JPH0316110B2 - - Google Patents

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Publication number
JPH0316110B2
JPH0316110B2 JP30647387A JP30647387A JPH0316110B2 JP H0316110 B2 JPH0316110 B2 JP H0316110B2 JP 30647387 A JP30647387 A JP 30647387A JP 30647387 A JP30647387 A JP 30647387A JP H0316110 B2 JPH0316110 B2 JP H0316110B2
Authority
JP
Japan
Prior art keywords
matsutake
sake
mushrooms
water
extract
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP30647387A
Other languages
Japanese (ja)
Other versions
JPH01148178A (en
Inventor
Takaaki Takeuchi
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.)
Individual
Original Assignee
Individual
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Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to JP62306473A priority Critical patent/JPH01148178A/en
Publication of JPH01148178A publication Critical patent/JPH01148178A/en
Publication of JPH0316110B2 publication Critical patent/JPH0316110B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

産業上の利用分野 この発明は、清酒原酒を規格アルコール度数に
調整するために実施される割水工程において、特
に優雅な香気を有することで知られる松茸を、割
水用水中に浸漬して、当該松茸のエキス分を滲出
して得られた松茸エキス滲出液を、清酒原酒に添
加して規格のアルコール度数に調整することを特
徴とする、松茸酒(リキユール酒)の製造方法に
関する。 従来の技術 近年、微生物食品であるきのこ類の薬用効果の
研究が進むにつれて、上記きのこ類の一部種類は
ビタミンの強化、コレステロール低下作用及び、
抗腫瘍効果などの優れた薬効を有することが明ら
かにされ、これらの確認に基づき、上記きのこ類
を清酒中に浸漬させて、当該きのこ類のエキス分
を滲出させる、薬用酒としても意義深いきのこ酒
が種々製造されるようになつた。一方、きのこ類
を用いた酒類の製造方法は、既に幾つか提案が成
されており、例えば、特公昭59−13185号「きの
こ等を原料とする酒の製造法」、特開昭62−65677
号「きのこ類を原料とする酒の製造方法」及び、
特公昭57−5509号「酒精飲料の製造法」等であ
る。即ち、特公昭59−13185号においては、特に
乾燥きのこを用い、当該きのこ類の成分を抽出
し、これを原料として発酵させて酒類を製造する
ものであり、さらに特開昭62−65677号は、特公
昭59−13185号の幾つかの問題点を解決する目的
によつて成されたものであつて、乾燥きのこ類の
成分を抽出したものと、梅果実成分を抽出したも
のの混合液を原料に、発酵させて酒類を製造する
ものであつた。一方、特公昭57−5509号において
は、きのこ類の中で特に抗腫瘍効果があるとされ
るマンネンタケ属のきのこ種を用いるものであ
り、上記きのこを酒精、糖類、水よりなる液中に
浸漬して得たアルコール液、または、上記きのこ
を水で煎じ、煮出した浸出液を、梅酒原液に添
加、混合した酒精飲料の製造法であつた。以上、
これらの製造方法においては、明細書中にも一部
記載があるように、きのこ類のきのこ臭を排除し
て、当該きのこ類が含有するエキス分(特に薬効
成分)を、特定な液中に滲出したものを原料とし
て発酵させるか、別の酒類とブレンドすることに
要旨があるものである。また、これらの製造方法
においては、きのこ類の腐敗は問題となり難いも
のであつたが、上記の酒類において古来より広く
日本人に親しまれて来た清酒中に、きのこ類(例
えば、松茸)を浸漬させて、そのエキス分を滲出
させてきのこ酒とする場合には、しばしば瓶等容
器に封入後に常温で放置する間に、上記清酒中に
投入されたきのこが腐敗してしまうことが多々見
受けられるという問題点があつた。そこで、本発
明者は上記の問題点を解決したきのこ酒の製造方
法として、きのこ類においては、特に優雅な香気
を有することで知られる松茸を選択することによ
つて、既に特開昭63−214174号「松茸酒の製造方
法」及び、昭和62年11月4日付提出の「松茸酒の
製造方法」によつて、瓶等容器中の清酒に松茸を
浸漬、密封して、松茸のエキス分を滲出させるた
めに、長時間常温で放置する場合であつても、清
酒中の松茸が腐敗することのない、而も優雅な松
茸特有の香気を発する、松茸酒の製造方法を開示
している。即ち、特開昭63−214174号「松茸酒の
製造方法」においては、生の松茸に含まれている
殺菌等の活動を抑制するために、生の松茸を密封
し瞬時にマイナス10℃以下の低温状態で10日間以
上凍結殺菌するようにし、次に徐々に解凍して常
温に戻し、雑菌が混入しないように速やかに清酒
中に浸漬することによつて、上記の問題点を解決
したものであり、一方、昭和62年11月4日付提出
の「松茸酒の製造方法」によつては、容器中の原
料清酒に松茸を浸漬し、95℃で5分間以上加熱殺
菌することによつて、生の松茸に含まれている細
菌等を殺菌し、上記の問題点を解決すると共に、
簡易な装置によつて松茸エキス分の滲出率が高い
松茸酒の製造方法を提供するものであつた。 発明が解決しようとする問題点 上述のように、本発明者が既に開示した発明に
おいては、特定手段によつて生の松茸を殺菌処理
し、清酒中に当該松茸のエキス分を滲出させると
共に、松茸特有の優雅な香気をも移行させるもの
であるが、さらに本発明者は鋭意研究を重ね、新
規な方法による松茸酒の製造方法に到達したもの
である。 問題点を解決するための手段 そこで、本発明に係る松茸酒の製造方法は以下
の構成による。即ち、清酒原酒を規格のアルコー
ル度数に調整するために行なわれる割水工程にお
いて、特に優雅な香気を有することで知られる松
茸を殺菌処理した後に、割水用水中に浸漬して、
当該松茸のエキス分を滲出するか、直接松茸を割
水用水中に浸漬して、殺菌処理すると共に当該松
茸のエキス分を滲出して得られた松茸エキス滲出
液から、当該松茸を一端分離し、また当該松茸エ
キス滲出液を、単独又は割水用水と共に清酒原酒
に添加して、全体を規格のアルコール度数に調整
するようにし、上記分離した松茸を瓶等容器の瓶
口より挿入して(この際、上記松茸は組織構造が
変化して海綿状となつているため、カサと茎部分
が分離することなく、細い瓶口より挿入可能であ
り、その後は当初の形状に復元するものであ
る。)、さらに上記のように規格のアルコール度数
に調整さた松茸酒を、清酒製造上における通常の
殺菌法と同様に、60℃〜65℃の熱酒として加熱殺
菌して、次に上記瓶等容器にこれを注入し、その
後雑菌が混入しないように、王冠等により密封す
るようにして松茸酒(リキユール酒)を製造する
ものである。また、上記松茸の殺菌処理として
は、生の松茸を密封の上マイナス10℃以下の低温
状態で、10日間以上凍結殺菌することにより、上
記割水用水中での松茸の殺菌処理としては、生の
松茸を直接割水用水中に浸漬後95℃で5分間以上
加熱殺菌した後、15℃以下に急冷することによ
る。さらに、上述のように松茸エキス滲出後、松
茸エキス滲出液より分離された松茸は、上記のよ
うに予め松茸酒(熱酒)が注入される瓶等容器に
挿入されていることに限定されることなく、松茸
酒(熱酒)の注入後に挿入される場合でも、本発
明の要旨を変更するものではない。 作 用 上述のように、本発明に用いられる松茸は殺菌
処理が成されるものであつて、生の松茸にあつて
は、これに含有される細菌等が採取後も一定期間
比較的活発な活動を継続することから、清酒程度
のアルコール濃度による液中(アルコール濃度が
高い液ほど、細菌等の細胞分裂抑止力が大きい。)
であつては、上記細菌等の活動を完全に抑制する
ことができず、上記液中に浸漬されている松茸に
腐敗がもたらされる場合がある。そこで、当該松
茸を殺菌処理することが必要であるが、例えば、
加熱殺菌において、100℃以上の水蒸気中で殺菌
処理を施こす場合には、松茸のエキス分及び香気
分が相当に消失するという欠点があり、本発明が
目的とするような、優れた香気分を有した松茸酒
を製造するためには適当ではないものである。ま
た一方、凍結殺菌において、高い殺菌効果を得る
ためには、断続的な凍結融解を繰返す方法が最適
であることが、既に公知の技術ではあるが、この
際においても、融解状態で松茸中のエキス分の滲
出や香気分の消失が相当大であることが判明した
ため、本発明においては不適当であるとした。さ
らに、凍結殺菌において、凍結速度によつても被
凍結物の細胞中に含まれる水分の形態が異なるこ
とが明らかになつており、徐々に冷却した場合に
は、上記細胞内に水の結晶が析出されて、細胞構
造が破壊されるものであつて、これにより細菌等
の殺菌が成されるのに対して、急激に冷却する場
合には、細胞中の水分が水の結晶を析出せずに、
ガラス様の固体となるので、細胞構造の破壊が起
こらないとされ、従つて一般に殺菌効果が弱いと
されている。しかしながら、本発明による松茸の
凍結殺菌において知見したところによれば、松茸
酒の製造を工業的に成立させるために、大量の松
茸を冷凍保存する目的において用いられる機械装
置及び設備により、瞬時にマイナス10℃以下の条
件下に生の松茸を晒しても、上記松茸は一種の保
温的組織構造であるから、細胞中の水分は徐々に
冷却されるようになり、細胞内に水の結晶が析出
されて細胞構造が破壊されるので、殺菌効果が充
分得られることが明らかとなつた。以上のような
作用性並び得失を踏まえた上で、本発明における
松茸の殺菌処理においては、上述のように、生の
松茸を直接割水用水中に浸漬後95℃で5分間以上
加熱殺菌した後、15℃以下に急冷するか、生の松
茸を密封してマイナス10℃以下の低温状態で、10
日間以上凍結殺菌する方法が選択され、このよう
にして処理された松茸は、当該松茸のエキス分及
び香気成分を割水用水中に良好に滲出するもので
ある。 実施例 以下、実施例に基づき更に本発明を詳説するも
のとする。そこで、松茸酒の製造方法において、
下記の実験を実施した。 実施例 1 清酒原酒を清酒2級の規格アルコール度数に調
整するために、常法に従い割水を実施した。即
ち、清酒原酒(アルコール分20.4%)1367mlに対
し割水用水(日本酒度+0.1、PH6.48)433mlを添
加して、清酒2級(アルコール分15.5%)1800ml
を得た。また、上記清酒原酒並びに得られた清酒
2級の成分分析表を、それぞれ第1表及び第2表
に示した。尚、この際の成分分析法は国税庁所定
分析法によつた。
Industrial Application Field This invention involves soaking matsutake mushrooms, which are known to have a particularly elegant aroma, in water for splitting water in the water splitting process that is carried out to adjust sake to a standard alcohol content. This invention relates to a method for producing matsutake sake (liqueur sake) characterized by adding a matsutake extract exudate obtained by exuding the matsutake mushroom extract to unprocessed sake to adjust the alcohol content to a standard. BACKGROUND ART In recent years, as research into the medicinal effects of mushrooms, which are microbial foods, has progressed, some types of mushrooms have been found to have vitamin-enriching, cholesterol-lowering, and
It has been revealed that the mushrooms have excellent medicinal effects such as antitumor effects, and based on these confirmations, the above mushrooms are soaked in sake to exude the extract of the mushrooms, which is meaningful as a medicinal sake. Various types of alcoholic beverages began to be produced. On the other hand, several proposals have already been made regarding methods for producing alcoholic beverages using mushrooms, such as JP-B No. 59-13185 ``Method for producing alcoholic beverages using mushrooms, etc.'', JP-A No. 62-65677;
No. ``Method for producing alcoholic beverages using mushrooms'' and
Special Publication No. 57-5509 ``Method for producing alcoholic beverages'' etc. That is, in Japanese Patent Publication No. 59-13185, alcoholic beverages are produced by using dried mushrooms, extracting the components of the mushrooms, and fermenting them as raw materials, and Japanese Patent Publication No. 62-65677 , was created with the purpose of solving some of the problems of Special Publication No. 59-13185, and the raw material is a mixture of extracted ingredients of dried mushrooms and extracted plum fruit ingredients. First, alcoholic beverages were produced by fermentation. On the other hand, in Japanese Patent Publication No. 57-5509, mushrooms of the genus Stonecrop, which are said to have a particularly antitumor effect among mushrooms, are used, and the mushrooms are immersed in a liquid consisting of alcohol, sugar, and water. This was a method for producing an alcoholic beverage by adding and mixing the alcoholic liquid obtained by decocting the above-mentioned mushrooms with water, or the infusion liquid obtained by decocting and boiling the above-mentioned mushrooms into a stock solution of plum wine. that's all,
In these manufacturing methods, as described in part in the specifications, the mushroom odor of the mushrooms is eliminated and the extracts (especially medicinal ingredients) contained in the mushrooms are added to a specific liquid. The idea is to ferment the exuded material as a raw material or blend it with another alcoholic beverage. In addition, in these production methods, spoilage of mushrooms is unlikely to be a problem, but mushrooms (for example, matsutake mushrooms) are added to the above-mentioned sake, which has been widely enjoyed by Japanese people since ancient times. When mushroom sake is made by steeping the mushrooms to exude their extract, it is often seen that the mushrooms put into the sake spoil while being left at room temperature after being sealed in a container such as a bottle. There was a problem with being exposed. Therefore, the present inventor has developed a method for producing mushroom sake that solves the above-mentioned problems by selecting matsutake mushrooms, which are known to have a particularly elegant aroma among mushrooms. According to No. 214174 "Method for producing matsutake sake" and "Method for manufacturing matsutake sake" submitted on November 4, 1986, matsutake mushrooms are immersed in sake in a container such as a bottle, sealed, and the extract of matsutake mushrooms is extracted. Discloses a method for producing matsutake sake in which the matsutake mushrooms in the sake do not rot even when left at room temperature for a long period of time in order to exude the matsutake mushrooms, and still emit an elegant aroma unique to matsutake mushrooms. . In other words, in JP-A-63-214174 ``Method for producing matsutake sake'', raw matsutake mushrooms are sealed and instantly heated to temperatures below -10℃ in order to suppress the sterilization activities contained in raw matsutake mushrooms. The above problem was solved by freezing and sterilizing it at a low temperature for at least 10 days, then gradually thawing it back to room temperature, and immediately immersing it in sake to prevent contamination with bacteria. On the other hand, according to the "Method for producing matsutake sake" submitted on November 4, 1988, matsutake mushrooms are immersed in raw sake in a container and sterilized by heating at 95℃ for 5 minutes or more. In addition to sterilizing the bacteria contained in raw matsutake mushrooms and solving the above problems,
The object of the present invention was to provide a method for producing matsutake sake with a high leaching rate of matsutake extract using a simple device. Problems to be Solved by the Invention As mentioned above, in the invention already disclosed by the present inventor, raw matsutake mushrooms are sterilized by specific means, and the extract of the matsutake mushrooms is exuded into sake, Although the elegant aroma unique to matsutake mushrooms is also transferred, the present inventor has conducted extensive research and has arrived at a novel method for producing matsutake mushroom wine. Means for Solving the Problems Therefore, the method for producing matsutake sake according to the present invention has the following configuration. That is, in the water splitting process that is performed to adjust the alcohol content of sake to the standard, matsutake mushrooms, which are known to have a particularly elegant aroma, are sterilized and then soaked in water for water splitting.
Either the matsutake mushroom extract is leached out, or the matsutake mushrooms are directly immersed in water for sterilization, and the matsutake mushrooms are sterilized and the matsutake mushroom extract is exuded. In addition, the matsutake mushroom extract exudate is added to the sake base alone or together with water for dilution to adjust the alcohol content of the whole to the standard alcohol content, and the separated matsutake mushrooms are inserted into the mouth of a container such as a bottle ( At this time, the tissue structure of the matsutake mushroom has changed and it has become spongy, so it can be inserted through the narrow bottle mouth without the cap and stem separating, and it will then return to its original shape. ), the matsutake mushroom sake adjusted to the standard alcohol content as described above is heat sterilized as a hot sake at 60°C to 65°C in the same way as the normal sterilization method in sake production, and then heated in the above bottle. Matsutake sake (liqueur sake) is produced by pouring this into a similar container and then sealing it with a crown or the like to prevent contamination with bacteria. In addition, the above-mentioned sterilization treatment of matsutake mushrooms involves freezing and sterilization of raw matsutake mushrooms in a sealed container at a low temperature of -10℃ or less for 10 days or more. Matsutake mushrooms are directly immersed in diluted water, sterilized by heating at 95℃ for 5 minutes or more, and then rapidly cooled to below 15℃. Furthermore, as described above, the matsutake mushrooms separated from the matsutake extract exudate after matsutake extract exudation are limited to being inserted into a container such as a bottle into which matsutake sake (hot sake) is injected in advance as described above. Even if it is inserted after injecting matsutake sake (hot sake) without changing the gist of the present invention. Function As mentioned above, the matsutake mushrooms used in the present invention are sterilized, and in the case of raw matsutake mushrooms, the bacteria contained therein remain relatively active for a certain period of time after being collected. Because it continues its activity, it is placed in a liquid with an alcohol concentration similar to that of Japanese sake (the higher the alcohol concentration, the greater the ability to inhibit cell division of bacteria, etc.).
In this case, the activities of the bacteria, etc. cannot be completely suppressed, and the matsutake mushrooms immersed in the liquid may rot. Therefore, it is necessary to sterilize the matsutake mushrooms, for example,
In heat sterilization, when sterilization is performed in steam at a temperature of 100°C or higher, there is a drawback that the matsutake mushroom extract and aroma are considerably lost. It is not suitable for producing matsutake sake with On the other hand, in freeze sterilization, it is already known that in order to obtain a high sterilization effect, the best method is to repeat intermittent freezing and thawing. It was found that the exudation of the extract component and the loss of aroma were quite large, so it was judged to be unsuitable for the present invention. Furthermore, in freeze sterilization, it has become clear that the form of water contained in the cells of the frozen object differs depending on the freezing speed, and when cooling gradually, water crystals form within the cells. This precipitates and destroys the cell structure, which sterilizes bacteria, etc. However, when rapidly cooled, the water in the cells does not precipitate water crystals. To,
Since it becomes a glass-like solid, it is said that destruction of cell structure does not occur, and therefore, it is generally considered to have a weak bactericidal effect. However, according to what was discovered in the freezing and sterilization of matsutake mushrooms according to the present invention, in order to commercialize the production of matsutake sake, the machinery and equipment used to freeze and preserve large quantities of matsutake mushrooms instantly Even if raw matsutake mushrooms are exposed to temperatures below 10℃, the matsutake mushrooms have a kind of heat-retaining tissue structure, so the water in the cells will gradually cool down and water crystals will precipitate inside the cells. It has become clear that a sufficient bactericidal effect can be obtained because the cell structure is destroyed. Based on the above-mentioned effects and advantages and disadvantages, in the sterilization treatment of matsutake mushrooms in the present invention, as described above, raw matsutake mushrooms are directly immersed in water for splitting water and then heat sterilized at 95°C for 5 minutes or more. After that, either rapidly cool the mushrooms to below 15 degrees Celsius, or seal the raw matsutake mushrooms and store them at a low temperature of -10 degrees Celsius or below for 10 minutes.
A method of freezing and sterilizing the matsutake mushrooms for at least one day was selected, and the matsutake mushrooms treated in this manner are capable of exuding the extract and aroma components of the matsutake mushrooms well into the water for diluting water. EXAMPLES Hereinafter, the present invention will be further explained in detail based on examples. Therefore, in the manufacturing method of matsutake sake,
The following experiment was conducted. Example 1 In order to adjust the alcohol content of unprocessed sake to the standard alcohol content of grade 2 sake, water was added according to a conventional method. In other words, 1,367 ml of unprocessed sake (alcohol content: 20.4%) is added with 433 ml of water for splitting water (sake content +0.1, PH 6.48) to produce 1,800 ml of second grade sake (alcohol content: 15.5%).
I got it. In addition, the component analysis tables of the above-mentioned sake unprocessed sake and the obtained second grade sake are shown in Tables 1 and 2, respectively. The component analysis method used in this case was the one prescribed by the National Tax Agency.

【表】【table】

【表】 実施例 2 割水用水(日本酒度+1.0、PH6.48)433mlに生
の松茸20gを浸漬して、95℃で5分間加熱殺菌処
理した後、15℃以下に急冷して、松茸エキス滲出
液A433mlを得て、上記松茸エキス滲出液Aより
松茸を一端分離した。次に、清酒原酒(第1表の
成分分析の通り)1367mlに、松茸エキス滲出液
A433mlを全量添加して、清酒2級の規格アルコ
ール度数に割水した松茸酒A(アルコール分15.5
%)1800mlを得た。さらに、1.8詰瓶等容器に
前記松茸を細い瓶口よりカサと茎部分を分離する
ことなく挿入し、上記の松茸酒Aを62℃の熱酒に
して加熱殺菌の上、上記1.8詰瓶容器に注入し
直ちに雑菌が混入しないように王冠によつて密封
した。また、上記松茸エキス滲出液A並びに松茸
酒Aの成分分析表を、それぞれ第3表及び第4表
に示した。さらに、上記松茸酒Aを常温で20日間
放置したものを松茸酒Bとし、その成分分析表を
第5表に示した。
[Table] Example 2 20g of raw matsutake mushrooms were immersed in 433ml of water for splitting water (sake content +1.0, PH6.48), heat sterilized at 95°C for 5 minutes, and then rapidly cooled to below 15°C. 433 ml of matsutake extract exudate A was obtained, and the matsutake mushroom was partially separated from the matsutake extract exudate A. Next, add matsutake extract exudate to 1367 ml of refined sake (as per the ingredient analysis in Table 1).
Matsutake sake A (alcohol content: 15.5
%) 1800ml was obtained. Furthermore, insert the matsutake mushrooms into a container such as a 1.8-sized bottle through the narrow bottle opening without separating the cap and stem, heat the matsutake sake A to 62℃, heat sterilize it, and heat it to the above-mentioned 1.8-sized bottle. The tube was injected into the tube and immediately sealed with a crown to prevent contamination by bacteria. In addition, the component analysis tables of the matsutake extract exudate A and matsutake sake A are shown in Tables 3 and 4, respectively. Furthermore, Matsutake Sake B was obtained by leaving the Matsutake Sake A at room temperature for 20 days, and its component analysis table is shown in Table 5.

【表】【table】

【表】【table】

【表】【table】

【表】 実施例 3 割水用水(日本酒度+1.0、PH6.48)200mlに生
の松茸10gを浸漬して、95℃で5分間加熱殺菌処
理した後、15℃以下急冷して、松茸エキス滲出液
C200mlを得た。次に、清酒原酒(第1表の成分
分析の通り)1367mlに対し、上記松茸エキス滲出
液C200ml及び割水用水(日本酒度+1.0、PH6.48)
233mlを添加して、清酒2級の規格アルコール度
数に割水した松茸酒C(アルコール分15.5%)
1800mlを得た。また、上記松茸エキス滲出液C並
びに松茸酒Cの成分分析表を、それぞれ第6表及
び第7表に示した。尚、この際の成分分析法は国
税庁所定分析法によつた。
[Table] Example 3 10g of raw matsutake mushrooms were immersed in 200ml of water for dilution (sake content +1.0, PH6.48), heat sterilized at 95°C for 5 minutes, and then rapidly cooled to 15°C or below. extract exudate
Obtained 200ml of C. Next, for 1367 ml of unprocessed sake (according to the component analysis in Table 1), 200 ml of the above matsutake extract exudate C and water for dilution (sake level +1.0, PH6.48)
Matsutake Sake C (alcohol content: 15.5%) with 233ml added and diluted to the standard alcohol content of grade 2 sake
Obtained 1800ml. In addition, the component analysis tables of the matsutake extract exudate C and matsutake sake C are shown in Table 6 and Table 7, respectively. The component analysis method used in this case was the one prescribed by the National Tax Agency.

【表】【table】

【表】 実施例 4 生の松茸10gを密封してマイナス10℃で10日間
凍結して殺菌した後、徐々に常温(24℃)に戻
し、割水用水(日本酒度+1.0、PH6.48)200mlに
常温(24℃)で10日間浸漬して、松茸エキス滲出
液D200mlを得た。次に、清酒原酒(第一表の成
分分析の通り)1367mlに対し、上記松茸エキス滲
出液D200ml及び割水用水(日本酒度+1.0、PH
6.48)233mlを添加して、清酒2級の規格アルコ
ール度数に割水した松茸酒D(アルコール分15.5
%)1800mlを得た。また、上記松茸エキス滲出液
D並びに松茸酒Dの成分分析表を、それぞれ第8
表及び第9表に示した。尚、この際の成分分析法
は国税庁所定分析法によつた。
[Table] Example 4 10g of raw matsutake mushrooms were sealed and sterilized by freezing at -10℃ for 10 days, then gradually returned to room temperature (24℃), and water for dilution (sake level +1.0, PH6.48 ) for 10 days at room temperature (24°C) to obtain 200 ml of Matsutake mushroom extract exudate D. Next, for 1367 ml of sake unblended sake (as per the component analysis in Table 1), add 200 ml of the above matsutake extract exudate D and diluted water (sake level + 1.0, PH
6.48) Matsutake Sake D (alcohol content: 15.5
%) 1800ml was obtained. In addition, the component analysis tables of the above matsutake extract exudate D and matsutake mushroom sake D are shown in Table 8.
It is shown in Table and Table 9. The component analysis method used in this case was the one prescribed by the National Tax Agency.

【表】【table】

【表】 以上、実施例2〜4によつて得られた松茸酒A
〜Dを試飲したところ、いずれも優雅な松茸の香
気を有する松茸酒であることを確認したが、香気
の強さで比較すれば、凍結処理によつた松茸酒D
が最も強く、また、松茸酒Aのように更に松茸酒
中に松茸を浸漬したものは、放置されている間に
アミノ酸量がやや増加する傾向であるが、最大値
1.0ml未満であるため極めてすつきりした口当た
りの松茸酒が得られた。 発明の効果 本発明は上記の通りであり、本発明に係る松茸
はその殺菌処理の際に組織構造が変化して、海綿
状となるので、松茸エキスの滲出液より取り出し
て、1.8詰瓶等の細い瓶口からでもカサと茎部
分を分離せずに挿入可能であり、本物の松茸入り
松茸酒として商品価値が高いという効果がある。
また、本発明によるように割水用水中に松茸を浸
漬して、松茸エキス滲出液を大量に作つておくよ
うにすれば、その都度清酒原酒に添加することに
よつて、容易に優れた松茸酒を製造できるという
効果もある。一方、清酒中に松茸を浸漬した上
で、加熱殺菌処理することは危険性が高く、且
つ、清酒中のアルコール分または香気分の蒸発や
清酒中の糖分のカラメル化等が問題となるが、本
発明においては加熱殺菌処理の場合であつても、
割水用水中であるので、極めて安全であると共
に、容易に加熱殺菌処理を施すことができるとい
う効果もある。
[Table] Matsutake mushroom sake A obtained in Examples 2 to 4
When I tasted ~D, I found that they were all matsutake sake with an elegant matsutake aroma, but when compared in terms of aroma strength, I found that matsutake sake D, which had undergone freezing treatment,
is the strongest, and when matsutake mushrooms are further soaked in matsutake sake, such as matsutake sake A, the amount of amino acids tends to increase slightly while left standing, but the maximum value
Since the amount was less than 1.0 ml, matsutake sake with an extremely smooth taste was obtained. Effects of the Invention The present invention is as described above, and the tissue structure of the matsutake mushroom according to the present invention changes during sterilization treatment and becomes spongy. It can be inserted through the narrow bottle mouth without separating the cap and stem, and has the effect of having high commercial value as a matsutake sake containing real matsutake mushrooms.
In addition, if a large amount of matsutake mushroom extract exudate is prepared by soaking matsutake mushrooms in dipping water as in the present invention, it is possible to easily produce superior matsutake mushroom extract by adding it to the sake base each time. It also has the effect of being able to produce alcohol. On the other hand, immersing matsutake mushrooms in sake and then heat sterilizing them is highly dangerous, and there are problems such as evaporation of the alcohol or aroma content in the sake and caramelization of the sugar in the sake. In the present invention, even in the case of heat sterilization treatment,
Since it is water for dilution, it is extremely safe and has the advantage that it can be easily heat sterilized.

Claims (1)

【特許請求の範囲】 1 清酒原酒を規格のアルコール度数に調整する
ために行なう割水工程において、生の松茸を割水
用水中に浸潰後、95℃で5分間以上加熱殺菌し、
次に15℃以下に急冷することによつて殺菌処理す
ると共に、当該松茸のエキス分を滲出して得た松
茸エキス滲出液を、単独又は割水用水と共に、清
酒原酒に添加して規格アルコール度数に調整する
ことを特徴とする、松茸酒の製造方法。 2 清酒原酒を規格のアルコール度数に調整する
ために行なう割水工程において、生の松茸を密封
して、マイナス10℃以下の低温状態で、10日間以
上凍結殺菌処理した後に、割水用水に浸潰して当
該松茸のエキス分を滲出して得た松茸エキス滲出
液を、単独又は割水用水と共に、清酒原酒に添加
して規格アルコール度数に調整することを特徴と
する、松茸酒の製造方法。 3 松茸エキスの滲出後、松茸エキス滲出液中よ
り松茸を分離して、規格のアルコール度数に調整
された松茸酒と共に、瓶等容器に密封されること
を特徴とする、特許請求の範囲第1項又は第2項
記載の松茸酒の製造方法。
[Scope of Claims] 1. In the water splitting process performed to adjust the alcohol content of unprocessed sake to the standard alcohol content, raw matsutake mushrooms are soaked in water for water splitting and then heat sterilized at 95°C for 5 minutes or more,
Next, it is sterilized by rapid cooling to 15℃ or less, and the matsutake extract exudate obtained by exuding the matsutake extract is added to the original sake, either alone or with water for dilution, to achieve the standard alcohol content. A method for producing matsutake mushroom wine, which is characterized by adjusting the following: 2 In the water splitting process that is performed to adjust the alcohol content of sake to the standard, raw matsutake mushrooms are sealed and freeze-sterilized for at least 10 days at a low temperature of -10°C or less, and then soaked in water for water splitting. A method for producing matsutake sake, which comprises adding a matsutake extract exudate obtained by exuding the extract of the matsutake mushroom by crushing the matsutake mushroom, alone or together with water for dilution, to a standard alcoholic content. 3. Claim 1, characterized in that after exudation of matsutake extract, matsutake mushrooms are separated from the matsutake extract exudate and sealed in a container such as a bottle together with matsutake sake adjusted to a standard alcohol content. 2. The method for producing matsutake mushroom wine according to item 2 or item 2.
JP62306473A 1987-12-03 1987-12-03 Preparation of 'matsutake' liquor Granted JPH01148178A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62306473A JPH01148178A (en) 1987-12-03 1987-12-03 Preparation of 'matsutake' liquor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62306473A JPH01148178A (en) 1987-12-03 1987-12-03 Preparation of 'matsutake' liquor

Publications (2)

Publication Number Publication Date
JPH01148178A JPH01148178A (en) 1989-06-09
JPH0316110B2 true JPH0316110B2 (en) 1991-03-04

Family

ID=17957436

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62306473A Granted JPH01148178A (en) 1987-12-03 1987-12-03 Preparation of 'matsutake' liquor

Country Status (1)

Country Link
JP (1) JPH01148178A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20020064597A (en) * 2001-02-02 2002-08-09 손동화 Novel compounded and extracted liquor using Tricholoma matsutake mycellium and process for preparation thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS575509A (en) * 1980-06-13 1982-01-12 Fuji Heavy Ind Ltd Chain lubrication device of internal combustion engine
JPS61185178A (en) * 1985-02-13 1986-08-18 Sadao Nakayama Production of modified refined sake

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS575509A (en) * 1980-06-13 1982-01-12 Fuji Heavy Ind Ltd Chain lubrication device of internal combustion engine
JPS61185178A (en) * 1985-02-13 1986-08-18 Sadao Nakayama Production of modified refined sake

Also Published As

Publication number Publication date
JPH01148178A (en) 1989-06-09

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