JP4705874B2 - Method for producing amino acid-rich food material, particularly amino acid-rich food material containing abundant ornithine, food material produced by using these production methods, and foods to which these food materials are added - Google Patents

Method for producing amino acid-rich food material, particularly amino acid-rich food material containing abundant ornithine, food material produced by using these production methods, and foods to which these food materials are added Download PDF

Info

Publication number
JP4705874B2
JP4705874B2 JP2006101292A JP2006101292A JP4705874B2 JP 4705874 B2 JP4705874 B2 JP 4705874B2 JP 2006101292 A JP2006101292 A JP 2006101292A JP 2006101292 A JP2006101292 A JP 2006101292A JP 4705874 B2 JP4705874 B2 JP 4705874B2
Authority
JP
Japan
Prior art keywords
ornithine
extract
amino acid
food material
enokitake
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.)
Expired - Fee Related
Application number
JP2006101292A
Other languages
Japanese (ja)
Other versions
JP2007274904A (en
Inventor
武 斉藤
Original Assignee
株式会社アセラ
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 株式会社アセラ filed Critical 株式会社アセラ
Priority to JP2006101292A priority Critical patent/JP4705874B2/en
Publication of JP2007274904A publication Critical patent/JP2007274904A/en
Application granted granted Critical
Publication of JP4705874B2 publication Critical patent/JP4705874B2/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Landscapes

  • Preparation Of Fruits And Vegetables (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)

Description

この発明は、アミノ酸高含有食品素材の製造方法、及び特にオルニチンを豊富に含有するアミノ酸高含有食品素材の製造方法、並びにこれらの製造方法を用いて製造される食品素材、及びこれらの食品素材を添加した食品に関するものである。   The present invention relates to a method for producing a food material with a high amino acid content, a method for producing a food material with a high amino acid content, particularly containing ornithine, a food material produced using these production methods, and these food materials. It relates to added food.

(イ)きのこ類を野菜や果物と同様の食材として捕らえ、温風乾燥や凍結乾燥などにより乾燥し粉末化したものはすでに存在している(特許文献1及び特許文献2)。
(ロ)生キノコを凍結させてからそのまま粉砕し、その後融解させてから回収すると(凍結粉砕法)高い遊離アミノ酸含有量のキノコエキスが得られる(特許文献3)。
(ハ)エノキタケは暗黒下で子実体(キノコ)を発生させ、柄が長く傘が小さいキノコが多数束になった形態で一般的に販売されている。
(ニ)子嚢菌類である酵母を自己消化処理あるいは酵素処理し、遊離アミノ酸を高濃度に含有させたエキス系調味料(酵母エキス)が市販されている。
(ホ)冷却処理をすることにより、シジミ貝中のオルニチン含有量を増加させる方法が報告されている(特許文献4)。
(I) Mushrooms that have been captured as foods similar to vegetables and fruits and dried and pulverized by hot air drying or freeze drying already exist (Patent Documents 1 and 2).
(B) Raw mushrooms are frozen and then pulverized as they are, and then thawed and then recovered (freeze pulverization method) to obtain a mushroom extract having a high free amino acid content (Patent Document 3).
(C) Enokitake mushrooms are generally sold in the form of many bundles of mushrooms that produce fruit bodies (mushrooms) in the dark and have long handles and small umbrellas.
(D) An extract-type seasoning (yeast extract) in which yeast, which is an ascomycete fungus, is self-digested or enzymatically treated to contain a high concentration of free amino acids is commercially available.
(E) A method for increasing the ornithine content in swordfish by cooling is reported (Patent Document 4).

特開2004−189710JP 2004-189710 A 特開昭50−46872JP 50-46872 A 特願2005−240561Japanese Patent Application No. 2005-240561 特開2001−204432JP 2001-204432 A

発明者は以前、生キノコを凍結させた後、そのまま粉砕し、その後融解させてからそのエキス回収すると、遊離アミノ酸を豊富に含むキノコエキスが得られることを知り、これに基づいて特許出願(発明の名称:食品素材、及びその製造方法、及びこの食品素材を添加した食品)をした事実がある(特許文献3)。
しかしながら、キノコエキスを得るための原料のキノコは、主に生食用として流通しており、エキス原料としては高価である。従って、より遊離アミノ酸含有量の高いキノコエキスの製造法が求められる。
又、キノコには機能性アミノ酸であるγ−アミノ酪酸(GABA)やオルニチンを含むものがあるが、これらの含有量を高めることはキノコエキスを原料とする食品素材及びこれを含有する食品の価値を高めることになる。
The inventor previously knew that raw mushrooms were frozen, then pulverized as they were, and then thawed before recovering the extract to obtain a mushroom extract rich in free amino acids. Name: food material, manufacturing method thereof, and food added with this food material) (Patent Document 3).
However, mushrooms, which are raw materials for obtaining mushroom extracts, are mainly distributed for raw consumption and are expensive as raw materials for extracts. Therefore, a method for producing a mushroom extract having a higher free amino acid content is required.
Some mushrooms contain functional amino acids such as γ-aminobutyric acid (GABA) and ornithine. Increasing the content of these mushrooms is the value of food materials made from mushroom extract and foods containing them. Will increase.

オルニチンは、成長ホルモンを分泌させて筋肉合成を促進させる、あるいは基礎代謝を高めて肥満を予防する食品素材として、米国を中心に使用されている。また、ヨーロッパでは、肝臓障害を改善する医薬品として用いられている。
日本でも、L−オルニチン塩酸塩の形態で、食品素材として使用可能である。オルニチンは成長ホルモンの分泌を促すことが知られており、また、オルニチン回路の成分としてアンモニアの解毒に関わると共に、ポリアミンの前駆体となる。また、オルニチン回路を活性化させて肝機能障害に伴う高アンモニア血症を改善したり、免疫増強作用を示したりすることも知られている。
従って、オルニチン含有量の高い食品素材を開発することは、非常に意義のあることである。
Ornithine is used mainly in the United States as a food material to secrete growth hormone to promote muscle synthesis or to increase basal metabolism to prevent obesity. In Europe, it is used as a medicine to improve liver damage.
In Japan, it can be used as a food material in the form of L-ornithine hydrochloride. Ornithine is known to promote the secretion of growth hormone, and is involved in the detoxification of ammonia as a component of the ornithine cycle and is a precursor of polyamine. It is also known to activate the ornithine circuit to improve hyperammonemia associated with liver dysfunction and to exhibit immune enhancement.
Therefore, it is very significant to develop food materials with high ornithine content.

オルニチンは、食品素材では特に二枚貝のシジミに多く、エキス100g中186mg含まれている。シジミを冷凍すると、オルニチン含量が約4倍に増加する(特許文献4)。
栽培キノコのエノキタケ、ブナシメジ、ハタケシメジ、マッシュルーム、雪霊茸のエキスには多量のオルニチンが含まれている。その含有量は94.5〜136.5mg/エキス100mlで、これらのエキスを乾燥させることにより、天然オルニチンを0.96g/100g〜1.23g/100g含む素材を得ることができる(特許文献3)。この含有量は計算上冷凍シジミに含まれるオルニチン含有量を超えるが、現在市販されているサプリメントによる1日当たりのオルニチン摂取量の目安は500mg〜1000mgとかなり多い。
Ornithine is abundant especially in bivalve swordfish as a food material, and is contained in 186 mg of 100 g of extract. Freezing shijimi increases the ornithine content about 4 times (Patent Document 4).
Large amounts of ornithine are contained in the extracts of cultivated mushrooms, Enokitake, Bunashimeji, Hatakeshimeji, mushrooms and snow mausoleum. The content is 94.5 to 136.5 mg / 100 ml of extract, and by drying these extracts, a material containing 0.96 g / 100 g to 1.23 g / 100 g of natural ornithine can be obtained (Patent Document 3). ). Although this content exceeds the ornithine content contained in frozen swordfish in calculation, the standard of the daily intake of ornithine with supplements currently on the market is considerably high at 500 mg to 1000 mg.

本発明は、キノコ類に豊富に含まれている遊離アミノ酸を自己消化処理によって更に増加させ、遊離アミノ酸含有量の非常に高いエキスを製造するとともに、このエキスを用いた遊離アミノ酸含有量の高い新しい食品素材、及びその製造方法、及びこの食品素材を添加した食品を提供することを目的とする。
また、特にキノコエキスにアルギニンを添加し、機能性アミノ酸であるオルニチンに変換させてオルニチン高含有量の新しい食品素材、及びその製造方法、及びこの食品素材を添加した食品をも提供することを目的とする。
The present invention further increases the amount of free amino acids contained in mushrooms by autolysis to produce an extract having a very high free amino acid content, and a new free amino acid content using the extract. An object of the present invention is to provide a food material, a production method thereof, and a food to which the food material is added.
In addition, the object is to provide a new food material with a high content of ornithine by adding arginine to mushroom extract and converting it to ornithine, which is a functional amino acid, and a method for producing the same, as well as a food containing this food material. And

本願発明は、下記の請求項1〜請求項167により構成されている。The present invention is constituted by the following claims 1 to 167.
〔請求項1〕 下記の(A)〜(C)の工程を順次経て生産されることを特徴とするアミノ酸高含有食品素材の製造方法。[Claim 1] A method for producing a food material having a high amino acid content, which is produced through the following steps (A) to (C).
(A)暗黒下で子実体を形成させた後、室温で光を照射して子実体の傘を大きくさせた生エノキタケを得る工程。(A) The process of obtaining the raw enokitake which formed the fruit body under darkness, and then irradiated with light at room temperature to enlarge the fruit body umbrella.
(B)前記生エノキタケ、又はエノキタケを凍結した後、これらを粉砕又はこれらに水を加えて粉砕し、エノキタケのスラリーを得る工程(B) A step of freezing the raw enokitake or enokitake and then pulverizing them or adding water to them to obtain a slurry of enokitake
(C)前記スラリーからエキス(液状物質)を分離する工程(C) The process of isolate | separating an extract (liquid substance) from the said slurry
〔請求項2〕 下記の(A)〜(C)の工程を順次経て生産されることを特徴とするアミノ酸高含有食品素材の製造方法。[Claim 2] A method for producing a food material having a high amino acid content, which is produced through the following steps (A) to (C).
(A)暗黒下で子実体を形成させた後、室温で光を照射して子実体の傘を大きくさせた生エノキタケを得る工程。(A) The process of obtaining the raw enokitake which formed the fruit body under darkness, and then irradiated with light at room temperature to enlarge the fruit body umbrella.
(B)前記生エノキタケ、又はエノキタケを凍結した後、これを保温して自己消化させ、エノキタケの自己消化物を得る工程(B) A step of freezing the enokitake mushroom or enokitake mushroom and then keeping it warm and self-digesting to obtain a self-digested enokitake mushroom
(C)前記自己消化物からエキス(液状物質)を分離する工程(C) The process of isolate | separating an extract (liquid substance) from the said autolysate
〔請求項3〕 下記の(A)〜(D)の工程を順次経て生産されることを特徴とするアミノ酸高含有食品素材の製造方法。[Claim 3] A method for producing a food material having a high amino acid content, which is produced through the following steps (A) to (D) in sequence.
(A)暗黒下で子実体を形成させた後、室温で光を照射して子実体の傘を大きくさせた生エノキタケを得る工程。(A) The process of obtaining the raw enokitake which formed the fruit body under darkness, and then irradiated with light at room temperature to enlarge the fruit body umbrella.
(B)前記生エノキタケ、又はエノキタケを凍結した後、これらを粉砕又はこれらに水を加えて粉砕し、エノキタケのスラリーを得る工程(B) A step of freezing the raw enokitake or enokitake and then pulverizing them or adding water to them to obtain a slurry of enokitake
(C)前記スラリーからエキス(液状物質)を分離する工程(C) The process of isolate | separating an extract (liquid substance) from the said slurry
(D)前記エキスを保温して自己消化させる工程(D) The process of keeping the extract warm and self-digesting
〔請求項4〕 エキスを濃縮又は(/及び)乾燥して、ペースト状又は粉末状とする請求項1〜請求項3に記載するアミノ酸高含有食品素材の製造方法。[Claim 4] The method for producing a food material having a high amino acid content according to claims 1 to 3, wherein the extract is concentrated or / and dried to make a paste or powder.
〔請求項5〕 自己消化させる条件が、下記の(a)及び(b)である請求項2〜請求項4に記載するアミノ酸高含有食品素材の製造方法。[5] The method for producing a food material with a high amino acid content according to [2] to [4], wherein the conditions for self-digestion are the following (a) and (b).
(a)温度:20℃〜80℃(より好ましくは、40℃〜60℃)  (A) Temperature: 20 ° C to 80 ° C (more preferably 40 ° C to 60 ° C)
(b)保持時間:2時間以上(より好ましくは、6時間〜10時間)  (B) Holding time: 2 hours or more (more preferably, 6 hours to 10 hours)
〔請求項6〕 請求項1〜請求項5に記載する製造方法を用いて製造されるアミノ酸高含有食品素材。[Claim 6] A food material with a high amino acid content produced using the production method according to any one of claims 1 to 5.
〔請求項7〕 請求項6に記載する食品素材を添加して栄養を強化し、かつ呈味性を改善したことを特徴とする食品。[Claim 7] A food comprising the food material according to claim 6 added to enhance nutrition and improve taste.
〔請求項8〕 下記の(A)〜(C)の工程を順次経て生産されることを特徴とする特にオルニチンを豊富に含有するアミノ酸高含有食品素材の製造方法。[Claim 8] A method for producing a food material having a high amino acid content, particularly rich in ornithine, which is produced through the following steps (A) to (C).
(A)生キノコ、又は凍結生キノコを破砕してキノコのスラリーを得る工程(A) A step of obtaining a mushroom slurry by crushing raw mushrooms or frozen raw mushrooms
(B)前記スラリーにアルギニンを添加して、スラリー中のオルニチン合成酵素(アルギナーゼ)を作用させる工程(B) A step of adding arginine to the slurry to cause ornithine synthase (arginase) in the slurry to act.
(C)前記スラリーからエキスを分離する工程(C) The process of isolate | separating an extract from the said slurry
〔請求項9〕 下記の(A)〜(C)の工程を順次経て生産されることを特徴とする特にオルニチンを豊富に含有するアミノ酸高含有食品素材の製造方法。[Claim 9] A method for producing a food material with a high amino acid content, particularly rich in ornithine, which is produced through the following steps (A) to (C).
(A)生キノコ、又は凍結生キノコを破砕してキノコのスラリーを得る工程(A) A step of obtaining a mushroom slurry by crushing raw mushrooms or frozen raw mushrooms
(B)前記スラリーからエキス(液状物質)を分離する工程(B) The process of isolate | separating an extract (liquid substance) from the said slurry
(C)前記エキスにアルギニンを添加して、エキス中のオルニチン合成酵素(アルギナーゼ)を作用させる工程(C) adding arginine to the extract and causing ornithine synthase (arginase) in the extract to act
〔請求項10〕 請求項8、又は請求項9の(A)工程に代えて、「酵素が失活しない温度帯で乾燥したキノコの粉末に水を加えてキノコのスラリーを得る工程」とする特にオルニチンを豊富に含有するアミノ酸高含有食品素材の製造方法。[Claim 10] Instead of the step (A) of claim 8 or 9, it is referred to as "a step of obtaining a mushroom slurry by adding water to mushroom powder dried in a temperature zone where the enzyme is not inactivated". In particular, a method for producing a food material with a high amino acid content, which is rich in ornithine.
〔請求項11〕 請求項8〜請求項10のオルニチン合成酵素(アルギナーゼ)を作用させた後のエキスを、濃縮又は(/及び)乾燥して、ペースト状又は粉末状とし、特にオルニチンを豊富に含有するアミノ酸高含有食品素材の製造方法。[Claim 11] The extract after the action of the ornithine synthase (arginase) according to claims 8 to 10 is concentrated or / and dried to form a paste or powder, particularly rich in ornithine. A method for producing a food material containing a high amino acid content.
〔請求項12〕 アルギニンの添加量が、請求項8〜請求項10に記載するエキス1Lに付き、1g〜50gである請求項8〜請求項11に記載する特にオルニチンを豊富に含有するアミノ酸高含有食品素材の製造方法。[Claim 12] The amount of arginine added is 1 g to 50 g per 1 L of the extract according to claims 8 to 10, and the amino acid content particularly rich in ornithine according to claims 8 to 11 is high. A method for producing a contained food material.
〔請求項13〕 オルニチン合成酵素(アルギナーゼ)を作用させる条件が、下記の(a)〜(c)である請求項8〜請求項10に記載する特にオルニチンを豊富に含有するアミノ酸高含有食品素材の製造方法。[Claim 13] Conditions for causing ornithine synthase (arginase) to act are the following (a) to (c): The food material with high amino acid content, particularly rich in ornithine, according to claims 8 to 10 Manufacturing method.
(a)温度:30℃〜70℃(より好ましくは、40℃〜60℃)  (A) Temperature: 30 ° C. to 70 ° C. (more preferably, 40 ° C. to 60 ° C.)
(b)pH:5.0〜11.0(より好ましくは、7.0〜10.0)  (B) pH: 5.0 to 11.0 (more preferably 7.0 to 10.0)
(c)保持時間:2時間以上(より好ましくは、6時間〜8時間)  (C) Holding time: 2 hours or more (more preferably, 6 hours to 8 hours)
〔請求項14〕 キノコにエノキタケ、ヒラタケ、バイリング(雪霊茸、白嶺茸)、タモギタケ、ハタケシメジ、ブナシメジ、エリンギ、アガリクスを使用する請求項8〜請求項13に記載する特にオルニチンを豊富に含有するアミノ酸高含有食品素材の製造方法。[Claim 14] Enriched with ornithine according to claims 8 to 13, wherein enokitake mushrooms, oyster mushrooms, bilings (snow mausoleum, birch), tamogitake, hatake shimeji, bunashimeji, eringi, agaricus are used as mushrooms. A method for producing a food material with a high amino acid content.
〔請求項15〕 キノコにエノキタケを用い、暗黒下で子実体を形成させた後、室温で光を照射して子実体の傘を大きくさせた生エノキタケを用いる請求項8〜請求項13に記載するアミノ酸高含有食品素材の製造方法。[Claim 15] Claims 8 to 13, wherein enokitake is used as a mushroom, and a fruit body is formed in the dark, and then a raw enokitake that is irradiated with light at room temperature to enlarge the fruit body umbrella is used. A method for producing a food material with a high amino acid content.
〔請求項16〕 請求項8〜請求項15に記載する製造方法を用いて製造される特にオルニチンを豊富に含有するアミノ酸高含有食品素材。[Claim 16] A food material with a high amino acid content, particularly rich in ornithine, produced using the production method according to claims 8 to 15.
〔請求項17〕 請求項16に記載する特にオルニチンを豊富に含有するアミノ酸高含有食品素材を添加して栄養を強化し、かつ呈味性を改善したことを特徴とする食品。[Claim 17] A food comprising the amino acid-rich food material particularly rich in ornithine according to claim 16 added to enhance nutrition and improve taste.

本願発明を以上のように構成する理由は、下記のとおりである。
(a)生キノコは、自己消化の工程を経ることによってキノコ自身の持つ酵素類により細胞内外のタンパク質が分解されるので、例えば、凍結粉砕法で回収したキノコエキス(特許文献3)に比べて遊離アミノ酸含有量のより高いエキスが容易に回収できることが判明したこと。
すなわち、キノコの子実体を生のまま、若しくは凍結した後、保温して自己消化させることにより、生のキノコの子実体中に多量に含まれている遊離アミノ酸を効率よく抽出できること、又キノコの子実体を生のまま、若しくは凍結したものをそのまま破砕してエキスを分離し、これを保温して自己消化させることにより、エキス中の遊離アミノ酸量を増加させることができること(請求項1、請求項2)。
(b)生キノコ、又は凍結生キノコを破砕して得られるキノコのスラリー、又はスラリーから分離して得られるエキスに、アルギニンを添加して保温すれば、キノコエキス中のオルニチン合成酵素(アルギナーゼ)により、アルギニンからオルニチンが効率よく生成されることが判明したこと(請求項10、請求項11)。
又、前記キノコエキス中のオルニチン合成酵素(アルギナーゼ)は、生キノコに限らず、酵素が失活しない温度帯で乾燥したキノコの粉末に水を加えて戻したスラリー又はスラリーから分離されたエキスにおいても、十分な活性があることが判明したこと(請求項12)。
(c)エノキタケは、終始暗黒下で栽培するよりも、暗黒下で子実体を形成させた後、室温で光を照射して子実体の傘を大きくさせたものを使用する方が、遊離アミノ酸を多量に得られることが判明したこと(請求項6、請求項16)。
(d)生キノコを自己消化させて得られるエキスを濃縮又は乾燥すれば、遊離アミノ酸高含有食品素材(請求項3及び請求項8)が容易に得られることが判明したこと。(e)生キノコのエキス(スラリ−中のエキスも含む)にアルギニンを添加して、生キノコエキス中に含まれるオルニチン合成酵素(アルギナーゼ)によりオルニチンを生成(増加)させたエキスを濃縮又は乾燥すれば、特にオルニチンを豊富に含有するアミノ酸高含有食品素材(請求項12、請求項17)が容易に得られることが判明したこと。
(f)前記(d)又は(e)に記載した遊離アミノ酸高含有食品素材、又は特にオルニチンを豊富に含有するアミノ酸高含有食品素材を一般食品に添加すれば、食品に容易に旨味を付与することができ、又かてて加えて毎日オルニチンの必要量を容易に摂取することができること(請求項9、請求項18)。
The reason why the present invention is configured as described above is as follows.
(A) Since raw mushrooms undergo a self-digestion process, proteins inside and outside the cell are decomposed by enzymes possessed by the mushrooms themselves, for example, compared with a mushroom extract recovered by freeze grinding (Patent Document 3). It has been found that an extract having a higher free amino acid content can be easily recovered.
That is, by freezing the mushroom fruit body as it is or after freezing, it is possible to efficiently extract free amino acids contained in a large amount in the fruit body of the raw mushroom by heating and self-digesting. The fruit body can be crushed raw or frozen as it is, and the extract can be separated, and the amount of free amino acids in the extract can be increased by keeping it warm and self-digesting (Claim 1, Claim) Item 2).
(B) Ornithine synthase (arginase) in a mushroom extract by adding arginine to a slurry of mushrooms obtained by crushing raw mushrooms or frozen raw mushrooms, or an extract obtained by separating from the slurry, and keeping the mixture warm. Thus, it has been found that ornithine is efficiently produced from arginine (claims 10 and 11).
In addition, the ornithine synthase (arginase) in the mushroom extract is not limited to raw mushrooms, but is a slurry obtained by adding water to mushroom powder dried in a temperature zone where the enzyme is not deactivated or an extract separated from the slurry. Has been found to have sufficient activity (claim 12).
(C) Enokitake is a free amino acid, rather than cultivating in the dark all the time, using a fruit body that has been grown under darkness and then irradiated with light at room temperature to enlarge the fruit body umbrella. Was found to be obtained in a large amount (Claim 6 and Claim 16).
(D) It has been found that if an extract obtained by self-digesting raw mushrooms is concentrated or dried, a food material containing high free amino acids (claims 3 and 8) can be easily obtained. (E) Arginine is added to the raw mushroom extract (including the extract in the slurry), and the extract produced or increased by ornithine synthase (arginase) contained in the raw mushroom extract is concentrated or dried. In particular, it was found that a food material containing a high amount of ornithine and containing a high amount of amino acid (claims 12 and 17) can be easily obtained.
(F) If a food material with a high free amino acid content described in (d) or (e) above, or a food material with a high amino acid content especially containing ornithine is added to a general food, the food is easily imparted with umami. In addition, the necessary amount of ornithine can be easily ingested every day (Claims 9 and 18).

本願発明に用いる原料のキノコは生キノコでも、生キノコの凍結品でもよい。   The raw material mushroom used in the present invention may be a raw mushroom or a frozen product of a raw mushroom.

本願発明において、自己消化とは、生キノコ(生キノコを凍結したものを含む)をそのまま、若しくは破砕したもの(スラリー)を一定範囲の温度に保温すること、又は生キノコ(生キノコを凍結したものを含む)を破砕したもの(スラリー)から分離したエキスを一定範囲の温度に保温することを言う。
自己消化は、通常下記の条件により行う。
(a)温度:20℃〜80℃(より好ましくは、40℃〜60℃)
(b)保持時間:2時間以上(より好ましくは、6時間〜10時間)
より具体的には、キノコに水を加えてから保温して自己消化させたり、ジューサー等で生キノコ或いは凍結キノコを破砕した後に自己消化させたりしても良い。この自己消化の工程を経ることによってキノコ自身の持つ酵素類により細胞内外のタンパク質が分解され、凍結粉砕法で回収したキノコエキスに比べて遊離アミノ酸含有量のより高いエキスが回収できる。
エキスの回収は、自己消化させた後にそのまま或いは一度凍結・融解、もしくは凍結・粉砕・融解後に圧搾又は遠心分離等の手段により行う。
In the present invention, self-digestion means keeping raw mushrooms (including those obtained by freezing raw mushrooms) as they are or by crushing (slurry) at a certain range of temperature, or raw mushrooms (freezing raw mushrooms). This means that the extract separated from the crushed product (slurry) is kept at a certain temperature range.
Autolysis is usually performed under the following conditions.
(A) Temperature: 20 ° C to 80 ° C (more preferably 40 ° C to 60 ° C)
(B) Holding time: 2 hours or more (more preferably, 6 hours to 10 hours)
More specifically, water may be added to the mushroom and then kept warm to be self-digested, or the raw mushroom or frozen mushroom may be crushed with a juicer or the like and then self-digested. Through this self-digestion process, intracellular and extracellular proteins are decomposed by enzymes possessed by the mushroom itself, and an extract having a higher free amino acid content can be recovered as compared with a mushroom extract recovered by freeze-grinding.
The extract is collected after self-digestion as it is or once by freezing / thawing, or after freezing / pulverizing / thawing, by pressing or centrifuging.

市販されているキノコ中、エノキタケは、通常暗黒下で5〜10℃に保つことにより、子実体の傘が小さく(直径1cm以下)、柄の長いキノコを束生させたものが栽培され、販売されている。   Among the commercially available mushrooms, enokitake is usually grown at a temperature of 5 to 10 ° C. under dark conditions, so that the fruit body umbrella is small (1 cm or less in diameter) and bundles of long mushrooms are grown and sold. Has been.

しかし、エノキタケは、柄が5〜10cm程度に伸びたところで、15〜25℃程度の室温で蛍光灯のような電灯の下で1〜2日間栽培すると傘が大きくなり、最大直径が2.5cm程度に達する。このように傘を大きくしたエニキタケのエキスは、同じ時間、5〜10℃、暗黒化で栽培したキノコのエキスに比べ、遊離アミノ酸含有量が顕著に増加することが判明した。
このように栽培されたエノキタケに、自己消化処理を行うことにより遊離アミノ酸含有量の非常に高いエキスを得ることができる。
However, the enokitake mushroom grows about 5-10 cm in the handle, and when grown at room temperature of about 15-25 ° C. under a lamp like a fluorescent lamp for 1-2 days, the umbrella grows and the maximum diameter is 2.5 cm. Reach the degree. Thus, it was found that the enokitake mushroom extract with an enlarged umbrella has a significantly increased free amino acid content compared to the mushroom extract grown in the dark at 5 to 10 ° C. for the same time.
An extract with a very high free amino acid content can be obtained by subjecting the enokitake cultivated in this way to self-digestion treatment.

自己消化処理により得られたキノコエキス、又はオルニチンを増やして得られたキノコエキスを濃縮してペースト状製品、又は真空凍結乾燥や温風乾燥、噴霧乾燥、ドラム乾燥等の効率の良い乾燥法で乾燥することにより、遊離アミノ酸含有量の非常に高い食品素材を製造することが可能である。
乾燥温度は、120℃以上になるとエキスが炭化してしまうため80℃以下が望ましい。
Mushroom extract obtained by self-digestion treatment or mushroom extract obtained by increasing ornithine is concentrated to a paste-like product, or an efficient drying method such as vacuum freeze drying, hot air drying, spray drying, drum drying, etc. By drying, a food material having a very high free amino acid content can be produced.
The drying temperature is preferably 80 ° C. or lower because the extract is carbonized at 120 ° C. or higher.

本願発明においては、オルニチン合成酵素(アルギナーゼ)の基質であるアルギニンを、キノコエキス(生キノコ又は凍結生キノコを破砕して得られるキノコのスラリー、又はスラリーから分離して得られるキノコエキス)に添加することにより、オルニチンを多量に生成させることができる。
原料キノコからエキスを得るには、生キノコ又はその凍結品をホモジナイザー又はジューサー等で粉砕した後、圧搾や遠心分離等でエキスを回収する。キノコに水を加えて粉砕した後エキス溶液を回収しても良い。
又、前記キノコエキス中のオルニチン合成酵素(アルギナーゼ)は、生キノコに限らず、酵素が失活しない温度帯で乾燥したキノコの粉末に水を加えて戻したスラリー又はスラリーから分離されたエキスを使用してもよい。
また、乾燥キノコ粉末とアルギニンを予め混合しておき、これに水を添加したものを、以下に記載する条件下に保持してもよい。
In the present invention, arginine which is a substrate of ornithine synthase (arginase) is added to a mushroom extract (a mushroom slurry obtained by crushing raw mushrooms or frozen raw mushrooms, or a mushroom extract obtained by separating from a slurry). By doing so, a large amount of ornithine can be produced.
In order to obtain an extract from a raw material mushroom, the raw mushroom or a frozen product thereof is pulverized with a homogenizer, a juicer, or the like, and then the extract is recovered by pressing or centrifuging. The extract solution may be recovered after adding water to the mushroom and crushing it.
In addition, the ornithine synthase (arginase) in the mushroom extract is not limited to raw mushrooms, but is a slurry obtained by adding water to mushroom powder dried in a temperature zone where the enzyme is not deactivated, or an extract separated from the slurry. May be used.
Alternatively, a dry mushroom powder and arginine mixed in advance and water added thereto may be kept under the conditions described below.

アルギニンを添加してオルニチンを生成させる好適な条件(反応条件)は下記のとおりである。
(a)温度:30℃〜70℃(より好ましくは、40℃〜60℃)
(b)pH:5.0〜11.0(より好ましくは、7.0〜10.0)
(c)保持時間:2時間以上(より好ましくは、6時間〜8時間)
(d)添加するアルギニンの量(アルギニン/エキス):1g/L〜50g/L
前記条件に保持した後、80℃以上の熱水中で酵素を失活させ、濾過或いは遠心分離等にて沈殿物を除去する。
Suitable conditions (reaction conditions) for adding arginine to produce ornithine are as follows.
(A) Temperature: 30 ° C. to 70 ° C. (more preferably, 40 ° C. to 60 ° C.)
(B) pH: 5.0 to 11.0 (more preferably 7.0 to 10.0)
(C) Holding time: 2 hours or more (more preferably, 6 hours to 8 hours)
(D) Amount of arginine to be added (arginine / extract): 1 g / L to 50 g / L
After maintaining the above conditions, the enzyme is deactivated in hot water at 80 ° C. or higher, and the precipitate is removed by filtration or centrifugation.

種々のキノコについて調べた結果、オルニチン生成量は、キノコの種類によって異なるが、エノキタケ、ヒラタケ、バイリング、ブナシメジ、エリンギ、アガリクス等のキノコにおいて、オルニチン生産性が非常に高いことが判明した(後記する実施例10参照)。 As a result of investigating various mushrooms, the production of ornithine varies depending on the type of mushroom, but it has been found that ornithine productivity is very high in mushrooms such as enokitake, oyster mushrooms, biling, bunashimeji, eringi and agaricus (see below). See Example 10).

前記アルギニンを基質とするアルギナーゼによる反応では、オルニチンのほかに副産物として尿素やアンモニアが生成する。
ヒラタケ、バイリングで高濃度の尿素が検出された。
又,エノキタケ、ブナシメジ、エリンギ、アガリクスでは尿素の代わりに高濃度のアンモニアが生成した。このアンモニアは、エキス成分を濃縮するための乾燥工程で容易に除去される。尿素は、人体ではアンモニアを無毒化するために尿素サイクルで合成され、毒性は非常に低いことが(社)日本化学物質安全・情報センターの資料で示されている(http://www.jetoc.or.jp/HP_SIDS/htmlfiles/57-13-6.html)。
以上のようにして得られたエキスを真空凍結乾燥や温風乾燥、噴霧乾燥、ドラム乾燥等の効率の良い乾燥法で乾燥することにより、重量百分率で10%以上のオルニチンを含む食品素材を製造することが可能である。
In the reaction with arginase using arginine as a substrate, urea and ammonia are produced as by-products in addition to ornithine.
High concentrations of urea were detected in oyster mushrooms and bilings.
Enokitake, Bunashimeji, Eringi, and Agaricus produced high concentrations of ammonia instead of urea. This ammonia is easily removed in the drying step for concentrating the extract components. Urea is synthesized in the urea cycle to detoxify ammonia in the human body, and the toxicity is very low, as shown in the materials of the Japan Chemical Safety and Information Center (http: //www.jetoc .or.jp / HP_SIDS / htmlfiles / 57-13-6.html).
The extract obtained as described above is dried by an efficient drying method such as vacuum freeze drying, hot air drying, spray drying, drum drying or the like, thereby producing a food material containing ornithine of 10% or more by weight. Is possible.

本願発明によれば、大量に生産可能な市販のキノコから、アミノ酸高含有食品素材,及び特にオルニチンを豊富に含有するアミノ酸高含有食品素材を容易に生産することができるので、旨味を付与する調味料として、又旨味を付与すると共にオルニチンを強化した調味料を提供することができるという効果を有する。   According to the present invention, it is possible to easily produce a food material with a high amino acid content and particularly a food material with a high amino acid content rich in ornithine from commercially available mushrooms that can be produced in large quantities. As a seasoning, there is an effect that it can provide a seasoning that imparts umami and enhances ornithine.

(1)エノキタケエキスの調製
市販のエノキタケを購入し、以下の方法で凍結粉砕エキス、自己消化エキスを調製した。
(A)凍結粉砕エキス
エノキタケを-20℃のフリーザー(チェストフリーザーHF-10CG,三洋電機株式会社)に入れて凍結させた後、凍結したままミル(TM807、株式会社テスコム)で粉砕した。この粉砕物を50 mlの遠心チューブに入れてしばらく室温に放置し、完全に融解させた。その後、遠心機(CN-1050、アズワン株式会社)で約3000×g、10分間遠心して残渣とエキスを分離し、エキスのみを回収した。
(B)自己消化エキス
生エノキタケを50 ml遠心チューブに詰め、30℃、40℃、50℃、60℃、70℃のそれぞれの温度で6時間保温した後、遠心機(CN-1050、アズワン株式会社)で約3,000×g、10分間遠心して残渣とエキスを分離し、エキスのみを回収した。
(2)エノキタケエキスの遊離アミノ酸分析
回収したエキスは回収量を測定後80℃の温浴に10分間浸して酵素を失活させ、一部を卓上微量高速遠心機(CT13R、日立工機株式会社)で16,000×g、10分間遠心した。上清をポアサイズ0.2μmのメンブランフィルター(ミニザルトRC15、ザルトリウス株式会社)で濾過し、濾液をサンプル希釈液(クエン酸リチウム緩衝液:6.9g/Lクエン酸リチウム(4H2O)、1.3g/L塩化リチウム、8.8g/Lクエン酸、4.0 ml/L塩酸、40.0 ml/Lエタノール、3.1 ml/L BRIJ-35(20%)、2.5 ml/Lチオジグリコール、0.1 ml/L n-カプリル酸; 日本電子(株)で販売)で適宜希釈してアミノ酸分析用サンプル溶液とした。サンプル溶液を全自動アミノ酸分析機(JLC-500/V、日本電子株式会社)用のバイアル瓶に入れてセットし、50μlを注入して分析を行った。装置の操作は付属の操作マニュアルに従った。
(3)アミノ酸分析結果
図1に各回収エキス中の総遊離アミノ酸量とエキス回収量を示す。尚、総遊離アミノ酸量は回収したエキス100 ml中の含有量、エキス回収量は試験に供したキノコ1 kg当たりの量で記載した。
図1の結果によれば、30〜60℃、6時間の自己消化処理でエキスの総遊離アミノ酸量は凍結粉砕処理エキスを上回り(特許文献3参照)、特に40℃で約1.58倍、50℃で約1.54倍と高かった。また、40〜70℃、6時間の自己消化処理で凍結粉砕処理(特許文献3参照)と同等量のエキスが回収できた。総遊離アミノ酸量とエキス回収量から考えて、自己消化処理の最適温度は40℃〜60℃であることがわかる。
(1) Preparation of enokitake mushroom extract Commercially available enokitake mushrooms were purchased, and freeze-ground and self-digested extracts were prepared by the following method.
(A) Freeze-pulverized extract Enokitake was placed in a freezer (chest freezer HF-10CG, Sanyo Electric Co., Ltd.) at −20 ° C. and frozen, and then pulverized with a mill (TM807, Tescom Co., Ltd.) while frozen. This pulverized product was placed in a 50 ml centrifuge tube and left at room temperature for a while to completely melt. Thereafter, the residue and the extract were separated by centrifugation at about 3000 × g for 10 minutes with a centrifuge (CN-1050, ASONE Co., Ltd.), and only the extract was recovered.
(B) Self-digested raw enokitake is packed in a 50 ml centrifuge tube and incubated at 30 ° C, 40 ° C, 50 ° C, 60 ° C, and 70 ° C for 6 hours, and then centrifuged (CN-1050, ASONE Stock) Company) was centrifuged at about 3,000 xg for 10 minutes to separate the residue and the extract, and only the extract was recovered.
(2) Analysis of free amino acids in enokitake mushroom extract The recovered extract was measured for volume and then immersed in a warm bath at 80 ° C for 10 minutes to inactivate the enzyme. Part of the tabletop microcentrifuge (CT13R, Hitachi Koki Co., Ltd.) And centrifuged at 16,000 xg for 10 minutes. The supernatant was filtered through a membrane filter (Minisart RC15, Sartorius Co., Ltd.) having a pore size of 0.2 μm, and the filtrate was a sample diluent (lithium citrate buffer: 6.9 g / L lithium citrate (4H 2 O), 1.3 g / L). Lithium chloride, 8.8 g / L citric acid, 4.0 ml / L hydrochloric acid, 40.0 ml / L ethanol, 3.1 ml / L BRIJ-35 (20%), 2.5 ml / L thiodiglycol, 0.1 ml / L n-caprylic acid A sample solution for amino acid analysis was appropriately diluted with JEOL Ltd.). The sample solution was set in a vial for a fully automatic amino acid analyzer (JLC-500 / V, JEOL Ltd.), and 50 μl was injected for analysis. The operation of the device followed the attached operation manual.
(3) Amino acid analysis results Figure 1 shows the total free amino acid content and extract recovery amount in each recovered extract. The total free amino acid content was described as the content in 100 ml of the recovered extract, and the extract recovery amount was described as the amount per 1 kg of mushrooms used in the test.
According to the results in FIG. 1, the total free amino acid content of the extract exceeds that of the freeze-pulverized extract after 30 hours at 60 to 60 ° C. for 6 hours (see Patent Document 3), especially about 1.58 times at 40 ° C. and 50 ° C. It was about 1.54 times higher. In addition, an amount of extract equivalent to that of the freeze pulverization process (see Patent Document 3) could be recovered by self-digestion treatment at 40 to 70 ° C. for 6 hours. Considering the total amount of free amino acids and the amount of recovered extract, it can be seen that the optimum temperature for the self-digestion treatment is 40 ° C to 60 ° C.

生エノキタケを詰めた50 ml遠心チューブを数本ずつ40℃及び50℃の孵卵器に入れ、一定時間経過ごとに取り出した。取り出した遠心チューブはすぐに遠心機(CN-1050、アズワン株式会社)で約3,000×g、10分間遠心して残渣とエキスを分離し、エキスのみを回収した。エキスから実施例1の場合と同様にサンプル溶液を調製し、アミノ酸分析を行って総遊離アミノ酸量を算出した。図2に結果を示す。
15時間まで自己消化処理を行ったが、40℃と50℃で総遊離アミノ酸量の増加の仕方はほとんど変わらなかった。しかしながら、雑菌の繁殖を考慮した場合、50℃、6〜8時間の処理が良い。
Several 50 ml centrifuge tubes filled with fresh enokitake were placed in an incubator at 40 ° C. and 50 ° C., and taken out at regular intervals. The removed centrifuge tube was immediately centrifuged at about 3,000 × g for 10 minutes with a centrifuge (CN-1050, ASONE Co., Ltd.) to separate the residue and the extract, and only the extract was recovered. A sample solution was prepared from the extract in the same manner as in Example 1, and amino acid analysis was performed to calculate the total amount of free amino acids. The results are shown in FIG.
Although self-digestion treatment was performed for up to 15 hours, the way of increasing the total free amino acid content at 40 ° C and 50 ° C was almost the same. However, when considering the propagation of various bacteria, treatment at 50 ° C. for 6 to 8 hours is good.

生エノキタケを詰めた50 ml遠心チューブを16本用意し、8本をフリーザー(チェストフリーザーHF-10CG,三洋電機株式会社)で凍結させた。全てのチューブを40℃の孵卵器に入れ、一定時間経過ごとに生キノコと凍結キノコのチュ−ブを1本ずつ取り出した。取り出した遠心チューブはすぐに遠心機(CN-1050、アズワン株式会社)で約3,000×g、10分間遠心して残渣とエキスを分離し、エキスのみを回収した。エキスから実施例1の場合と同様にサンプル溶液を調製し、アミノ酸分析を行って総遊離アミノ酸量を算出した。図3に結果を示す。
総遊離アミノ酸量は、凍結キノコを自己消化処理した方が、処理時間が同じ場合高くなることがわかった。原料のキノコを安定に供給するためには何らかの方法でキノコを保存しなければならないが、図3の結果は凍結保存が遊離アミノ酸高含有量エキスを製造する際に非常に有効な手段であることを示している。
Sixteen 50 ml centrifuge tubes filled with fresh enokitake were prepared, and eight were frozen in a freezer (chest freezer HF-10CG, Sanyo Electric Co., Ltd.). All the tubes were placed in an incubator at 40 ° C., and a tube of fresh mushrooms and frozen mushrooms was taken out at regular intervals. The removed centrifuge tube was immediately centrifuged at about 3,000 × g for 10 minutes with a centrifuge (CN-1050, ASONE Co., Ltd.) to separate the residue and the extract, and only the extract was recovered. A sample solution was prepared from the extract in the same manner as in Example 1, and amino acid analysis was performed to calculate the total amount of free amino acids. The results are shown in FIG.
The total amount of free amino acids was found to be higher when the frozen mushrooms were self-digested when the treatment time was the same. In order to stably supply the raw material mushrooms, the mushrooms must be preserved in some way, but the results in Fig. 3 show that cryopreservation is a very effective means for producing high free amino acid extract. Is shown.

1000 ml種菌瓶で栽培し、10℃、暗黒下で子実体(キノコ)を発生させたエノキタケを4本用意し、2本を室温(20〜24℃)、蛍光灯下(約1000 lux)で2日間栽培した。他の2本は、コントロールとして10℃、暗黒下で2日間栽培した。栽培後収穫したそれぞれのエノキタケの形態を図4に示す。重量は室温、蛍光灯下栽培品が平均273.5 g、コントロール品が279.4 gで、ほとんど変わらなかったが、室温、蛍光灯下栽培品の傘の直径は最大2.5 cmに達し、中心付近の子実体の柄は約3.5 cm伸びた。
これらのキノコをフリーザー(チェストフリーザーHF-10CG,三洋電機株式会社)で凍結し、実施例1と同様に凍結粉砕エキスを調製した。これらエキスから実施例1の場合と同様にサンプル溶液を調製し、アミノ酸分析を行った。
さらにこれらキノコの凍結品を50℃の孵卵器に入れ、6時間保温して自己消化処理した。処理後再び凍結し、実施例1と同様に凍結粉砕エキスを調製した。これらエキスから実施例1の場合と同様にサンプル溶液を調製し、アミノ酸分析を行った。結果を表1に示す。
Prepare 4 enokitake mushrooms grown in 1000 ml inoculum bottles and generate fruit bodies (mushrooms) at 10 ° C in the dark, 2 at room temperature (20-24 ° C), under fluorescent light (about 1000 lux) Cultivated for 2 days. The other two were grown for 2 days in the dark at 10 ° C as a control. The form of each enokitake mushroom harvested after cultivation is shown in FIG. The weight was room temperature, the average was 273.5 g for the cultivated products under fluorescent light, and 279.4 g for the control product, but the umbrella diameter of the cultivated products under the room temperature and fluorescent light reached a maximum of 2.5 cm. The handle stretched about 3.5 cm.
These mushrooms were frozen with a freezer (chest freezer HF-10CG, Sanyo Electric Co., Ltd.), and a freeze-pulverized extract was prepared in the same manner as in Example 1. Sample solutions were prepared from these extracts in the same manner as in Example 1, and amino acid analysis was performed.
Furthermore, these frozen mushrooms were placed in an incubator at 50 ° C. and kept for 6 hours to self-digest. After the treatment, it was frozen again, and a freeze-ground extract was prepared in the same manner as in Example 1. Sample solutions were prepared from these extracts in the same manner as in Example 1, and amino acid analysis was performed. The results are shown in Table 1.

Figure 0004705874
Figure 0004705874

室温、蛍光灯下栽培品の総遊離アミノ酸含有量は、コントロール品の約1.7倍という高い値を示した。特に旨味の主成分であるグルタミン酸の含有量は、コントロールの約1.96倍であった。
また、自己消化により、総遊離アミノ酸含有量は、収穫後の場合と比べてコントロールでは、約1.36倍、室温、蛍光下栽培品は約1.31倍に増加した。上記エノキタケエキス中のアミノ酸含有量が増加し、更に自己消化処理することによって非常に高濃度アミノ酸を含むエキスを回収できることがわかった。
自己消化処理の場合、キノコ自身の酵素を働かせるためには、20℃〜80℃、より好ましくは40℃〜60℃での保温が必要だが、この温度帯は雑菌も繁殖しやすいため、長時間の保温は危険である。
これに対し、キノコ栽培の最後に、温度と光の条件を少し変えてキノコの傘を大きく成長させることは、極めて容易であり、この方法は、高濃度遊離アミノ酸含有エキスを得るための前処理として優れている。
The total free amino acid content of the product cultivated under fluorescent light at room temperature was about 1.7 times higher than that of the control product. In particular, the content of glutamic acid, which is the main component of umami, was about 1.96 times that of the control.
In addition, due to self-digestion, the total free amino acid content increased by about 1.36 times in the control and about 1.31 times in the room temperature and fluorescently cultivated products compared to the case after harvesting. It was found that the amino acid content in the enokitake mushroom extract increased, and an extract containing a very high concentration amino acid can be recovered by further self-digestion treatment.
In the case of self-digestion treatment, it is necessary to keep the temperature at 20 ° C. to 80 ° C., more preferably 40 ° C. to 60 ° C., in order to make the mushroom's own enzyme work. Keeping warm is dangerous.
On the other hand, at the end of mushroom cultivation, it is extremely easy to grow mushroom umbrellas a little by changing the conditions of temperature and light a little, and this method is a pretreatment to obtain an extract containing high concentration free amino acids As excellent.

市販されている種々のキノコについて、購入後直ちに凍結させたものとその凍結品を50℃、6時間自己消化処理したものから実施例1の場合と同様の方法でキノコエキスサンプルを作製し、アミノ酸分析を行って総遊離アミノ酸量を算出した。結果を図5に示す。
各キノコともに自己消化処理を行うことによって、回収したエキスの総遊離アミノ酸量が未処理の場合と比べて約1.4〜3倍に増加することを確認した。自己消化後の各キノコエキスを60℃、48時間乾燥した場合に得られたペーストと市販されている酵母エキスの総遊離アミノ酸量、γ−アミノ酪酸含有量およびオルニチン含有量を表2に示す。
A variety of commercially available mushrooms were frozen immediately after purchase and the frozen products were self-digested at 50 ° C. for 6 hours to prepare mushroom extract samples in the same manner as in Example 1, and amino acids Analysis was performed to calculate the total amount of free amino acids. The results are shown in FIG.
It was confirmed that by performing autolysis treatment for each mushroom, the total amount of free amino acids in the recovered extract was increased by about 1.4 to 3 times compared to the case of untreated. Table 2 shows the total free amino acid content, γ-aminobutyric acid content, and ornithine content of the paste obtained when each mushroom extract after self-digestion was dried at 60 ° C. for 48 hours and the commercially available yeast extract.

Figure 0004705874
Figure 0004705874

総遊離アミノ酸量は全てのキノコペーストで酵母エキス1及び2のそれを大きく上回り、キノコの自己消化処理エキスを乾燥させることにより非常に高濃度の遊離アミノ酸を含有する食品素材を製造することが可能であることが判明した。また、エノキタケペースト、アガリクスペーストでγ−アミノ酪酸、エノキタケペースト、ヒラタケペースト、ブナシメジペースト、ハタケシメジペースト、シイタケペースト、ツクリタケペースト、アガリクスペースト、バイリングペーストでオルニチン含有量が高かった。   The total amount of free amino acids greatly exceeds that of yeast extracts 1 and 2 in all mushroom pastes, and it is possible to produce food materials containing very high levels of free amino acids by drying mushroom self-digested extracts. It turned out to be. In addition, γ-aminobutyric acid, enokitake paste, oyster mushroom paste, bunashimeji paste, mushroom shimeji paste, shiitake paste, tsutake mushroom paste, agaric paste, and biling paste had high ornithine content in enokitake paste and agaric paste.

生のエノキタケをジューサー(TM807、株式会社テスコム)に入れ、純水をキノコの半分の重量加えて粉砕した。粉砕物を50 ml遠心チューブに入れ、遠心機(CN-1050、アズワン株式会社)で約3,000×g、10分間遠心して残渣とエキスジュースを分離し、エキスジュースのみを回収した(生キノコエキスジュース)。
凍結したエノキタケについても同様の方法でエキスジュースを作製した(凍結キノコエキスジュース)。これらのエキスジュース20 mlにアルギニン0.2 g(1.148 mmol)を加え、50℃、6時間保温後溶液を1 ml採取して80℃の水浴に10分間浸し、酵素を失活させた。卓上微量高速遠心機(CT13R、日立工機株式会社)で16,000×g、10分間遠心した後、上清をポアサイズ0.2μmのメンブランフィルター(ミニザルトRC15、ザルトリウス株式会社)で濾過した。この濾液から実施例1に準じてアミノ酸分析用サンプルを調整し、アミノ酸分析を行ってオルニチン、アルギニン、アンモニアの含有量を測定した。さらに、生キノコエキスジュースを一晩冷凍及び冷蔵(5℃)保存した後室温に戻し、同様にアルギニンを加えて反応を行いオルニチン、アルギニン、アンモニアの含有量を測定した。結果を図6に示す。
オルニチンの生産効率は、エキスジュースを生キノコ、凍結キノコいずれから調製してもほぼ同じであったが、残存するアルギニン量は凍結キノコの場合の方が多かった。また、生キノコエキスジュースを凍結保存した場合オルニチン生産効率がエキスジュース調製直後に比べて約半分となり、冷蔵保存の場合はほとんど生産されなくなることが判明した。
Raw enokitake was placed in a juicer (TM807, Tescom Co., Ltd.), and pure water was added to half the weight of the mushroom and pulverized. The pulverized product was placed in a 50 ml centrifuge tube and centrifuged at approximately 3,000 xg for 10 minutes in a centrifuge (CN-1050, ASONE CORPORATION) to separate the residue and extract juice, and only the extract juice was collected (raw mushroom extract juice ).
Extract juice was prepared in the same manner for frozen enokitake (frozen mushroom extract juice). Arginine 0.2 g (1.148 mmol) was added to 20 ml of these extract juices, and after keeping the temperature at 50 ° C. for 6 hours, 1 ml of the solution was taken and immersed in an 80 ° C. water bath for 10 minutes to inactivate the enzyme. After centrifugation at 16,000 × g for 10 minutes with a desktop micro high-speed centrifuge (CT13R, Hitachi Koki Co., Ltd.), the supernatant was filtered through a membrane filter (Minisart RC15, Sartorius Co., Ltd.) having a pore size of 0.2 μm. A sample for amino acid analysis was prepared from this filtrate according to Example 1, and amino acid analysis was performed to measure the contents of ornithine, arginine, and ammonia. Further, the raw mushroom extract juice was frozen and refrigerated overnight (5 ° C.) and then returned to room temperature. Similarly, arginine was added to react to measure the contents of ornithine, arginine and ammonia. The results are shown in FIG.
The production efficiency of ornithine was almost the same regardless of whether the extract juice was prepared from raw mushrooms or frozen mushrooms, but the amount of remaining arginine was higher in the case of frozen mushrooms. In addition, it was found that the ornithine production efficiency was about half when the raw mushroom extract juice was stored frozen, and almost no product was produced when stored refrigerated.

冷凍エノキタケから実施例6と同様の方法でエキスジュースを調製し、エキスジュース20 mlにアルギニン0.4 g(2.296 mmol)を加えて30℃、40℃、50℃、60℃の各温度で6時間保温した。この溶液を実施例5の場合と同様に加熱処理、フィルター濾過等を行い、アミノ酸分析用サンプルを調製して分析を行った。各温度によるオルニチン、アルギニン、アンモニア量の比較結果を図7に示す。
この結果より、50℃での保温が最も効率良くオルニチンを生産できることが判明した。
Extract juice is prepared from frozen enokitake mushrooms in the same manner as in Example 6, and 0.4 g (2.296 mmol) of arginine is added to 20 ml of extract juice and kept at 30 ° C, 40 ° C, 50 ° C, and 60 ° C for 6 hours. did. This solution was subjected to heat treatment, filter filtration and the like in the same manner as in Example 5 to prepare a sample for amino acid analysis and perform analysis. FIG. 7 shows a comparison result of the amounts of ornithine, arginine, and ammonia at each temperature.
From this result, it was found that incubation at 50 ° C. can produce ornithine most efficiently.

実施例7と同様に調製したエノキタケジュース20 mlにアルギニン0.4 g(2.296 mmol)を加え、90%酢酸及び1N水酸化ナトリウムでpHを4、5、6、7、8、9、10、11に調製して50℃、6時間保温した。保温後実施例5の場合と同様に加熱処理、フィルター濾過等を行い、アミノ酸分析用サンプルを調製して分析を行った。溶液のpHの違いによるオルニチン、アルギニン、アンモニア量の比較結果を図8に示す。
この結果より、pH8〜10でオルニチンは効率良く生産されることが判明した。原料のアルギニンは塩基性アミノ酸で、エノキタケエキスジュースに1〜5%加えるとこの溶液のpH値は9〜10となるため、pH調製を行うことなしにオルニチン生成を効率良く行うことができる。
0.4 g (2.296 mmol) of arginine was added to 20 ml of enokitake mushroom juice prepared in the same manner as in Example 7, and the pH was adjusted to 4, 5, 6, 7, 8, 9, 10, 11 with 90% acetic acid and 1N sodium hydroxide. Prepared and incubated at 50 ° C. for 6 hours. After heat retention, the sample was subjected to heat treatment, filter filtration, etc. in the same manner as in Example 5 to prepare an amino acid analysis sample for analysis. FIG. 8 shows a comparison result of the amounts of ornithine, arginine and ammonia depending on the pH of the solution.
From this result, it was found that ornithine was efficiently produced at pH 8-10. The raw material arginine is a basic amino acid. When 1-5% is added to the enokitake extract juice, the pH value of this solution becomes 9-10. Therefore, it is possible to efficiently produce ornithine without adjusting the pH.

実施例7と同様に調製したエノキタケジュース20 mlにアルギニンを0.2 g(1.148 mmol)加え、50℃で保温しながら2時間、4時間、6時間、8時間経過時に1 mlずつサンプリングし、80℃、10分間加熱して酵素を失活させた。実施例5の場合と同様にアミノ酸分析用サンプルを調製し、アミノ酸分析を行ってオルニチン、アルギニン、
アンモニア量を測定した。結果を図9に示す。
保温時間6〜8時間でオルニチン生成量の増加及びアルギニン残存量の減少がほぼ止まることがわかった。8時間程度でアルギナーゼが失活することが推察される。
0.2 g (1.148 mmol) of arginine was added to 20 ml of enokitake mushroom juice prepared in the same manner as in Example 7, and 1 ml each was sampled after 2 hours, 4 hours, 6 hours, and 8 hours while keeping at 50 ° C. The enzyme was inactivated by heating for 10 minutes. A sample for amino acid analysis was prepared in the same manner as in Example 5, and amino acid analysis was performed to obtain ornithine, arginine,
The amount of ammonia was measured. The results are shown in FIG.
It was found that the increase in the production of ornithine and the decrease in the residual amount of arginine ceased after 6 to 8 hours of incubation. It is assumed that arginase is deactivated in about 8 hours.

市販されているヒラタケ、バイリング、タモギタケ、ヤマブシタケ、ハタケシメジ、ブナシメジ、マッシュルーム、マイタケ、シイタケ、エリンギ、アガリクスからエノキタケの場合と同様に生キノコエキスジュースを調製し、ジュース20 mlに対してアルギニン0.4 g(2.296 mmol)を加えて50℃、6時間保温した。なお、これらのジュースのpHは9〜10の範囲であった。これらのジュースからエノキタケの場合と同様にアミノ酸分析用サンプルを調製し、アミノ酸分析を行ってオルニチンとアンモニアの生成量とアルギニンの残存量を測定した。結果を図10に示す。
ヒラタケ、バイリング、ブナシメジ、エリンギ、アガリクスでエノキタケと同様のオルニチン生産能が認められた。また、ヒラタケとバイリングでは副産物であるアンモニアがほとんど生成しなかったが、尿素が高濃度(ヒラタケ:108.3μmol/ml, バイリング:107.6μmol/ml)に生成した。さらに、ジュースにアルギニンを添加した後90%酢酸を用いてpH値をジュースのpH値近くまで下げ、50℃、6時間保温してオルニチンの生産能を比較した。結果を図11に示す。
pH値が5〜7の中性付近では、各種キノコエキスジュースのオルニチン生産能は非常に低いことが判明した。
Prepare fresh mushroom extract juice from commercially available oyster mushroom, biling, tamagotake, yamabushitake, hatakeshimeji, bunashimeji, mushroom, maitake, shiitake, eringi, agaricus as in the case of enokitake, 0.4 g of arginine for 20 ml of juice (2.296 mmol) was added and kept at 50 ° C. for 6 hours. The pH of these juices was in the range of 9-10. Samples for amino acid analysis were prepared from these juices in the same manner as enokitake, and amino acid analysis was performed to measure the amounts of ornithine and ammonia produced and the remaining amount of arginine. The results are shown in FIG.
The ability to produce ornithine was found in oyster mushrooms, bilings, beech shimeji mushrooms, eringgi and agaricus. In addition, oyster mushrooms and biling produced almost no by-product ammonia, but urea was produced at a high concentration (oyster mushroom: 108.3 μmol / ml, biring: 107.6 μmol / ml). Furthermore, after adding arginine to the juice, the pH value was lowered to near the pH value of the juice using 90% acetic acid and incubated at 50 ° C. for 6 hours to compare the ornithine production ability. The results are shown in FIG.
It was found that the ornithine-producing ability of various mushroom extract juices was very low in the vicinity of neutral pH values of 5-7.

市販のエノキタケ1 kgに500 gの純水を加え、ジューサー(TM807、株式会社テスコム)で粉砕した。粉砕物を50 ml遠心チューブ30 本に約40 gづつ詰め、遠心機(CN-1050、アズワン株式会社)で約3,000×g、10分間遠心して残渣とエキスを分離し、400 mlのエキスを回収した。このエキスに6 g(1.5%(w/v))のアルギニンを添加し、50℃、6時間保温した。保温後溶液を1000 mlのガラスビーカーに移して80℃のウォ−タ−バス(BM400、ヤマト科学株式会社)に入れて加熱後、濾過して沈殿物を除去した。回収した濾液350 ml中のアンモニアを蒸発除去するため、濾液を入れた1000 mlガラスビーカーを再度80℃のウォーターバスに入れて時々攪拌しながら加熱した。濾液の温度が80℃に達してから30分後に加熱を止めてウォーターバスからビーカーを取り出し、オルニチン高含有量エノキタケエキスを得た。このエキス1 mlをポアサイズ0.2μmのメンブランフィルター(ミニザルトRC15、ザルトリウス株式会社)で濾過し、アミノ酸分析用サンプル希釈液(実施例1参照)で適宜希釈してアミノ酸分析を行った。結果を表3に示す。   500 g of pure water was added to 1 kg of commercially available enokitake mushrooms and ground with a juicer (TM807, Tescom Co., Ltd.). About 40 g of each pulverized product is packed in 30 50 ml centrifuge tubes and centrifuged at about 3,000 xg for 10 minutes in a centrifuge (CN-1050, ASONE Co., Ltd.) to separate the residue from the extract and collect 400 ml of extract. did. 6 g (1.5% (w / v)) arginine was added to this extract, and the mixture was incubated at 50 ° C. for 6 hours. After incubation, the solution was transferred to a 1000 ml glass beaker, placed in an 80 ° C. water bath (BM400, Yamato Scientific Co., Ltd.), heated, and then filtered to remove precipitates. In order to evaporate and remove ammonia in 350 ml of the collected filtrate, the 1000 ml glass beaker containing the filtrate was again placed in an 80 ° C. water bath and heated with occasional stirring. 30 minutes after the temperature of the filtrate reached 80 ° C., the heating was stopped and the beaker was taken out of the water bath to obtain an ornithine high content enokitake extract. 1 ml of this extract was filtered through a membrane filter (Minisart RC15, Sartorius Co., Ltd.) having a pore size of 0.2 μm and appropriately diluted with a sample diluent for amino acid analysis (see Example 1) for amino acid analysis. The results are shown in Table 3.

Figure 0004705874
Figure 0004705874

上記結果のように、1.5 g/100 ml(86.1μmol/ml)のアルギニン添加により、1.0137 g/100 ml(76.696μmol/ml)のオルニチンを含むエノキタケエキスが得られた。アルギニン添加前のエキスのオルニチン含有量は79.6 mg/100 ml(6.02μmol/ml)、アルギニン含有量は21.6 mg/100 ml(1.24μmol/ml)であったので、添加したアルギニンのオルニチンへの変換率は82.8%と推定される。このエキスを80℃、48時間乾燥したところ水分含量約5%の褐色のペ−ストが得られた。このペーストを水に溶かしてポアサイズ0.2μmのメンブレンフィルター(ミニザルトRC15、ザルトリウス株式会社)で濾過し、濾液をアミノ酸分析用サンプル希釈液で適宜希釈してアミノ酸分析を行ったところ、オルニチン含有量は約11.3 g/100 g、γ−アミノ酪酸は約1.1 g/100 gであった。 As described above, enokitake mushroom extract containing 1.0137 g / 100 ml (76.696 μmol / ml) ornithine was obtained by adding 1.5 g / 100 ml (86.1 μmol / ml) arginine. Since the ornithine content of the extract before addition of arginine was 79.6 mg / 100 ml (6.02 μmol / ml) and the arginine content was 21.6 mg / 100 ml (1.24 μmol / ml), conversion of the added arginine to ornithine The rate is estimated at 82.8%. When this extract was dried at 80 ° C. for 48 hours, a brown paste having a water content of about 5% was obtained. When this paste was dissolved in water and filtered through a membrane filter (Minisart RC15, Sartorius Co., Ltd.) having a pore size of 0.2 μm, the filtrate was appropriately diluted with a sample diluent for amino acid analysis, and amino acid analysis was performed. 11.3 g / 100 g and γ-aminobutyric acid were about 1.1 g / 100 g.

市販のエノキタケ約150gを凍結乾燥機(FRD-50M、岩城硝子(株))で凍結乾燥し、ミル(TM807、(株)テスコム)で粉末化した。この粉末3gとアルギニン0.3gを混合し水を加えて20mlの溶液に調製した(アルギニン添加量1.5%(w/v))。この溶液を50℃、6時間保持した後、実施6の場合と同様に加熱処理及びフィルター濾過を行い、アミノ酸分析用サンプルを調製して分析を行った。オルニチンとアンモニア生成量及びアルギニン残存量の定量結果を表4に示す。 About 150 g of commercially available enokitake was lyophilized with a freeze dryer (FRD-50M, Iwaki Glass Co., Ltd.) and powdered with a mill (TM807, Tescom Co., Ltd.). 3 g of this powder and 0.3 g of arginine were mixed and water was added to prepare a 20 ml solution (arginine addition amount 1.5% (w / v)). This solution was held at 50 ° C. for 6 hours, and then subjected to heat treatment and filter filtration in the same manner as in Example 6 to prepare a sample for amino acid analysis for analysis. Table 4 shows the quantification results of the amount of ornithine and ammonia produced and the residual amount of arginine.

Figure 0004705874
Figure 0004705874

次に、前記処理した濾液10mlを80℃、48時間乾燥したところ、水分含量約5%の褐色ペーストが得られた。このペーストを水に溶かしてポアサイズ0.2μmのメンブランフィルター(ミニザルトRC15、ザルトリウス株式会社)で濾過し、濾液をサンプル希釈液で適宜希釈してアミノ酸分析を行ったところ、オルニチン含有量は約12.3g/100gであった。
この結果より、凍結乾燥エノキタケ粉末はオルニチン生産用酵素製剤として使用できることが判明した。
Next, 10 ml of the treated filtrate was dried at 80 ° C. for 48 hours to obtain a brown paste having a water content of about 5%. When this paste was dissolved in water and filtered through a membrane filter (Minisart RC15, Sartorius Co., Ltd.) having a pore size of 0.2 μm, the filtrate was appropriately diluted with a sample diluent, and amino acid analysis was performed. As a result, the ornithine content was about 12.3 g / It was 100 g.
From this result, it was found that freeze-dried enokitake powder can be used as an enzyme preparation for ornithine production.

本願発明に係る食品素材は、下記の用途を期待できる。
(a)キノコ自己消化処理によるアミノ酸高含有量食品素材
万能型のエキス調味料として酵母エキスと同様に使用できる。例えば、自己消化エキスは液体スープ、ジュース等の飲料の味付けに使用できる。エキス粉末やペーストは各種複合調味料、調味液、調味味噌、粉末スープ等の調味素材として使用できる。さらに、アミノ酸含有を謳った健康飲料や健康食品等の素材として、特に天然物由来のアミノ酸原料として使用できる。
(b)キノコ由来のオルニチン高含有量食品素材
実施例11のエノキタケエキスペーストを用いた場合、以下の様な用途が考えられる。いずれも1食分に付き500 mg以上のオルニチンを含む。
The food material according to the present invention can be expected to have the following uses.
(A) Amino acid high content by mushroom self-digestion treatment As a food material all-purpose extract seasoning, it can be used in the same manner as yeast extract. For example, the self-digesting extract can be used for seasoning beverages such as liquid soups and juices. The extract powder and paste can be used as a seasoning material for various complex seasonings, seasoning liquids, seasoning miso, powder soups and the like. Furthermore, it can be used as a raw material for amino acids derived from natural products, particularly as a material for health drinks and health foods that contain amino acids.
(B) Mushroom-derived ornithine high content food material When the enokitake mushroom extract paste of Example 11 is used, the following uses are conceivable. Both contain more than 500 mg ornithine per serving.

A.味噌汁用調味味噌
味噌汁は塩分0.8%、150 ml/杯として、塩分12%の味噌を使用するとすれば、味噌10 gに上記オルニチン高含有量エノキタケエキスペーストを4.5 g以上混ぜ込む。
B.液体ス−プ類
缶入りスープのような液状スープの場合、缶1本分に上記エキスペーストを4.5 g以上加えて溶かす。
C.粉末スープ類
従来の粉末状のスープの素1杯分に上記エキスペーストを4.5 g以上加え、完全に水分がなくなるまで乾燥させ粉末化する。
D.インスタントカレー、シチュー
固形のルー1皿分(約20 g)の原料に上記エキスペーストを4.5 g以上加えて固める。
E.なめ茸
1食で30 g食べると仮定すると、内容量150 gの製品に対して上記エキスペーストを22.5 g以上加える。
F.サプリメント
例えば、上記エキスペースト45 gに賦形剤を55g加え、50粒の錠剤を作る。5粒/日の摂取を目安とする。
A. Seasoned miso for miso soup Miso soup is 0.8% salt, 150 ml / cup, and if you use miso soy with 12% salt, mix 4.5 g or more of the above ornithine extract paste with high ornithine content into 10 g of miso.
B. Liquid soup In the case of liquid soup such as canned soup, add 4.5 g or more of the above extract paste to one can and dissolve.
C. Powdered soups Add 4.5 g or more of the above extract paste to one serving of conventional powdered soup, and dry to powder until it is completely free of moisture.
D. Instant curry, stew Add 4.5 g or more of the above extract paste to the ingredients for 1 plate of solid roux (about 20 g) and harden.
E. Name candy
Assuming that you eat 30 g per serving, add 22.5 g or more of the above extract paste to a 150 g product.
F. Supplement For example, 55 g of an excipient is added to 45 g of the above extract paste to make 50 tablets. Use 5 tablets / day as a guide.

これらA〜Eのオルニチン高含有量食品には1食分に付き49.5 mg以上のγ−アミノ酪酸が同時に含まれる。この含有量は、ヤクルト本社販売の特定保健用食品プレティオに含まれるγ−アミノ酪酸(10 mg/本)の約5倍である。さらにこれらA〜Eの食品を製造する際にキノコ自己消化処理エキスまたは自己消化処理エキスペーストや粉末を加えれば、キノコの旨味や風味をさらに強化した食品ができる。 These ornithine high-content foods A to E contain 49.5 mg or more of γ-aminobutyric acid per serving. This content is about 5 times that of γ-aminobutyric acid (10 mg / tube) contained in the pleio for specific health foods sold by Yakult Honsha. Furthermore, if the mushroom self-digested extract or the self-digested extract paste or powder is added when producing these foods A to E, a food that further enhances the taste and flavor of the mushrooms can be obtained.

温度別自己消化処理を行ったエノキタケのエキス中の総遊離アミノ酸量とエキス回収量を示す図である(実施例1)。It is a figure which shows the total amount of free amino acids in the extract of the enokitake mushroom which performed the self-digestion process according to temperature, and extract recovery amount (Example 1). エノキタケ自己消化処理時間に伴うエキスの総遊離アミノ酸量の変化を示す図である(実施例2)。It is a figure which shows the change of the total free amino acid content of the extract accompanying enokitake self-digestion processing time (Example 2). エノキタケの生と凍結キノコを40℃で自己消化処理したときの総遊離アミノ酸量の変化を示す図である(実施例3)。(Example 3) which is a figure which shows the change of the amount of total free amino acids when the enokitake mushroom raw and frozen mushroom are autodigested at 40 degreeC. 10℃、暗黒下で発生させた後、20〜24℃、1000 luxで2日間栽培したエノキタケを示す図である(実施例4)。A:真上から撮影、B:横から撮影(右:20〜24℃、1000 lux、2日、左:10℃、暗黒下、2日)(Example 4) which is a figure which shows the enokitake mushroom which was cultivated at 20-24 degreeC and 1000 lux for 2 days after generating in 10 degreeC and darkness. A: Taken from directly above, B: Taken from the side (right: 20-24 ° C, 1000 lux, 2 days, left: 10 ° C, under dark, 2 days) 種々のキノコの自己消化処理と未処理の場合の総遊離アミノ酸量を示す図である(実施例5)。It is a figure which shows the amount of total free amino acids in the case of the autolysis process of various mushrooms, and un-processing (Example 5). エノキタケエキスジュースの作製法及び保存法の違いによるオルニチン生産能の比較を示す図である(実施例6)。It is a figure which shows the comparison of the ornithine production ability by the difference in the preparation method and preservation | save method of enokitake mushroom extract juice (Example 6). 保温温度の違いによるオルニチン、アンモニアの生成量及びアルギニンの残存量の比較を示す図である(実施例7)。It is a figure which shows the comparison of the production amount of ornithine and ammonia by the difference in heat retention temperature, and the residual amount of arginine (Example 7). 溶液のpHの違いによるオルニチン、アンモニアの生成量及びアルギニンの残存量の比較を示す図である(実施例8)。It is a figure which shows the comparison of the production amount of ornithine and ammonia by the difference in pH of a solution, and the residual amount of arginine (Example 8). 50℃保温におけるオルニチン、アンモニアの生成量及びアルギニン残存量の経時変化を示す図である(実施例9)。It is a figure which shows the time-dependent change of the production amount of ornithine and ammonia in 50 degreeC heat retention, and arginine residual amount (Example 9). 各種市販キノコエキスジュースのオルニチン生産能の比較(pH9〜10)を示す図である(実施例10)。It is a figure which shows the comparison (pH 9-10) of the ornithine production ability of various commercially available mushroom extract juices (Example 10). 各種市販キノコエキスジュースのオルニチン生産能の比較(pH5〜7)を示す図である(実施例10)。It is a figure which shows the comparison (pH 5-7) of the ornithine production ability of various commercially available mushroom extract juice (Example 10).

Claims (17)

下記の(A)〜(C)の工程を順次経て生産されることを特徴とするアミノ酸高含有食品素材の製造方法。A method for producing a food material having a high amino acid content, which is produced through the following steps (A) to (C).
(A)暗黒下で子実体を形成させた後、室温で光を照射して子実体の傘を大きくさせた生エノキタケを得る工程。(A) The process of obtaining the raw enokitake which formed the fruit body under darkness, and then irradiated with light at room temperature to enlarge the fruit body umbrella.
(B)前記生エノキタケ、又はエノキタケを凍結した後、これらを粉砕又はこれらに水を加えて粉砕し、エノキタケのスラリーを得る工程(B) A step of freezing the raw enokitake or enokitake and then pulverizing them or adding water to them to obtain a slurry of enokitake
(C)前記スラリーからエキス(液状物質)を分離する工程(C) The process of isolate | separating an extract (liquid substance) from the said slurry
下記の(A)〜(C)の工程を順次経て生産されることを特徴とするアミノ酸高含有食品素材の製造方法。A method for producing a food material having a high amino acid content, which is produced through the following steps (A) to (C).
(A)暗黒下で子実体を形成させた後、室温で光を照射して子実体の傘を大きくさせた生エノキタケを得る工程。(A) The process of obtaining the raw enokitake which formed the fruit body under darkness, and then irradiated with light at room temperature to enlarge the fruit body umbrella.
(B)前記生エノキタケ、又はエノキタケを凍結した後、これを保温して自己消化させ、エノキタケの自己消化物を得る工程(B) A step of freezing the enokitake mushroom or enokitake mushroom and then keeping it warm and self-digesting to obtain a self-digested enokitake mushroom
(C)前記自己消化物からエキス(液状物質)を分離する工程(C) The process of isolate | separating an extract (liquid substance) from the said autolysate
下記の(A)〜(D)の工程を順次経て生産されることを特徴とするアミノ酸高含有食品素材の製造方法。A method for producing a food material having a high amino acid content, which is produced through the following steps (A) to (D).
(A)暗黒下で子実体を形成させた後、室温で光を照射して子実体の傘を大きくさせた生エノキタケを得る工程。(A) The process of obtaining the raw enokitake which formed the fruit body under darkness, and then irradiated with light at room temperature to enlarge the fruit body umbrella.
(B)前記生エノキタケ、又はエノキタケを凍結した後、これらを粉砕又はこれらに水を加えて粉砕し、エノキタケのスラリーを得る工程(B) A step of freezing the raw enokitake or enokitake and then pulverizing them or adding water to them to obtain a slurry of enokitake
(C)前記スラリーからエキス(液状物質)を分離する工程(C) The process of isolate | separating an extract (liquid substance) from the said slurry
(D)前記エキスを保温して自己消化させる工程(D) The process of keeping the extract warm and self-digesting
エキスを濃縮又は(/及び)乾燥して、ペースト状又は粉末状とする請求項1〜請求項3に記載するアミノ酸高含有食品素材の製造方法。The method for producing a food material with a high amino acid content according to any one of claims 1 to 3, wherein the extract is concentrated or / and dried to form a paste or powder. 自己消化させる条件が、下記の(a)及び(b)である請求項2〜請求項4に記載するアミノ酸高含有食品素材の製造方法。The conditions for self-digestion are the following (a) and (b): The method for producing a food material with a high amino acid content according to claims 2 to 4.
(a)温度:20℃〜80℃(より好ましくは、40℃〜60℃)  (A) Temperature: 20 ° C to 80 ° C (more preferably 40 ° C to 60 ° C)
(b)保持時間:2時間以上(より好ましくは、6時間〜10時間)  (B) Holding time: 2 hours or more (more preferably, 6 hours to 10 hours)
請求項1〜請求項5に記載する製造方法を用いて製造されるアミノ酸高含有食品素材。A food material with a high amino acid content produced using the production method according to claim 1. 請求項6に記載する食品素材を添加して栄養を強化し、かつ呈味性を改善したことを特徴とする食品。The foodstuff characterized by adding the foodstuff material of Claim 6, strengthening nutrition, and improving taste property. 下記の(A)〜(C)の工程を順次経て生産されることを特徴とする特にオルニチンを豊富に含有するアミノ酸高含有食品素材の製造方法。A method for producing a food material with a high amino acid content, particularly rich in ornithine, characterized by being produced through the following steps (A) to (C).
(A)生キノコ、又は凍結生キノコを破砕してキノコのスラリーを得る工程(A) A step of obtaining a mushroom slurry by crushing raw mushrooms or frozen raw mushrooms
(B)前記スラリーにアルギニンを添加して、スラリー中のオルニチン合成酵素(アルギナーゼ)を作用させる工程(B) A step of adding arginine to the slurry to cause ornithine synthase (arginase) in the slurry to act.
(C)前記スラリーからエキスを分離する工程(C) The process of isolate | separating an extract from the said slurry
下記の(A)〜(C)の工程を順次経て生産されることを特徴とする特にオルニチンを豊富に含有するアミノ酸高含有食品素材の製造方法。A method for producing a food material with a high amino acid content, particularly rich in ornithine, characterized by being produced through the following steps (A) to (C).
(A)生キノコ、又は凍結生キノコを破砕してキノコのスラリーを得る工程(A) A step of obtaining a mushroom slurry by crushing raw mushrooms or frozen raw mushrooms
(B)前記スラリーからエキス(液状物質)を分離する工程(B) The process of isolate | separating an extract (liquid substance) from the said slurry
(C)前記エキスにアルギニンを添加して、エキス中のオルニチン合成酵素(アルギナーゼ)を作用させる工程(C) adding arginine to the extract and causing ornithine synthase (arginase) in the extract to act
請求項8、又は請求項9の(A)工程に代えて、「酵素が失活しない温度帯で乾燥したキノコの粉末に水を加えてキノコのスラリーを得る工程」とする特にオルニチンを豊富に含有するアミノ酸高含有食品素材の製造方法。In place of the step (A) of claim 8 or 9, the ornithine is particularly rich in "a step of adding water to a mushroom powder dried in a temperature zone where the enzyme is not inactivated to obtain a mushroom slurry". A method for producing a food material containing a high amino acid content. 請求項8〜請求項10のオルニチン合成酵素(アルギナーゼ)を作用させた後のエキスを、濃縮又は(/及び)乾燥して、ペースト状又は粉末状とし、特にオルニチンを豊富に含有するアミノ酸高含有食品素材の製造方法。The extract after the action of ornithine synthase (arginase) according to claims 8 to 10 is concentrated or (and / or) dried to form a paste or a powder, and is particularly rich in ornithine. A method of manufacturing food ingredients. アルギニンの添加量が、請求項8〜請求項10に記載するエキス1Lに付き、1g〜50gである請求項8〜請求項11に記載する特にオルニチンを豊富に含有するアミノ酸高含有食品素材の製造方法。The amount of arginine added is 1 g to 50 g per 1 L of the extract according to claim 8 to claim 10. Production of a food material with a high amino acid content, particularly rich in ornithine, according to claims 8 to 11. Method. オルニチン合成酵素(アルギナーゼ)を作用させる条件が、下記の(a)〜(c)である請求項8〜請求項10に記載する特にオルニチンを豊富に含有するアミノ酸高含有食品素材の製造方法。The conditions for causing ornithine synthase (arginase) to act are the following (a) to (c): The method for producing a food material with a high amino acid content, particularly rich in ornithine, according to claims 8 to 10.
(a)温度:30℃〜70℃(より好ましくは、40℃〜60℃)  (A) Temperature: 30 ° C. to 70 ° C. (more preferably, 40 ° C. to 60 ° C.)
(b)pH:5.0〜11.0(より好ましくは、7.0〜10.0)  (B) pH: 5.0 to 11.0 (more preferably 7.0 to 10.0)
(c)保持時間:2時間以上(より好ましくは、6時間〜8時間)  (C) Holding time: 2 hours or more (more preferably, 6 hours to 8 hours)
キノコにエノキタケ、ヒラタケ、バイリング(雪霊茸、白嶺茸)、タモギタケ、ハタケシメジ、ブナシメジ、エリンギ、アガリクスを使用する請求項8〜請求項13に記載する特にオルニチンを豊富に含有するアミノ酸高含有食品素材の製造方法。Use of enokitake mushrooms, oyster mushrooms, bilings (snow mackerel, birch), tamogitake, hatakeshimeji, bunashimeji, eringi, agaricus, particularly high ornithine-rich foods rich in ornithine Material manufacturing method. キノコにエノキタケを用い、暗黒下で子実体を形成させた後、室温で光を照射して子実体の傘を大きくさせた生エノキタケを用いる請求項8〜請求項13に記載するアミノ酸高含有食品素材の製造方法。Food containing high amino acids according to claims 8 to 13, wherein enokitake is used for mushrooms, and fruit bodies are formed in the dark, and then raw enokitake is used to enlarge the fruit bodies by irradiating light at room temperature. Material manufacturing method. 請求項8〜請求項15に記載する製造方法を用いて製造される特にオルニチンを豊富に含有するアミノ酸高含有食品素材。A food material with a high amino acid content, particularly rich in ornithine, produced using the production method according to claim 8. 請求項16に記載する特にオルニチンを豊富に含有するアミノ酸高含有食品素材を添加して栄養を強化し、かつ呈味性を改善したことを特徴とする食品。The foodstuff characterized by adding the amino acid high content food material which contains abundantly ornithine as described in Claim 16, strengthening nutrition, and improving taste property.
JP2006101292A 2006-04-03 2006-04-03 Method for producing amino acid-rich food material, particularly amino acid-rich food material containing abundant ornithine, food material produced by using these production methods, and foods to which these food materials are added Expired - Fee Related JP4705874B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2006101292A JP4705874B2 (en) 2006-04-03 2006-04-03 Method for producing amino acid-rich food material, particularly amino acid-rich food material containing abundant ornithine, food material produced by using these production methods, and foods to which these food materials are added

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2006101292A JP4705874B2 (en) 2006-04-03 2006-04-03 Method for producing amino acid-rich food material, particularly amino acid-rich food material containing abundant ornithine, food material produced by using these production methods, and foods to which these food materials are added

Publications (2)

Publication Number Publication Date
JP2007274904A JP2007274904A (en) 2007-10-25
JP4705874B2 true JP4705874B2 (en) 2011-06-22

Family

ID=38677105

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006101292A Expired - Fee Related JP4705874B2 (en) 2006-04-03 2006-04-03 Method for producing amino acid-rich food material, particularly amino acid-rich food material containing abundant ornithine, food material produced by using these production methods, and foods to which these food materials are added

Country Status (1)

Country Link
JP (1) JP4705874B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104256267A (en) * 2014-07-17 2015-01-07 张久兵 Pleurotus nebrodensis nutritional wheat paste and preparation method thereof

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103371371A (en) * 2012-04-27 2013-10-30 株式会社镰田工业 Food material containing ornithine
JP6546482B2 (en) * 2015-08-31 2019-07-17 株式会社 伊藤園 Container-packed liquid food and drink, method for producing the same, and method for suppressing taste deterioration of container-packed liquid food and beverage
CN108576196A (en) * 2018-04-12 2018-09-28 南京财经大学 A kind of freezing-thawing method of high-quality quick Frozen Double Spore Mushroom

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62294069A (en) * 1986-06-13 1987-12-21 Togo Kuroiwa Nutrition supplying solution containing high unit of l-ornithine
JP2001346538A (en) * 2000-04-06 2001-12-18 Maruasaen:Kk Method for producing cortinellus shiitake processed food
JP2002247966A (en) * 2000-12-22 2002-09-03 Yaegaki Hakko Giken Kk Health food and method for producing the same
JP2004256513A (en) * 2003-02-04 2004-09-16 Ezaki Glico Co Ltd Agent for increasing amount of muscle
JP2005097133A (en) * 2003-09-22 2005-04-14 Unitika Ltd IgA PRODUCTION PROMOTER DERIVED FROM SPARASSIS CRISPA
WO2005107496A1 (en) * 2004-05-06 2005-11-17 Maruasaen Corporation Method of producing fresh mushroom extract, extract and extract-containing material
JP2006050934A (en) * 2004-08-11 2006-02-23 Fujimi Yohoen:Kk Method for producing Agaricus koji extract, Agaricus koji extract, and health food composition containing the same

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62294069A (en) * 1986-06-13 1987-12-21 Togo Kuroiwa Nutrition supplying solution containing high unit of l-ornithine
JP2001346538A (en) * 2000-04-06 2001-12-18 Maruasaen:Kk Method for producing cortinellus shiitake processed food
JP2002247966A (en) * 2000-12-22 2002-09-03 Yaegaki Hakko Giken Kk Health food and method for producing the same
JP2004256513A (en) * 2003-02-04 2004-09-16 Ezaki Glico Co Ltd Agent for increasing amount of muscle
JP2005097133A (en) * 2003-09-22 2005-04-14 Unitika Ltd IgA PRODUCTION PROMOTER DERIVED FROM SPARASSIS CRISPA
WO2005107496A1 (en) * 2004-05-06 2005-11-17 Maruasaen Corporation Method of producing fresh mushroom extract, extract and extract-containing material
JP2006050934A (en) * 2004-08-11 2006-02-23 Fujimi Yohoen:Kk Method for producing Agaricus koji extract, Agaricus koji extract, and health food composition containing the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104256267A (en) * 2014-07-17 2015-01-07 张久兵 Pleurotus nebrodensis nutritional wheat paste and preparation method thereof

Also Published As

Publication number Publication date
JP2007274904A (en) 2007-10-25

Similar Documents

Publication Publication Date Title
JP5467433B2 (en) Seaweed fermentation composition and method for producing the same
KR101323893B1 (en) Preparation method of beef extraction using fermentation by lactobacillus
JP2011512130A (en) Yeast extract containing inosinic acid disodium salt and guanylic acid disodium salt and method for preparing the same
JP2004215529A (en) Method for producing lactic acid bacterium fermentation food product, beverage product, and seasoned food product all having good flavor and high gaba content
JP2004345986A (en) Fermented material and method for producing the same
JP2008017703A (en) METHOD FOR PRODUCING FOOD COMPRISING gamma-AMINOBUTYRIC ACID AND ORNITHINE
JP4705874B2 (en) Method for producing amino acid-rich food material, particularly amino acid-rich food material containing abundant ornithine, food material produced by using these production methods, and foods to which these food materials are added
JP2012187068A (en) γ-AMINO BUTYRIC ACID-CONTAINING FOOD, AND METHOD FOR PRODUCING THE SAME
CN103461947A (en) Method for preparing nutritional flavoring agent by using cold-pressed soybean cakes
JP2008019170A (en) Food and drink having ameliorating and prophylactic action on gastrointestinal injury
CN101401659B (en) Ham soup-stock and preparing process thereof
CN102498935A (en) Method for preparing flammulina velutipes nutrient solution by utilizing remains of food processing
CN102578521A (en) Scallop skirt seafood sauce and preparation method thereof
KR20140072595A (en) A natural seasoning containing an extract of ramie leaves and the preparation method thereof
JP2003024015A (en) Food material highly containing gamma-aminobutyric acid from sesame as raw material and method for producing the same
KR100216338B1 (en) Clear Shrimp Sauce
CN108185109A (en) A kind of processing method of star eel enzymolysis protein concentrate
CN103907882B (en) A kind of production method of plum halogen straw mushroom flavouring
JP3564119B2 (en) Treated product with increased vitamin U content in plants
CN1788608A (en) Pleurotus ferulae nutritious flavoring and its production method
KR101146151B1 (en) Antihypertensive natural seasoning for Muchim containing soybean hydrolysate and preparation thereof
JP2002000213A (en) Method for enhancing gamma-aminobutyric acid content of cruciferous plant
JP3422972B2 (en) Method for increasing gamma-aminobutyric acid content in grasses
JP7477273B2 (en) Method for cultivating shiitake mushrooms using coffee grounds and method for increasing yields of functional ingredients
JP2007053924A (en) Food raw material, method for producing the same, and food comprising the food raw material

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20090324

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20100720

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20100817

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20101001

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20101116

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20110222

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20110314

R150 Certificate of patent or registration of utility model

Ref document number: 4705874

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

LAPS Cancellation because of no payment of annual fees