Fat-reduced soybean protein material and soybean emulsion composition, and processes for production thereof

摘要

A fat-reduced soybean protein material containing a protein and a carbohydrate at a total content of 80 wt % or more in terms of dried form content, containing a fat (as an extract from a chloroform/methanol mixed solvent) at a content of less than 10 wt % relative to the content of the protein, and containing campesterol and stigmasterol (as plant-derived sterols) at a total content of 200 mg or more relative to 100 g of a fat; and a soybean emulsion composition containing a protein at a content of 25 wt % or more in terms of dried form content, containing a fat at a content of 100 wt % or more in terms of dried form content relative to the content of the protein in terms of dried form content, and having an LCI value of 60% or more.

主权项

1. A process for producing a soybean emulsion composition, which comprises the steps of:
(1) adding water to a modified fat-containing soybean, which comprises, as a raw material, a fat at a content of 15 wt % or more (as an extract with a chloroform/methanol mixed solvent) in terms of dry basis and having a Nitrogen Solubility Index (NSI) value in a range of from 20 to 65, wherein “modified” means that protein in the fat-containing soybean is denatured to 20 to 65 of NSI, to prepare a suspension liquid; (2) subjecting the suspension liquid of the modified fat-containing soybean to a solid-liquid separation to transfer a neutral lipid, a polar lipid and a protein comprising lipophilic protein as a major component to an insoluble fraction comprising fiber, removing a soluble fraction comprising sugar and a protein comprising glycinin and β-conglycinin as major components, and then recovering the insoluble fraction; (3) homogenizing the recovered insoluble fraction; and (4) subjecting the homogenized insoluble fraction to a solid-liquid separation to remove the fiber, and then recovering a supernatant to obtain the soybean emulsion composition, wherein the NSI value is determined by the following procedure: (a) adding 100 ml of water to 2.0 g of a sample to obtain a first mixture, (b) stirring the first mixture at 40° C. for 60 minutes, and then subjecting the first mixture to centrifugation at 1400×g for 10 minutes to obtain a supernatant 1, (c) adding 100 ml of water to a residual precipitate to obtain a second mixture, (d) stirring the second mixture obtained in step (c) at 40° C. for 60 minutes, and then subjecting the second mixture to centrifugation at 1400×g for 10 minutes to obtain a supernatant 2, (e) combining supernatant 1 and supernatant 2, and adding water to 250 ml to obtain a third mixture, (f) filtering the third mixture with No. 5A filter paper to obtain a filtrate, (g) determining a nitrogen content in the filtrate by the Kjeldahl method, (h) determining a nitrogen content in the sample by the Kjeldahl method, and (i) calculating the NSI value as wt % by dividing the nitrogen content in the filtrate by the nitrogen content in the sample.