Method for enriching and separating helicobacter pylori

Abstract

The invention discloses a method for enriching and separating helicobacter pylori (Helicobacter pylori, Hp), provides a basis for subsequent research on target bacteria and relates to the technical field of biology. The method comprises the following steps: performing covalent coupling on a hyperbranched polymer and an antibody, coating a long-chain biotin molecule on the antibody-modified hyperbranched polymer, capturing the target bacteria in a sample solution through the dendriform hyperbranched polymer modified by the antibody and the long-chain biotin, identifying streptavidin-modified nano magnetic beads and coupling the long-chain biotin dendriform hyperbranched polymer in the sample solution, separating and suspending the captured bacteria, wherein suspension can be directly analyzed later. Compared with the traditional bacteria magnetic separation method, the method is suitable for performing magnetic separation on the bacteria in a complex substrate, and the separation efficiency of target bacteria in the sample is improved.

Description

Technical field [0001] The invention relates to the field of biotechnology, in particular to a method for separating food-borne pathogenic bacteria based on nano magnetic beads. Background technique [0002] Food-borne pathogen contamination is one of the major problems of food safety in my country. According to WHO statistics, about one-third of people in developed countries are infected with foodborne diseases each year, and 2.2 million people worldwide die each year due to foodborne diseases. In my country, there are 200,000 to 400,000 food poisoning cases each year. Except for accidents, most of them are caused by food-borne pathogens. Helicobacter pylori (Helicobacter Pylor, HP) It is a microaerobe, which requires 5-8% of environmental oxygen. It cannot survive in the atmosphere or absolutely anaerobic environment, but it can be transmitted through hands, unclean food, unclean tableware, feces, etc. It is chronic active gastritis, digestion The main pathogenic bacteria of ...

AI Technical Summary

Problems solved by technology

However, the current separation technology based on micron-scale immunomagnetic beads has many limitations: 1) The specific surface area of ​​micron-sized magnetic beads is relatively small, which reduces the capture efficiency of magnetic beads; Bacterial cells are combined through a multiphase reaction (multiphase reaction), and it usually takes longer to specifically capture bacterial cells in the food matrix; 3) Micron magnetic beads have poor monodispersity and are prone to self-disruption in the food matrix solution. Aggregation or formation of precipitates; 4) Traditional immunomagnetic separation techniques often directly couple antibody molecules to immunomagnetic beads, which often leads to greatly reduced antibody activity and changes in the spatial direction of antibodies. The steric hindrance effect between antibodies reduces the capture efficiency of antibodies. 5) The nature of the food matrix is ​​complex and the concentration of non-target pathogenic bacteria is large. Micron magnetic beads are prone to non-specific adsorption, and it is difficult to realize the detection of food samples. Specific isolation of target bacteria; 6) Too high concentration of micron magnetic beads will cause damage to bacterial cells (the magnetic field causes the magnetic beads on the cell surface to attract each other, causing the cells to be squeezed or even ruptured, resulting in failure of separation

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