A method for preparing high-protein feed by fermenting citric acid cornstarch residue and mycelia residue as base material
A technology of corn starch slag and high-protein feed, applied in animal feed, animal feed, animal husbandry, etc., can solve the problems of limited protein content, difficult absorption and utilization, and high crude fiber content of citric acid slag, and the method is safe and efficient Green, limited nutritional value, simple preparation process
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Embodiment 1
[0031] (1) Activation of strains: Inoculate the cryopreserved Candida, Bacillus subtilis and Aspergillus oryzae on the potato agar slant medium respectively, and culture at 33° C. for 28 hours.
[0032] (2) Strain expansion culture: the activated strains were respectively inoculated into Erlenmeyer flasks equipped with potato liquid medium to carry out shaker expansion culture. The culture temperature was 33° C., cultivated for 42 hours, and the shaker speed was 200 rpm, and each strain was obtained. Bacterial fluids of strains, wherein the number of viable bacteria in the bacterial fluids of Candida ruthenicum, Bacillus subtilis and Aspergillus oryzae was 3.5×10 9 cfu / mL, 5.9×10 9 cfu / mL, 2.6×10 9 cfu / mL.
[0033] (3) Preparation of solid-state fermentation medium: take citric acid cornstarch residue and mycelia residue and mix and stir evenly according to the mass ratio of 1:2.5, add a small amount of water to make the residue humidity 60%; Add 1.2% ammonium sulfate, 0.5%...
Embodiment 2
[0039] (1) Activation of strains: Inoculate the cryopreserved Candida, Bacillus subtilis and Aspergillus oryzae on the potato agar slant medium respectively, and culture at 33° C. for 28 hours.
[0040] (2) Strain expansion culture: the activated strains were respectively inoculated into Erlenmeyer flasks equipped with potato liquid medium to carry out shaker expansion culture. The culture temperature was 33° C., cultivated for 42 hours, and the shaker speed was 200 rpm, and each strain was obtained. Bacterial fluids of strains, wherein the number of viable bacteria in the bacterial fluids of Candida rutatus, Bacillus subtilis and Aspergillus oryzae was 3.6×10 9 cfu / mL, 5.5×10 9 cfu / mL, 2.8×10 9 cfu / mL.
[0041] (3) Preparation of solid-state fermentation medium: take citric acid cornstarch residue and mycelium residue and mix and stir evenly according to the mass ratio of 1:2.5, add a small amount of water to make the residue humidity 60%; use 10wt% sodium hydroxide solutio...
Embodiment 3
[0047] (1) Activation of strains: Inoculate the cryopreserved Candida, Bacillus subtilis and Aspergillus oryzae on the potato agar slant medium respectively, and culture at 30° C. for 32 hours.
[0048] (2) Strain expansion culture: the activated strains were respectively inoculated into Erlenmeyer flasks equipped with potato liquid medium to carry out shaker expansion culture. The culture temperature was 30°C, cultivated for 48 hours, and the shaker speed was 250rpm, and each strain was obtained. Bacterial fluids of strains, wherein the number of viable bacteria in the bacterial fluids of Candida ruthenicum, Bacillus subtilis and Aspergillus oryzae was 3.0×10 9 cfu / mL, 5.8×10 9 cfu / mL, 2.3×10 9 cfu / mL.
[0049] (3) Preparation of solid-state fermentation medium: take citric acid cornstarch residue and mycelia residue according to the mass ratio of 1:4, mix and stir evenly, add a small amount of water to make the residue humidity 65%. Use 10wt% sodium hydroxide solution to ...
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