JPH0640796B2 - Lactic acid fermented product manufacturing method - Google Patents

Lactic acid fermented product manufacturing method

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Publication number
JPH0640796B2
JPH0640796B2 JP61309345A JP30934586A JPH0640796B2 JP H0640796 B2 JPH0640796 B2 JP H0640796B2 JP 61309345 A JP61309345 A JP 61309345A JP 30934586 A JP30934586 A JP 30934586A JP H0640796 B2 JPH0640796 B2 JP H0640796B2
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JP
Japan
Prior art keywords
lactic acid
acid fermentation
oligopeptide mixture
chain length
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
JP61309345A
Other languages
Japanese (ja)
Other versions
JPS63164841A (en
Inventor
有見子 藤田
高明 松尾
良介 木綿
実 木本
征雄 橋本
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.)
Fuji Oil Co Ltd
Original Assignee
Fuji Oil Co Ltd
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Filing date
Publication date
Application filed by Fuji Oil Co Ltd filed Critical Fuji Oil Co Ltd
Priority to JP61309345A priority Critical patent/JPH0640796B2/en
Publication of JPS63164841A publication Critical patent/JPS63164841A/en
Publication of JPH0640796B2 publication Critical patent/JPH0640796B2/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】 (産業上の利用分野) 本発明は乳酸醗酵物を短時間に製造(乳酸醗酵促進)で
きる方法を提供するものである。
DETAILED DESCRIPTION OF THE INVENTION (Industrial field of application) The present invention provides a method for producing a lactic acid fermentation product in a short time (accelerating lactic acid fermentation).

(従来技術) 従来から乳酸醗酵の促進剤としてアミノ糖(特公昭45-3
189)、特定動物肉の酵素分解低分子ペプチド(特公昭5
6-5134)、麦芽エキスとホエー蛋白水解物の併用(特開
昭59-220153)、蛋白原料の水解物を醤油乳酸菌処理す
る方法(特公昭55-39308,同51-36340等)が知られてい
る。しかし、アミノ糖は煩雑な処理を必要とし、特定動
物肉は大量入手が困難であり実用的でない。本願は醤油
等のようにオリゴペプチド自体を乳酸醗酵するものでは
なく、乳成分含有原料に添加して乳成分含有原料の乳酸
醗酵を促進するものである。
(Prior Art) Conventionally, amino sugar (Japanese Patent Publication No. 45-3
189), enzyme-degraded low molecular weight peptide of specific animal meat (Japanese Patent Publication No.
6-5134), a combination of malt extract and whey protein hydrolyzate (Japanese Patent Laid-Open No. 59-220153), and a method of treating a hydrolyzate of a protein raw material with soy sauce lactic acid bacteria (Japanese Patent Publication No. 55-39308, 51-36340, etc.) are known. ing. However, amino sugars require complicated processing, and it is not practical because it is difficult to obtain specific animal meat in large quantities. The present application does not lactic acid-ferment the oligopeptide itself such as soy sauce, but promotes the lactic acid fermentation of the dairy ingredient-containing raw material by adding it to the dairy ingredient-containing raw material.

(解決しようとする問題点) 本発明者等は乳成分含有原料の乳酸醗酵促進を目的とし
た。より好ましくは出来るだけ入手容易な原料を用い、
風味の優れた短時間乳酸醗酵促進を目的とした。
(Problems to be Solved) The present inventors aimed to promote lactic acid fermentation of a milk component-containing raw material. More preferably, use raw materials that are as easily available as possible,
The purpose was to promote short-term lactic acid fermentation with excellent flavor.

(問題を解決する為の手段) 本発明者等は前記目的を達成すべく種々の蛋白、その水
解物を検討するなかで、カゼイン等の乳成分蛋白及びそ
の水解物は乳酸醗酵促進効果が極めて少ないのに、これ
ら乳成分に含まれる蛋白以外の蛋白の水解物、例えば卵
白又は大豆蛋白等の油糧種子蛋白等の水解物のうち特定
鎖長の範囲のものが、乳成分含有原料の乳酸醗酵促進効
果を有することを見出し本発明を完成するに到った。
(Means for Solving the Problem) Among the various proteins and their hydrolyzates to be achieved by the inventors of the present invention, milk component proteins such as casein and hydrolyzates thereof have a very lactic acid fermentation promoting effect. Although small, hydrolysates of proteins other than the proteins contained in these dairy ingredients, for example, hydrolyzates such as oil seed proteins such as egg white or soybean proteins, etc. having a specific chain length range are lactic acid as a raw material containing dairy ingredients. They have found that they have a fermentation promoting effect and have completed the present invention.

即ち、本発明は乳成分含有原料に対し乳成分含有蛋白以
外の蛋白由来の平均鎖長15以下のオリゴペプチド混合物
を加え、乳酸醗酵することを特徴とする乳酸醗酵物の製
造法である。
That is, the present invention is a method for producing a lactic acid fermented product, which comprises adding a mixture of oligopeptides having an average chain length of 15 or less derived from a protein other than a milk component-containing protein to a milk component-containing raw material and performing lactic acid fermentation.

本発明の乳成分含有原料の乳成分の少なくとも一つ以上
を含むことが必要である。例えば、カゼイン、ラクトア
ルブミン、乳糖、ホエー、脱脂粉乳等を含むことが必要
である。又、これらの成分の酵素水解物を含んでもよ
い。例えば、カゼイン、ラクトアルブミン成分の一部又
は全部をこれらの酵素水解物(分子量は平均鎖長2以上
であれば特に限定しない)とすることは妨げない。前記
乳成分と本願のオリゴペプチド混合物との組合せにより
乳酸醗酵促進効果がある。
It is necessary to include at least one or more milk components of the milk component-containing raw material of the present invention. For example, it is necessary to include casein, lactalbumin, lactose, whey, skim milk powder and the like. Moreover, you may contain the enzyme hydrolyzate of these components. For example, part or all of the casein and lactalbumin components can be made into these enzyme hydrolyzates (the molecular weight is not particularly limited as long as the average chain length is 2 or more), which is not hindered. The combination of the milk component and the oligopeptide mixture of the present application has a lactic acid fermentation promoting effect.

本発明に用いるオリゴペプチド混合物は乳成分含有蛋白
以外の蛋白由来の平均鎖長15以下(2〜15)のオリゴペ
プチド混合物が適当である。カゼインやラクトアルブミ
ン等の乳成分含有蛋白由来のオリゴペプチド混合物は乳
酸醗酵促進効果が極めて少ない。通常、卵白、大豆蛋白
等の油糧種子蛋白が入手が容易なうえに、蛋白含量も高
く工業レベルで実用容易であり好ましい。特殊な蛋白は
大量入手が困難なばかりでなく、工業的に安価に大量生
産が困難であり産業上のメリットがない。例えば、特殊
なシカ科動物骨格筋等の入手容易でない動物由来の蛋白
は実用的でなく不適である。又、麦芽等は、従来からエ
キスとして各種醗酵に用いられているものの、蛋白含量
が少なく、本発明のオリゴペプチド混合物原料として実
用的でなく不適である。
The oligopeptide mixture used in the present invention is preferably an oligopeptide mixture having an average chain length of 15 or less (2 to 15) derived from a protein other than the milk component-containing protein. Oligopeptide mixtures derived from milk-containing proteins such as casein and lactalbumin have very little effect of promoting lactic acid fermentation. Usually, oil-seed proteins such as egg white and soybean protein are preferred because they are easily available and have a high protein content and are easy to put into practical use on an industrial level. Not only is it difficult to obtain a special protein in large quantities, but it is also industrially inexpensive and difficult to mass produce, so there is no industrial advantage. For example, a protein derived from an animal such as a special cervical skeletal muscle that is not readily available is not practical and is not suitable. Although malt and the like have been conventionally used as an extract in various fermentations, they have a low protein content and are not practical or suitable as a raw material for the oligopeptide mixture of the present invention.

本発明に用いるオリゴペプチド混合物の平均鎖長が15を
越えると乳酸醗酵促進効果が減少する。又、平均鎖長が
短くアミノ酸程度では、乳酸醗酵促進効果が減少するば
かりか、得られる乳酸醗酵物がアミノ酸特有の嫌な風味
がして好ましくない。通常平均鎖長2以上が適当であ
る。又、遊離アミノ酸が25%を越えると、乳酸醗酵促進
効果が減少したり、アミノ酸特有な嫌な風味が発生する
ことがある。
If the average chain length of the oligopeptide mixture used in the present invention exceeds 15, the lactic acid fermentation promoting effect is reduced. Further, when the average chain length is short and about amino acids are used, not only the lactic acid fermentation promoting effect is reduced but also the resulting lactic acid fermentation product has an unpleasant flavor peculiar to amino acids, which is not preferable. Usually, an average chain length of 2 or more is suitable. On the other hand, if the content of free amino acids exceeds 25%, the lactic acid fermentation promoting effect may be reduced, or the unpleasant flavor peculiar to amino acids may be generated.

オリゴペプチド混合物の製造態様は蛋白を公知の方法に
よりプロテアーゼを用いて水系下に水解して得ることが
できるが、通常苦味が発生することが多く、好ましく
は、特願昭60-281685等に開示されるように蛋白を、エ
ンド型プロテアーゼ及びエキソ型プロテアーゼ共存水系
下に、0.5〜10時間酵素分解して苦味のない風味の優れ
たオリゴペプチド混合物を得ることが適当である。
The oligopeptide mixture can be produced by hydrolyzing the protein in a water system using a protease by a known method, but usually bitterness is often generated, and preferably disclosed in Japanese Patent Application No. 60-281685. As described above, it is appropriate to enzymatically decompose the protein for 0.5 to 10 hours in an aqueous system coexisting with an endo-type protease and an exo-type protease to obtain an oligopeptide mixture having a good taste and no bitterness.

本発明において、平均鎖長15以下のオリゴペプチド混合
物(乾燥物として)を乳成分含有原料100重量部に対し
0.05〜10重量部、好ましくは0.1〜5重量部加え、乳酸
醗酵することが適当である。0,05重量部未満では乳酸醗
酵促進効果が少なく、10重量部を越えても乳酸醗酵促進
効果が少なくなる。これは本願に用いるオリゴペプチド
混合物の浸透圧に起因するものと推察される。
In the present invention, an oligopeptide mixture having an average chain length of 15 or less (as a dried product) is used with respect to 100 parts by weight of a raw material containing a milk component
It is suitable to add 0.05 to 10 parts by weight, preferably 0.1 to 5 parts by weight, and to ferment lactic acid. If it is less than 0.05 part by weight, the lactic acid fermentation promoting effect is small, and if it exceeds 10 parts by weight, the lactic acid fermentation promoting effect is small. It is speculated that this is due to the osmotic pressure of the oligopeptide mixture used in the present application.

本発明は乳酸飲料、ヨーグルト、ケフィア、チーズ等の
主に乳酸菌による乳酸醗酵の促進効果がある。例えば、
牛乳を用いたヨーグルトの製造において、目的の酸度に
達するまでに約8時間要するものを、本発明のオリゴペ
プチド混合物添加により約1/2の時間で目的の酸度に
達することができる。又、脱脂粉乳を用いたヨーグルト
の製造において、目的の酸度に達するまでの約5時間要
するものを、本発明のオリゴペプチド混合物添加により
約3.5時間で目的の酸度に達することができる。更に得
られるヨーグルトの風味を改良して美味しいものとする
こともできる。
The present invention has an effect of promoting lactic acid fermentation mainly by lactic acid bacteria such as lactic acid drinks, yogurt, kefir, and cheese. For example,
In the production of yogurt using milk, what takes about 8 hours to reach the desired acidity can be reached in about 1/2 time by adding the oligopeptide mixture of the present invention. Further, in the production of yogurt using skim milk powder, it takes about 5 hours to reach the desired acidity, but the desired acidity can be reached in about 3.5 hours by adding the oligopeptide mixture of the present invention. Furthermore, the flavor of the obtained yogurt can be improved to make it delicious.

以上説明したように、本発明は乳酸醗酵を促進された乳
酸醗酵物のみならず風味的にも優れた乳酸醗酵物を提供
できるものである。又、本発明に用いるオリゴペプチド
混合物を乳酸醗酵のみならず、酵母醗酵、カビ醗酵、そ
の他のバクテリア醗酵若しくはこれらの共存した醗酵に
用いることは妨げない。
As described above, the present invention can provide not only a lactic acid fermentation product in which lactic acid fermentation is promoted but also a lactic acid fermentation product excellent in flavor. The oligopeptide mixture used in the present invention can be used not only for lactic acid fermentation but also for yeast fermentation, mold fermentation, other bacterial fermentation, or fermentation in which these coexist.

(実施例) 以下実施例により本発明の実施態様を説明する。(Examples) The embodiments of the present invention will be described with reference to the following examples.

実験例1 分離大豆蛋白(フジプロ−R「不二製油(株)製)100gの
5%水溶液(pH7)をエンド型及びエキソ型プロテアー
ゼ共存するアクチナーゼAS(科研製薬製)1gを用いて
50℃で5時間酵素分解し、pH7に再調整後70℃で30分間
加熱して酵素失活させ、5000rpm×20分間遠心分離して
得た上澄みを噴霧乾燥して大豆オリゴペプチド混合物を
得た。尚、平均鎖長は特願昭60-281685記載の方法を用
いて測定した結果7.7(尚、遊離アミノ酸含量は18%)
であった。
Experimental Example 1 100 g of isolated soybean protein (Fuji Pro-R "Fuji Oil Co., Ltd.") in 5% aqueous solution (pH 7) was used with 1 g of actinase AS (manufactured by Kaken Pharmaceutical) coexisting with endo-type and exo-type proteases.
Enzymatic digestion at 50 ° C for 5 hours, readjustment to pH 7 and heating at 70 ° C for 30 minutes to inactivate the enzyme, centrifugation at 5000 rpm x 20 minutes, and spray drying of the resulting supernatant to obtain a soybean oligopeptide mixture. . The average chain length is 7.7 as measured by the method described in Japanese Patent Application No. 60-281685 (the free amino acid content is 18%).
Met.

実施例1 牛乳100mlに脱脂粉乳4.8g及び実施例1で得られた大豆
オリゴペプチド混合物0.2gを加えた混合液を50〜60℃に
加熱し、ホモゲナイザーを用いて150kg/cm2にて均質化
し、80〜90℃にて10分間加熱し、後42℃まで冷却し、カ
ルチャースクーター(Lactobacillus bulgaricus及びSt
reptococcus thermophillusの混合スターターを牛乳培
地で17時間培養した酸度1,菌数9×10の8乗個/ml)
1mlを添加し、42℃で乳酸醗酵を行い、酸度、菌数の経
時的変化をみた。結果を第1図に示す。
Example 1 A mixed solution of 4.8 g of skim milk powder and 0.2 g of the soybean oligopeptide mixture obtained in Example 1 in 100 ml of milk was heated to 50 to 60 ° C. and homogenized at 150 kg / cm 2 using a homogenizer. , Heat at 80-90 ℃ for 10 minutes, then cool to 42 ℃, culture scooter (Lactobacillus bulgaricus and St
A reptococcus thermophillus mixed starter was cultivated in milk medium for 17 hours, acidity 1, bacterial number 9 × 10 8 / ml)
1 ml was added and lactic acid fermentation was carried out at 42 ° C., and changes with time of acidity and number of bacteria were observed. The results are shown in Fig. 1.

尚、コントロールは該ペプチドの代わりに脱脂粉乳5.0g
を用いた。
The control is 5.0 g of skim milk powder instead of the peptide.
Was used.

第1図から明らかなようにヨーグルトの完成である酸度
0.8に達するまでに、コントロールは5時間かかったも
のを、大豆オリゴペプチド混合物を加えたものは3.5時
間しかかからなかった。
As is clear from Fig. 1, acidity is the completion of yogurt.
The control took 5 hours to reach 0.8, while the soy oligopeptide mixture was added only 3.5 hours.

又、得られたヨーグルトもコントロールより美味しいも
のであった。
The yogurt obtained was also tastier than the control.

実験例2 卵白を用い実験例1と同様にして平均鎖長5.3、遊離ア
ミノ酸15%の卵白オリゴペプチド混合物を得た。
Experimental Example 2 An egg white oligopeptide mixture having an average chain length of 5.3 and free amino acids of 15% was obtained in the same manner as in Experimental Example 1 using egg white.

実施例2 実験例1で得られた卵白オリゴペプチド混合物を実施例
1の大豆オリゴペプチド混合物の代わりに用い、実施例
1と同様にしてヨーグルトを製造した。
Example 2 Using the egg white oligopeptide mixture obtained in Experimental Example 1 instead of the soybean oligopeptide mixture of Example 1, yogurt was produced in the same manner as in Example 1.

酸度が0.8に達する時間は実施例1の大豆オリゴペプチ
ド混合物のときと同様3.5時間で、風味のよいヨーグル
トが得られた。
The time required for the acidity to reach 0.8 was 3.5 hours as in the case of the soybean oligopeptide mixture of Example 1, and a yogurt with a good taste was obtained.

実験例3 実験例1と同様にして市販カゼインを水解して平均鎖長
5.4、遊離アミノ酸13.3%ののカゼインオリゴペプチド
混合物を得た。
Experimental Example 3 In the same manner as in Experimental Example 1, commercially available casein was hydrolyzed to obtain an average chain length.
A casein oligopeptide mixture of 5.4, 13.3% free amino acids was obtained.

比較例1 実験例3で得られたカゼインオリゴペプチド混合物を大
豆オリゴペプチド混合物の代わりに用い、実施例1と同
様にしてヨーグルトを得た。
Comparative Example 1 Yogurt was obtained in the same manner as in Example 1 except that the casein oligopeptide mixture obtained in Experimental Example 3 was used instead of the soybean oligopeptide mixture.

酸度が0.8に達する時間は5時間で、乳酸醗酵促進効果
は認められなかった。
The time required for the acidity to reach 0.8 was 5 hours, and no lactic acid fermentation promoting effect was observed.

比較例2 アミノ酸組成物(平均鎖長1.0、アミノ酸組成は大豆オ
リゴペプチド混合物のそれと同一組成になるように調製
した)、分離大豆蛋白(不二製油(株)製フジプロ−R
(未分解))を実施例1の大豆蛋白ペプチド混合物の代
わりに用い、実施例1と同様にしてヨーグルトを製造し
た。酸度0.8に達するまでの醗酵時間及び風味は、アミ
ノ酸組成物の場合5.0時間かかり、アミノ酸特有の嫌な
味がし、大豆蛋白の場合5時間かかり、風味的には普通
のものであった。
Comparative Example 2 Amino acid composition (average chain length 1.0, amino acid composition was prepared to have the same composition as that of soybean oligopeptide mixture), isolated soybean protein (Fuji Pro-R manufactured by Fuji Oil Co., Ltd.)
(Undegraded) was used instead of the soybean protein peptide mixture of Example 1 to produce yogurt in the same manner as in Example 1. The fermentation time and flavor required to reach an acidity of 0.8 took 5.0 hours in the case of the amino acid composition, the unpleasant taste peculiar to amino acids, and 5 hours in the case of soybean protein, and the flavor was normal.

実施例3 実験例1と同様にして得た大豆ペプチド混合物の添加量
を表−1のように変えて、実施例1と同様にしてヨーグ
ルトを得た。酸度が0.8に達するまでの時間を併せ表−
1に示す。
Example 3 Yogurt was obtained in the same manner as in Example 1 except that the addition amount of the soybean peptide mixture obtained in the same manner as in Experimental Example 1 was changed as shown in Table 1. Also show the time until the acidity reaches 0.8-
Shown in 1.

実験例4 分離大豆蛋白10%水溶液(pH7.0)2kgをプロチン−AC
(大和化成(株)製)200mgを用いて、50℃で5〜10時間
水解し、pH7に再調整後70℃で30分間加熱して酵素失活
させ、5000RPMで遠心分離して上澄みを得、凍結乾燥し
て、平均鎖長6.8、遊離アミノ酸0.5%の大豆オリゴペ
プチド混合物、平均鎖長17.0、遊離アミノ酸0.5%の
大豆オリゴペプチド混合物を得た。
Experimental Example 4 2 kg of 10% aqueous solution of isolated soybean protein (pH 7.0) was used as Protin-AC.
Using 200 mg (manufactured by Daiwa Kasei Co., Ltd.), hydrolyzed at 50 ° C. for 5 to 10 hours, readjusted to pH 7 and heated at 70 ° C. for 30 minutes to inactivate the enzyme, and centrifuged at 5000 RPM to obtain a supernatant. After freeze-drying, a soybean oligopeptide mixture having an average chain length of 6.8 and 0.5% free amino acids and a soybean oligopeptide mixture having an average chain length of 17.0 and 0.5% free amino acids were obtained.

実施例4 実験例4で得られた大豆オリゴペプチド混合物を用い、
実施例1と同様にしてヨーグルトを得た。平均鎖長6.
8、遊離アミノ酸0.5%の大豆オリゴペプチド混合物の場
合、酸度0.8に達するのに4.0時間要し、平均鎖長17.
0、遊離アミノ酸0.5%の大豆オリゴペプチド混合物場
合、酸度0.8に達するのに5.0時間要した。各々、若干苦
い風味を呈した。
Example 4 Using the soybean oligopeptide mixture obtained in Experimental Example 4,
A yogurt was obtained in the same manner as in Example 1. Average chain length 6.
8.For soybean oligopeptide mixture with 0.5% free amino acids, it takes 4.0 hours to reach acidity 0.8, average chain length 17.
In the case of the soybean oligopeptide mixture containing 0 and 0.5% of free amino acid, it took 5.0 hours to reach the acidity of 0.8. Each had a slightly bitter taste.

(効果) 以上説明したように、本発明により、ヨーグルト、チー
ズ等の乳酸醗酵に際し、乳酸醗酵の時間を短縮(乳酸醗
酵促進)することが可能になったものである。
(Effect) As described above, according to the present invention, it is possible to shorten the time of lactic acid fermentation (accelerate lactic acid fermentation) during lactic acid fermentation of yogurt, cheese and the like.

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

第1図は牛乳−脱脂粉乳水溶液の乳酸醗酵の酸度と時間
の関係を表す図面であり、 は大豆オリゴペプチド混合物添加、 は無添加を表す。
FIG. 1 is a drawing showing the relationship between the acidity and the time of lactic acid fermentation of milk-skim milk powder aqueous solution, Is a soy oligopeptide mixture addition, Indicates no addition.

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭54−35243(JP,A) 特開 昭51−54976(JP,A) 特公 昭35−15425(JP,B1) 特公 昭51−36340(JP,B1) ─────────────────────────────────────────────────── ─── Continuation of the front page (56) References JP-A-54-35243 (JP, A) JP-A-51-54976 (JP, A) JP-B-35-15425 (JP, B1) JP-B-51- 36340 (JP, B1)

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】乳成分含有原料に対し油糧種子蛋白由来の
平均鎖長2〜15、かつ遊離アミノ酸25%以下のオリ
ゴペプチド混合物を加え、短時間乳酸発酵することを特
徴とする乳酸発酵物の製造法。
1. A lactic acid fermented product characterized in that a mixture of oligopeptides having an average chain length of 2 to 15 and free amino acids of 25% or less derived from oil seed protein is added to a raw material containing milk components, and lactic acid fermentation is carried out for a short time. Manufacturing method.
JP61309345A 1986-12-26 1986-12-26 Lactic acid fermented product manufacturing method Expired - Fee Related JPH0640796B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61309345A JPH0640796B2 (en) 1986-12-26 1986-12-26 Lactic acid fermented product manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61309345A JPH0640796B2 (en) 1986-12-26 1986-12-26 Lactic acid fermented product manufacturing method

Publications (2)

Publication Number Publication Date
JPS63164841A JPS63164841A (en) 1988-07-08
JPH0640796B2 true JPH0640796B2 (en) 1994-06-01

Family

ID=17991889

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61309345A Expired - Fee Related JPH0640796B2 (en) 1986-12-26 1986-12-26 Lactic acid fermented product manufacturing method

Country Status (1)

Country Link
JP (1) JPH0640796B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2873231B2 (en) * 1988-10-14 1999-03-24 味の素ゼネラルフーヅ株式会社 Coffee whitener
KR20080003637A (en) * 2006-07-03 2008-01-08 한상기 New functional fermented milk (yogurt) for use in dieting
JP4853443B2 (en) * 2007-09-27 2012-01-11 不二製油株式会社 Method for producing fermented foods with little quality deterioration

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS509877B2 (en) * 1972-09-13 1975-04-16
GB1516333A (en) * 1974-09-05 1978-07-05 Borden Inc Phage resistant cheese culture media
JPS5136340A (en) * 1974-09-18 1976-03-27 Tsuya Wakamatsu SHITAHARANO DEBARIOOSAHERUBYOHARAMAKI
JPS5435243A (en) * 1977-08-23 1979-03-15 Nippon Yuukon Kk Quality improver for lactic acid bacillus drink and food
JPS57146546A (en) * 1981-03-06 1982-09-10 Eisai Co Ltd Production of fermented dairy products
JPS59220153A (en) * 1983-05-30 1984-12-11 Kagome Kk Lactic acid fermentation beverage and production thereof

Also Published As

Publication number Publication date
JPS63164841A (en) 1988-07-08

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