JPH0459875B2 - - Google Patents
Info
- Publication number
- JPH0459875B2 JPH0459875B2 JP60070069A JP7006985A JPH0459875B2 JP H0459875 B2 JPH0459875 B2 JP H0459875B2 JP 60070069 A JP60070069 A JP 60070069A JP 7006985 A JP7006985 A JP 7006985A JP H0459875 B2 JPH0459875 B2 JP H0459875B2
- Authority
- JP
- Japan
- Prior art keywords
- moromi
- vinegar
- aged
- acetic acid
- fermentation
- 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
Links
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 75
- 235000021419 vinegar Nutrition 0.000 claims description 40
- 239000000052 vinegar Substances 0.000 claims description 39
- 238000000855 fermentation Methods 0.000 claims description 33
- 230000004151 fermentation Effects 0.000 claims description 33
- 239000007788 liquid Substances 0.000 claims description 20
- 239000002994 raw material Substances 0.000 claims description 19
- 238000003825 pressing Methods 0.000 claims description 12
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims description 10
- 230000001476 alcoholic effect Effects 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 9
- 230000032683 aging Effects 0.000 claims description 7
- 238000001914 filtration Methods 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 102000004169 proteins and genes Human genes 0.000 claims description 6
- 108090000623 proteins and genes Proteins 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 3
- 238000000354 decomposition reaction Methods 0.000 claims description 2
- 230000002255 enzymatic effect Effects 0.000 claims description 2
- 235000019614 sour taste Nutrition 0.000 description 10
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 9
- 238000003756 stirring Methods 0.000 description 9
- 240000007594 Oryza sativa Species 0.000 description 8
- 235000007164 Oryza sativa Nutrition 0.000 description 8
- 235000009566 rice Nutrition 0.000 description 8
- 102000004190 Enzymes Human genes 0.000 description 7
- 108090000790 Enzymes Proteins 0.000 description 7
- 238000000034 method Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 235000018102 proteins Nutrition 0.000 description 5
- 240000008620 Fagopyrum esculentum Species 0.000 description 4
- 235000009419 Fagopyrum esculentum Nutrition 0.000 description 4
- 241000209140 Triticum Species 0.000 description 4
- 235000021307 Triticum Nutrition 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 4
- 235000013339 cereals Nutrition 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 235000013305 food Nutrition 0.000 description 4
- 210000000582 semen Anatomy 0.000 description 4
- 241000228212 Aspergillus Species 0.000 description 3
- 244000068988 Glycine max Species 0.000 description 3
- 235000010469 Glycine max Nutrition 0.000 description 3
- 239000005909 Kieselgur Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 235000005822 corn Nutrition 0.000 description 3
- 239000000796 flavoring agent Substances 0.000 description 3
- 235000019634 flavors Nutrition 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 108010068370 Glutens Proteins 0.000 description 2
- 244000062793 Sorghum vulgare Species 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 235000021312 gluten Nutrition 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 235000019713 millet Nutrition 0.000 description 2
- 230000001953 sensory effect Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 235000019640 taste Nutrition 0.000 description 2
- 102000013142 Amylases Human genes 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- 244000176051 Apios tuberosa Species 0.000 description 1
- 235000003276 Apios tuberosa Nutrition 0.000 description 1
- 241000193830 Bacillus <bacterium> Species 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 1
- 241000235527 Rhizopus Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000009754 Vitis X bourquina Nutrition 0.000 description 1
- 235000012333 Vitis X labruscana Nutrition 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 235000014787 Vitis vinifera Nutrition 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000010903 husk Substances 0.000 description 1
- 235000021374 legumes Nutrition 0.000 description 1
- 238000009630 liquid culture Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
Landscapes
- Distillation Of Fermentation Liquor, Processing Of Alcohols, Vinegar And Beer (AREA)
Description
〔産業上の利用分野〕
本発明は食酢の製造方法、詳しくは優れた香味
を有する食酢の製造方法に関する。
〔従来の技術〕
常法の食酢製造法においては種々の穀物、果実
等を用いた酢酸発酵調製醪または酢酸発酵調製液
を酢酸発酵させ、発酵終了後常温で熟成させるこ
とが知られている。しかし、これら従来の方法に
より作られる米酢、粕酢、ぶどう酢等の食酢は、
酸味、酸臭が強く感じられ、一般に酢が好まれな
い原因の1つとなつている。
〔発明が解決しようとする問題点〕
上述の様に、従来法で製造される食酢には特有
の酸味、酸臭があり、これが一般に酢が好まれな
い原因の1つであり、食酢の需要拡大を防げる大
きな要因となつている。
本発明は、この問題を解決したもので、優れた
香味を有し、酸味、酸臭を感じさせない食酢を製
造する方法を提供することを目的とするものであ
る。
〔問題点を解決するための手段〕
上記問題を解決するための手段である本発明
は、澱粉質原料または澱粉質原料と蛋白質原料を
酵素による分解と酵母による発酵を行つて得た酒
精発酵醪を圧搾および/または過し得られた酒
精含有液もしくはこれに必要に応じて酒精を加え
た酒精含有液に種酢と水を加え混合した酢酸発酵
調製液に、〓を20%(W/V)以下の範囲で添加
して酢酸発酵を行い、発酵終了後、この醪を二分
し、一方の醪は更に〓と種酢を加えて混合熟成さ
せ、他方の醪は70〜80℃で熟成させ、これらの熟
成醪を、圧搾または過してもしくは圧搾または
過することなく、混合し、熟成させることを特
徴そする食酢の製造方法である。
本発明において澱粉質原料としては、たとえば
米、小麦、大麦、コーン、高粱、粟などの穀類や
これらの副産物(例えばふすま)等様々のものを
単独でまたは組合せて用いることができる。
また、蛋白質原料としては、各種のものが用い
られ、たとえば大豆、豌豆などの豆類、その副産
物、小麦グルテン、コーングルテンなどを単独で
または組合せて使用することができる。
上記原料については、常法による処理、たとえ
ば原料組織の軟化、澱粉のα化、殺菌、磨砕等が
適宜行われる。
また、本発明に使用される酵素としては、各種
起源のものが使用でき、微生物由来のものが好適
で、具体的には澱粉質原料または澱粉質原料と蛋
白質原料とを分解する酵素を生産する微生物、た
とえば黄麹菌、黒麹菌、リゾプス属およびバチル
ス属の微生物の固体培養物(すなわち麹)または
液体培養物もしくはこれら培養物から常法によつ
て得た粗酵素や精製酵素が挙げられ、これらは単
独で、あるいは適宜組合せて用いることができ
る。
また、酵母は澱粉質原料または澱粉質原料料と
蛋白質原料を上記の酵素による分解したものを酒
精発酵させる場合に用いられ、この酵母として
は、醸造食品等の食品の製造に使用されているも
のを任意に使用でき、その具体例としてたとえば
清酒酵母、ビール酵母、ワイン酵母、パン酵母な
どが挙げられる。
本発明では、澱粉質原料または澱粉質原料と蛋
白質原料を酵素による分解と酵母による発酵を行
なつて得た酒精発酵醪を圧搾および/または過
して得られた酒精含有液もしくはこれに必要に応
じて酒精を加えた酒精含有液に種酢と水を加えて
調製した酢酸発酵調製液に、〓を20%(W/V)
以下の範囲、好ましくは5〜15%(W/V)の範
囲で添加して酢酸発酵を行う。
これに使用する〓は、小麦粉を製造する際に生
じる副産物であり、通常市販されているものを用
いても何らさしつかえなく、また使用時に蒸煮、
殺菌を行うことは必ずしも必要ではない。
また、酢酸発酵調製液に〓を添加する場合、同
時に他の穀類の副産物、例えばそばがら、粟が
ら、もみがらなどを〓と併用しても何らさしつか
えはない。
酢酸発酵の条件は常法の酢酸発酵の条件と同様
でよく、〓を加えたことにより、特別な条件を設
定する必要はない。
発酵終了後の醪を二分するにあたつては、特に
その割合に限定はないが、1:1〜1:2が適当
であり、どちらの醪を上記した2つの熟成手段の
いずれで熟成させてもよい。
そして発酵終了後、更に〓と種酢を添加する醪
の場合、特にその添加量は限定はないが、〓につ
いては、醪内に含まれる酢酸発酵液に酢酸発酵調
製液作成時に添加された〓量との合計が35%
(W/V)以下となる様に添加することが適当で
あり、種酢については、醪内に含まれる酢酸発酵
調製液量の1/2から等量までが適当である。この
醪は熟成後、そのまま他方の熟成醪またはこれを
圧搾もしくは過して得た圧搾液もしくは液に
混合してもよく、またこの醪を圧搾もしくは過
して圧搾液もしくは液を得、これを他方の熟成
醪またはこれを圧搾もしくは過して得た圧搾液
もしくは液と混合してもよい。
他方の醪は、熟成を、好ましくは密ぺい槽内
で、70〜80℃で行い、必要に応じて撹拌する。熟
成の時間には特に限定はないが、通常は1〜10日
間、好ましくは4〜6日間である。熟成終了後の
醪はそのまま一方の熟成醪またはこれを圧搾もし
くは過して得た圧搾液もしくは液と混合して
もよく、またこの醪を圧搾もしくは過して得た
圧搾液もしくは液を一方の熟成醪またはこれを
圧搾もしくは過して得た圧搾液もしくは液と
混合してもよい。
上記のように両者を混合し充分撹拌後、約1ケ
月間常温で熟成させ過を行い食酢を得る。
本発明によつて得られる食酢は、〓を添加して
酢酸発酵を行い、発酵終了後の醪を二分し、一方
の醪は更に〓と種酢を添加し熟成させ、他方の醪
は70〜80℃で熟成させ、これらの醪またはこの醪
を圧搾もしくは過して得た圧搾液もしくは液
を混合して再度熟成させているため、特有の酸
味、酸臭が感じられず、まろやかで優れた香味を
有する食酢である。
〔発明の効果〕
本発明によれば、下記試験例から認められるよ
うに、従来の食酢に特有の酸味、酸臭が感じられ
ない、まろやかな食酢が得られ、したがつて嗜好
上の制約が解消し、食酢の需要拡大が期待され
る。
試験例
後記する実施例1により得られた本発明製品で
ある食酢(酢酸濃度4.5%、以下、試料Aとい
う)、常法によつて得られた醸造粕酢(酢酸濃度
4.5%、以下、試料Bという)について習熟した
パネル20名により、酸味、酸臭に関し官能評価を
行つた。官能評価は2点識別試験法(「食品の品
質測定」−食品工学シリーズ、第15巻、40〜42頁、
1961年光琳書院発行)を用いて行い、酸味、酸臭
について弱いと思う方を選択し、有意差検定を行
つた。その結果を第1表に示す。
[Industrial Application Field] The present invention relates to a method for producing vinegar, and more particularly, to a method for producing vinegar having excellent flavor. [Prior Art] It is known that in the conventional vinegar production method, acetic acid fermentation prepared moromi or acetic acid fermentation prepared moromi using various grains, fruits, etc. is subjected to acetic acid fermentation, and after completion of fermentation, it is aged at room temperature. However, the vinegars made using these traditional methods, such as rice vinegar, lees vinegar, and grape vinegar, are
Vinegar has a strong sour taste and odor, which is one of the reasons why vinegar is generally not liked. [Problems to be solved by the invention] As mentioned above, vinegar produced by conventional methods has a unique sour taste and odor, and this is one of the reasons why vinegar is not generally liked, and the demand for vinegar has increased. This is a major factor in preventing the spread. The present invention solves this problem and aims to provide a method for producing vinegar that has excellent flavor and does not give a sour taste or odor. [Means for Solving the Problems] The present invention, which is a means for solving the above-mentioned problems, provides a fermented sake mash obtained by decomposing starchy raw materials or starchy raw materials and protein raw materials with enzymes and fermenting with yeast. 20% (W/V ) Add in the following range to carry out acetic acid fermentation. After fermentation, divide this moromi into two. One moromi is further mixed and aged with 〓 and seed vinegar, and the other moromi is aged at 70-80℃. This method of producing vinegar is characterized by mixing and aging these aged moromi, either by pressing or filtering, or without pressing or filtering. In the present invention, various starchy raw materials can be used alone or in combination, such as grains such as rice, wheat, barley, corn, corn, millet, and their by-products (eg, bran). In addition, various types of protein raw materials can be used, such as legumes such as soybeans and potato beans, by-products thereof, wheat gluten, corn gluten, etc., alone or in combination. The above-mentioned raw materials are appropriately subjected to conventional treatments such as softening of the raw material structure, gelatinization of starch, sterilization, and grinding. In addition, the enzymes used in the present invention can be of various origins, and those derived from microorganisms are preferred. Specifically, enzymes used to produce enzymes that decompose starchy raw materials or starchy raw materials and protein raw materials are used. Examples include solid cultures (i.e., koji) or liquid cultures of microorganisms of the genus Aspergillus yellow, Aspergillus aspergillus, Rhizopus, and Bacillus, as well as crude enzymes and purified enzymes obtained from these cultures by conventional methods. can be used alone or in appropriate combination. In addition, yeast is used for alcoholic fermentation of starchy raw materials or starchy raw materials and protein raw materials decomposed by the enzymes mentioned above, and this yeast is used in the production of foods such as brewed foods. Any yeast can be used, and specific examples thereof include sake yeast, beer yeast, wine yeast, and baker's yeast. In the present invention, an alcohol-containing liquid obtained by squeezing and/or filtering an alcoholic fermented mash obtained by decomposing a starchy raw material or a starchy raw material and a protein raw material by enzymatic decomposition and fermentation by yeast, or an alcoholic liquor necessary for this, is used. Add 20% (W/V) of 〓 to the acetic acid fermentation preparation liquid prepared by adding seed vinegar and water to the alcoholic liquid containing alcoholic spirit.
Acetic acid fermentation is performed by adding in the following range, preferably in the range of 5 to 15% (W/V). The 〓 used for this is a by-product produced during the production of flour, and there is no problem even if you use a commercially available one.
It is not always necessary to sterilize. Furthermore, when adding 〓 to the acetic acid fermentation preparation, there is no problem in using other grain by-products, such as buckwheat hulls, millet hulls, and rice husks, in combination with 〓 at the same time. The conditions for acetic acid fermentation may be the same as those for conventional acetic acid fermentation, and by adding 〓, there is no need to set any special conditions. When dividing the moromi after fermentation into two parts, there is no particular limitation on the ratio, but a ratio of 1:1 to 1:2 is appropriate, and which moromi should be aged by either of the two aging methods mentioned above. It's okay. In the case of moromi in which 〓 and seed vinegar are added after fermentation, there is no particular limitation on the amount of addition, but 〓 is added to the acetic acid fermentation liquid contained in the moromi when preparing the acetic acid fermentation preparation liquid. Total with quantity is 35%
(W/V) It is appropriate to add the seed vinegar in an amount of 1/2 to the same amount as the amount of the acetic acid fermentation preparation liquid contained in the moromi. After maturing, this moromi may be mixed as it is with another aged moromi or a squeezed liquor or liquid obtained by pressing or passing this, or by pressing or passing this moromi to obtain a pressed liquor or liquid, and then It may be mixed with the other aged moromi or a squeezed liquor or liquid obtained by pressing or filtering it. The other moromi is aged, preferably in a tightly sealed tank, at 70 to 80°C, and stirred as necessary. The aging time is not particularly limited, but is usually 1 to 10 days, preferably 4 to 6 days. The moromi after aging may be mixed with one of the aged moromi or the squeezed liquor or liquor obtained by pressing or passing this moromi, or the pressed liquor or liquor obtained by pressing or passing this moromi may be mixed with one of the aged moromi. It may be mixed with aged moromi or a squeezed liquor or liquid obtained by pressing or filtering this. After mixing the two and stirring thoroughly as described above, the mixture is aged and filtered at room temperature for about one month to obtain vinegar. Vinegar obtained by the present invention is obtained by adding 〓 to carry out acetic acid fermentation, dividing the moromi after fermentation into two parts, adding 〓 and seed vinegar to mature the other moromi, and leaving the other moromi at a temperature of 70 to 70%. The moromi is aged at 80℃, and the moromi, or the squeezed liquid or liquid obtained by pressing or filtering this moromi, is mixed and aged again, so there is no characteristic sour taste or sour odor, and it has a mellow and excellent taste. It is a vinegar with flavor. [Effects of the Invention] According to the present invention, as can be seen from the test examples below, it is possible to obtain mild vinegar that does not have the sour taste and sour odor characteristic of conventional vinegar, and therefore has no restrictions on taste. The situation is expected to be resolved, and demand for vinegar is expected to increase. Test Example Vinegar (acetic acid concentration 4.5%, hereinafter referred to as sample A), which is a product of the present invention obtained in Example 1 described later, and brewed lees vinegar obtained by a conventional method (acetic acid concentration
4.5% (hereinafter referred to as sample B)), a sensory evaluation of sour taste and sour odor was conducted by a panel of 20 experts. Sensory evaluation is carried out using the two-point discrimination test method ("Food quality measurement" - Food Engineering Series, Vol. 15, pp. 40-42,
(Published by Korin Shoin in 1961), and selected those that were considered to be weak in sour taste and sour odor, and conducted a significant difference test. The results are shown in Table 1.
次に本発明の実施例を示すが、本発明はこれに
より制限されるものではない。
実施例 1
小麦100Kgと米100Kgを混合し、120℃で45分間
蒸煮し、これに常法に従つて製麹された米麹160
Kgと温水を加え1000とした後、55〜60℃で24時
間糖化した。これに酒母10を添加混合し、5日
間30℃で酒精発酵を行い、得られた醪を圧搾して
エタノール濃度13%の酒精液を得た。
この酒精液250と種酢500に水を加えて1000
とし、〓100Kgを添加して充分撹拌後、30℃で
30日間酢酸発酵を行つた。
この醪を二等分し、一方の醪には〓50Kgと種酢
500を添加して充分撹拌し、常温で1ケ月熟成
させた後、醪を過し液を得た。
残りの醪は70℃で6日間、密ぺい槽内で1回/
日撹拌しながら熟成させた。熟成終了後の醪に、
上記の液を加え、充分撹拌した後、常温で1ケ
月間熟成し、この醪を過し、さらにケイソウ土
過し、殺菌し、ビン詰して酢酸濃度4.5%の酸
味、酸臭の感じられない食酢を得た。
実施例 2
ソバ粒180Kgを冷水に20〜24時間浸漬後、100℃
で60分間蒸煮したものに、常法通り製麹されたソ
粒麹180Kgを混合し、水を加えて1000とし、こ
れに酒母10を加え混合して5日間30℃で平行複
発酵を行つた。得られた醪を圧搾してエタノール
濃度9%のソバ酒を得た。このソバ酒300に種
酢500を加え、水で1000とした後、〓100Kgと
もみがら20Kgを添加し、充分撹拌したのち、30℃
で30日間酢酸発酵を行つて酢酸発酵醪1200を得
た。
発酵終了後の醪の内400に対して〓30Kgと種
酢150を添加し、充分撹拌し、常温で1ケ月間
熟成させた後、この醪を圧搾して圧搾液を得た。
残りの発酵終了の醪800を75℃で4日間、密
ぺい槽内で1回/日撹拌しながら熟成させた。熟
成終了後の醪に上記の圧搾液を加え、充分撹拌し
た後、1ケ月間常温で熟成させ、この醪を過
し、常法に従いケイソウ土過、殺菌、ビン詰を
行なつて酢酸濃度5.0%の、酸味、酸臭の感じら
れないきわめて高品質の食酢を得た。
実施例 3
脱脂大豆150Kgと小麦粉150Kgに、アスペルギル
ス・ソーヤIFO4239を使用して固体麹をつくり、
この麹100Kgと、米200Kgを一夜冷水に浸漬後、
100℃で60分間蒸煮したものとを混合し、水を加
えて1000とした。この醪に市販のアミラーゼ酵
素剤0.5Kgとプロテアーゼ酵素剤0.9Kgを添加して
充分混合して57℃で18時間糖化した後、酒母10
を添加混合し、4日間30℃で酒精発酵を行い、得
られた醪を圧搾してエタノール濃度9.5%の酒精
液を得た。
この酒精液300に種酢540を加え水で1000
とした後、〓75Kgを添加し、充分撹拌したのち、
30℃で30日間酢酸発酵を行つて酢酸発酵醪1100
を得た。
発酵終了後の醪の内、500に対して〓50Kgと
種酢400を添加し、充分撹拌し、常温で1ケ月
間熟成させた後、この醪を過して液を得た。
残りの発酵終了後の醪600を80℃で5日間、
密ぺい槽内で1回/日撹拌しながら熟成させた。
熟成終了後の醪に上記の液を加え、充分撹拌し
た後、1ケ月間常温で熟成させ、この醪を過
し、常法に従いケイソウ土過、殺菌、ビン詰を
して酢酸濃度5.0%の酸味、酸臭の感じられない
食酢を得た。
Next, examples of the present invention will be shown, but the present invention is not limited thereto. Example 1 100 kg of wheat and 100 kg of rice were mixed and steamed at 120°C for 45 minutes, and 160 kg of rice malt was made using the conventional method.
Kg and warm water were added to bring the concentration to 1000, and the mixture was saccharified at 55 to 60°C for 24 hours. Sake mash 10 was added and mixed, alcoholic fermentation was carried out at 30°C for 5 days, and the resulting moromi was pressed to obtain sake semen with an ethanol concentration of 13%. Add water to this sake semen 250 and seed vinegar 500 to make 1000.
After adding 100 kg and stirring thoroughly, it was heated to 30℃.
Acetic acid fermentation was carried out for 30 days. Divide this moromi into two equal parts, and one half contains 50 kg and vinegar seeds.
500 was added, thoroughly stirred, and aged at room temperature for one month, the moromi was filtered to obtain a liquid. The remaining moromi was heated once in a tightly sealed tank for 6 days at 70℃.
The mixture was aged with stirring for days. In the moromi after aging,
After adding the above liquid and stirring thoroughly, it is aged for one month at room temperature, the moromi is filtered, further filtered through diatomaceous earth, sterilized, and bottled to produce a sour taste and sour odor with an acetic acid concentration of 4.5%. Got no vinegar. Example 2 180 kg of buckwheat grains were soaked in cold water for 20 to 24 hours and then heated to 100°C.
After steaming for 60 minutes, 180 kg of so-grain koji made in the usual manner was mixed, water was added to make a total of 1000, 10 shubo was added to this, mixed, and parallel multiple fermentation was carried out at 30℃ for 5 days. . The resulting moromi was pressed to obtain buckwheat liquor with an ethanol concentration of 9%. Add 500 parts of vinegar to this buckwheat sake, make 1,000 parts of vinegar with water, add 100 kg of rice hulls and 20 kg of rice hulls, stir thoroughly, and hold at 30°C.
Acetic acid fermentation was carried out for 30 days to obtain acetic acid fermented mash 1200 g. After fermentation, 30kg and 150kg of vinegar were added to 400ml of the fermented moromi, thoroughly stirred, and aged at room temperature for one month.The moromi was then pressed to obtain a pressed liquid. The remaining fermented moromi 800 was aged at 75°C for 4 days in a tightly sealed tank with stirring once a day. The above-mentioned pressing liquid was added to the moromi after ripening, stirred thoroughly, and then aged at room temperature for one month. The moromi was filtered, filtered with diatomaceous earth, sterilized, and bottled according to the usual method to obtain an acetic acid concentration of 5.0. % of extremely high quality vinegar with no sour taste or sour odor was obtained. Example 3 Solid koji was made using Aspergillus soya IFO4239 with 150 kg of defatted soybeans and 150 kg of wheat flour.
After soaking 100kg of this koji and 200kg of rice in cold water overnight,
The mixture was steamed at 100°C for 60 minutes, and water was added to bring the temperature to 1000. To this moromi, 0.5 kg of commercially available amylase enzyme and 0.9 kg of protease enzyme were added, thoroughly mixed, and saccharified at 57℃ for 18 hours.
were added and mixed, and alcoholic fermentation was performed at 30°C for 4 days, and the resulting moromi was pressed to obtain alcoholic semen with an ethanol concentration of 9.5%. Add 540% of seed vinegar to this sake semen 300% and add 1000% of water.
After that, add 〓75Kg and stir well,
Perform acetic acid fermentation at 30℃ for 30 days to make acetic acid fermented mash 1100
I got it. After fermentation, 50 kg of the mash and 400 g of vinegar were added to the mash, thoroughly stirred, and aged at room temperature for one month.The mash was filtered to obtain a liquid. The remaining 600 mash after fermentation was heated at 80℃ for 5 days.
The mixture was aged in a tightly sealed tank with stirring once a day.
After aging, add the above liquid to the moromi, stir thoroughly, and age at room temperature for one month.The moromi is filtered, filtered with diatomaceous earth, sterilized, and bottled according to the usual method to obtain an acetic acid concentration of 5.0%. Vinegar with no sour taste or odor was obtained.
Claims (1)
酵素による分解と酵母による発酵を行つて得た酒
精発酵醪を圧搾および/または過して得られた
酒精含有液もしくはこれに必要に応じて酒精を加
えた酒精含有液に種酢と水を加え混合した酢酸発
酵調製液に、〓を20%(W/V)以下の範囲で添
加し、酢酸発酵を行い、発酵終了後、この醪を二
分し、一方の醪は更に〓と種酢を加えて混合熟成
させ、他方の醪は70〜80℃で熟成させ、これらの
熟成醪を、圧搾または過してもしくは圧搾また
は過することなく、混合し、熟成させることを
特徴とする食酢の製造方法。1 Alcohol-containing liquid obtained by squeezing and/or filtering the fermented alcoholic moromi obtained by decomposing starchy raw materials or starchy raw materials and protein raw materials by enzymatic decomposition and fermentation by yeast, or adding alcoholic spirit to this as necessary. Add 〓 to the acetic acid fermentation preparation solution made by adding and mixing seed vinegar and water to the alcohol-containing liquid to carry out acetic acid fermentation in a range of 20% (W/V) or less. After fermentation is complete, this moromi is divided into two. , one moromi is further mixed and aged with 〓 and vinegar seeds, and the other moromi is aged at 70 to 80℃, and these aged moromi are mixed by pressing or straining or without pressing or straining. , a method for producing table vinegar characterized by aging it.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60070069A JPS61231991A (en) | 1985-04-04 | 1985-04-04 | Production of edible vinegar |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60070069A JPS61231991A (en) | 1985-04-04 | 1985-04-04 | Production of edible vinegar |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61231991A JPS61231991A (en) | 1986-10-16 |
| JPH0459875B2 true JPH0459875B2 (en) | 1992-09-24 |
Family
ID=13420878
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60070069A Granted JPS61231991A (en) | 1985-04-04 | 1985-04-04 | Production of edible vinegar |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61231991A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103497884B (en) * | 2013-09-28 | 2014-08-13 | 吉林农业大学 | Efficient and clean brewing method of corn vinegar |
-
1985
- 1985-04-04 JP JP60070069A patent/JPS61231991A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61231991A (en) | 1986-10-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |