JP4739036B2 - Process for producing a processed tea extraction product with improved flavor - Google Patents

Process for producing a processed tea extraction product with improved flavor Download PDF

Info

Publication number
JP4739036B2
JP4739036B2 JP2006018062A JP2006018062A JP4739036B2 JP 4739036 B2 JP4739036 B2 JP 4739036B2 JP 2006018062 A JP2006018062 A JP 2006018062A JP 2006018062 A JP2006018062 A JP 2006018062A JP 4739036 B2 JP4739036 B2 JP 4739036B2
Authority
JP
Japan
Prior art keywords
gallic acid
catechins
tea
gallate
polymer catechins
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.)
Expired - Fee Related
Application number
JP2006018062A
Other languages
Japanese (ja)
Other versions
JP2007195458A (en
Inventor
利彦 大多和
和種 長野
健介 野尻
亮 岩崎
博 長谷川
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
T Hasegawa Co Ltd
Original Assignee
T Hasegawa Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by T Hasegawa Co Ltd filed Critical T Hasegawa Co Ltd
Priority to JP2006018062A priority Critical patent/JP4739036B2/en
Publication of JP2007195458A publication Critical patent/JP2007195458A/en
Application granted granted Critical
Publication of JP4739036B2 publication Critical patent/JP4739036B2/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Tea And Coffee (AREA)

Description

本発明は、カテキン類特有の苦渋味・収斂味が低減され、かつ、酸味・えぐ味を有さない風味の改善された茶抽出処理物の製造方法に関する。   The present invention relates to a method for producing a tea extraction processed product that has reduced bitter astringency and astringent taste peculiar to catechins and has an improved flavor that does not have a sour taste or a gummy taste.

茶は古くより、嗜好飲料として親しまれてきたが、最近十数年前より手軽に飲用することができる缶あるいはペットボトル等に充填した容器詰め飲料が提供されており、消費者の甘味ばなれから高い支持を得てその生産量は増加の一途をたどっている。一方、茶はまた、近年その機能性においても注目され、盛んに研究が行われており、カテキン類のヒトの体脂肪蓄積抑制(非特許文献1)等の生理効果が報告されている。しかしながら容器詰め飲料としてカテキン類を多く配合しようとすると苦渋味・収斂味が強くなってしまい風味的に非常に摂取しづらくなってしまうという欠点がみられた。   Tea has long been popular as a favorite beverage, but recently, canned beverages filled in cans or plastic bottles, etc., that can be easily consumed have been provided for more than a decade ago, and consumers can become sweet. As a result, the production volume has been increasing steadily. On the other hand, tea has recently attracted attention in terms of its functionality and has been actively studied, and physiological effects such as suppression of human body fat accumulation by catechins (Non-patent Document 1) have been reported. However, when a large amount of catechins were added as a container-packed beverage, the bitter astringency and astringent taste became strong, and the disadvantage of being very difficult to take in flavor was observed.

茶中の非重合体カテキン類の主な成分として遊離型カテキン(エピカテキン、エピガロカテキン、カテキン、ガロカテキン)およびエステル型カテキン(エピカテキンガレート、エピガロカテキンガレート、カテキンガレート、ガロカテキンガレート)が挙げられるが、これらのうち遊離型カテキンは渋味、収斂味の閾値が高く、エステル型カテキンは渋味、収斂味の閾値が低いことが報告されている(特許文献1)。   The main components of non-polymer catechins in tea are free catechin (epicatechin, epigallocatechin, catechin, gallocatechin) and ester catechin (epicatechin gallate, epigallocatechin gallate, catechin gallate, gallocatechin gallate) Among them, it is reported that free catechins have high astringency and astringency taste thresholds, and ester catechins have low astringency and astringency taste thresholds (Patent Document 1).

一方、タンナーゼは茶飲料の清澄化に用いることが出来ることが知られているが、カテキンと没食子酸とのエステル結合に作用してカテキンと没食子酸に加水分解する酵素である。茶飲料中のクリームダウン(沈殿生成)は、ガレート型カテキン(エステル型カテキンと同義)とカフェインなどが複合体を形成することにより発生することが知られているが、その防止策としてタンナーゼ処理を行うことでガレート型カテキンを非ガレート型カテキン(遊離型カテキンと同義)に分解し、カフェインとの複合体形成をしづらくする方法が報告されている(非特許文献2)。   On the other hand, it is known that tannase can be used for clarifying tea beverages, but it is an enzyme that acts on an ester bond between catechin and gallic acid to hydrolyze it into catechin and gallic acid. Cream-down (precipitation) in tea beverages is known to occur when gallate-type catechin (synonymous with ester-type catechin) and caffeine form a complex. A method has been reported in which gallate-type catechins are decomposed into non-gallate-type catechins (synonymous with free-type catechins) to make complex formation with caffeine difficult (Non-patent Document 2).

また、前記タンナーゼ処理を緑茶の製茶工程に応用し、茶葉中に含まれる苦渋味の強いエピカテキンガレート、エピガロカテキンガレートをタンナーゼにて処理することで、没食子酸と爽快な苦みを持つエピカテキン、エピガロカテキンに分解する方法が開示されている(特許文献2)。   In addition, by applying the tannase treatment to the tea-making process of green tea and treating epicatechin gallate and epigallocatechin gallate with strong bitter taste contained in tea leaves with tannase, epicatechin having refreshing bitterness with gallic acid And a method for decomposing it into epigallocatechin is disclosed (Patent Document 2).

一方、容器詰め飲料においても、前記の通りカテキン類の機能性に着目し、カテキン類を多く配合することが求められているが、カテキン類を高濃度に含有する茶飲料を、タンナーゼ処理することによりカテキン類の苦渋味を低減する方法が開示されている(特許文献3)。   On the other hand, as described above, attention is paid to the functionality of catechins in container-packed beverages, and it is required to add a large amount of catechins. However, a tea beverage containing a high concentration of catechins should be treated with tannase. Discloses a method for reducing the bitter and astringent taste of catechins (Patent Document 3).

しかしながら、特許文献3の方法では、カテキン類をタンナーゼ処理することによりエステル型カテキンが遊離型カテキンと没食子酸に分解し、エステル型カテキン由来の渋味・収斂味は低減するものの、それにより没食子酸由来の酸味・えぐ味が発生してしまい、やはり風味的に満足できるものとはいえない。   However, in the method of Patent Document 3, ester catechin is decomposed into free catechin and gallic acid by treating catechins with tannase, and the astringency and astringent taste derived from ester catechins are reduced. The sour and savory tastes that originate from it occur, and it cannot be said that the flavor is still satisfactory.

また、一方では非重合体カテキン類のタンナーゼによる分解を制御し、カテキン類における、ガレート体率を40〜60重量%の範囲内にコントロ−ルすることにより、エステル型カテキン由来の渋味・収斂味を低減させ、かつ風味を改善する方法(特許文献4)が開示されている。   On the other hand, by controlling the degradation of non-polymer catechins by tannase and controlling the gallate content in catechins within the range of 40 to 60% by weight, the astringency and astringency derived from ester-type catechins A method for reducing the taste and improving the flavor (Patent Document 4) is disclosed.

特開平6−343389号公報JP-A-6-343389 特開平5−308901号公報JP-A-5-308901 特開2005−130809号公報JP 2005-130809 A 特開2004−321105号公報JP 2004-321105 A Journal of Oleo Science Vol.50(2001),No.9 p717−728Journal of Oleo Science Vol. 50 (2001), no. 9 p717-728 「食品と開発」32(12),1997年,p14−16"Food and Development" 32 (12), 1997, p14-16

特許文献4には、非重合体カテキン類中のガレート体率が40〜60重量%である風味の改善された緑茶抽出物が開示されているが、この方法においてもやはりタンナーゼ処理により遊離の没食子酸が生成し、没食子酸由来のえぐ味を伴った酸味を呈するという課題が依然として未解決のままであった。また、これまでに報告されている茶抽出液のタンナーゼ処理は、非重合体カテキン類濃度として1重量%未満の水溶液で行われており、製造コスト、生産効率の面で問題があると考えられる。   Patent Document 4 discloses a green tea extract with an improved flavor in which the percentage of gallate body in non-polymer catechins is 40 to 60% by weight, but also in this method, free gallic is also obtained by tannase treatment. The problem of acid generation and the sour taste associated with the gallic acid-derived taste remained unresolved. In addition, the tannase treatment of tea extract reported so far is carried out in an aqueous solution having a non-polymer catechin concentration of less than 1% by weight, which is considered to be problematic in terms of production cost and production efficiency. .

したがって、本発明の目的は、茶抽出液から、高濃度非重合体カテキン含有飲料においても苦渋味・収斂味および酸味・えぐ味などの不快感を感じさせる味を有さない優れた風味を有する茶抽出物を効率よく製造する方法を提供することにある。   Therefore, an object of the present invention is to have an excellent flavor that does not have a taste that makes a bitter astringent taste, astringent taste, sour taste, gummy taste, etc. even in a beverage containing a high concentration non-polymer catechin from a tea extract. It is providing the method of manufacturing a tea extract efficiently.

本発明者等は緑茶抽出物の風味を改善すべく鋭意検討したところ、茶抽出液をタンナーゼ処理することにより、非重合体カテキン類の総量に対するガレート型カテキンの含量を0〜40%に調整することでエステル型カテキン由来の渋味・収斂味を低減させ、さらにこのタンナーゼ処理した茶抽出物をイオン交換樹脂処理することで、遊離した没食子酸を効率的に除去し、没食子酸特有の酸味・えぐ味を有さない茶抽出物が得られることを見出し、本発明の完成に至った。   When the present inventors diligently studied to improve the flavor of the green tea extract, the content of gallate-type catechins with respect to the total amount of non-polymer catechins is adjusted to 0 to 40% by treating the tea extract with tannase. By reducing the astringent taste and astringent taste derived from ester-type catechins, and further treating the tea extract treated with tannase with an ion exchange resin, the free gallic acid is efficiently removed, and the sourness peculiar to gallic acid It has been found that a tea extract having no savory taste can be obtained, and the present invention has been completed.

また、非重合体カテキン類の濃度として1〜10重量%含有する状態にてタンナーゼ処理を行うことにより、大量製造においても効率よく、苦渋味・収斂味の低減した非重合体カテキン類含有水性溶液を製造できることを見出した。
かくして本発明は、茶抽出液をタンナーゼ処理した後、遊離する没食子酸を陰イオン交換樹脂と接触して除去することを特徴とする茶抽出処理物の製造方法を提供するものである。
Moreover, the non-polymer catechins-containing aqueous solution with reduced bitterness, astringency and taste can be efficiently produced even in mass production by performing tannase treatment in a state of containing 1 to 10% by weight as the concentration of non-polymer catechins. It was found that can be manufactured.
Thus, the present invention provides a method for producing a tea extraction processed product, characterized in that after the tea extract is tannase treated, the released gallic acid is removed by contact with an anion exchange resin.

また、本発明は前記茶抽出処理物における
(a)非重合体カテキン類中のガレート体率が0〜40重量%であり、かつ
(b)没食子酸/(非重合体カテキン類+没食子酸)が0〜0.15
である請求項1に記載の茶抽出処理物の製造方法を提供するものである。
Further, in the present invention, (a) the gallate content in the non-polymer catechins is 0 to 40% by weight in the tea extraction processed product, and (b) gallic acid / (non-polymer catechins + gallic acid) Is 0-0.15
The method for producing a tea extraction processed product according to claim 1 is provided.

さらに、本発明では前記茶抽出液中の非重合体カテキン類の濃度が1〜10重量%である前記に記載の茶抽出処理物の製造方法も提供される。
また、本発明は、茶抽出液をタンナーゼ処理した後、遊離する没食子酸を陰イオン交換樹脂と接触して除去して得られる茶抽出処理物であって、
前記茶抽出処理物における
(a)非重合体カテキン類中のガレート体率が0〜8.5重量%であり、かつ
(b)没食子酸/(非重合体カテキン類+没食子酸)が0〜0.15
である茶抽出処理物を提供するものである。
本発明にはまた、前記茶抽出処理物を含有する飲食品も含まれる。

Furthermore, in this invention, the manufacturing method of the tea extraction processed material as described in the above, wherein the concentration of non-polymer catechins in the tea extract is 1 to 10% by weight.
Further, the present invention is a tea extraction treatment product obtained by tannase treatment of a tea extract and then removing gallic acid released by contact with an anion exchange resin,
In the tea extraction processed product
(A) The gallate content in the non-polymer catechins is 0 to 8.5% by weight, and
(B) Gallic acid / (non-polymer catechins + gallic acid) is 0 to 0.15
A tea extraction processed product is provided.
The present invention also includes foods and drinks containing the tea extraction processed product.

本発明によればタンナーゼ処理により非重合カテキン中のガレート型カテキン類含量を低減させることにより苦渋味・収斂味を低減させ、さらにタンナーゼ処理により遊離した没食子酸含量を低減させることにより酸味・えぐ味を除くことができ、風味の良好な茶抽出物の製造方法を提供することができる。また、従来の方法に比べて高濃度でタンナーゼ処理を行うことにより、生産効率・製造コストの観点から有利である。   According to the present invention, the bitter and astringent taste is reduced by reducing the content of gallate-type catechins in the non-polymerized catechin by tannase treatment, and the sourness and gummy taste is reduced by reducing the content of gallic acid released by tannase treatment. Can be removed, and a method for producing a tea extract with good flavor can be provided. In addition, performing tannase treatment at a higher concentration than conventional methods is advantageous from the viewpoint of production efficiency and manufacturing cost.

本発明における非重合体カテキン類とは、カテキン、ガロカテキン、カテキンガレート、ガロカテキンガレートなどの非エピ体カテキン類及びエピカテキン、エピガロカテキン、エピカテキンガレート、エピガロカテキンガレートなどのエピ体カテキン類を8種あわせての総称である。本発明のガレート型カテキン類(エステル型カテキン類と同義)とは、前記のカテキン類のうちカテキンガレート、ガロカテキンガレート、エピガロカテキンガレート、エピカテキンガレート等の没食子酸エステル型のカテキン類の総称を意味する。本発明におけるガレート体率とは、前記ガレート型カテキン類4種の重量和の、前記8種からなる非重合体カテキン類の重量和に対する100分率である。   Non-polymer catechins in the present invention are non-epimeric catechins such as catechin, gallocatechin, catechin gallate and gallocatechin gallate and epi-catechins such as epicatechin, epigallocatechin, epicatechin gallate and epigallocatechin gallate Is a collective term for eight types. The gallate-type catechins (synonymous with ester-type catechins) of the present invention are generic names of gallate-type catechins such as catechin gallate, gallocatechin gallate, epigallocatechin gallate, and epicatechin gallate among the above catechins. Means. The gallate body ratio in the present invention is a 100 fraction of the weight sum of the four gallate catechins to the weight sum of the eight non-polymer catechins.

本発明に用いられる茶葉としては、ツバキ科の常緑樹であるチャ(学名:Camellia sinensis(L)O.Kuntze)から得られる茶葉から製茶された煎茶、番茶、玉露、てん茶、釜入り茶などの不発酵茶である緑茶;前記茶葉から半発酵又は発酵工程を経て製茶された烏龍茶、紅茶、黒茶などが挙げられる。   The tea leaves used in the present invention include sencha, bancha, gyokuro, tencha, tea in a pot, etc. made from tea leaves obtained from tea (Camellia sinensis (L) O. Kuntze), which is an evergreen tree of the camellia family. Examples include green tea that is non-fermented tea; oolong tea, black tea, black tea, and the like that are made from the tea leaves through a semi-fermentation or fermentation process.

本発明の茶抽出液としては、例えば、上記した茶葉の抽出物又はその濃縮物が挙げられる。茶葉の抽出物としては、上記した茶葉を水又は水溶性有機溶媒で、例えば、10〜100℃にて、3分〜2時間、攪拌又はカラム抽出し、遠心分離など適宜な分離手段を採用して抽出液を分離した抽出物を例示することができ、茶葉抽出物の濃縮物としては、茶葉抽出物を有機溶媒、減圧濃縮、膜濃縮等により濃縮した濃縮物を例示することができる。また、市販の「ポリフェノン」(三井農林(株))、「テアフラン」((株)伊藤園)、「サンフェノン」(太陽化学(株))、「サンウーロン」(サントリー(株))、「PF−TP」((株)ファーマフーズ)、「ポリフェノンHG」(東京フードテクノ(株))などのカテキン粉末を水又は水溶性有機溶媒に溶解して茶抽出液とすることもできる。茶抽出液の非重合体カテキン類濃度は、1〜10%、好ましくは1〜5%、更に好ましくは1〜3%が適当である。非重合体カテキン類濃度が10%を越えると、非重合体カテキン類の浸透圧によりタンナーゼの活性が低下し、同じガレート体率を得るためにはタンナーゼ使用量を増やす必要があり効率が悪い。また非重合体カテキン類濃度が1%未満の場合、処理する液体の量が増えてしまい、生産効率が低下し製造コストの増大を引き起こす。この非重合体カテキン類濃度範囲内でタンナーゼ処理を行うことにより、工業的規模において効率よく作業を行うことが出来る。   Examples of the tea extract of the present invention include the tea leaf extract described above or a concentrate thereof. As an extract of tea leaves, the above-mentioned tea leaves are stirred with water or a water-soluble organic solvent, for example, at 10 to 100 ° C. for 3 minutes to 2 hours, or subjected to appropriate separation means such as centrifugation. The extract obtained by separating the extract liquid can be exemplified, and the concentrate of the tea leaf extract can be exemplified by a concentrate obtained by concentrating the tea leaf extract with an organic solvent, vacuum concentration, membrane concentration or the like. In addition, commercially available “Polyphenone” (Mitsui Norin Co., Ltd.), “Theafranc” (Itoen Co., Ltd.), “Sanphenon” (Taiyo Kagaku Co., Ltd.), “Sun Oolong” (Suntory Ltd.), “PF-” Catechin powders such as “TP” (Pharma Foods Co., Ltd.) and “Polyphenone HG” (Tokyo Food Techno Co., Ltd.) can be dissolved in water or a water-soluble organic solvent to obtain a tea extract. The concentration of non-polymer catechins in the tea extract is 1 to 10%, preferably 1 to 5%, more preferably 1 to 3%. If the concentration of non-polymer catechins exceeds 10%, the activity of tannase decreases due to the osmotic pressure of non-polymer catechins, and in order to obtain the same gallate body rate, it is necessary to increase the amount of tannase, which is inefficient. Further, when the concentration of non-polymer catechins is less than 1%, the amount of liquid to be processed increases, resulting in a decrease in production efficiency and an increase in manufacturing cost. By performing tannase treatment within this non-polymer catechin concentration range, work can be efficiently performed on an industrial scale.

本発明で使用されるタンナーゼは、非重合体カテキン類の没食子酸エステル結合を分解する活性を有するものであればいずれでも使用可能であり、具体的には、アスペルギルス属、ペニシリウム属、リゾプス属などのタンナーゼ生産菌を培養して得られるタンナーゼが使用できる。このうち、アスペルギルス・オリゼ由来のものが特に好ましい。   Any tannase used in the present invention can be used as long as it has an activity of decomposing gallate ester bonds of non-polymer catechins, and specifically, Aspergillus, Penicillium, Rhizopus, etc. A tannase obtained by culturing a tannase-producing bacterium can be used. Of these, those derived from Aspergillus oryzae are particularly preferred.

茶抽出液に対するタンナーゼの添加量は非重合体カテキン類量1mgあたりに換算すると、約0.02〜約2.0Unit、好ましくは約0.05〜約0.4Unitである。ここで1Unitは、30℃の水中においてタンニン酸に含まれるエステル結合を1分間に1マイクロモル加水分解する酵素量で定義される。タンナーゼ処理条件としては、その水溶液のpHは4.0〜6.0、好ましくは4.5〜5.5にすることが適当であり、その水溶液の温度は30〜45℃、好ましくは35〜40℃で行うことが適当である。タンナーゼ処理後はできるだけ速やかに70〜90℃に昇温し、タンナーゼを失活させ反応を停止する。   The amount of tannase added to the tea extract is about 0.02 to about 2.0 Units, preferably about 0.05 to about 0.4 Units, per 1 mg of non-polymer catechins. Here, 1 Unit is defined as the amount of enzyme that hydrolyzes the ester bond contained in tannic acid 1 micromole per minute in 30 ° C. water. As tannase treatment conditions, the pH of the aqueous solution is suitably 4.0 to 6.0, preferably 4.5 to 5.5, and the temperature of the aqueous solution is 30 to 45 ° C., preferably 35 to It is appropriate to carry out at 40 ° C. After the tannase treatment, the temperature is raised to 70 to 90 ° C. as soon as possible to deactivate the tannase and stop the reaction.

非重合体カテキン総量に対するエステル型カテキン含量はタンナーゼ処理時間、処理温度、処理濃度を制御することで目的にあったものに調整することが可能で、その反応の挙動は、反応液のpH変化により判断することができる。   The ester type catechin content relative to the total amount of non-polymer catechins can be adjusted to the target by controlling the tannase treatment time, treatment temperature, treatment concentration, and the reaction behavior depends on the pH change of the reaction solution. Judgment can be made.

以上の方法により、茶抽出液中の非重合体カテキン総量に対するエステル型カテキン含量を0〜40重量%となるように調整する。非重合体カテキン総量に対するエステル型カテキン含量を0〜40重量%に調整することにより苦渋味・収斂味を低減させることができる。エステル型カテキン含量が40重量%を越えた場合、苦渋味・収斂味が強く感じられ好ましくない。   By the above method, the ester type catechin content with respect to the total amount of non-polymer catechin in the tea extract is adjusted to 0 to 40% by weight. By adjusting the ester-type catechin content to 0 to 40% by weight relative to the total amount of non-polymer catechins, bitterness and astringency can be reduced. When the ester type catechin content exceeds 40% by weight, the bitter and astringent taste and the astringent taste are strongly felt, which is not preferable.

タンナーゼ処理により、エステル型カテキンは分解され没食子酸が遊離する。この没食子酸はえぐ味のある酸味を有している。本発明ではタンナーゼ処理後のカテキン類含有水溶液を陰イオン交換樹脂と接触させることにより遊離した没食子酸を除去する。使用する陰イオン交換樹脂は特に限定されるものではなく、市販品の陰イオン交換樹脂を使用することが出来る。   By tannase treatment, ester-type catechin is decomposed and gallic acid is released. This gallic acid has a sour taste. In the present invention, free gallic acid is removed by bringing the catechins-containing aqueous solution after tannase treatment into contact with an anion exchange resin. The anion exchange resin to be used is not particularly limited, and a commercially available anion exchange resin can be used.

使用可能な陰イオン交換樹脂としては、例えば、強塩基性のイオン交換樹脂としてはダイヤイオンSA−10A、SA−11A、SA−20A、SA−21A(以上、三菱化成社製)、アンバーライト IRA−400、IRA−410、IR−45(以上ローム・アンド・ハース社製)、ダウエックスAG−1、21K、2、3、AG−4(以上ザ・ダウ・ケミカル社製)、また弱塩基性陰イオン交換樹脂処理の例としては、ダイヤイオンWA20、WA21、WA30(以上、三菱化成社製)、アンバーライトIRA−93ZU、IRA94S、IRA−94S−HG(以上ローム・アンド・ハース社製)、ダウエックスS40285(ザ・ダウ・ケミカル社製)等が挙げられる。   Usable anion exchange resins include, for example, Diaion SA-10A, SA-11A, SA-20A, SA-21A (above, manufactured by Mitsubishi Kasei Co., Ltd.), Amberlite IRA as strongly basic ion exchange resins. -400, IRA-410, IR-45 (above Rohm & Haas), Dowex AG-1, 21K, 2, 3, AG-4 (above The Dow Chemical), and weak base Examples of the anionic ion exchange resin treatment are Diaion WA20, WA21, WA30 (above, manufactured by Mitsubishi Kasei), Amberlite IRA-93ZU, IRA94S, IRA-94S-HG (above, manufactured by Rohm and Haas) , Dowex S40285 (The Dow Chemical Co., Ltd.) and the like.

イオン交換樹脂処理は、バッチ方式あるいはカラム方式のいずれも採用できるが、作業性の点からカラム方式を好ましく採用することができる。カラム方式で処理する方法としては、例えば、上記のようなイオン交換樹脂を充填したカラムに、該樹脂の10倍〜1000倍の茶抽出液をSV=1〜100の流速で通液し、没食子酸を吸着させ、その未吸着部を採取することにより本発明の苦渋味、収斂味の低減された茶抽出処理物を得ることができる。本発明では、タンナーゼ処理液中の非重合体カテキン類の濃度、タンナーゼ処理液のブリックス、イオン交換樹脂の使用量、イオン交換樹脂への通液速度等を調整し、茶抽出処理物中の遊離没食子酸の含有量を没食子酸/(非重合体カテキン類+没食子酸)として0〜0.15、好ましくは0.02〜0.15、より好ましくは0.05〜0.15に制御することが可能であり、酸味・えぐ味の低減された茶抽出処理物を得ることができる。茶抽出処理物中の遊離没食子酸の含有量が没食子酸/(非重合体カテキン類+没食子酸)として0.15を越えた場合、没食子酸特有のえぐ味のある酸味が感じられるようになり好ましくない。没食子酸/(非重合体カテキン類+没食子酸)はできる限り小さな値とすることが好ましいが、イオン交換樹脂の必要量が多くなりすぎてしまい、工業的には実用的でない。   As the ion exchange resin treatment, either a batch method or a column method can be adopted, but the column method can be preferably adopted from the viewpoint of workability. As a method of processing in the column system, for example, a tea extract liquid 10 to 1000 times the resin is passed at a flow rate of SV = 1 to 100 through a column filled with the ion exchange resin as described above, and gallic By adsorbing the acid and collecting the non-adsorbed portion, the tea extraction processed product with reduced bitterness and astringency of the present invention can be obtained. In the present invention, the concentration of non-polymer catechins in the tannase treatment liquid, the brix of the tannase treatment liquid, the amount of ion exchange resin used, the flow rate through the ion exchange resin, etc. are adjusted, and the free in the tea extraction treatment product Control the content of gallic acid as gallic acid / (non-polymer catechins + gallic acid), 0 to 0.15, preferably 0.02 to 0.15, more preferably 0.05 to 0.15. It is possible to obtain a tea extraction processed product with reduced sourness and gummy taste. When the content of free gallic acid in the tea extraction product exceeds 0.15 as gallic acid / (non-polymer catechins + gallic acid), the sour taste peculiar to gallic acid can be felt. It is not preferable. The gallic acid / (non-polymer catechins + gallic acid) is preferably as small as possible, but the required amount of ion exchange resin becomes too large, which is not practical industrially.

上記した方法により得られる本発明の茶抽出処理物は、そのまま水溶液の形態として使用することもできるが、所望により適宜な濃縮手段を採用して濃縮物の形態とする
こともできる。また、さらに所望により該水溶液にデキストリン、加工澱粉、サイクロデキストリン、アラビアガム等の賦形剤を添加又は添加しないで噴霧乾燥、真空乾燥、凍結乾燥などの適宜な乾燥手段を採用して乾燥することにより粉末状とすることもできる。
The tea extraction product of the present invention obtained by the above-described method can be used as it is in the form of an aqueous solution as it is, but if desired, an appropriate concentration means can be adopted to form a concentrate. Further, if desired, the aqueous solution may be dried by adding appropriate drying means such as spray drying, vacuum drying, freeze drying or the like without adding or adding excipients such as dextrin, modified starch, cyclodextrin, gum arabic and the like. It can also be made into a powder form.

かくして、本発明によれば、苦渋味、収斂味の低減されかつ酸味・えぐ味を有しない非重合体カテキン類を含有する飲食品類、香粧品類、保健・衛生・医薬品類等を提供することができる。これらの例としては、例えば、茶類飲料、スポーツ飲料、炭酸飲料、果汁飲料、乳飲料、酒類などの飲料類;アイスクリーム類、シャーベット類、アイスキャンディー類などの冷菓類;和・洋菓子、チューインガム類、チョコレート類、パン類、コーヒー、紅茶などの嗜好品類;各種のスナック類などに本発明の製造方法によって得られる非重合体カテキン類を配合することにより、各種の機能性が付与された飲食品類を提供することができる。
以下、実施例および比較例を挙げて、本発明をさらに具体的に説明する。
Thus, according to the present invention, food / beverage products, cosmetics, health / hygiene / pharmaceuticals, etc. containing non-polymer catechins with reduced bitter and astringent taste and reduced astringency and no sour / paste taste are provided. Can do. Examples of these include, for example, beverages such as tea beverages, sports beverages, carbonated beverages, fruit juice beverages, milk beverages, alcoholic beverages; , Chocolate, bread, coffee, tea and other favorite products; foods and drinks with various functionalities by adding non-polymer catechins obtained by the production method of the present invention to various snacks Goods can be provided.
Hereinafter, the present invention will be described more specifically with reference to examples and comparative examples.

実施例1
ポリフェノンHG(東京フードテクノ製:非重合体カテキン類含有量33.7重量%、ガレート体率50%)5.94重量%水溶液2,000gを調整し(非重合体カテキン類2.0%、ガレート体率50%、pH5.0)、35℃に加温した後タンナーゼ(キッコーマン社製5000Unit/g)を1.2g(非重合体カテキン類1mgに対し0.15Unit)添加した。同温度にて30分間静置保持した後、80℃に昇温することでタンナーゼを失活し反応を停止した(pH4.2、非重合体カテキン類1.74%、ガレート体率8.5%、没食子酸0.49%)。その後、重曹にてpH5.0に調整し、カテキン類含有水溶液2000gを得た(参考品1:非重合体カテキン類1.74%、ガレート体率8.5%、没食子酸含量0.49%、没食子酸/(没食子酸+非重合体カテキン類)=0.220)。
Example 1
Polyphenone HG (manufactured by Tokyo Food Techno: non-polymer catechin content: 33.7% by weight, gallate content: 50%) 5.94% by weight aqueous solution of 2,000 g (2.0% non-polymer catechins, After heating to 35 ° C. at a gallate ratio of 50%, pH 5.0), 1.2 g of tannase (5000 Unit / g manufactured by Kikkoman) was added (0.15 Unit for 1 mg of non-polymer catechins). After standing still at the same temperature for 30 minutes, the temperature was raised to 80 ° C. to deactivate tannase and stop the reaction (pH 4.2, non-polymer catechins 1.74%, gallate body ratio 8.5 %, Gallic acid 0.49%). Thereafter, the pH was adjusted to 5.0 with sodium bicarbonate to obtain 2000 g of an aqueous solution containing catechins (reference product 1: 1.74% of non-polymer catechins, 8.5% gallate body ratio, 0.49% gallic acid content) Gallic acid / (gallic acid + non-polymer catechins) = 0.220).

参考品1のうち1050gを陰イオン交換樹脂(ダイヤイオンSA10A、三菱化学社製)35mlに通液し、通過液980gを得た(本発明品1:非重合体カテキン類1.71%、ガレート体率8.5%、没食子酸含量0.13%、没食子酸/(没食子酸+非重合体カテキン類)=0.071)。   1050 g of the reference product 1 was passed through 35 ml of an anion exchange resin (Diaion SA10A, manufactured by Mitsubishi Chemical Corporation) to obtain 980 g of a passing solution (present product 1: 1.71% non-polymer catechins, gallate) Body ratio 8.5%, gallic acid content 0.13%, gallic acid / (gallic acid + non-polymer catechins) = 0.071).

カテキン類類の測定方法
試料を蒸留水で希釈した後、フィルター(0.45μm)でろ過し、Waters製高速液体クロマトグラフィー(Waters2695型セパレーションモジュール、Waters2996フォトダイオードアレーモジュール)を用い、オクタデシル基導入液体クロマトグラフ用パックドカラム L−カラムTM ODS(4.6mmφ×250mm:(財)化学物質評価研究機構製)を装着し、カラム温度35℃でグラジエント法で行い、移動相A液は酢酸を0.1モル/リットル含有の水溶液、B液は酢酸を0.1モル/リットル含有のアセトニトリル溶液とし、試料注入量は10μL、UV検出波長は280nmの条件で行った。
Method for measuring catechins After diluting a sample with distilled water, the sample is filtered with a filter (0.45 μm), and using a high-performance liquid chromatography manufactured by Waters (Waters 2695 type separation module, Waters 2996 photodiode array module) A chromatographic packed column L-column TM ODS (4.6 mmφ × 250 mm: manufactured by Chemical Substances Research Institute) is attached, and the gradient is carried out at a column temperature of 35 ° C. The aqueous solution containing 1 mol / liter and B solution were acetonitrile solutions containing acetic acid at 0.1 mol / liter, the sample injection volume was 10 μL, and the UV detection wavelength was 280 nm.

実施例2
ポリフェノンHG(東京フードテクノ製:非重合体カテキン類含有量33.7重量%、ガレート体率50%)5.94重量%水溶液2,000gを調整し(非重合体カテキン類2.0%、ガレート体率50%、pH5.0)、35℃に加温した後タンナーゼ(キッコーマン社製5000Unit/g)を1.2g(非重合体カテキン類1mgに対し0.15Unit)添加した。同温度にて120分間静置保持した後、80℃に昇温することでタンナーゼを失活し反応を停止した(pH4.1、非重合体カテキン類1.72%、ガレート体率1.5%、没食子酸0.60%)。その後、重曹にてpH5.0に調整し、カテキン類含有水溶液2000gを得た(参考品2:非重合体カテキン類1.72%、ガレート体率1.5%、没食子酸0.60%、没食子酸/(没食子酸+非重合体カテキン類)=0.259)。
Example 2
Polyphenone HG (manufactured by Tokyo Food Techno: non-polymer catechin content: 33.7% by weight, gallate content: 50%) 5.94% by weight aqueous solution of 2,000 g (2.0% non-polymer catechins, After heating to 35 ° C. at a gallate ratio of 50%, pH 5.0), 1.2 g of tannase (5000 Unit / g manufactured by Kikkoman) was added (0.15 Unit for 1 mg of non-polymer catechins). After standing at the same temperature for 120 minutes, the temperature was raised to 80 ° C. to deactivate tannase and stop the reaction (pH 4.1, non-polymer catechins 1.72%, gallate body ratio 1.5 %, Gallic acid 0.60%). Thereafter, the pH was adjusted to 5.0 with sodium bicarbonate to obtain 2000 g of an aqueous solution containing catechins (Reference 2: 1.72% non-polymer catechins, 1.5% gallate body ratio, 0.60% gallic acid, Gallic acid / (gallic acid + non-polymer catechins) = 0.259).

参考品2のうち1050gを陰イオン交換樹脂(ダイヤイオンSA10A、三菱化学社製)35mlに通液し、通過液980gを得た(本発明品2:非重合体カテキン類1.72%、ガレート体率1.5%、没食子酸含量0.24%、没食子酸/(没食子酸+非重合体カテキン類)=0.122)。   1050 g of the reference product 2 was passed through 35 ml of an anion exchange resin (Diaion SA10A, manufactured by Mitsubishi Chemical Corporation) to obtain 980 g of a passing solution (present product 2: 1.72% non-polymer catechins, gallate) Body ratio 1.5%, gallic acid content 0.24%, gallic acid / (gallic acid + non-polymer catechins) = 0.122).

比較例1
ポリフェノンHG(東京フードテクノ製:非重合体カテキン類含有量33.7重量%、ガレート体率50%)5.94重量%水溶液1,000gを調整し(非重合体カテキン類2.0%、ガレート体率50.0%、pH5.0)、80℃に昇温した(比較品1:非重合体カテキン類2.0%、ガレート体率50.0%、pH5.0、没食子酸含量0.05%、没食子酸/(没食子酸+非重合体カテキン類)=0.024)。
Comparative Example 1
Polyphenone HG (manufactured by Tokyo Food Techno: non-polymer catechin content: 33.7% by weight, gallate content: 50%) 5.94% by weight of 1,000 g aqueous solution (2.0% non-polymer catechins, Galate body ratio 50.0%, pH 5.0), heated to 80 ° C. (Comparative product 1: non-polymer catechins 2.0%, gallate body ratio 50.0%, pH 5.0, gallic acid content 0 0.05%, gallic acid / (gallic acid + non-polymer catechins) = 0.024).

比較例2
ポリフェノンHG(東京フードテクノ製:非重合体カテキン類含有量33.7重量%、ガレート体率50%)5.94重量%水溶液2,000gを調整し(非重合体カテキン類2.0%、ガレート体率50%、pH5.0)、35℃に加温した後タンナーゼ(キッコーマン社製5000Unit/g)を0.12g(非重合体カテキン類1mgに対し0.015Unit)添加した。同温度にて30分間静置保持した後、80℃に昇温することでタンナーゼを失活し反応を停止した(pH4.8、非重合体カテキン類2.0%、ガレート体率44.2%、没食子酸0.09%)。その後、重曹にてpH5.0に調整し、カテキン類含有水溶液2000gを得た(比較品2:非重合体カテキン類2.0%、ガレート体率44.2%、没食子酸0.09%、没食子酸/(没食子酸+非重合体カテキン類)=0.043)。
Comparative Example 2
Polyphenone HG (manufactured by Tokyo Food Techno: non-polymer catechin content: 33.7% by weight, gallate content: 50%) 5.94% by weight aqueous solution of 2,000 g (2.0% non-polymer catechins, After heating to 35 ° C. at a gallate ratio of 50%, pH 5.0), 0.12 g of tannase (5000 Unit / g manufactured by Kikkoman Corporation) was added (0.015 Unit for 1 mg of non-polymer catechins). After standing at the same temperature for 30 minutes, the temperature was raised to 80 ° C. to deactivate tannase and stop the reaction (pH 4.8, non-polymer catechins 2.0%, gallate body ratio 44.2). %, Gallic acid 0.09%). Thereafter, the pH was adjusted to 5.0 with sodium bicarbonate to obtain 2000 g of an aqueous solution containing catechins (Comparative product 2: 2.0% non-polymer catechins, 44.2% gallate content, 0.09% gallic acid, Gallic acid / (gallic acid + non-polymer catechins) = 0.043).

実施例3
ポリフェノンHG(東京フードテクノ製:非重合体カテキン類含有量33.7重量%、ガレート体率50%)23.74%水溶液500gを調整し(非重合体カテキン類8.0%、ガレート体率50%、pH5.0)、35℃に加温した後タンナーゼ(キッコーマン社製5000Unit/g)を2.4g(非重合体カテキン類1mgに対し0.3Unit)添加した。同温度にて180分間静置保持した後、80℃に昇温することでタンナーゼを失活し反応を停止した(pH4.2、非重合体カテキン類7.2%、ガレート体率4.9%、没食子酸1.92%)。その後、重曹にてpH5.0に調整し、カテキン類含有水溶液500gを得た(参考品3:非重合体カテキン類7.2%、ガレート体率4.9%、没食子酸1.92%)。
Example 3
Polyphenone HG (manufactured by Tokyo Food Techno: non-polymer catechin content: 33.7% by weight, gallate body ratio 50%) 23.74% 500 g of aqueous solution (non-polymer catechins 8.0%, gallate body ratio) After heating to 35 ° C., 2.4 g of tannase (5000 Unit / g manufactured by Kikkoman) was added (0.3 Unit for 1 mg of non-polymer catechins). After standing at the same temperature for 180 minutes, the temperature was raised to 80 ° C. to deactivate tannase and stop the reaction (pH 4.2, non-polymer catechins 7.2%, gallate body ratio 4.9). %, Gallic acid 1.92%). Thereafter, the pH was adjusted to 5.0 with sodium bicarbonate to obtain 500 g of a catechins-containing aqueous solution (reference product 3: non-polymer catechins 7.2%, gallate ratio 4.9%, gallic acid 1.92%). .

参考品3のうち260gを陰イオン交換樹脂(ダイヤイオンSA10A、三菱化学社製)35mlに通液し、通過液245gを得た(本発明品3:非重合体カテキン類7.2%、ガレート体率4.9%、没食子酸含量0.58%、没食子酸/(没食子酸+非重合体カテキン類)=0.075)。   260 g of the reference product 3 was passed through 35 ml of an anion exchange resin (Diaion SA10A, manufactured by Mitsubishi Chemical Corporation) to obtain 245 g of a passing solution (present product 3: non-polymer catechins 7.2%, gallate). Body ratio 4.9%, gallic acid content 0.58%, gallic acid / (gallic acid + non-polymer catechins) = 0.075).

比較例3
ポリフェノンHG(東京フードテクノ製:非重合体カテキン類含有量33.7重量%、ガレート体率50%)37.1%水溶液320gを調整し(非重合体カテキン類12.5%、ガレート体率50%、pH5.0)、35℃に加温した後タンナーゼ(キッコーマン社製5000Unit/g)を2.4g(非重合体カテキン類1mgに対し0.3Unit)添加した。同温度にて120分間静置保持したところ反応後のガレート体率は42.9%であった。そこでさらに、同温度にて60分間静置保持したが、ガレート体率は40.9%までしか低下しておらず、水溶液中の非重合体カテキン類濃度が10重量%越えた場合には、タンナーゼの活性が十分に発揮されなないことが示された。
Comparative Example 3
Polyphenone HG (manufactured by Tokyo Food Techno: non-polymer catechin content: 33.7% by weight, gallate body ratio: 50%) 37.1% aqueous solution 320 g was prepared (non-polymer catechins: 12.5%, gallate body ratio After heating to 35 ° C., 2.4 g of tannase (5000 Unit / g manufactured by Kikkoman) was added (0.3 Unit for 1 mg of non-polymer catechins). When the mixture was kept standing at the same temperature for 120 minutes, the gallate body ratio after the reaction was 42.9%. Then, furthermore, it was kept still at the same temperature for 60 minutes, but the gallate body ratio was reduced only to 40.9%, and when the concentration of non-polymer catechins in the aqueous solution exceeded 10% by weight, It was shown that the activity of tannase was not fully exhibited.

本発明品1〜3、参考品1、2及び比較品1、2のカテキン類含有水溶液の(a)非重合体カテキン類中のガレート体率および(b)没食子酸/(非重合体カテキン類+没食子酸)の値を表1に示す。   (A) gallate content in non-polymer catechins of catechins-containing aqueous solutions of the present invention products 1 to 3, reference products 1 and 2, and comparative products 1 and 2, and (b) gallic acid / (non-polymer catechins The value of (+ gallic acid) is shown in Table 1.

Figure 0004739036
Figure 0004739036

実施例4(緑茶飲料に配合した例)
煎茶100gに60℃イオン交換水2000gを加え、時々攪拌しながら10分間静置した後、40メッシュ金網にて茶葉を分離した。茶葉の残渣をイオン交換水1000gにて洗浄し、抽出液と洗浄液をあわせNo.2濾紙を使用して吸引ろ過した後、ろ液にL−アスコルビン酸ナトリウム4gと重曹0.2gを加え、イオン交換水にて非重合体カテキン類濃度として500ppmとなるよう調製した(全体量約10Kg)。この緑茶飲料に本発明品1〜3、参考品1、2及び比較品1、2の緑茶抽出処理物をそれぞれ非重合体カテキン類濃度として1000ppmとなるように配合し、138℃、30秒UHT殺菌を行い、88℃に冷却しペットボトルに充填し、さらに30℃まで水冷した。それぞれのペットボトル飲料は常温で2週間保存後、20名の良く訓練されたパネラーにて官能評価を行った。官能評価結果は苦渋味・収斂味、酸味・えぐ味、総合評価を対象としそれぞれ20点を満点とし、非常に好ましい:17〜20点、やや良い:14〜17点、普通:11〜14点、やや劣る:8〜11点、劣る:8点以下の評価基準で採点し20名のパネラーの平均点を表2に示す。
Example 4 (example blended in green tea beverage)
After adding 2000 g of 60 ° C. ion exchange water to 100 g of sencha and leaving it to stand for 10 minutes with occasional stirring, the tea leaves were separated with a 40 mesh wire mesh. The tea leaf residue was washed with 1000 g of ion-exchanged water. After suction filtration using 2 filter papers, 4 g of sodium L-ascorbate and 0.2 g of sodium bicarbonate were added to the filtrate, and the concentration was adjusted to 500 ppm as a non-polymer catechin concentration in ion-exchanged water (total amount of about 10 kg). The green tea beverages of the present invention products 1 to 3, the reference products 1 and 2, and the comparative products 1 and 2 were blended so that the concentration of non-polymer catechins was 1000 ppm, respectively, and 138 ° C., 30 seconds UHT Sterilized, cooled to 88 ° C., filled into a PET bottle, and further water cooled to 30 ° C. Each plastic bottle drink was stored at room temperature for 2 weeks and then subjected to sensory evaluation by 20 well-trained panelists. The sensory evaluation results are bitter astringent / astringent taste, sour / egu taste, and comprehensive evaluation, each with a perfect score of 20 points, very preferable: 17 to 20 points, slightly good: 14 to 17 points, normal: 11 to 14 points Slightly inferior: 8 to 11 points, inferior: Scored on an evaluation standard of 8 points or less, and the average score of 20 panelists is shown in Table 2.

Figure 0004739036
Figure 0004739036

表2に示すとおり本発明品を添加した緑茶飲料は、1000ppmという高濃度の非重合体カテキン類を含有するにもかかわらず、苦渋味・収斂味および酸味・えぐ味等の不自然な味は全く感じられなかった。一方、比較品1(タンナーゼ処理未処理:ガレート体率50%)および比較品2(タンナーゼ処理を行ったがガレート体率が44.2%)を添加した緑茶飲料は苦渋味・収斂味が強く、顕著に感じられた。また、タンナーゼ処理し、ガレート率を40%以下としたが、陰イオン交換樹脂処理を行っていない参考品1および参考品2を添加した緑茶飲料は酸味・えぐ味が強く感じられた。

As shown in Table 2, the green tea beverage to which the product of the present invention is added contains non-polymer catechins at a high concentration of 1000 ppm. I couldn't feel it at all. On the other hand, green tea beverages to which comparative product 1 (untreated tannase treatment: gallate body rate 50%) and comparative product 2 (tannase treated but gallate body rate 44.2%) have a strong bitter taste and astringent taste. , Felt noticeable. In addition, the green tea beverage to which the reference product 1 and the reference product 2 to which the tannase treatment was applied and the gallate rate was 40% or less but the anion exchange resin treatment was not performed strongly felt sourness and gummy taste.

Claims (4)

茶抽出液をタンナーゼ処理した後、遊離する没食子酸を陰イオン交換樹脂と接触して除去することを特徴とする茶抽出処理物の製造方法。   A method for producing a tea extract-treated product, comprising: treating a tea extract with tannase, and then removing liberated gallic acid by contacting with an anion exchange resin. 前記茶抽出処理物における
(a)非重合体カテキン類中のガレート体率が0〜40重量%であり、かつ
(b)没食子酸/(非重合体カテキン類+没食子酸)が0〜0.15
である請求項1に記載の茶抽出処理物の製造方法。
The gallate content in (a) non-polymer catechins in the tea extraction product is 0 to 40% by weight, and (b) gallic acid / (non-polymer catechins + gallic acid) is 0 to 0.00. 15
The method for producing a tea extraction processed product according to claim 1.
前記茶抽出液中の非重合体カテキン類の濃度が1〜10重量%である請求項1または2のいずれかに記載の茶抽出処理物の製造方法。   The method for producing a tea extraction processed product according to any one of claims 1 and 2, wherein the concentration of the non-polymer catechins in the tea extract is 1 to 10% by weight. 茶抽出液をタンナーゼ処理した後、遊離する没食子酸を陰イオン交換樹脂と接触して除去して得られる茶抽出処理物であって、
前記茶抽出処理物における
(a)非重合体カテキン類中のガレート体率が0〜8.5重量%であり、かつ
(b)没食子酸/(非重合体カテキン類+没食子酸)が0〜0.15
である茶抽出処理物。
After the tea extract is tannase-treated, it is a tea extraction treatment product obtained by removing free gallic acid in contact with an anion exchange resin,
In the tea extraction processed product
(A) The gallate content in the non-polymer catechins is 0 to 8.5% by weight, and
(B) Gallic acid / (non-polymer catechins + gallic acid) is 0 to 0.15
Tea extract-treated product is.
JP2006018062A 2006-01-26 2006-01-26 Process for producing a processed tea extraction product with improved flavor Expired - Fee Related JP4739036B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2006018062A JP4739036B2 (en) 2006-01-26 2006-01-26 Process for producing a processed tea extraction product with improved flavor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2006018062A JP4739036B2 (en) 2006-01-26 2006-01-26 Process for producing a processed tea extraction product with improved flavor

Publications (2)

Publication Number Publication Date
JP2007195458A JP2007195458A (en) 2007-08-09
JP4739036B2 true JP4739036B2 (en) 2011-08-03

Family

ID=38450676

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006018062A Expired - Fee Related JP4739036B2 (en) 2006-01-26 2006-01-26 Process for producing a processed tea extraction product with improved flavor

Country Status (1)

Country Link
JP (1) JP4739036B2 (en)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8945655B2 (en) 2007-07-10 2015-02-03 Conopco, Inc. Stable and consumable compositions
KR20100055448A (en) * 2007-09-05 2010-05-26 가오 가부시키가이샤 Method for producing purified tea extract
JP5238993B2 (en) * 2007-09-26 2013-07-17 サントリー食品インターナショナル株式会社 Tea extract, tea beverage and method for producing them
JP5081028B2 (en) * 2008-03-24 2012-11-21 花王株式会社 Method for producing purified green tea extract containing non-polymer catechins
EP2343987B1 (en) * 2008-11-11 2012-12-05 Unilever NV Tea composition
JP5593026B2 (en) * 2008-12-02 2014-09-17 オルガノ株式会社 Method for producing catechins
US20110311705A1 (en) * 2009-02-27 2011-12-22 Ito En, Ltd. Roasted green tea beverage packed in container
JP5336340B2 (en) 2009-12-09 2013-11-06 花王株式会社 Method for producing purified tea extract
JP2012147782A (en) 2010-12-28 2012-08-09 Kao Corp Method for producing purified tea extract
JP5634858B2 (en) * 2010-12-28 2014-12-03 花王株式会社 Method for producing purified tea extract
JP5480940B2 (en) * 2012-07-03 2014-04-23 花王株式会社 Method for producing purified green tea extract containing non-polymer catechins
JP7272809B2 (en) * 2019-02-07 2023-05-12 三井農林株式会社 Packaged green tea beverage
JP7260338B2 (en) * 2019-03-01 2023-04-18 ポッカサッポロフード&ビバレッジ株式会社 Roasted tea beverage, method for producing roasted tea beverage, and method for suppressing bitterness of roasted tea beverage and improving aftertaste

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5069925A (en) * 1990-06-07 1991-12-03 Nestec S.A. Preparation of tea products
JP2866711B2 (en) * 1990-06-22 1999-03-08 三井化学株式会社 Method for separating phenolic compounds
JPH07112404B2 (en) * 1992-05-08 1995-12-06 協同組合ティーライフクリエイティブ How to make green tea
JP3347822B2 (en) * 1993-06-28 2002-11-20 株式会社不二家 Extraction and purification method of quinic acid
EP1148790A2 (en) * 1999-02-08 2001-10-31 Unilever Plc Cold brew tea
JP3859930B2 (en) * 2000-04-19 2006-12-20 株式会社 伊藤園 Manganese-containing tea extract, method for producing tea extract, and manganese-containing tea extract
JP3589623B2 (en) * 2000-07-13 2004-11-17 独立行政法人 科学技術振興機構 Separation method of antioxidant components of food and drink
JP3592681B2 (en) * 2001-05-16 2004-11-24 花王株式会社 Packaged beverage
JP3706370B2 (en) * 2003-04-25 2005-10-12 花王株式会社 Tannase-treated green tea extract
JP4554184B2 (en) * 2003-10-31 2010-09-29 アサヒ飲料株式会社 Tea beverage astringency treatment method and tea beverage obtained by the method
JP4800779B2 (en) * 2005-03-15 2011-10-26 花王株式会社 Method for producing purified green tea extract

Also Published As

Publication number Publication date
JP2007195458A (en) 2007-08-09

Similar Documents

Publication Publication Date Title
JP4739036B2 (en) Process for producing a processed tea extraction product with improved flavor
JP4902655B2 (en) Tea extract
KR101414422B1 (en) Process for producing purified green tea extract
KR101391063B1 (en) Process for producing purified green tea extract
JP5081028B2 (en) Method for producing purified green tea extract containing non-polymer catechins
JP5228229B2 (en) Method for producing low caffeine tea extract
WO2007099715A1 (en) Process for producing purified tea extract
JP4327707B2 (en) Method for producing non-polymer catechins composition
CN107580455A (en) Green tea extracts composition
JP4634409B2 (en) Process for producing a flavor-modified tea extraction product
JP4690741B2 (en) Method for producing non-polymer catechins composition
JP4242908B2 (en) Method for producing purified tea extract
JP4927137B2 (en) Tea extract
JP5162594B2 (en) Method for producing purified tea extract
JP4773696B2 (en) Method for producing non-polymer catechins composition
JP5336340B2 (en) Method for producing purified tea extract
JP4630295B2 (en) Production method of tea extract
JP4242877B2 (en) Production method of green tea extract
JP4673247B2 (en) Process for producing a processed tea extraction product with improved flavor
JP4242891B2 (en) Method for producing purified tea extract
JP5307649B2 (en) Method for producing purified tea extract
JP4838999B2 (en) Method for producing non-polymer catechins composition
JP4545640B2 (en) Tea extract
JP5480940B2 (en) Method for producing purified green tea extract containing non-polymer catechins
JP5183567B2 (en) Method for producing purified tea extract

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20081110

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20100823

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20100831

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20101018

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20110426

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20110427

R150 Certificate of patent or registration of utility model

Ref document number: 4739036

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20140513

Year of fee payment: 3

LAPS Cancellation because of no payment of annual fees