JPS6149943B2 - - Google Patents

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Publication number
JPS6149943B2
JPS6149943B2 JP6232283A JP6232283A JPS6149943B2 JP S6149943 B2 JPS6149943 B2 JP S6149943B2 JP 6232283 A JP6232283 A JP 6232283A JP 6232283 A JP6232283 A JP 6232283A JP S6149943 B2 JPS6149943 B2 JP S6149943B2
Authority
JP
Japan
Prior art keywords
rhizopus
yeast
acid
pearl barley
culture solution
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
Application number
JP6232283A
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Japanese (ja)
Other versions
JPS59187773A (en
Inventor
Masahisa Takeda
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.)
KIKUNOKA SHUZO KK
Original Assignee
KIKUNOKA SHUZO KK
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Priority to JP58062322A priority Critical patent/JPS59187773A/en
Publication of JPS59187773A publication Critical patent/JPS59187773A/en
Publication of JPS6149943B2 publication Critical patent/JPS6149943B2/ja
Granted legal-status Critical Current

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Description

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

本発明は淡白な味と爽快な酸味を有するハトム
ギ酒の製造方法に関する。 ハトムギを原料とするハトムギ酒は、日本では
製造、販売されていないが、中国においては昔か
ら製造されている。ハトムギは熱帯アジア原産の
イネ科の一年草で〓苡仁(ヨクイニン)という。
ハトムギから醸造したハトムギ酒を〓苡仁酒また
は〓酒といつている。 中国での〓苡仁酒(以下、ハトムギ酒と称す
る。)の製造方法は、山崎百治著「東亜醗酵論
攻」(第1出版)によれば、酒薬、生ハトムギ
粉、蒸米(うるち白米)および水を混合して酵母
で醗酵させてつくるようにしている。ここで酒薬
は日本での麹に相当するが、日本でのカビが子の
う菌類のアスペルギルス・オリーゼ
(Aspergillus oryzae)群が主体をなすのに対
し、中国における酒薬のカビは藻菌類のリゾープ
ス(Rhizopus)属、ムコール(Mucor)属、ア
ブシデイア(Absidia)属等であり、通常これら
のカビ類が混在している。また酒薬は、桜井芳人
ら編、三訂総合食料工業、(恒星社厚生閣版)に
よれば、生のうるち白米と小麦ふすまおよび薬草
を水で混ぜて小さい塊を作り、暖いところに放置
して造つている。そして、酒薬に繁殖しているリ
ゾープス属のカビは、酸の生成が強く、ハトムギ
酒に酸味を付加する働きをしている。 また近年日本での清酒醸造においても、麹菌
(アスペルギルス属)の代りにリゾープス属で造
つた米麹(以下、酒薬および米麹を固体麹を総称
する)。を用いて高酸度の醸造酒が製造されてい
る。 しかしながら、上記従来の醸造酒においては、
酸味の付加が末だ充分でなく、また固体麹中に含
まれる蛋白解酵素や脂肪分解酵素により、原料中
に含まれる蛋白や脂肪が分解され、風味を害する
欠点があつた。 したがつて、本発明の目的は、酸の生成量を高
め、蛋白や脂肪の分解を抑えられるようにして、
淡白な味と爽快な酸味を有するハトムギ酒の製造
方法を提供するにある。 本発明者は、米等の穀類に水を加えて熱殺菌
し、この液体培地にリゾープス属に属する菌株を
接種して振盪または弾気培養すると、上記固体麹
よりも10〜20倍量の酸が生成され、かつこの液体
培養液においては酸素が失活していることを見出
し、本発明を完成するに至つた。 すなわち、本発明は、穀類を原料とした液体培
地にリゾープス属に属する菌株を接種して振盪ま
たは通気培養し、この培養液とハトムギ、酵素
剤、水を混合し、酵母を添加してアルコール醗酵
せしめることを特徴といるハトムギ酒の製造方法
である。 振盪(通気)培養で使用する穀類としては、玄
米、白米、米糖、押麦、玄小麦、ハトムギ等種々
のものが適用可能であるが、特に白米、白糖、押
麦が酸の生成量が多いので好ましい。これらの原
料に水を加えて加熱殺菌し、液体培地を作る。 本発明で使用する菌株は、酸生成量の高いリゾ
ープス属に属するものであればよく、例えばリゾ
ープス・ジヤパニカス(Rhizopus
javanicus055)、リゾープス・アルヒザス
(Rhizopus arrhizus059)、リゾープス・トンキ
ネンシス(Rhizopus tokinensis192)、リゾープ
ス・オリゴスポラス(Rhizobus
oligosporus058)、リゾープス・デレマ
(Rhizopus delemar056)等が挙げられる。 培養は振盪培養または通気培養を行い、培養温
度は、30℃前後が好ましく、培養時間は培養条件
によつても異るが、通常2〜4時間が適当であ
る。培養によつて穀類の原料は糖化されると共に
酸が生成される。この酸は主としてフマル酸また
は乳酸からなり、その他にリンゴ酸、コハク酸、
酢酸等も少量含まれているが、フマル酸の生成能
の強い菌株が好ましい。フマル酸は酵母の作用で
リンゴ酸に変化する。酸の生成量は従来の固体麹
の約10〜20倍量に達する。また培養液はカビ臭が
少く、糖、アミン酸も少く、爽快な酸味を呈する
のでそのまま醸造に利用することができる。 この培養液は酵母が失活しているので、しこみ
時に、糖化酵素を主体とした酵素剤を加える必要
がある。しかし他の酵素類例えば蛋白分解酵素や
脂肪分解酵素なども失活しているので、原料中の
蛋白や脂肪が分解されないため、製品の味は淡白
でさわやかな味を呈する。特に、ハトムギは、他
の穀類と異り風味に害のある脂肪を多く含むが、
本発明では上記のように脂肪の分解がなく、風味
に悪影響を与えない。 次に、この培養液に、蒸しハトムギ(糖白した
ハトムギを洗浄し浸漬後、常圧で約1時間蒸した
もの)と、水と、酵素剤とを加え、酵母を添加し
て醗酵させる。酵素剤としては、糖化酵素を主体
としたものが好ましく、例えばグルクSB(商品
名、天野製薬株式会社製)等が使用できる。ま
た、清酒醸造においては、酒母や初添で乳酸を添
加した腐造防止を行つているが、本発明において
は、リゾープス属の培養液中に酸が含まれるた
め、乳酸の添加を省略することができる。そし
て、前記した醗酵液中では、糖化酵素剤による澱
粉の糖化と、酵母による醗酵とが併行して行わ
れ、アルコールが生成される。醗酵温度は20℃前
後が適当であり、醗酵を開始してから15〜20日目
に上槽するのが好ましい。なお、蒸しハトムギ、
水および酵素剤は、従来より一次仕込み、二次仕
込みとして行われているように2〜3回に分けて
段階的に添加してもよい。このようにして熟成し
た醗酵液は、公知の方法で水圧圧搾機にかけて粕
と液とに分離し、さらに液をおりびきして清澄
化、60〜55℃にて加熱殺菌して製品とする。 こうしてできた製品は、アミノ酸が少く、リン
ゴ酸を主体とした酸を含むため、淡白な味と爽快
な酸味を有する酒となる。また、このハトムギ酒
は、リゾープス属による固体麹を用いて造つたハ
トムギ酒の風味とも異るが、その理由は、前述し
たように、固体麹を用いた場合には麹に含まれる
蛋白分解酵素や脂肪分解酵素による分解生成物、
特にハトムギに多い脂肪の分解生成物ができ、さ
らに麹自体の分解生成物もできるため、それらが
味と香りに影響を与えるのに対し、本発明による
振盪または通気培養液中では、ほとんどの酵素類
が失活しているので、酵素分解生成物による影響
が少いためと考えられる。 以上説明したように、本発明によれば、穀類を
主体とした液体培地にリゾープス属に属する菌株
を接種して振盪または液体培養をするので、酸が
多量に生成し、反面脂肪分解酵素や蛋白分解酵素
等が失活する。したがつてこの培養液を用いて醗
酵させることにより。ハトムギに多く含まれる脂
肪や蛋白の分解物の溶出を少くした淡白な味と、
多量の酸による爽快な酸味とを負荷した新しいタ
イプのハトムギ酒を製造することができる。また
本発明では、液体培地を用いるので、加熱殺菌し
易く、雑菌汚染を防止することができる。さら
に、リゾープス属による培養液中に多量が含まれ
るため、醗酵液中に汚染防止用の乳酸を添加する
必要がない。 以下、本発明の実施例を説明する。 実施例 1 肩付フラスコに第1表に原料と水とを加え、
110〜120℃、10〜15分間殺菌後、リゾープス・ジ
ヤパニカス(Rhizopus javanicus)を接種し
て、30℃にて3〜4日間振盪培養した。この培養
液中に成分を分析した結果を第1表に示す。な
お、第1表中、酸度は試験10mlに対する
0.1NNaOHによる中和量をmlで表示した値であ
り、アミノ酸度は試料10mlを中和し、ホルマリン
溶体を加えた後、0.1NNaOHの中和量をmlで表示
した値である。 実施例 2
The present invention relates to a method for producing pearl barley wine that has a light taste and refreshing sourness. Coix barley sake, which is made from coix barley, is not produced or sold in Japan, but it has been produced in China for a long time. Coix seed is an annual herb of the Poaceae family that is native to tropical Asia.
Coix barley wine brewed from pearl barley is called 〓茡人酒 or 〓sake. According to Hyakuji Yamazaki's ``Toa Hakko Rongo'' (1st edition), the manufacturing method for 〓茡仁酒 (hereinafter referred to as adlay wine) in China consists of alcoholic medicine, raw adlay flour, and steamed rice (Uruchi). It is made by mixing white rice (white rice) and water and fermenting it with yeast. Alcoholic medicine here corresponds to koji in Japan, but while the mold in Japan is mainly made up of the Aspergillus oryzae group, the mold used in alcoholic medicine in China is made up of algae. These include the genus Rhizopus, Mucor, and Absidia, and these molds are usually mixed together. In addition, alcoholic medicine is made by mixing raw non-glutinous white rice, wheat bran, and medicinal herbs with water to form small lumps, and then making a hot It is being built by leaving it somewhere. The mold of the Rhizopus genus that grows in alcoholic beverages is a strong acid generator, and has the function of adding sourness to pearl barley wine. In addition, in recent years in sake brewing in Japan, rice koji (liquor medicine and rice koji are collectively referred to as solid koji) has been produced using Rhizopus spp. instead of koji mold (Aspergillus spp.). A highly acidic brewed liquor is produced using this. However, in the above conventional brewed liquor,
The addition of sourness was not sufficient, and the proteolytic and lipolytic enzymes contained in the solid koji degraded the proteins and fats contained in the raw materials, resulting in poor flavor. Therefore, the purpose of the present invention is to increase the amount of acid produced and suppress the decomposition of proteins and fats.
To provide a method for producing pearl barley wine having a light taste and refreshing sourness. The present inventor has discovered that when grains such as rice are heat sterilized by adding water, and a strain belonging to the genus Rhizopus is inoculated into this liquid medium and shaken or blast cultured, the amount of acid is 10 to 20 times that of the solid koji. was produced and that oxygen was deactivated in this liquid culture solution, leading to the completion of the present invention. That is, in the present invention, a strain belonging to the genus Rhizopus is inoculated into a liquid medium made from grains, shaken or aerated, the culture solution is mixed with adlay, an enzyme agent, and water, yeast is added, and alcoholic fermentation is carried out. This is a method for producing pigeon barley sake that is characterized by the addition of rice wine. Various grains can be used for shaking (aeration) culture, such as brown rice, white rice, rice sugar, rolled barley, brown wheat, and adlay, but especially white rice, white sugar, and rolled barley produce a large amount of acid. preferable. Water is added to these raw materials and sterilized by heating to create a liquid medium. The strain used in the present invention may be any strain belonging to the genus Rhizopus that produces a high amount of acid, such as Rhizopus japanicus (Rhizopus
javanicus055), Rhizopus arrhizus059, Rhizopus tokinensis192, Rhizopus oligosporus
oligosporus058), Rhizopus delemar (Rhizopus delemar056), etc. The culture is carried out by shaking culture or aerated culture, and the culture temperature is preferably around 30°C, and the culture time varies depending on the culture conditions, but usually 2 to 4 hours is appropriate. Through cultivation, grain raw materials are saccharified and acids are produced. This acid mainly consists of fumaric acid or lactic acid, but also malic acid, succinic acid,
Although a small amount of acetic acid is also included, a strain with a strong ability to produce fumaric acid is preferred. Fumaric acid is converted to malic acid by the action of yeast. The amount of acid produced is about 10 to 20 times that of conventional solid koji. In addition, the culture solution has little mold odor, low sugar and amino acid content, and has a refreshing sour taste, so it can be used as is for brewing. Since the yeast in this culture solution is inactivated, it is necessary to add an enzyme agent mainly consisting of saccharifying enzymes at the time of straining. However, since other enzymes such as proteolytic enzymes and lipolytic enzymes are inactivated, the proteins and fats in the raw materials are not decomposed, so the product has a light and refreshing taste. In particular, pearl barley, unlike other grains, contains a lot of fat that is harmful to flavor.
In the present invention, as described above, there is no decomposition of fat, and the flavor is not adversely affected. Next, steamed pearl barley (white pearl barley washed and soaked, then steamed for about 1 hour at normal pressure), water, and an enzyme agent are added to this culture solution, and yeast is added for fermentation. The enzyme agent is preferably one based on a saccharifying enzyme, such as Gluk SB (trade name, manufactured by Amano Pharmaceutical Co., Ltd.). In addition, in sake brewing, lactic acid is added to the yeast base or the initial addition to prevent spoilage, but in the present invention, since acid is contained in the Rhizopus culture solution, the addition of lactic acid is omitted. I can do it. In the above-mentioned fermentation liquid, saccharification of starch by a saccharifying enzyme agent and fermentation by yeast are performed in parallel to produce alcohol. The appropriate fermentation temperature is around 20°C, and it is preferable to top the fermentation tank 15 to 20 days after starting the fermentation. In addition, steamed pearl barley,
Water and the enzyme agent may be added stepwise in 2 to 3 times, as has conventionally been done as a primary charge and a secondary charge. The fermented liquor thus aged is separated into lees and liquid by a known method using a hydraulic press, and the liquid is further drawn to clarify and heat sterilized at 60 to 55°C to produce a product. The product thus produced is low in amino acids and contains acids, mainly malic acid, resulting in alcoholic beverages with a light taste and refreshing sourness. In addition, the flavor of this Hatomugi sake is different from that of Hatomugi sake made using solid koji from the genus Rhizopus, and the reason for this is that, as mentioned above, when solid koji is used, the proteolytic enzymes contained in the koji and decomposition products by lipolytic enzymes,
In particular, decomposition products of fat, which is common in adlays, and decomposition products of koji itself are produced, which affect taste and aroma, whereas in the shaking or aerated culture medium of the present invention, most enzymes This is thought to be because the effects of enzymatic decomposition products are small because the enzymes are inactivated. As explained above, according to the present invention, a strain belonging to the genus Rhizopus is inoculated into a liquid medium mainly composed of grains, and shaken or liquid cultured. Degrading enzymes etc. are deactivated. Therefore, by fermenting using this culture solution. A light taste with less elution of fat and protein decomposition products that are abundant in pearl barley,
A new type of pearl barley wine loaded with refreshing sourness due to a large amount of acid can be produced. Furthermore, in the present invention, since a liquid medium is used, heat sterilization is easy and bacterial contamination can be prevented. Furthermore, since a large amount of Rhizopus is contained in the culture solution, there is no need to add lactic acid to the fermentation solution to prevent contamination. Examples of the present invention will be described below. Example 1 Add the raw materials and water listed in Table 1 to a shoulder flask,
After sterilization at 110-120°C for 10-15 minutes, Rhizopus javanicus was inoculated and cultured with shaking at 30°C for 3-4 days. Table 1 shows the results of analyzing the components in this culture solution. In addition, in Table 1, acidity is for 10ml of test.
The value is the amount of neutralization with 0.1N NaOH expressed in ml, and the amino acid content is the value expressed in ml of the amount of neutralization with 0.1N NaOH after neutralizing 10 ml of the sample and adding formalin solution. Example 2

【表】 上記仕込配合に示すように、ハトムギを原料と
した振盪培養液(第1表のNo.1)にハトムギ(精
白ハトムギを洗浄し、浸漬後、水切りして約1時
間常圧した。以下の実施例の一次、二次仕込に用
いるハトムギも同様である。)580gと、酵素剤
0.35gと、水80mlと、酵母とを仕込み、20℃にお
いて20日間醗酵させて上槽した。上槽後の成分分
析結果を第2表に示す。 実施例 3
[Table] As shown in the above-mentioned formulation, pearl barley (white pearl barley) was washed and immersed in a shaking culture solution made from pearl barley (No. 1 in Table 1), then drained and kept under normal pressure for about 1 hour. The same applies to the pearl barley used for the primary and secondary preparations in the following examples.) 580g and enzyme agent
0.35 g, 80 ml of water, and yeast were added, fermented at 20°C for 20 days, and then prepared in an upper tank. Table 2 shows the results of component analysis after the upper tank. Example 3

【表】 上記仕込配合に示すように、白糖を原料とした
振盪培養液(第1表のNo.2)にハトムギ604gと
酵素剤0.3gと水400ml及び酵母とを仕込み、20℃
にて20日間醗酵させた後、上槽した、上槽後の成
分分析結果を第2表に示す。 実施例 4
[Table] As shown in the above ingredients, 604 g of pearl barley, 0.3 g of enzyme agent, 400 ml of water, and yeast were added to a shaking culture solution made from white sugar (No. 2 in Table 1), and the mixture was heated to 20°C.
After fermentation for 20 days, the product was fermented in a tank. The results of the component analysis after the top tank are shown in Table 2. Example 4

【表】 上記仕込配合に示すように、白米を原料とした
振盪培養液(第1表のNo.3)にハトムギ604gと
酵素剤0.3gと水400ml及び酵母とを仕込み、20℃
にて20日間醗酵させて上槽した。上槽後の成分分
析結果を第2表に示す。 実施例 5
[Table] As shown in the above ingredients, 604 g of adlay, 0.3 g of enzyme agent, 400 ml of water, and yeast were added to a shaking culture solution made from polished rice (No. 3 in Table 1), and the mixture was heated to 20°C.
The mixture was fermented for 20 days in a tank. Table 2 shows the results of component analysis after the upper tank. Example 5

【表】 酵 母 少量
上記仕込配合に示すように、押麦を原料とした
振盪培養液(第1畢のNo.4)に、予めハトムギ
400gを蒸したものに温水600mlを加え酵素剤0.2
gを添加して55〜57℃で20日間糖化した醪と酵母
とを仕込み、28℃で3日間醗酵させ、さらに、二
次仕込みでハトムギ400gと水170mlと酵素剤0.2
gとを加え20℃で18日間醗酵させて上槽した。上
槽の成分分析結果第2表で示す。 以上、実施例1,2,3,4,5は本発明によ
るハトムギ酒の製造法である。 比較例
[Table] Yeast Small amount As shown in the above recipe, add pearl barley to the shaking culture solution (No. 4 in the first row) made from rolled barley.
Steam 400g and add 600ml of warm water to make enzyme agent 0.2
The moromi and yeast were saccharified for 20 days at 55-57℃ with the addition of 1.5g of the mixture, and then fermented for 3 days at 28℃.Furthermore, in the secondary preparation, 400g of pearl barley, 170ml of water, and 0.2ml of enzyme agent were added.
g was added and fermented at 20°C for 18 days, followed by an upper tank. Table 2 shows the results of component analysis of the upper tank. As described above, Examples 1, 2, 3, 4, and 5 are methods for producing pearl barley wine according to the present invention. Comparative example

【表】 上記仕込配合に示すように、ハトムギ固体麹を
用いたが、このハトムギ固体麹は蒸しハトムギに
リゾープス・ジヤパニカス(Rhizopus
Javanicus055)を接種し、30℃で2日間製麹した
ものである。一次仕込みで、このリゾープスのハ
トムギ固体麹80gと水200mlび酵母を仕込み28℃
にて2日間醗酵させた後、二次仕込みでハトムギ
220g、酵素剤0.09g、水220mlを加え、20℃で22
日間醗酵させた後、上槽した。上槽後の成分分析
結果を第2表に示す。 次に、実施例4と比較例について、それぞれの
有機酸含量を分析した。その結果を第3表に示
す。
[Table] As shown in the above-mentioned mixing ratio, solid adlay koji was used.
Javanicus 055) and made koji at 30℃ for 2 days. For the first preparation, add 80g of this Rhizopus pearl barley solid koji, 200ml of water, and yeast, and heat to 28℃.
After fermentation for 2 days in
Add 220 g, enzyme agent 0.09 g, and 220 ml of water, and heat at 20℃ for 22 hours.
After fermentation for one day, it was poured into an upper tank. Table 2 shows the results of component analysis after the upper tank. Next, the organic acid content of Example 4 and Comparative Example was analyzed. The results are shown in Table 3.

【表】【table】

【表】【table】

【表】 第2表から明らかなように、本発明によるハト
ムギ酒は、高い酸度を示し、アミノ酸度が少い。
また第3表から分るように、本発明によるハトム
ギ酒の有機酸は爽快な酸味を有するリンゴ酸とフ
マール酸が多い。 なお、実施例で使用した酵素剤は市販のグルク
SB(商品名、天野製薬株式会社製)であるが、
糖化酵素を体とした醸造用の酵素剤であれば、い
ずれの酵素剤でも使用可能である。また使用した
酵母はワイン酵母のサツカロミセス・セレビシエ
1F02300(Saccharomyces cerevisiae)である
が、醗酵力の強いサツカロミセス属例えばサツカ
ロミセス・サケ・キヨウカイNo.7
(Sacchanmyces sake kyokaiNo.7)でもよい。
実施例で振盪培養液の使用のみを記載したが通気
培養液でも同じ結果である。
[Table] As is clear from Table 2, the pearl barley wine according to the present invention exhibits high acidity and low amino acid content.
Further, as can be seen from Table 3, the organic acids in the pearl barley wine according to the present invention are mainly malic acid and fumaric acid, which have a refreshing sour taste. The enzyme used in the examples was commercially available glucose.
SB (trade name, manufactured by Amano Pharmaceutical Co., Ltd.),
Any enzyme agent for brewing containing saccharifying enzymes can be used. The yeast used was the wine yeast Satucharomyces cerevisiae.
1F02300 (Saccharomyces cerevisiae), but the Saccharomyces genus with strong fermentation power, such as Saccharomyces, Salmon, Kiyokai No. 7
(Sacchanmyces sake kyokai No.7) may also be used.
In the examples, only the use of a shaken culture solution was described, but the same results can be obtained using an aerated culture solution.

Claims (1)

【特許請求の範囲】[Claims] 1 穀類を原料とした液体培地にリゾープス属に
属する菌株を接種して振盪または通気培養し、こ
の培養液とハトムギ、酵素剤、水を混合し、酵母
を添加してアルコール醗酵せしめることを特徴と
するハトムギ酒の製造方法。
1. A strain belonging to the genus Rhizopus is inoculated into a liquid medium made from grains, shaken or aerated, cultured, this culture solution is mixed with adlay, an enzyme agent, and water, and yeast is added to carry out alcoholic fermentation. A method for producing pigeon barley sake.
JP58062322A 1983-04-11 1983-04-11 Preparation of adlay liquor Granted JPS59187773A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58062322A JPS59187773A (en) 1983-04-11 1983-04-11 Preparation of adlay liquor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58062322A JPS59187773A (en) 1983-04-11 1983-04-11 Preparation of adlay liquor

Publications (2)

Publication Number Publication Date
JPS59187773A JPS59187773A (en) 1984-10-24
JPS6149943B2 true JPS6149943B2 (en) 1986-10-31

Family

ID=13196785

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58062322A Granted JPS59187773A (en) 1983-04-11 1983-04-11 Preparation of adlay liquor

Country Status (1)

Country Link
JP (1) JPS59187773A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1049919C (en) * 1994-10-24 2000-03-01 北海道酒株式会社 Process for the production of novel beer-like sparkling alcoholic beverage
CN1101466C (en) * 1994-12-22 2003-02-12 北海道酒株式会社 Process for producing beer-like sparkling liquid
JP2009225685A (en) * 2008-03-19 2009-10-08 Kumamoto Technology & Industry Foundation Brewage using adlay as raw material and method for producing the same

Also Published As

Publication number Publication date
JPS59187773A (en) 1984-10-24

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