Method for preparing bean flour and functional soybean protein rich in glyceollin by adopting solid fermentation method
A technology of soybean antitoxin and solid fermentation method, which is applied in the field of food processing, and achieves the effect of mild process conditions and good safety
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Embodiment 1
[0028] Undamaged group: take 6g of soybean seeds, soak them with 70% alcohol for 2 minutes, then soak them with sterile water for 3 times, and finally soak them with sterile water at 25°C for 12 hours, and peel them off. With 1.5mL spore suspension (Aspergillus oryzae spore number is 1×10 7 pcs) into soybeans and mix well with a sterile spoon. Place the infected soybeans in petri dishes, 25-30 cloves per dish, seal with a parafilm, culture in a dark box at 25°C, and freeze-dry the fermented soybeans for later use.
[0029] Injury group: Soybean seeds were taken, soaked with 70% alcohol for 2 minutes, then soaked with sterile water for 3 times, and finally soaked in sterile water at 25°C for 12 hours, peeled, and scored 3 times on the surface of the beans with a scalpel Damage treatment.
[0030] With 1.5mL spore suspension (Aspergillus oryzae spore number is 1×10 7 ) into the damaged soybeans, and mix evenly with a sterile spoon. Put 6 g of soybeans that have been infected...
Embodiment 2
[0036] Take 6g of soybean seeds, soak them in alcohol with a mass concentration of 70% for 2 minutes, then soak them in sterile water for 3 times, and finally soak them in sterile water at 25°C for 12 hours, peel and damage them. With 1.5mL spore suspension (Aspergillus oryzae spore number is 1×10 7 pcs) into the damaged soybeans and mix well with a sterile spoon. Place the contaminated soybeans in petri dishes, 25-30 petri dishes per dish, seal with a parafilm, and culture in a dark box at 25°C for 0d, 1d, 3d, 5d, respectively, and the obtained fermented soybeans are freeze-dried, crushed, and set aside. Non-inoculated soybeans (0) were used as blank control. The test method is the same as in Example 1, and the test results are shown in Table 2.
[0037] Aglycone content (mg / kg) and Glys content (mg DE / kg DW) change in the embodiment 2 of table 2
[0038]
[0039] After calculation, as can be known from the results in Example 2, taking soybean as raw material, when the ...
Embodiment 3
[0041] Take 6g of soybean seeds, soak them with 70% alcohol for 2 minutes, then soak them with sterile water for 3 times, and finally soak them with sterile water at 25°C for 12 hours, peel and damage them. Inoculate 10 spores per gram of beans 7 a, 10 8 and 10 9 The spore suspension (1.5mL) was added to the damaged soybean and mixed with a sterile spoon. Put the contaminated soybeans in petri dishes, 25-30 petri dishes per dish, seal with parafilm, and culture in a dark box at 25°C for 3 days respectively. Non-inoculated soybeans (0) were used as blank control. The test method is the same as in Example 1, and the test results are shown in Table 3.
[0042] Aglycone content (mg / kg) and Glys content (mg DE / kg DW) change in the embodiment 3 of table 3
[0043]
[0044] Using high-isoflavone soybeans as raw materials, when the conditions such as the cultivation time are constant, the number of spores is 10 7 、10 8 、10 9 The bacteria inoculated into the treated soybeans...
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