A kind of probiotic isolated from intestinal tract and its application
A technology of probiotics and intestines, applied in the direction of application, medical preparations containing active ingredients, bacteria, etc., can solve the problems of drug resistance and drug residues, endanger human health, etc., achieve good application prospects, improve survival rate and anti-bacteria The effect of disease ability
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Embodiment 1
[0016] Screening and separation of embodiment 1 probiotics
[0017] 1) Sampling: 5-10 healthy turbot (body length 10-15cm) were randomly selected, anesthetized with 100-200ul of 1-2% pentobarbital sodium, dissected under sterile conditions, and their intestines were taken. Quickly wash with sterile 2216E liquid medium (ingredients: peptone 5g, yeast extract 1g, ferric phosphate 0.1g, aged sea water 1000mL, pH 7.5, sterilized at 121°C for 20min) or sterile PBS, 5-10mL glass homogenate Homogenate, homogenate with sterile 2216E liquid medium or PBS according to 10 -1 、10 -2 、10 -3 、10 -4 、10 -5 、10 -6 Gradient dilution. choose 10 -3 and 10 -6 The diluted homogenate was uniformly coated on TSB, LB, and 2216E solid plates. 28-30°C, culture upside down for 24-48h.
[0018] 2) Preliminary screening: the single colony grown on the above-mentioned plate is picked up according to the morphological and structural characteristics of the colony, and cultivated to OD with the liqu...
Embodiment 2
[0022] Example 2: Identification and activity analysis of P115
[0023] 1.16S rDNA analysis
[0024] a) Extraction of P115 genomic DNA: culture P115 to OD 600 =1.0-1.5, use the phenol-chloroform method to extract the genomic DNA of P115 to produce a protein-free layer, and dissolve it with a certain amount of TE solution.
[0025] b) PCR amplification of 16SrDNA: PCR reaction system: 0.5 μl P115 genomic DNA, 1 μl 27F, 1 μl 1492R, 4 μl dNTP, 5 μl Taqbuf, 0.4 μl Taq enzyme, 36.1 μl ddH 2 O. The reaction conditions were pre-denaturation at 95°C for 5 min, denaturation at 95°C for 1 min, renaturation at 54°C for 30 s, extension at 72°C for 1 min, and 30 cycles. Extend at 72°C for 10 min. The PCR product was detected as a single band by electrophoresis, with a size of about 1.6 kb, which was in line with expectations. Among them, specific primers 27F and 1492R are commonly used primers and belong to the public domain.
[0026]
[0027]
[0028] c) Sequencing and analysis...
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