A kind of pathogenic Vibrio phage vmyzu10474 and its application
A technology of pathogenic vibrio and phage, which is applied in the field of bioengineering, can solve the problems of few reports of pathogenic vibrio phage, and achieve the effects of reducing pollution and transmission risks, reducing pollution, and efficiently lysing activity
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Embodiment 1
[0037] Phage isolation and purification preparation
[0038] Phage isolation
[0039] Sewage samples were collected from the farmers' market in Lianyungang City, Jiangsu Province. Take 30mL of sewage samples into a 50mL centrifuge tube, centrifuge at 5000×g for 10min, take 5mL of the supernatant and add it to 5mL of LBS liquid medium (10g of tryptone, 5g of yeast extract, 35g of NaCl, 950mL of deionized water, pH 7.0), At the same time, 100 μL of Vibrio mimicus strain CICC10474 in the logarithmic growth phase was added, and cultured on a shaker at 37°C and 100 rpm overnight; the culture in the test tube was transferred to a sterile centrifuge tube, centrifuged at 5000×g for 10 minutes at 4°C, and the supernatant was passed through 0.22 μm filter membrane to obtain the phage stock solution.
[0040] With SM buffer (1L: NaCl 5.8g, MgSO 4 .7H 2 O 2.0g, 1M Tris-HCl (pH7.4) 50mL) carry out 10-fold ratio gradient dilution to the phage stock solution by volume ratio, take 100 μ L...
Embodiment 2
[0045] Characteristic Analysis of Phage VmYZU10474
[0046] Phage Morphological Characteristics
[0047] The microscopic morphological characteristics of phage were observed by transmission electron microscope. Using phosphotungstic acid negative staining method, with the membrane side of the copper grid facing up, take 10 μL of the purified phage VmYZU10474 obtained in Example 1 (10 11 PFU / mL) was dropped on the copper grid, absorbed for 15 minutes, then blotted dry, took out the copper grid, and dried naturally for 2-3 minutes. Then add 2% phosphotungstic acid (PTA) aqueous solution to the copper mesh for staining, take it off after 2 minutes, absorb the water with absorbent paper, dry it in the air for 5 minutes, observe with a transmission electron microscope, and select a clear phage image for photo analysis. The microscopic morphology of VmYZU10474 is as figure 2 As shown, the phage VmYZU10474 presents a symmetrical head, a diameter of about 54.84nm, and no tail.
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Embodiment 3
[0052] Bacteriostatic effect of phage VmYZU10474 on host bacteria in culture medium
[0053] Inoculate 10 mL of LBS liquid medium with Vibrio mimeticus CICC 10474 bacteria liquid, and place it in a 25°C incubator for constant temperature cultivation until about 10 7 CFU / mL, add 100 μL VmYZU10474 (10 9 PFU / mL) purified liquid, add an equal volume of SM buffer (0PFU / mL) to the negative control group, place constant temperature culture and continue to cultivate, sample 1mL every 2h, measure the absorbance value at the wavelength of 600nm with a spectrophotometer, each group Set up 3 parallels and take the average value for analysis.
[0054] The implementation results are as follows Figure 4 As shown, with the extension of culture time, the negative control group OD 600nmRapid growth, reaching 0.85 in 8h, while adding phage VmYZU10474 treatment group maintained at the original concentration in 8h, showing that phage VmYZU10474 in the present invention plays a significant role...
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