JPS61249363A - Production of yeast extract - Google Patents

Production of yeast extract

Info

Publication number
JPS61249363A
JPS61249363A JP60093270A JP9327085A JPS61249363A JP S61249363 A JPS61249363 A JP S61249363A JP 60093270 A JP60093270 A JP 60093270A JP 9327085 A JP9327085 A JP 9327085A JP S61249363 A JPS61249363 A JP S61249363A
Authority
JP
Japan
Prior art keywords
glutathione
yeast
yeast extract
extracted
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.)
Granted
Application number
JP60093270A
Other languages
Japanese (ja)
Other versions
JPS6237949B2 (en
Inventor
Kazutoshi Kinoshita
和俊 木下
Shunetsuro Oka
岡 俊悦郎
Masahiko Tabata
雅彦 把田
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.)
Sanyo Kokusaku Pulp Co Ltd
Original Assignee
Sanyo Kokusaku Pulp 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 Sanyo Kokusaku Pulp Co Ltd filed Critical Sanyo Kokusaku Pulp Co Ltd
Priority to JP60093270A priority Critical patent/JPS61249363A/en
Publication of JPS61249363A publication Critical patent/JPS61249363A/en
Publication of JPS6237949B2 publication Critical patent/JPS6237949B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:To obtain a yeast extract having high glutathione content and useful as a health food, etc., by extracting glutathione from yeast, extracting other cell components from the residue, mixing the extracted components to the glutathione, adjusting to an acidic state, and concentrating, neutralizing and spray-drying the mixture. CONSTITUTION:Yeast (e.g. Saccharomyces cerevisiae IMA 4220) is treated with e.g. an acid to effect the extraction of glutathione. The other cell components are extracted from the extraction residue with e.g. a cell wall lyase. The extracted components are mixed with the glutathione, and the mixture is adjusted to 2-4pH, concentrated, neutralized to 5-6pH and spray-dried to obtain the objective yeast extract.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は酵母エキスの製造方法に関するものであり、そ
の目的とする処はグルタチオン含有率の高い酵母エキス
を製造する方法を提供することにある。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a method for producing a yeast extract, and an object thereof is to provide a method for producing a yeast extract with a high glutathione content. .

グルタチオンは化学名が、γ−グルタミル・システイニ
ル・グリシンであるトリペプチドであり、生体内の酸化
還元系に関与して諸酵素の賦活および解毒作用などの重
要な役割を果たすものである。
Glutathione is a tripeptide whose chemical name is γ-glutamyl cysteinyl glycine, and it participates in the redox system in living organisms and plays important roles such as activation of various enzymes and detoxification.

酵母エキスは従来から調味料として用いられているが、
最近ではグルタミン酸ソーダなどの化学調味料が天然物
志向の影響を受けて敬遠され、天然物である酵母エキス
が好まれる傾向にある。
Yeast extract has traditionally been used as a seasoning, but
Recently, chemical seasonings such as monosodium glutamate have been avoided due to the preference for natural products, and yeast extract, which is a natural product, is being preferred.

本発明者等はグルタチオン含有率の高い酵母エキスの効
能について検討した結果、健康食品として有効である以
外にフレーバーエンハンサ−としての効果も極めて強い
ことを見い出した。
The present inventors investigated the efficacy of yeast extract with a high glutathione content and found that it is not only effective as a health food but also extremely effective as a flavor enhancer.

〔従来の技術〕[Conventional technology]

ところで、従来の酵母エキスの製造方法としては、酵素
法、アルカリ抽出法など各種の方法があるが、何れの場
合にも酵母中のグルタチオンは抽出、精製の工程で大部
分が消失して了っていた。
By the way, there are various conventional methods for producing yeast extract, such as enzymatic methods and alkaline extraction methods, but in either case, most of the glutathione in the yeast is lost during the extraction and purification process. was.

〔問題点を解決するための手段〕[Means for solving problems]

本発明者等は鋭意検討を進めた結果、次のようなグルタ
チオン高含有酵母エキスの製造方法を完成するに至った
As a result of intensive studies, the present inventors have completed the following method for producing a yeast extract containing high glutathione content.

先ず、酵母より酸または熱水にてグルタチオンを抽出し
、その抽出液をpH2〜4に調節して保存しておく、一
方、残金酵母から残りの菌体内成分(主にタンパク質)
を通常の方法で、例えば細胞壁溶解酵素を働かせて抽出
し、その抽出液と先のグルタチオン抽出液とを混合しp
Hを5に調節して噴霧乾燥することにより酵母中に含有
していたグルタチオンを殆ど減少させること無くグルタ
チオン高含有の酵母エキスを得る方法を発明するに至っ
たのである。
First, glutathione is extracted from yeast with acid or hot water, and the extract is adjusted to pH 2 to 4 and stored. Meanwhile, the remaining intracellular components (mainly proteins) are extracted from the remaining yeast.
is extracted by a normal method, for example by using a cell wall lytic enzyme, and the extract is mixed with the glutathione extract.
By adjusting H to 5 and spray drying, they have invented a method for obtaining a yeast extract with a high glutathione content without almost reducing the glutathione contained in the yeast.

この方法に用いる酵母の種類としては通常、パン酵母、
ビール酵母などに用いられるサツカロミセス属であるの
が普通であるが、その種類は問わない。
The types of yeast used in this method are usually baker's yeast,
Usually, it is from the genus Satucharomyces, which is used for brewer's yeast, etc., but the type does not matter.

また酵母の培養に用いる借地も糖蜜を糖源とするのが普
通であるが、その種類及びその他の栄養源に関しても特
に制限するものではない。
In addition, the rented land used for culturing yeast usually uses molasses as a sugar source, but there are no particular restrictions on the type or other nutritional sources.

〔実施例〕〔Example〕

以下、実施例によって本発明の詳細な説明するが、本発
明は之等に限定されるものではない。
EXAMPLES Hereinafter, the present invention will be explained in detail with reference to Examples, but the present invention is not limited thereto.

実施例1 サツカロミセス・セレビシェIAM4220を次の借地
で2日間培養した。
Example 1 Satucharomyces cerevisiae IAM4220 was cultured for 2 days on the following leased land.

ル 借地組成 糖蜜(糖濃度3%に調製) 尿素 29g、塩化カリウム Log リン安 23g、硫酸マグネシウム 10gを10Qに
調整し、培養液を遠心分離、洗浄して酵母スラリーIQ
 (固形分10%v/v)を得た。各500tanにつ
いて次の2つの方法により酵母エキスを製造した。
Molasses composition (adjusted to 3% sugar concentration) Urea 29g, potassium chloride Log Ammonium phosphorus 23g, magnesium sulfate 10g adjusted to 10Q, culture solution centrifuged and washed to make yeast slurry IQ
(solid content 10% v/v) was obtained. Yeast extracts were produced using the following two methods for each 500 tan.

A法(従来方法) 酵母スラリー500m mに細胞壁溶解酵素(商品名Y
L−5;天野製薬社製)0.5 gを添加し、45℃に
て24時間反応させた後、遠心分離し、上澄液を濃縮後
、噴霧乾燥して酵母エキス35gを得た。得られた酵母
エキスのDTNB法によるグルタチオン含有率は0.1
%(対絶乾)であった。
Method A (conventional method) Add cell wall lytic enzyme (product name Y) to 500 m of yeast slurry.
After adding 0.5 g of L-5 (manufactured by Amano Pharmaceutical Co., Ltd.) and reacting at 45° C. for 24 hours, centrifugation was performed, and the supernatant was concentrated and spray-dried to obtain 35 g of yeast extract. The glutathione content of the obtained yeast extract by the DTNB method was 0.1.
% (relative to bone dry).

B法(本発明方法) 前記酵母スラリー500IIQを塩酸にてpnを2に調
節し、60℃にて30分間撹拌抽出し、冷却後、遠心分
離し、上澄液はpH2に調節し冷却した侭保存して置き
、他方、抽出残差酵母の方は10%v/vになるように
水で分散させpH6に調節し、実施例Aと同じ細胞壁溶
解酵素を0.5 g添加し、45℃にて24時間反応さ
せた後、遠心分離し、上澄液を前記上澄液と併せ、 p
H2,0に調節した。該混合液を濃縮後、再度pH5に
調節し噴霧乾燥して酵母エキス34gを得た。得られた
酵母エキスのグルタチオン含有率は0.8%であった。
Method B (method of the present invention) The yeast slurry 500IIQ was adjusted to pn 2 with hydrochloric acid, stirred and extracted at 60°C for 30 minutes, cooled and centrifuged, and the supernatant was adjusted to pH 2 and cooled. On the other hand, the extracted residual yeast was dispersed with water to 10% v/v, adjusted to pH 6, added 0.5 g of the same cell wall lytic enzyme as in Example A, and incubated at 45°C. After reacting for 24 hours at p
Adjusted to H2.0. After concentrating the mixture, the pH was adjusted to 5 again and spray-dried to obtain 34 g of yeast extract. The glutathione content of the obtained yeast extract was 0.8%.

実施例2 サツカロミセス・セレビシェIAM4220を親株とす
る山場国策パルプ社変異株を実施例1と同様に培養し同
様の処理で酵母スラリー900+mff1 (固形分1
0%w/v)を得た。
Example 2 A mutant strain of Yamaba Kokusaku Pulp Co., Ltd. whose parent strain is Satscharomyces cerevisiae IAM4220 was cultured in the same manner as in Example 1, and yeast slurry 900+mff1 (solid content 1
0% w/v) was obtained.

各450@αについて実施例1と同様に処理して酵母エ
キスを製造した。
Each 450@α was treated in the same manner as in Example 1 to produce yeast extract.

A法(従来方法): 実施例1と全く同様にして酵母エキス30gを得た。得
られた酵母エキスのDTNB法によるグルタチオン含有
率は0.3%であった。
Method A (conventional method): 30 g of yeast extract was obtained in exactly the same manner as in Example 1. The glutathione content of the obtained yeast extract by the DTNB method was 0.3%.

B法(本発明方法) 実施例1と全く同様にして酵母エキス31gを得た。得
られた酵母エキスのDTNB法によるグルタチオン含有
率は2.2%であった。
Method B (method of the present invention) In exactly the same manner as in Example 1, 31 g of yeast extract was obtained. The glutathione content of the obtained yeast extract as determined by the DTNB method was 2.2%.

Claims (1)

【特許請求の範囲】[Claims] 1 酵母スラリーから、予め菌体中のグルタチオンを抽
出しておき、その抽出残査から更に残りの菌体成分を抽
出し、前者のグルタチオン抽出液と後者の菌体成分抽出
液とを混合し、pH2〜4に調節、濃縮後、pH5〜6
に中和して噴霧乾燥することを特徴とする酵母エキス製
造方法。
1. Glutathione in the bacterial cells is extracted from the yeast slurry in advance, the remaining bacterial components are further extracted from the extraction residue, and the former glutathione extract and the latter bacterial component extract are mixed, Adjust to pH 2-4, and after concentration, pH 5-6
A method for producing yeast extract, which comprises neutralizing and spray-drying the yeast extract.
JP60093270A 1985-04-30 1985-04-30 Production of yeast extract Granted JPS61249363A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60093270A JPS61249363A (en) 1985-04-30 1985-04-30 Production of yeast extract

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60093270A JPS61249363A (en) 1985-04-30 1985-04-30 Production of yeast extract

Publications (2)

Publication Number Publication Date
JPS61249363A true JPS61249363A (en) 1986-11-06
JPS6237949B2 JPS6237949B2 (en) 1987-08-14

Family

ID=14077767

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60093270A Granted JPS61249363A (en) 1985-04-30 1985-04-30 Production of yeast extract

Country Status (1)

Country Link
JP (1) JPS61249363A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01281057A (en) * 1988-05-06 1989-11-13 Ajinomoto Co Inc Production of yeast extract with high nucleic acid and glutathione content
WO2018043632A1 (en) * 2016-09-02 2018-03-08 興人ライフサイエンス株式会社 Yeast extract for enhancing richness and creamy feel

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51144788A (en) * 1975-06-04 1976-12-13 Kanegafuchi Chem Ind Co Ltd Process for preparing glutathione- containing liquid from yeast cells

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51144788A (en) * 1975-06-04 1976-12-13 Kanegafuchi Chem Ind Co Ltd Process for preparing glutathione- containing liquid from yeast cells

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01281057A (en) * 1988-05-06 1989-11-13 Ajinomoto Co Inc Production of yeast extract with high nucleic acid and glutathione content
WO2018043632A1 (en) * 2016-09-02 2018-03-08 興人ライフサイエンス株式会社 Yeast extract for enhancing richness and creamy feel
CN109640701A (en) * 2016-09-02 2019-04-16 兴人生命科学株式会社 Enhance the yeast extract of strong sense and cream sense
JPWO2018043632A1 (en) * 2016-09-02 2019-06-24 興人ライフサイエンス株式会社 Yeast extract to enhance body and creamy feeling
EP3508074A4 (en) * 2016-09-02 2020-04-29 KOHJIN Life Sciences Co., Ltd. Yeast extract for enhancing richness and creamy feel

Also Published As

Publication number Publication date
JPS6237949B2 (en) 1987-08-14

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