CN104430868B - A kind of preparation method for digesting oat dairy products and ultrahigh-pressure sterilization - Google Patents

A kind of preparation method for digesting oat dairy products and ultrahigh-pressure sterilization Download PDF

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CN104430868B
CN104430868B CN201410766464.3A CN201410766464A CN104430868B CN 104430868 B CN104430868 B CN 104430868B CN 201410766464 A CN201410766464 A CN 201410766464A CN 104430868 B CN104430868 B CN 104430868B
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oat
preparation
pressure
oatmeal
ultrahigh
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CN104430868A (en
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蔡涛
于鹏
杨思行
肖扬
任璐
王辉
姜雪
刘振民
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Shanghai Bright Dairy and Food Co Ltd
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Abstract

The invention discloses a kind of preparation method for digesting oat dairy products and ultrahigh-pressure sterilization.Its raw material includes following component:Fresh milk, oatmeal, stabilizer and water, above-mentioned percentage are all the mass percent relative to the raw material;Described preparation method comprises the following steps:1. after enzyme preparation is well mixed with water, being mixed with oatmeal, oat slurry is filtered to obtain after enzymolysis;2. after stabilizer and fresh milk are well mixed, it is well mixed with 1. oat slurry that step obtains;3. by step, 2. products therefrom adds water constant volume after milling treatment of colloid, obtains precursor;4. by step, 3. obtained precursor progress is high-pressure homogeneous;5. the precursor after step 4. homogeneous is subjected to destroy the enzyme treatment;6. after the precursor after step 5. sterilization treatment is carried out into ultrahigh-pressure sterilization, you can.The preparation method of the present invention, solve the problems, such as protein precipitation, retain the nutritional ingredient of oat and fresh milk, finished product smooth in taste, nature, color and luster are milky white, have good stability.

Description

A kind of preparation method for digesting oat dairy products and ultrahigh-pressure sterilization
Technical field
The present invention relates to a kind of preparation method for digesting oat dairy products and ultrahigh-pressure sterilization.
Background technology
Oat (Avena sativa L.) is grass, and the 6th is occupied in the production of world's cereal.It is common with other Cereal crops are compared, and oat is rich in protein, beta glucan, unrighted acid, polyphenol etc., in preventing and treating as caused by high fat of blood The effect of cardiovascular and cerebrovascular disease, control blood sugar for human body and fat-reducing etc., has been widely recognized, U.S.'s food and medicine pipe Reason office (FDA) announced the function of oat " having reduces heart disease risk " in 1997.
At present, major part oat in China's is formed to oatmeal, oatmeal and Oat Cracker.These products do not have Thoroughly solves the problems such as oat food single varieties, palatability difference.
Oats milk beverage is a kind of milk substitute products in good taste, nutritious.American-European countries treats as oat milk after ox The 3rd kind of most important protein drink after breast, soya-bean milk.But oat prepares oat milk and larger technical barrier always be present, Starch mainly in oat easily forms the very big colloid of viscosity with beta glucan, and even gel, protein easily precipitates Deng.External oat dairy products mass selling, and China's oat milk product does not obtain good exploitation also.
Oat (Avena sativa L.) is grass, is one of comprehensive nutritive food best in cereal preparation, Rich in saponin(e exclusive in protein, unrighted acid, dietary fiber and cereal, in preventing and treating heart and brain as caused by high fat of blood The effect of vascular diseases, control blood sugar for human body and fat-reducing etc., has been widely recognized.In addition, the water solubility in oat Beta glucan has reducing blood lipid, hypoglycemic, strengthen immunity, resisting oxidation and delaying senility and other effects, and healthy nutritive value is high.
At present, the processing for oat milk directly soaks slurrying using oat more or the allotment of oat water extract forms, fresh There are the dairy products compounded using oat and fresh milk.This is due to starch and β-Portugal in oat in oat milk process Glycan easily forms the very big colloid of viscosity, even gel, and easily precipitation causes system unstable etc. to protein.Asked for above-mentioned Topic, also there is the method digested by high temperature to improve at present, but because hydrolysis temperature is general higher, easily causes protein denaturation and sink Form sediment, therefore the product effect obtained is general.Therefore, how to overcome above-mentioned technical problem, prepare the breast system of oat and fresh milk compounding Product are urgent problems to be solved.
The content of the invention
The technical problems to be solved by the invention are that the starch overcome in prior art oat is easily formed with beta glucan The very big colloid of viscosity, even gel, and the defects of protein easily precipitates, there is provided one kind enzymolysis oat dairy products and The preparation method of ultrahigh-pressure sterilization.The present invention uses the preparation method of ultrahigh-pressure sterilization, can be in the temperature near normal temperature or normal temperature The effect of sterilization, enzyme deactivation is issued to, can effectively reduce protein precipitation problem in oat Milk drink, and pressure treatment is not destroyed The covalent bond of food ingredients, so as to reduce the deterioration of the loss of nutritional ingredient caused by high temperature and color, smell and taste, at utmost protect The nutritional ingredient of oat and fresh milk is stayed, the oat dairy products smooth in taste of preparation, nature, color and luster are milky white, have well Stability.
The present invention solves above-mentioned technical problem by the following technical programs.
The invention provides a kind of preparation method for the ultrahigh-pressure sterilization for digesting oat dairy products, its raw material includes such as the following group Point:Fresh milk 60-80%, oatmeal 3-6%, stabilizer 0.15-0.25% and water, above-mentioned percentage are all relative to the original The mass percent of material;
Described preparation method comprises the following steps:
(1) after enzyme preparation is well mixed with water, mixed with the oatmeal after baking, oat slurry is filtered to obtain after enzymolysis; Wherein, described enzyme preparation is amylase and carbohydrase, and the addition of described amylase is 0.3-0.4g/100g oatmeals, The addition of described carbohydrase is 0.6-0.8g/100g oatmeals, and the temperature of the enzymolysis is 60-70 DEG C;
(2) after being well mixed stabilizer and fresh milk, the oat slurry obtained with step (1) is well mixed;
(3) step (2) products therefrom is added into water constant volume after milling treatment of colloid, obtains precursor;
(4) precursor made from step (3) is carried out high-pressure homogeneous;
(5) precursor after step (4) homogeneous is subjected to destroy the enzyme treatment;
(6) after the precursor after step (5) sterilization treatment being carried out into ultrahigh-pressure sterilization, described oat dairy products are produced;Its In, the temperature of described ultrahigh-pressure sterilization is 10-25 DEG C, and the pressure of described ultrahigh-pressure sterilization is 450-800MPa, described The time of ultrahigh-pressure sterilization is 10-20min.
In step (1), described oatmeal is preferably the oatmeal that 200 mesh sieving rates are higher than 95%, is more preferably flat Equal fineness is less than 20 μm of oatmeal, and above-mentioned percentage is the mass percent for accounting for described oatmeal.
In step (1), described oatmeal is preferably crushed by oat raw mill and is made.Described oat raw material is this Conventional oat raw material in field.The advance for the operating procedure that the operation of described baking preferably crushes in oat raw mill OK.Described baking is this area common process, and described baking is preferably by oat raw material parch;The temperature of described parch Preferably 180-250 DEG C of degree, is more preferably 180-220 DEG C, optimal for 190-210 DEG C;The time of described parch is preferable Ground is 10-40min, is more preferably 20-35min;Preferably first by oat before the operating procedure of described oat raw material parch Raw material successively through past dirt, remove heterochromatic grain and remove magnetic impurity the step of.Routinely grind the described this area that is ground to Technique, described grinding technics is preferably to be refined using ultra micro of the temperature not higher than 10 DEG C.The equipment of the grinding is ability Domain conventional grinding machine, preferably nonmetal medium Refining apparatus.
In step (1), described amylase is amylase in the art conventional, preferably alpha amylase, more preferably for Amylex LT amylase.Described amylase is purchased from Co., Ltd in Danisco.The addition of described amylase is preferable Ground is 0.32-0.36g/100g oatmeals.
In step (1), described carbohydrase is carbohydrase in the art conventional, preferably beta glucan enzyme, more preferably For Diazyme P25 carbohydrase.Described carbohydrase is purchased from Co., Ltd in Danisco.The addition of described carbohydrase Preferably 0.65-0.72g/100g oatmeals.
In step (1), the temperature of described water is preferably 60-70 DEG C, is more preferably 63-65 DEG C.
In step (1), the temperature of described enzymolysis is preferably 63-65 DEG C.
In step (1), the mass ratio of described oatmeal and described water is preferably (1:4)-(1:6), more preferably for (1:4.5)-(1:5)。
In step (1), the time of described enzymolysis is preferably 25-35min, is more preferably 28-32min.
In step (1), described filtering is preferably filtered by the sieve of 90-120 mesh.
In step (2), described stabilizer is the conventional emulsion stabilizer for food, preferably selected from single diglycerol Fatty acid ester, sucrose fatty ester, any one or more in gellan gum and xanthans, more preferably single diglycerine fatty acid The mass ratio of ester, sucrose fatty ester, gellan gum and xanthans is 8:5:2:3 compound stabilizer.Described stabilizer is purchased from Co., Ltd in Danisco.
In the present invention, described raw material preferably also includes sweetener.Described sweetener is the conventional generation in this area The auxiliary material of sweet taste, preferably any one or more in white granulated sugar, brown granulated sugar, polydextrose and xylo-oligosaccharide, more preferably Ground is polydextrose.The dosage of described sweetener is 3-5%, and above-mentioned percentage is the quality percentage relative to the raw material Than.
In step (2), before the operating procedure that described stabilizer and fresh milk are well mixed, it is preferred that described is steady It is first dry-mixed with sweetener to determine agent.
In step (2), described fresh milk can be the one or more in raw milk, raw sheep breast and raw camel breast, preferably Ground is raw milk.Fresh milk of the present invention is to meet《National food safety standard --- lactogenesis》GB19301-2010 examination Standard, general fat content >=3.1%, protein content >=2.8%, nonfat milk solids content >=8.1%, above-mentioned percentage Respectively each component accounts for the mass percent of the fresh milk.The temperature of described fresh milk is preferably 70-85 DEG C, more preferably For 75-80 DEG C.
Milling treatment of colloid described in step (3) is conventional method in food technology, the rotating speed of described milling treatment of colloid compared with It is 3000-3500rpm goodly, is more preferably 3200-3400rpm.The operation of described constant volume is conventional method in food technology, After the operating procedure of described constant volume, stirring 10-15min preferably, 10 ± 3 DEG C are cooled to.
In step (4), described high-pressure homogeneous method is the conventional method in food technology, typically in high pressure homogenizer Middle progress, described high-pressure homogeneous temperature are preferably 65-75 DEG C.Described high-pressure homogeneous pressure is preferably 150- 160bar。
In step (5), the temperature of described enzyme deactivation is preferably 90-95 DEG C, and the time is preferably 5-10 minutes.
In step (6), the temperature of described ultrahigh-pressure sterilization is preferably 15-20 DEG C.The pressure of described ultrahigh-pressure sterilization Power is preferably 600-700MPa.The time of described ultrahigh-pressure sterilization is preferably 15-18min.
In step (6), the rate of pressure rise of described ultrahigh-pressure sterilization is preferably 800-1000MPa/min, more preferably for 900-950MPa/min.The venting duration of described ultrahigh-pressure sterilization is preferably the 5-30 seconds, is more preferably the 5-10 seconds.
Preferably, after oat dairy products progress hot filling prepared by step (6), cool down preservation.Described filling behaviour Make generally to meet SSOP (SSOP), Good Manufacture Practice (GMP) and hazard (HACCP) requirement.
Oat dairy products are digested as made from the preparation method of above-mentioned ultrahigh-pressure sterilization present invention also offers a kind of.
It on the basis of common sense in the field is met, above-mentioned each optimum condition, can be combined, it is each preferably real to produce the present invention Example.
Agents useful for same and raw material of the present invention are commercially available.
The positive effect of the present invention is:
1st, in enzymolysis oat dairy products of the invention, sweetener addition is few, without addition essence.It is not only in good taste, and And meet the demand of existing healthy living pattern.Meanwhile enzyme preparation reaction temperature is at 70 DEG C, less than conventional hydrolysis temperature, favorably In the reservation of nutritional ingredient, reduce it is unstable caused by protein denaturation, and during actual factorial praluction, two kinds Enzyme adds simultaneously, can greatly reduce operating process, reduces factory's power consumption, has great application prospect.
2nd, preparation method of the invention, sterilization, enzyme deactivation can be haveed the function that at the temperature near normal temperature or normal temperature, effectively Reduce oat Milk drink in protein precipitation problem, reduce nutritional ingredient caused by high temperature loss and color, smell and taste it is bad Change, and pressure treatment does not destroy the covalent bond of food ingredients, it is fragrant so as to reduce the loss of nutritional ingredient caused by high temperature and color The deterioration of taste, the quality factors such as the texture of product are had some improvement.Pressure transmission speed is fast, uniform simultaneously, in the absence of pressure Power gradient and dead angle, processing procedure are not influenceed by the size and shape of food, greatly remain the nutrition of oat into Divide and good mouthfeel.
3rd, enzymolysis oat dairy products smooth in taste provided by the invention, nature, color and luster are milky white, have good stability, Protein is not easy to precipitate, to improving the dietary structure of people and then improving compatriots' constitution highly significant.And cereal intake mode Change, a kind of fresh and new sensation can not only be given people, while also incorporated more modern fast pace fashionable elements, more can Meet nutritional need and psychological needs of the modern to life.
Embodiment
The present invention is further illustrated below by the mode of embodiment, but does not therefore limit the present invention to described reality Apply among a scope.The experimental method of unreceipted actual conditions in the following example, conventionally and condition, or according to business Product specification selects.
The specific source of raw material is as follows in following embodiments:
Raw milk is purchased from Shanghai Bright Dairy & Food Co., Ltd., and oatmeal is purchased from Beijing North Shang De Co., Ltds, white granulated sugar Purchased from Shanghai City sugar industry tobacco and wine group, stabilizer and enzyme are purchased from Co., Ltd in Danisco.
Embodiment 1
Raw material contains following component:Raw milk 80%, oatmeal 3%, white granulated sugar 5%, stabilizer 0.15% and water, each group It is 100% to divide mass percent sum;Above-mentioned percentage is mass percent;
Wherein, described stabilizer is single diglycerine fatty acid ester, sucrose fatty ester, the quality of gellan gum and xanthans Than for 8:5:2:3 compound stabilizer.Enzyme preparation is Amylex LT amylase 0.09g (with addition 0.3g/100g oatmeals Calculate) and the carbohydrase 0.18g of Diazyme P 25 (with addition 0.6g/100g oatmeals calculating) compounded.
Described preparation method comprises the following steps:
(1) by oat at 180 DEG C after parch 40min, by low temperature ultra micro fine grinding technology, by raw mill into powder, Temperature is controlled to be not higher than 10 DEG C in process of lapping, the equipment for grinding use is nonmetal medium Refining apparatus, powder 200 after grinding Mesh sieving rate is higher than 95%, and average fineness is less than 20 μm of ultimate attainment level, obtains oatmeal;
(2) enzyme preparation is added in 70 DEG C of hot water and stirred, then add the mass ratio of oatmeal, oatmeal and water For 1:6;Digest 35min, after through 90 mesh sieves, be filtrated to get oat slurry;
(3) by stabilizer and white granulated sugar it is dry-mixed after add under high velocity agitation in 70 DEG C of warm milk, obtained with step (2) Oat slurry is well mixed;
(4) slurries of the step (3) after well mixed are added into water constant volume after colloid mill 3000rpm processing, stir 10min, And 7 DEG C are cooled to, obtain precursor;
(5) it is precursor made from step (4) is high-pressure homogeneous as being carried out in 75 DEG C, 150bar environment;
(6) precursor after step (5) homogeneous is heated to 90 DEG C, enzyme deactivation 10min;
(7) by precursor after step (6) sterilizing in 25 DEG C, ultrahigh-pressure sterilization 20min under 800MPa, wherein, rate of pressure rise is 800MPa/min, venting duration 30s;
(8) after hot filling, cooling, you can.
Embodiment 2
Raw material contains following component:Raw milk 65%, oatmeal 4%, polydextrose 3.5%, stabilizer 0.18% and water, Each component mass percent sum is 100%;Above-mentioned percentage is mass percent;
Wherein, described stabilizer is single diglycerine fatty acid ester, sucrose fatty ester, the quality of gellan gum and xanthans Than for 8:5:2:3 compound stabilizer.Enzyme preparation is Amylex LT amylase 0.136g (with addition 0.34g/100g oats Powder calculate) and the carbohydrase 0.272g of Diazyme P 25 (with addition 0.68g/100g oatmeals calculating) compounded.
Described preparation method comprises the following steps:
(1) by oat at 200 DEG C after parch 20min, by low temperature ultra micro fine grinding technology, by raw mill into powder, Temperature is controlled to be not higher than 10 DEG C in process of lapping, the equipment for grinding use is nonmetal medium Refining apparatus, powder 200 after grinding Mesh sieving rate is higher than 95%, and average fineness is less than 20 μm of ultimate attainment level, obtains oatmeal;
(2) enzyme preparation is added in 63 DEG C of hot water and stirred, then add oatmeal, oatmeal is with water quality ratio 1:5;Digest 30min, after through 100 mesh sieves, be filtrated to get oat slurry;
(3) by stabilizer and polydextrose it is dry-mixed after add under high velocity agitation in 80 DEG C of warm milk, obtained with step (2) Oat slurry be well mixed;
(4) slurries of the step (3) after well mixed are added into water constant volume after colloid mill 3300rpm processing, stir 10min, And 10 DEG C are cooled to, obtain precursor;
(5) it is precursor made from step (4) is high-pressure homogeneous as being carried out in 65 DEG C, 160bar environment;
(6) precursor after step (5) homogeneous is heated to 95 DEG C, enzyme deactivation 8min;
(7) by precursor after step (6) sterilizing in 15 DEG C, ultrahigh-pressure sterilization 15min under 700MPa, wherein, rate of pressure rise is 950MPa/min, venting duration 5s;
(8) after hot filling, cooling, you can.
Embodiment 3
Raw material contains following component:Raw milk 60%, oatmeal 6%, brown granulated sugar 3%, stabilizer 0.25% and water, each group It is 100% to divide mass percent sum;Above-mentioned percentage is mass percent;
Wherein, described stabilizer is single diglycerine fatty acid ester, sucrose fatty ester, the quality of gellan gum and xanthans Than for 8:5:2:3 compound stabilizer.Described enzyme preparation is Amylex LT amylase 0.24g (with addition 0.4g/100g Oatmeal calculate) and the carbohydrase 0.48g of Diazyme P 25 (with addition 0.8g/100g oatmeals calculating) answered.
Described preparation method comprises the following steps:
(1) by oat at 250 DEG C after parch 10min, by low temperature ultra micro fine grinding technology, by raw mill into powder, Temperature is controlled to be not higher than 10 DEG C in process of lapping, the equipment for grinding use is nonmetal medium Refining apparatus, powder 200 after grinding Mesh sieving rate is higher than 95%, and average fineness is less than 20 μm of ultimate attainment level, obtains oatmeal;
(2) enzyme preparation is added in 60 DEG C of hot water and stirred, then add the mass ratio of oatmeal, oatmeal and water For 1:6;Digest 25min, after through 120 mesh sieves, be filtrated to get oat slurry;
(3) by stabilizer and brown granulated sugar it is dry-mixed after add under high velocity agitation in 85 DEG C of warm milk, obtained with step (2) Oat slurry is well mixed;
(4) slurries of the step (3) after well mixed are added into water constant volume after colloid mill 3500rpm processing, stir 10min, And 13 DEG C are cooled to, obtain precursor;
(5) it is precursor made from step (4) is high-pressure homogeneous as being carried out in 65 DEG C, 160bar environment;
(6) precursor after step (5) homogeneous is heated to 95 DEG C, enzyme deactivation 5min;
(7) by precursor after step (6) sterilizing in 10 DEG C, ultrahigh-pressure sterilization 10min under 450MPa, wherein, rate of pressure rise is 1000MPa/min, venting duration 5s;
(8) after hot filling, cooling, you can.
Embodiment 4
Raw material contains following component:Raw milk 68%, oatmeal 5%, polydextrose 4%, stabilizer 0.18% and water, respectively Constituent mass percentage sum is 100%;Above-mentioned percentage is mass percent;
Wherein, described stabilizer is single diglycerine fatty acid ester, sucrose fatty ester, the quality of gellan gum and xanthans Than for 8:5:2:3 compound stabilizer.Enzyme preparation is Amylex LT amylase 0.175g (with addition 0.35g/100g oats Powder calculate) and the carbohydrase 0.335g of Diazyme P 25 (with addition 0.67g/100g oatmeals calculating) compounded.
Described preparation method comprises the following steps:
(1) by oat at 200 DEG C after parch 20min, by low temperature ultra micro fine grinding technology, by raw mill into powder, Temperature is controlled to be not higher than 10 DEG C in process of lapping, the equipment for grinding use is nonmetal medium Refining apparatus, powder 200 after grinding Mesh sieving rate is higher than 95%, and average fineness is less than 20 μm of ultimate attainment level, obtains oatmeal;
(2) enzyme preparation is added in 65 DEG C of hot water and stirred, then add the mass ratio of oatmeal, oatmeal and water For 1:5;Digest 35min, after through 100 mesh sieves, be filtrated to get oat slurry;
(3) by stabilizer and polydextrose it is dry-mixed after add under high velocity agitation in 80 DEG C of warm milk, obtained with step (2) Oat slurry be well mixed;
(4) slurries of the step (3) after well mixed are added into water constant volume after colloid mill 3300rpm processing, stir 10min, And 12 DEG C are cooled to, obtain precursor;
(5) it is precursor made from step (4) is high-pressure homogeneous as being carried out in 65 DEG C, 160bar environment;
(6) precursor after step (5) homogeneous is heated to 95 DEG C, enzyme deactivation 10min;
(7) by precursor after step (6) sterilizing in 15 DEG C, ultrahigh-pressure sterilization 15min under 650MPa, wherein, rate of pressure rise is 900MPa/min, venting duration 7s;
(8) after hot filling, cooling, you can.
Embodiment 5
Raw material contains following component:Raw milk 75%, oatmeal 5.5%, xylo-oligosaccharide 5%, stabilizer 0.25% and water, Each component mass percent sum is 100%;Above-mentioned percentage is mass percent;
Wherein, described stabilizer is single diglycerine fatty acid ester, sucrose fatty ester, the quality of gellan gum and xanthans Than for 8:5:2:3 compound stabilizer.Enzyme preparation is Amylex LT amylase 0.193g (with addition 0.35g/100g oats Powder calculate) and the carbohydrase 0.374g of Diazyme P 25 (with addition 0.68g/100g oatmeals calculating) compounded.
Described preparation method comprises the following steps:
(1) by oat at 240 DEG C after parch 15min, by low temperature ultra micro fine grinding technology, by raw mill into powder, Temperature is controlled to be not higher than 10 DEG C in process of lapping, the equipment for grinding use is nonmetal medium Refining apparatus, powder 200 after grinding Mesh sieving rate is higher than 95%, and average fineness is less than 20 μm of ultimate attainment level, obtains oatmeal;
(2) enzyme preparation is added in 65 DEG C of hot water and stirred, then add the mass ratio of oatmeal, oatmeal and water For 1:4;Digest 30min, after through 100 mesh sieves, be filtrated to get oat slurry;
(3) by stabilizer and xylo-oligosaccharide it is dry-mixed after add under high velocity agitation in 75 DEG C of warm milk, obtained with step (2) Oat slurry be well mixed;
(4) slurries of the step (3) after well mixed are added into water constant volume after colloid mill 3500rpm processing, stir 15min, And 10 DEG C are cooled to, obtain precursor;
(5) it is precursor made from step (4) is high-pressure homogeneous as being carried out in 70 DEG C, 160bar environment;
(6) precursor after step (5) homogeneous is heated to 95 DEG C, enzyme deactivation 10min;
(7) by precursor after step (6) sterilizing in 20 DEG C, ultrahigh-pressure sterilization 20min under 550MPa, wherein, rate of pressure rise is 930MPa/min, venting duration 10s;
(8) after hot filling, cooling, you can.
Embodiment 6
Raw material contains following component:Raw milk 68%, oatmeal 4%, sweetener 3.5%, stabilizer 0.18% and water, respectively Constituent mass percentage sum is 100%;Above-mentioned percentage is mass percent;
Wherein, described stabilizer is single diglycerine fatty acid ester, sucrose fatty ester, the quality of gellan gum and xanthans Than for 8:5:2:3 compound stabilizer.Enzyme preparation is Amylex LT amylase 0.132g (with addition 0.33g/100g oats Powder calculate) and the carbohydrase 0.268g of Diazyme P 25 (with addition 0.67g/100g oatmeals calculating) compounded.
Described preparation method comprises the following steps:
(1) by oat at 200 DEG C after parch 25min, by low temperature ultra micro fine grinding technology, by raw mill into powder, Temperature is controlled to be not higher than 10 DEG C in process of lapping, the equipment for grinding use is nonmetal medium Refining apparatus, powder 200 after grinding Mesh sieving rate is higher than 95%, and average fineness is less than 20 μm of ultimate attainment level, obtains oatmeal;
(2) enzyme preparation is added in 61 DEG C of hot water and stirred, then add the mass ratio of oatmeal, oatmeal and water For 1:5;Digest 30min, after through 100 mesh sieves, be filtrated to get oat slurry;
(3) by stabilizer and polydextrose it is dry-mixed after add under high velocity agitation in 80 DEG C of warm milk, obtained with step (2) Oat slurry be well mixed;
(4) slurries of the step (3) after well mixed are added into water constant volume after colloid mill 3300rpm processing, stir 10min, And 10 DEG C are cooled to, obtain precursor;
(5) it is precursor made from step (4) is high-pressure homogeneous as being carried out in 65 DEG C, 160bar environment;
(6) precursor after step (5) homogeneous is heated to 95 DEG C, enzyme deactivation 7min;
(7) by precursor after step (6) sterilizing in 18 DEG C, ultrahigh-pressure sterilization 17min under 650MPa, wherein, rate of pressure rise is 940MPa/min, venting duration 6s;
(8) after hot filling, cooling, you can.
Effect example 1
Subjective appreciation is carried out to enzymolysis oat dairy products (by taking embodiment 2,4,6 as an example) of the present invention, with the good lattice in Taiwan The osmanthus lattice oat milk of food limited company production is control, and subjective appreciation is completed by 20 assessment officers.Index score is high Then effect is good by person, and evaluation is high, and as a result as shown in table 1, standards of grading are shown in Table 2.
Table 1
Table 2
For in stability test, size distribution is measured using Mastersizer Hydro3000;Stable dynamics Parameter (stability index, SI) represents average backscattered light rate of change (△ BS), the smaller stability of SI within observing time Better.
Data above shows that the embodiment of the present invention 2,4, the product prepared by 6 is in outward appearance, color and luster, texture, flavor, mouthfeel It is superior to compare set product with stability aspect.The enzymolysis oat dairy products of the present invention are because without additionally adding essence, having more Add soft full flavor and taste, obtain consumer Geng Gao preference degree, make product that there is higher added value.

Claims (9)

1. a kind of preparation method for the ultrahigh-pressure sterilization for digesting oat dairy products, its raw material include following component:Fresh milk 60- 80%, oatmeal 3-6%, stabilizer 0.15-0.25% and water, above-mentioned percentage are all the quality percentage relative to the raw material Than;Described stabilizer is single diglycerine fatty acid ester, sucrose fatty ester, and the mass ratio of gellan gum and xanthans is 8:5:2: 3 compound stabilizer;
Described preparation method comprises the following steps:
(1) after enzyme preparation is well mixed with water, mixed with the oatmeal after baking, oat slurry is filtered to obtain after enzymolysis;Wherein, Described enzyme preparation is amylase and carbohydrase, and the addition of described amylase is 0.3-0.4g/100g oatmeals, described The addition of carbohydrase is 0.6-0.8g/100g oatmeals, and the temperature of the enzymolysis is 60-70 DEG C;
(2) after being well mixed stabilizer and fresh milk, the oat slurry obtained with step (1) is well mixed;
(3) step (2) products therefrom is added into water constant volume after milling treatment of colloid, obtains precursor;
(4) precursor made from step (3) is carried out high-pressure homogeneous;
(5) precursor after step (4) homogeneous is subjected to destroy the enzyme treatment;
(6) after the precursor after step (5) sterilization treatment being carried out into ultrahigh-pressure sterilization, described oat dairy products are produced;Wherein, institute The temperature for the ultrahigh-pressure sterilization stated is 10-25 DEG C, and the pressure of described ultrahigh-pressure sterilization is 450-800MPa, described super-pressure The time of sterilization is 10-20min.
2. preparation method as claimed in claim 1, it is characterised in that in step (1), described oatmeal sieves for 200 mesh Rate is higher than 95% oatmeal, and above-mentioned percentage is the mass percent for accounting for described oatmeal;
In step (1), described oatmeal is crushed by oat raw mill and is made;The operation of described baking is ground in oat raw material Carried out before the broken operating procedure that is milled, described baking is by oat raw material parch;The temperature of described parch is 180-250 ℃;The time of described parch is 10-40min;Before the operating procedure of described oat raw material parch first by oat raw material according to It is secondary through past dirt, remove heterochromatic grain and remove magnetic impurity the step of;The technique of described grinding is to be not higher than using temperature 10 DEG C of ultra micro fine grinding;The equipment of the grinding is nonmetal medium Refining apparatus.
3. preparation method as claimed in claim 2, it is characterised in that in step (1), described oatmeal is that average fineness is small In 20 μm of oatmeal.
4. preparation method as claimed in claim 1, it is characterised in that in step (1), described amylase is alpha amylase, institute The addition for the amylase stated is 0.32-0.36g/100g oatmeals;
In step (1), described carbohydrase is beta glucan enzyme, and the addition of described carbohydrase is 0.65-0.72g/100g swallows Flour;
In step (1), the temperature of described water is 60-70 DEG C;
In step (1), the mass ratio of described oatmeal and described water is (1:4)-(1:6);
In step (1), the time of described enzymolysis is 25-35min;
In step (1), described being filtered into is filtered by the sieve of 90-120 mesh.
5. preparation method as claimed in claim 4, it is characterised in that in step (1), described amylase is Amylex LT Amylase;Described carbohydrase is Diazyme P25 carbohydrase.
6. preparation method as claimed in claim 1, it is characterised in that described raw material also includes sweetener, described sweet taste Any one or more of agent in white granulated sugar, brown granulated sugar, polydextrose and xylo-oligosaccharide, the dosage of described sweetener are 3-5%, above-mentioned percentage are the mass percent relative to the raw material;
In step (2), before the operating procedure that described stabilizer and fresh milk are well mixed, described stabilizer elder generation and sweet taste Agent is dry-mixed;
In step (2), described fresh milk be raw milk, raw sheep breast and raw camel it is newborn in one or more, the fresh butterfat Fat content >=3.1%, protein content >=2.8%, nonfat milk solids content >=8.1%, above-mentioned percentage are respectively each component The mass percent of the fresh milk is accounted for, the temperature of described fresh milk is 70-85 DEG C.
7. preparation method as claimed in claim 1, it is characterised in that the rotating speed of the milling treatment of colloid described in step (3) is 3000-3500rpm;After the operating procedure of described constant volume, 10-15min is stirred, is cooled to 10 ± 3 DEG C;
In step (4), it is described it is high-pressure homogeneous carried out in high pressure homogenizer, described high-pressure homogeneous temperature is 65-75 DEG C, Described high-pressure homogeneous pressure is 150-160bar;
In step (5), the temperature of described enzyme deactivation is 90-95 DEG C, and the time is 5-10 minutes.
8. preparation method as claimed in claim 1, it is characterised in that in step (6), the temperature of described ultrahigh-pressure sterilization is 15-20 DEG C, the pressure of described ultrahigh-pressure sterilization is 600-700MPa, and the time of described ultrahigh-pressure sterilization is 15-18min;
In step (6), the rate of pressure rise of described ultrahigh-pressure sterilization is 800-1000MPa/min, described ultrahigh-pressure sterilization Venting duration is the 5-30 seconds.
9. oat dairy products are digested made from a kind of preparation method as described in claim any one of 1-8.
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