JP2007215421A - Vinegar and method for producing the same - Google Patents

Vinegar and method for producing the same Download PDF

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JP2007215421A
JP2007215421A JP2006036941A JP2006036941A JP2007215421A JP 2007215421 A JP2007215421 A JP 2007215421A JP 2006036941 A JP2006036941 A JP 2006036941A JP 2006036941 A JP2006036941 A JP 2006036941A JP 2007215421 A JP2007215421 A JP 2007215421A
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vinegar
acetic acid
fermentation
amino acids
protease
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JP4901235B2 (en
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Yoshiharu Noda
野田義治
Toshio Kadowaki
門脇利夫
Kazunori Oba
大場和徳
Tatsuro Ueki
植木達朗
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FUKUOKA PREFECTURE SHOYU JOZO KYODO KUMIAI
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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12JVINEGAR; PREPARATION OR PURIFICATION THEREOF
    • C12J1/00Vinegar; Preparation or purification thereof
    • C12J1/04Vinegar; Preparation or purification thereof from alcohol

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Abstract

<P>PROBLEM TO BE SOLVED: To provide a method for producing vinegar easily ingested compared with conventional vinegar or black vinegar by generating a large quantity of amino acids, and the vinegar produced by the method. <P>SOLUTION: The vinegar is produced by decomposing plant proteins and/or animal proteins by contacting a protease-containing enzyme in the presence of an aqueous ethyl alcohol solution to decompose them into amino acids, subsequently carrying out acetic acid fermentation. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

本発明は、アミノ酸を多量に含有した飲料や調味料に適した食酢及びその製造方法に関する。   The present invention relates to vinegar suitable for beverages and seasonings containing a large amount of amino acids and a method for producing the same.

従来から、食酢は、食品に酸味を添えるため調味料として古くから利用され、また、清涼感が得られることから飲料にも使用されている。昨今は、食酢の健康イメージが強く、リンゴ酢、黒酢、もろみ酢、香酢などが健康酢として供されている。   Traditionally, vinegar has been used as a seasoning to add a sour taste to food, and has also been used in beverages because it provides a refreshing feeling. Recently, the health image of vinegar is strong, and apple vinegar, black vinegar, moromi vinegar, fragrant vinegar, etc. are served as healthy vinegar.

食酢は、通常、デンプン質原料を麹菌酵素で分解し、酵母菌を作用させてアルコール発酵させ、次に酢酸菌を作用させて酢酸発酵させることにより製造されている。   Vinegar is usually produced by decomposing starchy raw material with a koji mold enzyme, allowing yeast to act and subjecting it to alcohol fermentation, and then allowing acetic acid bacteria to act and acetic acid fermenting.

しかし、前記特許文献1に示されるような従来の食酢の製造方法では、食酢のアミノ酸含量が少なく、ほとんどが有機酸で飲みにくいため、希釈して蜂蜜などを加えて飲用し易くしているのが実情である。   However, in the conventional method for producing vinegar as shown in Patent Document 1, since the amino acid content of vinegar is low and most of it is difficult to drink with organic acid, it is diluted and made easy to drink by adding honey and the like. Is the actual situation.

そこで、本発明は、アミノ酸を多量に生成させることにより、従来の食酢や黒酢などに比べて飲みやすい食酢及びその製造方法を提供するものである。   Therefore, the present invention provides a vinegar that is easier to drink than conventional vinegar or black vinegar by producing a large amount of amino acid, and a method for producing the vinegar.

本発明の食酢は、エチルアルコール水溶液の存在下で植物性蛋白質及び/又は動物性蛋白質にプロテアーゼ含有酵素類を接触させてアミノ酸に分解した後、酢酸菌を作用させて酢酸発酵させることにより製造する。   The vinegar of the present invention is produced by contacting a plant protein and / or animal protein with a protease-containing enzyme in the presence of an aqueous ethyl alcohol solution to decompose it into amino acids, and then allowing acetic acid bacteria to act to carry out acetic acid fermentation. .

エチルアルコール濃度は、4.0〜5.0%が適している。植物性蛋白質としては、蒸煮した大豆、小麦、グルテン、米、トウモロコシ、ピーナツ等を使用することができる。又、動物性蛋白質としては、生及び/又は煮熟した鰯、鰹、イカ、エビ、貝等の魚介類や牛、豚、鳥等肉類を使用することができる。なお、植物性蛋白質は1種又は2種以上、動物性蛋白質も1種又は2種以上で、植物性蛋白質と動物性蛋白質を混和することもできる。   A suitable ethyl alcohol concentration is 4.0 to 5.0%. As the vegetable protein, steamed soybean, wheat, gluten, rice, corn, peanut and the like can be used. As animal protein, raw and / or boiled seafood such as salmon, salmon, squid, shrimp and shellfish and meat such as cow, pig and bird can be used. In addition, vegetable protein is 1 type, or 2 or more types, animal protein is also 1 type or 2 or more types, and vegetable protein and animal protein can also be mixed.

プロテアーゼ含有酵素類として、市販のプロテアーゼ製剤を使用することができる。例えば、ノボ社の商品名フレーバーザイム等である。又、プロテアーゼ含有の麹として、醤油麹、米麹、麦麹等、菌種としてアスペルギルス属、リゾープス属、バチルス属等を使用することができる。その際に、椎茸、霊芝、アガリクスなどのキノコ類や海藻類、茶、松、イチョウ等のポリフェノール含有物、野菜、果実等の1種又は2種以上の原料を配合して製造することができる。
酢酸発酵は、特に限定しないが、全窒素1.5〜2.0%、純エキス20〜30%、エタノール5〜15%、pH5.5〜6.5の発酵原液及び/又は水や果汁などによる希釈液が好ましい。また、酢酸発酵時に、卵殻、貝殻、炭酸カルシウム等のカルシウム含有物を加えて酸度及び/又はpH調整を図ることができる。
Commercially available protease preparations can be used as protease-containing enzymes. For example, Novo's brand name Flavorzyme. Moreover, as a protease-containing koji, soy sauce koji, rice koji, wheat straw, etc., and Aspergillus genus, Rhizopus genus, Bacillus genus, etc. can be used as bacterial species. In that case, it can be produced by blending one or more raw materials such as mushrooms such as shiitake mushrooms, ganoderma, agaricus, seaweeds, polyphenol-containing materials such as tea, pine, ginkgo, vegetables, fruits, etc. it can.
Acetic acid fermentation is not particularly limited, but total nitrogen 1.5-2.0%, pure extract 20-30%, ethanol 5-15%, pH 5.5-6.5 fermentation stock solution and / or water and fruit juice, etc. The diluted solution by is preferred. Moreover, at the time of acetic acid fermentation, acidity and / or pH adjustment can be aimed at by adding calcium containing materials, such as eggshell, shellfish, and calcium carbonate.

本発明のアミノ酸高含有の食酢は、例えば、次の方法で製造する。   The amino acid-rich vinegar of the present invention is produced, for example, by the following method.

(1)植物性蛋白原料や動物性蛋白原料に、プロテアーゼ製剤やプロテアーゼ含有の麹もしくは魚の自己消化酵素などを混和した後、これをエチルアルコール存在下で酵素分解し、アミノ酸を生成させた後に酢酸発酵させる。 (1) Protease preparations, protease-containing salmon or fish autolysis enzymes, etc. are mixed with plant protein raw materials or animal protein raw materials, then enzymatically decomposed in the presence of ethyl alcohol to produce amino acids, and then acetic acid Ferment.

(2)自己消化酵素(プロテアーゼ)を有する生の鰯や鰹などの動物性蛋白質をエチルアルコール存在下で酵素分解し、アミノ酸を生成させた後に酢酸発酵させる。 (2) Enzymatic degradation of animal proteins such as raw cocoons and cocoons having autolytic enzymes (proteases) in the presence of ethyl alcohol to produce amino acids, followed by acetic acid fermentation.

(3)生及び/又は煮熟した、鰯や鰹などにプロテアーゼ製剤やプロテアーゼ含有の麹などを混和した後、これをエチルアルコール存在下で酵素分解し、アミノ酸を生成させた後に酢酸発酵させる。 (3) A protease preparation or protease-containing koji is mixed with raw and / or boiled koji, koji, etc., and this is enzymatically decomposed in the presence of ethyl alcohol to produce amino acids and then subjected to acetic acid fermentation.

(4)エチルアルコールの一部を酢酸などの有機酸に置き換えて、アミノ酸に分解した後、酢酸発酵させる。 (4) A portion of ethyl alcohol is replaced with an organic acid such as acetic acid, decomposed into amino acids, and then fermented with acetic acid.

本発明によるアミノ酸高含有の食酢は、総アミノ酸量が1,000mg/dl以上で、好ましくは、1,500mg/dl以上、さらに好ましくは3,000mg/dl以上がよい。また、酢酸濃度は、1.0〜6.0%で、好ましくは、2.5〜4.5%がよい。   The vinegar with a high amino acid content according to the present invention has a total amino acid content of 1,000 mg / dl or more, preferably 1,500 mg / dl or more, more preferably 3,000 mg / dl or more. The acetic acid concentration is 1.0 to 6.0%, preferably 2.5 to 4.5%.

また、エチルアルコールの一部を酢酸などの有機酸に置き換えて、アミノ酸に分解した後、酢酸発酵させてアミノ酸高含有の食酢を製造することもできる。   Moreover, after replacing a part of ethyl alcohol with an organic acid such as acetic acid and decomposing it into amino acids, it can be fermented with acetic acid to produce vinegar containing a high content of amino acids.

本発明は、エチルアルコール水溶液の存在下で動植物性蛋白質にプロテアーゼ含有酵素類を接触させてアミノ酸に分解した後、酢酸発酵させることにより、アミノ酸高含有の食酢ができるので、従来の食酢や黒酢などに比べて旨味や甘みがあり、極めて飲みやすく、また、調味料としても適している。   In the present invention, vinegar with high amino acid content can be obtained by bringing protease-containing enzymes into contact with animal and plant proteins in the presence of an ethyl alcohol aqueous solution and decomposing them into amino acids, followed by acetic acid fermentation. Compared to the above, it has a umami and sweetness, is very easy to drink, and is also suitable as a seasoning.

以下に本発明の実施例について説明する。   Examples of the present invention will be described below.

蒸煮大豆1.2kgに醤油麹4kgを混合したものを20%エタノール水溶液8.3リットルに仕込み、15℃で1ヶ月間、さらに30℃で1ヶ月間酵素分解した後、圧搾して濾液(発酵原液)を得た。温度を変えて酵素分解させることにより、醸造期間の短縮やアミノ化率及びペプチド比率を調整することができる。   A mixture of 1.2 kg of steamed soybeans and 4 kg of soy sauce cake in 8.3 liters of 20% ethanol aqueous solution, enzymatically decomposed at 15 ° C. for 1 month, and further at 30 ° C. for 1 month, and then pressed and filtrated (fermented) Stock solution) was obtained. By performing enzymatic degradation at different temperatures, the brewing period can be shortened and the amination rate and peptide ratio can be adjusted.

発酵原液(エタノール濃度10%)、発酵原液を水で2倍水溶液に希釈してエタノール濃度を5%に調整したもの、3倍及び4倍水溶液に希釈し、アルコールを添加してエタノール濃度を5%に調整したものに、それぞれ酢酸菌(Acetobacter acetic)を添加して32℃で6日間の表面酢酸発酵を実施した。表1にその結果を示す。

Figure 2007215421
Fermentation stock solution (ethanol concentration 10%), fermentation stock solution diluted to 2 times aqueous solution with water to adjust ethanol concentration to 5%, diluted to 3 times and 4 times aqueous solution, alcohol added to increase ethanol concentration to 5 The acetic acid bacteria (Acetobacteracetic) was added to each adjusted to%, and surface acetic acid fermentation was performed at 32 ° C. for 6 days. Table 1 shows the results.
Figure 2007215421

表1より、6日間の表面酢酸発酵した結果、発酵原液は総アミノ酸量は多いが、酸度から明らかなとおりほとんど酢酸発酵しなかった。また、2倍希釈液の酢酸発酵は緩慢であった。しかし、4倍希釈液の酢酸発酵は、旺盛であったが、総アミノ酸量が他の試験区に比べて少なかった。   From Table 1, as a result of the surface acetic acid fermentation for 6 days, the fermentation stock solution had a large amount of total amino acids, but it was hardly acetic acid fermentation as apparent from the acidity. The acetic acid fermentation of the 2-fold diluted solution was slow. However, the acetic acid fermentation of the 4-fold diluted solution was vigorous, but the total amino acid amount was small compared to other test sections.

前記と同一の条件に調整した後、酢酸菌(Acetobacter pasteurianus SKV1108)を添加して32℃で2日間の深部酢酸発酵を実施した。

Figure 2007215421
After adjusting to the same conditions as described above, acetic acid bacteria (Acetobacter pasteurianus SKV1108) was added, and deep acetic acid fermentation was performed at 32 ° C. for 2 days.
Figure 2007215421

表2より、2日間の深部酢酸発酵をした結果、発酵原液は、酢酸発酵しなかった。しかし、2倍希釈の酢酸発酵は、旺盛で高アミノ酸含有の食酢が得られた。   From Table 2, as a result of the deep acetic acid fermentation for 2 days, the fermentation stock solution did not undergo acetic acid fermentation. However, the 2-fold dilution of acetic acid fermentation gave a vigorous and high amino acid content vinegar.

生の鰹ミンチ1Kgに醤油麹1kgを混合して20%エタノール水溶液2.6リットルで仕込んだ後、15℃で1ヶ月間、さらに30℃で1ヶ月間酵素分解した後、圧搾して濾液(鰹発酵原液A)を得た。この鰹発酵原液Aを2倍水溶液に希釈してエタノール濃度を5%に調整したものに、酢酸菌(Acetobacter pasteurianus SKV1108)を添加して、32℃で2日間の深部酢酸発酵を実施した。

Figure 2007215421
Mix 1 kg of soy sauce koji with 1 kg of raw minced minced meat and charge it with 2.6 liters of 20% ethanol aqueous solution. Then, it is enzymatically decomposed at 15 ° C for 1 month and further at 30 ° C for 1 month, and then pressed and filtrated ( A fermentation broth stock solution A) was obtained. Acetic acid bacteria (Acetobacter pasteurianus SKV1108) was added to a solution obtained by diluting this koji fermentation undiluted solution A into a 2-fold aqueous solution to adjust the ethanol concentration to 5%, and a deep acetic acid fermentation was performed at 32 ° C. for 2 days.
Figure 2007215421

表3より、2日間の深部酢酸発酵の結果、2倍希釈液の酢酸発酵は、旺盛でアミノ酸高含有の飲用食酢が得られた。なお、鰹発酵原液Aには、酢酸菌は添加していない。   From Table 3, as a result of the deep acetic acid fermentation for 2 days, acetic acid fermentation of the 2-fold diluted solution was vigorous and a drinking vinegar with a high amino acid content was obtained. In addition, acetic acid bacteria are not added to the fermentation broth A.

生の鰹ミンチ1kgに20%エタノール水溶液1.3リットルを混合して仕込み、15℃で1ヶ月間、さらに30℃で1ヶ月自己消化酵素で分解した後、圧搾して得られた濾液(鰹発酵原液B)を水で2倍水溶液に希釈してエタノール濃度を5%に調整したものに、酢酸菌(Acetobacter pasteurianus SKV1108)を添加して、32℃で2日間の深部酢酸発酵を実施した。

Figure 2007215421
1 kg of raw minced mince mixed with 1.3 liters of 20% ethanol aqueous solution, decomposed with autolysis enzyme at 15 ° C. for 1 month and further at 30 ° C. for 1 month, and then squeezed into the filtrate (鰹Acetobacter pasteurianus SKV1108 was added to the fermentation stock solution B) diluted to a 2-fold aqueous solution with water to adjust the ethanol concentration to 5%, and deep acetic acid fermentation was performed at 32 ° C. for 2 days.
Figure 2007215421

表4より、2日間の深部酢酸発酵の結果、2倍希釈液の酢酸発酵は、旺盛でアミノ酸高含有の食酢が得られた。なお、鰹発酵原液Bには、酢酸菌は添加していない。   From Table 4, as a result of deep acetic acid fermentation for 2 days, acetic acid fermentation of the 2-fold diluted solution was vigorous, and vinegar with high amino acid content was obtained. In addition, acetic acid bacteria are not added to the fermentation broth B.

実施例1〜3で得られた本発明の食酢と市販されている健康酢の総アミノ酸量及びアミノ酸組成は次のとおりであった。なお、実施例1は深部酢酸発酵したものである。

Figure 2007215421
The total amino acid amount and amino acid composition of the vinegar of the present invention obtained in Examples 1 to 3 and the commercially available healthy vinegar were as follows. In addition, Example 1 is a deep acetic acid fermented product.
Figure 2007215421

表5より、本発明の食酢のアミノ酸量が市販されている健康酢のアミノ酸量に比べて桁違いに多いことが確認できた。   From Table 5, it has confirmed that the amino acid amount of the vinegar of this invention was many orders of magnitude compared with the amino acid amount of the healthy vinegar marketed.

次ぎに、市販の黒酢、もろみ酢と本発明の食酢の飲みやすさについて官能評価の比較を実施した。

Figure 2007215421
Next, the sensory evaluation was compared about the ease of drinking of commercially available black vinegar, moromi vinegar, and the vinegar of this invention.
Figure 2007215421

本発明によるアミノ酸含有量の多い食酢は、従来の食酢に比べて飲みやすい評価が得られた。   The vinegar with a high amino acid content according to the present invention was evaluated to be easier to drink than conventional vinegar.

Claims (1)

エチルアルコール水溶液の存在下で植物性蛋白質及び/又は動物性蛋白質にプロテアーゼ含有酵素類を接触させてアミノ酸に分解した溶液(アミノ酸発酵原液)をさらに酢酸発酵させることを特徴とする食酢及びその製造方法。   A method for producing vinegar and a method for producing the same, characterized by further subjecting a vegetable protein and / or animal protein to protease-containing enzymes in contact with a protease-containing enzyme in the presence of an ethyl alcohol aqueous solution to further decompose into amino acids (amino acid fermentation stock solution), followed by acetic acid fermentation .
JP2006036941A 2006-02-14 2006-02-14 Beverage vinegar Active JP4901235B2 (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010172198A (en) * 2009-01-27 2010-08-12 Ninben:Kk Method for producing seasoning
JP2011036157A (en) * 2009-08-07 2011-02-24 Q P Corp Method for producing enzyme-treated black vinegar and application of enzyme-treated black vinegar obtained by the method
KR101293499B1 (en) * 2011-06-03 2013-08-06 손호환 Producing method for fermentation vinegar from fish, and vinegar using it
JP2014512836A (en) * 2011-05-03 2014-05-29 アセタイア ジュゼッペ クレモニーニ エス.アール.エル. Beverage

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH048281A (en) * 1990-04-26 1992-01-13 Toshio Mizobuchi Production of acidic fermentation composition
JPH04311367A (en) * 1991-04-08 1992-11-04 Takeda Shokuhin Kogyo Kk Low salt fermented acidic seasoning
JPH08256754A (en) * 1995-03-23 1996-10-08 Saiseidou Yakuhin Kk Healthy vinegar and its production
JPH09154563A (en) * 1995-12-11 1997-06-17 Suya Shoten:Kk Soybean vinegar

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH048281A (en) * 1990-04-26 1992-01-13 Toshio Mizobuchi Production of acidic fermentation composition
JPH04311367A (en) * 1991-04-08 1992-11-04 Takeda Shokuhin Kogyo Kk Low salt fermented acidic seasoning
JPH08256754A (en) * 1995-03-23 1996-10-08 Saiseidou Yakuhin Kk Healthy vinegar and its production
JPH09154563A (en) * 1995-12-11 1997-06-17 Suya Shoten:Kk Soybean vinegar

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010172198A (en) * 2009-01-27 2010-08-12 Ninben:Kk Method for producing seasoning
JP2011036157A (en) * 2009-08-07 2011-02-24 Q P Corp Method for producing enzyme-treated black vinegar and application of enzyme-treated black vinegar obtained by the method
JP2014512836A (en) * 2011-05-03 2014-05-29 アセタイア ジュゼッペ クレモニーニ エス.アール.エル. Beverage
KR101293499B1 (en) * 2011-06-03 2013-08-06 손호환 Producing method for fermentation vinegar from fish, and vinegar using it

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