Method for preparing straw ammoniation feed from oilseed rape straw as raw material
A technology of rape straw and straw, which is applied in animal feed, animal feed, application, etc., can solve the problems of difficult digestion and absorption of lignin, low organic matter digestibility, and limited feed intake of poultry, so as to be easy to popularize, promote secretion, and produce low cost effect
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Embodiment 1
[0017] 1. Preparation of fermentation agent
[0018] (1) Weigh the materials according to the following parts by weight: 18 parts of molasses, 80 parts of water, 0.5 parts of urea, 0.2 parts of potassium dihydrogen phosphate, adjust the pH value to 5.5, and steam sterilize at 115 °C for 20 minutes to obtain the expanded culture liquid;
[0019] (2) After the expanded culture medium is cooled to room temperature, the following bacterial species: Candidautilis, Candidatropicalis, Humicolainsolens, Trichodermallongibrachiatum, Geotrichum candidum Link and Aspergillus niger were respectively inoculated in the expansion culture medium, and under aerobic conditions, the expansion culture was carried out at 28°C for 0.8 days. 8 CFU / g;
[0020] (3) Take each bacterial agent according to the following volume percentage content: 15% of Candida utilis, 25% of Candida tropicalis, 14% of Humicola solitary, 10% of Trichoderma longhandle, 20% of Geotrichum candidum, 16% of Aspergillus nige...
Embodiment 2
[0026] 1. Preparation of fermentation agent
[0027] (1) Weigh the materials according to the following parts by weight: 16 parts of molasses, 75 parts of water, 0.8 parts of urea, 0.3 parts of potassium dihydrogen phosphate, adjust the pH value to 5.0, and steam sterilize at 115°C for 20 minutes to obtain the expanded culture liquid;
[0028] (2) After the expanded culture medium is cooled to room temperature, the following bacterial species: Candidautilis, Candidatropicalis, Humicolainsolens, Trichodermallongibrachiatum, Geotrichum candidum Link and Aspergillus niger were respectively inoculated in the expansion culture medium, and under aerobic conditions, the expansion culture was carried out at 30°C for 0.5 days. 8 CFU / g;
[0029] (3) Take each bacterial agent according to the following volume percentage content: Candida utilis 10%, Candida tropicalis 34%, Humicola solitaryus 18%, Trichoderma longiole 8%, Geotrichum candidum 15%, Aspergillus niger 15% %, mixed to obtai...
Embodiment 3
[0035] 1. Preparation of fermentation agent
[0036] (1) Weigh the materials according to the following parts by weight: 20 parts of molasses, 75 parts of water, 0.3 parts of urea, 0.2 parts of potassium dihydrogen phosphate, adjust the pH value to 6.0, and steam sterilize at 115 °C for 20 minutes to obtain the expanded culture liquid;
[0037] (2) After the expanded culture medium is cooled to room temperature, the following bacterial species: Candidautilis, Candidatropicalis, Humicolainsolens, Trichodermallongibrachiatum, Geotrichum candidum Link and Aspergillus niger were respectively inoculated in the expansion culture medium, under aerobic conditions, expanded culture at 25°C for 1 day, and the effective number of viable bacteria obtained from the bacterial preparation was ≧1×10 8 CFU / g;
[0038] (3) Take each bacterial agent according to the following volume percentage content: 20% of Candida utilis, 20% of Candida tropicalis, 10% of Humicola solitary, 15% of Trichoder...
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