Bacillus coagulans having aquatic pathogen antagonistic characteristic and application of bacillus coagulans
A technology of bacillus coagulans and aquatic pathogens, applied in the field of microorganisms, can solve the problems of difficult preservation, easy inactivation, poor stress resistance, etc., and achieve the effect of reducing pollutant content and improving the quality of aquaculture water
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Embodiment 1
[0024] Embodiment 1: Screening and isolation of strains
[0025] Allogenetic gibel carp samples were collected in Wuxi Goose Lake breeding pond, the fish body was dissected to take the intestinal tract, added physiological saline, and ground to make a homogenate, each sample was absorbed 1.0mL, heated at 80°C for 10min, and pipette gun to absorb 0.1mL Spread on YPD solid medium and culture at 37°C. According to the size of the colony, the well-growing colony was selected and screened repeatedly until a uniform single colony was obtained, which was named JSSW-LA-07-1.
Embodiment 2
[0026] Embodiment 2: strain identification
[0027] (1) Morphological characteristics
[0028] Strain JSSW-LA-07-1, Gram staining was positive, microscopic examination was rod-shaped, cell diameter <1 μm, and could form spores. The diameter of the colony on the MRS plate is 2.0-3.0mm, the shape is irregular, the surface is wrinkled, opaque, and no pigment. A large number of round, wrinkled, opaque, white colonies can be obtained on LB medium.
[0029] (2) Biochemical properties
[0030] Strain JSSW-LA-07-1 is positive for Gram staining, catalase, β-galactosidase, VP test and methyl red test, and can grow at 50°C. Oxidase, urease, arginine dihydrolase, ornithine decarboxylase, lysine decarboxylase tests are negative, can not hydrolyze starch, gelatin, casein, and do not produce indole and H 2 S, cannot grow on citric acid.
[0031] The results of growth experiments showed that the strain could utilize D-cellobiose, α-D-glucose, D-mannose, D-fructose, D-trehalose, dextrin, ...
Embodiment 3
[0039] Embodiment 3: Bacteriostasis determination
[0040] Place a piece of sterile filter paper at a concentration of 1.0×10 7 CFU / mL Bacillus coagulans JSSW-LA-07-1 soaked in fresh culture solution for 1.0h. Take the concentration as 5.0×10 6 Common pathogenic bacteria in aquaculture in CFU / mL Aeromonas hydrophila, Aeromonas sobria, Aeromonas victoria, Aeromonas caviae, Listonia eelensis, Edwardsiella parahaemolyticus Vibrio vibrio, Escherichia coli, Vibrio alginolyticus liquid culture solution 0.1mL, spread on the LB agar medium plate respectively, and then paste the filter paper soaked in the bacterial solution on the petri dish, stick 3 pieces on each plate , and each plate was replicated 3 times. The plates were placed in a 28°C incubator for 24 and 48 hours, and the size of the inhibition zone was measured. The measurement results are shown in Table 1:
[0041] Table 1 Bacillus coagulans JSSW-LA-07-1 antibacterial assay results (inhibition zone diameter: mm)
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