Biological demoulding agent and preparation method
A mold remover, biological technology, applied in animal feed, animal feed, application and other directions, can solve the problems of restricting large-scale application and promotion, high price, and achieve the effect of simple and flexible use, low price, and protection of intestinal mucosa
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0021] The biological mold removal agent of the present invention is formed by mixing and drying the Bacillus subtilis / yeast cell wall conjugate and glucose. The colonization time of the Bacillus subtilis in the digestive tract of the host is at least 12 hours. The mass ratio of the compound to the glucose is 1:15.
[0022] Follow the steps below to prepare:
[0023] a. Inoculate the seed solution of Bacillus subtilis (Accession No.: CICC 20683) that has been colonized in the digestive tract of the host for at least 12 hours in a 1:100 (VN) ratio in a 1000 mL / 5000 mL Erlenmeyer flask filled with medium, 37 Shake culture at ℃ overnight, after the strain grows to the late logarithmic stage, centrifuge to collect the bacterial pellet, then wash with sterile PBS (pH 8.0) for 2-3 times, and finally use an appropriate volume of PBS buffer (pH 8.0) to make a bacterial suspension for later use ;
[0024] b. Add yeast cell wall (MOS) to the bacterial suspension according to the ratio...
Embodiment 3
[0061] The biological mildew remover of the present invention is formed by mixing and drying the Enterococcus faecium / yeast cell wall conjugate and soluble starch. The colonization time of the Enterococcus faecium in the digestive tract of the host is at least 48 hours. The mass ratio of conjugate to soluble starch is 1:25.
[0062] Follow the steps below to prepare:
[0063] a. Inoculate the seed solution of Enterococcus faecium (Accession No.: CICC 6078) that has been colonized in the digestive tract of the host for at least 48 hours in a 1:100 (VN) ratio in a 1000 mL / 5000 mL Erlenmeyer flask filled with medium, 37 Shake culture at ℃ overnight, after the strain grows to the late logarithmic stage, centrifuge to collect the bacterial pellet, then wash with sterile PBS (pH 8.0) for 2-3 times, and finally use an appropriate volume of PBS buffer (pH 8.0) to make a bacterial suspension for later use ;
[0064] b. Add yeast cell wall (MOS) to the bacterial suspension according t...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


