Preparation method of composite probiotic preparation added into ruminant feed
A compound probiotic and ruminant technology, applied in animal feed, animal feed, microbial-based methods, etc., can solve the problems of low binding rate, high toxicity, pollution, etc., and achieve the effect of increased binding rate and enhanced absorption capacity
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example 1
[0026]First, the Candida krusei strain stored at 4°C was inoculated in solid activation medium, cultured at 30°C for 24 hours, and then transferred three times to restore the viability of the strain. After the activation was completed, the g Candida russii slant was inoculated in the seed medium, put it into a constant temperature shaker incubator, and cultured at 30°C at a speed of 100r / min for 24 hours to obtain seed liquid 1; In the solid activation medium, culture at 28°C for 30 hours, and then repeat the transfer 3 times, so that the vitality of the strain can be restored. The seed solution 2 was obtained by constant temperature cultivation for 18 hours; then the Streptococcus thermophilus strain was inoculated in the solid activation medium, cultured at 38°C for 36 hours, and then repeated transfer 3 times, so that the vitality of the strain could be restored. After the activation was completed, the produced Candida ruthenica slant was inoculated in the seed medium, and ...
example 2
[0029] Firstly, the Candida krusei strain stored at 5°C was inoculated in a solid activation medium, cultured at 35°C for 26 hours, and then transferred four times to restore the viability of the strain. After the activation was completed, the g Candida russii slant was inoculated in the seed medium, put it into a constant temperature shaker incubator, and cultured at 33°C at a speed of 130r / min for 26 hours to obtain seed solution 1; then the Candida russii strain was inoculated In the solid activation medium, culture at 29°C for 33h, and then repeat the transfer 4 times to restore the vigor of the strain. The seed liquid 2 was obtained by constant temperature cultivation for 22 hours; then the Streptococcus thermophilus strain was inoculated in the solid activation medium, cultured at 40°C for 42 hours, and then repeated transfer 4 times, so that the vitality of the strain was restored. After the activation was completed, the produced Candida ruthenica slant was inoculated i...
example 3
[0032] Firstly, the Candida krusei strain stored at 6°C was inoculated in a solid activation medium, cultured at 40°C for 30 hours, and then transferred 5 times to restore the viability of the strain. After the activation was completed, the g Candida russii slant was inoculated in the seed medium, placed in a constant temperature shaker incubator, and incubated at 35°C at a speed of 150r / min for 30 hours to obtain seed liquid 1; In the solid activation medium, culture at 30°C for 36h, and then repeat the transfer 5 times, so that the vigor of the strain can be restored. The seed liquid 2 was obtained by constant temperature cultivation for 24 hours; then the Streptococcus thermophilus strain was inoculated in the solid activation medium, cultured at 42°C for 48 hours, and then repeated transfer 5 times, so that the vitality of the strain was restored. After the activation was completed, the produced Candida ruthenica slant was inoculated in the seed medium, and cultured at 40°...
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