JPH06225734A - Functional powdery beverage and its production - Google Patents

Functional powdery beverage and its production

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Publication number
JPH06225734A
JPH06225734A JP50A JP4190393A JPH06225734A JP H06225734 A JPH06225734 A JP H06225734A JP 50 A JP50 A JP 50A JP 4190393 A JP4190393 A JP 4190393A JP H06225734 A JPH06225734 A JP H06225734A
Authority
JP
Japan
Prior art keywords
bacteria
useful
galactomannan
beverage
human
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.)
Granted
Application number
JP50A
Other languages
Japanese (ja)
Other versions
JP3441756B2 (en
Inventor
Noriyuki Ishihara
則幸 石原
Tsutomu Okubo
勉 大久保
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.)
Taiyo Kagaku KK
Original Assignee
Taiyo Kagaku KK
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Filing date
Publication date
Application filed by Taiyo Kagaku KK filed Critical Taiyo Kagaku KK
Priority to JP04190393A priority Critical patent/JP3441756B2/en
Publication of JPH06225734A publication Critical patent/JPH06225734A/en
Application granted granted Critical
Publication of JP3441756B2 publication Critical patent/JP3441756B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To obtain a powdery beverage having proliferating effects on useful enterobacteria effective for enhancing the human health by improving the human enterobacterial flora, i.e., increasing the microbial cell number of the useful enterobacteria such as bifidus bacteria or lactic acid bacteria. CONSTITUTION:This powdery beverage is obtained by adding a galactomannan having a reduced molecular weight and has proliferating effects on useful enterobacteria.

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、腸内有用菌増殖効果を
有する粉末飲料及びその製造方法に関する。より詳しく
は、ヒトの腸内細菌叢の改善、すなわち、腸内のビフィ
ズス菌、乳酸菌等の有用菌の菌数を増加させることによ
って、ヒトの健康の増進に有効な粉末飲料及びその製造
方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a powdered beverage having an effect of multiplying intestinal useful bacteria and a method for producing the same. More specifically, improvement of human intestinal microflora, that is, by increasing the number of useful bacteria such as bifidobacteria and lactic acid bacteria in the intestine, a powdered beverage effective for promoting human health and a method for producing the same. .

【0002】[0002]

【従来の技術】従来、腸内の細菌を観察することは困難
であった。しかし、近年の嫌気培養技術の著しい進歩に
より、糞便中の菌数が腸内の菌数を反映するようになり
腸内細菌叢に関する研究が多く行われるようになった。
その結果、腸内細菌が、ヒトの健康と深い関わりを有
し、ヒトの生理状態に影響を及ぼしていることが明らか
にされている。
2. Description of the Related Art Conventionally, it has been difficult to observe bacteria in the intestine. However, due to remarkable progress in anaerobic culture technology in recent years, the number of bacteria in feces reflects the number of bacteria in the intestine, and many studies on intestinal bacterial flora have been conducted.
As a result, it has been clarified that the intestinal bacterium is closely related to human health and affects human physiological condition.

【0003】又、これらの腸内細菌は食物や薬物に由来
するさまざまな物質や内因性物質の代謝に関与してい
て、ヒトの栄養、生理機能、感染免疫、発癌、老化、薬
効等に重要な役割を果たしている(光岡知足 ”腸内菌
の世界”叢文社、1980年;D.J.Hentges
”Human Intestinal Microf
lora in Health and Diseas
e” AcademicPress,1983)。
Further, these intestinal bacteria are involved in the metabolism of various substances derived from foods and drugs and endogenous substances, and are important for human nutrition, physiological functions, infectious immunity, carcinogenesis, aging, drug efficacy and the like. Playing an important role (Michioka Tomohi "The World of Enterobacteriaceae", Moubunsha, 1980; DJ Hentges
"Human Intestinal Microf
lora in Health and Diseases
e "Academic Press, 1983).

【0004】これらの腸内細菌の中には、ビフィズス菌
や乳酸菌のようにヒトの病原菌,ウイルス等に対する感
染防御,栄養,有害菌増殖抑制等の面で有利に働く有用
菌や、クロストリジウム菌,病原性大腸菌のように発
癌,肝臓疾患,動脈硬化症,高血圧症,感染症等に関係
している有害菌がある。又、有害菌の中には、日和味感
染を起こし、敗血症,心内膜炎,脳・肝・肺の腫瘍,膀
胱炎,膣炎等、好ましからぬ状況をもたらすことが多
い。(光岡知足 ”腸内細菌の話”岩波書店、1978
年)。
Among these intestinal bacteria, useful bacteria, such as bifidobacteria and lactic acid bacteria, which are advantageous in terms of defense against infection by human pathogens and viruses, nutrition, suppression of harmful bacterial growth, and Clostridium bacteria, There are harmful bacteria related to carcinogenesis, liver disease, arteriosclerosis, hypertension, infectious diseases, etc. such as pathogenic Escherichia coli. In addition, some harmful bacteria cause opportunistic infections and often bring about unfavorable situations such as sepsis, endocarditis, brain / liver / lung tumor, cystitis, vaginitis. (Michioka Chizu, "The story of intestinal bacteria", Iwanami Shoten, 1978.
Year).

【0005】このようなことから、ヒトの腸内で有用菌
を定着させ、増殖させることが最適な腸内細菌叢である
と考えられている。このために、腸内の有用菌を増加さ
せるために種々のビフィズス菌製剤や、ヨーグルトなど
が開発されているが、ヒトの生体内での胃酸,胆汁酸な
どの上部消化管のバリヤーの通過、増殖部位としての下
部消化管における増殖可能性といった生菌の定着ならび
に増殖能力が大きな問題となっている。
From the above, it is considered that the optimum intestinal bacterial flora is to establish and grow useful bacteria in the human intestine. For this reason, various bifidobacteria preparations and yogurt have been developed in order to increase useful bacteria in the intestine, but gastric acid in the human body, passage through the upper gastrointestinal barrier such as bile acids, The establishment and growth ability of viable bacteria, such as the possibility of growth in the lower digestive tract as a growth site, is a serious problem.

【0006】一方、腸内における有用菌の増殖に必要な
因子として最も重要なものは糖類であると考えられ、ラ
クチュロース,パラチノース,フラクトオリゴ糖,ラフ
ィノース,スタキオース,キシロオリゴ糖などの種々の
糖類が有用菌の増殖にとって有効であるとされており、
これらを含有した飲食物も提案されているが、これらの
糖類は、一部の大腸菌,クロストリジウム属細菌等の有
害菌に対しても資化性があり、それらの増殖にも関与し
ている。従って、上記糖類が有用菌に選択的に資化され
るわけではなく、ヒトの腸内で有用菌の菌数のみが特異
的には増加しないのが現状である。以上のことより、未
だ満足のいく結果が得られていない。
On the other hand, the most important factor necessary for the growth of useful bacteria in the intestine is considered to be sugars, and various sugars such as lactulose, palatinose, fructooligosaccharides, raffinose, stachyose, and xylooligosaccharides are useful bacteria. Is said to be effective for the growth of
Although foods and drinks containing them have been proposed, these saccharides have assimilation to some harmful bacteria such as Escherichia coli and Clostridium bacteria, and are involved in their growth. Therefore, the saccharides are not selectively assimilated to useful bacteria, and the number of useful bacteria in the human intestine is not specifically increased under the present circumstances. From the above, satisfactory results have not yet been obtained.

【0007】[0007]

【発明が解決しようとする課題】本発明は、腸内細菌の
うちビフィズス菌,乳酸菌等の有用菌のみを選択的に増
殖させることができる粉末飲料及びその製造方法を提供
することを目的とする。本発明でいう有用菌とは、ビフ
ィズス菌,乳酸菌等の宿主の健康に有益に作用する腸内
細菌を指し、また有害菌とはクロストリジウム菌,病原
性大腸菌等の宿主の健康に悪影響を及ぼす腸内細菌を指
す。
DISCLOSURE OF THE INVENTION An object of the present invention is to provide a powdered beverage capable of selectively growing only useful bacteria such as bifidobacteria and lactic acid bacteria among intestinal bacteria and a method for producing the same. . The useful bacteria referred to in the present invention refer to enterobacteria such as bifidobacteria and lactic acid bacteria that beneficially act on the health of the host, and harmful bacteria are intestinal bacteria such as Clostridium and pathogenic Escherichia coli that adversely affect the health of the host. Refers to inner bacteria.

【0008】[0008]

【課題を解決するための手段】本発明者らは、ヒト腸内
で有用菌を選択的に増殖させる粉末飲料を供する目的で
鋭意研究を重ねた結果、マンノース直鎖の鎖長が30〜
200単位の範囲内に80%以上分布するように低分子
化したガラクトマンナンを含有すると、有用菌を選択的
に増殖させ、かつロ当たりの非常によい粉末飲料を得ら
れることを初めて見い出し、本発明を完成させるに至っ
た。
[Means for Solving the Problems] As a result of intensive studies conducted by the present inventors for the purpose of providing a powdered beverage that selectively grows useful bacteria in the human intestine, the mannose straight chain has a chain length of 30 to 30.
For the first time, it was found that by containing a galactomannan whose molecular weight is reduced to 80% or more in the range of 200 units, useful bacteria can be selectively grown and a very good powdered beverage per lot can be obtained. The invention was completed.

【0009】本発明で使用する低分子化したガラクトマ
ンナンは、例えば、グアーガム,ローカストビーンガ
ム,タラガムあるいはキャロブガム等をアスペルギルス
属菌やリゾープス属菌等に由来するβ−マンナナーゼを
用いて酵素的にマンノース直鎖のみを加水分解すること
によって得ることができる。該ガラクトマンナンは酵素
の反応時間を変えることにより分子量を変化させること
ができるが、本発明の粉末飲料に添加される該ガラクト
マンナンは、腸内有用菌増殖効果を保持する目的ではマ
ンノース直鎖の鎖長が30〜200単位の範囲内に80
%以上分布するものが良く、さらに好ましくは50〜1
50単位の範囲内に分布していることが良い。なお本発
明のマンノース直鎖の鎖長とはガラクトマンナンの主鎖
であるマンノースの結合している数をさし、その測定法
は特に限定するものではないが、たとえば分解された多
糖類を水に溶解しTOSO 803D型の高速液体クロ
マトグラフィー(HPLC)を用い水を移動相にしてG
3000PWのカラムにてゲル濾過を行い、示唆屈折計
にて検出する。この際にグルコース数が既知の直鎖デキ
ストリン(グルコース数30,100,200)を指標
物質として測定することにより図1のようなグラフが得
られる。これから30〜200単位を面積から算出でき
る。マンノースの鎖長が30単位より短い場合は、還元
糖の含量が多くなるため腸内有用菌だけの選択的な増殖
効果が期待できず、一方、マンノース鎖長が200単位
以上であると、高粘度となり飲用したときの口当たりが
非常に悪いばかりか、高分子量のため腸内有用菌の増殖
効果が期待できない。また、本発明による粉末飲料の希
釈度は、該粉末10gに対し水をコップ一杯程度(18
0〜200cc)が望ましい。
The low-molecular-weight galactomannan used in the present invention is, for example, guar gum, locust bean gum, tara gum, or carob gum, which is enzymatically mannose using β-mannanase derived from Aspergillus or Rhizopus. It can be obtained by hydrolyzing only a straight chain. The galactomannan can be changed in molecular weight by changing the reaction time of the enzyme, but the galactomannan added to the powdered beverage of the present invention is a mannose linear chain for the purpose of retaining the effect of growing intestinal useful bacteria. 80 within the range of chain length of 30 to 200 units
% Or more is preferable, and more preferably 50 to 1
The distribution is preferably within the range of 50 units. The chain length of the mannose linear chain of the present invention refers to the number of mannose that is the main chain of galactomannan bound, and the measuring method is not particularly limited, but for example, decomposed polysaccharides can be treated with water. Dissolved in water and using TOSO 803D type high performance liquid chromatography (HPLC) with water as the mobile phase.
Gel filtration is performed with a 3000 PW column and detection is performed with a suggestive refractometer. At this time, a linear dextrin having a known glucose number (glucose number 30, 100, 200) is measured as an index substance to obtain a graph as shown in FIG. From this, 30 to 200 units can be calculated from the area. If the chain length of mannose is shorter than 30 units, the content of reducing sugars will be high and the selective growth effect of only useful enteric bacteria cannot be expected. On the other hand, if the chain length of mannose is 200 units or more, Not only does it become viscous and has a very bad mouth feel when it is drunk, but it cannot be expected to have a proliferative effect on useful enteric bacteria due to its high molecular weight. Further, the dilution degree of the powdered beverage according to the present invention is such that 10 g of the powdered beverage has about one glass of water (18
0 to 200 cc) is desirable.

【0010】尚、腸内有用菌増殖効果を得るための有効
量に関しては、該ガラクトマンナンとして、1日当たり
0.08〜0.83g/体重kgが好ましく、0.08
g/体重kgより少ない投与量では効果が弱く、0.8
3g/体重kgより多い場合は腹部の満腹感等、ヒトに
とって好ましくない影響が生じる。
The galactomannan is preferably used in an amount of 0.08 to 0.83 g / kg of body weight per day, preferably 0.08, for obtaining an effective intestinal bacteria-proliferating effect.
If the dose is less than g / kg of body weight, the effect is weak.
If the amount is more than 3 g / kg body weight, unpleasant effects on humans such as abdominal satiety may occur.

【0011】以下、実施例により詳細に説明する。A detailed description will be given below with reference to embodiments.

【実施例】【Example】

実施例1 水900部にクエン酸を加えてpHを3.0に調整し
た。これにアスペルギルス属菌由来のβ−マンナナーゼ
0.2部とグアーガム粉末100部を添加混合して40
〜45℃で24時間酵素を作用させた。反応後90℃,
15分間加熱して酵素を失活させた。ロ過分離して不溶
物を除去して得られた透明な溶液を減圧濃縮した後(固
形分20%)、噴霧乾燥したところ低分子化したガラク
トマンナンの白色粉末65部が得られた。酵素重量法に
従う水溶性食物繊維含有量は80%であった。また、固
定層として、カラムにG3000PW(東ソー(株)
製)を用いて高速液体クロマトグラフィーで測定した結
果、該ガラクトマンナンの糖鎖の80%以上はマンノー
スの鎖長が50〜150単位の範囲内に包含されてい
た。このとき糖鎖単位の標準試薬として、グルコース数
が既知の直鎖デキストリン(グルコース数50,10
0,150)を用いた。
Example 1 Citric acid was added to 900 parts of water to adjust the pH to 3.0. To this, 0.2 part of β-mannanase derived from Aspergillus and 100 parts of guar gum powder were added and mixed to obtain 40 parts.
The enzyme was allowed to act for 24 hours at ˜45 ° C. 90 ° C after reaction,
The enzyme was inactivated by heating for 15 minutes. The transparent solution obtained by separating the insoluble matters by filtration was concentrated under reduced pressure (solid content: 20%) and then spray-dried to obtain 65 parts of a white powder of low-molecular-weight galactomannan. The water-soluble dietary fiber content according to the enzyme gravimetric method was 80%. As a fixed bed, G3000PW (Tosoh Corp.) was used for the column.
As a result of measurement by high performance liquid chromatography using 80% or more of the sugar chains of the galactomannan, the chain length of mannose was within the range of 50 to 150 units. At this time, as a standard reagent of sugar chain unit, linear dextrin with known glucose number (glucose number 50, 10
0,150) was used.

【0012】実施例2 実施例1で得られた該ガラクトマンナンを用いて表1に
示すような配合比でオレンジ味の微紛状の粉末飲料を調
製した。
Example 2 Using the galactomannan obtained in Example 1, an orange-taste fine powdery beverage was prepared at the compounding ratio shown in Table 1.

【0013】[0013]

【表1】 [Table 1]

【0014】試験例1 健康な成人9名を対象に通常の食生活をしているコント
ロールの期間中に2回糞便を採取し、その後、実施例2
により得られた粉末飲料10gを1カップ(180c
c)の水に混ぜ、よく攪拌してから、毎食1本ずつ12
日間摂取させ、その5日目,7日目,11日目,13日
目の4回糞便を採取した。その後、上記ドリンクの摂取
を中止し、中止してから13日目,15日目の2回糞便
を採取した。
Test Example 1 Feces were collected twice during a control period in which 9 healthy adults were eating normally, and then Example 2 was used.
1 cup (180c) of 10g of the powdered beverage obtained by
Mix with water from c) and stir well, then take 12 each
It was ingested for a day, and feces were collected 4 times on the 5th, 7th, 11th and 13th days. Then, the ingestion of the drink was stopped, and feces were collected twice on the 13th and 15th days after the stop.

【0015】以上合計8回の糞便採取時に、糞便中の腸
内細菌の菌数,検出率及び占有率を求めた。菌数と検出
率については表2に、占有率については表3に、それぞ
れ示した。なお、表2と表3は、本発明粉末飲料の飲用
前,飲用中−1(飲用開始5日目と7日目),飲用中−
2(飲用開始11日目と13日目),飲用後の4つの期
間に分けて結果が示されている。又、各期間において2
回ずつ糞便の採取を行ったので、数値は合計18の平均
を示している。
At the time of collecting feces 8 times in total, the number of intestinal bacteria in the feces, the detection rate and the occupation rate were determined. The number of bacteria and the detection rate are shown in Table 2, and the occupancy rate is shown in Table 3. It should be noted that Tables 2 and 3 show that the powdered beverage of the present invention is before drinking, during drinking-1 (5th and 7th days after the start of drinking), during drinking-
2 (11th day and 13th day of drinking), the results are shown divided into 4 periods after drinking. Also, 2 in each period
Since the feces were collected each time, the numerical value shows the average of 18 in total.

【0016】[0016]

【表2】 [Table 2]

【0017】表2に示したように本発明粉末飲料を飲用
することにより各種腸内細菌中で有用菌であるビフィズ
ス菌の菌数の有意な増加が認められ、検出率については
有用菌である乳酸菌の有意な増加が、それぞれ認められ
た。
As shown in Table 2, by drinking the powdered beverage of the present invention, a significant increase in the number of Bifidobacterium, which is a useful bacterium among various intestinal bacteria, was observed, and the detection rate was a useful bacterium. A significant increase in lactic acid bacteria was observed respectively.

【0018】[0018]

【表3】 [Table 3]

【0019】一方、表3に示したように本発明品摂取に
より有用菌であるビフィズス菌の占有率の有意な増加が
認めらた。
On the other hand, as shown in Table 3, a significant increase in the occupancy rate of the bifidobacteria, which is a useful bacterium, was observed by ingesting the product of the present invention.

【0020】これらより明らかなように、本発明品はビ
フィズス菌や乳酸菌といった腸内有用菌を選択的に増殖
させる効果を有することが判った。
As is clear from these, it was found that the product of the present invention has the effect of selectively growing useful enteric bacteria such as bifidobacteria and lactic acid bacteria.

【0021】比較例1 実施例1と同様の方法で反応時間のみを48時間と変える
ことにより、マンノース直鎖の短いガラクトマンナン
(マンノースの鎖長の80%以上が5〜25単位の範囲
内に包含されていた。)を調製し、さらにそれを添加し
た粉末飲料を実施例2と同様の方法で調製し、健康な成
人9名を対象に同様の試験を行った。その結果について
は、菌数と検出率については表4に、占有率については
表5に、それぞれ示した。
Comparative Example 1 In the same manner as in Example 1, except that the reaction time was changed to 48 hours, galactomannan having a short mannose straight chain (80% or more of the chain length of mannose was within the range of 5 to 25 units). Was added to the powdered beverage) and a powdered beverage to which it was added was prepared in the same manner as in Example 2, and the same test was conducted on 9 healthy adults. The results are shown in Table 4 for the number of bacteria and the detection rate, and in Table 5 for the occupancy rate.

【0022】[0022]

【表4】 [Table 4]

【0023】[0023]

【表5】 [Table 5]

【0024】表4と表5より明らなように、マンノース
の鎖長が実施例2と比較して短いガラクトマンナンを添
加した粉末飲料を飲用しても腸内有用菌増殖効果は得ら
れなかった。
As is clear from Tables 4 and 5, even if the powdered beverage containing galactomannan having a shorter mannose chain length than that of Example 2 is ingested, no beneficial intestinal bacteria-proliferating effect is obtained. It was

【0025】[0025]

【発明の効果】本発明の粉末飲料は、ヒトの腸内のビフ
ィズス菌や乳酸菌といった腸内有用菌に対し極めて優れ
た増殖効果を有し、さらには口当たりや風味が非常に良
いことから、本発明はヒトの健康増進に貢献するところ
は多大である。
EFFECTS OF THE INVENTION The powdered beverage of the present invention has an extremely excellent proliferative effect on useful enteric bacteria such as bifidobacteria and lactic acid bacteria in the human intestine, and further has a very good mouthfeel and flavor. The invention contributes greatly to the promotion of human health.

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

【図1】示唆屈折計にて検出したゲル濾過の溶出パター
ンの図である。
FIG. 1 is a diagram of an elution pattern of gel filtration detected by a suggestive refractometer.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 マンノース直鎖の鎖長が30〜200単
位の範囲内に80%以上分布するように低分子化したガ
ラクトマンナンを添加することを特徴とする腸内有用菌
増殖効果を有する粉末飲料及びその製造方法。
1. A powder having an intestinal beneficial bacterial growth effect, which comprises adding galactomannan having a low molecular weight so that the mannose straight chain has a chain length of 80% or more distributed in the range of 30 to 200 units. Beverage and manufacturing method thereof.
【請求項2】 腸内有用菌がビフィズス菌及び/叉は乳
酸菌であることを特徴とする請求項1記載の粉末飲料及
びその製造方法。
2. The powdery beverage according to claim 1, and the method for producing the same, wherein the useful enteric bacteria are bifidobacteria and / or lactic acid bacteria.
JP04190393A 1993-02-05 1993-02-05 Functional powdered beverage and method for producing the same Expired - Lifetime JP3441756B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP04190393A JP3441756B2 (en) 1993-02-05 1993-02-05 Functional powdered beverage and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP04190393A JP3441756B2 (en) 1993-02-05 1993-02-05 Functional powdered beverage and method for producing the same

Publications (2)

Publication Number Publication Date
JPH06225734A true JPH06225734A (en) 1994-08-16
JP3441756B2 JP3441756B2 (en) 2003-09-02

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Country Status (1)

Country Link
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Cited By (7)

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WO1999064506A1 (en) * 1998-06-11 1999-12-16 Teijin Limited η-RAY STABILIZER AND THERMOPLASTIC POLYMER COMPOSITION CONTAINING THE SAME
JP2002114690A (en) * 2000-10-12 2002-04-16 Taiyo Kagaku Co Ltd Deodorant for excrement
WO2005056022A1 (en) * 2003-12-12 2005-06-23 Taiyo Kagaku Co., Ltd. Enteropathy ameliorating composition
JP2007282587A (en) * 2006-04-18 2007-11-01 Taiyo Kagaku Co Ltd Method for producing galactomannan enzyme degradation product
JP2008054508A (en) * 2006-08-29 2008-03-13 Taiyo Kagaku Co Ltd Method for producing enzymatically hydrolyzed galactomannan
JP2020078552A (en) * 2018-11-12 2020-05-28 ユニ・チャーム株式会社 Fecal indicator for absorbent article, fecal indicator material, use of them, and absorbent article
WO2021177208A1 (en) * 2020-03-02 2021-09-10 太陽化学株式会社 Galactomannan decomposition product

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999064506A1 (en) * 1998-06-11 1999-12-16 Teijin Limited η-RAY STABILIZER AND THERMOPLASTIC POLYMER COMPOSITION CONTAINING THE SAME
JP2002114690A (en) * 2000-10-12 2002-04-16 Taiyo Kagaku Co Ltd Deodorant for excrement
WO2005056022A1 (en) * 2003-12-12 2005-06-23 Taiyo Kagaku Co., Ltd. Enteropathy ameliorating composition
JPWO2005056022A1 (en) * 2003-12-12 2007-07-05 太陽化学株式会社 Composition for improving bowel disease
US8148351B2 (en) 2003-12-12 2012-04-03 Taiyo Kagaku Co., Ltd. Enteropathy ameliorating composition
JP4956002B2 (en) * 2003-12-12 2012-06-20 太陽化学株式会社 Composition for improving bowel disease
JP2007282587A (en) * 2006-04-18 2007-11-01 Taiyo Kagaku Co Ltd Method for producing galactomannan enzyme degradation product
JP2008054508A (en) * 2006-08-29 2008-03-13 Taiyo Kagaku Co Ltd Method for producing enzymatically hydrolyzed galactomannan
JP2020078552A (en) * 2018-11-12 2020-05-28 ユニ・チャーム株式会社 Fecal indicator for absorbent article, fecal indicator material, use of them, and absorbent article
WO2021177208A1 (en) * 2020-03-02 2021-09-10 太陽化学株式会社 Galactomannan decomposition product
CN115151575A (en) * 2020-03-02 2022-10-04 太阳化学株式会社 Galactomannan decomposition product
CN115151575B (en) * 2020-03-02 2023-10-13 太阳化学株式会社 Galactomannan decomposition product

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