首页> 外文期刊>Journal of Rapid Methods and Automation in Microbiology >Luminescent methods to detect viable and total Escherichia coli O157:H7 in ground beef.
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Luminescent methods to detect viable and total Escherichia coli O157:H7 in ground beef.

机译:发光方法检测碎牛肉中的活菌和总大肠杆菌O157:H7。

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Escherichia coli O157:H7 was inoculated into ground beef. Samples were incubated in E. coli broth plus novobiocin growth media at 37C for 5 h. Bacteria were captured by magnetic beads coated with anti-E. coli O157:H7 antibodies and were treated with menadione, a membrane-permeable electron-transfer shuttering reagent, to oxidize the cellular nicotinamide adenine dinucleotide phosphate (NAD[P]H). Alternatively, bead-captured bacteria were sandwiched by second anti-E. coli O157:H7 antibodies labeled with peroxidase. The level of NAD(P)H and the enzyme activity of antibody-bound peroxidase were then measured by luminol-linked luminescence. The treatment of the E. coli O157:H7 with a bacterial protein extraction reagent diminished the luminescence associated with cellular NAD(P)H but not the luminescence associated with the sandwiched peroxidase label. Thus, the NAD(P)H-linked luminescence, not the luminescence that was associated with the sandwiched complexes, was related to the viability of the E. coli O157:H7..
机译:将大肠杆菌O157:H7接种到碎牛肉中。将样品在大肠杆菌肉汤加新霉素生长培养基中于37°C孵育5小时。细菌被涂有抗E的磁珠捕获。大肠杆菌O157:H7抗体,并用甲萘醌(一种膜可透过的电子转移模板试剂)处理,以氧化细胞烟酰胺腺嘌呤二核苷酸磷酸(NAD [P] H)。备选地,捕获珠子的细菌被第二抗E夹在中间。用过氧化物酶标记的大肠杆菌O157:H7抗体。然后通过鲁米诺连接的发光测量NAD(P)H的水平和抗体结合的过氧化物酶的酶活性。用细菌蛋白提取试剂处理大肠杆菌O157:H7可减少与细胞NAD(P)H相关的发光,但不会减少与夹心的过氧化物酶标记相关的发光。因此,NAD(P)H连接的发光,而不是与夹心复合物相关的发光,与大肠杆菌O157:H7的生存能力有关。

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