Method for detecting pathogenic microorganism
A pathogenic microorganism and bio-nano technology, applied in the field of nano-biotechnology detection, can solve the problems of complex preparation of antibody molecules, limited wide application, poor stability, etc., and achieve the effects of low price, good selectivity and high stability
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Embodiment 1
[0028] 1) Preparation of peptide ligands displayed on the surface of phage
[0029] Using the food-borne pathogen Vibrio parahaemolyticus as the target, the landscape phage f8 / 9 library was panned using biopanning technology, and through the specificity test, a phage monoclonal capable of specifically recognizing Vibrio parahaemolyticus was successfully obtained . The phages were further amplified in large quantities and the phage fusion pVIII displaying specific polypeptides were separated and purified by saturated phenol.
[0030] First, V. parahaemolyticus was inoculated into a 96-well plate and allowed to dry overnight. Take 10 μl of the f8 / 9 landscape phage library (approximately 10 13phage / ml) was mixed with 45 μl library blocking solution, left at room temperature for 1 h, and then the phage library that could not bind to the target cells after incubation was aspirated. Add 100 μl of washing buffer (containing 0.5% BSA, 0.1% Tween-20) to the Vibrio parahaemolyticus c...
Embodiment 2
[0043] Detection of Vibrio parahaemolyticus:
[0044] Using the MnO obtained above 2 Based on the peroxidase-like activity of NSs and the specific binding performance of fusion pVIII to Vibrio parahaemolyticus, a method for detecting Vibrio parahaemolyticus with an unlabeled enzyme-like nanoprobe based on the specific phage pVIII fusion protein was constructed.
[0045] Detection: 100 μl of 40 μg / ml fusion pVIII was added to a 96-well plate, and fixed overnight at 4°C. Wash with PBS buffer (10 mM, pH 7.4) 3 times to remove unfixed fusion pVIII. Block with 10mg / ml BSA solution for 1h, wash twice with PBS buffer (10mM, pH 7.4), add target microorganism Vibrio parahaemolyticus, incubate at 37°C for 2h, then add 100μl 0.5mg / ml multifunctional nano The probe was incubated at 37°C for 1 h, washed three times with PBS buffer (10 mM, pH 7.4), and then added 140 μl acetic acid-sodium acetate buffer (10 mM, pH 4), 20 μl 10 mM H 2 o 2 And 20μl 6mM TMB, react at room temperature for ...
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