JP2008148615A - Fermented vinegar and method for producing the same - Google Patents
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Abstract
Description
本発明は、小豆等の雑豆類の餡粒子を酵素分解しながら酵母を添加しアルコール発酵させ、ついで酢酸発酵をすることにより得られる小豆等雑豆類を用いた醸造酢及びその製造方法に関する。 The present invention relates to a brewed vinegar using miso beans such as red beans obtained by adding yeast and subjecting it to alcoholic fermentation while enzymatically decomposing rice cake particles of miso beans such as red beans, and then acetic acid fermentation, and a method for producing the same.
清酒等の穀物を原料とした醸造酒のアルコール発酵は、穀物のでんぷん質を麹等を用いた酵素分解により麦芽糖あるいはぶどう糖に分解し、酵母の発酵を行う。ところが、小豆など雑豆類は大豆と比較して以下のようにでんぷん含有量が多いにもかかわらず、通常の穀物のようにアルコール発酵の原料として利用されていない。
・雑豆類: 炭水化物約60%、タンパク質20%、脂肪分2%
・大 豆: 炭水化物約30%、タンパク質35%、脂肪分20%
Alcohol fermentation of brewed liquor made from cereals such as refined sake is performed by fermenting yeast by degrading the starch of the cereal into maltose or glucose by enzymatic decomposition using koji or the like. However, miscellaneous beans such as red beans are not used as a raw material for alcoholic fermentation unlike ordinary grains, although they have a higher starch content than soybeans as described below.
・ Soybeans: About 60% carbohydrate, 20% protein, 2% fat
・ Bean: About 30% carbohydrate, 35% protein, 20% fat
その理由は小豆等に吸水させて加熱すると餡になるからであり、餡粒子はでんぷんをタンパク質やペクチン、キシランなどが取り囲んだ構造であることから、でんぷん分解酵素による分解が容易には進まないからである。 The reason is that when red beans are absorbed and heated, they become soot.Since the soot particles are surrounded by starch, protein, pectin, xylan, etc., the degradation by starch degrading enzymes does not proceed easily. It is.
そこで、各種酵素(タンパク質分解酵素・デンプン分解酵素・ペクチン分解酵素・キシラン分解酵素)により餡粒子を分解することにより、発酵に利用できる糖分の生成方法を検討したところ、酵素添加による餡粒子の分解による内部のデンプン分解による糖分の増加が認められた。 Therefore, we examined the production method of sugar that can be used for fermentation by degrading soot particles with various enzymes (proteolytic enzyme, starch degrading enzyme, pectin degrading enzyme, xylan degrading enzyme). Increased sugar content due to internal starch degradation was observed.
次いで、この糖分を酵母によるアルコール発酵に供し、さらにアルコール発酵液に酢酸菌による酢酸発酵に供したところ良好に酢酸発酵することを見いだした。
でんぷん質が多いにもかかわらず、これまで、発酵食品の原料とすることが出来なかった雑豆類を原料に食酢を製造とすることができれば好ましい。 It is preferable that vinegar can be produced from miscellaneous beans, which have not been able to be used as raw materials for fermented foods, despite the high starch quality.
そのためには、餡粒子を分解し内部のでんぷんを酵素分解し麦芽糖あるいはぶどう糖に分解する必要がある。 For this purpose, it is necessary to decompose the cocoon particles and enzymatically decompose the starch inside to decompose into maltose or glucose.
各種酵素による分解で餡粒子を分解し内部のでんぷんから麦芽糖あるいはぶどう糖を生成させることが出来る。 Maltose or glucose can be produced from starch in the starch by decomposing with various enzymes.
しかしながら、この方法では、糖分が増加する一方で、原料由来による雑菌汚染が進行する。すなわち、豆類にはバチルス属菌が付着しており、生菌は加熱により死滅するものの、胞子が残りこれが酵素分解時に発芽生育し腐敗を起こすという問題がある。 However, in this method, while the sugar content increases, contamination with germs from the raw material proceeds. That is, Bacillus spp. Are attached to the beans, and live bacteria are killed by heating, but there is a problem that spores remain and germinate and grow during enzymatic degradation, causing spoilage.
本発明は上記課題を達成するために、雑豆類を酵素分解と同時に酵母による発酵を並行させ、次いで酢酸発酵を行う。 In order to achieve the above object, the present invention parallels fermentation with yeasts simultaneously with enzymatic decomposition, and then performs acetic acid fermentation.
この発明によると、酢酸発酵に充分なアルコールの確保と、同時に雑菌属類の腐敗を防止することができた。また、得られたアルコール発酵液は各種酵素作用により多用な成分を含んでおり、次いで行う酢酸発酵に於いて酢酸菌の生育を促進し、良好に食酢を製造することが可能となった。 According to this invention, it was possible to secure sufficient alcohol for acetic acid fermentation and at the same time to prevent the rot of miscellaneous bacteria. In addition, the obtained alcohol fermentation broth contained various components due to various enzyme actions, and in the subsequent acetic acid fermentation, it was possible to promote the growth of acetic acid bacteria and to produce vinegar satisfactorily.
本発明の実施の形態を図1を参照しながら詳細に説明する。 An embodiment of the present invention will be described in detail with reference to FIG.
乾豆の雑豆類、主に小豆を原料に用いる。その他、金時、手亡、中長等を原料にする。 We use dried soybeans, mainly red beans. In addition, use gold, hand loss, medium length etc. as raw materials.
これら乾豆を秤量後、淡水にて洗浄する。 These dried beans are weighed and then washed with fresh water.
次に、乾豆の状態で水又は温水から炊き上げ(煮熟)る。この際、乾豆を予め水浸した状態から炊き上げることも可能である。炊き込み時間、水分量については、季節、乾豆の水分量などを鑑みながら調整する。 Next, it is cooked (boiled) from water or warm water in the form of dried beans. At this time, it is also possible to cook the dried beans from a state in which they are preliminarily immersed in water. The cooking time and moisture content are adjusted in consideration of the season and moisture content of dried beans.
次に、煮熟後の豆及び煮汁をマスコロイダーにて摩砕する。摩砕はマスコロイダー機器によるものの他、ミキサー等あるいはハンマーミルなど、煮豆をできるだけ潰砕できるものであればどのような機器でもよい。 Next, the beans and the broth after ripening are ground with a mass colloider. In addition to using a mass collider device, the grinding may be any device that can crush boiled beans as much as possible, such as a mixer or a hammer mill.
次に、上記の生成物に、速やかに酵素を添加し、恒温状態で攪拌し、でんぷん質の加水分解を促す。本実施例では、50℃で、2〜3時間の反応時間とする。 Next, an enzyme is quickly added to the above product, and the mixture is stirred at a constant temperature to promote hydrolysis of starch. In this example, the reaction time is 2 to 3 hours at 50 ° C.
加水分解の進んだ生成物の糖度を確認し、酵母活性の至適温度に調整し、酵母を添加・攪拌する。糖度はブリックスで10%以上、至適温度(酵母活性温度)25℃である。この酵母添加を速やかに行うことにより、雑菌の繁殖が防げ、なおかつ、酵素処理と酵母による発酵が同時に行われるため効率のよい処理が可能になる。 Confirm the sugar content of the hydrolyzed product, adjust to the optimum temperature for yeast activity, and add and stir the yeast. The sugar content is 10% or more in Brix, and the optimum temperature (yeast activation temperature) is 25 ° C. By promptly adding this yeast, it is possible to prevent the propagation of miscellaneous bacteria, and the enzyme treatment and the fermentation with yeast are performed simultaneously, so that an efficient treatment is possible.
次は、アルコール発酵の段階であり、恒温室にて、酵素反応、アルコール発酵が並行して進行する。恒温室の温度20℃に設定し、発酵時間約72時間、アルコール発酵を行う。この時アルコール度数は6%以上になる。 Next is the stage of alcohol fermentation, in which the enzymatic reaction and alcohol fermentation proceed in parallel in a constant temperature room. The temperature of the temperature-controlled room is set to 20 ° C., and alcoholic fermentation is performed for about 72 hours. At this time, the alcohol content becomes 6% or more.
次に、フィルタープレス機器等を用いて、固形物を分離する。分離は遠心分離機等でも可能である。 Next, a solid substance is separated using a filter press machine or the like. Separation is also possible with a centrifuge or the like.
上澄み液を70℃前後で10〜20分間加熱し、酵素の失活と酵母の殺菌処理を行う。加熱処理後は速やかに冷却する。本工程はあった方がより良いが必ずしも必要ではない。 The supernatant is heated at around 70 ° C. for 10 to 20 minutes to inactivate the enzyme and sterilize the yeast. Cool immediately after heat treatment. Although it is better to have this step, it is not always necessary.
次に、本液に酢酸菌を添加し発酵温度は30℃で酢酸発酵を行う。添加する酢酸菌は種酢として加えることが望ましい。 Next, acetic acid bacteria are added to this liquid, and acetic acid fermentation is performed at a fermentation temperature of 30 ° C. The acetic acid bacteria to be added are preferably added as seed vinegar.
次に、酢酸発酵が終了した後、濾過を行い、熟成、おり下げ及び火入れ殺菌を行う。 Next, after acetic acid fermentation is completed, filtration is performed, and aging, lowering and sterilization are performed.
以上の工程により、雑豆類を原料とする醸造酢が完成する。 The brewing vinegar which uses miscellaneous beans as a raw material is completed according to the above process.
本実施例では、雑豆類として小豆を使用し、酵素はペクチナーゼ製剤、アミラーゼ製剤、キシラナーゼ製剤の3種類を使用した。 In this example, red beans were used as miscellaneous beans, and three types of enzymes were used: pectinase preparation, amylase preparation, and xylanase preparation.
また、酵母はアルコール発酵に使用されているものであれば何れでもよく、乳糖発酵性酵母でもよい。本実施例で使用した酵母は清酒用きょうかい701号(日本醸造協会)である。 The yeast may be any yeast as long as it is used for alcoholic fermentation, and may be lactose-fermenting yeast. The yeast used in this example is sake 701 for sake (Japan Brewing Association).
酢酸菌は醸造酢に用いることができるものであれば何れでもよい。本実施例で使用した酢酸菌はIFO14814である。 Any acetic acid bacteria may be used as long as it can be used for brewing vinegar. The acetic acid bacterium used in this example is IFO 14814.
雑豆類として小豆を使用する場合につき説明する。まず、小豆を炊き、熱いままマスコロイダーにて磨砕する。 The case where red beans are used as miscellaneous beans will be described. First, cook the red beans and grind them with a mascolloy while hot.
磨砕された小豆を50℃に冷却し3種類の酵素を添加し、2時間、酵素反応を行う。2時間後にはブリックス値が約2上昇する。 The ground red beans are cooled to 50 ° C, 3 kinds of enzymes are added, and the enzyme reaction is carried out for 2 hours. The Brix value rises by about 2 after 2 hours.
次いで、25℃まで冷却し酵母の添加を行う。 Subsequently, it cools to 25 degreeC and adds yeast.
20℃で4日間酵母によるアルコール発酵を行う。アルコール発酵を行うことにより本磨砕物中のアルコール濃度は約7%となる。 Perform alcoholic fermentation with yeast at 20 ℃ for 4 days. By performing alcoholic fermentation, the alcohol concentration in the ground product becomes about 7%.
次いで、プレスにより固液分離を行い、液体部分を回収する。 Next, solid-liquid separation is performed by a press, and the liquid portion is recovered.
小豆アルコール発酵液は70℃、10分の加熱により添加酵素の失活と酵母の殺菌を行う。 The red bean alcohol fermentation liquid inactivates the added enzyme and sterilizes the yeast by heating at 70 ° C for 10 minutes.
次いで、酢酸菌を添加し、30℃で静置発酵を行う。 Subsequently, acetic acid bacteria are added and stationary fermentation is performed at 30 ° C.
酢酸発酵終了すると約5%の酢酸を含んだ小豆酢が得られる。 Upon completion of acetic acid fermentation, red beans vinegar containing about 5% acetic acid is obtained.
出来上がった小豆酢は、図2に示すように多くの市販食酢と比較してポリフェノールが豊富で、図3に示すように抗酸化性が強いものになる。
また、図4に示すように、カリウムとマグネシウムが非常に高い食酢となる。
The completed red bean vinegar is rich in polyphenols as shown in FIG. 2 as compared with many commercially available vinegars, and has strong antioxidant properties as shown in FIG.
In addition, as shown in FIG. 4, the vinegar is very high in potassium and magnesium.
手亡、金時を原料として用いた場合は、図2、図3に示したように小豆酢と同等の高いポリフェノールを含有しており、抗酸化性においては、小豆酢には及ばないが市販食酢よりも高い活性を持つ。 When Tetsuo and Kintoki are used as raw materials, as shown in FIG. 2 and FIG. 3, it contains a high polyphenol equivalent to red bean vinegar. Has higher activity than vinegar.
小豆同様にカリウムとマグネシウムが非常に高い食酢となる。 Like red beans, vinegar is very high in potassium and magnesium.
また、小豆とは異なり粘性の高い食酢になる。この粘性の高さは従来の酢にはない大きな特徴である。粘性が高くなると、酢独特の刺激が弱められる。 Also, unlike red beans, it becomes a highly viscous vinegar. This high viscosity is a major feature not found in conventional vinegar. When the viscosity increases, the irritation unique to vinegar is weakened.
また、酢の物等に使用した場合には、通常の食酢を使用した場合と比べ、食材表面の滑りが良くなり喉の通りがよくなる。喉の通りが悪くなっている嚥下障害者の介護的食材にすることもできる。 In addition, when used for vinegar, etc., the surface of the food material is more slippery and the throat is better than when using ordinary vinegar. It can also be used as a nursing food for people with dysphagia who have poor throat passage.
また、いずれの原料を用いた場合でも、原料の特長を生かした食酢とすることが出来る。 Moreover, even if any raw material is used, it can be set as the vinegar which utilized the characteristic of the raw material.
本実施例では、雑豆類として小豆を使用し、酵素製剤はセルロイシンTP25(HBI社製)、及びサンスーパー(ノボエンザイムジャパン社製)を各0.2%添加した。なお、酵素製剤はこれに限るものではない。 In this Example, red beans were used as miscellaneous beans, and cellulosine TP25 (manufactured by HBI) and sun super (manufactured by Novoenzyme Japan) were each added 0.2% as enzyme preparations. The enzyme preparation is not limited to this.
磨砕された小豆を50℃に冷却、酵素を添加して攪拌、2時間酵素反応を先行させる。酵素反応前の煮熟し磨砕した小豆は、ブリックス値で8.0程度を示し、酵素反応2時間後には1程度上昇してブリックス値で9.0程度になる(図5のbrixのライン参照)。
ここで、図5について説明する。図5は、時系列による糖分変化(brix変化)とアルコール生成量を示している。
具体的には、餡粒子に酵母を添加することなく、酵素だけを添加して酵素反応だけを進めると、brix値は20%位になるが、腐敗する。その為、酵素分解とアルコール発酵と並行して行うと、アルコールは7%位になることを示している。
Cool the ground red beans to 50 ° C, add the enzyme, stir, and precede the enzyme reaction for 2 hours. Boiled and ground red beans before the enzyme reaction show a Brix value of about 8.0, and after 2 hours of the enzyme reaction, increase by about 1 to a Brix value of about 9.0 (brix line in FIG. 5). reference).
Here, FIG. 5 will be described. FIG. 5 shows the change in sugar (brix change) and the amount of alcohol produced over time.
Specifically, if only the enzyme is added and the enzyme reaction is allowed to proceed without adding yeast to the soot particles, the brix value will be about 20%, but it will rot. Therefore, it is shown that alcohol is about 7% when it is performed in parallel with enzymatic decomposition and alcohol fermentation.
酵素反応のみを継続すると24時間後にはブリックス値は20程度に上昇するが(図5のbrixのライン参照)、原料由来のバチルス菌が繁殖し腐敗を起こす。原料に付着しているバチルス菌は、生菌が煮熟工程による加熱により死滅しているが、耐熱性の胞子が残り、酵素反応工程で発芽し繁殖する。 If only the enzyme reaction is continued, the Brix value rises to about 20 after 24 hours (see the brix line in FIG. 5), but the Bacillus derived from the raw material propagates and causes corruption. The Bacillus bacteria adhering to the raw material have been killed by heating during the cooking process, but heat-resistant spores remain and germinate and propagate in the enzyme reaction process.
酵素反応を2時間先行させることで、添加する酵母の利用する糖源を生成させ、速やかな増殖を促すことができる。酵素反応の先行は必ずしも必要ではなく、同時に添加することもできる。同時に添加する場合は、酵素反応と酵母の増殖を行うため25℃で酵素分解と発酵を並行して行う。 By preceding the enzyme reaction for 2 hours, a sugar source used by the yeast to be added can be generated and prompt growth can be promoted. The preceding enzyme reaction is not necessarily required, and can be added simultaneously. If they are added simultaneously, enzymatic degradation and fermentation are performed in parallel at 25 ° C in order to carry out enzymatic reaction and yeast growth.
50℃で酵素反応を2時間先行させた後、25℃に冷却し酵母を添加する。 The enzyme reaction is allowed to proceed for 2 hours at 50 ° C, then cooled to 25 ° C and yeast is added.
25℃で酵素反応と酵母によるアルコール発酵を3乃至4日間並行して行う。すると、約7%のアルコールを含む小豆磨砕物となる(図5のアルコールのライン参照)。 Enzyme reaction and yeast alcohol fermentation at 25 ° C are performed in parallel for 3 to 4 days. Then, it becomes a red bean grind containing about 7% alcohol (see the alcohol line in FIG. 5).
酵素分解とアルコール発酵を並行して行うことにより、酵母の圧倒的多数、嫌気状態の形成およびアルコールの生成によりバチルス菌の発生を抑制できる。 By performing the enzymatic degradation and alcohol fermentation in parallel, the generation of Bacillus can be suppressed by the overwhelming majority of yeast, the formation of anaerobic conditions, and the production of alcohol.
酵素分解によりでんぷんから生成するぶどう糖あるいは麦芽糖を、酵母が速やかに取り込み消費することにより、反応生生物の蓄積が生じず、酵素反応が促進する。 By rapidly taking in and consuming glucose or maltose produced from starch by enzymatic degradation, the reaction living organisms do not accumulate and the enzyme reaction is promoted.
本実施例では、雑豆類として小豆を使用し、酵素はペクチナーゼ製剤、アミラーゼ製剤、キシラナーゼ製剤の3種類を使用した。 In this example, red beans were used as miscellaneous beans, and three types of enzymes were used: pectinase preparation, amylase preparation, and xylanase preparation.
磨砕された小豆を50℃に冷却し3種類の酵素を添加し、2時間、酵素反応を行う。2時間後にはブリックス値が約2上昇する。 Cool the ground bean to 50 ° C, add 3 kinds of enzymes, and perform the enzyme reaction for 2 hours. The Brix value rises by about 2 after 2 hours.
次いで、25℃まで冷却し酵母の添加を行う。 Subsequently, it cools to 25 degreeC and adds yeast.
20℃で4日間酵母によるアルコール発酵を行う。アルコール発酵を行うことにより本磨砕物中のアルコール濃度は約7%となる。 Alcohol fermentation with yeast is performed at 20 ° C. for 4 days. By performing alcoholic fermentation, the alcohol concentration in the ground product becomes about 7%.
次いで、プレスにより固液分離を行い、液体部分を回収する。 Next, solid-liquid separation is performed by a press, and the liquid portion is recovered.
小豆アルコール発酵液は70℃、10分の加熱により添加酵素の失活と酵母の殺菌を行う。 Azuki bean alcohol fermentation liquid inactivates the added enzyme and sterilizes the yeast by heating at 70 ° C. for 10 minutes.
次いで、酢酸菌を添加し、30℃で静置発酵を行う。 Subsequently, acetic acid bacteria are added and stationary fermentation is performed at 30 ° C.
酢酸発酵終了すると約5%の酢酸を含んだ小豆酢が得られる。 When acetic acid fermentation is completed, red beans vinegar containing about 5% acetic acid is obtained.
Claims (4)
The method for producing brewed vinegar according to claim 2, wherein the enzyme agent used for enzymatic degradation is protease, amylase, pectinase or xylanase.
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JP2014166145A (en) * | 2013-02-28 | 2014-09-11 | Q P Corp | Vinegar |
KR20160066830A (en) * | 2014-12-03 | 2016-06-13 | 광주여자대학교 산학협력단 | Method for producing a diet drink |
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JP2014150760A (en) * | 2013-02-08 | 2014-08-25 | Q P Corp | Rice aroma enhancing composition or rice aroma enhancing agent, and cooked rice with use of the same |
JP2014166145A (en) * | 2013-02-28 | 2014-09-11 | Q P Corp | Vinegar |
KR20160066830A (en) * | 2014-12-03 | 2016-06-13 | 광주여자대학교 산학협력단 | Method for producing a diet drink |
KR101694732B1 (en) | 2014-12-03 | 2017-01-10 | 광주여자대학교 산학협력단 | Method for producing a diet drink |
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