JPH06287554A - Production of oxidation-resistant substance from soybean meal or lees of bean curd - Google Patents

Production of oxidation-resistant substance from soybean meal or lees of bean curd

Info

Publication number
JPH06287554A
JPH06287554A JP9869993A JP9869993A JPH06287554A JP H06287554 A JPH06287554 A JP H06287554A JP 9869993 A JP9869993 A JP 9869993A JP 9869993 A JP9869993 A JP 9869993A JP H06287554 A JPH06287554 A JP H06287554A
Authority
JP
Japan
Prior art keywords
soybean meal
lees
bean curd
antioxidant
resistant substance
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.)
Pending
Application number
JP9869993A
Other languages
Japanese (ja)
Inventor
Shinya Yamaguchi
信哉 山口
Tetsushi Naraoka
哲志 奈良岡
Kaoru Abe
馨 阿部
Junji Ichida
淳治 市田
Hajime Matsue
一 松江
Kouichi Kazaharu
浩一 風晴
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.)
AOMORI PREF GOV
MARUYA JOZO KK
Aomori Prefecture
Original Assignee
AOMORI PREF GOV
MARUYA JOZO KK
Aomori Prefecture
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 AOMORI PREF GOV, MARUYA JOZO KK, Aomori Prefecture filed Critical AOMORI PREF GOV
Priority to JP9869993A priority Critical patent/JPH06287554A/en
Publication of JPH06287554A publication Critical patent/JPH06287554A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a water-sol. thermally stable oxidation-resistant substance in large amt. from a soybean meal or the lees of bean curd. CONSTITUTION:A water-sol. thermally stable oxidation-resistant substance is obtd. by solubilizing a soybean meal or the lees of bean curd enzymatically or physically and separating the resulting product.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は大豆粕又はおからから酵
素的、物理的方法を用いて、水溶性で熱安定性な抗酸化
性物質を効率よく安価にかつ大量に製造する方法に関す
るものである。
FIELD OF THE INVENTION The present invention relates to a method for efficiently and inexpensively producing a large amount of a water-soluble and heat-stable antioxidant from soybean meal or okara by enzymatic and physical methods. Is.

【0002】[0002]

【従来の技術】従来から油の自動酸化を抑止する抗酸化
剤は、天然由来のものとしてはアスコルビン酸、トコフ
ェロール、合成のものとしてはBHA、BHT等が知ら
れている。一方、豆乳、豆腐等の加工食品の製造過程に
おいて大豆粕やおからが生じるが、それらは一部、飼料
として処理されている以外は、有効利用されていない。
大豆粕又はおからの原料である大豆の中には、抗酸化能
を有するトコフェロール、イソフラボン、サポニンやフ
ィチンが含まれていることは知られているが、大豆粕又
はおからからそれらを効率よく、大量に製造することは
その存在様式上、物性上困難であった。
2. Description of the Related Art Conventionally, ascorbic acid and tocopherol are known as naturally occurring antioxidants and BHA and BHT are known as synthetic antioxidants. On the other hand, soybean meal and okara are produced in the process of producing processed foods such as soymilk and tofu, but they are not used effectively except for being partially treated as feed.
Soybean that is a raw material of soybean meal or okara is known to contain tocopherol, isoflavone, saponin, and phytin, which have antioxidant ability, but soybean meal or okara efficiently extracts them. However, it was difficult to manufacture it in a large amount because of its existence and physical properties.

【0003】[0003]

【発明が解決しようとする問題点】しかしながら、食品
に添加して使用する抗酸化剤は人体に対して安全である
ことが第一の条件であり、更に食品加工の過程において
も安定であり、毒性や反応性を有しないことが要求され
る。その点、合成BHA、BHT等は人体に対して安全
性の面で問題点があり、近年使用頻度は低い。一方天然
物質であるアスコルビン酸は熱安定性やアルカリ性に弱
く、トコフェロールは脂溶性であり、高価なため適用範
囲が限定される。
However, the first condition is that the antioxidant used by adding it to food is safe for human body, and it is stable in the process of food processing. It is required to have no toxicity or reactivity. On the other hand, synthetic BHA, BHT and the like have a problem in terms of safety for the human body and have been used less frequently in recent years. On the other hand, ascorbic acid, which is a natural substance, is weak in thermal stability and alkalinity, and tocopherol is fat-soluble and expensive, so its application range is limited.

【0004】そこで、本発明者らは、大豆粕又はおから
から一度に大量にかつ水溶性で熱安定性を有する抗酸化
性物質を製造することに着目した。すなわち、大豆粕又
はおからを原料とし酵素的、物理的に可溶化させ、抗酸
化性物質を効率よく安価に製造することを目的として検
討を行い、本発明に至った。
Therefore, the present inventors have paid attention to the production of a large amount of water-soluble and heat-stable antioxidant substances from soybean meal or okara at one time. That is, the present invention was carried out for the purpose of enzymatically and physically solubilizing soybean meal or okara as a raw material to efficiently and inexpensively produce an antioxidant substance, and arrived at the present invention.

【0005】[0005]

【問題点を解決するための手段】即ち、本発明における
抗酸化性物質の製造方法は、大豆粕又はおからに水を加
えて、加熱滅菌し、各種の多糖類分解酵素を添加し、数
日間、酵素反応を行い可溶化させた後、得られた可溶化
物を分離し、得られた抗酸化性物質は水溶性で熱安定性
であることを特徴とするものである。
[Means for Solving the Problems] That is, the method for producing an antioxidant according to the present invention comprises adding water to soybean meal or okara, sterilizing by heating, adding various polysaccharide degrading enzymes, The solubilized product thus obtained is separated after the enzyme reaction is carried out for solubilization for a day, and the obtained antioxidant is water-soluble and thermostable.

【0006】以下、本発明の手段を具体的に説明する。The means of the present invention will be specifically described below.

【0007】最初に大豆粕又はおからを物理的、機械的
に破砕し、大豆粕又はおからに水を加えて、微生物によ
る汚染を防ぐため、約120℃で加熱滅菌する。必要な
らば間欠滅菌した方がよい、これにセルラーゼ、ヘミセ
ルラーゼやペクチナーゼのような複数の多糖類分解酵
素、又はそれらの活性を有する酵素を加えて20℃〜6
0℃で数日間振盪させ酵素反応を行う。酵素が最大の活
性を有する温度で反応させると期間は短くてもよい。こ
の際、多糖類分解酵素と一緒にリグニン分解酵素を併用
しても差し支えない。酵素反応後、可溶化物を遠心や、
ろ過により不溶化物と分離する。この時、可溶化率は1
0%から80%の範囲である。このようにして製造され
た可溶化物は、水溶性で熱安定性な抗酸化性物質として
用いることができる。
First, the soybean meal or okara is crushed physically and mechanically, water is added to the soybean meal or okara, and heat sterilization is performed at about 120 ° C. to prevent contamination by microorganisms. If necessary, intermittent sterilization is recommended. To this, a plurality of polysaccharide degrading enzymes such as cellulase, hemicellulase and pectinase, or enzymes having those activities are added and the temperature is kept at 20 ° C to 6 ° C.
Shake at 0 ° C for several days to carry out enzymatic reaction. The period may be short if the enzyme is allowed to react at the temperature at which it has maximal activity. At this time, a lignin degrading enzyme may be used together with the polysaccharide degrading enzyme. After enzymatic reaction, centrifuge the solubilized product,
Separated from insoluble matter by filtration. At this time, the solubilization rate is 1
It is in the range of 0% to 80%. The solubilized product produced in this manner can be used as a water-soluble and heat-stable antioxidant.

【0008】本発明の方法は、大豆粕やおからを原料に
用い、単に、加熱と多糖類分解酵素反応を組み合わせる
のみであるため、工程が極めて簡単であり、従来の抗酸
化性物質の製造方法にとって替わるのは明白である。し
かも、水溶性で熱安定性の高い天然の抗酸化性物質を安
価にかつ大量に得ることができる。
Since the method of the present invention uses soybean meal or okara as a raw material and simply combines heating and a polysaccharide-degrading enzyme reaction, the process is extremely simple, and conventional antioxidant substances are produced. Obviously, there is an alternative to the method. In addition, it is possible to obtain a large amount of a water-soluble and highly heat-stable natural antioxidant substance at low cost.

【0009】実施例1Example 1

【0010】市販のおから250gを冷凍したままマス
コロイダーで機械的に破砕する。これと水1リットルを
2リットルのバッフル付三角フラスコに入れ、15分、
121℃で間欠滅菌する。これに市販の多糖類分解酵素
としてドリセラーゼ(協和発酵(株)製)100mgと
ペクチナーゼ(シグマ社製)0.1mlを添加し、30
℃で7日間、100rpm/分で振盪しながら酵素反応
を行い、おからを可溶化させた。これを、8000rp
m、30分間遠心分離し、可溶化物を分離し、再び12
1℃、15分滅菌した。この可溶化物を凍結乾燥するこ
とにより抗酸化性物質を16.5g得た。この得られた
抗酸化性物質の抗酸化能を以下のように測定した。
250 g of commercially available tofu is mechanically crushed with a mass colloider while being frozen. Pour this and 1 liter of water into a 2 liter Erlenmeyer flask with baffle for 15 minutes.
Sterilize intermittently at 121 ° C. To this, 100 mg of commercially available polysaccharide degrading enzyme dolicerase (manufactured by Kyowa Hakko Co., Ltd.) and 0.1 ml of pectinase (manufactured by Sigma) were added, and 30
Enzyme reaction was carried out by shaking at 100 rpm / min for 7 days at 0 ° C to solubilize okara. This is 8000rp
Centrifuge for 30 minutes to separate the solubilized product, and
Sterilized at 1 ° C for 15 minutes. The solubilized product was freeze-dried to obtain 16.5 g of an antioxidant substance. The antioxidant ability of the obtained antioxidant substance was measured as follows.

【0011】30mlのバイアル瓶(胴径3cm)に
0.1Mホウ酸緩衝液(pH9.0)10ml入れ、N
aOHで中和したリノール酸10mM、上記製造された
抗酸化性物質を2mg/mlと0.2mg/mlになる
ように加えた。なお、対照としてはリノール酸のみ、ア
スコルビン酸2mg/mlとジメチルスルホキシドに溶
解したトコフェロール2mg/ml、盲検として各々の
リノール酸無添加を用意した。このバイアル瓶を50℃
のオーブンにいれ、遮光して、リノール酸の自動酸化に
よる過酸化物価を経時的に測定した。
10 ml of 0.1M borate buffer solution (pH 9.0) was placed in a 30 ml vial (body diameter: 3 cm).
10 mM of linoleic acid neutralized with aOH and the above-prepared antioxidant were added to 2 mg / ml and 0.2 mg / ml. As controls, linoleic acid alone, ascorbic acid 2 mg / ml and tocopherol 2 mg / ml dissolved in dimethylsulfoxide, and no linoleic acid added were prepared as a blind test. This vial is 50 ℃
Was placed in an oven, and was protected from light, and the peroxide value by autoxidation of linoleic acid was measured with time.

【0012】過酸化物価は上記バイアルから0.1ml
とり、これに75%エタノール2.35ml、0.05
mlの3%ロダンアンモニアを加え、0.05mlの塩
化第一鉄試薬(塩化バリウム水溶液(0.5g/50m
l)に硫酸第一鉄水溶液(0.6g/50ml)と濃塩
酸10mlを加えた液)を加えて3分後に500nmの
吸光度を測定し盲検との差から求めた。図1にその結果
を示すが、この製造された抗酸化性物質をリノール酸に
添加することにより、リノール酸は長時間経ても自動酸
化されることなく、抗酸化能は非常に高いことが示され
た。
Peroxide value is 0.1 ml from the above vial
Take this, 2.35 ml of 75% ethanol, 0.05
Add 3 ml of 3% rhodan ammonia and add 0.05 ml of ferrous chloride reagent (barium chloride aqueous solution (0.5 g / 50 m
An aqueous solution of ferrous sulfate (0.6 g / 50 ml) and concentrated hydrochloric acid (10 ml) was added to 1) and after 3 minutes, the absorbance at 500 nm was measured and the difference from the blind was determined. The results are shown in Fig. 1. By adding the produced antioxidant to linoleic acid, it is shown that the linoleic acid is not auto-oxidized even after a long time and the antioxidant ability is very high. Was done.

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

【図1】抗酸化能の結果を示す図であり、過酸物価の増
加は吸光度の増加として表している。
FIG. 1 is a graph showing the results of antioxidative ability, in which an increase in peracid value is expressed as an increase in absorbance.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 阿部 馨 青森県青森市大字八ツ役字芦谷202の4 青森県産業技術開発センター内 (72)発明者 市田 淳治 青森県青森市大字八ツ役字芦谷202の4 青森県産業技術開発センター内 (72)発明者 松江 一 青森県青森市大字八ツ役字芦谷202の4 青森県産業技術開発センター内 (72)発明者 風晴 浩一 青森県青森市大字八幡林字品川4番地1 丸屋醸造株式会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Kaoru Abe Yatsu, Aomori City, Aomori Prefecture, character 4 of Ashiya 202-4, Aomori Industrial Technology Development Center (72) Inventor Junji Ichida, Aomori City, Aomori Prefecture Ashiya 202-4, Aomori Prefecture Industrial Technology Development Center (72) Inventor, Hajime Matsue Aomori, Aomori Prefecture, Yatsu Katsushi Ashiya 202-4, Aomori Industrial Technology Development Center (72) Inventor, Koichi Kazeharu Aomori, Aomori Prefecture Maruya Brewery Co., Ltd. 1 Shinagawa 4

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 大豆粕又はおからを酵素的、物理的に可
溶化させることを特徴とする抗酸化性物質の製造方法。
1. A method for producing an antioxidant, which comprises solubilizing soybean meal or okara soybeans enzymatically and physically.
【請求項2】 大豆粕又はおからからの水溶性で熱安定
性を特徴とする抗酸化性物質の製造方法。
2. A method for producing a water-soluble and heat-stable antioxidant substance from soybean meal or okara.
JP9869993A 1993-04-01 1993-04-01 Production of oxidation-resistant substance from soybean meal or lees of bean curd Pending JPH06287554A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9869993A JPH06287554A (en) 1993-04-01 1993-04-01 Production of oxidation-resistant substance from soybean meal or lees of bean curd

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9869993A JPH06287554A (en) 1993-04-01 1993-04-01 Production of oxidation-resistant substance from soybean meal or lees of bean curd

Publications (1)

Publication Number Publication Date
JPH06287554A true JPH06287554A (en) 1994-10-11

Family

ID=14226759

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9869993A Pending JPH06287554A (en) 1993-04-01 1993-04-01 Production of oxidation-resistant substance from soybean meal or lees of bean curd

Country Status (1)

Country Link
JP (1) JPH06287554A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5919921A (en) * 1996-06-11 1999-07-06 Protein Technologies International, Inc. Recovery of isoflavones from soy molasses
CN1048283C (en) * 1996-03-12 2000-01-12 金凤燮 Method for extracting asponin composition from traditional Chinese medicinal material with enzymic processing
US6083553A (en) * 1998-06-05 2000-07-04 Protein Technologies International, Inc. Recovery of isoflavones from soy molasses
US6132795A (en) * 1998-03-15 2000-10-17 Protein Technologies International, Inc. Vegetable protein composition containing an isoflavone depleted vegetable protein material with an isoflavone containing material
US6521282B1 (en) 1996-08-09 2003-02-18 Protein Technologies International, Inc. Aglucone isoflavone enriched vegetable flour and grit
US6544566B1 (en) 1999-04-23 2003-04-08 Protein Technologies International, Inc. Composition containing plant sterol, soy protein and isoflavone for reducing LDL cholesterol
US6579561B2 (en) 1996-08-09 2003-06-17 Protein Technologies International, Inc. Aglucone isoflavone enriched vegetable flour and vegetable grit and process for making the same from a vegetable material containing isoflavone
US6582739B1 (en) * 1998-02-20 2003-06-24 Sawa Industrial Co., Ltd. Processes for producing functional okara milks and functional tofus
US7015339B2 (en) 2001-07-24 2006-03-21 Cargill, Incorporated Process for isolating phenolic compounds
US7285297B1 (en) 1999-04-23 2007-10-23 Archer-Daniels-Midland Company Method of reducing low density liproprotein cholesterol concentration

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1048283C (en) * 1996-03-12 2000-01-12 金凤燮 Method for extracting asponin composition from traditional Chinese medicinal material with enzymic processing
US5990291A (en) * 1996-06-11 1999-11-23 Protein Technologies International, Inc. Recovery of isoflavones from soy molasses
US6706292B2 (en) 1996-06-11 2004-03-16 Solae, Llc Recovery of isoflavones from soy molasses
US5919921A (en) * 1996-06-11 1999-07-06 Protein Technologies International, Inc. Recovery of isoflavones from soy molasses
US6323018B1 (en) 1996-06-11 2001-11-27 Protein Technologies Int'l Lnc. Recovery of isoflavones from soy molasses
US6495141B2 (en) 1996-06-11 2002-12-17 Protein Technologies International, Inc. Recovery of isoflavones from soy molasses
US6680381B1 (en) 1996-06-11 2004-01-20 Solae, Llc Recovery of isoflavones from soy molasses
US6664382B2 (en) 1996-06-11 2003-12-16 Solae, Llc Recovery of isoflavones from soy molasses
US6521282B1 (en) 1996-08-09 2003-02-18 Protein Technologies International, Inc. Aglucone isoflavone enriched vegetable flour and grit
US6579561B2 (en) 1996-08-09 2003-06-17 Protein Technologies International, Inc. Aglucone isoflavone enriched vegetable flour and vegetable grit and process for making the same from a vegetable material containing isoflavone
US6582739B1 (en) * 1998-02-20 2003-06-24 Sawa Industrial Co., Ltd. Processes for producing functional okara milks and functional tofus
US6132795A (en) * 1998-03-15 2000-10-17 Protein Technologies International, Inc. Vegetable protein composition containing an isoflavone depleted vegetable protein material with an isoflavone containing material
US6083553A (en) * 1998-06-05 2000-07-04 Protein Technologies International, Inc. Recovery of isoflavones from soy molasses
US6579534B2 (en) 1999-04-23 2003-06-17 Solae, Llc Composition containing soy hypocotyl material and plant sterol for reducing LDL-cholesterol
US6572876B2 (en) 1999-04-23 2003-06-03 Solae, Llc Administering a composition containing plant sterol, soy protein and isoflavone for reducing LDL-cholesterol
US6669952B2 (en) 1999-04-23 2003-12-30 Solae, Llc Composition containing isoflavone material and plant sterol for reducing LDL-cholesterol
US6544566B1 (en) 1999-04-23 2003-04-08 Protein Technologies International, Inc. Composition containing plant sterol, soy protein and isoflavone for reducing LDL cholesterol
US7285297B1 (en) 1999-04-23 2007-10-23 Archer-Daniels-Midland Company Method of reducing low density liproprotein cholesterol concentration
US7015339B2 (en) 2001-07-24 2006-03-21 Cargill, Incorporated Process for isolating phenolic compounds

Similar Documents

Publication Publication Date Title
JP4491698B2 (en) Method for producing soy protein hydrolyzate
JP3881494B2 (en) Natto bacteria culture extract
US3761353A (en) Enzymatic protein solubilization
EP0562171B1 (en) Water-Soluble polysaccharide and a process for producing the same
US8603552B2 (en) Method for producing foods from culture of Bacillus natto
US20060216281A1 (en) Process for producing aglycon and flavor-improved food containing the aglycon by diglycosidase, and converting agent to be used in the process
JPH06287554A (en) Production of oxidation-resistant substance from soybean meal or lees of bean curd
AU2005320635B2 (en) Antioxidant material, anti-deterioration agent and food or beverage
JPH0560893B2 (en)
Wang et al. Release of bound trypsin inhibitors in soybeans by Rhizopus oligosporus
KIM et al. Recovery of fish bone from hoki (Johnius belengeri) frame using a proteolytic enzyme isolated from mackerel intestine
EP0320717A2 (en) Process for the enzymatic hydrolysis of a protein material
JP2002000288A (en) Method for producing isoflavone aglycone and ang-khak comprising isoflavone aglycone
WO2022059754A1 (en) Method of manufacturing processed chickpea milk
JP2003102417A (en) Method for enzymatically treating onion
JP2631202B2 (en) Peptide production method
JP3813055B2 (en) Method for producing high purity plant protein material
WO2007080599A2 (en) Enyzmatic process for debittering of protein hydro-lysate using immobilized peptidases
JPH07327666A (en) Microorganism having high activity to produce thiol protease inhibiting substance, production of the substance using the microorganism, preparation of food using the substance and quality improver composed of the substance
JP7442777B2 (en) protein hydrolyzate
JP2007044009A (en) Method for producing soybean embryo processed product, and soybean embryo processed product obtained by the same
JP3911282B2 (en) How to recover vitamin K2
AU2001244631B2 (en) Process for producing aglycon by using diglycosidase and flavor-improved food containing the aglycon and converting agent to be used in the process
JPH03123484A (en) Enzymatic agent for production of peptide and peptide-production process
JP3479716B2 (en) Producing protein seasoning liquid