JP2958831B2 - Seasoning liquid production method - Google Patents

Seasoning liquid production method

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Publication number
JP2958831B2
JP2958831B2 JP3288802A JP28880291A JP2958831B2 JP 2958831 B2 JP2958831 B2 JP 2958831B2 JP 3288802 A JP3288802 A JP 3288802A JP 28880291 A JP28880291 A JP 28880291A JP 2958831 B2 JP2958831 B2 JP 2958831B2
Authority
JP
Japan
Prior art keywords
seasoning liquid
extraction
koji
salt
protein
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 - Fee Related
Application number
JP3288802A
Other languages
Japanese (ja)
Other versions
JPH05123131A (en
Inventor
二郎 片岡
晴樹 大村
正樹 柏原
早苗 井田
長義 北田
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.)
Ajinomoto Co Inc
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Ajinomoto Co Inc
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Publication date
Application filed by Ajinomoto Co Inc filed Critical Ajinomoto Co Inc
Priority to JP3288802A priority Critical patent/JP2958831B2/en
Publication of JPH05123131A publication Critical patent/JPH05123131A/en
Application granted granted Critical
Publication of JP2958831B2 publication Critical patent/JP2958831B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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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、大豆蛋白質を麹菌酵素
で分解してアミノ酸、ペプチド及びオリゴ糖を含み醤油
に代替しうる調味液を製造する方法に関するものであ
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a seasoning solution containing amino acids, peptides and oligosaccharides, which can be substituted for soy sauce, by decomposing soybean protein with a koji mold enzyme.

【0002】[0002]

【従来の技術】大豆蛋白質を麹菌を液体培養した麹菌酵
素で分解してアミノ酸、ペプチドを含む調味液の製造に
ついては過去多くの方法が報告されている。醤油の場合
には、製造原料を全量固体麹製麹したのち、高濃度の食
塩水で長期間諸味発酵する為に、多大な麹製造設備と諸
味発酵設備と圧搾設備を使用し、4ヵ月から1年の長期
間を掛けて製造することに比較してこれらの方法は簡易
な設備で短期間に製造する利点を有している。
2. Description of the Related Art Many methods have been reported in the past for producing a seasoning solution containing amino acids and peptides by decomposing a soybean protein with an enzyme of koji mold obtained by liquid culture of koji mold. In the case of soy sauce, after all production raw materials are solid koji-made koji, a large amount of koji production equipment, moromi fermentation equipment, and pressing equipment are used in order to ferment moromi for a long time with high-concentration saline, and from 4 months These methods have the advantage that they can be manufactured in a short time with simple equipment, as compared to manufacturing over a long period of one year.

【0003】防腐効果があるが酵素活性を阻害する食塩
の影響を防ぐ為、この酵素法は無菌状態で培養した麹菌
を酵素源として使用して、無塩かつ無菌状態での長時間
分解する方法が主流であったが、最近では酵素源として
は通常の固体麹を使用して低食塩下で分解する方法や食
塩耐性のある麹菌を使用する方法等が開発されている。
これらの方法は、バイオリアクターの使用により主呈味
源としてのグルタミン酸を増加させている。
In order to prevent the effect of salt which has an antiseptic effect but inhibits enzyme activity, this enzymatic method is a method of decomposing for a long time in a salt-free and aseptic condition using a koji mold aseptically cultured as an enzyme source. Recently, a method of decomposing under a low salt using ordinary solid koji and a method of using a koji mold having salt tolerance have been developed.
These methods increase glutamic acid as the main taste source by using a bioreactor.

【0004】[0004]

【発明が解決しようとする課題】前述のように、液体麹
を用いる方法は無塩かつ無菌状態で長時間酵素反応させ
なければならなかった。
As described above, the method using liquid koji requires a long enzymatic reaction under salt-free and sterile conditions.

【0005】本発明は、このような問題点があるが作業
性が容易な液体麹法を改良して、風味の優れた新規な調
味液の製造方法を提供することを目的としている。
An object of the present invention is to improve the liquid koji method which has such problems but is easy to work, and to provide a novel method for producing a seasoning liquid having an excellent flavor.

【0006】[0006]

【課題を解決するための手段】本発明は、上記目的を達
成した調味液の製造方法を提供するものである。この製
造方法は、原料脱脂大豆に含まれている少糖類を水又は
含水アルコールで抽出し、該抽出液を抽出残渣から分離
してこれに麹菌を接種して培養し、該培養液を前記の抽
出残渣又はこれからアルカリ抽出して得られた蛋白溶液
と混合してpH3〜8で40〜60℃で酵素分解した後、濾過
することを特徴としている。
SUMMARY OF THE INVENTION The present invention provides a method for producing a seasoning liquid which achieves the above object. In this production method, oligosaccharides contained in raw defatted soybeans are extracted with water or hydrous alcohol, the extract is separated from the extraction residue, and this is inoculated with a koji mold and cultured, and the culture solution is subjected to the method described above. It is characterized in that it is mixed with an extraction residue or a protein solution obtained by alkali extraction therefrom, and is subjected to enzymatic decomposition at pH 3 to 8 at 40 to 60 ° C., followed by filtration.

【0007】脱脂大豆からの可溶性の少糖類の分離方法
は通常2〜10倍量、好ましくは3〜5倍量の水でもよい
が、その場合脱脂大豆の変性度で異なるが、蛋白の可溶
化が起こり抽出液への蛋白漏出量が多くなる。この防止
方法として、抽出時のpHを微酸性として蛋白の等電点近
くにすることが有効であり、この方法として抽出水を塩
酸、乳酸等の酸で調整する方法がある。しかしながら、
抽出時に遊離型の陽イオン交換樹脂を通過させて陽イオ
ンを吸着されることにより、脱脂大豆中のクエン酸等の
有機酸を遊離させて自動的にpHを3.0から4.0にする方法
は糖の抽出率を高め、糖の他無機質を多く含み麹菌の培
養には更に良好である。更に、抽出の温度は常温でよい
が温度を高くすれば抽出時間の短縮や腐敗防止に有効で
ある。含水アルコール、例えば80%のエチルアルコール
を使用して同様に脱脂大豆を抽出し糖類を抽出する方法
でも、水抽出法と同様の手法で実施可能であるが、培養
液とする際にアルコールを濃縮蒸留除去する必要があ
る。蛋白区分は脱アルコール時に変性されており、酵素
分解時に加熱変性が不要である利点がある。
[0007] The method of separating soluble oligosaccharides from defatted soybeans may be usually 2 to 10 times, preferably 3 to 5 times the amount of water. In such a case, the degree of denaturation of the defatted soybeans varies. Occurs and the amount of protein leaked into the extract increases. As a method for preventing this, it is effective to make the pH at the time of extraction slightly acidic so as to be close to the isoelectric point of the protein, and there is a method of adjusting the extraction water with an acid such as hydrochloric acid or lactic acid. However,
The method of releasing organic acids such as citric acid in defatted soybeans and automatically adjusting the pH from 3.0 to 4.0 by absorbing cations by passing through a free cation exchange resin at the time of extraction is the method of sugar. It enhances the extraction rate and contains a lot of minerals in addition to sugar, which is even better for culturing Aspergillus oryzae. Further, the temperature for extraction may be room temperature, but increasing the temperature is effective for shortening the extraction time and preventing rot. The method of extracting defatted soybeans and extracting sugars in the same manner using aqueous alcohol, for example, 80% ethyl alcohol, can be carried out in the same manner as in the water extraction method. It needs to be distilled off. The protein section is denatured at the time of dealcoholation, and has the advantage that heat denaturation is not required at the time of enzymatic decomposition.

【0008】抽出液には、グルコース等の単糖類、2糖
類のショ糖およびオリゴ糖よりなる少糖類と大豆から抽
出される各種の無機質、ビタミンを含み麹菌の培養には
特に他の成分を添加せずに培地として使用可能である。
この抽出液は、pHが3.5前後の微酸性であり、加熱殺菌
して初期の雑菌を無くしたのち麹菌を接種することによ
り、無菌状態での管理をすることなく麹菌を培養し、分
解に必要な酵素量を蓄積することが可能である。
The extract contains monosaccharides such as glucose, disaccharides such as disaccharides sucrose and oligosaccharides, various inorganic substances extracted from soybeans and vitamins, and other components are particularly added to the culture of Aspergillus oryzae. It can be used as a medium without using.
This extract is slightly acidic with a pH of around 3.5, and is sterilized by heat to eliminate the initial bacteria, and then inoculated with koji mold to culture the koji mold without control under aseptic conditions and required for decomposition. It is possible to accumulate a large amount of enzyme.

【0009】抽出残渣は、糖類等が抽出除去されている
ため蛋白純度が向上しており、このまま適宜量の水を加
えて殺菌を兼ねた加熱変性をし、次いで、麹菌の培養液
を混合して酵素分解させることができる。酵素分解時に
は、糖類が殆ど存在しない為粘度が顕著に減少してお
り、防腐の為の食塩等の添加をせずに酵素反応を行なっ
ても腐敗菌の増殖はない。この場合、抽出残渣をさらに
0.5〜1.0N程度のアルカリで抽出する事により、蛋白を
溶液状として麹菌培養液を添加して酵素分解することに
より、濾過圧搾工程を軽減することも可能である。
[0009] The extraction residue has an improved protein purity because sugars and the like have been extracted and removed. An appropriate amount of water is added to the residue for heat denaturation, which also serves as sterilization, and then a culture solution of Aspergillus is mixed. Enzymatic degradation. At the time of enzymatic decomposition, the viscosity is remarkably reduced because almost no saccharides are present. Even if the enzyme reaction is carried out without adding salt or the like for preservation, there is no growth of putrefactive bacteria. In this case, the extraction residue is further
Extraction with an alkali of about 0.5 to 1.0 N makes it possible to reduce the filtration and pressing step by converting the protein into a solution and adding a koji mold culture solution to perform enzymatic decomposition.

【0010】酵素分解はpH3〜8程度で40〜60℃程度、
好ましくは40〜50℃程度で行なう。その際、必要に応じ
て少量のペプチダーゼ活性の高い酵素剤を追加すること
ができる。この反応に小麦蛋白質等や酵母の混合添加は
アミノ酸、ペプチド構成に良好に結果を与え、風味の増
強に有効な手段である。
[0010] Enzymatic degradation is about pH 3-8, about 40-60 ° C,
Preferably, it is carried out at about 40 to 50 ° C. At that time, a small amount of an enzymatic agent having a high peptidase activity can be added as needed. Mixed addition of wheat protein or yeast or yeast to this reaction gives good results for amino acid and peptide composition and is an effective means for enhancing flavor.

【0011】本発明の方法で得られる調味液はアミノ
酸、ペプチド及びオリゴ糖を含む風味に優れたものであ
る。褐変性が少なく、また低食塩である。この調味液は
乾燥して粉末状にしてもよい。
The seasoning obtained by the method of the present invention has an excellent flavor containing amino acids, peptides and oligosaccharides. Low browning and low salt. This seasoning liquid may be dried to a powder.

【0012】[0012]

【作用】従来の液体麹を用いた方法においては、酵素分
解時に糖分が存在するが、醤油諸味とは異なって乳酸
菌、酵母等の微生物による糖の資化がないため、雑菌の
好餌となり腐敗の原因となっていた。また、原料の加熱
変性時に糖とアミノ酸の反応物が酵素の活性を阻害等の
問題があった。本発明においては、脱脂大豆中の糖分を
製麹に使用して消費させており、その結果、酵素分解時
に存在する可溶性糖分の量を大幅に減少させて腐敗を防
止している。また、原料から可溶性糖分のほとんどを抽
出していることから原料中の蛋白を加熱変性する際に、
糖とアミノ酸との褐変反応がほとんど起こらない。
[Action] In the conventional method using liquid koji, there is a sugar content at the time of enzymatic decomposition, but unlike soy sauce moromi, there is no assimilation of sugar by microorganisms such as lactic acid bacteria and yeast, so that it becomes a bait for various bacteria and becomes putrefactive. Was the cause. In addition, there has been a problem that a reaction product of a sugar and an amino acid inhibits the activity of an enzyme during heat denaturation of a raw material. In the present invention, sugars in defatted soybeans are used in koji making and consumed. As a result, the amount of soluble sugars present at the time of enzymatic decomposition is significantly reduced to prevent spoilage. Also, since most of the soluble sugars are extracted from the raw material, when heating and denaturing the protein in the raw material,
Almost no browning reaction between sugar and amino acid occurs.

【0013】[0013]

【実施例】【Example】

実施例1 10リッターの塔に脱脂大豆1kgを入れ、5リッターの水
を上部から添加し、塔下部に溶出した水をポンプで循環
しつつ連続浸漬する。この際に、環境水を700mlの遊離
型の強酸性陽イオン交換樹脂(SK#1B)を通過させ
る。脱脂大豆を通過した液のpHが3.5前後になってから2
0分後に循環を中止し、浸漬水を集める(約3リッタ
ー)。この1,000mlを100℃で20分加熱したのち冷却し、
500mlの坂口フラスコに分注する。市販の種麹菌を接種
し、30℃で40時間培養して酵素源とする。
Example 1 1 kg of defatted soybeans was placed in a 10 liter tower, 5 liters of water was added from the top, and water eluted at the bottom of the tower was continuously immersed while circulating with a pump. At this time, environmental water is passed through 700 ml of a free strong acid cation exchange resin (SK # 1B). After the pH of the liquid that passed through the defatted soybean reached around 3.5, 2
After 0 minutes, the circulation is stopped and the immersion water is collected (about 3 liters). This 1,000 ml is heated at 100 ° C for 20 minutes, then cooled,
Dispense into a 500 ml Sakaguchi flask. A commercial koji mold is inoculated and cultured at 30 ° C. for 40 hours to obtain an enzyme source.

【0014】塔より脱脂大豆を取り出し、等量の水を加
えて100℃で30分加熱する。冷却後に麹菌培養液を混合
し、45℃で4日間攪拌分解する。次いで95℃、20分加熱
後濾過する。こうして、分解率40%の調味液を得た。
The defatted soybeans are taken out of the tower, an equal amount of water is added, and the mixture is heated at 100 ° C. for 30 minutes. After cooling, the koji mold is mixed and decomposed with stirring at 45 ° C. for 4 days. Then, the mixture is heated at 95 ° C. for 20 minutes and filtered. Thus, a seasoning liquid having a decomposition rate of 40% was obtained.

【0015】実施例2 実施例1と同様にして、可溶性少糖類を抽出した後の抽
出残渣を塔内に入れたまま、更に脱脂大豆重量の5倍量
の0.85NのNaOHで循環浸漬し、蛋白質のみを液体状
に抽出する。この蛋白溶液を90℃、10分加熱後冷却し、
乳酸または塩酸でpHを6.0とする。次いで、実施例1と
同様に培養した麹菌培養液を添加し、50℃で5日間攪拌
分解する。この分解液を95℃、20分加熱後に濾過する。
分解率45%の調味液を得た。
Example 2 In the same manner as in Example 1, while the extraction residue after extracting the soluble oligosaccharides was kept in the tower, it was further circulated and immersed in 0.85N NaOH five times the weight of defatted soybeans. Extract only protein in liquid form. This protein solution was heated at 90 ° C for 10 minutes and then cooled,
Adjust the pH to 6.0 with lactic acid or hydrochloric acid. Next, a koji mold culture solution cultured in the same manner as in Example 1 is added, and the mixture is stirred and decomposed at 50 ° C. for 5 days. This decomposition solution is filtered after heating at 95 ° C. for 20 minutes.
A seasoning solution having a decomposition rate of 45% was obtained.

【0016】この工程でアルカリ抽出した蛋白液の中和
に乳酸を使用すると無塩の調味液を得ることが出来、こ
の方法では実施例1に比較して圧搾濾過工程は著しく軽
減された。
When lactic acid is used to neutralize the protein solution extracted by the alkali in this step, a salt-free seasoning liquid can be obtained. In this method, the compression filtration step is remarkably reduced as compared with Example 1.

【0017】塩酸中和の場合でも分解液の窒素に対する
食塩量は3%であり、低食塩の調味液の製造が可能であ
った。
Even in the case of neutralization with hydrochloric acid, the amount of salt relative to nitrogen in the decomposition solution was 3%, and a seasoning solution with low salt could be produced.

【0018】実施例3 実施例1で得られた調味液に、さらに酵素製剤(ペプチ
ダーゼ活性の高いプロテアーゼ・アマノM(天野製薬
製)、スミチームMP(新日本化学(株)製)を添加、も
しくはこれを固定化したバイオリアクターを用いて分解
を行い、分解率55%の調味液を得た。
Example 3 An enzyme preparation (protease Amano M having high peptidase activity (manufactured by Amano Pharmaceutical Co., Ltd.) and Sumiteam MP (manufactured by Shin Nippon Chemical Co., Ltd.) are added to the seasoning solution obtained in Example 1, or This was decomposed using the immobilized bioreactor to obtain a seasoning liquid having a decomposition rate of 55%.

【0019】グルタミン酸の遊離率を45%から60%とす
ることにより、うま味とこく味を増強する効果があっ
た。
By setting the release rate of glutamic acid from 45% to 60%, there was an effect of enhancing umami and kokumi.

【0020】実施例に示した方法で製造した調味液と、
脱脂大豆と小麦を当量使用して製造した醤油とを比較す
る官能評価を実施した。
A seasoning liquid produced by the method shown in the Examples,
Sensory evaluation was performed to compare soy sauce produced using equivalent amounts of defatted soybeans and wheat.

【0021】醤油と本方法で製造した調味液の窒素濃度
と食塩濃度が異なるため、醤油及び各調味液の窒素濃度
を1.0g/dl、食塩を10g/dlと同一濃度として呈味につい
て比較したる。
Since the nitrogen concentration and the salt concentration of the soy sauce and the seasoning liquid produced by this method are different, the taste was compared with the same concentration of 1.0 g / dl for the soy sauce and each seasoning liquid and 10 g / dl for the salt. You.

【0022】評価方法は10点法で行い、醤油を5.0とし
て判定した。
The evaluation was performed according to a 10-point method, and the evaluation was made with soy sauce being 5.0.

【0023】[0023]

【表1】 [Table 1]

【0024】うまみ、こくみについては醤油とほぼ同等
であったが、実施例3の酵素剤を併用するとグルタミン
酸が多く呈味は更に改善されていた。こくみはペプチド
が多いため醤油より良好で、その結果塩角が減少した。
酵素分解でよく発現するペプチド由来の苦みについて
は、各実施例とも認められなかった。
The umami and kokumi were almost the same as soy sauce, but when the enzyme preparation of Example 3 was used in combination, the amount of glutamic acid was large and the taste was further improved. Kokumi was better than soy sauce due to its high peptide content, resulting in reduced salt angle.
No bitterness derived from the peptide, which is often expressed by enzymatic degradation, was observed in any of the examples.

【0025】[0025]

【発明の効果】本発明の方法は、麹菌の培養に原料脱脂
大豆中の糖その他の成分を利用し、かつ無塩に近い状態
でも特別の無菌容器を必要とせずにアミノ酸ペプチドを
含む調味液を製造可能である。
Industrial Applicability The method of the present invention utilizes a sugar or other component in a raw defatted soybean for cultivation of a koji mold, and a seasoning solution containing an amino acid peptide without the need for a special sterile container even in a salt-free state. Can be manufactured.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 井田 早苗 神奈川県川崎市川崎区鈴木町1−1 味 の素株式会社 川崎工場内 (72)発明者 北田 長義 神奈川県川崎市川崎区鈴木町1−1 味 の素株式会社 川崎工場内 (56)参考文献 特許164280(JP,C2) 特許129860(JP,C2) 特許143082(JP,C2) (58)調査した分野(Int.Cl.6,DB名) A23L 1/238 A23L 1/22 ──────────────────────────────────────────────────続 き Continuing on the front page (72) Sanae Ida 1-1, Suzukicho, Kawasaki-ku, Kawasaki-shi, Kanagawa Prefecture Ajinomoto Co., Inc. Kawasaki Plant (72) Inventor Nagayoshi Kitada 1-Suzukicho, Kawasaki-ku, Kawasaki-shi, Kanagawa Prefecture 1 Kawasaki Plant, Ajinomoto Co., Inc. (56) References Patent 164280 (JP, C2) Patent 129860 (JP, C2) Patent 143082 (JP, C2) (58) Fields investigated (Int. Cl. 6 , DB name) ) A23L 1/238 A23L 1/22

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 原料脱脂大豆に含まれている少糖類を水
又は含水アルコールで抽出し、該抽出液を抽出残渣から
分離してこれに麹菌を接種して培養し、該培養液を前記
の抽出残渣又はこれからアルカリ抽出して得られた蛋白
溶液と混合してpH3〜8で40〜60℃で酵素分解した後、
濾過することを特徴とする調味液の製造方法。
1. An oligosaccharide contained in a raw material defatted soybean is extracted with water or hydrous alcohol, the extract is separated from an extraction residue, and this is inoculated with a koji mold and cultured. After mixing with an extraction residue or a protein solution obtained by alkali extraction from this, and enzymatically decomposing at 40 to 60 ° C. at pH 3 to 8,
A method for producing a seasoning liquid, which comprises filtering.
JP3288802A 1991-11-05 1991-11-05 Seasoning liquid production method Expired - Fee Related JP2958831B2 (en)

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JP2958831B2 true JP2958831B2 (en) 1999-10-06

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