JPH0217151B2 - - Google Patents

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Publication number
JPH0217151B2
JPH0217151B2 JP61136005A JP13600586A JPH0217151B2 JP H0217151 B2 JPH0217151 B2 JP H0217151B2 JP 61136005 A JP61136005 A JP 61136005A JP 13600586 A JP13600586 A JP 13600586A JP H0217151 B2 JPH0217151 B2 JP H0217151B2
Authority
JP
Japan
Prior art keywords
ornithine
fermentation
temperature
content
urea
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
JP61136005A
Other languages
Japanese (ja)
Other versions
JPS62294069A (en
Inventor
Togo Kuroiwa
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to JP61136005A priority Critical patent/JPS62294069A/en
Publication of JPS62294069A publication Critical patent/JPS62294069A/en
Publication of JPH0217151B2 publication Critical patent/JPH0217151B2/ja
Granted legal-status Critical Current

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  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Non-Alcoholic Beverages (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Medicines Containing Plant Substances (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は人体の細胞蛋白質のアミノ酸の分解に
より生じたアンモニアを尿素に転換して解毒し、
窒素終末代謝を促進するL−オルニチンを高単位
(50mg/100ml)に含有した栄養補給液に関するも
のである。 〔従来の技術〕 塩基性アミノ酸の一種であるL−オルニチン
は、ヒトを含む尿素排出動物の肝臓に存在し、代
謝回路の中で最初に発見された尿素回路に関与す
る重要なアミノ酸である。 尿素回路の理論は、クレブス(Krebs)とヘン
ゼライト(Henseleit)により提唱され、さらに
コーエン(Cohen)とラツトナー(Ratner)ら
によりその詳細が発見された。 L−オルニチンは、通常の蛋白質には含まれて
いないとされているが、ニンヒドリン法ではヒト
の血漿中に約1mg/100ml(正常値)が含有され
ていることが確認されている。L−オルニチンは
カルバモイルリン酸と結合して、L−シトルリン
となる。これにアスパラギン酸が結合してアルギ
ニノコハク酸となり、さらに、コハク酸部分がは
ずれてL−アルギニンとなつたのち、アルギナー
ゼの作用によつて再びL−オルニチンとなる。 この一連の反応を尿素回路(オルニチンサイク
ル)と呼び、高等動物の尿素生成機構としてきわ
めて重要である。 L−オルニチンは、アンモニア解毒作用のほか
抗脂肪肝作用、肝機能亢進作用をもつているが、
これまでL−オルニチンを高単位に含有した食物
の製造は技術的にも、また経済的にも不可能であ
るとされてきた。 〔発明が解決しようとする問題点〕 本発明者は尿素回路を促進するのに有効なL−
オルニチンを高単位に含有する栄養補給液を、特
殊な技法によることなく、しかも経済的にも充分
成り立つようにして、得るべく鋭意研究を進めた
ところ、米麹と穀類と水を料として、通常の醗酵
温度よりも高い45〜60℃の高温度を維持して醗酵
させた醗酵液中に、必須アミノ酸を始め、人体の
細胞を構成する蛋白質の生合成に必要なL−アミ
ノ酸とともに、L−オルニチンが高単位に含有さ
れていることを見いだし、本発明を完成するに至
つたものである。 〔問題点を解決するための手段〕 本発明を詳述すれば、尿素回路(オルニチンサ
イクル)を促進するための飲料であつて、米麹、
穀物及び水を原料として通常の醗酵温度よりも高
い45〜60℃の高温度で醗酵させた醗酵液中より、
諸味の固形分を分離除去して得られることを特徴
とするL−オルニチンを高単位に含有した栄養補
給液、である。 通常の米麹を穀物と水を混合して醗酵させ食酢
等を醸造する場合の醗酵温度は、15〜35℃で比較
的長期の醗酵日数を要する。そのような、醗酵温
度によつて得られた醗酵液は、酸度4〜7%、総
アミノ態窒素150mg/100ml以内の数値を示し、L
−オルニチンの含有量はごく少量の10mg/100ml
以内であるのが通常である。15〜35℃程度の醗酵
温度では澱粉分解酵素のアミラーゼの活動がさか
んで、ブドウ糖→アルコール→酢酸への一連の醗
酵が進行して高酸度の醗酵液が生成される。醗酵
中酸度が上昇するにつれて、蛋白質分解酵素のプ
ロテアーゼ、特にL−アルギニンをL−オルニチ
ンに生成する酵素、アルギナーゼの活動が制限さ
れ、L−オルニチンの含量は上昇しない。 しかしながら、本発明者が到達した醗酵温度の
45〜60℃の高温醗酵では、澱粉質分解酵素の活動
が低下してごく低度の酸度しか得られない。従つ
て、低酸度と高温下の醗酵条件によつて、アルギ
ナーゼの活動が促進されL−オルニチンの含量が
上昇した醗酵液を得ることができたのであると推
定される。 なお、実験の結果、醗酵温度を60℃以上とした
場合は、温度上昇に比例して酵素活動が低下し、
ついには全く停止状態となりL−オルニチンが生
成されなくなることが判明した。 清酒や米酢の醸造では、醗酵温度の上昇が致命
的な失敗を招く要因となるが、本発明者はこの要
因を逆に利用することにより、高単位のL−オル
ニチンの生成を促進し、全く新規な醗酵液を得る
に至つたものである。 〔実施例〕 表1に示す力価を有する米麹の乾燥粉末12Kgに
対し、黒大豆の炒粉3Kgと水50をよく撹拌混合
して陶器製の容器内に仕込み、醗酵温度約55℃
(陶器製容器を静置した仕込室の室温を55℃前後
とすることによつた。)で、28日間醗酵させた。
なお、仕込み開始から4週経過までの醗酵過程を
表2に示す。そして、4週目の醗酵液中に溶解せ
ずに残つている諸味の固形分を常法によつて分離
除去し、固形分を含まない本発明醗酵液を得た。
この醗酵液は、表2に示されているように、酸度
が1.18%の低酸度であり、総アミノ態窒素は312
mg/100mlの数値を有していた。 このように、本発明の温度条件下による高温醗
酵では澱粉質分解酵素の活動が低下して酢酸への
醗酵が進行せず、従つて低酸度の醗酵液が生成さ
れる代りに、L−アルギニンをL−オルニチンに
生成する酵炊、アルギナーゼの活動が促進され、
表3に示すようにL−オルニチンの含量が突出
(151.84mg/100ml)していることが顕著である。 〔比較例〕 前記実施例と同様の力価を有する米麹の乾燥粉
末12Kgに対し、黒大豆の炒粉3Kgと水50をよく
撹拌混合して陶器製の容器内に仕込み、醗酵温度
を約30℃として28日間醗酵させた。 この比較例の4週目の尿素回路液は、表4に示
すように、酸度が2.49%となつており、総アミノ
態窒素は246mg/100mlの数値を示していた。 そして、この比較例によつた醗酵液では、表5
に示すようにL−オルニチンの含有量は僅かに
3.22mg/100mlであつたが、L−アルギニンの含
有量は267.04mg/100mlと高単位の数値を示した。 これらのことから、醗酵温度が低く且つ高酸度
の場合は、L−アルギニンの含量は多いが、L−
オルニチンの含量は少なくなる傾向にあることが
判つた。一方、高温度で且つ低酸度の醗酵では、
L−アルギニンの含量は低下し、それに比例して
L−オルニチンの含量が上昇することが判り、こ
れらのことは尿素回路におけるL−アルギニンと
L−オルニチンの関連を立証するのに役立つもの
と考えられる。 〔発明の効果〕 窒素終末代謝を行う重要な代謝回路である尿素
回路の主役をなすL−オルニチンは、通常は肝臓
で合成され肝臓に存在するが、肝機能低下の場合
L−オルニチンの生合成は阻害され高アンモニア
血症を招く。小児の急性脳症の一型であるライ症
候群もその主症状の一つで、尿素合成の阻害が原
因と予想される。また、肝炎、肝硬変、肝臓癌な
どの重症の肝疾患などにも、肝機能亢進作用を促
進するL−オルニチンの投与は栄養補給上きわめ
て重要なことであるが、本発明によれば、L−オ
ルニチンを高単位に含有した栄養補給液を特別な
技法によらず、しかも経済的に提供することがで
き、前記した症例の回復に多大な効果があるもの
である。また、本発明の栄養補給液は米麹、穀類
及び水を原料とするもので、化学的に合成された
ものは一切含まないので、保健衛生上も何等問題
はない。
[Industrial Application Field] The present invention detoxifies ammonia produced by the decomposition of amino acids in human cell proteins by converting it into urea.
The present invention relates to a nutritional supplement containing a high amount (50 mg/100 ml) of L-ornithine, which promotes nitrogen terminal metabolism. [Prior Art] L-ornithine, a type of basic amino acid, is present in the liver of urea-excreting animals including humans, and is an important amino acid involved in the urea cycle, which was first discovered in the metabolic cycle. The theory of the urea cycle was proposed by Krebs and Henseleit, and its details were discovered by Cohen, Ratner, and others. Although it is said that L-ornithine is not contained in normal proteins, it has been confirmed by the ninhydrin method that it is contained in human plasma at approximately 1 mg/100 ml (normal value). L-ornithine combines with carbamoyl phosphate to become L-citrulline. Aspartic acid is bonded to this to form argininosuccinic acid, and then the succinic acid moiety is removed to form L-arginine, which then becomes L-ornithine again by the action of arginase. This series of reactions is called the urea cycle (ornithine cycle), and is extremely important as a urea production mechanism in higher animals. L-ornithine has an ammonia detoxifying effect, an anti-fatty liver effect, and a liver function enhancing effect.
Until now, it has been thought that it is technically and economically impossible to produce foods containing a large amount of L-ornithine. [Problems to be Solved by the Invention] The present inventor has discovered that L-
We conducted intensive research to obtain a nutritional solution containing a high amount of ornithine without using any special techniques and in an economically viable manner. In the fermentation liquid, which is maintained at a high temperature of 45 to 60 degrees Celsius, which is higher than the fermentation temperature of It was discovered that ornithine is contained in high units, leading to the completion of the present invention. [Means for Solving the Problems] In detail, the present invention is a beverage for promoting the urea cycle (ornithine cycle), which comprises rice malt,
From the fermented liquid made from grains and water at a high temperature of 45 to 60 degrees Celsius, which is higher than the normal fermentation temperature.
This is a nutritional supplement containing a high unit of L-ornithine, which is obtained by separating and removing the solid content of moromi. When fermenting ordinary rice koji by mixing grains and water to brew vinegar, etc., the fermentation temperature is 15 to 35°C, and a relatively long fermentation period is required. The fermented liquid obtained at such fermentation temperature shows an acidity of 4 to 7%, total amino nitrogen of 150 mg/100 ml or less, and L
-Ornithine content is very small at 10mg/100ml
Normally, it is within the range. At fermentation temperatures of about 15 to 35 degrees Celsius, the activity of the starch-degrading enzyme amylase increases, and a series of fermentations from glucose to alcohol to acetic acid progresses, producing a highly acidic fermented liquid. As the acidity increases during fermentation, the activity of protease, especially arginase, an enzyme that converts L-arginine into L-ornithine, is limited, and the content of L-ornithine does not increase. However, the fermentation temperature reached by the inventor
In high-temperature fermentation at 45-60℃, the activity of starch-degrading enzymes decreases, resulting in only a very low level of acidity. Therefore, it is presumed that the fermentation conditions of low acidity and high temperature promoted the activity of arginase and made it possible to obtain a fermentation solution with an increased content of L-ornithine. In addition, as a result of experiments, when the fermentation temperature was set to 60℃ or higher, enzyme activity decreased in proportion to the rise in temperature.
It was finally found that the process stopped completely and L-ornithine was no longer produced. In the brewing of sake and rice vinegar, an increase in fermentation temperature is a factor that can lead to fatal failure, but the present inventor has reversely utilized this factor to promote the production of high units of L-ornithine. This led to the creation of a completely new fermentation liquid. [Example] 12 kg of dry powder of rice malt having the titer shown in Table 1, 3 kg of fried black soybean powder and 50 kg of water were well stirred and mixed and placed in a ceramic container, and fermented at a temperature of approximately 55°C.
(This was done by setting the room temperature of the preparation room where the ceramic container was kept at around 55°C) for 28 days.
Table 2 shows the fermentation process from the start of preparation until 4 weeks have elapsed. Then, the solid content of moromi remaining undissolved in the fermentation liquid after the fourth week was separated and removed by a conventional method to obtain a fermentation liquid of the present invention that does not contain any solid content.
As shown in Table 2, this fermentation liquid has a low acidity of 1.18%, and the total amino nitrogen is 312%.
It had a value of mg/100ml. As described above, in the high temperature fermentation under the temperature conditions of the present invention, the activity of starch-degrading enzymes decreases and fermentation to acetic acid does not proceed, and therefore, instead of producing a fermentation solution with low acidity, L-arginine Fermentation that produces L-ornithine and the activity of arginase are promoted,
As shown in Table 3, it is remarkable that the content of L-ornithine is prominent (151.84 mg/100 ml). [Comparative Example] To 12 kg of dry powder of rice malt having the same potency as in the above example, 3 kg of fried black soybean powder and 50 kg of water were thoroughly stirred and mixed, and the mixture was charged into a ceramic container and the fermentation temperature was adjusted to approx. Fermentation was carried out at 30°C for 28 days. As shown in Table 4, the 4th week urea circuit solution of this comparative example had an acidity of 2.49% and a total amino nitrogen of 246 mg/100 ml. In the fermentation liquid according to this comparative example, Table 5
As shown in the figure, the content of L-ornithine is small.
The content of L-arginine was 3.22 mg/100 ml, but the content of L-arginine was high at 267.04 mg/100 ml. From these facts, when the fermentation temperature is low and the acidity is high, the content of L-arginine is high, but the L-arginine content is high.
It was found that the content of ornithine tended to decrease. On the other hand, in fermentation at high temperature and low acidity,
It was found that the content of L-arginine decreased and the content of L-ornithine increased proportionally, and these findings are considered to be useful in proving the relationship between L-arginine and L-ornithine in the urea cycle. It will be done. [Effect of the invention] L-ornithine, which plays the main role in the urea cycle, which is an important metabolic circuit that performs nitrogen terminal metabolism, is normally synthesized and exists in the liver, but in cases of decreased liver function, L-ornithine biosynthesis is activated. is inhibited, leading to hyperammonemia. Reye's syndrome, a type of acute encephalopathy in children, is one of its main symptoms, and inhibition of urea synthesis is thought to be the cause. Furthermore, administration of L-ornithine, which promotes liver function enhancement, is extremely important for nutritional support in severe liver diseases such as hepatitis, cirrhosis, and liver cancer. A nutritional supplement containing a high amount of ornithine can be provided economically without any special technique, and is highly effective in the recovery of the above-mentioned cases. Furthermore, the nutritional supplement of the present invention is made from rice malt, grains, and water, and does not contain any chemically synthesized substances, so there is no problem in terms of health and hygiene.

【表】【table】

【表】【table】

【表】 (注) 総アミノ態窒素はホルモール法、酸度は
アルカリ滴定法、糖度はアタゴ屈折計によ
る。
[Table] (Note) Total amino nitrogen is measured by the formol method, acidity is measured by the alkaline titration method, and sugar content is measured by the Atago refractometer.

【表】【table】

【表】 (注) アミノ酸分析は日立高速ア
ミノ酸分析計835=50型使用
分析法は生体分析法。
[Table] (Note) Hitachi High Speed Amino Acid Analyzer Model 835=50 was used for amino acid analysis.The analysis method was bioanalysis.

【表】 アルカリ滴定法、糖度はアタゴ屈折計によ
る。
[Table] Alkaline titration method and sugar content using Atago refractometer.

【表】【table】

【表】 分析法は生体分析法。
[Table] The analysis method is bioanalysis.

Claims (1)

【特許請求の範囲】[Claims] 1 尿素回路(オルニチンサイクル)を促進する
ための飲料であつて、米麹、穀物及び水を原料と
して通常の醗酵温度よりも高い45〜60℃の高温度
で醗酵させた醗酵液中より、諸味の固形分を分離
除去して得られることを特徴とするL−オルニチ
ンを高単位に含有した栄養補給液。
1. It is a drink to promote the urea cycle (ornithine cycle), and is made from fermented liquid made from rice malt, grains, and water at a high temperature of 45 to 60 degrees Celsius, which is higher than the normal fermentation temperature. A nutritional supplement containing a high unit of L-ornithine, which is obtained by separating and removing the solid content of.
JP61136005A 1986-06-13 1986-06-13 Nutrition supplying solution containing high unit of l-ornithine Granted JPS62294069A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61136005A JPS62294069A (en) 1986-06-13 1986-06-13 Nutrition supplying solution containing high unit of l-ornithine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61136005A JPS62294069A (en) 1986-06-13 1986-06-13 Nutrition supplying solution containing high unit of l-ornithine

Publications (2)

Publication Number Publication Date
JPS62294069A JPS62294069A (en) 1987-12-21
JPH0217151B2 true JPH0217151B2 (en) 1990-04-19

Family

ID=15164961

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61136005A Granted JPS62294069A (en) 1986-06-13 1986-06-13 Nutrition supplying solution containing high unit of l-ornithine

Country Status (1)

Country Link
JP (1) JPS62294069A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4020980C1 (en) * 1990-07-02 1991-09-26 Degussa Ag, 6000 Frankfurt, De
WO2004052125A1 (en) * 2002-12-06 2004-06-24 Kyowa Hakko Kogyo Co., Ltd. Beverage containing amino acid and method of diminishing bitterness of amino acid
JP2007031375A (en) * 2005-07-28 2007-02-08 Kyowa Hakko Kogyo Co Ltd Oral agent for ameliorating skin quality
JP4705874B2 (en) * 2006-04-03 2011-06-22 株式会社アセラ Method for producing amino acid-rich food material, particularly amino acid-rich food material containing abundant ornithine, food material produced by using these production methods, and foods to which these food materials are added

Also Published As

Publication number Publication date
JPS62294069A (en) 1987-12-21

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