JPS5920357A - Production of conversion product of gardenia pigment - Google Patents

Production of conversion product of gardenia pigment

Info

Publication number
JPS5920357A
JPS5920357A JP13009282A JP13009282A JPS5920357A JP S5920357 A JPS5920357 A JP S5920357A JP 13009282 A JP13009282 A JP 13009282A JP 13009282 A JP13009282 A JP 13009282A JP S5920357 A JPS5920357 A JP S5920357A
Authority
JP
Japan
Prior art keywords
gardenia pigment
gardenia
medium
green
extract
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
JP13009282A
Other languages
Japanese (ja)
Inventor
Moritaka Wada
和田 盛隆
Shigemasa Ishihara
石原 茂正
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.)
Tokiwa Phytochemical Co Ltd
Original Assignee
Tokiwa Phytochemical 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 Tokiwa Phytochemical Co Ltd filed Critical Tokiwa Phytochemical Co Ltd
Priority to JP13009282A priority Critical patent/JPS5920357A/en
Publication of JPS5920357A publication Critical patent/JPS5920357A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To produce a conversion product of gardenia pigment (yellowish green to blue), by culturing a specified microorganism of genus Streptomyces in a medium contg. a gardenia pigment extract. CONSTITUTION:Streptomyces canescens (ISP5001) or Streptomyces chatanoogensis (ISP5001) is used. Crushed gardenia fruit is extracted with an aq. ethanol soln. The resultant gardenia pigment extract is added to a medium, pref. a liquid medium which is then inoculated with the above microorganism. The inoculated medium is aerated and stirred at 27-37 deg.C and at a pH of 5.5-8. When the medium assumes the desired color tone [the color tone continuously changes from yellow (the color of the gardenia pigment extract) to yellowish green, green and then blue], the medium is sterilized and the culture is stopped. Cells are then removed and the resultant clear soln. is concentrated to obtain conversion product of a gardenia pigment.

Description

【発明の詳細な説明】 本発明はクチナシ色素抽出物にストレプトマイセス属に
属する微生物を作用せしめ、もとのクチナシ色素抽出物
の色調、即ち黄色と異る黄緑、緑ないしは青色系クチナ
シ色素転換物を製造する方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention involves treating a gardenia pigment extract with a microorganism belonging to the genus Streptomyces, thereby producing gardenia pigments that are different in color from the original gardenia pigment extract, such as yellow-green, green, or blue. The present invention relates to a method for producing a converted product.

従来、クチナシ色素は耐光性、耐熱性などの安定性に優
れた天然黄色色素として飲食物などの着色料として広く
利用されてきた。このクチナシ色素の一般的性質として
、クチナシ色素抽出物を含有した標準寒天培地に、ある
種の枯草菌を培養することにより緑色のコロニーが得ら
れることが知られていた。
Traditionally, gardenia pigment has been widely used as a coloring agent for foods and drinks as a natural yellow pigment with excellent stability such as light resistance and heat resistance. As a general property of this gardenia pigment, it has been known that green colonies can be obtained by culturing a type of Bacillus subtilis on a standard agar medium containing a gardenia pigment extract.

この様な性質を利用してクチナシ色素抽出物に枯草菌を
作用せしめ、クチナシ色素抽出物の色調と異るクチナシ
色素転換物を製造する方法についての提案がなされてい
る。(特公昭52−13971) 本発明者らはクチナシ色素抽出物に対する枯草菌の作用
に注目し、クチナシ色素抽出物の色調と異るクチナシ色
素転換物を産生ずる能力を有する菌種について種々検討
を加えた結果、その様な能力を有することが全く知られ
てぃなかったストレプトマイセス属に属する微生物がク
チナシ色素抽出物の色調と異るクチナシ色素転換物特に
黄緑、緑々いしは青色系クチナシ色素転換物を産生ずる
ことを見い出した。
Utilizing such properties, a method has been proposed in which Bacillus subtilis is allowed to act on a gardenia pigment extract to produce a gardenia pigment conversion product having a color tone different from that of the gardenia pigment extract. (Japanese Patent Publication No. 52-13971) The present inventors focused on the action of Bacillus subtilis on gardenia pigment extracts, and conducted various studies on bacterial species that have the ability to produce gardenia pigment conversion products that differ in color tone from gardenia pigment extracts. As a result, microorganisms belonging to the genus Streptomyces, which have never been known to have such abilities, produce gardenia pigment conversion products that have a color tone different from that of gardenia pigment extracts, especially yellow-green, greenish, or blue colors. It was discovered that gardenia pigment conversion products were produced.

本発明に用いるクチナシ色素抽出物は水又は水−アルコ
ール特にメタノール、エタノールトの混合溶媒で抽出し
たものを用いることが望ましい。水で抽出する場合には
抽出液をそのま\用いて′も良く、水−アルコールの混
合溶媒で抽出する場合には濃縮後そのま\か又は水で希
釈して用いると良い。
The gardenia pigment extract used in the present invention is preferably extracted with water or a mixed solvent of water-alcohol, particularly methanol and ethanol. In the case of extraction with water, the extract may be used as it is; in the case of extraction with a water-alcohol mixed solvent, it may be used either after concentration or after dilution with water.

本発明に使用し得る微生物はストレプトマイセス属に属
する微生物であれば適宜使用し得るが、鋭意努力を重ね
た結果、 ストレプトマイセス カネセンス(strθpto −
myces canescens I S P 500
1 )ストレプトマイセス チャタノオゲンシス(St
r、chattanoogensis I S P 5
0 Mストレフトマイセス ミシガネンシス(Str。
As the microorganisms that can be used in the present invention, any microorganisms belonging to the genus Streptomyces can be used as appropriate.
myces canescens ISP 500
1) Streptomyces chatanoogensis (St
r, chattanogensis I S P 5
0 M Streftomyces michiganensis (Str.

michiganensis X S P 5015 
)ストレプトマイセス ブラストマイセチクス(Str
、bl、astmyceticus I S P 50
29 )ストレプトマイセス ピリドクロモゲネス(S
tr、viridOchromogenes工5P51
10)ストレプトマイセス フエレウス(S、tr。
michiganensis X S P 5015
) Streptomyces blastomyceticus (Str
, bl, astmyceticus I S P 50
29) Streptomyces pyridochromogenes (S
tr, virid Ochromogenes engineering 5P51
10) Streptomyces fuereus (S, tr.

felleus工5p5130) ストレプトマイセス クリセウス(Str。felleus engineering 5p5130) Streptomyces chryseus (Str.

griseus工5P5236) ヌトレブトマイセス フラボトリシニ(str。griseus engineering 5P5236) Nutrebutomyces flavotrichini (str.

flavotricini  I S P 5152 
)などがクチナシ色素転換物の産生能力が高いことが明
らかとなった。
flavotricini I SP 5152
) etc. were found to have a high production capacity for gardenia pigment conversion products.

捷だ、本発明における培地は、ストレプトマイセス属に
属する微生物が資化し得る炭素源、窒素源およびその他
の生育に必要々栄養源を有する通常の微生物培地でか捷
わないが、液体培地を用いる方が好捷しい。培養温度、
PHはストレプトマイセス属に属する微生物が生育でき
る範囲ならばか捷わないが、通常、27’−37°、P
H5,5−8の条件で攪拌通気培養することが望ましい
However, the culture medium of the present invention can only be used as a normal microbial culture medium containing a carbon source, nitrogen source, and other nutrients necessary for growth that can be assimilated by microorganisms belonging to the genus Streptomyces, but a liquid medium can be used. It is better to use it. culture temperature,
The pH is only within the range where microorganisms belonging to the genus Streptomyces can grow, but it is usually 27'-37°, P
It is desirable to carry out stirring aeration culture under conditions of H5, 5-8.

上記条件で培養後、目的とする色調が得られた段階で滅
菌処理し、菌体をろ別して清澄液を得る。それを濃縮し
てエキス状にするかあるいは粉末化することによシ黄緑
、緑ないしは青色系クチナシ色素転換物が容易に得られ
、こ\に本発明の目的を達した。
After culturing under the above conditions, sterilization is performed when the desired color tone is obtained, and the cells are filtered to obtain a clear liquid. By concentrating it into an extract form or powdering it, a yellow-green, green or blue gardenia pigment conversion product can be easily obtained, thereby achieving the object of the present invention.

本発明のクチナシ色素転換物の製造過程においては、培
養時間の経過に伴い、培養液の色調が初期のクチナシ色
素抽出物の黄色から黄緑、緑を経て青色に連続的に変化
するため、目的とする色調が得られた段階で培養を停止
することによって任意に黄緑、緑、青色系のクチナシ色
素転換物を得ることが出来る。
In the manufacturing process of the gardenia pigment conversion product of the present invention, the color tone of the culture solution changes continuously from the initial yellow of the gardenia pigment extract to yellow-green, green, and blue as the culture time progresses. By stopping the culture at the stage when the desired color tone is obtained, it is possible to optionally obtain yellow-green, green, or blue gardenia pigment conversion products.

こ\に得られた黄緑、緑ないしは青色系クチナシ色素転
換物は水溶性かつ耐光性、耐熱性などの安定性に優れた
天然色素として飲食物、医薬品、化粧品などの着色に有
用である。
The thus obtained yellow-green, green or blue gardenia pigment conversion product is useful for coloring foods, drinks, medicines, cosmetics, etc. as a water-soluble natural pigment with excellent stability such as light resistance and heat resistance.

以下、実施例によって本発明の方法について説明する。The method of the present invention will be explained below with reference to Examples.

実施例1 クチナシの果実500fを粉砕し、50%含水エタノー
ル2tを加え、2時間攪拌抽出する。得られた抽出液を
減圧濃縮し、クチナシ色素抽出物186.6Fを得た。
Example 1 500 f of gardenia fruit is crushed, 2 tons of 50% aqueous ethanol is added, and the mixture is stirred and extracted for 2 hours. The obtained extract was concentrated under reduced pressure to obtain gardenia pigment extract 186.6F.

(固形分67.7%)これを精製水にて10倍に希釈し
試料溶液としたO L字管中にTSB培地(トリプトン15f1ソイペプト
ン5 t 、Na(4159、蒸留水1000 ml。
(Solid content 67.7%) This was diluted 10 times with purified water and used as a sample solution. TSB medium (tryptone 15f1 soy peptone 5t, Na (4159), distilled water 1000 ml.

PH7,3)、GKMB培地(ポテトエキス−ポテト2
002から作成−1000−、デン粉102、ビーフェ
キス6゜02、グリコース2.02、ペグトン5.Of
 、 K、HPo、 0.8 ?、Fe80.−7H,
00,12、グリセロール60.0ml、P H7,0
)、YMB培地(バクトイ−ストエキス4t、)(クト
マルトエキス102、バントテキストロース4y、蒸留
水1ooo−1PH7,3)各々8 mlを入れ、12
06.20分高圧蒸気滅菌をほどこした後、各菌株を一
白金線量ずつ接種し、27゜にて振とり培養した。24
時間後、ろ過滅菌をほどこしたクチナシ試料液0.5−
をこれに加え、更に48時間振とう培養した後、色調今
肉眼的に観察した。その結果、表1に示す菌株に著しい
色調の変化が認められた。
PH7,3), GKMB medium (potato extract - potato 2)
Made from 002-1000-, starch 102, Beefex 6°02, glycose 2.02, pegton 5. Of
, K, HPo, 0.8? , Fe80. -7H,
00,12, glycerol 60.0ml, pH7,0
), YMB medium (Bacto yeast extract 4t,) (Bactomalt extract 102, Bunt textulose 4y, distilled water 1ooo-1PH7,3), add 8 ml each,
06. After autoclaving for 20 minutes, each strain was inoculated with one platinum dose and cultured by shaking at 27°. 24
After 0.5 hours, the gardenia sample solution was sterilized by filtration.
was added to this, and after further shaking culture for 48 hours, the color tone was visually observed. As a result, a significant change in color tone was observed in the strains shown in Table 1.

実施例2 実施例1と同様のTSB培地3tを作成し、これに実施
例1で作成したクチナシ色素抽出物49.69を添加す
る。120@、20分高圧蒸気滅菌後、あらかじめ27
°、48時間培養しておいたストレグトマイセス カネ
センス(工5P5001)培養液300−をこれに加え
る。これを30°、2500 rpmで攪拌通気培養し
、各時間毎に一部試料液としてぬきとり、120・、2
0分高圧蒸気滅菌後ろ過して清澄液を得た。
Example 2 3 tons of the same TSB medium as in Example 1 is prepared, and 49.69 g of the gardenia pigment extract prepared in Example 1 is added thereto. 120 @, after 20 minutes high pressure steam sterilization, 27
300° of Stregutomyces canescens (5P5001) culture solution that had been cultured for 48 hours was added thereto. This was cultured with aeration at 30° and 2500 rpm, and a portion was removed as a sample solution at each hour.
After 0 minutes of high-pressure steam sterilization, the mixture was filtered to obtain a clear liquid.

これら清澄液の440nm 、  59Onm付近の極
太吸収における−当りの吸光度及び肉眼的観察による色
調を表2に示す。
Table 2 shows the absorbance of these clear liquids in extremely thick absorption near 440 nm and 59 Onm and the color tone as determined by visual observation.

表2 120時間培養後、120°、20分高圧蒸気滅菌し、
ろ過、減圧濃縮して青色系クチナシ色素転換物をエキス
として得た。
Table 2 After culturing for 120 hours, autoclave sterilized at 120° for 20 minutes.
It was filtered and concentrated under reduced pressure to obtain a blue gardenia pigment conversion product as an extract.

実施例3 ペグトン452、ソイペプトン152、Nac115f
1蒸留水3tで1作成した培地に実施例1で作成したク
チナシ色素抽出物41.3Fを添加し、120’、20
分高圧滅菌後、あらかじめ27゜48時間培養しておい
たストレブトマイセスミシガネンシス(より p 53
 A 15 )培養液200−を加える。これを30°
、2500 ramで攪拌通気培養し、各時間毎に実施
f1」2と一様処理して表3に示す結果を得た。
Example 3 Pegton 452, Soy Peptone 152, Nac115f
41.3F of the gardenia pigment extract prepared in Example 1 was added to a medium prepared with 3 tons of distilled water, and 120', 20
After high-pressure sterilization for 1 minute, Strebtomyces miciganensis (from p. 53) was cultured for 27° and 48 hours.
A15) Add 200- of the culture solution. This is 30°
, 2500 ram with agitation and aeration, and uniform treatment was carried out at each time with the procedure f1''2 to obtain the results shown in Table 3.

20.60,120時間後一部試料液をぬきとり、各々
を実施例2と同様、滅菌後ろ過して清澄液を得、これを
減圧濃縮することによって、黄緑、緑、青色系クチナシ
色素転換物を得ることができた。
20. After 60 and 120 hours, a portion of the sample solution was removed, each sample was sterilized and filtered in the same manner as in Example 2 to obtain a clear solution, which was concentrated under reduced pressure to obtain yellow-green, green, and blue gardenia pigments. I was able to get a convertible.

Claims (1)

【特許請求の範囲】[Claims] クチナシ色素抽出物の色調と異るクチナシ色素転換物を
産生ずる能力を有しかつストレプトマイセス属に属する
微生物をクチナシ色素抽出物を添加した培地に接種培養
し、黄緑、緑ないしは青色系クチナシ色素転換物を製造
する方法。
A microorganism belonging to the genus Streptomyces that has the ability to produce a gardenia pigment conversion product different in color tone from the gardenia pigment extract is inoculated and cultured in a medium supplemented with a gardenia pigment extract, and a yellow-green, green or blue gardenia is produced. A method of producing a dye conversion product.
JP13009282A 1982-07-26 1982-07-26 Production of conversion product of gardenia pigment Pending JPS5920357A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13009282A JPS5920357A (en) 1982-07-26 1982-07-26 Production of conversion product of gardenia pigment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13009282A JPS5920357A (en) 1982-07-26 1982-07-26 Production of conversion product of gardenia pigment

Publications (1)

Publication Number Publication Date
JPS5920357A true JPS5920357A (en) 1984-02-02

Family

ID=15025770

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13009282A Pending JPS5920357A (en) 1982-07-26 1982-07-26 Production of conversion product of gardenia pigment

Country Status (1)

Country Link
JP (1) JPS5920357A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6261582A (en) * 1985-09-11 1987-03-18 Kao Corp Production of lipase formulation
JPS6485089A (en) * 1987-09-26 1989-03-30 Japan Res & Dev Ass Synthesis of ester using lipase
JPH02138986A (en) * 1987-12-22 1990-05-28 Unilever Nv Method for producing an aliphatic acid
CN102732050A (en) * 2012-06-06 2012-10-17 浙江科技学院 Method for preparing gardenia pigments from Gardenia jasminoides Ellis
TWI676684B (en) * 2017-06-15 2019-11-11 財團法人食品工業發展研究所 Lactobacillus spp., method for producing pigment by using the same, a lactobacillus spp. culture and a pigment composition comprising the same

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6261582A (en) * 1985-09-11 1987-03-18 Kao Corp Production of lipase formulation
JPS6485089A (en) * 1987-09-26 1989-03-30 Japan Res & Dev Ass Synthesis of ester using lipase
JPH0412716B2 (en) * 1987-09-26 1992-03-05 Shokuhin Sangyo Baioriakutaa Shisutemu Gijutsu Kenkyu Kumiai
JPH02138986A (en) * 1987-12-22 1990-05-28 Unilever Nv Method for producing an aliphatic acid
JPH0458958B2 (en) * 1987-12-22 1992-09-18 Unilever Nv
CN102732050A (en) * 2012-06-06 2012-10-17 浙江科技学院 Method for preparing gardenia pigments from Gardenia jasminoides Ellis
TWI676684B (en) * 2017-06-15 2019-11-11 財團法人食品工業發展研究所 Lactobacillus spp., method for producing pigment by using the same, a lactobacillus spp. culture and a pigment composition comprising the same

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