JPS61271969A - Quality improver for drink and method of improving quality of drink - Google Patents
Quality improver for drink and method of improving quality of drinkInfo
- Publication number
- JPS61271969A JPS61271969A JP60115170A JP11517085A JPS61271969A JP S61271969 A JPS61271969 A JP S61271969A JP 60115170 A JP60115170 A JP 60115170A JP 11517085 A JP11517085 A JP 11517085A JP S61271969 A JPS61271969 A JP S61271969A
- Authority
- JP
- Japan
- Prior art keywords
- drink
- glutamate
- quality
- sodium
- cyclodextrin
- 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.)
- Pending
Links
Landscapes
- Tea And Coffee (AREA)
- Alcoholic Beverages (AREA)
- Non-Alcoholic Beverages (AREA)
- Dairy Products (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、サイクロデキストリント、5′−リボヌクレ
オタイド類または/およびグルタミン酸塩を用いること
からなる飲料用品質改良剤および飲料の品質改良法に関
する。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a beverage quality improving agent and a beverage quality improving method comprising the use of cyclodextrins, 5'-ribonucleotides or/and glutamates.
従来の技術
]−ヒー、紅茶の風味改良を目的にサイクロデキスFり
ンを単独添加する方法として米国特許第8.528,8
19号が、また柑橘類飲料にサイクロデキストリンを単
独添加して品質改良をはかる方法として特開昭56−4
8849号が知られている。Prior art] - U.S. Patent No. 8.528,8 describes a method of adding cyclodextrin alone for the purpose of improving the flavor of tea and tea.
No. 19 is also published in JP-A-56-4 as a method for improving the quality of citrus beverages by adding cyclodextrin alone.
No. 8849 is known.
発明が解決しようとする問題点
飲料は、たとえばコーヒー、ココア、茶類あるいは各種
の清涼飲料にみられるように、他の食品に比較して嗜好
的な面が強く、それだけに特有の風味が重んぜられるが
、この要望は近年の★生活の高級化に伴なって従来以上
に強くなってきている。Problems to be Solved by the Invention Beverages, for example, coffee, cocoa, tea, and various soft drinks, are more palatable than other foods, and their unique flavor is therefore important. However, this demand has become stronger than ever as the lifestyle has become more luxurious in recent years.
一方、飲料の風味は製造後から経時的に変化し、その品
質が損なわれるものが多い。九とえば、コーヒーの場合
、焙煎して破砕したコーヒー豆を常法によシ熱水抽出し
た液は、抽出直後の良好な風味が保温貯蔵しておくこと
によシ次第に苦味や酸味が増加して風味が悪くなる。紅
茶、緑茶などの茶葉の熱水抽出液も経時的に苦味や渋味
が増加すると共に、抽出液の混濁が生ずる。この混濁は
進行度合が強くなると、遂にはミルクダウンと呼ばれる
乳濁状頷に至る。この状態になると、抽出液の渋味はも
はや飲用に適さないほど強くなる。On the other hand, the flavor of beverages changes over time after they are manufactured, and the quality of the beverages often deteriorates. For example, in the case of coffee, the liquid obtained by extracting roasted and crushed coffee beans with hot water in a conventional manner has a good flavor immediately after extraction, but when stored at a warm temperature, the bitterness and sourness gradually change. It increases and the flavor deteriorates. Hot water extracts of tea leaves such as black tea and green tea also become bitter and astringent over time, and the extract becomes cloudy. As this turbidity progresses to a greater degree, it eventually develops into a milky state called milk down. In this state, the astringent taste of the extract becomes so strong that it is no longer suitable for drinking.
このために、コーヒー、茶類は風味良好な状態で飲用し
ようとすれば、そのつと抽出する必要があって手間と時
間を要し、と)わけ喫茶店、レストラン、列車食堂など
のように多数の人の注文に手早く応じたい場合、個々に
調製することは極めて非能率的である。さらに、コーヒ
ー、茶類の抽出液を容器詰めで販売するときにも、やは
シ飲用時までに風味が低下するという問題点がある。For this reason, if you want to drink coffee and tea in a good-flavored state, you have to extract them each time, which takes time and effort. If you want to quickly respond to people's orders, it is extremely inefficient to prepare the food individually. Furthermore, when coffee and tea extracts are sold in containers, there is a problem in that the flavor deteriorates by the time it is consumed.
上記のような問題点に!li与沫発明者らは飲料の品質
改良法について種々研究をかさねた結果、飲料中にサイ
クロデキストリンと、6′−リボヌクレオタイド類また
は/およびグルタミン酸塩を含有せしめることにより、
品質改良効果が相乗的に高まり品質も安定に保持できる
ことを見出し、さらに研究をして本発明を完成した。Problems like the above! The inventors conducted various studies on methods for improving the quality of beverages, and found that by incorporating cyclodextrin, 6'-ribonucleotides or/and glutamate into beverages,
They found that the quality improvement effect increases synergistically and the quality can be maintained stably, and after further research, they completed the present invention.
すなわち、本発明は(1)サイクロデキストリンと、5
−リボヌクレオタイド類または/およびグルタミンam
とを含有してなる飲料用品質改良剤、および(2)サイ
クロデキストリンと、5′−リボヌクレオタイド類また
は/およびグルタミン酸塩を飲料中に含有せしめること
を特徴とする飲料の品質改良法である。That is, the present invention provides (1) cyclodextrin;
- ribonucleotides or/and glutamine am
and (2) a method for improving the quality of a beverage, characterized in that the beverage contains a cyclodextrin and a 5'-ribonucleotide or/and a glutamate. .
本発明でいう飲料壓ト、コーヒー、ココア、コーラ、ガ
ラナなどの植物種実飲料、紅茶、緑茶、ウーロン茶など
の茶類飲料、乳酸菌飲料類(例、ヨーグルト)、薬用酒
(例、クコ酒6層蘇酒、陶陶11!I)などが挙げられ
る。In the present invention, beverage bottles, coffee, cocoa, cola, plant seed drinks such as guarana, tea drinks such as black tea, green tea, and oolong tea, lactic acid bacteria drinks (e.g., yogurt), medicinal liquors (e.g., goji liquor 6-layer) Examples include Sushu and Totou 11!I).
本発明で使用するサイクロデキストリンとしては、α−
サイクロデキストリン、β−サイクロデキストリン、r
−サイクロデキストリンが挙げられ、これらは1種でも
よくまた2種以上を併用してもよい。The cyclodextrin used in the present invention includes α-
cyclodextrin, β-cyclodextrin, r
- Cyclodextrins can be mentioned, and these may be used alone or in combination of two or more.
本発明で使用する5′−リボヌクレオタイド類としては
、5′−イノシン酸、6′−グアニル酸が挙げられ、こ
れらの5′−リボヌクレオタイド類は遊離のものでもよ
いし、その可食性塩たとえばナトリウム塩、カリウム塩
、力μシウム壜などでもよい。The 5'-ribonucleotides used in the present invention include 5'-inosinic acid and 6'-guanylic acid, and these 5'-ribonucleotides may be free or edible. Salts such as sodium salts, potassium salts, salts, etc. may also be used.
5−リボヌクレオタイド類はその1mを用いてもよく、
2種以上を併用してもよい。本発明では、6′−イノシ
ン酸ナトリウムと5′−グアニル酸ナトリウムの混合物
が特に好ましく用いられる。次に、グルタミン酸塩とし
ては、L−グルタミン酸の可食性塩、特にL−グルタミ
ン酸ナトリウムが好ましく用いられる。1 m of 5-ribonucleotides may be used,
Two or more types may be used in combination. In the present invention, a mixture of sodium 6'-inosinate and sodium 5'-guanylate is particularly preferably used. Next, as the glutamate, edible salts of L-glutamic acid, particularly sodium L-glutamate, are preferably used.
本発明の飲料用品質改良剤は、通常サイクロデキストリ
ン100重量部と、これに対し5′−リボヌクレオタイ
ド類を約0.01〜toot量部および/またはグルタ
ミン酸塩を約0.1〜1000重量部の割合となるよう
に混合することによって調製される。混合方法自体は特
に限定されず、たとえばこれらの粉末品をV型混合機、
スピードミキサー等を使用し常法によシ製造でき、この
際に砂糖などの甘味料を混和しておいてもよい。The beverage quality improving agent of the present invention usually contains 100 parts by weight of cyclodextrin, and about 0.01 to 1,000 parts by weight of 5'-ribonucleotides and/or about 0.1 to 1000 parts by weight of glutamate. It is prepared by mixing in the following proportions: The mixing method itself is not particularly limited; for example, these powder products may be mixed in a V-type mixer,
It can be produced by a conventional method using a speed mixer or the like, and a sweetener such as sugar may be mixed in at this time.
該改良剤は飲料に対して飲用時濃度で約0.01〜1重
量%程度添加される。The improving agent is added to the drink at a drinking concentration of about 0.01 to 1% by weight.
次に本発明の壱判の品質改良法は従来公知の製造段階で
、サイクロデキストリンと、5′−リボヌクレオタイド
類または/およびグルタミン酸塩を飲料中に含有せしめ
れば良い。サイクロデキストリント、5′−リボヌクレ
オタイド類または/およびグルタミン酸塩を飲料に添加
するに際し、これらは個々に加えてもよいが通常は、前
述のように、予じめ配合した組成物として添加するのが
便利である。Next, one of the most important quality improvement methods of the present invention is to incorporate cyclodextrin, 5'-ribonucleotides or/and glutamate into a beverage at a conventionally known manufacturing step. When adding cyclodextrins, 5'-ribonucleotides or/and glutamate to a beverage, they may be added individually but are usually added as a pre-formulated composition, as described above. It is convenient.
サイクロデキストリン、5′−リボヌクレオタイド類、
グルタミン酸塩の使用量は、飲料の種類。cyclodextrin, 5'-ribonucleotides,
The amount of glutamate used depends on the type of beverage.
目的とする効果などによシ適宜選定されるが、通常、飲
用時の濃度でサイクロデキストリンは約0.01〜1重
量%、5′−リボヌクレオタイドaは約0.0001〜
0.01重量%、グルタミン酸塩は約o、oot〜0.
1重量/容量%となるように、好ましくは、サイクロデ
キストリン約0.05〜0.6重量%、5′−リボヌク
レオタイド類約0.0005〜0.005重量%、グル
タミン酸塩約0.005〜0.02恵量%程度となるよ
うに用いられる。The concentration is selected as appropriate depending on the desired effect, etc., but the concentration at the time of drinking is usually about 0.01 to 1% by weight for cyclodextrin and about 0.0001 to 1% by weight for 5'-ribonucleotide a.
0.01% by weight, glutamate is approximately o,oot~0.
1% w/v, preferably about 0.05-0.6% cyclodextrin, about 0.0005-0.005% 5'-ribonucleotides, about 0.005% glutamate. It is used so that the amount is about 0.02%.
サイクロデキストリンと、5′−リボヌクレオタイド類
または/およびグルタミン酸塩の飲料への添加は、飲用
前の適宜の段階で実施できるが、たとえば紅茶、緑茶、
ウーロン茶などの茶類のように熱水抽出するもので経時
的変化が苦味、渋味および混濁であるものに対する添加
時期は抽出直後の液、あるいは抽出するに際し熱水の方
Km解しておくのが好ましい。一方、経時的変化が酸味
、苦味の増加であって混濁が問題とならないコーヒー等
の場合は、飲用前の任意の時期でよく、その他の飲料の
場合も同様である。またインスタントコーヒーの場合は
、その製造工程中に添加したシ、あるいは乾燥後の製品
に粉末状態で混和しておくこともできる。インスタント
紅茶の場合はティーパックへの封入に際し、またバック
飲料の場合は容器へ充填するに際し、混和せしめておい
てもよい。Cyclodextrin and 5'-ribonucleotide or/and glutamate can be added to the beverage at an appropriate stage before drinking; for example, black tea, green tea,
For teas such as oolong tea that are extracted with hot water and whose taste changes over time such as bitterness, astringency, and turbidity, the timing of addition is to the liquid immediately after extraction, or to the hot water used during extraction. is preferred. On the other hand, in the case of coffee or the like where the change over time is an increase in sourness or bitterness and turbidity is not a problem, it may be done at any time before drinking, and the same applies to other beverages. In the case of instant coffee, it can also be added during the manufacturing process or mixed into the dried product in powder form. In the case of instant black tea, the ingredients may be mixed before being packed into a tea bag, and in the case of a bag beverage, when being filled into a container.
実施例
次に、実験例と共に実施例を挙げて本発明をさらに具体
的に説明する。EXAMPLES Next, the present invention will be explained in more detail by giving examples together with experimental examples.
実験例1゜
紅茶18Fを沸騰水1aoosZ中に加え、1分間煮沸
後、v紙で濾過して紅茶抽出液を得た。この抽出液を2
00 mlづつ小分けして、β−サイクロデキスtリン
(以下、β−CDと略す)(商品名“セμデツクスNT
”松谷化学製造)、6′−リボヌクレオタイドナトリウ
ム(商品名″リボタイド”大田薬品工業■製造、6′−
イノシン酸ナトリウムト5′−グアニ)vIIIナトリ
ウムの等量混合物)、をそれぞれ単独または併用して加
えたのち、直ちに水冷し、20℃まで冷却したのち冷蔵
庫中で20時間放置した。これらの各紅茶液について、
渋味の強さをバネfi/10名による官能検査によって
調べた。その結果を第1表に示す。Experimental Example 1 Black tea 18F was added to boiling water 1aoosZ, boiled for 1 minute, and filtered through V paper to obtain a black tea extract. Add this extract to 2
Divide into 00 ml portions and add β-cyclodextrin (hereinafter abbreviated as β-CD) (trade name “Seμdex NT”).
"Matsutani Chemical Manufacturing), 6'-Ribonucleotide Sodium (Product name: Ribotide" manufactured by Ota Pharmaceutical Co., Ltd., 6'-
A mixture of equal amounts of sodium inosinate, 5'-guani)vIII, and sodium inosinate were added alone or in combination, and immediately cooled with water, cooled to 20°C, and then left in a refrigerator for 20 hours. For each of these black tea liquids,
The strength of astringency was investigated by a sensory test conducted by 10 people. The results are shown in Table 1.
第1表
注1)バネ/I/には次の尺度の評点を与え、渋味の程
度を評価させた。Table 1 Note 1) Spring/I/ was given a score using the following scale to evaluate the degree of astringency.
非常に弱い・・・・・・・・・2点1弱い・・・・・・
・・・1点、普通・・・・・・・・・0点9強い・・・
・・・・・・−1点、非常に強い・・・・・・・・・−
2点
注2)官能検査の結果を一元配置のためのTukeyO
表(「食品の品質測定法」、吉川誠次ら著、昭和42年
、光琳書院)を用いて有意差検定を行ない、そのときの
試料点6と各試料間の差の検定結果を示す。Very weak...2 points, 1 weak...
...1 point, average...0 points, 9 strong...
・・・・・・−1 point, very strong・・・・・・・・・−
2 points Note 2) TukeyO for unified arrangement of sensory test results
A significant difference test was performed using a table ("Food Quality Measuring Method", written by Seiji Yoshikawa et al., 1962, Korin Shoin), and the test results of the difference between sample point 6 and each sample are shown.
※・・・・・・・・・危険率5%で有意差あり。*・・・・・・・・・There is a significant difference at a risk rate of 5%.
※※・・・・・・・・・危険率1%で有意差あり。※※・・・・・・・・・There is a significant difference at a risk rate of 1%.
第1表の結果に示されるように、β−CDとぎ的に極め
て顕著に渋味抑制効果が認められた。As shown in the results in Table 1, β-CD significantly suppressed astringency.
実験例2゜ 実験例1と同様にして得た紅茶抽出液にβ−CD。Experimental example 2゜ β-CD was added to the black tea extract obtained in the same manner as in Experimental Example 1.
5′−リボヌクレオタイドナトリウム、L−グルタミン
酸ナトリウムを第2表に示す量で添加し、以下実験例1
と同様の保存条件及び官能検査法で渋味の程度を評価し
た。Sodium 5'-ribonucleotide and sodium L-glutamate were added in the amounts shown in Table 2, and the following Experimental Example 1 was carried out.
The degree of astringency was evaluated using the same storage conditions and sensory testing methods.
第2表 注1)第1表と同意義を示す。Table 2 Note 1) Shows the same meaning as Table 1.
注2)試料A6と各試料間の有意差検定結果を示す。Note 2) Shows the results of significant difference test between sample A6 and each sample.
注8)試料A7と各試料間の有意差検定結果を示す。Note 8) Shows the results of significant difference test between sample A7 and each sample.
注4)試料A8と各試料間の有意差検定結果を示す。Note 4) Shows the results of significant difference test between sample A8 and each sample.
第2表の結果に示されるように、紅茶の渋味は、β−C
Dと、5′〜リボヌクレオタイドナトリウムまたは/お
よびL−グルタミン酸ナトリウムの併用によってこれら
単独添加区よりも著しく軽減される。As shown in the results in Table 2, the astringency of black tea is caused by β-C
The combined use of D and sodium 5'-ribonucleotide or/and sodium L-glutamate results in a more significant reduction than when these are added alone.
実施例1
焙煎コーヒーの粉末aOfを沸騰本釣600g?で抽出
してコーヒー抽出液を得た。これを200m1づつ2個
のフフスコにとり、一方を対照とし、他方に、β−CD
l&9.L−グμタミン酸ナトリウム4fシナトリウム
4fヌクレオタイドナトリウム0.2fを乳鉢で混合し
て得た品質改良剤1fを加えて栓をし、80〜90℃で
5時間保存した。Example 1 Boil 600g of roasted coffee powder aOf? A coffee extract was obtained by extraction. Transfer 200ml of this to two fufuscos, one as a control, and the other with β-CD.
l&9. 1f of a quality improver obtained by mixing 4f of sodium L-μ glutamate, 4f of sodium nucleotide, and 0.2f of sodium nucleotide in a mortar was added, the mixture was stoppered, and the mixture was stored at 80 to 90°C for 5 hours.
5時間後両者を飲み比べると、添加区は対照に比べて苦
味と酸味が抑制され、良好な風味を保つことが出来た。When comparing the two after 5 hours, it was found that the bitterness and sourness in the added group was suppressed compared to the control, and a good flavor was maintained.
実施例2
市販のインスタントコーヒー11Fに熱湯1jを加えて
飲用濃度とし、フラスコ中80〜90℃−思夜貯蔵した
。これに、β−CD95F、5’−リボヌクレオタイド
ナトリウム0.5fおよびL−グルタミン酸ナトリウム
4.5fを乳鉢で混合して得た品質改良剤を前記コーヒ
ーに対し0.4%となるように加えて添加区とし、一方
これらを加えないものを対照区とし飲み比べると、添加
区では苦味や酸味などの不快味が抑制され、対照と比較
して良好な風味を有していた。Example 2 Hot water 1j was added to commercially available instant coffee 11F to make it drinkable, and the mixture was stored overnight at 80 to 90°C in a flask. To this, a quality improver obtained by mixing β-CD95F, 0.5f of sodium 5'-ribonucleotide, and 4.5f of sodium L-glutamate in a mortar was added to the coffee at a concentration of 0.4%. When comparing the samples with the additives and the controls without these additives, the additives suppressed unpleasant tastes such as bitterness and sourness, and had a better flavor than the control.
実施例8
紅茶葉18Fを沸騰水llに加えて1分間煮沸したのち
p紙濾過し、紅茶的1gを得た。紅茶200m1に砂糖
6f、β−CD粉末0.8 f 、 5’−リボヌクレ
オタイドナトリウム0.004FおよびL−グルタミン
酸ナトリウム0.04Fの混合物を加え、試料Aとした
。ま九、紅茶200g/に砂糖6fを加え九本のを試料
Bとした。試料Aおよび試料δ を24時間冷蔵し九の
ち飲み比べると、試料Bは強い渋味を有していたが、試
料Aは適度な渋味があシ良好な風味を有していた。Example 8 18F black tea leaves were added to 1 liter of boiling water, boiled for 1 minute, and then filtered through p paper to obtain 1 g of black tea. Sample A was prepared by adding a mixture of 6 f sugar, 0.8 f β-CD powder, 0.004 F sodium 5'-ribonucleotide, and 0.04 F sodium L-glutamate to 200 ml black tea. Sample B was prepared by adding 6 grams of sugar to 200 g of black tea. When Sample A and Sample δ were refrigerated for 24 hours and drank after nine hours, Sample B had a strong astringent taste, while Sample A had a moderate astringent taste and a good flavor.
実施例4
β−CD粉末1#、L−グルタミン酸ナトリウム6fお
よび5′−リボヌクレオタイドナトリウム1fを別々に
秤量した。まずL−グルタミン酸ナトリウムと5′−リ
ボヌクレオタイドナトリウムを乳鉢で混合したのち、こ
れにβ−CD粉末約2゜fを加えて混合した。この混合
物を21容のポリ袋に移し、これにβ−CD粉末の残部
を加え、よく振って混合して飲料用品質改良剤を得た。Example 4 1 # of β-CD powder, 6 f of sodium L-glutamate, and 1 f of sodium 5'-ribonucleotide were weighed separately. First, sodium L-glutamate and sodium 5'-ribonucleotide were mixed in a mortar, and then approximately 2°F of β-CD powder was added and mixed. This mixture was transferred to a 21-volume plastic bag, the remainder of the β-CD powder was added thereto, and the mixture was thoroughly shaken and mixed to obtain a beverage quality improver.
上記に飲料用品質改良剤を、常法にょシ得た紅茶抽出液
に0.5%添加して5時間放置したところ、混濁の発生
はみられず、風味良好な紅茶が得られた。When 0.5% of the above-mentioned beverage quality improver was added to the black tea extract obtained by a conventional method and left to stand for 5 hours, no turbidity was observed and black tea with good flavor was obtained.
実施例5
緑茶葉10Fを沸騰水11に加えて1分間煮沸したのち
v紙濾過し、緑茶抽出液を得た。Example 5 Green tea leaves 10F were added to boiling water 11 and boiled for 1 minute, and then filtered through V paper to obtain a green tea extract.
この紅茶抽出液200 mlに、実施例4で得た品質改
良剤1Fを加えて6時間放置した。かくして得られたも
のを、本品質改良剤を加えないで6時間放置したものと
飲み比べてみると、明らかに風味が良好であった。The quality improver 1F obtained in Example 4 was added to 200 ml of this black tea extract and left for 6 hours. When the thus obtained product was compared with a product that had been left for 6 hours without the addition of the present quality improving agent, the flavor was clearly better.
発明の効果
本発明方法を適用することによシ、飲料の不必要な苦味
、渋味酸味等が軽減され、その風味を一段と向上させる
ことができる。この効果は、サイクロデキストリンと、
5−リボヌクレオタイド類または/およびグルタミン酸
塩とを使用する併用効果に基づくものである。すなわち
、本発明による飲料の風味改良効果は、上記各添加物を
単独使用したときに比較して著しく大きく、併用使用す
ることにより相乗的に風味が改良される。Effects of the Invention By applying the method of the present invention, unnecessary bitterness, astringency, sourness, etc. of the beverage can be reduced, and its flavor can be further improved. This effect is due to cyclodextrin and
It is based on the combined effect of using 5-ribonucleotides and/or glutamate. That is, the effect of improving the flavor of the beverage according to the present invention is significantly greater than when each of the above additives is used alone, and when used in combination, the flavor is synergistically improved.
Claims (2)
イド類または/およびグルタミン酸塩とを含有してなる
飲料用品質改良剤(1) Beverage quality improving agent containing cyclodextrin and 5'-ribonucleotides or/and glutamate
イド類または/およびグルタミン酸塩を飲料中に含有せ
しめることを特徴とする飲料の品質改良法(2) A method for improving the quality of a beverage, which comprises incorporating cyclodextrin and 5'-ribonucleotides or/and glutamate into the beverage.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60115170A JPS61271969A (en) | 1985-05-27 | 1985-05-27 | Quality improver for drink and method of improving quality of drink |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60115170A JPS61271969A (en) | 1985-05-27 | 1985-05-27 | Quality improver for drink and method of improving quality of drink |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS61271969A true JPS61271969A (en) | 1986-12-02 |
Family
ID=14656075
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60115170A Pending JPS61271969A (en) | 1985-05-27 | 1985-05-27 | Quality improver for drink and method of improving quality of drink |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61271969A (en) |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63126556A (en) * | 1986-11-17 | 1988-05-30 | Nippon Shokubai Kagaku Kogyo Co Ltd | Catalyst for vapor phase intramolecular dehydration reaction of alkanol amines |
JPS63126558A (en) * | 1986-11-17 | 1988-05-30 | Nippon Shokubai Kagaku Kogyo Co Ltd | Catalyst for vapor phase intramolecular dehydration reaction of alkanol amines |
JPS63152945A (en) * | 1986-12-17 | 1988-06-25 | Hikoshige Fujii | Compression formed product of coffee bean |
JPH01196257A (en) * | 1988-01-29 | 1989-08-08 | Ajinomoto General Foods Kk | Method of preventing coffee beverage from becoming turbid |
WO2000038536A3 (en) * | 1998-12-23 | 2000-11-16 | Sinai School Medicine | Inhibitors of the bitter taste response |
JP2006067895A (en) * | 2004-09-02 | 2006-03-16 | Mitsui Norin Co Ltd | Inhibitory agent of bitterness and astringency |
EP1836899A1 (en) * | 2006-03-20 | 2007-09-26 | Ito En, Ltd. | Bottleable green tea beverage |
US7314716B2 (en) | 1999-11-19 | 2008-01-01 | Mount Sinai School Of Medicine | Gustducin γ subunit materials and methods |
US7452563B2 (en) | 2005-06-20 | 2008-11-18 | Redpoint Bio Corporation | Compositions and methods for producing flavored seasonings that contain reduced quantities of common salt |
US7455872B2 (en) | 2005-06-20 | 2008-11-25 | Redpoint Bio Corporation | Compositions and methods for producing a salty taste in foods or beverages |
WO2009013240A2 (en) * | 2007-07-20 | 2009-01-29 | Dsm Ip Assets B.V. | Foodstuffs with enhanced chocolate taste |
US7972644B2 (en) | 2006-03-22 | 2011-07-05 | Ito En, Ltd. | Bottleable green tea beverage |
JP2012165659A (en) * | 2011-02-10 | 2012-09-06 | Mitsui Norin Co Ltd | Tea beverage enhanced in deliciousness and reduced in bitterness and astringency |
JP2012165753A (en) * | 2012-05-01 | 2012-09-06 | Mitsui Norin Co Ltd | Tea beverage enhanced in deliciousness and reduced in bitterness and astringency |
JP2012179042A (en) * | 2011-02-10 | 2012-09-20 | Mitsui Norin Co Ltd | Nucleotide-containing tea extract and method for producing the same |
TWI403273B (en) * | 2004-08-06 | 2013-08-01 | Suntory Holdings Ltd | Tea drinks containing amino acids |
US20220248702A1 (en) * | 2021-02-08 | 2022-08-11 | Kodimule Shyam Prasad | Method of making a plant-based protein composition rich in glutamic acid |
-
1985
- 1985-05-27 JP JP60115170A patent/JPS61271969A/en active Pending
Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63126558A (en) * | 1986-11-17 | 1988-05-30 | Nippon Shokubai Kagaku Kogyo Co Ltd | Catalyst for vapor phase intramolecular dehydration reaction of alkanol amines |
JPS63126556A (en) * | 1986-11-17 | 1988-05-30 | Nippon Shokubai Kagaku Kogyo Co Ltd | Catalyst for vapor phase intramolecular dehydration reaction of alkanol amines |
JPS63152945A (en) * | 1986-12-17 | 1988-06-25 | Hikoshige Fujii | Compression formed product of coffee bean |
JPH01196257A (en) * | 1988-01-29 | 1989-08-08 | Ajinomoto General Foods Kk | Method of preventing coffee beverage from becoming turbid |
USRE40594E1 (en) | 1998-12-23 | 2008-12-02 | Mount Sinai School Of Medicine Of New York University | Inhibitors of the bitter taste response |
WO2000038536A3 (en) * | 1998-12-23 | 2000-11-16 | Sinai School Medicine | Inhibitors of the bitter taste response |
US7314716B2 (en) | 1999-11-19 | 2008-01-01 | Mount Sinai School Of Medicine | Gustducin γ subunit materials and methods |
TWI403273B (en) * | 2004-08-06 | 2013-08-01 | Suntory Holdings Ltd | Tea drinks containing amino acids |
JP2006067895A (en) * | 2004-09-02 | 2006-03-16 | Mitsui Norin Co Ltd | Inhibitory agent of bitterness and astringency |
US7455872B2 (en) | 2005-06-20 | 2008-11-25 | Redpoint Bio Corporation | Compositions and methods for producing a salty taste in foods or beverages |
US7452563B2 (en) | 2005-06-20 | 2008-11-18 | Redpoint Bio Corporation | Compositions and methods for producing flavored seasonings that contain reduced quantities of common salt |
EP1836899A1 (en) * | 2006-03-20 | 2007-09-26 | Ito En, Ltd. | Bottleable green tea beverage |
US7972644B2 (en) | 2006-03-22 | 2011-07-05 | Ito En, Ltd. | Bottleable green tea beverage |
WO2009013240A2 (en) * | 2007-07-20 | 2009-01-29 | Dsm Ip Assets B.V. | Foodstuffs with enhanced chocolate taste |
WO2009013240A3 (en) * | 2007-07-20 | 2009-04-02 | Dsm Ip Assets Bv | Foodstuffs with enhanced chocolate taste |
JP2012165659A (en) * | 2011-02-10 | 2012-09-06 | Mitsui Norin Co Ltd | Tea beverage enhanced in deliciousness and reduced in bitterness and astringency |
JP2012179042A (en) * | 2011-02-10 | 2012-09-20 | Mitsui Norin Co Ltd | Nucleotide-containing tea extract and method for producing the same |
JP2012165753A (en) * | 2012-05-01 | 2012-09-06 | Mitsui Norin Co Ltd | Tea beverage enhanced in deliciousness and reduced in bitterness and astringency |
US20220248702A1 (en) * | 2021-02-08 | 2022-08-11 | Kodimule Shyam Prasad | Method of making a plant-based protein composition rich in glutamic acid |
US11957134B2 (en) * | 2021-02-08 | 2024-04-16 | Vidya Herbs, Inc. | Method of making a plant-based protein composition rich in glutamic acid |
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