JPH0718194A - Production of crocetin - Google Patents

Production of crocetin

Info

Publication number
JPH0718194A
JPH0718194A JP5209840A JP20984093A JPH0718194A JP H0718194 A JPH0718194 A JP H0718194A JP 5209840 A JP5209840 A JP 5209840A JP 20984093 A JP20984093 A JP 20984093A JP H0718194 A JPH0718194 A JP H0718194A
Authority
JP
Japan
Prior art keywords
crocetin
pts
cellulase
enzymatic reaction
aqueous solution
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
Application number
JP5209840A
Other languages
Japanese (ja)
Inventor
Nobuyoshi Nosaka
宜嘉 野坂
Nobuo Miyano
信雄 宮野
Mikinori Asano
幹則 浅野
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.)
TAISHIYOO TECHNOS KK
Original Assignee
TAISHIYOO TECHNOS KK
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 TAISHIYOO TECHNOS KK filed Critical TAISHIYOO TECHNOS KK
Priority to JP5209840A priority Critical patent/JPH0718194A/en
Publication of JPH0718194A publication Critical patent/JPH0718194A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To safely and hygienically obtain the subject compound excellent in brightness of yellow and useful for coloring of foods by reacting an aqueous solution of crocetin with a specific enzyme. CONSTITUTION:100 pts.wt. of an aqueous solution of crocetin is mixed with 0.01-10 pts.wt. of glucoamylase and subject to enzymatic reaction to provide the objective compound. Furthermore, the objective compound can also be obtained by mixing 100 pts.wt. of an aqueous solution of crocetin with 0.01-10 pts.wt. of (hemi)cellulase and subjecting the solution to enzymatic reaction with the (hemi)cellulase.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野 】本発明は、酵素を利用したクロ
セチンの製造方法に関するものである。
TECHNICAL FIELD The present invention relates to a method for producing crocetin using an enzyme.

【0002】[0002]

【従来の技術】クチナシ色素の主成分であるクロシン
は、アカネ科のくちなし(Gardenia augu
sta MERR.Var.grandiflora
HORT.)の果実あるいは、アヤメ科のサフラン(
rocus sativus L.)の花の柱頭などに
含まれている色素であり、漬物・和菓子・栗きんとん・
餅などの着色に利用されている。
2. Description of the Related Art Crocin, which is the main component of gardenia pigments, is known as Gardenia augu
sta MERR. Var. grandiflora
HORT. ) Fruit or saffron of the family Iridaceae ( C
rocus sativus L. ) It is a pigment contained in stigmas of flowers, such as pickles, Japanese sweets, chestnuts,
It is used for coloring rice cakes.

【0003】クチナシ色素の主成分は、クロシンであり
その他の成分としてクロセチンが少量含まれている。ク
ロシンとクロセチンの色調を比較するとクロセチンはク
ロシンに比べて明るい鮮明な黄色、言い替えれば青みを
有する黄色を呈し、食品に利用する際に有用性が高いも
のである。
The main component of gardenia pigment is crocin, and a small amount of crocetin is contained as the other component. When the color tones of crocin and crocetin are compared, crocetin exhibits a brighter and clearer yellow color than crocin, in other words, it has a bluish yellow color, and is highly useful when used in foods.

【0004】[0004]

【発明が解決しようとする課題】クロシンを加水分解す
ることによって構造中に存在するゲンチオビオースがは
ずれクロセチンが生成するが、加水分解するには 通常
水酸化ナトリウム等のアルカリが使用され、作業上危険
が伴うことはもちろん、労働衛生上も好ましいことでは
なかった。
When crocin is hydrolyzed, gentiobiose existing in the structure is released and crocetin is produced. However, alkali such as sodium hydroxide is usually used for hydrolysis, which is dangerous for work. Of course, it was not good for occupational health.

【0005】[0005]

【課題を解決するための手段】本発明者等は、前記した
課題を解決すべく鋭意努力して実験を重ねた結果、グル
コアミラーゼ、セルラーゼ、ヘミセルラーゼの1種また
は数種を併用することによって、作業上安全でかつ労働
衛生上好ましい方法でクロセチンを製造する方法を見い
出すに至ったのである。
Means for Solving the Problems The inventors of the present invention have made diligent efforts to solve the above-mentioned problems, and as a result, have conducted experiments, and as a result, by using one or several kinds of glucoamylase, cellulase and hemicellulase in combination. The inventors have come to find a method for producing crocetin by a method that is safe for work and is favorable for occupational health.

【0006】即ち、クロシンの水溶液0.01部ないし
10部好ましくは、0.5部ないし5部のグルコアミラ
ーゼ及びまたは0.01部ないし10部好ましくは、
0.05部ないし5部のセルラーゼ及びまたは0.01
部あいし10部好ましくは、0.05部ないし5部のヘ
ミセルラーゼを混合後、10℃ないし70C℃好ましく
は40℃ないし60℃に一定時間酵素反応させることに
よって、クロセチンを製造することが可能になったので
ある。
That is, 0.01 to 10 parts of an aqueous solution of crocin, preferably 0.5 to 5 parts of glucoamylase and / or 0.01 to 10 parts, preferably,
0.05 to 5 parts of cellulase and or 0.01
It is possible to produce crocetin by mixing 10 parts, preferably 0.05 part to 5 parts of hemicellulase and then enzymatically reacting at 10 ° C. to 70 ° C., preferably 40 ° C. to 60 ° C. for a certain period of time. It has become.

【0007】本発明を実施するための酵素は、その起源
を問わず、また精製品でも目的とする酵素活性を有する
粗抽出液でも使用でき、本発明の実行を妨げるものでは
ない。
The enzyme for carrying out the present invention can be used regardless of its origin, and can be used as a purified product or a crude extract having a desired enzymatic activity, and does not impede the practice of the present invention.

【0008】本発明で酵素を作用させる温度は、使用す
る酵素の作用適温であれば良く特に限定されるものでは
ない。
The temperature at which the enzyme acts in the present invention is not particularly limited as long as it is a temperature suitable for the action of the enzyme used.

【実施例】【Example】

【0009】以下に実施例を挙げて説明するが、本発明
は、以下の実施例に制約されるものではない。
Examples will be described below, but the present invention is not limited to the following examples.

【0010】実施例1 セルラーゼ(繊維消化力30,000u/g pH4.
5)を5g混合した。この溶液を50℃に調整した恒温
器中で20時間酵素反応させた後、No.2の濾紙で濾
過を行い、 約3.9g得られた。
Example 1 Cellulase (fiber digestion 30,000 u / g pH 4.
5 g of 5) was mixed. The solution was subjected to an enzymatic reaction for 20 hours in a thermostat adjusted to 50 ° C., and then No. Filter with 2 filter paper, About 3.9 g was obtained.

【0011 】得られたクロセチンは、約421nmに
吸収極大を持ち、クロシンと比較すると、顕著に青みが
あり食品に添加した処、きれいな青みのある黄色を呈し
た。
The obtained crocetin had an absorption maximum at about 421 nm and had a noticeably bluish color as compared with crocin, and when added to food, it exhibited a clear bluish yellow color.

【0012】実施例2 ヘミセルラーゼ(キシラナーゼ力価90,000u/g
pH4.5)を5g混合した。この溶液を45℃に調
整した恒温器中で17時間酵素反応させた後、No.2
の濾紙で濾 の粉末が約2.2g得られた。
Embodiment 2 Hemicellulase (xylanase titer 90,000 u / g
5g of pH 4.5) was mixed. This solution was subjected to an enzymatic reaction for 17 hours in an incubator adjusted to 45 ° C., and then No. Two
With a filter paper About 2.2 g of powder was obtained.

【0013】得られたクロセチンは、約421nmに吸
収極大を持ち、クロシンと比較すると、顕著に青みがあ
り食品に添加した処、きれいな青みのある黄色を呈し
た。
The crocetin thus obtained had an absorption maximum at about 421 nm and was markedly bluish in comparison with crocin, and when added to food, it exhibited a beautiful bluish yellow color.

【0014】実施例 3 にグルコアミラーゼ(澱粉糖化力価6,000u/g
pH4.5)を10g混合した。この溶液を55℃に調
整した恒温器中で15時間酵素反応させた後、No.2
の濾紙で濾 0)の粉末が約6.1g得られた。
Example 3 Glucoamylase (starch saccharification titer 6,000u / g
pH 4.5) was mixed with 10 g. This solution was subjected to an enzymatic reaction for 15 hours in an incubator adjusted to 55 ° C., and then No. Two
With a filter paper About 6.1 g of the powder of 0) was obtained.

【0015】得られたクロセチンは、約421nmに吸
収極大を持ち、クロシンと比較すると、顕著に青みがあ
り食品に添加した処、きれいな青みのある黄色を呈し
た。
The crocetin thus obtained had an absorption maximum at about 421 nm and was markedly bluish in comparison with crocin, and when added to food, it exhibited a beautiful bluish yellow color.

【0016】比較例1 実施例1 に於て、セルラーゼの代わりにβ−アミラー
ゼを使用する以外は実施例1 と全く同様の方法で酵素
反応を行った。本酵素反応からは、クロセチンの沈澱は
殆ど得られなかった。
Comparative Example 1 The enzymatic reaction was carried out in the same manner as in Example 1 except that β-amylase was used instead of cellulase. From this enzymatic reaction, almost no precipitation of crocetin was obtained.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 浅野 幹則 静岡県駿東郡小山町湯船1157番16号 ハイ テクパーク富士小山 株式会社タイショー テクノス内 ─────────────────────────────────────────────────── ─── Continuation of front page (72) Inventor Mikinori Asano No. 1157-16 Yubune, Oyama-cho, Sunto-gun, Shizuoka High-tech park Fuji Oyama Taisho Technos Co., Ltd.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】グルコアミラーゼを使用することを特徴と
するクロセチンの製造方法
1. A method for producing crocetin, which comprises using glucoamylase.
【請求項2】セルラーゼを使用することを特徴とするク
ロセチンの製造方法
2. A method for producing crocetin, which comprises using cellulase.
【請求項3】ヘミセルラーゼを使用することを特徴とす
るクロセチンの製造方法
3. A method for producing crocetin, which comprises using hemicellulase.
JP5209840A 1993-06-30 1993-06-30 Production of crocetin Pending JPH0718194A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5209840A JPH0718194A (en) 1993-06-30 1993-06-30 Production of crocetin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5209840A JPH0718194A (en) 1993-06-30 1993-06-30 Production of crocetin

Publications (1)

Publication Number Publication Date
JPH0718194A true JPH0718194A (en) 1995-01-20

Family

ID=16579495

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5209840A Pending JPH0718194A (en) 1993-06-30 1993-06-30 Production of crocetin

Country Status (1)

Country Link
JP (1) JPH0718194A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010094745A1 (en) * 2009-02-18 2010-08-26 Omnica Gmbh Hydrolysate of crocin
JP2012171887A (en) * 2011-02-18 2012-09-10 Kao Corp Tyrosinase activity inhibitor, and cosmetic for whitening
CN108558645A (en) * 2018-05-18 2018-09-21 武汉雅仕博科技有限公司 The method that crocin is extracted from cape jasmine

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010094745A1 (en) * 2009-02-18 2010-08-26 Omnica Gmbh Hydrolysate of crocin
US8569247B2 (en) 2009-02-18 2013-10-29 Omnica Gmbh Hydrolysate of crocin
JP2012171887A (en) * 2011-02-18 2012-09-10 Kao Corp Tyrosinase activity inhibitor, and cosmetic for whitening
CN108558645A (en) * 2018-05-18 2018-09-21 武汉雅仕博科技有限公司 The method that crocin is extracted from cape jasmine

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