Probiotics with antibacterial ability and their application
A technology of probiotics and ability, applied in the field of probiotics, can solve problems such as drug resistance and drug residues, endangering human health, etc., and achieve the effect of good application prospects
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Embodiment 1
[0023] Example 1 Screening and isolation of probiotic Enterobacter ludwigii PC88
[0024] 1) Sampling: 5-10 healthy flounder (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 use sterile TSB liquid medium (ingredients: tryptone 17g, polyvalent peptone 3g, yeast extract 6g, sodium chloride 5g, dipotassium hydrogen phosphate 2.5g, glucose 2.5g, add water to 1L, pH=7.2-7.5) Or wash with sterile PBS, homogenize with 5-10mL glass homogenizer, use sterile TSB 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 evenly spread on TSB and LB solid plates respectively. 28-30°C, culture upside down for 24-48h.
[0025] 2) Preliminary screening: the single colony grown on the above plate, according to the morphological and structural characteristics of the colo...
Embodiment 2
[0029] Example 2: Identification and activity analysis of PC88
[0030] 1) 16S rDNA analysis
[0031] a) Extraction of PC88 genomic DNA: culture PC88 to OD 600 =1.0-1.5, use the phenol-chloroform method to extract the genomic DNA of PC88 to produce a protein-free layer, and dissolve it with a certain amount of TE solution.
[0032] b) PCR amplification of 16SrDNA: PCR reaction system: 0.5 μl PC88 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.
[0033] c) Sequencing and analysis: After recovering the gel of the PCR product, send it to a sequencing company for sequencing. Results After nBlast analysis,...
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