JPS5828243A - Preparation of mushroom extract - Google Patents

Preparation of mushroom extract

Info

Publication number
JPS5828243A
JPS5828243A JP56123840A JP12384081A JPS5828243A JP S5828243 A JPS5828243 A JP S5828243A JP 56123840 A JP56123840 A JP 56123840A JP 12384081 A JP12384081 A JP 12384081A JP S5828243 A JPS5828243 A JP S5828243A
Authority
JP
Japan
Prior art keywords
extract
mushroom
mushrooms
residue
extracting
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
JP56123840A
Other languages
Japanese (ja)
Other versions
JPS5933338B2 (en
Inventor
Kazuya Hashimoto
一哉 橋本
Tetsuhiko Tominaga
富永 哲彦
Yoshitomo Iwamoto
岩本 喜伴
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.)
Toyo Seikan Group Holdings Ltd
Original Assignee
Toyo Seikan Kaisha 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 Toyo Seikan Kaisha Ltd filed Critical Toyo Seikan Kaisha Ltd
Priority to JP56123840A priority Critical patent/JPS5933338B2/en
Publication of JPS5828243A publication Critical patent/JPS5828243A/en
Publication of JPS5933338B2 publication Critical patent/JPS5933338B2/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L31/00Edible extracts or preparations of fungi; Preparation or treatment thereof

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Microbiology (AREA)
  • Mycology (AREA)
  • Health & Medical Sciences (AREA)
  • Nutrition Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Food Science & Technology (AREA)
  • Polymers & Plastics (AREA)
  • Preparation Of Fruits And Vegetables (AREA)
  • Seasonings (AREA)

Abstract

PURPOSE:To prepare a mushroom extract in high yield, by dipping a mushroom in an alcoholic solution containing phosphoric acid under reduced pressure, extracting the mushroom with vitamin C, and a metallic chelating agent and then an alkaline saline solution, and extracting the resultant residue with an enzymic treatment. CONSTITUTION:An edible mushroom, e.g. SHIITAKE mushroom, is dipped in 30-100% alcohol containing 0.2-3.0% citric acid under reduced pressure, heated with vitamin C and a metallic chelating agent, e.g. sodium citrate, and homogenized. The resultant homogenate is then centrifuged to extract the first extract. The remaining residue is heated with an alkaline saline solution of 8-9 pH to separate the second extract. The remaining residue is then treated with a cell wall lytic enzyme, e.g. cellulase, and the residue is then centrifuged to give the third extract. The first - the third extracts are then combined and used as a mushroom extract for a seasoning.

Description

【発明の詳細な説明】 本発明は、キノコエキスの製造方法に@する。[Detailed description of the invention] The present invention is directed to a method for producing a mushroom extract.

食用キノコは香味に丁ぐれている上に多檎幸のアミノ酸
を含む良質の蛋白質とビタずン頌を豊富に含有し栄養価
の極めて高い食品である。その蛋1白質は必須アミノ酸
であるスレオニン、バリン。
Edible mushrooms are extremely nutritious foods, rich in flavor and rich in high-quality proteins, including amino acids, and vitamins. The protein contains essential amino acids threonine and valine.

メチオニン、イソロイシン、ロイシン、フェニールアラ
ニン、リシン、トリプトファンのほかアス珊によって比
較的安定な状態でアスコルビン酸。
Methionine, isoleucine, leucine, phenylalanine, lysine, tryptophan as well as ascorbic acid in a relatively stable state by ascoral.

サイアンン、リボフラビン、ニコチン酸、バントティン
酸、ビオチン等を残存し1%にリボフラビンとニコチン
酸の含有量が高い。また食用キイコのm質中にはマンニ
ットとトレハロースが、高<。
Cyanine, riboflavin, nicotinic acid, bantotic acid, biotin, etc. remain, and the content of riboflavin and nicotinic acid is high at 1%. In addition, mannitol and trehalose are high in the substance of edible keystone.

キノコ特有のうまみの構成分となっている。It is a component of the unique flavor of mushrooms.

キノコの子実体は周知のように檀々の方法で調理して食
用に供するほか1缶詰等として加工もされているが、こ
れら従来の1lllI珊、加工の方法はいずれもキノコ
の子実体を固体として丸のま−あるいは切断して食用に
供するものである。また従来製造されている缶詰やカッ
プ入りのマッシュルームスープや粉末状のマツシュルー
ムスープの素等和しても、クリームスープ等に固体のキ
ノコの細片を混入したものであって、キノコの子実体を
液化し飲料として利用したものはない。
As is well known, the fruiting bodies of mushrooms are cooked and eaten using various methods, and are also processed into canned foods, etc., but all of these conventional processing methods produce solid mushroom fruiting bodies. It is eaten by rolling it or cutting it into pieces. Furthermore, even if conventionally produced canned or cupped mushroom soups or powdered pine mushroom soups are mixed with cream soup, solid mushroom pieces are mixed into the cream soup. There is no substance that has been liquefied and used as a drink.

キノコを上記のように固体として食用に供するかわりに
その岨畿馨完全に崩壊して含有取分を抽出するようにし
てキノコのエキスを製a″fれば。
Instead of edible mushrooms as solids as described above, mushroom extracts can be produced by completely disintegrating the mushrooms and extracting the fraction contained therein.

このキノコエキスはこれを希釈した上に適宜の調味料を
加えることKより香味がすぐれかつ栄養価の高いスープ
として食膳に供することができるし。
By diluting this mushroom extract and adding appropriate seasonings, it can be served as a soup with excellent flavor and high nutritional value.

また一種の「だしの素」として調味料としての利用も可
能である等1食品工業忙おける利用価値は極めて高いと
考えられる。
It is also considered to have extremely high utility value in the food industry, as it can be used as a seasoning as a type of "dashi base".

しかるに、従来キノコのエキスは商品として市場に視れ
たことはな(、キノコエキスを抽出する方法%なんら仰
られていない。従来缶結工業においては、キノコの子実
体ケグライン中で加熱処理する際に生じる処場液馨マツ
シュルーム缶詰(以下の説明において1マツシユルーム
」とは市場において「マツシュルーム」と呼ばれて取引
されている学名ムgaricum biaporus、
和名ハラタケと呼ばれるキノコを指称する)の注入液や
!141味液として利用しているが、この場合、被処理
子実体中エキスとして抽出される成分は子実体全体の乙
チ程度に過ぎない。また、上記従来のプライン中での単
純な煮熱処理でを:キノコの蛋白質はほとんど分解、抽
出さtt rxいので、キノコに含まれる必須アミノ酸
を含む多種類のアミノ酸をすべてエキス中に抽出てるこ
とはとうてい不可能である。
However, until now, mushroom extracts have never been seen on the market as a commercial product (no mention has been made of any methods for extracting mushroom extracts.) In the past, in the canning industry, mushroom fruiting bodies were heat-treated in keglines. canned pine mushrooms (in the following explanation, 1 pine mushroom) refers to the scientific name Garicum biaporus, which is traded as ``pine mushrooms'' in the market.
The Japanese name refers to the mushroom called Haratake ) infusion and! 141 is used as a taste liquid, but in this case, the components extracted as an extract from the fruiting body to be processed are only about the amount of ochi from the whole fruiting body. In addition, with the above-mentioned simple boiling heat treatment in the conventional brine, most of the mushroom proteins are decomposed and extracted, so all the various types of amino acids, including essential amino acids, contained in mushrooms are extracted into the extract. is simply impossible.

キノコエキスの上記のような食品工業における高い利用
価値にもかかわらずキノコエキスが商品としていまだ市
場に現れていないのは、キノコの上記各種栄養分を含む
成分を食品としての価値を損わずに抽出″′rりことが
極めて困難であることに帰因する。′rなわち、上記プ
ライン中での煮熱処理より%l長い時間を、かけてキノ
コを煮熱すれば。
Despite the high utility value of mushroom extracts in the food industry as described above, mushroom extracts have not yet appeared on the market as commercial products.The reason why mushroom extracts have not yet appeared on the market is because the components containing the various nutrients mentioned above can be extracted from mushrooms without sacrificing their value as food. This is due to the fact that it is extremely difficult to boil the mushrooms. That is, if the mushrooms are boiled for a period of time that is %l longer than the boiling treatment in the prine described above.

キノコ成分の収率馨ある程度高めることは可能であるが
、キノコには各種の酵素が含まれており、これらの酵素
の中のあるものはエキス抽出のためキノコを加熱処理す
る過程において活性化し、その作用によりキノコは黒変
したり異臭を放つようになるので、得られたエキスはと
うてい食品としての価値を有しないものになってしまう
。したがって、単lfC&時間にわたる煮熱処理を行う
だけでは食用に耐えつるキノコエキスを得ることは不可
能である。
Although it is possible to increase the yield of mushroom components to some extent, mushrooms contain various enzymes, and some of these enzymes are activated during the process of heating the mushrooms for extract extraction. As a result of this action, the mushrooms turn black and emit a strange odor, so the resulting extract has no value as a food. Therefore, it is impossible to obtain an edible mushroom extract by simply performing a boiling heat treatment for a single lfC & hours.

そこで、本発明は、キノコのすべての栄養分を含むエキ
スを食品としての価値を損わずに最大限に抽出しつる新
規な方法!提供することt目的とするものである。
Therefore, the present invention is a novel method for extracting the maximum amount of mushroom extract containing all the nutrients without sacrificing its value as a food! The purpose is to provide.

上記目的を達成する本発明の構成は、特許請求の範囲に
記載のとおりであるが、これt喪てるにエキスの抽出工
程を3段階に分けて、第1の段階では原料固形キノコを
クエン酸添加アルコール水浴液中和減圧下に浸漬してキ
ノコ中の酵素を不活性化した後ビタミンCおよび金属キ
レート剤水溶液中で酸化、着色を防止しつへ加熱して第
1の抽出液を分離抽出し%@−2+の段階では該第1の
抽出gv抽出した後の残渣Yμs8ないし9の弱アルカ
リ性の食塩水中で加熱し組織崩壊を促進させて第2の抽
出液を分離抽出し、さらVC1!3の段階では該m2の
抽出液を抽出した後の残渣をキノコの細胞膜を崩壊させ
る能力を有する酵素と接触せしめることによりm解して
第3の抽出液を分離抽出し、か(して3段階の各抽出工
程で得た第1、第2および第3の抽出液を合せ濃縮して
キノコエキスを得るものである。
The structure of the present invention that achieves the above object is as described in the claims, but the extraction process of the mushroom extract is divided into three stages, and in the first stage, the solid mushroom raw material is extracted with citric acid. Neutralize the mushrooms in a water bath with added alcohol. After immersing them under reduced pressure to inactivate the enzymes in the mushrooms, heat in an aqueous solution of vitamin C and a metal chelating agent to prevent oxidation and coloring, and then separate and extract the first extract. At the %@-2+ stage, the residue after the first gv extraction is heated in a weakly alkaline saline solution of Yμs 8 to 9 to promote tissue disintegration, and the second extract is separated and extracted, and further VC1! In step 3, the residue after extracting the m2 extract is brought into contact with an enzyme capable of disrupting the cell membrane of mushrooms, and a third extract is separated and extracted. A mushroom extract is obtained by combining and concentrating the first, second, and third extracts obtained in each extraction step.

本発明にかかる方法を適用しつるキノコとしては、その
生産量が多く、比較的安価に入手でき、スープにした場
合の風味においてもすぐれている 、マツシュルームが
好適であるが、その他シイタケ。
Preferred vine mushrooms to which the method of the present invention can be applied are pine mushrooms, which are produced in large quantities, are relatively inexpensive, and have excellent flavor when made into soup, but other mushrooms may also be used.

エノキダケ、ヒラタケ、ナメコ、キクラゲ等地の食用キ
ノコにも適用しうるものである。また原料として使用す
るキノコはその子実体のみならず。
It can also be applied to edible mushrooms such as enoki mushrooms, oyster mushrooms, nameko mushrooms, and wood ear mushrooms. In addition, the mushrooms used as raw materials are not limited to their fruiting bodies.

根茎部、株などの]1!+富廃棄される部分をも利用て
 ゛ることができる。
rhizome, stock, etc.] 1! +You can also use the part that would be discarded.

ここで、実施例の説明に先立ち、本発明にかかるキノコ
エキスめ製造方法について一般的説明を行う。なお以下
の説明において成分室有料数値はすべて重量憾で示す。
Here, prior to describing Examples, a general explanation will be given of the method for producing mushroom extract according to the present invention. In the following explanation, all component room charges are expressed by weight.

キノコKtXフェノールオキシダーゼやチロシナーゼ等
各種の酵素が含まれており、これらの酵素作用はその肯
および温度条件KJ:つて大きく影響を受ける。エキス
抽出のためキノコを加熱処理する過5lllcおいて活
性化したこれらの酵素の作用圧よりキノコは黒変し、ま
た異臭を放つようになる。
Mushroom KtX contains various enzymes such as phenol oxidase and tyrosinase, and the action of these enzymes is greatly affected by the temperature and temperature conditions. Due to the action pressure of these enzymes activated during the heat treatment of mushrooms for extraction of extracts, the mushrooms turn black and emit a strange odor.

ソコで本発明の方法においては、まず原料キノコ40.
2 %ないし3.04のクエン酸Y含む加傷ないし10
0%アルコール中忙浸漬することKより、クエン酸の存
在lCよりキノコのpHヲ酵素が活性化する値以下に抑
えるとともにアルコールの酵素失活作用により酵素反応
を抑止する。酵素はその本体が蛋白質であるため、蛋白
質を凝固させる性質を有するアルコール忙接触させるこ
とによりその活性を失うのである。アルコールとしては
エタノールが好適であるが、メタノールまたはグロパノ
ールを、その他アセトン等を用いてもよい、アルコール
中にクエン酸のほか、JII糖脂肪酸エステル。
In the method of the present invention, first, raw material mushroom 40.
Containing 2% to 3.04% of Y citric acid to 10%
By immersing the mushrooms in 0% alcohol, the presence of citric acid keeps the pH of the mushrooms below the level at which enzymes are activated, and the enzyme deactivation effect of alcohol suppresses the enzyme reaction. Since enzymes are essentially proteins, they lose their activity when brought into contact with alcohol, which has the property of coagulating proteins. Ethanol is preferred as the alcohol, but methanol or gropanol, acetone, etc. may also be used.In addition to citric acid, JII sugar fatty acid ester may be used in the alcohol.

ソルビタン脂肪酸エステル等通宜の界面活性剤を県加す
れば、後の工程でキノコの酸化を防止し抽出液の抽出を
容rijにすることができる。キノコをクエン酸含有ア
ルコール中に浸漬しつ〜減圧するのは、キノコの組織中
に含まれる空気を除去し、クエン酸およびアルコール音
キノコ組織中にあまね(浸透させることにより充分な酸
化防止や酵素失活効果をあげるためである。
By adding a commonly used surfactant such as sorbitan fatty acid ester, oxidation of the mushrooms can be prevented in the subsequent process and the extraction of the extract can be made easier. Immersing mushrooms in citric acid-containing alcohol and reducing the pressure removes the air contained in the mushroom tissue, and allows the citric acid and alcohol to penetrate into the mushroom tissue to provide sufficient antioxidant protection and enzymes. This is to achieve a deactivation effect.

次にアルコールから取出したキノコをビタミンCおよび
金属キレート剤の水溶液をホモゲナイズしている中に添
加破砕し加熱する。ビタミンCは酸化防止と酵素活性抑
制作用を有し、その添加量は0.01憾ないし2.0係
程度が適当である。また。
Next, the mushrooms removed from the alcohol are crushed and heated in a homogenized aqueous solution of vitamin C and a metal chelating agent. Vitamin C has antioxidant and enzyme activity inhibiting effects, and the appropriate amount of vitamin C to be added is about 0.01 to 2.0 parts. Also.

金属キレート剤はキノコの組織中の酸性多糖類と結合し
ている金属(鉄、鋼、カリ、カルシウム等)を取除(こ
とにより細織の崩壊を助長するとともに、チロシナーゼ
等キノコ中の金属酵素に含まれる鋼等の酵素活性の発現
に必要な金属原子7に取除くことにより、これら金属酵
素を失活させる効果−ダのほか、ポリリン酸、メタリン
酸、フィチン酸等のリン酸塩、EDTA等を用いること
ができる。
Metal chelating agents remove metals (iron, steel, potassium, calcium, etc.) that are bound to acidic polysaccharides in mushroom tissues (thereby promoting the breakdown of microstructures, as well as promoting the disintegration of metal enzymes in mushrooms such as tyrosinase). In addition to the effect of deactivating these metal enzymes by removing the metal atoms necessary for the expression of enzyme activity such as steel contained in steel, phosphates such as polyphosphoric acid, metaphosphoric acid, phytic acid, EDTA etc. can be used.

これらの金属キレート剤の中−檀のみを用いてもよいが
、充分な効果?あげるためには2檀以上を組合せて用い
るのがよい。金属キレート剤の添加量は全体で0.11
ないし4.0優楊度が適当である。
Among these metal chelating agents, only Dan may be used, but is it sufficiently effective? In order to increase the performance, it is best to use two or more dans in combination. The total amount of metal chelating agent added is 0.11
A rating of 4.0 to 4.0 is appropriate.

加熱処理の温度および時間は被処理原料キノコの檀拳、
品質等圧応じ適宜設定しつる。マツシュルーム子実体の
場合は、最大限に抽出液を得るためKは、加熱処理は7
05以上で5ないし加分間行うことが望ましい。
The temperature and time of heat treatment are determined by the temperature and time of the mushroom to be treated.
Set as appropriate depending on the quality and pressure. In the case of pine mushroom fruiting bodies, K is 7 for heat treatment to obtain maximum extract liquid.
It is desirable to carry out the addition for 5 or more minutes at 0.05 or more.

加熱溶液中で加熱されホモゲナイズされたキノコは加熱
処理後公知の遠心分離機にかけ第1の抽出液が分離抽出
される。この第1の抽出液は0T溶性糖頷、遊離アt)
酸、プリン体、糖アルコール。
The mushrooms that have been heated and homogenized in a heated solution are heated and then placed in a known centrifuge to separate and extract a first extract. This first extract contains 0T soluble sugar (free attenuate)
Acids, purines, sugar alcohols.

グルコーゲンおよび塩基を含有し、抽出後の残渣は蛋白
質、キチン、ヘミセルローズを含有している。
It contains glucose and bases, and the residue after extraction contains proteins, chitin, and hemicellulose.

上記8Ilの抽出液を抽出した債残存する残渣か!(す
、硼酸ソーダ、リン酸ソーダ等の中から適宜選択したも
のを用いる。アルカリ剤の添加量ソーダ塩としては0.
011ないし0.596a度、食塩水の濃度は0.1憾
ないし2.0係が好適であり、加熱110℃以上で15
分間以上行うことが望ましい。
Is it the residue that remains after extracting the above 8Il extract? (Use an appropriate one selected from sodium borate, sodium phosphate, etc.) Addition amount of alkaline agent As soda salt, 0.
0.1 to 0.596 degrees Celsius, the concentration of saline solution is preferably 0.1 to 2.0 degrees, and heating to 110 degrees Celsius or higher
It is desirable to do this for at least a minute.

アルカリ剤で処理されたキノコは遠心分離機にかけて第
2の抽出液が分離抽出される。lW2の抽出液はへiセ
ルローズ、多糖類および糖類を含有し、第2の抽出液を
抽出した後の残渣は蛋白質およびキチンを含有している
The mushrooms treated with the alkaline agent are centrifuged to separate and extract a second extract. The IW2 extract contains cellulose, polysaccharides and saccharides, and the residue after extracting the second extract contains proteins and chitin.

第2の抽出液馨抽出した後の残渣から第3の抽出液を抽
出する工程において使用するキノコの細胞膜崩壊活性を
有する酵素はセルラーゼ、ヘミセルラーゼ、キチナーゼ
、プロチアーゼ等である。
Enzymes having mushroom cell membrane disrupting activity used in the step of extracting the third extract from the residue after the second extract are cellulase, hemicellulase, chitinase, protease, and the like.

これらの酵素としては市販の各種酵素剤のほか、ナメコ
、シイタケ、エノキダケ、ヒラタケ、マツシュルーム、
キクラゲ、フクロタケ等の担子菌を培養して得た酵素を
用いることができる。酵素の特異性により、−糖類の酵
素が作用する基′j[は限られているので、完全な細胞
膜崩壊効果を挙げるため、これらの酵素を数檀類組み合
せて便用し。
In addition to various commercially available enzymes, these enzymes include nameko mushrooms, shiitake mushrooms, enoki mushrooms, oyster mushrooms, pine mushrooms,
Enzymes obtained by culturing basidiomycetes such as wood ear fungus and fungus fungus can be used. Due to the specificity of the enzyme, there are only a limited number of saccharide groups that the enzyme can act on, so in order to achieve a complete cell membrane disruption effect, several combinations of these enzymes are used.

これら酵素の協同作用によりキノコの細胞膜な崩壊、溶
解させる。これらの酵素はおおむねpH4,0ないし5
.0.温度あ℃ないし45℃で最大の活性を示す。した
がって酵素処理工程はI℃ないしく資)℃。
The cooperative action of these enzymes causes the mushroom cell membrane to collapse and dissolve. These enzymes generally have a pH of 4.0 to 5.
.. 0. It exhibits maximum activity at temperatures between 0°C and 45°C. Therefore, the temperature of the enzyme treatment step is 1°C or 1°C.

pki3.4Txいし6.3で行うのが適当である。It is appropriate to use pki3.4Tx to pki6.3.

酵素処理されたキノコ残渣からは遠心分離によりIll
3の抽出液が抽出される。第3の抽出液はアミノ酸、ベ
グチド’s、グルコサミン、糖@を含有し、最後にキチ
ン、リグニンを含む残渣が残る。
The enzyme-treated mushroom residue is separated by centrifugation.
The extract of No. 3 is extracted. The third extract contains amino acids, vegutide's, glucosamine, and sugar@, and finally a residue containing chitin and lignin remains.

上記各工程において抽出されたIIIないし第3の抽出
液1合せ、濃縮した優過当な濾過材により一過すること
Kより脱色処理を行い、所望のキノコエキス製品を得る
A combination of extracts III to 3 extracted in each of the above steps is passed through a concentrated and suitable filter medium, and decolorized by K to obtain a desired mushroom extract product.

次に本発明のキノコエキス製造方法の好ましい実施例を
挙げる。
Next, preferred examples of the mushroom extract manufacturing method of the present invention will be described.

実施例1 1時の生鮮マツシュルームを水洗し0.4参クエン酸と
0.o5暢の界面活性剤(蔗糖脂肪酸エステルおよびン
ルビタン脂肪酸エステル(商品名Sp凰n加と8pan
 85 ’P9t 2 : 1 : 1の割合で混合し
たもの)を含んだ80係エタノール中に浸漬し、室温で
減圧とし、子実体の組織内にこれt浸透させた。約10
〜15分後、子実体のみを採取し、0.1幅フィチン酸
、0.1%ビタミンC,0,31メタリン酸ソーダを含
んだ加熱溶液5を中く上記子実体音ホモゲナイズしなが
ら添加した。全部添加後95℃以上で10分間加熱した
elk、 400Orpmで連続遠心分離を行って5.
2tのIllの抽出液を得た。沈殿物はo、in炭績ソ
ーダを含んだ0.3優食塩水5tで帥℃以上で加分間抽
出し、4.71のwE2の抽出液を得た。  5最優に
残った抽出残渣は≠4.0のクエン酸−衝板1を中に分
散させて、重版のオセロチーム(ヤクルト薬品工業製)
2PとグロテアーゼYPSBCヤ、クルト薬ム工業11
1り5ハ加えて、70rpmで振盪、40℃で明分間反
応させた1心分%Lr、、6竺1な°、いし第3の抽出
液を合せて、高a−ia+aにより2tK濃縮し、。活
性炭とナイ・ロア66(100メツ゛シユ)にて脱色処
理した俊再び一権、L 200−のエキス【優た。
Example 1 1 hour fresh pine mushrooms were washed with water and mixed with 0.4 citric acid and 0.4 hour fresh pine mushrooms. O5's surfactant (sucrose fatty acid ester and nrubitan fatty acid ester (trade name: Sp 凰nka and 8pan)
The seeds were immersed in 80% ethanol containing 85'P9t (mixed at a ratio of 1:1), and the pressure was reduced at room temperature to allow this to penetrate into the tissue of the fruiting body. about 10
~15 minutes later, only the fruiting bodies were collected, and heated solution 5 containing 0.1% phytic acid, 0.1% vitamin C, and 0.31% sodium metaphosphate was added to the fruiting bodies while homogenizing the fruiting bodies. . After adding everything, heat the elk at 95°C or higher for 10 minutes, and perform continuous centrifugation at 400 rpm.5.
2t of Ill extract was obtained. The precipitate was extracted with 5 tons of 0.3 euthanized saline solution containing carbonated soda at a temperature above 30°C to obtain an extract with a wE2 of 4.71. 5. The most remaining extraction residue is dispersed in ≠4.0 citric acid-blocking plate 1 and reprinted with Othellozyme (manufactured by Yakult Pharmaceutical Co., Ltd.).
2P and Grotease YPSBC Ya, Kurt Yakumu Kogyo 11
Add 1 x 5 extracts, shake at 70 rpm, react for 1 hour at 40°C, add 1% Lr, 6x1°, and combine the third extract and concentrate to 2tK using high a-ia + a. ,. Extract of L 200 - decolorized with activated carbon and Nai Loa 66 (100 mesh) [excellent].

実施へ2 o、sKfの生鮮マッシュルームト0.2Kfのマツシ
ュルーム根茎部を水洗優実施例1と同−會のクエン酸お
よび界面活性剤を含む8otlIメタノール中に浸漬し
、40Cで10分間減圧処理した優収出し、0.3暢ポ
リリン酸ソーダ、0.3彊クエン酸ソーダ、0.1優ビ
タミンCt−含む加熱浴液5を中にホモゲナイズしなが
ら添加した。全部添加5に90℃以上で、加分間抽出し
、4.71 (D@ 2の抽出液を得た。以後実施例1
と同じ方圧で酵素処理を行い、1g3の抽出液を抽出し
、実施例1と同様に第1〜I!3の抽出液を合せて濃a
、脱色処珈を行い200−のエキスケ4た◎ 実施例3 1−の生鮮マツシュルームについて実施例1と同じ方法
でクエン#、アルコール浸漬、減圧処理、金I14除去
処堆、加熱も理を行って第1および第2抽出液χ得た優
の残渣vpH4,0の0.1Mクエン酸−緩衝液(クエ
ン*およびクエン敵ソーダからなる)KII11濁しK
u*hn@romyc@s nam@ko (ナメコ)
の生産した菌体外酵素のアセトン粉末0.3/−Y添加
し切℃で7Orpmで振盪させながらω分間反応させる
ことKよりWJ3の抽出液2.81 Y得た。上記第1
〜第3の抽出液を合せ第1の実施例と同様に濃縮。
To implementation 2 o, sKf of fresh mushrooms 0.2Kf of pine mushroom rhizomes were immersed in 8otlI methanol containing the same citric acid and surfactant as in Example 1, and treated under reduced pressure at 40C for 10 minutes. Heating bath solution 5 containing 0.3% sodium polyphosphate, 0.3% sodium citrate, and 0.1% vitamin Ct was added therein while homogenizing. After addition of all 5, extraction was carried out at 90°C or higher to obtain an extract of 4.71 (D@2).Hereinafter, Example 1
Enzyme treatment was performed under the same pressure as in Example 1, and 1g3 of the extract was extracted. Combine the extracts from step 3 and make concentrated a.
Example 3 The fresh pine mushrooms of 1- were treated in the same manner as in Example 1, including quench #, alcohol immersion, vacuum treatment, gold I14 removal treatment, and heating. 1st and 2nd extract
u*hn@romyc@s nam@ko (Nameko)
An extract of WJ3 (2.81 Y) was obtained by adding 0.3/-Y of acetone powder of the extracellular enzyme produced by K and reacting for ω minutes at 70° C. with shaking at 7 Orpm. 1st above
- Combine the third extract and concentrate in the same manner as in the first example.

脱色して200mのエキスを得た。After decolorization, a 200m extract was obtained.

以上に述べたよりに、本発明によれば、加熱処理、アル
カリ処理、酵素処理というそれぞれ興る処理工程により
段階的にキノコの組織を破壊し、各工i/’Uにおいて
それぞれ抽出液を得た優、これらの抽出液を介せるよう
にしたので、従来のブライン中での加熱処理による方法
に比べてはるかに高い歩留Qk挙げることができる。本
発明d抽出方法によるキノコエキスの収率を従来方法と
比較して示すと下表のとおりであるが、従来方法の収率
皮憾に対し本発明の方法によれは87憾の収率tあげる
ことができるのであって本発明の有利性は明白である。
As described above, according to the present invention, mushroom tissue is destroyed in stages through the respective treatment steps of heat treatment, alkali treatment, and enzyme treatment, and extracts are obtained in each step i/'U. Since these extracts can be passed through, a much higher yield Qk can be achieved than in the conventional method of heat treatment in brine. The yield of mushroom extract obtained by the extraction method of the present invention is compared with the conventional method as shown in the table below.The yield of the conventional method is 87% lower than that of the conventional method. The advantages of the present invention are obvious.

秦 缶詰工業においてマツシュルームをプライン中で加
熱処理する方法 また栄養価の点においても1本発明の方法KJ。
Hata: A method of heat treating pine mushrooms in prine in the canning industry, and also a method of the present invention in terms of nutritional value KJ.

つて製造されたキノコエキスは水分48.3 %、蛋白
(N X 6.25 ) 18.1係、脂質0.1%糖
’![20,2係、繊m 1.8、灰分11.5憾の組
成を有し、極めて栄養価の高い食品である。特に本発明
の方法によれば。
The mushroom extract produced using this method contains 48.3% moisture, 18.1% protein (N x 6.25), 0.1% fat and sugar! [It has a composition of 20.2%, fiber m 1.8, and ash content 11.5, and is an extremely nutritious food. Especially according to the method of the invention.

キノコの組織をほぼ完全に破壊し、含有アξ)酸成分馨
はとんど残らず駿り出てことができるので。
The structure of the mushroom is almost completely destroyed, and almost all of the acid components contained in it can escape.

本発明の万去によって製造されたキノコエキスは下表に
示すように’fべての必須アミノ酸を含む各檀アミノ!
!ヲ含有している。これだけの種類のアミノ酸をこれだ
け多量に含むキノコエキスン製造すること【工従米の方
法によってはとうてい不可能である。
The mushroom extract produced by the method of the present invention contains all the essential amino acids as shown in the table below.
! Contains wo. It would be impossible to produce a mushroom extract that contains so many types of amino acids in such large amounts using traditional methods.

さらに、本発明の方法によれは、エキス抽出に際して生
じ得る酵素作用によるキノコの黒変、異臭発生その他の
品質の変化を完全に防止することができるので、生°の
キノコと同様の風味を有する丁ぐれた品質のエキス製品
Y:得ることができる。
Furthermore, the method of the present invention can completely prevent mushrooms from turning black, producing off-flavors, and other quality changes that may occur during extract extraction, resulting in mushrooms having a flavor similar to that of fresh mushrooms. Extract product Y of excellent quality can be obtained.

本発明の方法忙より製造されたキノコエキスは水で希釈
してみりん、食塩等適宜の調味料を加え、さらに必要に
応じ、野菜の細片等を加えてキノコスープとして用いる
ことができるほか、単独でまたは他の!i4味料やだし
の累と混合して一種のだしの素として利用する等広い用
途に用いることができる。
The mushroom extract produced by the method of the present invention can be diluted with water and added with appropriate seasonings such as mirin and salt, and if necessary, can be used as a mushroom soup by adding vegetable pieces, etc. Alone or other! It can be used for a wide range of purposes, such as being mixed with i4 seasonings and stock ingredients and used as a type of stock base.

出願人   東洋製罐株式会社Applicant: Toyo Seikan Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 原料固形キノコをクエン酸添加アルコール水溶液中に#
!圧下で浸漬し、次いでこの原料固形キノコをビタiン
Cおよび金鋼キレート剤水溶液中に投下加熱して@1の
抽出液を分離抽出し1次いで111111の抽出液を抽
出した後の残渣&pH8ないし90弱アルカリ性の食塩
水中で加熱して第2の抽a液を分離抽出し、さらKII
fl[2の抽出液を抽出した後の残渣をキノコの細胞膜
を崩壊させる能力を有する酵素と接触せしめてs1!3
の抽出液を分離抽出し、前記第1.第2および@3の抽
出液1合せて濃縮することV特徴とするキノコエキスの
製造方法。
Raw material solid mushrooms in citric acid-added alcohol solution #
! After soaking under pressure, this raw material solid mushroom was dropped into an aqueous solution of Vitamin I C and a gold steel chelating agent and heated to separate and extract the extract of @1, and then the residue after extracting the extract of 111111 & pH 8 to The second extract was separated and extracted by heating in a slightly alkaline saline solution of 90%, and further KII
The residue after extracting fl[2 was brought into contact with an enzyme capable of disrupting mushroom cell membranes, and s1!3 was extracted.
Separate and extract the extract of 1. A method for producing a mushroom extract, characterized by concentrating the second and @3 extracts together.
JP56123840A 1981-08-07 1981-08-07 Method for producing mushroom extract Expired JPS5933338B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56123840A JPS5933338B2 (en) 1981-08-07 1981-08-07 Method for producing mushroom extract

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56123840A JPS5933338B2 (en) 1981-08-07 1981-08-07 Method for producing mushroom extract

Publications (2)

Publication Number Publication Date
JPS5828243A true JPS5828243A (en) 1983-02-19
JPS5933338B2 JPS5933338B2 (en) 1984-08-15

Family

ID=14870680

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56123840A Expired JPS5933338B2 (en) 1981-08-07 1981-08-07 Method for producing mushroom extract

Country Status (1)

Country Link
JP (1) JPS5933338B2 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2259709A (en) * 1991-09-19 1993-03-24 British Textile Tech Production of chitin/chitosan
EP0700641A3 (en) * 1994-08-23 1996-04-17 Braunschweigische Masch Bau
EP1190627A3 (en) * 2000-09-14 2003-10-22 Bestfoods Process for the production of a mushroom flavouring
CN103210997A (en) * 2013-04-17 2013-07-24 西华大学 Preparation method of natural coating antistaling agent for fresh meat preservation
CN104187620A (en) * 2014-08-04 2014-12-10 宁波北仑锐晟明杰生物科技发展有限公司 Chinese caterpillar fungus health powder
JP2015042151A (en) * 2013-08-26 2015-03-05 理研ビタミン株式会社 Mushroom extract processed product and method for producing the same
CN104738639A (en) * 2015-04-21 2015-07-01 青岛金麦谷润食品有限公司 Health maintenance nourishing health food

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102586521B1 (en) 2017-12-12 2023-10-06 산쇼가부시키가이샤 Method for producing cyclic sodium phosphatidate

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2259709A (en) * 1991-09-19 1993-03-24 British Textile Tech Production of chitin/chitosan
EP0700641A3 (en) * 1994-08-23 1996-04-17 Braunschweigische Masch Bau
EP1190627A3 (en) * 2000-09-14 2003-10-22 Bestfoods Process for the production of a mushroom flavouring
CN103210997A (en) * 2013-04-17 2013-07-24 西华大学 Preparation method of natural coating antistaling agent for fresh meat preservation
JP2015042151A (en) * 2013-08-26 2015-03-05 理研ビタミン株式会社 Mushroom extract processed product and method for producing the same
CN104187620A (en) * 2014-08-04 2014-12-10 宁波北仑锐晟明杰生物科技发展有限公司 Chinese caterpillar fungus health powder
CN104738639A (en) * 2015-04-21 2015-07-01 青岛金麦谷润食品有限公司 Health maintenance nourishing health food

Also Published As

Publication number Publication date
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