JPS5948974B2 - Method for producing aroma composition - Google Patents
Method for producing aroma compositionInfo
- Publication number
- JPS5948974B2 JPS5948974B2 JP52108290A JP10829077A JPS5948974B2 JP S5948974 B2 JPS5948974 B2 JP S5948974B2 JP 52108290 A JP52108290 A JP 52108290A JP 10829077 A JP10829077 A JP 10829077A JP S5948974 B2 JPS5948974 B2 JP S5948974B2
- Authority
- JP
- Japan
- Prior art keywords
- aroma
- lecithin
- reaction
- aroma composition
- weight
- 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
Links
Landscapes
- Seasonings (AREA)
- Fats And Perfumes (AREA)
Description
【発明の詳細な説明】
本発明はアーモンド様乃至カステラ様香気組成物の製法
に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing an almond-like to castella-like aroma composition.
従来、アミノ酸と糖類との加燃反応、いわゆるアミノ−
カルボニル反応を利用して飲食品の香気改良や増強させ
る試みが種々検討され米菓、しょうゆ、チョコレー1〜
等の賦香あるいは魚肉練製品の矯臭に一部実用化されて
いる。Conventionally, the combustion reaction between amino acids and sugars, the so-called amino-
Various attempts have been made to improve and enhance the aroma of foods and drinks using carbonyl reactions, including rice crackers, soy sauce, and chocolate.
It has been partially put into practical use for flavoring products such as fish paste and for flavoring fish paste products.
しかしながらアミノ−カルボニル反応は別名褐変反応と
も呼ばれており、その生成物は著しく着色しているため
、利用可能な飲食品が限定される難点があった。However, the amino-carbonyl reaction is also called a browning reaction, and the product is extremely colored, which has the disadvantage that the food and drink products that can be used for it are limited.
またこの反応は非常にテ゛リゲートな反応であり、アミ
ノ酸や糖の種類、混合比、量、および反応状性(温度、
時間、pH等)によっては生成する香気の質や量が異な
ったり、反応時には好ましい香気であっても経時的に消
失したり、あるいは飲食品成分と反応して好ましくない
香気に変化したりして使用法が非常に難しい難点もあっ
た。In addition, this reaction is a very dependent reaction, and the types of amino acids and sugars, mixing ratios, amounts, and reaction conditions (temperature,
The quality and quantity of the aroma produced may differ depending on the time, pH, etc., and even if the aroma is favorable at the time of reaction, it may disappear over time, or it may change to an unfavorable aroma due to reaction with food and beverage components. It also had the disadvantage that it was very difficult to use.
本発明者等は種々研究を重ねた結果、リジンもしくはア
ルギニンまたはそれらの塩酸塩と糖類とをレシチンの存
在下に加熱反応させるようにすれば、着色度の少なく、
経時的にも安定なアーモンド様乃至カステラ様香気組成
物が得られることを見出し、従来のアミノ−カルボニル
反応における難点を著しく改良し得ることが判った。As a result of various studies, the present inventors have found that if lysine or arginine or their hydrochloride and saccharide are heated and reacted in the presence of lecithin, the degree of coloration will be reduced and the coloring will be reduced.
It has been found that an almond-like or castella-like aroma composition that is stable over time can be obtained, and that the difficulties in conventional amino-carbonyl reactions can be significantly improved.
すなわち、本発明によれば、アーモンド様乃至カステラ
様香気組成物はリジンもしくはアルギニンまたはそれら
の塩酸塩と糖類とをレシチンの存在下に加熱反応させる
ことにより製することが出来る。That is, according to the present invention, an almond-like or castella-like aroma composition can be produced by subjecting lysine or arginine or their hydrochloride salts to a saccharide and a saccharide in the presence of lecithin.
本発明において、アーモンド様乃至カステラ様香気組成
物の製造に用いるアミノ酸としてはリジン、リジン塩酸
塩、アルギニン、アルギニン塩酸塩等があげられ、これ
らのアミノ酸は光学活性体であっても光学的に不活性な
ラセミ体であってもよい。In the present invention, the amino acids used for producing the almond-like or castella-like aroma composition include lysine, lysine hydrochloride, arginine, arginine hydrochloride, etc. Even if these amino acids are optically active forms, they are optically inactive. It may also be an active racemate.
しかし上記と同じ塩基性アミノ酸の一つであるヒスチジ
ンおよびその塩酸塩の場合は生成する香気が不安定で経
時的に消失したり、また好ましいものではなかった。However, in the case of histidine, which is one of the basic amino acids mentioned above, and its hydrochloride, the produced aroma was unstable and disappeared over time, and was not desirable.
また糖類としては、例えばグルコース、フラグ1〜−ス
、キシロースの如き単糖類、シュークロースの如き多糖
類等が上げられ、これらの糖類をいずれも好適に用いる
ことが出来るが、経済的にはグルコース、シュークロー
ス等が適当である。Examples of saccharides include monosaccharides such as glucose, flag-1--xylose, and polysaccharides such as sucrose, and any of these saccharides can be suitably used, but economically, glucose , sucrose, etc. are suitable.
また上記アミノ酸と糖類との加熱反応系に存在させるレ
シチンとしては卵、大豆等から抽出されるものをいずれ
も好適に用いることが出来るが、これらのレシチンの構
成成分であるコリンおよびオレイン酸を存在させても、
また同ヒリン脂質であるケファリンを存在させても香気
の改良効果は認められなかった。In addition, lecithin extracted from eggs, soybeans, etc. can be suitably used as the lecithin to be present in the heating reaction system of the amino acids and sugars, but choline and oleic acid, which are the constituent components of these lecithins, are present. Even if I let you,
Furthermore, even when cephalin, a phospholipid, was present, no improvement in aroma was observed.
本発明において、上記アミノ酸と糖類との混合割合は如
何なる割合であってもよいが、とりわけアミノ酸1重量
部に対して糖類を約0.5〜2重量部程度とするのが好
ましい。In the present invention, the mixing ratio of the amino acid and saccharide may be any ratio, but it is particularly preferable that the amount of saccharide is approximately 0.5 to 2 parts by weight per 1 part by weight of the amino acid.
また存在させるレシチンの使用量も特に限定はないが、
とりわけアミノ酸1重量部に対して約0.1〜0.5重
量部程度であるのが適当である。There is also no particular limitation on the amount of lecithin used, but
In particular, it is appropriate that the amount is about 0.1 to 0.5 parts by weight per 1 part by weight of the amino acid.
また上記アミノ酸の塩酸塩を用いる場合には、重曹を該
塩酸塩1重量部に対して1重量部程度使用すれば、香気
の生成に好結果を期待することが出来る。In addition, when using the hydrochloride of the above-mentioned amino acid, good results can be expected in aroma production by using about 1 part by weight of baking soda per 1 part by weight of the hydrochloride.
加熱反応は、例えば上記アミノ酸、糖類およびレシチン
の混合物を加熱して実施するとよく、加熱温度は概ね1
00〜230℃であればよいが、特に150〜200℃
附近にあるのが好ましい。The heating reaction is preferably carried out by heating the above-mentioned mixture of amino acids, saccharides and lecithin, and the heating temperature is approximately 1.
00~230℃, especially 150~200℃
Preferably nearby.
また加熱時間はそれ稈長時間を必要とせず、概ね2〜1
0分間程度もあれば充分である。In addition, the heating time does not require a long time, and is approximately 2 to 1
Approximately 0 minutes is sufficient.
かくして香気組成物は反応液中に生成してくるが、該香
気組成物は取り出すことなくその反応物のまま対象とす
る飲食品に適当な割合で混合使用すればよい。Thus, the aroma composition is generated in the reaction solution, but the aroma composition may be mixed and used in the target food/beverage product in an appropriate ratio without being taken out.
尚、上記方法において、リジンもしくはその塩酸塩と糖
類とを組合せた場合にはカステラ様香気組成物が得られ
、アルギニンもしくはその塩酸塩と糖類とを組合せた場
合にはアーモンド様香気組成物が得られる。In the above method, when lysine or its hydrochloride and saccharide are combined, a castella-like aroma composition is obtained, and when arginine or its hydrochloride and saccharide are combined, an almond-like aroma composition is obtained. It will be done.
本発明方法により得られた香気組成物は着色が少なく、
甘味をおびた好ましいアーモンド様もしくはカステラ様
の香気を有し、またその香気は経済的に好ましくない香
気に変わることがなく安定であった。The aroma composition obtained by the method of the present invention has little coloring,
It had a pleasant almond-like or castella-like aroma with a sweet taste, and the aroma was stable without changing to an economically undesirable aroma.
このようなことは従来のアミノ−カルボニル反応を利用
した香気物質には認められなかったことであり、加熱反
応系に存在させるレシチンが香気組成物の経済的な安定
化に寄与しているものと推定される。This has not been observed in conventional aroma substances that utilize amino-carbonyl reactions, and it appears that lecithin present in the heating reaction system contributes to the economical stability of the aroma composition. Presumed.
実験例 1
下記第1表に示すアミノ酸、糖類およびレシチンの混合
物を加熱反応させた。Experimental Example 1 A mixture of amino acids, saccharides and lecithin shown in Table 1 below was heated and reacted.
また上記加熱反応においてレシチンを非存在の場合、レ
シチンに代えてコリン、オレイン酸もしくはケファリン
を存在させた場合、およびヒスチジンを用いた場合をそ
れぞれ対照とした。Further, in the heating reaction, the cases where lecithin was not present, the case where choline, oleic acid, or cephalin was present in place of lecithin, and the case where histidine was used were used as controls.
反応直後生成した香気組成物の香気について官能検査を
行なうと共に、それらの香気組成物を密閉容器中−20
℃で1ケ月間保持したのち上記同様に官能検査を行なっ
た。A sensory test was conducted on the aroma of the aroma compositions produced immediately after the reaction, and the aroma compositions were placed in a closed container at -20°C.
After being kept at ℃ for one month, a sensory test was conducted in the same manner as above.
それらの結果は第1表に示す通りであった。The results are shown in Table 1.
実施例 1
リジン塩酸塩1重量部、グルコース1重量部、レシチン
0.2重量部および重曹1重量部を約180℃にて5分
間かくはんする。Example 1 1 part by weight of lysine hydrochloride, 1 part by weight of glucose, 0.2 part by weight of lecithin and 1 part by weight of sodium bicarbonate are stirred at about 180° C. for 5 minutes.
反応後反応物を急激に冷却することにより、カステラ様
香気を有する粉末を得る。After the reaction, the reactant is rapidly cooled to obtain a powder having a castella-like odor.
カステラの製造に際し、本品を少量その原料に添加した
ところ、カステラの風味が著しく向上したことが認めら
れた。When a small amount of this product was added to the raw materials for making castella, it was observed that the flavor of castella was significantly improved.
実施例 2
アルギニン1重量部、キシロース0.8重量部およびレ
シチン0.3重量部を約190℃にて5分間かくはんし
、冷却することにより、アーモンド様香気を有する粉末
を得る。Example 2 1 part by weight of arginine, 0.8 parts by weight of xylose and 0.3 parts by weight of lecithin are stirred at about 190° C. for 5 minutes and cooled to obtain a powder having an almond-like aroma.
本品を焼上り直後のクツキーの表面に少量塗布したとこ
ろ、クツキーの風味が著しく向上し、1週間後において
も風味の低下は認められなかった。When a small amount of this product was applied to the surface of kutsky immediately after baking, the flavor of the kutsky was significantly improved, and no deterioration in flavor was observed even after one week.
Claims (1)
糖類とをレシチンの存在下に加熱反応させることを特徴
とするアーモンド様乃至カステラ様香気組成物の製法。1. A method for producing an almond-like or castella-like aroma composition, which comprises subjecting lysine or arginine or their hydrochloride salts to a saccharide in the presence of lecithin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP52108290A JPS5948974B2 (en) | 1977-09-07 | 1977-09-07 | Method for producing aroma composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP52108290A JPS5948974B2 (en) | 1977-09-07 | 1977-09-07 | Method for producing aroma composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5441338A JPS5441338A (en) | 1979-04-02 |
JPS5948974B2 true JPS5948974B2 (en) | 1984-11-30 |
Family
ID=14480912
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP52108290A Expired JPS5948974B2 (en) | 1977-09-07 | 1977-09-07 | Method for producing aroma composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5948974B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20190003986A1 (en) * | 2015-12-24 | 2019-01-03 | Posco | Pinhole or hole detection device and method |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5075061A (en) * | 1973-11-01 | 1975-06-20 |
-
1977
- 1977-09-07 JP JP52108290A patent/JPS5948974B2/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20190003986A1 (en) * | 2015-12-24 | 2019-01-03 | Posco | Pinhole or hole detection device and method |
Also Published As
Publication number | Publication date |
---|---|
JPS5441338A (en) | 1979-04-02 |
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