Method for preparing vegetable seed active peptide by microbial solid state fermentation
A solid-state fermentation and active peptide technology, which is applied in the direction of microorganism-based methods, biochemical equipment and methods, and peptide preparation methods, can solve the problems of destroying the original configuration of amino acids, severe reaction conditions, and low degree of hydrolysis. It is beneficial to environmental protection, the production process is simple, and the effect of wide source of raw materials
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Embodiment 1
[0019] Example 1 Screening of solid-state fermented rapeseed meal to produce rapeseed active peptide strains
[0020] Fermentation strains: Aspergillus niger, Rhizopus niger, Geotrichum candidum, Aspergillus oryzae, Aspergillus usami, Mucor actinosa, Lactic acid bacteria, Candida utilis, Bacillus licheniformis and Bacillus subtilis.
[0021] Preparation of starter: After the activated strains were expanded and cultivated according to conventional methods, the fermented seeds were diluted with sterile distilled water to make the cell concentration reach 3×10 7 Each / mL is the starter.
[0022] The double-low rapeseed meal was crushed to a particle size of about 500 μm, and sterilized by moist heat at 121°C for 30 minutes. In the fermenter, the starter is added according to the solid-liquid ratio of 1:1-1:2 (mass ratio), the fermentation temperature is 28°C-35°C, the ambient humidity is 80%-90%, stirring and ventilating. After 3 days of fermentation, add distilled water to diss...
Embodiment 4
[0024] Example 4 Rapeseed Active Peptide Production by Aspergillus Usami Solid-state Fermentation of Rapeseed Meal
[0025] Slant medium: 300g potato, 20g glucose, 20g agar, 1000mL tap water.
[0026] Plate expansion medium: 300g potato, 20g glucose, 20g agar, 1000mL tap water.
[0027] Nutrient solution composition: glucose 50g, KH 2 PO 4 2g, tap water 1000mL, pH 6.0.
[0028] Fermentation medium: rapeseed meal, nutrient solution.
[0029] Preparation of starter: Aspergillus Usami was inoculated on a slant medium and cultured at a constant temperature of 28°C for 4 days, then inoculated on a flat plate and expanded at 28°C, after 4 days, the spores were washed with sterile nutrient solution, and the concentration was adjusted to 10 7 individual / mL.
[0030] Crush the common rapeseed meal to a particle size of about 400 μm, sterilize, add a starter in a fermenter at a solid-to-liquid ratio of 1:1 (mass ratio), adjust the fermentation temperature to 30°C, and the ambient h...
Embodiment 5
[0032] Example 5 Candida utilis solid-state fermentation of rapeseed meal to produce rapeseed active peptide
[0033] Incline medium: 3g of malt extract, 10g of glucose, 3g of yeast extract, 5g of peptone, 20g of agar, 1000mL of tap water.
[0034] Seed medium: malt extract 3g, glucose 10g, yeast extract 3g, peptone 5g, tap water 1000mL.
[0035] Nutrient solution: glucose 3g, KH 2 PO 4 3g, tap water 1000mL, pH 7.0.
[0036] Fermentation medium: rapeseed meal, nutrient solution.
[0037] Preparation of starter: Pick two rings of Candida utilis from the slant of preserved strains after activation and inoculate it in the seed medium, seal with 8 layers of gauze, culture at 35°C, 120r / min, on a shaking table for 24h, the bacteria Concentration up to 10 8 individual / mL. Adjust its concentration to 10 with sterile nutrient solution 7 pcs / mL
[0038] Crush the rapeseed meal to a particle size of about 300 μm, and sterilize at 121°C for 30 minutes. In the fermenter, add the ...
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