JPH0843B2 - Propionic acid fermentation product and soybean fermentation product using the same - Google Patents

Propionic acid fermentation product and soybean fermentation product using the same

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Publication number
JPH0843B2
JPH0843B2 JP4358545A JP35854592A JPH0843B2 JP H0843 B2 JPH0843 B2 JP H0843B2 JP 4358545 A JP4358545 A JP 4358545A JP 35854592 A JP35854592 A JP 35854592A JP H0843 B2 JPH0843 B2 JP H0843B2
Authority
JP
Japan
Prior art keywords
propionic acid
streptococcus
fermentation product
soybean
lactic acid
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
Application number
JP4358545A
Other languages
Japanese (ja)
Other versions
JPH06197719A (en
Inventor
禮三郎 石垣
Original Assignee
株式会社ソーイ
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 株式会社ソーイ filed Critical 株式会社ソーイ
Priority to JP4358545A priority Critical patent/JPH0843B2/en
Priority to CA002110415A priority patent/CA2110415A1/en
Publication of JPH06197719A publication Critical patent/JPH06197719A/en
Publication of JPH0843B2 publication Critical patent/JPH0843B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L11/00Pulses, i.e. fruits of leguminous plants, for production of food; Products from legumes; Preparation or treatment thereof
    • A23L11/30Removing undesirable substances, e.g. bitter substances
    • A23L11/37Removing undesirable substances, e.g. bitter substances using microorganisms
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2400/00Lactic or propionic acid bacteria
    • A23V2400/11Lactobacillus
    • A23V2400/123Bulgaricus
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2400/00Lactic or propionic acid bacteria
    • A23V2400/21Streptococcus, lactococcus
    • A23V2400/249Thermophilus
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2400/00Lactic or propionic acid bacteria
    • A23V2400/51Bifidobacterium
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2400/00Lactic or propionic acid bacteria
    • A23V2400/61Propionibacterium
    • A23V2400/623Shermanii

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  • Life Sciences & Earth Sciences (AREA)
  • Microbiology (AREA)
  • Agronomy & Crop Science (AREA)
  • Botany (AREA)
  • Health & Medical Sciences (AREA)
  • Nutrition Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Food Science & Technology (AREA)
  • Polymers & Plastics (AREA)
  • Beans For Foods Or Fodder (AREA)

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】この発明は、短期間に原料大豆の
臭気及び大豆の蒸煮臭を完全に消すとともに、黴の発生
を完全に防止したプロピオン酸醗酵物及びこれを用いた
大豆醗酵物に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a propionic acid fermented product which completely eliminates the odor of raw material soybeans and the steamed odor of soybeans in a short period of time, and completely prevents the generation of mold, and a soybean fermented product using the same. It is a thing.

【0002】[0002]

【従来の技術】従来の大豆発酵物は、大豆臭が残存し、
かつ黴が生えやい欠点があった。前記大豆臭を除去する
ものとしては、例えば特公昭59−48621号公報が
知られている。本号においては、脱皮大豆を微粉砕して
高度の酸素活性のある全脂大豆粉とし、これを水蒸気処
理(蒸煮)して酵素破壊するとともに、大豆の揮発性成
分を除去し、この蒸煮された大豆粉を水に溶解して乳酸
醗酵させ、この乳酸醗酵液に酵母を添加して大豆醗酵物
を得ている。
2. Description of the Related Art Conventional soybean fermented products retain the soybean odor,
And there was a defect that mold was not easy to grow. As a means for removing the soybean odor, for example, Japanese Patent Publication No. 59-48621 is known. In this issue, dehulled soybeans are finely pulverized to obtain full-fat soybean flour with a high degree of oxygen activity, which is steamed (steamed) to enzymatically destroy it, and the volatile components of soybeans are removed. Soybean flour is dissolved in water to ferment lactic acid, and yeast is added to the lactic acid fermentation solution to obtain a soybean fermented product.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、大豆の
蒸煮物を乳酸菌と酵母で発酵しただけでは、保存中に黴
が生えやすい。そこで本発明者は、この大豆発酵物に、
更にプロピオン酸菌を添加して発酵させれば、生成する
プロピオン酸により黴の発生を防止することができるこ
とを知り本発明を完成した(プロピオン酸発酵に関して
は、JOURNAL OF FERMENTATION
AND BIOENGINEERINGVo1.7
4,No.2,95−99.1992を参考にした)。
本発明は、脱皮大豆の粉末に、酵素、乳酸菌、及びプロ
ピオン酸菌、又はこれらに加えて酵母を作用させて大豆
臭と黴の発生を防止するものである。
[Problems to be Solved by the Invention] However, if the steamed soybean product is fermented with lactic acid bacteria and yeast, mildew tends to grow during storage. Therefore, the present inventor, in this soybean fermented product,
Further, the present invention was completed by knowing that the generation of mold can be prevented by the generated propionic acid by adding and fermenting the propionic acid bacterium (for the propionic acid fermentation, JOURNAL OF FERMENTATION).
AND BIO ENGINEERING Vo1.7
4, No. 2, 95-99.1992).
According to the present invention, an enzyme, a lactic acid bacterium, a propionic acid bacterium, or a yeast in addition to these is allowed to act on the dehulled soybean powder to prevent generation of soybean odor and mold.

【0004】[0004]

【課題を解決するための手段】本願発明は下記の(イ)
及び(ロ)の請求項により構成されている。 (イ)下記の(1)〜(3)の工程を順次経ることを特
徴とするプロピオン酸醗酵物。 (1)脱皮大豆の粉末を蒸煮した後、これをアスペルギ
ルスオリザエ(Aspergillus 0ryza
e)起源の酵素により酵素消化する工程 (2)前記(1)で得られる酵素消化物に、ラクトバチ
ルスブルガリクス(Lactobacillus bu
lgaricus)とストレプトコッカスサーモフィル
ス(Streptococcus thermophi
lus)を接種して培養する工程 (3)前記(2)で得られる乳酸発酵物にプロピオニバ
クテリウムシェルマーニ(Propionibacte
riun shermanii)を接種して培養する工
程 (ロ)下記の(1)〜(3)の工程を順次経て得られる
プロピオン酸醗酵物(A)と、下記(イ)〜(ハ)の工
程を順次経て得られる酵母発酵物(B)とを混合するこ
とを特徴とするプロピオン酸発酵物を用いた大豆醗酵
物。 <プロピオン酸醗酵物(A)> (1)脱皮大豆の粉末を蒸煮した後、これを酵素消化す
る工程 (2)前記(1)で得られる酵素消化物に、ラクトバチ
ルスブルガリクス(Lactobacillus bu
lgaricus)とストレプトコッカスサーモフィル
ス(Streptococcus thermophi
lus)を接種して培養する工程 (3)前記(2)で得られる乳酸発酵物にプロピオニバ
クテリウムシェルマーニ(Propionibacte
riun shermanii)を接種して培養する工
程 <酵母醗酵物(B)> (イ)脱皮大豆の粉末を蒸煮した後、これをアスペルギ
ルスオリザエ(Aspergillus Oryza
e)起源の酵素により酵素消化する工程 (ロ)前記(イ)で得られる酵素消化物に、ラクトバチ
ルスブルガリクス(Lactobacillus bu
lgaricus)とストレプトコッカスサーモフィル
ス(Streptococcus thermophi
lus)を接種して培養する工程 (ハ)前記(ロ)で得られる乳酸発酵物に酵母を接種し
て培養する工程
Means for Solving the Problems The present invention has the following (a)
And (b). (A) A propionic acid fermented product characterized by sequentially undergoing the following steps (1) to (3). (1) After steaming the powder of dehulled soybeans, the powdered Aspergillus oryzae (Aspergillus 0ryza)
e) Step of enzymatically digesting with an enzyme of origin (2) The enzymatically digested product obtained in the above (1) is added to Lactobacillus bulgaricus (Lactobacillus bu).
lgaricus) and Streptococcus thermophilus (Streptococcus thermophi)
(3) a step of inoculating and culturing the lactic acid fermented product obtained in (2) above with Propionibacterium shellmani (Propionibacte)
(b) Propionic acid fermentation product (A) obtained by sequentially performing the following steps (1) to (3) and the following steps (a) to (c). A soybean fermented product using a propionic acid fermented product, which is characterized by being mixed with the yeast fermented product (B) obtained. <Propionic Acid Fermented Product (A)> (1) Step of steaming dehulled soybean powder and enzymatically digesting it (2) The enzymatically digested product obtained in (1) above is added to Lactobacillus bulgaricus (Lactobacillus bu)
lgaricus) and Streptococcus thermophilus (Streptococcus thermophi)
(3) a step of inoculating and culturing the lactic acid fermented product obtained in (2) above with Propionibacterium shellmani (Propionibacte)
riun hermanii) inoculation and culturing <Yeast fermented product (B)> (a) After steaming powder of dehulled soybeans, this is used as Aspergillus Oryzae (Aspergillus Oryzae).
e) Step of enzymatically digesting with the enzyme of origin (b) Lactobacillus bulgaricus (Lactobacillus bu) is added to the enzymatically digested product obtained in (a) above.
lgaricus) and Streptococcus thermophilus (Streptococcus thermophi)
and incubating and culturing (c) the lactic acid fermented product obtained in (b) above with yeast

【0005】この発明に係るプロピオン酸醗酵物及び大
豆発酵物にあっては、プロピオン酸発酵が始まる前に、
培地となる脱皮大豆の微粉末が、アスペルギルスオリザ
エ(Aspergillus Oryzae)起源の酵
素によって分解される。次いで、この大豆消化物にラク
トバチルスブルガリクス(Lactobacillus
bulgaricus)とストレプトコッカスサーモ
フィルス(Streptococcus thermo
philus)を共生させる(請求項2の発明にあって
は、前記の乳酸菌以外に更に酵母も接種して培養す
る。)。そのため、前記発酵物には、プロピオン酸菌の
成育に不可欠な複雑な窒素化合物や、パントテン酸、ビ
オチン等のビタミンが生成されるので、従来不安定であ
ったプロピオン酸発酵が安定して進行するのである。
In the propionic acid fermented product and the soybean fermented product according to the present invention, before the propionic acid fermentation is started,
A dehulled soybean fine powder, which is a medium, is decomposed by an enzyme originating from Aspergillus Oryzae. Next, this soybean digest was applied to Lactobacillus bulgaricus (Lactobacillus).
bulgaricus) and Streptococcus thermophilus
philus) is symbiotic (in the invention of claim 2, yeast is further inoculated and cultured in addition to the lactic acid bacterium). Therefore, in the fermented product, since complicated nitrogen compounds and pantothenic acid, vitamins such as biotin are indispensable for the growth of propionic acid bacteria, conventionally unstable propionic acid fermentation proceeds stably. Of.

【0006】この発明に係るプロピオン酸醗酵(発酵物
及び大豆発酵物)にあっては、酵母エキスを少量添加す
ることにより、プロピオン酸と醋酸はモル比が、2:1
と安定した。さらに収量については、2種類の乳酸菌と
プロピオン酸菌を共生させることによって揮発酸の生成
が促進され、消費される基質、すなわち乳酸は平行醗酵
による生酸がなされ、前記乳酸の約75%がプロピオン
酸と醋酸として得られ、高収率であった。
In the propionic acid fermentation (fermented product and soybean fermented product) according to the present invention, by adding a small amount of yeast extract, the molar ratio of propionic acid and acetic acid is 2: 1.
And stable. Further, regarding the yield, the coexistence of two kinds of lactic acid bacteria and propionic acid bacteria promotes the production of volatile acid, and the consumed substrate, that is, lactic acid, is produced by parallel fermentation, and about 75% of the lactic acid is propione. The acid and acetic acid were obtained in high yield.

【0007】この発明に係るプロピオン酸醗酵物及び大
豆発酵物の製造において、プロピオン酸発酵に先立って
行われる乳酸発酵及び酵母発酵により生産されるパント
テン酸、及びビオチンの量を知るために下記の試験をし
た。蒸煮大豆粉100部、殺菌水200部、アスペルギ
ルスオリザェ(Aspergillus Oryza
e)酵素0.02部を加え、酵素消化、乳酸醗酵を行
い、これにサッカロマイセスセルビアシエ(Sacch
aromyces serevisiae)を接種して
乳酸醗酵させた。その結果、乳酸醗酵液にパントテン酸
0.25mg/100g、ビオチン6.2μg/100
gの生成が見られた。これによりプロピオン酸醗酵が容
易に進行するが予想された。
In the production of the propionic acid-fermented product and the soybean-fermented product according to the present invention, the following tests were carried out in order to know the amounts of pantothenic acid and biotin produced by lactic acid fermentation and yeast fermentation carried out prior to propionic acid fermentation. Did. 100 parts steamed soybean powder, 200 parts sterilized water, Aspergillus Oryza
e) 0.02 parts of enzyme was added, enzyme digestion and lactic acid fermentation were carried out, and Saccharomyces serbia sie (Sacch
lactic acid fermentation was carried out by inoculating amyces cerevisiae). As a result, 0.25 mg / 100 g of pantothenic acid and 6.2 μg / 100 of biotin were added to the lactic acid fermentation solution.
Production of g was seen. It was expected that this would facilitate the propionic acid fermentation.

【0008】さらに、得られたプロピオン酸醗酵液と酵
素消化させた大豆液、これらにさらに乳酸醗酵、酵母醗
酵されたものを混合し、熟成(調熟)させ、約10日後
にチーズ様の醗酵食品となり、試食によれば大豆臭はも
ちろんのこと大豆の蒸煮臭も全く感じることができなか
った。
Furthermore, the resulting propionic acid fermentation broth and enzyme-digested soybean liquor, which are further mixed with lactic acid fermentation and yeast fermentation, are aged (ripened), and after about 10 days, cheese-like fermentation. It became a food, and according to the tasting, not only the soybean odor but also the steamed odor of soybean could not be felt at all.

【0009】またプロピオン酸醗酵物を用いたこの発明
に係る大豆醗酵物は、黴の発育を阻止し、またこの醗酵
物に炭酸カルシウム(CaCO)を添加したものを製
パン工程中に加えると、パンの防黴を図るのみならず、
風味の改善とエクステンソグラフ(Extensogr
aph)における製パン適正が向上し、カルシウム強化
食品となる。
Further, the soybean fermented product according to the present invention using the propionic acid fermented product inhibits the growth of mold, and when the product obtained by adding calcium carbonate (CaCO 3 ) to the fermented product is added during the baking process. , Not only to protect the mold from mold,
Flavor improvement and extensograph (Extensogr
aph) improves bread-making suitability and becomes a calcium-fortified food.

【0010】[0010]

【実施例】実施例1 培地となる乳酸醗酵液は、脱皮生大豆粉を20分間蒸煮
したもの20%、殺菌水77.9%、アスペルギルスオ
リザエ(Aspergillus Oryzae)起源
の酵素0.02%を加え、40℃で30分消化し、これ
にラクトバチルスブルガリクス(Lactobacil
lus bulgaricus)及びストレプトコッカ
スサーモフィルス(Streptococcus th
ermophilus)を接種したスターター2%を添
加し、37℃で5時間培養した乳酸醗酵液をさらに4倍
に希釈した液にイーストエキス0.05%を加え、プロ
ピオン酸菌用培地とし、これにプロピオニバクテリウム
シェルマーニ(Propionibacteriun
shermanii)を接種すると、培地中の乳酸2%
に対しプロピオン酸0.81%、醋酸0.43%の割合
で生酸される。これを30℃で8日間培養した。さらに
醗酵を継続すると収量は上昇する。
Example 1 A lactic acid fermentation broth used as a medium was prepared by steaming 20 minutes of dehulled soybean flour, 77.9% of sterilized water, and 0.02% of an enzyme originating from Aspergillus Oryzae. In addition, digestion was carried out at 40 ° C for 30 minutes, and this was digested with Lactobacillus bulgaricus.
lus bulgaricus) and Streptococcus thermophilus (Streptococcus th)
2% of the starter inoculated with E. thermophilus) was added, and 0.05% of yeast extract was added to a solution obtained by further diluting the lactic acid fermentation broth cultured at 37 ° C for 5 hours to prepare a medium for propionic acid bacteria. Pionibacterium shellmani (Propionibacterium)
inoculation with Shermanii), 2% lactic acid in the medium
On the other hand, the propionic acid is 0.81% and the acetic acid is 0.43%. This was cultured at 30 ° C. for 8 days. If fermentation is further continued, the yield will increase.

【0011】実施例2 培地となる乳酸醗酵液は、脱皮生大豆粉を20分間蒸煮
したもの20%、殺菌水77.9%、アスペルギルスオ
リザエ(Aspergillus Oryzae)起源
の酵素0.05%を加え、40℃で30分消化し、これ
にラクトバチルスブルガリクス(Lactobacil
lus bulgaricus)及びストレプトコッカ
スサーモフィルス(Streptococcus th
ermophilus)を接種したスターター2%を添
加し、37℃で5時間培養した乳酸醗酵液をさらに4倍
に希釈した液に炭酸カルシウム1%、酵母エキス0.1
%を添加した液をプロピオン酸菌用培地とし、これにプ
ロピオニバクテリウムシェルマーニ(Propioni
bacteriun shermanii)を接種する
と、培地中の乳酸2%に対しプロピオン酸0.93%、
醋酸0.47%の割合で生酸される。これを30℃で1
2日間培養した。さらに醗酵を継続すると収量は上昇す
る。
Example 2 A lactic acid fermentation broth serving as a medium was prepared by adding 20% of dehulled raw soybean flour cooked for 20 minutes, 77.9% of sterilized water, and 0.05% of an enzyme originating from Aspergillus Oryzae. Digested at 40 ℃ for 30 minutes, and add it to Lactobacillus bulgaricus.
lus bulgaricus) and Streptococcus thermophilus (Streptococcus th)
2% of the starter inoculated with E. thermophilus) was added, and the lactic acid fermentation broth cultured at 37 ° C. for 5 hours was further diluted 4-fold to give 1% calcium carbonate and 0.1% yeast extract.
% Was added to the medium as a medium for propionic acid bacteria, to which Propionibacterium shellmani (Propioni) was added.
When inoculated with Bacteriun hermanii), 0.93% of propionic acid to 2% of lactic acid in the medium,
It is produced in the proportion of 0.47% acetic acid. 1 at 30 ℃
Cultured for 2 days. If fermentation is further continued, the yield will increase.

【0012】実施例3 培地となる乳酸醗酵液は、脱皮生大豆粉を20分間蒸煮
したもの30%、殺菌水65.9%、アスペルギルスオ
リザエ(Aspergillus Oryzae)起源
の酵素0.02%を加え、30℃で30分消化し、これ
にラクトバチルスブルガリクス(Lactobacil
lus bulgaricus)及びストレプトコッカ
スサーモフィルス(Streptococcus th
ermophilus)を接種したスターター2%を添
加し、30分後に酵母サッカロマイセスセルビシアエ
(Sacchromyces cerevisiae)
2%を接種して35〜37℃で4時間培養し、15℃に
冷却した醗酵液100部に対して、前記実施例1記載の
プロピオン酸醗酵液20部と混同し、7日間の熟成し、
製品とする。
Example 3 A lactic acid fermentation broth used as a medium was prepared by adding 30% steamed dehulled soybean flour for 20 minutes, sterilized water 65.9%, and 0.02% enzyme derived from Aspergillus Oryzae. Digested at 30 ℃ for 30 minutes, and add it to Lactobacillus bulgaricus.
lus bulgaricus) and Streptococcus thermophilus (Streptococcus th)
2% of a starter inoculated with E. thermophilus was added, and 30 minutes later, the yeast Saccharomyces cerevisiae was added.
2% was inoculated and cultivated at 35 to 37 ° C. for 4 hours, and 100 parts of the fermentation liquid cooled to 15 ° C. was confused with 20 parts of the propionic acid fermentation liquid described in Example 1, and aged for 7 days. ,
The product.

【0013】実施例4 培地となる乳酸醗酵液は、脱皮生大豆粉を20分間蒸煮
したもの30%、殺菌水65.9%、アスペルギルスオ
リザエ(Aspergillus Oryzae)起源
の酵素0.02%を加え、38℃で消化し、これに直ち
にラクトバチルスブルガリクス(Lactobacil
lus bulgaricus)及びストレプトコッカ
スサーモフィルス(Streptococcus th
ermophilus)を接種したスターター2%を添
加し、30分後に酵母サッカロマイセスセルビシアエ
(Sacchromyces cerevisiae)
2%を接種して35〜38℃で4時間培養し、30℃に
冷却した醗酵液1部に対して、前記実施例2記載のプロ
ピオン酸醗酵液1部と混同し、7日間の熟成する。これ
を炭酸カルシウムでpH5.0に調整し、乾燥させて製
品とする。
Example 4 A lactic acid fermentation broth used as a medium was prepared by adding 30% steamed dehulled soybean flour for 20 minutes, 65.9% sterilized water, and 0.02% of an enzyme originating from Aspergillus Oryzae. Digested at 38 ° C and immediately added to Lactobacillus bulgaricus.
lus bulgaricus) and Streptococcus thermophilus (Streptococcus th)
2% of a starter inoculated with E. thermophilus was added, and 30 minutes later, the yeast Saccharomyces cerevisiae was added.
2% was inoculated and cultivated at 35 to 38 ° C. for 4 hours, and 1 part of the fermentation liquid cooled to 30 ° C. was confused with 1 part of the propionic acid fermentation liquid described in Example 2, and aged for 7 days. . This is adjusted to pH 5.0 with calcium carbonate and dried to obtain a product.

【0014】前記実施例1〜4で得られたプロピオン酸
醗酵物及びこれを用いた大豆醗酵物を適宜混合し、熟成
(調熟)させたところ、約10日後にチーズ様の醗酵食
品となり、試食によれば大豆臭はもちろんのこと大豆の
蒸煮臭も全く感じることができなかった。
When the propionic acid fermented product obtained in Examples 1 to 4 and the soybean fermented product using the same were appropriately mixed and aged (aged), a cheese-like fermented food was obtained after about 10 days, According to the tasting, not only the soybean smell but also the steamed smell of soybean could not be felt at all.

【0015】また前記実施例1〜4で得られたプロピオ
ン酸醗酵物及びこれを用いた大豆醗酵物は、黴の発育を
阻止しするものであった。またこれらの醗酵物に炭酸カ
ルシウム(CaCo)を添加したものを製パン工程中
に加えると、パンの防黴を図るのみならず、風味の改善
とエクステンソグラフ(Extensograph)に
おける製パン適正が向上し、カルシウム強化食品となっ
た。
Further, the propionic acid fermented product obtained in Examples 1 to 4 and the soybean fermented product using the same inhibited the growth of mold. If calcium carbonate (CaCo 3 ) is added to these fermented products during the bread making process, not only the fungus mold of the bread is prevented but also the flavor is improved and the bread making suitability in the Extensograph is improved. Improved and became a calcium fortified food.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 下記の(1)〜(3)の工程を順次経る
ことを特徴とするプロピオン酸醗酵物。 (1)脱皮大豆の粉末を蒸煮した後、これをアスペルギ
ルスオリザエ(Aspergillus Oryza
e)起源の酵素により酵素消化する工程 (2)前記(1)で得られる酵素消化物に、ラクトバチ
ルスブルガリクス(Lactobacillus bu
lgaricus)とストレプトコッカスサーモフィル
ス(Streptococcus thermophi
lus)を接種して培養する工程 (3)前記(2)で得られる乳酸発酵物にプロピオニバ
クテリウムシェルマーニ(Propionibacte
riun shermanii)を接種して培養する工
1. The following steps (1) to (3) are sequentially performed.
A propionic acid fermented product characterized by the following. (1) After steaming the dehulled soybean powder, add this to Aspergi
Aspergillus Oryza
e) Step of enzymatically digesting with the enzyme of origin (2) The enzymatically digested product obtained in (1) above is
Ruth Bulgari s (Lactobacillus bu
lgaricus) and Streptococcus thermophile
Su (Streptococcus thermophi)
(3) a step of inoculating and culturing the lactic acid fermentation product obtained in (2) above with propioniva
Cterium shellmani (Propionibacte
riun hermanii) inoculation and culture
Degree
【請求項2】 下記の(1)〜(3)の工程を順次経て
得られるプロピオン酸醗酵物(A)と、下記(イ)〜
(ハ)の工程を順次経て得られる酵母発酵物(B)とを
混合することを特徴とするプロピオン酸発酵物を用いた
大豆醗酵物。 <プロピオン酸醗酵物(A)> (1)脱皮大豆の粉末を蒸煮した後、これをアスペルギ
ルスオリザエ(Aspergillus Oryza
e)起源の酵素により酵素消化する工程 (2)前記(1)で得られる酵素消化物に、ラクトバチ
ルスブルガリクス(Lactobacillus bu
lgaricus)とストレプトコッカスサーモフィル
ス(Streptococcus thermophi
lus)を接種して培養する工程 (3)前記(2)で得られる乳酸発酵物にプロピオニバ
クテリウムシェルマーニ(Propionibacte
riun shermanii)を接種して培養する工
<酵母醗酵物(B)> (イ)脱皮大豆の粉末を蒸着した後、これを酵素消化す
る工程 (ロ)前記(イ)で得られる酵素消化物に、ラクトバチ
ルスブルガリクス(Lactobacillus bu
lgaricus)とストレプトコッカスサーモフィル
ス(Streptococcus thermophi
lus)を接種して培養する工程 (ハ)前記(ロ)で得られる乳酸発酵物に酵母を接種し
て培養する工程
2. The steps (1) to (3) below are sequentially performed.
The resulting propionic acid fermentation product (A) and the following (a) to
The yeast fermented product (B) obtained by sequentially performing the step (C)
Using a propionic acid fermented product characterized by mixing
Fermented soybeans. <Fermented propionic acid (A)> (1) After steaming the powder of dehulled soybeans, use this asperghi
Aspergillus Oryza
e) Step of enzymatically digesting with the enzyme of origin (2) The enzymatically digested product obtained in (1) above is
Ruth Bulgari s (Lactobacillus bu
lgaricus) and Streptococcus thermophile
Su (Streptococcus thermophi)
(3) a step of inoculating and culturing the lactic acid fermentation product obtained in (2) above with propioniva
Cterium shellmani (Propionibacte
riun hermanii) inoculation and culture
Extent after depositing the powder of <yeast fermentations (B)> (b) dehulled soybeans, which to enzymatic digestion
Step (b) Lactobacillus was added to the enzyme digest obtained in (a) above.
Ruth Bulgari s (Lactobacillus bu
lgaricus) and Streptococcus thermophile
Su (Streptococcus thermophi)
and inoculating the lactic acid fermentation product obtained in (b) above with yeast
Culture process
JP4358545A 1992-12-28 1992-12-28 Propionic acid fermentation product and soybean fermentation product using the same Expired - Lifetime JPH0843B2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP4358545A JPH0843B2 (en) 1992-12-28 1992-12-28 Propionic acid fermentation product and soybean fermentation product using the same
CA002110415A CA2110415A1 (en) 1992-12-28 1993-12-01 Propionic acid fermentation product and soy bean fermentation product obtained using the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4358545A JPH0843B2 (en) 1992-12-28 1992-12-28 Propionic acid fermentation product and soybean fermentation product using the same

Publications (2)

Publication Number Publication Date
JPH06197719A JPH06197719A (en) 1994-07-19
JPH0843B2 true JPH0843B2 (en) 1996-01-10

Family

ID=18459875

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4358545A Expired - Lifetime JPH0843B2 (en) 1992-12-28 1992-12-28 Propionic acid fermentation product and soybean fermentation product using the same

Country Status (2)

Country Link
JP (1) JPH0843B2 (en)
CA (1) CA2110415A1 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2360418C2 (en) * 2003-12-04 2009-07-10 Фудзи Ойл Компани, Лимитед Bread, containing bread improving agent and its manufacturing method
CN114145428B (en) * 2021-12-16 2024-01-05 广东广益科技实业有限公司 Fermented soybean steamed cake and preparation method thereof

Also Published As

Publication number Publication date
JPH06197719A (en) 1994-07-19
CA2110415A1 (en) 1994-06-29

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