JP2020191830A - Beverage composition - Google Patents
Beverage composition Download PDFInfo
- Publication number
- JP2020191830A JP2020191830A JP2019100178A JP2019100178A JP2020191830A JP 2020191830 A JP2020191830 A JP 2020191830A JP 2019100178 A JP2019100178 A JP 2019100178A JP 2019100178 A JP2019100178 A JP 2019100178A JP 2020191830 A JP2020191830 A JP 2020191830A
- Authority
- JP
- Japan
- Prior art keywords
- beverage
- dextrin
- concentration
- beverage composition
- comparative example
- 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
Links
- 235000013361 beverage Nutrition 0.000 title claims abstract description 229
- 239000000203 mixture Substances 0.000 title claims abstract description 131
- 239000007787 solid Substances 0.000 claims abstract description 147
- 229920001353 Dextrin Polymers 0.000 claims abstract description 102
- 239000004375 Dextrin Substances 0.000 claims abstract description 102
- 235000019425 dextrin Nutrition 0.000 claims abstract description 102
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 claims abstract description 48
- 229920001864 tannin Polymers 0.000 claims abstract description 33
- 239000001648 tannin Substances 0.000 claims abstract description 33
- 235000018553 tannin Nutrition 0.000 claims abstract description 33
- 235000001671 coumarin Nutrition 0.000 claims abstract description 23
- 229960000956 coumarin Drugs 0.000 claims abstract description 23
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- 235000013616 tea Nutrition 0.000 claims description 103
- 235000009569 green tea Nutrition 0.000 claims description 59
- 235000006468 Thea sinensis Nutrition 0.000 claims description 23
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- 240000006914 Aspalathus linearis Species 0.000 claims description 19
- 235000012984 Aspalathus linearis Nutrition 0.000 claims description 17
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- ADRVNXBAWSRFAJ-UHFFFAOYSA-N catechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3ccc(O)c(O)c3 ADRVNXBAWSRFAJ-UHFFFAOYSA-N 0.000 claims description 16
- 235000005487 catechin Nutrition 0.000 claims description 16
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- 150000001765 catechin Chemical class 0.000 claims description 12
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Abstract
Description
本発明は、飲料組成物に関する。 The present invention relates to beverage compositions.
タンニンは茶葉等に含まれるポリフェノールの1種であり、抗酸化作用をはじめとする様々な生理活性を有することが知られている。このような生理効果を発現させるためには、タンニンを継続して摂取する必要があり、それを生活習慣として簡便に摂取する手段として飲料がある。しかしながら、タンニンは強い渋味を有するため、飲料を継続して摂取するうえで障害となりやすい。そこで、ポリフェノールの渋味の抑制について検討され、例えば、シクロデキストリンやソーマチンがタンニン等のポリフェノールの渋味に対してマスキング作用を有するとの報告がある(特許文献1)。 Tannin is one of the polyphenols contained in tea leaves and the like, and is known to have various physiological activities including antioxidant activity. In order to exert such a physiological effect, it is necessary to continuously ingest tannin, and there is a beverage as a means for easily ingesting it as a lifestyle. However, since tannin has a strong astringency, it tends to be an obstacle to continuous intake of beverages. Therefore, suppression of astringency of polyphenols has been studied, and it has been reported that, for example, cyclodextrin and thaumatin have a masking effect on the astringency of polyphenols such as tannin (Patent Document 1).
しかしながら、タンニン等のポリフェノールにデキストリンを添加すると、口に含んだ際に感じる渋味は抑制できるものの、口に含んだ後に渋味が余韻として残り、後に引きやすい。このような後に引く渋味を抑制するために、デキストリンを増量することが考えられるが、デキストリンは、粉っぽさ、苦味、雑味といった独特の異味を有するため、多量に添加するには限界がある。以下、本明細書において、口を含んだ後に余韻として残り、後に引く渋味を「後渋味」という。
本発明の課題は、デキストリン由来の異味を抑制しつつ、タンニン由来の後渋味が低減された飲料組成物を提供することにある。
However, when dextrin is added to a polyphenol such as tannin, the astringency felt when it is contained in the mouth can be suppressed, but the astringency remains as a lingering finish after being contained in the mouth, and it is easy to pull back later. It is conceivable to increase the amount of dextrin in order to suppress such astringency that is drawn afterwards, but dextrin has a unique taste such as powderiness, bitterness, and miscellaneous taste, so it is limited to be added in a large amount. There is. Hereinafter, in the present specification, the astringency that remains as a lingering finish after including the mouth and is drawn later is referred to as "post-astringency".
An object of the present invention is to provide a beverage composition in which the aftertaste derived from tannin is reduced while suppressing the unpleasant taste derived from dextrin.
本発明者らは、上記課題に鑑み、鋭意研究を重ねた結果、タンニンとデキストリンをそれぞれ特定量含有させ、タンニンに対して特定の香気成分を特定の質量比で含有させることで、デキストリン由来の異味を抑制しつつ、タンニン由来の後渋味が低減された飲料組成物が得られることを見出した。 In view of the above problems, the present inventors have conducted intensive studies and found that tannin and dextrin are each contained in a specific amount, and a specific aroma component is contained in a specific mass ratio with respect to tannin, thereby being derived from dextrin. It has been found that a beverage composition having a reduced aftertaste derived from tannin can be obtained while suppressing an offensive taste.
すなわち、本発明は、次の成分(A)、(B)及び(C);
(A)タンニン 固形分中に1.2〜12質量%
(B)デキストリン 固形分中に18〜95質量%
(C)クマリン及びその誘導体から選択される少なくとも1種
を含有し、
成分(A)と成分(C)との質量比[(C)/(A)]が0.70×10−4以上300×10−4以下である、
飲料組成物を提供するものである。
That is, the present invention describes the following components (A), (B) and (C);
(A) 1.2-12% by mass of tannin solids
(B) 18-95% by mass in the dextrin solid content
(C) Containing at least one selected from coumarin and its derivatives,
The mass ratio [(C) / (A)] of the component (A) to the component (C) is 0.70 × 10 -4 or more and 300 × 10 -4 or less.
It provides a beverage composition.
本発明によれば、デキストリン由来の異味を抑制しつつ、タンニン由来の後渋味が低減された飲料組成物を提供することができる。 According to the present invention, it is possible to provide a beverage composition in which the aftertaste derived from tannin is reduced while suppressing the unpleasant taste derived from dextrin.
本発明の飲料組成物は、例えば、液状でも、固形状でもよく、適宜の形態を採り得る。
例えば、本発明の飲料組成物が液状である場合、飲料の形態は、RTD飲料のみならず、濃縮還元飲料、ゼリー状、濃縮液状、スラリー状等の形態でもよい。中でも、利便性の観点から、RTD飲料が好ましい。ここで、本明細書において「RTD飲料」とは、希釈せずにそのまま飲用できる飲料をいう。ゼリー状である場合、容器に備え付けられた吸い口やストローから飲料組成物を吸引できれば、その固形分濃度は特に限定されず、適宜選択可能である。また、本発明の飲料組成物が固形状である場合、常温(20℃±15℃)において固体であればその形状は特に限定されず、粉末状、顆粒状、錠状、棒状、板状、ブロック状等の種々の形状とすることができる。固形飲料組成物は、固形分量が通常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」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をいい、「固形分量」とは、その残分の質量をいう。
The beverage composition of the present invention may be, for example, liquid or solid, and may take an appropriate form.
For example, when the beverage composition of the present invention is liquid, the form of the beverage may be not only an RTD beverage but also a concentrated reduced beverage, a jelly-like, a concentrated liquid, a slurry-like form, or the like. Among them, RTD beverages are preferable from the viewpoint of convenience. Here, the term "RTD beverage" as used herein refers to a beverage that can be drunk as it is without being diluted. In the case of a jelly-like substance, the solid content concentration is not particularly limited and can be appropriately selected as long as the beverage composition can be sucked from the mouthpiece or straw provided in the container. When the beverage composition of the present invention is solid, its shape is not particularly limited as long as it is solid at room temperature (20 ° C ± 15 ° C), and is powdery, granular, tablet-like, rod-like, plate-like, or It can have various shapes such as a block shape. The solid beverage composition usually has a solid content of 95% by mass or more, preferably 97% by mass or more. The upper limit of the solid content is not particularly limited and may be 100% by mass. Here, in the present specification, the “solid content” refers to the residue obtained by drying the sample in an electric constant temperature dryer at 105 ° C. for 3 hours to remove volatile substances, and the “solid content” refers to the residue thereof. Refers to mass.
本発明の飲料組成物は、本発明の効果を享受しやすい点で、茶飲料組成物が好ましい。ここで、本明細書において「茶飲料組成物」とは、植物抽出物を茶原料として含み、専ら飲用に供される組成物をいう。
植物抽出物の原料としては特に限定されないが、例えば、Camellia属の茶葉、穀物、Camellia属以外の茎葉、根を挙げることができる。なお、植物抽出物の抽出方法及び抽出条件は特に限定されず、植物の種類に応じて公知の方法を採用することができる。
The beverage composition of the present invention is preferably a tea beverage composition in that the effects of the present invention can be easily enjoyed. Here, the term "tea beverage composition" as used herein refers to a composition containing a plant extract as a tea raw material and used exclusively for drinking.
The raw material of the plant extract is not particularly limited, and examples thereof include tea leaves and grains of the genus Camellia, foliage and roots of the genus Camellia. The extraction method and extraction conditions of the plant extract are not particularly limited, and a known method can be adopted depending on the type of plant.
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)が挙げられる。茶葉は、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、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、芽茶等の緑茶葉が挙げられる。また、半発酵茶としては、例えば、鉄観音、色種、黄金桂、武夷岩茶等のウーロン茶葉が挙げられる。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葉が挙げられる。
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、コーン(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。穀物は、1種又は2種以上を使用することができる。
Camellia属以外の茎葉、根としては、例えば、イチョウの葉、柿の葉、ビワの葉、桑の葉、ゴボウ、チコリの葉、タンポポの葉又は根、クコの葉、杜仲の葉、エゴマの葉、小松菜、ルイボス、クマザサ、ヨモギ、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属以外の茎葉、根は、1種又は2種以上を使用することができる。
Examples of tea leaves of the genus Camellia include C. sinensis.var.sinensis (including Camellia seeds), C. sinensis.var. Assamica and tea leaves (Camellia sinensis) selected from hybrids thereof. Tea leaves can be classified into non-fermented tea, semi-fermented tea, and fermented tea according to the processing method, and one kind or two or more kinds can be used. The tea variety and collection time of the tea leaves are not particularly limited, and the tea leaves may be fired. Examples of the non-fermented tea include green tea leaves such as sencha, deep-steamed sencha, roasted tea, bancha, gyokuro, kabusecha, tencha, potted tea, kukicha, bar tea, and mecha. In addition, examples of semi-fermented tea include oolong tea leaves such as Tieguanyin, color species, golden katsura, and Wuyi tea. Further, examples of fermented tea include black tea leaves such as Darjeeling, Assam and Sri Lanka.
Examples of grains include barley, wheat, pigeon barley, rye, swallow barley, bare barley and other wheat; brown rice and other rice; soybeans, black soybeans, soybeans, green beans, red beans, shrimp, sage, lacquer, pea, ryokuto and the like. Beans: Millets such as buckwheat, corn, white sesame, black sesame, millet, Japanese millet, millet, and kinuwa can be mentioned. One kind or two or more kinds of grains can be used.
Stems and roots other than the genus Camellia include, for example, ginkgo leaves, persimmon leaves, biwa leaves, mulberry leaves, gobos, chicory leaves, dandelion leaves or roots, spider leaves, tochu leaves, and egoma. Examples include leaves, Komatsuna, Louis Boss, Kumazasa, Yomogi, Dokudami, Amachazuru, Watermelon, Tsukimisou, Kakidooshi, Kawaraketsumei, Gymnema sylvestre, Yellow tea (Walnut family), Sweet tea (Rose family), Kidachi aloe and the like. In addition, herbs such as chamomile, hibiscus, peppermint, lemongrass, lemon peel, lemon balm, rose hips and rosemary can also be used. One or more kinds of foliage and roots other than Camellia can be used.
中でも、本発明の効果を享受しやすい点から、Camellia属の茶葉、穀物及びルイボスから選択される少なくとも1種を原料とすることが好ましく、Camellia属の茶葉及びルイボスから選択される少なくとも1種を原料とすることが更に好ましい。
茶飲料組成物の種類としては、例えば、緑茶飲料、ウーロン茶飲料、紅茶飲料、ルイボス茶飲料、麦茶飲料、コーン茶飲料が好ましく、緑茶飲料、ウーロン茶飲料、ルイボス茶飲料が更に好ましい。
Among them, it is preferable to use at least one selected from Camellia tea leaves, grains and rooibos as a raw material from the viewpoint of easily enjoying the effects of the present invention, and at least one selected from Camellia tea leaves and rooibos. It is more preferable to use it as a raw material.
As the type of the tea beverage composition, for example, a green tea beverage, an oolong tea beverage, a black tea beverage, a Louis Boss tea beverage, a barley tea beverage, and a corn tea beverage are preferable, and a green tea beverage, an oolong tea beverage, and a Louis Boss tea beverage are further preferable.
本発明の飲料組成物は、成分(A)としてタンニンを含有する。ここで、本明細書において「タンニン」とは、後掲の実施例に記載の方法により測定されるものであって、非重合体カテキン類、没食子酸、そのエステル及びそれらの縮合物、並びにクロロゲン酸類及びその縮合物を包含する概念である。また、本明細書において「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り、本発明においては上記8種のうち少なくとも1種を含有すればよい。また、「クロロゲン酸類」とは、3−カフェオイルキナ酸、4−カフェオイルキナ酸及び5−カフェオイルキナ酸のモノカフェオイルキナ酸と、3−フェルラキナ酸、4−フェルラキナ酸及び5−フェルラキナ酸のモノフェルラキナ酸を併せての総称であり、本発明においては上記6種のうち少なくとも1種を含有すればよい。 The beverage composition of the present invention contains tannin as the component (A). Here, the term "tannin" as used herein is measured by the method described in Examples described later, and is a non-polymer catechin, gallic acid, an ester thereof and a condensate thereof, and a chlorogen. It is a concept that includes acids and their condensates. In addition, in the present specification, "non-polymer catechins" refers to non-gallates such as catechin, galocatechin, epicatechin and epigallocatechin, and catechin gallate, galocatechin gallate, epicatechin gallate and epigallocatechin gallate. It is a general term for gallates together, and in the present invention, at least one of the above eight types may be contained. The "chlorogenic acids" are 3-cafe oil quinic acid, 4-cafe oil quinic acid and 5-cafe oil quinic acid monocafe oil quinic acid, and 3-ferlaquinic acid, 4-ferlaquinic acid and 5-ferlacina. It is a general term for the acid monoferlaquinic acid, and in the present invention, at least one of the above six types may be contained.
本発明の飲料組成物は、固形分中の成分(A)の含有量が1.2〜12質量%であるが、生理活性の観点から、1.3質量%以上が好ましく、1.5質量%以上がより好ましく、1.7質量%以上が更に好ましく、また後渋味抑制の観点から、10質量%以下が好ましく、8.5質量%以下がより好ましく、7質量%以下が更に好ましい。かかる成分(A)の範囲としては、飲料組成物の固形分中に、好ましくは1.3〜10質量%であり、より好ましくは1.5〜8.5質量%であり、更に好ましくは1.7〜7質量%である。なお、成分(A)の分析は、後掲の実施例に記載の方法にしたがうものとする。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 beverage composition of the present invention has a content of the component (A) in the solid content of 1.2 to 12% by mass, preferably 1.3% by mass or more, preferably 1.5% by mass, from the viewpoint of physiological activity. % Or more is more preferable, 1.7% by mass or more is further preferable, and from the viewpoint of suppressing post-astringency, 10% by mass or less is more preferable, 8.5% by mass or less is more preferable, and 7% by mass or less is further preferable. The range of the component (A) is preferably 1.3 to 10% by mass, more preferably 1.5 to 8.5% by mass, and further preferably 1 in the solid content of the beverage composition. .7 to 7% by mass. The analysis of the component (A) shall be in accordance with the method described in the examples below. At the time of measurement, appropriate treatment is performed as necessary, such as freeze-drying the sample to match the detection range of the device and removing impurities in the sample to match the separability of the device. May be good.
本発明の飲料組成物は、成分(A)として、少なくとも非重合体カテキン類(以下、「成分(A1)」とも称する)を含有することが好ましい。
本発明の飲料組成物中の成分(A)と成分(A1)との質量比[(A1)/(A)]は、渋味の観点から、0.01以上が好ましく、0.015以上がより好ましく、0.018以上が更に好ましい。なお、かかる質量比[(A1)/(A)]の上限は特に限定されないが、1であってもよい。かかる質量比[(A1)/(A)]の範囲としては、好ましくは0.01〜1であり、より好ましくは0.015〜1であり、更に好ましくは0.018〜1である。
The beverage composition of the present invention preferably contains at least non-polymer catechins (hereinafter, also referred to as "component (A1)") as the component (A).
The mass ratio [(A1) / (A)] of the component (A) to the component (A1) in the beverage composition of the present invention is preferably 0.01 or more, preferably 0.015 or more, from the viewpoint of astringency. More preferably, 0.018 or more is further preferable. The upper limit of the mass ratio [(A1) / (A)] is not particularly limited, but may be 1. The range of the mass ratio [(A1) / (A)] is preferably 0.01 to 1, more preferably 0.015 to 1, and even more preferably 0.018 to 1.
本発明の飲料組成物は、固形分中の成分(A1)の含有量が、0.01質量%以上であることが好ましく、0.02質量%以上がより好ましく、0.03質量%以上が更に好ましく、また後渋味抑制の観点から、9質量%以下が好ましく、8質量%以下がより好ましく、7質量%以下が更に好ましい。かかる成分(A1)の範囲としては、飲料組成物の固形分中に、好ましくは0.01〜9質量%であり、より好ましくは0.02〜8質量%であり、更に好ましくは0.03〜7質量%である。なお、成分(A1)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(A1)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。 In the beverage composition of the present invention, the content of the component (A1) in the solid content is preferably 0.01% by mass or more, more preferably 0.02% by mass or more, and 0.03% by mass or more. Further, from the viewpoint of suppressing post-astringency, 9% by mass or less is preferable, 8% by mass or less is more preferable, and 7% by mass or less is further preferable. The range of the component (A1) is preferably 0.01 to 9% by mass, more preferably 0.02 to 8% by mass, and further preferably 0.03 in the solid content of the beverage composition. ~ 7% by mass. The content of the component (A1) is defined based on the total amount of the above eight types of non-polymer catechins. Further, the content of the component (A1) can be measured by an analysis method suitable for the condition of the measurement sample among the commonly known measurement methods, and can be analyzed by, for example, liquid chromatography. .. Specifically, the method described in the examples described later can be mentioned. At the time of measurement, appropriate treatment is performed as necessary, such as freeze-drying the sample to match the detection range of the device and removing impurities in the sample to match the separability of the device. May be given.
本発明の飲料組成物は、成分(B)としてデキストリンを含有する。ここで、本明細書において「デキストリン」とは、でんぷん分解物の一種であり、でんぷんを酸処理又は加熱処理して部分的に加水分解し低分子化した化合物である。デキストリンは、糖がグリコシド結合によって重合した分子構造を有しており、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、α−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。 The beverage composition of the present invention contains dextrin as the component (B). Here, the term "dextrin" as used herein is a kind of starch decomposition product, and is a compound obtained by partially hydrolyzing starch by acid treatment or heat treatment to reduce its molecular weight. Dextrin has a molecular structure in which sugars are polymerized by glycosidic bonds, and the glycosidic bonds may be chain-bonded, cyclically bonded, or a mixture thereof. Examples of the sugar binding method include α-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. It may be mentioned that only a single bonding method or two or more types of bonding methods may be used.
成分(B)は、本発明の効果を享受しやすい点から、デキストロース当量(DE)が、1以上が好ましく、2以上が更に好ましく、そして30以下が好ましく、21以下がより好ましく、13以下が更に好ましく、5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1〜30であり、より好ましくは2〜21であり、更に好ましくは2〜13であり、殊更に好ましくは2〜5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が挙げられる。 The component (B) has a dextrose equivalent (DE) of 1 or more, more preferably 2 or more, preferably 30 or less, more preferably 21 or less, and 13 or less, from the viewpoint of easily enjoying the effects of the present invention. More preferably, 5 or less is further preferable. The range of such DE is preferably 1 to 30, more preferably 2 to 21, still more preferably 2 to 13, and even more preferably 2 to 5. The dextrose equivalent (DE) can be measured by an analytical method suitable for the condition of the measurement sample among the commonly known measuring methods for dextrose. Specifically, the method described in the examples described later can be mentioned.
本発明の飲料組成物は、固形分中の成分(B)の含有量が18〜95質量%であるが、後渋味抑制の観点から、20質量%以上であることが好ましく、35質量%以上がより好ましく、50質量%以上が更に好ましく、また異味抑制の観点から、93質量%以下が好ましく、90質量%以下が更に好ましい。かかる成分(B)の範囲としては、飲料組成物の固形分中に、好ましくは20〜95質量%であり、より好ましくは35〜93質量%であり、更に好ましくは50〜90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、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 beverage composition of the present invention has a content of the component (B) in the solid content of 18 to 95% by mass, but is preferably 20% by mass or more, preferably 35% by mass, from the viewpoint of suppressing post-astringency. The above is more preferable, 50% by mass or more is further preferable, and from the viewpoint of suppressing unpleasant taste, 93% by mass or less is preferable, and 90% by mass or less is further preferable. The range of the component (B) is preferably 20 to 95% by mass, more preferably 35 to 93% by mass, and further preferably 50 to 90% by mass in the solid content of the beverage composition. .. The content of the component (B) can be measured by an analytical method suitable for the condition of the measurement sample among the commonly known measurement methods. For example, the method described in the following Examples can be used. Can be mentioned. At the time of measurement, appropriate treatment is performed as necessary, such as freeze-drying the sample to match the detection range of the device and removing impurities in the sample to match the separability of the device. May be given.
本発明の飲料組成物は、成分(C)としてクマリン及びその誘導体から選択される少なくとも1種を含有する。ここで、本明細書において「クマリン」とは、ベンゾ−α−ピロンであり、また「クマリン誘導体」とは、7−メトキシクマリン、4−ヒドロキシクマリン及び3,4−ジヒドロクマリンである。クマリン及びその誘導体は、甘い香りを有する香気成分として知られているが、同様に甘い香りを有するバニリンやマルトールは、デキストリン由来の異味抑制効果やタンニン由来の渋味低減効果が不十分であり、クマリン及びその誘導体がデキストリン由来の異味抑制やタンニン由来の渋味低減に有効であることを本発明者らは見出した。中でも、本発明の効果を享受しやすい点から、成分(C)として、少なくともクマリンを含有することが好ましく、クマリン及びその誘導体を含有することが更に好ましい。なお、成分(C)として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、天然由来品でも、化学合成品でも、市販品でも、原料由来のものでもよい。 The beverage composition of the present invention contains at least one selected from coumarin and its derivatives as the component (C). Here, the "coumarin" in the present specification is benzo-α-pyrone, and the "coumarin derivative" is 7-methoxycoumarin, 4-hydroxycoumarin and 3,4-dihydrocoumarin. Coumarin and its derivatives are known as aroma components having a sweet scent, but vanillin and maltol, which also have a sweet scent, have insufficient dextrin-derived taste-suppressing effect and tannin-derived astringency-reducing effect. The present inventors have found that coumarin and its derivatives are effective in suppressing the unpleasant taste derived from dextrin and reducing the astringency derived from tannin. Above all, from the viewpoint that the effect of the present invention can be easily enjoyed, it is preferable to contain at least coumarin as the component (C), and it is more preferable to contain coumarin and its derivative. The origin of the component (C) is not particularly limited as long as it is normally used in the field of food and drink. For example, it may be a naturally derived product, a chemically synthesized product, a commercially available product, or a raw material-derived product. Good.
本発明の飲料組成物は、固形分中の成分(C)の含有量が、渋味抑制の観点から、1.8質量ppm以上が好ましく、2.3質量ppm以上がより好ましく、2.8質量ppm以上が更に好ましく、また異味抑制の観点から、18質量ppm以下が好ましく、14質量ppm以下がより好ましく、10質量ppm以下が更に好ましい。成分(C)の含有量の範囲としては、飲料組成物の固形分中に、好ましくは1.8〜18質量ppmであり、より好ましくは2.3〜14質量ppmであり、更に好ましくは2.8〜10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、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。 In the beverage composition of the present invention, the content of the component (C) in the solid content is preferably 1.8 mass ppm or more, more preferably 2.3 mass ppm or more, and 2.8 from the viewpoint of suppressing astringency. It is more preferably mass ppm or more, more preferably 18 mass ppm or less, still more preferably 14 mass ppm or less, still more preferably 10 mass ppm or less, from the viewpoint of suppressing unpleasant taste. The range of the content of the component (C) is preferably 1.8 to 18 mass ppm, more preferably 2.3 to 14 mass ppm, and further preferably 2 in the solid content of the beverage composition. It is .8 to 10 mass ppm. The content of the component (C) can be measured by an analytical method suitable for the condition of the measurement sample among the commonly known measurement methods, and can be measured by, for example, the GC / MS method. .. Specifically, the method described in the examples described later can be mentioned. At the time of measurement, appropriate treatment is performed as necessary, such as freeze-drying the sample to match the detection range of the device and removing impurities in the sample to match the separability of the device. May be given.
本発明の飲料組成物は、成分(A)と成分(C)との質量比[(C)/(A)]が0.70×10−4以上300×10−4以下であるが、後渋味及び異味の抑制の観点から、0.75×10−4以上が好ましく、0.85×10−4以上がより好ましく、0.95×10−4以上が更に好ましく、また風味バランスの観点から、250×10−4以下が好ましく、200×10−4以下がより好ましく、150×10−4以下が更に好ましい。かかる質量比[(C)/(A)]の範囲としては、好ましくは0.75×10−4以上250×10−4以下であり、より好ましくは0.85×10−4以上200×10−4以下であり、更に好ましくは0.95×10−4以上150×10−4以下である。なお、質量比[(C)/(A)]は、成分(A)と成分(C)の含有量の単位を揃えて算出するものとする。 The beverage composition of the present invention has a mass ratio [(C) / (A)] of the component (A) to the component (C) of 0.70 × 10 -4 or more and 300 × 10 -4 or less, but later. From the viewpoint of suppressing astringency and unpleasant taste, 0.75 × 10 -4 or more is preferable, 0.85 × 10 -4 or more is more preferable, 0.95 × 10 -4 or more is more preferable, and flavor balance is also considered. Therefore , 250 × 10 -4 or less is preferable, 200 × 10 -4 or less is more preferable, and 150 × 10 -4 or less is further preferable. The range of the mass ratio [(C) / (A)] is preferably 0.75 × 10 -4 or more and 250 × 10 -4 or less, and more preferably 0.85 × 10 -4 or more and 200 × 10 It is -4 or less, more preferably 0.95 × 10 -4 or more and 150 × 10 -4 or less. The mass ratio [(C) / (A)] shall be calculated by aligning the units of the contents of the component (A) and the component (C).
本発明の飲料組成物は、所望により、甘味料、酸味料、アミノ酸、たんぱく質、ビタミン、ミネラル、エステル、花蜜エキス、色素、乳化剤、乳成分、ココアパウダー、保存料、調味料、品質安定剤等の添加剤を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 beverage composition of the present invention can be used as a sweetener, acidulant, amino acid, protein, vitamin, mineral, ester, nectar extract, pigment, emulsifier, milk component, cocoa powder, preservative, seasoning, quality stabilizer and the like, if desired. Can contain one or more of the additives of. The content of the additive can be appropriately set within a range that does not impair the object of the present invention.
また、本発明の飲料組成物が固形飲料組成物である場合、必要に応じて許容される担体を含有することができる。例えば、賦形剤(例えば、グルコース、ガラクトース、フルクトース等の単糖類、スクロース、ラクトース、ラクトース、パラチノース等の二糖類、マルチトール、キシリトール、ソルビトール、還元パラチノース等の糖アルコール);結合剤(例えば、ヒドロキシプロピルメチルセルロース、ヒドロキシプロピルセルロース、ゼラチン、アルファー化デンプン、ポリビニルピロリドン、ポリビニルアルコール、プルラン、メチルセルロース、硬化油等);崩壊剤(例えば、カルメロース、カルメロースカルシウム、クロスカルメロースナトリウム、クロスポピドン、トウモロコシデンプン、低置換度ヒドロキシプロピルセルロース等);滑沢剤(例えば、ステアリン酸カルシウム、ステアリン酸マグネシウム、ショ糖脂肪酸エステル、フマル酸ステアリルナトリウム、タルク、二酸化ケイ素等);嬌味剤(例えば、ステビア等);オリゴ糖、寒天、結晶セルロース、軽質無水ケイ酸、リン酸水素カルシウム、増量剤、界面活性剤、分散剤、緩衝剤、希釈剤等の担体が挙げられる。なお、担体の含有量は、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可能である。 Further, when the beverage composition of the present invention is a solid beverage composition, an acceptable carrier can be contained, if necessary. For example, excipients (eg, monosaccharides such as glucose, galactose, fructose, disaccharides such as sucrose, lactose, lactose, palatinose, sugar alcohols such as maltulose, xylitol, sorbitol, reduced palatinose); binders (eg, eg Hydroxypropyl methylcellulose, hydroxypropylcellulose, gelatin, pregelatinized starch, polyvinylpyrrolidone, polyvinyl alcohol, purulan, methylcellulose, hardened oil, etc.; Disintegrants (eg, carmellose, carmellose calcium, croscarmellose sodium, crospopidone, corn starch) , Low-substituted hydroxypropyl cellulose, etc.); Lubricants (eg, calcium stearate, magnesium stearate, sucrose fatty acid ester, sodium stearyl fumarate, talc, silicon dioxide, etc.); Flavoring agents (eg, stevia, etc.); Examples thereof include carriers such as oligosaccharides, agar, crystalline cellulose, light anhydrous silicic acid, calcium hydrogen phosphate, bulking agents, surfactants, dispersants, buffers, and diluents. The content of the carrier can be appropriately set within a range that does not impair the object of the present invention.
本発明の飲料組成物がRTD飲料である場合、あるいは本発明の飲料組成物が固形飲料組成物又は濃縮飲料組成物であって、該固形飲料組成物又は濃縮飲料組成物を還元飲料とした場合、pH(20℃)は、4以上が好ましく、4.5以上がより好ましく、5以上が更に好ましく、そして7以下が好ましく、6.8以下がより好ましく、6.5以下が更に好ましい。かかるpHの範囲としては、好ましくは4〜7であり、より好ましくは4.5〜6.8であり、更に好ましくは5〜6.5である。なお、固形飲料組成物又は濃縮飲料組成物を還元飲料とする場合、固形飲料組成物又は濃縮飲料組成物を液体に希釈溶解すればよく、液体の温度は問わない。液体は飲料に還元できれば特に限定されないが、例えば、水、炭酸水、牛乳、豆乳等を挙げることができる。また、pHは、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。 When the beverage composition of the present invention is an RTD beverage, or when the beverage composition of the present invention is a solid beverage composition or a concentrated beverage composition and the solid beverage composition or the concentrated beverage composition is a reduced beverage. , PH (20 ° C.) is preferably 4 or more, more preferably 4.5 or more, further preferably 5 or more, and preferably 7 or less, more preferably 6.8 or less, still more preferably 6.5 or less. The pH range is preferably 4 to 7, more preferably 4.5 to 6.8, and even more preferably 5 to 6.5. When the solid beverage composition or the concentrated beverage composition is used as a reduced beverage, the solid beverage composition or the concentrated beverage composition may be diluted and dissolved in a liquid, and the temperature of the liquid does not matter. The liquid is not particularly limited as long as it can be reduced to a beverage, and examples thereof include water, carbonated water, milk, and soymilk. Further, the pH shall be measured by a pH meter after adjusting the temperature to 20 ° C.
本発明の飲料組成物がRTD飲料である場合、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に充填して容器詰飲料とすることができる。
また、RTD飲料の場合、加熱殺菌済でもよい。殺菌方法としては、適用されるべき法規(日本にあっては食品衛生法)に定められた条件に適合するものであれば特に限定されない。例えば、茶飲料を容器包装に充填し、密栓若しくは密封した後殺菌するか、又は自記温度計をつけた殺菌器等で殺菌したもの若しくはろ過器等で除菌したものを自動的に容器包装に充填した後、密栓若しくは密封すればよい。より具体的には、レトルト殺菌法、高温短時間殺菌法(HTST法)、超高温殺菌法(UHT法)等を挙げることができる。
When the beverage composition of the present invention is an RTD beverage, it is a normal packaging container such as a molded container (so-called PET bottle) containing polyethylene terephthalate as a main component, a metal can, a paper container compounded with a metal foil or a plastic film, and a bottle. Can be filled into a packaged beverage.
Further, in the case of RTD beverage, it may be sterilized by heating. The sterilization method is not particularly limited as long as it meets the conditions stipulated in the applicable regulations (Food Sanitation Law in Japan). For example, tea beverages are filled in containers and packaging and sterilized after being sealed or sealed, or sterilized with a sterilizer equipped with a self-recording thermometer or sterilized with a filter etc. After filling, it may be sealed or sealed. More specifically, a retort sterilization method, a high-temperature short-time sterilization method (HTST method), an ultra-high-temperature sterilization method (UHT method), and the like can be mentioned.
また、本発明の飲料組成物が固形飲料組成物である場合、例えば、瓶等に容器詰し飲用する際にカップ1杯分をスプーン等で計量するもの、1杯分を収容したカップタイプ、カップ1杯分毎に小分け包装したスティックタイプ等とすることができる。更に、本発明の飲料組成物が濃縮飲料組成物である場合、例えば、カップ1杯分毎に小分け包装したポーションタイプの希釈飲料とすることができる。なお、カップの容量は30〜320mLであることが好ましく、また小分け包装の内容量はカップ容量に適合するように適宜設定することが可能である。小分け包装は、アルミ蒸着フィルム等を材質とする包装材料で包装することができる。なお、容器内及び包材内は窒素ガスを充填してもよく、また包材は酸素透過性の低いものが品質維持の点で好ましい。 When the beverage composition of the present invention is a solid beverage composition, for example, one cup is weighed with a spoon or the like when it is packed in a bottle or the like and drunk, and a cup type containing one cup. It can be a stick type or the like that is packaged in small portions for each cup. Further, when the beverage composition of the present invention is a concentrated beverage composition, for example, it can be a portion-type diluted beverage that is packaged in small portions for each cup. The capacity of the cup is preferably 30 to 320 mL, and the content of the subdivided package can be appropriately set so as to match the capacity of the cup. The subdivided packaging can be packaged with a packaging material made of an aluminum vapor-deposited film or the like. The inside of the container and the inside of the packaging material may be filled with nitrogen gas, and the packaging material having low oxygen permeability is preferable from the viewpoint of maintaining quality.
本発明の飲料組成物は適宜の方法で製造することができるが、例えば、成分(A)、(B)及び(C)、必要により他の成分を配合し、成分(A)及び(B)の含有量、並びに質量比[(C)/(A)]を調整して製造することができる。 The beverage composition of the present invention can be produced by an appropriate method, and for example, the components (A), (B) and (C), and if necessary, other components may be blended to form the components (A) and (B). It can be produced by adjusting the content of and the mass ratio [(C) / (A)].
成分(A)としては、市販の試薬を用いてもよいが、成分(A)を豊富に含む植物の抽出物の形態で含有させることができる。
植物としては、成分(A)を含み、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特に限定されないが、例えば、Camellia属の茶葉、柿葉、栗皮、ヒマワリ種子、リンゴ、コーヒー豆、シモン葉、マツ、サトウキビ、南天の葉、ゴボウ、ナスの皮、ウメの果実、フキタンポポ、ブドウ種子、ブドウ果皮等が挙げられ、1種又は2種以上を使用することができる。中でも、タンニン含量、風味の観点から、Camellia属の茶葉、コーヒー豆及びリンゴから選ばれる1種又は2種以上が好ましい。なお、コーヒー豆は、生コーヒー豆でも、焙煎コーヒー豆でもよく、焙煎条件は、適宜選択することができる。また、抽出方法及び抽出条件は特に限定されず、公知の方法を採用することができる。
As the component (A), a commercially available reagent may be used, but it can be contained in the form of a plant extract rich in the component (A).
The plant is not particularly limited as long as it contains the component (A) and is usually used in the field of food and drink, but for example, tea leaves of the genus Camellia, pericarp, chestnut bark, sunflower seeds, apples, coffee beans. , Simon leaf, pine, sugar cane, southern sky leaf, gobo, eggplant skin, sea urchin fruit, sunflower popo, grape seed, grape skin and the like, and one or more kinds can be used. Among them, one or more selected from Camellia tea leaves, coffee beans and apples are preferable from the viewpoint of tannin content and flavor. The coffee beans may be raw coffee beans or roasted coffee beans, and the roasting conditions can be appropriately selected. Further, the extraction method and the extraction conditions are not particularly limited, and a known method can be adopted.
1.タンニンの分析
試料中のタンニン量の測定は酒石酸鉄法により、標準液として没食子酸エチルを用い、没食子酸の換算量として求めた(参考文献:「緑茶ポリフェノール」飲食料品用機能性素材有効利用技術シリーズNo.10)。
純水で溶解した試料5mLを酒石酸鉄標準溶液5mLで発色させ、リン酸緩衝液で25mLに定溶し、540nmで吸光度を測定し、没食子酸エチルによる検量線からタンニン量を求めた。
酒石酸鉄標準液の調製:硫酸第一鉄・7水和物100mg、酒石酸ナトリウム・カリウム(ロッシェル塩)500mgを蒸留水で100mLとした。
リン酸緩衝液の調製 :1/15mol/Lリン酸水素二ナトリウム溶液と1/15mol/Lリン酸二水素ナトリウム溶液を混合しpH7.5に調整した。
1. 1. Analysis of tannin The amount of tannin in the sample was measured by the iron tartrate method using ethyl gallate as a standard solution and calculated as a conversion amount of gallate (Reference: "Green tea polyphenol" Effective use of functional materials for food and drink). Technology series No. 10).
5 mL of the sample dissolved in pure water was colored with 5 mL of an iron tartrate standard solution, dissolved in 25 mL with a phosphate buffer solution, the absorbance was measured at 540 nm, and the amount of tannin was determined from the calibration curve with ethyl gallate.
Preparation of iron tartrate standard solution: 100 mg of ferrous sulfate heptahydrate and 500 mg of sodium tartrate (Rochelle salt) were added to 100 mL of distilled water.
Preparation of phosphate buffer: A 1/15 mol / L disodium hydrogen phosphate solution and a 1/15 mol / L sodium dihydrogen phosphate solution were mixed to adjust the pH to 7.5.
2.非重合体カテキン類の分析
純水で溶解希釈した試料を、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ODS、4.6mmφ×250mm 粒子径5μm:財団法人 化学物質評価研究機構製)を装着し、カラム温度35℃でグラジエント法により測定する。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、流速は1mL/分、試料注入量は10μL、UV検出器波長は280nmの条件で行う。なお、グラジエント条件は以下の通りである。
2. 2. Analysis of non-polymer catechins
A sample dissolved and diluted with pure water is used on a high performance liquid chromatograph (model SCL-10AVP, manufactured by Shimadzu Corporation), and a packed column for an octadecyl group-introduced liquid chromatograph (L-column ODS, 4.6 mmφ × 250 mm, particle size 5 μm: It is equipped with a chemical substance evaluation research organization) and measured by the gradient method at a column temperature of 35 ° C. The mobile phase A solution is a distilled aqueous solution containing 0.1 mol / L of acetic acid, the B solution is an acetonitrile solution containing 0.1 mol / L of acetic acid, the flow velocity is 1 mL / min, the sample injection amount is 10 μL, and the UV detector wavelength is The condition is 280 nm. The gradient conditions are as follows.
濃度勾配条件(体積%)
時間 A液濃度 B液濃度
0分 97% 3%
5分 97% 3%
37分 80% 20%
43分 80% 20%
43.5分 0% 100%
48.5分 0% 100%
49分 97% 3%
60分 97% 3%
Concentration gradient condition (% by volume)
Time A liquid concentration B liquid concentration 0 minutes 97% 3%
5 minutes 97% 3%
37 minutes 80% 20%
43 minutes 80% 20%
43.5 minutes 0% 100%
48.5 minutes 0% 100%
49 minutes 97% 3%
60 minutes 97% 3%
3.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質量分析を用い、下記条件にて測定する。
3. 3. Analysis of dextrin (1) Quantitative method 250 μL of 1N-NaOH aqueous solution and 0.5 M PMP (3-methyl-1-phenyl-5-pyrazolone) -methanol solution in 1.5 mL of sample and standard solution of each concentration Add 500 μL and heat at 70 ° C. for 30 minutes. A 1N-HCl aqueous solution is neutralized with 250 μL to the obtained 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 chromatograph 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
Analytical conditions-HPLC device: model ACQUITY UPLC, made by Waters-MS device: model SYNAPT G2-S HDMS type, made by Waters-ionization: ESI
-Mass range: m / z 100-2500
-Column: Model Unison UK-C18 UP (2.0 x 100 mm, 3 μm), manufactured by Intact Co., Ltd.-Mobile phase: Liquid E: 0.05% aqueous solution of formic acid, Liquid F: acetonitrile (% F = 15 → 90)
・ Flow rate: 0.6 mL / min
・ Injection volume: 1 μL
(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) Dextrose equivalent (I) analysis is applied when the reduced sugar content such as glucose and maltose contained in dextrin is quantified as glucose, and is performed according to the following procedure.
・ Quantification of water ・ Quantification of reducing sugar by Rain-Ainon 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
スクロース(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
G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。
H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 determination of titer (II-A) Preparation of sample (II-1) Standard invert sugar solution Weigh accurately 4.75 g of sucrose (reagent) and use 90 mL of water to measure 500 mL. Transfer to a measuring flask. To this, 5 mL of hydrochloric acid (specific gravity 1.18) is added, and the mixture is left at 20 to 30 ° C. for 3 days, then water is added to the volume, and the mixture is stored in a cool and dark place. 50 mL of the flask is placed in a 200 mL volumetric flask, neutralized with a 1 mol / L sodium hydroxide solution using phenolphthalein as an indicator, and then water is added to control the volume. This is used as an invert sugar solution to determine the titer of Fehling's solution.
(II-2) Methylene blue solution Dissolve 1 g of 1% methylene blue in water to make 100 mL.
(II-3) Fehling solution G solution: copper sulfate (CuSO 4 · 5H 2 O) 34.639g and 500mL dissolved in water and filtered after standing for 2 days.
H solution: sodium potassium sodium tartrate and (KNaC 4 H 4 O 6 · 4H 2 O) 173g hydroxide 50g and 500mL dissolved in water, which is filtered after standing for 2 days.
(II-B)フェーリング溶液の力価の標定
フェーリング溶液G液5.0mL及びH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) Indication of the titer of Fehling's solution Take 5.0 mL of Fehling's solution G solution and 5 mL of H solution in a 200 mL Erlenmeyer flask, and add 19.5 mL of standard invert sugar solution using a 50 mL volume 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 end point is where the blue color disappears. Titration is completed within 3 minutes of beginning to boil. This titration is performed 3 times and the average value is calculated. However, the average value of 3 times is taken as the titration value, but the difference between each titration value is within 0.1 mL. In addition, the fourth decimal place of the titer is rounded off to 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 the formula, A indicates the amount (mL) of the consumed standard invert sugar solution. ]
(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 The analysis sample is prepared as follows according to the properties of the sample.
(III-1) Liquid sample If crystals or lumps are precipitated in the liquid, put them in a closed container, immerse them in a water bath at 60 to 70 ° C to dissolve them, shake them well, mix them, and then cool them to room temperature. To do.
(III-2) Solid sample Make powder or crystal, crush if there is a lump, 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 water content The water content is quantified by the following method depending on the properties of the sample.
(IV-1) Liquid sample As a drying aid, take about 15 g of sea sand in a weighing bottle in advance and dry it with a glass rod in a dryer at 105 ° C to determine the constant amount. Next, weigh accurately the amount equivalent to about 2 g of the uniform sample prepared in (III) above as a solid content, add a small amount of water if necessary until the whole is immersed, and stir occasionally with a glass rod on the water bath. Heat with to volatilize most of the water. Further, it is stirred occasionally 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. Vacuum drying is repeated for 1 hour to obtain a constant amount. When the weight loss changes to 2 mg or less, it is considered that the constant dose has been reached.
(IV-2) Solid sample About 2 g of the uniform sample prepared in (III) above is accurately weighed in a pre-constant weight weighing bottle 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. Further, vacuum drying is repeated for 1 hour each, and when the weight loss changes to 2 mg or less, it is considered that the constant dose has been reached.
(IV-3) Calculation of water content The water content 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。〕 [In the formula, W 0 indicates the amount of sample collected (g), and W 1 indicates 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G液5.0mL及びH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) Quantification of DE value (V-1) Preparation of test solution Weigh accurately about 10 g of the uniform sample prepared in (III) above, dissolve it in water, transfer it to a 500 mL volumetric flask, and add water. Set and use as a test solution.
(V-2) Titration operation Take 5.0 mL of Fehling's solution G solution and 5 mL of H solution into a 200 mL Erlenmeyer flask, add 15 mL of the test solution prepared in (V-1) using a 50 mL volume burette, and add (II-). Titrate according to the procedure in B), and use this as a preliminary titration. Further, in the same manner, add an amount of the test solution about 1 mL less than the titration constant obtained by the preliminary titration, and titrate according to the procedure of (II-B). Multiply the consumption of the test solution obtained here by the titer of the Fehling's solution, and from this value, use the rain-Ainon sugar amount table (glucose) shown in Table 1 to determine the reducing sugar concentration (DE value, mg / 100 mL) of glucose. Ask as.
(V-3) Calculation of DE value The DE value calculated as glucose in the dry state of the sample is calculated by the following formula. 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。〕
[In the formula,
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 indicates the water content (%) of the sample weighed in (IV).
S indicates the collected amount (g) of the sample weighed in (V-1). ]
4.クマリン及びその誘導体の分析
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を添加した。その後、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た。吸着後、SPMEファイバーを注入口で加熱脱着し、GC/MS測定を行った。分析機器は、Agilent 7890A/5975Cinert(アジレント・テクノロジー社製)を使用した。
4. Analysis of coumarin and its derivatives 10 mL of a sample was collected in a GC headspace vial (20 mL), and 4 g of sodium chloride was added. Then, a stirrer was placed in a vial, the vial was tightly closed, and the components were adsorbed on SPME fiber (manufactured by Sigma-Aldrich, 50/30 μm, DVB / CAR / PDMS) while stirring with a stirrer for 30 minutes. After adsorption, SPME fiber was heated and desorbed at the injection port, and GC / MS measurement was performed. The analytical instrument used was Agilent 7890A / 5975Cinert (manufactured by Agilent Technologies).
分析条件は次のとおりである。
・カラム :VF−WAX(60m(長さ)、0.25mm(内径)、1.0μm(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 :250℃
・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:m/z10〜500
・定量イオン :クマリン m/z146、7−メトキシクマリン m/z176、4−ヒドロキシクマリン m/z162、3,4−ジヒドロクマリン m/z148
The analysis conditions are as follows.
-Column: VF-WAX (60 m (length), 0.25 mm (inner diameter), 1.0 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: lmL / min (He)
・ Inlet temperature: 250 ℃
・ Injection method: Splitless ・ Detector: MS
・ Ion source temperature: 230 ℃
-Ionization method: EI (70eV)
-Scan range: m / z 10-500
-Quantitative ions: coumarin m / z 146, 7-methoxycoumarin m / z 176, 4-hydroxycoumarin m / z 162, 3,4-dihydrocoumarin m / z 148
定量は以下の手順にて行った。
各成分の標準試薬をエタノールで溶解し、段階希釈して標品を調製した。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測定を行った。そして、測定された各成分の定量イオンのピーク面積と調製濃度から検量線を作成し、試料中のクマリン及びその誘導体の含有量を求めた。
The quantification was performed according to the following procedure.
Standard reagents for each component were dissolved in ethanol and serially diluted to prepare a standard. A standard having a predetermined concentration was added to the sample, and the sample was adsorbed on the SPME fiber in the same manner as the sample alone, and GC / MS measurement was performed. Then, a calibration curve was prepared from the measured peak area of the quantitative ion of each component and the prepared concentration, and the content of coumarin and its derivative in the sample was determined.
5.pHの測定
茶飲料を20℃に温度調整し、pHメータ(HORIBA コンパクトpHメータ、堀場製作所製)を用いて測定した。
5. Measurement of pH The temperature of the tea beverage was adjusted to 20 ° C., and the temperature was measured using a pH meter (HORIBA compact pH meter, manufactured by HORIBA, Ltd.).
製造例1
茶抽出液IIの製造
煎茶葉(宮崎県産、鹿児島県産)30gを90℃の熱水2000gに投入し、3分間抽出を行い、茶殻を除去した後、液温20℃まで冷却し、緑茶抽出液を得た。当該緑茶抽出液を「茶抽出液II」とする。得られた茶抽出液IIは、タンニンの含有量が0.028質量%であり、非重合体カテキン類の含有量が0.02質量%であり、クマリンの含有量が10質量ppbであった。
Manufacturing example 1
Production of Tea Extract II 30 g of sencha leaves (produced in Miyazaki and Kagoshima prefectures) was put into 2000 g of hot water at 90 ° C, extracted for 3 minutes, the tea leaves were removed, and then cooled to a liquid temperature of 20 ° C to make green tea. An extract was obtained. The green tea extract is referred to as "tea extract II". The obtained tea extract II had a tannin content of 0.028% by mass, a non-polymer catechin content of 0.02% by mass, and a coumarin content of 10% by mass ppb. ..
製造例2
茶抽出液IIIの製造
烏龍茶葉(ユニリーバ社)3gを90℃の熱水150gに投入し、8分間抽出を行い、茶殻を除去した後、液温20℃まで冷却し、ウーロン茶抽出液を得た。当該ウーロン茶抽出液を「茶抽出液III」とする。得られた茶抽出液IIIは、タンニンの含有量が0.020質量%であり、非重合体カテキン類の含有量が0.007質量%であり、クマリンの含有量が10質量ppbであった。
Manufacturing example 2
Production of Tea Extract III 3 g of oolong tea leaves (Unilever plc) was put into 150 g of hot water at 90 ° C, extracted for 8 minutes, the tea leaves were removed, and then cooled to a liquid temperature of 20 ° C to obtain an oolong tea extract. .. The oolong tea extract is referred to as "tea extract III". The obtained tea extract III had a tannin content of 0.020% by mass, a non-polymer catechin content of 0.007% by mass, and a coumarin content of 10% by mass ppb. ..
製造例3
茶抽出液IVの製造
ルイボス茶ティーパック(株式会社 国太楼)2gを90℃の熱水200gに投入し、30秒抽出を行い、ティーパックを除去した後、液温20℃まで冷却し、ルイボス茶抽出液を得た。当該ルイボス茶抽出液を「茶抽出液IV」とする。得られた茶抽出液IVは、タンニンの含有量が0.016質量%であり、クマリンの含有量が5.6質量ppbであった。なお、非重合体カテキン類は検出されなかった。
Manufacturing example 3
Manufacture of Tea Extract IV Rooibos Tea Tea Pack (Kunitaro Co., Ltd.) 2 g is put into 200 g of hot water at 90 ° C, extracted for 30 seconds, the tea pack is removed, and then cooled to a liquid temperature of 20 ° C. A rooibos tea extract was obtained. The rooibos tea extract is referred to as "tea extract IV". The obtained tea extract IV had a tannin content of 0.016% by mass and a coumarin content of 5.6% by mass ppb. No non-polymer catechins were detected.
製造例4
茶抽出液Vの製造
コーン茶葉(株式会社 ほんぢ園)4gを90℃の熱水150gに投入し、5分間抽出を行い、茶殻を除去した後、液温20℃まで冷却し、コーン茶抽出液を得た。当該コーン茶抽出液を「茶抽出液V」とする。得られた茶抽出液Vは、クマリン含有量が11.3質量ppbであった。なお、タンニン及び非重合体カテキン類は検出されなかった。
Manufacturing example 4
Manufacture of tea extract V 4 g of corn tea leaves (Honjien Co., Ltd.) was put into 150 g of hot water at 90 ° C, extracted for 5 minutes, the tea leaves were removed, and then cooled to a liquid temperature of 20 ° C to extract corn tea. I got the liquid. The corn tea extract is referred to as "tea extract V". The obtained tea extract V had a coumarin content of 11.3 mass ppb. In addition, tannin and non-polymer catechins were not detected.
製造例5
茶抽出液VIの製造
麦茶葉(株式会社 小川生薬)2gを90℃の熱水140gに投入し、3分間抽出を行い、茶殻を除去した後、液温20℃まで冷却し、麦茶抽出液を得た。当該麦茶抽出液を「茶抽出液VI」とする。得られた茶抽出液VIは、クマリン含有量が5.4質量ppbであった。なお、タンニン及び非重合体カテキン類は検出されなかった。
Production example 5
Manufacture of tea extract VI 2 g of barley tea leaves (Ogawa Seiyaku Co., Ltd.) was put into 140 g of hot water at 90 ° C, extracted for 3 minutes, the tea leaves were removed, and then cooled to a liquid temperature of 20 ° C to prepare the barley tea extract. Obtained. The barley tea extract is referred to as "tea extract VI". The obtained tea extract VI had a coumarin content of 5.4 mass ppb. In addition, tannin and non-polymer catechins were not detected.
参考例1
重曹と、賦形剤とを表4に示す割合で配合して固形飲料組成物を得た。次いで、得られた固形飲料組成物について分析を行い、官能評価1にしたがって評価した。その結果を表4に示す。なお、表4中の計算値又は分析値の濃度は、固形分濃度である。
Reference example 1
Baking soda and excipients were blended in the proportions shown in Table 4 to obtain a solid beverage composition. Next, the obtained solid beverage composition was analyzed and evaluated according to the sensory evaluation 1. The results are shown in Table 4. The concentration of the calculated value or the analytical value in Table 4 is the solid content concentration.
比較例1
茶抽出物I(Teavigo、太陽化学社製、タンニン94質量%、非重合体カテキン類94質量%、クマリン未検出、以下、同様である。)と、重曹と、賦形剤とを表4に示す割合で配合して固形緑茶飲料組成物を得た。次いで、得られた固形緑茶飲料組成物について、参考例1と同様に分析及び官能評価を行った。その結果を表4に示す。なお、表4中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 1
Table 4 shows tea extract I (Teavigo, manufactured by Taiyo Kagaku Co., Ltd., tannin 94% by mass, non-polymer catechins 94% by mass, coumarin not detected, the same applies hereinafter), baking soda, and excipients. A solid green tea beverage composition was obtained by blending in the ratio shown. Next, the obtained solid green tea beverage composition was analyzed and sensory evaluated in the same manner as in Reference Example 1. The results are shown in Table 4. The concentration of the calculated value or the analytical value in Table 4 is the solid content concentration.
比較例2
更に、デキストリンを表4に示す割合で配合したこと以外は、比較例1と同様の操作により固形緑茶飲料組成物を得た。得られた各固形緑茶飲料組成物について、比較例1と同様に分析及び官能評価を行った。その結果を表4に示す。なお、表4中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 2
Further, a solid green tea beverage composition was obtained by the same operation as in Comparative Example 1 except that dextrin was blended in the ratio shown in Table 4. Each of the obtained solid green tea beverage compositions was analyzed and sensory evaluated in the same manner as in Comparative Example 1. The results are shown in Table 4. The concentration of the calculated value or the analytical value in Table 4 is the solid content concentration.
実施例1〜5
更に、ジヒドロクマリンを表4に示す割合で配合したこと以外は、比較例2と同様の操作により固形緑茶飲料組成物を得た。得られた各固形緑茶飲料組成物について、比較例2と同様に分析及び官能評価を行った。その結果を表4に示す。なお、表4中の計算値又は分析値の濃度は、固形分濃度である。
Examples 1-5
Further, a solid green tea beverage composition was obtained by the same operation as in Comparative Example 2 except that dihydrocoumarin was blended in the ratio shown in Table 4. Each of the obtained solid green tea beverage compositions was analyzed and sensory evaluated in the same manner as in Comparative Example 2. The results are shown in Table 4. The concentration of the calculated value or the analytical value in Table 4 is the solid content concentration.
比較例3
リンゴ抽出物(リンゴポリフェノール アップリン、ユニテックフーズ株式会社、タンニン22質量%、非重合体カテキン類0.4質量%、クマリン未検出、以下、同様である。)と、重曹と、賦形剤とを表4に示す割合で配合して固形飲料組成物を得た。次いで、得られた固形飲料組成物について分析を行い、官能評価1にしたがって評価した。その結果を表4に示す。なお、表4中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 3
Apple extract (apple polyphenol apprin, Unitech Foods Co., Ltd., tannin 22% by mass, non-polymer catechins 0.4% by mass, coumarin not detected, the same applies hereinafter), baking soda, excipients. Was blended in the proportions shown in Table 4 to obtain a solid beverage composition. Next, the obtained solid beverage composition was analyzed and evaluated according to the sensory evaluation 1. The results are shown in Table 4. The concentration of the calculated value or the analytical value in Table 4 is the solid content concentration.
比較例4
更に、デキストリンを表4に示す割合で配合したこと以外は、比較例3と同様の操作により固形飲料組成物を得た。得られた各固形飲料組成物について、比較例3と同様に分析及び官能評価を行った。その結果を表4に示す。なお、表4中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 4
Further, a solid beverage composition was obtained by the same operation as in Comparative Example 3 except that dextrin was blended in the ratio shown in Table 4. Each of the obtained solid beverage compositions was analyzed and sensory evaluated in the same manner as in Comparative Example 3. The results are shown in Table 4. The concentration of the calculated value or the analytical value in Table 4 is the solid content concentration.
実施例6〜9
更に、ジヒドロクマリンを表4に示す割合で配合したこと以外は、比較例4と同様の操作により固形飲料組成物を得た。得られた各固形飲料組成物について、比較例4と同様に分析及び官能評価を行った。その結果を表4に示す。なお、表4中の計算値又は分析値の濃度は、固形分濃度である。
Examples 6-9
Further, a solid beverage composition was obtained by the same operation as in Comparative Example 4 except that dihydrocoumarin was blended in the ratio shown in Table 4. Each of the obtained solid beverage compositions was analyzed and sensory evaluated in the same manner as in Comparative Example 4. The results are shown in Table 4. The concentration of the calculated value or the analytical value in Table 4 is the solid content concentration.
比較例5
コーヒー抽出物(クロロゲン酸含有製剤、長谷川香料株式会社、タンニン20質量%、非重合体カテキン類0質量%、クマリン未検出、以下、同様である。)と、重曹と、賦形剤とを表4に示す割合で配合して固形飲料組成物を得た。次いで、得られた固形飲料組成物について分析を行い、官能評価1にしたがって評価した。その結果を表4に示す。なお、表4中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 5
Table shows coffee extract (chlorogenic acid-containing preparation, Hasegawa Fragrance Co., Ltd., tannin 20% by mass, non-polymer catechins 0% by mass, coumarin not detected, the same applies hereinafter), baking soda, and excipients. A solid beverage composition was obtained by blending in the ratio shown in 4. Next, the obtained solid beverage composition was analyzed and evaluated according to the sensory evaluation 1. The results are shown in Table 4. The concentration of the calculated value or the analytical value in Table 4 is the solid content concentration.
比較例6
更に、デキストリンを表4に示す割合で配合したこと以外は、比較例5と同様の操作により固形飲料組成物を得た。得られた各固形飲料組成物について、比較例5と同様に分析及び官能評価を行った。その結果を表4に示す。なお、表4中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 6
Further, a solid beverage composition was obtained by the same operation as in Comparative Example 5 except that dextrin was blended in the ratio shown in Table 4. Each of the obtained solid beverage compositions was analyzed and sensory evaluated in the same manner as in Comparative Example 5. The results are shown in Table 4. The concentration of the calculated value or the analytical value in Table 4 is the solid content concentration.
実施例10
更に、ジヒドロクマリンを表4に示す割合で配合したこと以外は、比較例6と同様の操作により固形飲料組成物を得た。得られた各固形飲料組成物について、比較例6と同様に分析及び官能評価を行った。その結果を表4に示す。なお、表4中の計算値又は分析値の濃度は、固形分濃度である。
Example 10
Further, a solid beverage composition was obtained by the same operation as in Comparative Example 6 except that dihydrocoumarin was blended in the ratio shown in Table 4. Each of the obtained solid beverage compositions was analyzed and sensory evaluated in the same manner as in Comparative Example 6. The results are shown in Table 4. The concentration of the calculated value or the analytical value in Table 4 is the solid content concentration.
比較例7
茶抽出物Iと、コーヒー抽出物と、重曹と、賦形剤とを表4に示す割合で配合して固形飲料組成物を得た。次いで、得られた固形飲料組成物について分析を行い、官能評価1にしたがって評価した。その結果を表4に示す。なお、表4中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 7
A solid beverage composition was obtained by blending tea extract I, coffee extract, baking soda, and excipients in the proportions shown in Table 4. Next, the obtained solid beverage composition was analyzed and evaluated according to the sensory evaluation 1. The results are shown in Table 4. The concentration of the calculated value or the analytical value in Table 4 is the solid content concentration.
比較例8
更に、デキストリンを表4に示す割合で配合したこと以外は、比較例7と同様の操作により固形飲料組成物を調製した。得られた各固形飲料組成物について、比較例7と同様に分析及び官能評価を行った。その結果を表4に示す。なお、表4中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 8
Further, a solid beverage composition was prepared by the same operation as in Comparative Example 7 except that dextrin was blended in the ratio shown in Table 4. Each of the obtained solid beverage compositions was analyzed and sensory evaluated in the same manner as in Comparative Example 7. The results are shown in Table 4. The concentration of the calculated value or the analytical value in Table 4 is the solid content concentration.
実施例11
更に、ジヒドロクマリンを表4に示す割合で配合したこと以外は、比較例8と同様の操作により固形飲料組成物を調製した。得られた各固形飲料組成物について、比較例8と同様に分析及び官能評価を行った。その結果を表4に示す。なお、表4中の計算値又は分析値の濃度は、固形分濃度である。
Example 11
Further, a solid beverage composition was prepared by the same procedure as in Comparative Example 8 except that dihydrocoumarin was blended in the ratio shown in Table 4. Each of the obtained solid beverage compositions was analyzed and sensory evaluated in the same manner as in Comparative Example 8. The results are shown in Table 4. The concentration of the calculated value or the analytical value in Table 4 is the solid content concentration.
官能評価1
各固形飲料組成物2gを20℃のイオン交換水で希釈し、全量を120gとして還元飲料を調製した。そして、還元飲料の「後渋味」、「デキストリンの異味」について専門パネル4名が官能試験を行った。官能試験は、次の手順で行った。
Sensory evaluation 1
2 g of each solid beverage composition was diluted with ion-exchanged water at 20 ° C. to make a total amount of 120 g to prepare a reduced beverage. Then, four specialized panels conducted sensory tests on the "after astringency" and "dextrin's offensive taste" of the reduced beverage. The sensory test was performed according to the following procedure.
(1)後渋味の評価
先ず、参考例1の還元飲料にエピガロカテキンガレート(EGCG)を表2に示す割合で配合して「後渋味」の強さを10段階に調整した「後渋味標準飲料」を調製した。次に、専門パネル4名が各濃度の「後渋味標準飲料」について、表2に示す評点とすることを合意した。次いで、各専門パネルがEGCG濃度の低い「後渋味標準飲料」から順に摂取し、「後渋味」の強さを記憶した。次いで、各専門パネルが各還元飲料を摂取し、「後渋味」の程度を評価し、「後渋味標準飲料」の中から「後渋味」が最も近いものを決定した。そして、各専門パネルが決定した評点に基づいて、協議により「0.5」刻みで最終評点を決定した。なお、評点は、数値が大きいほど、「後渋味」が強く感じられることを意味する。
(1) Evaluation of post-astringency First, epigallocatechin gallate (EGCG) was added to the reduced beverage of Reference Example 1 at the ratio shown in Table 2, and the strength of "post-astringency" was adjusted in 10 steps. "Astringent standard beverage" was prepared. Next, four expert panels agreed to give the scores shown in Table 2 for each concentration of "after-astringent standard beverage". Next, each specialized panel ingested the "post-astringent standard beverage" having the lowest EGCG concentration in order, and memorized the strength of the "post-astringent taste". Next, each specialized panel ingested each reduced beverage, evaluated the degree of "after-astringency", and determined the one with the closest "after-astringency" from the "after-astringency standard beverages". Then, based on the scores decided by each specialized panel, the final score was decided in "0.5" increments by consultation. In addition, the score means that the larger the numerical value, the stronger the "after astringency" is felt.
(2)デキストリンの異味の評価
先ず、参考例1の還元飲料にデキストリン(サンデック#30、三和澱粉株式会社)を表3に示す割合で配合して「デキストリンの異味」の強さを5段階に調整した「異味標準飲料」を調製した。次に、専門パネル4名が各濃度の「異味標準飲料」について、表3に示す評点とすることを合意した。次いで、各専門パネルがデキストリン濃度の低い「異味標準飲料」から順に摂取し、「デキストリンの異味」の強さを記憶した。次いで、各専門パネルが各還元飲料を摂取し、「デキストリンの異味」の程度を評価し、「異味標準飲料」の中から「デキストリンの異味」が最も近いものを決定した。そして、各専門パネルが決定した評点に基づいて、協議により「0.5」刻みで最終評点を決定した。なお、評点は、数値が大きいほど、「異味」が強く感じられることを意味する。
(2) Evaluation of the taste of dextrin First, dextrin (Sandeck # 30, Sanwa Cornstarch Co., Ltd.) was added to the reduced beverage of Reference Example 1 at the ratio shown in Table 3, and the strength of the "dextrin taste" was graded in 5 levels. A "dextrin standard beverage" adjusted to the above was prepared. Next, four expert panels agreed to give the scores shown in Table 3 for each concentration of "unusual standard beverage". Next, each specialized panel ingested in order from the "dextrin standard beverage" with the lowest dextrin concentration, and memorized the strength of the "dextrin off-flavor". Next, each specialized panel ingested each reduced beverage, evaluated the degree of "dextrin offensive taste", and determined the one with the closest "dextrin offensive taste" from the "dextrin standard beverages". Then, based on the scores decided by each specialized panel, the final score was decided in "0.5" increments by consultation. In addition, the score means that the larger the numerical value, the stronger the "unpleasant taste" is felt.
比較例9
茶抽出物Iと、重曹と、賦形剤とを表5に示す割合で配合して固形緑茶飲料組成物を得た。次いで、得られた固形緑茶飲料組成物について分析を行い、官能評価1にしたがって評価した。その結果を、参考例1の結果とともに表5に示す。なお、表5中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 9
Tea extract I, baking soda, and excipients were blended in the proportions shown in Table 5 to obtain a solid green tea beverage composition. Next, the obtained solid green tea beverage composition was analyzed and evaluated according to sensory evaluation 1. The results are shown in Table 5 together with the results of Reference Example 1. The concentration of the calculated value or the analytical value in Table 5 is the solid content concentration.
比較例10
更に、デキストリンを表5に示す割合で配合したこと以外は、比較例9と同様の操作により固形緑茶飲料組成物を得た。得られた固形緑茶飲料組成物について、比較例9と同様に分析及び官能評価を行った。その結果を表5に示す。なお、表5中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 10
Further, a solid green tea beverage composition was obtained by the same operation as in Comparative Example 9 except that dextrin was blended in the ratio shown in Table 5. The obtained solid green tea beverage composition was analyzed and sensory evaluated in the same manner as in Comparative Example 9. The results are shown in Table 5. The concentration of the calculated value or the analytical value in Table 5 is the solid content concentration.
実施例12〜14
更に、ジヒドロクマリンを表5に示す割合で配合したこと以外は、比較例10と同様の操作により固形緑茶飲料組成物を得た。得られた各固形緑茶飲料組成物について、比較例10と同様に分析及び官能評価を行った。その結果を、参考例1の結果とともに表5に示す。なお、表5中の計算値又は分析値の濃度は、固形分濃度である。
Examples 12-14
Further, a solid green tea beverage composition was obtained by the same operation as in Comparative Example 10 except that dihydrocoumarin was blended in the ratio shown in Table 5. Each of the obtained solid green tea beverage compositions was analyzed and sensory evaluated in the same manner as in Comparative Example 10. The results are shown in Table 5 together with the results of Reference Example 1. The concentration of the calculated value or the analytical value in Table 5 is the solid content concentration.
比較例11
リンゴ抽出物と、重曹と、賦形剤とを表5に示す割合で配合して固形飲料組成物を得た。次いで、得られた固形飲料組成物について分析を行い、官能評価1にしたがって評価した。その結果を、参考例1の結果とともに表5に示す。なお、表5中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 11
The apple extract, baking soda, and excipient were blended in the proportions shown in Table 5 to obtain a solid beverage composition. Next, the obtained solid beverage composition was analyzed and evaluated according to the sensory evaluation 1. The results are shown in Table 5 together with the results of Reference Example 1. The concentration of the calculated value or the analytical value in Table 5 is the solid content concentration.
比較例12
更に、デキストリンを表5に示す割合で配合したこと以外は、比較例11と同様の操作により固形飲料組成物を得た。得られた固形飲料組成物について、比較例11と同様に分析及び官能評価を行った。その結果を表5に示す。なお、表5中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 12
Further, a solid beverage composition was obtained by the same operation as in Comparative Example 11 except that dextrin was blended in the ratio shown in Table 5. The obtained solid beverage composition was analyzed and sensory evaluated in the same manner as in Comparative Example 11. The results are shown in Table 5. The concentration of the calculated value or the analytical value in Table 5 is the solid content concentration.
実施例15〜17
更に、ジヒドロクマリンを表5に示す割合で配合したこと以外は、比較例12と同様の操作により固形飲料組成物を得た。得られた各固形飲料組成物について、比較例12と同様に分析及び官能評価を行った。その結果を、参考例1の結果とともに表5に示す。なお、表5中の計算値又は分析値の濃度は、固形分濃度である。
Examples 15-17
Further, a solid beverage composition was obtained by the same operation as in Comparative Example 12 except that dihydrocoumarin was blended in the ratio shown in Table 5. Each of the obtained solid beverage compositions was analyzed and sensory evaluated in the same manner as in Comparative Example 12. The results are shown in Table 5 together with the results of Reference Example 1. The concentration of the calculated value or the analytical value in Table 5 is the solid content concentration.
比較例13
茶抽出物Iと、重曹と、賦形剤とを表6に示す割合で配合して固形緑茶飲料組成物を得た。次いで、得られた固形緑茶飲料組成物について分析を行い、官能評価1にしたがって評価した。その結果を、参考例1の結果とともに表6に示す。なお、表6中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 13
Tea extract I, baking soda, and excipients were blended in the proportions shown in Table 6 to obtain a solid green tea beverage composition. Next, the obtained solid green tea beverage composition was analyzed and evaluated according to sensory evaluation 1. The results are shown in Table 6 together with the results of Reference Example 1. The concentration of the calculated value or the analytical value in Table 6 is the solid content concentration.
比較例14
更に、デキストリンを表6に示す割合で配合したこと以外は、比較例13と同様の操作により固形緑茶飲料組成物を得た。得られた各固形緑茶飲料組成物について、比較例13と同様に分析及び官能評価を行った。その結果を、参考例1の結果とともに表6に示す。なお、表6中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 14
Further, a solid green tea beverage composition was obtained by the same operation as in Comparative Example 13 except that dextrin was blended in the ratio shown in Table 6. Each of the obtained solid green tea beverage compositions was analyzed and sensory evaluated in the same manner as in Comparative Example 13. The results are shown in Table 6 together with the results of Reference Example 1. The concentration of the calculated value or the analytical value in Table 6 is the solid content concentration.
実施例18、19及び比較例15
更に、ジヒドロクマリンを表6に示す割合で配合したこと以外は、比較例14と同様の操作により固形緑茶飲料組成物を得た。得られた各固形緑茶飲料組成物について、比較例14と同様に分析及び官能評価を行った。その結果を、参考例1の結果とともに表6に示す。なお、表6中の計算値又は分析値の濃度は、固形分濃度である。
Examples 18 and 19 and Comparative Example 15
Further, a solid green tea beverage composition was obtained by the same operation as in Comparative Example 14 except that dihydrocoumarin was blended in the ratio shown in Table 6. Each of the obtained solid green tea beverage compositions was analyzed and sensory evaluated in the same manner as in Comparative Example 14. The results are shown in Table 6 together with the results of Reference Example 1. The concentration of the calculated value or the analytical value in Table 6 is the solid content concentration.
比較例16
茶抽出物Iと、重曹と、賦形剤とを表7に示す割合で配合して固形緑茶飲料組成物を得た。次いで、得られた固形緑茶飲料組成物について分析を行い、官能評価1にしたがって評価した。その結果を、参考例1の結果とともに表7に示す。なお、表7中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 16
Tea extract I, baking soda, and excipients were blended in the proportions shown in Table 7 to obtain a solid green tea beverage composition. Next, the obtained solid green tea beverage composition was analyzed and evaluated according to sensory evaluation 1. The results are shown in Table 7 together with the results of Reference Example 1. The concentration of the calculated value or the analytical value in Table 7 is the solid content concentration.
比較例17
更に、デキストリンを表7に示す割合で配合したこと以外は、比較例16と同様の操作により固形緑茶飲料組成物を得た。得られた各固形緑茶飲料組成物について、比較例16と同様に分析及び官能評価を行った。その結果を、参考例1の結果とともに表7に示す。なお、表7中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 17
Further, a solid green tea beverage composition was obtained by the same operation as in Comparative Example 16 except that dextrin was blended in the ratio shown in Table 7. Each of the obtained solid green tea beverage compositions was analyzed and sensory evaluated in the same manner as in Comparative Example 16. The results are shown in Table 7 together with the results of Reference Example 1. The concentration of the calculated value or the analytical value in Table 7 is the solid content concentration.
実施例20
更に、ジヒドロクマリンを表7に示す割合で配合したこと以外は、比較例17と同様の操作により固形緑茶飲料組成物を得た。得られた各固形緑茶飲料組成物について、比較例17と同様に分析及び官能評価を行った。その結果を、参考例1の結果とともに表7に示す。なお、表7中の計算値又は分析値の濃度は、固形分濃度である。
Example 20
Further, a solid green tea beverage composition was obtained by the same operation as in Comparative Example 17 except that dihydrocoumarin was blended in the ratio shown in Table 7. Each of the obtained solid green tea beverage compositions was analyzed and sensory evaluated in the same manner as in Comparative Example 17. The results are shown in Table 7 together with the results of Reference Example 1. The concentration of the calculated value or the analytical value in Table 7 is the solid content concentration.
比較例18、19
デキストリンを表8に示す割合に変更したこと以外は、比較例2と同様の操作により固形緑茶飲料組成物を得た。得られた各固形緑茶飲料組成物について、比較例2と同様に分析及び官能評価を行った。その結果を、比較例2及び参考例1の結果とともに表8に示す。なお、表8中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Examples 18, 19
A solid green tea beverage composition was obtained by the same operation as in Comparative Example 2 except that the dextrin was changed to the ratio shown in Table 8. Each of the obtained solid green tea beverage compositions was analyzed and sensory evaluated in the same manner as in Comparative Example 2. The results are shown in Table 8 together with the results of Comparative Example 2 and Reference Example 1. The concentration of the calculated value or the analytical value in Table 8 is the solid content concentration.
実施例21、22
デキストリンを表8に示す割合に変更したこと以外は、実施例2と同様の操作により固形緑茶飲料組成物を得た。得られた各固形緑茶飲料組成物について、実施例2と同様に分析及び官能評価を行った。その結果を、実施例2及び参考例1の結果とともに表8に示す。なお、表8中の計算値又は分析値の濃度は、固形分濃度である。
Examples 21 and 22
A solid green tea beverage composition was obtained by the same operation as in Example 2 except that the dextrin was changed to the ratio shown in Table 8. Each of the obtained solid green tea beverage compositions was analyzed and sensory evaluated in the same manner as in Example 2. The results are shown in Table 8 together with the results of Example 2 and Reference Example 1. The concentration of the calculated value or the analytical value in Table 8 is the solid content concentration.
比較例20
更に、バニリンを表9に示す割合で配合したこと以外は、比較例2と同様の操作により固形緑茶飲料組成物を得た。得られた固形緑茶飲料組成物について、比較例2と同様に分析及び官能評価を行った。その結果を、比較例2及び参考例1の結果とともに表9に示す。なお、表9中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 20
Further, a solid green tea beverage composition was obtained by the same operation as in Comparative Example 2 except that vanillin was blended in the ratio shown in Table 9. The obtained solid green tea beverage composition was analyzed and sensory evaluated in the same manner as in Comparative Example 2. The results are shown in Table 9 together with the results of Comparative Example 2 and Reference Example 1. The concentration of the calculated value or the analytical value in Table 9 is the solid content concentration.
比較例21
更に、マルトールを表9に示す割合で配合したこと以外は、比較例2と同様の操作により固形緑茶飲料組成物を得た。得られた固形緑茶飲料組成物について、比較例2と同様に分析及び官能評価を行った。その結果を、比較例2及び参考例1の結果とともに表9に示す。なお、表9中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 21
Further, a solid green tea beverage composition was obtained by the same operation as in Comparative Example 2 except that maltol was blended in the ratio shown in Table 9. The obtained solid green tea beverage composition was analyzed and sensory evaluated in the same manner as in Comparative Example 2. The results are shown in Table 9 together with the results of Comparative Example 2 and Reference Example 1. The concentration of the calculated value or the analytical value in Table 9 is the solid content concentration.
実施例23〜27
ジヒドロクマリンに代えて、表8に示す割合のクマリン及び/又はクマリン誘導体を配合したこと以外は、実施例2と同様の操作により固形緑茶飲料組成物を得た。得られた各固形緑茶飲料組成物について、実施例2と同様に分析及び官能評価を行った。その結果を、実施例2及び参考例1の結果とともに表9に示す。なお、表9中の計算値又は分析値の濃度は、固形分濃度である。
Examples 23-27
A solid green tea beverage composition was obtained by the same operation as in Example 2 except that the proportions of coumarin and / or coumarin derivative shown in Table 8 were blended in place of dihydrocoumarin. Each of the obtained solid green tea beverage compositions was analyzed and sensory evaluated in the same manner as in Example 2. The results are shown in Table 9 together with the results of Example 2 and Reference Example 1. The concentration of the calculated value or the analytical value in Table 9 is the solid content concentration.
参考例2
製造例1で得られた茶抽出液IIと、重曹と、イオン交換水とを表12に示す割合で配合して緑茶飲料(RTD飲料)を得た。次いで、得られた緑茶飲料について分析を行い、官能評価2にしたがって評価した。その結果を表12に示す。なお、表12中の計算値又は分析値の濃度は、固形分濃度である。
Reference example 2
The tea extract II obtained in Production Example 1, baking soda, and ion-exchanged water were blended in the proportions shown in Table 12 to obtain a green tea beverage (RTD beverage). Next, the obtained green tea beverage was analyzed and evaluated according to the sensory evaluation 2. The results are shown in Table 12. The concentration of the calculated value or the analytical value in Table 12 is the solid content concentration.
比較例22
茶抽出物Iと、製造例1で得られた茶抽出液IIと、重曹と、イオン交換水とを表12に示す割合で配合して緑茶飲料(RTD飲料)を得た。次いで、得られた緑茶飲料について、参考例2と同様に分析及び官能評価を行った。その結果を表12に示す。なお、表12中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 22
A green tea beverage (RTD beverage) was obtained by blending tea extract I, the tea extract II obtained in Production Example 1, baking soda, and ion-exchanged water at the ratios shown in Table 12. Next, the obtained green tea beverage was analyzed and sensory evaluated in the same manner as in Reference Example 2. The results are shown in Table 12. The concentration of the calculated value or the analytical value in Table 12 is the solid content concentration.
比較例23
更に、デキストリンを表12に示す割合で配合したこと以外は、比較例22と同様の操作により緑茶飲料(RTD飲料)を得た。得られた緑茶飲料について、比較例22と同様に分析及び官能評価を行った。その結果を表12に示す。なお、表12中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 23
Further, a green tea beverage (RTD beverage) was obtained by the same operation as in Comparative Example 22 except that dextrin was blended in the ratio shown in Table 12. The obtained green tea beverage was analyzed and sensory evaluated in the same manner as in Comparative Example 22. The results are shown in Table 12. The concentration of the calculated value or the analytical value in Table 12 is the solid content concentration.
比較例24
製造例1で得られた茶抽出液IIと、リンゴ抽出物と、重曹と、イオン交換水とを表12に示す割合で配合して緑茶飲料(RTD飲料)を得た。次いで、得られた緑茶飲料について、参考例2と同様に分析及び官能評価を行った。その結果を表12に示す。なお、表12中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 24
A green tea beverage (RTD beverage) was obtained by blending the tea extract II obtained in Production Example 1, an apple extract, baking soda, and ion-exchanged water at the ratios shown in Table 12. Next, the obtained green tea beverage was analyzed and sensory evaluated in the same manner as in Reference Example 2. The results are shown in Table 12. The concentration of the calculated value or the analytical value in Table 12 is the solid content concentration.
比較例25
更に、デキストリンを表12に示す割合で配合したこと以外は、比較例24と同様の操作により緑茶飲料(RTD飲料)を調製した。得られた緑茶飲料について、比較例24と同様に分析及び官能評価を行った。その結果を表12に示す。なお、表12中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 25
Further, a green tea beverage (RTD beverage) was prepared by the same operation as in Comparative Example 24 except that dextrin was blended in the ratio shown in Table 12. The obtained green tea beverage was analyzed and sensory evaluated in the same manner as in Comparative Example 24. The results are shown in Table 12. The concentration of the calculated value or the analytical value in Table 12 is the solid content concentration.
実施例28〜30
更に、ジヒドロクマリンを表12に示す割合で配合したこと以外は、比較例23と同様の操作により緑茶飲料(RTD飲料)を得た。得られた緑茶飲料について、比較例23と同様に分析及び官能評価を行った。その結果を表12に示す。なお、表12中の計算値又は分析値の濃度は、固形分濃度である。
Examples 28-30
Further, a green tea beverage (RTD beverage) was obtained by the same operation as in Comparative Example 23 except that dihydrocoumarin was blended in the ratio shown in Table 12. The obtained green tea beverage was analyzed and sensory evaluated in the same manner as in Comparative Example 23. The results are shown in Table 12. The concentration of the calculated value or the analytical value in Table 12 is the solid content concentration.
実施例31〜33
更に、ジヒドロクマリンを表12に示す割合で配合したこと以外は、比較例25と同様の操作により緑茶飲料(RTD飲料)を得た。得られた緑茶飲料について、比較例25と同様に分析及び官能評価を行った。その結果を表12に示す。なお、表12中の計算値又は分析値の濃度は、固形分濃度である。
Examples 31 to 33
Further, a green tea beverage (RTD beverage) was obtained by the same operation as in Comparative Example 25 except that dihydrocoumarin was blended in the ratio shown in Table 12. The obtained green tea beverage was analyzed and sensory evaluated in the same manner as in Comparative Example 25. The results are shown in Table 12. The concentration of the calculated value or the analytical value in Table 12 is the solid content concentration.
官能評価2
各緑茶飲料の「後渋味」、「デキストリンの異味」について専門パネル4名が官能試験を行った。官能試験は、次の手順で行った。
Sensory evaluation 2
Four expert panels conducted sensory tests on the "after astringency" and "dextrin's offensive taste" of each green tea beverage. The sensory test was performed according to the following procedure.
(1)後渋味の評価
先ず、参考例2の緑茶飲料にエピガロカテキンガレート(EGCG)を表10に示す割合で配合して「後渋味」の強さを10段階に調整した「後渋味標準飲料」を調製した。次に、専門パネル4名が各濃度の「後渋味標準飲料」について、表10に示す評点とすることを合意した。次いで、各専門パネルがEGCG濃度の低い「後渋味標準飲料」から順に摂取し、「後渋味」の強さを記憶した。次いで、各専門パネルが各緑茶飲料を摂取し、「後渋味」の程度を評価し、「後渋味標準飲料」の中から「後渋味」が最も近いものを決定した。そして、各専門パネルが決定した評点に基づいて、協議により「0.5」刻みで最終評点を決定した。なお、評点は、数値が大きいほど、「後渋味」が強く感じられることを意味する。
(1) Evaluation of post-astringency First, epigallocatechin gallate (EGCG) was added to the green tea beverage of Reference Example 2 at the ratio shown in Table 10, and the strength of "post-astringency" was adjusted in 10 steps. "Astringent standard beverage" was prepared. Next, four expert panels agreed to give the scores shown in Table 10 for each concentration of "after-astringent standard beverage". Next, each specialized panel ingested the "post-astringent standard beverage" having the lowest EGCG concentration in order, and memorized the strength of the "post-astringent taste". Next, each specialized panel ingested each green tea beverage, evaluated the degree of "after-astringency", and determined the one with the closest "after-astringency" from the "after-astringency standard beverages". Then, based on the scores decided by each specialized panel, the final score was decided in "0.5" increments by consultation. In addition, the score means that the larger the numerical value, the stronger the "after astringency" is felt.
(2)デキストリンの異味の評価
先ず、参考例2の緑茶飲料にデキストリン(サンデック#30、三和澱粉株式会社)を表11に示す割合で配合して「デキストリンの異味」の強さを5段階に調整した「異味標準飲料」を調製した。次に、専門パネル4名が各濃度の「異味標準飲料」について、表11に示す評点とすることを合意した。次いで、各専門パネルがデキストリン濃度の低い「異味標準飲料」から順に摂取し、「デキストリンの異味」の強さを記憶した。次いで、各専門パネルが各緑茶飲料を摂取し、「デキストリンの異味」の程度を評価し、「異味標準飲料」の中から「デキストリンの異味」が最も近いものを決定した。そして、各専門パネルが決定した評点に基づいて、協議により「0.5」刻みで最終評点を決定した。なお、評点は、数値が大きいほど、「異味」が強く感じられることを意味する。
(2) Evaluation of the taste of dextrin First, dextrin (Sandeck # 30, Sanwa Cornstarch Co., Ltd.) was added to the green tea beverage of Reference Example 2 at the ratio shown in Table 11, and the strength of the "dextrin taste" was graded in 5 levels. A "dextrin standard beverage" adjusted to the above was prepared. Next, four expert panels agreed to give the scores shown in Table 11 for each concentration of "unusual standard beverage". Next, each specialized panel ingested in order from the "dextrin standard beverage" with the lowest dextrin concentration, and memorized the strength of the "dextrin off-flavor". Next, each specialized panel ingested each green tea beverage, evaluated the degree of "dextrin offensive taste", and determined the one with the closest "dextrin offensive taste" from the "dextrin standard beverages". Then, based on the scores decided by each specialized panel, the final score was decided in "0.5" increments by consultation. In addition, the score means that the larger the numerical value, the stronger the "unpleasant taste" is felt.
参考例3
製造例2で得られた茶抽出液IIIと、重曹と、イオン交換水とを表15に示す割合で配合してウーロン茶飲料(RTD飲料)を得た。次いで、得られたウーロン茶飲料について分析を行い、官能評価3にしたがって評価した。その結果を表15に示す。なお、表15中の計算値又は分析値の濃度は、固形分濃度である。
Reference example 3
The tea extract III obtained in Production Example 2, baking soda, and ion-exchanged water were blended in the proportions shown in Table 15 to obtain an oolong tea beverage (RTD beverage). Next, the obtained oolong tea beverage was analyzed and evaluated according to the sensory evaluation 3. The results are shown in Table 15. The concentration of the calculated value or the analytical value in Table 15 is the solid content concentration.
比較例26
茶抽出物Iと、製造例2で得られた茶抽出液IIIと、重曹と、イオン交換水とを表15に示す割合で配合してウーロン茶飲料(RTD飲料)を得た。次いで、得られたウーロン茶飲料について、参考例3と同様に分析及び官能評価を行った。その結果を表15に示す。なお、表15中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 26
The tea extract I, the tea extract III obtained in Production Example 2, the baking soda, and the ion-exchanged water were blended in the proportions shown in Table 15 to obtain an oolong tea beverage (RTD beverage). Next, the obtained oolong tea beverage was analyzed and sensory evaluated in the same manner as in Reference Example 3. The results are shown in Table 15. The concentration of the calculated value or the analytical value in Table 15 is the solid content concentration.
比較例27
更に、デキストリンを表15に示す割合で配合したこと以外は、比較例26と同様の操作によりウーロン茶飲料(RTD飲料)を得た。得られたウーロン茶飲料について、比較例26と同様に分析及び官能評価を行った。その結果を表15に示す。なお、表15中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 27
Further, an oolong tea beverage (RTD beverage) was obtained by the same operation as in Comparative Example 26 except that dextrin was blended in the ratio shown in Table 15. The obtained oolong tea beverage was analyzed and sensory evaluated in the same manner as in Comparative Example 26. The results are shown in Table 15. The concentration of the calculated value or the analytical value in Table 15 is the solid content concentration.
実施例34〜36
更に、ジヒドロクマリンを表15に示す割合で配合したこと以外は、比較例27と同様の操作によりウーロン茶飲料(RTD飲料)を得た。得られたウーロン茶飲料について、比較例27と同様に分析及び官能評価を行った。その結果を表15に示す。なお、表15中の計算値又は分析値の濃度は、固形分濃度である。
Examples 34-36
Further, an oolong tea beverage (RTD beverage) was obtained by the same operation as in Comparative Example 27 except that dihydrocoumarin was blended in the ratio shown in Table 15. The obtained oolong tea beverage was analyzed and sensory evaluated in the same manner as in Comparative Example 27. The results are shown in Table 15. The concentration of the calculated value or the analytical value in Table 15 is the solid content concentration.
官能評価3
各ウーロン茶飲料の「後渋味」、「デキストリンの異味」について専門パネル4名が官能試験を行った。官能試験は、次の手順で行った。
Sensory evaluation 3
Four specialized panels conducted sensory tests on the "after-astringency" and "dextrin taste" of each oolong tea beverage. The sensory test was performed according to the following procedure.
(1)後渋味の評価
先ず、参考例3のウーロン茶飲料にエピガロカテキンガレート(EGCG)を表13に示す割合で配合して「後渋味」の強さを10段階に調整した「後渋味標準飲料」を調製した。次に、専門パネル4名が各濃度の「後渋味標準飲料」について、表13に示す評点とすることを合意した。次いで、各専門パネルがEGCG濃度の低い「後渋味標準飲料」から順に摂取し、「後渋味」の強さを記憶した。次いで、各専門パネルが各ウーロン茶飲料を摂取し、「後渋味」の程度を評価し、「後渋味標準飲料」の中から「後渋味」が最も近いものを決定した。そして、各専門パネルが決定した評点に基づいて、協議により「0.5」刻みで最終評点を決定した。なお、評点は、数値が大きいほど、「後渋味」が強く感じられることを意味する。
(1) Evaluation of post-astringency First, epigallocatechin gallate (EGCG) was added to the oolong tea beverage of Reference Example 3 at the ratio shown in Table 13, and the strength of "post-astringency" was adjusted in 10 steps. "Astringent standard beverage" was prepared. Next, four expert panels agreed to give the scores shown in Table 13 for each concentration of "after-astringent standard beverage". Next, each specialized panel ingested the "post-astringent standard beverage" having the lowest EGCG concentration in order, and memorized the strength of the "post-astringent taste". Next, each specialized panel ingested each oolong tea beverage, evaluated the degree of "after-astringency", and determined the one with the closest "after-astringency" from the "after-astringency standard beverages". Then, based on the scores decided by each specialized panel, the final score was decided in "0.5" increments by consultation. In addition, the score means that the larger the numerical value, the stronger the "after astringency" is felt.
(2)デキストリンの異味の評価
先ず、参考例3のウーロン茶飲料にデキストリン(サンデック#30、三和澱粉株式会社)を表14に示す割合で配合して「デキストリンの異味」の強さを5段階に調整した「異味標準飲料」を調製した。次に、専門パネル4名が各濃度の「異味標準飲料」について、表14に示す評点とすることを合意した。次いで、各専門パネルがデキストリン濃度の低い「異味標準飲料」から順に摂取し、「デキストリンの異味」の強さを記憶した。次いで、各専門パネルが各ウーロン茶飲料を摂取し、「デキストリンの異味」の程度を評価し、「異味標準飲料」の中から「デキストリンの異味」が最も近いものを決定した。そして、各専門パネルが決定した評点に基づいて、協議により「0.5」刻みで最終評点を決定した。なお、評点は、数値が大きいほど、「異味」が強く感じられることを意味する。
(2) Evaluation of the taste of dextrin First, dextrin (Sandeck # 30, Sanwa Cornstarch Co., Ltd.) was added to the oolong tea beverage of Reference Example 3 at the ratio shown in Table 14, and the strength of the "dextrin taste" was graded in 5 levels. A "dextrin standard beverage" adjusted to the above was prepared. Next, four expert panels agreed to give the scores shown in Table 14 for each concentration of "unusual standard beverage". Next, each specialized panel ingested in order from the "dextrin standard beverage" with the lowest dextrin concentration, and memorized the strength of the "dextrin off-flavor". Next, each specialized panel ingested each oolong tea beverage, evaluated the degree of "dextrin offensive taste", and determined the one with the closest "dextrin offensive taste" from the "dextrin standard beverages". Then, based on the scores decided by each specialized panel, the final score was decided in "0.5" increments by consultation. In addition, the score means that the larger the numerical value, the stronger the "unpleasant taste" is felt.
参考例4
製造例3で得られた茶抽出液IVと、重曹とイオン交換水とを表18に示す割合で配合してルイボス茶飲料(RTD飲料)を得た。次いで、得られたルイボス茶飲料について分析を行い、官能評価4にしたがって評価した。その結果を表18に示す。なお、表18中の計算値又は分析値の濃度は、固形分濃度である。
Reference example 4
A rooibos tea beverage (RTD beverage) was obtained by blending the tea extract IV obtained in Production Example 3 with baking soda and ion-exchanged water in the proportions shown in Table 18. Next, the obtained rooibos tea beverage was analyzed and evaluated according to the sensory evaluation 4. The results are shown in Table 18. The concentration of the calculated value or the analytical value in Table 18 is the solid content concentration.
比較例28
茶抽出物Iと、製造例3で得られた茶抽出液IVと、重曹とを表18に示す割合で配合してルイボス茶飲料(RTD飲料)を得た。次いで、得られたルイボス茶飲料について、参考例4と同様に分析及び官能評価を行った。その結果を表18に示す。なお、表18中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 28
A rooibos tea beverage (RTD beverage) was obtained by blending tea extract I, the tea extract IV obtained in Production Example 3, and baking soda in the proportions shown in Table 18. Next, the obtained rooibos tea beverage was analyzed and sensory evaluated in the same manner as in Reference Example 4. The results are shown in Table 18. The concentration of the calculated value or the analytical value in Table 18 is the solid content concentration.
比較例29
更に、デキストリンを表18に示す割合で配合したこと以外は、比較例28と同様の操作によりルイボス茶飲料(RTD飲料)を得た。得られたルイボス茶飲料について、比較例28と同様に分析及び官能評価を行った。その結果を表18に示す。なお、表18中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 29
Further, a rooibos tea beverage (RTD beverage) was obtained by the same operation as in Comparative Example 28 except that dextrin was blended in the ratio shown in Table 18. The obtained rooibos tea beverage was analyzed and sensory evaluated in the same manner as in Comparative Example 28. The results are shown in Table 18. The concentration of the calculated value or the analytical value in Table 18 is the solid content concentration.
実施例37〜39
更に、ジヒドロクマリンを表18に示す割合で配合したこと以外は、比較例29と同様の操作によりルイボス茶飲料(RTD飲料)を得た。得られたルイボス茶飲料について、比較例29と同様に分析及び官能評価を行った。その結果を表18に示す。なお、表18中の計算値又は分析値の濃度は、固形分濃度である。
Examples 37-39
Further, a rooibos tea beverage (RTD beverage) was obtained by the same operation as in Comparative Example 29 except that dihydrocoumarin was blended in the ratio shown in Table 18. The obtained rooibos tea beverage was analyzed and sensory evaluated in the same manner as in Comparative Example 29. The results are shown in Table 18. The concentration of the calculated value or the analytical value in Table 18 is the solid content concentration.
官能評価4
各ルイボス茶飲料の「後渋味」、「デキストリンの異味」について専門パネル4名が官能試験を行った。官能試験は、次の手順で行った。
Sensory evaluation 4
Four expert panels conducted sensory tests on the "after-astringency" and "dextrin taste" of each rooibos tea beverage. The sensory test was performed according to the following procedure.
(1)後渋味の評価
先ず、参考例4のルイボス茶飲料にエピガロカテキンガレート(EGCG)を表16に示す割合で配合して「後渋味」の強さを10段階に調整した「後渋味標準飲料」を調製した。次に、専門パネル4名が各濃度の「後渋味標準飲料」について、表16に示す評点とすることを合意した。次いで、各専門パネルがEGCG濃度の低い「後渋味標準飲料」から順に摂取し、「後渋味」の強さを記憶した。次いで、各専門パネルが各ルイボス茶飲料を摂取し、「後渋味」の程度を評価し、「後渋味標準飲料」の中から「後渋味」が最も近いものを決定した。そして、各専門パネルが決定した評点に基づいて、協議により「0.5」刻みで最終評点を決定した。なお、評点は、数値が大きいほど、「後渋味」が強く感じられることを意味する。
(1) Evaluation of post-astringency First, epigallocatechin gallate (EGCG) was added to the rooibos tea beverage of Reference Example 4 at the ratio shown in Table 16, and the strength of "post-astringency" was adjusted in 10 steps. "Post-astringent standard beverage" was prepared. Next, four expert panels agreed to give the scores shown in Table 16 for each concentration of "after-astringent standard beverage". Next, each specialized panel ingested the "post-astringent standard beverage" having the lowest EGCG concentration in order, and memorized the strength of the "post-astringent taste". Next, each specialized panel ingested each rooibos tea beverage, evaluated the degree of "after-astringency", and determined the one with the closest "after-astringency" from the "after-astringency standard beverages". Then, based on the scores decided by each specialized panel, the final score was decided in "0.5" increments by consultation. In addition, the score means that the larger the numerical value, the stronger the "after astringency" is felt.
(2)デキストリンの異味の評価
先ず、参考例4のルイボス茶飲料にデキストリン(サンデック#30、三和澱粉株式会社)を表17に示す割合で配合して「デキストリンの異味」の強さを5段階に調整した「異味標準飲料」を調製した。次に、専門パネル4名が各濃度の「異味標準飲料」について、表17に示す評点とすることを合意した。次いで、各専門パネルがデキストリン濃度の低い「異味標準飲料」から順に摂取し、「デキストリンの異味」の強さを記憶した。次いで、各専門パネルが各ルイボス茶飲料を摂取し、「デキストリンの異味」の程度を評価し、「異味標準飲料」の中から「デキストリンの異味」が最も近いものを決定した。そして、各専門パネルが決定した評点に基づいて、協議により「0.5」刻みで最終評点を決定した。なお、評点は、数値が大きいほど、「異味」が強く感じられることを意味する。
(2) Evaluation of dextrin taste First, dextrin (Sandeck # 30, Sanwa Cornstarch Co., Ltd.) was added to the rooibos tea beverage of Reference Example 4 at the ratio shown in Table 17, and the strength of "dextrin taste" was 5 A step-adjusted "dextrin standard beverage" was prepared. Next, four expert panels agreed to give the scores shown in Table 17 for each concentration of "unusual standard beverage". Next, each specialized panel ingested in order from the "dextrin standard beverage" with the lowest dextrin concentration, and memorized the strength of the "dextrin off-flavor". Next, each specialized panel ingested each rooibos tea beverage, evaluated the degree of "dextrin offensive taste", and determined the one with the closest "dextrin offensive taste" from the "dextrin standard beverages". Then, based on the scores decided by each specialized panel, the final score was decided in "0.5" increments by consultation. In addition, the score means that the larger the numerical value, the stronger the "unpleasant taste" is felt.
参考例5
製造例4で得られた茶抽出液Vと、重曹と、イオン交換水とを表21に示す割合で配合してコーン茶飲料(RTD飲料)を得た。次いで、得られたコーン茶飲料について分析を行い、官能評価5にしたがって評価した。その結果を表21に示す。なお、表21中の計算値又は分析値の濃度は、固形分濃度である。
Reference example 5
The tea extract V obtained in Production Example 4, baking soda, and ion-exchanged water were blended in the proportions shown in Table 21 to obtain a corn tea beverage (RTD beverage). Next, the obtained corn tea beverage was analyzed and evaluated according to the sensory evaluation 5. The results are shown in Table 21. The concentration of the calculated value or the analytical value in Table 21 is the solid content concentration.
比較例30
茶抽出物Iと、製造例4で得られた茶抽出液Vと、重曹と、イオン交換水とを表21に示す割合で配合してコーン茶飲料(RTD飲料)を得た。次いで、得られたコーン茶飲料について、参考例5と同様に分析及び官能評価を行った。その結果を表21に示す。なお、表21中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 30
A corn tea beverage (RTD beverage) was obtained by blending tea extract I, the tea extract V obtained in Production Example 4, baking soda, and ion-exchanged water in the proportions shown in Table 21. Next, the obtained corn tea beverage was analyzed and sensory evaluated in the same manner as in Reference Example 5. The results are shown in Table 21. The concentration of the calculated value or the analytical value in Table 21 is the solid content concentration.
比較例31
更に、デキストリンを表21に示す割合で配合したこと以外は、比較例30と同様の操作によりコーン茶飲料(RTD飲料)を得た。得られたコーン茶飲料について、比較例30と同様に分析及び官能評価を行った。その結果を表21に示す。なお、表21中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 31
Further, a corn tea beverage (RTD beverage) was obtained by the same operation as in Comparative Example 30 except that dextrin was blended in the ratio shown in Table 21. The obtained corn tea beverage was analyzed and sensory evaluated in the same manner as in Comparative Example 30. The results are shown in Table 21. The concentration of the calculated value or the analytical value in Table 21 is the solid content concentration.
実施例40〜42
更に、ジヒドロクマリンを表21に示す割合で配合したこと以外は、比較例31と同様の操作によりコーン茶飲料(RTD飲料)を得た。得られたコーン茶飲料について、比較例31と同様に分析及び官能評価を行った。その結果を表21に示す。なお、表21中の計算値又は分析値の濃度は、固形分濃度である。
Examples 40-42
Further, a corn tea beverage (RTD beverage) was obtained by the same operation as in Comparative Example 31 except that dihydrocoumarin was blended in the ratio shown in Table 21. The obtained corn tea beverage was analyzed and sensory evaluated in the same manner as in Comparative Example 31. The results are shown in Table 21. The concentration of the calculated value or the analytical value in Table 21 is the solid content concentration.
官能評価5
各コーン茶飲料の「後渋味」、「デキストリンの異味」について専門パネル4名が官能試験を行った。官能試験は、次の手順で行った。
Sensory evaluation 5
Four specialized panels conducted sensory tests on the "after-astringency" and "dextrin taste" of each corn tea beverage. The sensory test was performed according to the following procedure.
(1)後渋味の評価
先ず、参考例5のコーン茶飲料にエピガロカテキンガレート(EGCG)を表19に示す割合で配合して「後渋味」の強さを10段階に調整した「後渋味標準飲料」を調製した。次に、専門パネル4名が各濃度の「後渋味標準飲料」について、表19に示す評点とすることを合意した。次いで、各専門パネルがEGCG濃度の低い「後渋味標準飲料」から順に摂取し、「後渋味」の強さを記憶した。次いで、各専門パネルが各コーン茶飲料を摂取し、「後渋味」の程度を評価し、「後渋味標準飲料」の中から「後渋味」が最も近いものを決定した。そして、各専門パネルが決定した評点に基づいて、協議により「0.5」刻みで最終評点を決定した。なお、評点は、数値が大きいほど、「後渋味」が強く感じられることを意味する。
(1) Evaluation of post-astringency First, epigallocatechin gallate (EGCG) was added to the corn tea beverage of Reference Example 5 at the ratio shown in Table 19, and the strength of "post-astringency" was adjusted in 10 steps. "Post-astringent standard beverage" was prepared. Next, four expert panels agreed to give the scores shown in Table 19 for each concentration of "after-astringent standard beverage". Next, each specialized panel ingested the "post-astringent standard beverage" having the lowest EGCG concentration in order, and memorized the strength of the "post-astringent taste". Next, each specialized panel ingested each corn tea beverage, evaluated the degree of "after-astringency", and determined the one with the closest "after-astringency" from the "after-astringency standard beverages". Then, based on the scores decided by each specialized panel, the final score was decided in "0.5" increments by consultation. In addition, the score means that the larger the numerical value, the stronger the "after astringency" is felt.
(2)デキストリンの異味の評価
先ず、参考例5のコーン茶飲料にデキストリン(サンデック#30、三和澱粉株式会社)を表20に示す割合で配合して「デキストリンの異味」の強さを5段階に調整した「異味標準飲料」を調製した。次に、専門パネル4名が各濃度の「異味標準飲料」について、表20に示す評点とすることを合意した。次いで、各専門パネルがデキストリン濃度の低い「異味標準飲料」から順に摂取し、「デキストリンの異味」の強さを記憶した。次いで、各専門パネルが各コーン茶飲料を摂取し、「デキストリンの異味」の程度を評価し、「異味標準飲料」の中から「デキストリンの異味」が最も近いものを決定した。そして、各専門パネルが決定した評点に基づいて、協議により「0.5」刻みで最終評点を決定した。なお、評点は、数値が大きいほど、「異味」が強く感じられることを意味する。
(2) Evaluation of Dextrin's Disappearance First, dextrin (Sandeck # 30, Sanwa Cornstarch Co., Ltd.) was added to the corn tea beverage of Reference Example 5 at the ratio shown in Table 20, and the strength of "dextrin's discomfort" was 5 A step-adjusted "dextrin standard beverage" was prepared. Next, four expert panels agreed to give the scores shown in Table 20 for each concentration of "unusual standard beverage". Next, each specialized panel ingested in order from the "dextrin standard beverage" with the lowest dextrin concentration, and memorized the strength of the "dextrin off-flavor". Next, each specialized panel ingested each corn tea beverage, evaluated the degree of "dextrin taste", and determined the one with the closest "dextrin taste" from the "dextrin standard drinks". Then, based on the scores decided by each specialized panel, the final score was decided in "0.5" increments by consultation. In addition, the score means that the larger the numerical value, the stronger the "unpleasant taste" is felt.
参考例6
製造例5で得られた茶抽出液VIと、重曹と、イオン交換水とを表24に示す割合で配合して麦茶飲料(RTD飲料)を得た。次いで、得られた麦茶飲料について分析を行い、官能評価6にしたがって評価した。その結果を表24に示す。なお、表24中の計算値又は分析値の濃度は、固形分濃度である。
Reference example 6
The tea extract VI obtained in Production Example 5, baking soda, and ion-exchanged water were blended in the proportions shown in Table 24 to obtain a barley tea beverage (RTD beverage). Next, the obtained barley tea beverage was analyzed and evaluated according to the sensory evaluation 6. The results are shown in Table 24. The concentration of the calculated value or the analytical value in Table 24 is the solid content concentration.
比較例32
茶抽出物Iと、製造例5で得られた茶抽出液VIと、重曹と、イオン交換水とを表24に示す割合で配合して麦茶飲料(RTD飲料)を得た。次いで、得られた麦茶飲料について、参考例6と同様に分析及び官能評価を行った。その結果を表24に示す。なお、表24中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 32
A barley tea beverage (RTD beverage) was obtained by blending tea extract I, the tea extract VI obtained in Production Example 5, baking soda, and ion-exchanged water in the proportions shown in Table 24. Next, the obtained barley tea beverage was analyzed and sensory evaluated in the same manner as in Reference Example 6. The results are shown in Table 24. The concentration of the calculated value or the analytical value in Table 24 is the solid content concentration.
比較例33
更に、デキストリンを表24に示す割合で配合したこと以外は、比較例32と同様の操作により麦茶飲料(RTD飲料)を得た。得られた麦茶飲料について、比較例32と同様に分析及び官能評価を行った。その結果を表24に示す。なお、表24中の計算値又は分析値の濃度は、固形分濃度である。
Comparative Example 33
Further, a barley tea beverage (RTD beverage) was obtained by the same operation as in Comparative Example 32 except that dextrin was blended in the ratio shown in Table 24. The obtained barley tea beverage was analyzed and sensory evaluated in the same manner as in Comparative Example 32. The results are shown in Table 24. The concentration of the calculated value or the analytical value in Table 24 is the solid content concentration.
実施例43〜45
更に、ジヒドロクマリンを表24に示す割合で配合したこと以外は、比較例33と同様の操作により麦茶飲料(RTD飲料)を得た。得られた麦茶飲料について、比較例33と同様に分析及び官能評価を行った。その結果を表24に示す。なお、表24中の計算値又は分析値の濃度は、固形分濃度である。
Examples 43-45
Further, a barley tea beverage (RTD beverage) was obtained by the same operation as in Comparative Example 33 except that dihydrocoumarin was blended in the ratio shown in Table 24. The obtained barley tea beverage was analyzed and sensory evaluated in the same manner as in Comparative Example 33. The results are shown in Table 24. The concentration of the calculated value or the analytical value in Table 24 is the solid content concentration.
官能評価6
各麦茶飲料の「後渋味」、「デキストリンの異味」について専門パネル4名が官能試験を行った。官能試験は、次の手順で行った。
Sensory evaluation 6
Four specialized panels conducted sensory tests on the "after-astringency" and "dextrin taste" of each barley tea beverage. The sensory test was performed according to the following procedure.
(1)後渋味の評価
先ず、参考例6の麦茶飲料にエピガロカテキンガレート(EGCG)を表22に示す割合で配合して「後渋味」の強さを10段階に調整した「後渋味標準飲料」を調製した。次に、専門パネル4名が各濃度の「後渋味標準飲料」について、表22に示す評点とすることを合意した。次いで、各専門パネルがEGCG濃度の低い「後渋味標準飲料」から順に摂取し、「後渋味」の強さを記憶した。次いで、各専門パネルが各麦茶飲料を摂取し、「後渋味」の程度を評価し、「後渋味標準飲料」の中から「後渋味」が最も近いものを決定した。そして、各専門パネルが決定した評点に基づいて、協議により「0.5」刻みで最終評点を決定した。なお、評点は、数値が大きいほど、「後渋味」が強く感じられることを意味する。
(1) Evaluation of post-astringency First, epigallocatechin gallate (EGCG) was added to the barley tea beverage of Reference Example 6 at the ratio shown in Table 22, and the strength of "post-astringency" was adjusted in 10 steps. "Astringent standard beverage" was prepared. Next, four expert panels agreed to give the scores shown in Table 22 for each concentration of "after-astringent standard beverage". Next, each specialized panel ingested the "post-astringent standard beverage" having the lowest EGCG concentration in order, and memorized the strength of the "post-astringent taste". Next, each specialized panel ingested each barley tea beverage, evaluated the degree of "after-astringency", and determined the one with the closest "after-astringency" from the "after-astringency standard beverages". Then, based on the scores decided by each specialized panel, the final score was decided in "0.5" increments by consultation. In addition, the score means that the larger the numerical value, the stronger the "after astringency" is felt.
(2)デキストリンの異味の評価
先ず、参考例6の麦茶飲料にデキストリン(サンデック#30、三和澱粉株式会社)を表23に示す割合で配合して「デキストリンの異味」の強さを5段階に調整した「異味標準飲料」を調製した。次に、専門パネル4名が各濃度の「異味標準飲料」について、表23に示す評点とすることを合意した。次いで、各専門パネルがデキストリン濃度の低い「異味標準飲料」から順に摂取し、「デキストリンの異味」の強さを記憶した。次いで、各専門パネルが各麦茶飲料を摂取し、「デキストリンの異味」の程度を評価し、「異味標準飲料」の中から「デキストリンの異味」が最も近いものを決定した。そして、各専門パネルが決定した評点に基づいて、協議により「0.5」刻みで最終評点を決定した。なお、評点は、数値が大きいほど、「異味」が強く感じられることを意味する。
(2) Evaluation of dextrin taste First, dextrin (Sandeck # 30, Sanwa Cornstarch Co., Ltd.) was added to the barley tea beverage of Reference Example 6 at the ratio shown in Table 23, and the strength of "dextrin taste" was graded in 5 levels. A "dextrin standard beverage" adjusted to the above was prepared. Next, four expert panels agreed to give the scores shown in Table 23 for each concentration of "unusual standard beverage". Next, each specialized panel ingested in order from the "dextrin standard beverage" with the lowest dextrin concentration, and memorized the strength of the "dextrin off-flavor". Next, each specialized panel ingested each barley tea beverage, evaluated the degree of "dextrin offensive taste", and determined the one with the closest "dextrin offensive taste" from the "dextrin standard beverages". Then, based on the scores decided by each specialized panel, the final score was decided in "0.5" increments by consultation. In addition, the score means that the larger the numerical value, the stronger the "unpleasant taste" is felt.
表4〜9、12、15、18、21及び24から、タンニンとデキストリンをそれぞれ特定量含有させ、タンニンに対してクマリン及び/又はその誘導体を特定の質量比で含有させることで、デキストリン由来の異味を抑制しつつ、タンニン由来の後渋味が低減された飲料組成物が得られることがわかる。 From Tables 4 to 9, 12, 15, 18, 21 and 24, tannin and dextrin are contained in specific amounts, respectively, and coumarin and / or a derivative thereof is contained in a specific mass ratio with respect to tannin to be derived from dextrin. It can be seen that a beverage composition with reduced tannin-derived after-astringency while suppressing offensive taste can be obtained.
Claims (7)
(A)タンニン 固形分中に1.2〜12質量%
(B)デキストリン 固形分中に18〜95質量%
(C)クマリン及びその誘導体から選択される少なくとも1種
を含有し、
成分(A)と成分(B)との質量比[(C)/(A)]が0.70×10−4以上300×10−4以下である、
飲料組成物。 The following components (A), (B) and (C);
(A) 1.2-12% by mass of tannin solids
(B) 18-95% by mass in the dextrin solid content
(C) Containing at least one selected from coumarin and its derivatives,
The mass ratio [(C) / (A)] of the component (A) to the component (B) is 0.70 × 10 -4 or more and 300 × 10 -4 or less.
Beverage composition.
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JPH0335898B2 (en) * | 1984-04-04 | 1991-05-29 | Sato Shokuhin Kogyo Kk | |
JP2009017867A (en) * | 2007-07-13 | 2009-01-29 | Sato Shokuhin Kogyo Kk | Method for producing digestion-resistant dextrin-containing instant tea |
US20130243935A1 (en) * | 2012-03-19 | 2013-09-19 | Symrise Ag | Substance Mixtures |
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JPH0335898B2 (en) * | 1984-04-04 | 1991-05-29 | Sato Shokuhin Kogyo Kk | |
JP2009017867A (en) * | 2007-07-13 | 2009-01-29 | Sato Shokuhin Kogyo Kk | Method for producing digestion-resistant dextrin-containing instant tea |
US20130243935A1 (en) * | 2012-03-19 | 2013-09-19 | Symrise Ag | Substance Mixtures |
Non-Patent Citations (2)
Title |
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YANG Z. ET AL.: "Analysis of coumarin and its glycosidically bound precursor in Japanese green tea having sweet-herba", FOOD CHEM., vol. 114, no. 1, JPN6020024582, 2009, pages 289 - 294, XP025874471, ISSN: 0004982353, DOI: 10.1016/j.foodchem.2008.09.014 * |
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