JPH0889230A - Production of sake - Google Patents

Production of sake

Info

Publication number
JPH0889230A
JPH0889230A JP25418894A JP25418894A JPH0889230A JP H0889230 A JPH0889230 A JP H0889230A JP 25418894 A JP25418894 A JP 25418894A JP 25418894 A JP25418894 A JP 25418894A JP H0889230 A JPH0889230 A JP H0889230A
Authority
JP
Japan
Prior art keywords
sake
rice
added
acid
ester hydrolase
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.)
Pending
Application number
JP25418894A
Other languages
Japanese (ja)
Inventor
Michio Harada
倫夫 原田
Shigemichi Okamura
成通 岡村
Tsunahiko Saegusa
維彦 三枝
Yoshihiko Endo
善彦 遠藤
Yoshimi Shimazu
善美 島津
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.)
Kikkoman Corp
Original Assignee
Kikkoman Corp
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 Kikkoman Corp filed Critical Kikkoman Corp
Priority to JP25418894A priority Critical patent/JPH0889230A/en
Publication of JPH0889230A publication Critical patent/JPH0889230A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE: To obtain SAKE(Japanese rice wine) containing a large amount of a flavoring component such as ferulic acid, its ethyl ester, vanillin or vanillic acid and having a mellow flavor by reacting a hydroxycinnamic ester hydrolase in a step for saccharifying, fermenting and aging unrefined SAKE for SAKE. CONSTITUTION: A hydroxycinnamic ester hydrolase in an amount of >=1 unit, preferably 3-100 units based on 1kg raw material rice is added and reacted in a step for saccharifying, fermenting and aging an unrefined SAKE for SAKE. Thereby, SAKE containing a relatively large amount of a flavoring ingredient having depth is obtained without using a specific yeast.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、清酒の製造法、特にフ
ェルラ酸、フェルラ酸エチルエステル、バニリン、バニ
リン酸等の芳醇な香味成分の豊かな清酒の製造法に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing sake, and more particularly to a method for producing sake with rich flavor components such as ferulic acid, ethyl ferulic acid, vanillin and vanillic acid.

【0002】[0002]

【従来の技術】従来、清酒の香味を改良するには、清酒
酵母701号と清酒酵母901号由来の一倍体株同士の
交雑により育種される芳香性の高い新規酵母菌を用いて
酢酸イソアミル及びカプロン酸エチルの多い、芳香性に
富んだ清酒を得る方法が知られている(特開平5−31
7034号公報参照)。また、イソアミルアルコ−ル、
酢酸イソアミル等の香味成分を多量に生成する変異酵母
を使用することを特徴とする清酒の製造法(特開昭62
−6669号公報参照)が知られている。
2. Description of the Related Art Conventionally, in order to improve the flavor of sake, isoamyl acetate having a high aromaticity has been used by using a novel yeast having high aromaticity bred by crossing haploid strains derived from sake yeast 701 and sake yeast 901. And a method of obtaining sake having a high aromatic content and containing a lot of ethyl caproate are known (Japanese Patent Laid-Open No. 5-31).
No. 7034). Also, isoamyl alcohol,
A method for producing sake characterized by using a mutant yeast which produces a large amount of a flavor component such as isoamyl acetate (Japanese Patent Laid-Open No. Sho 62-62).
No. 6669) is known.

【0003】[0003]

【発明が解決しようとする課題】しかしこれらの方法は
特殊な酵母を創生するのに高度な技術を必要とする欠点
を有する。
However, these methods have the drawback that they require sophisticated techniques to create specialized yeast.

【0004】従って、本発明は特殊な酵母を創生したり
することなく芳醇な香味を有する清酒を得ることを目的
とする。
Therefore, an object of the present invention is to obtain sake having a rich flavor without creating a special yeast.

【0005】[0005]

【課題を解決するための手段】本発明者らは、上記課題
を解決するため鋭意検討を重ねた結果、通常の清酒の醪
糖化発酵熟成工程において、ヒドロキシシナミック酸エ
ステル加水分解酵素を添加作用せしめるときは、フェル
ラ酸、フェルラ酸エチルエステル、バニリン、バニリン
酸等、重厚な香味成分の豊かな清酒が得られることを知
り、この知見に基ずいて本発明を完成した。即ち、本発
明は清酒の醪糖化発酵熟成工程において、ヒドロキシシ
ナミック酸エステル加水分解酵素を添加作用せしめるこ
とを特徴とする清酒の製造法である。
Means for Solving the Problems As a result of intensive studies to solve the above-mentioned problems, the present inventors have found that the action of adding hydroxycinamic acid ester hydrolase in the process of normal saccharification and fermentation of sake. Based on this finding, the present invention was completed based on the knowledge that when simmering, fermented acid, ferulic acid ethyl ester, vanillin, vanillic acid, and the like can be obtained. That is, the present invention is a method for producing sake, which comprises adding a hydroxycinamic acid ester hydrolase in the process of saccharification, fermentation and aging of sake.

【0006】以下本発明を詳細に説明する。先ず、本発
明でいう清酒の醪としては、通常の精白米を洗滌、浸漬
して膨潤させた後、常法により蒸きょうして蒸米を得、
これを一部麹とし、一部を掛米として水と共に仕込み、
これに酸及び清酒酵母を添加して、酸を含んだ糖液で該
酵母を淘汰的に培養して(もと発酵を行わせ)熟成酒母
を調製し、この酒母に麹、掛米、汲水の3者を3段階に
わたって仕込み(それぞれ初添、仲添、留添という)を
行い得た醪が挙げられる。なお、酒母に麹、掛米、汲水
の3者を4段階にわけて仕込みを行った醪でもよい。
The present invention will be described in detail below. First, as the sake liquor referred to in the present invention, normal polished rice is washed, soaked to swell, and then steamed by a conventional method to obtain steamed rice,
Part of this is koji, and part is rice with water,
An acid and sake yeast are added to this, and the yeast is selectively cultivated with a sugar solution containing acid (to be originally fermented) to prepare an aged sake mother. One example is the mash that has been able to prepare three people for water in three stages (each called Hatsuzo, Nakazoe, and Tomezo). It should be noted that the mash made from koji, rice, and water can be divided into four stages for the sake mother.

【0007】このようにして得られた醪は、通常の方法
により麹による糖化と酵母による酒精発酵とを並行して
営ませ、熟成醪とした後圧搾、濾過、火入れ等を行って
清酒を得る。
The mash thus obtained is subjected to saccharification with koji and liquor fermentation with yeast in parallel by an ordinary method, and then subjected to aging, squeezing, filtering, burning, etc. to obtain sake. .

【0008】本発明を実施するには、上記清酒の醪糖化
発酵熟成工程において、ヒドロキシシナミック酸エステ
ル加水分解酵素生産能を有するアスペルギルス属微生物
の培養物又はその処理物(本発明では、これらをまとめ
てヒドロキシシナミック酸エステル加水分解酵素と言
う)を添加作用せしめる。
In order to carry out the present invention, a culture of a microorganism of the genus Aspergillus or a processed product thereof having the ability to produce a hydroxycinamic acid ester hydrolase in the above-mentioned process of saccharification, fermentation and aging of sake (in the present invention, these are Collectively referred to as hydroxycinnamic acid ester hydrolase).

【0009】本発明に用いるヒドロキシシナミック酸エ
ステル加水分解酵素は、既に本発明者らが特開昭57−
99193号において詳細に開示したものであって、例
えばアスペルギルス・ヤポニカスATCC20236、
アスペルギルス・ニガ−IAM3002、アスペルギル
ス・サイトイATCC14332等の菌株を糸状菌の培
養に用いられる栄養培地を用い常法に従って固体培養ま
たは液体培養し得られた培養物をそのまま使用する。
The hydroxycinamic acid ester hydrolase used in the present invention has already been disclosed by the present inventors in JP-A-57-
No. 99193, which is disclosed in detail, for example, Aspergillus japonicas ATCC20236,
A culture obtained by subjecting strains such as Aspergillus niger-IAM3002 and Aspergillus cytoii ATCC14332 to solid culture or liquid culture according to a conventional method using a nutrient medium used for culture of filamentous fungi is used as it is.

【0010】あるいは、その固体培養物の水抽出液ある
いは液体培養物の濾液にセライトなどを添加し清澄濾過
して粗酵素液を得、この水抽出液または粗酵素液に硫安
等を添加するか(塩析法)またはアルコ−ルを添加する
か(有機溶媒沈殿法)して、沈殿物を得、これを集め真
空乾燥等して得られた粗酵素粉末を使用する。
Alternatively, celite or the like may be added to the water extract of the solid culture or the filtrate of the liquid culture and clarified by filtration to obtain a crude enzyme solution. Ammonium sulfate or the like may be added to the water extract or the crude enzyme solution. A crude enzyme powder obtained by (salting out method) or adding alcohol (organic solvent precipitation method) to obtain a precipitate, which is collected by vacuum drying and the like is used.

【0011】あるいは、上記粗酵素粉末を緩衝液等に溶
解後、DEAE−セファデックスA−50、QAE−セ
ファデックスA−50、またはCM−セファデックス等
のイオン交換セファデックスや、セファデックスG−2
00等のセファデックスを用いるゲル濾過法、アンフォ
ラインを用いる等電点分画法、アセテ−ト膜澱粉、アク
リルアマイドゲルを用いる電気泳動法、その他等電点沈
殿法等の個々の手段、またはこれらの適当な組合せを適
宜利用することによって、精製酵素を得、これを使用す
る(本発明では、上記粗酵素、精製酵素を「培養物の処
理物」という)。
Alternatively, after the crude enzyme powder is dissolved in a buffer solution or the like, an ion exchange Sephadex such as DEAE-Sephadex A-50, QAE-Sephadex A-50 or CM-Sephadex, or Sephadex G- is used. Two
Individual means such as gel filtration using Sephadex such as 00, isoelectric focusing using ampholine, electrophoresis using acetate membrane starch, acrylamide gel, and other isoelectric precipitation, or A purified enzyme is obtained by appropriately utilizing these appropriate combinations and is used (in the present invention, the above-mentioned crude enzyme and purified enzyme are referred to as "treated product of culture").

【0012】これらの微生物は下記Aの製麹方法条件で
製麹した場合の麹中のヒドロキシシナミック酸エステル
加水分解酵素活性が、下記Bの活性測定法において0.
5単位/g麹以上のヒドロキシシナミック酸エステル加
水分解酵素生産能を示す微生物を用いるときは、その培
養物中に該酵素を著量生成蓄積させることができるの
で、粗酵素あるいは精製酵素のような形態とする必要が
なくなり、そのまま添加作用させることができるので好
ましい。
[0012] These microorganisms have a hydroxycinnamic acid ester hydrolase activity in the koji of 0.
When using a microorganism having a hydroxycinamic acid ester hydrolase-producing ability of 5 units / g or more of koji, a large amount of the enzyme can be produced and accumulated in the culture, so that it may be used as a crude enzyme or a purified enzyme. It is preferable because it does not need to be in such a form and can be added and act as it is.

【0013】A 製麹方法条件 1リットル容フェルンバッハフラスコに80%撒水した
フスマを36gを投入し、120℃で1時間加圧殺菌
し、冷却後アスペルギルス属微生物を接種し、30℃で
72時間培養する。
A Method for making koji: 36 g of 80% sprinkled bran was put in a 1 liter Fernbach flask, sterilized under pressure at 120 ° C. for 1 hour, and after cooling, inoculated with Aspergillus microorganisms, and 72 at 30 ° C. Incubate for hours.

【0014】B ヒドロキシシナミック酸エステル加水
分解酵素活性測定法 アグリカルチュラルバイオロジカルケミストリ−46
巻、297頁(1982)により以下のようにして測定
する。0.05Mリン酸緩衝液(pH6.5)に市販の
クロロゲン酸(3−カフエオイルキナ酸)(東京化成工
業社製)を530mg/l濃度で溶解した。この溶液
0.5mlに同緩衝液に溶解した酵素溶液0.03ml
を添加し、30℃で反応させる。一定時間後に80%メ
タノ−ル水10mlを加えて反応を止め、350nmに
おける吸光度を測定する。上記方法において、「酵素溶
液」に代えて「該酵素溶液を70℃で分保持して酵素の
熱失活処理したもの」を用いる以外は全く同様にして吸
光度を測定し、ブランク値とした。活性は1分間に基質
1マイクロモルを加水分解することのできる酵素の量を
1単位(U)と定める。酵素活性は以下の式ににより求
めたものである。 t2−t1:反応時間(分) Et1 :t1時におけるOD値からブランク値を差引
いた値 Et2 :t2時におけるOD値からブランク値を差引
いた値
B Hydroxycinamic acid ester hydrolase activity assay method Agricultural biological chemistry-46
Vol., P. 297 (1982). Commercially available chlorogenic acid (3-caphoeoylquinic acid) (manufactured by Tokyo Kasei Kogyo Co., Ltd.) was dissolved in a 0.05 M phosphate buffer (pH 6.5) at a concentration of 530 mg / l. 0.03 ml of enzyme solution dissolved in the same buffer solution in 0.5 ml of this solution
Is added and reacted at 30 ° C. After a certain period of time, 10 ml of 80% methanol water was added to stop the reaction, and the absorbance at 350 nm was measured. In the above method, the absorbance was measured in exactly the same manner except that the "enzyme solution was heat-inactivated by holding the enzyme solution at 70 ° C for minutes" was used in place of the "enzyme solution" to give a blank value. The activity is defined as 1 unit (U) of the enzyme capable of hydrolyzing 1 micromol of the substrate in 1 minute. The enzyme activity is calculated by the following formula. t2-t1: Reaction time (min) Et1: Value obtained by subtracting blank value from OD value at t1 time Et2: Value obtained by subtracting blank value from OD value at t2 time

【0015】清酒醪糖化発酵熟成工程において添加作用
せしめる上記酵素は、形態、酵素の比活性、酵素を作用
せしめる方法等の相違により異なるが、出発原料である
原料米1Kg当たり、1単位以上、好ましくは3〜10
0単位使用することが好ましい。
The above-mentioned enzyme to be added and acted in the sake saccharification and fermentation aging step varies depending on the form, the specific activity of the enzyme, the method of making the enzyme act, etc., but it is preferably 1 unit or more per 1 kg of the starting rice rice. Is 3 to 10
It is preferred to use 0 units.

【0016】添加する時期は、醪糖化発酵熟成工程中の
任意の時期が挙げられるが、仕込み初期の醪、即ち、初
添、仲添あるいは留添時に添加すると、原料由来の遊離
のフェルラ酸を醪中に著量生成蓄積せしめることができ
るので好ましい。
The time of addition may be any time during the saccharification and fermentation ripening step, but if added during the initial stage of preparation, that is, during the initial addition, Nakazo or distillation, free ferulic acid derived from the raw material is added. It is preferable because a large amount can be produced and accumulated in the mash.

【0017】[0017]

【作用】このようにヒドロキシシナミック酸エステル加
水分解酵素を清酒醪糖化発酵熟成工程において添加使用
すると、該酵素が原料米に作用して、該原料由来の遊離
のフェルラ酸を醪中に生成蓄積せしめる。そして、この
フェルラ酸自身、甘い香りを有することが知られている
が、フェルラ酸の一部は分解してバニリン酸、バニリン
等の甘い香味を有する物質となるため、清酒の風味は次
第に良好になり、一方、フェルラ酸及びバニリン酸は清
酒中に存在するアルコ−ルと反応して、それぞれ重厚な
香味を有するフェルラ酸エチルエステル、バニリン酸エ
チルエステルとなる。
[Function] When a hydroxycinamic acid ester hydrolase is added and used in the sake saccharification and fermentation ripening process as described above, the enzyme acts on the raw material rice to produce and accumulate free ferulic acid derived from the raw material in the mash. Excuse me. And, it is known that this ferulic acid itself has a sweet fragrance, but part of the ferulic acid is decomposed into vanillic acid, a substance having a sweet flavor such as vanillin, so that the flavor of sake is gradually improved. On the other hand, ferulic acid and vanillic acid react with the alcohol present in sake to form ferulic acid ethyl ester and vanillic acid ethyl ester, each of which has a heavy flavor.

【0018】従って本発明によれば、それ自身重厚な甘
い香り、即ち芳醇な香味を有する清酒を得ることができ
る。
Therefore, according to the present invention, it is possible to obtain sake having a heavy sweet scent, that is, a rich flavor.

【0019】以下、実施例を示して本発明をより具体的
に説明する。なお、下記実施例において用いられるヒド
ロキシシナミック酸エステル加水分解酵素の高生産能を
有するアスペルギルス属微生物の培養物、及び該酵素の
粗酵素粉末は以下の方法により調製した。
Hereinafter, the present invention will be described more specifically by showing examples. The cultures of Aspergillus microorganisms having a high productivity of the hydroxycinamic acid ester hydrolase used in the following examples, and the crude enzyme powder of the enzyme were prepared by the following method.

【0020】(黒麹菌アスペルギルス・ヤポニカスAT
CC20236の菌株の培養物の調製)殺菌した扁平な
プラスチック製容器に、80%撒水したフスマを120
℃で1時間加圧殺菌し、冷却したものを入れ、これにア
スペルギルス・ヤポニカスATCC20236の菌株を
接種し、時々攪拌しながら30℃で72時間培養し、ヒ
ドロキシシナミック酸エステル加水分解酵素活性が、2
単位/g麹を示す固体培養物を得た。
(Aspergillus japonicas AT of Aspergillus niger
Preparation of culture of CC20236 strain) 120% sprinkled bran in a sterilized flat plastic container
After sterilizing under pressure for 1 hour at ℃, put what was cooled, inoculate the strain of Aspergillus japonicas ATCC20236 into this, and cultivate for 72 hours at 30 ℃ while stirring occasionally, hydroxycinamic acid ester hydrolase activity, Two
A solid culture showing units / g koji was obtained.

【0021】(ヒドロキシシナミック酸エステル加水分
解酵素の粗酵素粉末の調製)上記固体培養物に5重量倍
の水を添加し時々攪拌しながら室温で2時間放置し後搾
汁し、得られた濾液にセライトを添加し濾過して透明な
酵素液を得る。この酵素液を5℃に冷却し、これに同温
度に冷却したアルコ−ルを3容量倍添加し生成した沈殿
を集めて、20℃の低温下で真空乾燥して、粗酵素粉末
を得る。
(Preparation of Crude Enzyme Powder of Hydroxycinamic Acid Ester Hydrolase) 5 times by weight of water was added to the above solid culture and left for 2 hours at room temperature with occasional stirring to obtain juice. Celite is added to the filtrate and filtered to obtain a transparent enzyme solution. The enzyme solution was cooled to 5 ° C., and 3 volumes of alcohol cooled to the same temperature was added thereto, and the produced precipitates were collected and vacuum dried at a low temperature of 20 ° C. to obtain a crude enzyme powder.

【0022】[0022]

【実施例1】 (芳醇な風味を有する清酒の製造法) (1)米麹の調製 精白した粳米225gを常法により洗米、浸漬、水切り
し、蒸きょうした後放冷し、これに市販の清酒用種麹菌
を接種し、常法により製麹し、米麹を得た。 (2)蒸粳米の調製 精白した粳米450gを常法により洗米、浸漬、水切り
し、蒸きょうした後放冷して、蒸粳米を得た。 (3)酒母の調製 汲水700mlに上記米麹及び上記蒸粳米を混和し、こ
れに種酵母(2×108個/ml)及び乳酸(10倍希
釈液)をそれぞれ20ml、4mlを混和し、10〜1
5℃で15日間糖化発酵させ、酸を含んだ糖液で該酵母
を淘汰的に増殖して酒母を調製した。 (4)清酒の製造(初添) 上記の酒母1200mlに米麹400g(生米換算)、
蒸米950g(同)及び汲水1150mlを混和して、
これを48時間発酵させた。 (5)同(仲添) 上記初添醪に蒸米2075g(生米換算)、米麹625
g(同)及び汲水3250mlを混和して、これを24
時間発酵させた。 (6)同(留添) 上記仲添醪に、蒸米3450g(生米換算)、米麹82
5g(同)及び汲水6250mlを混和して、これを1
0ー15℃で20日間発酵熟成させ、常法により圧搾濾
過し、醪液汁(清酒)を得た。 (7)上記熟成醪の調製に際し留添時に本発明区1には
ヒドロキシシナミック酸エステル加水分解酵素の粗酵素
粉末50単位を、また本発明区2には同酵素100単位
を、そして対照区には同粗酵素粉末を添加することなく
そのまま放置した。 (8)このようにして得られた熟成醪から液汁を採取し
そのアルコ−ルと香気成分を分析し、また官能検査を行
なった。 (9)なお、醪液汁中のアルコ−ルは、国税庁所定分析
法により、また香気成分のフェルラ酸、バニリン及びバ
ニリン酸は、それぞれO.D.Sを分離用の樹脂(東ソ
−社製TSKgel・ODS−120T)とする高速液
体クロマトグラフィ−を用いて測定した。 (10)また、官能検査は識別能力を有する10名のパ
ネルにより、清酒の香味について、評点法により行い、
対照区のものに比べて、優れているを+2、やや優れて
いるを+1、差がないを0、やや劣るを−1、劣るを−
2と評価し、その平均値を示した。それらの結果をまと
めて表1に示す。
Example 1 (Manufacturing Method of Sake with Rich Flavor) (1) Preparation of Rice Koji 225 g of polished white rice was washed, dipped, drained, steamed and allowed to cool, and then commercially available. The rice koji was obtained by inoculating the seed koji mold for sake and making the koji by a conventional method. (2) Preparation of steamed rice 450 g of whitened steamed rice was washed, soaked, drained, steamed and allowed to cool by ordinary methods to obtain steamed rice. (3) Preparation of liquor Mother 700 ml of pumped water was mixed with the above rice koji and the above steamed rice, and 20 ml and 4 ml of seed yeast (2 × 10 8 cells / ml) and lactic acid (10-fold diluted solution) were mixed therein. , 10-1
Saccharification and fermentation was carried out at 5 ° C. for 15 days, and the yeast was selectively grown in a sugar solution containing an acid to prepare a liquor. (4) Manufacture of sake (first addition) To 1200 ml of the above-mentioned sake mother, 400 g of rice koji (raw rice equivalent),
Mix 950 g of steamed rice (same) and 1150 ml of pumped water,
This was fermented for 48 hours. (5) Same (Nakazoe) 2075 g of steamed rice (converted to raw rice), rice malt 625 in addition to Hatsuzou
g (the same) and 3250 ml of pumped water were mixed, and this was added to 24
Fermented for hours. (6) Same (Tozoe) In addition to Nakazoe, steamed rice 3450 g (raw rice equivalent), rice koji 82
5 g (same) and 6250 ml of pumped water are mixed, and this is 1
The mixture was fermented and aged at 0-15 ° C. for 20 days and squeezed and filtered by a conventional method to obtain a beer juice (sake). (7) When preparing the above-mentioned aged mash, at the time of distillation, 50 units of crude enzyme powder of hydroxycinamic acid ester hydrolase was added to the present invention group 1, 100 units of the same enzyme to the present invention group 2, and the control group. The crude enzyme powder was not added to the above, but allowed to stand. (8) A soup was sampled from the thus-obtained aged mash, the alcohol and aroma components thereof were analyzed, and a sensory test was conducted. (9) The alcohol in the liquid broth was analyzed by the National Tax Agency analysis method, and the aroma components ferulic acid, vanillin, and vanillic acid were treated with O. D. S was measured using high performance liquid chromatography using a resin for separation (TSKgel ODS-120T manufactured by Tosoh Corporation). (10) In addition, a sensory test is performed by a panel of 10 persons having discrimination ability, and the flavor of sake is evaluated by a scoring method.
Compared to the control group, +2 is excellent, +1 is slightly excellent, 0 is no difference, -1 is slightly inferior, -1 is inferior.
It was evaluated as 2, and the average value was shown. The results are summarized in Table 1.

【0023】 仕 込 配 合 酒母 初添 仲添 留添 合計 総米 675g 1350g 2700g 4275g 9000g 掛米 450g 950g 2075g 3450g 6925g 麹米 225g 400g 625g 825g 2075g 汲水 700ml 1150ml 3250ml 6250ml 11350ml 乳酸 4ml 酵母 20ml Ingredients Sake Mother Hatsuzou Nakazoe Tosekizo Total Total Rice 675g 1350g 2700g 4275g 9000g Kakemi 450g 950g 2075g 3450g 6925g Koji Rice 225g 400ml 625ml 825g 2075g 1 50ml 150ml 6 50ml 150ml 6

【0024】[0024]

【表1】 [Table 1]

【0025】実施例1の結果から、ヒドロキシシナミッ
ク酸エステル加水分解酵素を清酒の醪糖化発酵熟成に際
し添加使用すると、醪液汁中に、フェルラ酸エチルエス
テル、バニリン、バニリン酸の、重厚な香味成分が豊か
になり、風味良好な清酒が得られることが判る。
From the results of Example 1, when a hydroxycinnamic acid ester hydrolase was added and used during the saccharification and fermentation aging of sake, a heavy flavor component of ferulic acid ethyl ester, vanillin and vanillic acid was added to the beer juice. It can be seen that the sake is enriched and the sake with good flavor can be obtained.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 遠藤 善彦 千葉県野田市野田339番地 キッコーマン 株式会社内 (72)発明者 島津 善美 千葉県野田市野田339番地 キッコーマン 株式会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Yoshihiko Endo, 339 Noda, Noda, Chiba Prefecture, Kikkoman Corporation (72) Yoshimi Shimazu, 339, Noda, Noda, Chiba Prefecture, Kikkoman Corporation

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】清酒の醪糖化発酵熟成工程において、ヒド
ロキシシナミック酸エステル加水分解酵素を添加作用せ
しめることを特徴とする清酒の製造法。
1. A method for producing sake, which comprises adding a hydroxycinamic acid ester hydrolase in the step of saccharification, fermentation and aging of sake.
【請求項2】ヒドロキシシナミック酸エステル加水分解
酵素を原料米1kg当り1単位以上添加作用せしめる請
求項1に記載の清酒の製造法。
2. The method for producing sake according to claim 1, wherein 1 unit or more of hydroxycinamic acid ester hydrolase is added to 1 kg of the raw material rice.
JP25418894A 1994-09-26 1994-09-26 Production of sake Pending JPH0889230A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP25418894A JPH0889230A (en) 1994-09-26 1994-09-26 Production of sake

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP25418894A JPH0889230A (en) 1994-09-26 1994-09-26 Production of sake

Publications (1)

Publication Number Publication Date
JPH0889230A true JPH0889230A (en) 1996-04-09

Family

ID=17261466

Family Applications (1)

Application Number Title Priority Date Filing Date
JP25418894A Pending JPH0889230A (en) 1994-09-26 1994-09-26 Production of sake

Country Status (1)

Country Link
JP (1) JPH0889230A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006180809A (en) * 2004-12-28 2006-07-13 Asahi Breweries Ltd Method for producing liquors using liquid koji and solid koji in combination
JP2007195435A (en) * 2006-01-25 2007-08-09 Suntory Ltd Plum liquor having improved flavor and taste and method for producing the same
JP2007202504A (en) * 2006-02-03 2007-08-16 Takara Shuzo Co Ltd Method for producing alcoholic drink and seasoning
JP2015149972A (en) * 2014-02-19 2015-08-24 長谷川香料株式会社 Manufacturing method of enzyme treated plant extract

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006180809A (en) * 2004-12-28 2006-07-13 Asahi Breweries Ltd Method for producing liquors using liquid koji and solid koji in combination
JP2007195435A (en) * 2006-01-25 2007-08-09 Suntory Ltd Plum liquor having improved flavor and taste and method for producing the same
JP4585458B2 (en) * 2006-01-25 2010-11-24 サントリーホールディングス株式会社 Plum wine with improved flavor and taste and method for producing the same
JP2007202504A (en) * 2006-02-03 2007-08-16 Takara Shuzo Co Ltd Method for producing alcoholic drink and seasoning
JP4601071B2 (en) * 2006-02-03 2010-12-22 宝酒造株式会社 Method for producing alcoholic beverages and seasonings
JP2015149972A (en) * 2014-02-19 2015-08-24 長谷川香料株式会社 Manufacturing method of enzyme treated plant extract
WO2015125629A1 (en) * 2014-02-19 2015-08-27 長谷川香料株式会社 Method for producing enzymatically treated plant extract

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