Feed additive containing lysozyme
A feed additive, lysozyme technology, applied in the field of feed, can solve the problems of less microbial lysozyme, limited application, limited application scope, etc., and achieve good results
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Embodiment 1
[0028] Prepare liquid culture medium, wherein glucose 10g / L, peptone 5g / L. Get 25mL liquid culture medium and place in Erlenmeyer flask, insert the thalline seed of Streptomyces griseus S-35 by the inoculum size of 4% (v / v), carry out shaking flask fermentation, fermentation condition is 30 ℃, 200r / min, After 24 hours of fermentation and cultivation, the fermentation liquid was centrifuged to remove the bacteria, and the supernatant was successively salted out with ammonium sulfate (add ammonium sulfate to the supernatant to 20% saturation, stirred for 1 hour, then stood still for 1 hour, centrifuged at 10,000 r / min, precipitated Dissolve it in distilled water, put it into a dialysis bag with a molecular weight of 10,000, and place it in 10mmol / LPBS for full dialysis; add ammonium sulfate to the supernatant in the dialysis bag to 70% saturation, stir for 1 hour, let it stand for 1 hour, and centrifuge at 10,000r / min. The precipitate was dialyzed in the same way as above to obt...
Embodiment 2
[0030] Prepare liquid culture medium, wherein glucose 10g / L, peptone 5g / L. Get 25mL liquid culture medium and place in Erlenmeyer flask, insert the thalline seed of Streptomyces griseus S-35 by the inoculum size of 4% (v / v), carry out shaking flask fermentation, fermentation condition is 20 ℃, 150r / min, After 24 hours of fermentation and cultivation, the fermentation liquid was centrifuged to remove the bacteria, and the supernatant was successively salted out with ammonium sulfate (add ammonium sulfate to the supernatant to 20% saturation, stirred for 1 hour, then stood still for 1 hour, centrifuged at 10,000 r / min, precipitated Dissolve it in distilled water, put it into a dialysis bag with a molecular weight of 10,000, and place it in 10mmol / LPBS for full dialysis; add ammonium sulfate to the supernatant in the dialysis bag to 70% saturation, stir for 1 hour, let it stand for 1 hour, and centrifuge at 10,000r / min. Take the precipitate and dialyze, the method is the same as ...
Embodiment 3
[0032]Prepare liquid culture medium, wherein glucose 10g / L, peptone 5g / L. Get 25mL liquid culture medium and place in Erlenmeyer flask, insert the thalline seed of Streptomyces griseus S-35 by 4% (v / v) inoculum size, carry out shaking flask fermentation, fermentation condition is 40 ℃, 300r / min, After 24 hours of fermentation and cultivation, the fermentation liquid was centrifuged to remove the bacteria, and the supernatant was successively salted out with ammonium sulfate (add ammonium sulfate to the supernatant to 20% saturation, stirred for 1 hour, then stood still for 1 hour, centrifuged at 10,000 r / min, precipitated Dissolve it in distilled water, put it into a dialysis bag with a molecular weight of 10,000, and place it in 10mmol / LPBS for full dialysis; add ammonium sulfate to the supernatant in the dialysis bag to 70% saturation, stir for 1 hour, let it stand for 1 hour, and centrifuge at 10,000r / min. The precipitate was dialyzed, and the dialysate was obtained in the ...
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