Use of UV induction mutation for reinforcing cracking performance of Bdellovibrio
A technology of Bdellovibrio and its performance, which is applied in the application field of ultraviolet-induced mutation in enhancing the lysis performance of Bdellovibrio, can solve the problems of difficult screening, long time, and difficult recovery of mutation frequency, etc., and achieves convenient operation, simple method, and improved The effect of lytic capacity
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Embodiment 1
[0027] The application of UV-induced mutagenesis, supplemented by infrared light source and LiCl-enhanced mutagenesis includes the following specific steps and conditions:
[0028] 1. Stabilized light waves
[0029] In the dark room, place a 15W ultraviolet lamp above the operating table, and place an infrared lamp with a power of 20W as an auxiliary infrared light source on both sides of the operating table, and turn on the ultraviolet light source 30 minutes in advance to stabilize the light wave;
[0030] 2. Sterile Induced Mutagenesis
[0031] 100mL of Bdellovibrio wild strain Bdellovibrio sp.BDJ01 culture solution, which has been preserved in the Chinese Type Culture Collection Center of Wuhan University in Wuhan City, China, with the preservation number CCTCC NO: M 208011, was kept at 4°C and at a speed of 5000×g. Centrifuge for 20 minutes, take the centrifuged supernatant and centrifuge at 12000×g for 20 minutes at 4°C, and suspend the precipitate with 10 mL of DNB liq...
Embodiment 2
[0051] The application of UV-induced mutagenesis, supplemented by infrared light source and LiCl-enhanced mutagenesis includes the following specific steps and conditions:
[0052] 1. Stabilized light waves
[0053] In the dark room, place a 20W ultraviolet lamp above the operating table, and place 25W infrared lamps as auxiliary infrared light sources on both sides of the operating table. Turn on the ultraviolet light source 60 minutes in advance to stabilize the light wave.
[0054] 2. Sterile Induced Mutagenesis
[0055] The concentrating method of Bdellovibrio wild strain BDJ01 is the same as Example 1, and the obtained concentration is 2×10 7 Pfu / mL Bdellovibrio wild strain concentrate; under the state of filtering visible light, the above 2×10 7 Add 5 mL of pfu / mL concentrated solution into a 9 cm sterile petri dish, then add 1.67 mL of LiCl solution with a concentration of 1.0% to the petri dish to make the final concentration reach 0.25%, add a sterile magnetic rotor...
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