JPS58141761A - Preparation of soy - Google Patents

Preparation of soy

Info

Publication number
JPS58141761A
JPS58141761A JP57023380A JP2338082A JPS58141761A JP S58141761 A JPS58141761 A JP S58141761A JP 57023380 A JP57023380 A JP 57023380A JP 2338082 A JP2338082 A JP 2338082A JP S58141761 A JPS58141761 A JP S58141761A
Authority
JP
Japan
Prior art keywords
soy
yeast
soy sauce
days
strains
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.)
Granted
Application number
JP57023380A
Other languages
Japanese (ja)
Other versions
JPS606183B2 (en
Inventor
Kazuo Uchida
内田 一生
Kazuo Inamori
稲森 和夫
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.)
Yamasa Shoyu KK
Original Assignee
Yamasa Shoyu KK
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 Yamasa Shoyu KK filed Critical Yamasa Shoyu KK
Priority to JP57023380A priority Critical patent/JPS606183B2/en
Publication of JPS58141761A publication Critical patent/JPS58141761A/en
Publication of JPS606183B2 publication Critical patent/JPS606183B2/en
Expired legal-status Critical Current

Links

Abstract

PURPOSE:To carry out the brewing of soy, in a short time, by fermenting or digesting unrefined soy, adding a specific amount of lactobacillus to the soy, keeping the soy at a specific temperature for a specific period, and subjecting the product to a combination of the process for adding yeast, the process for decreasing the amount of the yeast, and the process for aging the soy. CONSTITUTION:Unrefined soy is fermented or digested, and added with 10<7>-10<8> cells of lactobacillus per 1g of the unrefined soy, and subjected to the lactic fermentation at 15-20 deg.C for 10-20 days. After the fermentation, the soy is added with 10<6>-10<8> cells of yeast per 1g of the unrefined soy, and subjected to the alcoholic fermentation at 20-25 deg.C for 10-15 days. In the third step, the unrefined soy is treated at 32-36 deg.C to decrease the number of the yeast cells to <=10<6> per 1g of the unrefined soy, and in the fourth step, the unrefined soy is aged at 25-35 deg.C for 30-50 days. Soy sauce similar to the naturally brewed soy can be prepared by this process in a short time.

Description

【発明の詳細な説明】 本発明は、短期間で醤油を醸造する醤油の製造法に関す
るものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing soy sauce that brews soy sauce in a short period of time.

従来、醤油を短期間に醸造する方法の一つとして、通常
の方法で製麹した麹を食塩濃度θ〜14%にして仕込み
、40’C以上の高温条件下で酵素分解して消化諸株を
得、これに乳酸菌、酵母を添加して短期間に両発酵を行
なう方法が知られている。しかし、この方法により得ら
れる醤油製品は、醸造醤油としての香味が調わず、醤油
とは異質の醸造調味液の域を出ない製品にすぎなかった
。また、蛋白質原料を麹菌あるいは他の微生物起源の酵
素で消化分解したものに醤油醸造関連微生物を添加して
発酵熟成させる速醸法によっても、得られる製品は同様
に醤油様調味液の域を出るものて偉 はなかった。このような■1法において、14%以下の
食塩濃度で仕込んだ減塩諸株の場合には、贋造の問題が
あった。この問題を解決するため、たとえば細菌汚染の
ない麹を作り、無菌の低濃度食塩水で仕込み、加温して
乳酸菌、酵母を添加して発酵させた後、高濃度食塩水を
加えてさらに熟成させる方法(たとえば特開昭56−8
9762号公報参照)などの無菌的操作による方法が工
夫されている。しかし、これらの方法は、全工程ないし
主要工程を無菌的に、操作する必要があるたy〕、大量
生産には適さず、かつ多額の設備費、維持費を要する欠
°点がある。
Conventionally, as one of the methods for brewing soy sauce in a short period of time, koji made by the usual method is prepared with a salt concentration of θ ~ 14%, and then enzymatically decomposed under high temperature conditions of 40'C or higher to digest various strains. A known method is to add lactic acid bacteria and yeast to this mixture to carry out both types of fermentation in a short period of time. However, the soy sauce product obtained by this method did not have the flavor of a brewed soy sauce, and was nothing more than a brewed seasoning liquid different from soy sauce. In addition, the product obtained also goes beyond the soy sauce-like seasoning liquid by using the quick brewing method, in which protein raw materials are digested and decomposed with enzymes originating from koji mold or other microorganisms, and microorganisms related to soy sauce brewing are added to ferment and mature the product. It wasn't great. In such method (1), there was a problem of counterfeiting in the case of low-salt strains prepared with a salt concentration of 14% or less. To solve this problem, for example, we make koji that is free of bacterial contamination, prepare it with sterile low-concentration saline, heat it, add lactic acid bacteria and yeast, ferment it, and then add high-concentration saline and further ripen it. method (for example, Japanese Patent Application Laid-Open No. 56-8
Methods using aseptic operations such as (see Japanese Patent No. 9762) have been devised. However, these methods have the disadvantage that they are not suitable for mass production because all or the main steps must be operated aseptically, and that they require large equipment and maintenance costs.

醸造醤油の香味形成に関与するファクターには、原料の
種類と配合割合、原料処理方法とその条件、麹菌の種類
と製麹法、仕込塩水量と濃度、諸株の品温経過、撹拌方
法、乳酸菌発酵、酵母発酵、火入条件などがある。この
中で乳酸菌と酵母の発酵が特に良好な香味形成に重要で
あることはよく知られている。乳酸菌、酵母による発酵
は遂次発酵とされ、まず乳酸発酵によって酵母1の生育
に適した環境がつくられ、その後に酵母によるアルコー
ル発酵が行われて諸株の熟成が進行するといわれている
。後熟酵母の生成する微量成分が熟成に関与するとの説
もある。
Factors involved in the flavor formation of brewed soy sauce include the type and blending ratio of raw materials, the raw material processing method and its conditions, the type of koji mold and koji production method, the amount and concentration of brine, the temperature progression of various strains, the stirring method, These include lactic acid bacteria fermentation, yeast fermentation, and firing conditions. It is well known that the fermentation of lactic acid bacteria and yeast is particularly important for the formation of good flavor. Fermentation by lactic acid bacteria and yeast is said to be sequential fermentation, in which an environment suitable for the growth of yeast 1 is first created by lactic acid fermentation, and then alcoholic fermentation by yeast is carried out to advance the ripening of the strains. There is also a theory that trace components produced by post-ripening yeast are involved in ripening.

一方、近年、防パイ剤(たとえばPOBB%PBなど)
が消費者に忌避され、その代替物としてアルコールが利
用されるようになった。そのため諸株中のアルコール生
成量が少ない場合、アルコールを防パイ効果のある濃度
まで添加する必要かあり、製造コストの上昇を招いてい
る。諸株中のアルコール生成量を増強する目的で諸株へ
の酵母添加が盛んに行われるようになった。しかし酵母
添加を行って熟成させると、醤油製品に酵母エキス臭、
果実様エステル臭などが付与し、品質が著しく劣下する
問題点がある。
On the other hand, in recent years, anti-piping agents (for example, POBB%PB, etc.)
However, consumers began to avoid it, and alcohol began to be used as a substitute. Therefore, if the amount of alcohol produced in the various strains is small, it is necessary to add alcohol to a concentration that is effective for preventing pimples, leading to an increase in manufacturing costs. Addition of yeast to various strains has become popular for the purpose of increasing the amount of alcohol produced in the strains. However, when yeast is added and ripened, the soy sauce product has a yeast extract smell.
There is a problem in that it imparts a fruit-like ester odor, resulting in a significant deterioration in quality.

本発明者らは、従来の速醸法、酵母添加法の欠点を克服
すべく鋭意研究を重ねた結果、■醤油諸株の乳酸発酵に
おいて15〜20°Cという低温条件を設定し、かつ乳
酸菌の添加を菌体数107〜108/諸味りとなるよう
に多量に行なって10〜20日間保持すると、十分乳酸
発酵が行われ、しかも諸株に異臭が付与しないこと、■
酵母発酵において20〜25°Cという低温条件を設定
し、かつ酵母の添加を菌体数106〜108/諸味9と
なるように多量に行って10〜15日間保持することに
より、十分アルコールを生成させることができ、しかも
酵母エキス臭、エステル臭の生成が認められないこと、
■■および■の工程を経た諸株を、諸株中の酵母数を1
06/諸味q以下の天然醸造工程の諸株中の酵母数レベ
°ルに調整して25〜85℃で調熟させることにより、
酵母エキス臭、エステル臭を付与させずに、非常に芳醇
な醤油醸造香気のみを生成させることができること、0
0番こおける酵母数の調整工程として諸株を32〜36
8Cに保温する工程を採用すればよいことなどを知見し
、これらの工程を結合することによって高品質の醤油を
短期間に製造することができる方法を確立した。すなわ
ち、本発明方法は、醤油諸株を発酵熟成させる方法にお
いて、仕込みないし消化後の諸株に対して乳酸菌を10
7〜108/諸味qになるように添加して15’−20
°Cで10〜20日間保持する第1工程、次いで酵母を
106〜108/諸味9になるように添加して20〜2
5°Cで10〜15日間保持する第2工程、82〜86
°Cで処理して酵母数を106/”諸株q以下に減少さ
せる第3工程、および25〜85°Cで調熟させる第4
工程を結合することを特徴とする醤油の製造法である。
As a result of intensive research to overcome the shortcomings of the conventional quick brewing method and yeast addition method, the present inventors have established a low-temperature condition of 15 to 20°C for lactic acid fermentation of various soy sauce strains, and If a large amount is added so that the number of bacterial cells is 107 to 108/moromi and kept for 10 to 20 days, lactic acid fermentation will be carried out sufficiently and the strains will not have any off-flavor.
In yeast fermentation, low temperature conditions of 20-25°C are set, and a large amount of yeast is added so that the number of bacterial cells is 106-108 / Moromi 9, and it is maintained for 10-15 days to produce enough alcohol. and that no yeast extract odor or ester odor is observed.
The strains that have gone through the steps of ■■ and ■, the number of yeast in each strain is reduced to 1.
By adjusting the number of yeast in the strains in the natural brewing process below 06/Moromi q and ripening at 25 to 85 °C,
Ability to generate only a very rich soy sauce brewing aroma without imparting yeast extract odor or ester odor, 0
As a step to adjust the number of yeast in the 0th cage, 32 to 36 strains were added.
They discovered that it was sufficient to adopt a process of keeping the temperature at 8C, and established a method that could produce high-quality soy sauce in a short period of time by combining these processes. That is, the method of the present invention is a method of fermenting and aging various soy sauce strains, and 10 lactic acid bacteria are added to the strains after preparation or digestion.
Add to make 7-108/moromi q 15'-20
The first step is holding at °C for 10-20 days, then yeast is added to give a ratio of 106-108/moromi 9 to 20-20%.
Second step of holding at 5°C for 10-15 days, 82-86
The third step is to treat the yeast at 10°C to reduce the number of yeast to less than 10 6 /'' strains, and the fourth step is to ripen at 25 to 85°C.
This is a soy sauce manufacturing method characterized by combining steps.

従来の速醸法では乳酸菌、酵母の管理が十分できないた
め、品質、特に香気のバラツキが大きく、一定品質の製
品を得ることは困難であったが、本発明方法によれば微
生物の添加によって発酵を促進しつつ、しかも発酵期に
異臭を生成することなく醸造できるために、常に品質の
安定した醤油を短期間に製造することが可能となった。
In the conventional fast brewing method, lactic acid bacteria and yeast cannot be sufficiently controlled, resulting in large variations in quality, especially aroma, and it is difficult to obtain products of constant quality.However, according to the method of the present invention, fermentation is improved by adding microorganisms. Because it can be brewed while promoting the fermentation process and without producing any off-flavors during the fermentation period, it has become possible to produce soy sauce of consistently stable quality in a short period of time.

特に低温発酵条件を採用したため、グルタミン酸の溶出
も良好になった。
In particular, because low-temperature fermentation conditions were adopted, the elution of glutamic acid was also improved.

以下、本発明方法について詳細に説明する。The method of the present invention will be explained in detail below.

本発明方法において発酵熟成の対象とされる醤油諸株は
、醤油麹を適当濃度の食塩水と仕込んだもの、またはそ
れを加温消化させたものなどを適用することができる。
As the soy sauce strains to be fermented and matured in the method of the present invention, soy sauce koji prepared with a saline solution of an appropriate concentration, or prepared by heating and digesting the soy sauce koji can be used.

醤油麹の仕込み方法には特に制約はなく、たとえば常法
により丸大豆、脱脂大豆、小麦、米、トウモロコシなど
を原料にして得られた醤油麹を21〜2596食塩水を
用いて仕込んで調製すればよい。また、消化諸株は、醤
油麹を水または食塩水で仕込み、無塩条件では45〜6
0°Cて15〜80時間、食塩濃度5〜18%では40
〜45℃で7〜10日間消化させ、必要に応じて補塩す
ればよい。また、醤油麹とともに未製麹原料を加えて加
温消化、する方法、あるいは醤油原料を酸素剤を利用し
て加水分解する方法によって得られた諸株を適用するこ
ともてきる。
There are no particular restrictions on the method of preparing soy sauce koji, and for example, soy sauce koji obtained from whole soybeans, defatted soybeans, wheat, rice, corn, etc. as raw materials may be prepared using a 21-2596 salt solution using a conventional method. Bye. In addition, for the digested stocks, soy sauce koji is prepared with water or salt water, and under unsalted conditions, 45 to 6
40 at 0°C for 15-80 hours and at a salt concentration of 5-18%.
Digestion may be carried out at ~45°C for 7 to 10 days, and salt may be supplemented as necessary. In addition, it is also possible to apply strains obtained by adding unmade koji raw materials together with soy sauce koji and heating and digesting them, or by hydrolyzing soy sauce raw materials using an oxygen agent.

本発明方法の第1工程においては、醤油諸株に乳酸菌を
107〜108/諸味9になるように添加し、20〜2
5°Cで10〜20日間保持して乳酸発酵を行なう。
In the first step of the method of the present invention, lactic acid bacteria are added to various soy sauce strains at a ratio of 107 to 108/moromi 9, and 20 to 2
The mixture is kept at 5°C for 10 to 20 days to carry out lactic acid fermentation.

諸株温度の調節は常法によればよく、たとえば通常の仕
込みの場合には使用する仕込み食塩水を冷却し、仕込み
後の諸株品温が15〜25°Cになるようにする。消化
諸株の場合は、諸株を冷却して15〜25°Cにする。
The temperature of each strain may be adjusted by a conventional method; for example, in the case of normal preparation, the saline solution used is cooled so that the temperature of each strain after preparation is 15 to 25°C. For digested stocks, cool the stocks to 15-25°C.

添加される乳酸菌としては、醤油醸造における代表的菌
株を単独もしくは混合して用い、たとえば、ペディオコ
ッカス・ハロフィラス(pediococcushal
ophilus) I A M 16 T 8、ペデイ
tコy力x −v −’r (pediococcus
soyae)  I AM1678、テトラコツカス・
ソーヤ(7etracoccussoyae)I AM
 1676などが適用できる。乳酸菌の添加は、その前
培養物を添加する方法によればよい。前培養は、適当な
培養基で好適な条件を設定して行うことができ、たとえ
ば培養基として醤油5.096、ペプトン1.0%、酵
母エキス0,5%、りん酸二水素カリウム1.0%、グ
ルコース1.0%、食塩17%、pH7,0の培地を用
い、28〜80℃で96時間の培養条件を設定して行う
ことができる。
As the lactic acid bacteria to be added, representative strains used in soy sauce brewing may be used alone or in combination, such as Pediococcus halophilus (Pediococcus halophilus).
ophilus) I A M 16 T 8, pedi t coy force x -v -'r (pediococcus
soyae) I AM1678, Tetracoccuscus
Sawyer (7etracoccus soyae) I AM
1676 etc. can be applied. The lactic acid bacteria may be added by adding a preculture thereof. Pre-culture can be carried out using a suitable culture medium under suitable conditions. For example, the culture medium may be soy sauce 5.096, peptone 1.0%, yeast extract 0.5%, potassium dihydrogen phosphate 1.0%. This can be carried out by using a medium containing 1.0% glucose, 17% sodium chloride, and pH 7.0, and setting culture conditions at 28 to 80° C. for 96 hours.

乳酸発酵の温度条件を20〜25℃という低温条件に設
定したことより、十分な乳酸発酵を行わせるために乳・
酸閑の添加量を107〜108/諸味9になるようにす
ることが必須である。このような乳酸菌の多量添加と低
温発酵により、10〜20日間で乳酸を十分に生成させ
、しかも異臭の生成を防止することができる。
By setting the temperature conditions for lactic acid fermentation at a low temperature of 20 to 25°C, milk and
It is essential that the amount of acid added is 107 to 108/moromi 9. By adding a large amount of lactic acid bacteria and fermenting at low temperature, it is possible to sufficiently produce lactic acid in 10 to 20 days and prevent the production of off-flavors.

乳酸菌の乳酸、香気生成に対する温度条件の影響につい
てモデル実験した結果は次のとおりであった。
The results of a model experiment on the influence of temperature conditions on lactic acid and aroma production by lactic acid bacteria were as follows.

実験 1 常法により調製した醤油麹を1096食塩水を用いて1
1水仕込みを行い、50°Cで48時間消化させ、濾過
し、濾液を食塩濃・度18%およびpH6,0に調整し
、これにペディオコッカス・/′−ロフイラスIAM1
678を2. Ox 107/ mlになるように接種
し、10’C,15°Cl2O℃、25℃、28°Cの
各温度条件下でlO日間静置培養した。
Experiment 1 Soy sauce koji prepared by a conventional method was mixed with 1096 saline solution.
1 water was prepared, digested at 50°C for 48 hours, filtered, and the filtrate was adjusted to a salt concentration of 18% and pH 6.0.
678 2. The cells were inoculated at 107 Ox/ml and statically cultured for 10 days at 10'C, 15°C, 25°C, and 28°C.

なお培地中の全窒素濃度は1.60%であった。Note that the total nitrogen concentration in the medium was 1.60%.

これらについての乳酸の生成量およびI)Hの分析結果
、ならびに香気の官能検査結果は第1表のとおりであっ
た。
Table 1 shows the analysis results for the amount of lactic acid produced and I)H, and the sensory test results for aroma.

第1表 本発明方法における第2工程では、乳酸発酵させたpH
5,、o以下の諸株−こ酵母を106〜108/諸d萄
なるように添加し、20〜25°Cで10〜15日間保
持してアルコール発酵を行う。
Table 1 In the second step of the method of the present invention, the pH of the lactic acid fermentation
The following strains of yeast are added at a concentration of 106 to 108/d and held at 20 to 25°C for 10 to 15 days to carry out alcoholic fermentation.

添加酵′母としては、醤油酵母として代表的な菌株を用
いることができ、たとえば、サツカロミセス・ルーキシ
−(3accharomyces rouxii) I
 F 00517、サツカロミセス・ルーキシ−・バリ
エフ)−ハoメンブ5 二x (3accharomy
ctts rouzijvari halomenbr
anis) I F OO494、トルロプシx −ハ
ーサチリy、 (7orulopsisversati
lis)AHU8788、)ルロブシス・エッチエリシ
ー(7orulopsis etchellisii)
 A HU 4141、トルロプシス・マグノリア<7
orutopSis magnotia) A Hu4
215、トルロプシx ・f ヶ(7orulopsi
s 5ake)杢 AHU4260、トルプシス・スフエリ力(7orul
opsis 5pherica)、トルロプシy、 −
yノv5 (Torulopsis anomala)
などを単独または組合せて添#を 加することができる。酵母の添加法−前培養物を添加す
る方法を採用すればよく、その前培養の方法条件も常法
による。たとえば、醤油80.096、食塩5.096
、グルコース5.096、pH5,0の培地に好気的に
培養したものを使用する。
As the additive yeast, typical strains of soy sauce yeast can be used, such as Saccharomyces rouxii (3accharomyces rouxii) I
F 00517, Saccharomyces luxii variev) - Haomenbu 5 2
ctts rouzijvari halomenbr
anis) I F OO494, torulopsis x -hersatiliy, (7orulopsisversati
lis) AHU8788,) 7orulopsis etchellisii
A HU 4141, Torulopsis Magnolia <7
orutopSis magnotia) A Hu4
215, torulopsi x ・f months (7orulopsi
s 5ake) heather AHU4260, Torpsis spheeri force (7orul
opsis 5pherica), Torulopsis y, −
yno v5 (Torulopsis anomala)
These can be added alone or in combination. Yeast addition method - A method of adding a preculture may be adopted, and the conditions for the preculture are also the same as conventional methods. For example, soy sauce 80.096, salt 5.096
, glucose 5.096, pH 5.0 cultured aerobically.

醤油諸株に対する酵母2添加によるアルコール発酵の温
度条件は、従来は28〜80℃であった。
Conventionally, the temperature conditions for alcoholic fermentation by adding yeast 2 to various soy sauce strains were 28 to 80°C.

この条件下ではアルコールを短時間に多量生成させるこ
とが可能であるが、アルコールと同時に酵母エキス臭、
エステル臭などの異臭を生成する欠点があった。アルコ
ール発酵時の温度条件を20〜25°Cという低温に設
定することにより、異臭の生成が起らないことが判明し
た。本発明方法においては、このような低温条件で発酵
させるのでアルコール生成速度が遅くなり、短期間で十
分なアルコール生成を行わせるために酵母の添加を10
6〜108/諸味りになるようにすることが必要である
。これらの条件設定により、10〜15日間で十分なア
ルコール発酵を行うことができる。
Under these conditions, it is possible to produce a large amount of alcohol in a short period of time, but at the same time, the yeast extract odor,
It has the disadvantage of producing off-flavors such as ester odor. It has been found that by setting the temperature conditions during alcohol fermentation to a low temperature of 20 to 25°C, no off-flavors are generated. In the method of the present invention, since fermentation is carried out under such low-temperature conditions, the rate of alcohol production is slow, and in order to produce sufficient alcohol in a short period of time, the addition of yeast is
It is necessary to make it 6 to 108/moromi. By setting these conditions, sufficient alcoholic fermentation can be performed in 10 to 15 days.

酵母のアルコール、香気生成に対する温度条件の影響に
ついてモデル実験した結果は、次のとおりであった。
The results of a model experiment on the influence of temperature conditions on alcohol and aroma production by yeast were as follows.

実験 2 実験1と同様にして調製した消□゛化諸味液を食塩濃度
18%、I)H4,9に調整し、サツカロミセス・ルー
キシ−IFOO517またはトルロプシス・バーサチリ
スAHU878Bをそれぞれ1.0×107/s+/に
なるように接種し、10°C115°Cl2O’C,2
5°C128°C180°C185°Cの各温度条件下
で10日間静置培養した。
Experiment 2 The quenched moromi liquid prepared in the same manner as in Experiment 1 was adjusted to a salt concentration of 18% and I) H4.9, and Saccharomyces luxi-IFOO517 or Torulopsis versatilis AHU878B was added at 1.0 x 107/s+, respectively. / 10°C115°Cl2O'C,2
The cells were statically cultured for 10 days under various temperature conditions of 5°C, 128°C, 180°C, and 185°C.

これらについてのアルコール生成量の分析結果および香
気の官能試験結果は第2表のとおりてあった。
The analysis results of the amount of alcohol produced and the results of the aroma sensory test are shown in Table 2.

第2表 本発明方法の第3工程では、諸株を82〜360Cに加
温して諸株中の酵母数を106/諸味q以下に減少させ
る。
Table 2 In the third step of the method of the present invention, the strains are heated to 82 to 360 C to reduce the number of yeast in the strains to 10 6 /moromi q or less.

第2工程のアルコール発酵により、諸株中にアルコール
が十分に生成された段階では、諸株をIll、温で管理
してきたために諸株の熟成度合が不十分である。しかし
、熟成を完了させる目的で第2工程のアルコール発酵終
了後、そのまま低温条件下に長時間維持すると、やはり
異臭が生成する。このような異臭生成を防止して諸株熟
成を行−う条件Jこついて検討したところ、諸株熟成を
天然醸造諸株の酵母数と同レベル、すなわち106/諸
味q以下の酵母の存在下で行えばよいことが判明した。
At the stage where sufficient alcohol has been produced in the strains through the alcoholic fermentation in the second step, the degree of ripening of the strains is insufficient because the strains have been kept at a constant temperature. However, if the product is kept under low-temperature conditions for a long time after the second step of alcohol fermentation for the purpose of completing ripening, an off-flavor will still be produced. Conditions for ripening the strains while preventing the production of such off-odors J After careful consideration, we found that the ripening of the strains was carried out in the presence of yeast at the same level as the yeast number of the naturally brewed strains, that is, 106/moromi q or less. It turns out that you can do it with.

さらに第1図に示したように諸株品温を82〜86°C
に高めると、酵母は急速に死滅し、容易に諸株中の酵母
数を減6dことが可能であることを知見した。
Furthermore, as shown in Figure 1, the temperature of each plant was adjusted to 82 to 86°C.
It has been found that when the yeast is raised to 60%, the yeast rapidly dies, and it is possible to easily reduce the number of yeast in the strains by 6 days.

第4工程における諸株の熟成は、諸株品温を25〜85
℃にして80〜50日間管理して行纏う。色度の淡い醤
油を得る場合には温度条件を25°Cよりに、色度の濃
いものの場合には85°Cよりに設定する。第4工・程
を経ることにより、芳醇な醤油醸造香気を有する色沢あ
ざやかな熟成諸味を得ることができる。
In the fourth step, the strains are aged at a temperature of 25 to 85.
It is maintained at ℃ for 80 to 50 days. When obtaining a soy sauce with a light color, the temperature condition is set at 25°C or higher, and when obtaining a soy sauce with a deep color, the temperature is set at 85°C or higher. By going through the fourth step, it is possible to obtain mature moromi with a bright color and a rich soy sauce brewing aroma.

以上のように本発明方法によれば、全熟成期間90日以
内で天然醸造醤油と何ら変わらない醤油製品を得ること
ができる。
As described above, according to the method of the present invention, a soy sauce product that is no different from naturally brewed soy sauce can be obtained within a total aging period of 90 days.

以下 本発明方法の実施例を挙げてより具体的な説明と
する。
A more specific explanation of the method of the present invention will be given below with reference to Examples.

実施例1 脱脂大豆100&Li、小麦100#をそれぞれ常法に
より蒸煮処理、または炒蒸割砕して混合し、これに醤油
麹菌を接種し、製麹して醤油麹を得た。
Example 1 Defatted soybeans 100&Li and wheat 100# were each steamed or roasted and crushed in a conventional manner and mixed, inoculated with soy sauce koji mold, and made into koji to obtain soy sauce koji.

醤油麹を5°Cに冷却した24%食塩水を用いて11水
で仕込んだ。諸株品温は17℃であった。
Soy sauce koji was prepared with 11 water using 24% saline solution cooled to 5°C. The temperature of each strain was 17°C.

諸株g1どなるように添加し、通常の撹拌をしながら品
温を17°Cに保持して12:月間乳酸発酵させた。こ
の諸株の pHは4.90であった。
G1 of each strain was added to the mixture, and the product temperature was maintained at 17°C while stirring normally, and lactic acid fermentation was carried out for 12 months. The pH of these strains was 4.90.

この諸株に、別に培養したサツカロミセス・ルーキシ−
IF00571をlX107/諸味q、トルロプシス・
バーサチリスAHU8788を1×106/諸味9にな
るように添加し、通常の撹拌をして20°Cで15日間
発酵させた。この時の諸法中の乳酸の生成量は9801
197diで、アルコールは2.4096であった。
Separately cultured Satucharomyces rukisi
IF00571 lX107/Moromi q, Torulopsis
Versatillis AHU8788 was added at a ratio of 1 x 10 6 /moromi 9, and fermented at 20°C for 15 days with regular stirring. The amount of lactic acid produced in the various methods at this time was 9801
At 197di, alcohol was 2.4096.

この諸株を直ちに34°Cにして4日間経過させ、た後
、80℃で50日間熟成させた。この熟成諸株を常法に
より圧搾、火入れして製品とした。
These strains were immediately heated to 34°C for 4 days, and then aged at 80°C for 50 days. These matured stocks were pressed and pasteurized using conventional methods to produce products.

一方従来の温醸法で6力月間醸造して得た醤油と成分分
析および咀味試験により比較した。結果は第8表のとお
りてあった。なお、哨味試験は熟練したパネル20名に
より二点嗜好試験法で付属った。表中の数字は、試料の
香味を好む人数を示す。批評は、批評会の結果をまとめ
たものである。
On the other hand, it was compared with soy sauce obtained by brewing for 6 months using the conventional hot brewing method by component analysis and chewing taste test. The results are shown in Table 8. The taste test was conducted by a panel of 20 experts using a two-point preference test method. The numbers in the table indicate the number of people who like the flavor of the sample. A critique is a summary of the results of a critique meeting.

第3表−1 第3表−2 本実施例醤油の成分分析結果を従来法のものと比べると
、本発明方法による低温発酵でも、窒素成分の溶出は全
く影響を受けないこと、グルタミン酸の生成がすぐれて
いることが明らかである。
Table 3-1 Table 3-2 Comparing the component analysis results of the soy sauce of this example with those of the conventional method, it was found that even at low temperature fermentation by the method of the present invention, the elution of nitrogen components was not affected at all, and the production of glutamic acid is clearly superior.

本実施例による醤油と従来の温醸法醤油とは官能検査の
結果にも有意差があり、本実施例醤油の方が品質的に優
れていることが認められた。
There was also a significant difference in the results of sensory tests between the soy sauce according to this example and the conventional hot-brewed soy sauce, and it was recognized that the soy sauce of this example was superior in terms of quality.

実施例 2 脱脂大豆4800 kg、小麦480(lりをそれぞれ
常法により蒸煮処理、または炒蒸割砕して混合し、これ
に醤油麹菌を接種し、製麹して醤油麹を得た。
Example 2 4800 kg of defatted soybeans and 480 liters of wheat were each steamed or roasted and crushed in a conventional manner and mixed, inoculated with soy sauce koji mold, and made into koji to obtain soy sauce koji.

醤油麹を5°Cに冷却した23.5%食塩水を用いて1
2水で仕込んだ。諸株品温は15°Cてあった。
1 using 23.5% salt solution cooled to 5°C soy sauce koji
2 Prepared with water. The temperature of the plants was 15°C.

この諸株に、別に培養した乳酸菌(ペディオコッカス・
ハロフィラスIAM1678)を5 X 107/諸味
qになるように添加し、品温を保持して通常の撹拌を行
ないながら14日間乳酸発酵させた。
These strains were combined with separately cultured lactic acid bacteria (Pediococcus spp.
Halophilus IAM1678) was added at a ratio of 5 x 107/q of moromi, and lactic acid fermentation was carried out for 14 days while maintaining the product temperature and performing normal stirring.

この時、諸株 pHは4.84であった。At this time, the pH of each strain was 4.84.

この諸株に、別に培養したサツカロミセス・ルーキシ−
IF00571を1.5X107/諸味9、トルロプシ
ス・エッチエリシーAHU414141×106/諸味
q、トルロプシス・サケAHU4260をI X 10
6 /諸味9になるように添加し、通常の撹拌をして2
2℃で10日間発酵させた。
Separately cultured Satucharomyces rukisi
IF00571 to 1.5 x 107/Moromi 9, Torulopsis etcherisii AHU414141 x 106/Moromi q, Torulopsis salmon AHU4260 to I x 10
Add so that the ratio is 6/moromi 9, stir as usual and add 2
Fermentation was carried out at 2°C for 10 days.

この時の諸株の乳酸生成量は1040■/dl、アルコ
ール生成量は2.824であった。
At this time, the lactic acid production amount of each strain was 1040 μ/dl, and the alcohol production amount was 2.824.

この諸株を直ちに86°Cにして8日間経過させた後、
88°Cて48日間熟成させた。この熟成諸株を常法に
より圧搾、火入れして製品にした。
These strains were immediately heated to 86°C for 8 days, and then
It was aged for 48 days at 88°C. These matured stocks were pressed and pasteurized using conventional methods to produce products.

一方従来の温醸法で6力月間醸造して得た醤油と成分分
析および晰味試験をして比較した。結果は第4表のとお
りてあった。
On the other hand, we conducted a component analysis and taste test to compare it with soy sauce obtained by brewing for 6 months using the conventional hot brewing method. The results are shown in Table 4.

第4表−1 第4表−2 両供試醤油間の比較結果は有意差は認められず、両者の
品質の差異は認められなかった。
Table 4-1 Table 4-2 No significant difference was observed between the two test soy sauces, and no difference in quality was observed between the two.

実施例 3 脱脂大豆100 Ag、小麦100kri@−それぞれ
常て13水で仕込んだ。諸−品温は15℃であった。
Example 3 Defatted soybean 100 Ag, wheat 100 kri@- each was prepared with 13 water. Item temperature was 15°C.

この諸株に、別に培養した乳酸菌(ペディオコッカ7.
− ハ0 フイ5スIAM1678)を5 X 107
/諸味gになるように添加し、通常の撹拌を行■いなが
ら品温を保持して8日間乳酸発酵させた。
These strains were combined with separately cultured lactic acid bacteria (Pediococca 7.
- 5 x 107
/g of moromi was added, and lactic acid fermentation was carried out for 8 days while maintaining the temperature while stirring normally.

諸株pHは4.98であった。The pH of each strain was 4.98.

この諸株に、別に培養したサツカロミセス・ルーキシ−
IF00571を5x107/諸味9、トル台ブシス・
エッチエリシーAHU4141 ヲ2X 106 /諸
味9になるように添加し、20℃で14日間発酵させた
。この時の諸株中の乳酸生成量は75211f / d
L 、アルコール生成量は2.76%であった。
Separately cultured Satucharomyces rukisi
IF00571 5x107/Moromi 9, Torudai Bushis・
H. Elysee AHU4141 was added at a ratio of 2 x 106/moromi 9, and fermented at 20°C for 14 days. The amount of lactic acid produced in each strain at this time was 75211f/d
L, the amount of alcohol produced was 2.76%.

この諸株を直ちに82°Cで6日経過させた後、諸株品
温を26°Cにして45日間熟成させ、常法により圧搾
、火入れして淡口醤油とした。
These stocks were immediately incubated at 82°C for 6 days, then brought to a temperature of 26°C and aged for 45 days, and then pressed and pasteurized using conventional methods to obtain light soy sauce.

一方、従来法で6力月醸造して得た淡口醤油と成分分析
および一哨味試験をして比較した。結果は第5表のとお
りであった。
On the other hand, we conducted a component analysis and a taste test and compared it with the light soy sauce obtained by brewing it using the conventional method. The results are shown in Table 5.

第5表−1 第5表−2 両供試淡口醤油間番こ哨味試験の結果は有意差があり、
本実施例製品のほうが品質が優れていることか認められ
た。
Table 5-1 Table 5-2 There is a significant difference between the results of the light soy sauce sample taste test,
It was recognized that the product of this example was superior in quality.

実施例 4 脱脂大豆100 kg、小麦100 kQを用いて常法
により製造した醤油麹を12%食塩水で11水に仕込み
、40℃で7日間消化し、この消化諸株を食塩濃度17
.0%、pH5,9に調整後、18°Cにして、別に培
養した乳酸菌(ペディオコッカス・ハロフィラスIAM
1678)を2 x 107 /諸株qになるように添
加し、15日間乳酸発酵を行1った。この時諸株pHは
4.82であった。
Example 4 Soy sauce koji produced by a conventional method using 100 kg of defatted soybeans and 100 kQ of wheat was added to 11 water with 12% salt solution, digested at 40°C for 7 days, and the digested strains were prepared at a salt concentration of 17.
.. After adjusting the pH to 0% and pH 5.9, the lactic acid bacteria (Pediococcus halophilus IAM) were cultured separately at 18°C.
1678) was added at 2 x 107/q of strains, and lactic acid fermentation was carried out for 15 days. At this time, the pH of each strain was 4.82.

この諸株1こ、別に培養したサツカロミセス・ルーキシ
−IF00571を8×107/諸味g、トルロプシス
・サケ−AHU4260およびトルロプシス・バーサチ
リスAHU8788をそれぞ第15 X 105 /諸
株qになるように添加し、22°Cで14日間発酵させ
た。
To each of these strains, separately cultured Satucharomyces ruxi-IF00571 was added at 8 x 10/g of moromi, Torulopsis salmon-AHU4260 and Torulopsis versatilis AHU8788 were added at 15 x 10/q of each strain, Fermentation was performed at 22°C for 14 days.

この諸株を84℃で4日経過させた後、諸株品温を27
°Cにして45日間熟成させ、常法により圧搾、火入れ
して製品とした。
After keeping these stocks at 84°C for 4 days, the temperature of the stocks was adjusted to 27°C.
The mixture was aged at °C for 45 days, then pressed and pasteurized using conventional methods to obtain a product.

一方従来法で6力月醸造して得た醤油と成分号析、晰味
試験をして比較した。結果は第6表のとおりであった。
On the other hand, we conducted a component analysis and taste test to compare it with soy sauce obtained by brewing it using the conventional method. The results are shown in Table 6.

第6表−1 第6表−2 両供試醤油間に有意差はなく、両者の品質の差異は認め
られなかった。
Table 6-1 Table 6-2 There was no significant difference between the two test soy sauces, and no difference in quality was observed between the two.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は、酵母の死滅と温度との関係を示すものである
。 特許出願人 (677)ヤマサ醤油株式会社第1図 4ek
FIG. 1 shows the relationship between yeast death and temperature. Patent applicant (677) Yamasa Soy Sauce Co., Ltd. Figure 1 4ek

Claims (1)

【特許請求の範囲】[Claims] 醤油諸株を発酵熟成させる方法において、仕込みないし
消化後の諸株に対して乳酸菌を107〜108/諸味q
になるように添加して15〜20°Cて10〜20日間
保持する第1工程、酵母を106〜108/諸味りにな
るように添加して20〜25る第3工程、および25〜
35°Cで調熟させる第4工程を結合することを特徴と
する醤油の製造法。
In the method of fermenting and maturing soy sauce strains, lactic acid bacteria are added to the strains after preparation or digestion at a concentration of 107 to 108 q/moromi q.
The first step is to add the yeast to a ratio of 10 to 20°C and hold it for 10 to 20 days, the third step is to add yeast to a ratio of 10 to 108/moromi to 20 to 25, and
A method for producing soy sauce characterized by combining a fourth step of ripening at 35°C.
JP57023380A 1982-02-16 1982-02-16 Soy sauce manufacturing method Expired JPS606183B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57023380A JPS606183B2 (en) 1982-02-16 1982-02-16 Soy sauce manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57023380A JPS606183B2 (en) 1982-02-16 1982-02-16 Soy sauce manufacturing method

Publications (2)

Publication Number Publication Date
JPS58141761A true JPS58141761A (en) 1983-08-23
JPS606183B2 JPS606183B2 (en) 1985-02-16

Family

ID=12108918

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57023380A Expired JPS606183B2 (en) 1982-02-16 1982-02-16 Soy sauce manufacturing method

Country Status (1)

Country Link
JP (1) JPS606183B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6387961A (en) * 1986-10-01 1988-04-19 Higeta Shoyu Kk Method for improving quality of low-quality soy sauce
JPS642550A (en) * 1987-06-25 1989-01-06 Takeda Shokuryo Kk Process for quick brewing of soy
EP1512407A1 (en) * 2003-09-02 2005-03-09 Microbio Company, Ltd. Use of fermented glycine max (L.) extract in inhibiting 15-lipoxygenase
US7056543B2 (en) 2001-12-21 2006-06-06 Kikkoman Corporation Method of brewing soy sauce

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3688471T2 (en) * 1985-03-20 1993-12-09 Nec Corp Key intercom system.

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6387961A (en) * 1986-10-01 1988-04-19 Higeta Shoyu Kk Method for improving quality of low-quality soy sauce
JPS642550A (en) * 1987-06-25 1989-01-06 Takeda Shokuryo Kk Process for quick brewing of soy
US7056543B2 (en) 2001-12-21 2006-06-06 Kikkoman Corporation Method of brewing soy sauce
EP1512407A1 (en) * 2003-09-02 2005-03-09 Microbio Company, Ltd. Use of fermented glycine max (L.) extract in inhibiting 15-lipoxygenase

Also Published As

Publication number Publication date
JPS606183B2 (en) 1985-02-16

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