A kind of bean sprouts of the genus Vigna with low phytic acid and production method thereof
A production method and technology of cowpea, applied in the field of low-phytic acid cowpea bean sprouts and its production, can solve the differences in soaking medium, culture solution components and phytic acid degradation rate, and do not involve the impact of phytic acid degradation. Involves phytic acid degradation and other issues to achieve the effects of shortening the germination cycle, high yield, and improving physiological metabolism
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Embodiment 1
[0021] Select mung bean seeds with plump granules, high germination rate and no damage, disinfect them with 1% sodium hypochlorite by volume according to known methods, put them in clear water with a mass ratio of water to mung beans of 1:4, and soak them at 30°C for 5 hours; Put the soaked mung bean seeds into a germination machine and germinate them in the dark at 30°C for 2 days. During this period, 5 μmol / L H 2 o 2 Spray with an aqueous solution mixed with 50 μmol / L SNP for 2 minutes, the spray flow rate is 150 mL / min, and the culture medium is replaced every 24 hours. The degradation rate of phytic acid in mung bean sprouts was 45%.
Embodiment 2
[0023] Red bean grain selection, disinfection, soaking methods are the same as in Example 1. The soaked red bean seeds were placed in a germination machine and germinated at 30°C in the dark for 3 days. During this period, 20 μmol / L H 2 o 2 The aqueous solution mixed with 600 μmol / L SNP was sprayed for 2 minutes, the flow rate of the spray solution was the same as in Example 1, and the culture solution was replaced every 24 hours. The phytic acid degradation rate of the prepared red bean sprouts was 65%.
Embodiment 3
[0025] Mung bean grain selection and disinfection method are the same as in Example 1. The sterilized mung bean grains were placed in clear water with a mass ratio of water to mung beans of 1:3, and soaked at 30°C for 6h; the soaked mung bean grains were placed in a germination machine, and germinated at 30°C in the dark for 3 days, during which, Use 10μmol / L H every 1h 2 o 2 Spray with an aqueous solution mixed with 200 μmol / L SNP for 3 minutes, the spray flow rate is 200 mL / min, and the culture medium is replaced every 24 hours. The phytic acid degradation rate of the prepared mung bean sprouts was 70%.
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