Polypeptide preparation for microorganism ferment making feed and preparation method
A microbial fermentation and feed technology, which is applied in animal feed, animal feed, microbial/single-cell algae protein processing, etc., can solve problems such as limited application range and potential safety hazards, and achieve guaranteed survival time, low site requirements, and improved daily The effect of feed intake
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Embodiment 1
[0042] Step 1: Breeding of Fermentation Strains
[0043] a. Subculture of strains: Bacillus subtilis strains, Lactobacillus plantarum and Lactobacillus casei provided by the Culture Preservation Center of the Ministry of Agriculture are used to subculture through nutrient agar medium, and line separation is drawn during the cultivation process to select for fast growth and colony characteristics For obvious strains, the strains should be preserved at 4°C;
[0044] b. Composite induction of strains: the Bacillus subtilis preserved in step a is diluted to 10 with 0.9% normal saline -5 , treat the bacterial suspension with a low fire for 30 seconds in a microwave oven, count by hemocytometer, compare the number of viable bacteria before and after treatment, spread the processed bacterial suspension with a higher survival rate on a flat plate of starch medium, Inverted culture at 35°C for 48 hours, select colonies with a ratio of transparent circle diameter to colony diameter gre...
Embodiment 2
[0062] Step 1: Breeding of Fermentation Strains
[0063] a. Bacterial strain passage: Same as Example 1.
[0064] b. Compound induction of strains: the preserved Bacillus subtilis was diluted to 10 with 0.9% normal saline -7 , treat the bacterial suspension with low heat in a microwave oven for 45S, count by hemocytometer, spread the treated bacterial suspension on a starch medium plate, and culture it upside down at 37°C for 48 hours, and select the culture medium The colony with the larger ratio of the diameter of the middle transparent circle to the diameter of the colony (HC value) was inoculated into a nutrient agar test tube for preservation. Dilute the preserved strain to 10 -7 . At 30cm place, use a power of 20W UV lamp (wavelength is 260nm) to treat for 25s, and the bacteria suspension after treatment is cultivated upside down at 35°C for 48h on the nutrient agar plate, and the colony with fast growth rate is selected for shake flask experiment. Observe the growth...
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