Method for preparing straw ammoniation feed by adopting sorgo straws
A technology of sweet sorghum straw and straw, which is applied in the field of straw ammoniated feed production, can solve the problems of difficult digestion and absorption of lignin, low organic matter digestibility, and limited feed intake of poultry, and achieves easy popularization, secretion promotion, and low production cost. Effect
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[0017] Example 1
[0018] 1. Preparation of fermented bacteria
[0019] (1) Weigh the materials according to the following parts by weight: 18 parts of molasses, 80 parts of water, 0.5 part of urea, 0.2 part of potassium dihydrogen phosphate, adjust the pH value to 5.5, and sterilize by steam at 115°C for 20 minutes, to expand the culture liquid;
[0020] (2) After the expanded culture medium is cooled to room temperature, the following strains are added: Candida utilis, Humicolainsolens, Penicillium funiculosum, Trichodermalongibrachiatum, Geotrichum candidumLink and Aspergillus niger were respectively inoculated into the expanded culture medium and expanded at 28°C for 0.8 days under aerobic conditions. 8 CFU / g;
[0021] (3) Take each bacterial agent according to the following volume percentages: Candida utilis 15%, Humicola solitarius 15%, Penicillium solani 15%, Trichoderma longiformis 15%, Geotrichum candidum 20%, Aspergillus niger 20% %, mixed to obtain a combined liq
Example Embodiment
[0026] Example 2
[0027] 1. Preparation of fermented bacteria
[0028] (1) Weigh the materials according to the following parts by weight: 16 parts of molasses, 75 parts of water, 0.8 part of urea, 0.3 part of potassium dihydrogen phosphate, adjust the pH value to 5.0, and sterilize it with steam at 115°C for 20 minutes to expand the culture. liquid;
[0029] (2) After the expanded culture medium is cooled to room temperature, the following strains are added: Candida utilis, Humicolainsolens, Penicillium funiculosum, Trichodermalongibrachiatum, Geotrichum candidumLink and Aspergillus niger were respectively inoculated into the expanded culture medium and expanded at 30°C for 0.5 days under aerobic conditions. 8 CFU / g;
[0030] (3) Take each bacterial agent according to the following volume percentages: Candida utilis 10%, Humicola solitarius 10%, Penicillium solani 10%, Trichoderma longiformis 10%, Geotrichum candidum 30%, Aspergillus niger 30% %, mixed to obtain a combine
Example Embodiment
[0035] Example 3
[0036] 1. Preparation of fermented bacteria
[0037] (1) Weigh the materials according to the following parts by weight: 20 parts of molasses, 75 parts of water, 0.3 part of urea, 0.2 part of potassium dihydrogen phosphate, adjust the pH value to 6.0, and sterilize by steam at 115° C. for 20 minutes to expand the culture liquid;
[0038] (2) After the expanded culture medium is cooled to room temperature, the following strains are added: Candida utilis, Humicolainsolens, Penicillium funiculosum, Trichodermalongibrachiatum, Geotrichum candidumLink and Aspergillus niger were respectively inoculated into the expanded culture medium and expanded for 1 day at 25°C under aerobic conditions, and the number of effective viable bacteria of the obtained bacterial agent was ≧1×10 8 CFU / g;
[0039] (3) Take each bacterial agent according to the following volume percentages: Candida utilis 25%, Humicola solitarius 10%, Penicillium solani 15%, Trichoderma longiformis 10
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