Wide-lysis-spectrum Escherichia coli phage and composition, kit and application thereof
A technology of Escherichia coli and bacteriophage, which is applied in the direction of bacteriophage, virus/phage, medical raw materials derived from virus/phage, etc., to achieve the effect of excellent strain resources and good application and development prospects
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Embodiment 1
[0041] Example 1: Isolation, preparation and purification of phage
[0042] In the present invention, the source sample of Escherichia coli phage CL1 is collected from the sewage of Zhongcai farmer's market in Jiangning District, Nanjing City, Jiangsu Province, the source sample of CL6 is collected from cow dung in Jiangnan Dairy Farm, Jiangning District, Nanjing City, Jiangsu Province, and the source sample of CL7 is collected in Jiangsu Province The underground sewage in Jiangning University City, Nanjing City was filtered through double-layer filter paper, then centrifuged at low speed and normal temperature, and then the supernatant was filtered with a 0.22 μm filter membrane.
[0043] Isolation of phage: take 10mL filtered supernatant, add it to 10mL 2 times TSB medium, add 1mL phage host bacteria logarithmic phase bacteria liquid at the same time, place it at 37°C for 6 hours, take the above culture, and put it under the condition of 8000rpm Centrifuge for 10 min, filter...
Embodiment 2
[0045] Embodiment 2: Electron microscope observation of phage
[0046] Take the supernatant of each phage culture obtained in Example 1 for electron microscope observation: take 20 μ L of sample and drop it on the copper grid, wait for its natural precipitation for 15 minutes, absorb excess liquid from the side with filter paper, add 1 drop of 2% phosphotungstic acid (PTA ) on a copper grid, dyed for 10 minutes, sucked the dye solution from the side with filter paper, and observed with an electron microscope after drying: the results are as follows: figure 1 As shown, coliphage CL1 has a polyhedral symmetric head and a long tail with a long diameter L of about 60nm and a transverse diameter W of about 15nm; the tail is about 60nm long and 2nm wide with retractable Muscle sheath (see figure 1 ); the morphology of Escherichia coli phage CL6 was found to be tadpole-shaped, with a polyhedral symmetrical head structure and a long tail. About 3 nm, with a contractile muscle sheath...
Embodiment 3
[0047] Example 3: Extraction and sequencing of phage genome
[0048] Take 100 mL of each phage prepared in Example 1, add DNaseI and RNaseA at a final concentration of 1 μg / mL, incubate at 37°C for 60 min, add 5.84 g NaCl (final concentration 1 mol / L), dissolve and place in an ice bath for 1 h. Centrifuge at 11,000 rpm for 10 min at 4°C, and transfer the supernatant to a new centrifuge tube. Add solid PEG8000 (final concentration 10%, that is, add 10 g to 100 mL), and after complete dissolution, ice bath for at least 1 h. Centrifuge at 11,000 rpm for 20 min at 4°C, and resuspend the pellet with a small amount of SM solution. Add an equal volume of chloroform and isoamyl alcohol for extraction, shake gently for 30 s, centrifuge at 8000 rpm for 1 min, absorb the supernatant, and repeat the extraction until clarification. Add DNase I and RNase A again to a final concentration of 1 μg / mL, and react at 37°C for 30-60 minutes. Add EDTA to a final concentration of 20 mmol / L (that ...
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