CN109700035A - A kind of high-intensitive and high retentiveness double protein plural gel preparation process - Google Patents

A kind of high-intensitive and high retentiveness double protein plural gel preparation process Download PDF

Info

Publication number
CN109700035A
CN109700035A CN201910135877.4A CN201910135877A CN109700035A CN 109700035 A CN109700035 A CN 109700035A CN 201910135877 A CN201910135877 A CN 201910135877A CN 109700035 A CN109700035 A CN 109700035A
Authority
CN
China
Prior art keywords
protein
intensitive
preparation process
retentiveness
gel preparation
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201910135877.4A
Other languages
Chinese (zh)
Inventor
李杨
王中江
郑丽
腾飞
周艳
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Northeast Agricultural University
Original Assignee
Northeast Agricultural University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Northeast Agricultural University filed Critical Northeast Agricultural University
Priority to CN201910135877.4A priority Critical patent/CN109700035A/en
Publication of CN109700035A publication Critical patent/CN109700035A/en
Pending legal-status Critical Current

Links

Abstract

The present invention provides a kind of high-intensitive and high retentiveness double protein plural gel preparation process, is related to food processing technology field.Described high-intensitive and high retentiveness plural gel preparation process specifically includes that enzymolysis modified soybean protein isolate lower bound degree, extraction of silver carp fribrillin, purifying, two kinds of albumen mixing crosslinkings, two steps heat.The present invention overcomes the deficiencies in the prior art, a kind of high-intensitive and high retentiveness double protein plural gel preparation process is provided, the problems such as solving silver carp myofibrillar protein gel deterioration, gel products fishlike smell weight, simultaneously, soybean protein isolate is improved in the application of field of food, double protein gel products of the present invention have high nutrition, it is easy to digest, low fat, raciness, the advantages that mouthfeel is good may advantageously facilitate the development of meat products and soybean processing industry, realize the synthesis complete utilization of soybean processing industry.

Description

A kind of high-intensitive and high retentiveness double protein plural gel preparation process
The present invention relates to food and meat products materials processing technology field, and in particular to a kind of high-intensitive and high retentiveness is double Albumen plural gel preparation process.
Background technique
Lower bound degree enzyme modification is exactly to obtain modified protein with the method for enzymatic hydrolysis within the scope of Lower degrees of hydrolysis.Lower bound degree enzyme Modification can be different degrees of raising and improve the certain nutritive peculiarities of protein and functional character.The enzymolysis protein of Lower degrees of hydrolysis is The texture feature of non-enzymolysis protein is remained, and remains original characteristic flavor on basis in non-enzymolysis protein, to expand protein The range used is added in varieties of food items.
Silver carp is that biomass is maximum in aquatic food in the world, the minimum biomass of cost, as minced fish production Raw material, since the problems such as gel collapse, fishlike smell limits the use of silver carp.Soybean protein isolate is economical, trophism, The advantages that functional, but its application in fields such as food, medicine, health care products is also somewhat limited, major embodiment At two aspects, first is that soybean protein isolate will cause nutrient component damages in extracting process and functional character weakens; Second is that some natural function characteristics such as gelation, dissolubility etc. of soybean protein isolate have certain limit.Soybean is separated Albumen carries out lower bound degree enzyme modification to improve its gelation.What is played a major role in chub surimi gel is fribrillin, Silver carp fribrillin is mixed with the soybean protein isolate of enzyme modification, double protein gel products are made.But at this stage to it Study less, commercialization degree is relatively low.Enzymatic hydrolysis of soybean protein isolate and the silver carp fribrillin for studying Lower degrees of hydrolysis are multiple The double protein gel products formed are closed, the purpose is to combine the healthy advantage of the nutritional advantages of animal protein and vegetable protein, The health type food that quality plant albumen and high-quality animal protein combine is promoted in fitness-for-all diet.
Summary of the invention
In view of the shortcomings of the prior art, the present invention provides a kind of high-intensitive and high retentiveness double protein plural gel preparation work Skill solves the problems such as chub surimi gel strength deteriorates, fishlike smell is heavy, Soybean Protein Isolate Gel is poor, it is multiple to improve gained The healthy advantage of the intensity and retentiveness of hop protein gel, the nutritional advantages and vegetable protein of realizing animal protein combines, and increases Add the output value, while creating favorable conditions for the actual production of double protein plural gel and industrial application.
In order to achieve the above object, technical solution of the present invention is achieved by the following technical programs:
A kind of high-intensitive and high retentiveness double protein plural gel preparation process, comprising the following steps: (1) separate soybean Albumen is mixed with deionized water, carries out low limited enzymatic hydrolysis, the soybean separation protein of gained difference degree of hydrolysis with alkali protease White powder is spare;(2) the meat crusher of silver carp white muscle is rubbed, buffer solution washing is added, centrifugation, is precipitated;(3) it will sink It forms sediment and is added that buffer solution is washed, is centrifuged, washed again, filtered, is centrifuged, to obtain silver carp fribrillin spare;It (4) will be upper The soybean separation protein white powder and silver carp fribrillin of different degree of hydrolysis are mixed according to different proportion, and it is standby to obtain compound protein solution With;(5) above-mentioned mixed protein solution is heated in digital display thermostat water bath, is handled by two step heatings;It (6) will be upper Solution of stating that treated carry out it is cooling, store, obtain soybean protein isolate and silver carp protein plural gel product of the present invention.It is preferred that , soybean protein isolate mixes (concentration of substrate 3%) with deionized water in step (1), low limited enzymatic hydrolysis, degree of hydrolysis DH2 =5%.Preferably, the requirement for buffer solution being added in step (2) is 4 times of volume (V/W) buffer solutions (50mM, pH7.5), 4 DEG C, 15min is centrifuged under the conditions of 8500 × g.Preferably, the requirement that buffer solution is added in step (3) is that 4 times of volumes (V/W) are slow Solution (0.1M NaCl) is rushed, using 6 layers of filtered through gauze.Preferably, soybean separation protein white powder and silver carp myogen are fine in step (4) Fibrillarin is mixed according to 1:3, and the total protein content of all mixed solutions is 60mg/mL.Preferably, two steps add in step (5) Thermal method is to heat 30min in 40 DEG C of water-baths, heats 30min in 90 DEG C of water-baths.Preferably, ice-water bath is used in step (6) It is cooled to room temperature, stores 12h in 4 DEG C of refrigerators.Preferably, the soybean protein isolate is digested by alkali protease lower bound degree Afterwards, it obtains degree of hydrolysis and is 5% modified soybean protein isolate, and mixed with silver carp fribrillin by 1:3, added by two steps Thermal method prepares gel products, wherein acid extraction is to heat 30min in 40 DEG C of water-baths, is heated in 90 DEG C of water-baths 30min。
The present invention provides a kind of high-intensitive and high retentiveness double protein plural gel preparation process, excellent compared with prior art Point is: (1) present invention digests soybean using Alcalase FG 2.4L alkali protease, can effectively make in soybean Protein macromolecule is converted to micromolecule polypeptide, is convenient for absorption of human body, the trophic function of enhancing gained gel.(2) present invention will The condition that the soybean protein isolate and silver carp fribrillin of lower bound degree enzymatic hydrolysis are compounded in two heating prepares egg-pair white gel, The bioavailability of silver carp is improved, the gel strength and water retention property of acquisition are significantly improved.(3) present invention first passes through low temperature Heating (40 DEG C, 30min) cure mixed solution, then be heated at high temperature (90 DEG C, 30min) can effectively prevent it is solidifying There is gel collapse phenomenon, enhances the purity and stability of gel in glue product, and reduces the beany flavor and fish raw meat of products obtained therefrom Taste enhances the integrated quality of product.
Detailed description of the invention
Influence of Fig. 1 degree of hydrolysis to double protein gel strength;
Influence of Fig. 2 degree of hydrolysis to egg-pair white gel retentiveness;
Influence of the two kinds of albumen different mixing proportions of Fig. 3 to double protein gel strength;
Influence of the two kinds of albumen different mixing proportions of Fig. 4 to egg-pair white gel retentiveness;
Specific embodiment
In order to make the object, technical scheme and advantages of the embodiment of the invention clearer, below with reference to the embodiment of the present invention pair Technical solution in the embodiment of the present invention is clearly and completely described, it is clear that described embodiment is a part of the invention Embodiment, instead of all the embodiments.Based on the embodiments of the present invention, those of ordinary skill in the art are not making wound Every other embodiment obtained under the premise of the property made labour, shall fall within the protection scope of the present invention.
A kind of high-intensitive and high retentiveness double protein plural gel preparation process, comprising the following steps: (1) separate soybean Albumen is mixed with deionized water, carries out low limited enzymatic hydrolysis, the soybean separation protein of gained difference degree of hydrolysis with alkali protease White powder is spare;(2) the meat crusher of silver carp white muscle is rubbed, buffer solution washing is added, centrifugation, is precipitated;(3) it will sink It forms sediment and is added that buffer solution is washed, is centrifuged, washed again, filtered, is centrifuged, to obtain silver carp fribrillin spare;It (4) will be upper The soybean separation protein white powder and silver carp fribrillin of different degree of hydrolysis are mixed according to different proportion, and it is standby to obtain compound protein solution With;(5) above-mentioned mixed protein solution is heated in digital display thermostat water bath, is handled by two step heatings.It (6) will be upper Solution of stating that treated carry out it is cooling, store, obtain soybean protein isolate and silver carp protein plural gel product of the present invention.
Embodiment 1:
A kind of high-intensitive and high retentiveness double protein plural gel preparation process, comprising the following steps: soybean in step (1) Protein isolate mixes (concentration of substrate 3%) with deionized water, low limited enzymatic hydrolysis, degree of hydrolysis DH2=5%;Add in step (2) The requirement for entering buffer solution is that 4 times of volume (V/W) buffer solutions (50mM, pH7.5) are centrifuged under the conditions of 8500 × g at 4 DEG C 15min;It is 4 times of volume (V/W) buffer solutions (0.1M NaCl) that the requirement of buffer solution is added in step (3), using 6 layers of yarn Cloth filtering;Soybean separation protein white powder and silver carp fribrillin are mixed according to 1:3 in step (4), all mixed solutions it is total Protein content is 60mg/mL;Two step heatings are that 30min is heated in 40 DEG C of water-baths in step (5), are added in 90 DEG C of water-baths Hot 30min;Room temperature is cooled to using ice-water bath in step (6), stores 12h in 4 DEG C of refrigerators, the soybean protein isolate passes through alkali Property protease lower bound degree enzymatic hydrolysis after, obtain the modified soybean protein isolate that degree of hydrolysis is 5%, and pressed with silver carp fribrillin 1:3 mixing, is heated by digital display thermostat water bath, and acid extraction is to heat 30min, 90 DEG C of water-baths in 40 DEG C of water-baths 30min is heated in pot.Wherein, the mixed proportion of two kinds of albumen is 1:3, and degree of hydrolysis is respectively set to DH1=2%, DH2=5%, DH3=10%.
It detects under soybean protein isolate difference degree of hydrolysis, the intensity and retentiveness of product gel change, as a result such as Fig. 1 and figure Shown in 2.
Embodiment 2:
A kind of high-intensitive and high retentiveness double protein plural gel preparation process, comprising the following steps: soybean in step (1) Protein isolate mixes (concentration of substrate 3%) with deionized water, low limited enzymatic hydrolysis, degree of hydrolysis DH2=5%;Add in step (2) The requirement for entering buffer solution is that 4 times of volume (V/W) buffer solutions (50mM, pH7.5) are centrifuged under the conditions of 8500 × g at 4 DEG C 15min;It is 4 times of volume (V/W) buffer solutions (0.1M NaCl) that the requirement of buffer solution is added in step (3), using 6 layers of yarn Cloth filtering;Soybean separation protein white powder and silver carp fribrillin are mixed according to 1:3 in step (4), all mixed solutions it is total Protein content is 60mg/mL;Two step heatings are that 30min is heated in 40 DEG C of water-baths in step (5), are added in 90 DEG C of water-baths Hot 30min;Room temperature is cooled to using ice-water bath in step (6), stores 12h in 4 DEG C of refrigerators, the soybean protein isolate passes through alkali Property protease lower bound degree enzymatic hydrolysis after, obtain the modified soybean protein isolate that degree of hydrolysis is 5%, and pressed with silver carp fribrillin 1:3 mixing, is heated by digital display thermostat water bath, and acid extraction is to heat 30min, 90 DEG C of water-baths in 40 DEG C of water-baths 30min is heated in pot.Wherein, the degree of hydrolysis of soybean protein isolate is DH2=5%, the mixed proportion of two kinds of albumen is set as 1: 1,1:2 and 1:3.
It detects under two kinds of albumen different mixing proportions, intensity and the retentiveness variation of product gel, as a result such as Fig. 3 and Fig. 4 It is shown.
Embodiment 3:
A kind of high-intensitive and high retentiveness double protein plural gel preparation process, comprising the following steps: measurement embodiment 1~ 2 double protein plural gel performances, the specific steps are as follows: (1) gel strength measures: (20 ± 1 DEG C) are by gel products system at room temperature At the square gel piece with a thickness of 30mm, measured using TA-XT plus type texture analyser.Model of popping one's head in selects P/ 0.5 (diameter 12mm), the penetration power pushed are the gel strength of albumen.The physical property instrument location parameter of selection is as follows: Speed before testing: 2.0mm/s;Test speed: 0.5mm/s;Trigger force is 5g;Speed after test: 2.0mm/s;Puncture distance: 5.0mm.Each sample carries out parallel test three times, is averaged.(2) gel retentiveness measures: the protein gel of 10g is placed in 15min is centrifuged at 1600 × g, 4 DEG C in 50mL centrifuge tube.Record the weight M of centrifuge tube0, the preceding gel sample of centrifuge tube and centrifugation Product weight M1With gel sample weight M after centrifuge tube and centrifugation2.WHC is expressed as after the percentage centrifugation of gel weight relative to first The weight of beginning gel.
According to Figure of description experimental result it is found that becoming larger with soybean separation proteolysis degree, egg-pair white gel Intensity becomes larger, and egg-pair white gel retentiveness first increases to be reduced afterwards.This may be because the hydrolysis of soybean protein isolate enhances The interaction of itself and silver carp fribrillin, still, hydrolysis degree is excessively high, cause most of protein to be hydrolyzed into small Molecular peptide, to reduce its relative molecular mass distribution, viscosity is reduced, while will lead to the reduction of gelation.Therefore, it selects Select the soybean protein isolate of DH=5%.With the soybean protein isolate and silver carp fribrillin mixing ratio of lower bound degree enzymatic hydrolysis Example changes to 1:3 by 1:1, and protein gel intensity and retentiveness significantly increase.This is because the egg-pair being thermally formed by two steps White gel network structure and silver carp fribrillin have very big relationship, and silver carp fribrillin proportion is higher, coagulate Glue hardness is relatively bigger.The double protein plural gel network structure formed as SPI:FP=1:1 is poor, it may be possible to because of mixing When SPI additive amount is excessive in system, hydrophobic interaction is caused to enhance, reduces the ability of gel network Bound Water Moleculess, When centrifugation, hydrone is easy to separate out, when SPI additive amount very little, can promote gel network structure to a certain extent Enhancing.To sum up, DH=5%, SPI:FP=1:3 are selected.
Although the present invention has been disclosed in the preferred embodiment as above, it is not intended to limit the invention, any to be familiar with this The people of technology can do various changes and modification, therefore protection of the invention without departing from the spirit and scope of the present invention Range should subject to the definition of the claims.

Claims (8)

1. a kind of high-intensitive and high retentiveness double protein plural gel preparation process, which comprises the following steps: (1) Soybean protein isolate is mixed with deionized water, carries out low limited enzymatic hydrolysis with alkali protease, gained difference degree of hydrolysis Soybean separation protein white powder is spare;(2) the meat crusher of silver carp white muscle is rubbed, buffer solution washing is added, centrifugation, is sunk It forms sediment;(3) precipitating is added that buffer solution is washed, is centrifuged, washed again, filtered, is centrifuged, to obtain silver carp fribrillin standby With;(4) soybean separation protein white powder of upper different degree of hydrolysis and silver carp fribrillin are mixed according to different proportion, is obtained compound Protein solution is spare;(5) above-mentioned mixed protein solution is heated in digital display thermostat water bath, at two step heatings Reason.(6) treated solution is subjected to cooling, stored, it is compound solidifying to obtain soybean protein isolate and silver carp protein of the present invention Glue product.
2. according to a kind of high-intensitive and high retentiveness plural gel preparation process as described in claim 1, it is characterised in that: step Suddenly soybean protein isolate mixes (concentration of substrate 3%) with deionized water in (1), low limited enzymatic hydrolysis, degree of hydrolysis DH2= 5%.
3. a kind of high-intensitive and high retentiveness plural gel preparation process as described in claim 1, it is characterised in that: step (2) it is 4 times of volume (V/W) buffer solutions (50mM, pH7.5) that the requirement of buffer solution is added in, at 4 DEG C, under the conditions of 8500 × g It is centrifuged 15min.
4. a kind of high-intensitive and high retentiveness plural gel preparation process as described in claim 1, it is characterised in that: step (3) it is 4 times of volume (V/W) buffer solutions (0.1M NaCl) that the requirement of buffer solution is added in, using 6 layers of filtered through gauze.
5. a kind of high-intensitive and high retentiveness plural gel preparation process as described in claim 1, it is characterised in that: step (4) soybean separation protein white powder and silver carp fribrillin are mixed according to 1:3 in, and the total protein content of all mixed solutions is 60mg/mL。
6. a kind of high-intensitive and high retentiveness plural gel preparation process as described in claim 1, it is characterised in that: step (5) two step heatings are to heat 30min in 40 DEG C of water-baths in, heat 30min in 90 DEG C of water-baths.
7. a kind of high-intensitive and high retentiveness plural gel preparation process as described in claim 1, it is characterised in that: step (6) room temperature is cooled to using ice-water bath in, stores 12h in 4 DEG C of refrigerators.
8. a kind of high-intensitive and high retentiveness plural gel preparation process as described in claim 1, it is characterised in that: described big Beans protein isolate obtains the modified soybean protein isolate of degree of hydrolysis 5%, and and silver carp after alkali protease lower bound degree enzymatic hydrolysis Fribrillin is mixed by 1:3, prepares gel products by two step heatings, wherein acid extraction is 40 DEG C of water 30min is heated in bath, heats 30min in 90 DEG C of water-baths.
CN201910135877.4A 2019-02-25 2019-02-25 A kind of high-intensitive and high retentiveness double protein plural gel preparation process Pending CN109700035A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910135877.4A CN109700035A (en) 2019-02-25 2019-02-25 A kind of high-intensitive and high retentiveness double protein plural gel preparation process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910135877.4A CN109700035A (en) 2019-02-25 2019-02-25 A kind of high-intensitive and high retentiveness double protein plural gel preparation process

Publications (1)

Publication Number Publication Date
CN109700035A true CN109700035A (en) 2019-05-03

Family

ID=66263787

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910135877.4A Pending CN109700035A (en) 2019-02-25 2019-02-25 A kind of high-intensitive and high retentiveness double protein plural gel preparation process

Country Status (1)

Country Link
CN (1) CN109700035A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111109427A (en) * 2019-12-25 2020-05-08 中国肉类食品综合研究中心 Method for improving myofibrillar protein gel strength and application thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111109427A (en) * 2019-12-25 2020-05-08 中国肉类食品综合研究中心 Method for improving myofibrillar protein gel strength and application thereof

Similar Documents

Publication Publication Date Title
WO2017004903A1 (en) Edible bird's nest product and preparation method thereof
US20200037654A1 (en) Peanut protein vegetarian sausage and preparation method thereof
CN106359638B (en) Sour pulp milk-flavored bean curd and preparation method thereof
CN101990955B (en) Sour milk bean curd and manufacturing method thereof
CN101356966A (en) Method for producing sea-crab seasoner products material
CN102630999A (en) Walnut lactic acid bacteria fermented beverage and preparation method thereof
CN102028171A (en) Method for producing chicken flavor collagen concentrated soup by utilizing chicken skeletons and chicken claws
CN102356834A (en) Sargassum fusiforme health care jelly and production method thereof
CN109007746A (en) A kind of preparation method of sturgeon head seasoning
Li et al. Comparative study of chemical composition and texture profile analysis between camembert cheese and Chinese sufu
CN105660985A (en) Preparation technology of natural fish protein powder by biological fermentation
CN107439955B (en) Health nutrient puffed food and preparation process thereof
CN105661377A (en) High-protein and low-calorie fish flesh crisp slice preparation method
CN109700035A (en) A kind of high-intensitive and high retentiveness double protein plural gel preparation process
CN105029572B (en) A kind of black soya bean antioxidation polypeptide beverage and preparation method thereof
CN103059745A (en) Preparation method of tilapia skin gelatin
CN107058437B (en) Hairtail minced fillet protein powder for pizza embryo and preparation method thereof
CN102845760B (en) Preparation method of duck blood polypeptide nutrient sausage
CN105982123A (en) Preparation method of earthworm protein beverage and product obtained by preparation method
CN105286022A (en) Compound protein powder rich in content of essential amino acids and reasonable in composition and preparation method of compound protein powder
CN105876726B (en) A kind of natural shrimp taste sea-food cream and preparation method thereof
Yao et al. Fermentation process improvement of a Chinese traditional food: soybean residue cake
JP4663954B2 (en) Fermented food and coagulation treatment method thereof
CN103651849B (en) Dairy product containing cloverleaf proteins and preparation method thereof
CN113812506A (en) Modified silver carp muscle protein, processing method and application thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20190503

WD01 Invention patent application deemed withdrawn after publication