A kind of production method of Bdellovibrio microecological preparation
A micro-ecological preparation, Bdellovibrio phage technology, applied in the field of breeding, can solve the problems of reduced cracking activity and short shelf life of Bdellovibrio phage, and achieve the effect of reducing dosage, reducing production cost and extending shelf life
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Embodiment 1
[0027] Embodiment 1: host bacterium is fixed with polyvinyl alcohol, and specific process is as follows:
[0028] (1) Preparation of host bacteria suspension
[0029] The cultured Escherichia coli was sterilized under high pressure at 115°C for 30 minutes, then centrifuged at 10,000 rpm in a tubular high-speed centrifuge, and the bacteria were collected and diluted to a concentration of 10 with phosphate buffer. 12 cfu / mL host bacterial suspension, stored at 4°C for later use;
[0030] (2) Preparation of sustained-release granules
[0031] Dilute the host bacterial suspension by 2 times with water, then add 10% polyvinyl alcohol, fully mix and dissolve, add 1 volume of vegetable oil and stir thoroughly to form a sphere, set and solidify at -20°C for 8 hours, and wash for later use. (3) Preparation of culture medium
[0032] Dilute the pH7.4 phosphate buffer 100 times with water, then add 40mg / L CaCl 2 and 40mg / L of MgCl 2 .
[0033] (4) Preparation of seeds
[0034] Add...
Embodiment 2
[0037] Embodiment 2: The host bacterium is fixed with sodium alginate, and the specific process is as follows:
[0038] (1) Preparation of host bacteria suspension
[0039] The cultured Escherichia coli was sterilized under high pressure at 115°C for 30 minutes, then centrifuged at 10,000 rpm in a tubular high-speed centrifuge, and the bacteria were collected and diluted to a concentration of 10 with phosphate buffer. 12 cfu / mL host bacterial suspension, stored at 4°C for later use;
[0040] (2) Preparation of sustained-release granules
[0041] Dilute the host bacterial suspension by 1 time with water, add 2% sodium alginate, mix well to dissolve, and then drop in 3% CaCl 2 , cross-link for 30 minutes, and wash for later use.
[0042] (3) Preparation of culture medium
[0043] Dilute the pH7.2 phosphate buffer 20 times with water, then add 20mg / L CaCl 2 and 20mg / L of MgCl 2 .
[0044] (4) Preparation of seeds
[0045] Add 5% of the host bacteria suspension prepared in...
Embodiment 3
[0048] Embodiment 3: use gelatin and sodium alginate to fix the host bacteria, the specific process is as follows:
[0049] (1) Preparation of host bacteria suspension
[0050] The cultured Escherichia coli was sterilized under high pressure at 115°C for 30 minutes, then centrifuged at 10,000 rpm in a tubular high-speed centrifuge, and the bacteria were collected and diluted to a concentration of 10 with phosphate buffer. 12 cfu / mL host bacterial suspension, stored at 4°C for later use;
[0051] (2) Preparation of sustained-release granules
[0052] Dilute the host bacterial suspension by 1 time with water, add 7% gelatin and 3% sodium alginate, mix well to dissolve, and then add 4% CaCl dropwise 2 , cross-link for 60 minutes, and wash for later use.
[0053](3) Preparation of culture medium
[0054] Dilute the pH7.2 phosphate buffer 10 times with water, then add 60mg / L CaCl 2 and 60mg / L of MgCl 2 .
[0055] (4) Preparation of seeds
[0056] Add 15% of the host bacteri...
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