JPS62275669A - Production of yeast extract - Google Patents

Production of yeast extract

Info

Publication number
JPS62275669A
JPS62275669A JP61119086A JP11908686A JPS62275669A JP S62275669 A JPS62275669 A JP S62275669A JP 61119086 A JP61119086 A JP 61119086A JP 11908686 A JP11908686 A JP 11908686A JP S62275669 A JPS62275669 A JP S62275669A
Authority
JP
Japan
Prior art keywords
yeast
basidiomycetes
extract
yeast extract
soft
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
JP61119086A
Other languages
Japanese (ja)
Inventor
Yoshinori Masuda
増田 芳宣
Kozo Kamata
鎌田 耕造
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.)
Sapporo Breweries Ltd
Original Assignee
Sapporo Breweries 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 Sapporo Breweries Ltd filed Critical Sapporo Breweries Ltd
Priority to JP61119086A priority Critical patent/JPS62275669A/en
Publication of JPS62275669A publication Critical patent/JPS62275669A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To produce a yeast extract having improved flavor and seasoning powder free from a yeast smell, by treating yeast with soft Basidiomycetes. CONSTITUTION:In producing a yeast extract by a conventional procedure, in a proper period of the production process, yeast is treated with a fruit body of soft Basidiomycetes such as Ganoderma lucidum, Pleurotus ostreatus, Lentinus edodes, etc., a mycelium, a ground mold, an extract, a mold culture solution, a supernatant liquid or a mixture thereof, for example, the Basidiomycetes is added to a yeast suspension and brought into contact with the Basidiomycetes for a given time under a condition such as pH, temperature, etc., to readily show enzymatic reactions.

Description

【発明の詳細な説明】 3、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法に関し、詳しくは香味の改
良された酵母エキスを効率的に製造する方法に関する。
Detailed Description of the Invention 3. Detailed Description of the Invention [Field of Industrial Application] The present invention relates to a method for producing a yeast extract, and more particularly to a method for efficiently producing a yeast extract with improved flavor.

〔従来の技術とその問題点〕[Conventional technology and its problems]

酵母エキスは天然調味料として肉エキス、野菜エキス、
魚介類エキス等と共に化学調味料にはない複雑な呈味性
を有しているため、近年広く利用されてきている。
Yeast extract is used as a natural seasoning for meat extract, vegetable extract,
It has been widely used in recent years because, along with seafood extracts, it has a complex taste that is not found in chemical seasonings.

しかしながら、酵母エキスは特有の香味を有するため、
その使用量や用途などに制約を受けるなどの問題点があ
った。
However, since yeast extract has a unique flavor,
There were problems such as restrictions on the amount of use and applications.

一般に、酵母エキスは自己消化法、酸分解法。Generally, yeast extract is produced by autolysis or acid decomposition.

酸素分解法などによって製造されているが、自己消化法
では酵母の持つ酵素力を利用するため、その作用が緩慢
であり、かつ強固な酵母細胞壁が残留する。また、酸分
解法では酸により強制的に加熱加水分解するため、その
香味は好ましいものではない。さらに、酵素分解法では
各種の酵素を用いているけれども、これら酵素はカビや
ハタテリア等から得られたものが多く、食品添加物とし
てあまり好ましいものではなかった。
It is produced using oxygen decomposition methods, etc., but since the autolysis method uses the enzymatic power of yeast, its action is slow and strong yeast cell walls remain. In addition, in the acid decomposition method, the flavor is not desirable because the acid is used to forcibly heat and hydrolyze the product. Furthermore, although various enzymes are used in the enzymatic decomposition method, many of these enzymes are obtained from molds, groupers, etc., and are not very desirable as food additives.

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

本発明者らは、これら酵母エキスの香味の改良、製造条
件の改善、収率の向上等を目指して研究を重ねた結果、
本発明を完成するに至ったのである。
As a result of repeated research aimed at improving the flavor, manufacturing conditions, and yield of these yeast extracts, the present inventors found that
This led to the completion of the present invention.

すなわち本発明は、酵母エキスを製造するにあたり、酵
母に軟質を旦子菌類を作用させることを特徴とする酵母
エキスの製造法である。
That is, the present invention is a method for producing a yeast extract, which is characterized in that, in producing the yeast extract, a yeast fungus is applied to soften the yeast.

本発明は酵素分解法による酵母エキスの製造法に分類さ
れるものであるが、まんねんたけ、ひらたけ、しいたけ
、なめたけ等の軟質担子菌類、好ましくは食用、薬用担
子菌類の1種もしくは2種以上の培養によって得られる
酵素を利用して酵母エキスを製造するものである。
The present invention is classified as a method for producing yeast extract by enzymatic decomposition method, and the method uses soft basidiomycetes such as Mannentake mushroom, Hiratake mushroom, Shiitake mushroom, Nametake mushroom, etc., preferably one or two types of edible and medicinal basidiomycete fungi. Yeast extract is produced using the enzyme obtained by the above culture.

本発明は、主にこれら菌類を培養する工程と、その培養
物を利用して酵母エキスを得る工程から成っている。
The present invention mainly consists of a step of culturing these fungi and a step of obtaining yeast extract using the culture.

軟質担子菌類は通常、ホダ木やオガ屑、堆肥等に固体培
養され、その子実体は好んで食用とされるが、これら菌
類はセルロース、ヘミセルロース。
Soft basidiomycetes are usually cultivated on solid wood, sawdust, compost, etc., and their fruiting bodies are often eaten, but these fungi produce cellulose and hemicellulose.

リグニン等を分解する酵素力を有しており、さらに種々
の核酸分解酵素をも含有している。本発明はこれら担子
菌類の酵素力をそのままあるいは部分的に利用して酵母
エキスを製造するものであり、担子菌類の利用法はそれ
が子実体であるか菌糸であるかを問わない。また、担子
菌体の破砕物や抽出物などであってもよい。さらには、
担子菌類を液体培養した培養液そのものや該培養液から
固液分離して得られる上清であってもよい。また、これ
らを精製処理したものであってもよい。担子菌類を液体
培養すると、菌糸の生育と共に菌糸は勿論のこと培養液
中にも強力な酵素を蓄積する。したがって、担子菌体破
砕物あるいは抽出物等の利用も可能であるが、培養液(
担子菌体の有無に拘らず)の利用の方が容易であり、実
用性に富むものである。なお、これら菌類は混合物とし
て用いることが出来ることは勿論である。
It has enzymatic power to decompose lignin, etc., and also contains various nucleolytic enzymes. The present invention uses the enzymatic power of these basidiomycetes directly or partially to produce a yeast extract, and the basidiomycetes can be used regardless of whether they are fruiting bodies or hyphae. It may also be a crushed product or extract of basidiomycete cells. Furthermore,
The culture solution itself obtained by liquid culturing Basidiomycetes or the supernatant obtained by solid-liquid separation from the culture solution may be used. Moreover, these may be purified. When basidiomycetes are cultured in liquid, strong enzymes accumulate not only in the hyphae but also in the culture solution as the hyphae grow. Therefore, it is possible to use crushed basidiomycete cells or extracts, but culture fluid (
It is easier to use basidiomycetes (with or without basidiomycetes) and is more practical. It goes without saying that these fungi can be used as a mixture.

担子菌類を液体培養するために用いる培地としては通常
の栄養培地でよく、特殊な成分を加えたりする必要はな
い。具体的には、一般に用いられる培地素材、たとえば
ペプトン、肉エキス、麦芽エキス、酵母エキス、ブドウ
糖、無機塩類等を適宜組合わせ、水に希釈して用いれば
よく、各成分の濃度は1〜5%程度で十分である。
The medium used for liquid culture of basidiomycetes may be a normal nutrient medium, and there is no need to add special ingredients. Specifically, commonly used culture medium materials such as peptone, meat extract, malt extract, yeast extract, glucose, inorganic salts, etc. may be appropriately combined and used after being diluted with water, and the concentration of each component may be 1 to 5. % is sufficient.

担子菌類培養物は強力なβ−グルカナーゼ活性を有して
おり、これはβ−グルカンから還元垢を生成することか
ら確認できる(第1図参照)。この酵素は酵母細胞壁に
も作用して、これを溶解することが検鏡により観察され
た。さらに、この培養物はキシラナーゼ活性を有してい
ることが認められた。
Basidiomycete cultures have strong β-glucanase activity, which is confirmed by the production of reduced plaque from β-glucans (see Figure 1). Using a microscope, it was observed that this enzyme also acts on yeast cell walls and dissolves them. Furthermore, this culture was found to have xylanase activity.

酵母に担子菌類に作用させるには、酵母エキス製造過程
の適宜時期に行なえばよいが、通常は酵母懸濁液に該担
子菌類を加え、pH,温度などを酵素作用が発現しやす
い条件として所定時間(通常1〜20時間)接触させれ
ばよい。この場合、酵母懸濁液の濃度は圧搾酵母濃度を
5〜45%、好ましくは15〜35%として用いるとよ
く、担子菌類として液体培養物を用いるときは、培養開
始後約1ケ月経過したものを0.3〜10%程度、好ま
しくは1〜5%程度の割合で添加するのがよい。さらに
、酵素の作用温度、 pHについては、β−グルカナー
ゼ活性が発現し、かつ良好な呈味を持つ酵母エキスを得
るための条件として、pHが4.5〜9.0、好ましく
は6.5〜8.5、温度が30〜60℃、好ましくは4
0〜55℃で作用させるのがよい。また、酵母は生酵母
を用いて自己消化法による酵母エキスの製造法と併用す
る形式としてもよく、乾燥酵母や熱変性処理した酵母な
どを用いてもよく、特に制約されることはない。
To make yeast act on the basidiomycetes, it can be done at an appropriate time during the yeast extract production process, but usually the basidiomycetes are added to the yeast suspension and the pH, temperature, etc. are adjusted to certain conditions that facilitate the expression of enzyme action. The contact may be made for a period of time (usually 1 to 20 hours). In this case, the concentration of the yeast suspension should be 5 to 45%, preferably 15 to 35%, of the compressed yeast concentration, and when using a liquid culture as the basidiomycete, the yeast suspension should be used after about 1 month has passed after the start of culture. It is preferable to add about 0.3 to 10%, preferably about 1 to 5%. Furthermore, regarding the action temperature and pH of the enzyme, the pH is 4.5 to 9.0, preferably 6.5, as conditions for expressing β-glucanase activity and obtaining a yeast extract with good taste. ~8.5, temperature is 30-60℃, preferably 4
It is preferable to act at a temperature of 0 to 55°C. Further, the yeast may be used in combination with the method for producing yeast extract by autolysis using fresh yeast, or dried yeast or heat-denatured yeast may be used, and there are no particular restrictions.

〔発明の効果および作用〕[Effects and operations of the invention]

本発明によれば、酵母臭がなく香味の改善された呈味力
のある酵母エキスが得られる。たとえば、実施例2にお
いて得られた酵母エキスの分析を行なったところ、グル
タミン酸、アラニン、リジンなどのアミノ酸類を多く含
み、かつ種々の5′−ヌクレオチド類、とりわけ5゛−
グアニル酸を多量に含んでいることが判明した。したが
って、本発明による酵母エキスが呈味性に優れている理
由は、これらアミノ酸類と5′−ヌクレオチド類の相互
作用によるものであると認められる。このことは、本発
明に用いる担子菌類に含まれる酵素が単に細胞壁溶解酵
素としてだけでなく、蛋白質分解酵素、核酸分解酵素な
どをも含む複合酵素として作用していると考えられるば
かりでなく、酵母エキス製造時の自己消化酵素系とも連
動して作用し、その呈味性を増幅しているものと思われ
る。
According to the present invention, a yeast extract with no yeast odor, improved flavor, and strong taste can be obtained. For example, analysis of the yeast extract obtained in Example 2 revealed that it contained a large amount of amino acids such as glutamic acid, alanine, and lysine, as well as various 5'-nucleotides, especially 5'-nucleotides.
It was found that it contains a large amount of guanylic acid. Therefore, it is recognized that the reason why the yeast extract according to the present invention has excellent taste is due to the interaction between these amino acids and 5'-nucleotides. This suggests that the enzymes contained in the basidiomycetes used in the present invention not only act as cell wall lytic enzymes but also as complex enzymes that include proteolytic enzymes, nucleolytic enzymes, etc. It is thought that it acts in conjunction with the autolytic enzyme system during extract production to amplify its taste.

また、本発明の方法によれば、酵母エキスの製造時間を
短縮することが出来る上に、その収率も向上する。
Moreover, according to the method of the present invention, not only can the manufacturing time of yeast extract be shortened, but also its yield can be improved.

〔実施例〕〔Example〕

次に、本発明を実施例により説明するが、本発明はこれ
らによって制限されるものではない。
Next, the present invention will be explained by examples, but the present invention is not limited thereto.

実施例1 麦汁(温度約1.5%)1)に粉末酵母エキス2.5g
(0,25%)およびグルコース20g(2,0%)を
添加し、オートクレーブで120℃、15分の殺菌を行
なった。冷却後、この培地にまんねんたけを接種し、2
0℃で静置培養を行なった。
Example 1 2.5 g of powdered yeast extract in wort (temperature approximately 1.5%) 1)
(0.25%) and 20 g (2.0%) of glucose were added and sterilized in an autoclave at 120° C. for 15 minutes. After cooling, this medium was inoculated with Mannentake mushrooms, and 2
Static culture was performed at 0°C.

約1週間後には培養液表面に白色の菌糸が観察され、さ
らに培養を続けると、約1ケ月後には厚い菌糸蓋となり
、β−グルカナーゼ活性が最大となる。この培養液を濾
過して得た濾液を粗酵素とした。
After about one week, white hyphae are observed on the surface of the culture solution, and if the culture is continued further, after about one month a thick hyphae is formed and the β-glucanase activity reaches its maximum. The filtrate obtained by filtering this culture solution was used as a crude enzyme.

ビール酵母を洗浄して得た圧搾酵母200g(酵母乾物
21%)を水に分散し、これに上記まんねんたけ粗酵素
20m1を加え、加水して1)とした。次に、pH6,
5、温度45℃で保持し、20時間後に遠心分離を行な
い、液部と粕部に分けた。液部に一定量の食塩を添加し
たのち濃縮し温度約55%として殺菌した。このときの
酵母エキス収率は52%であった。一方、対照として粗
酵素を加えることなく自己消化法としたこと以外は同様
にして得た酵母エキスは収率が約10%も低いものであ
った。また、官能検査(パネル4名による2%溶液の試
飲による比較)により酵母エキスの香味について検討し
たところ、第1表に示した如く、本発明による製品は香
味も優れていることが判明した。
200 g of compressed yeast (21% yeast dry matter) obtained by washing beer yeast was dispersed in water, and 20 ml of the above-mentioned Mannake mushroom crude enzyme was added thereto and water was added to obtain 1). Next, pH 6,
5. The temperature was maintained at 45°C, and after 20 hours, centrifugation was performed to separate the liquid part and the lees part. After adding a certain amount of common salt to the liquid part, it was concentrated and sterilized at a temperature of about 55%. The yeast extract yield at this time was 52%. On the other hand, as a control, the yield of yeast extract obtained in the same manner except that the autolysis method was used without adding crude enzyme was about 10% lower. Furthermore, when the flavor of the yeast extract was investigated through a sensory test (comparison by tasting 2% solutions by four panelists), it was found that the product according to the present invention also had an excellent flavor, as shown in Table 1.

第  1  表 1♂L−評        価 対照品    酵母臭あり、呈味力やや乏しい本発明品
   酵母臭なし、呈味力あり実施例2 麦汁(温度約1.5%)1)に肉エキス2.0g(0,
2%)およびグルコース20g(2,0%)を添加し、
オートクレーブで120℃、15分の殺菌を行なった。
Table 1 ♂L-Evaluation control product Inventive product with yeast odor and slightly poor taste power Example 2: Wort (temperature approx. 1.5%) 1) with meat extract 2 .0g(0,
2%) and glucose 20g (2,0%),
Sterilization was performed in an autoclave at 120°C for 15 minutes.

冷却後、この培地にひらたけを接種し、20℃で静置培
養を行なった。
After cooling, this medium was inoculated with oyster mushrooms and statically cultured at 20°C.

約1ケ月後に培養液表面に生育した菌糸を採取し、これ
に水を加えて磨砕し、次いぞ遠心分離して得た上清を粗
酵素とした。
After about one month, the mycelium grown on the surface of the culture solution was collected, ground by adding water, and then centrifuged to obtain a supernatant, which was used as crude enzyme.

ビール乾燥酵母45gを水に分散し、上記ひらたけ粗酵
素20mlを加え、加水して1)とした。
45 g of beer dry yeast was dispersed in water, 20 ml of the above-mentioned Hiratake crude enzyme was added, and water was added to prepare 1).

次に、pH8,0,温度45℃で保持し、10時間後に
遠心分離を行ない、液部と粗部に分けた。液部に一定量
の食塩を添加したのち濃縮し温度約55%として殺菌し
た。
Next, the mixture was maintained at a pH of 8.0 and a temperature of 45° C., and centrifuged after 10 hours to separate a liquid portion and a coarse portion. After adding a certain amount of common salt to the liquid part, it was concentrated and sterilized at a temperature of about 55%.

この酵母エキスについて分析を行なったところ、グルタ
ミン酸4.5%、アラニン3.1%、リジン2.0%、
5゛−グアニル酸0.6%を含有しており、対照の酵素
無添加で調製した酵母エキスよりも香味が優れていた。
Analysis of this yeast extract revealed that glutamic acid 4.5%, alanine 3.1%, lysine 2.0%,
It contained 0.6% of 5'-guanylic acid, and had a better flavor than the control yeast extract prepared without the addition of enzyme.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は実施例1で得た粗酵素をpH6,0,温度45
℃の条件でβ−グルカンに作用させたときの還元糖の経
時的生成率を示すグラフである。
Figure 1 shows the crude enzyme obtained in Example 1 at pH 6.0 and temperature 45.
It is a graph showing the production rate of reducing sugar over time when it is made to act on β-glucan under conditions of °C.

Claims (3)

【特許請求の範囲】[Claims] (1)酵母エキスを製造するにあたり、酵母に軟質担子
菌類を作用させることを特徴とする酵母エキスの製造法
(1) A method for producing a yeast extract, which comprises reacting yeast with a soft basidiomycete.
(2)軟質担子菌類がまんねんたけ、ひらたけ、しいた
け、なめたけ等の中から選ばれたものである特許請求の
範囲第1項記載の方法。
(2) The method according to claim 1, wherein the soft basidiomycete is selected from Mannentake mushroom, Oyster mushroom, Shiitake mushroom, Nametake mushroom, etc.
(3)軟質担子菌類が子実体、菌糸、菌体破砕物もしく
は抽出物、菌体培養液もしくはその培養上清またはこれ
らの混合物である特許請求の範囲第1項記載の方法。
(3) The method according to claim 1, wherein the soft basidiomycete is a fruiting body, mycelium, a fungal cell fragment or extract, a fungal cell culture solution, a culture supernatant thereof, or a mixture thereof.
JP61119086A 1986-05-26 1986-05-26 Production of yeast extract Pending JPS62275669A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61119086A JPS62275669A (en) 1986-05-26 1986-05-26 Production of yeast extract

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61119086A JPS62275669A (en) 1986-05-26 1986-05-26 Production of yeast extract

Publications (1)

Publication Number Publication Date
JPS62275669A true JPS62275669A (en) 1987-11-30

Family

ID=14752543

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61119086A Pending JPS62275669A (en) 1986-05-26 1986-05-26 Production of yeast extract

Country Status (1)

Country Link
JP (1) JPS62275669A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1078452C (en) * 1992-12-02 2002-01-30 Cpc国际有限公司 Flavored yeast extracts
JP2006129835A (en) * 2004-11-09 2006-05-25 Takeda-Kirin Foods Corp Yeast essence highly containing glutamic acid and method for producing the same
JP2019129795A (en) * 2018-02-02 2019-08-08 三菱商事ライフサイエンス株式会社 Flavor improver

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1078452C (en) * 1992-12-02 2002-01-30 Cpc国际有限公司 Flavored yeast extracts
JP2006129835A (en) * 2004-11-09 2006-05-25 Takeda-Kirin Foods Corp Yeast essence highly containing glutamic acid and method for producing the same
JP4651361B2 (en) * 2004-11-09 2011-03-16 キリンフードテック株式会社 Glutamic acid-rich yeast extract and method for producing the same
JP2019129795A (en) * 2018-02-02 2019-08-08 三菱商事ライフサイエンス株式会社 Flavor improver

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