Keratin degrading bacteria NJK4
A technology of keratin degrading bacteria and strains, applied in the directions of bacteria, microorganisms, animal feed, etc., can solve problems such as shortage of feed protein resources, and achieve the effect of promoting sustainable development, protecting the environment, and having broad application prospects.
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Embodiment 1
[0014] Example 1: Isolation of Keratin Degrading Strains
[0015] Collect 2 g of samples from the soil environment where feathers have accumulated for a long time, add 10 mL of sterile saline, shake for 1 min, let stand for 5 min, absorb the supernatant to inoculate the nutrient broth medium, and culture at 37 ° C for 48 h.
[0016] Streak inoculation of the above-mentioned cultured strains on a feather meal medium plate, and culture at 37° C. for 24 hours. The formula of the feather meal culture medium is that 1L of distilled water contains: 5.0g sodium chloride, 20.0g feather meal, and 20.0g agar powder. Heat to dissolve, adjust pH to 7.5, and autoclave at 121°C for 15 minutes.
[0017] Purify the bacteria that produce larger hydrolysis circles in the above medium. A bacterium with a strong ability to hydrolyze keratin was obtained and named: NJK4. The bacterial strain NJK4 is classified and named as: Bacillus pumilus, and was deposited in the General Microorganism Center...
Embodiment 2
[0018] Embodiment 2: the expansion culture of above-mentioned bacterial strain NJK4
[0019] The formula of the seed medium is that 1L of distilled water contains: 10.0g peptone, 3.0g beef extract, 2.0g yeast extract, and 5.0g sodium chloride. Heat to dissolve, adjust pH to 7.5, and autoclave at 121°C for 15 minutes.
[0020] The bacterial strain NJK4 obtained above was inoculated into a 250mL Erlenmeyer flask containing 50mL of seed medium, and cultivated on a shaker at a speed of 120r / min for 24h at a temperature of 37°C to obtain a NJK4 liquid culture. The number of cells was 8×1013CFU / mL.
Embodiment 3
[0021] Embodiment 3: Utilize strain NJK4 to ferment and degrade feather keratin in feather fermentation medium
[0022] Take 1 mL of the NJK4 liquid culture obtained in Example 2 and inoculate it into a 500 mL Erlenmeyer flask containing 100 mL of feather fermentation medium, and culture it on a shaker at a speed of 180 r / min for 3 days at a temperature of 37° C. The formula of the feather fermentation medium is, 1L distilled water contains: 0.05g calcium chloride, 0.15g magnesium sulfate heptahydrate, 0.15g sodium chloride, 0.54g dipotassium hydrogen phosphate, 0.09g potassium dihydrogen phosphate, 20g feathers, adjusted pH7.5, autoclave at 121°C for 15 minutes.
[0023] The feathers in the culture medium increased with time, first the feather twigs gradually fell off, and then the feather stalks gradually broke, and the feathers were completely degraded after 3 days; the culture medium gradually became turbid, and the color gradually deepened, and finally became a uniform da...
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Abstract
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