JPH0420592B2 - - Google Patents
Info
- Publication number
- JPH0420592B2 JPH0420592B2 JP30833787A JP30833787A JPH0420592B2 JP H0420592 B2 JPH0420592 B2 JP H0420592B2 JP 30833787 A JP30833787 A JP 30833787A JP 30833787 A JP30833787 A JP 30833787A JP H0420592 B2 JPH0420592 B2 JP H0420592B2
- Authority
- JP
- Japan
- Prior art keywords
- koji
- ratio
- fermentation
- sake
- reduction
- 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
- 240000006439 Aspergillus oryzae Species 0.000 claims description 7
- 235000002247 Aspergillus oryzae Nutrition 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 5
- 238000009630 liquid culture Methods 0.000 claims description 3
- 239000004570 mortar (masonry) Substances 0.000 claims description 2
- 238000000855 fermentation Methods 0.000 description 8
- 230000004151 fermentation Effects 0.000 description 8
- 108090000790 Enzymes Proteins 0.000 description 6
- 102000004190 Enzymes Human genes 0.000 description 6
- 229940088598 enzyme Drugs 0.000 description 6
- 240000007594 Oryza sativa Species 0.000 description 5
- 235000007164 Oryza sativa Nutrition 0.000 description 5
- 235000009566 rice Nutrition 0.000 description 4
- 108010073178 Glucan 1,4-alpha-Glucosidase Proteins 0.000 description 3
- 102100022624 Glucoamylase Human genes 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 229940088594 vitamin Drugs 0.000 description 3
- 239000011782 vitamin Substances 0.000 description 3
- 235000013343 vitamin Nutrition 0.000 description 3
- 229930003231 vitamin Natural products 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- 108091005804 Peptidases Proteins 0.000 description 2
- 239000004365 Protease Substances 0.000 description 2
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 2
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 2
- 238000012258 culturing Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000004382 Amylase Substances 0.000 description 1
- 102000013142 Amylases Human genes 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- SQUHHTBVTRBESD-UHFFFAOYSA-N Hexa-Ac-myo-Inositol Natural products CC(=O)OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O SQUHHTBVTRBESD-UHFFFAOYSA-N 0.000 description 1
- 235000007189 Oryza longistaminata Nutrition 0.000 description 1
- 102000016202 Proteolipids Human genes 0.000 description 1
- 108010010974 Proteolipids Proteins 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000005273 aeration Methods 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 235000019418 amylase Nutrition 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- FAPWYRCQGJNNSJ-UBKPKTQASA-L calcium D-pantothenic acid Chemical compound [Ca+2].OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O.OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O FAPWYRCQGJNNSJ-UBKPKTQASA-L 0.000 description 1
- 229960002079 calcium pantothenate Drugs 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 229940079919 digestives enzyme preparation Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 229960000367 inositol Drugs 0.000 description 1
- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 235000012149 noodles Nutrition 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
Landscapes
- Alcoholic Beverages (AREA)
Description
[産業上の利用分野]
本発明は、清酒醸造における麹歩合の低減を目
的とし、その際に不足する麹由来の持込み成分
を、液体培養により得られた麹菌体を加えること
により補い、醗酵経過も従来と大差のない清酒を
醸造するための麹歩合の低減法に関する。
[発明の技術的背景とその課題]
多大なる労力、および、経費を要する製麹プロ
セスにおいて麹歩合を低減することは、麹の生産
量を減少し得ることになり、製麹プロセスの省力
化、および、低コスト化に大きく貢献する。ま
た、醪中で溶解しにくい麹米の量を減少させ得る
ことにもつながり、原料利用率、あるいは、酒化
率の向上をも生みだし、製造コストの低減化をも
たらすなど、極めて大きな利点を有するものであ
ると考えられる。しかし一方、清酒醸造における
麹の最も重要な役割は、アミラーゼ、および、プ
ロテアーゼなどの加水分解酵素を供給することで
あり、醗酵とバランスのとれた蒸米の溶解に必要
な酵素量を補うには、通常約20%の麹歩合が必要
であつた。また、麹の持つもう一つの意義は、そ
の持込み成分にあり、酵母が順調に増殖醗酵する
ためや、清酒独特の味や香りを生成するためには
必須のものである。従つて、麹歩合を低減するほ
ど、醗酵と溶解のバランスが崩れ、酒質も悪影響
を被る。特に、麹歩合を約10%以下に減らした場
合には、各種酵素剤を充分補添しても醗酵が顕著
に遅れだし、エステルなどの香気成分も著るしく
減少し、明らかに官能的にも有意差が認められて
くる。これは先に述べたように、麹菌体由来の持
込み成分の欠乏によるものである。
[課題を解決するための手段]
従来技術の課題を解決する本発明の構造は、清
酒醸造に際して麹歩合を低減するとともに、この
麹歩合の低減により不足する麹由来の持込み成分
として、液体培養により得られた麹菌体を醪に添
加するものである。
[発明の作用]
このように本発明によれば、麹エキスや麹の水
抽出液、あるいは、ビタミン混液などを加えれ
ば、この現象は改善させることが確認できた。ま
た、この事実は、酵素剤仕込みの際に、イノシト
ール、パントテン酸カルシウムなどのビタミン混
液を加えれば、醗酵の遅れが回復するとの報告か
らも裏付けられる。以上のようなことから、約10
%以下の麹歩合の低減を望めば、麹由来の持込み
成分を添加する必要があることは明らかである。
しかし、麹の持込み成分として考えられる物質は
かなり複雑であると考えられ、単にビタンミン類
だけでなく、脂肪酸やプロテオリピツドなど多種
多様の麹の代謝産物が、酵母の増殖醗酵や微妙な
清酒の味や香りに影響しているものと考えられ
る。このような観点から、麺由来の持込み成分の
代用となり得るものは、麹菌体そのものしかない
ことが、幾多の実験の結果が得られた。尚、培養
後分離した麹菌体は、真空乾燥、あるいは、通常
乾燥すれば、長期保存が可能である。
[実施例]
蒸留水100mlに炭素源として粉砕白米2g、ま
た、窒素源として赤糠1gを加え、120℃で15分
間殺菌したものを培地として、これに麹菌、例え
ば、Asp・oryzae(RIB 647)の胞子を1白金耳
植菌し、30℃、撹拌速度200r.p.m、通気量1vvm
の条件下で48時間、通気撹拌培養を行い、培養
後、ガーゼにて集菌し、麹菌体を取得した。
醗酵試験は、表2に示した仕込配合にて、総米
1Kgの仕込みを行い、麹歩合3%とし、麹歩合の
低減量に応じたグルコアミラーゼを麹のグルコア
ミラーゼ力価より換算し補添した。尚、対照とし
ては、表1に示した麹歩合20%にて仕込みを行つ
た場合(対照1)、ならびに、表2に示すように、
麹歩合3%で麹菌体を補添しない場合の結果(対
照2)を示した。表3は、表2で示した仕込配合
に麹菌体を使用したものを示している。尚、上記
表1、表2に示した酵素剤は、市販のグルコアミ
ラーゼ0.8g、および、市販のプロテアーゼ2g
を100mlの蒸留水に溶解したものを用いた。
表4には、得られた上槽酒の一般分析値を示
し、また、表5には、香気成分の分析結果を示し
た。図は、CO2発生量を示す特性図で、1は麹、
2は酵素、3は、菌体の特性曲線を示している。
[Industrial Application Field] The purpose of the present invention is to reduce the koji ratio in sake brewing, by supplementing the insufficient components derived from koji by adding koji cells obtained by liquid culture, and increasing the fermentation process. This paper also relates to a method for reducing the koji ratio in order to brew sake that is not much different from conventional sake. [Technical background of the invention and its problems] Reducing the koji ratio in the koji making process, which requires a great deal of labor and expense, can reduce the production amount of koji, which leads to labor saving in the koji making process, It also greatly contributes to cost reduction. It also leads to the reduction of the amount of koji rice that is difficult to dissolve in the mortar, which leads to an improvement in the raw material utilization rate or the alcoholization rate, which has extremely large advantages such as reducing production costs. It is considered to be a thing. However, the most important role of koji in sake brewing is to supply hydrolytic enzymes such as amylase and protease, and to supplement the amount of enzymes required for fermentation and balanced dissolution of steamed rice, Usually, a koji ratio of about 20% was required. Another significance of koji lies in its ingredients, which are essential for the smooth growth and fermentation of yeast and for producing the unique taste and aroma of sake. Therefore, the lower the koji ratio, the more the balance between fermentation and dissolution will be disrupted, and the quality of sake will be adversely affected. In particular, if the koji ratio is reduced to about 10% or less, fermentation will be significantly delayed even if various enzymes are sufficiently supplemented, and aromatic components such as esters will also be significantly reduced, making it clearly sensual. A significant difference is also recognized. As mentioned above, this is due to the lack of components derived from the koji mold cells. [Means for Solving the Problems] The structure of the present invention, which solves the problems of the prior art, reduces the koji ratio during sake brewing, and uses liquid culture to replace the koji-derived ingredients that are insufficient due to the reduction in the koji ratio. The obtained koji mold bodies are added to moromi. [Effect of the Invention] As described above, according to the present invention, it has been confirmed that this phenomenon can be improved by adding koji extract, water extract of koji, or mixed vitamin solution. This fact is also supported by reports that the delay in fermentation can be recovered by adding a mixture of vitamins such as inositol and calcium pantothenate when preparing the enzyme preparation. From the above, about 10
It is clear that if it is desired to reduce the koji ratio by less than %, it is necessary to add components derived from koji.
However, the substances that are considered to be brought in by koji are thought to be quite complex, and include not only vitamins but also a wide variety of koji metabolites such as fatty acids and proteolipids, which contribute to yeast growth and fermentation, as well as the delicate taste of sake. This is thought to have an effect on the scent. From this point of view, the results of numerous experiments have shown that the only thing that can substitute for the noodle-derived ingredients is the koji mold itself. The koji mold cells separated after culturing can be stored for a long period of time by vacuum drying or normal drying. [Example] Add 2 g of ground white rice as a carbon source and 1 g of red rice bran as a nitrogen source to 100 ml of distilled water, and sterilize the mixture at 120°C for 15 minutes as a medium. ) spores were inoculated with a platinum loop, 30℃, stirring speed 200r.pm, aeration rate 1vvm.
Aerated agitation culture was carried out under the following conditions for 48 hours, and after culturing, the bacteria were collected using gauze to obtain koji mold bodies. In the fermentation test, 1 kg of total rice was prepared using the mixing ratio shown in Table 2, the koji ratio was 3%, and glucoamylase was added according to the amount of reduction in the koji ratio, calculated from the glucoamylase titer of the koji. did. As a control, as shown in Table 1, the koji ratio was 20% (Control 1), and as shown in Table 2,
The results are shown (Control 2) when the koji ratio is 3% and no koji cells are supplemented. Table 3 shows the preparations shown in Table 2 using koji mold bodies. The enzyme preparations shown in Tables 1 and 2 above include 0.8g of commercially available glucoamylase and 2g of commercially available protease.
was dissolved in 100 ml of distilled water. Table 4 shows the general analysis values of the obtained Jotansake, and Table 5 shows the analysis results of aroma components. The figure is a characteristic diagram showing the amount of CO 2 generated. 1 is koji;
2 shows the enzyme, and 3 shows the characteristic curve of the bacterial cell.
【表】【table】
【表】 表3(本試験) 表2(対照2)+麹菌体【table】 Table 3 (main test) Table 2 (Control 2) + Aspergillus cells
【表】【table】
図はCO2発生量の特性図である。 1……麹、2……酵素、3……菌体。 The figure is a characteristic diagram of the amount of CO 2 generated. 1...Koji, 2...Enzyme, 3...Bacteria.
Claims (1)
に、この麹歩合の低減により不足する麹由来の持
込み成分として、液体培養により得られた麹菌体
を醪に添加することを特徴とする清酒醸造におけ
る麹歩合の低減法。1. A method of reducing the koji ratio in sake brewing, which is characterized by reducing the koji ratio during sake brewing and adding koji mold bodies obtained by liquid culture to the mortar as a component derived from the koji that is insufficient due to the reduction of the koji ratio. Reduction method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62308337A JPH01148176A (en) | 1987-12-04 | 1987-12-04 | Method for reducing yield of malt in brewing of 'sake' |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62308337A JPH01148176A (en) | 1987-12-04 | 1987-12-04 | Method for reducing yield of malt in brewing of 'sake' |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01148176A JPH01148176A (en) | 1989-06-09 |
JPH0420592B2 true JPH0420592B2 (en) | 1992-04-03 |
Family
ID=17979846
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62308337A Granted JPH01148176A (en) | 1987-12-04 | 1987-12-04 | Method for reducing yield of malt in brewing of 'sake' |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01148176A (en) |
Families Citing this family (1)
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 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59118078A (en) * | 1982-12-24 | 1984-07-07 | Tax Adm Agency | Preparation of seed malt |
JPS59140872A (en) * | 1983-02-02 | 1984-08-13 | Kikunoka Syuzo Kk | Production of brewed liquor |
JPS60141282A (en) * | 1983-12-27 | 1985-07-26 | Wakamoto Pharmaceut Co Ltd | Liquid cultivation of aspergillus |
-
1987
- 1987-12-04 JP JP62308337A patent/JPH01148176A/en active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59118078A (en) * | 1982-12-24 | 1984-07-07 | Tax Adm Agency | Preparation of seed malt |
JPS59140872A (en) * | 1983-02-02 | 1984-08-13 | Kikunoka Syuzo Kk | Production of brewed liquor |
JPS60141282A (en) * | 1983-12-27 | 1985-07-26 | Wakamoto Pharmaceut Co Ltd | Liquid cultivation of aspergillus |
Also Published As
Publication number | Publication date |
---|---|
JPH01148176A (en) | 1989-06-09 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |