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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[0026] Example 1
[0027] The application of UV-induced mutations, with the aid of infrared light sources and LiCl enhanced mutagenesis includes the following specific steps and conditions:
[0028] 1. Stable light waves
[0029] In the dark room, place the 15W ultraviolet lamp above the operating table, and place the 20W infrared lamp as the auxiliary infrared light source on both sides of the operating table. Turn on the ultraviolet light source 30 minutes in advance to stabilize the light wave;
[0030] 2. Aseptic induced mutation
[0031] 100mL of Bdellovibrio sp.BDJ01 culture broth of the wild strain Bdellovibrio sp.BDJ01, which has been deposited in the Chinese Type Culture Collection in Wuhan University, Wuhan City, Wuhan, China, with the deposit number CCTCC NO: M 208011, at 4°C and at a speed of 5000×g Centrifuge for 20 min, take the supernatant after centrifugation and centrifuge at 12000×g for 20 min at 4°C, and suspend the precipitate in 10 mL DNB liquid medium. The su...
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[0050] Example 2
[0051] The application of UV-induced mutations, with the aid of infrared light sources and LiCl enhanced mutagenesis includes the following specific steps and conditions:
[0052] 1. Stable light waves
[0053] In the dark room, place a 20W ultraviolet lamp above the operating table, and place the 25W infrared lamp as an auxiliary infrared light source on both sides of the operating table. Turn on the ultraviolet light source 60 minutes in advance to stabilize the light wave.
[0054] 2. Aseptic induced mutation
[0055] The concentration method of Budovibrus wild strain BDJ01 is the same as in Example 1, and the concentration is 2×10 7 pfu / mL of the concentrated liquid of the wild strain of Budovibrio; under the state of filtering visible light, the above 2×10 7 Add 5mL of pfu / mL concentrated solution to a 9cm sterile petri dish, and then add 1.67mL LiCl solution with a concentration of 1.0% to the petri dish to make the final concentration reach 0.25%. Add a s...
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