A nucleic acid aptamer h7 capable of targeting and inhibiting Vibrio anguillarum and its application
A technology of nucleic acid aptamer and Vibrio anguillarum, which is applied to medical preparations containing active ingredients, antibacterial drugs, and pharmaceutical formulas, etc., and can solve problems such as hidden dangers, increased number of vibriosis infections, and quality and safety risks of aquatic products , to achieve the effects of simple chemical synthesis, short screening cycle and good application prospects
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Publication Date
- 2021-08-17
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Abstract
Description
technical field
[0001] The present invention relates to a nucleic acid aptamer, in particular to a nucleic acid aptamer H7 capable of targeting and inhibiting Vibrio anguillarum and its application. Background technique
[0002] foreword
[0003] Vibrio anguillarum is one of the most common opportunistic pathogens in aquaculture. The aquaculture animal diseases caused by it are prevalent in the world, and can infect more than 50 kinds of sea and freshwater organisms, including rainbow trout, eel, sweetfish, perch, cod, Turbot, flounder, yellow croaker, etc. At present, with the development of high-density and intensive aquaculture, the number of vibriosis in farmed animals is also increasing, which brings huge economic losses to the aquaculture industry. Due to the serious harm caused by Vibrio anguillaris to aquaculture, a large amount of antibiotics are mainly used to prevent and control Vibrio, which not only leads to the emergence of bacterial resistance, but also brin...
Examples
Embodiment Construction
[0020] 1 SELEX screening of nucleic acid aptamers
[0021] (1) Bacteria treatment: Take the cultured Vibrio anguillarum in a centrifuge tube, centrifuge at 6000r / min for 5min, discard the supernatant, wash the bacteria 3 times, add sterile culture medium and mix evenly, measure the OD value of the bacteria solution, and then Take Vibrio anguillarum bacteria liquid containing about 4×108 cells, centrifuge at 6000r / min for 5min, discard the supernatant, wash the bacterial pellet three times with 0.9% normal saline, wash the bacterial pellet once with 1×binding buffer, and finally Add 100 μL of 2× binding buffer to resuspend.
[0022] (2) Binding: take ssDNA random library, dilute to 3 μmol / L 100 μL with 2× binding buffer, denature in 95°C constant temperature metal bath for 5 minutes, then ice-bath for 10 minutes, then add to the previous bacterial suspension, mix well Afterwards, combine in a shaker at 30°C and 100r / min for 2h.
[0023] (3) Washing: After the binding is compl...