Method for rapidly screening microorganism strain capable of generating gonyautoxin and digoxin labeled DNA (Deoxyribonucleic Acid) probe used by method
A technology for labeling of gonitoxin and digoxin, which is applied in the field of marine biology, can solve the problems of rapid screening of bacterial strains, heavy workload, long cycle, etc., and achieve the effect of not easy to operate errors and low errors
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Embodiment 1
[0029] Sensitivity test sample strain cultivation, take samples of nitrate-reducing bacteria (Nitratireductor sp.LZ3-1, chemical analysis of its metabolites confirmed to produce GTXs toxin), pick a single colony of the LZ3-1 strain on the plate, and extract its For DNA samples, dilute it 5-10 times.
Embodiment 2
[0031]Specific detection sample strain cultivation, take samples of 1 strain of toxin-producing bacteria (nitrate-reducing bacteria), 9 strains of non-toxin-producing bacteria (including Escherichia coli, Shigella sonneri, Staphylococcus aureus, Bacillus subtilis, Pseudomonas aeruginosa bacterium, Vibrio harveii, Vibrio salmonicida, Moraxella lacunae, Pseudomonas shigellai), pick single colonies on the plate of each strain, and extract their DNA samples according to the conventional method of molecular cloning, Dilute it 5-10 times.
Embodiment 3
[0033] A method for rapid screening of microorganism strains producing gonitoxins, said method comprising the following steps:
[0034] 1) Take 2 μL of the sample prepared in Example 1 or Example 2 and put it on a nitrocellulose membrane to make the membrane to be tested, soak the membrane to be tested in 0.3mol / L NaOH solution for 5min, and place it at 60°C after immersion Dry for 1 hour to immobilize DNA, then place it in 3 mg / mL lysozyme solution with pH 7.6, warm water bath at 35°C for 15 minutes, wash off bacterial cell residues on the membrane surface with TE buffer to obtain pretreated DNA membrane , placing the obtained pre-treated DNA membrane in a hybridization solution, and incubating at 40°C for 40 minutes to obtain a pre-hybridization solution;
[0035] 2) Put the digoxin-labeled DNA in boiling water for 8 minutes and cool it in an ice bath to obtain a labeled DNA solution. Take the labeled DNA solution and add it to the pre-hybridization solution obtained in step...
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