JPH10316992A - Preparation of natural vanilla aroma - Google Patents

Preparation of natural vanilla aroma

Info

Publication number
JPH10316992A
JPH10316992A JP9129321A JP12932197A JPH10316992A JP H10316992 A JPH10316992 A JP H10316992A JP 9129321 A JP9129321 A JP 9129321A JP 12932197 A JP12932197 A JP 12932197A JP H10316992 A JPH10316992 A JP H10316992A
Authority
JP
Japan
Prior art keywords
vanilla
organic solvent
hydrophilic organic
extract
tannase
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
Application number
JP9129321A
Other languages
Japanese (ja)
Other versions
JP3471561B2 (en
Inventor
Makoto Takahashi
誠 高橋
Hideko Hirai
秀子 平井
Satoru Shiraishi
悟 白石
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 JP12932197A priority Critical patent/JP3471561B2/en
Publication of JPH10316992A publication Critical patent/JPH10316992A/en
Application granted granted Critical
Publication of JP3471561B2 publication Critical patent/JP3471561B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain a Vanilla aroma which has improved fragrance and flavor and is free of grassy, astringent, or harsh smell, which is characteristic of Vanilla Bean, by providing an extract of Vanilla Bean with a hydrophilic organic solvent and treating the extract with β-glucosidase and tannase. SOLUTION: Some pieces of Vanilla Bean which have been cut into a length of about 0.2 to 2.0 cm are mixed with equal to 5 times amount of a mixture of a hydrophilic organic solvent and water in a ratio of 3:7 to 8:2, and subjected to extraction under stirring or refluxing at 20 to 90 deg.C for 1 to 6 hr. The resulting mixture is subjected to solid-liquid separation by centrifugal separation or the like, and the obtained liquid portion is concentrated by removing the hydrophilic organic solvent to provide an extract of Vanilla Bean with a hydrophilic organic solvent. Then, 100 pts.wt. of the extract is mixed with 0.01 to 2.0 pts.wt. of β-glucosidase and subjected to treating at a pH of 4.0 to 8.0 at 30 to 60 deg.C for 8 to 48 hr, and thereafter, is mixed with 0.01 to 2.0 pts.wt. of tannase and subjected to treating at a pH of 4.0 to 8.0 at 30 to 60 deg.C for 1 to 3 hr. The resulting mixture is heated at 80 to 95 deg.C for 5 min to 1 hr, thereby deactivating the enzymes.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、天然バニラ香料の
製造方法、詳しくは、バニラ青莢(greenvani
lla pods)の親水性有機溶媒抽出物を、酵素で
処理することを特徴とする天然バニラ香料の製造方法に
関する。
TECHNICAL FIELD The present invention relates to a method for producing a natural vanilla flavor, and more particularly, to a green vanilla pod.
The present invention relates to a method for producing a natural vanilla fragrance, which comprises treating an extract of a hydrophilic organic solvent (Ila pods) with an enzyme.

【0002】[0002]

【従来の技術】バニラ香料は、古くから、飲食品に対し
て、広く利用されている重要な香料の一種であり、バニ
ラ青莢から得られる天然バニラ香料と香料成分を化学的
に合成した合成バニラ香料とがある。天然バニラ香料
は、通常、キュアリング工程と呼ばれる工程、すなわ
ち、収穫直後のバニラ青莢を加温して、バニラ青莢自体
がもつ酵素の活性を高め、その酵素の働きにより熟成を
促進させた後、乾燥する工程、を経たバニラビーンズ
を、各種有機溶媒で抽出処理したバニラエキストラクト
等の形で市場に供給されている。
2. Description of the Related Art Vanilla fragrance is one of important fragrances widely used for foods and drinks since ancient times, and is obtained by chemically synthesizing a natural vanilla fragrance obtained from a vanilla blue pod and a fragrance component. There is vanilla flavoring. The natural vanilla flavoring is usually called a curing step, i.e., heating the vanilla blue pods immediately after harvesting, increasing the activity of the enzymes possessed by the vanilla blue pods themselves, and promoting the ripening by the action of the enzymes. After that, the dried vanilla beans are supplied to the market in the form of vanilla extract or the like obtained by extracting with various organic solvents.

【0003】しかしながら、キュアリング工程は、通
常、約9カ月以上を要する、手数のかかる工程であるた
め、この工程を経て得られる天然バニラ香料はコスト高
となる。また、キュアリング工程中の長期間にわたる温
度等の管理状態によって、品質等にバラツキが生ずると
いう問題もあった。
[0003] However, the curing step is a tedious step that usually takes about 9 months or more, and the natural vanilla flavor obtained through this step is costly. There is also a problem that quality and the like vary depending on a long-term management state such as a temperature during the curing process.

【0004】そこで、上記問題点を解決するため、キュ
アリング工程が不要な天然バニラ香料の製造方法、具体
的には、植物細胞の膜組織を破壊し、グルコシドを加水
分解することのできる酵素系、特にβ−グルコシダーゼ
活性を有する酵素系によって、バニラ青莢の粉砕物を処
理することを特徴とする天然バニラ香料の製造方法(特
表平6−502685号公報参照)が提案されている。
Therefore, in order to solve the above problems, a method for producing a natural vanilla fragrance which does not require a curing step, specifically, an enzyme system which can destroy the membrane tissue of plant cells and hydrolyze glucosides In particular, there has been proposed a method for producing a natural vanilla flavor, which comprises treating a ground vanilla green pod with an enzyme system having β-glucosidase activity (see Japanese Patent Application Laid-Open No. 6-502687).

【0005】[0005]

【発明が解決しようとする課題】しかしながら、上記公
報で提案されている天然バニラ香料の製造方法は、従来
の製造方法の欠点である、長期間のキュアリング工程に
よるコスト高および品質のバラツキの解消という点では
優れているが、上記方法で得られる天然バニラ香料に
は、バニラ青莢特有の青臭さ、渋み、エグ味が残るた
め、必ずしも満足できる品質をもった天然バニラ香料の
製造方法であるとは言い難かった。そこで、本発明は、
キュアリング工程が不要で、短期間かつ簡便に製造で
き、しかもバニラ青莢特有の青臭さ、渋み、エグ味がな
く、良好な香気・香味を有する天然バニラ香料を得るこ
とができる、天然バニラ香料の製造方法を提供すること
を目的とする。
However, the method for producing a natural vanilla flavor proposed in the above-mentioned publication eliminates the disadvantages of the conventional production method, that is, high cost and quality variation due to a long-term curing step. Although it is excellent in that point, the natural vanilla flavor obtained by the above method has a peculiar blue odor, astringency, and astringency unique to vanilla blue pods, so it is a method for producing a natural vanilla flavor with necessarily satisfactory quality. It was hard to say. Therefore, the present invention
A natural vanilla flavor that does not require a curing step, can be manufactured in a short period of time and is simple, and has no blue odor, astringency, or astringency peculiar to vanilla blue pods, and can provide a natural vanilla flavor having good aroma and flavor. It is an object of the present invention to provide a method for producing the same.

【0006】[0006]

【課題を解決するための手段】本発明者らは、上記課題
を解決するため、鋭意研究を重ねた結果、バニラ青莢を
親水性有機溶媒で抽出して、バニラ青莢特有の青臭さ、
渋味、エグ味のある夾雑物を、ある程度除去した後、抽
出物をβ−グルコシダーゼおよびタンナーゼで処理する
ことにより、バニラ青莢特有の青臭み、渋み、エグ味が
全く感じられない、良好な香気・香味を有する天然バニ
ラ香料を、短期間かつ簡便に製造することができること
を見出し、本発明を完成するに至った。すなわち、本発
明は、バニラ青莢の親水性有機溶媒抽出物を、β−グル
コシダーゼおよびタンナーゼで処理することを特徴とす
る天然バニラ香料の製造方法である。
Means for Solving the Problems The present inventors have conducted intensive studies in order to solve the above-mentioned problems. As a result, the vanilla blue pods were extracted with a hydrophilic organic solvent, and the green odor peculiar to the vanilla blue pods,
Astringency, astringent contaminants are removed to some extent, and then the extract is treated with β-glucosidase and tannase. The present inventors have found that a natural vanilla flavor having an aroma and a flavor can be easily produced in a short period of time, and have completed the present invention. That is, the present invention is a method for producing a natural vanilla flavor, comprising treating a hydrophilic organic solvent extract of vanilla blue pods with β-glucosidase and tannase.

【0007】[0007]

【発明の実施の形態】以下、本発明について、更に詳し
く説明する。本発明で使用するバニラ青莢は、Vanilla
planifolia、Vanilla tahitiense またはVanilla pompon
a に属する植物であって、緑色かつ生のものであれば、
産地や品種は特に限定されない。ここで、「バニラ青
莢」とは、開花・(人工)受粉後、結実したものを指
す。バニラ青莢は、通常、結実後4〜5カ月目の時点で
収穫されるものであるが、本発明では、結実後のバニラ
青莢であれば、どの時期に収穫したものでも使用するこ
とができる。
BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in more detail. The vanilla blue pod used in the present invention is Vanilla
planifolia, Vanilla tahitiense or Vanilla pompon
If the plant belongs to a and is green and raw,
The place of production and variety are not particularly limited. Here, the "vanilla blue pod" refers to a fruit that has been fruited after flowering and (artificial) pollination. Vanilla blue pods are usually harvested 4 to 5 months after fruiting, but in the present invention, any harvested vanilla blue pods may be used at any time. it can.

【0008】バニラ青莢の親水性有機溶媒抽出物を調製
するには、通常の植物成分を抽出する方法を利用して行
えばよく、その方法は特に限定されるものではない。以
下に、好ましい一例を説明する。
In order to prepare a hydrophilic organic solvent extract of vanilla blue pods, a conventional method for extracting plant components may be used, and the method is not particularly limited. Hereinafter, a preferred example will be described.

【0009】バニラ青莢は、抽出効率を高めるため、
0.2〜2.0cm程度に切断したものを用いる。好ま
しくは、切断したバニラ青莢をそのままの状態または親
水性有機溶媒とともに、更に、ミキサー等で粉砕する。
[0009] In order to increase the extraction efficiency,
The one cut to about 0.2 to 2.0 cm is used. Preferably, the cut vanilla blue pods are pulverized as they are or together with a hydrophilic organic solvent using a mixer or the like.

【0010】次に、切断または粉砕したバニラ青莢に、
等倍〜5倍量の親水性有機溶媒を加え、20〜90℃
で、攪拌または還流しながら、1〜6時間抽出を行う。
その際、親水性有機溶媒の種類は、特に限定されない。
例えば、メタノール、エタノール、アセトン、酢酸エチ
ルを挙げることができる。また、親水性有機溶媒は、単
独溶媒ではなく混合溶媒でもよい。特に、親水性有機溶
媒と水との混合溶媒、とりわけ、親水性有機溶媒:水=
3:7〜8:2の割合からなる混合溶媒が好ましい。抽
出後、遠心分離等により固液分離して、液相部分を適
宜、濃縮し、親水性有機溶媒を除去することにより、バ
ニラ青莢の親水性有機溶媒抽出物が得られる。
Next, the cut or crushed vanilla blue pods are
Add 1 to 5 times the amount of the hydrophilic organic solvent and add 20 to 90 ° C.
Then, extraction is performed for 1 to 6 hours while stirring or refluxing.
At that time, the kind of the hydrophilic organic solvent is not particularly limited.
For example, methanol, ethanol, acetone, and ethyl acetate can be mentioned. The hydrophilic organic solvent may be a mixed solvent instead of a single solvent. In particular, a mixed solvent of a hydrophilic organic solvent and water, especially a hydrophilic organic solvent: water =
A mixed solvent having a ratio of 3: 7 to 8: 2 is preferable. After the extraction, solid-liquid separation is performed by centrifugation or the like, the liquid phase portion is appropriately concentrated, and the hydrophilic organic solvent is removed, whereby a hydrophilic organic solvent extract of vanilla blue pod is obtained.

【0011】次に、バニラ青莢の親水性有機溶媒抽出物
を、β−グルコシダーゼおよびタンナーゼで処理する。
本発明で使用するβ−グルコシダーゼは、特に限定され
ず、グルコシド結合を加水分解できるβ−グルコシダー
ゼ活性を有する酵素や該酵素活性を有する微生物等が挙
げられる。β−グルコシダーゼ活性を有する酵素は、市
販されていて、容易に得ることができ、例えば、プロテ
アーゼ「アマノ」(天野製薬社製、商品名)、「コクラ
ーゼ」(三共社製、商品名)、「リパーゼAP」(天野
製薬社製、商品名)、「コクラーゼSS」(三共社製、
商品名)、「Rohapect 7104」( ROEH
M社製、商品名) が市販されている。β−グルコシダー
ゼの使用量は、その酵素活性によって異なるが、バニラ
青莢の親水性有機溶媒抽出物100重量部に対して、
0.01〜2.0重量部が例示される。また、β−グル
コシダーゼの処理条件は、特に限定されないが、pH
4.0〜8.0、30〜60℃の温度範囲で、8〜48
時間の処理を行うのが一般的である。
Next, the hydrophilic organic solvent extract of the vanilla blue pod is treated with β-glucosidase and tannase.
The β-glucosidase used in the present invention is not particularly limited, and examples thereof include an enzyme having β-glucosidase activity capable of hydrolyzing a glucoside bond, and a microorganism having the enzyme activity. Enzymes having β-glucosidase activity are commercially available and can be easily obtained. For example, proteases “Amano” (trade name, manufactured by Amano Pharmaceutical Co., Ltd.), “Coclase” (trade name, manufactured by Sankyo Co., Ltd.), “ "Lipase AP" (manufactured by Amano Pharmaceutical Co., Ltd.), "Coclase SS" (manufactured by Sankyo)
Product name), “Rohapect 7104” (ROEH
M (trade name) is commercially available. The amount of β-glucosidase used depends on its enzymatic activity, but is based on 100 parts by weight of the hydrophilic organic solvent extract of the vanilla blue pod.
0.01 to 2.0 parts by weight is exemplified. Further, the treatment conditions of β-glucosidase are not particularly limited,
4.0 to 8.0, 30 to 60 ° C, 8 to 48
In general, time processing is performed.

【0012】本発明で使用するタンナーゼは、タンナー
ゼであれば任意のものを使用できる。特には、タンニン
酸を唯一の炭素源として培養した、アスペルギルス(As
pergillus )属やペニシリウム(Penicillium )属等に
属するタンナーゼ生産菌から得たタンナーゼが好適であ
る。タンナーゼは、市販されていて、容易に得ることが
でき、例えば、「タンナーゼ」(キッコーマン社製、商
品名)が市販されている。タンナーゼの使用量は、その
酵素活性によって異なるが、バニラ青莢の親水性有機溶
媒抽出物100重量部に対して、0.01〜2.0重量
部が例示される。また、タンナーゼの処理条件は、特に
限定されないが、一般的には,pH4.0〜8.0、3
0〜60℃の温度範囲で、1〜3時間の処理を行うのが
一般的である。
As the tannase used in the present invention, any tannase can be used. In particular, Aspergillus (Aspergillus) cultured using tannic acid as the sole carbon source
Preferred is tannase obtained from a tannase-producing bacterium belonging to the genus pergillus or the genus Penicillium. Tannase is commercially available and can be easily obtained. For example, “tannase” (trade name, manufactured by Kikkoman Corporation) is commercially available. The amount of tannase used varies depending on its enzymatic activity, and is, for example, 0.01 to 2.0 parts by weight based on 100 parts by weight of the hydrophilic organic solvent extract of vanilla blue pod. Further, the treatment conditions of tannase are not particularly limited, but generally, pH 4.0 to 8.0, 3
Generally, the treatment is performed for 1 to 3 hours in a temperature range of 0 to 60 ° C.

【0013】本発明において、バニラ青莢の親水性有機
溶媒抽出物を、β−グルコシダーゼおよびタンナーゼで
処理する方法は特に限定されない。例えば、β−グルコ
シダーゼとタンナーゼで同時に処理する方法、β−グル
コシダーゼで処理した後、タンナーゼで処理する方法、
あるいは、タンナーゼで処理した後、β−グルコシダー
ゼで処理する方法等、任意に選択することができる。
In the present invention, the method of treating the hydrophilic organic solvent extract of the vanilla blue pod with β-glucosidase and tannase is not particularly limited. For example, a method of simultaneously treating with β-glucosidase and tannase, a method of treating with β-glucosidase, followed by treatment with tannase,
Alternatively, a method of treating with tannase and then treating with β-glucosidase can be arbitrarily selected.

【0014】β−グルコシダーゼおよびタンナーゼで処
理したバニラ青莢の親水性有機溶媒抽出物は、例えば、
80〜95℃の温度で、5分〜1時間加熱して、上記酵
素を失活させることにより、溶液状の天然バニラ香料が
得られる。得られた天然バニラ香料は、その後、希望に
より、濃縮液状、ペースト状、粉末状その他の任意の形
態にして、各種飲食品や化粧品等に利用することができ
る。特に、水蒸気蒸留法、膜濃縮法、樹脂吸着法、超臨
界抽出法、減圧濃縮法等の濃縮法を利用して濃縮液状に
することにより、良好な天然バニラ香料が得られる。特
に好ましい濃縮法としては、樹脂吸着法を挙げることが
でき、以下、樹脂吸着法を用いて濃縮する方法について
詳細に説明する。
The hydrophilic organic solvent extract of vanilla blue pods treated with β-glucosidase and tannase is, for example,
By heating at a temperature of 80 to 95 ° C. for 5 minutes to 1 hour to inactivate the enzyme, a natural vanilla flavor in a solution form can be obtained. The obtained natural vanilla flavor can then be converted into a concentrated liquid, paste, powder, or any other form as desired, and used in various foods and drinks, cosmetics, and the like. In particular, a good natural vanilla flavor can be obtained by making a concentrated liquid by using a concentration method such as a steam distillation method, a membrane concentration method, a resin adsorption method, a supercritical extraction method, and a vacuum concentration method. As a particularly preferred concentration method, a resin adsorption method can be mentioned. Hereinafter, a method of concentration using the resin adsorption method will be described in detail.

【0015】まず、β−グルコシダーゼおよびタンナー
ゼで処理したバニラ青莢の親水性有機溶媒抽出物を、ス
チレンとジビニルベンゼンの共重合体、2,6−ジフェ
ニル−9−フェニルオキサイドの単独重合体、あるいは
メタクリル酸とジオールの重縮合体等からなる多孔性樹
脂に接触させて、天然バニラ香料成分を多孔性樹脂に吸
着させる。そして、エチルアルコール、メチルアルコー
ル、アセトン、酢酸エチル、およびこれらの含水物等で
抽出することにより、濃縮液状の天然バニラ香料が得ら
れる。なお、上記した多孔性樹脂は、表面積が300m
2 /g以上、細孔分布が10〜500Åであるものが好
ましく、「HP樹脂」(三菱化学社製、商品名)、「S
P樹脂」(三菱化学社製、商品名)、「XAD−4」
(ローム・ハース社製、商品名)等が市販されていて、
容易に入手することができる。また、メタクリル酸系樹
脂として、「XAD−7」や「XAD−8」(ローム・
ハース社製、商品名)等が市販されている。
First, a hydrophilic organic solvent extract of vanilla blue pods treated with β-glucosidase and tannase was used as a copolymer of styrene and divinylbenzene, a homopolymer of 2,6-diphenyl-9-phenyloxide, or The natural vanilla flavor component is adsorbed on the porous resin by contact with a porous resin composed of a polycondensate of methacrylic acid and a diol. Then, by extraction with ethyl alcohol, methyl alcohol, acetone, ethyl acetate, and hydrates thereof, a concentrated liquid natural vanilla flavor is obtained. The above-mentioned porous resin has a surface area of 300 m.
2 / g or more and those having a pore distribution of 10 to 500 ° are preferable, and “HP resin” (trade name, manufactured by Mitsubishi Chemical Corporation), “S
P resin "(Mitsubishi Chemical Corporation, trade name)," XAD-4 "
(Rohm Haas, product name) etc. are commercially available,
It can be easily obtained. In addition, as methacrylic acid-based resins, “XAD-7” and “XAD-8” (ROHM
Haas Co., trade name) is commercially available.

【0016】[0016]

【実施例】以下、実施例を挙げて本発明を更に詳しく説
明する。なお、本発明は、以下の実施例に限定されるも
のではない。
EXAMPLES Hereinafter, the present invention will be described in more detail by way of examples. Note that the present invention is not limited to the following embodiments.

【0017】(実施例1)バニラ青莢の粉砕物1000
gに、70%エチルアルコール1500gを加えて、7
0〜75℃で2時間、攪拌抽出を行った。抽出後、40
℃に冷却して固液分離を行い、抽出液1350gを得
た。得られた抽出液を、更に減圧濃縮して、バニラ青莢
の親水性有機溶媒抽出物を400g調製した。この抽出
物に軟水400gを加えて混合し、β−グルコシダーゼ
「Rohapect 7104」(ROEHM社製、商
品名)0.5gおよびタンナーゼ「タンナーゼ」(キッ
コーマン社製、商品名)0.1gを添加して、50℃〜
55℃で24時間酵素処理を行った。酵素処理後、90
〜95℃で10分間加熱して、酵素を失活させた。そし
て、酵素処理液を減圧濃縮し、得られた濃縮液400g
に、95%エチルアルコール400gを添加混合した
後、不溶物を遠心分離して除去することにより、天然バ
ニラ香料750gを得た。この天然バニラ香料には、バ
ニラ青莢特有の青臭み、渋味、エグ味がなく、芳醇な甘
味、清涼感、ミルク感を有していた。
(Example 1) Crushed vanilla blue pod 1000
g, add 1500 g of 70% ethyl alcohol and add 7 g
Stirring extraction was performed at 0 to 75 ° C for 2 hours. After extraction, 40
After cooling to ℃, solid-liquid separation was performed to obtain 1350 g of an extract. The obtained extract was further concentrated under reduced pressure to prepare 400 g of a hydrophilic organic solvent extract of vanilla blue pods. 400 g of soft water was added to this extract and mixed, and 0.5 g of β-glucosidase “Rohapect 7104” (trade name, manufactured by ROEHM) and 0.1 g of tannase “tannase” (trade name, manufactured by Kikkoman) were added. , 50 ° C ~
The enzyme treatment was performed at 55 ° C. for 24 hours. After enzyme treatment, 90
The enzyme was inactivated by heating at 9595 ° C. for 10 minutes. Then, the enzyme-treated solution was concentrated under reduced pressure, and the obtained concentrated solution 400 g was obtained.
After adding and mixing 400 g of 95% ethyl alcohol, 750 g of natural vanilla flavor was obtained by removing the insoluble matter by centrifugation. This natural vanilla flavor had no odor, astringency, or astringent taste unique to vanilla blue pods, and had a rich sweetness, refreshing feeling, and milky feeling.

【0018】(比較例1)実施例1において、タンナー
ゼを添加しなかった以外は、すべて実施例1と同様に処
理して、天然バニラ香料を得た。この天然バニラ香料
は、実施例1で得られた天然バニラ香料に比べて、青臭
み、渋味、エグ味が強かった。
Comparative Example 1 A natural vanilla flavor was obtained in the same manner as in Example 1 except that tannase was not added. This natural vanilla flavor had a stronger blue odor, astringency, and astringency than the natural vanilla flavor obtained in Example 1.

【0019】(実施例2)バニラ青莢の粉砕物2000
gに、80%メチルアルコール4000gを加えて、6
0〜65℃で2時間、攪拌抽出を行った。抽出後、40
℃に冷却して固液分離を行い、抽出液3800gを得
た。得られた抽出液を、更に減圧濃縮、減圧乾燥して、
乾燥したバニラ青莢の親水性有機溶媒抽出物を112g
調製した。この抽出物5gに軟水100gを加えて混合
し、「タンナーゼ」(同上)0.025gを添加して、
30〜35℃で1時間酵素処理を行った。次いで、「R
ohapect 7104」(同上)0.05gを添加
して、50〜55℃で24時間酵素処理を行った後、9
0〜95℃で10分間加熱して、酵素を失活させた。そ
して、多孔性樹脂「HP−20」(三菱化学社製、商品
名)25mlを充填したカラムに、酵素処理液を、SV
=3の流量で通過させ、バニラの香気成分を該樹脂に吸
着させた。通液終了後、125mlの水で該樹脂を洗浄
し、95%エチルアルコールで脱着して天然バニラ香料
25gを得た。この天然バニラ香料には、バニラ青莢特
有の青臭み、渋味、エグ味がなく、芳醇な甘味、清涼
感、ミルク感を有していた。
Example 2 Pulverized Vanilla Blue Pods 2000
g, add 4000 g of 80% methyl alcohol, and add
Stirring extraction was performed at 0 to 65 ° C for 2 hours. After extraction, 40
After cooling to ℃, solid-liquid separation was performed to obtain 3800 g of an extract. The obtained extract is further concentrated under reduced pressure and dried under reduced pressure,
112 g of hydrophilic organic solvent extract of dried vanilla blue pods
Prepared. 100 g of soft water was added to 5 g of this extract, mixed, and 0.025 g of "tannase" (same as above) was added.
The enzyme treatment was performed at 30 to 35 ° C for 1 hour. Then, "R
After adding 0.05 g of “Ohpect 7104” (same as above) and performing the enzyme treatment at 50 to 55 ° C. for 24 hours, 9
Heating at 0-95 ° C for 10 minutes inactivated the enzyme. Then, the enzyme treatment liquid was added to a column filled with 25 ml of a porous resin “HP-20” (trade name, manufactured by Mitsubishi Chemical Corporation),
= 3, and the fragrance component of vanilla was adsorbed on the resin. After the completion of the passage, the resin was washed with 125 ml of water and desorbed with 95% ethyl alcohol to obtain 25 g of a natural vanilla flavor. This natural vanilla flavor had no odor, astringency, or astringent taste unique to vanilla blue pods, and had a mellow sweetness, a refreshing feeling, and a milky feeling.

【0020】[0020]

【発明の効果】本発明は、キュアリング工程が不要であ
るため、短期間かつ簡便に天然バニラ香料を得ることが
できる。また、本発明により得られる天然バニラ香料に
は、バニラ青莢特有の青臭さ、渋み、エグ味がなく、良
好な香気・香味を有し、例えば、アイスクリーム、シャ
ーベット等の冷菓類;チョコレート、ビスケット、シュ
ークリーム、プリン、ババロア、ムース等の洋菓子類;
パン類;キャンディ、チョコレート、焼物等のセンター
に詰めるフィリング材;ホイップクリーム、ファットク
リーム等のクリーム類;ココアドリンク等の飲料類、あ
るいはベビーパウダー、ボディー用消臭スプレー、フッ
トスプレー、液状または粉末状の制汗剤、看護用身体洗
浄剤、ヘアムース、ヘアコンディショナー等の頭髪化粧
料等の化粧品類の香気・香味賦与剤あるいは変調剤の調
合素材として利用することができる。
According to the present invention, since a curing step is not required, a natural vanilla flavor can be easily obtained in a short period of time. In addition, the natural vanilla flavor obtained according to the present invention does not have a peculiar blue odor, astringency, or astringent taste of vanilla blue pods, has a good aroma and flavor, and includes, for example, ice creams, frozen desserts such as sherbet; chocolate, Western sweets such as biscuits, cream puffs, puddings, bavarois, and mousses;
Breads; Filling materials to be packed in centers such as candy, chocolate, and baked goods; Creams such as whipped cream and fat cream; Beverages such as cocoa drinks; baby powder; The present invention can be used as a compounding material of a fragrance / flavor imparting agent or a modulator for cosmetics such as antiperspirants, nursing body cleansing agents, hair mousses, hair conditioners and other hair cosmetics.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 バニラ青莢の親水性有機溶媒抽出物を、
β−グルコシダーゼおよびタンナーゼで処理することを
特徴とする天然バニラ香料の製造方法。
1. A hydrophilic organic solvent extract of vanilla blue pods,
A method for producing a natural vanilla flavor, wherein the natural vanilla flavor is treated with β-glucosidase and tannase.
JP12932197A 1997-05-20 1997-05-20 Method for producing natural vanilla fragrance Expired - Lifetime JP3471561B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12932197A JP3471561B2 (en) 1997-05-20 1997-05-20 Method for producing natural vanilla fragrance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12932197A JP3471561B2 (en) 1997-05-20 1997-05-20 Method for producing natural vanilla fragrance

Publications (2)

Publication Number Publication Date
JPH10316992A true JPH10316992A (en) 1998-12-02
JP3471561B2 JP3471561B2 (en) 2003-12-02

Family

ID=15006698

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12932197A Expired - Lifetime JP3471561B2 (en) 1997-05-20 1997-05-20 Method for producing natural vanilla fragrance

Country Status (1)

Country Link
JP (1) JP3471561B2 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002171993A (en) * 2000-09-27 2002-06-18 Ikeda Shokken Kk Method of manufacturing fatty acid ester of sterol for foods
SG121100A1 (en) * 2004-09-10 2006-04-26 Hasegawa T Co Ltd Method of preparing tea extract and tea flavor
WO2010066060A1 (en) * 2008-12-12 2010-06-17 Givaudan Sa Enzymatic process
JP2015149971A (en) * 2014-02-19 2015-08-24 長谷川香料株式会社 Manufacturing method of enzyme-treated vanilla extract
CN106028825A (en) * 2014-02-19 2016-10-12 长谷川香料株式会社 Method for producing enzymatically treated plant extract
JP2017063753A (en) * 2015-10-01 2017-04-06 長谷川香料株式会社 Manufacturing method of heat treated vanilla extract
CN107474959A (en) * 2017-06-09 2017-12-15 珠海市美绿达香料有限公司 A kind of spices and its preparation method and application

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002171993A (en) * 2000-09-27 2002-06-18 Ikeda Shokken Kk Method of manufacturing fatty acid ester of sterol for foods
SG121100A1 (en) * 2004-09-10 2006-04-26 Hasegawa T Co Ltd Method of preparing tea extract and tea flavor
KR101089533B1 (en) 2004-09-10 2011-12-05 하세가와 고오료오 가부시끼가이샤 Method of preparing tea extract and tea flavor
US9408408B2 (en) 2008-12-12 2016-08-09 Givaudan Sa Enzymatic process
WO2010066060A1 (en) * 2008-12-12 2010-06-17 Givaudan Sa Enzymatic process
JP2012511308A (en) * 2008-12-12 2012-05-24 ジボダン エス エー Enzymatic process
US8580322B2 (en) 2008-12-12 2013-11-12 Givaudan Sa Enzymatic process
EP2679102A3 (en) * 2008-12-12 2014-02-26 Givaudan SA Enzymatic process
JP2015051003A (en) * 2008-12-12 2015-03-19 ジボダン エス エー Enzymatic processing
US11497233B2 (en) 2008-12-12 2022-11-15 Givaudan Sa Enzymatic process
JP2015149971A (en) * 2014-02-19 2015-08-24 長谷川香料株式会社 Manufacturing method of enzyme-treated vanilla extract
CN106028836A (en) * 2014-02-19 2016-10-12 长谷川香料株式会社 Method of producing enzyme-treated vanilla extract
CN106028825A (en) * 2014-02-19 2016-10-12 长谷川香料株式会社 Method for producing enzymatically treated plant extract
WO2015125628A1 (en) * 2014-02-19 2015-08-27 長谷川香料株式会社 Method of producing enzyme-treated vanilla extract
JP2017063753A (en) * 2015-10-01 2017-04-06 長谷川香料株式会社 Manufacturing method of heat treated vanilla extract
CN107474959A (en) * 2017-06-09 2017-12-15 珠海市美绿达香料有限公司 A kind of spices and its preparation method and application

Also Published As

Publication number Publication date
JP3471561B2 (en) 2003-12-02

Similar Documents

Publication Publication Date Title
WO2005039301A1 (en) Fresh tea leaf powder and processed product, extract, oil and aroma obtained from fresh tea leaf powder
WO2006047404A2 (en) Methods for the production of food grade extracts
FR2542318A1 (en) FOOD PRODUCTS BASED ON SOYA GLYCOSIDE AND PROCESS FOR PREPARING THE SAME
WO2006062133A1 (en) Methods of producing enzymatically treated tea extract, natural aroma of enzymatically treated tea and concentrated natural aroma extract of enzymatically treated tea, and enzymatically treated tea extract, natural aroma of enzymatically treated tea and concentrated natural aroma extract of enzymatically treated tea obtaine
CN102613370B (en) Chocolate flavour manipulation
CN1582117B (en) Manipulation of chocolate flavor
JP3471561B2 (en) Method for producing natural vanilla fragrance
JP6297354B2 (en) Method for producing enzyme-treated plant extract
JPH03277247A (en) Preparation of edible raw material using ginseng
US20050074521A1 (en) Method for the production of natural botanical extracts
JP4122391B2 (en) Flavor improving agent, perfume composition and food containing the same
JP3432255B2 (en) How to make chocolate drinks
JP4106429B2 (en) Production method of new vanilla extract
JPS6251099B2 (en)
JPH034766A (en) Production of dried fruit extract and flavor modifier
JPH0484855A (en) Production of cheese-flavored composition
KR101891885B1 (en) Method of manufacturing vanilla extract by heat-treatment
JP5877854B2 (en) Method for producing enzyme-treated vanilla extract
JPH06225721A (en) Fermented seasoning and its production and pickle seasoning using the same
JP2002142713A (en) Dairy product flavor
JPH0683656B2 (en) Method for producing ginseng cream
JP2001252091A (en) Material highly containing gamma-aminobutyric acid, its preparation method and food and drink containing the same
JPH08154619A (en) Taste and flavor improver and beverage and food products improved in taste and flavor
JP2665978B2 (en) How to make dairy flavors
JPS60234563A (en) Low smell "miso" paste containing highly hydrolyzed protein

Legal Events

Date Code Title Description
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080912

Year of fee payment: 5

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

Free format text: PAYMENT UNTIL: 20090912

Year of fee payment: 6

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

Free format text: PAYMENT UNTIL: 20090912

Year of fee payment: 6

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

Free format text: PAYMENT UNTIL: 20100912

Year of fee payment: 7

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

Free format text: PAYMENT UNTIL: 20100912

Year of fee payment: 7

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

Free format text: PAYMENT UNTIL: 20110912

Year of fee payment: 8

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

Free format text: PAYMENT UNTIL: 20110912

Year of fee payment: 8

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

Free format text: PAYMENT UNTIL: 20120912

Year of fee payment: 9

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

Free format text: PAYMENT UNTIL: 20130912

Year of fee payment: 10

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

Free format text: PAYMENT UNTIL: 20130912

Year of fee payment: 10

EXPY Cancellation because of completion of term