CN105533371A - Preparation method of prebiotic anti-oxidization peptide beverage - Google Patents
Preparation method of prebiotic anti-oxidization peptide beverage Download PDFInfo
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- CN105533371A CN105533371A CN201511024059.5A CN201511024059A CN105533371A CN 105533371 A CN105533371 A CN 105533371A CN 201511024059 A CN201511024059 A CN 201511024059A CN 105533371 A CN105533371 A CN 105533371A
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- prebiotic
- casein
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- antioxidant peptide
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- 235000013406 prebiotics Nutrition 0.000 title claims abstract description 56
- 235000013361 beverage Nutrition 0.000 title claims abstract description 35
- 238000002360 preparation method Methods 0.000 title claims abstract description 16
- 108090000765 processed proteins & peptides Proteins 0.000 title description 2
- 238000007254 oxidation reaction Methods 0.000 title 1
- 239000005018 casein Substances 0.000 claims abstract description 52
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 claims abstract description 52
- 235000021240 caseins Nutrition 0.000 claims abstract description 52
- 101800000068 Antioxidant peptide Proteins 0.000 claims abstract description 37
- 239000002244 precipitate Substances 0.000 claims abstract description 33
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims abstract description 24
- 150000008442 polyphenolic compounds Chemical class 0.000 claims abstract description 20
- 235000013824 polyphenols Nutrition 0.000 claims abstract description 20
- 239000000843 powder Substances 0.000 claims abstract description 16
- 239000006228 supernatant Substances 0.000 claims abstract description 16
- 238000003756 stirring Methods 0.000 claims abstract description 15
- 230000007071 enzymatic hydrolysis Effects 0.000 claims abstract description 14
- 238000006047 enzymatic hydrolysis reaction Methods 0.000 claims abstract description 14
- 238000000034 method Methods 0.000 claims abstract description 13
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- WHGYBXFWUBPSRW-FOUAGVGXSA-N beta-cyclodextrin Chemical compound OC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)CO)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1CO WHGYBXFWUBPSRW-FOUAGVGXSA-N 0.000 claims abstract description 10
- 235000011175 beta-cyclodextrine Nutrition 0.000 claims abstract description 10
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- 239000000243 solution Substances 0.000 claims description 90
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 54
- 244000269722 Thea sinensis Species 0.000 claims description 31
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 27
- 235000013616 tea Nutrition 0.000 claims description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 12
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 12
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- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims description 9
- 229920002907 Guar gum Polymers 0.000 claims description 9
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 9
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- UQZIYBXSHAGNOE-USOSMYMVSA-N Stachyose Natural products O(C[C@H]1[C@@H](O)[C@H](O)[C@H](O)[C@@H](O[C@@]2(CO)[C@H](O)[C@@H](O)[C@@H](CO)O2)O1)[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](CO[C@@H]2[C@@H](O)[C@@H](O)[C@@H](O)[C@H](CO)O2)O1 UQZIYBXSHAGNOE-USOSMYMVSA-N 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 7
- 239000006084 composite stabilizer Substances 0.000 claims description 7
- UQZIYBXSHAGNOE-XNSRJBNMSA-N stachyose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO[C@@H]3[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O3)O)O2)O)O1 UQZIYBXSHAGNOE-XNSRJBNMSA-N 0.000 claims description 7
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- 238000005119 centrifugation Methods 0.000 claims description 5
- HDTRYLNUVZCQOY-UHFFFAOYSA-N α-D-glucopyranosyl-α-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OC1C(O)C(O)C(O)C(CO)O1 HDTRYLNUVZCQOY-UHFFFAOYSA-N 0.000 claims description 4
- HDTRYLNUVZCQOY-WSWWMNSNSA-N Trehalose Natural products O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-WSWWMNSNSA-N 0.000 claims description 4
- HDTRYLNUVZCQOY-LIZSDCNHSA-N alpha,alpha-trehalose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-LIZSDCNHSA-N 0.000 claims description 4
- RQFQJYYMBWVMQG-IXDPLRRUSA-N chitotriose Chemical compound O[C@@H]1[C@@H](N)[C@H](O)O[C@H](CO)[C@H]1O[C@H]1[C@H](N)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)N)[C@@H](CO)O1 RQFQJYYMBWVMQG-IXDPLRRUSA-N 0.000 claims description 4
- FTSSQIKWUOOEGC-RULYVFMPSA-N fructooligosaccharide Chemical compound OC[C@H]1O[C@@](CO)(OC[C@@]2(OC[C@@]3(OC[C@@]4(OC[C@@]5(OC[C@@]6(OC[C@@]7(OC[C@@]8(OC[C@@]9(OC[C@@]%10(OC[C@@]%11(O[C@H]%12O[C@H](CO)[C@@H](O)[C@H](O)[C@H]%12O)O[C@H](CO)[C@@H](O)[C@@H]%11O)O[C@H](CO)[C@@H](O)[C@@H]%10O)O[C@H](CO)[C@@H](O)[C@@H]9O)O[C@H](CO)[C@@H](O)[C@@H]8O)O[C@H](CO)[C@@H](O)[C@@H]7O)O[C@H](CO)[C@@H](O)[C@@H]6O)O[C@H](CO)[C@@H](O)[C@@H]5O)O[C@H](CO)[C@@H](O)[C@@H]4O)O[C@H](CO)[C@@H](O)[C@@H]3O)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@@H](O)[C@@H]1O FTSSQIKWUOOEGC-RULYVFMPSA-N 0.000 claims description 4
- 229940107187 fructooligosaccharide Drugs 0.000 claims description 4
- 235000021255 galacto-oligosaccharides Nutrition 0.000 claims description 4
- 150000003271 galactooligosaccharides Chemical class 0.000 claims description 4
- 230000001954 sterilising effect Effects 0.000 claims description 4
- 238000004659 sterilization and disinfection Methods 0.000 claims description 4
- SERLAGPUMNYUCK-DCUALPFSSA-N 1-O-alpha-D-glucopyranosyl-D-mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O SERLAGPUMNYUCK-DCUALPFSSA-N 0.000 claims description 3
- 239000000905 isomalt Substances 0.000 claims description 3
- 235000010439 isomalt Nutrition 0.000 claims description 3
- HPIGCVXMBGOWTF-UHFFFAOYSA-N isomaltol Natural products CC(=O)C=1OC=CC=1O HPIGCVXMBGOWTF-UHFFFAOYSA-N 0.000 claims description 3
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- 238000010438 heat treatment Methods 0.000 claims description 2
- 238000003760 magnetic stirring Methods 0.000 claims description 2
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- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 abstract description 2
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- HHEAADYXPMHMCT-UHFFFAOYSA-N dpph Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C1[N]N(C=1C=CC=CC=1)C1=CC=CC=C1 HHEAADYXPMHMCT-UHFFFAOYSA-N 0.000 description 5
- 230000002000 scavenging effect Effects 0.000 description 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
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- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical class OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 2
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- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
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- 230000018109 developmental process Effects 0.000 description 1
- 238000006911 enzymatic reaction Methods 0.000 description 1
- 235000012041 food component Nutrition 0.000 description 1
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- 230000036541 health Effects 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 230000007366 host health Effects 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
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- 230000003902 lesion Effects 0.000 description 1
- 230000003859 lipid peroxidation Effects 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 235000020124 milk-based beverage Nutrition 0.000 description 1
- 150000002482 oligosaccharides Chemical class 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
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- 230000035790 physiological processes and functions Effects 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
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- 238000000108 ultra-filtration Methods 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Preparation or treatment thereof
- A23L2/38—Other non-alcoholic beverages
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
- A23J3/00—Working-up of proteins for foodstuffs
- A23J3/30—Working-up of proteins for foodstuffs by hydrolysis
- A23J3/32—Working-up of proteins for foodstuffs by hydrolysis using chemical agents
- A23J3/34—Working-up of proteins for foodstuffs by hydrolysis using chemical agents using enzymes
- A23J3/341—Working-up of proteins for foodstuffs by hydrolysis using chemical agents using enzymes of animal proteins
- A23J3/343—Working-up of proteins for foodstuffs by hydrolysis using chemical agents using enzymes of animal proteins of dairy proteins
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Preparation or treatment thereof
- A23L2/52—Adding ingredients
- A23L2/60—Sweeteners
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Preparation or treatment thereof
- A23L2/52—Adding ingredients
- A23L2/68—Acidifying substances
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Preparation or treatment thereof
- A23L2/70—Clarifying or fining of non-alcoholic beverages; Removing unwanted matter
- A23L2/84—Clarifying or fining of non-alcoholic beverages; Removing unwanted matter using microorganisms or biological material, e.g. enzymes
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
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- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Nutrition Science (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Zoology (AREA)
- Molecular Biology (AREA)
- Microbiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Biochemistry (AREA)
- Non-Alcoholic Beverages (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Abstract
一种益生元抗氧化肽饮料的制备方法,向脱脂羊乳滴加盐酸磁力搅拌弃去上清液,将沉淀进行冷冻干燥得到酪蛋白干粉;将酪蛋白干粉制成酪蛋白溶液并向其中加入Alcalase酶水解结束后取上清液得到酶解液;向酶解液中添加β-环状糊精、白砂糖、混合酸、复合稳定剂、茶多酚以及益生元进行饮料复配;最后,进行灭菌即得到益生元抗氧化肽饮料;按本发明的制备方法制得的益生元抗氧化肽饮料可以降低体内自由基水平,帮助机体抵御疾病;同时,食物和药物的抗氧化性相比,可以长期食用,不仅可以预防和治疗如心血管、糖尿病、癌症和衰老等慢性病有很好的帮助;而且饮料中因含有益生元,经常饮用对调节肠道,帮助消化,调节体内毒素也有很好的帮助。A method for preparing a prebiotic antioxidant peptide beverage, comprising: adding hydrochloric acid dropwise to skimmed goat milk, magnetically stirring, discarding the supernatant, and freeze-drying the precipitate to obtain dry casein powder; making the dry casein powder into a casein solution and adding After Alcalase enzymatic hydrolysis, take the supernatant to obtain the enzymolysis solution; add β-cyclodextrin, white sugar, mixed acid, compound stabilizer, tea polyphenols and prebiotics to the enzymolysis solution for beverage compounding; finally, Sterilize to obtain the prebiotic antioxidant peptide beverage; the prebiotic antioxidant peptide beverage prepared according to the preparation method of the present invention can reduce the level of free radicals in the body and help the body resist diseases; at the same time, the antioxidant properties of food and medicine are compared , can be consumed for a long time, not only can prevent and treat chronic diseases such as cardiovascular, diabetes, cancer and aging, but also has a good effect on the prevention and treatment of chronic diseases such as cardiovascular disease, diabetes, cancer and aging; and because the beverage contains prebiotics, regular drinking can help regulate the intestinal tract, help digestion, and regulate toxins in the body. good help.
Description
技术领域technical field
本发明属于食品保健领域,涉及酶法制备抗氧化肽饮料,特别涉及一种益生元抗氧化肽饮料的制备方法。The invention belongs to the field of food health care, and relates to an enzymatic method for preparing an antioxidant peptide beverage, in particular to a preparation method of a prebiotic antioxidant peptide beverage.
背景技术Background technique
自由基是生物体新陈代谢过程中产生的一类可以单独存在的具有高度氧化活性的带有一个或几个不配对电子的分子或原子,化学性质极活泼。自由基可攻击生命大分子物质及细胞壁,造成机体的多种损伤和病变,加速机体的衰老。在正常生理状态下,机体内自由基的产生与清除处于动态平衡状态,但当机体处于不良环境状态下,以及随着年龄的增长,体内的自由基将会产生过多或清除过慢。抗氧化肽作为生物活性肽的一种,具有抑制脂质过氧化和清除自由基、维持机体自由基平衡和提高机体抗衰老、抗疾病功能。Free radicals are a class of molecules or atoms with one or several unpaired electrons that can exist alone and have high oxidative activity produced during the metabolism of organisms. The chemical properties are extremely active. Free radicals can attack life macromolecules and cell walls, causing various damages and lesions in the body, and accelerating the aging of the body. Under normal physiological conditions, the production and removal of free radicals in the body are in a state of dynamic balance, but when the body is in an unfavorable environment and with age, the free radicals in the body will be produced too much or cleared too slowly. As a kind of biologically active peptides, antioxidant peptides can inhibit lipid peroxidation and scavenge free radicals, maintain the balance of free radicals in the body, and improve the body's anti-aging and anti-disease functions.
天然抗氧化肽具有重金属清道夫和过氧化氢分解促进剂作用,可降低自氧化速率,减少脂肪过氧化氢含量,减少自由基的生成,其不仅具有较强的抗氧化活性,而且具有很高的安全性,在动物饲料和人类食品市场中具有巨大的开发前景。Natural antioxidant peptide has the functions of heavy metal scavenger and hydrogen peroxide decomposition accelerator, which can reduce the rate of autoxidation, reduce the content of hydrogen peroxide in fat, and reduce the generation of free radicals. It not only has strong antioxidant activity, but also has a high It has great development prospects in the animal feed and human food markets.
益生元(Prebiotics)是一种膳食补充剂,通过选择性的刺激一种或少数种菌落中的细菌的生长与活性而对寄主产生有益的影响从而改善寄主健康的不可被消化的食品成分。它不能直接对机体起作用,而是通过益生菌发挥生理功能。益生菌通过调理人体肠道菌群,产生一些有益物质直接起作用。大多数商业用益生元为寡糖,如低聚异麦芽糖、低聚果糖、低聚半乳糖等,它们都具有健康肠道的作用。益生元在各类食品中已被广泛应用,消费者对其认知度虽不如益生菌高,但随着益生元促进肠道健康的功能已获得越来越多的科学数据支持,益生元的市场正在呈现良好的增长趋势。Prebiotics are non-digestible food ingredients that beneficially affect the host by selectively stimulating the growth and activity of one or a small number of bacteria in the colony to improve the health of the host. It cannot directly act on the body, but exerts physiological functions through probiotics. Probiotics work directly by regulating the intestinal flora of the human body and producing some beneficial substances. Most commercial prebiotics are oligosaccharides, such as isomaltooligosaccharides, fructooligosaccharides, galactooligosaccharides, etc., which all have the effect of healthy intestinal tract. Prebiotics have been widely used in various foods. Although consumers’ awareness of them is not as high as that of probiotics, as the function of prebiotics in promoting intestinal health has been supported by more and more scientific data, prebiotics’ The market is showing a good growth trend.
目前,利用酶法酶解蛋白制备抗氧化肽的报道已有很多。专利CN103320489A中公开了一种松籽蛋白源抗氧化肽的制备方法,它是通过将提取的松籽蛋白用液体碱性蛋白酶进行水解,并进行超滤浓缩、真空干燥从而得到抗氧化肽。专利CN103421875B中公开了一种酶法水解小白杏杏仁蛋白制备抗氧化肽的方法,该方法通过加入了碱性蛋白酶和胰蛋白酶复合质量比1:3进行水解。目前国内外对于抗氧化肽的研究主要集中在制备方法,关于含抗氧化肽饮料等产品也是未涉及。At present, there have been many reports on the preparation of antioxidant peptides by enzymatic hydrolysis of proteins. Patent CN103320489A discloses a preparation method of pine nut protein-derived antioxidant peptide, which is to obtain the antioxidant peptide by hydrolyzing the extracted pine nut protein with liquid alkaline protease, performing ultrafiltration concentration, and vacuum drying. Patent CN103421875B discloses a method of enzymatically hydrolyzing almond almond protein to prepare antioxidant peptides. The method is hydrolyzed by adding alkaline protease and trypsin in a compound mass ratio of 1:3. At present, the research on antioxidant peptides at home and abroad is mainly focused on the preparation method, and the products such as beverages containing antioxidant peptides are not involved.
目前含有益生元食品主要是酸奶、乳饮料和果汁饮料等。CN102266107A公开了一种复合益生元饮料及其制备方法,通过将高纯度低聚果糖,水苏糖,低聚乳糖,低聚木糖按一定比例混合,再与水和果汁调配而成。陈金玲等(陈金玲,陈晓磊,郭默婷,黄雪松.大蒜益生元饮料生产工艺研究,食品科技,2009,34(4):85—87)报道了以大蒜中的果聚糖为益生元调配的益生元饮料。相反,在生产益生元抗氧化肽饮料方面目前还未见报道涉及。At present, foods containing prebiotics are mainly yogurt, milk drinks and juice drinks. CN102266107A discloses a compound prebiotic beverage and a preparation method thereof, which is prepared by mixing high-purity fructo-oligosaccharides, stachyose, lacto-oligosaccharides and xylo-oligosaccharides in a certain proportion, and then blending them with water and fruit juice. Chen Jinling et al. (Chen Jinling, Chen Xiaolei, Guo Moting, Huang Xuesong. Research on the Production Technology of Garlic Prebiotic Beverage, Food Science and Technology, 2009, 34(4):85-87) reported the preparation of prebiotics with fructan in garlic. Prebiotic drink. On the contrary, there have been no reports concerning the production of prebiotic antioxidant peptide beverages.
发明内容Contents of the invention
本发明的目的在于提供一种益生元抗氧化肽饮料的制备方法,饮用后发挥不仅可以降低体内自由基水平,而且能帮助消化,排除体内毒素,便秘的人长期饮用,可以慢慢调节肠道,缓解和治疗便秘。The purpose of the present invention is to provide a preparation method of a prebiotic antioxidant peptide beverage, which can not only reduce the level of free radicals in the body after drinking, but also help digestion and eliminate toxins in the body. People with constipation can drink it for a long time, and can slowly regulate the intestinal tract , relieve and treat constipation.
为了实现上述目的,本发明所采用的技术方案是:In order to achieve the above object, the technical solution adopted in the present invention is:
1)将脱脂羊乳加热到45℃,然后滴加盐酸磁力搅拌至pH值达4.6,使酪蛋白沉淀后离心,弃去上清液,将沉淀进行冷冻干燥得到酪蛋白干粉;1) Heating skim goat milk to 45°C, then adding hydrochloric acid dropwise and magnetically stirring until the pH value reaches 4.6, centrifuging the casein after precipitation, discarding the supernatant, and freeze-drying the precipitate to obtain dry casein powder;
2)将酪蛋白干粉制成质量浓度为2%–5%的酪蛋白溶液,然后放入恒温水浴锅中,加热至45℃–60℃,通过滴加NaOH溶液调节酪蛋白溶液pH为6.5–8.0;2) Make casein dry powder into a casein solution with a mass concentration of 2%–5%, then put it in a constant temperature water bath, heat it to 45°C–60°C, and adjust the pH of the casein solution to 6.5–6.5 by dropping NaOH solution 8.0;
3)向酪蛋白溶液加入酪蛋白溶液质量1%–2%的Alcalase酶,反应过程中滴加NaOH溶液保持pH不变,水解结束后进行灭酶、离心后弃沉淀取上清液得到酶解液;3) Add Alcalase enzyme of 1%-2% of the casein solution mass to the casein solution, add NaOH solution dropwise during the reaction to keep the pH constant, inactivate the enzyme after hydrolysis, centrifuge, discard the precipitate and take the supernatant to obtain enzymolysis liquid;
4)向酶解液中添加酶解液质量0.6%~1.0%的β-环状糊精,在室温下搅拌进行脱苦处理,然后加入酶解液质量6%~10%的白砂糖、0.5%~0.8%的柠檬酸与苹果酸的混合酸、0.2%~0.35%的瓜尔豆胶、黄原胶和CMC-Na的复合稳定剂、0.02%~0.03%的茶多酚以及4%~8%的益生元进行饮料复配;最后,进行灭菌即得到益生元抗氧化肽饮料。4) Add β-cyclodextrin of 0.6% to 1.0% of the mass of the enzymatic hydrolysis solution to the enzymatic hydrolysis solution, stir at room temperature for debittering treatment, then add 6% to 10% of the mass of the enzymatic hydrolysis solution of white granulated sugar, 0.5 %~0.8% of mixed acid of citric acid and malic acid, 0.2%~0.35% of guar gum, xanthan gum and CMC-Na composite stabilizer, 0.02%~0.03% of tea polyphenols and 4%~ 8% prebiotics are used for beverage compounding; finally, prebiotics and antioxidant peptide beverages are obtained through sterilization.
所述步骤1)的盐酸为1mol/L的盐酸,磁力搅拌强度为1200rpm,离心采用8000rmp离心15min。The hydrochloric acid in the step 1) is 1mol/L hydrochloric acid, the magnetic stirring intensity is 1200rpm, and the centrifugation adopts 8000rmp centrifugation for 15min.
所述步骤2)NaOH溶液的浓度为1mol/L。Said step 2) the concentration of NaOH solution is 1mol/L.
所述步骤3)NaOH溶液的浓度为0.1mol/L,水解时间为60min–150min,灭酶在90℃水浴中灭酶10min,离心为8000rmp离心15min。Step 3) The concentration of NaOH solution is 0.1mol/L, the hydrolysis time is 60min-150min, the enzyme is inactivated in a 90°C water bath for 10min, and the centrifugation is 8000rmp for 15min.
所述的混合酸中柠檬酸与苹果酸按2:1的质量比混合。In the mixed acid, citric acid and malic acid are mixed in a mass ratio of 2:1.
所述的复合稳定剂中瓜尔豆胶、黄原胶和CMC-Na按1:3:3的质量比混合。In the composite stabilizer, guar gum, xanthan gum and CMC-Na are mixed in a mass ratio of 1:3:3.
所述步骤4)的灭菌在85℃进行15min。The sterilization in step 4) is carried out at 85° C. for 15 minutes.
所述的茶多酚采用下述方法制备:取5g的绿茶,用沸水浸泡过滤出茶汁,调节溶液的pH至5.0~6.5,然后加入10~16gCaCl2和AlCl3混合的复合型沉淀剂,其中CaCl2与AlCl3按1:1-3或1-2:1的质量比混合,将得到的沉淀加入到质量浓度为40%的硫酸溶液中至沉淀完全溶解得混合溶液,然后,再加入混合溶液质量20%~80%的乙醇溶液,在55℃~75℃、超声功率在200W~380W下提取30~90min,将得到的沉淀经冷冻干燥制得茶多酚。The tea polyphenols are prepared by the following method: take 5g of green tea, soak and filter the tea juice with boiling water, adjust the pH of the solution to 5.0-6.5, and then add 10-16g of CaCl 2 and AlCl 3 mixed composite precipitant, Wherein CaCl 2 and AlCl 3 are mixed according to the mass ratio of 1:1-3 or 1-2:1, and the obtained precipitate is added to a sulfuric acid solution with a mass concentration of 40% until the precipitate is completely dissolved to obtain a mixed solution, and then added The mixed solution is 20%-80% ethanol solution, extracted at 55°C-75°C and ultrasonic power at 200W-380W for 30-90min, and the obtained precipitate is freeze-dried to obtain tea polyphenols.
所述的益生元为水苏糖,低聚壳聚糖,海藻糖,低聚半乳糖,低聚果糖,异麦芽酮糖醇中一种或两种以上的混合物。The prebiotic is one or a mixture of stachyose, chitosan oligosaccharide, trehalose, galactooligosaccharide, fructooligosaccharide and isomalt.
按本发明的制备方法制得的益生元抗氧化肽饮料可以降低体内自由基水平,帮助机体抵御疾病。同时,食物和药物的抗氧化性相比,可以长期食用,不仅可以预防和治疗如心血管、糖尿病、癌症和衰老等慢性病有很好的帮助。而且饮料中因含有益生元,经常饮用对调节肠道,帮助消化,调节体内毒素也有很好的帮助。The prebiotic antioxidant peptide drink prepared according to the preparation method of the invention can reduce the level of free radicals in the body and help the body resist diseases. At the same time, compared with the antioxidant properties of food and medicine, it can be eaten for a long time, which can not only help prevent and treat chronic diseases such as cardiovascular, diabetes, cancer and aging. Moreover, because the beverage contains prebiotics, regular drinking is also very helpful for regulating the intestinal tract, helping digestion, and regulating toxins in the body.
具体实施方式detailed description
实施例1:Example 1:
1)将脱脂羊乳加热到45℃,然后滴加1mol/L的盐酸,在1200rpm磁力搅拌至pH值达4.6,使酪蛋白沉淀后在8000rmp离心15min,弃去上清液,将沉淀进行冷冻干燥得到酪蛋白干粉;1) Heat skim goat milk to 45°C, then add 1mol/L hydrochloric acid dropwise, stir magnetically at 1200rpm until the pH value reaches 4.6, centrifuge at 8000rmp for 15min after the casein is precipitated, discard the supernatant, and freeze the precipitate Dried to obtain casein dry powder;
2)将酪蛋白干粉制成质量浓度为2%的酪蛋白溶液,然后放入恒温水浴锅中,加热至45℃,通过滴加1mol/L的NaOH溶液调节酪蛋白溶液pH为6.5;2) Make a casein solution with a mass concentration of 2% from the dry casein powder, then put it into a constant temperature water bath, heat it to 45° C., and adjust the pH of the casein solution to 6.5 by adding 1 mol/L NaOH solution dropwise;
3)向酪蛋白溶液加入酪蛋白溶液质量1%的Alcalase酶,反应过程中滴加0.1mol/L的NaOH溶液保持pH不变,水解60min后,在90℃水浴中灭酶10min,再在8000rmp离心15min后弃沉淀取上清液得到酶解液;用紫外分光光度计测得DPPH自由基清除能力为51.34%;3) Add the Alcalase enzyme of 1% of the casein solution quality to the casein solution, drop the NaOH solution of 0.1mol/L in the reaction process to keep the pH constant, after hydrolysis for 60min, inactivate the enzyme in a 90°C water bath for 10min, and then in 8000rmp After centrifuging for 15 minutes, the precipitate was discarded and the supernatant was taken to obtain the enzymatic hydrolysis solution; the scavenging ability of DPPH free radicals was measured to be 51.34% by an ultraviolet spectrophotometer;
4)向酶解液中添加酶解液质量0.6%的β-环状糊精,在室温下搅拌进行脱苦处理,然后加入酶解液质量6%的白砂糖、0.5%的按2:1的质量比混合的柠檬酸与苹果酸的混合酸、0.2%的按1:3:3的质量比混合的瓜尔豆胶、黄原胶和CMC-Na的复合稳定剂以及0.02%的茶多酚以及4%的益生元进行饮料复配;最后,在85℃进行15min灭菌即得到益生元抗氧化肽饮料。将经过杀菌的益生元抗氧化肽饮料在4℃条件下进行保藏。4) Add 0.6% β-cyclodextrin of enzymolysis solution mass to the enzymolysis solution, stir at room temperature for debittering treatment, then add 6% enzymolysis solution mass white granulated sugar, 0.5% β-cyclodextrin at a ratio of 2:1 The mass ratio of mixed citric acid and malic acid mixed acid, 0.2% of guar gum, xanthan gum and CMC-Na compound stabilizer mixed in a mass ratio of 1:3:3 and 0.02% tea poly phenol and 4% prebiotics for beverage compounding; finally, sterilized at 85°C for 15 minutes to obtain the prebiotic antioxidant peptide beverage. Preserve the sterilized prebiotic antioxidant peptide drink at 4°C.
本实施例的益生元采用水苏糖。The prebiotic of this embodiment uses stachyose.
实施例2:Example 2:
1)将脱脂羊乳加热到45℃,然后滴加1mol/L的盐酸,在1200rpm磁力搅拌至pH值达4.6,使酪蛋白沉淀后在8000rmp离心15min,弃去上清液,将沉淀进行冷冻干燥得到酪蛋白干粉;1) Heat skim goat milk to 45°C, then add 1mol/L hydrochloric acid dropwise, stir magnetically at 1200rpm until the pH value reaches 4.6, centrifuge at 8000rmp for 15min after the casein is precipitated, discard the supernatant, and freeze the precipitate Dried to obtain casein dry powder;
2)将酪蛋白干粉制成质量浓度为3%的酪蛋白溶液,然后放入恒温水浴锅中,加热至50℃,通过滴加1mol/L的NaOH溶液调节酪蛋白溶液pH为7.0;2) Make the casein dry powder into a casein solution with a mass concentration of 3%, then put it into a constant temperature water bath, heat it to 50°C, and adjust the pH of the casein solution to 7.0 by adding 1mol/L NaOH solution dropwise;
3)向酪蛋白溶液加入酪蛋白溶液质量1.5%的Alcalase酶,反应过程中滴加0.1mol/L的NaOH溶液保持pH不变,水解90min后,在90℃水浴中灭酶10min,再在8000rmp离心15min后弃沉淀取上清液得到酶解液;用紫外分光光度计测得DPPH自由基清除能力为56.19%;3) Add the Alcalase enzyme of 1.5% of the casein solution quality to the casein solution, drop the NaOH solution of 0.1mol/L in the reaction process to keep the pH constant, after hydrolysis for 90min, inactivate the enzyme in a 90°C water bath for 10min, and then in 8000rmp After centrifuging for 15 minutes, the precipitate was discarded and the supernatant was taken to obtain the enzymatic hydrolysis solution; the scavenging ability of DPPH free radicals was 56.19% as measured by an ultraviolet spectrophotometer;
4)向酶解液中添加酶解液质量0.8%的β-环状糊精,在室温下搅拌进行脱苦处理,然后加入酶解液质量8%的白砂糖、0.6%的按2:1的质量比混合的柠檬酸与苹果酸的混合酸、0.25%的按1:3:3的质量比混合的瓜尔豆胶、黄原胶和CMC-Na的复合稳定剂以及0.025%的茶多酚以及5%的益生元进行饮料复配;最后,在85℃进行15min灭菌即得到益生元抗氧化肽饮料。将经过杀菌的益生元抗氧化肽饮料在4℃条件下进行保藏。4) Add 0.8% β-cyclodextrin of enzymolysis solution mass to the enzymolysis solution, stir at room temperature for debittering treatment, then add 8% enzymolysis solution mass white granulated sugar, 0.6% of The mass ratio of mixed citric acid and malic acid mixed acid, 0.25% of guar gum, xanthan gum and CMC-Na composite stabilizer mixed in a mass ratio of 1:3:3 and 0.025% tea poly phenol and 5% prebiotics for beverage compounding; finally, sterilized at 85°C for 15 minutes to obtain the prebiotic antioxidant peptide beverage. Preserve the sterilized prebiotic antioxidant peptide drink at 4°C.
本实施例的益生元采用水苏糖与低聚壳聚糖的混合物。The prebiotic of this embodiment adopts the mixture of stachyose and chitosan oligosaccharide.
本实施例的茶多酚采用下述方法制备:取10g的绿茶,用沸水浸泡过滤出茶汁,调节溶液的pH至5.0,然后加入10gCaCl2和AlCl3混合的复合型沉淀剂,其中CaCl2与AlCl3按1:1的质量比混合,将得到的沉淀加入到质量浓度为40%的硫酸溶液中至沉淀完全溶解得混合溶液,然后,再加入混合溶液质量20%的乙醇溶液,在55℃、超声功率在200W下提取30min,将得到的沉淀经冷冻干燥制得茶多酚。The tea polyphenols of this embodiment are prepared by the following method: take 10g of green tea, soak and filter the tea juice with boiling water, adjust the pH of the solution to 5.0, and then add 10g of CaCl 2 and AlCl 3 mixed composite precipitant, wherein CaCl 2 Mix with AlCl in a mass ratio of 1 :1, add the obtained precipitate into a 40% sulfuric acid solution until the precipitate is completely dissolved to obtain a mixed solution, and then add 20% ethanol solution of the mixed solution quality, at 55 ℃ and ultrasonic power at 200W for 30min, and freeze-dry the obtained precipitate to obtain tea polyphenols.
实施例3:Example 3:
1)将脱脂羊乳加热到45℃,然后滴加1mol/L的盐酸,在1200rpm磁力搅拌至pH值达4.6,使酪蛋白沉淀后在8000rmp离心15min,弃去上清液,将沉淀进行冷冻干燥得到酪蛋白干粉;1) Heat skim goat milk to 45°C, then add 1mol/L hydrochloric acid dropwise, stir magnetically at 1200rpm until the pH value reaches 4.6, centrifuge at 8000rmp for 15min after the casein is precipitated, discard the supernatant, and freeze the precipitate Dried to obtain casein dry powder;
2)将酪蛋白干粉制成质量浓度为4%的酪蛋白溶液,然后放入恒温水浴锅中,加热至55℃,通过滴加1mol/L的NaOH溶液调节酪蛋白溶液pH为7.5;2) Make the casein dry powder into a casein solution with a mass concentration of 4%, then put it into a constant temperature water bath, heat it to 55° C., and adjust the pH of the casein solution to 7.5 by adding 1 mol/L NaOH solution dropwise;
3)向酪蛋白溶液加入酪蛋白溶液质量1.5%的Alcalase酶,反应过程中滴加0.1mol/L的NaOH溶液保持pH不变,水解150min后,在90℃水浴中灭酶10min,再在8000rmp离心15min后弃沉淀取上清液得到酶解液;用紫外分光光度计测得DPPH自由基清除能力为61.53%;3) Add the Alcalase enzyme of 1.5% of the casein solution quality to the casein solution, drop the NaOH solution of 0.1mol/L in the reaction process to keep the pH constant, after hydrolysis for 150min, inactivate the enzyme in a 90°C water bath for 10min, and then in 8000rmp After centrifuging for 15 minutes, the precipitate was discarded and the supernatant was taken to obtain the enzymatic hydrolysis solution; the scavenging ability of DPPH free radicals was 61.53% as measured by an ultraviolet spectrophotometer;
4)向酶解液中添加酶解液质量1.0%的β-环状糊精,在室温下搅拌进行脱苦处理,然后加入酶解液质量8%的白砂糖、0.7%的按2:1的质量比混合的柠檬酸与苹果酸的混合酸、0.25%的按1:3:3的质量比混合的瓜尔豆胶、黄原胶和CMC-Na的复合稳定剂以及0.025%的茶多酚以及7%的益生元进行饮料复配;最后,在85℃进行15min灭菌即得到益生元抗氧化肽饮料。将经过杀菌的益生元抗氧化肽饮料在4℃条件下进行保藏。4) Add β-cyclodextrin of 1.0% mass of the enzymolysis solution to the enzymatic hydrolysis solution, stir at room temperature for debittering treatment, then add 8% white granulated sugar of the enzymolysis solution mass, 0.7% of The mass ratio of mixed citric acid and malic acid mixed acid, 0.25% of guar gum, xanthan gum and CMC-Na composite stabilizer mixed in a mass ratio of 1:3:3 and 0.025% tea poly phenol and 7% prebiotics for beverage compounding; finally, sterilized at 85°C for 15 minutes to obtain the prebiotic antioxidant peptide beverage. Preserve the sterilized prebiotic antioxidant peptide drink at 4°C.
本实施例的益生元采用水苏糖,低聚壳聚糖与海藻糖的混合物。The prebiotic of this embodiment uses a mixture of stachyose, chitosan oligosaccharide and trehalose.
本实施例的茶多酚采用下述方法制备:取10g的绿茶,用沸水浸泡过滤出茶汁,调节溶液的pH至5.5,然后加入12gCaCl2和AlCl3混合的复合型沉淀剂,其中CaCl2与AlCl3按1:2的质量比混合,将得到的沉淀加入到质量浓度为40%的硫酸溶液中至沉淀完全溶解得混合溶液,然后,再加入混合溶液质量40%的乙醇溶液,在60℃、超声功率在260W下提取60min,将得到的沉淀经冷冻干燥制得茶多酚。The tea polyphenols of this embodiment are prepared by the following method: take 10g of green tea, soak and filter the tea juice with boiling water, adjust the pH of the solution to 5.5, and then add 12g of CaCl 2 and AlCl 3 mixed compound precipitant, wherein CaCl 2 Mix with AlCl3 in a mass ratio of 1: 2 , add the precipitate obtained into the sulfuric acid solution with a mass concentration of 40% until the precipitate is completely dissolved to obtain a mixed solution, and then add a 40% ethanol solution with a mixed solution quality, at 60 ℃ and ultrasonic power at 260W for 60min, and freeze-dry the obtained precipitate to obtain tea polyphenols.
实施例4:Example 4:
1)将脱脂羊乳加热到45℃,然后滴加1mol/L的盐酸,在1200rpm磁力搅拌至pH值达4.6,使酪蛋白沉淀后在8000rmp离心15min,弃去上清液,将沉淀进行冷冻干燥得到酪蛋白干粉;1) Heat skim goat milk to 45°C, then add 1mol/L hydrochloric acid dropwise, stir magnetically at 1200rpm until the pH value reaches 4.6, centrifuge at 8000rmp for 15min after the casein is precipitated, discard the supernatant, and freeze the precipitate Dried to obtain casein dry powder;
2)将酪蛋白干粉制成质量浓度为4%的酪蛋白溶液,然后放入恒温水浴锅中,加热至60℃,通过滴加1mol/L的NaOH溶液调节酪蛋白溶液pH为8.0;2) Make the casein dry powder into a casein solution with a mass concentration of 4%, then put it into a constant temperature water bath, heat it to 60° C., and adjust the pH of the casein solution to 8.0 by adding 1 mol/L NaOH solution dropwise;
3)向酪蛋白溶液加入酪蛋白溶液质量2%的Alcalase酶,反应过程中滴加0.1mol/L的NaOH溶液保持pH不变,水解90min后,在90℃水浴中灭酶10min,再在8000rmp离心15min后弃沉淀取上清液得到酶解液;用紫外分光光度计测得DPPH自由基清除能力为58.23%;3) Add the Alcalase enzyme of casein solution quality 2% to casein solution, drop the NaOH solution of 0.1mol/L in the reaction process and keep pH constant, after hydrolysis 90min, in 90 ℃ of water baths, go out enzyme 10min, again in 8000rmp After centrifuging for 15 minutes, the precipitate was discarded and the supernatant was taken to obtain the enzymatic hydrolysis solution; the scavenging ability of DPPH free radicals was 58.23% as measured by an ultraviolet spectrophotometer;
4)向酶解液中添加酶解液质量1.0%的β-环状糊精,在室温下搅拌进行脱苦处理,然后加入酶解液质量10%的白砂糖、0.8%的按2:1的质量比混合的柠檬酸与苹果酸的混合酸、0.3%的按1:3:3的质量比混合的瓜尔豆胶、黄原胶和CMC-Na的复合稳定剂以及0.03%的茶多酚以及8%的益生元进行饮料复配;最后,在85℃进行15min灭菌即得到益生元抗氧化肽饮料。将经过杀菌的益生元抗氧化肽饮料在4℃条件下进行保藏。4) Add β-cyclodextrin of 1.0% mass of the enzymolysis solution to the enzymolysis solution, stir at room temperature for debittering treatment, then add 10% white granulated sugar of the enzymolysis solution mass, 0.8% of The mass ratio of mixed citric acid and malic acid mixed acid, 0.3% of guar gum, xanthan gum and CMC-Na composite stabilizer mixed in a mass ratio of 1:3:3 and 0.03% tea poly phenol and 8% prebiotics for beverage compounding; finally, sterilized at 85°C for 15 minutes to obtain the prebiotic antioxidant peptide beverage. Preserve the sterilized prebiotic antioxidant peptide drink at 4°C.
本实施例的益生元采用海藻糖、低聚半乳糖与低聚果糖的混合物。The prebiotic of this embodiment uses a mixture of trehalose, galacto-oligosaccharide and fructo-oligosaccharide.
本实施例的茶多酚采用下述方法制备:取10g的绿茶,用沸水浸泡过滤出茶汁,调节溶液的pH至5.5,然后加入14gCaCl2和AlCl3混合的复合型沉淀剂,其中CaCl2与AlCl3按1:3的质量比混合,将得到的沉淀加入到质量浓度为40%的硫酸溶液中至沉淀完全溶解得混合溶液,然后,再加入混合溶液质量60%的乙醇溶液,在65℃、超声功率在320W下提取60min,将得到的沉淀经冷冻干燥制得茶多酚。The tea polyphenol of this embodiment is prepared by the following method: take 10g of green tea, soak and filter the tea juice with boiling water, adjust the pH of the solution to 5.5, and then add 14g of CaCl 2 and AlCl 3 mixed compound precipitant, wherein CaCl 2 Mix with AlCl at a mass ratio of 1: 3 , add the precipitate obtained into a 40% sulfuric acid solution until the precipitate is completely dissolved to obtain a mixed solution, and then add 60% ethanol solution of the mixed solution quality, at 65 ℃ and ultrasonic power at 320W for 60 min, and freeze-dry the obtained precipitate to obtain tea polyphenols.
实施例5:Example 5:
1)将脱脂羊乳加热到45℃,然后滴加1mol/L的盐酸,在1200rpm磁力搅拌至pH值达4.6,使酪蛋白沉淀后在8000rmp离心15min,弃去上清液,将沉淀进行冷冻干燥得到酪蛋白干粉;1) Heat skim goat milk to 45°C, then add 1mol/L hydrochloric acid dropwise, stir magnetically at 1200rpm until the pH value reaches 4.6, centrifuge at 8000rmp for 15min after the casein is precipitated, discard the supernatant, and freeze the precipitate Dried to obtain casein dry powder;
2)将酪蛋白干粉制成质量浓度为5%的酪蛋白溶液,然后放入恒温水浴锅中,加热至50℃,通过滴加1mol/L的NaOH溶液调节酪蛋白溶液pH为7.0;2) Make a casein solution with a mass concentration of 5% from the dry casein powder, then put it into a constant temperature water bath, heat it to 50° C., and adjust the pH of the casein solution to 7.0 by adding 1 mol/L NaOH solution dropwise;
3)向酪蛋白溶液加入酪蛋白溶液质量1.8%的Alcalase酶,反应过程中滴加0.1mol/L的NaOH溶液保持pH不变,水解120min后,在90℃水浴中灭酶10min,再在8000rmp离心15min后弃沉淀取上清液得到酶解液;用紫外分光光度计测得DPPH自由基清除能力为59.44%;3) Add the Alcalase enzyme of casein solution quality 1.8% to the casein solution, drop the NaOH solution of 0.1mol/L in the reaction process to keep the pH constant, after hydrolysis for 120min, inactivate the enzyme in 90 DEG C water bath for 10min, then in 8000rmp After centrifuging for 15 minutes, the precipitate was discarded and the supernatant was taken to obtain the enzymatic hydrolysis solution; the scavenging ability of DPPH free radicals was 59.44% as measured by an ultraviolet spectrophotometer;
4)向酶解液中添加酶解液质量0.9%的β-环状糊精,在室温下搅拌进行脱苦处理,然后加入酶解液质量9%的白砂糖、0.6%的按2:1的质量比混合的柠檬酸与苹果酸的混合酸、0.35%的按1:3:3的质量比混合的瓜尔豆胶、黄原胶和CMC-Na的复合稳定剂以及0.03%的茶多酚以及6%的益生元进行饮料复配;最后,在85℃进行15min灭菌即得到益生元抗氧化肽饮料。将经过杀菌的益生元抗氧化肽饮料在4℃条件下进行保藏。4) Add 0.9% β-cyclodextrin to the enzymolysis solution, stir at room temperature for debittering treatment, then add 9% enzymolysis solution white sugar, 0.6% β-cyclodextrin at a ratio of 2:1 The mass ratio of mixed citric acid and malic acid mixed acid, 0.35% of guar gum, xanthan gum and CMC-Na compound stabilizer mixed in a mass ratio of 1:3:3 and 0.03% tea poly phenol and 6% prebiotics for beverage compounding; finally, sterilized at 85°C for 15 minutes to obtain the prebiotic antioxidant peptide beverage. Preserve the sterilized prebiotic antioxidant peptide drink at 4°C.
本实施例的益生元采用水苏糖、低聚果糖与异麦芽酮糖醇的混合物。The prebiotic of this embodiment is a mixture of stachyose, fructooligosaccharide and isomalt.
本实施例的茶多酚采用下述方法制备:取10g的绿茶,用沸水浸泡过滤出茶汁,调节溶液的pH至6.5,然后加入16gCaCl2和AlCl3混合的复合型沉淀剂,其中CaCl2与AlCl3按2:1的质量比混合,将得到的沉淀加入到质量浓度为40%的硫酸溶液中至沉淀完全溶解得混合溶液,然后,再加入混合溶液质量80%的乙醇溶液,在75℃、超声功率在380W下提取90min,将得到的沉淀经冷冻干燥制得茶多酚。The tea polyphenols of this embodiment are prepared by the following method: take 10g of green tea, soak and filter the tea juice with boiling water, adjust the pH of the solution to 6.5, and then add 16g of CaCl 2 and AlCl 3 mixed compound precipitant, wherein CaCl 2 Mix with AlCl in a mass ratio of 2 :1, add the precipitate obtained into the sulfuric acid solution with a mass concentration of 40% until the precipitate is completely dissolved to obtain a mixed solution, then add an ethanol solution with a mixed solution quality of 80%, at 75 ℃ and ultrasonic power at 380W for 90 minutes, and freeze-dry the obtained precipitate to obtain tea polyphenols.
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