Bdellovibrio bacteriovorus preparation, and fermentation method and applications thereof
A fermentation method and technology of Bdellovibrio, which is applied in the field of fermentation, can solve the problems of low content of Bdellovibrio preparations and low cracking activity, achieve the effects of shortening the fermentation cycle, high activity, and solving excessive energy consumption
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Embodiment 1
[0051] Bacillus subtilis (strain number: GIM1.136, obtained from the Guangdong Provincial Culture Collection Center for Microorganisms) and Escherichia coli (strain number: GIM1.137, obtained from the Guangdong Provincial Culture Collection Center for Microorganisms) were used as The host bacterium prepares Bdellovibrio preparation A and Bdellovibrio preparation B, and the specific process is as follows:
[0052] (1) Preparation of Bacillus subtilis suspension
[0053] Inoculate Bacillus subtilis in nutrient broth medium (peptone 10g, beef extract powder 3g, sodium chloride 5g, pH 7.4±0.2), and place it in a shaker at 33°C for 18h to make it in the logarithmic growth phase , the culture solution was centrifuged at 5000rpm for 25min at 4°C, the precipitate was retained and the supernatant was discarded, and sodium potassium phosphate buffer (concentration: 0.2mol / L, p H7.6), resulting in a concentration of 10 19 cfu / mL of the Bacillus subtilis suspension, then placed in a ref...
Embodiment 2
[0062] Using Bacillus natto (strain number: CGMCC1.1086, from the General Microbiology Center of the China Microbial Culture Collection Management Committee) and Escherichia coli as the host bacteria to prepare leech vibrio preparation A and leech vibrio preparation B, the specific process is as follows:
[0063] (1) Preparation of Bacillus natto suspension
[0064] Bacillus natto was inoculated into the nutrient broth medium (10g peptone, 3g beef extract powder, 5g sodium chloride, pH 7.4±0.2), and placed in a shaker at 35°C for 15h to keep it in logarithmic growth. The culture medium was centrifuged at 6000 rpm for 25 min at 4°C, the supernatant was discarded and the precipitation was retained, and sodium phosphate buffer (concentration 0.1 mol / L, pH 7.4) was added to the precipitation to obtain a concentration of 10 18 cfu / mL of Bacillus natto suspension, and then stored in a 2°C refrigerator for later use;
[0065] The same method as above, the preparation concentration i...
Embodiment 3
[0073] Bifidobacterium bifidum (strain number: GIM1.169, from the Guangdong Provincial Microbial Culture Collection Center) and Salmonella typhimurium were used as host bacteria to prepare Hirudovibrio preparation A and Hirudovibrio preparation B. The specific process is as follows:
[0074] (1) Preparation of Bifidobacterium bifidum suspension
[0075] Bifidobacterium bifidum was inoculated into PTYG medium, placed in a shaker at 37°C for 24h to make it in the logarithmic growth phase, the culture medium was centrifuged at 7000rpm for 20min at 8°C, the precipitate was retained and the supernatant was discarded. , adding potassium phosphate buffer (concentration 0.3mol / L, pH7.5) to the precipitate to obtain a concentration of 10 22 cfu / mL of Bifidobacterium bifidum suspension, and then stored in an 8°C refrigerator for later use;
[0076] The same method as above, using the nutrient broth medium to prepare a concentration of 10 22 cfu / mL Salmonella typhimurium suspension, st...
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