JP2019170307A - Instant tea beverage - Google Patents
Instant tea beverage Download PDFInfo
- Publication number
- JP2019170307A JP2019170307A JP2018064290A JP2018064290A JP2019170307A JP 2019170307 A JP2019170307 A JP 2019170307A JP 2018064290 A JP2018064290 A JP 2018064290A JP 2018064290 A JP2018064290 A JP 2018064290A JP 2019170307 A JP2019170307 A JP 2019170307A
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- JP
- Japan
- Prior art keywords
- mass
- tea
- instant tea
- instant
- beverage
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 235000013361 beverage Nutrition 0.000 title claims abstract description 80
- 235000020344 instant tea Nutrition 0.000 title claims abstract description 71
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- CXQXSVUQTKDNFP-UHFFFAOYSA-N octamethyltrisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C CXQXSVUQTKDNFP-UHFFFAOYSA-N 0.000 description 1
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Landscapes
- Tea And Coffee (AREA)
Abstract
Description
本発明は、インスタント茶飲料に関する。 The present invention relates to instant tea beverages.
非重合体カテキン類は、Camellia属の茶葉に含まれるポリフェノールの1種であり、様々な生理活性を有することから、飲食品への応用が注目されている。中でも、生活習慣として手軽に摂取できることから、近年急須やティーポット等を用いることなく、カップ等の容器に入れ温水等を注ぐだけで手軽に飲用できるインスタント茶飲料が多数上市されている。 Non-polymer catechins are a kind of polyphenol contained in tea leaves belonging to the genus Camellia, and have various physiological activities, and thus are attracting attention for application to foods and drinks. Among them, since it can be easily ingested as a lifestyle, a number of instant tea beverages that can be easily drunk simply by pouring hot water into a container such as a cup without using a teapot or teapot have been put on the market in recent years.
従来、インスタント茶飲料として、例えば、エタノールと水との質量比が99/1〜75/25の混合溶液中で緑茶抽出物を精製して得られた緑茶抽出物の精製物0.5〜20.0質量%と、ヒドロキシカルボン酸若しくはそのラクトン又はそれらの塩0.01〜10.0質量%を配合し、非重合体カテキン類の含有量を0.5〜15.0質量%とすることで、非重合体カテキン類を高濃度に含有しながら、苦味及び収斂味が低減されて風味が良好であり、しかも飲料に還元した後も風味や外観安定性を長時間保持できるインスタント粉末飲料(特許文献1)、茶ポリフェノール、カテキン類及びストリクチニンを含有させ、カテキン類のうちの70重量%以上をエピ体カテキン類とすることで、茶ポリフェノールを高濃度に含有しているにも拘わらず、茶本来の香味・滋味及び口当たりに優れ、嗜好性と機能性を兼ね備えたインスタント粉末茶(特許文献2)、緑茶抽出物、抗酸化物、粉末茶及びカリウムを含有させ、カリウムの含有量を0.8〜5.6質量%とすることで、飲用時に旨味及び香りが十分に得られ、粉体色及び飲用時の水色が鮮やかな緑色を示し、かつ粉体の溶解時から飲用終了時まで粉末茶が沈降し難いインスタント緑茶(特許文献3)等が提案されている。 Conventionally, as an instant tea beverage, for example, a purified product of green tea extract 0.5 to 20 obtained by purifying a green tea extract in a mixed solution having a mass ratio of ethanol and water of 99/1 to 75/25. 0.0 mass% and hydroxycarboxylic acid or lactone thereof or a salt thereof 0.01 to 10.0 mass% are blended, and the content of non-polymer catechins is 0.5 to 15.0 mass%. In addition, an instant powdered beverage that has a high concentration of non-polymer catechins, has a good bitterness and astringent taste, has a good flavor, and can maintain flavor and appearance stability for a long time after being reduced to a beverage ( Patent Document 1), tea polyphenol, catechins and strictinin are contained, and 70% by weight or more of catechins are epi-catechins, thereby containing tea polyphenols at a high concentration. Regardless of its original flavor, taste and taste, it contains instant powder tea (Patent Document 2), green tea extract, antioxidant, powder tea and potassium, which has both taste and functionality, and contains potassium. By setting the amount to 0.8 to 5.6% by mass, sufficient umami and aroma are obtained at the time of drinking, the powder color and light blue at the time of drinking show a vivid green color, and drinking from the time of dissolution of the powder Instant green tea (Patent Document 3) and the like in which powdered tea does not easily settle until the end is proposed.
一方、アストラガリンは、柿の葉や桑の葉に含まれるポリフェノールの1種であり、抗アレルギー作用を有することが報告されている。このようなアストラガリンの生理作用に着目し、飲食品への応用が検討されており、例えば、アストラガリンに、果糖、ガラクトース、乳糖及びブドウ糖からなる群から選ばれる糖の1種又は2種以上を配合することで、アストラガリンの吸収性が向上するとの報告がある(特許文献4)。 On the other hand, astragalin is a kind of polyphenol contained in bamboo leaves and mulberry leaves, and has been reported to have antiallergic action. Paying attention to such physiological effects of astragalin, its application to foods and beverages has been studied. For example, astragalin has one or more sugars selected from the group consisting of fructose, galactose, lactose and glucose. There has been a report that the astragalin absorbability is improved by blending (Patent Document 4).
非重合体カテキン類を高含有させたインスタント茶飲料は、還元飲料としたときに強い苦味を伴うことがある。本発明の課題は、非重合体カテキン類を強化しながらも、非重合体カテキン類の苦味の抑制されたインスタント茶飲料を提供することにある。 An instant tea beverage containing a high amount of non-polymer catechins may have a strong bitter taste when used as a reduced beverage. The subject of this invention is providing the instant tea drink by which the bitterness of non-polymer catechins was suppressed, strengthening non-polymer catechins.
本発明者は、上記課題に鑑み、鋭意研究を重ねた結果、非重合体カテキン類を高含有するインスタント茶飲料に、渋味物質として知られるアストラガリンを含有させ、非重合体カテキン類とアストラガリンとの質量比を特定範囲内に制御することで、意外なことに、非重合体カテキン類を強化しながらも、苦味を顕著に低減できることを見出した。 As a result of intensive research in view of the above problems, the inventor of the present invention contains an astragalin known as an astringent substance in an instant tea beverage that contains a high amount of non-polymer catechins, and the non-polymer catechins and astra It was surprisingly found that the bitterness can be remarkably reduced while reinforcing the non-polymer catechins by controlling the mass ratio with galine within a specific range.
すなわち、本発明は、次の成分(A)及び(B);
(A)非重合体カテキン類 7.5〜20質量%、及び
(B)アストラガリン
を含有し、
成分(A)と成分(B)との質量比[(B)/(A)]が1×10-3以上30×10-3以下である、インスタント茶飲料を提供するものである。
That is, the present invention includes the following components (A) and (B);
(A) Non-polymer catechins 7.5 to 20% by mass, and (B) containing astragalin,
An instant tea beverage having a mass ratio [(B) / (A)] of the component (A) to the component (B) of 1 × 10 −3 or more and 30 × 10 −3 or less is provided.
本発明によれば、非重合体カテキン類を強化しながらも、苦味の抑制されたインスタント茶飲料を提供することができる。 ADVANTAGE OF THE INVENTION According to this invention, while strengthening non-polymer catechins, the instant tea drink by which bitterness was suppressed can be provided.
本明細書において「インスタント茶飲料」とは、液体に希釈溶解して茶飲料として飲用に供される還元食品をいう。茶飲料としては、例えば、緑茶飲料、焙じ茶飲料、紅茶飲料、烏龍茶飲料等を挙げられ、特に限定されない。また、液体は飲料に還元できれば特に限定されず、例えば、水、炭酸水、牛乳、豆乳等が挙げられ、液体の温度は問わない。 As used herein, “instant tea beverage” refers to a reduced food that is diluted and dissolved in a liquid and used for drinking as a tea beverage. Examples of the tea beverage include, but are not particularly limited to, a green tea beverage, a roasted tea beverage, a black tea beverage, and a oolong tea beverage. The liquid is not particularly limited as long as it can be reduced to a beverage, and examples thereof include water, carbonated water, milk, soy milk, and the temperature of the liquid does not matter.
本発明のインスタント茶飲料は、成分(A)として非重合体カテキン類を含有する。ここで、本明細書において「(A)非重合体カテキン類」とは、カテキン、ガロカテキン、エピカテキン及びエピガロカテキン等の非ガレート体と、カテキンガレート、ガロカテキンガレート、エピカテキンガレート及びエピガロカテキンガレート等のガレート体を併せての総称である。本発明においては、上記8種の非重合体カテキン類のうち少なくとも1種を含有すればよい。 The instant tea beverage of the present invention contains non-polymer catechins as the component (A). As used herein, “(A) non-polymer catechins” refers to non-gallate compounds such as catechin, gallocatechin, epicatechin and epigallocatechin, catechin gallate, gallocatechin gallate, epicatechin gallate and epigallo It is a general term that includes gallate bodies such as catechin gallate. In this invention, what is necessary is just to contain at least 1 sort (s) among the said 8 types of non-polymer catechins.
本発明のインスタント茶飲料中の成分(A)の含有量は7.5〜20質量%であるが、非重合体カテキン類の強化、生理効果の観点から、8質量%以上が好ましく、8.5質量%以上がより好ましく、9質量%以上が更に好ましく、また苦味低減の観点から、18質量%以下が好ましく、15質量%以下がより好ましく、12質量%以下が更に好ましい。成分(A)の含有量の範囲としては、本発明のインスタント茶飲料中に、好ましくは8〜18質量%であり、より好ましくは8.5〜15質量%であり、更に好ましくは9〜12質量%である。なお、成分(A)の含有量は、上記8種の非重合体カテキン類の合計量に基づいて定義される。また、成分(A)の含有量は、通常知られている測定法のうち測定試料の状況に適した分析法により測定することが可能であり、例えば、液体クロマトグラフィーで分析することが可能である。具体的には、後掲の実施例に記載の方法が挙げられる。なお、測定の際には装置の検出域に適合させるため、試料を凍結乾燥したり、装置の分離能に適合させるため試料中の夾雑物を除去したりする等、必要に応じて適宜処理を施してもよい。 The content of the component (A) in the instant tea beverage of the present invention is 7.5 to 20% by mass, and is preferably 8% by mass or more from the viewpoint of strengthening non-polymer catechins and physiological effects. 5 mass% or more is more preferable, 9 mass% or more is still more preferable, and from a viewpoint of bitterness reduction, 18 mass% or less is preferable, 15 mass% or less is more preferable, and 12 mass% or less is still more preferable. As a range of content of a component (A), in the instant tea drink of this invention, Preferably it is 8-18 mass%, More preferably, it is 8.5-15 mass%, More preferably, it is 9-12. % By mass. In addition, content of a component (A) is defined based on the total amount of said 8 types of non-polymer catechins. The content of the component (A) can be measured by an analysis method suitable for the state of the measurement sample among the commonly known measurement methods, and can be analyzed by, for example, liquid chromatography. is there. Specifically, the methods described in the examples described later can be mentioned. In addition, in order to adapt to the detection range of the device at the time of measurement, the sample is freeze-dried, or impurities in the sample are removed to adapt to the separation performance of the device. You may give it.
本発明のインスタント茶飲料は、成分(B)としてアストラガリンを含有する。ここで、本明細書において「アストラガリン」とは、ケンフェロールの3位にグルコースが結合した化合物である。成分(B)は、原料に由来するものでも、新たに加えられたものでもよい。 The instant tea beverage of the present invention contains astragalin as the component (B). As used herein, “astragalin” is a compound in which glucose is bonded to the 3-position of kaempferol. The component (B) may be derived from a raw material or newly added.
本発明のインスタント茶飲料中の成分(B)の含有量は、苦味低減の観点から、0.02質量%以上が好ましく、0.04質量%以上がより好ましく、また風味の観点から、0.3質量%以下が好ましく、0.2質量%以下がより好ましく、0.15質量%以下が更に好ましく、0.07質量%以下が殊更に好ましい。成分(B)の含有量の範囲としては、本発明のインスタント茶飲料中に、好ましくは0.02〜0.3質量%であり、より好ましくは0.04〜0.2質量%であり、更に好ましくは0.04〜0.15質量%であり、殊更に好ましくは0.04〜0.07質量%である。なお、成分(B)の含有量は、通常知られている測定法のうち測定試料の状況に適した分析法により測定することが可能であり、例えば、液体クロマトグラフィーで分析することが可能である。具体的には、後掲の実施例に記載の方法が挙げられる。なお、測定の際には装置の検出域に適合させるため、試料を凍結乾燥したり、装置の分離能に適合させるため試料中の夾雑物を除去したりする等、必要に応じて適宜処理を施してもよい。 The content of the component (B) in the instant tea beverage of the present invention is preferably 0.02% by mass or more, more preferably 0.04% by mass or more from the viewpoint of bitterness reduction, and from the viewpoint of flavor, the content of the component (B) is preferably 0.0. 3 mass% or less is preferable, 0.2 mass% or less is more preferable, 0.15 mass% or less is further more preferable, and 0.07 mass% or less is especially preferable. As a range of content of a component (B), in the instant tea drink of this invention, Preferably it is 0.02-0.3 mass%, More preferably, it is 0.04-0.2 mass%, More preferably, it is 0.04-0.15 mass%, More preferably, it is 0.04-0.07 mass%. The content of the component (B) can be measured by an analysis method suitable for the state of the measurement sample among the commonly known measurement methods, and can be analyzed by, for example, liquid chromatography. is there. Specifically, the methods described in the examples described later can be mentioned. In addition, in order to adapt to the detection range of the device at the time of measurement, the sample is freeze-dried, or impurities in the sample are removed to adapt to the separation performance of the device. You may give it.
本発明のインスタント茶飲料は、成分(A)と成分(B)との質量比[(B)/(A)]が1×10-3以上30×10-3以下であるが、苦味低減の観点から、2×10-3以上が好ましく、2.5×10-3以上がより好ましく、5.5×10-3以上が更に好ましく、また風味の観点から、25×10-3以下が好ましく、20×10-3以下がより好ましく、15×10-3以下が更に好ましく、9×10-3以下が殊更に好ましい。かかる質量比[(B)/(A)]の範囲としては、好ましくは2×10-3以上25×10-3以下であり、より好ましくは2.5×10-3以上20×10-3以下であり、更に好ましくは5.5×10-3以上15×10-3以下であり、殊更に好ましくは5.5×10-3以上9×10-3以下である。 In the instant tea beverage of the present invention, the mass ratio [(B) / (A)] of the component (A) and the component (B) is 1 × 10 −3 or more and 30 × 10 −3 or less. From the viewpoint, 2 × 10 −3 or more is preferable, 2.5 × 10 −3 or more is more preferable, 5.5 × 10 −3 or more is further preferable, and from the viewpoint of flavor, 25 × 10 −3 or less is preferable. 20 × 10 −3 or less is more preferable, 15 × 10 −3 or less is further preferable, and 9 × 10 −3 or less is particularly preferable. The mass ratio [(B) / (A)] is preferably 2 × 10 −3 or more and 25 × 10 −3 or less, more preferably 2.5 × 10 −3 or more and 20 × 10 −3 or less. Or less, more preferably 5.5 × 10 −3 or more and 15 × 10 −3 or less, and particularly preferably 5.5 × 10 −3 or more and 9 × 10 −3 or less.
本発明のインスタント茶飲料は、成分(C)としてバニリンを含有することができる。ここで、本明細書において「バニリン」とは、バニラの香りの主要成分であり、飲食品の分野においてフレーバーとして一般に使用されている。成分(C)は、原料に由来するものでも、新たに加えられたものでもよい。また、成分(C)は、飲食品の分野において通常使用されているものであれば由来は特に限定されず、例えば、化学合成品でも、バニラ豆より抽出したものでもよい。 The instant tea beverage of the present invention can contain vanillin as the component (C). Here, “vanillin” in the present specification is a main component of the scent of vanilla and is generally used as a flavor in the field of food and drink. Component (C) may be derived from raw materials or newly added. In addition, the origin of the component (C) is not particularly limited as long as it is usually used in the field of foods and drinks. For example, the component (C) may be a chemically synthesized product or a product extracted from vanilla beans.
本発明のインスタント茶飲料中の成分(C)の含有量は、苦味低減の観点から、0.1質量ppm以上が好ましく、0.5質量ppm以上がより好ましく、1質量ppm以上が更に好ましく、2質量ppm以上がより更に好ましく、4質量ppm以上が殊更に好ましく、そして100質量ppm以下が好ましく、50質量ppm以下がより好ましく、30質量ppm以下が更に好ましく、10質量ppm以下が殊更に好ましい。かかる成分(C)の含有量の範囲としては、本発明のインスタント茶飲料中に、好ましくは0.1〜100質量ppmであり、より好ましくは0.5〜50質量ppmであり、更に好ましくは1〜30質量ppmであり、より更に好ましくは2〜10質量ppmであり、殊更に好ましくは4〜10質量ppmである。なお、成分(C)の含有量は、通常知られている分析法のうち測定試料の状況に適した分析法、例えば、GC/MS法により測定することができる。具体的には、後掲の実施例に記載の方法が挙げられる。なお、測定の際には装置の検出域に適合させるため、試料を凍結乾燥したり、装置の分離能に適合させるため試料中の夾雑物を除去したりする等、必要に応じて適宜処理を施してもよい。 From the viewpoint of reducing bitterness, the content of the component (C) in the instant tea beverage of the present invention is preferably 0.1 mass ppm or more, more preferably 0.5 mass ppm or more, and even more preferably 1 mass ppm or more, More preferably 2 ppm by mass or more, more preferably 4 ppm by mass or more, more preferably 100 ppm by mass or less, more preferably 50 ppm by mass or less, still more preferably 30 ppm by mass or less, and still more preferably 10 ppm by mass or less. . As a range of content of this component (C), in the instant tea drink of this invention, Preferably it is 0.1-100 mass ppm, More preferably, it is 0.5-50 mass ppm, More preferably It is 1-30 mass ppm, More preferably, it is 2-10 mass ppm, Most preferably, it is 4-10 mass ppm. In addition, content of a component (C) can be measured by the analysis method suitable for the condition of the measurement sample among the analysis methods generally known, for example, GC / MS method. Specifically, the methods described in the examples described later can be mentioned. In addition, in order to adapt to the detection range of the device at the time of measurement, the sample is freeze-dried, or impurities in the sample are removed to adapt to the separation performance of the device. You may give it.
更に、本発明のインスタント茶飲料は、成分(D)としてデキストリンを含有することができる。ここで、本明細書において「デキストリン」とは、各種の糖がグリコシド結合によって重合した高分子化合物をいう。グリコシド結合は、鎖状に結合していても、環状に結合していても、これらの混合物であっても構わない。糖の結合方式としては、1,4−結合、α−1,6結合、β−1,2結合、β−1,3結合、β−1,4結合、β−1,6結合等が挙げられ、単一の結合方式のみでも、2種以上の結合方式でも構わない。 Furthermore, the instant tea beverage of the present invention can contain dextrin as component (D). As used herein, “dextrin” refers to a polymer compound in which various sugars are polymerized by glycosidic bonds. The glycosidic bond may be linked in a chain, cyclically bonded, or a mixture thereof. Examples of the sugar bonding method include 1,4-bond, α-1,6 bond, β-1,2 bond, β-1,3 bond, β-1,4 bond, β-1,6 bond, and the like. However, only a single coupling method or two or more coupling methods may be used.
成分(D)は、苦味低減の観点から、デキストロース当量(DE)が、1以上が好ましく、2以上がより好ましく、3以上が更に好ましく、そして40以下が好ましく、25以下がより好ましく、11以下が更に好ましく、9以下が更に好ましい。かかるDEの範囲としては、好ましくは1〜40であり、より好ましくは2〜25であり、更に好ましくは3〜11であり、殊更に好ましくは3〜9である。なお、デキストロース当量(DE)は、通常知られているデキストロースの測定法のうち測定試料の状況に適した分析法により測定することができる。具体的には、後掲の実施例に記載の方法により測定することができる。なお、成分(D)の含有量は、所望する最終形態に応じて適宜選択することができる。 Component (D) has a dextrose equivalent (DE) of preferably 1 or more, more preferably 2 or more, still more preferably 3 or more, and preferably 40 or less, more preferably 25 or less, and 11 or less, from the viewpoint of reducing bitterness. Is more preferable, and 9 or less is more preferable. The range of DE is preferably 1 to 40, more preferably 2 to 25, still more preferably 3 to 11, and even more preferably 3 to 9. The dextrose equivalent (DE) can be measured by an analysis method suitable for the state of the measurement sample among the commonly known methods for measuring dextrose. Specifically, it can be measured by the method described in Examples below. In addition, content of a component (D) can be suitably selected according to the final form to desire.
本発明のインスタント茶飲料は、所望により、甘味料、酸味料、香料、ビタミン、ミネラル、酸化防止剤、エステル、乳化剤、品質安定剤、保存料、調味料、果汁エキス、野菜エキス、花蜜エキス等の添加剤を1種又は2種以上を含有することができる。添加剤の含有量は、本発明の目的を損なわない範囲内で適宜設定することができる。 The instant tea beverage of the present invention may be sweetened, sour, flavor, vitamin, mineral, antioxidant, ester, emulsifier, quality stabilizer, preservative, seasoning, fruit juice extract, vegetable extract, nectar extract, etc. One or two or more additives may be contained. The content of the additive can be appropriately set within a range that does not impair the object of the present invention.
本発明のインスタント茶飲料の形態は、常温(20℃±15℃)において固形でも濃縮液状でもよく、特に限定されない。例えば、固形としては、粉末状、顆粒状、錠状、棒状、板状、ブロック状等を挙げることができる。本発明のインスタント茶飲料が固形である場合、インスタント茶飲料中の固形分量は通常95質量%以上、好ましくは97質量%以上である。なお、かかる固形分量の上限は特に限定されず、100質量%であってもよい。ここで、本明細書において「固形分量」とは、試料を105℃の電気恒温乾燥機で3時間乾燥して揮発物質を除いた残分の質量をいう。濃縮液状としては、濃縮液、ゲル状、ゼリー状、スラリー状等を挙げることができる。なお、本発明のインスタント茶飲料が濃縮液状である場合、その濃度はそのまま飲料可能なストレート飲料よりも高濃度であれば適宜選択可能であり、特に限定されない。中でも、本発明のインスタント茶飲料の形態としては、ハンドリング性の観点から、固形が好ましく、粉末が更に好ましい。 The form of the instant tea beverage of the present invention may be solid or concentrated at normal temperature (20 ° C. ± 15 ° C.), and is not particularly limited. For example, examples of solids include powder, granules, tablets, rods, plates, and blocks. When the instant tea beverage of the present invention is solid, the solid content in the instant tea beverage is usually 95% by mass or more, preferably 97% by mass or more. In addition, the upper limit of this amount of solid content is not specifically limited, 100 mass% may be sufficient. Here, the “solid content” in this specification refers to the mass of a residue obtained by drying a sample for 3 hours with an electric constant temperature dryer at 105 ° C. to remove volatile substances. Examples of the concentrated liquid include concentrated liquid, gel, jelly, and slurry. In addition, when the instant tea drink of this invention is concentrated liquid form, if the density | concentration is higher than the straight drink which can drink as it is, it can select suitably, and it will not specifically limit. Especially, as a form of the instant tea drink of this invention, solid is preferable from a viewpoint of handling property, and a powder is still more preferable.
本発明のインスタント茶飲料の希釈倍率は所定の用法にしたがえばよい。例えば、インスタント茶飲料が固形の場合、希釈倍率は、通常20〜600質量倍、好ましくは30〜500質量倍、より好ましくは50〜250質量倍、更に好ましくは100〜200質量倍である。また、インスタント茶飲料が濃縮液状である場合、希釈倍率は、通常1.5〜100質量倍であり、好ましくは1.5〜50質量倍であり、より好ましくは1.8〜30質量倍であり、更に好ましくは2〜100質量倍である。 The dilution rate of the instant tea beverage of the present invention may be in accordance with a predetermined usage. For example, when the instant tea beverage is solid, the dilution ratio is usually 20 to 600 times by mass, preferably 30 to 500 times by mass, more preferably 50 to 250 times by mass, and still more preferably 100 to 200 times by mass. When the instant tea beverage is a concentrated liquid, the dilution ratio is usually 1.5 to 100 times by mass, preferably 1.5 to 50 times by mass, more preferably 1.8 to 30 times by mass. Yes, more preferably 2 to 100 times mass.
本発明のインスタント茶飲料は、所定の用法にしたがって希釈したときに、次の特性を具備することができる。例えば、本発明のインスタント茶飲料を水で66質量倍に希釈したときに、還元飲料中の非重合体カテキン類の含有量は、通常0.06〜0.5質量%であり、より好ましくは0.08〜0.4質量%であり、更に好ましくは0.1〜0.3質量%であり、殊更に好ましくは0.12〜0.25質量%である。この場合、還元飲料のpH(20℃)は、通常3〜7であり、好ましくは3.5〜6.8であり、更に好ましくは4〜6.6であり、殊更に好ましくは5〜6.4である。なお、pHは、還元飲料100mLを300mLのビーカーに量り取り、20℃に温度調整をしてpHメータにより測定するものとする。 The instant tea beverage of the present invention can have the following characteristics when diluted according to a predetermined usage. For example, when the instant tea beverage of the present invention is diluted 66 times by mass with water, the content of non-polymer catechins in the reduced beverage is usually 0.06 to 0.5% by mass, more preferably It is 0.08-0.4 mass%, More preferably, it is 0.1-0.3 mass%, Most preferably, it is 0.12-0.25 mass%. In this case, the pH (20 ° C.) of the reduced beverage is usually 3 to 7, preferably 3.5 to 6.8, more preferably 4 to 6.6, and even more preferably 5 to 6. .4. The pH is measured with a pH meter by weighing 100 mL of the reduced beverage into a 300 mL beaker, adjusting the temperature to 20 ° C.
本発明のインスタント茶飲料は、常法にしたがって製造することが可能であり、適宜の方法を採り得る。例えば、成分(A)及び(B)、必要により他の成分を配合し、成分(A)の含有量とともに、質量比[(B)/(A)]を調整して製造することができる。成分(A)及び(B)の混合順序は特に限定されず、任意の順序で添加しても、両者を同時に添加してもよい。混合方法としては、撹拌、震盪等の適宜の方法を採用することができるが、混合装置を使用しても構わない。混合装置の混合方式は、容器回転型でも、容器固定型でもよい。容器回転型として、例えば、水平円筒型、V型、ダブルコーン型、立方体型等を採用することができる。また、容器固定型として、例えば、リボン型、スクリュー型、円錐形スクリュー型、パドル型、流動層型、フィリップスブレンダ−等を採用することができる。また、公知の造粒法により造粒物としてもよい。造粒方法としては、例えば、噴霧造粒、流動層造粒、圧縮造粒、転動造粒、撹拌造粒、押出造粒、粉末被覆造粒等が挙げられる。なお、造粒条件は、造粒方法により適宜選択することができる。更に、濃縮液状である場合、例えば、常圧にて溶媒の蒸発を行う常圧濃縮法、減圧にて溶媒の蒸発を行う減圧濃縮法、膜分離により溶媒を除去する膜濃縮法等の公知の濃縮方法を採用することができる。 The instant tea beverage of the present invention can be produced according to a conventional method, and an appropriate method can be adopted. For example, components (A) and (B), and other components as necessary, can be blended, and the mass ratio [(B) / (A)] can be adjusted together with the content of the component (A). The mixing order of components (A) and (B) is not particularly limited, and they may be added in any order or both may be added simultaneously. As a mixing method, an appropriate method such as stirring and shaking can be adopted, but a mixing device may be used. The mixing system of the mixing device may be a container rotating type or a container fixing type. As the container rotation type, for example, a horizontal cylindrical type, a V type, a double cone type, a cubic type, or the like can be adopted. As the container fixing type, for example, a ribbon type, a screw type, a conical screw type, a paddle type, a fluidized bed type, a Philips blender, or the like can be adopted. Moreover, it is good also as a granulated material by a well-known granulation method. Examples of the granulation method include spray granulation, fluidized bed granulation, compression granulation, rolling granulation, stirring granulation, extrusion granulation, powder-coated granulation and the like. The granulation conditions can be appropriately selected depending on the granulation method. Furthermore, in the case of a concentrated liquid, for example, a known atmospheric pressure concentration method in which the solvent is evaporated at normal pressure, a reduced pressure concentration method in which the solvent is evaporated at reduced pressure, a membrane concentration method in which the solvent is removed by membrane separation, and the like Concentration methods can be employed.
成分(A)は、飲食品の分野において通常使用されているものであれば由来は特に限定されず、市販の試薬でも、成分(A)を豊富に含む植物でもよく、これらを併用することもできる。成分(A)を豊富に含む植物としては、例えば、Camellia属の茶葉が挙げられ、その態様は、例えば、茶葉からの茶抽出物でも、茶葉粉砕物でもよい。
茶抽出物の場合、茶葉を溶媒で抽出して得られた茶抽出液でも、該茶抽出液の濃縮物でも乾燥物でもよく、インスタント茶飲料の製造方法に応じて適宜選択することができる。なお、抽出方法としては、例えば、ニーダー抽出、攪拌抽出(バッチ抽出)、向流抽出(ドリップ抽出)、カラム抽出等の公知の方法を採用することができる。また、抽出条件は特に限定されず、抽出方法により適宜選択することが可能である。また、茶抽出物は、インスタント茶飲料の製造方法に応じて、濃縮又は乾燥することができる。濃縮方法としては、上記と同様の方法が挙げられ、乾燥方法としては、例えば、噴霧乾燥、凍結乾燥等の公知の方法を採用することができる。
茶葉粉砕物としては茶葉を粉砕したものであれば特に限定されないが、例えば、抹茶を挙げることができる。茶葉粉砕物は、通常平均粒子径(d50)が100μm以下となるように茶葉を粉砕したものである。かかる平均粒子径の範囲としては、好ましくは0.1〜100μm、より好ましくは0.1〜50μm、更に好ましくは1〜30μmである。ここで、本明細書において「平均粒子径(d50)」とは、試料の粒度分布を体積基準で作成したときに積算分布曲線の50%に相当する粒子径(d50)を意味する。なお、茶葉の粉砕方法は公知の方法を採用することが可能であり、特に限定されない。
The origin of the component (A) is not particularly limited as long as it is normally used in the field of food and drink, and it may be a commercially available reagent or a plant rich in the component (A), and these may be used in combination. it can. Examples of plants rich in the component (A) include tea leaves of the genus Camellia, and the mode thereof may be, for example, a tea extract from tea leaves or a ground tea leaf.
In the case of a tea extract, it may be a tea extract obtained by extracting tea leaves with a solvent, a concentrate of the tea extract or a dried product, and can be appropriately selected according to the method for producing an instant tea beverage. In addition, as an extraction method, well-known methods, such as a kneader extraction, stirring extraction (batch extraction), countercurrent extraction (drip extraction), column extraction, are employable, for example. The extraction conditions are not particularly limited, and can be appropriately selected depending on the extraction method. Also, the tea extract can be concentrated or dried according to the method for producing an instant tea beverage. Examples of the concentration method include the same methods as described above. As the drying method, for example, a known method such as spray drying or freeze drying can be employed.
The tea leaf pulverized product is not particularly limited as long as it is obtained by pulverizing tea leaves, and examples thereof include matcha tea. The tea leaf pulverized product is obtained by pulverizing tea leaves so that the average particle diameter (d 50 ) is usually 100 μm or less. The range of the average particle diameter is preferably 0.1 to 100 μm, more preferably 0.1 to 50 μm, and still more preferably 1 to 30 μm. In the present specification, the "average particle diameter (d 50)" means the particle diameter (d 50) which corresponds to 50% of the cumulative distribution curve when creating a particle size distribution of the sample by volume. In addition, the grinding | pulverization method of a tea leaf can employ | adopt a well-known method, and is not specifically limited.
Camellia属の茶葉としては、例えば、C.sinensis.var.sinensis(やぶきた種を含む)、C.sinensis.var.assamica及びそれらの雑種から選択される茶葉(Camellia sinensis)が挙げられ、その加工方法により、不発酵茶、半発酵茶、発酵茶に分類することができる。Camellia属の茶葉は、1種又は2種以上を使用することができる。なお、茶葉の茶品種及び採取時期は特に限定されず、また茶葉は火入れ加工が施されていてもよい。
不発酵茶としては、例えば、煎茶、深蒸し煎茶、焙じ茶、番茶、玉露、かぶせ茶、碾茶、釜入り茶、茎茶、棒茶、芽茶等の緑茶が挙げられる。また、半発酵茶としては、例えば、鉄観音、色種、黄金桂、武夷岩茶等の烏龍茶が挙げられる。更に、発酵茶としては、ダージリン、アッサム、スリランカ等の紅茶が挙げられる。
Examples of tea leaves belonging to the genus Camellia include C. sinensis. Var. Sinensis (including Yabutaki species), C. sinensis. Var. Assamica, and tea leaves (Camellia sinensis) selected from those hybrids. According to the method, it can be classified into non-fermented tea, semi-fermented tea, and fermented tea. One or more kinds of tea leaves belonging to the genus Camellia can be used. In addition, the tea varieties and collection times of tea leaves are not particularly limited, and the tea leaves may be subjected to a burning process.
Examples of the non-fermented tea include green tea such as sencha, deep-steamed sencha, roasted tea, bancha, gyokuro, kabusecha, mochi tea, kettle tea, stem tea, stick tea, and bud tea. Examples of the semi-fermented tea include oolong tea such as iron kannon, color type, golden katsura, and martial arts tea. Further, examples of fermented tea include black teas such as Darjeeling, Assam, Sri Lanka and the like.
また、本発明のインスタント茶飲料は、原料としてCamellia属の茶葉を含んでいれば、穀物やCamellia属以外の茶葉を原料として使用してもよい。穀物としては、例えば、大麦、小麦、ハト麦、ライ麦、燕麦、裸麦等の麦;玄米等の米;大豆、黒大豆、ソラマメ、インゲン豆、小豆、エビスクサ、ササゲ、ラッカセイ、エンドウ、リョクトウ等の豆;ソバ、トウモロコシ、白ゴマ、黒ゴマ、粟、稗、黍、キヌワ等の雑穀を挙げることができる。また、Camellia属以外の茶葉としては、例えば、イチョウの葉、柿の葉、ビワの葉、桑の葉、クコの葉、杜仲の葉、小松菜、ルイボス、クマザサ、ドクダミ、アマチャヅル、スイカズラ、ツキミソウ、カキドオシ、カワラケツメイ、ギムネマ・シルベスタ、黄杞茶(クルミ科)、甜茶(バラ科)、キダチアロエ等が挙げられる。更に、カモミール、ハイビスカス、ペパーミント、レモングラス、レモンピール、レモンバーム、ローズヒップ、ローズマリー等のハーブも用いることができる。Camellia属の茶葉以外の原料茶葉は、1種又は2種以上を使用することができる。ここで、本明細書でいう「Camellia属の茶葉以外の原料茶葉」は上述のとおりCamellia属以外の茶葉に加え、穀物やハーブを包含するものとする。 In addition, the instant tea beverage of the present invention may use cereals or tea leaves other than Camellia as raw materials, as long as they contain tea leaves belonging to the genus Camellia as raw materials. Examples of grains include barley, wheat, pigeons, rye, buckwheat, and bare wheat; rice such as brown rice; soybeans, black soybeans, broad beans, kidney beans, red beans, shrimp, cowpeas, peanuts, peas, mung bean, etc. Beans; minor grains such as buckwheat, corn, white sesame, black sesame, persimmon, persimmon, persimmon, and kinuwa. In addition, tea leaves other than the genus Camellia include, for example, ginkgo biloba leaves, bamboo leaves, loquat leaves, mulberry leaves, wolfberry leaves, bamboo leaves, komatsuna, rooibos, kumazasa, dokudami, amacha eel, honeysuckle, primrose, Kakidooshi, Kawaraketsumei, Gymnema sylvestre, twilight tea (walnut family), persimmon tea (rose family), kidachi aloe and the like. Furthermore, herbs such as chamomile, hibiscus, peppermint, lemongrass, lemon peel, lemon balm, rosehip and rosemary can also be used. One type or two or more types of raw tea leaves other than Camellia tea leaves can be used. Here, “raw material tea leaves other than Camellia genus tea leaves” as used in the present specification include grains and herbs in addition to tea leaves other than Camellia genus as described above.
なお、本明細書では、Camellia属の茶葉として不発酵茶葉を最も多く使用するインスタント茶飲料を「インスタント緑茶飲料」とし、「半発酵茶葉」を最も多く使用するインスタント茶飲料を「インスタント烏龍飲料」とし、「発酵茶葉」を最も多く使用するインスタント茶飲料を「インスタント紅茶飲料」とする。 In this specification, instant tea drinks that use the most non-fermented tea leaves as Camellia genus are called “instant green tea drinks”, and instant tea drinks that use the most semi-fermented tea leaves are called “instant oolong drinks”. "Instant tea beverages that most use" fermented tea leaves "are referred to as" instant tea beverages ".
また、成分(B)は、飲食品の分野において通常使用されているものであれば由来は特に限定されず、例えば、化学合成品でも、市販の試薬を用いても、成分(B)を含有する植物からの抽出物でもよい。 In addition, the origin of the component (B) is not particularly limited as long as it is normally used in the field of foods and drinks. For example, the component (B) contains a component (B), whether it is a chemically synthesized product or a commercially available reagent. It may be an extract from a plant.
1.非重合体カテキン類の分析
試料溶液をフィルター(0.45μm)で濾過し、高速液体クロマトグラフ(型式SCL−10AVP、島津製作所製)を用い、オクタデシル基導入液体クロマトグラフ用パックドカラムL−カラムTM ODS(4.6mmφ×250mm:財団法人 化学物質評価研究機構製)を装着し、カラム温度40℃にてグラジエント法により分析した。非重合体カテキン類の標準品として、栗田工業製のものを使用し、検量線法で定量した。移動相A液は酢酸を0.1mol/L含有する蒸留水溶液、B液は酢酸を0.1mol/L含有するアセトニトリル溶液とし、試料注入量は20μL、UV検出器波長は280nmの条件で行った。なお、グラジエントの条件は、以下のとおりである。
1. Analysis of non-polymer catechins The sample solution is filtered through a filter (0.45 μm), and a high-performance liquid chromatograph (model SCL-10AVP, manufactured by Shimadzu Corporation) is used to pack an octadecyl group-introduced packed column L-column TM. An ODS (4.6 mmφ × 250 mm: manufactured by the Chemical Substance Evaluation Research Organization) was attached and analyzed by a gradient method at a column temperature of 40 ° C. As a standard product of non-polymer catechins, a product made by Kurita Kogyo was used and quantified by a calibration curve method. The mobile phase A solution was a distilled aqueous solution containing 0.1 mol / L of acetic acid, the B solution was an acetonitrile solution containing 0.1 mol / L of acetic acid, the sample injection amount was 20 μL, and the UV detector wavelength was 280 nm. . The gradient conditions are as follows.
濃度勾配条件
時間(分) A液濃度(体積%) B液濃度(体積%)
0 97% 3%
5 97% 3%
37 80% 20%
43 80% 20%
43.5 0% 100%
48.5 0% 100%
49 97% 3%
60 97% 3%
Concentration gradient condition Time (min) A solution concentration (volume%) B solution concentration (volume%)
0 97% 3%
5 97% 3%
37 80% 20%
43 80% 20%
43.50% 100%
48.5 0% 100%
49 97% 3%
60 97% 3%
2.アストラガリンの分析
試料2gを採取し、メタノール20mLを加えて5分間超音波抽出した後、25mLに定容する。次いで、1mLを分取し、25mLに定容した後、高速液体クロマトグラフ−タンデム型質量分析計を用いて分析する。
2. Analysis of astragalin Take 2 g of sample, add 20 mL of methanol and ultrasonically extract for 5 minutes, then adjust to a volume of 25 mL. Next, 1 mL is fractioned and the volume is adjusted to 25 mL, and then analyzed using a high performance liquid chromatograph-tandem mass spectrometer.
分析条件は次のとおりである。
・カラム :InertSustain C18、φ2.1mm×150mm、粒径3μm
・移動相 :水、アセトニトリル及び酢酸の混液
・流量 :0.2mL/min
・カラム温度 :40℃
・イオン化法 :エレクトロスプレー(負イオン検出モード)
・設定イオン数:m/z 446.8→254.9
The analysis conditions are as follows.
Column: InertSustain C18, φ2.1mm x 150mm, particle size 3μm
-Mobile phase: Water, acetonitrile and acetic acid mixture-Flow rate: 0.2 mL / min
-Column temperature: 40 ° C
・ Ionization method: Electrospray (negative ion detection mode)
-Number of set ions: m / z 446.8 → 254.9
また、アストラガ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、アストラガリンを指標として、前記試料溶液中のアストラガリンの定量を行う。 A standard solution of astragalin is prepared, a calibration curve is prepared by subjecting it to high performance liquid chromatographic analysis, and the amount of astragalin in the sample solution is determined using astragalin as an index. .
3.バニリンの分析
試料10mLをGC用ヘッドスペースバイアル(20mL)に採取し、塩化ナトリウム4gを添加する。バイアルに攪拌子を入れて密栓し、スターラーで30分間撹拌しながら、SPMEファイバー(シグマアルドリッチ社製、50/30μm、DVB/CAR/PDMS)に含有成分を吸着させる。吸着後、SPMEファイバーを注入口で加熱脱着し、GC/MS測定を行う。分析機器は、Agilent 7890A/5975Cinert(アジレント・テクノロジー社製)を使用する。
3. Analysis of vanillin Take a 10 mL sample into a GC headspace vial (20 mL) and add 4 g of sodium chloride. A stirrer is placed in the vial and sealed, and the components are adsorbed onto SPME fiber (Sigma Aldrich, 50/30 μm, DVB / CAR / PDMS) while stirring with a stirrer for 30 minutes. After adsorption, the SPME fiber is heated and desorbed at the inlet and GC / MS measurement is performed. The analytical instrument is Agilent 7890A / 5975Cinert (manufactured by Agilent Technologies).
分析条件は次のとおりである。
・カラム :TC―WAX(30m(長さ),0.25mm(内径),0.25μm(膜厚))
・カラム温度 :40℃ (3min)→ 20℃/min→ 250℃
・カラム圧力 :定流量モード(31kPa)
・カラム流量 :lmL/min(He)
・注入口温度 :260℃
・注入方式 :スプリットレス
・検出器 :MS
・イオン源温度:230℃
・イオン化方法:EI(70eV)
・スキャン範囲:SCAN
・ゲイン :1729V
The analysis conditions are as follows.
Column: TC-WAX (30 m (length), 0.25 mm (inner diameter), 0.25 μm (film thickness))
Column temperature: 40 ° C. (3 min) → 20 ° C./min→250° C.
-Column pressure: Constant flow rate mode (31 kPa)
-Column flow rate: 1 mL / min (He)
・ Inlet temperature: 260 ° C
・ Injection method: Splitless ・ Detector: MS
-Ion source temperature: 230 ° C
-Ionization method: EI (70 eV)
・ Scan range: SCAN
・ Gain: 1729V
購入試薬をエタノールで溶解させて、段階希釈し、標品を調製した。所定濃度の標品を試料に添加し、試料単体と同様にSPMEファイバーに吸着させ、GC/MS測定を行う。なお、定量にはm/z151のイオンのピーク面積を用いる。 The purchased reagent was dissolved in ethanol and serially diluted to prepare a sample. A sample with a predetermined concentration is added to the sample, and the sample is adsorbed on the SPME fiber in the same manner as the sample itself, and GC / MS measurement is performed. Note that the peak area of ions of m / z 151 is used for quantification.
4.デキストリンの分析
(1)定量法
試料、及び各濃度の標準溶液1.5mLに、1N−NaOH水溶液を250μLと0.5 MのPMP(3−メチル−1−フェニル−5−ピラゾロン)−メタノール溶液を500μL加え、70℃で30分加熱する。得られた溶液に 対し、1N−HCl水溶液を250μLにて中和し、5mLのクロロホルムを加え分配し、水層を測定試料とする。上記操作により得られた測定試料について、高速液体クロマト グラフィ質量分析を用い、下記条件にて測定する。
4). Analysis of dextrin (1) Quantitative method Sample and 1.5 mL of standard solution of each concentration, 250 μL of 1N-NaOH aqueous solution and 0.5 M PMP (3-methyl-1-phenyl-5-pyrazolone) -methanol solution Is heated at 70 ° C. for 30 minutes. The obtained solution is neutralized with 250 μL of 1N HCl aqueous solution, 5 mL of chloroform is added and distributed, and the aqueous layer is used as a measurement sample. The measurement sample obtained by the above operation is measured under the following conditions using high performance liquid chromatography / mass spectrometry.
分析条件
・HPLC装置:型式ACQUITY UPLC、Waters製
・MS装置 :型式SYNAPT G2−S HDMS型、Waters製
・イオン化 :ESI
・質量範囲 :m/z 100−2500
・カラム :型式Unison UK−C18 UP(2.0×100mm,3μm),インタクト社製
・移動相 :E液:ギ酸0.05%水溶液、F液:アセトニトリル(%F=15→90)
・流量 :0.6mL/min
・注入量 :1μL
Analysis conditions / HPLC apparatus: Model ACQUITY UPLC, manufactured by Waters / MS apparatus: Model SYNAPT G2-S HDMS, manufactured by Waters / ionization: ESI
Mass range: m / z 100-2500
Column: Model Unison UK-C18 UP (2.0 × 100 mm, 3 μm), manufactured by Intact ・ Mobile phase: E solution: 0.05% formic acid aqueous solution, F solution: acetonitrile (% F = 15 → 90)
・ Flow rate: 0.6mL / min
・ Injection volume: 1μL
(2)デキストロース当量
(I)分析は、デキストリンに含まれているぶどう糖、麦芽糖などの還元糖分をぶどう糖として定量する場合に適用し、次の手順にしたがって行う。
・水分の定量
・レイン・エイノン法による還元糖分の定量
・ぶどう糖として計算した還元糖の含有率(DE値、%)の計算
(2) The dextrose equivalent (I) analysis is applied when quantifying reducing sugars such as glucose and maltose contained in dextrin as glucose, and is performed according to the following procedure.
・ Quantification of moisture ・ Rain ・ Quantification of reducing sugar content by Einon method ・ Calculation of reducing sugar content (DE value,%) calculated as glucose
(II)試料の調製及び力価の標定
(II-A)試料の調製
(II-1)標準転化糖溶液
しょ糖(試薬)4.75gを正確に量り取り、90mLの水を使用して500mL容メスフラスコに移し入れる。これに塩酸(比重1.18)5mLを加え、20〜30℃で3日間放置した後、水を加えて定容し、冷暗所に保存する。その50mLを200mL容メスフラスコにとり、フェノールフタレインを指示薬として1mol/L水酸化ナトリウム溶液で中和した後、水を加えて定容する。これを転化糖溶液としてフェーリング溶液の力価の標定に用いる。
(II-2)メチレンブルー溶液
1%メチレンブルー1gを水に溶かして100mLとする。
(II-3)フェーリング溶液
A液:硫酸銅(CuSO4・5H2O)34.639gを水に溶かして500mLとし、2日間放置後ろ過する。
B液:酒石酸カリウムナトリウム(KNaC4H4O6・4H2O)173gと水酸化ナトリウム50gを水に溶かして500mLとし、これを2日間放置後ろ過する。
(II) Preparation of sample and standardization of titer (II-A) Preparation of sample (II-1) Standard invert sugar solution 4.75 g of sucrose (reagent) is accurately weighed and 500 mL using 90 mL of water. Transfer to volumetric flask. To this is added 5 mL of hydrochloric acid (specific gravity 1.18), and the mixture is allowed to stand at 20-30 ° C. for 3 days, and then added with water to make a constant volume and stored in a cool and dark place. 50 mL of the solution is taken into a 200 mL volumetric flask, neutralized with 1 mol / L sodium hydroxide solution using phenolphthalein as an indicator, and then added with water to make a constant volume. This is used as an invert sugar solution for standardizing the titer of the Fering solution.
(II-2) Methylene blue solution 1 g of 1% methylene blue is dissolved in water to make 100 mL.
(II-3) Falling solution A solution: 34.639 g of copper sulfate (CuSO 4 .5H 2 O) is dissolved in water to make 500 mL, and the solution is allowed to stand for 2 days and then filtered.
Liquid B: 173 g of potassium sodium tartrate (KNaC 4 H 4 O 6 · 4H 2 O) and 50 g of sodium hydroxide are dissolved in water to make 500 mL, and this is left for 2 days and then filtered.
(II-B)フェーリング溶液の力価の標定
フェーリング溶液A液5.0mL及びB液5mLを200mL容三角フラスコにとり、50mL容ビュレットを用いて標準転化糖溶液19.5mLを加える。電熱器上で2分間沸騰させた後、メチレンブルー溶液4滴を加え、沸騰しながら標準転化糖溶液を滴下し、青色が消失したところを終点とする。滴定は沸騰し始めてから3分以内に終了する。この滴定を3回行い、平均値を求める。但し、3回の平均値を滴定値とするが、各滴定値の差は0.1mL以内とする。また、力価の小数点以下第4位を四捨五入し、1±0.02の範囲内に収める。
(II-B) Standardization of the titer of the failing solution Take 5.0 mL of the failing solution A and 5 mL of the solution B in a 200 mL Erlenmeyer flask and add 19.5 mL of the standard invert sugar solution using a 50 mL burette. After boiling for 2 minutes on an electric heater, 4 drops of methylene blue solution is added, and the standard invert sugar solution is dropped while boiling, and the point where the blue color disappears is taken as the end point. The titration ends within 3 minutes after starting to boil. This titration is performed 3 times, and the average value is obtained. However, the average of three times is used as the titration value, but the difference between the titration values is within 0.1 mL. Round off the fourth decimal place of the titer and keep it within the range of 1 ± 0.02.
〔式中、Aは、消費した標準転化糖溶液の量(mL)を示す。〕 [In formula, A shows the quantity (mL) of the standard invert sugar solution consumed. ]
(III)試料の調製
分析試料は、試料の性状に応じて、次により調製する。
(III-1)液体試料
液体中に結晶又は塊状物が析出している場合には、密閉容器に入れ、60〜70℃の水浴に浸漬して溶解し、よく振り混合した後、室温に冷却する。
(III-2)固体試料
粉末又は結晶状とし、塊がある場合には砕き、よく混合する。
(III) Preparation of sample Analytical samples are prepared as follows according to the properties of the samples.
(III-1) Liquid sample If crystals or lumps are precipitated in the liquid, put in a sealed container, dissolve in a 60-70 ° C water bath, dissolve well, and cool to room temperature. To do.
(III-2) Solid sample Powder or crystal form. If there is a lump, crush it and mix well.
(IV)水分の定量
水分の定量は、試料の性状により、次の方法で行う。
(IV-1)液体試料
乾燥助剤として、予め秤量瓶に海砂を約15g取り、ガラス棒とともに105℃の乾燥機中で乾燥して恒量を求める。次に、前記(III)で調製した均一試料を固形分として約2gに相当する量を正確に量り取り、必要があれば少量の水を全体が浸るまで加え、時々ガラス棒でかき混ぜながら水浴上で加熱して大部分の水を揮散させる。更に、105℃の乾燥機内で時々かき混ぜ、ほとんど乾燥するまで乾かした後、真空乾燥機に移し、70℃で4時間乾燥する。デシケータ中で室温まで放冷した後、重量を量る。1時間ずつ真空乾燥を繰り返して恒量を求める。減量が、2mg以下の変化になった時を恒量に達したとみなす。
(IV-2)固体試料
前記(III)で調製した均一試料約2gを予め恒量にした秤量瓶に正確に量り取り、真空乾燥機で70℃、4時間乾燥する。次に、デシケータ中で室温まで放冷した後、重量を量る。更に、1時間ずつ真空乾燥を繰り返して、減量が2mg以下の変化になった時を恒量に達したとみなす。
(IV-3)水分の計算
試料中の水分は、次式により算出する。数値は小数点以下第2位を四捨五入する。
(IV) Quantification of moisture The moisture is quantified by the following method according to the properties of the sample.
(IV-1) Liquid Sample As a drying aid, about 15 g of sea sand is taken in a weighing bottle in advance and dried in a dryer at 105 ° C. together with a glass rod to obtain a constant weight. Next, accurately measure the amount corresponding to about 2 g of the solid sample prepared in the above (III) as a solid content, add a small amount of water if necessary until it is completely immersed, and occasionally stir with a glass rod on a water bath. Heat up to volatilize most of the water. Further, the mixture is occasionally stirred in a dryer at 105 ° C., dried until almost dry, then transferred to a vacuum dryer and dried at 70 ° C. for 4 hours. Allow to cool to room temperature in a desiccator and then weigh. Repeat the vacuum drying for 1 hour to obtain the constant weight. When the weight loss changes by 2 mg or less, it is considered that the constant weight has been reached.
(IV-2) Solid Sample About 2 g of the uniform sample prepared in the above (III) is accurately weighed in a weighing bottle previously made constant, and dried in a vacuum dryer at 70 ° C. for 4 hours. Next, it is allowed to cool to room temperature in a desiccator and then weighed. Furthermore, vacuum drying is repeated for 1 hour, and when the weight loss changes to 2 mg or less, it is considered that the constant weight has been reached.
(IV-3) Calculation of moisture The moisture in the sample is calculated by the following formula. Numbers are rounded to the first decimal place.
〔式中、W0は試料の採取量(g)を示し、W1は乾燥後の試料の重量(g)を示す。〕 [Wherein W 0 represents the amount of sample collected (g), and W 1 represents the weight (g) of the sample after drying. ]
(V)DE値の定量
(V-1)検液の調製
前記(III)で調製した均一試料約10gを正確に量り取り、水に溶かして500mL容メスフラスコに移し入れ、水を加えて容定し検液とする。
(V-2)滴定操作
フェーリング溶液A液5.0mL及びB液5mLを200mL容三角フラスコに採り、50mL容ビュレットを用いて、(V-1)で調製した検液15mLを加え、(II-B)の要領にしたがって滴定し、これを予備滴定とする。更に同様にして、予備滴定で得た滴定数より約1mL少ない量の検液を加え、(II-B)の要領にしたがって滴定する。ここで得た検液の消費量にフェーリング溶液の力価を乗じ、この数値から表1に示すレイン・エイノン糖量表(ぶどう糖)を用いて還元糖濃度(DE値,mg/100mL)をぶどう糖として求める。
(V-3)DE値の計算
試料の乾燥状態におけるぶどう糖として計算したDE値は、次式により算出する。数値は、小数点以下第2位を四捨五入する。
(V) DE value determination (V-1) Preparation of test solution About 10 g of the uniform sample prepared in (III) above is accurately weighed, dissolved in water, transferred to a 500 mL volumetric flask, and water is added to the solution. Use the test solution.
(V-2) Titration operation Take 5.0 mL of the Falling Solution A and 5 mL of Solution B in a 200 mL Erlenmeyer flask, add 15 mL of the test solution prepared in (V-1) using a 50 mL burette, and add (II- Titrate according to the procedure in B), and use this as the preliminary titration. Further, in the same manner, a test solution of about 1 mL less than the titration constant obtained by preliminary titration is added, and titration is performed according to the procedure of (II-B). The consumption of the test solution obtained here is multiplied by the titer of the Fehring solution, and from this value, the reducing sugar concentration (DE value, mg / 100 mL) is obtained by using the Rain-Eynon sugar content table (glucose) shown in Table 1. Asking.
(V-3) Calculation of DE Value The DE value calculated as glucose in the dry state of the sample is calculated by the following equation. Numbers are rounded to the first decimal place.
〔式中、
DSは、表1に示すレイン・エイノン糖量表(ぶどう糖)を用いて求めた検液100mL中のぶどう糖量(mg)を示し、
Mは、(IV)で秤量した試料の水分(%)を示し、
Sは、(V-1)で秤量した試料の採取量(g)を示す。〕
[Where,
D S indicates rain Einon sugar amount table shown in Table 1 (glucose) glucose amount in the test solution 100mL was determined using the (mg),
M represents the moisture content (%) of the sample weighed in (IV),
S represents the amount (g) of the sample weighed in (V-1). ]
5.pH測定
各インスタント茶飲料を20℃の水で66質量倍に希釈し、還元飲料100mLを300mLのビーカーに量り取り、pHメータ(HORIBA コンパクトpHメータ、堀場製作所製)を用いて、20℃に温度調整をして測定した。
5. pH measurement Each instant tea beverage was diluted 66 times by mass with water at 20 ° C., 100 mL of reduced beverage was weighed into a 300 mL beaker, and the temperature was adjusted to 20 ° C. using a pH meter (HORIBA Compact pH meter, manufactured by HORIBA, Ltd.). Measured with adjustment.
6.官能評価
各インスタント茶飲料を20℃の水で66質量倍に希釈した還元飲料の「苦味」について専門パネル4名が官能試験を行った。官能試験では、各パネリストが下記の評価基準とすることに合意したうえで実施した。その後、専門パネルの評点の平均値を求めた。なお、評点の平均値は、小数第2位を四捨五入するものとする。
6). Sensory evaluation Four expert panels conducted a sensory test on the “bitter taste” of a reduced beverage obtained by diluting each instant tea beverage 66 times by mass with 20 ° C. water. The sensory test was conducted after each panelist agreed to the following evaluation criteria. Then, the average value of the score of the specialized panel was calculated. The average score shall be rounded to the first decimal place.
苦味の評価基準
苦味は、飲用したときの苦味の強さを評価した。
1:苦味が非常に強い
2:苦味が強い
3:苦味がやや強い
4:苦味がごくわずかに強い
5:苦味が程よい
Criteria for evaluating bitterness Bitterness was evaluated by evaluating the strength of bitterness when consumed.
1: Very strong bitterness 2: Strong bitterness 3: Slightly strong bitterness 4: Very slightly bitterness 5: Moderate bitterness
製造例1
緑茶粉末の製造
2番煎茶葉(宮崎県産(2016年度産))を石臼で挽き、平均粒子径(d50)が20μmの緑茶粉末を得た。緑茶粉末は、非重合体カテキン類の含有量が11.1質量%であり、アストラガリンの含有量が0.034質量%であった。
Production Example 1
Manufacture of Green Tea Powder No. 2 Sencha leaves (produced in Miyazaki Prefecture (produced in 2016)) were ground with a stone mill to obtain a green tea powder having an average particle size (d 50 ) of 20 μm. The green tea powder had a non-polymer catechin content of 11.1% by mass and an astragalin content of 0.034% by mass.
実施例1〜6及び比較例1、2
表2に示す各成分を混合し、粉末状のインスタント茶飲料を得た。得られたインスタント茶飲料について分析及び官能評価を行った。得られたインスタント茶飲料はいずれも固形分量が97.0質量%であった。なお、実施例1〜6及び比較例1、2のインスタント茶飲料を20℃の水で66質量倍に希釈して調製された還元飲料は、非重合体カテキン類の含有量が0.14質量%であり、pH(20℃)が5.8であった。また、官能評価は、実施例6のインスタント茶飲料から調製された還元飲料の苦味の強度を評点「5」とし、比較例1のインスタント茶飲料から調製された還元飲料の苦味の強度を評点「1」として、上記評価基準にしたがって行った。その結果を表2に示す。
Examples 1 to 6 and Comparative Examples 1 and 2
Each component shown in Table 2 was mixed to obtain a powdered instant tea beverage. The obtained instant tea beverage was analyzed and subjected to sensory evaluation. All of the obtained instant tea beverages had a solid content of 97.0% by mass. In addition, the reduced beverages prepared by diluting the instant tea beverages of Examples 1 to 6 and Comparative Examples 1 and 2 with water at 20 ° C. by 66 times by mass have a non-polymer catechin content of 0.14 mass. % And pH (20 ° C.) was 5.8. The sensory evaluation was based on the bitterness intensity of the reduced beverage prepared from the instant tea beverage of Example 6 as “5”, and the bitterness intensity of the reduced beverage prepared from the instant tea beverage of Comparative Example 1 as “ 1 ”was performed according to the above evaluation criteria. The results are shown in Table 2.
実施例7及び比較例3
表3に示す各成分を混合し、粉末状のインスタント茶飲料を得た。得られたインスタント茶飲料について分析及び官能評価を行った。得られたインスタント茶飲料はいずれも固形分量が97.0質量%であった。なお、実施例7及び比較例3のインスタント茶飲料を20℃の水で66質量倍に希釈して調製された還元飲料は、非重合体カテキン類の含有量が0.28質量%であり、pH(20℃)が5.8であった。また、官能評価は、比較例3のインスタント茶飲料から調製された還元飲料の苦味の強度を評点「1」として、上記評価基準にしたがって行った。その結果を表3に示す。
Example 7 and Comparative Example 3
Each component shown in Table 3 was mixed to obtain a powdered instant tea beverage. The obtained instant tea beverage was analyzed and subjected to sensory evaluation. All of the obtained instant tea beverages had a solid content of 97.0% by mass. In addition, the reduced beverage prepared by diluting the instant tea beverage of Example 7 and Comparative Example 3 with water at 20 ° C. by 66 mass times has a non-polymer catechin content of 0.28% by mass, The pH (20 ° C.) was 5.8. Moreover, sensory evaluation was performed according to the said evaluation criteria by setting the bitterness intensity | strength of the reduced drink prepared from the instant tea drink of the comparative example 3 as the score "1". The results are shown in Table 3.
実施例8、9及び比較例4
表4に示す各成分を混合し、粉末状のインスタント茶飲料を得た。得られたインスタント茶飲料について分析及び官能評価を行った。得られたインスタント茶飲料はいずれも固形分量が97.0質量%であった。なお、実施例8及び比較例4のインスタント茶飲料を20℃の水で66質量倍に希釈して調製された還元飲料は、非重合体カテキン類の含有量が0.11質量%であり、実施例9のインスタント茶飲料から調製された還元飲料は、非重合体カテキン類の含有量が0.12質量%であった。また、いずれの還元飲料もpH(20℃)は、5.8であった。また、官能評価は、実施例1と同一基準で行った。その結果を表4に示す。
Examples 8 and 9 and Comparative Example 4
Each component shown in Table 4 was mixed to obtain a powdered instant tea beverage. The obtained instant tea beverage was analyzed and subjected to sensory evaluation. All of the obtained instant tea beverages had a solid content of 97.0% by mass. In addition, the reduced beverage prepared by diluting the instant tea beverage of Example 8 and Comparative Example 4 with water at 20 ° C. by 66 times by mass has a non-polymer catechin content of 0.11% by mass, The reduced beverage prepared from the instant tea beverage of Example 9 had a non-polymer catechin content of 0.12% by mass. Moreover, pH (20 degreeC) of all the reduced drinks was 5.8. The sensory evaluation was performed based on the same criteria as in Example 1. The results are shown in Table 4.
実施例10〜12
表5に示す各成分を混合し、粉末状のインスタント緑茶飲料を得た。得られたインスタント茶飲料について分析及び官能評価を行った。得られたインスタント茶飲料はいずれも固形分量が97.0質量%であった。なお、実施例10〜12のインスタント茶飲料を20℃の水で66質量倍に希釈して調製された還元飲料は、非重合体カテキン類の含有量が0.15質量%であり、pH(20℃)が5.8であった。また、官能評価は、実施例1と同一基準で行った。その結果を表5に示す。
Examples 10-12
Each component shown in Table 5 was mixed to obtain a powdery instant green tea beverage. The obtained instant tea beverage was analyzed and subjected to sensory evaluation. All of the obtained instant tea beverages had a solid content of 97.0% by mass. In addition, the reduced beverage prepared by diluting the instant tea beverages of Examples 10 to 12 with water at 20 ° C. by 66 times by mass has a non-polymer catechin content of 0.15% by mass, and has a pH ( 20 ° C.) was 5.8. The sensory evaluation was performed based on the same criteria as in Example 1. The results are shown in Table 5.
実施例13、14
表6に示す各成分を混合し、濃縮液状のインスタント緑茶飲料を得た。得られたインスタント茶飲料について分析及び官能評価を行った。なお、実施例13,14のインスタント茶飲料を20℃の水で66質量倍に希釈して調製された還元飲料は、非重合体カテキン類の含有量が0.15質量%であり、pH(20℃)が5.8であった。また、官能評価は、実施例1と同一基準で行った。その結果を表6に示す。
Examples 13 and 14
Each component shown in Table 6 was mixed to obtain a concentrated liquid instant green tea beverage. The obtained instant tea beverage was analyzed and subjected to sensory evaluation. In addition, the reduced beverage prepared by diluting the instant tea beverages of Examples 13 and 14 with water at 20 ° C. by 66 times by mass has a non-polymer catechin content of 0.15% by mass, and has a pH ( 20 ° C.) was 5.8. The sensory evaluation was performed based on the same criteria as in Example 1. The results are shown in Table 6.
表2〜6から、高濃度の非重合体カテキン類に、アストラガリンを含有させ、非重合体カテキン類とアストラガリンとの質量比を特定範囲内に制御することで、非重合体カテキン類を強化しながらも、非重合体カテキン類の苦味が低減されたインスタント茶飲料が得られることがわかる。 From Tables 2 to 6, high-concentration non-polymer catechins contain astragalin, and the non-polymer catechins are controlled by controlling the mass ratio of non-polymer catechins and astragalin within a specific range. It can be seen that an instant tea beverage in which the bitterness of non-polymer catechins is reduced while being strengthened can be obtained.
Claims (5)
(A)非重合体カテキン類 7.5〜20質量%、及び
(B)アストラガリン
を含有し、
成分(A)と成分(B)との質量比[(B)/(A)]が1×10-3以上30×10-3以下である、インスタント茶飲料。 The following components (A) and (B);
(A) Non-polymer catechins 7.5 to 20% by mass, and (B) containing astragalin,
Instant tea drink whose mass ratio [(B) / (A)] of an ingredient (A) and an ingredient (B) is 1x10-3 or more and 30x10-3 or less.
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