JP3448344B2 - Peptide composition - Google Patents

Peptide composition

Info

Publication number
JP3448344B2
JP3448344B2 JP10339194A JP10339194A JP3448344B2 JP 3448344 B2 JP3448344 B2 JP 3448344B2 JP 10339194 A JP10339194 A JP 10339194A JP 10339194 A JP10339194 A JP 10339194A JP 3448344 B2 JP3448344 B2 JP 3448344B2
Authority
JP
Japan
Prior art keywords
peptide
protein
amino acids
amino acid
peptide composition
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
JP10339194A
Other languages
Japanese (ja)
Other versions
JPH07284369A (en
Inventor
孫一 山口
正保 高田
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.)
Nihon Shokuhin Kako Co Ltd
Original Assignee
Nihon Shokuhin Kako Co Ltd
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 Nihon Shokuhin Kako Co Ltd filed Critical Nihon Shokuhin Kako Co Ltd
Priority to JP10339194A priority Critical patent/JP3448344B2/en
Publication of JPH07284369A publication Critical patent/JPH07284369A/en
Application granted granted Critical
Publication of JP3448344B2 publication Critical patent/JP3448344B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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、植物性蛋白質の2種以
上の混合物を酵素で加水分解して得られる、遊離アミノ
酸をほとんど含まないペプチド態からなるペプチド組成
に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a peptide composition which is obtained by hydrolyzing a mixture of two or more kinds of vegetable proteins with an enzyme and which has a peptide form containing almost no free amino acid .

【0002】[0002]

【従来の技術】従来から、植物性蛋白質の加水分解物と
しては、酸や酵素を用いて分解したものが知られている
が、最近、植物性蛋白質や動物性蛋白質から各種のプロ
テアーゼにより得られるペプチドが報告されている。ペ
プチドには、蛋白質やアミノ酸とは異なる生理的な機
能、例えばモルヒネ様沈痛作用、免疫賦活作用、血圧調
節作用、あるいはカルシウム吸収促進作用、脂質代謝調
節作用などの機能が見い出されている。
2. Description of the Related Art Heretofore, as a hydrolyzate of a vegetable protein, one obtained by decomposing it with an acid or an enzyme has been known, but recently, it has been obtained by various proteases from a vegetable protein or an animal protein. Peptides have been reported. Peptides have been found to have physiological functions different from those of proteins and amino acids, such as morphine-like analgesic action, immunostimulatory action, blood pressure regulating action, calcium absorption promoting action, and lipid metabolism regulating action.

【0003】また、ペプチドは、その吸収特性から、ス
ポーツ、その他の激しい体力消耗時における即効的栄養
補給剤や、外科手術後の栄養補給剤や、各種疾患の栄養
療法としての経腸栄養剤に有効に利用できる。
[0003] Peptides, due to their absorption properties, are also effective nutritional supplements for sports and other intense physical exhaustion, nutritional supplements after surgery, and enteral nutritional supplements as nutritional therapy for various diseases. It can be used effectively.

【0004】これまでに知られている主なペプチドとし
ては、乳清ペプチド、米蛋白質由来ペプチド、卵白由来
ペプチド、イワシ等の魚肉蛋白質由来ペプチド、大豆ペ
プチドや、小麦ペプチド等が挙げられる。
Major peptides known so far include whey peptide, rice protein-derived peptide, egg white-derived peptide, fish meat protein-derived peptide such as sardines, soybean peptide and wheat peptide.

【0005】例えば、特開昭63-287462 号には、大豆ペ
プチドを栄養補給剤として利用することが開示されてお
り、特開平5-236906号には、小麦ペプチドからのグルタ
ミンに富んだペプチド組成物が、外科手術後の経腸栄養
剤などの窒素源として有用であることが開示されてい
る。
For example, JP-A-63-287462 discloses the use of soybean peptide as a nutritional supplement, and JP-A-5-236906 discloses a glutamine-rich peptide composition from wheat peptide. It is disclosed that the article is useful as a nitrogen source such as enteral nutrition after surgery.

【0006】一方、各種アミノ酸を含有する健康飲料も
種々提案されている。この場合、アミノ酸の種類により
その特性が異なるため、それぞれのアミノ酸の持つ機能
を発揮させるためにアミノ酸を直接添加する方法がとら
れている。
On the other hand, various health drinks containing various amino acids have been proposed. In this case, since the characteristics differ depending on the type of amino acid, a method of directly adding the amino acid has been adopted in order to exert the function of each amino acid.

【0007】[0007]

【発明が解決しようとする課題】しかしながら、アミノ
酸は、一般的に強い苦みを有するため、添加濃度が高く
なると風味が損なわれる他、経腸栄養剤においては投与
量を多くすると下痢を引き起こすという副作用があるた
め、投与量に限界があった。
However, since amino acids generally have a strong bitterness, the flavor is impaired when the added concentration is high, and in the enteral nutritional supplement, a side effect of causing diarrhea when the dose is increased. Therefore, the dose was limited.

【0008】また、アミノ酸を主体とした経腸栄養剤の
調製においては、アミノ酸を自由に配合できるが、吸収
効率を考慮する場合や、グルタミン等の不安定なアミノ
酸を利用する場合には、ペプチド態の方が有効と思われ
る。
Further, in the preparation of enteral nutritional supplements mainly composed of amino acids, amino acids can be freely mixed, but when considering absorption efficiency or when unstable amino acids such as glutamine are used, the peptide It seems that the state is more effective.

【0009】すなわち、蛋白質は、その起源によりアミ
ノ酸組成が異なることから、蛋白質の種類を選択し、こ
れらをペプチド化し配合することにより、目的のアミノ
酸を多く含むペプチド組成物を得ることが可能となる。
That is, since the amino acid composition of a protein varies depending on its origin, it is possible to obtain a peptide composition containing a large amount of the target amino acid by selecting the type of protein and peptide-mixing these. .

【0010】水溶液中で不安定なグルタミンは、他のア
ミノ酸とのペプチド態として合成されるか、あるいは誘
導体の形にして利用されているが、蛋白質由来のグルタ
ミンを含むペプチドを用いれば、これらの問題点を解決
できる。
Glutamine, which is unstable in an aqueous solution, is synthesized as a peptide form with other amino acids or is used in the form of a derivative, but if a peptide containing a glutamine derived from a protein is used, these are used. Can solve problems.

【0011】一方、栄養効果を考えると、一種類の蛋白
質からのペプチドは、その原料由来のアミノ酸組成に左
右され、一部のアミノ酸の含量が低くなる。これを補う
方法としては、アミノ酸を直接添加することも考えられ
るが、ペプチドの形で補う方が理想的である。この場
合、補充されるペプチドとしては、他の蛋白質からのペ
プチドが有効である。
On the other hand, considering the nutritional effect, a peptide derived from one kind of protein has a low content of some amino acids depending on the amino acid composition derived from the raw material. As a method of compensating for this, it is possible to add an amino acid directly, but it is ideal to supplement it in the form of a peptide. In this case, peptides from other proteins are effective as the supplemented peptides.

【0012】このように各種のアミノ酸をペプチドの形
で相互に補充できれば、種々の病態に対応した特殊栄養
食品や経腸栄養剤等の調製が可能となる。
Thus, if various amino acids can be mutually supplemented in the form of peptides, it becomes possible to prepare special nutritional foods, enteral nutritional products and the like corresponding to various pathological conditions.

【0013】しかしながら、従来のペプチド組成物は、
プロテアーゼの種類や、酵素反応系が適切でなかったた
め、遊離アミノ酸が生成しやすく、経腸栄養剤等を調製
する際の殺菌処理等の加熱により、糖類との反応が起こ
りやすかった。そのために、着色や風味が悪くなるばか
りでなく、刺激味も伴うため、経口投与する際に抵抗が
あるという問題点があった。
However, conventional peptide compositions are
Since the type of protease and the enzyme reaction system were not appropriate, free amino acids were likely to be produced, and the reaction with saccharides was likely to occur due to heating such as sterilization during preparation of enteral nutritional supplements. Therefore, not only the coloring and flavor are deteriorated, but also an irritating taste is accompanied, which causes a problem that there is resistance in oral administration.

【0014】したがって、本発明の目的は、目的に応じ
て選択された各種の植物性蛋白質から自由に調製でき
る、遊離アミノ酸含量が極めて少ないペプチド組成物を
提供することにある。
Therefore, an object of the present invention is to provide a peptide composition having a very low free amino acid content, which can be freely prepared from various plant proteins selected according to the purpose.

【0015】[0015]

【課題を解決するための手段】本発明者らは、上記目的
を達成するため、種々の研究を重ねた結果、2種以上の
植物性蛋白質の混合物を含有する原料から不純物を除去
し、高アルカリ下においてアルカリ性プロテアーゼで加
水分解し、必要に応じて、イオン交換樹脂や吸着樹脂、
活性炭等により精製することにより、遊離アミノ酸をほ
とんど含まないペプチド態からなるペプチド組成物が得
られることを見い出し、本発明を完成させるに至った。
Means for Solving the Problems As a result of various studies to achieve the above object, the present inventors have found that impurities are extracted from a raw material containing a mixture of two or more vegetable proteins. Removed and hydrolyzed with alkaline protease under high alkali, if necessary, ion exchange resin or adsorption resin,
It was found that a peptide composition consisting of a peptide containing almost no free amino acid can be obtained by purifying with activated carbon or the like, and completed the present invention.

【0016】すなわち、本発明のペプチド組成物は、2
種以上の植物性蛋白質の混合物を酵素で加水分解して得
られる分子量200〜4000のペプチドを主成分と
し、遊離アミノ酸含量が全アミノ酸に対して1%以下で
り、下記表1に示すアミノ酸組成を有することを特徴
とする。
That is, the peptide composition of the present invention comprises 2
The mixture of species or vegetable proteins as a main component a peptide of molecular weight 200 to 4000 obtained by enzymatic hydrolysis, free amino acid content of Ri <br/> Ah 1% or less of the total amino acids, the following Table It has the amino acid composition shown in 1 .

【表1】 また、本発明のペプチド組成物においては、とうもろこ
し蛋白質、小麦蛋白質、じゃがいも蛋白質、大豆蛋白質
より選ばれた2種以上から得られたペプチドを 含有する
ことが好ましい。 更に、本発明においては、固形分中、
ペプチド80〜99重量%、糖2〜10重量%、アミノ
酸0〜1重量%、その他0〜5重量%含有することが好
ましい。
[Table 1] In addition, in the peptide composition of the present invention, corn
Soy protein, wheat protein, potato protein, soy protein
Containing peptides obtained from a more selected two or more
It is preferable. Furthermore, in the present invention, in the solid content,
Peptide 80-99% by weight, sugar 2-10% by weight, amino
It is preferable to contain 0 to 1% by weight of acid and 0 to 5% by weight of others.
Good

【0017】[0017]

【0018】以下、本発明について好ましい態様を挙げ
て更に詳細に説明する。本発明において、植物性蛋白質
としては、各種のものが使用できるが、特にとうもろこ
し蛋白質、小麦蛋白質、じゃがいも蛋白質、大豆蛋白質
から選ばれた二種以上の混合物が好ましく用いられる。
とうもろこし蛋白質は、構成アミノ酸中、分岐鎖アミノ
酸、グルタミン、アラニン、プロリンの含量が高く、小
麦蛋白質は、グルタミン、プロリンの含量が高く、じゃ
がいも蛋白質は、アスパラギン、分岐鎖アミノ酸、リジ
ンの含量が高く、大豆蛋白質は、アスパラギン、グルタ
ミン、リジン、アルギニンの含量が高いという特徴を有
している。
Hereinafter, the present invention will be described in more detail with reference to preferred embodiments. In the present invention, various kinds of vegetable proteins can be used, but a mixture of two or more kinds selected from corn protein, wheat protein, potato protein and soybean protein is particularly preferably used.
Corn protein has a high content of branched chain amino acids, glutamine, alanine, and proline among constituent amino acids, wheat protein has a high content of glutamine and proline, and potato protein has a high content of asparagine, branched chain amino acids, and lysine. Soy protein is characterized by a high content of asparagine, glutamine, lysine, and arginine.

【0019】とうもろこし蛋白質としては、コーンスタ
ーチの製造過程において、とうもろこしからウエットミ
リングを経て得られるとうもろこし蛋白質の懸濁液、例
えばコーングルテンミール懸濁液や、コーングルテンリ
カーや、とうもろこし蛋白質画分から70%の含水アルコ
ール又はアルカリにて溶出してくるツエインなどが好ま
しく用いられる。また、小麦蛋白質としては、小麦粉か
ら分離した小麦グルテンが好ましく用いられ、じゃがい
も蛋白質としては、じゃがいも澱粉の製造過程におい
て、じゃがいもから分離して得られる蛋白質区分が好ま
しく用いられ、大豆蛋白質としては、脱脂大豆粉や濃縮
大豆蛋白質、分離大豆蛋白質及び脱脂豆乳等が好ましく
用いられる。これらの蛋白質懸濁液を原料とする場合、
その固形分濃度は5〜15重量%程度に調整することが
好ましい。
As the corn protein, a corn protein suspension obtained by subjecting corn to wet milling in the manufacturing process of corn starch, for example, a corn gluten meal suspension, a corn gluten liquor, or a corn protein fraction containing 70% of corn protein is used. Tween and the like which are eluted with hydrous alcohol or alkali are preferably used. Further, as the wheat protein, wheat gluten separated from wheat flour is preferably used, and as the potato protein, a protein category obtained by separating from potato is preferably used in the production process of potato starch, and as soybean protein, defatted Soybean powder, concentrated soybean protein, separated soybean protein, defatted soybean milk and the like are preferably used. When using these protein suspensions as raw materials,
The solid content concentration is preferably adjusted to about 5 to 15% by weight.

【0020】製造方法としては、これらの原料を予め生
澱粉分解酵素で処理して澱粉を分解、除去する。好まし
い態様によれば、上記植物性蛋白質の2種以上の混合物
の懸濁液に、水酸化ナトリウム、水酸化カリウム、水酸
化カルシウム等のアルカリを添加して、pH5〜6程度に
調整し、生澱粉分解酵素、例えば「ダビアーゼ」(商品
名、ダイキン工業株式会社製)を原料固形分当たり0.02
〜0.2 wt%添加して、50〜60℃にて3〜20時間攪拌して
反応させ、脱水、濾過することにより、澱粉を分解、除
去する。
As a manufacturing method, these raw materials are previously treated with a raw starch degrading enzyme to decompose and remove the starch. According to a preferred embodiment, an alkali such as sodium hydroxide, potassium hydroxide or calcium hydroxide is added to a suspension of a mixture of two or more of the above vegetable proteins to adjust the pH to about 5 to 6, A starch degrading enzyme, such as "Daviase" (trade name, manufactured by Daikin Industries, Ltd.), was added to 0.02
˜0.2 wt% is added, the mixture is stirred at 50 to 60 ° C. for 3 to 20 hours to react, dehydrated and filtered to decompose and remove starch.

【0021】次に、この処理物を固形分濃度5〜20wt
%、好ましくは、10〜15wt%になるように再懸濁し、こ
の懸濁液に、水酸化ナトリウム、水酸化カリウム、水酸
化カルシウム等のアルカリを添加して、好ましくはpH9
以上、より好ましくはpH12以上に調整し、50℃にてアル
カリ性プロテアーゼを原料固形分当たり0.02〜0.2wt %
添加して、50〜60℃にて3〜20時間攪拌して反応させ
る。この処理によって植物性蛋白質が適当な長さに加水
分解される。
Next, the treated product is treated with a solid content concentration of 5 to 20 wt.
%, Preferably 10 to 15 wt% and resuspended, and an alkali such as sodium hydroxide, potassium hydroxide or calcium hydroxide is added to this suspension to adjust the pH to preferably 9%.
More preferably, the pH is adjusted to 12 or more, and the alkaline protease is added at 0.02 to 0.2 wt% per solid material at 50 ° C.
Add and stir at 50-60 ° C. for 3-20 hours to react. This treatment hydrolyzes the vegetable protein to an appropriate length.

【0022】この場合のアルカリ性プロテアーゼとして
は、例えば掘越らの「Agric. Biol.Chem, 35(9), 1407
〜1414」に報告されている好アルカリ性細菌(Bacillu
s. No.221)由来のアルカリ性プロテアーゼ(名糖産業
株式会社製)や、好アルカリ性変異株由来の「エスペラ
ーゼ8.OL」、「サビナーゼ」(商品名、ノボ社製)など
が好適である。これらのアルカリ性プロテアーゼは、酵
素作用の最適pHが10〜12であり、耐熱性に優れており、
通常はエンド型の酵素で、遊離アミノ酸を生成しにくい
酵素である。
The alkaline protease in this case is, for example, “Agric. Biol. Chem, 35 (9), 1407” by Hikoshi et al.
~ 1414 "reported by Bacillu
s. No. 221) derived from alkaline protease (manufactured by Meito Sangyo Co., Ltd.), and "esperase 8.OL" and "sabinase" (trade name, manufactured by Novo Co.) derived from an alkaliphilic mutant strain are preferable. These alkaline proteases have an optimum pH for enzyme action of 10 to 12, and have excellent heat resistance,
Usually, it is an endo-type enzyme, and it is an enzyme that hardly produces free amino acids.

【0023】本発明のペプチド組成物は、例えば上記の
製造方法により得られるが、製品化に際しては、必要に
応じて、最後の処理液を濃縮し、pHを調整した後に、酸
処理や、アミダーゼ、デアミナーゼ等の酵素処理により
苦みを低減し、イオン交換樹脂やイオン交換膜、逆浸透
膜(RO膜)等により脱塩処理し、更に活性炭処理、殺
菌処理し、蒸発乾固して粉末化することが好ましい。た
だし、用途によっては、溶液のまま用いることもでき
る。
The peptide composition of the present invention can be obtained, for example, by the above-mentioned production method. In commercialization, if necessary, the final treatment solution is concentrated and the pH is adjusted, followed by acid treatment or amidase. , Bitterness is reduced by enzyme treatment such as deaminase, desalting treatment is performed by ion exchange resin, ion exchange membrane, reverse osmosis membrane (RO membrane), etc., further activated carbon treatment, sterilization treatment, evaporation to dryness and powderization. It is preferable. However, depending on the application, the solution may be used as it is.

【0024】また、本発明においては、目的とするアミ
ノ酸組成のペプチドを得るために、異なる種類の植物性
蛋白質を原料として得られたペプチド組成物を2種以上
混合して、最終的なペプチド組成物を得ることもでき
る。
In the present invention, in order to obtain a peptide having a desired amino acid composition, two or more peptide compositions obtained by using different types of plant proteins as raw materials are mixed to obtain a final peptide composition. You can also get things.

【0025】本発明のペプチド組成物は、植物性蛋白質
を上記のように酵素で加水分解したものからなり、分子
量分布200 〜4,000 、平均分子量500 〜2,000 程度のペ
プチドを主成分とし、遊離アミノ酸含量が全アミノ酸に
対して1%以下である。このペプチド組成物の成分は、
好ましい例として、固形分中、ペプチド80〜99重量
%、糖2〜10重量%、アミノ酸0〜1重量%、その他
0〜5重量%からなっている。
The peptide composition of the present invention comprises a vegetable protein hydrolyzed with an enzyme as described above, which is mainly composed of a peptide having a molecular weight distribution of 200 to 4,000 and an average molecular weight of about 500 to 2,000, and a free amino acid content. Is 1% or less with respect to all amino acids. The components of this peptide composition are
As a preferred example, the solid content is composed of 80 to 99% by weight of peptide, 2 to 10% by weight of sugar, 0 to 1% by weight of amino acid, and 0 to 5% by weight of others.

【0026】本発明のペプチド組成物は下記表2に示
すようなアミノ酸組成を有している。
The peptide compositions of the present invention has the amino acid composition shown in Table 2 below.

【0027】[0027]

【表2】 [Table 2]

【0028】[0028]

【作用】本発明のペプチド組成物は、2種以上の植物性
蛋白質の混合物を酵素で加水分解して得られる分子量分
布200 〜4,000 のペプチドを主成分とするものであり、
アミノ酸と同様に消化管よりの吸収が急速かつ良好であ
るために、激しい運動などに伴う体力低下時の栄養補給
剤や、消化機能の不十分な病態への経腸栄養剤に適して
いる。
The peptide composition of the present invention is mainly composed of a peptide having a molecular weight distribution of 200 to 4,000 obtained by hydrolyzing a mixture of two or more kinds of vegetable proteins with an enzyme,
As with amino acids, its rapid and good absorption from the digestive tract makes it suitable as a nutritional supplement when physical strength decreases due to intense exercise, and as an enteral nutritional supplement for the condition of poor digestive function.

【0029】本発明のペプチド組成物は、遊離アミノ酸
がほとんど含まれていないので、アミノ酸に比べて苦み
が少なく、臭いや味等が改善され、また、不安定なグル
タミンをペプチドの状態で存在させたり、不足しがちな
アミノ酸を他の蛋白質由来ペプチドで補うことができる
ので、広い範囲の食品に応用できる。
Since the peptide composition of the present invention contains almost no free amino acids, it has less bitterness than amino acids, has improved odor and taste, and has unstable glutamine in the form of peptides. In addition, amino acids that tend to be deficient can be supplemented with peptides derived from other proteins, so that they can be applied to a wide range of foods.

【0030】[0030]

【0031】[0031]

【実施例】以下、本発明を実施例により更に詳細に説明
する。参考例1 コーンスターチを製造する際のウエットミリング工程か
ら得られるとうもろこし蛋白質区分450 Lに、水酸化ナ
トリウムを添加してpH5.5 に調整し、生澱粉分解酵素
「ダビアーゼ」(商品名、ダイキン工業株式会社製)70
g を添加し、50℃で5時間反応させた後、フィルタープ
レスにて固液分離し、とうもろこし蛋白質のウエットケ
ーキ90kgを得る。
EXAMPLES The present invention will now be described in more detail with reference to examples. Reference Example 1 Sodium hydroxide was added to 450 L of the corn protein category obtained from the wet milling process when producing corn starch, and the pH was adjusted to 5.5 by adding sodium hydroxide, and the raw starch degrading enzyme "Daviase" (trade name, Daikin Industries, Ltd.) Company made) 70
After adding g and reacting at 50 ° C. for 5 hours, solid-liquid separation is performed with a filter press to obtain 90 kg of wet cake of corn protein.

【0032】このウエットケーキを蒸留水350 Lに再懸
濁させ、水酸化ナトリウムを添加してpH12に調整し、好
アルカリ性細菌由来の高アルカリ性プロテアーゼ(名糖
産業株式会社製)80g を添加し、pHを9.0 に調整しつ
つ、20時間反応させる。反応液をフィルタープレスにて
固液分離し、とうもろこし蛋白質の酵素加水分解物を得
る。
This wet cake was resuspended in 350 L of distilled water, sodium hydroxide was added to adjust the pH to 12, and 80 g of a highly alkaline protease derived from alkalophilic bacteria (manufactured by Meito Sangyo Co., Ltd.) was added, Incubate for 20 hours while adjusting pH to 9.0. The reaction solution is subjected to solid-liquid separation with a filter press to obtain an enzymatic hydrolyzate of corn protein.

【0033】上記加水分解物をイオン交換樹脂にて脱塩
し、吸着樹脂にて脱色、脱臭後、活性炭処理及び加熱殺
菌を行い、濃縮、乾燥して白色粉末であるコーンペプチ
ド組成物を得る。
The above hydrolyzate is desalted with an ion exchange resin, decolorized with an adsorption resin, deodorized, treated with activated carbon and sterilized by heating, concentrated and dried to obtain a corn peptide composition as a white powder.

【0034】参考例2 上記参考例1におけるとうもろこし蛋白質を、小麦蛋白
質に代え、参考例1と同様な操作を繰り返し、乾燥して
白色粉末である小麦ペプチド組成物を得る。
Reference Example 2 The same procedure as in Reference Example 1 was repeated except that the corn protein in Reference Example 1 was replaced with wheat protein, and the wheat peptide composition was obtained as a white powder by drying.

【0035】参考例3 上記参考例1におけるとうもろこし蛋白質を、じゃがい
も蛋白質に代え、参考例1と同様な操作を繰り返し、乾
燥して淡黄色粉末であるポテトペプチド組成物を得る。
Reference Example 3 The potato protein was used in place of the corn protein in Reference Example 1 above, and the same operation as in Reference Example 1 was repeated and dried to obtain a potato peptide composition which was a pale yellow powder.

【0036】参考例4 上記参考例1におけるとうもろこし蛋白質を、脱脂大豆
蛋白質に代え、参考例1と同様な操作を繰り返し、乾燥
して淡黄色粉末である大豆ペプチド組成物を得る。
Reference Example 4 The corn protein in the above Reference Example 1 was replaced with defatted soybean protein, and the same operation as in Reference Example 1 was repeated and dried to obtain a soybean peptide composition which was a pale yellow powder.

【0037】実施例1 上記参考例1におけるとうもろこし蛋白質区分200 L
に、小麦蛋白質22kgを添加し、参考例1と同様な操作を
繰り返し、乾燥して白色粉末である、とうもろこし+小
麦ペプチド組成物を得る。
Example 1 200 L of corn protein category in Reference Example 1 above
To this, 22 kg of wheat protein is added, the same operation as in Reference Example 1 is repeated, and dried to obtain a corn + wheat peptide composition as a white powder.

【0038】実施例2 上記参考例1におけるとうもろこし蛋白質区分200 L
に、じゃがいも蛋白質20kgを添加し、参考例1と同様な
操作を繰り返し、乾燥して白色粉末である、とうもろこ
し+じゃがいもペプチド組成物を得る。
Example 2 200 L of corn protein category in Reference Example 1 above
Then, 20 kg of potato protein is added, and the same procedure as in Reference Example 1 is repeated to obtain a corn + potato peptide composition which is a white powder after drying.

【0039】実施例3 小麦蛋白質20kgと、分離大豆蛋白質20kgとを、400 Lの
水に懸濁し、水酸化ナトリウムを添加してpH5.5 に調整
し、生澱粉分解酵素「ダビアーゼ」(商品名、ダイキン
工業株式会社製)50g を添加し、50℃で5時間反応させ
た後、参考例1と同様な操作を繰り返し、乾燥して淡黄
色粉末である、小麦+大豆ペプチド組成物を得る。
Example 3 20 kg of wheat protein and 20 kg of isolated soybean protein were suspended in 400 L of water, and sodium hydroxide was added to adjust the pH to 5.5. The raw starch degrading enzyme "Daviase" (trade name) (Manufactured by Daikin Industries, Ltd.) and reacted at 50 ° C. for 5 hours, and then the same operation as in Reference Example 1 is repeated and dried to obtain a wheat + soybean peptide composition which is a pale yellow powder.

【0040】試験例1参考例1〜4、実施例1〜3 で得られたペプチド組成物
のアミノ酸組成を表3、4に示す。なお、表3、4に
は、芳香族アミノ酸であるトリプトファンのデータが記
載されていないが、これはトリプトファンがほとんど含
まれてなかったためである。
Test Example 1 Tables 3 and 4 show the amino acid compositions of the peptide compositions obtained in Reference Examples 1 to 4 and Examples 1 to 3. It should be noted that data of tryptophan, which is an aromatic amino acid, is not shown in Tables 3 and 4 because it contains almost no tryptophan.

【0041】[0041]

【表3】 [Table 3]

【0042】[0042]

【表4】 [Table 4]

【0043】試験例2参考例1 で得られたペプチド組成物をアミノ酸自動分析
機器にかけて、ニンヒドリン発色による遊離アミノ酸量
(1mg 当たりのng)を測定した結果を表5に示す。
Test Example 2 The peptide composition obtained in Reference Example 1 was applied to an amino acid automatic analyzer to measure the amount of free amino acid (ng per 1 mg) by ninhydrin color development.

【0044】[0044]

【表5】 [Table 5]

【0045】試験例3参考例1〜4、実施例1〜3 で得られたペプチド組成物
と、対照として芳香族アミノ酸であるチロシン、フェニ
ルアラニンとを、高速液体クロマトグラフィー(HPLC)
にかけて分析を行い、ペプチド組成物の分子量分布及
び遊離アミノ酸量をそれぞれ求めた。
Test Example 3 The peptide compositions obtained in Reference Examples 1 to 4 and Examples 1 to 3 and aromatic amino acids tyrosine and phenylalanine as controls were subjected to high performance liquid chromatography (HPLC).
Analysis was carried out to determine the molecular weight distribution and free amino acid content of the peptide composition.

【0046】分離カラムとして「OH Pak KB-802.5 」
(商品名、昭和電工株式会社製)を用い、0〜1%トリ
フルオロ酢酸−40%アセトニトリル系の溶離液を用い、
流速0.5ml/min.とし、検出器はUV270nm として分析を
行った。
[OH Pak KB-802.5] as a separation column
(Trade name, manufactured by Showa Denko KK) using 0 to 1% trifluoroacetic acid-40% acetonitrile eluent,
The flow rate was 0.5 ml / min., And the detector was UV270 nm for analysis.

【0047】この分析結果を表6、7に示す。表6、7
は溶出位置を時間で比較してある。また、参考例1で得
られたペプチド組成物を高速液体クロマトグラフィー
(HPLC) にかけたときの溶出曲線を図1に示す。
The results of this analysis are shown in Tables 6 and 7. Tables 6 and 7
Shows the elution positions compared in time. Further, the elution curve when the peptide composition obtained in Reference Example 1 was subjected to high performance liquid chromatography (HPLC) is shown in FIG.

【0048】[0048]

【表6】 [Table 6]

【0049】[0049]

【表7】 [Table 7]

【0050】表5では参考例1で得られたペプチド組成
物のチロシン、フェニルアラニンの遊離アミノ酸量がそ
れぞれ40.69 %、33.56 %となっているが、表6では0.
27%である。表5ではペプチド区分がニンヒドリンによ
り発色し、検出されたものと考えられることから、表
6、7から判断すると、参考例1〜4、実施例1〜3
ペプチド組成物の遊離アミノ酸量は1.0 %以下であるこ
とがわかる。
In Table 5, the free amino acid amounts of tyrosine and phenylalanine of the peptide composition obtained in Reference Example 1 are 40.69% and 33.56%, respectively.
27%. In Table 5, it is considered that the peptide category was colored by ninhydrin and was detected. Therefore, judging from Tables 6 and 7, the free amino acid content of the peptide compositions of Reference Examples 1 to 4 and Examples 1 to 3 was 1.0. It can be seen that it is less than or equal to%.

【0051】[0051]

【発明の効果】以上説明したように、本発明のペプチド
組成物は、2種以上の植物性蛋白質の混合物を酵素分解
して得られた分子量200 〜4,000 のペプチドを主成分と
するので、アミノ酸と同様に消化管よりの吸収が急速か
つ良好であり、激しい運動などに伴う体力低下時の栄養
補給剤や、消化機能の不十分な病態への経腸栄養剤に適
している。
Industrial Applicability As described above, the peptide composition of the present invention contains as a main component a peptide having a molecular weight of 200 to 4,000 obtained by enzymatically decomposing a mixture of two or more plant proteins. As with the above, absorption from the digestive tract is rapid and good, and it is suitable as a nutritional supplement when physical strength decreases due to vigorous exercise, or as an enteral nutritional supplement for the condition of poor digestive function.

【0052】また、本発明のペプチド組成物は、遊離ア
ミノ酸をほとんど含まないので、アミノ酸に比べて苦み
が少なく、臭いや味等が改善される。更に、不安定なグ
ルタミンをペプチドの状態で存在させたり、不足しがち
なアミノ酸を他の蛋白質由来ペプチドで補うことができ
るので、広い範囲の食品に応用できる。
Further, since the peptide composition of the present invention contains almost no free amino acids, it has less bitterness than amino acids and has improved odor, taste and the like. Further, unstable glutamine can be present in the form of a peptide, and amino acids that tend to be deficient can be supplemented with peptides derived from other proteins, so that it can be applied to a wide range of foods.

【0053】[0053]

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

【図1】参考例1で得られたペプチド組成物を高速液体
クトマトグラフィー(HPLC)にかけたときの溶出曲線を示
す図表である。
FIG. 1 is a chart showing an elution curve when the peptide composition obtained in Reference Example 1 was subjected to high performance liquid chromatography (HPLC).

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 2種以上の植物性蛋白質の混合物を酵素
で加水分解して得られる分子量200〜4000のペプ
チドを主成分とし、遊離アミノ酸含量が全アミノ酸に対
して1%以下であり、下記表1に示すアミノ酸組成を有
することを特徴とするペプチド組成物。 【表1】
1. A two or more mixtures of vegetable protein as a main component a peptide of molecular weight 200 to 4000 obtained by enzymatic hydrolysis, the free amino acid content of not more than 1% of the total amino acids, the following The amino acid composition shown in Table 1
A peptide composition comprising: [Table 1]
【請求項2】 とうもろこし蛋白質、小麦蛋白質、じゃ
がいも蛋白質、大豆蛋白質より選ばれた2種以上から得
られたペプチドを含有する請求項1記載のペプチド組成
物。
2. The peptide composition according to claim 1, which contains a peptide obtained from two or more kinds selected from corn protein, wheat protein, potato protein, and soybean protein.
【請求項3】 固形分中、ペプチド80〜99重量%、
糖2〜10重量%、アミノ酸0〜1重量%、その他0〜
5重量%含有する請求項1又は2記載のペプチド組成
物。
3. The solid content of the peptide is 80 to 99% by weight,
Sugar 2-10% by weight, amino acids 0-1% by weight, other 0
5 containing by weight% claim 1 or 2 peptide composition.
JP10339194A 1994-04-18 1994-04-18 Peptide composition Expired - Lifetime JP3448344B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10339194A JP3448344B2 (en) 1994-04-18 1994-04-18 Peptide composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10339194A JP3448344B2 (en) 1994-04-18 1994-04-18 Peptide composition

Publications (2)

Publication Number Publication Date
JPH07284369A JPH07284369A (en) 1995-10-31
JP3448344B2 true JP3448344B2 (en) 2003-09-22

Family

ID=14352778

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10339194A Expired - Lifetime JP3448344B2 (en) 1994-04-18 1994-04-18 Peptide composition

Country Status (1)

Country Link
JP (1) JP3448344B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102987275A (en) * 2012-12-28 2013-03-27 黑龙江新曙光牧业集团有限公司 Preparation method of soybean oligo saccharide peptide with high biological value

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69738806D1 (en) * 1996-10-10 2008-08-14 Invitrogen Corp ANIMAL CELL CULTURE MEDIUM WITH VEGETABLE NUTRIENTS
JP4227984B2 (en) * 2004-11-15 2009-02-18 コスモ食品株式会社 Composition for improving flavor and taste of food
JP5639803B2 (en) * 2010-07-12 2014-12-10 青葉化成株式会社 Meat card inhibitor
CN110117634A (en) * 2019-05-11 2019-08-13 世堃堂(广东)生物科技有限公司 A kind of five-cereal health-care peptide and preparation method thereof
CN110819675A (en) * 2019-11-20 2020-02-21 吉林云步科技有限公司 Preparation method for extracting high-activity small-molecule peptide from corn

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102987275A (en) * 2012-12-28 2013-03-27 黑龙江新曙光牧业集团有限公司 Preparation method of soybean oligo saccharide peptide with high biological value
CN102987275B (en) * 2012-12-28 2018-06-01 长春大学 A kind of preparation method of the soy oligosaccharides glycopeptide of high biological value

Also Published As

Publication number Publication date
JPH07284369A (en) 1995-10-31

Similar Documents

Publication Publication Date Title
US9609883B2 (en) Method for producing wheat glutamine peptide
CA2759424C (en) Collagen peptide composition having good ability to enter the blood and food or beverage containing the same
US4452888A (en) Process for producing a low-molecular weight peptide composition and nutrient agent containing the same
Oste et al. Effect of Maillard reaction products on protein digestion. In vitro studies
WO1996011584A1 (en) Peptide mixture and products thereof
US4016147A (en) Method for preparation of low-phenylalanine plastein
FI94088C (en) Process for removing phenylalanine from proteinaceous compositions
CA1237937A (en) Health food and drink
JP3448344B2 (en) Peptide composition
US5021338A (en) Enzyme extract from germinated sorghum for hydrolysis of protein material
JP2862418B2 (en) Functional foods effective for improving lipid metabolism
JP4619730B2 (en) Amino acid / peptide mixture with excellent flavor and method for producing the same
JP2944008B2 (en) Parenteral lipid metabolism improver
WO1990013228A1 (en) Oligopeptide mixture and composition containing the same
CN109661401B (en) Phenylalanine-free proteins for use in the treatment of PKU
WO2022168413A1 (en) Method for producing deprestatin-containing composition
KR20040067859A (en) Novel peptide sy
JP2006158390A (en) Food flavor/taste improving composition
JP2931022B2 (en) Edible peptide-containing substance and method for producing the same
EP0499306B1 (en) Starches with an improved flavour
ZA200306957B (en) Process for preparation of protein hydrolysate from soy flour.
JP2631202B2 (en) Peptide production method
JPH0581219B2 (en)
JP5717433B2 (en) Bile acid adsorption composition
JP2022146119A (en) Edible composition and method for producing the same

Legal Events

Date Code Title Description
A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20030212

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20030610

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080704

Year of fee payment: 5

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090704

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090704

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090704

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100704

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100704

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110704

Year of fee payment: 8

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110704

Year of fee payment: 8

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110704

Year of fee payment: 8

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120704

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120704

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120704

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120704

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130704

Year of fee payment: 10

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130704

Year of fee payment: 10

EXPY Cancellation because of completion of term