Method for preparing rapeseed peptide by mixed-strains liquid fermentation
A technology for liquid fermentation and rapeseed, applied in microorganism-based methods, biochemical equipment and methods, fermentation, etc., can solve the problem that the soluble nitrogen content and biological activity need to be further improved, it is difficult to form large-scale industrial production, and the protease activity is affected. problem, to achieve the effect of being conducive to environmental protection, low price, and increasing the content of soluble nitrogen
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Embodiment 1
[0020] (1) Preparation of liquid fermentation medium
[0021] Nutrient solution composition: glucose 5g, KH 2 PO 4 2g, 1000mL, pH 6.5. Crush the ordinary rapeseed meal to a particle size of about 100 μm, mix it evenly with the rapeseed meal with a nutrient solution at a solid-to-liquid ratio of 1:30 g / mL, and sterilize at 121°C for 30 minutes to obtain a liquid fermentation medium for fermentation inside the tank.
[0022] (2) Liquid fermentation
[0023] ①Preparation of seed solution of Mucor radiata Yazhi:
[0024] Slant medium: 300g potato, 20g glucose, 20g agar, 1000mL tap water.
[0025] Plate expansion medium: 300g potato, 20g glucose, 20g agar, 1000mL tap water.
[0026] Inoculate the spores of Mucor actinosa on the slant medium and incubate at 28°C for 4 days, then inoculate on the flat plate and carry out expansion culture at 28°C. After 4 days, wash the spores with sterile water, transfer them to the Erlenmeyer flask with glass beads, and shake Break up the sp...
Embodiment 2
[0043] The difference from Example 1 is that (4) purification is carried out as follows:
[0044] Adjust the pH of the rapeseed peptide crude extract to 7.0, add 10g / L activated carbon, decolorize and debitterize at 50°C for 1.5h, then centrifuge at a high speed (relative centrifugal force 10000g) to remove impurities, and the supernatant is passed through a desalting column (HiPrep TM 26 / 10, flow rate 30mL / min) after desalination, spray-dry the rapeseed peptide crude extract to obtain rapeseed peptide, its protein content (dry basis, N × 6.25) is 88%, soluble nitrogen content is 94%, molecular weight is 1000Da The peptide content of ~5000Da is 65%, and the glucosinolate content is 8 μmoL / g.
Embodiment 3
[0046] (1) Preparation of liquid fermentation medium
[0047] Nutrient solution composition: glucose 5g, KH 2 PO 4 2g, 1000mL, pH 6.0. Crush the ordinary rapeseed meal to a particle size of about 100 μm, mix the rapeseed meal with nutrient solution at a solid-to-liquid ratio of 1:15 g / mL, and sterilize at 121°C for 30 minutes to obtain a liquid fermentation medium for fermentation inside the tank.
[0048] (2) Liquid fermentation
[0049] ①Preparation of seed solution of Mucor radiata Yazhi:
[0050] Slant medium: 300g potato, 20g glucose, 20g agar, 1000mL tap water.
[0051] Plate expansion medium: 300g potato, 20g glucose, 20g agar, 1000mL tap water.
[0052] Inoculate the spores of Mucor actinosa on the slant medium and incubate at 28°C for 4 days, then inoculate on the flat plate and carry out expansion culture at 28°C. After 4 days, wash the spores with sterile water, transfer them to the Erlenmeyer flask with glass beads, and shake Break up the spores, filter the ...
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