Hemoglobin degrading bacterium NJM4
A hemoglobin and bacteria-degrading technology, which is applied in the direction of bacteria, microorganisms, animal feed, etc., can solve the problems of soaring prices and shortage of feed protein resources, and achieve the effects of protecting the environment, promoting sustainable development, and broad application prospects
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Embodiment 1
[0017] Embodiment 1: Efficient strain isolation
[0018] A total of 2 g of samples were collected from special environments such as the sewage ditch of the slaughterhouse, added to 10 mL of nutrient broth, shaken for 1 min, and allowed to stand for 5 min. The supernatant was drawn to inoculate the nutrient broth medium, and cultured at 37°C for 48 h.
[0019] Streak inoculation of the above-mentioned cultured strains on a blood agar medium plate, and culture at 37° C. for 24 hours. The formula of the blood agar medium is as follows: 1L of distilled water contains: 10.0g of peptone, 3.0g of beef extract, 5.0g of sodium chloride, and 20.0g of agar powder. Heat to dissolve, adjust pH to 7.5, and autoclave at 121°C for 15 minutes. Cool to 45°C-50°C, and add 50mL of fresh sheep blood.
[0020] Purely culture the bacteria that produce larger hemolytic circles in the above medium. A strain of bacteria with greater hemolytic ability was obtained and named: NJM4. The strain NJM4 is...
Embodiment 2
[0021] Embodiment 2: the expansion culture of above-mentioned bacterial strain NJM4
[0022] The formula of the seed medium is that 1L of distilled water contains: 6.0g of peptone, 4.0g of beef extract, 2.0g of yeast extract, and 5.0g of sodium chloride. Heat to dissolve, adjust pH to 7.5, and autoclave at 121°C for 15 minutes.
[0023] The bacterial strain NJM4 obtained above was inoculated into a 250mL Erlenmeyer flask containing 50mL of seed medium, and cultured on a shaker at a speed of 120r / min for 24h at a temperature of 37°C to obtain a NJM4 liquid culture. The number of bacteria was 4×10 11 CFU / mL.
Embodiment 3
[0024] Example 3: Using strain NJM4 to ferment and degrade hemoglobin in the hemoglobin fermentation medium Take 6 mL of the NJM4 liquid culture obtained in Example 2 and inoculate it in a 250 mL Erlenmeyer flask containing 150 mL of the hemoglobin fermentation medium at a temperature of 37°C. Cultivate for 24 h on a shaker at a speed of 120 r / min. The formula of hemoglobin fermentation medium is: 1L distilled water contains: 4.0g glucose, 0.4g dipotassium hydrogen phosphate, 0.5g sodium chloride, 0.6g potassium dihydrogen phosphate, 0.1g magnesium sulfate, 0.02g ferric sulfate, adjust pH7. Autoclave at 0,121°C for 15 minutes. Cool to 45°C-50°C, add 10.0g fresh sheep hemoglobin. The degradation rate of hemoglobin was measured by Kjeldahl method, and the degradation rate of hemoglobin was 53.6% after 24 hours of culture.
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