JPH08298930A - Tea extract or tea beverage reduced in astringency and its production - Google Patents
Tea extract or tea beverage reduced in astringency and its productionInfo
- Publication number
- JPH08298930A JPH08298930A JP7135701A JP13570195A JPH08298930A JP H08298930 A JPH08298930 A JP H08298930A JP 7135701 A JP7135701 A JP 7135701A JP 13570195 A JP13570195 A JP 13570195A JP H08298930 A JPH08298930 A JP H08298930A
- Authority
- JP
- Japan
- Prior art keywords
- tea
- astringency
- tea extract
- extract
- beverage
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、渋味を低減した茶抽出
物または茶飲料とその製造方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a tea extract or tea beverage with reduced astringency and a method for producing the same.
【0002】[0002]
【従来の技術】現在、缶飲料やインスタント飲料をはじ
めとして茶葉を原料として含む食品が大量に販売されて
いる。また、一方で茶の渋み成分が、コレステロール上
昇抑制作用(特公平2−44449号公報)、抗菌作用
(特開平2−276562号公報)、抗酸化作用(特公
平1−44234号公報)、抗腫瘍作用(特開昭60−
190719号公報)、血圧上昇抑制作用および酵素活
性阻害作用(特開平3−133928号公報)などの生
理活性作用を持つことが知られている。茶の渋み成分の
主成分であるポリフェノール類としては、緑茶や烏龍茶
ではエピガロカテキンガレートやエピガロカテキン,エ
ピカテキンガレートが、紅茶ではこれらの他に、さらに
テアルビジンやテアフラビンが知られている。しかしな
がら、茶はこれらのポリフェノール類の持つ特徴的な渋
みのために、いわゆる茶として飲用されている他には、
数種類の食品原料として使用されているのみであり,食
品原料としての使用用途は限定されている。2. Description of the Related Art At present, a large amount of foods containing tea leaves as raw materials, including canned drinks and instant drinks, are being sold. On the other hand, the astringency component of tea, on the other hand, has a cholesterol-suppressing action (Japanese Patent Publication No. 2-44449), an antibacterial action (Japanese Patent Laid-Open No. 2-276562), an antioxidant action (Japanese Patent Publication No. 1-44434), and an anti-oxidant action. Tumor action (JP-A-60-
No. 190719), a blood pressure increase suppressing action and an enzyme activity inhibiting action (JP-A-3-133928). As polyphenols, which are the main components of the astringency component of tea, epigallocatechin gallate, epigallocatechin, epicatechin gallate are known for green tea and oolong tea, and thearuvidin and theaflavin are also known for black tea. However, tea is drunk as so-called tea because of the characteristic astringency of these polyphenols.
It is only used as a raw material for several kinds of food, and its use as a raw material for food is limited.
【0003】食品原料としての用途開発のため、あるい
は茶飲料の呈味性改善のために、茶の渋みを低下させる
試みがなされており、これまでに提案された方法として
は、ポリビニルピロリドンで茶抽出液中の渋み成分を取
り除く方法(特開平1−218550号公報)、原茶製
造時にアルコール水溶液で処理する方法(特開昭60−
115170号公報)、サイクロデキストリンやグルタ
ミン酸塩を添加する方法(特開昭61−271969号
公報)、さらにはサポニンを配糖化することによって呈
味性を改善する方法(特開昭63−39597号公報、
特公平3−68664号公報)が挙げられる。しかしな
がら、ポリビニルピロリドンの使用では、茶の生理活性
成分であるポリフェノール類が除去されてしまう。ま
た、原茶製造時の処理方法は、該処理が可能な機械でし
か目的とする茶の製造ができないという課題がある。さ
らに、サイクロデキストリンやグルタミン酸塩の使用
は、一時的なマスキング効果しか持たない。また、茶サ
ポニンは茶の渋み成分の主成分ではないため、サポニン
を配糖化するだけで茶抽出物や茶飲料の渋みの低減を図
ることは困難である。従って、茶の特性を生かした上で
渋みを低減し、さらに茶飲料や茶抽出物の用途を拡大す
ることは従来の技術では困難であった。[0003] Attempts have been made to reduce the astringency of tea for the purpose of developing its use as a food material or for improving the taste of tea beverages. As a method proposed so far, polyvinylpyrrolidone A method of removing astringent components in the extract (Japanese Patent Laid-Open No. 1-218550) and a method of treating with an aqueous alcohol solution during the production of raw tea (Japanese Patent Laid-Open No. 60-
No. 115170), a method of adding cyclodextrin or glutamate (JP-A-61-271969), and a method of improving taste by glycosylating saponin (JP-A-63-39597). ,
Japanese Patent Publication No. 3-68664). However, the use of polyvinylpyrrolidone removes polyphenols, which are the physiologically active components of tea. Further, the processing method at the time of manufacturing the raw tea has a problem that the target tea can be manufactured only by a machine capable of the processing. Furthermore, the use of cyclodextrins and glutamate has only a temporary masking effect. Further, since tea saponin is not the main component of the astringency component of tea, it is difficult to reduce the astringency of the tea extract or the tea beverage by simply glycosylating the saponin. Therefore, it is difficult to reduce the astringency while making the best use of the characteristics of tea, and to expand the uses of tea beverages and tea extracts by the conventional techniques.
【0004】[0004]
【発明が解決しようとする課題】本発明の目的は、茶に
含まれる生理活性成分を含んだままで、渋みを低減した
茶抽出物または茶飲料を提供することである。さらに、
渋みを低減した茶抽出物または茶飲料を飲食物をはじめ
として、化粧品,医薬品などの広い分野で十分に活用で
きるようにすることである。SUMMARY OF THE INVENTION It is an object of the present invention to provide a tea extract or a tea beverage with reduced astringency while containing the physiologically active ingredient contained in tea. further,
The aim is to make tea extracts or tea beverages with reduced astringency sufficiently usable in a wide range of fields such as food and drink, cosmetics, pharmaceuticals and the like.
【0005】[0005]
【課題を解決するための手段】本発明者らは茶抽出物ま
たは茶飲料の渋みの低減に関して、鋭意研究を重ねた結
果、茶抽出物または茶飲料をデキストリン,サイクロデ
キストリン,澱粉もしくはこれらの混合物と混ぜ、これ
にサイクロマルトデキストリングルカノトランスフェラ
ーゼを作用させることによって、渋みを低減した茶抽出
物または茶飲料が得られることを見いだした。Means for Solving the Problems As a result of intensive studies conducted by the present inventors on reducing the astringency of tea extracts or tea beverages, the inventors have found that the tea extracts or tea beverages are dextrin, cyclodextrin, starch or a mixture thereof. It was found that a tea extract or a tea beverage with reduced astringency can be obtained by mixing with a cyclomaltodextrin glucanotransferase.
【0006】本発明は、渋みを低減した茶抽出物または
茶飲料、より具体的にはポリフェノール類を配糖化する
ことにより渋みを低減した茶抽出物または茶飲料に関
し、さらに茶抽出物または茶飲料をデキストリン,サイ
クロデキストリンおよび澱粉のうちの少なくとも1種と
混ぜ、これにサイクロマルトデキストリングルカノトラ
ンスフェラーゼを作用させることを特徴とする渋みを低
減した茶抽出物または茶飲料の製造方法に関する。ま
た、本発明は、上記の渋みを低減した茶抽出物または茶
飲料を含有する飲食物に関する。The present invention relates to a tea extract or tea beverage with reduced astringency, more specifically to a tea extract or tea beverage with reduced astringency by glycosylating polyphenols, and further to a tea extract or tea beverage. The present invention relates to a method for producing a tea extract or tea beverage with reduced astringency, which comprises mixing at least one of dextrin, cyclodextrin, and starch and allowing cyclomaltodextrin glucanotransferase to act on the mixture. The present invention also relates to food and drink containing the tea extract or tea beverage with reduced astringency described above.
【0007】以下に、本発明を詳しく説明する。本発明
に用いる茶抽出物や茶飲料は制限がなく、既知の方法に
よって得られるものを任意に使用できる。茶飲料の一般
的な製造方法は、緑茶,烏龍茶,紅茶,プアール茶など
の茶葉を原料として抽出を行い、濾過、遠心沈殿などに
より清澄化を行った後に、香料,添加物やビタミンCな
どを適宜添加して味を整え、さらに加熱殺菌を行い茶飲
料にする方法である。次に、茶抽出物の製造方法は、茶
飲料と同様、あるいはさらに濃い濃度で抽出を行った
後、清澄化等の処理を行ってから濃縮してエキスにする
方法、あるいは該エキスに凍結乾燥,噴霧乾燥等の乾燥
手段を適用して粉末にする方法である。The present invention will be described in detail below. There is no limitation on the tea extract and tea beverage used in the present invention, and those obtained by a known method can be arbitrarily used. The general method of manufacturing tea beverages is to extract tea leaves such as green tea, oolong tea, black tea, and puar tea as raw materials, and after filtering and clarification by centrifugal precipitation, etc., add flavors, additives, vitamin C, etc. This is a method of adding tea as needed to adjust the taste, and sterilizing by heating to obtain a tea beverage. Next, the method for producing a tea extract is the same as that for a tea beverage, or after extracting at a higher concentration, a process such as clarification and then concentration to obtain an extract, or freeze-drying on the extract. This is a method of applying a drying means such as spray drying to obtain a powder.
【0008】茶抽出物または茶飲料の渋みを低減する具
体的な方法としては、上記の茶抽出物(粉末の場合は液
化する)または茶飲料に、デキストリン,サイクロデキ
ストリン,澱粉あるいはこれらの混合物を添加し、これ
にサイクロマルトデキストリングルカノトランスフェラ
ーゼを作用させる方法を用いることができる。サイクロ
マルトデキストリングルカノトランスフェラーゼとして
は、バチルス・ステアロサーモフィラス(Bacillus ste
arothermophilus)由来の酵素がポリフェノール類への配
糖化能が高く、渋みをよく低減できるので、有利に利用
できる。As a specific method for reducing the astringency of a tea extract or tea beverage, dextrin, cyclodextrin, starch or a mixture thereof is added to the above tea extract (liquefied in the case of powder) or tea beverage. A method in which cyclomaltodextrin glucanotransferase is added to this and added thereto can be used. Cyclomaltodextrin glucanotransferases include Bacillus stearothermophilus.
The enzyme derived from (arothermophilus) has a high ability to glycosylate to polyphenols and can well reduce astringency, so that it can be advantageously used.
【0009】酵素反応の条件としては、反応のpHを3
〜9、好ましくは5〜8、反応温度を20〜80℃、好
ましくは30〜70℃とし、基質濃度としてポリフェノ
ール類を0.1〜20%(w/w)、好ましくは5〜1
5%(w/w)、デキストリン,サイクロデキストリン
および澱粉のうちの少なくとも1種を1〜40%(w/
w)、好ましくは2〜35%(w/w)含む反応液を用
いるのがよい。酵素量や反応時間は、上記反応条件に合
わせ適宜に設定することができる。本発明の方法には、
上記のように、茶抽出物や茶飲料に直接酵素を作用させ
て渋みを低減させる方法だけでなく、茶抽出物や茶飲料
の製造工程の途中で上記の酵素反応を行うことによっ
て、渋みを低減した茶抽出物や茶飲料を製造する方法も
包含される。The condition of the enzyme reaction is that the pH of the reaction is 3
-9, preferably 5-8, a reaction temperature of 20-80 ° C, preferably 30-70 ° C, and a substrate concentration of polyphenols of 0.1-20% (w / w), preferably 5-1.
5% (w / w), at least one of dextrin, cyclodextrin and starch is 1-40% (w / w).
It is advisable to use a reaction solution containing w), preferably 2-35% (w / w). The amount of enzyme and the reaction time can be appropriately set according to the above reaction conditions. The method of the present invention includes
As described above, not only a method of directly acting an enzyme on a tea extract or a tea beverage to reduce astringency, but by performing the above-mentioned enzymatic reaction during the manufacturing process of a tea extract or a tea beverage, astringency is reduced. Also included are methods of making reduced tea extracts and tea beverages.
【0010】以上述べたようにして得られる茶抽出物ま
たは茶飲料は、従来の茶抽出物や茶飲料と比べて苦味、
渋味、えぐみや収斂性などの嫌味がなく、そのままで渋
みを低減した茶飲料等として飲用に供することができる
だけでなく、他の素材と共に含有せしめて飲食物として
用いる他、嗜好品,医薬部外品,化粧品,医薬品などの
広い分野に自由に用いることができる。また、本発明の
渋みを低減した茶抽出物または茶飲料に含まれる配糖化
されたポリフェノール類は、これらを摂取したとき、体
内のα−アミラーゼ,α−グルコシダーゼなどの作用に
より容易に元のポリフェノール類に戻ることから、その
機能性の低下を懸念することなく、茶本来の例えば、コ
レステロール上昇抑制作用,生体内抗酸化作用などの生
理活性機能を発揮できるため、健康増進食品,健康維持
食品,健康回復食品などとして有利に利用することがで
きる。本発明の渋みを低減させた茶抽出物または茶飲料
の利用分野を例示すれば、調味料,和菓子,洋菓子,氷
菓子,シロップ類,果実加工品,野菜加工品,漬物類,
畜肉製品,魚肉製品,珍味類,缶・ビン詰類,酒類,清
涼飲料,即席飲食物などの食品類、タバコ,練り歯磨
き,口紅,リップクリーム,内服薬,トローチ,肝油ド
ロップ,口中清涼剤,口中香錠,うがい薬などの各種固
形状,ペースト状,液状の嗜好品、化粧品、医薬品など
である。The tea extract or tea beverage obtained as described above has a bitter taste, compared with conventional tea extracts or tea beverages.
It has no astringency, astringency, astringency, and other unpleasant tastes, and can be used as it is as a tea beverage with reduced astringency as it is. It is also used as a food or drink by including it with other ingredients. It can be used freely in a wide range of fields such as external products, cosmetics, and pharmaceuticals. Further, the glycosylated polyphenols contained in the tea extract or tea beverage with reduced astringency of the present invention, when these are ingested, α-amylase in the body, α- glucosidase and the like easily the original polyphenols. Since it returns to the class, it is possible to exert physiologically active functions such as an original cholesterol-suppressing effect and an in-vivo antioxidant effect without worrying about the deterioration of its functionality. It can be advantageously used as a food for recovering health. Examples of the field of use of the tea extract or tea beverage with reduced astringency of the present invention include seasonings, Japanese sweets, Western sweets, ice sweets, syrups, fruit processed products, vegetable processed products, pickles,
Meat products, fish products, delicacies, canned and bottled foods, alcoholic beverages, soft drinks, foods such as instant food and drink, tobacco, toothpaste, lipstick, lip balm, oral drug, troche, liver oil drop, mouthwash, mouthwash These include various solid, paste, and liquid items such as pastilles and mouthwashes, cosmetics, and pharmaceuticals.
【0011】[0011]
【実施例】以下に、本発明を実施例により説明するが、
本発明はかかる説明によって何ら制限されるものではな
い。 実施例1 紅茶濃縮エキス(三井農林株式会社製)60gを熱水1
590gで希釈して飲用濃度にした。この希釈液135
0gに対してデキストリン(商品名:パインデックス#
1、松谷化学株式会社製)50g(希釈紅茶エキスのB
rixの3倍量)を加え、さらにバチルス・ステアロサ
ーモフィラス由来のサイクロマルトデキストリングルカ
ノトランスフェラーゼ(株式会社林原生物化学研究所
製)をデキストリン1グラム当たり1000単位加え、
NaOHでpHを5.5に調整後、50℃で12時間反
応させた。EXAMPLES The present invention will be described below with reference to examples.
The present invention is not limited to the above description. Example 1 60 g of black tea concentrated extract (manufactured by Mitsui Norin Co., Ltd.) was added to hot water 1
It was diluted with 590 g to a drinking concentration. This diluent 135
0 g for dextrin (trade name: Pa index #
1, Matsutani Chemical Co., Ltd.) 50 g (diluted black tea extract B)
(3 times the amount of rix), and then 1000 units of cyclomaltodextrin glucanotransferase (produced by Hayashibara Biochemical Research Institute) derived from Bacillus stearothermophilus per 1 g of dextrin,
After adjusting the pH to 5.5 with NaOH, the mixture was reacted at 50 ° C. for 12 hours.
【0012】一方、対照例として上記の希釈紅茶エキス
のBrixに対して3倍量のデキストリン(上記と同
じ)を溶解したものを作成した。10人のパネラーによ
り、実施例と対照例の各製品の渋みについて3点比較法
で試験を行い、渋味が強いと感じられるものを選択して
貰い評価を行った。その結果を第1表に示す。On the other hand, as a control, a solution prepared by dissolving 3 times the amount of dextrin (the same as above) in Brix of the diluted black tea extract was prepared. The astringency of each product of the example and the control example was tested by 10 panelists by the three-point comparison method, and those having a strong astringency were selected and evaluated. The results are shown in Table 1.
【0013】[0013]
【表1】 第1表 実施例の製品 対照例の製品 渋味が強いと評価した人数 1人 9人[Table 1] 1 person nine the number of people product astringency of the product Control Example of Table 1 embodiment was evaluated as strong
【0014】第1表から明らかなように、渋みの弱いも
のとして実施例の製品を選択したパネラーが有意に多か
った。また、実施例と対照例の各製品を冷蔵庫中で保存
したところ、対照例の製品は紅茶特有のクリームダウン
現象による顕著な濁りを生じたのに対して、実施例の製
品は濁りの低減が認められた。従って、渋みを低減する
反応に伴って紅茶特有の問題であるクリームダウンも低
減できることが判った。このように呈味性が改善された
ことによって、本発明の渋みを低減した紅茶飲料は、飲
料の他に食品,嗜好品,化粧品等を問わず様々な物品に
応用することができる。As is clear from Table 1, a large number of panelists selected the products of the examples as those with weak astringency. Further, when each product of the example and the control example was stored in a refrigerator, the control product produced remarkable cloudiness due to the cream-down phenomenon peculiar to black tea, whereas the product of the example showed a reduction in cloudiness. Admitted. Therefore, it was found that cream down, which is a problem peculiar to black tea, can be reduced along with the reaction of reducing astringency. Due to the improved taste, the tea beverage of the present invention with reduced astringency can be applied to various products such as foods, luxury items, cosmetics and the like in addition to beverages.
【0015】実施例2 実施例1で得られた渋みを低減した紅茶エキスが、本発
明の方法により配糖化することによって渋みを低減した
茶抽出物であることを定性的に確認するため、以下のよ
うな操作を行った。実施例1で得られた紅茶エキス5m
lを秤取り、グルコアミラーゼ(商品名:グルクザイム
AF6、天野製薬株式会社製)1.6mgとα- グルコ
シダーゼ(シグマ社製)0.23mgを加えてよく撹拌
後、37℃で3時間インキュベートした。次いで、反応
液に酢酸エチル1mlを加えてよく混合した後、300
0回転/分で5分間遠心して、酢酸エチル層と水層に分
離し、酢酸エチル層を回収した。この操作を4回繰り返
した。得られた酢酸エチル層を遠心濃縮機で濃縮して酢
酸エチルを留去後、得られた固形物を水で25mlにメ
スアップした。これを処理画分とした。Example 2 In order to qualitatively confirm that the black tea extract with reduced astringency obtained in Example 1 is a tea extract with reduced astringency by glycosylation by the method of the present invention, the following is given. I performed an operation like. 5 m of the black tea extract obtained in Example 1
1 g was weighed, 1.6 mg of glucoamylase (trade name: Gluczyme AF6, manufactured by Amano Pharmaceutical Co., Ltd.) and 0.23 mg of α-glucosidase (manufactured by Sigma) were added, and after stirring well, the mixture was incubated at 37 ° C. for 3 hours. Then, 1 ml of ethyl acetate was added to the reaction mixture and mixed well.
The mixture was centrifuged at 0 rpm for 5 minutes to separate an ethyl acetate layer and an aqueous layer, and the ethyl acetate layer was collected. This operation was repeated 4 times. The obtained ethyl acetate layer was concentrated with a centrifugal concentrator to distill off the ethyl acetate, and the resulting solid was diluted to 25 ml with water. This was used as a treated fraction.
【0016】一方、実施例1で得られた紅茶エキスを5
ml秤取って酢酸エチル1mlを加えてよく混合した
後、3000回転/分で5分間遠心して、酢酸エチル層
と水層に分離し、酢酸エチル層を回収した。この操作を
4回繰り返した。得られた酢酸エチル層を遠心濃縮機で
濃縮して酢酸エチルを留去後、得られた固形物を水で2
5mlにメスアップした。これをコントロール画分とし
た。On the other hand, 5 parts of the black tea extract obtained in Example 1 were used.
After weighing 1 ml and adding 1 ml of ethyl acetate and mixing well, the mixture was centrifuged at 3000 rpm for 5 minutes to separate into an ethyl acetate layer and an aqueous layer, and the ethyl acetate layer was recovered. This operation was repeated 4 times. The obtained ethyl acetate layer was concentrated with a centrifugal concentrator to distill off the ethyl acetate, and then the obtained solid was diluted with water to 2%.
The volume was raised to 5 ml. This was used as a control fraction.
【0017】上記処理画分およびコントロール画分中の
茶ポリフェノールを酒石酸鉄法を用いて以下のように測
定した。処理画分とコントロール画分をそれぞれ5ml
ずつとり、硫酸第一鉄(1mg/ml)と酒石酸カリウ
ムナトリウム(5mg/ml)の混合溶液5mlを加え
た後で、1/15Mのリン酸ナトリウム−リン酸カリウ
ム緩衝液(pH7.5)で25mlにメスアップした。
得られた反応液の540nmにおける吸光度をそれぞれ
測定した。結果を第2表に示す。Tea polyphenols in the treated fraction and the control fraction were measured by the iron tartrate method as follows. 5 ml each of treated and control fractions
After each addition, 5 ml of a mixed solution of ferrous sulfate (1 mg / ml) and potassium sodium tartrate (5 mg / ml) was added, and then with 1/15 M sodium phosphate-potassium phosphate buffer (pH 7.5). The volume was raised to 25 ml.
The absorbance at 540 nm of each of the obtained reaction solutions was measured. The results are shown in Table 2.
【0018】[0018]
【表2】 第2表 540nmの吸光度 処理画分 0.549 コントロール画分 0.371Table 2 Table 2 Absorbance- treated fraction at 540 nm 0.549 Control fraction 0.371
【0019】第2表から明らかなように、処理画分では
コントロール画分に比べて吸光度が約20%増加した。
これは処理画分の方がコントロール画分に比べて酢酸エ
チル層に移りやすい遊離のポリフェノール類の量が多い
ことを示すものであり、実施例1で配糖化されていたポ
リフェノール類が元のポリフェノール類に戻ったことを
示すものである。従って、この結果は、本発明の方法に
よって紅茶中の渋み成分である茶ポリフェノールが配糖
化されていたことを示すものである。さらには、この方
法が本発明の渋みを低減した茶抽出物または茶飲料の確
認方法となることを示すものである。As is clear from Table 2, the absorbance of the treated fraction increased by about 20% as compared with the control fraction.
This indicates that the treated fraction has a larger amount of free polyphenols that are easily transferred to the ethyl acetate layer than the control fraction, and the polyphenols glycosylated in Example 1 are the original polyphenols. It is a sign that it has returned to the class. Therefore, this result indicates that the tea polyphenol, which is an astringent ingredient in black tea, was glycosylated by the method of the present invention. Furthermore, it is shown that this method is the method for confirming the tea extract or tea beverage with reduced astringency of the present invention.
【0020】実施例3 緑茶抽出物(商品名:ポリフェノン60、三井農林株式
会社製)1.5gとα−サイクロデキストリン(株式会
社林原生物化学研究所製)6.0gを10mM塩化カル
シウム溶液30mlに溶解後、pHを5.5に調整し
た。この溶液にバチルス・ステアロサーモフィラス由来
のサイクロマルトデキストリングルカノトランスフェラ
ーゼ(株式会社林原生物化学研究所製)500単位を添
加して50℃で24時間インキュベートした。酵素反応
を100℃で30分間加熱して停止後、反応生成物を凍
結乾燥して粉末7.6gを得た。Example 3 1.5 g of a green tea extract (trade name: Polyphenon 60, manufactured by Mitsui Norin Co., Ltd.) and 6.0 g of α-cyclodextrin (manufactured by Hayashibara Biochemical Laboratory Co., Ltd.) were added to 30 ml of a 10 mM calcium chloride solution. After dissolution, the pH was adjusted to 5.5. To this solution, 500 units of cyclomaltodextrin glucanotransferase (manufactured by Hayashibara Biochemical Laboratories) derived from Bacillus stearothermophilus was added and incubated at 50 ° C. for 24 hours. After stopping the enzymatic reaction by heating at 100 ° C. for 30 minutes, the reaction product was freeze-dried to obtain 7.6 g of a powder.
【0021】一方、対照例として、緑茶抽出物(上記と
同じ)1.5gとα−サイクロデキストリン(株式会社
林原生物化学研究所製)6.0gを10mM塩化カルシ
ウム溶液30mlに溶解してpHを5.5とした後、5
0℃で24時間インキュベートした。次に、バチルス・
ステアロサーモフィラス由来のサイクロマルトデキスト
リングルカノトランスフェラーゼ(株式会社林原生物化
学研究所製)500単位を添加して、直ちに100℃で
30分間加熱して酵素を失活させた。得られた溶液を凍
結乾燥して粉体7.7gを得た。On the other hand, as a control example, 1.5 g of the green tea extract (the same as above) and 6.0 g of α-cyclodextrin (manufactured by Hayashibara Biochemical Laboratory Co., Ltd.) were dissolved in 30 ml of 10 mM calcium chloride solution to adjust the pH. After setting to 5.5, 5
Incubated at 0 ° C for 24 hours. Next, Bacillus
500 units of cyclomaltodextrin glucanotransferase (manufactured by Hayashibara Biochemical Laboratories) derived from stearothermophilus was added and immediately heated at 100 ° C. for 30 minutes to inactivate the enzyme. The obtained solution was freeze-dried to obtain 7.7 g of powder.
【0022】上記の実施例および対照例で得た各粉末な
らびに原料の緑茶抽出物(商品名:ポリフェノン60、
三井農林株式会社製)を該緑茶抽出物の濃度で2000
ppm相当となるように溶解した。これら3種類のサン
プルについて3点比較法で試験を行い、渋味が少ないも
のを選択させ評価した。なお、官能検査は20人のパネ
ラーに対して行った。結果を第3表に示す。Each powder obtained in the above Examples and Controls and the green tea extract as a raw material (trade name: Polyphenon 60,
Mitsui Norin Co., Ltd.) at a concentration of the green tea extract of 2000
It was dissolved so as to be equivalent to ppm. Tests were carried out on these three types of samples by the three-point comparison method, and those with less astringency were selected and evaluated. The sensory test was conducted on 20 panelists. The results are shown in Table 3.
【0023】[0023]
【表3】 第3表 実施例の製品 対照例の製品 原料 渋味が弱いと評価した人数 17人 2人 1人[Table 3] Table 3 The number of people who evaluated that the astringency of the raw materials for the products of the control example of the example was weak 17 2 1
【0024】実施例の製品は、原料の緑茶抽出物に対し
ても、対照例の製品に対しても、明らかに渋みが低減し
ていた。このように、呈味性が改善されたことによっ
て、本発明の渋みを低減した茶抽出物は飲料原料以外に
も食品,嗜好品,化粧品等の別を問わず様々な物品に応
用できるものである。The products of the Examples had a clear reduction in astringency with respect to the raw material green tea extract and the control products. As described above, the tea extract of the present invention, which has reduced astringency due to the improved taste, can be applied not only to beverage raw materials but also to various articles such as foods, luxury items and cosmetics. is there.
【0025】実施例4 実施例3で得た緑茶抽出物約150mgを秤取り、水1
mlに溶解後、実施例2と同様の方法で酵素処理と酢酸
エチル抽出を行った。得られた酢酸エチル層を遠心濃縮
機で濃縮して酢酸エチルを留去し、得られた固形物を水
で50mlにメスアップした。これを処理画分とした。Example 4 About 150 mg of the green tea extract obtained in Example 3 was weighed, and water 1
After dissolving in ml, enzymatic treatment and extraction with ethyl acetate were carried out in the same manner as in Example 2. The obtained ethyl acetate layer was concentrated with a centrifugal concentrator to distill off the ethyl acetate, and the obtained solid substance was diluted to 50 ml with water. This was used as a treated fraction.
【0026】一方、実施例3で得た緑茶抽出物150m
gを秤取り、水1mlに溶解後、実施例2の対照例と同
様の方法で酢酸エチル抽出を行った。得られた酢酸エチ
ル層を遠心濃縮機で濃縮して酢酸エチルを留去し、得ら
れた固形物を水で50mlにメスアップした。これをコ
ントロール画分とした。処理画分とコントロール画分を
実施例2と同様にして酒石酸鉄法で分析した。結果を第
4表に示す。第4表から明らかなように、処理画分の吸
光度はコントロール画分に比べて約30%増加した。On the other hand, 150 m of green tea extract obtained in Example 3
g was weighed, dissolved in 1 ml of water, and extracted with ethyl acetate in the same manner as in the control example of Example 2. The obtained ethyl acetate layer was concentrated with a centrifugal concentrator to distill off the ethyl acetate, and the obtained solid substance was diluted to 50 ml with water. This was used as a control fraction. The treated fraction and the control fraction were analyzed by the iron tartrate method in the same manner as in Example 2. The results are shown in Table 4. As is clear from Table 4, the absorbance of the treated fraction was increased by about 30% as compared with the control fraction.
【0027】[0027]
【表4】 第4表 540nmの吸光度 処理画分 0.279 コントロール画分 0.215Table 4 Table 4 Absorbance- treated fraction at 540 nm 0.279 Control fraction 0.215
【0028】次に、上記の処理画分およびコントロール
画分を高速液体クロマトグラフィー(HPLC)法で以
下の通り分析した。カラムは資生堂 CAPCELLPAK C-18 A
G1204.6×250mmを40℃に加温して、移動相に
は酢酸エチル:アセトニトリル:0.05%リン酸水=
0.6:12:90の混合溶媒を移動相流速1ml/m
inで使用した。検出はUV280nmで行った。結果
を図1および図2に示す。すなわち、図1はコントロー
ル画分の、図2は処理画分のHPLCでの分析結果を示
す。図2における各ピークの保持時間(分)はピークA
が5.68、ピークBが7.83、ピークCが4.42
である。また、第5表に茶成分の中で配糖化反応で配糖
化されないことが明らかなカフェイン(ピークA)の面
積値を1としたときの主要なポリフェノールであるエピ
ガロカテキンガレート(ピークB)およびエピガロカテ
キン(ピークC)の相対面積値を示した。第5表から明
らかなように、処理画分ではコントロール画分に比べて
ピークBとピークCの相対面積値がそれぞれ約25%、
26%ずつ増加した。Next, the treated and control fractions were analyzed by the high performance liquid chromatography (HPLC) method as follows. Column is Shiseido CAPCELLPAK C-18 A
G1204.6 × 250 mm was heated to 40 ° C., and the mobile phase was ethyl acetate: acetonitrile: 0.05% phosphoric acid water =
A mixed solvent of 0.6: 12: 90 was used as a mobile phase flow rate of 1 ml / m.
Used in. Detection was performed at UV280 nm. The results are shown in FIGS. 1 and 2. That is, FIG. 1 shows the analytical results of the control fractions, and FIG. 2 shows the analytical results of the treated fractions by HPLC. The retention time (minutes) of each peak in FIG.
Is 5.68, peak B is 7.83, and peak C is 4.42.
Is. In addition, in Table 5, epigallocatechin gallate (peak B), which is a major polyphenol when the area value of caffeine (peak A), which is clearly not glycosylated by glycosylation reaction among tea components, is set to 1 And the relative area value of epigallocatechin (peak C) are shown. As is clear from Table 5, in the treated fraction, the relative area values of peak B and peak C were about 25% each, compared to the control fraction.
It increased by 26%.
【0029】[0029]
【表5】 第5表 ピークAに対するピークBとCの相対面積値 ピークB ピークC 処理画分 0.446 0.046 コントロール画分 0.361 0.037[Table 5] Table 5 Relative Area Values of Peaks B and C with respect to Peak A Peak B Peak C Treated Fraction 0.446 0.046 Control Fraction 0.361 0.037
【0030】酒石酸鉄法で測定した処理画分の吸光度が
増加していることは、実施例2の場合と同様に、本緑茶
抽出物が配糖化されていたことを示すものであり、HP
LC法で認められたピークBとピークCの面積値の増加
は、エピガロカテキンガレートやエピカテキンといった
ポリフェノール類が配糖化されていたことを示すもので
ある。従って、本緑茶抽出物が配糖化することによって
渋みが低減した緑茶抽出物が得られたことを示すもので
ある。さらに、本茶抽出物はα−グルコシダーゼやグル
コアミラーゼによって加水分解されてエピガロカテキン
ガレートやエピガロカテキンを遊離することから、本緑
茶抽出物も生体内のα−グルコシダーゼやα−アミラー
ゼ等の酵素によっても容易に加水分解されて、生理活性
機能を持つエピガロカテキンガレートなどのポリフェノ
ール類を遊離して、ポリフェノール類本来の生理活性機
能を示すものと考えられる。The increase in the absorbance of the treated fraction measured by the iron tartrate method indicates that the green tea extract was glycosylated, as in Example 2.
The increase in the area values of peak B and peak C observed by the LC method indicates that polyphenols such as epigallocatechin gallate and epicatechin were glycosylated. Therefore, it indicates that the green tea extract having reduced astringency was obtained by glycosylation of the green tea extract. Furthermore, since the green tea extract is hydrolyzed by α-glucosidase or glucoamylase to release epigallocatechin gallate or epigallocatechin, the green tea extract is also an enzyme such as α-glucosidase or α-amylase in vivo. It is considered that the polyphenols such as epigallocatechin gallate, which has a physiologically active function, are easily hydrolyzed to liberate the polyphenols and exhibit the original physiologically active function of the polyphenols.
【0031】実施例5 実施例3で得られた渋みを低減した茶抽出物を使用して
清涼飲料を試作した。レシピーは第6表の通りである。
また、対照例では緑茶抽出物(商品名:ポリフェノン6
0、三井農林株式会社製)を使用した。渋みの比較のた
めに実施例3の茶抽出物中の緑茶抽出物の量と対照例で
使用した緑茶抽出物の量を同じとした。結果を第6表に
示す。Example 5 A soft drink was experimentally produced using the tea extract having a reduced astringency obtained in Example 3. The recipe is shown in Table 6.
In the control example, a green tea extract (trade name: polyphenon 6
0, manufactured by Mitsui Norin Co., Ltd.) was used. For comparison of astringency, the amount of green tea extract in the tea extract of Example 3 and the amount of green tea extract used in the control were the same. The results are shown in Table 6.
【0032】[0032]
【表6】 第6表 清涼飲料のレシピー 原 料 実施例(kg) 対照例(kg) 果糖ぶどう糖液糖 5.0 5.0 砂 糖 4.0 4.0 クエン酸(結晶) 0.2 0.2 1/5柑橘混合果汁 6.0 6.0 カロチン色素 0.02 0.02 オレンジ香料 0.05 0.05 茶抽出物 1.2 0.2[Table 6] Table 6 Soft drink recipe Raw material Example (kg) Control example (kg) Fructose glucose liquid sugar 5.0 5.0 Sand sugar 4.0 4.0 Citric acid (crystal) 0.2 0 .2 1/5 citrus mixed fruit juice 6.0 6.0 carotene pigment 0.02 0.02 orange flavor 0.05 0.05 tea extract 1.2 0.2
【0033】上記レシピーで試作した2種類の清涼飲料
について、渋みに対する官能検査を実施した。試験は2
0人のパネラーに対して3点比較法を用いて行った。結
果を第7表に示す。実施例の飲料の方が有意に渋みが少
ないという結論であった。従って、渋みが低減して呈味
性を改善したことによって、本発明の渋みを低減した茶
抽出物は飲料の風味を損なうことなく飲料原料として使
用できることが確認された。A sensory test for astringency was carried out on the two types of soft drinks produced by the above recipe. Test 2
It was performed using a three-point comparison method for 0 panelists. The results are shown in Table 7. It was concluded that the beverages of the examples had significantly less astringency. Therefore, it was confirmed that the astringency-reduced tea extract of the present invention can be used as a beverage raw material without impairing the flavor of the beverage by reducing the astringency and improving the taste.
【0034】[0034]
【表7】 第7表 実施例の飲料 対照例の飲料 渋みが強いと評価した人数 2人 18人[Table 7] Table 7 Number of people evaluated as having strong drink astringency in the beverage control example of Example 2 2 18
【0035】実施例7 実施例1で得られた渋みを低減した紅茶飲料を使用して
ゼリー菓子の製造を行った。カップリングシュガー(登
録商標、株式会社林原生物化学研究所製)126g、オ
リゴメイト50(商品名、ヤクルト薬品工業株式会社
製)136g、乳糖6g、アスパルテーム(商品名、味
の素株式会社製)、実施例1で得られた渋みを低減した
紅茶飲料100gおよび水50gを加えて溶解した後、
撹拌しつつ加熱溶解した。この溶液にペクチン4.5g
を徐々に加えて溶解後、50%クエン酸溶液3.3g、
1/5濃縮レモン果汁6g天然色素0.1gおよびレモ
ンフレーバー0.2gを加えて十分に混合し、この溶液
を型に流し込み、室温で12時間放冷して固化させてペ
クチンゼリーを作成した。本品はポリフェノール類特有
の渋みがなく、風味が優れたゼリー菓子である。また、
ポリフェノール類の機能性を有するゼリー菓子として好
適である。Example 7 A jelly confectionery was produced using the tea beverage with reduced astringency obtained in Example 1. 126 g of coupling sugar (registered trademark, manufactured by Hayashibara Biochemical Laboratory Co., Ltd.), Oligomate 50 (trade name, manufactured by Yakult Chemical Industry Co., Ltd.) 136 g, lactose 6 g, aspartame (trade name, manufactured by Ajinomoto Co., Inc.), Example After adding 100 g of the tea beverage with reduced astringency obtained in 1 and 50 g of water and dissolving,
It was heated and dissolved with stirring. 4.5 g of pectin in this solution
Was gradually added to dissolve the solution, and then 3.3 g of 50% citric acid solution,
Pectin jelly was prepared by adding 6 g of 1/5 concentrated lemon juice, 0.1 g of natural pigment and 0.2 g of lemon flavor and mixing them well, pouring this solution into a mold and allowing it to cool at room temperature for 12 hours to solidify. This product is a jelly confectionery that has no astringency peculiar to polyphenols and has an excellent flavor. Also,
It is suitable as a jelly confectionery having the functionality of polyphenols.
【0036】[0036]
【発明の効果】本発明の渋みを低減した茶抽出物および
茶飲料は、生理活性成分であるポリフェノール類を含ん
だままで、従来の茶飲料や茶抽出物が持つ強い渋みが効
果的に改善されている。そのため、このものは飲食物の
みならず、嗜好品,化粧品,医薬部外品,医薬品などの
広い分野に応用可能である。The tea extract and tea beverage with reduced astringency of the present invention effectively improve the strong astringency of conventional tea beverages and tea extracts while containing the polyphenols which are physiologically active ingredients. ing. Therefore, this product can be applied not only to foods and drinks, but also to a wide range of fields such as favorite products, cosmetics, quasi drugs, and pharmaceutical products.
【図1】 実施例4のコントロール画分のHPLCでの
分析結果を示す。FIG. 1 shows the results of HPLC analysis of the control fractions of Example 4.
【図2】 実施例4の処理画分のHPLCでの分析結果
を示す。FIG. 2 shows the results of HPLC analysis of the treated fractions of Example 4.
フロントページの続き (72)発明者 万代 隆彦 岡山県岡山市政津1428番地 (72)発明者 渋谷 孝 岡山県総社市下原318番地Front page continuation (72) Inventor Takahiko Bandai 1428 Masatsu, Okayama, Okayama Prefecture (72) Inventor Takashi Shibuya, 318 Shimohara, Soja City, Okayama Prefecture
Claims (6)
り渋みを低減した茶抽出物または茶飲料。2. A tea extract or tea beverage having reduced astringency by glycosylation of polyphenols.
発酵茶,発酵茶,後発酵茶などの茶葉を原料としたもの
である請求項1記載の渋みを低減した茶抽出物または茶
飲料。3. The tea extract or tea extract with reduced astringency according to claim 1, wherein the tea extract or tea beverage is made from tea leaves such as unfermented tea, semi-fermented tea, fermented tea, and post-fermented tea. Tea drink.
サイクロデキストリンおよび澱粉のうちの少なくとも1
種と混ぜ、これにサイクロマルトデキストリングルカノ
トランスフェラーゼを作用させることを特徴とする渋み
を低減した茶抽出物または茶飲料の製造方法。4. The tea extract or tea beverage is dextrin,
At least one of cyclodextrin and starch
A method for producing a tea extract or tea beverage with reduced astringency, which comprises mixing with a seed and allowing cyclomaltodextrin glucanotransferase to act on it.
ランスフェラーゼがバチルス・ステアロサーモフィラス
由来のものである請求項4記載の茶抽出物または茶飲料
の製造方法。5. The method for producing a tea extract or tea beverage according to claim 4, wherein the cyclomaltodextrin glucanotransferase is derived from Bacillus stearothermophilus.
または茶飲料を含有する飲食物。6. A food or drink containing the tea extract or tea beverage with reduced astringency according to claim 1.
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JP13570195A JP3579496B2 (en) | 1995-05-10 | 1995-05-10 | Tea extract or tea beverage with reduced astringency and method for producing the same |
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ID=15157881
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WO2005060762A1 (en) | 2003-12-18 | 2005-07-07 | Kao Corporation | Bottled beverage |
JP2006129738A (en) * | 2004-11-04 | 2006-05-25 | Kao Corp | Non-tea-based packaged beverage |
JP2006217815A (en) * | 2005-02-08 | 2006-08-24 | Kao Corp | Non-tea-based packaged beverage |
JP2007151521A (en) * | 2005-12-09 | 2007-06-21 | ▲吉▼岡 嘉雄 | Product with functionality, and quasi-drug |
WO2008004339A1 (en) | 2006-07-04 | 2008-01-10 | Kao Corporation | Beverage packed in foam container |
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JPH06153875A (en) * | 1992-11-27 | 1994-06-03 | Sb Shokuhin Kk | Improvement of bitterness and astringency of drink |
JPH06303904A (en) * | 1993-04-22 | 1994-11-01 | Asahi Breweries Ltd | Tea beverage and its production |
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JP2007151521A (en) * | 2005-12-09 | 2007-06-21 | ▲吉▼岡 嘉雄 | Product with functionality, and quasi-drug |
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US8278088B2 (en) | 2007-01-19 | 2012-10-02 | Suntory Holdings Limited | Polynucleotide encoding a polypeptide having glycosylation activity on a flavonoid |
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WO2011065799A3 (en) * | 2009-11-30 | 2011-11-03 | (주)아모레퍼시픽 | Preparation method of tea water, and tea water obtained thereby |
US10111922B2 (en) | 2009-11-30 | 2018-10-30 | Amorepacific Corporation | Preparation method of tea water, and tea water obtained thereby |
US11806352B2 (en) | 2010-05-19 | 2023-11-07 | Upfield Europe B.V. | Theobromine for increasing HDL-cholesterol |
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WO2015022911A1 (en) * | 2013-08-12 | 2015-02-19 | 長谷川香料株式会社 | Method for manufacturing tea extract |
JPWO2015022911A1 (en) * | 2013-08-12 | 2017-03-02 | 長谷川香料株式会社 | Method for producing tea extracts |
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