JP2019024365A - Beverages containing tiliroside and plant extracts - Google Patents
Beverages containing tiliroside and plant extracts Download PDFInfo
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- JP2019024365A JP2019024365A JP2017145503A JP2017145503A JP2019024365A JP 2019024365 A JP2019024365 A JP 2019024365A JP 2017145503 A JP2017145503 A JP 2017145503A JP 2017145503 A JP2017145503 A JP 2017145503A JP 2019024365 A JP2019024365 A JP 2019024365A
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- Prior art keywords
- beverage
- tea
- tiliroside
- concentration
- extract
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- Non-Alcoholic Beverages (AREA)
Abstract
【課題】ティリロサイドを含有していながらも、後味においてティリロサイドの苦味が感じられにくい飲料の提供。【解決手段】0.01〜1.0mg/100mLのティリロサイドを含有する飲料に対して、植物抽出物を配合し、飲料中のアミノ態窒素の濃度を18〜60mg/100mLに調整した飲料。飲料のpHは5〜7であることが好ましく、植物抽出物は茶抽出物であることが好ましい。【選択図】なし[Problem] To provide a beverage in which the bitterness of tiliroside is difficult to be felt in the aftertaste while containing tiliroside. A beverage obtained by blending a plant extract with a beverage containing 0.01 to 1.0 mg / 100 mL of tiliroside and adjusting the concentration of amino nitrogen in the beverage to 18 to 60 mg / 100 mL. The pH of the beverage is preferably 5-7, and the plant extract is preferably a tea extract. [Selection figure] None
Description
本発明は、ティリロサイド及び植物抽出物を含有する飲料に関し、より詳細には、飲料の後味としてティリロサイドの苦味が感じられにくい、ティリロサイド及び植物抽出物を含有する飲料に関する。 The present invention relates to a beverage containing tiliroside and a plant extract, and more particularly, to a beverage containing tiliroside and a plant extract, in which the bitter taste of tiliroside is less likely to be felt as a beverage aftertaste.
近年、消費者の健康志向の高まりから、ポリフェノールやポリフェノールを含有する植物抽出物を配合した健康食品が数多く市販されている。しかしながら、このような健康食品は、ポリフェノール特有の苦味及び渋味を有しているため、飲食物に利用しにくいという問題がある。そこで、ポリフェノール由来の苦味や渋味を抑制するための簡便で安価な方法として、タンパクやペプチドを利用する方法が種々提案されている。このようなタンパクやペプチドとしては、プロタミン(特許文献1)、コラーゲン由来ペプチド(特許文献2)、大豆タンパク(特許文献3)、ポリアミノ酸(特許文献4)などが挙げられる。 In recent years, many health foods containing polyphenols and plant extracts containing polyphenols are on the market due to increasing consumer health-consciousness. However, such health foods have a problem that they are difficult to use for foods and drinks because they have the bitterness and astringency unique to polyphenols. Thus, various methods using proteins and peptides have been proposed as simple and inexpensive methods for suppressing the bitterness and astringency derived from polyphenols. Examples of such proteins and peptides include protamine (patent document 1), collagen-derived peptide (patent document 2), soybean protein (patent document 3), polyamino acid (patent document 4) and the like.
ところで、ローズヒップ等の植物には、ポリフェノールの一種であるティリロサイドが含まれていることが知られている。ローズヒップはバラ科バラ属の植物の果実であり、それに含まれる豊富な栄養成分によって、高い美肌効果が得られることや、抗菌、抗ウイルス及び免疫力強化等の効果が得られることが知られている(非特許文献1)。 By the way, it is known that plants such as rose hips contain tiliroside, which is a kind of polyphenol. Rosehip is a fruit of the plant of the genus Rosaceae, and it is known that the rich nutritional components contained in it can provide high skin-beautifying effects and antibacterial, antiviral and immunity enhancement effects. (Non-Patent Document 1).
本発明者らは、ティリロサイドを含有する飲料について研究開発を進めていたところ、ティリロサイドが飲料に含まれると、ティリロサイドの苦味が後味として残りやすく、飲料の嗜好性が低下する傾向があることに気が付いた。特に飲料が中性である場合には、その傾向が強くなった。 The present inventors have been researching and developing beverages containing tiliroside, and when tiliroside is included in the beverage, the bitterness of tiliroside tends to remain as an aftertaste, and the preference of the beverage tends to decrease. It was. This tendency was particularly strong when the beverage was neutral.
そこで、本発明は、ティリロサイドを含有していながらも、後味においてティリロサイドの苦味が感じられにくい飲料を提供することを目的とする。 Then, an object of this invention is to provide the drink which is hard to feel the bitterness of tiriloside in aftertaste, even though it contains tiriloside.
上記課題を解決すべく本発明者らは鋭意検討した結果、特定量のティリロサイドを含有する飲料において、アミノ酸を含有する植物抽出物を配合し、飲料中のアミノ態窒素の含有量が特定範囲となるように調整することによって、ティリロサイド由来の苦味が抑制又は低減され、後味においてその苦味が感じられにくい飲料となることを見出し、本発明を完成するに至った。本発明は、これに限定されるものではないが、以下に関する。
(1)ティリロサイド及び植物抽出物を含有する飲料であって、
飲料中のティリロサイドの濃度が0.01〜1.0mg/100mLであり、
飲料中のアミノ態窒素の濃度が18〜60mg/100mLである、前記飲料。
(2)飲料のpHが5〜7である、(1)に記載の飲料。
(3)植物抽出物が茶抽出物である、(1)又は(2)に記載の飲料。
As a result of intensive investigations by the present inventors to solve the above problems, in a beverage containing a specific amount of tiliroside, a plant extract containing an amino acid is blended, and the content of amino nitrogen in the beverage is within a specific range. By adjusting so that the bitterness derived from tiliroside was suppressed or reduced, it was found that the bitterness of the aftertaste is less likely to be felt, and the present invention was completed. The present invention is not limited to this, but relates to the following.
(1) A beverage containing tiliroside and a plant extract,
The concentration of tiliroside in the beverage is 0.01 to 1.0 mg / 100 mL,
The said drink whose density | concentration of the amino nitrogen in a drink is 18-60 mg / 100mL.
(2) The beverage according to (1), wherein the beverage has a pH of 5 to 7.
(3) The beverage according to (1) or (2), wherein the plant extract is a tea extract.
本発明によれば、ティリロサイドを含有していながらも、後味においてティリロサイドの苦味が感じられにくい飲料を提供することが可能となる。これにより、ティリロサイドを含有する飲料の後味を改善することができ、ティリロサイド又はこれを含む植物抽出物の有用な作用効果を有しつつ、飲みやすい飲料を提供することができる。 ADVANTAGE OF THE INVENTION According to this invention, it becomes possible to provide the drink which is hard to feel the bitterness of tiriloside in the aftertaste, although containing tiriloside. Thereby, the aftertaste of the drink containing tiliroside can be improved, and the drink which it is easy to drink can be provided, having the useful effect of tiliroside or a plant extract containing this.
本発明の一態様は、ティリロサイド及び植物抽出物を含有する飲料であって、飲料中のティリロサイドの濃度が0.01〜1.0mg/100mLであり、飲料中のアミノ態窒素の濃度が18〜60mg/100mLである、前記飲料である。 One aspect of the present invention is a beverage containing tiliroside and a plant extract, wherein the concentration of tiliroside in the beverage is 0.01 to 1.0 mg / 100 mL, and the concentration of amino nitrogen in the beverage is 18 to The beverage is 60 mg / 100 mL.
(ティリロサイド)
本発明の飲料は、0.01〜1.0mg/100mLのティリロサイドを含有する。ティリロサイド(Tiliroside)とは、フラボノイド配糖体に分類される有機化合物の一種であって、下式(1)の構造を有する化合物である。ティリロサイドの別名はKaempferol-3-O-glucoside-6''-E-coumaroylとも称され、そのCAS登録番号は20316−62−5である。構造名・構造式から自明な通り、ティリロサイドは、ケンフェロール、クマル酸、グルコースから構成されている。
(Tiriloside)
The beverage of the present invention contains 0.01 to 1.0 mg / 100 mL of tiliroside. Tiliroside is a kind of organic compound classified as a flavonoid glycoside, and is a compound having the structure of the following formula (1). Another name for Tiriloside is also called Kaempferol-3-O-glucoside-6 ″ -E-coumaroyl, and its CAS registry number is 20316-62-5. As is obvious from the structure name and structural formula, tiriloside is composed of kaempferol, coumaric acid, and glucose.
本発明の飲料において、ティリロサイドの含有量は0.015mg/100mL以上が好ましく、0.02mg/100mL以上がより好ましい。一方、飲料中のティリロサイド含有量が1.0mg/100mLを超えると、ティリロサイドの苦味が強くなりすぎて本発明の効果が得られないことがある。効果及び香味の観点から、飲料中のティリロサイドの含有量は0.8mg/100mL以下が好ましく、0.5mg/100mL以下がより好ましく、0.1mg/100mL以下がさらに好ましい。飲料中のティリロサイドの含有量は、HPLCを用いて測定することができる。HPLCによる測定条件を以下に示す。
・溶離液:37.5%アセトニトリル
・流速:1 mL
・検出:UV 254 nm
・カラム:資生堂CAPCELL PAK C18 (4.6 × 250 mm)
In the beverage of the present invention, the content of tiliroside is preferably 0.015 mg / 100 mL or more, and more preferably 0.02 mg / 100 mL or more. On the other hand, when the tiriloside content in the beverage exceeds 1.0 mg / 100 mL, the bitterness of tiriloside becomes too strong, and the effects of the present invention may not be obtained. From the viewpoint of effect and flavor, the content of tiriloside in the beverage is preferably 0.8 mg / 100 mL or less, more preferably 0.5 mg / 100 mL or less, and further preferably 0.1 mg / 100 mL or less. The content of tiliroside in the beverage can be measured using HPLC. The measurement conditions by HPLC are shown below.
・ Eluent: 37.5% acetonitrile ・ Flow rate: 1 mL
・ Detection: UV 254 nm
・ Column: Shiseido CAPCELL PAK C18 (4.6 x 250 mm)
ティリロサイドは、市販されている既知の化合物である。本発明では、ティリロサイドは純品又は植物抽出物の形態で用いることができる。ティリロサイドの市販品としては、フナコシより販売されているもの、Merck KGaAによって販売されているもの等が挙げられる。また、ティリロサイドを含有する植物抽出物としては、森下仁丹製のローズヒップ抽出物、オリザ油化製のイチゴ種子抽出物等が挙げられる。 Tiriloside is a known compound that is commercially available. In the present invention, tiliroside can be used in the form of a pure product or a plant extract. Examples of commercial products of Tiriroside include those sold by Funakoshi and those sold by Merck KGaA. Examples of the plant extract containing tiliroside include rosehip extract manufactured by Morishita Jintan and strawberry seed extract manufactured by Oriza Oil.
(植物抽出物)
本発明の飲料はまた、植物抽出物を含有する。本発明において植物抽出物は、植物の一部又は全体を、そのまま、或いは必要に応じて、乾燥、破砕、粉砕処理等を行った後に抽出することによって得ることができる。抽出手段は特に限定されず、エタノール等の有機溶媒、水又はそれらの混合物を用いた攪拌・振盪・浸漬抽出法や、減圧水蒸気蒸留抽出法、二酸化炭素等の超臨界流体を用いた超臨界ガス抽出法等、公知の抽出方法で行えばよい。
(Plant extract)
The beverage of the present invention also contains a plant extract. In the present invention, the plant extract can be obtained by extracting a part or the whole of the plant as it is or after performing drying, crushing, pulverizing treatment or the like as necessary. The extraction means is not particularly limited, and a supercritical gas using a supercritical fluid such as an organic solvent such as ethanol, a stirring / shaking / immersion extraction method using water or a mixture thereof, a reduced pressure steam distillation extraction method, carbon dioxide, etc. A known extraction method such as an extraction method may be used.
本発明で用いられる植物抽出物は、アミノ酸を含有する植物抽出物が好ましい。かかる植物抽出物に含まれるアミノ酸としては、分子内にアミノ基とカルボキシ基とを有する化合物であれば特に限定されないが、例えば、アスパラギン酸、スレオニン、セリン、グルタミン酸、グリシン、アラニン、システィン、バリン、メチオニン、イソロイシン、ロイシン、チロシン、フェニルアラニン、リジン、ヒスチジン、プロリン、アルギニンなどが挙げられる。本発明においてアミノ酸は1種のみが含まれていてもよいし、2種以上が含まれていてもよい。 The plant extract used in the present invention is preferably a plant extract containing an amino acid. The amino acid contained in the plant extract is not particularly limited as long as it is a compound having an amino group and a carboxy group in the molecule. For example, aspartic acid, threonine, serine, glutamic acid, glycine, alanine, cysteine, valine, Examples include methionine, isoleucine, leucine, tyrosine, phenylalanine, lysine, histidine, proline, and arginine. In the present invention, only one amino acid may be included, or two or more amino acids may be included.
本発明における植物抽出物は、飲料中のアミノ態窒素濃度が後述する特定範囲となるように、適宜配合量を設定することができる。特に限定されないが、飲料の香味や色味の観点から、植物抽出物は、例えば本発明の飲料中に固形分濃度で0.001〜0.5重量%(w/v)となるように含有させることができ、好ましくは0.01〜0.2重量%(w/v)、より好ましくは0.01〜0.2重量%(w/v)の量で含有させることができる。植物抽出物におけるアミノ酸の含有量は、植物抽出物の濃縮度合等に応じて適宜設定することができる。 The plant extract in the present invention can be appropriately mixed so that the amino nitrogen concentration in the beverage falls within a specific range described later. Although not particularly limited, from the viewpoint of the flavor and color of the beverage, the plant extract is contained, for example, in the beverage of the present invention so that the solid content concentration is 0.001 to 0.5% by weight (w / v). Preferably, it can be contained in an amount of 0.01 to 0.2% by weight (w / v), more preferably 0.01 to 0.2% by weight (w / v). The content of amino acids in the plant extract can be appropriately set according to the concentration degree of the plant extract and the like.
アミノ酸を含有する植物抽出物の植物原料としては、特に限定されないが、本発明の効果の大きさから、茶葉、コーヒー、ココア等を用いることが好ましい。すなわち、本発明において好ましい植物抽出物は、茶抽出物、コーヒー抽出物、又はココア抽出物であり、これらのうち茶抽出物が特に好ましい。本発明ではアミノ酸を含有する植物抽出物が好適に用いられるが、かかる植物抽出物を用いた場合は、単にアミノ酸を使用した場合と比較して、ティリロサイドの苦味を低減する作用効果が顕著に発現する。これは、植物抽出物中に含まれる植物性フェノール類等とアミノ酸との相加的又は相乗的な効果と推測できる。 Although it does not specifically limit as a plant raw material of the plant extract containing an amino acid, From the magnitude | size of the effect of this invention, it is preferable to use a tea leaf, coffee, cocoa, etc. That is, the preferred plant extract in the present invention is a tea extract, a coffee extract, or a cocoa extract, and among these, a tea extract is particularly preferable. In the present invention, a plant extract containing an amino acid is preferably used. However, when such a plant extract is used, the effect of reducing the bitter taste of tiliroside is significantly expressed as compared to the case of simply using an amino acid. To do. This can be presumed to be an additive or synergistic effect between the plant phenols contained in the plant extract and the amino acid.
ここで好適な態様の一つである茶抽出物について詳述する。本発明において茶抽出物とは、茶葉から得られる抽出物を意味する。抽出に使用する茶葉としては、例えば、Camellia属(例えば、C. sinensis var. sinensis(やぶきた種を含む)、C. sinensis var. assamica等のCamellia sinensis等)及びそれらの雑種から選択される茶葉が挙げられる。本発明で使用される茶葉は、加工方法により、不発酵茶、半発酵茶、発酵茶に分類することができる。不発酵茶としては、例えば、煎茶、番茶、碾茶、釜入り茶、茎茶、棒茶、芽茶等の緑茶が挙げられる。また、半発酵茶としては、例えば、鉄観音、色種、黄金桂、武夷岩茶等の烏龍茶が挙げられる。さらに、発酵茶としては、ダージリン、アッサム、スリランカ等の紅茶が挙げられる。茶葉は、1種又は2種以上を組み合わせて用いることができる。中でも、アミノ酸含有量の調整のしやすさから、本発明では緑茶を用いることが好ましい。 Here, the tea extract which is one of the preferred embodiments will be described in detail. In the present invention, the tea extract means an extract obtained from tea leaves. As tea leaves used for extraction, for example, tea leaves selected from the genus Camellia (for example, C. sinensis var. Sinensis (including Yabutaki species), C. sinensis var. Assamica, etc.) and hybrids thereof. Is mentioned. The tea leaves used in the present invention can be classified into non-fermented tea, semi-fermented tea, and fermented tea according to the processing method. Examples of non-fermented tea include green tea such as sencha, bancha, mochi tea, kettle tea, stem tea, stick tea, and bud tea. Examples of the semi-fermented tea include oolong tea such as iron kannon, color type, golden katsura, and martial arts tea. Furthermore, examples of fermented tea include black teas such as Darjeeling, Assam, and Sri Lanka. Tea leaves can be used alone or in combination of two or more. Especially, it is preferable to use green tea in this invention from the ease of adjustment of amino acid content.
茶葉の抽出方法としては、ニーダー抽出、バッチ抽出、ドリップ抽出、カラム抽出等の公知の方法を採用することができる。茶抽出物は、茶抽出液又は茶濃縮物を1種又は2種以上を組み合わせて使用することが可能である。ここで、本明細書において「茶抽出液」とは、茶葉から抽出溶媒を用いて抽出されたものであって、濃縮や精製操作が行われていないものをいう。また、「茶濃縮物」とは茶抽出液のうち溶媒の一部を除去するなどして可溶性固形分濃度を高めたものであり、例えば、濃縮方法として、常圧濃縮、減圧濃縮、膜濃縮等を挙げることができる。茶濃縮物としては市販品を使用してもよい。 As a method for extracting tea leaves, known methods such as kneader extraction, batch extraction, drip extraction, and column extraction can be employed. As the tea extract, a tea extract or a tea concentrate can be used alone or in combination of two or more. As used herein, “tea extract” refers to a product extracted from tea leaves using an extraction solvent and not subjected to concentration or purification operations. In addition, “tea concentrate” is a tea extract obtained by removing a part of the solvent to increase the soluble solid content concentration. For example, as a concentration method, atmospheric concentration, reduced pressure concentration, membrane concentration Etc. A commercial product may be used as the tea concentrate.
(アミノ態窒素)
本発明の飲料は、植物抽出物(好ましくは、アミノ酸を含有する植物抽出物)を含有し、飲料中のアミノ態窒素の濃度を所定の範囲とすることで、飲料中のティリロサイドに由来する苦味を抑制又は低減し、飲料の後味におけるその苦味を軽減することができる。一般に、苦味には、先味の苦味、中味の苦味、後味の苦味、またはそれらの組み合わせがあるが、本発明では、ティリロサイドが呈する後味の苦味を抑制又は低減するものである。本明細書においては、苦味を抑制又は低減する効果を単に「苦味抑制効果」と称することもある。ここで「苦味を抑制又は低減する」とは、対照物(例えば、ティリロサイドの濃度が0.01〜1.0mg/100mLであり、アミノ態窒素の濃度が18mg/100mL未満の飲料)と比較して、苦味の強さが小さくなっていることをいう。苦味の強さは、例えば専門パネルによる官能評価により決定できる。
(Amino nitrogen)
The beverage of the present invention contains a plant extract (preferably a plant extract containing an amino acid), and the bitterness derived from tiliroside in the beverage by making the concentration of amino nitrogen in the beverage a predetermined range Can be suppressed or reduced, and the bitterness in the aftertaste of the beverage can be reduced. In general, the bitterness includes an initial bitterness, a medium bitterness, an aftertaste bitterness, or a combination thereof, but in the present invention, the aftertaste bitterness exhibited by tiliroside is suppressed or reduced. In the present specification, the effect of suppressing or reducing bitterness may be simply referred to as “bitterness suppressing effect”. Here, “suppressing or reducing bitterness” is compared with a control (for example, a beverage having a concentration of tiriloside of 0.01 to 1.0 mg / 100 mL and a concentration of amino nitrogen of less than 18 mg / 100 mL). This means that the intensity of bitterness is decreasing. The intensity of bitterness can be determined, for example, by sensory evaluation using a specialized panel.
本発明において、アミノ態窒素とは、遊離α−アミノ酸の総量に該当する量のことである。ティリロサイドは、上述の式(1)に示すとおり、他のフラボノイドやその配糖体にはない特徴的な構造を持つものである。この特徴的な構造を有するティリロサイドと遊離α−アミノ酸との相互作用により、ティリロサイドの特異的な苦味を抑制又は低減することができると考えらえる。 In the present invention, amino nitrogen is an amount corresponding to the total amount of free α-amino acids. Tililoside has a characteristic structure not found in other flavonoids or glycosides thereof as shown in the above formula (1). It is considered that the specific bitter taste of tiliroside can be suppressed or reduced by the interaction between tiliroside having this characteristic structure and a free α-amino acid.
本発明の飲料中のアミノ態窒素の濃度は、18〜60mg/100mLであり、好ましくは18〜30mg/100mL、より好ましくは18〜27mg/100mLである。上記の濃度範囲であれば、本発明の効果を十分に得ることができる。これに対し、飲料中のアミノ態窒素の濃度が18mg/100mL未満であると、ティリロサイドの苦味抑制効果が十分に得られない傾向にある。また、飲料中のアミノ態窒素の濃度が60mg/100mLを超えると、遊離α−アミノ酸自体の風味が飲料に影響を及ぼすことがある。飲料中のアミノ態窒素の濃度は、TNBS法(trinitro benzen sulfonic acid法)により求めることができる。具体的には、試料を適度に希釈したのち、リン酸緩衝液とTNBS(2,4,6−トリニトロベンゼンスルホン酸)溶液とを加え、所定時間、所定濃度で保持した後、反応停止液を加え、吸光度を測定し(分光光度計波長340nm)、この吸光度を既知濃度のグリシン標準水溶液から求められた検量線に照らし合わせることにより、飲料中のアミノ態窒素の濃度を算出することができる。 The concentration of amino nitrogen in the beverage of the present invention is 18 to 60 mg / 100 mL, preferably 18 to 30 mg / 100 mL, more preferably 18 to 27 mg / 100 mL. If it is said density | concentration range, the effect of this invention can fully be acquired. On the other hand, when the concentration of amino nitrogen in the beverage is less than 18 mg / 100 mL, the bitterness suppressing effect of tiliroside tends not to be sufficiently obtained. In addition, when the concentration of amino nitrogen in the beverage exceeds 60 mg / 100 mL, the flavor of the free α-amino acid itself may affect the beverage. The concentration of amino nitrogen in the beverage can be determined by the TNBS method (trinitro benzen sulfonic acid method). Specifically, after appropriately diluting the sample, a phosphate buffer and a TNBS (2,4,6-trinitrobenzenesulfonic acid) solution are added and held at a predetermined concentration for a predetermined time. In addition, the concentration of amino nitrogen in the beverage can be calculated by measuring the absorbance (spectrophotometer wavelength 340 nm) and comparing the absorbance with a calibration curve obtained from a glycine standard aqueous solution having a known concentration.
(pH)
本発明では、飲料に含まれるティリロサイドの苦味を抑制又は低減し、飲料の後味においてその苦味を感じさせにくくするものであるが、後味におけるティリロサイドの苦味は、特に飲料が中性である場合に強くなる傾向にある。そのため、本発明の好適な態様は、飲料が中性であることである。具体的には、本発明の飲料は、好ましくはpH5〜7であり、より好ましくはpH5.5〜7である。
(PH)
In the present invention, the bitterness of tiliroside contained in the beverage is suppressed or reduced, and the bitterness of the aftertaste is made difficult to feel, but the bitterness of tiliroside in the aftertaste is particularly strong when the beverage is neutral. Tend to be. Therefore, a preferred aspect of the present invention is that the beverage is neutral. Specifically, the beverage of the present invention preferably has a pH of 5-7, more preferably a pH of 5.5-7.
本発明の飲料には、pHを上記範囲内に調整するために、pH調整剤を含有させることができる。pH調整剤としては、例えば、アスコルビン酸、クエン酸、グルコン酸、コハク酸、酒石酸、乳酸、フマル酸、リンゴ酸、アジピン酸等の有機酸、リン酸等の無機酸及びそれらの塩類から選ばれる1種又は2種以上を使用することができる。 In order to adjust pH in the said range, the drink of this invention can be made to contain a pH adjuster. The pH adjuster is selected from, for example, ascorbic acid, citric acid, gluconic acid, succinic acid, tartaric acid, organic acids such as lactic acid, fumaric acid, malic acid and adipic acid, inorganic acids such as phosphoric acid, and salts thereof. 1 type (s) or 2 or more types can be used.
(その他の成分)
本発明の飲料には、上記成分に加え、さらに香料、ビタミン、ミネラル、酸化防止剤、各種エステル類、色素類、乳化剤、保存料、調味料、甘味料、果汁エキス、野菜エキス、花蜜エキス、品質安定剤等の添加剤を含有させることができる。これら添加剤は、1種又は2種以上を組み合わせて含有させることができ、飲料中のその含有量は、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。
(Other ingredients)
In addition to the above ingredients, the beverage of the present invention further includes flavors, vitamins, minerals, antioxidants, various esters, pigments, emulsifiers, preservatives, seasonings, sweeteners, fruit juice extracts, vegetable extracts, nectar extracts, Additives such as quality stabilizers can be included. These additives can be contained alone or in combination of two or more thereof, and the content in the beverage can be appropriately set within a range not impairing the object of the present invention.
(飲料)
本発明の飲料の種類は特に限定されないが、好ましくは茶飲料である。茶飲料とは、茶葉の抽出物や穀類の抽出物を主成分として含有する飲料であり、具体的には、緑茶、ほうじ茶、ブレンド茶、麦茶、マテ茶、ジャスミン茶、紅茶、ウーロン茶、杜仲茶などが挙げられる。本発明において特に好ましい茶飲料は、緑茶飲料である。
(Beverage)
Although the kind of drink of this invention is not specifically limited, Preferably it is a tea drink. Tea beverages are beverages containing tea leaf extract or cereal extract as the main component, specifically, green tea, roasted tea, blended tea, barley tea, mate tea, jasmine tea, black tea, oolong tea, and Tochu tea. Etc. A particularly preferred tea beverage in the present invention is a green tea beverage.
本発明の飲料は、上述した成分を適宜配合することにより製造することができる。本発明の飲料を茶飲料とする場合は、茶葉、穀類種子又はそれらの抽出物等を配合して製造することができる。また、本発明の飲料は、必要に応じて殺菌等の工程を経て、容器詰め飲料とされる。例えば、飲料を容器に充填した後に加熱殺菌等を行う方法や、飲料を殺菌してから無菌環境下で容器に充填する方法により、殺菌された容器詰め飲料を製造することができる。 The beverage of the present invention can be produced by appropriately blending the components described above. When the beverage of the present invention is used as a tea beverage, it can be produced by blending tea leaves, cereal seeds or extracts thereof. Moreover, the drink of this invention is made into a container stuffed drink through processes, such as sterilization, as needed. For example, a sterilized container-packed beverage can be produced by a method of performing heat sterilization after filling a beverage into a container, or a method of sterilizing a beverage and then filling the container in an aseptic environment.
容器の種類は特に限定されず、PETボトル、缶、瓶、紙パックなどを挙げることができる。特に、無色透明のPETボトルは、容器中の飲料の色味が外部から視認しやすく、且つ充填後の飲料の取り扱いも容易であるため、好ましい。 The kind of container is not particularly limited, and examples thereof include PET bottles, cans, bottles, paper packs, and the like. In particular, a colorless and transparent PET bottle is preferable since the color of the beverage in the container is easily visible from the outside and the beverage after filling is easy to handle.
以下、実験例を示して本発明の詳細を具体的に説明するが、本発明はこれに限定されるものではない。また、本明細書において、特に記載しない限り、数値範囲はその端点を含むものとして記載される。 Hereinafter, although an experiment example is shown and the detail of this invention is demonstrated concretely, this invention is not limited to this. In this specification, unless otherwise specified, numerical ranges are described as including the end points.
本実施例中、飲料中のアミノ態窒素の濃度は以下の方法により測定した。 In this example, the concentration of amino nitrogen in the beverage was measured by the following method.
(アミノ態窒素濃度の測定)
アミノ態窒素は、TNBS法で測定した。まず、0.1、0.2、0.3、0.4、及び0.5mMのグリシン溶液を調製した(グリシン標準溶液)。そして、試料となる飲料及びグリシン標準溶液を0.5mLずつ量りとり、リン酸緩衝溶液2mL及び0.1% 2,4,6−Trinitro benzensulfonic acid−Na塩水溶液2mLをそれぞれに加えて攪拌混合し、45℃で90分間反応を行った。反応終了後、紫外可視分光光度計を用いて波長340nmで吸光度を測定した。グリシン標準溶液から検量線を作成し、試料中のアミノ態窒素の濃度(含有量)をグリシン相当量として算出した。
(Measurement of amino nitrogen concentration)
Amino nitrogen was measured by the TNBS method. First, 0.1, 0.2, 0.3, 0.4, and 0.5 mM glycine solutions were prepared (glycine standard solution). Then, 0.5 mL each of the sample beverage and glycine standard solution are weighed, and 2 mL of phosphate buffer solution and 2 mL of 0.1% 2,4,6-Trinitrobenzonic acid-Na salt aqueous solution are added to each and stirred and mixed. The reaction was performed at 45 ° C. for 90 minutes. After completion of the reaction, the absorbance was measured at a wavelength of 340 nm using an ultraviolet-visible spectrophotometer. A calibration curve was prepared from the glycine standard solution, and the concentration (content) of amino nitrogen in the sample was calculated as the glycine equivalent.
実験1:ティリロサイド含有茶飲料(1)
(1)茶抽出物の製造
まず、アミノ酸を含有する植物抽出物として茶抽出物を製造した。10gの緑茶葉に対し熱水(70〜80℃)1000mLを用いて5分間抽出処理を行った後、茶葉を分離し、さらに遠心分離処理(6000rpm、10分)して粗大な粉砕組織や茶粒子などの固形分を除去して、緑茶抽出液を得た(抽出液A)。この抽出液Aを希釈して、アミノ態窒素濃度が15mg/100mLとなる緑茶抽出液(試料1)を製造した。
Experiment 1: Tiriloside-containing tea beverage (1)
(1) Production of tea extract First, a tea extract was produced as a plant extract containing amino acids. 10 g of green tea leaves are extracted with hot water (70 to 80 ° C.) 1000 mL for 5 minutes, and then the tea leaves are separated and centrifuged (6000 rpm, 10 minutes) to obtain coarse crushed tissue or tea. Solid contents such as particles were removed to obtain a green tea extract (extract A). This extract A was diluted to produce a green tea extract (sample 1) having an amino nitrogen concentration of 15 mg / 100 mL.
(2)茶濃縮物の製造
次に、特許第5624633号公報(実施例3)に記載の方法に準じて茶濃縮物を製造した。すなわち、第一工程としてカラム型抽出機に10gの緑茶葉を封入し、抽出機上部から25℃のイオン交換水を100mL加え、緑茶葉を浸漬させた。そこに25℃のイオン交換水を50mL/minの流量にて連続的に20分通液し、低温抽出液を得た(試料B1)。第二工程として、試料B1抽出後の抽出残渣に75℃のイオン交換水を100mL加えた上で、75℃のイオン交換水を50mL/minの流量にて連続的に40分通液し、高温抽出液を得た(試料B2)。第三工程として、試料B2抽出後の抽出残渣に、酵素としてプロテアーゼ及びペクチナーゼを各0.2gずつ添加し、40℃のイオン交換水を加え総重量160gに調整し、40℃に保持したまま50mL/minにて16時間循環通液を行い、酵素処理(反応)を行った。その後、得られた酵素処理液を90℃で10分加熱して酵素を失活させ、酵素抽出液を得た(試料B3)。第四工程として、上記試料B1及びB3全量を混合し、茶抽出液の混合物を得た(茶濃縮物B)。茶濃縮物Bは苦味や渋味がなく、コクや厚みのある豊かな旨みを有するものであり、アミノ態窒素濃度は91mg/100mLであった。
(2) Production of tea concentrate Next, a tea concentrate was produced according to the method described in Japanese Patent No. 5624633 (Example 3). That is, as a first step, 10 g of green tea leaves were sealed in a column type extractor, and 100 mL of 25 ° C. ion-exchanged water was added from the top of the extractor to immerse the green tea leaves. Thereto, ion exchange water at 25 ° C. was continuously passed at a flow rate of 50 mL / min for 20 minutes to obtain a low temperature extract (sample B1). As a second step, 100 mL of 75 ° C. ion exchange water was added to the extraction residue after extraction of sample B1, and then 75 ° C. ion exchange water was continuously passed at a flow rate of 50 mL / min for 40 minutes, An extract was obtained (sample B2). As the third step, 0.2 g each of protease and pectinase as enzymes are added to the extraction residue after sample B2 extraction, adjusted to a total weight of 160 g by adding ion exchange water at 40 ° C., and kept at 40 ° C. The solution was circulated for 16 hours at / min to perform enzyme treatment (reaction). Thereafter, the obtained enzyme-treated solution was heated at 90 ° C. for 10 minutes to deactivate the enzyme to obtain an enzyme extract (sample B3). As a 4th process, the said sample B1 and B3 whole quantity was mixed and the mixture of the tea extract was obtained (tea concentrate B). Tea concentrate B had no bitter or astringent taste, had rich and rich umami, and the amino nitrogen concentration was 91 mg / 100 mL.
(3)ティリロサイド含有茶飲料の製造
試料1に0.02mg/100mLとなるようにティリロサイドを配合し、さらに茶濃縮物Bを表1の濃度となるように適宜添加して、アミノ態窒素濃度が異なる飲料を製造した。各飲料は、pH調整剤(炭酸水素ナトリウム)を用いてpHを6.5に調整した。pH調整後の飲料は500mLのPETボトル容器に充填して、容器詰め飲料とした。
(3) Manufacture of Tiriloside-Containing Tea Beverage Tiriloside is added to Sample 1 so as to be 0.02 mg / 100 mL, and tea concentrate B is appropriately added so as to have the concentration shown in Table 1, so that the amino nitrogen concentration is Different beverages were produced. Each beverage was adjusted to pH 6.5 using a pH adjuster (sodium bicarbonate). The beverage after pH adjustment was filled into a 500 mL PET bottle container to obtain a container-packed beverage.
得られた各種飲料について、パネル3名にて官能評価を行った。官能評価は、飲料の後味におけるティリロサイドの苦味の有無を調べ、各パネルが評価した結果に基づいて、3点:パネル3名が苦味を感じない、2点:パネル2名が苦味を感じない、1点:パネル2名が苦味を感じる、0点:パネル3名が苦味を感じる、として点数付けを行った。 About the obtained various drinks, sensory evaluation was performed by three panelists. The sensory evaluation is to examine the presence or absence of tiriloside bitterness in the aftertaste of the beverage, and based on the results evaluated by each panel, 3 points: panel 3 people do not feel bitter, 2 points: panel 2 people do not feel bitter, The score was given as 1 point: 2 panelists feel bitter, 0 point: 3 panelists feel bitter.
その結果を表1に示す。中性飲料においてはティリロサイドの飲料中の含有量が0.02mg/100mLであったとしても、苦味が強く後味が悪くなることが示された。ティリロサイドを含有する中性飲料において、飲料中のアミノ態窒素含有量を18mg/100mL以上とすると、ティリロサイドの苦味が効果的に低減でき、後味においてティリロサイドの苦味は感じられにくかった。 The results are shown in Table 1. In the neutral beverage, even if the content of tiriroside in the beverage was 0.02 mg / 100 mL, it was shown that the bitterness was strong and the aftertaste was poor. In a neutral beverage containing tiriroside, when the amino nitrogen content in the beverage was 18 mg / 100 mL or more, the bitterness of tiriloside could be effectively reduced, and the bitterness of tiriloside was hardly felt in the aftertaste.
実験2:ティリロサイド含有茶飲料(2)
ティリロサイドの濃度を0.1mg/100mLに変えること以外は、実験1と同様にして飲料を調製し、官能評価した。結果を表2に示す。ティリロサイドを含有する中性飲料において、飲料中のアミノ態窒素含有量を18mg/100mL以上とすると、ティリロサイドの苦味が効果的に低減でき、後味においてティリロサイドの苦味は感じられにくかった。
Experiment 2: Tiriloside-containing tea beverage (2)
A beverage was prepared and sensory evaluated in the same manner as in Experiment 1 except that the concentration of tiliroside was changed to 0.1 mg / 100 mL. The results are shown in Table 2. In a neutral beverage containing tiriroside, when the amino nitrogen content in the beverage was 18 mg / 100 mL or more, the bitterness of tiriloside could be effectively reduced, and the bitterness of tiriloside was hardly felt in the aftertaste.
試料2−7及び試料2−8の比較から、飲料中のアミノ態窒素含有量が60mg/100mLを超える量で茶濃縮物Bを配合しても、ティリロサイドの苦味抑制効果が高まることはないことがわかった。また、茶濃縮物Bを高濃度に配合することにより、茶濃縮物B由来の呈味が飲料に影響を及ぼすと知覚するパネルが存在した。これより、アミノ態窒素含有量の上限は60mg/100mLであることが示唆された。 From the comparison of Sample 2-7 and Sample 2-8, even if tea concentrate B is blended in an amount where the amino nitrogen content in the beverage exceeds 60 mg / 100 mL, the bitterness-inhibiting effect of tiliroside does not increase. I understood. Moreover, the panel which perceives that the taste derived from the tea concentrate B affects the beverage by blending the tea concentrate B at a high concentration exists. From this, it was suggested that the upper limit of amino nitrogen content is 60 mg / 100 mL.
実験3:ティリロサイド含有茶飲料(3)
ティリロサイドの濃度を0.5mg/100mLに変えること以外は、実験2の試料2−7及び2−8と同様にして飲料(試料3−1、3−2)を調製し、官能評価した。結果を表3に示す。実験2の結果と同様に、ティリロサイドを含有する中性飲料において、飲料中のアミノ態窒素含有量が60mg/100mLを超える量で茶濃縮物Bを配合しても、60mg/100mLの量で配合した場合と同程度の苦味抑制効果であった。
Experiment 3: Tea drink containing tiriroside (3)
Beverages (Samples 3-1, 3-2) were prepared and subjected to sensory evaluation in the same manner as Samples 2-7 and 2-8 in Experiment 2, except that the concentration of tiliroside was changed to 0.5 mg / 100 mL. The results are shown in Table 3. Similar to the result of Experiment 2, in a neutral beverage containing tiliroside, even if tea concentrate B is blended in an amount where the amino nitrogen content in the beverage exceeds 60 mg / 100 mL, it is blended in an amount of 60 mg / 100 mL The bitterness-inhibiting effect was the same as that of the case.
Claims (3)
飲料中のティリロサイドの濃度が0.01〜1.0mg/100mLであり、
飲料中のアミノ態窒素の濃度が18〜60mg/100mLである、前記飲料。 A beverage containing tililoside and a plant extract,
The concentration of tiliroside in the beverage is 0.01 to 1.0 mg / 100 mL,
The said drink whose density | concentration of the amino nitrogen in a drink is 18-60 mg / 100mL.
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