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Process for the preparation of protein hydrolysate from legumes

a technology of protein hydrolysate and legumes, which is applied in the field of process for the preparation of protein hydrolysate from legumes, can solve the problems of heat-denatured protein present in defatted cakes, direct un-extractable, and increase the salt content of the product, so as to achieve the effect of higher yield

Inactive Publication Date: 2006-08-31
RAO APPU RAO GOPALA RAO APPU +7
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0019] Yet another object of the present invention is to decrease the bitterness in the hydrolysate to the extent that the threshold perception of bitterness is greater than 2 g %.

Problems solved by technology

Following oil removal, the protein present in the defatted cakes is heat-denatured and therefore directly un-extractable.
The drawback in such hydrolysis is that it is likely to lead to racemisation of amino acids and the addition of acid increases the salt content in the product.
Such single enzyme systems are likely to result in bitter peptides and the process is energy intensive due to the high temperature (90° C.) used.
The drawback of the process is it involves the separation of the mixture of hydrolyzed products.
The drawback of the process is the starting material protein isolate, which is more expensive.
The process is a multi step process, energy intensive.
The drawback of the process is it is a multi-step process.
The drawback of the process is that due to partial defatting soy flour, left over oil comes in contact with protein phase, which could lead to off-flavors.
The drawback of the process is that it is a multi step process and due to partial defatting of soy flour, left over oil comes in contact with protein phase which could lead to off-flavors.
Enzyme inactivation is done by addition of acid, which is likely to lead to increased salt content in the product.
The starting material is not defatted and hence the residual oil could come in contact with the aqueous phase, which could lead to off-flavors.
The solubility of the substrate is low at the acidic pH which is likely to result in low yields.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example 1

[0053] Twenty-five gram of defatted soy flour is dispersed in 250 ml of water and the pH of the dispersion was adjusted to 7.2 by using 6N sodium hydroxide solution. It was kept stirring for 20 min with mechanical stirrer and temperature raised to 40° C. by heating. At this stage, 125 mg of fungal protease was added and stirring continued for 2 h. At the end of 2 h, temperature was raised to 50° C. by heating and the second enzyme, papain (125 mg), was added and kept stirring for 1 hr. After the hydrolysis, the resultant solution was boiled for 10 min for enzyme inactivation. The slurry was centrifuged using basket centrifuge. The clear solution was lyophilised. The yield was 65% on protein basis and degree of hydrolysis by TNBS method was found to be 43%.

example 2

[0054] Fifty gram of soy flour is dispersed in 500 ml of water and the pH of the dispersion was adjusted to 7.3. It was kept stirring for 20 min with mechanical stirrer and temperature raised to 43° C. At this stage 250 mg of fungal protease is added and stirring continued for 1.5 hours. At the end of 2 hours the temperature was raised to 53° C. and the second enzyme papain (250 mg) was added and kept stirring for 1 hours. After the hydrolysis the hydrolysate was boiled for 15 min. for enzyme inactivation and centrifuged. The clear solution was lyophilised. The yield was 68.0% on protein basis and degree of hydrolysis by TNBS method was 39%.

example 3

[0055] One hundred grams of defatted soybean flour is dispersed in 1 L of water and the pH of the dispersion was adjusted to 7.6. It was kept stirring for 20 min with mechanical stirrer and then temperature raised to 45° C. At this stage 500 mg of fungal protease is added and stirring continued for 2 hours. At the end of 2 hours the temperature was raised to 55° C. and the second enzyme papain 500 mg was added and kept stirring for 1.5 hours. After the hydrolysis the hydrolysate was boiled for 10 minutes for enzyme inactivation and centrifuged. The clear solution was spray dried. The yield was 70% on protein basis and degree of hydrolysis by TNBS method was 38%.

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Abstract

The present invention provides a process for the preparation of protein hydrolysate from soy flour, which comprises preparing aqueous slurry of defatted soy flour having 6-12% w / v of solid content, hydrolyzing the said slurry using fungal protease at pH 7-8 and temperature 43±5° C. to get 20-40% degree of hydrolysis (DH), further hydrolyzing using papain at temperature 53±5° C. under stirring till completion of hydrolysis to 30-45% DH, inactivating residual enzyme in a known manner, separating the solids and drying the clarified supernatant thus obtained to get protein hydrolysate.

Description

FIELD OF THE INVENTION [0001] The present invention relates to a process for the preparation of protein hydrolysate from soy flour using fungal protease. Particularly, the present invention relates to a process for the preparation of protein hydrolysate from defatted soy flour using fungal protease obtained from Aspergillus sp. BACKGROUND OF THE INVENTION [0002] Presently about 6.8 M tons of soybean is produced in India and extracted for oil and the solvent extracted flour is exported for feed purposes. By providing additional facilities for the hygienic processing of soybean in the solvent extraction units, it is possible to obtain edible grade defatted flour having the desired functional characteristics. After the recovery of oil, 4.9 M tons of soy flour is available for utilization in India. As a by-product of edible oil production, oilseed proteins are a potentially important source of human dietary protein throughout the world. Following oil removal, the protein present in the ...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A23L1/20C12P21/06A61K36/48A23L11/00C07K2/00
CPCC07K2/00C12P21/06
Inventor RAO, APPU RAO GOPALA RAO APPUGOVINDARAJU, KARADKAHARENDRANATH, RAMASWAMYJOSEPH, JOHNYPRAKASH, VISHWESHWARIAHRADHA, CHERUPPANPULLILSASTRY, MYSORE CHEELUVARAYA SHAMANTHAKASINGH, SRIDEVI ANNAPURNA
Owner RAO APPU RAO GOPALA RAO APPU
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