JPS6094076A - Fermented drink and its preparation - Google Patents

Fermented drink and its preparation

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Publication number
JPS6094076A
JPS6094076A JP58201574A JP20157483A JPS6094076A JP S6094076 A JPS6094076 A JP S6094076A JP 58201574 A JP58201574 A JP 58201574A JP 20157483 A JP20157483 A JP 20157483A JP S6094076 A JPS6094076 A JP S6094076A
Authority
JP
Japan
Prior art keywords
wort
fermentation
fermented
germinated
fermented beverage
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP58201574A
Other languages
Japanese (ja)
Other versions
JPH0357742B2 (en
Inventor
Tetsuya Yokota
徹也 横田
Hideki Sakamoto
秀樹 坂本
Toshibumi Arimura
有村 俊文
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.)
Kagome Co Ltd
Original Assignee
Kagome Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kagome Co Ltd filed Critical Kagome Co Ltd
Priority to JP58201574A priority Critical patent/JPS6094076A/en
Publication of JPS6094076A publication Critical patent/JPS6094076A/en
Publication of JPH0357742B2 publication Critical patent/JPH0357742B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:To obtain a fermented drink having excellent taste and flavor and low alcohol content, by adjusting the pH of wort, sterilizing the wort, and carrying out the alcoholic fermentation and lactic fermentation simultaneously by the addition of a specific yeast and normal lactobacillus for food. CONSTITUTION:Wort or a mixture of wort and treated vegetables and fruits, is adjusted to about 6.3pH, sterilized with heat, and cooled. The liquid is inoculated with preliminarily cultured yeasts such as Kluyveromyces lactis and/or Kluyveromyces fragilis in combination with separately precultured normal lactobacillus for food (e.g. Lactobacillus vulgaris) to effect the simultaneous alcoholic fermentation and lactic fermentation. The fermentation is terminated when the ethyl alcohol-content is <1% (W/V). The microbial cells are separated, and the fermented liquid is optionally concentrated, dried, or mixed with other components to obtain the objective fermented drink.

Description

【発明の詳細な説明】 本発明は発酵飲料及びその製造方法、更に詳しくは発芽
麦汁を主原料とし、これに含まれる各種の蛋白質、ミネ
ラル、ビタミン等を活用しつつ、その特定酵母を用いた
アルコール発酵及び食品用の一般乳酸菌を用いた乳酸発
酵の同時発酵による二次的香味を複合化して飲用に優れ
た香味を有する、低アルコール含量の発酵飲料及びその
製造方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a fermented beverage and a method for producing the same, and more specifically, to a fermented beverage that uses germinated wort as the main raw material, utilizes various proteins, minerals, vitamins, etc. contained therein, and uses its specific yeast. The present invention relates to a fermented beverage with a low alcohol content, which has an excellent flavor for drinking by combining secondary flavors resulting from simultaneous fermentation of alcoholic fermentation and lactic acid fermentation using common food-grade lactic acid bacteria, and a method for producing the same.

麦類の発芽物を主原料とし、これをアルコール発酵させ
た飲料、例えばビールが多量に飲用されている。しかし
、この種のアルコール飲料は通常、食品用に汎用されて
いるサツカロマイセス属の酵母を使用してアルコール発
酵させたもので、数−以上のアルコールを含有し、独特
の香味を有する0したがってこれらは、児童を含めて一
般的に、ある種の健康飲料として、手軽に飲用するには
誠に不向である。
BACKGROUND ART Beverages made from germinated barley as a main ingredient and alcoholic fermented from it, such as beer, are consumed in large quantities. However, this type of alcoholic beverage is usually alcohol-fermented using yeast of the genus Satucharomyces, which is commonly used for food, and contains several or more alcohols and has a unique flavor. It is really unsuitable for easy consumption by the general public, including children, as a kind of health drink.

一方、豆乳や蒸煮米処理物に酵母及び乳酸菌を共生させ
た発酵飲料が提案されている(特公昭51−36340
号、特公昭54−32078号)。
On the other hand, a fermented beverage in which yeast and lactic acid bacteria coexist in soybean milk or steamed rice has been proposed (Special Publication No. 51-36340).
No., Special Publication No. 54-32078).

これらは、アルコール発酵と乳酸発酵とを同時に行なう
ため、発酵が一工程で済み、得られる発酵液の香味も相
応に深さやこくがある。ところが、この種の共生による
従来手段は、発酵対象原料も大きな問題であるが、前記
の場合と同様、サツカロマイセス属の如き食品用に汎用
されている一般酵母を用い、これに食品用の一般乳酸菌
を共生させて、アルコール発酵と乳酸発酵とを同時に行
なうため、飲用に優れた香味を有する発酵飲料を得るに
対してのアルコール発酵と乳酸発酵との相互調整が困難
であり、得られる発酵液もこれを直接乃至その!.ま希
釈して飲用するには香味それ自体及び特にそのバランス
が欠ける。
These fermenters perform alcoholic fermentation and lactic acid fermentation at the same time, so the fermentation only takes place in one step, and the resulting fermented liquid has a correspondingly deep and rich flavor. However, with conventional means based on this kind of symbiosis, the raw material to be fermented is also a big problem, but as in the case above, common yeast commonly used for food such as Satucharomyces is used, and common food-grade lactic acid bacteria are used. Because alcoholic fermentation and lactic acid fermentation are carried out simultaneously, it is difficult to mutually adjust alcoholic fermentation and lactic acid fermentation to obtain a fermented beverage with an excellent flavor for drinking, and the resulting fermented liquid is also difficult to achieve. This directly or that! .. However, if it is diluted and drunk, the flavor itself and especially its balance are lacking.

本発明者らは、斜上の実情に鑑み、原料特性を活用した
低アルコール含量の新規発酵飲料を得るべく鋭意研究し
た結果、発芽麦汁を主原料とし、これに特定酵母と食品
用の一般乳酸菌とを共生させ、所定条件下にアルコール
発酵と乳酸発酵とを同時に行なうと、飲用に優れた複合
的香味を有する発酵飲料の得られることを見出し、本発
明を完成した。
In view of the current situation, the inventors of the present invention conducted intensive research to obtain a new fermented beverage with low alcohol content that takes advantage of the characteristics of raw materials. The present invention has been completed based on the discovery that a fermented beverage with a complex flavor that is excellent for drinking can be obtained by coexisting with lactic acid bacteria and performing alcoholic fermentation and lactic acid fermentation simultaneously under specified conditions.

すなわち本発明は、発芽麦汁又は、発芽麦汁と野菜及び
/又は果実処理物との混合系に、フレベロマイセス・ラ
クチス( Kluyveromyces lactis)及ヒ/又
ハクレベロマイセス・フラギリス(Kluyverom
yces fragilis)と、食品用の一般乳酸菌
とを共生させて、エチルアルコール含量1%(W/■)
未満にアルコール発酵と乳酸発酵とを同時に行なうこと
を骨子とする発酵飲料及びその製造方法に係る0本発明
において、発芽麦汁は、大、麦、小麦、ひえ麦、ライ麦
、エン麦等の麦類の単品又は混合品に適当な水分と温度
を与え、これらの胚乳中に含まれる栄養成分を利用して
発芽させたものから得られる汁質である。かかる発芽麦
汁として、既に市販されているような麦芽エキスを用い
ると、量産加工現場における入手や保管等の取扱い容易
性に加え、本発明の目的がより良く達成される。通常、
ビールの製造に用いられる麦芽は、幼芽が粒の2/3〜
3/4程度発芽した短麦芽といわれるものであるが、本
発明において好適例である麦芽エキスの原料は、幼芽が
粒の1.5〜2.0倍程度発芽した、酵素力が最も強く
なっている状態の長麦芽といわれるもので、これを乾燥
して苦味のある根部を除去し、更に荒砕きしたものを温
水でゆつくシ抽出し、得られる抽出液を例えばフィルタ
ー濃縮のような有効成分の分解のない濃縮法で濃縮した
ものが麦芽エキスである。この麦芽エキスは、ミネラル
やビタミン等に富む。
That is, the present invention provides a method for adding Kluyveromyces lactis and/or Kluyveromyces lactis to germinated wort or a mixed system of germinated wort and processed vegetables and/or fruits.
yces fragilis) and general food-grade lactic acid bacteria, the ethyl alcohol content is 1% (W/■).
In the present invention, the germinated wort is made from barley, barley, wheat, barley, rye, oats, etc. It is a juice obtained by giving appropriate moisture and temperature to single or mixed products of the same species and germinating them using the nutritional components contained in the endosperm. If a malt extract that is already commercially available is used as such germinated wort, the objects of the present invention can be better achieved in addition to ease of handling such as acquisition and storage in mass production processing sites. usually,
The malt used for beer production consists of 2/3 to 2/3 grains of young germs.
It is called short malt that has germinated to about 3/4, but the raw material for malt extract, which is a preferred example in the present invention, is short malt that has germinated young germs that are about 1.5 to 2.0 times the size of grains and has the strongest enzymatic power. This is called long malt, which is dried and the bitter roots are removed, and the coarsely ground malt is extracted with warm water and the resulting extract is filtered and concentrated. Malt extract is concentrated using a concentration method that does not degrade the active ingredients. This malt extract is rich in minerals and vitamins.

発酵対象として、発芽麦汁単独系でも、得られる発酵液
は飲用に優れた複合的香味を有するが、発芽麦汁に野菜
及び/又は果実処理物を加えた混合系の場合、得られる
発酵液は更に一層良好となる。野菜はトマト、ニンジン
等、また果実はリンゴ、ブドウ等、ともに所望する全て
のものが対象となり、これらは、洗浄・選別した後、必
要に応じて適宜剥皮・除芯し、例えばパルパーやフィニ
ッシャ−等で網濾過した搾汁液を使用すればよく、網沖
過の前後に加熱処理をしてもよい。
Even if the fermentation target is the germinated wort alone, the resulting fermented liquid will have a complex flavor that is excellent for drinking. However, if the fermented wort is mixed with vegetable and/or fruit processed materials, the resulting fermented liquid will have a complex flavor that is excellent for drinking. becomes even better. Vegetables include tomatoes, carrots, etc., and fruits include apples, grapes, and any other desired items. After cleaning and sorting, the fruits are peeled and cored as necessary, and processed through a pulper or finisher, for example. It is sufficient to use the squeezed liquid filtered through a net, and heat treatment may be performed before and after filtering through a net.

本発明では、以上説明したような発芽麦汁の単独系又は
、発芽麦汁と野菜及び/又は果実処理物との混合系を所
謂共生発酵する。該共生発酵において、アルコール発酵
に使用する酵母は、フレベロマイセス・ラクチス及び/
又はフレベロマイセス・フラギリスである。これらの酵
母は単品で使用してもよいし、併用してもよい。従来の
ように、サツカロマイセス・カールスベルゲンシス(S
accharomyces car 1 sbergens i s )やサツカロ
マイセス0セレビシエ(Saccharomycesc
erevi 5eae )等の食品用に汎用されている
一般酵母を使用すると、本発明の目的とする発酵液を得
るに、同時に進行する乳酸発酵との発酵調整が困難で、
得られる発酵液の香味が劣る〇一方、本発明の共生発酵
において、乳酸発酵に使用する乳酸菌は、ラフトノ(シ
ルレス・ブルガリカス(Lactobacillus bulugaricus)、ストレプトコッカス・サー
モフィラス(Streptococcusthermo
phi lus )、ビフィドバクテリウム・ロングム
( Bifidobacterium longum)等の
食品用の一般乳酸菌である。これらは2種以上を併用す
ることによって一層好ましい共生発酵をすることもでき
る。
In the present invention, a so-called symbiotic fermentation is performed on a single system of germinated wort or a mixed system of germinated wort and a processed vegetable and/or fruit as described above. In the symbiotic fermentation, the yeast used for alcoholic fermentation is Phlebellomyces lactis and/or
or Phlebelomyces fragilis. These yeasts may be used alone or in combination. As before, Satucharomyces Carlsbergensis (S
accharomyces car 1 sbergens is) and Saccharomyces 0 cerevisiae (Saccharomyces car 1 sbergens is)
When using general yeast commonly used for food such as E. erevi 5eae), it is difficult to adjust the fermentation with the lactic acid fermentation that is proceeding at the same time in order to obtain the fermented liquid that is the objective of the present invention.
The flavor of the resulting fermented liquid is inferior. On the other hand, in the symbiotic fermentation of the present invention, the lactic acid bacteria used for lactic acid fermentation are Lactobacillus bulgaricus, Streptococcus thermophilus
philus) and Bifidobacterium longum (Bifidobacterium longum). More preferable symbiotic fermentation can be achieved by using two or more of these in combination.

前述した単独系又は混合系に、フレベロマイセス・ラク
チス及び/又はフレペロマイセス・フラギリスを使用し
たアルコール発酵と、食品用の一般乳酸菌を使用した乳
酸発酵とを同時に進行させると、エチルアルコールの生
成が比較的緩慢で、香味との関連においてアルコール発
酵と乳酸発酵との調整がなされ、特にエチルアルコール
含量1−未満の共生発酵段階においてはそのまま飲用に
供し得る極めて優れた複合的香味の発酵飲料が得られる
のである。そしてこの際、いずれの系においても、発芽
麦汁として麦芽エキスを使用するのが好適であり、発酵
対象の各系中において、麦芽エキスの濃度を5〜50%
(W/V )にすると便利である。麦芽エキスを高濃度
で発酵させても、共生発酵に悪影響はなく、シかも得ら
れる発酵液もそれだけ高濃度になるため、発酵液の保存
等取扱い、他製品への展開利用が容易になる0具体的に
共生発酵は、前述した発芽麦汁等の発酵対象を、例えば
重炭酸カルシウムの如きアルカリ剤でp)I6.3程度
に調整し、95℃達温程度に加熱殺菌した後、冷却した
ものに、予備培養した前記の酵母及び別に予備培養した
食品用の一般乳酸菌を加えて行なう。酵母及び乳酸菌の
添加量は、それぞれの性質、活性度、所望する発酵液の
品質等にもよるが、大略、基質1 ml当りI X 1
05〜5X10’cellsとする0発酵中は外部から
の雑菌汚染を厳重防止し、発酵温度は20〜45℃の範
囲でよいが、25〜40℃に維持するのが好ましい。発
酵温度が低すぎると、共生発酵に長時間を要し、逆に発
酵温度が高すぎると、得られる発酵液の香味が悪い。所
定の系に、前述の如く酵母及び乳酸菌を加え、25〜4
0℃の温度で20〜35時間共生発酵させ、pH4,0
〜5.0、エチ/l/7/I/:I−ル0.5〜< 1
.0 % (W/V )、乳酸100〜500ツ%(W
/V 、滴定酸度を乳酸換算したもの、以下図面の場合
も含めて同じ)とした発酵液が最良である。
When alcohol fermentation using Fleperomyces lactis and/or Fleperomyces fragilis and lactic acid fermentation using general food-grade lactic acid bacteria proceed simultaneously in the above-mentioned single system or mixed system, the production of ethyl alcohol is relatively slow. Therefore, alcoholic fermentation and lactic acid fermentation are adjusted in relation to flavor, and especially in the symbiotic fermentation stage where the ethyl alcohol content is less than 1 -, a fermented beverage with an extremely excellent complex flavor that can be consumed as is is obtained. . At this time, it is preferable to use malt extract as the germination wort in any system, and the concentration of malt extract in each system to be fermented is 5 to 50%.
(W/V) is convenient. Even if malt extract is fermented at a high concentration, there is no negative effect on the symbiotic fermentation, and the fermented liquid obtained will be of a higher concentration, making it easier to store and handle the fermented liquid, and to use it in other products. Specifically, in symbiotic fermentation, the fermentation target such as the above-mentioned germinated wort is adjusted to a p)I of about 6.3 with an alkaline agent such as calcium bicarbonate, heat sterilized to a temperature of about 95 ° C, and then cooled. The above-mentioned pre-cultured yeast and separately pre-cultured general lactic acid bacteria for food are added to the mixture. The amount of yeast and lactic acid bacteria to be added depends on their properties, activity, desired quality of fermentation liquid, etc., but is approximately I x 1 per ml of substrate.
During fermentation with 0.05 to 5.times.10' cells, bacterial contamination from the outside is strictly prevented, and the fermentation temperature may be in the range of 20 to 45°C, but preferably maintained at 25 to 40°C. If the fermentation temperature is too low, the symbiotic fermentation will take a long time, and if the fermentation temperature is too high, the flavor of the resulting fermented liquid will be poor. Yeast and lactic acid bacteria were added to the predetermined system as described above, and 25 to 4
Symbiotic fermentation for 20-35 hours at a temperature of 0℃, pH 4.0
~5.0, Eth/l/7/I/:I-le 0.5~<1
.. 0% (W/V), lactic acid 100-500% (W
/V, titratable acidity converted into lactic acid (the same applies hereafter, including in the drawings) is best.

第1図は麦芽エキス(三共フーズ社製、三共モルトB2
、以下実施例も含めて、麦芽エキスは同じものを使用)
の15%(W/v、以下実施例も含めてチはいずれもW
/V表示)水溶液を、重炭酸カルシウムでpH7,3に
調整し、これを95℃達温で加熱殺菌して30℃に冷却
した後、各別に予備培養したフレベロマイセス・ラクチ
ス及びフレペロマイセス・フラギリスをそれぞれ同じ菌
数となるように加え、更に各別に予備培養したストレフ
トコツカス争す−モンィラス及びラクトバシルス・ブル
ガリカスを加えて、30℃で静置発酵したときの、共生
発酵状況を例示するグラフである。
Figure 1 shows malt extract (Sankyo Foods Co., Ltd., Sankyo Malt B2).
, the same malt extract is used in the following examples as well)
15% (W/v, below, including the examples, all values are W)
/V display) The aqueous solution was adjusted to pH 7.3 with calcium bicarbonate, heated to sterilize it at 95°C, cooled to 30°C, and then precultured Fleveromyces lactis and Fleperomyces fragilis, respectively. This is a graph illustrating the symbiotic fermentation situation when Streftococcus monillus and Lactobacillus bulgaricus, which were pre-cultured separately, were added to the same number of bacteria and fermented statically at 30°C. be.

また第2図は、麦芽エキスを18%及びニンジン処理物
(洗浄・選別したニンジンの2Mφ孔径濾過金網を装着
したパルパーによる搾汁液)を10チ含有する混合水溶
液を、重炭酸ナトリウムでpH7,0に調整し、以下第
1図の場合と同様に静置発酵したときの、共生発酵状況
を例示するグラフである〔各図中、曲線11.12−乳
酸(q%)、曲線21.22=エチルアルコール(%、
液体クロマトグラフィーで分析、以下同じ)、曲線31
.32=pH1曲線41.42=酵母生菌数(logN
/1ml、以下生菌数は同I、)、+tHI51.52
=ストレグトコッ力ス−サーモフィラス生菌数、曲線6
1.62=ラクトバシルス・ブルガリカス生菌数、横軸
は発酵時間(時)〕。
In addition, Figure 2 shows that a mixed aqueous solution containing 18% malt extract and 10 g of processed carrots (juice extracted from washed and sorted carrots using a pulper equipped with a 2Mφ pore size filtration wire mesh) was prepared with sodium bicarbonate to pH 7.0. This is a graph illustrating the symbiotic fermentation situation when static fermentation is carried out in the same manner as in the case of FIG. Ethyl alcohol(%,
Analyzed by liquid chromatography, the same applies hereafter), curve 31
.. 32=pH1 curve 41.42=Yeast viable count (logN
/1ml, hereinafter the number of viable bacteria is the same as I), +tHI51.52
= Streptococcus - thermophilus viable count, curve 6
1.62 = Lactobacillus bulgaricus viable count, horizontal axis is fermentation time (hours)].

第1図と第2図で例示するように、エチルアルコールの
生成は比較的緩慢であり、香味関連において、エチルア
ルコール1チ未満の段階でアルコール発酵と乳酸発酵と
の発酵バランスが程よく調整されていて、各図面の範囲
内では発酵時間が25〜30(時)の段階で飲用に好適
の発酵液が得られている。
As illustrated in Figures 1 and 2, the production of ethyl alcohol is relatively slow, and in terms of flavor, the fermentation balance between alcoholic fermentation and lactic acid fermentation is well adjusted at the stage of less than 1 gram of ethyl alcohol. Therefore, within the range of each drawing, a fermented liquid suitable for drinking was obtained at a fermentation time of 25 to 30 hours.

かくして得られる発酵液は、ここに含まれる菌体それ自
身も有用であるため、菌体を含有したままで、又は菌体
を濾過や遠心分離で除去した後に、そのまま製品(例え
ばチルド製品、又は殺菌後に通常の瓶や缶詰製品)化す
ることもでき、更に必要に応じて、該発酵液を濃縮、乾
燥及び/又は調整して製品化する。濃縮は例えば逆浸透
圧法や真空法で、また乾燥は例えば噴霧乾燥法や凍結乾
燥法等でよい。これらの製品化最終段階において、糖類
や香料等を加えることもできる。勿論、発芽麦汁を高濃
度で発酵した場合、発酵液を濃縮や乾燥した場合等には
、製品化の際に又は飲用の際に適宜希釈する。また、発
酵液をそのまま飲用し得る濃度溶液で製品化する場合に
は、カーボネーションすると、されやかな発酵飲料が得
られる。この場合のカーボネーションは、製品中の炭酸
ガスボリー−ムが2.0〜2.5程度となるようにする
のがよい。
The fermentation liquid obtained in this way is useful because the bacteria contained therein are themselves useful, so it can be used as a product (for example, a chilled product, or After sterilization, the fermented liquid can be made into ordinary bottled or canned products, and if necessary, the fermented liquid can be concentrated, dried and/or adjusted to be made into a product. Concentration may be carried out by, for example, reverse osmosis or vacuum, and drying may be carried out by, for example, spray drying or freeze drying. Sugars, fragrances, etc. can also be added at the final stage of commercialization. Of course, when the germinated wort is fermented at a high concentration, or when the fermented liquid is concentrated or dried, it is diluted as appropriate when producing a product or drinking it. In addition, when the fermented liquid is to be manufactured into a concentrated solution that can be drunk as it is, a refreshing fermented beverage can be obtained by carbonation. In this case, carbonation is preferably carried out so that the carbon dioxide volume in the product is about 2.0 to 2.5.

各製品はいずれも、原料である発芽麦汁や野菜及び/又
は果実処理物中に含まれる、各種の蛋白質、ミネラル、
ビタミン等が活用されており、飲用に優れた複合的香味
を有する。実際、これらの製品と、他の諸条件を同一に
しつつ単に酵母としてサツカロマイセス属を用いたこと
だけが異なる発酵飲料とを官能評価しても(発芽麦汁を
使用しない場合のように、原料内容が欠ける又は異なる
場合も同様であるが)、1チの危険率で、本発明に係る
発酵飲料について好結果が有意検定されるのである(検
査員20名×3回繰り返し×2点又は3点嗜好順位法)
Each product contains various proteins, minerals,
It contains vitamins, etc., and has a complex flavor that is excellent for drinking. In fact, even if we sensory-evaluate these products and fermented beverages that have the same other conditions but differ only in the use of Satucharomyces as the yeast (such as in the case of not using germinated wort), (The same applies to cases where the values are missing or different), a positive result for the fermented beverage according to the present invention is significantly tested at a risk rate of 1 (20 inspectors x 3 repetitions x 2 or 3 points). preference ranking method)
.

・実施例1 麦芽エキスの40%水溶液を重炭酸カルシウムでpH6
,8に調整し、これを95℃達温で加熱殺菌して35℃
に冷却した後、予備培養したフレベロマイセス・ラクチ
スを基質1 tttl当り5X106cells、及び
別に予備培養したストレプトコッカス拳サーモフィラス
とラクトバシルレス・フ゛ルガリカスを各々基質1屑l
当り2X10’cellsとなるように加え、外部から
の菌的汚染を厳重防止しつつ、30℃で28時間静置発
酵した。得られた発酵液のエチルアルコール1.0%弱
、乳酸(換算量) 440q%、pH8,9であった。
・Example 1 A 40% aqueous solution of malt extract was adjusted to pH 6 with calcium bicarbonate.
, 8, heat sterilize it until it reaches 95℃, and heat it to 35℃.
After cooling to 100 ml, pre-cultured Phlebellomyces lactis was added to 5 x 106 cells per tttl of substrate, and separately pre-cultured Streptococcus thermophilus and Lactobacillus fergaricus were added to 1 piece of substrate each.
The cells were added at 2×10' cells per cell, and fermented for 28 hours at 30° C. while strictly preventing bacterial contamination from the outside. The resulting fermentation liquid contained slightly less than 1.0% ethyl alcohol, 440q% lactic acid (converted amount), and had a pH of 8.9.

この発酵液を遠心分離して発酵母液を得た。This fermentation liquid was centrifuged to obtain a fermentation mother liquor.

そして、発酵母液を3倍水希釈し、希釈液99l十砂糖
200g+香料(レモン系)0.5gの割合で調整した
後、95℃達温で加熱殺菌して10℃に冷却し、発酵飲
料(実施例)を製造した。
Then, the fermentation mother liquor was diluted 3 times with water and adjusted to a ratio of 99 liters of diluted liquid, 200 g of ten sugar + 0.5 g of fragrance (lemon type), heated to 95°C, cooled to 10°C, and fermented beverage ( Example) was manufactured.

他の諸条件を同一にしつつ並行して、酵母にサツカロマ
イセス・セレビシェを用いたことだけが異なる発酵飲料
(比較例)を製造したが、実施例と比較例とを官能評価
すると、実施例に好結果が有意検定された(検査員20
名×2回繰り返し×2点嗜好×危険率1チ)。
A fermented beverage (comparative example) was produced in parallel with other conditions being the same, but the only difference was that Saccharomyces cerevisiae was used as the yeast. Sensory evaluation of the example and comparative example revealed that the example had a preference. The results were tested for significance (inspector 20
name x 2 repetitions x 2 points preference x risk rate 1).

・実施例2 実施例1と同様にして発酵母液を得だ。・Example 2 A fermentation mother liquor was obtained in the same manner as in Example 1.

そして、発酵母液を3倍水希釈し、希釈液99j十砂糖
200g+香料(柑橘系)0.5iiJの割合で調整し
、その寸まチルド(5℃)の発酵飲料を製造した。
Then, the fermentation mother liquor was diluted 3 times with water and adjusted to a ratio of 200 g of diluted solution 99j deca sugar + 0.5 iiJ of fragrance (citrus) to produce a chilled (5° C.) fermented beverage.

官能評価は実施例1の場合と同様であった。The sensory evaluation was the same as in Example 1.

・実施例3 実施例1と同様にして発酵母液を得た。・Example 3 Fermentation mother liquor was obtained in the same manner as in Example 1.

そして、発酵母液を3倍水希釈し、以下実施例1と同様
に調整、加熱殺菌、冷却(但し5℃)及び遠心分離した
後、炭酸ガスボリューム2.3を目標にカーボネーショ
ンして発酵飲料(実施例)を製造した。
Then, the fermentation mother liquor was diluted 3 times with water, adjusted in the same manner as in Example 1, heat sterilized, cooled (5°C) and centrifuged, and then carbonated with a target carbon dioxide volume of 2.3 to make a fermented beverage. (Example) was manufactured.

官能評価は実施例1の場合と同様であったO・実施例4 実施例1と同様にして発酵母液を得た。Sensory evaluation was the same as in Example 1.O Example 4 Fermentation mother liquor was obtained in the same manner as in Example 1.

そして、発酵母液を減圧下に濃縮しく80℃)、更に凍
結乾燥した。得られた乾燥物30g+砂糖6f/+香料
(レモン系)0.001gの割合で調整し、これを30
0jltに加水溶解して発酵飲料(実施例)を製造した
The fermentation mother liquor was then concentrated under reduced pressure (80°C) and further freeze-dried. The ratio of 30 g of the obtained dry matter + 6 f sugar/+ 0.001 g of fragrance (lemon type) was adjusted, and this was added to 30 g.
A fermented beverage (Example) was produced by dissolving it in 0jlt.

官能評価は実施例1の場合と同様であった。The sensory evaluation was the same as in Example 1.

・実施例5 麦芽エキスの15多水溶液80容量部と、トマト処理物
〔洗浄・選別したトマト(品種はカゴメ81)を破砕し
、85℃達温で加熱した後、2朋ψ孔径の沢過網を装着
、したパルパーで搾汁したもの〕20容量部との混合溶
液を、重炭酸カルシウムでpH6,5に調整し、これを
95℃達温で加熱殺菌して30℃に冷却した後、それぞ
れ各別に予備培養した、フレベロマイセス・ラクチス、
フレベロマイセス・フラキリス、ストレプトコッカス・
サーモフィラス、ラクトバシルス・ブルガリカスを各々
基質1 ml当り3X106cel1gとなるように加
え、外部からの菌的汚染を防止しつつ、30℃で25時
間静置発酵した。得られた発酵液のエチルアルコール0
.9 % 、乳酸(換算量)350qチ、pH4,1で
あった。
・Example 5 80 parts by volume of a 15% aqueous solution of malt extract and a processed tomato product [washed and sorted tomatoes (variety: Kagome 81) were crushed, heated to 85°C, and then filtered through a pore size of 2 mm. A mixed solution of 20 parts by volume of juice squeezed with a pulper equipped with a screen was adjusted to pH 6.5 with calcium bicarbonate, heated to sterilize it at 95°C, cooled to 30°C, Phlebellomyces lactis, each pre-cultured separately.
Phlebellomyces frachyris, Streptococcus
Thermophilus and Lactobacillus bulgaricus were each added in an amount of 3×10 6 cells per ml of substrate, and fermentation was allowed to stand at 30° C. for 25 hours while preventing bacterial contamination from the outside. Ethyl alcohol in the resulting fermented liquid: 0
.. 9%, lactic acid (converted amount) 350q, and pH 4.1.

そして、この発酵液の遠心分離液99j十砂糖200g
+香料(レモン系)0.5gの割合で調整した後、95
℃達温で加熱殺菌して10℃に冷却し、発酵飲料(実施
例)を製造した。
And 200 g of centrifuged liquid of this fermented liquid 99j ten sugar
After adjusting the ratio of + fragrance (lemon type) 0.5g, 95
The fermented beverage (Example) was produced by heat sterilization at a temperature of 10°C and cooling to 10°C.

官能評価は実施例1の場合と同様であっだ0The sensory evaluation was 0 as in Example 1.

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

第1図と第2図とは本発明における発酵状況を各別に例
示するグラフである。 11.12・・・乳酸曲線、 21.22・・・エチルアルコール曲線、31.32・
・・pH曲線、 51.52・・・ ストレプトコッカス・サーモフィラ
ス生菌数曲線、 61.62・・・ ラクトバシルス・ブルガリカス生菌
数曲線、 特許出願人 カゴメ株式会社 代理人 弁理士 入 山 宏 正
FIG. 1 and FIG. 2 are graphs illustrating each fermentation situation in the present invention. 11.12... Lactic acid curve, 21.22... Ethyl alcohol curve, 31.32.
...pH curve, 51.52... Streptococcus thermophilus viable cell count curve, 61.62... Lactobacillus bulgaricus viable cell count curve, patent applicant Kagome Co., Ltd. agent, patent attorney Hiroshi Iriyama

Claims (1)

【特許請求の範囲】 1 発芽麦汁のフレベロマイセス・ラクチス(Kluy
veromyces 1actis)及び/又はフレペ
ロマイセス会フラギリス(Kluyveromycea fragilis)と食品用の一般乳酸菌との共生によ
る発酵液、該発酵液の濃縮物又は該発酵液の乾燥物を主
成分とする、エチルアルコール含量1%(W/V)未満
の発酵飲料。 2発芽麦汁として麦芽エキスを用いる特許請求の範囲第
1項記載の発酵飲料。 3発芽麦汁のフレベロマイセス・ラクチス(Kluyv
eromyces 1actis)及び/又はフレベロ
マイセス・フラキリス(Kluyveromyces fragilis)と食品用の一般乳酸菌との共生によ
る発酵液、該発酵液の濃縮物又は該発酵液の乾燥物を主
成分とし、酵母及び乳酸菌を含有する、エチルアルコー
ル含量1%(W/V)未満の発酵飲料。 4発芽麦汁として麦芽エキスを用いる特許請求の範囲第
3項記載の発酵飲料。 5発芽麦汁と野菜及び/又は果実処理物との混合系のフ
レベロマイセス・ラクチス( Kluyverom7ces 1actis)及び/又
はフレベロマイセス・フラギリス(Klu)’vero
myces fragilis)と食品用の一般乳酸菌との共生によ
る発酵液、該発酵液の濃縮物又は該発酵液の乾燥物を主
成分とする、エチルアルコール含量1 % (W/V 
)未満の発酵飲料06発芽麦汁として麦芽エキスを用い
る特許請求の範囲第5項記載の発酵飲料。 7発芽麦汁をpH調整し、殺菌して冷却した後、予備培
養した酵母であるフレベロマイセス・ラクチス(Klu
yveromFces l a c t i s ) 及ヒ/又はフレベロマイ
セス・フラギリス(Kluyveromycesfra
gili8)と、別に予備培養した食品用の一般乳酸菌
とを加えて、所謂アルコール酵と乳酸発酵とを同時に行
ない、エチルアルコール 了させ、次いで酵母及び乳酸菌を分離して発酵液を得、
これを必要に応じて濃縮、乾燥及び/又は調整する発酵
飲料の製造方法。 8発酵したものをカーボネーションする特許請求の範囲
第7項記載の発酵飲料の製造方法09 発芽麦汁として
麦芽エキスを用いる特許請求の範囲第7項又は第8項記
載の発酵飲料の製造方法。 10麦芽エキスの濃度を5〜50%(、W/V)で発酵
する特許請求の範囲第9項記載の発酵飲料の製造方法。 11温度を25〜40℃で発酵する特許請求の範囲第7
項〜第10項のいずれか一つの項記載の発酵飲料の製造
方法。
[Scope of Claims] 1. Phlebellomyces lactis (Kluy) in germinated wort
1% ethyl alcohol content, mainly composed of a fermentation liquid produced by the symbiosis of Kluyveromyces 1actis and/or Kluyveromycetes fragilis and general food-grade lactic acid bacteria, a concentrate of the fermentation liquid, or a dried product of the fermentation liquid. (W/V) fermented beverage. 2. The fermented beverage according to claim 1, which uses malt extract as the germinated wort. 3 Phlebellomyces lactis (Kluyv) in germinated wort
A fermentation liquid resulting from the symbiosis of Kluyveromyces 1actis and/or Kluyveromyces fragilis with food-grade general lactic acid bacteria, a concentrate of the fermentation liquid, or a dried product of the fermentation liquid as the main component, and containing yeast and lactic acid bacteria. , a fermented beverage with an ethyl alcohol content of less than 1% (W/V). 4. The fermented beverage according to claim 3, which uses malt extract as the germinated wort. 5 Phleveromyces lactis (Kluyverom7ces 1actis) and/or Phleveromyces fragilis (Klu)'vero in a mixed system of germinated wort and processed vegetables and/or fruits
1% (W/V
) Fermented beverage according to claim 5, in which malt extract is used as the germinated wort. 7 After adjusting the pH of the germinated wort, sterilizing it, and cooling it, we added the pre-cultured yeast Phlebellomyces lactis (Klu
Kluyveromyces fragilis and/or Kluyveromyces fragilis
gili8) and food-grade general lactic acid bacteria precultured separately, so-called alcohol fermentation and lactic acid fermentation are performed simultaneously, ethyl alcohol is evaporated, and then yeast and lactic acid bacteria are separated to obtain a fermented liquid.
A method for producing a fermented beverage, in which the fermented beverage is concentrated, dried and/or adjusted as necessary. 8. A method for producing a fermented beverage according to claim 7, in which the fermented product is carbonated. 09. A method for producing a fermented beverage according to claim 7 or 8, which uses malt extract as the germinated wort. 10. The method for producing a fermented beverage according to claim 9, wherein the malt extract is fermented at a concentration of 5 to 50% (W/V). Claim 7: Fermenting at a temperature of 25 to 40°C
A method for producing a fermented beverage according to any one of Items 1 to 10.
JP58201574A 1983-10-27 1983-10-27 Fermented drink and its preparation Granted JPS6094076A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58201574A JPS6094076A (en) 1983-10-27 1983-10-27 Fermented drink and its preparation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58201574A JPS6094076A (en) 1983-10-27 1983-10-27 Fermented drink and its preparation

Publications (2)

Publication Number Publication Date
JPS6094076A true JPS6094076A (en) 1985-05-27
JPH0357742B2 JPH0357742B2 (en) 1991-09-03

Family

ID=16443313

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58201574A Granted JPS6094076A (en) 1983-10-27 1983-10-27 Fermented drink and its preparation

Country Status (1)

Country Link
JP (1) JPS6094076A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04320669A (en) * 1991-04-17 1992-11-11 Asahi Breweries Ltd Carrot fermented drink
WO2009124529A2 (en) * 2008-04-11 2009-10-15 Vlb Berlin E.V. Refreshment drink

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59135869A (en) * 1983-01-13 1984-08-04 ソシエテ・デ・プロデユイ・ネツスル・ソシエテ・アノニム Production of carbonated beverage

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59135869A (en) * 1983-01-13 1984-08-04 ソシエテ・デ・プロデユイ・ネツスル・ソシエテ・アノニム Production of carbonated beverage

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04320669A (en) * 1991-04-17 1992-11-11 Asahi Breweries Ltd Carrot fermented drink
JPH0675487B2 (en) * 1991-04-17 1994-09-28 アサヒビール株式会社 Ginseng fermented beverage
WO2009124529A2 (en) * 2008-04-11 2009-10-15 Vlb Berlin E.V. Refreshment drink
WO2009124529A3 (en) * 2008-04-11 2009-12-23 Vlb Berlin E.V. Refreshment drink

Also Published As

Publication number Publication date
JPH0357742B2 (en) 1991-09-03

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