JPH0522500B2 - - Google Patents
Info
- Publication number
- JPH0522500B2 JPH0522500B2 JP61120982A JP12098286A JPH0522500B2 JP H0522500 B2 JPH0522500 B2 JP H0522500B2 JP 61120982 A JP61120982 A JP 61120982A JP 12098286 A JP12098286 A JP 12098286A JP H0522500 B2 JPH0522500 B2 JP H0522500B2
- Authority
- JP
- Japan
- Prior art keywords
- soy sauce
- yeast
- raw soy
- alcohol
- low
- 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
Landscapes
- Soy Sauces And Products Related Thereto (AREA)
Description
本発明は低品質生醤油の品質の改良方法に関す
るものである。
更に詳細には、本発明は醤油諸味として3箇月
以上経過した生醤油で、酵母発酵が低調乃至は生
成アルコール量及び/又は4−エチルグアヤコー
ル及び/又は4−エチルフエノール及び/又はそ
の他の香気成分の量が低濃度であつた低品質生醤
油の品質の改良方法に関するものである。
一般に、醤油は蒸煮大豆に炒つた小麦を割砕し
たものをまぶし麹菌を接種し製麹し、出来上がつ
た麹を塩水と混合しコンクリートタンク、鉄タン
ク、FRP樹脂等のタンクに仕込み、発酵させ、
熟成させ、熟成した諸味を圧搾濾過して生醤油
(生揚醤油ともいう)を得、これを火入れして製
造されている。
醤油の製造には出来上がつた麹を塩水と混合
し、発酵タンクに仕込む工程がある。この工程
で、アミラーゼ、プロテアーゼ等の酵素群が塩水
によつて麹より抽出され、これによつて原料であ
る脱脂加工大豆、小麦が溶かされ、醤油中の旨
味、甘味成分となると同時に、微生物によつて、
アルコールがその他の香気成分等の主要な発酵生
産物も作られる。
しかし、通常麹の製造は無菌状態で行なわれる
訳ではなく、色々なバクテリア、酵母等が共存
し、所謂微生物同志が競合した状態となつている
のである。特に通風堆積麹の場合床下から麹層を
貫通して麹層表面に抜けるように空気を強制的に
送る為に外気等から持ち込れた細菌、酵母は麹層
をフイルターとしたように吸着されているのが普
通である。
一般的な固体麹は、この様に細菌や酵母等を一
緒に含んだまま塩水と混合されるが、塩水と混合
された細菌群、酵母群の中で耐塩性のない菌は短
期間のうちに死滅し、耐塩性のある菌群だけが生
き残ることになる。
また、一般に、醤油諸味の微生物の動態の典型
的なパターンは、先ず、耐塩性のない細菌、酵母
が死滅した後、耐塩性の乳酸菌が生育し、乳酸を
生成し、諸味のPHを低下させ、PHが酵母の至適PH
付近になると酵母の増殖が大となり主発酵酵母に
よつてアルコールの生成が行われ、次いでトルロ
プシス属などの後熟酵母による後熟発酵が行われ
る。
また、近年になつて、加温、微生物の添加等の
技術革新によつて醸造期間が短縮されたことによ
り、乳酸発酵、酵母発酵の期間も短かくなり、両
者の間に1つの工程が終つて次の工程という境界
がなくなり、乳酸発酵と酵母発酵とがほぼ並行し
て行なわれるような形となつた。その為乳酸菌と
酵母の微妙なバランスが重要となつた。また、同
様なことが酵母群の中でも、主発酵酵母が働く迄
の間にその時々で主役となる酵母の交代がある。
酵母間ででも微妙なバランスが要求される様にな
つた結果、時には仕込初期から発酵能の弱い野性
の酵母の生育が旺盛になり、本来必要な良性酵母
の生育が抑制されることもある。
抑制された酵母がサツカロミセス・ルキシーの
場合、アルコール発酵が弱く、アルコール濃度が
0〜2.3ml/100ml程度の醤油が出来てしまう。こ
の場合アルコールと他成分との誘導体に由来する
香の不足した醤油や、アルコールが低濃度の為防
黴力の弱い、すなわちサツカロミセス・ルキシ
ー・バリアント・ハロメンブラニス(白カビ)の
生じ易い、醤油となる。
また、生育の悪い酵母が後熟酵母であるトルロ
プシス・エチエルシやトルロプシス・バーサテイ
リスのような酵母である場合、アルコールと他成
分との誘導体に由来する香が不足した熟成感の乏
しい醤油や、アルコールが不足の為防黴力の弱い
醤油が出来る。
また後熟酵母は4−エチルグアヤコール、4−
エチルフエノール等のそれ自体防黴性を有する物
質を作るが、これも少量しか作られず白カビの生
じやすい醤油となつてしまう。しかし、低品質の
醤油となることが諸味の時点で推定されていても
これに対する対応手段は諸味では全くなかつた。
アルコール濃度が低く、香気成分の少い醤油
は、正常な発酵を終了したものと比べたとき著し
く劣つたものとなつているのである。
このようにして醸造された醤油諸味は、圧搾濾
過して、生醤油としたときに、アルコール濃度を
測定したり、香気成分の感能検査をして、酵母発
酵が低調であり低品質生醤油と判断されることに
なる。
このような低品質生醤油の最終的な対応として
はアルコールを添加しアルコール濃度を微調整し
たり、アルコール濃度を微調整した後良品質の生
醤油と混合するなどの方法もとらざるを得ないこ
ともあるが、香気、風味等全体の品質が低下する
などの問題がさけられない。
本発明は、醤油諸味として3箇月以上経過した
生醤油で、酵母発酵が低調乃至は生成アルコール
及び/又は4−エチルグアヤコール及び/又は4
−エチルフエノール及び/又は香気成分の量が低
濃度であつた低品質生醤油の品質を改良すること
を目的としている。
本発明は、醤油諸味として3箇月以上経過した
生醤油で、酵母発酵が低調乃至は生成アルコール
及び/又は4−エチルグアヤコール及び/又は4
−エチルフエノール及び/又はその他の香気成分
が低濃度であつた低品質生醤油を酵母又はその処
理物もしくは固定化した酵母で処理することを特
徴とする低品質生醤油の改良方法である。
本発明においては、低品質の生醤油と酵母やそ
の処理物で酸素系の活性を保持したもの、例えば
菌体磨砕物、その他固定化酵母などとを接触させ
ることによつて、アルコール量、4−エチルグア
ヤコール、4−エチルフエノール量及び香味の調
整をすることが可能となる。
使用する酵母としては、醤油醸造に関係する酵
母であればいずれでもよいが、例示すれば、サツ
カロミセス・ルキシー、トルロプシス・エチエル
シ、トルロプシス・バーサテイリスなどがあり、
これらの種から選択した一菌株もしくは二菌株以
上の混合菌株が用いられる。
酵母菌体を接触させる方法は、生醤油と直接接
触させ菌体を濾別する方法、遠心分離する方法ま
たは、酵母菌体をアルギン酸ゲル包括法、K(カ
ツパー)−カラーギナン包括法、ポリアクリルア
ミド包括法、多孔性のガラスビーズに吸着させる
方法等により固定化し、この固定化菌体を直接ま
たは固定化菌体カラムに生醤油を接触させること
により発酵を行わせ、アルコール濃度及び、4−
エチルグアヤコール、4−エチルフエノール及び
香味を整えることができる。
生醤油と酵母又はその処理物は10〜40℃程度で
接触させ、接触時間は酵母量によつても異なるが
アルコールが十分生成する時間、例えば10分から
100時間程度でよい。十分なアルコール生成及
び/又は4−エチルグアヤコール、4−エチルフ
エノールの生成があり、アルコール濃度及び/又
は4−エチルグアヤコール、4−エチルフエノー
ルの濃度が調整され、香味を整えることができた
ら、接触をやめればよい。
接触終了後は、酵母又はその処理物を分離し、
加熱殺菌することにより品質のすぐれた醤油が得
られる。
次に本発明の実施例を示す。
実施例 1
常法通り脱脂大豆、小麦、アスペルギルス・ソ
ヤを用いて製麹し、得られた麹を常法通り25g/
100mlの濃度の食塩水に混合し、仕込を行ない、
発酵熟成を経た後、常法により圧搾し、生醤油を
得た。この生醤油を仕込タンク毎のロツトで分析
を行なつた所正常な発酵を経たものが大部分であ
つたが中に第1表に示したアルコール発酵の不足
な生醤油A,B,Cが存在した。なお、Dは平均
的な正常のアルコール発酵醤油である。
The present invention relates to a method for improving the quality of low-quality raw soy sauce. More specifically, the present invention deals with raw soy sauce that has been used for soy sauce moromi for three months or more, and has low yeast fermentation or the amount of alcohol produced and/or 4-ethylguaiacol and/or 4-ethylphenol and/or other aroma components. The present invention relates to a method for improving the quality of low-quality raw soy sauce with a low concentration of soy sauce. Generally, soy sauce is made by coating steamed soybeans with crushed roasted wheat, inoculating them with koji mold, and making koji.The resulting koji is mixed with salt water and placed in a concrete tank, iron tank, FRP resin tank, etc., and then fermented. let me,
It is produced by aging and compressing and filtering the aged moromi to obtain raw soy sauce (also called raw soy sauce), which is then pasteurized. The production of soy sauce involves the process of mixing the finished koji with salt water and placing it in a fermentation tank. In this process, enzymes such as amylase and protease are extracted from the koji using salt water, which dissolves the defatted processed soybeans and wheat, which are the raw materials, and becomes the flavor and sweetness components of soy sauce, as well as being absorbed by microorganisms. Then,
Alcohol is also produced as the main fermentation product, along with other aroma components. However, the production of koji is not normally carried out under sterile conditions, and various bacteria, yeast, etc. coexist, creating a state of competition between so-called microorganisms. In particular, in the case of ventilation-deposited koji, air is forcibly sent from below the bed to penetrate the koji layer and reach the surface of the koji layer. Bacteria and yeast brought in from the outside air are absorbed by the koji layer as if it were a filter. It is normal to have General solid koji is mixed with salt water while containing bacteria, yeast, etc. in this way, but among the bacteria and yeast mixed with salt water, bacteria that are not salt tolerant are removed in a short period of time. The bacteria will die, and only salt-tolerant bacteria will survive. In addition, in general, the typical pattern of the dynamics of microorganisms in soy sauce moromi is that first, bacteria and yeast that are not salt-tolerant die, then salt-tolerant lactic acid bacteria grow, produce lactic acid, and lower the pH of moromi. , PH is the optimum pH for yeast
In the vicinity, yeast multiplication increases, and alcohol is produced by the main fermenting yeast, followed by post-ripening fermentation by post-ripening yeasts such as Torulopsis. In addition, in recent years, as the brewing period has been shortened due to technological innovations such as heating and the addition of microorganisms, the periods of lactic acid fermentation and yeast fermentation have also become shorter, and one process is completed between them. As a result, there were no boundaries between the next process, and lactic acid fermentation and yeast fermentation began to take place almost in parallel. Therefore, the delicate balance between lactic acid bacteria and yeast became important. Similarly, among yeast groups, there is a change in the dominant yeast from time to time until the main fermenting yeast works.
As a result of the delicate balance that is now required even among yeasts, wild yeasts with weak fermentation ability sometimes grow vigorously from the early stage of preparation, and the growth of naturally necessary benign yeasts is sometimes suppressed. If the suppressed yeast is Satucharomyces luxii, alcoholic fermentation is weak and soy sauce with an alcohol concentration of about 0 to 2.3ml/100ml is produced. In this case, soy sauce that lacks aroma derived from derivatives of alcohol and other ingredients, or soy sauce that has weak antifungal properties due to the low concentration of alcohol, in other words, soy sauce that is susceptible to Saccharomyces luxii variant Halomembranis (white mold). becomes. In addition, if the yeast with poor growth is a post-ripening yeast such as Torulopsis ethielsii or Torulopsis versateilis, soy sauce with a lack of ripeness due to the lack of aroma derived from derivatives of alcohol and other ingredients, or alcohol Due to the shortage, soy sauce with weak anti-mildew properties is produced. In addition, post-ripening yeasts include 4-ethylguaiacol, 4-
Substances such as ethylphenol that have anti-mold properties are produced, but these are produced in small amounts, resulting in soy sauce that is prone to mildew. However, even though it was assumed at the time of moromi that the soy sauce would be of low quality, moromi did not have any countermeasures against this. Soy sauce with a low alcohol concentration and few aromatic components is significantly inferior to one that has undergone normal fermentation. When the soy sauce moromi brewed in this way is pressed and filtered to make raw soy sauce, the alcohol concentration is measured and a sensory test for aroma components is performed to determine that yeast fermentation is slow and that the raw soy sauce is of low quality. It will be judged that. The final solution to such low-quality raw soy sauce is to add alcohol to fine-tune the alcohol concentration, or to fine-tune the alcohol concentration and then mix it with high-quality raw soy sauce. However, problems such as deterioration of overall quality such as aroma and flavor cannot be avoided. The present invention is a raw soy sauce that has been used for soy sauce moromi for three months or more, and has low yeast fermentation or produced alcohol and/or 4-ethylguaiacol and/or 4-ethylguaiacol.
- The purpose is to improve the quality of low-quality raw soy sauce containing low concentrations of ethylphenol and/or aroma components. The present invention is a raw soy sauce that has been used for soy sauce moromi for three months or more, and has low yeast fermentation or produced alcohol and/or 4-ethylguaiacol and/or 4-ethylguaiacol.
- A method for improving low-quality raw soy sauce characterized by treating low-quality raw soy sauce with a low concentration of ethylphenol and/or other aroma components with yeast or its treated product or immobilized yeast. In the present invention, by bringing low-quality raw soy sauce into contact with yeast or its processed product that retains oxygen-based activity, such as ground bacterial cells or other immobilized yeast, the alcohol content can be reduced by 4. - It becomes possible to adjust the amount and flavor of ethylguaiacol and 4-ethylphenol. The yeast used may be any yeast related to soy sauce brewing, but examples include Satucharomyces luxii, Torulopsis ethiersii, Torulopsis versateilis, etc.
One strain selected from these species or a mixed strain of two or more strains is used. Methods for contacting yeast cells include direct contact with raw soy sauce and filtration of the cells, centrifugation, alginate gel entrapment method, K (katsupa)-carrageenan entrapment method, polyacrylamide entrapment method. The immobilized cells are then fermented either directly or by contacting the immobilized cell column with raw soy sauce, and the alcohol concentration and 4-
Ethylguaiacol, 4-ethylphenol and flavor can be adjusted. Raw soy sauce and yeast or their processed products are brought into contact at a temperature of about 10 to 40°C, and the contact time varies depending on the amount of yeast, but the contact time is long enough to generate enough alcohol, e.g. 10 minutes.
About 100 hours is sufficient. When sufficient alcohol is produced and/or 4-ethylguaiacol and 4-ethylphenol are produced, the alcohol concentration and/or the concentration of 4-ethylguaiacol and 4-ethylphenol are adjusted, and the flavor can be adjusted, contact is carried out. Just stop. After the contact is completed, the yeast or its treated product is separated,
High-quality soy sauce can be obtained by heat sterilization. Next, examples of the present invention will be shown. Example 1 Koji was made using defatted soybeans, wheat, and Aspergillus soya in a conventional manner, and 25 g of the obtained koji was produced in a conventional manner.
Mix with 100ml of concentrated saline solution and prepare.
After fermentation and maturing, the soy sauce was pressed using a conventional method to obtain raw soy sauce. When we analyzed lots of this raw soy sauce for each preparation tank, we found that most of it had undergone normal fermentation, but among them were raw soy sauces A, B, and C that had insufficient alcoholic fermentation as shown in Table 1. Were present. Note that D is an average normal alcoholic fermented soy sauce.
【表】
ロマトグラフイーによる分析
別に、醤油酵母サツカロミセス・ルキシー
ATCC13356を生醤油10ml/100ml、食塩10g/
100ml、グルコース10g/100ml、リン酸−カリウ
ム0.01g/100ml、硫酸マグネシウム0.01g/100
ml、塩化カルシウム0.0025g/100ml、酵母エキス
0.01g/100ml、PH5.2(以下Y培地と称する)の組
成の培地を500ml容の三角フラスコ10本に各150ml
入れ減菌したものに各1白金耳接種し、30℃で72
時間振盪培養した。この培養物を更に100のY
培地を入れたジヤーフアーメンターで30℃、72時
間通気撹拌培養を行なつた。この培養物を10000
回転、15分遠心することにより集菌した。
この菌体を第1表の生醤油A,B,C各10に
108/mlになる様に懸濁し、菌体がまんべくなく
生揚醤油と接触出来るように撹拌羽根でゆつくり
撹拌しながら30℃で48時間接触させた。
この処理後のそれぞれの生醤油を10000回転15
分遠心することにより酵母菌体を除き、さらに常
法により火入及び〓引を行なつた。またA,B,
Cそれぞれについて本発明方法を適用する前の生
揚醤油を火入及び〓引を行ない、本発明適用後の
醤油との分析値、20名の専門パネルによる官能評
価を比較した。結果は第2表に示した。[Table] Analysis by romatography Separately, soy sauce yeast Satsucharomyces luxii
ATCC13356 with raw soy sauce 10ml/100ml, salt 10g/
100ml, glucose 10g/100ml, potassium phosphate 0.01g/100ml, magnesium sulfate 0.01g/100
ml, calcium chloride 0.0025g/100ml, yeast extract
0.01g/100ml, PH5.2 (hereinafter referred to as Y medium) culture medium in 10 500ml Erlenmeyer flasks, 150ml each.
Inoculate one platinum loopful into each sterilized container and inoculate at 30℃ for 72 hours.
Cultured with shaking for hours. Add this culture to 100 Y
Culture was carried out with aeration at 30°C for 72 hours in a jar fermenter containing a culture medium. 10000 of this culture
Bacteria were collected by rotation and centrifugation for 15 minutes. Add these bacteria to 10 each of raw soy sauce A, B, and C in Table 1.
The suspension was suspended at a concentration of 10 8 /ml, and the cells were left in contact at 30° C. for 48 hours while being gently stirred with a stirring blade so that the bacterial cells could evenly come into contact with the raw soy sauce. After this treatment, each raw soy sauce is rotated 10,000 times 15
Yeast cells were removed by centrifugation, and the mixture was fired and strained using conventional methods. Also A, B,
For each of C, the freshly fried soy sauce before applying the method of the present invention was fired and strained, and the analytical values and sensory evaluation by a panel of 20 experts were compared with the soy sauce after applying the method of the present invention. The results are shown in Table 2.
【表】
パネルが良いと評価した人数
第2表より明らかな様に本発明方法を適用する
ことによりエチルアルコールが増加し、官能評価
でも品質が向上した。
更にAについて本発明方法を適用せず火入及び
〓引した醤油と本発明方法を適用後火入及び〓引
した醤油それぞれに産膜酵母サツカロミセス・ル
キシー・バリアント・ハロメンブラニスを106/
mlになるように接種し、2のガラス壜に各1.5
詰め30℃に放置し、界面に産膜(白カビ)が発
生するかどうか観察した。本発明を適用せず火入
した醤油は20日目で産膜の発生が観察されたが本
発明方法を適用した後に火入した醤油には産膜の
発生は認められなかつた。
実施例 2
実施例1で使用したY培地を500ml容の三角フ
ラスコ10本に各150ml入り、滅菌後、その5本に
サツカロミセス・ルキシーATCC14679を1白金
耳接種し30℃で72時間振盪培養した。
この培養液500mlを2g/100ml濃度のアルギン
酸ナトリウム溶液20に加え混合し2.8×106/ml
の酵母−アルギン酸ナトリウム懸濁液とした。
この懸濁液を5℃に冷却した2g/100ml濃度の
塩化カルシウム溶液に内径2mmのチユーブをセツ
トした定流量ポンプを使うことにより滴下し直径
約3mmのビーズ状とし、更に24時間同溶液に浸漬
し十分に固化しATCC14679の固定化ゲルを調整
した。
残りの5本のY培地にはトルロプシス・エチエ
ルシーATCC20190を1白金耳接種し30℃で72時
間振盪培養した。
以下ATCC14679と同様にしてATCC20190の固
定化ゲルを調整した。
ATCC14679、ATCC20190それぞれの固定化ゲ
ルをそれぞれ別に新しいY培地に投入し、通気撹
拌しながら30℃、48時間培養し、ゲル内の菌数を
108〜109/gまで増加させた。
実施例1で使用した生醤油B100に先ず
ATCC14679固定化ゲル18を投入し、ゆつくり
と撹拌羽根で撹拌し30℃48時間接触させた。終了
後、サラン製のネツトでATCC14679固定化ゲル
を除いた後、生醤油B−1を100得た。このB
−1 50にATCC20190固定化ゲル10を投入
し同様撹拌羽根で撹拌し30℃48時間接触させた。
終了後同様にしてサラン製のネツトで
ATCC20190固定化ゲルを除去した(生醤油B−
2)。各処理段階の生醤油B−1、B−2それに
処理前の生醤油Bの分析値を第3表に示した。さ
らに、各生醤油を火入れ及び 引を行ないそれぞ
れについて官能評価を行なつた結果も同様第3表
に示した。[Table] Number of people who rated the panel as good As is clear from Table 2, by applying the method of the present invention, the amount of ethyl alcohol increased and the quality also improved in the sensory evaluation. Furthermore, for A, the soy sauce that was fired and reduced without applying the method of the present invention and the soy sauce that was fired and reduced after applying the method of the present invention were each treated with 10 6 /
Inoculate to 1.5 ml in 2 glass bottles each.
They were packed and left at 30°C to observe whether a film (mildew) would form on the interface. In the soy sauce that was pasteurized without applying the present invention, the formation of a film was observed on the 20th day, but no formation of a film was observed in the soy sauce that was fired after the method of the present invention was applied. Example 2 150 ml of the Y medium used in Example 1 was placed in 10 500 ml Erlenmeyer flasks each, and after sterilization, one platinum loop of Saccharomyces luxii ATCC 14679 was inoculated into the 5 flasks and cultured with shaking at 30° C. for 72 hours. Add 500ml of this culture solution to sodium alginate solution 20 with a concentration of 2g/100ml and mix to obtain a concentration of 2.8×10 6 /ml.
yeast-sodium alginate suspension. This suspension was dropped into a calcium chloride solution with a concentration of 2 g/100 ml cooled to 5°C using a constant flow pump equipped with a tube with an inner diameter of 2 mm to form beads with a diameter of approximately 3 mm, and the beads were further immersed in the same solution for 24 hours. The mixture was thoroughly solidified and a gel with ATCC14679 immobilized was prepared. One platinum loop of Torulopsis ethielci ATCC 20190 was inoculated into the remaining five Y medium bottles and cultured with shaking at 30°C for 72 hours. An immobilized gel for ATCC20190 was prepared in the same manner as for ATCC14679. The immobilized gels of ATCC14679 and ATCC20190 were placed separately in new Y medium and incubated at 30°C for 48 hours with aeration and agitation to determine the number of bacteria in the gel.
It was increased to 10 8 to 10 9 /g. First, add raw soy sauce B100 used in Example 1.
ATCC14679 immobilized gel 18 was added, slowly stirred with a stirring blade, and kept in contact at 30°C for 48 hours. After the completion of the reaction, the ATCC14679 immobilized gel was removed using a net made by Saran, and 100 grams of raw soy sauce B-1 was obtained. This B
-1 50 was charged with ATCC20190 immobilized gel 10, stirred with a stirring blade in the same manner, and kept in contact at 30°C for 48 hours.
After finishing, use Saran net in the same way.
ATCC20190 immobilized gel was removed (raw soy sauce B-
2). Table 3 shows the analytical values of raw soy sauce B-1 and B-2 at each treatment stage and raw soy sauce B before treatment. Furthermore, the results of sensory evaluation of each raw soy sauce after pasteurization and straining are also shown in Table 3.
【表】
BよりB−1ではエチルアルコールが増加し、
B−2ではさらにエチルアルコールの増加と4−
エチルフエノール、4−エチルグアヤコールの適
度の生成があつた。
更に、火入後のB、B−1、B−2それぞれに
産膜酵母サツカロミセス・ルキシー・バリアン
ト・ハロメンブラニスを106/mlになるように接
種し、2のガラス壜に各1.5ずつ詰め30℃に
放置し、界面に産膜が発生するかどうか観察し
た。本発明方法を適用しなかつたBは14日目でわ
ずかに産膜の発生が認められた。B−1、B−2
では1ケ月を経過してもカビの発生は全く認めら
れなかつた。1ケ月経過後のB−1、B−2を18
%塩水でそれぞれ2倍に稀釈し30℃に置いた所B
−1の方がわずかではあるが早目に産膜の発生が
認められた。
実施例 3
実施例2で得た固定化ゲル培養物、すなわちサ
ツカロミセス・ルキシーATCC14679とトルロプ
シス・エチエルシATCC20190の固定化ゲル培養
物をそれぞれを内径5cm、高さ100cmのカラムに
充填した。
この固定化ゲル充填カラムに実施例1で使用し
た生醤油Bを接触させ通過させた。
先ず生醤油BをATCC14679固定化ゲル充填カ
ラムに75〜100ml/時間(カラムの空塔基準の平
均滞留時間19〜25時間)の割合で供給し接触させ
た。
この通過後の生醤油をB−3とする。
このB−3を更にATCC20190固定化ゲル充填
カラムに同様に75〜100ml/時間の割合で供給し
接触させた。
この通過後の生醤油をB−4とする。
各処理段階の生醤油B−3、B−4それに処理
前の生醤油Bの分析値を第4表に示した。更に各
生醤油を火入及び〓引を行ない、それぞれについ
て官能評価を行なつた結果も同様に第4表に示し
た。[Table] Ethyl alcohol increases in B-1 compared to B,
B-2 further increases ethyl alcohol and 4-
Appropriate amounts of ethylphenol and 4-ethylguaiacol were produced. Furthermore, after firing, each of B, B-1, and B-2 was inoculated with the film-producing yeast Satucharomyces luxii variant Halomembranis at a concentration of 10 6 /ml, and 1.5 of each was packed in the second glass bottle. It was left at 30°C and observed whether a film formed at the interface. In case B, to which the method of the present invention was not applied, slight production of membranes was observed on the 14th day. B-1, B-2
No mold growth was observed even after one month had passed. 18 B-1 and B-2 after 1 month
% salt water diluted twice and placed at 30℃ B
In case of -1, the production of membranes was observed earlier, although to a lesser extent. Example 3 The immobilized gel cultures obtained in Example 2, that is, the immobilized gel cultures of Satucharomyces luxii ATCC 14679 and Torulopsis ethierci ATCC 20190, were each packed into a column with an inner diameter of 5 cm and a height of 100 cm. The raw soy sauce B used in Example 1 was brought into contact with and passed through this immobilized gel-packed column. First, raw soy sauce B was supplied and brought into contact with an ATCC14679 immobilized gel-packed column at a rate of 75 to 100 ml/hour (average residence time based on the empty column of the column, 19 to 25 hours). The raw soy sauce after this passage is referred to as B-3. This B-3 was further supplied and brought into contact with an ATCC20190 immobilized gel packed column at a rate of 75 to 100 ml/hour. The raw soy sauce after this passage is referred to as B-4. Table 4 shows the analytical values of raw soy sauce B-3 and B-4 at each treatment stage and raw soy sauce B before treatment. Furthermore, each raw soy sauce was heated and strained, and the sensory evaluation results were also shown in Table 4.
【表】
実施例2と同様BよりB−3ではエチルアルコ
ールが増加しB−4では更にエチルアルコールの
増加と4−エチルフエノール、4−エチルグアヤ
コールの生成があつた。
更に、火入後のB、B−3、B−4それぞれに
産膜酵母サツカロミセス・ルキシー・バリアン
ト・ハロメンブラニスを106/mlになるように接
種し、2のガラス壜に各1.5ずつ詰め、30℃
に放置し、界面に産膜が発生するかどうか観察し
た。
本発明方法を適用しなかつたBは12日目でわず
かに産膜の発生が認められた。B−3、B−4で
は1ケ月を経過しても産膜の発生は認められなか
つた。
1ケ月経過後のB−3、B−4を18%塩水でそ
れぞれ2倍に稀釈し、30℃に置いた所B−3の方
がわずかではあるが早目に産膜の発生が認められ
た。[Table] As in Example 2, ethyl alcohol increased in B-3 compared to B, and ethyl alcohol further increased in B-4, and 4-ethylphenol and 4-ethylguaiacol were produced. Furthermore, each of B, B-3, and B-4 after firing was inoculated with the film-producing yeast Satucharomyces luxii variant Halomembranis at a concentration of 10 6 /ml, and 1.5 of each was packed in 2 glass bottles. ,30℃
It was observed whether a film formed at the interface. In case B to which the method of the present invention was not applied, slight production of membranes was observed on the 12th day. In B-3 and B-4, no production of production membranes was observed even after one month had passed. After one month had passed, B-3 and B-4 were each diluted twice with 18% salt water and placed at 30°C, and formation of membranes was observed earlier in B-3, although slightly. Ta.
Claims (1)
で、酵母発酵が低調乃至は生成アルコール及び/
又は4−エチルグアヤコール及び/又は4−エチ
ルフエノール及び/又はその他の香気成分が低濃
度であつた低品質生醤油を酵母又はその処理物も
しくは固定化した酵母で処理することを特徴とす
る低品質生醤油の改良方法。1 Raw soy sauce that has been used as soy sauce moromi for more than 3 months, yeast fermentation is low, or alcohol and/or alcohol produced are low.
Or low-quality raw soy sauce containing low concentrations of 4-ethylguaiacol and/or 4-ethylphenol and/or other aromatic components is treated with yeast or its treated product or immobilized yeast. How to improve raw soy sauce.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61120982A JPS62278965A (en) | 1986-05-28 | 1986-05-28 | Method for improving raw soy sauce having low quality |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61120982A JPS62278965A (en) | 1986-05-28 | 1986-05-28 | Method for improving raw soy sauce having low quality |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62278965A JPS62278965A (en) | 1987-12-03 |
| JPH0522500B2 true JPH0522500B2 (en) | 1993-03-29 |
Family
ID=14799854
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61120982A Granted JPS62278965A (en) | 1986-05-28 | 1986-05-28 | Method for improving raw soy sauce having low quality |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62278965A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103416717A (en) * | 2013-08-19 | 2013-12-04 | 西峡县福到家食品有限公司 | Production method for brewing mushroom soy sauce |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014207881A (en) * | 2013-01-16 | 2014-11-06 | キッコーマン株式会社 | Soy sauce for enhancing broth taste |
| CN104621534B (en) * | 2015-02-09 | 2017-07-11 | 厦门古龙食品有限公司 | A kind of preparation method of soy sauce |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5911160A (en) * | 1982-07-08 | 1984-01-20 | Kikkoman Corp | Preparation of seasoning liquid |
| JPS6167459A (en) * | 1984-09-11 | 1986-04-07 | Kikkoman Corp | Production of seasoning solution |
-
1986
- 1986-05-28 JP JP61120982A patent/JPS62278965A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103416717A (en) * | 2013-08-19 | 2013-12-04 | 西峡县福到家食品有限公司 | Production method for brewing mushroom soy sauce |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62278965A (en) | 1987-12-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5141756A (en) | Process for producing soya sauce | |
| CN102268358B (en) | A kind of production process of using grape pomace to brew grape fruit vinegar | |
| CN104397791A (en) | Method for Ziziphus jujuba residues producing Ziziphus jujuba vinegar drink | |
| CN107227222A (en) | A kind of preparation method of the sweet shaddock fruit wine of red heart | |
| CN102911885B (en) | Saccharomyces cerevisiae strain and method for preparing blueberry fruit wine by using saccharomyces cerevisiae strain | |
| CN113397150B (en) | Fermentation method of soy sauce | |
| CN109593627B (en) | Electric field strengthening brewing process of sea-buckthorn and Chinese wolfberry health-care fruit wine | |
| CN102268384A (en) | Saccharomyces cerevisiae strain and method for preparing blackberry fruit wine by using same | |
| JPH03210172A (en) | Method for producing wine-style ginseng liquor | |
| KR102114184B1 (en) | Manufacturing method for fermentation vinegar using by-product of red-ginseng and fermentation vinegar manufactured by same method | |
| JPH0522500B2 (en) | ||
| JP3544921B2 (en) | Vinegar made from mushrooms | |
| CN101565667A (en) | Preparation method of Grifola frondosa-black plum fruit wine | |
| CN108660025A (en) | A kind of glutinous rice corn yellow rice wine manufacture craft | |
| JPH0516824B2 (en) | ||
| JPS6387961A (en) | Method for improving quality of low-quality soy sauce | |
| CN101565668A (en) | Preparation method of hericium erinaceus-black plum fruit wine | |
| KR100790502B1 (en) | Manufacturing method of Cheongju containing wild ginseng culture root | |
| CN118126786B (en) | Beer with good foam stability and preparation method thereof | |
| CN105695224B (en) | A kind of Lenlinus edodes black garlic wine | |
| JPS61124342A (en) | Production of food picked in fermented seasoning solution | |
| JPH0516823B2 (en) | ||
| JP2001245650A (en) | Method of producing alcoholic beverages | |
| CN110894445A (en) | Method for producing pure and high-alcohol yellow wine in inhibition mode | |
| KR100187450B1 (en) | Preparation process of citrus fermented vinegar |