Method for preparing straw ammoniated feed by using peanut vines as raw material
A peanut vine and straw technology, applied in animal feed, animal feed, application and other directions, can solve the problems of difficult digestion and absorption of lignin, low organic matter digestibility, limited feed intake of poultry, etc. low cost effect
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Embodiment 1
[0018] 1. Preparation of fermentation agent
[0019] (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;
[0020] (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;
[0021] (3) Each bacterial agent is taken according to the following volume percentage content: Candida utilis 15%, Candida tropicalis 15%, Humicola solitaryus 20%, Trichoderma longiole 20%, Geotrichum candidum 20%, Aspergillus niger 10% %, mixed to...
Embodiment 2
[0027] 1. Preparation of fermentation agent
[0028] (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;
[0029] (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;
[0030] (3) Take each bacterial agent according to the following volume percentage content: 20% of Candida utilis, 10% of Candida tropicalis, 15% of Humicola solitary, 20% of Trichoderma longhandle, 15% of Geotrichum candidum, 20% of Aspergillus niger...
Embodiment 3
[0036] 1. Preparation of fermentation agent
[0037] (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;
[0038] (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;
[0039] (3) Take each bacterial agent according to the following volume percentage content: 10% Candida utilis, 10% Candida tropicalis, 25% Humicola solitary, 15% Trichoderma longhandl...
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