Method for producing soybean trypsin inhibitor concentration
A technology of trypsin inhibition, manufacturing method, applied in the field of useful concentrates, which can solve the problems of lack of effective utilization of various components, and impossibility of industrialization
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manufacture example 1
[0031] Add 10 times the amount of warm water to low-denatured defatted soybeans to maintain pH = 7.0 while stirring for 1 hour for extraction. Okara which is an insoluble component was removed with a decanter to obtain a defatted soybean emulsion. Concentrated hydrochloric acid was added to the defatted soybean emulsion to make the pH = 4.5, and the precipitated soybean protein was separated to obtain soybean whey.
Embodiment 1
[0033]The soybean whey (solid content: 3% by weight, pH = 4.5) obtained in Production Example 1 above was subjected to a vacuum degree of 40 Torr, a heating temperature of 60° C., and an evaporation temperature of 35° C. using a thin-film flash evaporator (manufactured by Tokyo Rike Instruments Co., Ltd.). Concentrate under reduced pressure under certain conditions, and extract when the solid content concentration is 7%, 12%, 16%, and 27%. Sodium sulfate was added to the obtained concentrated whey of various concentrations in an amount of 0.5%, 3%, 6%, 9%, and 14% of the concentrated whey, further adjusted to pH = 4 with phosphoric acid, and refrigerated for one night.
[0034] Each sample was centrifuged at 3,000 rpm for 5 minutes, and the supernatant was subjected to SDS electrophoresis to quantify the concentration of the 20 kDa band corresponding to Kunitz-type trypsin inhibitor (hereinafter referred to as KSTI), and compare it with the whey of the raw material.
Embodiment 2
[0035] Example 2 (the example where the whey concentration is 28%)
[0036] In the same manner as in Example 1, the soybean whey was concentrated under reduced pressure in a thin-film flash evaporator to a solid content concentration of 28%. Sodium sulfate is added to the concentrated whey in an amount of 3% or 6% of the concentrated whey, further adjusted to pH = 4 with phosphoric acid, and stored overnight in refrigeration.
[0037] Each sample was centrifuged at 3000 rpm for 5 minutes, and the supernatant was subjected to SDS electrophoresis, and the concentration of the 20 kDa band corresponding to KSTI was quantified, and compared with the whey of the raw material.
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