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基于噬菌体的生物吸附剂与生物发光 ATP 分析相结合,快速浓缩和检测大肠杆菌。

Bacteriophage-based biosorbents coupled with bioluminescent ATP assay for rapid concentration and detection of Escherichia coli.

机构信息

Canadian Research Institute for Food Safety, University of Guelph, Guelph, Ontario, N1G 2W1 Canada.

出版信息

J Microbiol Methods. 2010 Aug;82(2):177-83. doi: 10.1016/j.mimet.2010.05.013. Epub 2010 Jun 1.

Abstract

Wild type T4 bacteriophage and recombinant T4 bacteriophages displaying biotin binding peptide (BCCP) and cellulose binding module (CBM) on their heads were immobilized on nano-aluminum fiber-based filter (Disruptor), streptavidin magnetic beads and microcrystalline cellulose, respectively. Infectivity of the immobilized phages was investigated by monitoring the phage-mediated growth inhibition of bioluminescent E. coli B and cell lysis using bioluminescent ATP assay. The results showed that phage immobilization resulted in a partial loss of infectivity as compared with the free phage. Nevertheless, the use of a biosorbent based on T4 bacteriophage immobilized on Disruptor filter coupled with a bioluminescent ATP assay allowed simultaneous concentration and detection of as low as 6 x 10(3)cfu/mL of E. coli in the sample within 2h with high accuracy (CV=1-5% in log scale). Excess of interfering microflora at levels 60-fold greater than the target organism did not affect the results when bacteriophage was immobilized on the filter prior to concentration of bacterial cells.

摘要

野生型 T4 噬菌体和展示生物素结合肽 (BCCP) 和纤维素结合模块 (CBM) 的重组 T4 噬菌体分别固定在纳米铝纤维滤器 (Disruptor)、链霉亲和素磁珠和微晶纤维素上。通过监测噬菌体介导的发光大肠杆菌 B 的生长抑制和使用发光 ATP 测定法的细胞裂解来研究固定噬菌体的感染力。结果表明,与游离噬菌体相比,噬菌体固定化导致部分感染力丧失。然而,使用固定在 Disruptor 滤器上的 T4 噬菌体作为生物吸附剂与发光 ATP 测定法相结合,可在 2 小时内以高准确度(对数标度下的 CV=1-5%)同时浓缩和检测低至 6×10(3)cfu/mL 的样品中的大肠杆菌,干扰微生物的数量超过目标生物 60 倍,当在浓缩细菌细胞之前将噬菌体固定在滤器上时,不会影响结果。

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