Screening and application of probiotic bacillus licheniformis of high-yield compound enzyme
The technology of Bacillus licheniformis and compound enzyme, which is applied in the field of agricultural microbiology, can solve the problems of being susceptible to the influence of internal and external environment, high cost of enzyme preparation preparation, poor growth-promoting effect, etc., and achieves fast growth and reproduction speed and obvious bacteriostatic effect. , the effect of strong resistance
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Embodiment 1
[0031] Example 1: Isolation and identification of strains
[0032] 1. Separation of strains
[0033] Isolate samples were taken from 90-day-old healthy broiler manure from a chicken farm in Wuhan, Hubei Province. After the sample is collected, use a sterile cotton swab to pick up a small amount of feces in a 7mL EP tube filled with 3mL sterile water. After 10 minutes in a water bath at 80°C, spread the bacterial solution on the LB solid medium and select the rough surface The dirty white colonies with pleats and irregular edges are purely cultured. The pure cultures are morphologically observed by Gram stain for preliminary screening. The bacteria are long rod-shaped, single, paired or chain-like gram-positive bacilli. After 20 hours, spores were formed, producing near-mesophytic ellipsoid spores with slightly enlarged cysts. The strain of the invention was named Bacillus licheniformis HDRaBLp, and it was subcultured and preserved. The colony characteristics of this strain on sol...
Embodiment 2
[0061] Example 2: Verification of antibacterial performance of strains
[0062] When preparing a suspension of indicator bacteria (enterpathogenic E. coli, Staphylococcus aureus, Clostridium weichii), use an inoculation needle to pick a small amount of indicator bacteria from the slope and inoculate them into the conventional nutrient broth respectively. Incubate at ℃ for 24h, adjust the concentration of the bacterial suspension to about 10 9 CFU / mL.
[0063] Using the method of plate diffusion (Lyver et al., 1998; Lin Dong et al., 2001), dip a small amount of Bacillus licheniformis with an inoculating rod and spot them in the center of the poured nutrient agar plate. Incubate at 37°C for 24 hours, then buckle the plate upside down. Cover the petri dish with a thin layer of chloroform and fumigate for about 30 minutes to kill the living cells and allow the colony to be fixed on the surface of the plate, then remove the petri dish cover and let the residual chloroform in the plate c...
Embodiment 3
[0066] Example 3: Stress resistance and growth characteristics of Bacillus licheniformis strain HDRaBLp
[0067] 1. Tolerance test
[0068] (1) Bile salt tolerance test
[0069] After the Bacillus licheniformis strain HDRaBLp (isolated from 90-day-old healthy broiler manure of a chicken farm in Wuhan, Hubei Province in December 2013) was activated for 2 generations, 1 mL was inoculated into 9 mL containing 0%, 0.15%, and 0.30% , 0.50% bile salt in conventional LB liquid culture medium, culture for 12h at 37°C, dilute to a suitable multiple, take 0.1mL and apply to solid LB plate, observe the growth and count, repeat each treatment 3 times. The results show that HDRaBLp can tolerate 0.15%, 0.30%, and 0.50% bile salt concentration (see Table 4). The concentration of bile in the digestive tract fluctuates in the range of 0.03% to 0.3%. Therefore, the Bacillus licheniformis strain HDRaBLp can tolerate the environment of intestinal bile salts.
[0070] Table 4 Tolerance of Bacillus liche...
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