JPS6049751A - Food composition - Google Patents
Food compositionInfo
- Publication number
- JPS6049751A JPS6049751A JP58157511A JP15751183A JPS6049751A JP S6049751 A JPS6049751 A JP S6049751A JP 58157511 A JP58157511 A JP 58157511A JP 15751183 A JP15751183 A JP 15751183A JP S6049751 A JPS6049751 A JP S6049751A
- Authority
- JP
- Japan
- Prior art keywords
- food composition
- taste
- coffee
- bitter
- food
- 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
Landscapes
- Non-Alcoholic Beverages (AREA)
- Confectionery (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- General Preparation And Processing Of Foods (AREA)
- Seasonings (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、食品組成物に関し、特許、アミノ酸又はペプ
チドを含有する食品組成物の嗜好性を改善し、その摂食
を容易にし、アミノ酸やペプチドに期待した栄養生理効
果の発揮を助長することを目的とするものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to food compositions, which improve the palatability of food compositions containing amino acids or peptides, make them easier to eat, and provide the nutritional and physiological effects expected from amino acids and peptides. The purpose is to encourage the performance of
近年、アミノ酸やペプチドの栄養生理学的効果について
の知見が増大するのに伴い、これを健康の維持増進や、
疾病の予防治療に利用しようとする試みも多くなされる
に至った。In recent years, as knowledge about the nutritional and physiological effects of amino acids and peptides has increased, it has become increasingly important to use them to maintain and improve health.
Many attempts have been made to use it for preventive treatment of diseases.
肝臓病の治療や、大きい負傷や手術を受けた時イソロイ
シン、ロイシン、バリン等を多く投与することがすすめ
られて、おシ、トリットファンを精神安定や、安眠のた
めに利用する試みがあることはその例である。ペプチド
にも特異な生理効果を有するものが多いことが知られて
いるが、タンパク質に代る栄養組材としての役割も見逃
がせない。It is recommended to administer large amounts of isoleucine, leucine, valine, etc. in the treatment of liver disease or when undergoing major injury or surgery, and there are attempts to use oshi and tritophane for mental stability and sleep. is an example. It is known that many peptides have unique physiological effects, but their role as nutritional components in place of proteins cannot be overlooked.
消化能力の弱い疾病患者又は虚弱者に対する栄養補給の
方法として、タンパク質の代シにアミノ酸混合物を以て
栄養補給を行うことは成分栄養法として既に確立してい
る。しかし、コストが安く出来ること、製品の浸透圧を
生体に好ましいレベルにおくものであること、及び多少
とも消化能を有する者にとっては、アミノ酸よシもむし
ろペプチドの方が吸収し易い利点があるとの説があるこ
となどの理由から、近年、タンパク質の部分分解により
調製したペプチドを栄養組材として利用することが活発
に試みられつつある。As a method of nutritional supplementation for sick or infirm patients with weak digestive ability, nutritional supplementation using an amino acid mixture in place of protein has already been established as a component nutrition method. However, peptides have the advantage of being cheaper to produce, the osmotic pressure of the product to be at a level favorable to living organisms, and that peptides are easier to absorb than amino acids for those with some digestive ability. For this reason, in recent years, active attempts have been made to utilize peptides prepared by partial protein decomposition as nutritional ingredients.
これ等の内、アミノ酸の投与は、中心静脈輸液法や末梢
血管への注射法によシ、目的を達し得る場合もあるが、
ペプチドについては、免疫反応のためこの種方法を採る
ことは不可能である。Among these, administration of amino acids can sometimes achieve the purpose by central venous infusion or injection into peripheral blood vessels;
For peptides, this type of method is not possible due to the immune reaction.
輸液、注射などの方法を採シ得る場合でも、それはいわ
ば非日常的な行為であシ、長期継続実施することは困難
である。他の多くの薬剤の如く少量の投与摂取で効果の
発揮されることは期待出来ず、食品成分として日常摂取
されている量に対し有意差をもつ量を摂ることか必要で
あって、上記諸方法によることを更に困難にしている。Even if methods such as infusions and injections are available, they are unconventional activities and difficult to implement on a long-term basis. Unlike many other drugs, it cannot be expected that the effect will be exerted by administering or ingesting a small amount, and it is necessary to take an amount that is significantly different from the amount that is ingested on a daily basis as a food ingredient. This makes it even more difficult to determine the method.
アミノ酸、ペプチドが、重要な栄養素であるタンパク質
の構成成分であるとの本質からみても、食品として、あ
るいは食品に添えられた形で給与することが最も自然で
あシ、長期多量の摂取にも適合した形態であるといえよ
う。Considering the fact that amino acids and peptides are components of protein, which is an important nutrient, it is most natural to provide them as food or as an accompaniment to food. It can be said that it is a suitable form.
しかるに、アミノ酸やペプチドの内には苦味を呈するも
のが多く、食品又は食品に添えた形での摂取に大きい障
害となっていた。However, many amino acids and peptides have a bitter taste, which poses a major obstacle to their ingestion as food or food supplements.
本発明者等は、この問題解決のため種々検討を重ねた結
果、苦味を呈するアミノ酸及び又は苦味を呈するペプチ
ドの1種または2種以上を含有する食品組成物に、カカ
オおよび/またはコーヒーの風味を附与することにより
、苦味に対する抵抗感が著しく低減され、所期の目的が
達成されることを発見し、本発明を完成した。As a result of various studies to solve this problem, the present inventors have discovered that a food composition containing one or more bitter-tasting amino acids and/or bitter-tasting peptides has a cacao and/or coffee flavor. The present invention has been completed based on the discovery that by adding , the resistance to bitterness can be significantly reduced and the intended purpose can be achieved.
これ等風味を有する原食品、チョコレート、コーヒー等
はいずれも本来多少の苦味を呈し、苦味がこれ等食品に
対する本来的な嗜好の一部を成しているため、摂食者も
自然な気持で、苦味を感じつつも摂取出来るようになる
ものと考えられる。All of these flavored raw foods, chocolate, coffee, etc., naturally have a slightly bitter taste, and since bitterness forms part of the natural preference for these foods, consumers naturally feel the same way. It is thought that it will be possible to ingest it even though it tastes bitter.
食生活の西欧化が進んだ今日において、チョコレートや
コーヒーは、ごく普通の日常的な嗜好品として定着して
おp、長期間の連用に対しても[あき」が米にくいこと
も、本発明の方法のすぐれた点である。In today's world, where dietary habits have become more Westernized, chocolate and coffee have become common everyday indulgences. This is an excellent point of this method.
本発明の方法において使用する風味附与物質としては、
カカオおよび/またはコーヒーの風味を呈するものであ
れば、天然物あるいは化学的合成物いずれでも使用出来
る。天然物については、それぞれ原料豆(ビーンズ)か
ら、チョコレート。The flavor imparting substances used in the method of the present invention include:
Any natural or chemically synthesized product can be used as long as it exhibits the flavor of cacao and/or coffee. Regarding natural products, we use raw beans and chocolate.
コーヒーとして市販されている形に至る各段階のもの、
風味成分を抽出したもの、更にそれを加工。Products at each stage leading to the form sold commercially as coffee,
The flavor components are extracted and then further processed.
精製したものに至る迄、使用の実態に合わせて適宜選択
すればよい。Until it reaches a purified product, it may be selected as appropriate depending on the actual situation of use.
風味附与物質の使用量は、製品を摂取する時に、カカオ
、及び/又はコーヒーの風味を有することを感じられる
に足りる量、濃度で使用すれは、本発明の目的は達せら
れる。製品が液体であるか、固体であるか等によって用
量が変動するが、たとえば、市販インスタント・コーヒ
ー粉末又はカカオ粉末を0.2チ添加した時に相当する
か、それ以上の風味の強さを与える程度であればよい。The purpose of the present invention can be achieved as long as the flavoring substance is used in an amount and concentration sufficient to make the product taste like cocoa and/or coffee when ingested. The dosage will vary depending on whether the product is liquid or solid, but will give a flavor intensity equivalent to or greater than, for example, adding 0.2 g of commercially available instant coffee powder or cocoa powder. It is sufficient as long as it is of a certain extent.
好ましくは、食品として摂取する時に1俤ないし30%
となるように添加すればよい。Preferably, 1 to 30% when ingested as food.
It should be added so that
アミノ酸としては、イソロイシン、ロイシン。Amino acids include isoleucine and leucine.
リジン、メチオニン、フ゛エニルアラニン、トリプトフ
ァン、バリン、アルギニン、ヒスチゾン、シトルリン、
オルニチン、fロリン等苦味を呈するアミノ酸が対象に
なる。ペプチドとしては、卵白粉、カゼイン等の動物性
タンパク質や大豆、小麦等の植物性タンパク質を原料と
し、酸や酵素を用いて部分加水分解にょシ調製したペプ
チド、これ等をもとにグラスティン反応にょシ修飾した
もの、アミノ酸モノマーを原料に化合的方法にょシ合成
したものなどが対象となる。投与対象者の条件に応じ、
使用目的にょシこれ等の内から選択使用する。更に使用
目的にまり、上記以外のアミノ酸等を併用することもさ
しつがえない。Lysine, methionine, phenylalanine, tryptophan, valine, arginine, histizone, citrulline,
Amino acids that exhibit a bitter taste, such as ornithine and f-loline, are targeted. Peptides are prepared from animal proteins such as egg white powder and casein, and vegetable proteins such as soybeans and wheat, and are partially hydrolyzed using acids and enzymes. Target products include those that have been modified, and those that have been synthesized using chemical methods using amino acid monomers as raw materials. Depending on the conditions of the recipient,
Select and use from among these depending on the purpose of use. Furthermore, depending on the purpose of use, amino acids other than those mentioned above may also be used in combination.
本発明による食品組成物の製品形態としては、溶液、懸
濁物、粉末、固体成形物等をとシ得、飲料、ムース、ゼ
リー、凍菜、飴、クラッカー、ケーキ、パン等多様であ
シ、これによって本発明が限定されるものではない。The product form of the food composition according to the present invention includes solutions, suspensions, powders, solid molded products, etc., and various forms such as drinks, mousses, jellies, frozen vegetables, candies, crackers, cakes, and breads. However, the present invention is not limited thereby.
このような製品形態に仕上げるため、それぞれの目的に
応じて他の食品原料素材、栄養素成分や呈味料賦形料、
乳化科、保存料等の食品添加物を併せ用いることも可能
である。In order to create such a product form, other food raw materials, nutritional ingredients, flavoring excipients,
It is also possible to use food additives such as emulsifiers and preservatives.
以下、実施例によって本発明を説明する。The present invention will be explained below with reference to Examples.
実施例1
表1に記した諸原料を混合し粉末状の製品とした。ここ
に得られた組成物は、粉体のまま、あるいは水又は温湯
と混練して軟餅状又は粥状とし、あるいは適量の水又は
温湯に懸濁して乳状とし供食したが、いずれも嗜好性良
く摂食出来た。同じ配合でインスタントコーヒーを除き
、バニラ、荀などの香料に代えた時は、(それぞれ適量
使用し、全量が100係に合するように粉糖で調整した
)苦味を強く感じ摂食に対し抵抗が大であった。Example 1 The raw materials listed in Table 1 were mixed to form a powdered product. The composition obtained here was eaten as a powder, or kneaded with water or hot water to form a soft rice cake or gruel, or suspended in an appropriate amount of water or hot water to form an emulsion, but both were edible. I was able to eat well. When using the same formulation but excluding instant coffee and replacing it with flavorings such as vanilla and sage, (using appropriate amounts of each and adjusting with powdered sugar so that the total amount was 100%), the taste was stronger and the patient resisted feeding. was large.
表1 食品組成物配合例 L−インロイシン 4.5チ L−ロイシン 4.0 L−バリン 2.0 L−アルギニン 4.0 卵白粉 58.0 コーンサラダ油 3.5 粉末クリーム 20.0 粉 糖 io、。Table 1 Food composition formulation example L-inleucine 4.5ch L-leucine 4.0 L-valine 2.0 L-arginine 4.0 Egg white powder 58.0 Corn salad oil 3.5 Powder cream 20.0 Powdered sugar io.
インスタントコーヒー 2.0
実施例2
カカオバター20gとカカオマス320,9.!=を6
0℃でニーグーにより混合した。得られた混合物に砂糖
395gを加え同じく60℃でニーグーによシ充分に混
合した。混合を尚続行しつつレシチン5g、カカオバタ
ー60g、L−イソロイシン45g、L−oイン:y4
01.L−パリ:/24gを順次加え、混練を続行した
。操作開始より24練
時間混線の続いたところで混−しつつ混合物を徐冷して
品温を28〜30℃に至らしめこの状態で2時間混練し
た。ついで品温をやや上昇させ31〜32℃に保って1
時間混練した。Instant coffee 2.0 Example 2 20g of cocoa butter and 320.9% of cocoa mass. ! = 6
Mixing was carried out using a niegu at 0°C. 395 g of sugar was added to the resulting mixture, and the mixture was thoroughly mixed at 60°C. While still mixing, add 5 g of lecithin, 60 g of cocoa butter, 45 g of L-isoleucine, L-in:y4
01. 24 g of L-Paris was added one after another and kneading was continued. After 24 hours of kneading from the start of the operation, the mixture was gradually cooled to a temperature of 28 to 30° C. and kneaded in this state for 2 hours. Next, raise the temperature of the product slightly and keep it at 31-32℃.
Kneaded for hours.
得られた混合物を型入れ一冷却して短棒(パー)状に成
形した。The resulting mixture was placed in a mold, cooled, and shaped into a short bar.
以上の工程によシ、市販のプラックチョコレートに類似
した外形食感、風味を有する製品が得られ、アミノ酸特
有の苦味は殆ど感じられなかった。Through the above steps, a product was obtained that had an external appearance, texture, and flavor similar to commercially available plaque chocolate, and the bitterness characteristic of amino acids was hardly felt.
実施例3 表−2に示す配合で常法によりキャラメルを試作した。Example 3 Caramel was trial-produced using the formulation shown in Table 2 using a conventional method.
表−2キャラメルの配合
サンプルA * B * Cについて、io名のパネル
に味覚テストを行なった。io点満点による平均点を表
−3に示した。Table 2: Caramel composition samples A*B*C were subjected to a taste test on a panel of io names. Table 3 shows the average score based on the io perfect score.
各試料間の5%有意差R=0.81
サングルAはアミノ酸特有の苦味がストレートに出て評
価は非常に低いが、コーヒー粉末、カカオ粉末を添加し
たものは、それらの風味によってアミノ酸の苦味がマス
キングされるため評価は高くなったO
実施例4
市販カゼイン(カゼイン・ナトリウムの形のもの)10
0.9を2tの水に溶解させ、水酸化ナトリウム溶液に
よJ pHを6.0に調整し、市販の・9ノ母イン(1
■当り0.00357ンソン単位の活性のもの)2gを
添7x+ L、40℃に24〜48時間保持した。この
保持時間中、適宜反応液の一部少量を取り、これに、終
濃度で0.2Mになるようト1ノクロロ酢酸を添加し、
沈澱生成の有無を観察して、反応の終点を探った。5% significant difference between each sample R = 0.81 Sangru A has a very low evaluation because the bitterness peculiar to amino acids comes out directly, but the ones with coffee powder and cacao powder added have the bitterness of amino acids due to their flavor. The evaluation was high because O was masked. Example 4 Commercially available casein (in the form of sodium casein) 10
0.9 was dissolved in 2 tons of water, the pH was adjusted to 6.0 with sodium hydroxide solution, and commercially available
2 g of 0.00357 units of activity per 1) was added to 7x+L and kept at 40°C for 24 to 48 hours. During this holding time, take a small portion of the reaction solution as appropriate, add 1-chloroacetic acid to the final concentration of 0.2M,
The end point of the reaction was determined by observing the presence or absence of precipitate formation.
上記の検査法で、沈澱が生じなくなった時点で、保温保
持中の反応液を100℃5分間加熱して、パ/J?イン
を失活させ反応を止めた。次いで、12.000 G
(10,00ORPM )の遠心分離・機によシ、不溶
性物質を除去し、得られた上清を凍結乾燥した。According to the above test method, when no precipitate is formed, the reaction solution that is being kept warm is heated to 100°C for 5 minutes, and Pa/J? The reaction was stopped by inactivating the in. Then 12.000 G
(10,00 ORPM) to remove insoluble substances, and the resulting supernatant was freeze-dried.
以上の処理によシタンパク質(カゼイン)の部分氷解物
、すなわちペグチド混合物82gが得られた。この物は
、単独ではかなシ強い苦味を有し、摂食にはかなりの抵
抗を覚えさせるものでちった。Through the above treatment, 82 g of a partially thawed protein (casein), ie, a pegutide mixture, was obtained. When taken alone, this substance had a very strong bitter taste and made me feel quite reluctant to eat it.
更に本イゾチド混合物40.9に蔗糖20g、インスタ
ント・コーヒー粉末5g1粉末クリーム20g、デキス
) IJン15&を混合して得た粉末は粉末のまま、あ
るいは、水に混じ餅状あるいは粥状として摂食すると、
嗜好性良く摂食出来た。Furthermore, the powder obtained by mixing the present isotide mixture 40.9 with 20 g of sucrose, 5 g of instant coffee powder, 20 g of powdered cream, and dextrose) can be eaten as a powder or mixed with water in the form of a rice cake or porridge. Then,
I was able to eat it with good taste.
この際インスタント・コーヒー粉末に代えてバニラ、レ
モン等のフレーバーを用いた時(それぞれ適量配合し、
全量が100gとなるようガキストリンで調整した)は
原ペグチド混合物に比しかなりの味の改良は認められた
が、コーヒーを用いた例には及ばなかった。At this time, when using flavors such as vanilla and lemon instead of instant coffee powder (mix appropriate amounts of each,
(adjusted with gakistrin so that the total amount was 100 g) was found to be considerably improved in taste compared to the original pegtide mixture, but it was not as good as the example using coffee.
実施例5
市販ラクトアルブミン100Iを21!の水に溶解させ
、塩酸を用いてPllを2,5に調整した。これに市販
のペゾシン製剤(1〜当り0.001アンソン単位の活
性のもの)を2I添加し、40℃で24〜48時間保温
保持した。Example 5 Commercially available lactalbumin 100I was added to 21! of water, and the Pll was adjusted to 2.5 using hydrochloric acid. To this was added 2 I of a commercially available Pezocin preparation (activity of 0.001 Anson unit per unit), and the mixture was kept at 40° C. for 24 to 48 hours.
以下、実施例4に於けると同様の方法で、反応の終点の
検出、酵素反応の停止を行い、水酸化ナトリウムを用い
て反応液のPIlをほぼ中性にもどし、遠心分離、凍結
乾燥を行ってペゾチド混合製品を得た。Thereafter, in the same manner as in Example 4, the end point of the reaction was detected, the enzyme reaction was stopped, the PIl of the reaction solution was returned to almost neutrality using sodium hydroxide, centrifugation, and freeze-drying were carried out. and obtained a pezotide mixed product.
この椰品も、同じくかなυの苦味を示したが、実施例4
に於ると同様な混合物としてコーヒーフレバーを与える
ことにより、苦味を嫌味として感じない嗜好性の良い食
品組成物を得ることが出来たO
特許出願人 味の素株式会社This coconut product also showed the same bitterness of kana υ, but Example 4
By adding coffee flavor as a mixture similar to that used in the above patent, it was possible to obtain a food composition with good palatability in which bitterness is not perceived as an unpleasant taste. Patent applicant: Ajinomoto Co., Inc.
Claims (3)
の1種または2種以上を含有し、且つカカオおよび/ま
たはコーヒーの風味が附与されていることを特徴とする
食品組成物。(1) A food composition characterized in that it contains one or more types of bitter-tasting amino acids or bitter-tasting peptides, and is flavored with cacao and/or coffee.
シン、リシン、メチオニン、フェニルアラニン、トリッ
トファン、バリン、アルプニン、ヒスチジン、シトルリ
ン、オルニチン、プロリンよシ成る群よシ選ばれた1種
または2種以上である特許請求の範囲第(1)項記載の
食品組成物。(2) One or more amino acids selected from the group consisting of inleucine, lysine, methionine, phenylalanine, tritophane, valine, alpnin, histidine, citrulline, ornithine, and proline, which exhibit bitter potassium. The food composition according to claim (1).
は酵素によって部分水解することによって得られたペプ
チドである特許請求の範囲第(1)項記載の食品組成物
。(3) The food composition according to claim (1), wherein the peptide exhibiting a bitter taste is a peptide obtained by partial hydrolysis with tongue/matric acid or an enzyme.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58157511A JPS6049751A (en) | 1983-08-29 | 1983-08-29 | Food composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58157511A JPS6049751A (en) | 1983-08-29 | 1983-08-29 | Food composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6049751A true JPS6049751A (en) | 1985-03-19 |
JPH0347829B2 JPH0347829B2 (en) | 1991-07-22 |
Family
ID=15651273
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58157511A Granted JPS6049751A (en) | 1983-08-29 | 1983-08-29 | Food composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6049751A (en) |
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02128669A (en) * | 1988-11-08 | 1990-05-17 | Ajinomoto Co Inc | Amino acid-containing food composition |
JPH02128670A (en) * | 1988-11-08 | 1990-05-17 | Ajinomoto Co Inc | Amino acid-containing food composition |
JPH02142449A (en) * | 1988-10-11 | 1990-05-31 | Holgates Nutritional Foods Ltd | Edible composition |
JPH04235136A (en) * | 1991-01-08 | 1992-08-24 | Kibun Foods Inc | Method for reducing bitterness and composition for reducing bitterness |
JPH04346937A (en) * | 1991-05-24 | 1992-12-02 | Kibun Foods Inc | Reduction of bitterness |
US6063432A (en) * | 1998-05-19 | 2000-05-16 | Cooke Pharma | Arginine or lysine containing fruit healthbar formulation |
JP2001226293A (en) * | 2000-02-17 | 2001-08-21 | Kotaro Kanpo Seiyaku Kk | Taking assisting agent |
WO2002030416A1 (en) * | 2000-10-10 | 2002-04-18 | Ajinomoto Co., Inc. | Medicinal suspensions containing branched amino acids |
WO2002030417A1 (en) * | 2000-10-10 | 2002-04-18 | Ajinomoto Co., Inc. | Medicinal suspensions containing branched amino acids |
WO2004052125A1 (en) * | 2002-12-06 | 2004-06-24 | Kyowa Hakko Kogyo Co., Ltd. | Beverage containing amino acid and method of diminishing bitterness of amino acid |
US6805883B2 (en) | 1998-03-12 | 2004-10-19 | Mars, Incorporated | Food products containing polyphenol(s) and L-arginine to stimulate nitric oxide |
JP2005272410A (en) * | 2004-03-26 | 2005-10-06 | Ajinomoto Co Inc | Oral amino acid composition for anti-arteriosclerotic and/or blood rheology improving use |
JP2007077173A (en) * | 2006-12-25 | 2007-03-29 | Ajinomoto Co Inc | Suspension for medicine, containing branched amino acid |
CN100358435C (en) * | 1998-03-12 | 2008-01-02 | 马尔斯公司 | Products containing polyphenol(S) and L-arginine to stimulate nitric oxide production |
JP2010148453A (en) * | 2008-12-25 | 2010-07-08 | Suntory Holdings Ltd | Bitterness masking agent for chlorogenic acid |
US8507018B2 (en) | 1998-03-12 | 2013-08-13 | Mars, Incorporated | Products containing polyphenol(s) and L-arginine and methods of use thereof |
JP5355395B2 (en) * | 2007-06-13 | 2013-11-27 | 大塚製薬株式会社 | Equol-containing extract and method for producing the same, equol extraction method, and food containing equol |
WO2014157696A1 (en) * | 2013-03-29 | 2014-10-02 | 株式会社カネカ | Protease-containing dough for bread or confectionery |
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JP6227304B2 (en) * | 2013-07-04 | 2017-11-08 | キリン株式会社 | Ornithine or salt derived masking method |
JP6951835B2 (en) * | 2016-06-02 | 2021-10-20 | キリンホールディングス株式会社 | Beer-taste beverage with reduced miscellaneous taste |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52110873A (en) * | 1976-03-11 | 1977-09-17 | Hasegawa Co Ltd | Coffee taste substance having coffee like flavor |
JPS52117470A (en) * | 1976-03-29 | 1977-10-01 | Gen Foods Corp | Antagonist substance against caffeine |
JPS5331943A (en) * | 1976-09-06 | 1978-03-25 | Nec Corp | Monostable multiple vibrator |
JPS5417014A (en) * | 1977-07-06 | 1979-02-08 | Nec Corp | Radiation sensitive composite |
JPS55135546A (en) * | 1979-04-12 | 1980-10-22 | Meiji Seika Kaisha Ltd | Production of cocoa powder |
-
1983
- 1983-08-29 JP JP58157511A patent/JPS6049751A/en active Granted
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52110873A (en) * | 1976-03-11 | 1977-09-17 | Hasegawa Co Ltd | Coffee taste substance having coffee like flavor |
JPS52117470A (en) * | 1976-03-29 | 1977-10-01 | Gen Foods Corp | Antagonist substance against caffeine |
JPS5331943A (en) * | 1976-09-06 | 1978-03-25 | Nec Corp | Monostable multiple vibrator |
JPS5417014A (en) * | 1977-07-06 | 1979-02-08 | Nec Corp | Radiation sensitive composite |
JPS55135546A (en) * | 1979-04-12 | 1980-10-22 | Meiji Seika Kaisha Ltd | Production of cocoa powder |
Cited By (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02142449A (en) * | 1988-10-11 | 1990-05-31 | Holgates Nutritional Foods Ltd | Edible composition |
JPH02128669A (en) * | 1988-11-08 | 1990-05-17 | Ajinomoto Co Inc | Amino acid-containing food composition |
JPH02128670A (en) * | 1988-11-08 | 1990-05-17 | Ajinomoto Co Inc | Amino acid-containing food composition |
JP2522367B2 (en) * | 1988-11-08 | 1996-08-07 | 味の素株式会社 | Amino acid-containing food composition |
JPH04235136A (en) * | 1991-01-08 | 1992-08-24 | Kibun Foods Inc | Method for reducing bitterness and composition for reducing bitterness |
JP2508547B2 (en) * | 1991-01-08 | 1996-06-19 | 株式会社紀文食品 | Bitterness reduction method and bitterness reduction composition |
JPH04346937A (en) * | 1991-05-24 | 1992-12-02 | Kibun Foods Inc | Reduction of bitterness |
JP2508555B2 (en) * | 1991-05-24 | 1996-06-19 | 株式会社紀文食品 | Bitterness reduction method |
US8715749B2 (en) | 1998-03-12 | 2014-05-06 | Mars, Incorporated | Products containing polyphenol(s) and L-arginine |
US8507018B2 (en) | 1998-03-12 | 2013-08-13 | Mars, Incorporated | Products containing polyphenol(s) and L-arginine and methods of use thereof |
US6805883B2 (en) | 1998-03-12 | 2004-10-19 | Mars, Incorporated | Food products containing polyphenol(s) and L-arginine to stimulate nitric oxide |
CN100358435C (en) * | 1998-03-12 | 2008-01-02 | 马尔斯公司 | Products containing polyphenol(S) and L-arginine to stimulate nitric oxide production |
US6063432A (en) * | 1998-05-19 | 2000-05-16 | Cooke Pharma | Arginine or lysine containing fruit healthbar formulation |
JP2001226293A (en) * | 2000-02-17 | 2001-08-21 | Kotaro Kanpo Seiyaku Kk | Taking assisting agent |
WO2002030416A1 (en) * | 2000-10-10 | 2002-04-18 | Ajinomoto Co., Inc. | Medicinal suspensions containing branched amino acids |
WO2002030417A1 (en) * | 2000-10-10 | 2002-04-18 | Ajinomoto Co., Inc. | Medicinal suspensions containing branched amino acids |
WO2004052125A1 (en) * | 2002-12-06 | 2004-06-24 | Kyowa Hakko Kogyo Co., Ltd. | Beverage containing amino acid and method of diminishing bitterness of amino acid |
CN100399948C (en) * | 2002-12-06 | 2008-07-09 | 协和发酵工业株式会社 | Beverage containing amino acid and method of diminishing bitterness of amino acid |
JP2005272410A (en) * | 2004-03-26 | 2005-10-06 | Ajinomoto Co Inc | Oral amino acid composition for anti-arteriosclerotic and/or blood rheology improving use |
JP2007077173A (en) * | 2006-12-25 | 2007-03-29 | Ajinomoto Co Inc | Suspension for medicine, containing branched amino acid |
JP5355395B2 (en) * | 2007-06-13 | 2013-11-27 | 大塚製薬株式会社 | Equol-containing extract and method for producing the same, equol extraction method, and food containing equol |
US8900645B2 (en) | 2007-06-13 | 2014-12-02 | Otsuka Pharmaceuticals Co., Ltd. | Equol-containing extract, method for production thereof, method for extraction of equol, and equol-containing food |
US8993014B2 (en) | 2007-06-13 | 2015-03-31 | Otsuka Pharmaceutical Co., Ltd. | Equol-containing extract, method for production thereof, method for extraction of equol, and equol-containing food |
US9192185B2 (en) | 2007-06-13 | 2015-11-24 | Otsuka Pharmaceutical Co., Ltd. | Equol-containing extract, method for production thereof, method for extraction of equol, and equol-containing food |
US10681930B2 (en) | 2007-06-13 | 2020-06-16 | Otsuka Pharmaceutical Co., Ltd. | Equol-containing extract, method for production thereof, method for extraction of equol, and equol-containing food |
JP2023182687A (en) * | 2007-06-13 | 2023-12-26 | 大塚製薬株式会社 | Equol-containing extract, method for production thereof, method for extraction of equol, and equol-containing food |
JP2010148453A (en) * | 2008-12-25 | 2010-07-08 | Suntory Holdings Ltd | Bitterness masking agent for chlorogenic acid |
WO2014157696A1 (en) * | 2013-03-29 | 2014-10-02 | 株式会社カネカ | Protease-containing dough for bread or confectionery |
JPWO2014157696A1 (en) * | 2013-03-29 | 2017-02-16 | 株式会社カネカ | Bread / confectionery dough containing protease |
Also Published As
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JPH0347829B2 (en) | 1991-07-22 |
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