WO2013047613A1 - Containerized beverage - Google Patents

Containerized beverage Download PDF

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Publication number
WO2013047613A1
WO2013047613A1 PCT/JP2012/074775 JP2012074775W WO2013047613A1 WO 2013047613 A1 WO2013047613 A1 WO 2013047613A1 JP 2012074775 W JP2012074775 W JP 2012074775W WO 2013047613 A1 WO2013047613 A1 WO 2013047613A1
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Prior art keywords
mass
isoquercitrin
aftertaste
less
component
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PCT/JP2012/074775
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French (fr)
Japanese (ja)
Inventor
俊 迫田
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花王株式会社
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    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L2/00Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
    • A23L2/52Adding ingredients
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L2/00Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
    • A23L2/52Adding ingredients
    • A23L2/68Acidifying substances

Definitions

  • the present invention relates to a packaged beverage.
  • Isoquercitrin is a flavonol glycoside in which one glucose is ⁇ -bonded at the 3-position of quercetin. Isoquercitrin has a strong antioxidant activity and is known to prevent discoloration of the pigment (Patent Document 1), and is also expected to act on the living body such as anti-arteriosclerosis and blood flow improvement. ing.
  • isoquercitrin is poorly soluble in water and thus works effectively in vitro, but is not sufficiently effective in vivo and has limited use as a water-based composition for beverages and the like. Therefore, in order to improve the solubility in water, “enzyme-treated isoquercitrin” obtained by allowing glycosyltransferase to act on isoquercitrin in the presence of starch is proposed (Patent Document 2). “Enzyme-treated isoquercitrin” is a mixture of isoquercitrin and ⁇ -glucosylisoquercitrin in which one or more glucoses are further added to the glucose residue of isoquercitrin with an ⁇ -1,4 bond.
  • Non-patent Document 3 a quercetin glycoside composition in which the composition of ⁇ -glucosyl isoquercitrin contained in enzyme-treated isoquercitrin is changed by fractionation to further enhance oral absorbability. Recently, it has been found that isoquercitrin has an action to reduce body fat of obese people, and it is reported that it is effective when ingested in the form of a beverage (Non-patent Document 1).
  • the present invention includes the following components (A) and (B): (A) Isoquercitrin and its sugar adduct 0.03-0.17% by mass, (B) Amino acids 0.0001-2% by mass And a packaged beverage having a pH of 2 to 5.
  • the present invention is a method for improving the aftertaste of a container-packed beverage containing isoquercitrin and its sugar adduct, wherein the following components (A) and (B) are: (A) Isoquercitrin and its sugar adduct 0.03-0.17% by mass, (B) Amino acids 0.0001-2% by mass The aftertaste is improved by adjusting the pH to 2-5.
  • the present invention is to provide a packaged beverage containing a high concentration of isoquercitrin and its sugar adduct and having a sour aftertaste and a bitter astringent aftertaste. Moreover, this invention is providing the improvement method of the aftertaste of the container-packed drink containing a high concentration isoquercitrin and its sugar adduct.
  • the inventor of the present invention contains an amino acid together with isoquercitrin and its sugar adduct, and controls the content and pH of each component in the container-packed beverage within a specific range, so that the aftertaste of bitterness and bitterness is obtained. It was found that a refreshing and easy-to-drink beverage can be obtained.
  • the present invention it is possible to provide a packaged beverage containing isoquercitrin and its sugar adduct that are refreshed and easy to drink, with a sour aftertaste and a bitter and bitter aftertaste suppressed. Moreover, according to this invention, the improvement method of the aftertaste of the container-packed drink containing a high concentration isoquercitrin and its sugar adduct can be provided.
  • the container-packed beverage of the present invention contains 0.03 to 0.17% by mass of (A) isoquercitrin and a sugar adduct thereof (hereinafter also referred to as “isoquercitrin sugar adduct etc.”).
  • the upper limit of the content of the component (A) is 0.15% by mass or less, further 0.12% by mass or less, and further 0.1% by mass or less from the viewpoint of suppressing the sour aftertaste and bitterness aftertaste. Is preferred.
  • content of a component (A) is 0.04 mass% or more from a viewpoint of a physiological effect, Furthermore, 0.05 mass% or more, Furthermore, 0.06 mass% or more is preferable.
  • the range of the content of component (A) is 0.04 to 0.15% by mass, further 0.05 to 0.12% by mass, further 0.06 to 0.12% by mass, and further 0.06 to 0%. .1% by mass is preferable.
  • Isoquercitrin is obtained by ⁇ -bonding one glucose at the 3-position of quercetin (quercetincet3-O- ⁇ -D-glucopyranoside).
  • the isoquercitrin sugar adduct can be obtained, for example, by allowing glycosyltransferase to act on isoquercitrin in the presence of a sugar donor (glucose source), and adding one or more glucose to the glucose residue of isoquercitrin.
  • ⁇ -Glucosylisoquercitrin further added with ⁇ -1,4 bond (FFI Journal, Vol.209, No.7, 2004, p.622-628; Food Hygiene Journal, Vol.41, No. .1, p.54-60).
  • the component (A) includes isoquercitrin in which the number of glucose residues (n) is 0 in the following formula (1) and an integer in which the number of glucose residues (n) is 1 or more (preferably A mixture with an isoquercitrin sugar adduct which is an integer of 1 to 15, more preferably an integer of 1 to 10, and still more preferably an integer of 1 to 8.
  • Glc represents a glucose residue
  • n represents 0 or an integer of 1 or more.
  • the mass ratio of isoquercitrin sugar adduct / isoquercitrin in component (A) is preferably 1 or more, more preferably 2 or more, and particularly preferably 4 or more, from the viewpoint of water solubility.
  • the mass ratio is preferably 1000 or less, further 500 or less, further 100 or less, further 50 or less, further 25 or less, and further 10 or less from the viewpoint of production efficiency.
  • the range of the mass ratio is preferably 1 to 1000, further 1 to 500, further 1 to 100, further 1 to 50, further 1 to 25, further 1 to 10, further 2 to 10, and further 4 to 10.
  • Such (A) isoquercitrin sugar adducts and the like are commercially available.
  • Sanmerin AO-1007, Sanmerin Powder C-10 and the like (manufactured by Saneigen FFI Co., Ltd.) Can be mentioned.
  • glycosyltransferases used for glycosylation of isoquercitrin include glucosidases such as ⁇ -amylase (EC 3.2.1.1) and ⁇ -glucosidase (EC 3.2.1.20), and cyclodextrin glucanotransferase (EC). And transglucosidase such as 2.4.1.19).
  • glycosyltransferases are all commercially available, and examples thereof include contizyme (manufactured by Amano Enzyme).
  • the amount of glycosyltransferase used is not uniform depending on the type of enzyme and the desired composition.
  • cyclodextrin glucanotransferase [enzyme specific activity of about 100 units ( ⁇ -cyclodextrin from soluble starch per 1 minute per minute)
  • the amount of enzyme produced is defined as 1 unit)] is usually 0.001 to 20 parts by weight, preferably 0.005 to 10 parts by weight, more preferably 0.01 to 10 parts by weight per 1 part by weight of isoquercitrin. 5 parts by mass.
  • the sugar donor (glucose source) used for glycosylation is not particularly limited as long as one or more molecules of the glucose residue can be transferred to one molecule of isoquercitrin.
  • the amount of glucose used is usually 0.1 to 20 parts by weight, preferably 0.5 to 15 parts by weight, and more preferably 1 to 10 parts by weight with respect to 1 part by weight of isoquercitrin.
  • composition of the resulting (A) isoquercitrin sugar adduct is not uniform depending on the reaction conditions.
  • the temperature is 80 ° C. or less, preferably 20 to 80 ° C., more preferably 40 to 75 ° C., pH 3 to 11
  • various compositions can be obtained by allowing glycosyltransferase to act on isoquercitrin in the presence of a sugar donor (glucose source), preferably under conditions of pH 4-8.
  • the analysis method of (A) isoquercitrin sugar adduct and the like shall follow the method described in the examples described later.
  • the above reaction can be performed while standing or stirring or shaking.
  • the head space of the reaction system may be replaced with an inert gas such as nitrogen, and an antioxidant such as ascorbic acid may be added to the reaction system.
  • Isoquercitrin sugar adducts and the like can be prepared starting from rutin as well as using isoquercitrin as a raw material as described above. For example, ⁇ -1,6-rhamnosidase (EC 3.2.1.40) is allowed to act on rutin to convert it to isoquercitrin, and then (A) an isoquercitrin sugar adduct is prepared according to the above-mentioned method. it can.
  • ⁇ -1,6-rhamnosidase is commercially available, and examples thereof include hesperidinase, naringinase (manufactured by Tanabe Seiyaku Co., Ltd.), and cellulase A “Amano” 3 (manufactured by Amano Enzyme).
  • isoquercitrin sugar adducts where n is 0 and isoquercitrin sugar adducts where n is 4 or more are reduced by fractionation and rich in isoquercitrin sugar adducts where n is 3
  • the fraction contained in may be collected and used.
  • the container-packed beverage of the present invention contains (A) an isoquercitrin sugar adduct or the like so as to be 0.01 to 0.07% by mass in terms of quercetin, so as to suppress the sour aftertaste and the aftertaste of bitter astringency. From the viewpoint of physiological effect, it is preferably 0.06% by mass or less, more preferably 0.05% by mass or less, and further preferably 0.04% by mass or less. 0.021% by mass or more, more preferably 0.025% by mass or more.
  • the content range of the component (A) is preferably 0.016 to 0.06% by mass, more preferably 0.021 to 0.05% by mass, and further preferably 0.025 to 0.04% by mass in terms of quercetin.
  • the container-packed beverage of the present invention contains (B) an amino acid in order to suppress the sour aftertaste and the aftertaste of bitter astringency.
  • amino acid any of acidic amino acid, neutral amino acid and basic amino acid can be used, and it may be a single optically active substance or a racemic body.
  • neutral amino acid refers to an amino acid having a nitrogen-containing basic group such as an amino group, an imino group, or a guanidyl group and one carboxyl group in one molecule.
  • “Amino acid” means an amino acid having more carboxyl groups than the nitrogen-containing basic group in one molecule, and “basic amino acid” has more nitrogen-containing basic groups than a carboxyl group in one molecule.
  • Examples of acidic amino acids include aspartic acid and glutamic acid.
  • Examples of neutral amino acids include leucine, proline, glycine, sarcosine, ⁇ -alanine, ⁇ -alanine, N-methyl- ⁇ -alanine, glutamine, asparagine, isoleucine, epsilon-aminocaproic acid, ⁇ -aminobutyric acid, Examples thereof include glycylglycine, cysteine, cystine, creatine, serine, tyrosine, tryptophan, threonine, valine, phenylalanine, proline, hydroxyproline, and methionine.
  • basic amino acids include lysine, arginine, ornithine, hydroxylysine, and histidine. These can be used alone or in combination of two or more. Among these, a neutral amino acid is preferable and leucine and proline are more preferable from the viewpoint of further improving the aftertaste of bitterness and bitterness.
  • the content of the amino acid (B) in the packaged beverage of the present invention is 0.0001 to 2% by mass, but preferably 1.9% by mass from the viewpoint of further suppressing the aftertaste of bitterness and bitterness.
  • % Or less more preferably 1.5% by mass or less, still more preferably 1.2% by mass or less, still more preferably 1% by mass or less, still more preferably 0.5% by mass or less, and even more preferably 0.3% by mass or less.
  • it is preferably 0.001% by mass or more, more preferably 0.005% by mass or more, further preferably 0.01% by mass or more, and still more preferably 0.02% by mass or more.
  • the range of the content of component (B) is from 0.001 to 1.9% by mass, more preferably from 0.005 to 1.5% by mass, and further preferably from the viewpoint of suppressing the sour aftertaste and the aftertaste of bitter and astringent taste. It is preferably 01 to 1.2% by mass, more preferably 0.02 to 1% by mass, further 0.02 to 0.5% by mass, and further preferably 0.02 to 0.3% by mass.
  • the content mass ratio [(B) / (A)] of the component (A) and the component (B) in the packaged beverage of the present invention is preferably from the viewpoint of suppressing the aftertaste of bitter and astringent taste. 20 or less, more preferably 10 or less, still more preferably 5 or less, still more preferably 3 or less, still more preferably 2 or less, still more preferably 1.5 or less, even more preferably 1 or less, and preferably 0.01 or more More preferably, it is 0.02 or more, More preferably, it is 0.05 or more, More preferably, it is 0.1 or more, Most preferably, it is 0.2 or more.
  • the range of the mass ratio [(B) / (A)] is preferably 0.01 to 20, more preferably 0.01 to 10, further 0.01 to 5, and more preferably 0.01 to 3. Further, it may be 0.02 to 2, further 0.05 to 1.5, further 0.1 to 1, and particularly 0.2 to 1.
  • the container-packed drink of this invention can be made to contain a sweetener.
  • sweeteners include, for example, monosaccharides such as fructose, glucose, tagatose, and arabinose, disaccharides such as lactose, trehalose, maltose, and sucrose; Oligosaccharides, non-crystalline saccharides such as syrup, and honey and the like in which sugars such as glucose and fructose account for about 70%.
  • These sweeteners can be used alone or in combination of two or more.
  • the content of the sweetener in the packaged beverage of the present invention can be appropriately determined, but is 0.02 to 1% by mass, further 0.05 to 0.8% by mass, and further 0.05 to 0. 0%. It is preferable that it is 6 mass% from the point of suppression of the sour aftertaste and the bitterness aftertaste.
  • the packaged beverage of the present invention can contain a high-intensity sweetener.
  • the “high-intensity sweetener” is a general term for sweeteners having a sweetness stronger than that of sucrose, and includes natural sweeteners and synthetic sweeteners. Specific examples include sucralose, stevia, licorice extract, thaumatin, glycyrrhizin, disodium glycyrrhizinate, ammonium glycyrrhizinate, saccharin, saccharin sodium, aspartame, acesulfame K, alitame, neotame and the like. These can be used alone or in combination of two or more.
  • the content of the high-intensity sweetener in the packaged beverage of the present invention can be appropriately selected depending on the type thereof, but is preferably 0.0001 to 0.00 in terms of suppressing the sour aftertaste and the aftertaste of bitter astringency. It is 5% by mass, more preferably 0.0001 to 0.25% by mass, and still more preferably 0.0001 to 0.1% by mass.
  • the content is preferably 1% by mass or less, more preferably 0.1 to 0.9% by mass, and still more preferably 0.2 to 0.8% by mass. %, More preferably 0.3 to 0.7% by mass.
  • a measuring method of a carbon dioxide gas it can measure with a gas volume meter and can convert into gas mass.
  • the gas volume refers to the ratio of the gas volume at 20 ° C. of the carbon dioxide dissolved in the beverage to the beverage volume.
  • the container-packed drink of this invention can contain a potassium ion.
  • the refreshing feeling is not diluted even during long-term storage, the refreshing feeling in the mouth is maintained, and it contributes to suppressing the after-taste of acidity and bitterness.
  • Potassium ions as potassium salts such as potassium chloride, potassium carbonate, potassium sulfate, potassium acetate, potassium bicarbonate, potassium citrate, potassium phosphate, potassium hydrogen phosphate, potassium tartrate, potassium sorbate etc. or mixtures thereof Can be blended.
  • the potassium ions include those derived from raw materials.
  • the content of potassium ions in the packaged beverage of the present invention is preferably 0.001% by mass or more, more preferably 0.002% by mass or more, still more preferably 0.003% by mass or more, and further preferably 0.005.
  • % By mass or more, particularly preferably 0.01% by mass or more, and preferably 0.2% by mass or less, more preferably 0.1% by mass or less, still more preferably 0.09% by mass or less, still more preferably 0%. 0.08% by mass or less, particularly preferably 0.07% by mass or less.
  • the range of the potassium ion content is preferably 0.001 to 0.2% by mass, more preferably 0.002 to 0.1% by mass, further 0.003 to 0.09%, and further 0.005 to 0.08. % By mass, especially 0.01 to 0.07% by mass is preferred.
  • acidulant such as preservatives, seasonings excluding amino acids, fruit juice, cereal extract, malt extract, vegetable extract, nectar extract, and quality stabilizer can be used alone or in combination of two or more.
  • content of an additive can be suitably selected within the range which does not prevent the objective of this invention.
  • the pH (20 ° C.) of the packaged beverage of the present invention is 2 to 5, but 3 to 4 is preferred from the viewpoint of further suppressing the aftertaste of bitterness and bitterness.
  • the container-packed beverage of the present invention preferably has a low viscosity in a container-packed state.
  • it is preferably not a high-viscosity food having shape-retaining properties such as jelly, but a viscosity that allows it to flow and be drunk only by tilting the container.
  • the specific viscosity is preferably 0.01 to 500 mPa ⁇ s, more preferably 0.01 to 400 mPa ⁇ s, and particularly preferably 0.01 to 200 mPa ⁇ s when measured at 20 ° C. with a vibration viscometer. .
  • the container-packed beverage of the present invention can be produced by, for example, blending the component (A) and the component (B) and adjusting the concentration and pH of each component.
  • a container which can be used for the container-packed beverage of the present invention a molded container mainly composed of polyethylene terephthalate (so-called PET bottle), a metal can, a paper container combined with a metal foil or a plastic film, a bottle or the like is used.
  • PET bottle polyethylene terephthalate
  • a packaging container is mentioned.
  • heat sterilization such as a metal can can be performed, it can be sterilized under the conditions stipulated in the applicable regulations (the Food Sanitation Law in Japan).
  • those that cannot be sterilized by retort such as PET bottles and paper containers, are preliminarily sterilized at a high temperature and short time using a plate heat exchanger, for example, and then cooled to a certain temperature and filled into containers. Etc. can be adopted. Moreover, you may mix
  • the container-packed drink of this invention was demonstrated, the structure similar to the above is employable also in the improvement method of the aftertaste of the container-packed drink containing isoquercitrin and its sugar adduct.
  • this invention discloses the following container-packed drinks or the improvement method of a aftertaste.
  • the content of the component (A) is preferably 0.04% by mass or more, more preferably 0.05% by mass or more, still more preferably 0.06% by mass or more, preferably 0.15% by mass or less, More preferably, it is 0.12% by mass or less, and still more preferably 0.1% by mass or less, in the above-mentioned [1-1].
  • the content of component (A) is preferably 0.04 to 0.15% by mass, more preferably 0.05 to 0.12% by mass, still more preferably 0.06 to 0.12% by mass, still more preferably The packaged beverage according to [1-1], which is 0.06 to 0.1% by mass.
  • the mass ratio of isoquercitrin sugar adduct / isoquercitrin is preferably 1 or more, more preferably 2 or more, further preferably 4 or more, preferably 1000 or less, more preferably 500.
  • Component (A) has an isoquercitrin sugar adduct / isoquercitrin mass ratio of preferably 1 to 1000, more preferably 1 to 500, still more preferably 1 to 100, still more preferably 1 to 50, and still more preferably. Is from 1 to 25, more preferably from 1 to 10, more preferably from 2 to 10, and even more preferably from 4 to 10, The packaged beverage according to any one of [1-1] to [1-3] above . [1-6] The content of the component (A) is preferably 0.01 to 0.07% by mass, more preferably 0.016 to 0.06% by mass, and still more preferably 0.021 to 0.05% by mass in terms of quercetin.
  • [1-7] The packaged beverage according to any one of [1-1] to [1-6] above, wherein the component (B) is a neutral amino acid.
  • [1-8] The packaged beverage according to [1-7] above, wherein the neutral amino acid is leucine or proline.
  • the content of the component (B) is preferably 0.001% by mass or more, more preferably 0.005% by mass or more, further preferably 0.01% by mass or more, and further preferably 0.02% by mass or more.
  • the container-packed beverage according to any one of [1-1] to [1-8], in which is 0.3% by mass or less.
  • the content of component (B) is preferably 0.001 to 1.9% by mass, more preferably 0.005 to 1.5% by mass, still more preferably 0.01 to 1.2% by mass, still more preferably Any of [1-1] to [1-8], which is 0.02 to 1% by mass, further 0.02 to 0.5% by mass, and further 0.02 to 0.3% by mass. Bottled beverage.
  • the mass ratio [(B) / (A)] of the component (A) and the component (B) is preferably 0.01 or more, more preferably 0.02 or more, still more preferably 0.05 or more, Preferably it is 0.1 or more, more preferably 0.2 or more, preferably 20 or less, more preferably 10 or less, more preferably 5 or less, still more preferably 3 or less, still more preferably 2 or less, still more preferably.
  • the packaged beverage according to any one of [1-1] to [1-10], which is 1.5 or less, more preferably 1 or less.
  • the mass ratio [(B) / (A)] of the component (A) and the component (B) is preferably 0.01 to 20, more preferably 0.01 to 10, and still more preferably 0.01 to 5.
  • the mass ratio [(B) / (A)] of the component (A) and the component (B) is preferably 0.02 to 2, more preferably 0.05 to 1.5, still more preferably 0.00.
  • the packaged beverage according to any one of [1-1] to [1-10] which is 1-1, more preferably 0.2-1.
  • the high-intensity sweetener is one or more selected from sucralose, stevia, licorice extract, thaumatin, glycyrrhizin, disodium glycyrrhizinate, ammonium glycyrrhizinate, saccharin, sodium saccharin, aspartame, acesulfame K, aritem and neotame
  • the content of the high-intensity sweetener is preferably 0.0001 to 0.5% by mass, more preferably 0.0001 to 0.25% by mass, and still more preferably 0.0001 to 0.1% by mass.
  • carbon dioxide is contained, and the content of carbon dioxide is preferably 1% by mass or less, more preferably 0.1 to 0.9% by mass, still more preferably 0.2 to 0.8% by mass, and still more preferably.
  • the packaged beverage contains potassium ions, and the content of potassium ions is preferably 0.001% by mass or more, more preferably 0.002% by mass or more, still more preferably 0.003% by mass or more, and further preferably 0.
  • the packaged beverage contains potassium ions, and the content of potassium ions is preferably 0.001 to 0.2% by mass, more preferably 0.002 to 0.1% by mass, and still more preferably 0.003 to 0%.
  • a method for improving the aftertaste of a packaged beverage containing isoquercitrin and its sugar adduct comprising the following components (A) and (B): (A) Isoquercitrin and its sugar adduct 0.03-0.17% by mass, (B) Amino acids 0.0001-2% by mass The aftertaste is improved by adjusting the pH to 2-5.
  • the component (A) is preferably 0.04% by mass or more, more preferably 0.05% by mass or more, still more preferably 0.06% by mass or more, preferably 0.15% by mass or less, more preferably The method for improving the aftertaste according to [2-1], wherein the blending is performed so that the content is 0.12% by mass or less, more preferably 0.1% by mass or less.
  • the component (A) is preferably 0.04 to 0.15% by mass, more preferably 0.05 to 0.12% by mass, still more preferably 0.06 to 0.12% by mass, and still more preferably 0.06. The method for improving aftertaste according to the above [2-1], which is blended in an amount of 0.1 to 0.1% by mass.
  • Component (B) is preferably at least 0.001% by mass, more preferably at least 0.005% by mass, even more preferably at least 0.01% by mass, even more preferably at least 0.02% by mass, preferably 1.9% by mass or less, more preferably 1.5% by mass or less, further preferably 1.2% by mass or less, still more preferably 1% by mass or less, still more preferably 0.5% by mass or less, still more preferably 0.00%.
  • Component (B) is preferably 0.001 to 1.9% by mass, more preferably 0.005 to 1.5% by mass, still more preferably 0.01 to 1.2% by mass, and still more preferably 0.02%.
  • the component (A) and the component (B) have a mass ratio [(B) / (A)] of preferably 0.01 or more, more preferably 0.02 or more, still more preferably 0.05 or more, Preferably it is 0.1 or more, more preferably 0.2 or more, preferably 20 or less, more preferably 10 or less, more preferably 5 or less, still more preferably 3 or less, still more preferably 2 or less, still more preferably.
  • the mass ratio [(B) / (A)] of the component (A) and the component (B) is preferably 0.01 to 20, more preferably 0.01 to 10, and still more preferably 0.01 to 5.
  • a sample for analysis was prepared by the following procedure. 1 g of a sample was weighed, 1 mL of methanol was added, and a mixed solution of methanol and water (1: 1) was further added to make a constant volume of 10 mL to obtain a sample solution. The prepared sample solution was subjected to high performance liquid chromatographic analysis.
  • quercetin equivalent amount of isoquercitrin sugar adducts and the like in the sample was calculated by calculating the content of the aglycone part from the respective molar concentrations of isoquercitrin and each sugar adduct.
  • a sample for analysis was prepared by the following procedure. 1) 6 g of a sample was weighed, and 25 mL of a 10 w / v% sulfosalicylic acid solution was added thereto, followed by extraction (mixing), and then a 3 mol / L sodium hydroxide solution was added. 2) The solution was adjusted to pH 2.2, and sodium citrate buffer (pH 2.2) was further added to adjust the volume to 50 mL. 3) After filtering the solution, it was diluted with a sodium citrate buffer (pH 2.2) as necessary to obtain a sample solution. 4) The sample solution was subjected to an amino acid automatic analyzer.
  • Examples 1 to 18 and Comparative Examples 1 to 3 Prepared with the composition shown in Table 1, then sterilized at 85 ° C. for 2 minutes, and filled in a 200 mL PET bottle with 160 mL to prepare a packaged beverage. Table 1 shows the component analysis and evaluation results of each packaged beverage.
  • the (A) isoquercitrin sugar adduct and the like (B) contain amino acids and control the concentration and pH of each component within a specific range, thereby suppressing the aftertaste of bitterness and bitterness. It was confirmed that a container-packed beverage that was clean and easy to drink was obtained.

Abstract

Provided is a containerized beverage containing a high concentration of isoquercitin and sugar adducts thereof, reducing the acidic aftertaste and the bitter, astringent aftertaste. This containerized beverage contains the following components (A) and (B): (A) 0.03-0.17 mass% of isoquercitin and sugar adducts thereof, and (B) 0.0001-2 mass% of an amino acid; and has pH of 2-5.

Description

容器詰飲料Container drink
 本発明は、容器詰飲料に関する。 The present invention relates to a packaged beverage.
 イソクエルシトリンは、ケルセチンの3位にグルコース1つがβ結合したフラボノール配糖体である。イソクエルシトリンは、強力な抗酸化活性を有し、色素の退色を防止することが知られており(特許文献1)、また、抗動脈硬化、血流改善等の生体への作用も期待されている。 Isoquercitrin is a flavonol glycoside in which one glucose is β-bonded at the 3-position of quercetin. Isoquercitrin has a strong antioxidant activity and is known to prevent discoloration of the pigment (Patent Document 1), and is also expected to act on the living body such as anti-arteriosclerosis and blood flow improvement. ing.
 しかしながら、イソクエルシトリンは水に難溶であるため生体外では有効に作用するものの、生体内における効果が十分ではなく、飲料等の水系の組成物としての利用が制限されるという問題あった。そこで、水への溶解性を改善すべく、イソクエルシトリンにでん粉質の存在下、糖転移酵素を作用させて得られる「酵素処理イソクエルシトリン」が提案されている(特許文献2)。「酵素処理イソクエルシトリン」は、イソクエルシトリンと、イソクエルシトリンのグルコース残基に1以上のグルコースをα-1,4結合で更に付加したα-グルコシルイソクエルシトリンとの混合物である。 However, isoquercitrin is poorly soluble in water and thus works effectively in vitro, but is not sufficiently effective in vivo and has limited use as a water-based composition for beverages and the like. Therefore, in order to improve the solubility in water, “enzyme-treated isoquercitrin” obtained by allowing glycosyltransferase to act on isoquercitrin in the presence of starch is proposed (Patent Document 2). “Enzyme-treated isoquercitrin” is a mixture of isoquercitrin and α-glucosylisoquercitrin in which one or more glucoses are further added to the glucose residue of isoquercitrin with an α-1,4 bond.
 また、酵素処理イソクエルシトリンに含まれるα-グルコシルイソクエルシトリンの組成を分画により変化させて、経口吸収性を更に高めたケルセチン配糖体組成物も提案されている(特許文献3)。そして、最近になりイソクエルシトリンには肥満者の体脂肪を低減させる作用があることが見出され、飲料の形態で摂取させて効果があることが報告されている(非特許文献1)。 Also proposed is a quercetin glycoside composition in which the composition of α-glucosyl isoquercitrin contained in enzyme-treated isoquercitrin is changed by fractionation to further enhance oral absorbability (Patent Document 3). Recently, it has been found that isoquercitrin has an action to reduce body fat of obese people, and it is reported that it is effective when ingested in the form of a beverage (Non-patent Document 1).
特開2008-131888号公報JP 2008-131888 A 特開平1-213293号公報JP-A-1-213293 国際公開第2006/070883号パンフレットInternational Publication No. 2006/070883 Pamphlet
 本発明は、次の成分(A)及び(B):
(A)イソクエルシトリン及びその糖付加物 0.03~0.17質量%、
(B)アミノ酸 0.0001~2質量%
を含有し、pHが2~5である容器詰飲料を提供するものである。
The present invention includes the following components (A) and (B):
(A) Isoquercitrin and its sugar adduct 0.03-0.17% by mass,
(B) Amino acids 0.0001-2% by mass
And a packaged beverage having a pH of 2 to 5.
 また、本発明は、イソクエルシトリン及びその糖付加物を含有する容器詰飲料の後味の改善方法であって、次の成分(A)及び(B)を、
(A)イソクエルシトリン及びその糖付加物 0.03~0.17質量%、
(B)アミノ酸 0.0001~2質量%
となるように配合し、pHを2~5に調整する、後味の改善方法を提供するものである。
Further, the present invention is a method for improving the aftertaste of a container-packed beverage containing isoquercitrin and its sugar adduct, wherein the following components (A) and (B) are:
(A) Isoquercitrin and its sugar adduct 0.03-0.17% by mass,
(B) Amino acids 0.0001-2% by mass
The aftertaste is improved by adjusting the pH to 2-5.
 イソクエルシトリンの生理作用を、より効果的に発現させるためには、酵素処理等によりイソクエルシトリンに糖を付加させてその摂取量及び体内吸収量を増やすことが有効であり、また、それを簡便に達成可能とする手段として飲料の形態とすることが挙げられる。
 本発明者は、酵素処理イソクエルシトリンを含有する飲料を開発すべく検討を行った。その結果、酵素処理イソクエルシトリンを飲料に配合し、それを高濃度化するに従い酸味や苦渋味が後に引きやすくなるため、高濃度の酵素処理イソクエルシトリンを飲料として継続摂取することは困難であることが判明した。一方、低水分の食品や、ゼリー等の高粘度食品においては、酵素処理イソクエルシトリンの含有量を高濃度化しても後味に酸味及び苦渋味が残らないことも確認された。このように、酵素処理イソクエルシトリンを含有する飲食品において、酸味の後味及び苦渋味の後味は低粘度の飲料の形態に特有の課題であることが判明した。なお、本明細書において「後味」とは、JIS Z 8144:2004に記載の「口内に残る感覚」をいう。
In order to express the physiological action of isoquercitrin more effectively, it is effective to add sugar to isoquercitrin by enzyme treatment or the like to increase its intake and absorption by the body. As a means that can be easily achieved, there is a form of a beverage.
The present inventor studied to develop a beverage containing enzyme-treated isoquercitrin. As a result, it is difficult to continuously ingest high-concentration enzyme-treated isoquercitrin as a beverage because enzyme-treated isoquercitrin is blended in beverages, and as it is concentrated, acidity and bitterness become easier to pull later. It turned out to be. On the other hand, in low-moisture foods and high-viscosity foods such as jelly, it was also confirmed that no sour and bitter taste remained in the aftertaste even when the concentration of enzyme-treated isoquercitrin was increased. Thus, in food and drink containing enzyme-treated isoquercitrin, it was found that the sour aftertaste and bitter astringent aftertaste are problems specific to the form of a low-viscosity beverage. In addition, in this specification, "aftertaste" means the "sensation remaining in the mouth" described in JIS Z 8144: 2004.
 本発明は、高濃度のイソクエルシトリン及びその糖付加物を含有し、酸味の後味及び苦渋味の後味の抑制された容器詰飲料を提供することにある。また、本発明は、高濃度のイソクエルシトリン及びその糖付加物を含有する容器詰飲料の後味の改善方法を提供することにある。 The present invention is to provide a packaged beverage containing a high concentration of isoquercitrin and its sugar adduct and having a sour aftertaste and a bitter astringent aftertaste. Moreover, this invention is providing the improvement method of the aftertaste of the container-packed drink containing a high concentration isoquercitrin and its sugar adduct.
 本発明者は、イソクエルシトリン及びその糖付加物とともにアミノ酸を含有せしめ、かつ各成分の容器詰飲料中の含有量及びpHを特定範囲内に制御することで、酸味の後味及び苦渋味の後味が抑制され、すっきりしていて飲みやすい飲料が得られることを見出した。 The inventor of the present invention contains an amino acid together with isoquercitrin and its sugar adduct, and controls the content and pH of each component in the container-packed beverage within a specific range, so that the aftertaste of bitterness and bitterness is obtained. It was found that a refreshing and easy-to-drink beverage can be obtained.
 本発明によれば、酸味の後味及び苦渋味の後味が抑制され、すっきりしていて飲みやすいイソクエルシトリン及びその糖付加物を含有する容器詰飲料を提供することができる。また、本発明によれば、高濃度のイソクエルシトリン及びその糖付加物を含有する容器詰飲料の後味の改善方法を提供することができる。 According to the present invention, it is possible to provide a packaged beverage containing isoquercitrin and its sugar adduct that are refreshed and easy to drink, with a sour aftertaste and a bitter and bitter aftertaste suppressed. Moreover, according to this invention, the improvement method of the aftertaste of the container-packed drink containing a high concentration isoquercitrin and its sugar adduct can be provided.
 本発明の容器詰飲料は(A)イソクエルシトリン及びその糖付加物(以下、「イソクエルシトリン糖付加物等」とも称する)を0.03~0.17質量%含有するものである。成分(A)の含有量の上限は、酸味の後味及び苦渋味の後味の抑制の点から、0.15質量%以下、更に0.12質量%以下、更に0.1質量%以下であることが好ましい。また、成分(A)の含有量は、生理効果の観点から、0.04量%以上、更に0.05質量%以上、更に0.06質量%以上が好ましい。成分(A)の含有量の範囲としては、0.04~0.15質量%、更に0.05~0.12質量%、更に0.06~0.12質量%、更に0.06~0.1質量%が好ましい。 The container-packed beverage of the present invention contains 0.03 to 0.17% by mass of (A) isoquercitrin and a sugar adduct thereof (hereinafter also referred to as “isoquercitrin sugar adduct etc.”). The upper limit of the content of the component (A) is 0.15% by mass or less, further 0.12% by mass or less, and further 0.1% by mass or less from the viewpoint of suppressing the sour aftertaste and bitterness aftertaste. Is preferred. Moreover, content of a component (A) is 0.04 mass% or more from a viewpoint of a physiological effect, Furthermore, 0.05 mass% or more, Furthermore, 0.06 mass% or more is preferable. The range of the content of component (A) is 0.04 to 0.15% by mass, further 0.05 to 0.12% by mass, further 0.06 to 0.12% by mass, and further 0.06 to 0%. .1% by mass is preferable.
 イソクエルシトリンは、ケルセチンの3位にグルコース1つがβ結合したものである(quercetin 3-O-β-D-glucopyranoside)。イソクエルシトリン糖付加物は、例えば、イソクエルシトリンに糖供与体(グルコース源)の存在下、糖転移酵素を作用させて得ることができ、イソクエルシトリンのグルコース残基に1以上のグルコースをα-1,4結合で更に付加したα-グルコシルイソクエルシトリンとなっている(FFIジャーナル,Vol.209,No.7,2004,p.622-628;食品衛生学雑誌,Vol.41,No.1,p.54-60)。 Isoquercitrin is obtained by β-bonding one glucose at the 3-position of quercetin (quercetincet3-O-β-D-glucopyranoside). The isoquercitrin sugar adduct can be obtained, for example, by allowing glycosyltransferase to act on isoquercitrin in the presence of a sugar donor (glucose source), and adding one or more glucose to the glucose residue of isoquercitrin. α-Glucosylisoquercitrin further added with α-1,4 bond (FFI Journal, Vol.209, No.7, 2004, p.622-628; Food Hygiene Journal, Vol.41, No. .1, p.54-60).
 成分(A)は、より具体的には、下記式(1)において、グルコース残基数(n)が0であるイソクエルシトリンと、グルコース残基数(n)が1以上の整数(好ましくは1~15の整数、より好ましくは1~10の整数、更に好ましくは1~8の整数)であるイソクエルシトリン糖付加物との混合物である。 More specifically, the component (A) includes isoquercitrin in which the number of glucose residues (n) is 0 in the following formula (1) and an integer in which the number of glucose residues (n) is 1 or more (preferably A mixture with an isoquercitrin sugar adduct which is an integer of 1 to 15, more preferably an integer of 1 to 10, and still more preferably an integer of 1 to 8.
Figure JPOXMLDOC01-appb-C000001
Figure JPOXMLDOC01-appb-C000001
〔式中、Glcはグルコース残基を示し、nは0又は1以上の整数を示す。〕 [Wherein Glc represents a glucose residue, and n represents 0 or an integer of 1 or more. ]
 また、成分(A)中のイソクエルシトリンの糖付加物/イソクエルシトリンの質量比は、水溶性の点から1以上であることが好ましく、更に2以上、殊更に4以上が好ましい。また、当該質量比は、製造効率の点から1000以下、更に500以下、更に100以下、更に50以下、更に25以下、更に10以下であることが好ましい。かかる質量比の範囲としては、1~1000、更に1~500、更に1~100、更に1~50、更に1~25、更に1~10、更に2~10、更に4~10が好ましい。 Further, the mass ratio of isoquercitrin sugar adduct / isoquercitrin in component (A) is preferably 1 or more, more preferably 2 or more, and particularly preferably 4 or more, from the viewpoint of water solubility. The mass ratio is preferably 1000 or less, further 500 or less, further 100 or less, further 50 or less, further 25 or less, and further 10 or less from the viewpoint of production efficiency. The range of the mass ratio is preferably 1 to 1000, further 1 to 500, further 1 to 100, further 1 to 50, further 1 to 25, further 1 to 10, further 2 to 10, and further 4 to 10.
 このような(A)イソクエルシトリン糖付加物等は商業的に入手可能であり、例えば、サンメリンAO-1007、サンメリンパウダーC-10等(以上、三栄源エフ・エフ・アイ社製)を挙げることができる。 Such (A) isoquercitrin sugar adducts and the like are commercially available. For example, Sanmerin AO-1007, Sanmerin Powder C-10 and the like (manufactured by Saneigen FFI Co., Ltd.) Can be mentioned.
 イソクエルシトリンの配糖化処理に使用される糖転移酵素としては、例えば、α-アミラーゼ(E.C.3.2.1.1)、α-グルコシダーゼ(E.C.3.2.1.20)等のグルコシダーゼや、シクロデキストリングルカノトランスフェラーゼ(E.C.2.4.1.19)等のトランスグルコシダーゼを挙げることができる。 Examples of glycosyltransferases used for glycosylation of isoquercitrin include glucosidases such as α-amylase (EC 3.2.1.1) and α-glucosidase (EC 3.2.1.20), and cyclodextrin glucanotransferase (EC). And transglucosidase such as 2.4.1.19).
 これらの糖転移酵素はいずれも商業的に入手可能であり、例えば、コンチザイム(天野エンザイム社製)を挙げることができる。なお、糖転移酵素の使用量は酵素の種類や所望の組成により一様ではないが、例えば、シクロデキストリングルカノトランスフェラーゼ〔酵素比活性約100単位(溶性デンプンからβ-シクロデキストリンを1分間当たり1mg生成する酵素量を1単位とする)〕の場合、イソクエルシトリン1質量部に対して、通常0.001~20質量部、好ましくは0.005~10質量部、より好ましくは0.01~5質量部である。 These glycosyltransferases are all commercially available, and examples thereof include contizyme (manufactured by Amano Enzyme). The amount of glycosyltransferase used is not uniform depending on the type of enzyme and the desired composition. For example, cyclodextrin glucanotransferase [enzyme specific activity of about 100 units (β-cyclodextrin from soluble starch per 1 minute per minute) The amount of enzyme produced is defined as 1 unit)] is usually 0.001 to 20 parts by weight, preferably 0.005 to 10 parts by weight, more preferably 0.01 to 10 parts by weight per 1 part by weight of isoquercitrin. 5 parts by mass.
 配糖化の際に用いられる糖供与体(グルコース源)としては、そのグルコース残基の1分子以上がイソクエルシトリンの1分子に転移され得るものであれば特に限定されるものではないが、例えば、グルコース、マルトース、アミロース、アミロペクチン、でん粉、でん粉液化物、でん粉糖化物、シクロデキストリン等を挙げることができる。グルコース源の使用量は、イソクエルシトリン1質量部に対して、通常0.1~20質量部、好ましくは0.5~15質量部、より好ましくは1~10質量部である。 The sugar donor (glucose source) used for glycosylation is not particularly limited as long as one or more molecules of the glucose residue can be transferred to one molecule of isoquercitrin. Glucose, maltose, amylose, amylopectin, starch, starch liquefied product, starch saccharified product, cyclodextrin and the like. The amount of glucose used is usually 0.1 to 20 parts by weight, preferably 0.5 to 15 parts by weight, and more preferably 1 to 10 parts by weight with respect to 1 part by weight of isoquercitrin.
 また、得られる(A)イソクエルシトリン糖付加物等の組成は反応条件によって一様ではなく、例えば、温度80℃以下、好ましくは20~80℃、より好ましくは40~75℃、pH3~11、好ましくはpH4~8の条件で、糖供与体(グルコース源)の存在下、イソクエルシトリンに糖転移酵素を作用させることにより、種々の組成のものが得られる。なお、(A)イソクエルシトリン糖付加物等の分析方法は、後掲の実施例に記載の方法にしたがうものとする。 Further, the composition of the resulting (A) isoquercitrin sugar adduct is not uniform depending on the reaction conditions. For example, the temperature is 80 ° C. or less, preferably 20 to 80 ° C., more preferably 40 to 75 ° C., pH 3 to 11 In addition, various compositions can be obtained by allowing glycosyltransferase to act on isoquercitrin in the presence of a sugar donor (glucose source), preferably under conditions of pH 4-8. In addition, the analysis method of (A) isoquercitrin sugar adduct and the like shall follow the method described in the examples described later.
 上記反応は、静置又は攪拌若しくは振盪しながら行うことができる。反応中の酸化を防止するために、反応系のヘッドスペースを窒素等の不活性ガスで置換してもよく、またアスコルビン酸等の酸化防止剤を反応系に添加することも可能である。 The above reaction can be performed while standing or stirring or shaking. In order to prevent oxidation during the reaction, the head space of the reaction system may be replaced with an inert gas such as nitrogen, and an antioxidant such as ascorbic acid may be added to the reaction system.
 (A)イソクエルシトリン糖付加物等は、前述のようにイソクエルシトリンを原料とする他、ルチンから出発して調製することも可能である。例えば、ルチンにα-1,6-ラムノシダーゼ(E.C.3.2.1.40)を作用させてイソクエルシトリンに変換してから、前述の方法にしたがって(A)イソクエルシトリン糖付加物等を調製することができる。α-1,6-ラムノシダーゼは商業的に入手可能であり、例えば、ヘスペリジナーゼ、ナリンジナーゼ(以上、田辺製薬社製)、セルラーゼA「アマノ」3(天野エンザイム社製)が挙げられる。 (A) Isoquercitrin sugar adducts and the like can be prepared starting from rutin as well as using isoquercitrin as a raw material as described above. For example, α-1,6-rhamnosidase (EC 3.2.1.40) is allowed to act on rutin to convert it to isoquercitrin, and then (A) an isoquercitrin sugar adduct is prepared according to the above-mentioned method. it can. α-1,6-rhamnosidase is commercially available, and examples thereof include hesperidinase, naringinase (manufactured by Tanabe Seiyaku Co., Ltd.), and cellulase A “Amano” 3 (manufactured by Amano Enzyme).
 また、本発明においては、上記式(1)で表わされる(A)イソクエルシトリン糖付加物等において、nが0であるイソクエルシトリンと、nが1以上の整数であるイソクエルシトリン糖付加物との混合物から、例えば、nが0であるイソクエルシトリンと、nが4以上であるイソクエルシトリン糖付加物を分画により低減し、nが3であるイソクエルシトリン糖付加物を豊富に含む画分を分取して使用してもよい。 In the present invention, in the (A) isoquercitrin sugar adduct represented by the above formula (1), isoquercitrin in which n is 0 and isoquercitrin sugar addition in which n is an integer of 1 or more For example, isoquercitrin sugar adducts where n is 0 and isoquercitrin sugar adducts where n is 4 or more are reduced by fractionation and rich in isoquercitrin sugar adducts where n is 3 The fraction contained in may be collected and used.
 本発明の容器詰飲料は、(A)イソクエルシトリン糖付加物等をケルセチン換算で0.01~0.07質量%となるように含有することが、酸味の後味及び苦渋味の後味の抑制の観点から好ましく、更に0.06質量%以下、更に0.05質量%以下、更に0.04質量%以下であるのが好ましく、また生理効果の観点から、0.016質量%以上、更に0.021質量%以上、更に0.025質量%以上が好ましい。成分(A)の含有量の範囲としては、ケルセチン換算で0.016~0.06質量%、更に0.021~0.05質量%、更に0.025~0.04質量%が好ましい。 The container-packed beverage of the present invention contains (A) an isoquercitrin sugar adduct or the like so as to be 0.01 to 0.07% by mass in terms of quercetin, so as to suppress the sour aftertaste and the aftertaste of bitter astringency. From the viewpoint of physiological effect, it is preferably 0.06% by mass or less, more preferably 0.05% by mass or less, and further preferably 0.04% by mass or less. 0.021% by mass or more, more preferably 0.025% by mass or more. The content range of the component (A) is preferably 0.016 to 0.06% by mass, more preferably 0.021 to 0.05% by mass, and further preferably 0.025 to 0.04% by mass in terms of quercetin.
 また、本発明の容器詰飲料は、酸味の後味及び苦渋味の後味を抑制するために、(B)アミノ酸を含有する。アミノ酸としては、酸性アミノ酸、中性アミノ酸及び塩基性アミノ酸のいずれも使用することが可能であり、また単一の光学活性体でもラセミ体でもよい。ここで、本明細書において「中性アミノ酸」とは、1分子中にアミノ基、イミノ基、グアニジル基等の含窒素塩基性基と、カルボキシル基を各1個有するアミノ酸をいい、また「酸性アミノ酸」とは1分子中に上記含窒素塩基性基よりもカルボキシル基を多く有するアミノ酸をいい、更に「塩基性アミノ酸」とは1分子中にカルボキシル基よりも上記含窒素塩基性基を多く有するアミノ酸をいう。 Moreover, the container-packed beverage of the present invention contains (B) an amino acid in order to suppress the sour aftertaste and the aftertaste of bitter astringency. As the amino acid, any of acidic amino acid, neutral amino acid and basic amino acid can be used, and it may be a single optically active substance or a racemic body. As used herein, the term “neutral amino acid” refers to an amino acid having a nitrogen-containing basic group such as an amino group, an imino group, or a guanidyl group and one carboxyl group in one molecule. “Amino acid” means an amino acid having more carboxyl groups than the nitrogen-containing basic group in one molecule, and “basic amino acid” has more nitrogen-containing basic groups than a carboxyl group in one molecule. An amino acid.
 酸性アミノ酸としては、アスパラギン酸、グルタミン酸が挙げられる。また、中性アミノ酸としては、例えば、ロイシン、プロリン、グリシン、サルコシン、α-アラニン、β-アラニン、N-メチル-β-アラニン、グルタミン、アスパラギン、イソロイシン、イプシロン-アミノカプロン酸、γ-アミノ酪酸、グリシルグリシン、システイン、シスチン、クレアチン、セリン、チロシン、トリプトファン、トレオニン、バリン、フェニルアラニン、プロリン、ハイドロキシプロリン、メチオニン等を挙げることができる。更に、塩基性アミノ酸としては、リジン、アルギニン、オルニチン、ヒドロキシリジン、ヒスチジンが挙げられる。これらは単独で又は2種以上を組み合わせて使用することができる。
 これらの中でも、より一層の酸味の後味及び苦渋味の後味の改善の観点から、中性アミノ酸が好ましく、ロイシン、プロリンがより好ましい。
Examples of acidic amino acids include aspartic acid and glutamic acid. Examples of neutral amino acids include leucine, proline, glycine, sarcosine, α-alanine, β-alanine, N-methyl-β-alanine, glutamine, asparagine, isoleucine, epsilon-aminocaproic acid, γ-aminobutyric acid, Examples thereof include glycylglycine, cysteine, cystine, creatine, serine, tyrosine, tryptophan, threonine, valine, phenylalanine, proline, hydroxyproline, and methionine. Furthermore, basic amino acids include lysine, arginine, ornithine, hydroxylysine, and histidine. These can be used alone or in combination of two or more.
Among these, a neutral amino acid is preferable and leucine and proline are more preferable from the viewpoint of further improving the aftertaste of bitterness and bitterness.
 本発明の容器詰飲料中の(B)アミノ酸の含有量は0.0001~2質量%であるが、より一層の酸味の後味及び苦渋味の後味の抑制の観点から、好ましくは1.9質量%以下、より好ましくは1.5質量%以下、更に好ましくは1.2質量%以下、更に好ましくは1質量以下、更に好ましくは0.5質量%以下、殊更に好ましくは0.3質量%以下、そして、好ましくは0.001質量%以上、より好ましくは0.005質量%以上、更に好ましくは0.01質量%以上、殊更に好ましくは0.02質量%以上である。成分(B)の含有量の範囲としては、酸味の後味及び苦渋味の後味の抑制の観点から、0.001~1.9質量%、更に0.005~1.5質量%、更に0.01~1.2質量%、更に0.02~1質量%、更に0.02~0.5質量%、更に0.02~0.3質量%が好ましい。 The content of the amino acid (B) in the packaged beverage of the present invention is 0.0001 to 2% by mass, but preferably 1.9% by mass from the viewpoint of further suppressing the aftertaste of bitterness and bitterness. % Or less, more preferably 1.5% by mass or less, still more preferably 1.2% by mass or less, still more preferably 1% by mass or less, still more preferably 0.5% by mass or less, and even more preferably 0.3% by mass or less. And, it is preferably 0.001% by mass or more, more preferably 0.005% by mass or more, further preferably 0.01% by mass or more, and still more preferably 0.02% by mass or more. The range of the content of component (B) is from 0.001 to 1.9% by mass, more preferably from 0.005 to 1.5% by mass, and further preferably from the viewpoint of suppressing the sour aftertaste and the aftertaste of bitter and astringent taste. It is preferably 01 to 1.2% by mass, more preferably 0.02 to 1% by mass, further 0.02 to 0.5% by mass, and further preferably 0.02 to 0.3% by mass.
 本発明の容器詰飲料中の成分(A)と、成分(B)との含有質量比[(B)/(A)]は、酸味の後味及び苦渋味の後味の抑制の点から、好ましくは20以下、より好ましくは10以下、更に好ましくは5以下、更に好ましくは3以下、更に好ましくは2以下、更に好ましくは1.5以下、殊更に好ましくは1以下、そして、好ましくは0.01以上、より好ましくは0.02以上、更に好ましくは0.05以上、更に好ましくは0.1以上、殊更に好ましくは0.2以上である。かかる質量比[(B)/(A)]の範囲としては、0.01~20、更に0.01~10、更に0.01~5、更に0.01~3であることが好ましい。また、0.02~2、更に0.05~1.5、更に0.1~1、殊更0.2~1とすることもできる。 The content mass ratio [(B) / (A)] of the component (A) and the component (B) in the packaged beverage of the present invention is preferably from the viewpoint of suppressing the aftertaste of bitter and astringent taste. 20 or less, more preferably 10 or less, still more preferably 5 or less, still more preferably 3 or less, still more preferably 2 or less, still more preferably 1.5 or less, even more preferably 1 or less, and preferably 0.01 or more More preferably, it is 0.02 or more, More preferably, it is 0.05 or more, More preferably, it is 0.1 or more, Most preferably, it is 0.2 or more. The range of the mass ratio [(B) / (A)] is preferably 0.01 to 20, more preferably 0.01 to 10, further 0.01 to 5, and more preferably 0.01 to 3. Further, it may be 0.02 to 2, further 0.05 to 1.5, further 0.1 to 1, and particularly 0.2 to 1.
 また、本発明の容器詰飲料には、甘味料を含有させることができる。かかる甘味料としては、例えば、果糖,ブドウ糖,タガトース,アラビノース等の単糖、乳糖,トレハロース,麦芽糖,ショ糖等の二糖、粉末水あめ等の多糖といった結晶性糖類や、マルトオリゴ糖、ガラクトオリゴ糖等のオリゴ糖、水あめ等の非結晶性糖類、更にはブドウ糖や果糖等の糖分が約7割を占める蜂蜜等を挙げることができる。これら甘味料は単独で又は2種以上を組み合わせて使用することができる。
 本発明の容器詰飲料中の甘味料の含有量は適宜決定することが可能であるが、0.02~1質量%、更に0.05~0.8質量%、更に0.05~0.6質量%であることが、酸味の後味及び苦渋味の後味の抑制の点から好ましい。
Moreover, the container-packed drink of this invention can be made to contain a sweetener. Such sweeteners include, for example, monosaccharides such as fructose, glucose, tagatose, and arabinose, disaccharides such as lactose, trehalose, maltose, and sucrose; Oligosaccharides, non-crystalline saccharides such as syrup, and honey and the like in which sugars such as glucose and fructose account for about 70%. These sweeteners can be used alone or in combination of two or more.
The content of the sweetener in the packaged beverage of the present invention can be appropriately determined, but is 0.02 to 1% by mass, further 0.05 to 0.8% by mass, and further 0.05 to 0. 0%. It is preferable that it is 6 mass% from the point of suppression of the sour aftertaste and the bitterness aftertaste.
 更に、本発明の容器詰飲料には、高甘味度甘味料を含有せしめることができる。ここで、本明細書において「高甘味度甘味料」とは、ショ糖に比べて強い甘味を有する甘味料の総称であり、天然甘味料、合成甘味料がある。具体的には、スクラロース、ステビア、甘草抽出物、ソーマチン、グリチルリチン、グリチルリチン酸2ナトリウム、グリチルリチン酸アンモニウム、サッカリン、サッカリンナトリウム、アスパルテーム、アセスルファムK、アリテーム、ネオテーム等を挙げることができる。これらは単独で又は2種以上を組み合わせて使用することができる。 Furthermore, the packaged beverage of the present invention can contain a high-intensity sweetener. Here, in the present specification, the “high-intensity sweetener” is a general term for sweeteners having a sweetness stronger than that of sucrose, and includes natural sweeteners and synthetic sweeteners. Specific examples include sucralose, stevia, licorice extract, thaumatin, glycyrrhizin, disodium glycyrrhizinate, ammonium glycyrrhizinate, saccharin, saccharin sodium, aspartame, acesulfame K, alitame, neotame and the like. These can be used alone or in combination of two or more.
 本発明の容器詰飲料中の高甘味度甘味料の含有量は、その種類により適宜選択可能であるが、酸味の後味及び苦渋味の後味の抑制の点から、好ましくは0.0001~0.5質量%、より好ましくは0.0001~0.25質量%、更に好ましくは0.0001~0.1質量%である。 The content of the high-intensity sweetener in the packaged beverage of the present invention can be appropriately selected depending on the type thereof, but is preferably 0.0001 to 0.00 in terms of suppressing the sour aftertaste and the aftertaste of bitter astringency. It is 5% by mass, more preferably 0.0001 to 0.25% by mass, and still more preferably 0.0001 to 0.1% by mass.
 また、本発明においては、炭酸ガスを含有せしめて炭酸飲料とすることも可能である。炭酸ガスの適度な起泡性により、酸味の後味及び苦渋味の後味を抑制することができる。
 本発明の容器詰飲料に炭酸ガスを含有させる場合、その含有量は、好ましくは1質量%以下、より好ましくは0.1~0.9質量%、更に好ましくは0.2~0.8質量%、更に好ましくは0.3~0.7質量%である。なお、炭酸ガスの測定方法としては、ガスボリューム計により計測し、ガス質量に換算することができる。ガスボリュームとは、飲料中に溶解している炭酸ガスの20℃における気体容量の飲料容量に対する比率をいい、本発明の容器詰飲料の場合、好ましくは0.5~4、更に1~3.8、更に2~3.5であることが好ましい。
Moreover, in this invention, it is also possible to make a carbonated drink by containing a carbon dioxide gas. Due to the moderate foaming property of carbon dioxide, it is possible to suppress the sour aftertaste and the aftertaste of bitter astringency.
When carbon dioxide is contained in the packaged beverage of the present invention, the content is preferably 1% by mass or less, more preferably 0.1 to 0.9% by mass, and still more preferably 0.2 to 0.8% by mass. %, More preferably 0.3 to 0.7% by mass. In addition, as a measuring method of a carbon dioxide gas, it can measure with a gas volume meter and can convert into gas mass. The gas volume refers to the ratio of the gas volume at 20 ° C. of the carbon dioxide dissolved in the beverage to the beverage volume. In the case of the packaged beverage of the present invention, preferably 0.5 to 4, and more preferably 1 to 3. 8, more preferably 2 to 3.5.
 更に、本発明の容器詰飲料は、カリウムイオンを含有することができる。これにより、長期保存時においても爽快感が希薄にならず、口中におけるスッキリ感が保持され、酸味の後味及び苦渋味の後味を抑制するのに寄与する。
 カリウムイオンは、塩化カリウム、炭酸カリウム、硫酸カリウム、酢酸カリウム、炭酸水素カリウム、クエン酸カリウム、リン酸カリウム、リン酸水素カリウム、酒石酸カリウム、ソルビン酸カリウム等又はそれらの混合物のようなカリウム塩として配合することができる。なお、カリウムイオンは、原料由来のものも含まれる。
 本発明の容器詰飲料中のカリウムイオンの含有量は、好ましくは0.001質量%以上、より好ましくは0.002質量%以上、更に好ましくは0.003質量%以上、更に好ましくは0.005質量%以上、殊更に好ましくは0.01質量%以上、そして、好ましくは0.2質量%以下、より好ましくは0.1質量%以下、更に好ましくは0.09質量%以下、更に好ましくは0.08質量%以下、殊更に好ましくは0.07質量%以下である。カリウムイオンの含有量の範囲としては0.001~0.2質量%が好ましく、更に0.002~0.1質量%、更に0.003~0.09質量、更に0.005~0.08質量%、殊更に0.01~0.07質量%が好ましい。
Furthermore, the container-packed drink of this invention can contain a potassium ion. Thereby, the refreshing feeling is not diluted even during long-term storage, the refreshing feeling in the mouth is maintained, and it contributes to suppressing the after-taste of acidity and bitterness.
Potassium ions as potassium salts such as potassium chloride, potassium carbonate, potassium sulfate, potassium acetate, potassium bicarbonate, potassium citrate, potassium phosphate, potassium hydrogen phosphate, potassium tartrate, potassium sorbate etc. or mixtures thereof Can be blended. The potassium ions include those derived from raw materials.
The content of potassium ions in the packaged beverage of the present invention is preferably 0.001% by mass or more, more preferably 0.002% by mass or more, still more preferably 0.003% by mass or more, and further preferably 0.005. % By mass or more, particularly preferably 0.01% by mass or more, and preferably 0.2% by mass or less, more preferably 0.1% by mass or less, still more preferably 0.09% by mass or less, still more preferably 0%. 0.08% by mass or less, particularly preferably 0.07% by mass or less. The range of the potassium ion content is preferably 0.001 to 0.2% by mass, more preferably 0.002 to 0.1% by mass, further 0.003 to 0.09%, and further 0.005 to 0.08. % By mass, especially 0.01 to 0.07% by mass is preferred.
 更に、本発明の容器詰飲料には、所望により、酸味料、香料(乳化香料を含む)、ビタミン、ミネラル、酸化防止剤、起泡剤、泡安定剤、各種エステル類、色素類、乳化剤、保存料、アミノ酸を除く調味料、果汁、穀物エキス、麦芽エキス、野菜エキス、花蜜エキス、品質安定剤等の添加剤を単独で又は2種以上を組み合わせて含有させることができる。なお、添加剤の含有量は、本発明の目的を妨げない範囲内で適宜選択可能である。 Furthermore, in the packaged beverage of the present invention, as desired, acidulant, flavor (including emulsified flavor), vitamin, mineral, antioxidant, foaming agent, foam stabilizer, various esters, pigments, emulsifier, Additives such as preservatives, seasonings excluding amino acids, fruit juice, cereal extract, malt extract, vegetable extract, nectar extract, and quality stabilizer can be used alone or in combination of two or more. In addition, content of an additive can be suitably selected within the range which does not prevent the objective of this invention.
 本発明の容器詰飲料のpH(20℃)は2~5であるが、より一層の酸味の後味及び苦渋味の後味の抑制の観点から、3~4が好ましい。 The pH (20 ° C.) of the packaged beverage of the present invention is 2 to 5, but 3 to 4 is preferred from the viewpoint of further suppressing the aftertaste of bitterness and bitterness.
 本発明の容器詰飲料は、容器詰めされた状態において低粘度のものであることが好ましい。例えば、ゼリー等の保形性を有する高粘度食品ではなく、容器を傾けるだけで流動して飲用できる程度の粘度のものであることが好ましい。具体的な粘度としては、振動式粘度計にて20℃で測定した場合に0.01~500mPa・s、更に0.01~400mPa・s、殊更0.01~200mPa・sであることが好ましい。 The container-packed beverage of the present invention preferably has a low viscosity in a container-packed state. For example, it is preferably not a high-viscosity food having shape-retaining properties such as jelly, but a viscosity that allows it to flow and be drunk only by tilting the container. The specific viscosity is preferably 0.01 to 500 mPa · s, more preferably 0.01 to 400 mPa · s, and particularly preferably 0.01 to 200 mPa · s when measured at 20 ° C. with a vibration viscometer. .
 本発明の容器詰飲料は、例えば、成分(A)と成分(B)を配合し、各成分の濃度及びpHを調整して製造することができる。 The container-packed beverage of the present invention can be produced by, for example, blending the component (A) and the component (B) and adjusting the concentration and pH of each component.
 また、本発明の容器詰飲料に使用できる容器としては、ポリエチレンテレフタレートを主成分とする成形容器(いわゆるPETボトル)、金属缶、金属箔やプラスチックフィルムと複合された紙容器、瓶等の通常の包装容器が挙げられる。
 更に、容器に充填後、例えば、金属缶のような加熱殺菌できる場合にあっては適用されるべき法規(日本にあっては食品衛生法)に定められた条件で殺菌することができる。他方、PETボトル、紙容器のようにレトルト殺菌できないものについては、あらかじめ上記と同等の殺菌条件、例えばプレート式熱交換器などで高温短時間殺菌後、一定の温度迄冷却して容器に充填する等の方法が採用できる。また無菌下で、充填された容器に別の成分を配合して充填してもよい。
Moreover, as a container which can be used for the container-packed beverage of the present invention, a molded container mainly composed of polyethylene terephthalate (so-called PET bottle), a metal can, a paper container combined with a metal foil or a plastic film, a bottle or the like is used. A packaging container is mentioned.
Furthermore, after filling the container, for example, when heat sterilization such as a metal can can be performed, it can be sterilized under the conditions stipulated in the applicable regulations (the Food Sanitation Law in Japan). On the other hand, those that cannot be sterilized by retort, such as PET bottles and paper containers, are preliminarily sterilized at a high temperature and short time using a plate heat exchanger, for example, and then cooled to a certain temperature and filled into containers. Etc. can be adopted. Moreover, you may mix | blend another component with the filled container under aseptic conditions.
 以上、本発明の容器詰飲料について説明したが、イソクエルシトリン及びその糖付加物を含有する容器詰飲料の後味の改善方法においても、上記と同様の構成を採用することができる。 As mentioned above, although the container-packed drink of this invention was demonstrated, the structure similar to the above is employable also in the improvement method of the aftertaste of the container-packed drink containing isoquercitrin and its sugar adduct.
 すなわち、上記実施形態に関し、本発明は更に以下の容器詰飲料、あるいは後味の改善方法を開示する。
〔1-1〕
 次の成分(A)及び(B):
(A)イソクエルシトリン及びその糖付加物 0.03~0.17質量%、
(B)アミノ酸 0.0001~2質量%
を含有し、pHが2~5である容器詰飲料。
〔1-2〕
 成分(A)の含有量が、好ましくは0.04量%以上、より好ましくは0.05質量%以上、更に好ましくは0.06質量%以上であって、好ましくは0.15質量%以下、より好ましくは0.12質量%以下、更に好ましくは0.1質量%以下である、前記〔1-1〕記載の容器詰飲料。
〔1-3〕
 成分(A)の含有量が、好ましくは0.04~0.15質量%、より好ましくは0.05~0.12質量%、更に好ましくは0.06~0.12質量%、更に好ましくは0.06~0.1質量%である、前記〔1-1〕記載の容器詰飲料。
〔1-4〕
 成分(A)は、イソクエルシトリン糖付加物/イソクエルシトリンの質量比が、好ましくは1以上、より好ましくは2以上、更に好ましくは4以上であって、好ましくは1000以下、より好ましくは500以下、更に好ましくは100以下、更に好ましくは50以下、更に好ましくは25以下、更に好ましくは10以下である、前記〔1-1〕~〔1-3〕のいずれか一に記載の容器詰飲料。
〔1-5〕
 成分(A)は、イソクエルシトリン糖付加物/イソクエルシトリンの質量比が、好ましくは1~1000、より好ましくは1~500、更に好ましくは1~100、更に好ましくは1~50、更に好ましくは1~25、更に好ましくは1~10、更に好ましくは2~10、更に好ましくは4~10である、前記〔1-1〕~〔1-3〕のいずれか一に記載の容器詰飲料。
〔1-6〕
 成分(A)の含有量が、ケルセチン換算で、好ましくは0.01~0.07質量%、より好ましくは0.016~0.06質量%、更に好ましくは0.021~0.05質量%、更に好ましくは0.025~0.04質量%である、前記〔1-1〕~〔1-5〕のいずれか一に記載の容器詰飲料。
〔1-7〕
 成分(B)が、中性アミノ酸である、前記〔1-1〕~〔1-6〕のいずれか一に記載の容器詰飲料。
〔1-8〕
 中性アミノ酸がロイシン又はプロリンである、前記〔1-7〕記載の容器詰飲料。
〔1-9〕
 成分(B)の含有量が、好ましくは0.001質量%以上、より好ましくは0.005質量%以上、更に好ましくは0.01質量%以上、更に好ましくは0.02質量%以上であって、好ましくは1.9質量%以下、より好ましくは1.5質量%以下、更に好ましくは1.2質量%以下、更に好ましくは1質量%以下、更に好ましくは0.5質量%以下、更に好ましくは0.3質量%以下である、前記〔1-1〕~〔1-8〕のいずれか一に記載の容器詰飲料。
〔1-10〕
 成分(B)の含有量が、好ましくは0.001~1.9質量%、より好ましくは0.005~1.5質量%、更に好ましくは0.01~1.2質量%、更に好ましくは0.02~1質量%、更に0.02~0.5質量%、更に0.02~0.3質量%である、前記〔1-1〕~〔1-8〕のいずれか一に記載の容器詰飲料。
That is, regarding the said embodiment, this invention discloses the following container-packed drinks or the improvement method of a aftertaste.
[1-1]
The following components (A) and (B):
(A) Isoquercitrin and its sugar adduct 0.03-0.17% by mass,
(B) Amino acids 0.0001-2% by mass
And a packaged beverage having a pH of 2-5.
[1-2]
The content of the component (A) is preferably 0.04% by mass or more, more preferably 0.05% by mass or more, still more preferably 0.06% by mass or more, preferably 0.15% by mass or less, More preferably, it is 0.12% by mass or less, and still more preferably 0.1% by mass or less, in the above-mentioned [1-1].
[1-3]
The content of component (A) is preferably 0.04 to 0.15% by mass, more preferably 0.05 to 0.12% by mass, still more preferably 0.06 to 0.12% by mass, still more preferably The packaged beverage according to [1-1], which is 0.06 to 0.1% by mass.
[1-4]
In the component (A), the mass ratio of isoquercitrin sugar adduct / isoquercitrin is preferably 1 or more, more preferably 2 or more, further preferably 4 or more, preferably 1000 or less, more preferably 500. The container-packed beverage according to any one of [1-1] to [1-3], more preferably 100 or less, more preferably 50 or less, more preferably 25 or less, and still more preferably 10 or less. .
[1-5]
Component (A) has an isoquercitrin sugar adduct / isoquercitrin mass ratio of preferably 1 to 1000, more preferably 1 to 500, still more preferably 1 to 100, still more preferably 1 to 50, and still more preferably. Is from 1 to 25, more preferably from 1 to 10, more preferably from 2 to 10, and even more preferably from 4 to 10, The packaged beverage according to any one of [1-1] to [1-3] above .
[1-6]
The content of the component (A) is preferably 0.01 to 0.07% by mass, more preferably 0.016 to 0.06% by mass, and still more preferably 0.021 to 0.05% by mass in terms of quercetin. More preferably, the packaged beverage according to any one of [1-1] to [1-5], which is 0.025 to 0.04% by mass.
[1-7]
The packaged beverage according to any one of [1-1] to [1-6] above, wherein the component (B) is a neutral amino acid.
[1-8]
The packaged beverage according to [1-7] above, wherein the neutral amino acid is leucine or proline.
[1-9]
The content of the component (B) is preferably 0.001% by mass or more, more preferably 0.005% by mass or more, further preferably 0.01% by mass or more, and further preferably 0.02% by mass or more. , Preferably 1.9% by mass or less, more preferably 1.5% by mass or less, further preferably 1.2% by mass or less, still more preferably 1% by mass or less, still more preferably 0.5% by mass or less, still more preferably. The container-packed beverage according to any one of [1-1] to [1-8], in which is 0.3% by mass or less.
[1-10]
The content of component (B) is preferably 0.001 to 1.9% by mass, more preferably 0.005 to 1.5% by mass, still more preferably 0.01 to 1.2% by mass, still more preferably Any of [1-1] to [1-8], which is 0.02 to 1% by mass, further 0.02 to 0.5% by mass, and further 0.02 to 0.3% by mass. Bottled beverage.
〔1-11〕
 成分(A)と、成分(B)との含有質量比[(B)/(A)]が、好ましくは0.01以上、より好ましくは0.02以上、更に好ましくは0.05以上、更に好ましくは0.1以上、更に好ましくは0.2以上であって、好ましくは20以下、より好ましくは10以下、更に好ましくは5以下、更に好ましくは3以下、更に好ましくは2以下、更に好ましくは1.5以下、更に好ましくは1以下である、前記〔1-1〕~〔1-10〕のいずれか一に記載の容器詰飲料。
〔1-12〕
 成分(A)と、成分(B)との含有質量比[(B)/(A)]が、好ましくは0.01~20、より好ましくは0.01~10、更に好ましくは0.01~5、更に好ましくは0.01~3である、前記〔1-1〕~〔1-10〕のいずれか一に記載の容器詰飲料。
〔1-13〕
 成分(A)と、成分(B)との含有質量比[(B)/(A)]が、好ましくは0.02~2、より好ましくは0.05~1.5、更に好ましくは0.1~1、更に好ましくは0.2~1である、前記〔1-1〕~〔1-10〕のいずれか一に記載の容器詰飲料。
〔1-14〕
 更に高甘味度甘味料を含有する、前記〔1-1〕~〔1-13〕のいずれか一に記載の容器詰飲料。
〔1-15〕
 高甘味度甘味料がスクラロース、ステビア、甘草抽出物、ソーマチン、グリチルリチン、グリチルリチン酸2ナトリウム、グリチルリチン酸アンモニウム、サッカリン、サッカリンナトリウム、アスパルテーム、アセスルファムK、アリテーム及びネオテームから選ばれる1種又は2種以上である、前記〔1-14〕記載の容器詰飲料。
〔1-16〕
 高甘味度甘味料の含有量が、好ましくは0.0001~0.5質量%、より好ましくは0.0001~0.25質量%、更に好ましくは0.0001~0.1質量%である、前記〔1-14〕又は〔1-15〕記載の容器詰飲料。
〔1-17〕
 更に炭酸ガスを含有し、炭酸ガスの含有量が、好ましくは1質量%以下、より好ましくは0.1~0.9質量%、更に好ましくは0.2~0.8質量%、更に好ましくは0.3~0.7質量%である、前記〔1-1〕~〔1-16〕のいずれか一に記載の容器詰飲料。
〔1-18〕
 当該容器詰飲料がカリウムイオンを含み、カリウムイオンの含有量が、好ましくは0.001質量%以上、より好ましくは0.002質量%以上、更に好ましくは0.003質量%以上、更に好ましくは0.005質量%以上、更に好ましくは0.01質量%以上であって、好ましくは0.2質量%以下、より好ましくは0.1質量%以下、更に好ましくは0.09質量%以下、更に好ましくは0.08質量%以下、更に好ましくは0.07質量%以下である、前記〔1-1〕~〔1-17〕のいずれか一に記載の容器詰飲料。
〔1-19〕
 当該容器詰飲料がカリウムイオンを含み、カリウムイオンの含有量が、好ましくは0.001~0.2質量%、より好ましくは0.002~0.1質量%、更に好ましくは0.003~0.09質量、更に好ましくは0.005~0.08質量%、更に好ましくは0.01~0.07質量%である、前記〔1-1〕~〔1-17〕のいずれか一に記載の容器詰飲料。
〔1-20〕
 pH(20℃)が、好ましくは3~4である、前記〔1-1〕~〔1-19〕のいずれか一に記載の容器詰飲料。
[1-11]
The mass ratio [(B) / (A)] of the component (A) and the component (B) is preferably 0.01 or more, more preferably 0.02 or more, still more preferably 0.05 or more, Preferably it is 0.1 or more, more preferably 0.2 or more, preferably 20 or less, more preferably 10 or less, more preferably 5 or less, still more preferably 3 or less, still more preferably 2 or less, still more preferably. The packaged beverage according to any one of [1-1] to [1-10], which is 1.5 or less, more preferably 1 or less.
[1-12]
The mass ratio [(B) / (A)] of the component (A) and the component (B) is preferably 0.01 to 20, more preferably 0.01 to 10, and still more preferably 0.01 to 5. The packaged beverage according to any one of [1-1] to [1-10], more preferably 0.01 to 3.
[1-13]
The mass ratio [(B) / (A)] of the component (A) and the component (B) is preferably 0.02 to 2, more preferably 0.05 to 1.5, still more preferably 0.00. The packaged beverage according to any one of [1-1] to [1-10], which is 1-1, more preferably 0.2-1.
[1-14]
The packaged beverage according to any one of [1-1] to [1-13], further comprising a high-intensity sweetener.
[1-15]
The high-intensity sweetener is one or more selected from sucralose, stevia, licorice extract, thaumatin, glycyrrhizin, disodium glycyrrhizinate, ammonium glycyrrhizinate, saccharin, sodium saccharin, aspartame, acesulfame K, aritem and neotame The container-packed beverage according to [1-14] above.
[1-16]
The content of the high-intensity sweetener is preferably 0.0001 to 0.5% by mass, more preferably 0.0001 to 0.25% by mass, and still more preferably 0.0001 to 0.1% by mass. The packaged beverage according to [1-14] or [1-15].
[1-17]
Further, carbon dioxide is contained, and the content of carbon dioxide is preferably 1% by mass or less, more preferably 0.1 to 0.9% by mass, still more preferably 0.2 to 0.8% by mass, and still more preferably. The packaged beverage according to any one of [1-1] to [1-16], which is 0.3 to 0.7% by mass.
[1-18]
The packaged beverage contains potassium ions, and the content of potassium ions is preferably 0.001% by mass or more, more preferably 0.002% by mass or more, still more preferably 0.003% by mass or more, and further preferably 0. 0.005% by mass or more, more preferably 0.01% by mass or more, preferably 0.2% by mass or less, more preferably 0.1% by mass or less, still more preferably 0.09% by mass or less, still more preferably. Is a packed beverage according to any one of the above [1-1] to [1-17], which is 0.08% by mass or less, more preferably 0.07% by mass or less.
[1-19]
The packaged beverage contains potassium ions, and the content of potassium ions is preferably 0.001 to 0.2% by mass, more preferably 0.002 to 0.1% by mass, and still more preferably 0.003 to 0%. 0.09 mass, more preferably 0.005 to 0.08 mass%, still more preferably 0.01 to 0.07 mass%, as described in any one of [1-1] to [1-17] above Bottled beverage.
[1-20]
The packaged beverage according to any one of [1-1] to [1-19] above, which has a pH (20 ° C.) of preferably 3 to 4.
〔2-1〕
 イソクエルシトリン及びその糖付加物を含有する容器詰飲料の後味の改善方法であって、次の成分(A)及び(B)を、
(A)イソクエルシトリン及びその糖付加物 0.03~0.17質量%、
(B)アミノ酸 0.0001~2質量%
となるように配合し、pHを2~5に調整する、後味の改善方法。
〔2-2〕
 成分(A)を、好ましくは0.04量%以上、より好ましくは0.05質量%以上、更に好ましくは0.06質量%以上であって、好ましくは0.15質量%以下、より好ましくは0.12質量%以下、更に好ましくは0.1質量%以下となるように配合する、前記〔2-1〕記載の後味の改善方法。
〔2-3〕
 成分(A)を、好ましくは0.04~0.15質量%、より好ましくは0.05~0.12質量%、更に好ましくは0.06~0.12質量%、更に好ましくは0.06~0.1質量%配合する、前記〔2-1〕記載の後味の改善方法。
〔2-4〕
 成分(B)として、中性アミノ酸を使用する、前記〔2-1〕~〔2-3〕のいずれか一に記載の後味の改善方法。
〔2-5〕
 中性アミノ酸として、ロイシン又はプロリンを使用する、前記〔2-4〕記載の後味の改善方法。
〔2-6〕
 成分(B)を、好ましくは0.001質量%以上、より好ましくは0.005質量%以上、更に好ましくは0.01質量%以上、更に好ましくは0.02質量%以上であって、好ましくは1.9質量%以下、より好ましくは1.5質量%以下、更に好ましくは1.2質量%以下、更に好ましくは1質量%以下、更に好ましくは0.5質量%以下、更に好ましくは0.3質量%以下となるように配合する、前記〔2-1〕~〔2-5〕のいずれか一に記載の後味の改善方法。
〔2-7〕
 成分(B)を、好ましくは0.001~1.9質量%、より好ましくは0.005~1.5質量%、更に好ましくは0.01~1.2質量%、更に好ましくは0.02~1質量%、更に0.02~0.5質量%、更に0.02~0.3質量%配合する、前記〔2-1〕~〔2-5〕のいずれか一に記載の後味の改善方法。
〔2-8〕
 成分(A)と、成分(B)とを、質量比[(B)/(A)]が、好ましくは0.01以上、より好ましくは0.02以上、更に好ましくは0.05以上、更に好ましくは0.1以上、更に好ましくは0.2以上であって、好ましくは20以下、より好ましくは10以下、更に好ましくは5以下、更に好ましくは3以下、更に好ましくは2以下、更に好ましくは1.5以下、更に好ましくは1以下となるように配合する、前記〔2-1〕~〔2-7〕のいずれか一に記載の後味の改善方法。
〔2-9〕
 成分(A)と、成分(B)とを、質量比[(B)/(A)]が、好ましくは0.01~20、より好ましくは0.01~10、更に好ましくは0.01~5、更に好ましくは0.01~3となるように配合する、前記〔2-1〕~〔2-7〕のいずれか一に記載の後味の改善方法。
〔2-10〕
 pH(20℃)を、好ましくは3~4に調整する、前記〔2-1〕~〔2-9〕のいずれか一に記載の後味の改善方法。
[2-1]
A method for improving the aftertaste of a packaged beverage containing isoquercitrin and its sugar adduct, comprising the following components (A) and (B):
(A) Isoquercitrin and its sugar adduct 0.03-0.17% by mass,
(B) Amino acids 0.0001-2% by mass
The aftertaste is improved by adjusting the pH to 2-5.
[2-2]
The component (A) is preferably 0.04% by mass or more, more preferably 0.05% by mass or more, still more preferably 0.06% by mass or more, preferably 0.15% by mass or less, more preferably The method for improving the aftertaste according to [2-1], wherein the blending is performed so that the content is 0.12% by mass or less, more preferably 0.1% by mass or less.
[2-3]
The component (A) is preferably 0.04 to 0.15% by mass, more preferably 0.05 to 0.12% by mass, still more preferably 0.06 to 0.12% by mass, and still more preferably 0.06. The method for improving aftertaste according to the above [2-1], which is blended in an amount of 0.1 to 0.1% by mass.
[2-4]
The method for improving aftertaste according to any one of [2-1] to [2-3] above, wherein a neutral amino acid is used as component (B).
[2-5]
The method for improving aftertaste according to the above [2-4], wherein leucine or proline is used as the neutral amino acid.
[2-6]
Component (B) is preferably at least 0.001% by mass, more preferably at least 0.005% by mass, even more preferably at least 0.01% by mass, even more preferably at least 0.02% by mass, preferably 1.9% by mass or less, more preferably 1.5% by mass or less, further preferably 1.2% by mass or less, still more preferably 1% by mass or less, still more preferably 0.5% by mass or less, still more preferably 0.00%. The method for improving aftertaste according to any one of [2-1] to [2-5], wherein the aftertaste is blended so as to be 3% by mass or less.
[2-7]
Component (B) is preferably 0.001 to 1.9% by mass, more preferably 0.005 to 1.5% by mass, still more preferably 0.01 to 1.2% by mass, and still more preferably 0.02%. The aftertaste according to any one of the above [2-1] to [2-5], which is added in an amount of ˜1% by mass, further 0.02 to 0.5% by mass, and further 0.02 to 0.3% by mass. How to improve.
[2-8]
The component (A) and the component (B) have a mass ratio [(B) / (A)] of preferably 0.01 or more, more preferably 0.02 or more, still more preferably 0.05 or more, Preferably it is 0.1 or more, more preferably 0.2 or more, preferably 20 or less, more preferably 10 or less, more preferably 5 or less, still more preferably 3 or less, still more preferably 2 or less, still more preferably. The method for improving aftertaste according to any one of [2-1] to [2-7] above, which is blended so as to be 1.5 or less, more preferably 1 or less.
[2-9]
The mass ratio [(B) / (A)] of the component (A) and the component (B) is preferably 0.01 to 20, more preferably 0.01 to 10, and still more preferably 0.01 to 5. The method for improving aftertaste according to any one of [2-1] to [2-7] above, which is preferably blended so as to be 0.01 to 3.
[2-10]
The method for improving aftertaste according to any one of [2-1] to [2-9] above, wherein the pH (20 ° C) is preferably adjusted to 3 to 4.
1.イソクエルシトリン糖付加物等の分析
 イソクエルシトリン糖付加物等の分析は、HPLC(高速液体クロマトグラフ)法に基づき、次の方法にしたがって行った。
 分析機器は、LC-10AD(島津製作所社製)を使用した。
 分析機器の装置構成は次の通りである。
検出器 :紫外可視吸光光度計 SPD-10AV(島津製作所社製)
カラム :YMC-Pack ODS-A AA12S05-1506WT、φ6mm×150mm(ワイエムシィ社製)
1. Analysis of isoquercitrin sugar adduct etc. Analysis of isoquercitrin sugar adduct etc. was performed according to the following method based on HPLC (high performance liquid chromatograph) method.
LC-10AD (manufactured by Shimadzu Corporation) was used as an analytical instrument.
The apparatus configuration of the analytical instrument is as follows.
Detector: UV-visible spectrophotometer SPD-10AV (manufactured by Shimadzu Corporation)
Column: YMC-Pack ODS-A AA12S05-1506WT, φ6mm x 150mm (manufactured by YMC)
 分析条件は次の通りである。
カラム温度:40℃
移動相  :水、アセトニトリル、2-プロパノール及び酢酸の混液(200:38:2:1)
流量   :1.0mL/min
試料注入量:10μL
測定波長 :360nm
The analysis conditions are as follows.
Column temperature: 40 ° C
Mobile phase: Mixture of water, acetonitrile, 2-propanol and acetic acid (200: 38: 2: 1)
Flow rate: 1.0 mL / min
Sample injection volume: 10 μL
Measurement wavelength: 360 nm
 以下の手順にて分析用試料を調製した。
 検体1gを量りとり、メタノール1mLを加え、更にメタノール及び水の混液(1:1)を加えて10mLに定容し、試料溶液とした。調製した試料溶液を高速液体クロマトグラフ分析に供した。
A sample for analysis was prepared by the following procedure.
1 g of a sample was weighed, 1 mL of methanol was added, and a mixed solution of methanol and water (1: 1) was further added to make a constant volume of 10 mL to obtain a sample solution. The prepared sample solution was subjected to high performance liquid chromatographic analysis.
 また、イソクエルシトリンの標準品を用いて濃度既知の溶液を調製し、高速液体クロマトグラフ分析に供することにより検量線を作成し、イソクエルシトリンを指標として、前記試料溶液中のイソクエルシトリン糖付加物等の定量を行った。即ち、前記検量線から、前記資料溶液のHPLC分析におけるイソクエルシトリン(前記式(1)におけるn=0)及びn≧1の各糖付加物についてそれぞれモル濃度を求め、更に各物質の分子量からその含有量(質量%)を計算し、試料中のイソクエルシトリン糖付加物等の定量を行った。また、試料中のイソクエルシトリン糖付加物等のケルセチン換算量は、上記イソクエルシトリン及び各糖付加物のそれぞれのモル濃度から、アグリコン部分の含有量を計算することにより算出した。 In addition, a standard solution of isoquercitrin is prepared, a calibration curve is prepared by subjecting it to high performance liquid chromatographic analysis, and isoquercitrin sugar in the sample solution is prepared using isoquercitrin as an index. Quantification of adducts and the like was performed. That is, from the calibration curve, the molar concentration was determined for each of the sugar adducts of isoquercitrin (n = 0 in the formula (1)) and n ≧ 1 in the HPLC analysis of the sample solution, and further from the molecular weight of each substance. The content (mass%) was calculated, and the amount of isoquercitrin sugar adducts in the sample was determined. In addition, the quercetin equivalent amount of isoquercitrin sugar adducts and the like in the sample was calculated by calculating the content of the aglycone part from the respective molar concentrations of isoquercitrin and each sugar adduct.
2.アミノ酸の分析
 アミノ酸の分析は、次の方法にしたがい、アミノ酸自動分析計に供することにより行った。
<アミノ酸自動分析計操作条件>
機種  :L-8800形高速アミノ酸分析計〔日立ハイテクノロジーズ社製〕
カラム :日立カスタムイオン交換樹脂、φ4.6mm×60mm〔日立ハイテクノロジーズ社製〕
移動相 :MCI BUFFER L-8500-PF(PF-1~PF-4)〔三菱化学社製〕
反応液 :ニンヒドリン試液〔和光純薬工業社製〕
流量  :移動相 0.35 mL/min、反応液 0.30 mL/min
測定波長:570nm(プロリンを除く)
     440nm(プロリン)
2. Analysis of amino acids Analysis of amino acids was performed by using an amino acid automatic analyzer according to the following method.
<Operating conditions for automatic amino acid analyzer>
Model: L-8800 type high-speed amino acid analyzer (manufactured by Hitachi High-Technologies Corporation)
Column: Hitachi custom ion exchange resin, φ4.6mm x 60mm [manufactured by Hitachi High-Technologies Corporation]
Mobile phase: MCI BUFFER L-8500-PF (PF-1 to PF-4) [Mitsubishi Chemical Corporation]
Reaction solution: Ninhydrin test solution [Wako Pure Chemical Industries, Ltd.]
Flow rate: Mobile phase 0.35 mL / min, reaction solution 0.30 mL / min
Measurement wavelength: 570nm (excluding proline)
440nm (proline)
 以下の手順にて分析用試料を調製した。
1)検体6gを量りとり、これに10w/v%スルホサリチル酸溶液25mLを加えて、抽出(混和)した後、3mol/L水酸化ナトリウム溶液を加えた。
2)その溶液をpH2.2に調整し、更にクエン酸ナトリウム緩衝液(pH2.2)を加えて50mLに定容した。
3)その溶液をろ過後、必要に応じてクエン酸ナトリウム緩衝液(pH2.2)で希釈し、試料溶液とした。
4)試料溶液をアミノ酸自動分析計に供した。
A sample for analysis was prepared by the following procedure.
1) 6 g of a sample was weighed, and 25 mL of a 10 w / v% sulfosalicylic acid solution was added thereto, followed by extraction (mixing), and then a 3 mol / L sodium hydroxide solution was added.
2) The solution was adjusted to pH 2.2, and sodium citrate buffer (pH 2.2) was further added to adjust the volume to 50 mL.
3) After filtering the solution, it was diluted with a sodium citrate buffer (pH 2.2) as necessary to obtain a sample solution.
4) The sample solution was subjected to an amino acid automatic analyzer.
3.カリウムイオンの分析
 カリウムは、「分析実務者が書いた五訂日本食品標準成分表分析マニュアルの解説」(財団法人日本食品分析センター編集、中央法規出版株式会社発行所、2001年7月10日発行)のp90-91及びp99-103にしたがい測定した。
 具体的には、検体2~5gを抽出容器に量り取り、1%塩酸溶液200mLを加え、室温下で30分振とう抽出した。抽出液を遠心管に移し、遠心分離後の上澄み液を原子吸光用試験溶液とした。原子吸光光度計の測定波長を766.5nmに設定し、カリウムを測定した。そして、予め作成した検量線を用いて試料中のカリウム量を定量した。
3. Analysis of Potassium Ion Potassium is “Explanation of the Manual for Analyzing the Five Standards of Japanese Food Standards Constructed by Analyzing Practitioners” (edited by the Japan Food Analysis Center, published by Chuo Law Publishing Co., Ltd., July 10, 2001) ) Of p90-91 and p99-103.
Specifically, 2 to 5 g of the sample was weighed into an extraction container, 200 mL of 1% hydrochloric acid solution was added, and the mixture was extracted by shaking at room temperature for 30 minutes. The extract was transferred to a centrifuge tube, and the supernatant after centrifugation was used as a test solution for atomic absorption. The measurement wavelength of the atomic absorption photometer was set to 766.5 nm, and potassium was measured. And the amount of potassium in a sample was quantified using the calibration curve prepared beforehand.
4.官能評価
 各容器詰飲料の酸味の後味及び苦渋味の後味について、専門パネル3名による飲料試験を行い、その平均値をもって評価値とした。飲用試験では、比較例2の容器詰飲料を標準とする相対評価とし、下記の基準にしたがって行った。
4). Sensory evaluation About the sour aftertaste and bitterness astringent aftertaste of each container-packed drink, the drink test by 3 expert panels was conducted, and the average value was made into the evaluation value. In the drinking test, a relative evaluation using the packaged beverage of Comparative Example 2 as a standard was used, and the following criteria were used.
酸味の後味の評価基準
  5:比較例2の容器詰飲料と比較して、酸味の後味が少ない
  4:比較例2の容器詰飲料と比較して、酸味の後味がやや少ない
  3:比較例2の容器詰飲料と比較して、酸味の後味が僅かに少ない
  2:比較例2の容器詰飲料と比較して、酸味の後味がやや多い
  1:比較例2の容器詰飲料と比較して、酸味の後味が多い
  0:比較例2の容器詰飲料と比較して、酸味がなさ過ぎて、すっきりしない
Evaluation criteria for sour aftertaste 5: Less sour aftertaste compared to the packaged beverage of Comparative Example 2: 4: Slightly less aftertaste compared to the packaged beverage of Comparative Example 2 3: Comparative Example 2 The sour aftertaste is slightly less compared to the containered beverage of No. 2: Compared to the containerized beverage of Comparative Example 2, the sour aftertaste is slightly higher 1: Compared to the containerized beverage of Comparative Example 2, There is much sour aftertaste 0: Compared with the container-packed beverage of Comparative Example 2, it is too sour and not refreshing
苦渋味の後味の評価基準
  5:比較例2の容器詰飲料と比較して、苦渋味の後味が少ない
  4:比較例2の容器詰飲料と比較して、苦渋味の後味がやや少ない
  3:比較例2の容器詰飲料と比較して、苦渋味の後味が僅かに少ない
  2:比較例2の容器詰飲料と比較して、苦渋味の後味がやや多い
  1:比較例2の容器詰飲料と比較して、苦渋味の後味が多い
Evaluation criteria for bitter and astringent aftertaste 5: Less aftertaste for bitter and astringent taste compared to the canned beverage of Comparative Example 2 4: Slightly less aftertaste for bitter and astringent taste compared to the canned beverage of Comparative Example 2 3: Compared with the packaged beverage of Comparative Example 2, the bitter and astringent aftertaste is slightly less 2: Compared with the packaged beverage of Comparative Example 2, the bitter and astringent aftertaste is slightly higher 1: Containerized beverage of Comparative Example 2 More aftertaste than bitter
実施例1~18、比較例1~3
 表1に示す組成で調合し、次いで85℃で2分殺菌を行い、200mLのPETボトルに160mL充填して容器詰飲料を調製した。各容器詰飲料の成分分析及び評価結果を表1に併せて示す。
Examples 1 to 18 and Comparative Examples 1 to 3
Prepared with the composition shown in Table 1, then sterilized at 85 ° C. for 2 minutes, and filled in a 200 mL PET bottle with 160 mL to prepare a packaged beverage. Table 1 shows the component analysis and evaluation results of each packaged beverage.
Figure JPOXMLDOC01-appb-T000002
Figure JPOXMLDOC01-appb-T000002
 表1から、(A)イソクエルシトリン糖付加物等とともに(B)アミノ酸を含有せしめ、かつ各成分の濃度及びpHを特定範囲内に制御することで、酸味の後味及び苦渋味の後味が抑制され、すっきりしていて飲みやすい容器詰飲料が得られることが確認された。 From Table 1, the (A) isoquercitrin sugar adduct and the like (B) contain amino acids and control the concentration and pH of each component within a specific range, thereby suppressing the aftertaste of bitterness and bitterness. It was confirmed that a container-packed beverage that was clean and easy to drink was obtained.

Claims (11)

  1.  次の成分(A)及び(B):
    (A)イソクエルシトリン及びその糖付加物 0.03~0.17質量%、
    (B)アミノ酸 0.0001~2質量%
    を含有し、pHが2~5である容器詰飲料。
    The following components (A) and (B):
    (A) Isoquercitrin and its sugar adduct 0.03-0.17% by mass,
    (B) Amino acids 0.0001-2% by mass
    And a packaged beverage having a pH of 2-5.
  2.  成分(A)に対する成分(B)の質量比[(B)/(A)]が0.01~20である、請求項1記載の容器詰飲料。 The packaged beverage according to claim 1, wherein the mass ratio [(B) / (A)] of component (B) to component (A) is 0.01-20.
  3.  アミノ酸が中性アミノ酸である、請求項1又は2記載の容器詰飲料。 The container-packed beverage according to claim 1 or 2, wherein the amino acid is a neutral amino acid.
  4.  中性アミノ酸がロイシン又はプロリンである、請求項3記載の容器詰飲料。 4. The packaged beverage according to claim 3, wherein the neutral amino acid is leucine or proline.
  5.  更に、高甘味度甘味料を0.0001~0.5質量%含有する、請求項1~4のいずれか1項に記載の容器詰飲料。 Furthermore, the packaged beverage according to any one of claims 1 to 4, further comprising 0.0001 to 0.5 mass% of a high-intensity sweetener.
  6.  更に、炭酸ガスを1質量%以下含有する、請求項1~5のいずれか1項に記載の容器詰飲料。 Furthermore, the packaged beverage according to any one of claims 1 to 5, further comprising carbon dioxide gas in an amount of 1% by mass or less.
  7.  カリウムイオンを0.001~0.2質量%含有する、請求項1~6のいずれか1項に記載の容器詰飲料。 The packaged beverage according to any one of claims 1 to 6, comprising 0.001 to 0.2% by mass of potassium ions.
  8.  イソクエルシトリン及びその糖付加物を含有する容器詰飲料の後味の改善方法であって、次の成分(A)及び(B)を、
    (A)イソクエルシトリン及びその糖付加物 0.03~0.17質量%、
    (B)アミノ酸 0.0001~2質量%
    となるように配合し、pHを2~5に調整する、後味の改善方法。
    A method for improving the aftertaste of a packaged beverage containing isoquercitrin and its sugar adduct, comprising the following components (A) and (B):
    (A) Isoquercitrin and its sugar adduct 0.03-0.17% by mass,
    (B) Amino acids 0.0001-2% by mass
    The aftertaste is improved by adjusting the pH to 2-5.
  9.  成分(A)と成分(B)を、成分(A)に対する成分(B)の質量比[(B)/(A)]が0.01~20となるように配合する、請求項8記載の後味の改善方法。 The component (A) and the component (B) are blended so that a mass ratio [(B) / (A)] of the component (B) to the component (A) is 0.01 to 20. How to improve aftertaste.
  10.  アミノ酸として、中性アミノ酸を使用する、請求項8又は9記載の後味の改善方法。 The method for improving aftertaste according to claim 8 or 9, wherein a neutral amino acid is used as the amino acid.
  11.  中性アミノ酸として、ロイシン又はプロリンを使用する、請求項10記載の後味の改善方法。
     
    The method for improving the aftertaste according to claim 10, wherein leucine or proline is used as the neutral amino acid.
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JP2015142562A (en) * 2013-12-27 2015-08-06 花王株式会社 Packed beverage
JP2016144409A (en) * 2015-02-06 2016-08-12 キリン株式会社 Non-alcohol beer taste beverage having drinking sensation and thickness

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WO2019009251A1 (en) * 2017-07-03 2019-01-10 味の素株式会社 Beverage
JP7154926B2 (en) * 2018-10-03 2022-10-18 サントリーホールディングス株式会社 Non-alcoholic beverage containing malic acid
JP7239315B2 (en) * 2018-12-25 2023-03-14 キリンホールディングス株式会社 Carbonated drink with caramel coloring

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WO2010036576A1 (en) * 2008-09-24 2010-04-01 Pepsico, Inc. Beverage composition and method of reducing degradation of monatin

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JPH0840923A (en) * 1994-07-28 1996-02-13 Masatoshi Nakano Nutrient-supplying agent
JP2003261593A (en) * 2002-03-08 2003-09-19 Toyo Seito Kk Enzyme-treated isoquercitrin composition
WO2010036576A1 (en) * 2008-09-24 2010-04-01 Pepsico, Inc. Beverage composition and method of reducing degradation of monatin

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015142562A (en) * 2013-12-27 2015-08-06 花王株式会社 Packed beverage
JP2016144409A (en) * 2015-02-06 2016-08-12 キリン株式会社 Non-alcohol beer taste beverage having drinking sensation and thickness

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