A phage capable of lysing bovine Streptococcus agalactiae and its application
A technology for Streptococcus lactis and Streptococcus, applied in the field of bioengineering, can solve the problems of narrow lysis spectrum and unclear sequence type of Streptococcus agalactiae, and achieve good killing effect, no toxic side effects, and high safety
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Embodiment 1
[0036] Example 1 Isolation and preparation of bacteriophage
[0037] The host bacteria of the test phage of the present invention is the clinical isolate HZJG1201 of Streptococcus agalactiae.
[0038] The samples of the present invention were collected from mastitis milk samples from experimental farms in Yangzhou City, Jiangsu Province. The milk samples were centrifuged at 12,000 rpm for 20 minutes, and the supernatant was filtered through a 0.22 μm filter membrane. Take 10 mL of filtered supernatant, add 0.5 mL of host bacteria overnight culture, and then add sterile CaCl 2 The mother liquor was mixed to a final concentration of 1.25mM, and 20mL of THB medium was added. After culturing in a 37°C incubator for 6-8 hours, the above culture was taken at 12000rpm, centrifuged for 30min, and the supernatant was taken; then 10mL of the supernatant was taken. , add 0.5 mL of the host bacteria overnight culture, add sterile CaCl 2 The mother liquor was mixed to a final concentrati...
Embodiment 2
[0041] Example 2 Amplification and purification of phage
[0042] On the double-layered plate with plaque formation in Example 1, use the pipette tip to pick a single plaque with a larger diameter, inoculate it into 3-5 mL of THB medium, and add 0.1 mL of phage host bacterial solution. Mix well, act at room temperature for 15 minutes, incubate at 37° C. for 10-14 hours, centrifuge at 12,000 rpm for 10 minutes at 4° C., take the supernatant, and add 0.3% chloroform. Repeatedly picking individual plaques 4-5 times until the phages were purified into plaques of the same size.
[0043] Take 1 mL of freshly cultured host bacteria and add 0.3 mL of phage lysate (in a ratio of 1:1, 1:10 and 1:100 for a single phage culture and host bacteria, respectively). Incubate at 37°C for 20 min to make the phage particles adsorb to the host bacteria; add 100 mL of THB liquid medium, and then add CaCl 2 The mother solution was brought to a final concentration of 1.25 mM, shaken at 37 °C for 12...
Embodiment 3
[0047] Example 3 Transmission electron microscope detection of bacteriophage
[0048] Take the purified phage particles (provided in Example 2) for electron microscope observation, add 10 μL of the sample and drop it on the copper grid, wait for it to settle for 15 minutes, absorb the excess liquid with filter paper, and stain with 2% phosphotungstic acid (PTA) for 1-2 minutes , and observed by transmission electron microscope (Hitachi H-7650) after drying.
[0049] observe as figure 2 As shown, the phage head is a regular polyhedron with a head diameter of about 50 nm and a tail length of about 200 nm. According to "The Taxonomy of Viruses - The Ninth Report of the International Committee on Taxonomy of Viruses" published by the International Committee on Taxonomy of Viruses (ICTV) in 2011, vB_SagS_FSN1 belongs to the family Siphoviridae.
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