WO2016056366A1 - Acidic protein beverage - Google Patents
Acidic protein beverage Download PDFInfo
- Publication number
- WO2016056366A1 WO2016056366A1 PCT/JP2015/076253 JP2015076253W WO2016056366A1 WO 2016056366 A1 WO2016056366 A1 WO 2016056366A1 JP 2015076253 W JP2015076253 W JP 2015076253W WO 2016056366 A1 WO2016056366 A1 WO 2016056366A1
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- WO
- WIPO (PCT)
- Prior art keywords
- protein
- beverage
- acidic
- powdered
- less
- Prior art date
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- 235000020124 milk-based beverage Nutrition 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 102000013415 peroxidase activity proteins Human genes 0.000 description 1
- 108040007629 peroxidase activity proteins Proteins 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 235000021118 plant-derived protein Nutrition 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 235000010409 propane-1,2-diol alginate Nutrition 0.000 description 1
- 239000000770 propane-1,2-diol alginate Substances 0.000 description 1
- 230000004845 protein aggregation Effects 0.000 description 1
- 239000012460 protein solution Substances 0.000 description 1
- 235000019423 pullulan Nutrition 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 235000019592 roughness Nutrition 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 235000017709 saponins Nutrition 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 235000013322 soy milk Nutrition 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- BAQAVOSOZGMPRM-QBMZZYIRSA-N sucralose Chemical compound O[C@@H]1[C@@H](O)[C@@H](Cl)[C@@H](CO)O[C@@H]1O[C@@]1(CCl)[C@@H](O)[C@H](O)[C@@H](CCl)O1 BAQAVOSOZGMPRM-QBMZZYIRSA-N 0.000 description 1
- 235000019408 sucralose Nutrition 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 235000019640 taste Nutrition 0.000 description 1
- 235000019587 texture Nutrition 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 235000021119 whey protein Nutrition 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
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
- A23L2/52—Adding ingredients
- A23L2/66—Proteins
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING OR TREATMENT THEREOF
- A23C9/00—Milk preparations; Milk powder or milk powder preparations
-
- 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
- A23J3/14—Vegetable proteins
- A23J3/16—Vegetable proteins from soybean
-
- 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
- A23J3/04—Animal proteins
- A23J3/08—Dairy proteins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Definitions
- the present invention relates to a liquid and acidic beverage containing protein.
- proteins are high molecular and amphiphilic, some have gelling properties, thickening properties, and water retention properties. Powdered protein materials such as separated protein that contain this in high concentrations are free of water and therefore easier to manage and distribute than liquid materials, and can be added to various processed foods because they can be formulated at high concentrations. It is widely used as a material for improving physical properties.
- soy protein has a well-balanced amino acid composition and has physiological functions such as cholesterol lowering action, and is also used in nutritional and health foods that expect nutritional supplementation and physiological functions. .
- an object of the present invention is to provide an acidic liquid beverage in which precipitation is not likely to occur over a long period of time even when a relatively large amount of protein is blended, and the dispersion of the protein in the liquid is stably maintained. There is.
- the present inventors initially tried to combine various water-soluble polysaccharides using a highly soluble powdered protein material to solve the above problems, but it was difficult to stabilize the dispersion of the protein. It was. Therefore, as a result of further earnest research, a relatively large amount of protein is contained, and a water-soluble polysaccharide is used in combination as a protein dispersion stabilizer, and as a water-soluble polysaccharide in a liquid and pH 3-5 acidic protein beverage system, We obtained knowledge that selecting soy polysaccharides or pea polysaccharides, selecting specific powdered protein materials, and combining them together is important for stabilizing protein dispersion in acidic beverages. The invention has been completed.
- the present invention includes the following configurations.
- At least one of the protein-containing raw materials is a powdered protein material that satisfies the following requirements a) to c), the protein content is 1% by weight or more, and a soybean polysaccharide and / or peas
- An acidic protein beverage comprising a saccharide as a protein dispersion stabilizer, being liquid and having a pH of 3 to 5, a) the powdered protein material is a protein hydrolyzate, and the degree of hydrolysis is 10 to 35% as 0.22M trichloroacetic acid (TCA) solubility; b) Nitrogen solubility index (NSI) of the powdered protein material is 10 to 80, c) The diluted protein NSI of the powdered protein material is 10 to 70, (2) The acidic protein beverage according to (1), wherein the protein content of the acidic protein beverage is 1 to 20% by weight, (3) The acidic protein beverage according to (1) or (2) above, wherein the protein content per dry matter of the
- the dispersion of the protein is stably maintained in the liquid over a long period of time, and the emulsifiability with fats and oils is also improved.
- An excellent liquid protein beverage having a pH of 3 to 5 can be provided.
- the protein dispersion stability can be maintained even when the viscosity is low, so that an acidic protein beverage can be finished into a clean drinking mouth with little roughness and no viscosity.
- the flavor derived from the powdered protein material can be finished to a good one.
- the powdered protein material is a protein hydrolyzate, and the degree of hydrolysis is 10 to 35% as 0.22M trichloroacetic acid (TCA) solubility; b) Nitrogen solubility index (NSI) of the powdered protein material is 10 to 80, c) The diluted protein NSI of the powdered protein material is 10 to 70, A powdery protein material satisfying the above three requirements, wherein the protein content is 1% by weight or more and soy polysaccharides and / or pea polysaccharides are contained as protein dispersion stabilizers, are liquid and have a pH of 3 to 5 It is characterized by being.
- TCA trichloroacetic acid
- liquid and acidic protein beverage The liquid and acidic protein beverage (hereinafter referred to as “the present beverage”), which is the subject of the present invention, is commercialized in a liquid state and consumed by consumers. Recently, drinks called RTD drinks (Ready-To-Drink) and enteral nutrients are also conceptually included.
- enteral nutrition is also called concentrated liquid food in Japan, and refers to liquid nutritional compositions that have forms such as soup, potage, milk drinks and fruit juice drinks without ingredients
- Calorie value is 1kcal / mL or more and contains at least protein, lipid, carbohydrate, mineral and vitamin as nutritional components.
- it has an energy composition of protein: 10-25%, lipid: 15-45%, carbohydrate: 35% or more, calcium: 20-110 mg / 100 kcal, magnesium: 10-70 mg / 100 kcal.
- it has an energy composition of protein: 16-20%, lipid: 20-30%, carbohydrate: 50-65%, calcium: 35-65mg / 100kcal, magnesium: 15-40mg / 100kcal is there.
- this beverage is filled and sealed in a sealed container and sold as it is to a consumer as a sealed container-packed beverage.
- it is put in a restaurant server and injected into a cup or the like according to consumer demand. For this reason, it is more strictly demanded that precipitation of insolubilized proteins hardly occurs even when stored in a liquid state for a long time.
- the effect of the present invention is particularly exerted in the form of a liquid beverage, and is most prominent in the form of a sealed container-packed beverage that is stored for a longer period of time.
- the liquidity of the present beverage exhibits an acidity of pH 3 to 5, and pH 3.4 to 4.6 is particularly preferable.
- the pH value to be selected within this range is appropriately determined by those skilled in the art in consideration of the quality of the product flavor and the like. However, when it is desired to make the sterilization conditions as mild as possible, the pH is 3 or more and less than 4 It is preferable to set in the range. On the other hand, the pH can be set in the range of 4 to 5 for the purpose of relieving acidity.
- This beverage is an acidic protein beverage containing at least protein as a nutrient component, and the protein content is 1% by weight or more per weight of the whole beverage.
- a higher protein content is preferable because the effect of the present invention can be effectively exhibited, preferably 1.5% by weight or more, more preferably 2% by weight or more, and further preferably 2.5% by weight or more.
- the upper limit can be 20 weight% or less, 15 weight% or less, or 10 weight% or less.
- Many proteins, such as soy protein and milk protein have an isoelectric point around pH 4.5, so in a liquid and acidic environment such as this beverage, the protein solubility is drastically reduced, so the protein is preserved. Precipitation tends to occur inside. That is, the protein dispersion stability deteriorates. And the degree of precipitation increases as it is stored for a long time. On the other hand, the present invention solves such a problem.
- Protein types include beans such as soybeans, peas and mung beans, plant-derived proteins such as canola seeds, and milk-derived proteins.
- a protein derived from soybean which is usually difficult to stabilize in an acidic dispersion, can effectively exert an effect in the present invention.
- the protein in the beverage is contained by blending the protein material containing the above protein into the beverage as a raw material.
- One essential and important ingredient is a specific powdered protein described in detail below. It is a material.
- two or more kinds of powdered protein materials can be used in combination, for example, a soy protein material and a milk protein material can be used in combination.
- the specific powdery protein material used in the present beverage is a food material mainly composed of protein and used in various processed foods and beverages.
- a food material mainly composed of protein and used in various processed foods and beverages.
- it is prepared by further processing soybean protein from soybean raw materials such as defatted soybeans and whole soybeans, and in general, isolated soybean protein, powdered soy milk, or various processed products thereof Is conceptually included.
- casein or concentrated milk protein MPC
- the powdered protein material suitably has a protein content per dry matter of at least 40% by weight, preferably 50% by weight or more, and more preferably 60% by weight or more.
- the content of insoluble dietary fiber is preferably as low as possible in order to prevent precipitation of insolubles during storage, and it is preferably 2% by weight or less per dry matter. % Or less is more preferable.
- the specific powdery protein material used in the present beverage satisfies at least the following requirements a) to c).
- the powdered protein material is a protein hydrolyzate, and the degree of hydrolysis is 10 to 35% as 0.22M trichloroacetic acid (TCA) solubility;
- Nitrogen solubility index (NSI) of the powdered protein material is 10 to 80,
- the dilute acid NSI of the powdered protein material is 10 to 70. It is important that the protein contained by blending a specific powdered protein material that satisfies all the requirements of a) to c) coexists with a specific polysaccharide described later in the beverage.
- TCA solubility 0.22M trichloroacetic acid solubility
- the 0.22M TCA solubility in the powdered protein material used in this beverage is in the range of 10 to 35%.
- the lower limit is preferably 11% or more, more preferably 12% or more, and further preferably 13% or more.
- the lower limit is preferably 30% or less, and more preferably 28% or less.
- the TCA solubility of the material is too low, that is, if it is not enzymatically decomposed or if it is too low, the protein in the beverage will be present even if a specific polysaccharide described later is present. Particles are not finely dispersed, precipitation during storage is likely to occur, and roughness is easily felt. Even when the TCA solubility of the material is too high, that is, as the enzymatic degradation further proceeds, the reason is unknown, but the protein particle size tends to increase, and in any case, precipitation during storage tends to occur. , Makes it easier to feel rough. In addition, as the degree of degradation increases, it becomes easier to feel the bitter taste of peptides with a reduced molecular weight.
- the average molecular weight is preferably about 10,000 to 100,000, more preferably about 20,000 to 90,000.
- the average molecular weight can be measured by the method described later.
- the powdered protein material used in this beverage has an NSI (Nitrogen Solubility Index) as an index of solubility in water of 10 to 80, particularly preferably 15 to 75, 20 More preferably, 70.
- NSI Nonrogen Solubility Index
- the solubility of the protein is too low, the amount of precipitation increases, and the roughness is strongly felt.
- powdered protein materials with reduced NSI tend to be more roughened by adding divalent metals such as calcium and magnesium during the production of powdered protein materials to react proteins and divalent metals.
- NSI is represented by a ratio (% by weight) of water-soluble nitrogen (crude protein) in the total amount of nitrogen based on a predetermined method, and is a value measured according to the method described later in the present invention.
- Dilute acid NSI The powdered protein material used in this beverage is an “acid-soluble protein” such as an acid-soluble soy protein or whey protein described in International Publication WO2002 / 67690, wherein the protein is highly soluble in the acidic region. Rather, it is characterized by being moderate or less.
- the solubility in the acidic region can be expressed using “dilute acid NSI” (NSI is an abbreviation for nitrogen solubility index) as an index, and the higher the value of the diluted acid NSI, the higher the solubility in the acidic region. It becomes. Note that dilute acid NSI is measured according to the method described below.
- the dilute acid NSI of the powdered protein material used in this beverage is 10 to 70, preferably 11 to 60. If the dilute acid NSI of the material is too high like an acidic soluble protein, the solubility of the protein in the acidic region is high, but agglomeration may occur due to reaction with minerals and it may solidify by heating. On the other hand, if the diluted acid NSI of the material is too low, the solubility of the protein is too low, resulting in a large amount of precipitation and a strong feeling of roughness.
- the powdered protein material used in this beverage is such that both NSI and dilute acid NSI are in a medium range, and the protein is only partially dissolved in water.
- the liquid is not transparent like an acidic soluble protein, and is cloudy.
- the transmittance of the dispersion (concentration at 5% by weight) is 1% T or less as a value measured at 600 nm with a spectrophotometer.
- the transmittance (% T) is a measure of the transparency of a dispersion containing protein, and is defined as follows.
- a dispersion obtained by dispersing protein powder in water so that the protein content is 5% by weight and stirring sufficiently is 1 cm by a spectrophotometer (manufactured by Hitachi High-Technologies Corporation: U-3210 self-recording spectrophotometer). Using a cell, the transmittance (% T) at 600 nm is measured.
- powdered protein materials that satisfy all of the above requirements a) to c) are commercially available and can be purchased and obtained.
- products such as “Prolina (R) 800”, “Prolina (R) HD101”, “Fujipro (R) CL” can be used, Any product other than these products may be used as long as it satisfies all the above requirements.
- “Fujipuro (R) F” such as a general powdery soybean protein material which is not hydrolyzed in the TCA solubility is less than 10%, and NSI of 90 or more.
- the "Purorina (R) SU” is one in which TCA solubility is more than 35%. Also known as powdery soybean protein acid soluble “Soyasawa (R)" is extremely high solubility of the proteins in the acidic region, NSI is not less 90 or more and diluted acid NSI also 90% or more, even transmittance It has a high transparency of 80% T or more. For this reason, these products do not correspond to the powdered protein material that satisfies the above-mentioned requirements for use in the present beverage.
- This beverage contains a specific polysaccharide (hereinafter sometimes referred to as “the present polysaccharide”) together with the above-described protein, and as the specific polysaccharide, soybean polysaccharide and / or pea polysaccharide is used. It is important to use it as a dispersion stabilizer for proteins.
- the polysaccharide is already known to have the effect of dispersing and stabilizing the protein in the liquid and acidic beverage, but the synergistic effect of the combination with the specific powdered protein material described above is remarkable in the present invention. It has been found.
- Soy polysaccharides and pea polysaccharides are water-soluble polysaccharides composed of saccharides such as rhamnose, fucose, arabinose, xylose, galactose, glucose and uronic acid, and are generally analyzed by gel filtration HPLC under the following conditions The average molecular weight is 1 million or less. These can be extracted from water containing raw materials containing soybean or pea insoluble dietary fiber (Okara) by water using a known method and purified if necessary. Soybean polysaccharides can be commercially available, such as the “Soya Five (R) ” series (Fuji Oil Co., Ltd.) and the “SM” series (San-Eigen FFI Co., Ltd.).
- Gel filtration HPLC uses standard pullulan (Showa Denko Co., Ltd.) as a standard substance, analytical column “TSKgel G5000PWXL” (manufactured by Tosoh Corporation, column size: 7.8 mm I.D. ⁇ 30 cm, packing material: methacrylate polymer , Filler particle size: 10 ⁇ m, exclusion limit molecular weight: 2.5 million).
- the average absolute molecular weight (MM) is obtained by multi-angle laser light scattering (MALLS) calibrated with toluene after passing through the column.
- MALLS multi-angle laser light scattering
- the eluent is, for example, 50 mM aqueous sodium acetate (pH 5.0)
- the column flow rate is 1.0 mL / min
- the detector is an RI detector and a MALLS detector.
- each analysis condition may be appropriately changed within a range in which a large error does not occur in the analysis value.
- water-soluble polysaccharides used as a protein dispersion stabilizer can be used in combination as long as the effects of the present invention are not impaired.
- propylene glycol alginate, high methoxyl pectin, carboxymethyl cellulose (CMC), xanthan gum, locust bean gum, guar gum, gum arabic and the like can be used. It is more preferable that the present polysaccharide is contained in the beverage before the step in which the raw material liquid is homogenized by homogenizer, stirring, heat sterilization, or the like in the production process of the beverage.
- the polysaccharide can be contained at any timing before or after the protein is contained in the beverage, and the polysaccharide and protein can be mixed well in an aqueous system and homogenized in advance. It is also possible to use a powdered protein material in which the polysaccharide is previously contained in an aqueous system or in a dry state.
- the content of the polysaccharide contained in the beverage is preferably 5 to 40% by weight, more preferably 7 to 35% by weight, based on the protein content. If the amount is within such a range, the present polysaccharide can sufficiently act with the protein, and the effect of dispersing and stabilizing the protein in an acidic solution can be further exerted.
- the content of this polysaccharide can be grasped by using the dietary fiber content as a guide, and it can be separated from insoluble dietary fiber using the official method for measuring dietary fiber using the enzyme-weight method (modified Prosky method). It can be analyzed as water-soluble dietary fiber.
- This beverage is made from protein particles introduced from a specific powdered protein material because it is homogenized and refined by the synergistic action with this polysaccharide, or even if stored for a long time under acidic and liquid conditions. Precipitation is unlikely to occur and the texture is not easily felt.
- the average particle size of the particles dispersed in the beverage can be at least 5 ⁇ m or less, preferably 3 ⁇ m or less, more preferably 2 ⁇ m or less, still more preferably 1.5 ⁇ m or less, and most preferably 1 ⁇ m or less. it can.
- centrifugal sedimentation rate of beverage This beverage has a low amount of sediment during long-term storage and is extremely excellent in protein dispersion stability.
- centrifugal precipitation rate indicating the ratio of the protein amount in the precipitate generated by centrifuging the beverage to the protein amount in the whole liquid. Specifically, a predetermined amount of the measurement sample solution is collected in a centrifuge tube, centrifuged at 700 G for 20 minutes with a centrifuge, and then the amount of precipitation (g) after discarding the supernatant is measured. The ratio (wt%) of the precipitation amount to the sample liquid amount (g) is defined as “centrifugal precipitation rate”. Thus, long-term dispersion stability in the protein solution can be easily confirmed.
- the centrifugal sedimentation rate can be 5% by weight or less, preferably 3% by weight or less.
- the viscosity of the beverage can be appropriately adjusted by adding a thickener or the like according to the taste, and is not particularly limited. However, if the user prefers a refreshing mouth, the viscosity is lower. Is preferable, and the effect of the present invention can be more enjoyed.
- the viscosity can be 50 mPa ⁇ s or less, preferably 20 mPa ⁇ s or less, and more preferably 10 mPa ⁇ s or less. Further, it can be set to 5 mPa ⁇ s or less.
- the viscosity is measured with a B-type viscometer at room temperature of 20 ° C.
- the present beverage can be blended with various ingredients according to the product design of those skilled in the art, and the types and addition amounts are not particularly limited.
- various fruit juices citrus fruits, grapes, etc.
- sugars saccharide, fructose glucose liquid sugar, dextrin, etc.
- sweeteners saccharide, aspartame, etc.
- fats and oils fats and oils
- emulsifiers Lecithin, fatty acid esters, etc.
- pH adjusters citric acid, fumaric acid, tartaric acid, phosphoric acid, etc.
- minerals potassium salt, sodium salt, magnesium salt, calcium salt, iron salt, etc.
- vitamins A, B, C) , D, E, P, K, etc.
- chelating agents sodium citrate, polymerized phosphate, etc.
- perfume physiologically functional materials
- This beverage can be produced by a known method, and can be produced through steps such as raw material preparation, water addition, stirring, dissolution, pH adjustment, homogenization (homogenizer, etc.), heat sterilization and the like.
- the analysis value in the present invention is determined according to the following measurement method.
- ⁇ NSI measurement method> Add 60 ml of water to 3 g of the sample, stir the propeller at 37 ° C. for 1 hour, and centrifuge at 1400 ⁇ g for 10 minutes to collect the supernatant (I). Next, 100 ml of water is again added to the remaining precipitate, and the mixture is again stirred with a propeller at 37 ° C. for 1 hour, and then centrifuged to collect the supernatant (II). The liquid (I) and liquid (II) are combined, and water is added to the mixture to make 250 ml. After filtering this with a filter paper (NO.
- the nitrogen content in the filtrate is measured by the Kjeldahl method.
- the amount of nitrogen in the sample is measured by the Kjeldahl method, and the ratio of the amount of nitrogen recovered as filtrate (water-soluble nitrogen) to the total amount of nitrogen in the sample is expressed as% by weight.
- ⁇ Measurement method of dilute acid NSI> Add 100 ml of 0.1% by weight citric acid aqueous solution to 2.0 g of sample, stir and extract at 40 ° C. for 60 minutes, and centrifuge at 1400 ⁇ g for 10 minutes to obtain supernatant 1. 100 ml of 0.1% by weight citric acid aqueous solution is again added to the remaining precipitate, followed by extraction with stirring at 40 ° C. for 60 minutes, and centrifugation at 1400 ⁇ g for 10 minutes to obtain supernatant 2. Supernatant 1 and supernatant 2 are combined, and further 0.1% by weight citric acid aqueous solution is added to make 250 ml. After filtering with No.
- the nitrogen content of the filtrate is measured by Kjeldahl method.
- the nitrogen content in the sample is measured by the Kjeldahl method, and the ratio of the nitrogen recovered as filtrate (water-soluble nitrogen) to the total nitrogen in the sample is expressed as weight%, which is diluted acid NSI.
- ⁇ Average molecular weight> The dispersion of the protein degradation product diluted with 50 mM phosphate buffer (1% (weight / volume) SDS, 1.2% (weight / volume) NaCl, pH 7.0) was sonicated for 10 minutes. Then, it filters using a 0.2 micrometer filter.
- “TSK gel G3000SWXL column” is “TSK gel G2000SWXL column” (both manufactured by Tosoh Corporation, column size: inner diameter 7.8 mm ⁇ length 30 cm) at a flow rate of 0.4 ml / min at room temperature of 20 ° C.
- the protein degradation product is eluted using the above phosphate buffer. Protein degradation products are detected by measuring absorbance at 220 nm using a UV detector. Thereby, the weight average molecular weight of the proteolysate separated and purified in each fraction is calculated from the chart obtained using GPC software (manufactured by Tosoh Corporation).
- the molecular weight marker the following molecular weight compounds are used. 335,000 (Thyrogloblin, manufactured by Wako Pure Chemical Industries, Ltd.) 150,000 ( ⁇ -globlin, manufactured by Wako Pure Chemical Industries, Ltd.) 67,000 (Albumin (BSA), manufactured by SIGMA) 43,000 (Peroxidase, Wako Pure Chemical Industries, Ltd.) 18,000 (Myoglobin, manufactured by SIGMA) 12,384 (Cytochrome-C, manufactured by SIGMA) 5,734 (Insulin, manufactured by SIGMA) 307 (Glutathione, manufactured by Wako Pure Chemical Industries, Ltd.) 137 (p-aminobenzoic acid, manufactured by Wako Pure Chemical Industries, Ltd.)
- % and part indicate “% by weight” and “part by weight” unless otherwise specified.
- the powdered protein materials used in the examples are all commercially available from Fuji Oil Co., Ltd., and the soy polysaccharide is “Soya Five (R) -S” manufactured by Fuji Oil Co., Ltd. Using.
- Test Example 1 (Tests T1 to T9) Undecomposed product type powdery soybean protein material "Fujipuro (R) F" (protein content: 90.8% dry basis) was prepared was prepared commercially A ⁇ H as a hydrolysis type powdery soybean protein material. These commercial products A to H can be obtained by contacting Fuji Oil Co., Ltd. The analytical values of these 0.22M TCA solubility (degradation degree), NSI, and dilute acid NSI are shown in Table 1 below.
- Each powdery soy protein material was mixed with water so that the protein concentration was 5% and mixed well to obtain a dispersion.
- the pH of these dispersions was adjusted to 4.0 with 50% citric acid solution.
- a commercial product H having a high T9 dilute acid NSI and excellent solubility in acidity in any case of T1 to T8, aggregation occurs alone, so that an acidic protein dispersion is obtained. It was not prepared, and its suitability for acidic protein beverages was poor.
- the protein dispersion using the commercial product H of T9 is in an acidic or transparent liquid state, and even when heated, no agglomeration occurred. There was room for improvement to use.
- Test Example 2 (Tests T10 to T18) Each powdered protein material of Test Example 1 and soybean polysaccharide were mixed so that the protein concentration would be 5% and the soybean polysaccharide concentration would be 1%, and dispersed well by adding water to obtain a dispersion. The pH of this mixture was adjusted to 4.0 with a 50% citric acid solution, homogenized at 20 MPa with a homogenizer, sterilized by heating to 93 ° C., and cooled to obtain an acidic protein dispersion. . About each obtained dispersion liquid, the physical property of each dispersion liquid was measured after standing still at 20 degreeC for 24 hours.
- the viscosity was measured with a B-type rotational viscometer (manufactured by Toki Sangyo Co., Ltd.), and the median diameter was measured with “SALD-2000” (manufactured by Shimadzu Corporation).
- SALD-2000 manufactured by Shimadzu Corporation.
- the sample amount (g) obtained by separating each dispersion into a centrifuge tube was used as the denominator, and the collected sample was centrifuged with a centrifuge at 700 ⁇ G for 20 minutes, and the supernatant was discarded. Using the amount of precipitation (g) as a molecule, “centrifugal precipitation rate”, which is an index of protein dispersion stability, was calculated.
- beverages using powdered soy protein materials A and B of T11 and T12 are degraded products, but the NSI was too high, or the dispersion stability of the protein is poor in terms of centrifugal sedimentation rate. The feeling was bad and unsuitable.
- beverages using T17 powdered soy protein material G were unsuitable in terms of median diameter after heating, centrifugal sedimentation rate, bitterness and astringency, probably because the degree of degradation was too high at 50%.
- the drink using the powdery soybean protein raw material H was not suitable in terms of astringency because the NSI and dilute acid NSI were too high, and the viscosity after heating was considerably high.
- Test Example 3 (Tests T19 to T20) An acidic protein dispersion was prepared in the same manner as in Test Example 2, except that powdered soy protein material D was used and HM pectin and sodium carboxymethylcellulose (CMC-Na) were used instead of soy polysaccharide. Measurement and sensory evaluation were performed. The results are shown in Table 4.
- Example 1 (Prescription example of acidic protein beverage) 50 g of soybean polysaccharide was added to 950 g of water, stirred and dissolved at 80 ° C. for 20 minutes, and then cooled to 20 ° C. to obtain a 5% soybean polysaccharide solution. Next, 200 g of a 5% soybean polysaccharide solution was stirred and mixed with 560 g of room temperature water, and then 28 g of powdered soybean protein material E having a degradation degree of 23% shown in Table 1 was mixed and dispersed uniformly. Next, 90 g of granulated sugar and 70 g of fructose-glucose liquid sugar were mixed and stirred until each raw material was uniformly dispersed.
- Example 5 summarizes the beverage formulation of Example 1.
- Example 2 (Prescription example of acidic enteral nutrient) 100 g of soybean polysaccharide was added to 900 g of water, stirred and dissolved at 80 ° C. for 20 minutes, and then cooled to 20 ° C. to obtain a 10% soybean polysaccharide solution. Subsequently, 100 g of a 10% soybean polysaccharide solution was stirred and mixed while 500 g of normal temperature water was stirred. Next, powdery soybean protein material E55 g having a decomposition degree of 23% in Table 1 and 76 g of granulated sugar and 80 g of dextrin were mixed with powder, mixed in room temperature water containing soybean polysaccharide, and stirred until each raw material was uniformly dispersed.
- the acidic protein beverage and enteral nutrient obtained in Examples 1 and 2 were stored at 20 ° C. for 24 hours, and then physical properties of each sample were measured and sensory evaluation was performed. The measurement method and sensory evaluation method followed Test Example 2. The results are shown in Table 7.
- All the beverages had a very low viscosity of less than 6 mPa ⁇ s, a median diameter of less than 2 ⁇ m and good physical properties, and because the particles were fine, the mouthfeel was good and the texture was low.
- a beverage having a very good protein dispersion stability with a centrifugal precipitation rate of less than 2% could be prepared.
- the enteral nutrient of Example 2 was not observed that fats and oils were separated during storage, and the emulsification stability was high. The flavor was a delicious beverage with very little bitterness and astringency.
- Example 3 In the formulation of Example 1, an acidic protein beverage was obtained in the same manner as in Example 1 except that the 50% citric acid solution was adjusted to pH 3.4 (Example 3) and pH 4.5 (Example 4), respectively. . Each of these beverages had a good texture and good dispersion stability of the protein as in Example 1.
- an acidic and liquid beverage excellent in flavor, texture and protein dispersion stability can be obtained by selectively combining a powdered protein material having a specific degree of degradation and soybean polysaccharide. It was.
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Abstract
Description
また、例えば大豆蛋白質はアミノ酸組成のバランスが良く、またコレステロール低下作用に代表されるような生理機能も有しており、栄養補給や生理機能を期待した栄養・健康訴求食品にも使用されている。 Since proteins are high molecular and amphiphilic, some have gelling properties, thickening properties, and water retention properties. Powdered protein materials such as separated protein that contain this in high concentrations are free of water and therefore easier to manage and distribute than liquid materials, and can be added to various processed foods because they can be formulated at high concentrations. It is widely used as a material for improving physical properties.
In addition, for example, soy protein has a well-balanced amino acid composition and has physiological functions such as cholesterol lowering action, and is also used in nutritional and health foods that expect nutritional supplementation and physiological functions. .
したがって、酸性かつ液状の飲料において蛋白質を高配合することができ、且つそれを長期に分散安定化させる技術が求められている。 However, since many proteins such as soy protein and milk protein have an isoelectric point in the acidic range, the protein precipitates under acidic conditions, reducing the commercial value in appearance and texture. In addition, health-oriented beverages and enteral nutrients often have enhanced minerals such as calcium and magnesium, and these minerals are more reactive with proteins and promote protein aggregation, further dispersing proteins. Make stabilization difficult. Furthermore, since enteral nutrients also contain fats and oils, long-term emulsification stability is also required.
Therefore, there is a need for a technique that can highly blend protein in an acidic and liquid beverage and that can stabilize the dispersion for a long period of time.
そこで本発明の目的は、蛋白質を比較的多量に配合する場合であっても、長期に渡って沈殿が生じにくく、蛋白質の液中での分散が安定に維持される酸性の液状飲料を提供することにある。 It is technically difficult to formulate a relatively large amount of protein in an acidic liquid beverage that has the worst dispersion stability for the protein. In particular, it is more difficult to stabilize a dispersion by hydrating a powdered protein material in a powder state and blending it in a large amount. Even if water-soluble polysaccharides that have been conventionally known as protein dispersion stabilizers in Patent Documents 1 to 6 and the like are added, precipitation occurs in a liquid beverage containing a relatively large amount of protein over a long period of time. It has been difficult to guarantee the dispersion stability of proteins.
Accordingly, an object of the present invention is to provide an acidic liquid beverage in which precipitation is not likely to occur over a long period of time even when a relatively large amount of protein is blended, and the dispersion of the protein in the liquid is stably maintained. There is.
(1)蛋白質を含有する原料の少なくとも一つが、下記a)~c)の要件を満たす粉末状蛋白素材であって、蛋白質含量が1重量%以上であり、かつ大豆多糖類又は/及びエンドウ多糖類を蛋白質の分散安定剤として含み、液状であってかつpH3~5であることを特徴とする、酸性蛋白質飲料、
a)該粉末状蛋白素材が蛋白質加水分解物であり、該加水分解度が0.22Mトリクロロ酢酸(TCA)可溶率として10~35%、
b)該粉末状蛋白素材の窒素溶解指数(NSI)が10~80、
c)該粉末状蛋白素材の希酸NSIが10~70、
(2)該酸性蛋白質飲料の蛋白質含量が、1~20重量%である、前記(1)記載の酸性蛋白質飲料、
(3)該粉末状蛋白素材の乾物あたりの蛋白質含量が40重量%以上である、前記(1)又は(2)記載の酸性蛋白質飲料、
(4)該粉末状蛋白素材の乾物あたりの不溶性食物繊維の含量が2重量%以下である、前記(1)~(3)の何れか1項記載の酸性蛋白質飲料、
(5)該粉末状蛋白素材の5重量%分散液を、分光光度計により600nmで測定したときの透過率が1%T以下である、前記(1)~(4)の何れか1項記載の酸性蛋白質飲料、
(6)該粉末状蛋白素材が大豆、エンドウ、緑豆及び乳から選ばれる1以上の由来である、前記(1)~(5)の何れか1項記載の酸性蛋白質飲料、
(7)該飲料を700×Gで20分間の条件にて遠心分離したときの遠心沈殿率が5重量%以下である、前記(1)~(6)の何れか1項記載の酸性蛋白質飲料、
(8)該飲料中に分散された粒子の平均粒子径が5μm以下である、前記(1)~(7)の何れか1項記載の酸性蛋白質飲料、
(9)該飲料の粘度が50mPa/s以下である、前記(1)~(8)の何れか1項記載の酸性蛋白質飲料、
(10)該飲料が経腸栄養剤である、前記(1)~(9)の何れか1項記載の酸性蛋白質飲料、
(11)該飲料が密封容器に充填され密封されている、前記(1)~(10)の何れか1項記載の酸性蛋白質飲料、
(12)該粉末状蛋白素材が大豆、エンドウ及び緑豆から選ばれる1以上の由来であり、該飲料を700×Gで20分間の条件にて遠心分離したときの遠心沈殿率が5重量%以下である、前記(1)~(5)の何れか記載の酸性蛋白質飲料、
(13)該飲料中に分散された粒子の平均粒子径が5μm以下である、前記(12)記載の酸性蛋白質飲料、
(14)該飲料の粘度が50mPa/s以下である、前記(13)記載の酸性蛋白質飲料、
(15)該飲料が経腸栄養剤であり、かつ該飲料が密封容器に充填され密封されている、前記(14)記載の酸性蛋白質飲料。 That is, the present invention includes the following configurations.
(1) At least one of the protein-containing raw materials is a powdered protein material that satisfies the following requirements a) to c), the protein content is 1% by weight or more, and a soybean polysaccharide and / or peas An acidic protein beverage comprising a saccharide as a protein dispersion stabilizer, being liquid and having a pH of 3 to 5,
a) the powdered protein material is a protein hydrolyzate, and the degree of hydrolysis is 10 to 35% as 0.22M trichloroacetic acid (TCA) solubility;
b) Nitrogen solubility index (NSI) of the powdered protein material is 10 to 80,
c) The diluted protein NSI of the powdered protein material is 10 to 70,
(2) The acidic protein beverage according to (1), wherein the protein content of the acidic protein beverage is 1 to 20% by weight,
(3) The acidic protein beverage according to (1) or (2) above, wherein the protein content per dry matter of the powdered protein material is 40% by weight or more,
(4) The acidic protein beverage according to any one of (1) to (3), wherein the content of insoluble dietary fiber per dry matter of the powdered protein material is 2% by weight or less,
(5) The transmittance according to any one of (1) to (4), wherein the 5% by weight dispersion of the proteinaceous protein material has a transmittance of 1% T or less when measured with a spectrophotometer at 600 nm. Of acidic protein beverages,
(6) The acidic protein beverage according to any one of (1) to (5), wherein the powdered protein material is derived from one or more selected from soybeans, peas, mung beans and milk,
(7) The acidic protein beverage according to any one of (1) to (6), wherein the centrifugal precipitation rate is 5% by weight or less when the beverage is centrifuged at 700 × G for 20 minutes. ,
(8) The acidic protein beverage according to any one of (1) to (7), wherein the average particle size of the particles dispersed in the beverage is 5 μm or less,
(9) The acidic protein beverage according to any one of (1) to (8), wherein the beverage has a viscosity of 50 mPa / s or less,
(10) The acidic protein beverage according to any one of (1) to (9), wherein the beverage is an enteral nutrient,
(11) The acidic protein beverage according to any one of (1) to (10), wherein the beverage is filled in a sealed container and sealed,
(12) The powdered protein material has one or more origins selected from soybeans, peas, and mung beans, and the centrifugal precipitation rate when the beverage is centrifuged at 700 × G for 20 minutes is 5% by weight or less. The acidic protein beverage according to any one of (1) to (5),
(13) The acidic protein beverage according to (12) above, wherein the average particle size of the particles dispersed in the beverage is 5 μm or less,
(14) The acidic protein beverage according to (13), wherein the beverage has a viscosity of 50 mPa / s or less,
(15) The acidic protein beverage according to (14), wherein the beverage is an enteral nutrient, and the beverage is filled in a sealed container and sealed.
a)該粉末状蛋白素材が蛋白質加水分解物であり、該加水分解度が0.22Mトリクロロ酢酸(TCA)可溶率として10~35%、
b)該粉末状蛋白素材の窒素溶解指数(NSI)が10~80、
c)該粉末状蛋白素材の希酸NSIが10~70、
の3要件を満たす粉末状蛋白素材であって、蛋白質含量が1重量%以上であり、かつ大豆多糖類又は/及びエンドウ多糖類を蛋白質の分散安定剤として含み、液状であってかつpH3~5であることを特徴とするものである。
以下、本発明の実施形態について詳細に説明する。 In the acidic protein beverage of the present invention, at least one of the raw materials containing protein is:
a) the powdered protein material is a protein hydrolyzate, and the degree of hydrolysis is 10 to 35% as 0.22M trichloroacetic acid (TCA) solubility;
b) Nitrogen solubility index (NSI) of the powdered protein material is 10 to 80,
c) The diluted protein NSI of the powdered protein material is 10 to 70,
A powdery protein material satisfying the above three requirements, wherein the protein content is 1% by weight or more and soy polysaccharides and / or pea polysaccharides are contained as protein dispersion stabilizers, are liquid and have a pH of 3 to 5 It is characterized by being.
Hereinafter, embodiments of the present invention will be described in detail.
本発明の対象である液状かつ酸性の蛋白質飲料(以下、「本飲料」と称する。)は、液状態で製品化されて消費者に飲用されるものである。最近ではRTD飲料(Ready-To-Drink)と呼ばれる飲料や、経腸栄養剤も概念的に包含されるものとする。 (Liquid and acidic protein beverage)
The liquid and acidic protein beverage (hereinafter referred to as “the present beverage”), which is the subject of the present invention, is commercialized in a liquid state and consumed by consumers. Recently, drinks called RTD drinks (Ready-To-Drink) and enteral nutrients are also conceptually included.
本飲料は、栄養成分として少なくとも蛋白質を含有する酸性蛋白質飲料であり、蛋白質含量は飲料全体の重量あたり1重量%以上である。さらに蛋白質の含有量が高い方が本発明の効果を有効に発揮することができ好ましく、1.5重量%以上が好ましく、2重量%以上がより好ましく、2.5重量%以上がさらに好ましい。またその上限は20重量%以下、15重量%以下、あるいは10重量%以下とすることができる。大豆蛋白質や乳蛋白質などの多くの蛋白質は等電点がpH4.5近辺に存在するため、本飲料のような液状かつ酸性の環境では、蛋白質の溶解性が急激に低下するため、蛋白質が保存中に沈殿が生じやすくなる。すなわち蛋白質の分散安定性が悪くなる。そして沈殿の程度は長期保存されるほど多くなる。一方、本発明ではこのような問題が解決されている。 (protein)
This beverage is an acidic protein beverage containing at least protein as a nutrient component, and the protein content is 1% by weight or more per weight of the whole beverage. A higher protein content is preferable because the effect of the present invention can be effectively exhibited, preferably 1.5% by weight or more, more preferably 2% by weight or more, and further preferably 2.5% by weight or more. Moreover, the upper limit can be 20 weight% or less, 15 weight% or less, or 10 weight% or less. Many proteins, such as soy protein and milk protein, have an isoelectric point around pH 4.5, so in a liquid and acidic environment such as this beverage, the protein solubility is drastically reduced, so the protein is preserved. Precipitation tends to occur inside. That is, the protein dispersion stability deteriorates. And the degree of precipitation increases as it is stored for a long time. On the other hand, the present invention solves such a problem.
本飲料に用いられる特定の粉末状蛋白素材は、蛋白質を主成分とし、各種加工食品や飲料に使用される食品素材である。例えば大豆由来の蛋白質の場合、脱脂大豆や丸大豆等の大豆原料からさらに大豆蛋白質を濃縮加工して調製されるものであり、一般には分離大豆蛋白質や粉末豆乳、あるいはそれらを種々加工したものなどが概念的に包含されるものである。また乳由来の蛋白質ではカゼインや濃縮乳蛋白(MPC)等を用いることができる。
該粉末状蛋白素材は、乾物あたりの蛋白質含量が少なくとも40重量%以上、好ましくは50重量%以上、さらに好ましくは60重量%以上であるのが適当である。
一方、液状飲料へ使用されることから、保存中の不溶物の沈殿を防止するために不溶性食物繊維の含量はなるべく低い方が好ましく、乾物あたりでは2重量%以下であるのが好ましく、1重量%以下であるのがより好ましい。 (Powdered protein material)
The specific powdery protein material used in the present beverage is a food material mainly composed of protein and used in various processed foods and beverages. For example, in the case of protein derived from soybeans, it is prepared by further processing soybean protein from soybean raw materials such as defatted soybeans and whole soybeans, and in general, isolated soybean protein, powdered soy milk, or various processed products thereof Is conceptually included. For milk-derived proteins, casein or concentrated milk protein (MPC) can be used.
The powdered protein material suitably has a protein content per dry matter of at least 40% by weight, preferably 50% by weight or more, and more preferably 60% by weight or more.
On the other hand, since it is used for liquid beverages, the content of insoluble dietary fiber is preferably as low as possible in order to prevent precipitation of insolubles during storage, and it is preferably 2% by weight or less per dry matter. % Or less is more preferable.
a)該粉末状蛋白素材が蛋白質加水分解物であり、該加水分解度が0.22Mトリクロロ酢酸(TCA)可溶率として10~35%、
b)該粉末状蛋白素材の窒素溶解指数(NSI)が10~80、
c)該粉末状蛋白素材の希酸NSIが10~70。
かかるa)~c)の要件を全て満たす特定の粉末状蛋白素材が配合されることにより含有される蛋白質が、本飲料中において後述する特定の多糖類と共存していることが重要である。そしてこの組合せが相乗的に作用することで、蛋白質の分散安定性に極めて不利な液状かつpH3~5の酸性という環境下において長期に保存されても、沈殿量が極めて少なく、ざらつきを感じにくく、外観が均一で良好であり、低粘度で風味良好な液状かつ酸性の蛋白質飲料を得ることができる。
以下、これらの要件についてより具体的に説明する。 In addition, it is essential that the specific powdery protein material used in the present beverage satisfies at least the following requirements a) to c).
a) the powdered protein material is a protein hydrolyzate, and the degree of hydrolysis is 10 to 35% as 0.22M trichloroacetic acid (TCA) solubility;
b) Nitrogen solubility index (NSI) of the powdered protein material is 10 to 80,
c) The dilute acid NSI of the powdered protein material is 10 to 70.
It is important that the protein contained by blending a specific powdered protein material that satisfies all the requirements of a) to c) coexists with a specific polysaccharide described later in the beverage. And this combination acts synergistically, even if stored for a long time in a liquid and pH 3-5 acidic environment that is extremely disadvantageous for protein dispersion stability, the amount of precipitation is extremely small, making it difficult to feel roughness, A liquid and acidic protein beverage having a uniform and good appearance, low viscosity and good flavor can be obtained.
Hereinafter, these requirements will be described more specifically.
本飲料で用いられる粉末状蛋白素材は、一定の分解度まで酵素分解された蛋白質加水分解物であることが重要である。蛋白質の分解度は、0.22M トリクロロ酢酸可溶率(TCA可溶率)を指標として表すことができる。この数値は粉末状蛋白素材を蛋白質含量として1.0重量%となるように水に分散させ十分撹拌した分散液について、全蛋白質に対する0.22M トリクロロ酢酸(TCA)に溶解する蛋白質の割合をケルダール法により測定したものである。蛋白質の分解が進行するにつれて、TCA可溶率は上昇する。
本飲料に用いられる粉末状蛋白素材は、この0.22M TCA可溶率が10~35%の範囲にあることが重要である。特に下限については11%以上が好ましく、12%以上がより好ましく、13%以上がさらに好ましい。また下限については30%以下が好ましく、28%以下がさらに好ましい。 a) 0.22M Trichloroacetic acid solubility It is important that the powdered protein material used in this beverage is a protein hydrolyzate that has been enzymatically degraded to a certain degree of degradation. The degree of protein degradation can be expressed using 0.22M trichloroacetic acid solubility (TCA solubility) as an index. This figure shows the ratio of protein dissolved in 0.22M trichloroacetic acid (TCA) to total protein in a dispersion in which powdered protein material is dispersed in water to a protein content of 1.0% by weight and sufficiently stirred. It was measured by the method. As protein degradation proceeds, the TCA solubility increases.
It is important that the 0.22M TCA solubility in the powdered protein material used in this beverage is in the range of 10 to 35%. In particular, the lower limit is preferably 11% or more, more preferably 12% or more, and further preferably 13% or more. The lower limit is preferably 30% or less, and more preferably 28% or less.
本飲料に用いられる粉末状蛋白素材は、水への溶解性の指標として、NSI(Nitrogen Solubility Index:窒素溶解指数)が10~80であるのが重要であり、特に15~75が好ましく、20~70がさらに好ましい。
ここで、NSIが低すぎると、蛋白質の溶解性が低すぎて沈殿が多くなり、ざらつきも強く感じるようになる。この点で、粉末状蛋白素材の製造時にカルシウムやマグネシウム等の2価金属を添加して蛋白質と2価金属を反応させ、NSIを低下させたような粉末状蛋白素材は、ざらつきが強くなる傾向にあるため、このようなミネラル反応を生じさせていない粉末状蛋白素材を用いるのがより好ましく、上記ア)の酵素分解によってNSIを低下させた粉末状蛋白素材を用いるのが好ましい。
なお、NSIは所定の方法に基づき、全窒素量に占める水溶性窒素(粗蛋白)の比率(重量%)で表すものとし、本発明においては後述の方法に準じて測定された値とする。 b) Nitrogen solubility index (NSI)
The powdered protein material used in this beverage has an NSI (Nitrogen Solubility Index) as an index of solubility in water of 10 to 80, particularly preferably 15 to 75, 20 More preferably, 70.
Here, if the NSI is too low, the solubility of the protein is too low, the amount of precipitation increases, and the roughness is strongly felt. In this regard, powdered protein materials with reduced NSI tend to be more roughened by adding divalent metals such as calcium and magnesium during the production of powdered protein materials to react proteins and divalent metals. Therefore, it is more preferable to use a powdered protein material that does not cause such a mineral reaction, and it is preferable to use a powdered protein material in which NSI is reduced by the enzymatic decomposition of a).
NSI is represented by a ratio (% by weight) of water-soluble nitrogen (crude protein) in the total amount of nitrogen based on a predetermined method, and is a value measured according to the method described later in the present invention.
本飲料に用いられる粉末状蛋白素材は、酸性領域において蛋白質が高溶解性である、国際公開WO2002/67690号に記載の酸性可溶大豆蛋白や乳清蛋白質などのような「酸性可溶蛋白」ではなく、むしろ中程度以下のものであることが特徴である。酸性領域での溶解性は、「希酸NSI」(NSIは、窒素溶解指数の略称)を指標として表すことができ、希酸NSIの値が高いほど酸性領域での溶解性が高いことの指標となる。なお希酸NSIは後述の方法に準じて測定するものとする。 c) Dilute acid NSI
The powdered protein material used in this beverage is an “acid-soluble protein” such as an acid-soluble soy protein or whey protein described in International Publication WO2002 / 67690, wherein the protein is highly soluble in the acidic region. Rather, it is characterized by being moderate or less. The solubility in the acidic region can be expressed using “dilute acid NSI” (NSI is an abbreviation for nitrogen solubility index) as an index, and the higher the value of the diluted acid NSI, the higher the solubility in the acidic region. It becomes. Note that dilute acid NSI is measured according to the method described below.
該素材の希酸NSIが酸性可溶蛋白のように高すぎると、酸性領域での蛋白質の溶解性は高いが、ミネラル類との反応により凝集が生じ、加熱により凝固してしまう場合がある。また該素材の希酸NSIが低すぎると、蛋白質の溶解性が低すぎて沈殿が多くなり、ざらつきも強く感じるようになる。 It is important that the dilute acid NSI of the powdered protein material used in this beverage is 10 to 70, preferably 11 to 60.
If the dilute acid NSI of the material is too high like an acidic soluble protein, the solubility of the protein in the acidic region is high, but agglomeration may occur due to reaction with minerals and it may solidify by heating. On the other hand, if the diluted acid NSI of the material is too low, the solubility of the protein is too low, resulting in a large amount of precipitation and a strong feeling of roughness.
なお透過率(%T)は、蛋白質を含んだ分散液の透明性の尺度であり、次のようにして定義する。つまり、蛋白質粉末を蛋白質分が5重量%になるように水に分散させ十分撹拌した分散液を、分光光度計((株)日立ハイテクノロジーズ製:U-3210形自記分光光度計)にて1cmセルを使用し600nmでの透過率(%T)を測定する。 The powdered protein material used in this beverage is such that both NSI and dilute acid NSI are in a medium range, and the protein is only partially dissolved in water. The liquid is not transparent like an acidic soluble protein, and is cloudy. The transmittance of the dispersion (concentration at 5% by weight) is 1% T or less as a value measured at 600 nm with a spectrophotometer.
The transmittance (% T) is a measure of the transparency of a dispersion containing protein, and is defined as follows. In other words, a dispersion obtained by dispersing protein powder in water so that the protein content is 5% by weight and stirring sufficiently is 1 cm by a spectrophotometer (manufactured by Hitachi High-Technologies Corporation: U-3210 self-recording spectrophotometer). Using a cell, the transmittance (% T) at 600 nm is measured.
一方、「フジプロ(R)F」等の加水分解していない一般的な粉末状大豆蛋白素材はTCA可溶率が10%未満、NSIが90以上である。また「プロリーナ(R)SU」はTCA可溶率が35%を超えるものである。また酸性可溶性の粉末状大豆蛋白として知られている「ソヤサワー(R)」は酸性領域における蛋白質の溶解性が極めて高く、NSIが90以上でかつ希酸NSIも90%以上であり、透過率も80%T以上の透明性の高いものである。このため、これらの製品は本飲料に用いられる上記要件を満たした粉末状蛋白素材には該当しないものである。 Various powdered protein materials that satisfy all of the above requirements a) to c) are commercially available and can be purchased and obtained. For example, among powdered soy protein materials manufactured by Fuji Oil Co., Ltd., products such as “Prolina (R) 800”, “Prolina (R) HD101”, “Fujipro (R) CL” can be used, Any product other than these products may be used as long as it satisfies all the above requirements.
On the other hand, "Fujipuro (R) F" such as a general powdery soybean protein material which is not hydrolyzed in the TCA solubility is less than 10%, and NSI of 90 or more. The "Purorina (R) SU" is one in which TCA solubility is more than 35%. Also known as powdery soybean protein acid soluble "Soyasawa (R)" is extremely high solubility of the proteins in the acidic region, NSI is not less 90 or more and diluted acid NSI also 90% or more, even transmittance It has a high transparency of 80% T or more. For this reason, these products do not correspond to the powdered protein material that satisfies the above-mentioned requirements for use in the present beverage.
本飲料は、上述した蛋白質と共に特定の多糖類(以下、「本多糖類」と称する場合がある。)を含有するものであり、特定の多糖類として、大豆多糖類又は/及びエンドウ多糖類を蛋白質の分散安定剤として用いることが重要である。該多糖類は蛋白質を液状かつ酸性の本飲料中で分散安定化させる効果がすでに知られているが、上述の特定の粉末状蛋白素材との組合せによる相乗効果が顕著であることが本発明で見出されたものである。
大豆多糖類やエンドウ多糖類はラムノース、フコース、アラビノース、キシロース、ガラクトース、グルコース及びウロン酸等の糖類から構成される水溶性多糖類であって、一般には以下の条件で分析されるゲルろ過HPLC法で平均分子量が100万以下のものである。これらは大豆やエンドウの不溶性食物繊維(オカラ)を含む原料から公知の方法により水で抽出し、必要により精製して調製されたものを用いることができる。大豆多糖類は市販品を使用することができ、例えば「ソヤファイブ(R)」シリーズ(不二製油(株)製)や「SM」シリーズ(三栄源エフ・エフ・アイ(株)製)などを用いることができる。またエンドウ多糖類は、例えば国際公開WO2012/176852号や国際公開WO2014/103833号に記載の方法で得られるものを用いることができる。
ゲルろ過HPLCは、標準プルラン(昭和電工(株))を標準物質として、分析カラム「TSKgel G5000PWXL」(東ソー(株)製、カラムサイズ:7.8mmI.D.×30cm、充填剤基材:メタクリレートポリマー、充填剤粒子径:10μm、排除限界分子量:250万)を用いる。平均絶対分子量(MM)は、カラム通液後にトルエンでキャリブレーションしたマルチアングルレーザーライトスキャッタリング(MALLS)により求める。溶離液は例えば50mM酢酸ナトリウム水溶液(pH5.0)を用い、カラムの流速は1.0mL/分とし、検出器はRI検出器及びMALLS検出器を用いる。ただし、分析値に大きな誤差が生じない範囲で各分析条件を適宜変更してもよい。 (Polysaccharide)
This beverage contains a specific polysaccharide (hereinafter sometimes referred to as “the present polysaccharide”) together with the above-described protein, and as the specific polysaccharide, soybean polysaccharide and / or pea polysaccharide is used. It is important to use it as a dispersion stabilizer for proteins. The polysaccharide is already known to have the effect of dispersing and stabilizing the protein in the liquid and acidic beverage, but the synergistic effect of the combination with the specific powdered protein material described above is remarkable in the present invention. It has been found.
Soy polysaccharides and pea polysaccharides are water-soluble polysaccharides composed of saccharides such as rhamnose, fucose, arabinose, xylose, galactose, glucose and uronic acid, and are generally analyzed by gel filtration HPLC under the following conditions The average molecular weight is 1 million or less. These can be extracted from water containing raw materials containing soybean or pea insoluble dietary fiber (Okara) by water using a known method and purified if necessary. Soybean polysaccharides can be commercially available, such as the “Soya Five (R) ” series (Fuji Oil Co., Ltd.) and the “SM” series (San-Eigen FFI Co., Ltd.). Can be used. Moreover, what is obtained by the method as described in international publication WO2012 / 176852 and international publication WO2014 / 103833 can be used for pea polysaccharide, for example.
Gel filtration HPLC uses standard pullulan (Showa Denko Co., Ltd.) as a standard substance, analytical column “TSKgel G5000PWXL” (manufactured by Tosoh Corporation, column size: 7.8 mm I.D. × 30 cm, packing material: methacrylate polymer , Filler particle size: 10 μm, exclusion limit molecular weight: 2.5 million). The average absolute molecular weight (MM) is obtained by multi-angle laser light scattering (MALLS) calibrated with toluene after passing through the column. The eluent is, for example, 50 mM aqueous sodium acetate (pH 5.0), the column flow rate is 1.0 mL / min, and the detector is an RI detector and a MALLS detector. However, each analysis condition may be appropriately changed within a range in which a large error does not occur in the analysis value.
本飲料は特定の粉末状蛋白素材から導入された蛋白質粒子が本多糖類との相乗作用で均質化され微細化されているためか、酸性で液状の条件下で長期に保存されても蛋白質の沈殿が生じにくく、食感のざらつきも感じにくいものである。本飲料中に分散された粒子の平均粒子径は少なくとも5μm以下とすることができ、好ましくは3μm以下、より好ましくは2μm以下、さらに好ましくは1.5μm以下、最も好ましくは1μm以下とすることができる。 (Average particle size in beverages)
This beverage is made from protein particles introduced from a specific powdered protein material because it is homogenized and refined by the synergistic action with this polysaccharide, or even if stored for a long time under acidic and liquid conditions. Precipitation is unlikely to occur and the texture is not easily felt. The average particle size of the particles dispersed in the beverage can be at least 5 μm or less, preferably 3 μm or less, more preferably 2 μm or less, still more preferably 1.5 μm or less, and most preferably 1 μm or less. it can.
本飲料は長期保存中の沈澱量が低く、極めて蛋白質の分散安定性に優れたものである。そのような分散安定性の指標としては、飲料を遠心分離して発生する沈殿中の蛋白質量の、全液中の蛋白質量に対する割合を示す「遠心沈殿率」を用いることができる。
具体的には測定サンプル液を一定量遠沈管に分取し、遠心分離器で700G、20分間の条件にて遠心分離後、上澄みを廃棄した後の沈殿量(g)を測定する。この沈殿量のサンプル液量(g)に対する割合(重量%)を「遠心沈殿率」とする。これによって蛋白質の液中での長期の分散安定性を簡便に確認することができる。本飲料では遠心沈殿率は5重量%以下とすることができ、好ましくは3重量%以下とすることができる。 (Centrifugal sedimentation rate of beverage)
This beverage has a low amount of sediment during long-term storage and is extremely excellent in protein dispersion stability. As an indicator of such dispersion stability, “centrifugal precipitation rate” indicating the ratio of the protein amount in the precipitate generated by centrifuging the beverage to the protein amount in the whole liquid can be used.
Specifically, a predetermined amount of the measurement sample solution is collected in a centrifuge tube, centrifuged at 700 G for 20 minutes with a centrifuge, and then the amount of precipitation (g) after discarding the supernatant is measured. The ratio (wt%) of the precipitation amount to the sample liquid amount (g) is defined as “centrifugal precipitation rate”. Thus, long-term dispersion stability in the protein solution can be easily confirmed. In this beverage, the centrifugal sedimentation rate can be 5% by weight or less, preferably 3% by weight or less.
本飲料は酸性のpHで低粘度であっても蛋白質が沈殿しにくく分散安定性が高い品質を維持することができる。飲料の粘度は嗜好に合わせて増粘剤等の添加により適宜調整することができるため、特に限定されるものではないが、すっきりとした飲み口を嗜好する場合には、より低粘度であるのが好ましく、またその方が本発明の効果をより享受することができる。該粘度は50mPa・s以下とすることができ、好ましくは20mPa・s以下とすることができ、より好ましくは10mPa・s以下とすることができる。またさらに5mPa・s以下にもすることもできる。なお粘度は20℃の室温にてB型粘度計で測定するものとする。 (Viscosity of beverage)
Even if the beverage has an acidic pH and a low viscosity, the protein is difficult to precipitate and can maintain a high dispersion stability. The viscosity of the beverage can be appropriately adjusted by adding a thickener or the like according to the taste, and is not particularly limited. However, if the user prefers a refreshing mouth, the viscosity is lower. Is preferable, and the effect of the present invention can be more enjoyed. The viscosity can be 50 mPa · s or less, preferably 20 mPa · s or less, and more preferably 10 mPa · s or less. Further, it can be set to 5 mPa · s or less. The viscosity is measured with a B-type viscometer at room temperature of 20 ° C.
本飲料には上述の原料の他に、当業者の製品設計に合わせて種々の原料を配合することができ、その種類や添加量は特に限定されるものではない。
例えば、各種の果汁(柑橘類、ブドウ等)、糖類(ショ糖、果糖ブドウ糖液糖、デキストリン等)、甘味料(スクラロース、アスパルテーム等)、油脂(菜種油、大豆油、EPA、DHA等)、乳化剤(レシチン、脂肪酸エステル等)、pH調整剤(クエン酸、フマル酸、酒石酸、リン酸等)、ミネラル(カリウム塩、ナトリウム塩、マグネシウム塩、カルシウム塩、鉄塩等)、ビタミン(A,B,C,D,E,P,K等)、キレート剤(クエン酸ナトリウム、重合リン酸塩等)香料、生理機能素材(イソフラボン、サポニン、乳酸菌末、ペプチド類、グルコサミン等)等を適宜配合することができる。
本飲料の製造工程においてpH調整剤を添加し、pHを3~5に調整するタイミングは、粉末状蛋白素材と本多糖類を添加した後が好ましい。 (Other ingredients blended in beverages)
In addition to the above-mentioned ingredients, the present beverage can be blended with various ingredients according to the product design of those skilled in the art, and the types and addition amounts are not particularly limited.
For example, various fruit juices (citrus fruits, grapes, etc.), sugars (sucrose, fructose glucose liquid sugar, dextrin, etc.), sweeteners (sucralose, aspartame, etc.), fats and oils (rapeseed oil, soybean oil, EPA, DHA, etc.), emulsifiers ( Lecithin, fatty acid esters, etc.), pH adjusters (citric acid, fumaric acid, tartaric acid, phosphoric acid, etc.), minerals (potassium salt, sodium salt, magnesium salt, calcium salt, iron salt, etc.), vitamins (A, B, C) , D, E, P, K, etc.), chelating agents (sodium citrate, polymerized phosphate, etc.) perfume, physiologically functional materials (isoflavones, saponins, lactic acid bacteria powder, peptides, glucosamine, etc.) it can.
The timing for adding a pH adjuster and adjusting the pH to 3 to 5 in the production process of the present beverage is preferably after adding the powdered protein material and the present polysaccharide.
本発明における分析値は以下の測定方法に従うものとする。
<NSIの測定方法>
試料3gに60mlの水を加え、37℃で1時間プロペラ攪拌した後、1400×gにて10分間遠心分離し、上澄み液(I)を採取する。次に、残った沈殿に再度水100mlを加え、再度37℃で1時間プロペラ撹拌した後、遠心分離し、上澄み液(II)を採取する。(I)液および(II)液を合わせ、その混合液に水を加えて250mlとする。これを濾紙(NO.5)にて濾過した後、濾液中の窒素含量をケルダール法にて測定する。同時に試料中の窒素量をケルダール法にて測定し、濾液として回収された窒素量(水溶性窒素)の試料中の全窒素量に対する割合を重量%として表したものをNSIとする。 (Measuring method)
The analysis value in the present invention is determined according to the following measurement method.
<NSI measurement method>
Add 60 ml of water to 3 g of the sample, stir the propeller at 37 ° C. for 1 hour, and centrifuge at 1400 × g for 10 minutes to collect the supernatant (I). Next, 100 ml of water is again added to the remaining precipitate, and the mixture is again stirred with a propeller at 37 ° C. for 1 hour, and then centrifuged to collect the supernatant (II). The liquid (I) and liquid (II) are combined, and water is added to the mixture to make 250 ml. After filtering this with a filter paper (NO. 5), the nitrogen content in the filtrate is measured by the Kjeldahl method. At the same time, the amount of nitrogen in the sample is measured by the Kjeldahl method, and the ratio of the amount of nitrogen recovered as filtrate (water-soluble nitrogen) to the total amount of nitrogen in the sample is expressed as% by weight.
試料2.0gに100mlの0.1重量%クエン酸水溶液を加え、40℃にて60分攪拌抽出し、1400×gにて10分間遠心分離し、上清1を得る。残った沈殿に再度100mlの0.1重量%クエン酸水溶液を加え、40℃にて60分攪拌抽出し、1400×gにて10分間遠心分離し、上清2を得る。上清1および上清2を合わせ、さらに0.1重量%クエン酸水溶液を加えて250mlとする。No.5Aろ紙にてろ過したのち、ろ液の窒素含量をケルダール法にて測定する。同時に試料中の窒素含量をケルダール法にて測定し、ろ液として回収された窒素(水溶性窒素)の試料中の全窒素に対する割合を重量%として表したものを希酸NSIとする。 <Measurement method of dilute acid NSI>
Add 100 ml of 0.1% by weight citric acid aqueous solution to 2.0 g of sample, stir and extract at 40 ° C. for 60 minutes, and centrifuge at 1400 × g for 10 minutes to obtain supernatant 1. 100 ml of 0.1% by weight citric acid aqueous solution is again added to the remaining precipitate, followed by extraction with stirring at 40 ° C. for 60 minutes, and centrifugation at 1400 × g for 10 minutes to obtain supernatant 2. Supernatant 1 and supernatant 2 are combined, and further 0.1% by weight citric acid aqueous solution is added to make 250 ml. After filtering with No. 5A filter paper, the nitrogen content of the filtrate is measured by Kjeldahl method. At the same time, the nitrogen content in the sample is measured by the Kjeldahl method, and the ratio of the nitrogen recovered as filtrate (water-soluble nitrogen) to the total nitrogen in the sample is expressed as weight%, which is diluted acid NSI.
50mMリン酸緩衝液(1%(重量/体積)SDS、1.2%(重量/体積)NaCl、pH7.0)を用いて希釈調整した蛋白質分解物の分散液を、10分間超音波処理を行った後、0.2μmフィルターを用いて濾過する。得られた濾液を0.4ml/minの流速、室温20℃で、「TSK gel G3000SWXLカラム」を「TSK gel G2000SWXLカラム」(何れも東ソー(株)製、カラムサイズ:内径7.8mm×長さ30cm)と直列につないで連続で通し、上記リン酸緩衝液を用いて蛋白質分解物を溶出する。蛋白質分解物の検出はUV検出器を用い、220nmの吸光度を測定して行う。これにより、各画分に分離精製された蛋白分解物の重量平均分子量を、GPCソフトウェア(東ソー(株)製)を使用して得られたチャートから算出する。 <Average molecular weight>
The dispersion of the protein degradation product diluted with 50 mM phosphate buffer (1% (weight / volume) SDS, 1.2% (weight / volume) NaCl, pH 7.0) was sonicated for 10 minutes. Then, it filters using a 0.2 micrometer filter. “TSK gel G3000SWXL column” is “TSK gel G2000SWXL column” (both manufactured by Tosoh Corporation, column size: inner diameter 7.8 mm × length 30 cm) at a flow rate of 0.4 ml / min at room temperature of 20 ° C. The protein degradation product is eluted using the above phosphate buffer. Protein degradation products are detected by measuring absorbance at 220 nm using a UV detector. Thereby, the weight average molecular weight of the proteolysate separated and purified in each fraction is calculated from the chart obtained using GPC software (manufactured by Tosoh Corporation).
335,000(Thyrogloblin、和光純薬工業(株)製)
150,000(γ-globlin、和光純薬工業(株)製)
67,000(Albumin(BSA)、SIGMA社製)
43,000(Peroxidase、和光純薬工業(株)製)
18,000(Myoglobin、SIGMA社製)
12,384(Cytochrome-C、SIGMA社製)
5,734(Insulin、SIGMA社製)
307(Glutathione、和光純薬工業(株)製)
137(p-アミノ安息香酸、和光純薬工業(株)製) As the molecular weight marker, the following molecular weight compounds are used.
335,000 (Thyrogloblin, manufactured by Wako Pure Chemical Industries, Ltd.)
150,000 (γ-globlin, manufactured by Wako Pure Chemical Industries, Ltd.)
67,000 (Albumin (BSA), manufactured by SIGMA)
43,000 (Peroxidase, Wako Pure Chemical Industries, Ltd.)
18,000 (Myoglobin, manufactured by SIGMA)
12,384 (Cytochrome-C, manufactured by SIGMA)
5,734 (Insulin, manufactured by SIGMA)
307 (Glutathione, manufactured by Wako Pure Chemical Industries, Ltd.)
137 (p-aminobenzoic acid, manufactured by Wako Pure Chemical Industries, Ltd.)
未分解品タイプの粉末状大豆蛋白素材「フジプロ(R)F」(蛋白質含量:乾物あたり90.8%)を用意し、加水分解タイプの粉末状大豆蛋白素材として市販品A~Hを用意した。この市販品A~Hは不二製油(株)に問い合わせれば入手することができる。
これらの0.22M TCA可溶率(分解度)、NSI、希酸NSIの分析値を下記表1に示した。 ■ Test Example 1 (Tests T1 to T9)
Undecomposed product type powdery soybean protein material "Fujipuro (R) F" (protein content: 90.8% dry basis) was prepared was prepared commercially A ~ H as a hydrolysis type powdery soybean protein material. These commercial products A to H can be obtained by contacting Fuji Oil Co., Ltd.
The analytical values of these 0.22M TCA solubility (degradation degree), NSI, and dilute acid NSI are shown in Table 1 below.
しかし、T9の希酸NSIが高く酸性での溶解性に優れた市販品Hを用いた場合を除き、T1~T8の何れの場合も単独では凝集が発生してしまい、酸性の蛋白質分散液を調製するには至らず、酸性蛋白飲料への適性は不良であった。
T9の市販品Hを用いた蛋白質分散液は酸性でも透明な液状となっており、これを加熱しても凝集は発生しなかったが、渋味が感じられて風味の点で酸性蛋白飲料に使用するには改良の余地があった。 Each powdery soy protein material was mixed with water so that the protein concentration was 5% and mixed well to obtain a dispersion. The pH of these dispersions was adjusted to 4.0 with 50% citric acid solution.
However, except in the case of using a commercial product H having a high T9 dilute acid NSI and excellent solubility in acidity, in any case of T1 to T8, aggregation occurs alone, so that an acidic protein dispersion is obtained. It was not prepared, and its suitability for acidic protein beverages was poor.
The protein dispersion using the commercial product H of T9 is in an acidic or transparent liquid state, and even when heated, no agglomeration occurred. There was room for improvement to use.
試験例1の各粉末状蛋白素材と大豆多糖類とを蛋白質濃度が5%、大豆多糖類濃度が1%となるように混合し、加水してよく分散させ、分散液を得た。この混合液のpHを50%クエン酸溶液で4.0に調整した後、ホモゲナイザーで20MPaで均質化し、93℃まで加熱して殺菌を行い、冷却することにより、酸性の蛋白質分散液を得た。
得られた各分散液について20℃にて24時間静置保存後に各分散液の物性を測定した。粘度はB型回転粘度計(東機産業(株)製)で、メジアン径を「SALD-2000」((株)島津製作所製)で測定した。また各分散液を一定量遠沈管に分取したサンプル量(g)を分母とし、分取したサンプルを遠心分離器で700×G、20分間の条件にて遠心後、上澄みを廃棄した後の沈殿量(g)を分子として、蛋白質の分散安定性の指標である「遠心沈澱率」を算出した。
また各分散液について、10人のパネラーに依頼し、ざらつき、苦味、渋味(収斂味)に関して下記表2の基準で官能評価を行い、各パネラーが与えた評価の平均値を算出した。そして、平均値が1.5点未満を評価「A」、1.5点以上2.5点未満を評価「B」、2.5点以上3.5点未満を評価「C」、3.5点以上4点以下を評価「D」とした。 ■ Test Example 2 (Tests T10 to T18)
Each powdered protein material of Test Example 1 and soybean polysaccharide were mixed so that the protein concentration would be 5% and the soybean polysaccharide concentration would be 1%, and dispersed well by adding water to obtain a dispersion. The pH of this mixture was adjusted to 4.0 with a 50% citric acid solution, homogenized at 20 MPa with a homogenizer, sterilized by heating to 93 ° C., and cooled to obtain an acidic protein dispersion. .
About each obtained dispersion liquid, the physical property of each dispersion liquid was measured after standing still at 20 degreeC for 24 hours. The viscosity was measured with a B-type rotational viscometer (manufactured by Toki Sangyo Co., Ltd.), and the median diameter was measured with “SALD-2000” (manufactured by Shimadzu Corporation). The sample amount (g) obtained by separating each dispersion into a centrifuge tube was used as the denominator, and the collected sample was centrifuged with a centrifuge at 700 × G for 20 minutes, and the supernatant was discarded. Using the amount of precipitation (g) as a molecule, “centrifugal precipitation rate”, which is an index of protein dispersion stability, was calculated.
For each dispersion, 10 panelists were requested, and sensory evaluation was performed with respect to roughness, bitterness, and astringency (astringency) according to the criteria shown in Table 2 below, and an average value of evaluations given by each panel was calculated. 2. An average value of less than 1.5 points is evaluated as “A”, 1.5 points or more and less than 2.5 points is evaluated as “B”, 2.5 points or more and less than 3.5 points are evaluated as “C”, An evaluation “D” was given between 5 and 4 points.
T13~T16の通り、粉末状大豆蛋白素材C~Fを選択して大豆多糖類と組み合わせて用いた飲料は、加熱後も低粘度で遠心沈殿率が5%以下と少なく、ざらつき、粘性、苦味、渋味が少ない傾向であり、総合的に酸性蛋白質飲料としての適性を有していた。特に苦味と渋味が少ないT13~T15の粉末状大豆蛋白素材C~Eを用いた飲料が好ましかった。
一方、T10の通り、粉末状大豆蛋白素材として「フジプロ(R)F」(未分解/NSI90)を用いた飲料は遠心沈殿率とざらつきの点で不適であった。
またT11、T12の粉末状大豆蛋白素材A,Bを用いた飲料は、分解物であるがNSIが高すぎたためか、遠心沈殿率の点で蛋白質の分散安定性が悪く、ざらつきの点で食感が悪く不適であった。
逆にT17の粉末状大豆蛋白素材Gを用いた飲料は、分解度が50%と高すぎたためか、加熱後メジアン径,遠心沈殿率,苦味及び渋味の点で不適であった。また粉末状大豆蛋白素材Hを用いた飲料は、NSIと希酸NSIが高すぎるためか、加熱後粘度がかなり高くなり、また渋味の点でも不適であった。
このように、T13~T16の粉末状大豆蛋白素材C~F以外の粉末状蛋白素材を用いた例では、蛋白質の分散安定剤である大豆多糖類と組み合わせても酸性蛋白飲料としての適性がなかった。
以上より、大豆多糖類と組み合わせて使用する粉末状蛋白素材としては、特定の範囲の分解度、NSI及び希酸NSIを有するものを選択することが、酸性蛋白飲料に適していた。 (Discussion)
As shown in T13 to T16, beverages selected from powdered soy protein materials C to F and used in combination with soy polysaccharides have a low viscosity even after heating and a low centrifugal sedimentation rate of 5% or less, and are rough, viscous and bitter. The astringency tends to be low, and it has an overall suitability as an acidic protein beverage. In particular, beverages using T13 to T15 powdered soy protein materials C to E with little bitterness and astringency were preferred.
On the other hand, as T10, as a powdery soybean protein material "Fujipuro (R) F '(undecomposed / NSI90) beverages with was unsuitable in terms of roughness and spun rate.
In addition, beverages using powdered soy protein materials A and B of T11 and T12 are degraded products, but the NSI was too high, or the dispersion stability of the protein is poor in terms of centrifugal sedimentation rate. The feeling was bad and unsuitable.
Conversely, beverages using T17 powdered soy protein material G were unsuitable in terms of median diameter after heating, centrifugal sedimentation rate, bitterness and astringency, probably because the degree of degradation was too high at 50%. Moreover, the drink using the powdery soybean protein raw material H was not suitable in terms of astringency because the NSI and dilute acid NSI were too high, and the viscosity after heating was considerably high.
Thus, in the examples using powdered protein materials other than T13 to T16 powdered soy protein materials C to F, there is no suitability as an acidic protein beverage even when combined with soy polysaccharide which is a protein dispersion stabilizer. It was.
From the above, it was suitable for acidic protein beverages to select a powdered protein material to be used in combination with soybean polysaccharide having a specific range of degree of degradation, NSI and dilute acid NSI.
粉末状大豆蛋白素材Dを使用し、大豆多糖類の代わりにHMペクチン、カルボキシメチルセルロースナトリウム(CMC-Na)を使用する以外は、試験例2と同様にして酸性の蛋白質分散液を調製し、物性測定と官能評価を行った。結果を表4に示した。 ■ Test Example 3 (Tests T19 to T20)
An acidic protein dispersion was prepared in the same manner as in Test Example 2, except that powdered soy protein material D was used and HM pectin and sodium carboxymethylcellulose (CMC-Na) were used instead of soy polysaccharide. Measurement and sensory evaluation were performed. The results are shown in Table 4.
T19,T20の通り、粉末状大豆蛋白素材DにHMペクチンやCMC-Naを組み合わせても、酸性蛋白飲料として不適な点が確認された。T19では得られる酸性蛋白飲料粘度が著しく上昇し、非常に粘性の強い飲み口であり、すっきりとした飲み口とはならなかった。T20では加熱後メジアン径が大きく、ざらつきが生じ、更に遠心沈澱量が多いため蛋白質の分散安定性が低く、製品の外観を損なうなどの点で不適であった。 (Discussion)
As shown in T19 and T20, even when HM pectin or CMC-Na was combined with the powdered soy protein material D, it was confirmed that it was not suitable as an acidic protein beverage. At T19, the viscosity of the obtained acidic protein beverage was remarkably increased, and it was a very viscous drinking mouth and did not become a clean drinking mouth. At T20, the median diameter after heating was large, roughening occurred, and the amount of centrifugal precipitation was large, so that the dispersion stability of the protein was low, and this was unsuitable in that the appearance of the product was impaired.
大豆多糖類50gを水950gに加え、80℃で20分間撹拌溶解後、20℃まで冷却し、5%大豆多糖類溶液を得た。次いで常温水560gに5%大豆多糖類溶液200gを撹拌混合後、表1の分解度が23%の粉末状大豆蛋白素材E28gを混合し均一に分散させた。次いで、グラニュー糖90gと果糖ブドウ糖液糖70gを混合し各原料が均一に分散するまで撹拌した。その後、50%クエン酸溶液でpHを4.0に調整した後、水で全量を1000gとし、150kg/cm2にて均質化を施した。均質化された分散液を90℃、20分間の条件にて殺菌し、容器に充填後、冷却し、蛋白質2.5%を含有する酸性蛋白質飲料を得た。実施例1の飲料配合を表5にまとめた。 ■ Example 1 (Prescription example of acidic protein beverage)
50 g of soybean polysaccharide was added to 950 g of water, stirred and dissolved at 80 ° C. for 20 minutes, and then cooled to 20 ° C. to obtain a 5% soybean polysaccharide solution. Next, 200 g of a 5% soybean polysaccharide solution was stirred and mixed with 560 g of room temperature water, and then 28 g of powdered soybean protein material E having a degradation degree of 23% shown in Table 1 was mixed and dispersed uniformly. Next, 90 g of granulated sugar and 70 g of fructose-glucose liquid sugar were mixed and stirred until each raw material was uniformly dispersed. Then, after adjusting pH to 4.0 with a 50% citric acid solution, the total amount was made 1000 g with water, and homogenization was performed at 150 kg / cm 2 . The homogenized dispersion was sterilized at 90 ° C. for 20 minutes, filled into a container and then cooled to obtain an acidic protein beverage containing 2.5% protein. Table 5 summarizes the beverage formulation of Example 1.
大豆多糖類100gを水900gに加え、80℃で20分間撹拌溶解後、20℃まで冷却し、10%大豆多糖類溶液を得た。次いで常温水500gを撹拌中に10%大豆多糖類溶液100gを撹拌混合した。次いで表1の分解度が23%の粉末状大豆蛋白素材E55gとグラニュー糖76g、デキストリン80gを粉粉混合し、大豆多糖類を含む常温水に混合し各原料が均一に分散するまで撹拌した。その後、50%クエン酸溶液でpHを4.0に調整した後、別途表5の配合で調製したミネラル溶液100gを加え、十分撹拌した。次いで菜種油25gを投入し、ホモミキサーで7000rpmにて10分間予備乳化を行い、最終的に水で全量を1000gとした後、1段目450kg/cm2、2段目50kg/cm2にて均質化を施した。均質化された分散液を90℃,20分間の条件にて殺菌し、容器に密封充填後、冷却し、蛋白質5%を含有する酸性経腸栄養剤を得た。実施例2の飲料配合を表6にまとめた。 ■ Example 2 (Prescription example of acidic enteral nutrient)
100 g of soybean polysaccharide was added to 900 g of water, stirred and dissolved at 80 ° C. for 20 minutes, and then cooled to 20 ° C. to obtain a 10% soybean polysaccharide solution. Subsequently, 100 g of a 10% soybean polysaccharide solution was stirred and mixed while 500 g of normal temperature water was stirred. Next, powdery soybean protein material E55 g having a decomposition degree of 23% in Table 1 and 76 g of granulated sugar and 80 g of dextrin were mixed with powder, mixed in room temperature water containing soybean polysaccharide, and stirred until each raw material was uniformly dispersed. Then, after adjusting pH to 4.0 with a 50% citric acid solution, 100 g of a mineral solution prepared separately according to the formulation shown in Table 5 was added and sufficiently stirred. Then charged rapeseed 25 g, performed 7000rpm for 10 minutes pre-emulsified with a homomixer, after finally the total volume of water was 1000 g, homogenized in 1 stage 450 kg / cm 2, 2-stage 50 kg / cm 2 Was applied. The homogenized dispersion was sterilized at 90 ° C. for 20 minutes, sealed and filled in a container, and then cooled to obtain an acidic enteral nutrient containing 5% protein. Table 6 summarizes the beverage formulation of Example 2.
実施例1の配合において、50%クエン酸溶液をpH3.4(実施例3)及びpH4.5(実施例4)にそれぞれ調整する以外は、実施例1と同様にして酸性蛋白飲料を得た。これらの飲料は、いずれも実施例1と同様に良好な食感と蛋白質の良好な分散安定性を有していた。 ■ Examples 3 and 4
In the formulation of Example 1, an acidic protein beverage was obtained in the same manner as in Example 1 except that the 50% citric acid solution was adjusted to pH 3.4 (Example 3) and pH 4.5 (Example 4), respectively. . Each of these beverages had a good texture and good dispersion stability of the protein as in Example 1.
Claims (15)
- 蛋白質を含有する原料の少なくとも一つが、下記a)~c)の要件を満たす粉末状蛋白素材であって、蛋白質含量が1重量%以上であり、かつ大豆多糖類又は/及びエンドウ多糖類を蛋白質の分散安定剤として含み、液状であってかつpH3~5であることを特徴とする、酸性蛋白質飲料。
a)該粉末状蛋白素材が蛋白質加水分解物であり、該加水分解度が0.22Mトリクロロ酢酸(TCA)可溶率として10~35%、
b)該粉末状蛋白素材の窒素溶解指数(NSI)が10~80、
c)該粉末状蛋白素材の希酸NSIが10~70。 At least one of the raw materials containing protein is a powdered protein material that satisfies the following requirements a) to c), the protein content is 1% by weight or more, and soybean polysaccharide and / or pea polysaccharide is protein An acidic protein beverage characterized in that it is liquid and has a pH of 3 to 5.
a) the powdered protein material is a protein hydrolyzate, and the degree of hydrolysis is 10 to 35% as 0.22M trichloroacetic acid (TCA) solubility;
b) Nitrogen solubility index (NSI) of the powdered protein material is 10 to 80,
c) The dilute acid NSI of the powdered protein material is 10 to 70. - 該酸性蛋白質飲料の蛋白質含量が、1~20重量%である、請求項1記載の酸性蛋白質飲料。 The acidic protein beverage according to claim 1, wherein the protein content of the acidic protein beverage is 1 to 20% by weight.
- 該粉末状蛋白素材の乾物あたりの蛋白質含量が40重量%以上である、請求項2記載の酸性蛋白質飲料。 The acidic protein beverage according to claim 2, wherein the protein content per dry matter of the powdered protein material is 40% by weight or more.
- 該粉末状蛋白素材の乾物あたりの不溶性食物繊維の含量が2重量%以下である、請求項3記載の酸性蛋白質飲料。 The acidic protein beverage according to claim 3, wherein the content of insoluble dietary fiber per dry matter of the powdered protein material is 2% by weight or less.
- 該粉末状蛋白素材の5重量%分散液を、分光光度計により600nmで測定したときの透過率が1%T以下である、請求項4記載の酸性蛋白質飲料。 The acidic protein beverage according to claim 4, which has a transmittance of 1% T or less when a 5 wt% dispersion of the powdered protein material is measured at 600 nm with a spectrophotometer.
- 該粉末状蛋白素材が大豆、エンドウ、緑豆及び乳から選ばれる1以上の由来である、請求項5記載の酸性蛋白質飲料。 The acidic protein beverage according to claim 5, wherein the powdered protein material has one or more origins selected from soybeans, peas, mung beans and milk.
- 該飲料を700×Gで20分間の条件にて遠心分離したときの遠心沈殿率が5重量%以下である、請求項1記載の酸性蛋白質飲料。 The acidic protein beverage according to claim 1, wherein the centrifugal precipitation rate is 5 wt% or less when the beverage is centrifuged at 700 × G for 20 minutes.
- 該飲料中に分散された粒子の平均粒子径が5μm以下である、請求項1記載の酸性蛋白質飲料。 The acidic protein beverage according to claim 1, wherein the average particle size of the particles dispersed in the beverage is 5 μm or less.
- 該飲料の粘度が50mPa/s以下である、請求項1記載の酸性蛋白質飲料。 The acidic protein drink of Claim 1 whose viscosity of this drink is 50 mPa / s or less.
- 該飲料が経腸栄養剤である、請求項1記載の酸性蛋白質飲料。 The acidic protein beverage according to claim 1, wherein the beverage is an enteral nutrient.
- 該飲料が密封容器に充填され密封されている、請求項1記載の酸性蛋白質飲料。 The acidic protein beverage according to claim 1, wherein the beverage is filled and sealed in a sealed container.
- 該粉末状蛋白素材が大豆、エンドウ及び緑豆から選ばれる1以上の由来であり、該飲料を700×Gで20分間の条件にて遠心分離したときの遠心沈殿率が5重量%以下である、請求項5記載の酸性蛋白質飲料。 The powdered protein material is derived from one or more selected from soybeans, peas and mung beans, and the centrifugal sedimentation rate when the beverage is centrifuged at 700 × G for 20 minutes is 5% by weight or less. The acidic protein drink according to claim 5.
- 該飲料中に分散された粒子の平均粒子径が5μm以下である、請求項12記載の酸性蛋白質飲料。 The acidic protein beverage according to claim 12, wherein the average particle size of the particles dispersed in the beverage is 5 µm or less.
- 該飲料の粘度が50mPa/s以下である、請求項13記載の酸性蛋白質飲料。 The acidic protein drink of Claim 13 whose viscosity of this drink is 50 mPa / s or less.
- 該飲料が経腸栄養剤であり、かつ該飲料が密封容器に充填され密封されている、請求項14記載の酸性蛋白質飲料。 The acidic protein beverage according to claim 14, wherein the beverage is an enteral nutrient, and the beverage is filled and sealed in a sealed container.
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Also Published As
Publication number | Publication date |
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MY178433A (en) | 2020-10-13 |
CN107105723A (en) | 2017-08-29 |
JP6673210B2 (en) | 2020-03-25 |
TW201613491A (en) | 2016-04-16 |
JPWO2016056366A1 (en) | 2017-07-20 |
KR102522320B1 (en) | 2023-04-14 |
SG11201702875XA (en) | 2017-05-30 |
TWI635805B (en) | 2018-09-21 |
KR20170069204A (en) | 2017-06-20 |
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