JP2698123B2 - Bifidobacterium growth promotion / intestinal harmful bacteria growth inhibitor - Google Patents

Bifidobacterium growth promotion / intestinal harmful bacteria growth inhibitor

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Publication number
JP2698123B2
JP2698123B2 JP63277300A JP27730088A JP2698123B2 JP 2698123 B2 JP2698123 B2 JP 2698123B2 JP 63277300 A JP63277300 A JP 63277300A JP 27730088 A JP27730088 A JP 27730088A JP 2698123 B2 JP2698123 B2 JP 2698123B2
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Japan
Prior art keywords
evening
growth
powder
bifidobacterium
cotton
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Japanese (ja)
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JPH02124089A (en
Inventor
靖彦 菊池
卓郎 山浦
実 内田
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東京田辺製薬株式会社
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Description

【発明の詳細な説明】 産業上の利用分野 本発明は夕顔の果実のワタ(以下、ワタという。)ま
たは夕顔の葉、葉柄およびつる(以下、葉茎という。)
を有効成分とするビフィドバクテリウム菌(Bifidobact
erium)増殖促進・腸内有害菌増殖抑制剤に関する。
Description: FIELD OF THE INVENTION The present invention relates to cotton of evening fruit (hereinafter referred to as cotton) or leaves, petiole and vine of evening meal (hereinafter referred to as leaf stem).
Containing Bifidobacterium as an active ingredient
erium) It relates to a growth promotion / intestinal harmful bacteria growth inhibitor.

従来の技術 夕顔はうり科の一年生つる草で、その果実は直径70セ
ンチ程の長円形になる。この果実の果肉を紐のように細
長くむいて乾燥したものが干瓢である。ワタとは夕顔果
実の果肉の中心部の柔かい部分であって、干瓢製造時に
は廃棄される。
Prior art Evening glory is an annual vine plant of the bollaceae, and its fruit is oval with a diameter of about 70 cm. The dried and dried pulp of the fruit is like a string. Cotton is the soft part of the center of the flesh of the evening grape fruit, which is discarded during the production of gourd.

ビフィドバクテリウム菌は病原性がなく、ヒトを始め
として、主に哺乳動物の腸内に存在し、腸内腐敗生成物
の抑制、下痢、便秘症の改善などの生理的意義が認めら
れている有用な菌である。
Bifidobacterium is not pathogenic and exists mainly in the intestines of mammals, including humans, and has been shown to have physiological significance such as suppression of intestinal putrefaction products, diarrhea, and improvement of constipation. Is a useful fungus.

近年、ビフィドバクテリウム菌の免疫力促進効果や抗
生物質を連続投与した時に起る菌交代症の防止効果、さ
らには発癌性物質の抑制効果などが明らかになり、臨床
への応用が盛んに行われている(「微生物」、1巻、4
号、2頁、1987年、医学出版センサー)。このように、
ビフィドバクテリウム菌は、ヒトを始めとする哺乳動物
の健康に深いかかわりを持ち、医療の分野において注目
されている。
In recent years, the immunity-promoting effect of Bifidobacterium bacteria, the preventive effect of bacterial alternation caused by continuous administration of antibiotics, and the inhibitory effect of carcinogenic substances have been clarified. ("Microorganisms", Volume 1, 4
No. 2, p. 1987, Medical Publishing Sensor). in this way,
Bifidobacterium is closely related to the health of mammals including humans, and is attracting attention in the medical field.

ビフィドバクテリウム菌を腸内で増殖させる方法とし
ては、ビフィドバクテリウム菌を経口投与する直接法と
ビフィドバクテリウム菌に利用される物質(以下、ビフ
ィズスファクターという。)を投与してビフィドバクテ
リウム菌を増殖させる間接法とがある。直接法ではビフ
ィドバクテリウム菌製剤の安定性が低い、投与後の菌の
定着率が低いなどの問題があり、最近は間接法が重視さ
れている。
As a method of growing Bifidobacterium in the intestine, there are a direct method of orally administering Bifidobacterium and a method of administering a substance used for Bifidobacterium (hereinafter referred to as Bifidobacterium). There is an indirect method of growing fidobacteria. The direct method has problems such as low stability of the Bifidobacterium preparation and a low colonization rate of the bacteria after administration. Recently, the indirect method has been emphasized.

従来、ビフィズスファクターとしては、N−アセチル
グルコサミン、その誘導体、ニンジン抽出液(主にパン
テティンを含有)、ラスチュロース、ラフィノース、ス
タキオース、マルトトリオース(「ビフィズス菌」、77
頁、1979年、株式会社ヤクルト本社)、フラクトオリゴ
糖(「化学と生物」、21巻、291頁、1983年、学会出版
センター)、ガラクトオリゴ糖(特公昭58−20266号公
報、特公昭61−46479号公報、特開昭60−41449号公
報)、イソマルトオリゴ糖(日本栄養食料学会発表、19
86年)、シクロデキストリン(特開昭57−138385号公
報)、コンニャクマンナン(「理研腸内フローラ シン
ポジュウムIII、腸内フローラと栄養」、89頁、1983
年、学会出版センター)、豆乳(特公昭45−9822号公
報、特開昭51−142566号公報、特開昭55−85390号公
報)、豆乳抽出物(特開昭59−17906号公報)、非病原
性大腸菌培養液の抽出液(特公昭50−13359号公報)な
どの種々の物質が知られている。
Conventionally, as the bifidogenic factor, N-acetylglucosamine, a derivative thereof, a carrot extract (mainly containing pantethine), rastulose, raffinose, stachyose, maltotriose ("Bifidobacterium", 77
1979, Yakult Honsha Co., Ltd., fructooligosaccharides ("Chemistry and Biology", 21, 291 pages, 1983, Gakkai Shuppan Center), galactooligosaccharides (JP-B-58-20266, JP-B-61-46479). JP, JP-A-60-41449), isomaltooligosaccharides (Presentation of Japanese Society of Nutrition and Food, 19
1986), cyclodextrin (JP-A-57-138385), konjac mannan (“RIKEN intestinal flora symposium III, intestinal flora and nutrition”, p. 89, 1983)
Soy Milk (JP-B-45-9822, JP-A-51-142566, JP-A-55-85390), soymilk extract (JP-A-59-17906), Various substances such as an extract of a non-pathogenic Escherichia coli culture (Japanese Patent Publication No. 50-13359) are known.

従来、夕顔のワタまたは葉茎がビフィドバクテリウム
菌の増殖を促進することおよび腸内有害菌の増殖を抑制
することは知られていない。
Conventionally, it has not been known that the cotton or leaf stem of the evening face promotes the growth of Bifidobacterium and suppresses the growth of intestinal harmful bacteria.

発明が解決しようとする課題 前述の既知ビフィズスファクターは生体内で他の腸内
細菌にも利用されるので、ビフィドバクテリウム菌の増
殖効果が充分でなく、また、それらの製造方法が繁雑で
ある、高価であるなどの欠点がある。従って、充分なビ
フィズス菌増殖促進効果、腸内有害菌増殖抑制効果があ
り、しかも、安価で容易に製造できるビフィズスファク
ターがあれば、産業上極めて有益である。
PROBLEM TO BE SOLVED BY THE INVENTION Since the above-mentioned known bifidobacterium is utilized also for other intestinal bacteria in vivo, the growth effect of bifidobacterium is not sufficient, and the production method thereof is complicated. There are drawbacks such as certain and expensive. Therefore, a bifidobacterium having sufficient bifidobacterium growth promoting effect and intestinal harmful bacterial growth inhibitory effect, as well as being inexpensive and easily producible, is extremely useful in industry.

課題を解決するための手段 既に、本発明者らの一部はビフィズスファクターにつ
いて鋭意研究した結果、夕顔果肉を加工した夕顔食品が
ビフィドバクテリウム菌の増殖を選択的に、かつ、顕著
に促進することを見出した(特願昭62−123761号明細
書)。今回、夕顔のワタまたは葉茎にも果肉と同様のビ
フィズス菌増殖促進効果があること、また、腸内有害菌
増殖抑制効果があることを見出し、本発明を完成した。
Means for Solving the Problems Already, some of the present inventors have conducted intensive studies on the bifidobacterium, and as a result, the evening meal obtained by processing the evening flesh selectively and remarkably promoted the growth of Bifidobacterium bacteria. (Japanese Patent Application No. 62-123761). The present inventors have found that the cotton or leaf stem of the evening face has the same effect of promoting the growth of bifidobacteria as the pulp, and also has the effect of suppressing the growth of harmful bacteria in the intestine, and completed the present invention.

本発明のビフィドバクテリウム菌増殖促進・腸内有害
菌増殖抑制剤は夕顔のワタまたは葉茎を粉剤、顆粒剤、
錠剤など所望の形状に加工したものであり、殺菌された
ものまたはされないものである。
The bifidobacterium growth promotion / intestinal harmful bacteria growth inhibitor of the present invention is a powder or granule of cotton or leaf stem of evening face,
It is processed into a desired shape, such as a tablet, and may or may not be sterilized.

本発明の、殺菌された増殖促進・腸内有害菌増殖抑制
剤は、蒸気圧0.2〜0.4kg/cm2、殺菌時間5〜20分の蒸気
殺菌またはアルコール添加量15〜150g/kg(夕顔乾燥
物)、殺菌日数1〜30日のアルコール殺菌により製造す
ることができる。この殺菌された増殖促進・腸内有害菌
増殖抑制剤は一般生菌数が5×103個/g以下、大腸菌群
およびサルモネラが陰性、水分含量が8%以下であり、
食品衛生上極めて安全である。
The sterilized growth-promoting / intestinal harmful bacteria growth inhibitor of the present invention has a steam pressure of 0.2 to 0.4 kg / cm 2 , and a sterilization time of 5 to 20 minutes by steam sterilization or an alcohol addition amount of 15 to 150 g / kg (evening face dried ), And can be manufactured by alcohol sterilization for 1 to 30 days of sterilization. The sterilized growth promoting / intestinal harmful bacteria growth inhibitor has a general viable cell count of 5 × 10 3 cells / g or less, is negative for Escherichia coli and Salmonella, and has a water content of 8% or less,
Very safe for food hygiene.

本発明の増殖促進・腸内有害菌増殖抑制剤には添加剤
を加えてもよく、添加剤としては、例えば、スイートコ
ーン、キャロットパウダー、コーンファイバー、アップ
ルファイバー、かぼちゃ粉末、アルギン酸などの繊維成
分、乳糖、でんぷんなどの賦形剤、白糖、麦芽糖、ソル
ビトール、マンニトールなどの甘味成分、ミルクパウダ
ー、肉エキス、ビタミンなどの栄養補給剤、アラビアゴ
ム末、ポリビニルピロリドン、ヒドロキシプロピルセル
ロース、カルボキシメチルセルロースナトリウムなどの
結合剤、ステアリン酸マグネシウム、ステアリン酸カル
シウム、ラブリワックス、タルクなどの滑沢剤が挙げら
れ、増殖促進剤食品の形状および/または好みに応じて
適宜選択して使用すればよい。
Additives may be added to the growth-promoting / intestinal harmful bacteria growth inhibitor of the present invention. Examples of the additives include sweet corn, carrot powder, corn fiber, apple fiber, pumpkin powder, and fiber components such as alginic acid. , Lactose, excipients such as starch, sweeteners such as sucrose, maltose, sorbitol, mannitol, nutritional supplements such as milk powder, meat extract, vitamins, gum arabic powder, polyvinylpyrrolidone, hydroxypropylcellulose, sodium carboxymethylcellulose, etc. And a lubricant such as magnesium stearate, calcium stearate, lubri wax, talc, etc., and may be appropriately selected and used depending on the shape and / or taste of the foodstuff for promoting growth.

本発明の増殖促進・腸内有害菌増殖抑制剤の内、粉
状、顆粒状のものはスープの素、ふりかけとして、ある
いは菓子、めん類、豆腐、その他の食品に添加してもよ
い。この他、牛、豚などの家畜の飼料添加物として、
犬、猫などのペットの餌料添加物としても使用すること
ができる。
Of the growth promoting / intestinal harmful bacteria growth inhibitor of the present invention, powdery and granular forms may be added to soup ingredients, sprinkles or to confectionery, noodles, tofu, and other foods. In addition, as a feed additive for livestock such as cattle and pigs,
It can also be used as a feed additive for pets such as dogs and cats.

作用 本発明のビフィドバクテリウム菌増殖促進・腸内有害
菌増殖抑制剤の作用について説明する。
Action The action of the bifidobacterium growth promotion / intestinal harmful bacteria growth inhibitor of the present invention will be described.

試料として、製造例1と同様の方法で製造した夕顔ワ
タ粉末、製造例6と同様の方法で製造した夕顔葉茎粉
末、製造例5と同様の方法で製造した殺菌夕顔ワタ粉末
および製造例10と同様の方法で製造した殺菌夕顔葉茎粉
末を使用した。対照として既知のビフィズスファクター
を用いた。
As samples, evening powder cotton powder produced by the same method as in Production Example 1, evening powder leaf stem powder produced by the same method as in Production Example 6, sterilized evening powder cotton powder produced by the same method as in Production Example 5, and Production Example 10 A pasteurized evening stalk powder produced in the same manner as in Example 1 was used. A known bifid factor was used as a control.

試験1 ビフィズスファクター検索用基礎培地として根岸寒天
培地(日本細菌学雑誌、13巻、519頁、1958年)を用
い、これに試料を0.5%添加し、9cmシャーレにコロニー
数が約50個となるようにビフィドバクテリウム ロング
ム(Bifidobacterium longum,ATCC 15707)を塗布し
た。これを37℃で48時間培養し、増殖状態を観察した。
結果を表1に示す。
Test 1 A Negishi agar medium (Bacteriological Journal of Japan, Vol. 13, p. 519, 1958) was used as a basal medium for searching for a bifidobacterial factor, and 0.5% of the sample was added to the medium. Bifidobacterium longum (ATCC 15707) was applied as described above. This was cultured at 37 ° C. for 48 hours, and the state of proliferation was observed.
Table 1 shows the results.

表中、増殖状態の欄の+は、その数が多い程、増殖状
態が良好であることを示す。
In the table, + in the column of the growth state indicates that the larger the number, the better the growth state.

表1から明らかなように、夕顔ワタ粉末、殺菌夕顔ワ
タ粉末、夕顔葉茎粉末および殺菌夕顔葉茎粉末は夕顔果
実粉末と同様に従来のビフィズスファクターよりも優れ
たビフィズス菌増殖促進効果が認められた。
As is clear from Table 1, the evening face cotton powder, the pasteurized evening face cotton powder, the evening face leaf stem powder and the pasteurized evening face leaf stem powder have the same effect as the evening face fruit powder in promoting the growth of bifidobacteria which is superior to the conventional bifidobacterium factor. Was.

試験2 夕顔ワタ粉末および夕顔葉茎粉末を基礎培地であるト
マレリ(Tomarelli)改変培地(ジャーナル オブ バ
イオケミカル ケミストリー、181巻、879頁、1949年)
にそれぞれ0〜2%添加し、ビフィドバクテリウム ロ
ングム(ATCC 15707)を37℃で48時間培養した。培養
後、ビフィドバクテリウム ロングムの培養液をBL寒天
培地に塗布し、37℃で48時間培養した後、培地の菌数を
測定した。結果を表2に示す。
Test 2 Evening cotton powder and evening leaf stem powder were converted from a base medium, Tomarelli modified medium (Journal of Biochemical Chemistry, 181: 879, 1949)
Was added, and Bifidobacterium longum (ATCC 15707) was cultured at 37 ° C. for 48 hours. After the culture, a culture solution of Bifidobacterium longum was applied to a BL agar medium, and cultured at 37 ° C. for 48 hours, and the number of cells in the medium was measured. Table 2 shows the results.

表2から明らかなように、夕顔ワタ粉末および夕顔葉
茎粉末はビフィドバクテリウム菌に対し、濃度0.10〜2.
00%で1000倍の増殖促進効果を示す。
As is clear from Table 2, the evening cotton cotton powder and the evening leaf stem powder had a concentration of 0.10 to 2.
It shows a 1000-fold growth promoting effect at 00%.

試験3 試料として夕顔ワタ粉末、夕顔葉茎粉末および夕顔果
肉粉末を用いた。
Test 3 Evening cotton powder, evening leaf stem powder and evening meal flesh powder were used as samples.

各々の試料をトマレリ改変培地に添加し、ビフィドバ
クテリウム菌およびその他の腸内細菌を37℃で48時間培
養した。培養後、培養液をBL寒天培地に塗布し、37℃で
48時間培養した後、菌数を測定した。結果を表3に示
す。
Each sample was added to the Tomarelli modified medium, and Bifidobacterium and other enterobacteria were cultured at 37 ° C for 48 hours. After culturing, apply the culture solution to BL agar medium and
After culturing for 48 hours, the number of bacteria was measured. Table 3 shows the results.

表3から明らかなように、夕顔ワタ粉末および夕顔葉
茎粉末は、夕顔果肉粉末と同様、ビフィズス菌に対して
著るしい増殖促進効果を示し、一方、腸球菌、緑膿菌、
大腸菌、ウェルシュ菌などの腸内有害菌には利用され
ず、むしろ、これらの菌に対して増殖抑制効果を示す。
As is clear from Table 3, evening face cotton powder and evening face leaf stem powder show a remarkable growth-promoting effect on bifidobacteria similarly to evening face pulp powder, while enterococci, Pseudomonas aeruginosa,
It is not used for intestinal harmful bacteria such as Escherichia coli and C. perfringens, but rather has a growth inhibitory effect on these bacteria.

製造例1 夕顔のワタを1日天日乾燥した後、70℃で5時間乾燥
して水分含量約3%の夕顔ワタを得た。この乾燥物30kg
をパルベライザー(細川鉄工所製)で粉砕して夕顔ワタ
粉末24kgを得た。
Production Example 1 Evening cotton was dried for one day in the sun and then dried at 70 ° C. for 5 hours to obtain evening cotton having a water content of about 3%. 30 kg of this dried product
Was ground with a pulverizer (manufactured by Hosokawa Iron Works) to obtain 24 kg of evening cotton powder.

製造例2 製造例1で得られた粉末950gとヒドロキシプロピルセ
ルロース40gとを混合撹拌機中で10分間混合した後、精
製水を加えて練合し、熱風乾燥した。これを放冷後、オ
シレーター(菊水製作所製)で整粒して夕顔ワタ顆粒96
0gを得た。
Production Example 2 After mixing 950 g of the powder obtained in Production Example 1 and 40 g of hydroxypropyl cellulose in a mixing stirrer for 10 minutes, purified water was added and kneaded, followed by hot-air drying. After allowing this to cool, it is sized with an oscillator (manufactured by Kikusui Seisakusho) and the evening cotton cotton granules 96
0 g was obtained.

製造例3 製造例2で得られた顆粒495gとステアリン酸マグネシ
ウム5gとを混合撹拌機中で10分間混合した後、打錠して
1錠110mgの夕顔ワタ錠剤4400錠を得た。
Production Example 3 After mixing 495 g of the granules obtained in Production Example 2 and 5 g of magnesium stearate in a mixing stirrer for 10 minutes, the mixture was tableted to obtain 4400 evening tablet cotton tablets of 110 mg each.

製造例4 1日天日乾燥した夕顔ワタ30kgを0.2kg/cm2の蒸気圧
下で20分間殺菌した後、水分含量が約3%になるまで60
℃で熱風乾燥した。ついで、これを粉砕して殺菌夕顔ワ
タ粉末25kgを得た。
Production Example 4 After 30 days of 30 kg of sun-dried cotton on the sun dried for 20 minutes under a vapor pressure of 0.2 kg / cm 2 , the water content was reduced to 60% until the water content became about 3%.
It dried with hot air at ° C. Then, this was crushed to obtain 25 kg of sterilized evening cotton powder.

この粉末は一般生菌数が3.4×102個/g、大腸菌および
サルモネラが陰性であった。
This powder had a general viable cell count of 3.4 × 10 2 cells / g and was negative for Escherichia coli and Salmonella.

製造例5 1日天日乾燥した夕顔ワタ30kgにエタノール2.7kgを
噴霧し、密封して室温で5日間放置した後、粉砕して殺
菌夕顔ワタ粉末26kgを得た。
Production Example 5 2.7 kg of ethanol was sprayed onto 30 kg of sun-dried cotton, which had been sun-dried for 1 day, sealed, allowed to stand at room temperature for 5 days, and then pulverized to obtain 26 kg of sterilized cotton powder.

この粉末は一般生菌数が2.5個×102/g、大腸菌および
サルモネラが陰性であった。
This powder had a general viable cell count of 2.5 × 10 2 / g, and was negative for Escherichia coli and Salmonella.

製造例6 夕顔の葉茎を1日天日乾燥した後、70℃で5時間乾燥
して水分含量約3%の夕顔葉茎を得た。この乾燥物30kg
をパルベライザー(細川鉄工所製)で粉砕して夕顔葉茎
粉末23kgを得た。
Production Example 6 Evening leaf stems were dried for one day in the sun and then dried at 70 ° C. for 5 hours to obtain evening leaf stems having a water content of about 3%. 30 kg of this dried product
Was pulverized with a pulverizer (manufactured by Hosokawa Iron Works) to obtain 23 kg of evening face leaf stem powder.

製造例7 製造例6で得られた粉末950gとヒドロキシプロピルセ
ルロース40gとを混合撹拌機中で10分間混合した後、精
製水を加えて練合し、熱風乾燥した。これを放冷後、オ
シレーター(菊水製作所製)で整粒して夕顔葉茎顆粒96
0gを得た。
Production Example 7 After mixing 950 g of the powder obtained in Production Example 6 and 40 g of hydroxypropyl cellulose in a mixing stirrer for 10 minutes, purified water was added and kneaded, followed by hot-air drying. After allowing it to cool, it is sized with an oscillator (manufactured by Kikusui Seisakusho) and the evening leaf stem granules 96
0 g was obtained.

製造例8 製造例3で得られた顆粒495gとステアリン酸マグネシ
ウム5gとを混合撹拌機中で10分間混合した後、打錠して
1錠110mgの夕顔葉茎錠剤4400錠を得た。
Production Example 8 After mixing 495 g of the granules obtained in Production Example 3 and 5 g of magnesium stearate in a mixing stirrer for 10 minutes, the mixture was tableted to obtain 4400 tablets of 110 mg of evening globe leaf stem tablets.

製造例9 1日天日乾燥した夕顔葉茎30kgを0.2kg/cm2の蒸気圧
下で20分間殺菌した後、水分含量が約3%になるまで60
℃で熱風乾燥した。ついで、これを粉砕して殺菌夕顔葉
茎粉末23kgを得た。
Production Example 9 30 kg of evening sun leaf stems dried in the sun for one day were sterilized under a vapor pressure of 0.2 kg / cm 2 for 20 minutes, and then 60 kg until the water content became about 3%.
It dried with hot air at ° C. Then, this was crushed to obtain 23 kg of sterilized evening stalk powder.

この粉末は一般生菌数が6.3×102個/g、大腸菌および
サルモネラが陰性であった。
This powder had a general viable cell count of 6.3 × 10 2 cells / g, and was negative for Escherichia coli and Salmonella.

製造例10 1日天日乾燥した夕顔葉茎30kgにエタノール2.7kgを
噴霧し、密封して室温で5日間放置した後、粉砕して殺
菌夕顔葉茎粉末25kgを得た。
Production Example 10 2.7 kg of ethanol was sprayed onto 30 kg of the sun-dried evening globe leaf stem, sealed, allowed to stand at room temperature for 5 days, and then pulverized to obtain a sterilized evening grape leaf stem powder of 25 kg.

この粉末は一般生菌数が3.1個×102/g、大腸菌および
サルモネラが陰性であった。
This powder had a general viable cell count of 3.1 × 10 2 / g, and was negative for Escherichia coli and Salmonella.

実施例 健康な成人5人に、製造例1と同様の方法で製造した
夕顔ワタ粉末を1日2gづつ7日間、および製造例6と同
様の方法で製造した夕顔葉茎粉末を1日2gづつ7日間、
それぞれ食前に投与した。各投与7日目に各人の糞便を
採取し、BS培地上で培養し、生育したビフィドバクテリ
ウム菌数、乳酸菌数および大腸菌数を測定し、その平均
値を求めた。結果を表4に示す。
EXAMPLE For 5 healthy adults, evening ginger cotton powder produced by the same method as in Production Example 1 was 2 g / day for 7 days, and evening glow leaf stem powder produced by the same method as in Production Example 6 was given 2 g per day. 7 days,
Each was administered before meals. On day 7 of each administration, feces of each individual were collected, cultured on a BS medium, and the number of bifidobacteria, lactic acid bacteria, and Escherichia coli grown were measured, and the average value was obtained. Table 4 shows the results.

表4から明らかなように、夕顔ワタ粉末および夕顔葉
茎粉末は腸内のビフィドバクテリウム菌の増殖を選択的
に、かつ、顕著に促進することが認められた。
As is evident from Table 4, it was confirmed that the evening meal cotton powder and the evening leaf stem powder selectively and significantly promoted the growth of bifidobacteria in the intestine.

発明の効果 本発明のビフィドバクテリウム菌増殖促進・腸内有害
菌増殖抑制剤はビフィドバクテリウム菌の増殖を選択
的、かつ、顕著に促進し、腸内有害菌の増殖を抑制する
ので、健康維持に役立つほか、免疫賦活剤、制癌剤など
の薬剤としても期待される。また、本発明は、今まで利
用価値のなかった夕顔ワタおよび葉茎の有効利用を可能
にしたので農業の発展にも寄与するものである。
Effect of the Invention The agent for promoting the growth of bifidobacteria and the growth of harmful intestinal bacteria according to the present invention selectively and remarkably promote the growth of bifidobacteria, and suppress the growth of harmful bacteria in the intestine. In addition to helping maintain health, it is also expected as a drug such as an immunostimulant or an anticancer drug. Further, the present invention contributes to the development of agriculture because it enables effective use of evening face cotton and leaf stems, which have not been used until now.

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】夕顔の果実のワタを有効成分とし、腸内有
害菌の増殖を抑制するビフィドバクテリウム菌増殖促進
剤。
1. An agent for promoting the growth of bifidobacteria, which comprises the cotton of evening fruit as an active ingredient and suppresses the growth of harmful intestinal bacteria.
【請求項2】夕顔の葉、葉柄およびつるを有効成分と
し、腸内有害菌の増殖を抑制するビフィドバクテリウム
菌増殖促進剤。
2. An agent for promoting the growth of bifidobacteria, which comprises evening leaves, petiole and vine as active ingredients and suppresses the growth of intestinal harmful bacteria.
JP63277300A 1988-11-04 1988-11-04 Bifidobacterium growth promotion / intestinal harmful bacteria growth inhibitor Expired - Lifetime JP2698123B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63277300A JP2698123B2 (en) 1988-11-04 1988-11-04 Bifidobacterium growth promotion / intestinal harmful bacteria growth inhibitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63277300A JP2698123B2 (en) 1988-11-04 1988-11-04 Bifidobacterium growth promotion / intestinal harmful bacteria growth inhibitor

Publications (2)

Publication Number Publication Date
JPH02124089A JPH02124089A (en) 1990-05-11
JP2698123B2 true JP2698123B2 (en) 1998-01-19

Family

ID=17581617

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP2698123B2 (en)

Also Published As

Publication number Publication date
JPH02124089A (en) 1990-05-11

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