A method for preparing compound amino acid liquid by using cottonseed cake
A compound amino acid and cottonseed cake technology, applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve the problems of high production cost and low utilization rate of raw materials, so as to improve utilization rate, reduce production cost, Avoid the effects of by-product formation
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[0032] A method for preparing compound amino acid liquid by utilizing cottonseed cake, the preparation method comprises the following processes in sequence:
[0033] Cottonseed meal pretreatment process: Mix the mechanically crushed cottonseed meal with water and cook at 110-130°C for 15-20 minutes to form the material to be hydrolyzed;
[0034] Bacterial enzymatic hydrolysis process: first cool the material to be hydrolyzed to 30-36°C, then inoculate Aspergillus niger, Aspergillus oryzae, and Saccharomyces cerevisiae at this temperature, and then inoculate them at a relative humidity of 80%- Cultivate under 88% and aerobic conditions for 15‐20 hours to form a primary enzymatic hydrolysis system, and then inoculate Bacillus subtilis and Bacillus licheniformis into the primary enzymatic hydrolysis system to continue aerobic culture for 18‐ 32h to form fermented liquid, wherein, the inoculation amount of described Aspergillus niger, Aspergillus oryzae, Saccharomyces cerevisiae, ...
Embodiment 1
[0074] A method for preparing compound amino acid liquid by utilizing cottonseed cake, the preparation method comprises the following processes in sequence:
[0075] Cottonseed cake pretreatment process: Mix the mechanically crushed cottonseed cake with water and cook at 121°C for 20 minutes to form the material to be hydrolyzed;
[0076] Bacterial enzyme hydrolysis process: first cool the material to be hydrolyzed to 30°C, and then inoculate Aspergillus niger, Aspergillus oryzae, and Saccharomycescerevisiae respectively at this temperature, and then inoculate them at a relative humidity of 80% and with Aerobic culture under oxygen conditions for 15 hours to form a primary enzymatic hydrolysis system, and then inoculate the primary enzymatic hydrolysis system with Bacillus subtilis and Bacillus licheniformis for 8 hours to form a secondary enzymatic hydrolysis system , and then add water to the secondary enzymatic hydrolysis system, then adjust the pH value of the secondary en...
Embodiment 2
[0087] Step is with embodiment 1, and difference is:
[0088] In the bacterial enzymatic hydrolysis process, the material to be hydrolyzed is first cooled to 34°C, and then inoculated with Aspergillus niger, Aspergillus oryzae, and Saccharomyces cerevisiae at this temperature, and then at a relative humidity of 85%. , and aerobic culture under aerobic conditions for 20 hours to form a primary enzymatic hydrolysis system, and then respectively inoculate Bacillus subtilis (Bacillus subtilis) and Bacillus licheniformis (Bacillus licheniformis) into the primary enzymatic hydrolysis system for 12 hours to form a secondary enzymatic hydrolysis system Enzymatic hydrolysis system, add water to the secondary enzymatic hydrolysis system, then adjust the pH value of the secondary enzymatic hydrolysis system after adding water to 5.0, and continue aerobic cultivation at 50°C for 15 hours to form a fermentation broth, wherein, The inoculation amounts of described Aspergillus niger, Aspergi...
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