D-glucuronide media.
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Distribution of uidA gene sequences in Escherichia coli isolates in water sources and comparison with the expression of beta-glucuronidase activity in 4-methylumbelliferyl-beta-D-glucuronide media.

机译:大肠杆菌分离株在水中的uidA基因序列的分布,并与4-甲基伞形酮-β-D-葡糖醛酸苷介质中的β-葡糖醛酸糖苷酶活性的表达进行比较。

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摘要

The uidA gene, which encodes the beta-glucuronidase enzyme, was detected in 97.7% of 435 Escherichia coli isolates from treated and raw water sources by DNA-DNA hybridization; 92.4% of the strains expressed the translational product in 4-methylumbelliferyl-beta-D-glucuronide-containing media after reinoculation. Upon initial isolation from water samples, the minimal medium o-nitrophenyl-beta-D-galactopyranoside-4-methylum-belliferyl -beta-D-glucuronide preparations failed to detect more than 50% of the E. coli isolates that possessed uidA gene. Treated water gave the lowest recovery, with Colilert producing 26% positive samples and Coliquik producing 48% positive samples. There appears to be no relationship between the intensity of the autoradiographic signals of the uidA gene and the expression of beta-glucuronidase activity. Therefore, another variable such as physiological condition of the bacteria could be responsible for the nonexpression of the enzyme activity.
机译:通过DNA-DNA杂交,在来自处理过的水源和原水源的435株大肠杆菌中97.7%检出了编码β-葡萄糖醛酸苷酶的uidA基因。重新接种后,有92.4%的菌株在含4-甲基伞形酮-β-D-葡糖醛酸苷的培养基中表达了翻译产物。从水样品中初步分离后,基本培养基邻硝基苯基-β-D-吡喃半乳糖苷-4-甲基-风铃草基-β-D-葡糖醛酸苷制剂未能检测到50%以上的具有uidA基因的大肠杆菌。经处理的水回收率最低,其中Colilert产生26%的阳性样品,Coliquik产生48%的阳性样品。 uidA基因的放射自显影信号的强度与β-葡萄糖醛酸苷酶活性的表达之间似乎没有关系。因此,另一个变量,例如细菌的生理状况,可能是导致酶活性无法表达的原因。

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