JPH02276556A - Composition for food containing edible fiber component and food prepared therefrom - Google Patents

Composition for food containing edible fiber component and food prepared therefrom

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Publication number
JPH02276556A
JPH02276556A JP1200828A JP20082889A JPH02276556A JP H02276556 A JPH02276556 A JP H02276556A JP 1200828 A JP1200828 A JP 1200828A JP 20082889 A JP20082889 A JP 20082889A JP H02276556 A JPH02276556 A JP H02276556A
Authority
JP
Japan
Prior art keywords
dextrin
oligosaccharide
food
amylase
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.)
Granted
Application number
JP1200828A
Other languages
Japanese (ja)
Other versions
JPH0473986B2 (en
Inventor
Takao Hanno
半野 敬夫
Makoto Okuda
誠 奥田
Yoshimi Mochizuki
望月 芳美
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.)
Matsutani Chemical Industries Co Ltd
Original Assignee
Matsutani Chemical Industries 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 Matsutani Chemical Industries Co Ltd filed Critical Matsutani Chemical Industries Co Ltd
Publication of JPH02276556A publication Critical patent/JPH02276556A/en
Publication of JPH0473986B2 publication Critical patent/JPH0473986B2/ja
Granted legal-status Critical Current

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  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

PURPOSE:To obtain a food containing edible fiber and effective in ameliorating constipation by dissolving roasted dextrin in water, treating the solution with alpha-amylase and using the obtained dextrin containing edible fiber in combination with an oligosaccharide. CONSTITUTION:The objective food composition is composed mainly of an oligosaccharide and a dextrin containing edible fiber and produced by treating an aqueous solution of roasted dextrin with alpha-amylase. In order to eliminate the irritant smell and disagreeable taste of the dextrin in high efficiency, the roasted dextrin used as a raw material is preferably the one produced by adding an aqueous solution of a mineral acid (preferably hydrochloric acid) to a starch raw material, preliminarily drying to a water-content of about 5% and roasting the product. Especially preferable oligosaccharide is the one assimilable with Bifidobacterium having intestinal function controlling action, e.g. fructo- oligosaccharide, isomerized lactose, galacto-oligosaccharide and partially decomposed inulin.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は食品用組成物乃至食品に関し、更に詳しくは食
物繊維分を含有する良便通性食品に関するものである。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Field of Application) The present invention relates to food compositions and foods, and more particularly to foods containing dietary fiber and having good bowel movements.

(従来の技術) 焙焼デキストリンは周知の通り澱粉を高熱処理したもの
であって、その処理により澱粉分子は加水分解及び再重
合が起こり、複雑な構造を呈していると言われ、水溶性
になると共に、難消化性のものがかなりの割合をしめて
いる。
(Prior art) As is well known, roasted dextrin is made by treating starch with high heat.As a result of this treatment, starch molecules are hydrolyzed and repolymerized, and are said to have a complex structure, making them water-soluble. In addition, a large proportion of the food is indigestible.

一方近時日本人の食生活が変化し、多様化した結果、繊
維分の摂取量が目立って減少しており、この繊維分の欠
乏は成人病の起因の一つにも上げられており、食物繊維
の必要性が注目を集め、蛋白質、I!類、脂質、ビタミ
ン、ミネラルに次ぐ六番口の栄養素と言われる様になっ
てきた。
On the other hand, as the Japanese diet has recently changed and become more diverse, the intake of fiber has decreased significantly, and this fiber deficiency has been cited as one of the causes of adult diseases. The need for dietary fiber has attracted attention, and protein, I! It has come to be said that it is the sixth most important nutrient, after fats, vitamins, and minerals.

現在食物繊維としては植物性のものや、動物性のもので
、水溶性、不溶性と色々挙げられており、又合成品とし
てポリデキストロースが挙げられている。これらはぶど
う糖或いはその誘導体、ぶどう糖尿外の糖類が多数結合
した形の繊維状をなしたもの、或いは蛋白質多糖と言っ
たもので形作られている。その構造は複雑でアミラーゼ
による消化が困難で、体外に排出されるため繊維として
の効果があるとされている。
Currently, there are a variety of dietary fibers, including plant-based and animal-based fibers, water-soluble and insoluble, and polydextrose as a synthetic product. These are made of glucose or its derivatives, fibrous forms in which many sugars other than glucose are bound together, or protein polysaccharides. It has a complex structure and is difficult to digest with amylase, so it is excreted from the body and is said to be effective as fiber.

尚食物繊維の定義としては現在プロスキー(Prosk
y) AOAC法又はサウスゲート(3outhgat
e)法で定量されたものをもって食物繊維としている。
The current definition of dietary fiber is Prosk.
y) AOAC method or Southgate (3outhgat)
e) Dietary fiber is determined by the method.

(発明が解決しようとする課題) 本発明者は従来から食物繊維について研究を続けて来た
が、この研究に於いて、従来その激しい刺激臭や望まし
くない味覚のために全く食物繊維として考えても見られ
なかった焙焼デキストリンを、新しい食物繊維として利
用することが出来ないであろうかという全く新しい着想
に至った。この新しい着想に基づきこれを実現するため
に引き続き鋭意研究し、焙焼デキストリンの上記食物繊
維としての難点を解消すると共に、食物繊維として本来
具有する難消化性をそのまま或いは更に高含量で維持で
きる手段の開発に着手した。この結果上記新しい着想を
実現し、食物繊維として充分に使用しうる難消化性物質
を焙焼デキストリンから製造しうる手段を開発すること
に成功し、すでに出願した。更にこの研究を押し進め、
この新しい難消化性成分の優れた特性を更に一段と向上
するための新しい研究に着手した。従って本発明の課題
は上記目的を達成することである。
(Problems to be Solved by the Invention) The present inventor has been researching dietary fiber for a long time, and in this research, it was found that due to its strong pungent odor and undesirable taste, it was not considered as dietary fiber at all. We came up with a completely new idea of whether it would be possible to use roasted dextrin, which had never been seen before, as a new dietary fiber. Based on this new idea, we will continue to conduct intensive research to realize this, and we will solve the above-mentioned difficulties of roasted dextrin as a dietary fiber, and at the same time, we will find a means to maintain the inherent indigestibility of dietary fiber as it is or at an even higher content. We have started development of . As a result, we realized the above-mentioned new idea and succeeded in developing a means for producing an indigestible substance from roasted dextrin that can be used satisfactorily as dietary fiber, and have already filed an application. Pushing this research further,
We have begun new research to further improve the excellent properties of this new indigestible ingredient. It is therefore an object of the invention to achieve the above object.

(課題を解決するための手段) この課題は、焙焼デキストリンを水に溶解し、これにα
−アミラーゼを作用させて得られる食物繊維分含有デキ
ストリンとオリゴ糖とを併用することにより基本的には
解決される。
(Means for solving the problem) This problem involves dissolving roasted dextrin in water and adding α
- The problem can basically be solved by using oligosaccharides and dietary fiber-containing dextrin obtained by the action of amylase.

(発明の構成並びに作用) 本発明に於いては上記本発明者が別途に新しく開発した
食物繊維分含有デキストリンとオリゴ糖を併用すること
により、これ等両者の相乗作用により著しく難消化性食
物繊維による便通作用が改善される。
(Structure and operation of the invention) In the present invention, by using together the dietary fiber-containing dextrin and oligosaccharide, which were newly developed by the present inventor, the synergistic effect of these two makes it possible to produce extremely indigestible dietary fiber. Improves bowel movements.

以下に順をおって各成分を説明する。Each component will be explained below in order.

本発明に於いては焙焼デキストリンを先ずα−アミラー
ゼで処理してデキストリンをα−リミットデキストリン
まで進行せしめて、焙焼デキストリンの有する刺激臭や
好ましくない味覚を解消する。
In the present invention, roasted dextrin is first treated with α-amylase to advance the dextrin to α-limit dextrin, thereby eliminating the pungent odor and unfavorable taste of roasted dextrin.

先ず焙焼デキストリンを原料とするが、この焙焼デキス
トリンとしては、従来から知られているものが使用でき
るが、特に本発明に於いては、その刺激臭や好ましくな
い味覚を効率良く除去するには、次のような方法で製造
された焙焼テキストリンを使用するのが好ましい。即ち
原料澱粉に鉱酸好ましくは塩酸の水溶液を加え、次いで
水分量が5%前後になるまで予備乾燥し、続いて焙焼し
て製造したものが好ましい、この際の原料澱粉としては
、広く各種のものがいずれも使用出来、たとえば馬鈴薯
、トーモロコシ、キャラサバなど何れでもよく、又食品
用加工澱粉として市販されているものでよい、これらの
原料澱粉に硫酸、塩酸、硝酸などの鉱酸好ましくは塩酸
を好ましくはその濃度を1重量%程度となして原料に対
して数乗量%の景を添加好ましくは噴霧して均一になる
様良く混合し、100〜120℃程度で予備乾燥する。
First, roasted dextrin is used as a raw material. As this roasted dextrin, conventionally known ones can be used, but especially in the present invention, in order to efficiently remove the irritating odor and unpleasant taste, It is preferable to use roasted texturin produced by the following method. That is, it is preferable to add an aqueous solution of a mineral acid, preferably hydrochloric acid, to the raw material starch, then pre-dry it until the moisture content becomes around 5%, and then roast it. Any type of starch can be used, such as potato, maize, mackerel, etc., or any commercially available processed starch for food. Preferably, the concentration is about 1% by weight, and a few percent of the powder is added to the raw material, preferably by spraying to mix well so that it becomes uniform, and pre-dried at about 100 to 120°C.

この予備乾燥では澱粉の水分を5%前後まで乾燥する。In this pre-drying, the water content of starch is dried to around 5%.

続いて150°C〜220℃に温度を上げて、1時間〜
5時間程度焙焼して焙焼デキストリンとする。ここで出
来た焙焼デキストリンはDE(デキストロース当量)1
〜lO位のものが好ましい。
Next, raise the temperature to 150°C to 220°C for 1 hour.
Roast for about 5 hours to obtain roasted dextrin. The roasted dextrin produced here has a DE (dextrose equivalent) of 1
-1O is preferable.

次にこの焙焼デキストリンを水に溶かし30〜50重量
%の液となし、中和してpH5,5〜6.5好ましくは
5.8となし、市販のα−アミラーゼ(カビ由来のもの
、細菌由来のもの等何れでもよい)を焙焼デキストリン
に対して0.05〜0.2重量%添加して該アミラーゼ
の作用温度85℃〜100°C前後となし、30分〜2
時間保持する。これにより酵素によるデキストリンの分
解がα−リミットデキストリンまで進む。次いで温度を
120℃まで上げα−アミラーゼの酵素作用を終了させ
る。
Next, dissolve this roasted dextrin in water to make a 30 to 50% by weight liquid, neutralize it to pH 5.5 to 6.5, preferably 5.8, and use commercially available α-amylase (derived from mold, Add 0.05 to 0.2% by weight of dextrin (which may be derived from bacteria, etc.) to the roasted dextrin to adjust the action temperature of the amylase to around 85°C to 100°C for 30 minutes to 2.
Hold time. This causes the enzymatic decomposition of dextrin to proceed to α-limit dextrin. Then, the temperature is raised to 120°C to terminate the enzymatic action of α-amylase.

以上の操作により得られた液を活性炭脱色、脱塩等の通
常の精製工程を通し、濃縮、噴霧乾燥して異臭、刺激味
のない食品用に利用できるデキストリン粉末を得ること
が出来る。
The liquid obtained by the above operations is subjected to conventional purification processes such as decolorization with activated carbon and desalination, concentrated and spray-dried to obtain a dextrin powder that can be used for food products and has no off-odor or irritating taste.

また本発明に於いてはα−アミラーゼ処理が終了した後
火にトランスグルコシダーゼを作用させることが出来る
Further, in the present invention, transglucosidase can be applied to the mixture after the α-amylase treatment is completed.

この酵素処理は上記α−アミラーゼ処理が終了した後、
この後液温を下げ、pHを調整し、トランスグルコシダ
ーゼ(市販品)を元の焙焼デキストリンに対して0.0
5〜0,2重量%添加し、24時間〜48時間作用させ
る。この反応は液中に存在することがあるぶとう糖やオ
リゴ糖の様な小さい分子を大きい分子の方へ再重合させ
ると共に、焙焼デキストリンの複雑な構造を更に増加さ
せるものである。かくして所定の時間後−旦温度を上げ
て(たとえば80℃前後に)トランスグルコシダーゼの
酵素作用を終了させる。尚このトランスグルコシダーゼ
の添加の際β−アミラーゼ(市販品)を同時に作用させ
てもよい。これにより反応が促進される。
This enzyme treatment is carried out after the above α-amylase treatment is completed.
After this, the liquid temperature was lowered, the pH was adjusted, and transglucosidase (commercially available) was added to
Add 5 to 0.2% by weight and let it act for 24 to 48 hours. This reaction repolymerizes small molecules such as glucose and oligosaccharides that may be present in the liquid into larger molecules and further increases the complex structure of the torrefied dextrin. Thus, after a predetermined period of time, the temperature is raised (eg, to around 80° C.) to terminate the enzymatic action of transglucosidase. Incidentally, when adding this transglucosidase, β-amylase (commercially available product) may be allowed to act simultaneously. This accelerates the reaction.

この処理により繊維分が更に高分子化され難消化性が更
に増加する。
This treatment further polymerizes the fiber content and further increases the indigestibility.

またトランスグルコシダーゼで処理する場合には、原料
焙焼デキストリンに単I!類やオリゴ糖を添加すること
ができる。これ等tJ!頻の添加は繊維分を増加せしめ
ることが出来、通常その糖含有量が40〜60重景%の
糖液を、澱粉に対し1〜lO重量%程度添加する。
In addition, when treating with transglucosidase, the raw material roasted dextrin has a single I! and oligosaccharides can be added. These are tJ! Addition of starch can increase the fiber content, and usually a sugar solution with a sugar content of 40 to 60% by weight is added to the starch in an amount of about 1 to 10% by weight.

また本発明に於いては上記処理が終了したデキストリン
に更に水素添加を施すことが出来る。この水素添加によ
り ■着色がなくなる。■還元基を取られたため還元性を無
くし、メーラード反応を出し難くする。
Further, in the present invention, the dextrin that has been subjected to the above treatment can be further subjected to hydrogenation. This hydrogenation eliminates coloring. ■Since the reducing group has been removed, it loses reducibility and makes it difficult for the Maillard reaction to occur.

■味が良くなり、また舌ざわりが良くなる。■難発酵性
になり、たとえば乳酸菌にアタックされなくなる等の顕
著な効果が発現する。
■It tastes better and has a better texture. - It becomes difficult to ferment, and produces remarkable effects such as being no longer attacked by lactic acid bacteria.

本発明に於いて使用される食物繊維分合をデキストリン
と併用されるもう一つの成分であるオリゴ糖としては通
常難消化性かつ易発酵性のオリゴ糖であり、ヒトの消化
管で分泌される消化酵素によってはほとんど消化されな
いが腸内細菌によって容易に資化されるもの(具体的に
は、新鮮なヒト糞便の4倍希釈液と混合し37°Cの嫌
気状態に保ったとき2時間以内に90%以上が消失する
ような発酵性のもの)である。一般に°°オリゴ糖゛と
いうときは2糖類を含むが、2tlQNの多くは易消化
性であり、また易消化性とはいえない2糖類も存在する
が、2tJ!1は本発明における”′オリゴ糖″”とし
ては特に好ましいとは言い難い。
The oligosaccharide used in the dietary fiber component used in the present invention in combination with dextrin is usually an indigestible and easily fermentable oligosaccharide, and is secreted in the human gastrointestinal tract. Items that are hardly digested by digestive enzymes but are easily assimilated by intestinal bacteria (specifically, within 2 hours when mixed with a 4-fold dilution of fresh human feces and kept in anaerobic conditions at 37°C) 90% or more of the product is fermentable). Generally speaking, when we talk about oligosaccharides, we include disaccharides, but most of 2tlQN are easily digestible, and there are also disaccharides that are not easily digestible, but 2tJ! 1 cannot be said to be particularly preferable as the "'oligosaccharide" in the present invention.

本発明におけるオリゴ糖として特に好ましいのは、整腸
作用を有するビフィットバクテリウム菌が資化し得るも
のである。その具体例としては、特開昭59−1790
64号公報に記載されているラフィノース系のもの、特
公昭58−20266号公報に記載されているガラクト
ース系のもの、特公昭59−53834号公報に記載さ
れているフルクトオリゴ糖、特開昭58−212780
号公報に記載されているコンニャクマンナンの分解物、
特開昭57−18982号公報に記載されているレバン
(β−2,6−フルクタン)、特開昭58−99497
号公報に記載されているガラクトース系のもの、特開昭
59−11190号公報に記載されているキチン部分加
水分解に記載されているラクトシュークロースなどが例
示出来る。
Particularly preferred oligosaccharides in the present invention are those that can be assimilated by Bifitobacterium bacteria, which have intestinal regulation effects. A specific example is JP-A-59-1790
Raffinose-based products described in Japanese Patent Publication No. 64, galactose-based products described in Japanese Patent Publication No. 58-20266, fructo-oligosaccharides described in Japanese Patent Publication No. 59-53834, 212780
The decomposition product of konjac mannan described in the publication No.
Levan (β-2,6-fructan) described in JP-A-57-18982, JP-A-58-99497
Examples include the galactose type described in JP-A-59-11190 and lactosucrose described in chitin partial hydrolysis described in JP-A-59-11190.

更に具体例を示せばフラクトオリゴ糖、異性化乳糖(ラ
クツロース)、ガラクトオリゴ糖、大豆オリゴ糖、イヌ
リン部分分解物、レバン部分分解物、コンニャクマンナ
ン部分分解物、イソマルトオリゴ糖、キシロオリゴ糖、
アガロオリゴ糖等を例示出来る。
Further specific examples include fructooligosaccharide, isomerized lactose (lactulose), galactooligosaccharide, soybean oligosaccharide, inulin partial decomposition product, levan partial decomposition product, konjac mannan partial decomposition product, isomaltooligosaccharide, xylooligosaccharide,
Examples include agarooligosaccharides.

本発明に於いて食物繊維含有デキストリンとオリゴ糖と
の配合割合は前者;後者が1;10〜20;l(を景)
程度である。
In the present invention, the mixing ratio of dietary fiber-containing dextrin and oligosaccharide is the former; the latter is 1; 10 to 20;
That's about it.

本発明組成物はこれをそのまま食品として供しても良い
が、またこれを食品用組成物として使用し、これから適
宜な手段で食品としても良い。たとえば水に溶解して流
動性食品としても良い。
The composition of the present invention may be used as a food as it is, but it may also be used as a food composition and made into a food by appropriate means. For example, it may be dissolved in water to make a liquid food.

本発明に於いては食物繊維部デキストリンとオリゴ糖と
から成る組成物を粉末状とすることも出来る。本発明に
於いて使用するオリゴ糖は通常は液状のものであり、こ
のオリゴ糖は粉末化の難しいものとされている。しかる
に本発明者の研究に依れば、食物繊維分含有デキストリ
ンとオリゴ糖を併用するときは、通常の粉末化の手段で
容易に粉末化することが出来、例えばスプレードライヤ
ーを用いる噴霧乾燥により面単且つ容易に粉末とするこ
とが出来、惹いては粉末状の最終目的物が収得出来るこ
ととなる。粉末化の方法としてはスプレードライヤーを
用いる方法が特に好ましいが、その他例えばドラム乾燥
、真空凍結乾燥、泡沫層乾燥の方法でも良い。スプレー
ドライヤー法を行う場合の条件も、通常の条件から適宜
に選択され、熱風温度iso ”c〜200 ’C1排
風温度100°C程度の条件で行うのが好ましい。この
際オリゴ糖の配合量が掻端に多くなりすぎると、粉末化
が円滑に行い難くなる場合もあり、好ましくはオリゴ糖
が70重量%以下である。
In the present invention, the composition consisting of the dietary fiber part dextrin and the oligosaccharide can also be made into powder form. The oligosaccharide used in the present invention is usually in liquid form, and it is said that this oligosaccharide is difficult to powder. However, according to the research of the present inventor, when a dietary fiber-containing dextrin and an oligosaccharide are used together, it can be easily powdered by ordinary powdering means, and for example, by spray drying using a spray dryer. It can be simply and easily made into a powder, and as a result, the final target product in powder form can be obtained. As a powdering method, a method using a spray dryer is particularly preferred, but other methods such as drum drying, vacuum freeze drying, and foam layer drying may also be used. The conditions for carrying out the spray dryer method are also appropriately selected from the usual conditions, and it is preferable to carry out under the conditions of hot air temperature iso''c~200'C1 exhaust air temperature of about 100°C.In this case, the blended amount of oligosaccharide If there is too much oligosaccharide on the edges, it may be difficult to powderize smoothly, so preferably the oligosaccharide content is 70% by weight or less.

(実施例) 以下に食物繊維分含有難消化性デキストリンの製造例を
示す参考例と実施例とを示す。
(Example) Reference examples and examples showing production examples of indigestible dextrin containing dietary fiber are shown below.

参考例1 市販の馬鈴薯澱粉100gに1.0%塩酸溶液5all
を加圧空気を用いてスプレーし、更にミキサーにて均一
に混合後、アルミバットに入れ、乾燥器で110℃で1
時間予備乾燥し、次いで150°Cで3時間焙焼した。
Reference Example 1 5all of 1.0% hydrochloric acid solution to 100g of commercially available potato starch
Spray it using pressurized air, mix it evenly with a mixer, put it in an aluminum vat, and dry it in a dryer at 110℃ for 1 hour.
It was pre-dried for 1 hour and then roasted at 150°C for 3 hours.

得られた焙焼デキストリンのDEは6.8、粘度160
cps(濃度50%、30℃)、難消化性デキストリン
含量57%であった。
The obtained roasted dextrin has a DE of 6.8 and a viscosity of 160.
cps (concentration 50%, 30°C), and the indigestible dextrin content was 57%.

上記の方法で調製した焙焼デキストリン100gに10
0gの熱水を加え溶解し、IN水酸化ナトリウムで中和
してpH5,8となし、更にα−アミラーゼ(ターマミ
ル120L)0.1%を添加し95 ’Cで反応、1時
間後115°Cまで昇温して反応を終了させた。次にp
)I s、s、温度55°Cに糖液を調製し、β−アミ
ラーゼ(天野製薬製) 0.05%、トランスグルコシ
ダーゼ(天野製薬製)0.1%を添加し、24時間反応
させ次のようなデキストリンを得た。
10 g for 100 g of roasted dextrin prepared by the above method.
Add 0g of hot water to dissolve, neutralize with IN sodium hydroxide to pH 5.8, add 0.1% α-amylase (Termamyl 120L) and react at 95'C, 1 hour later at 115°C. The reaction was terminated by raising the temperature to C. Then p
) Is, s, Prepare a sugar solution at a temperature of 55°C, add 0.05% of β-amylase (manufactured by Amano Pharmaceutical) and 0.1% of transglucosidase (manufactured by Amano Pharmaceutical), and let it react for 24 hours. Obtained dextrin like.

キ唐組成り P 1 15.8%、D P 2 10.
7%(マルトース0.6、コージビオース0.3、イソ
マルトース9.8%)、DP3 5.3% DP4以上
68.2%粘度 75cps(1度50%、30°C)
、難消化性デキストリン含量72%。
Kikara composition P 1 15.8%, D P 2 10.
7% (maltose 0.6, cordibiose 0.3, isomaltose 9.8%), DP3 5.3% DP4 or higher 68.2% Viscosity 75 cps (1 degree 50%, 30°C)
, indigestible dextrin content 72%.

参考例2 タピオカ澱粉10000 kgを硫酸ナトリウム150
0kg含む水1200Ofに懸濁せしめ、撹はん下、3
%水酸化ナトリウム水溶液3000 fを滴下し、更に
プロピレンオキサイド800!を加え、43°Cで20
時間反応後、硫酸で中和し、水洗、遠心分離機で脱水、
フラッシュドライヤーで乾燥してヒドロキシプロピル澱
粉を得た。ここで得たヒドロキシプロピル澱粉は水分1
2.5%、DS、 0.145であった。
Reference example 2 10,000 kg of tapioca starch and 150 kg of sodium sulfate
Suspend in 1200Of water containing 0kg, stir, 3
% sodium hydroxide aqueous solution was added dropwise, followed by propylene oxide 800%! and incubate at 43°C for 20
After reaction time, neutralize with sulfuric acid, wash with water, dehydrate with centrifuge,
Hydroxypropyl starch was obtained by drying with a flash dryer. The hydroxypropyl starch obtained here has a water content of 1
2.5%, DS, 0.145.

上記で得たヒドロキシプロピル澱粉5000kgをリボ
ン式ミキサーに入れ、撹はんしながら1.2%塩酸20
02.50%に濃度調整した市販ハイマルトースシラツ
ブ(MC−75、日本食品化工製)500kgを加圧空
気を用いてスプレーし、1時間混合、粉砕機を通して均
一にした後、更にリボン式ミキサー中で12時間熟成し
た。この混合物をフラッシュドライヤーで水分3.5%
に予備乾燥した後、ロータリーキルン式焙焼機に連続的
に投入し、175°Cで1.5時間 焙焼機中に滞留せ
しめ焙焼した。得られた焙焼デキストリンのDEは9.
0で粘度200cps  (50%、30°C)、難消
化性デキストリン含M45%であった。
Add 5,000 kg of the hydroxypropyl starch obtained above to a ribbon mixer, and while stirring, add 200 kg of 1.2% hydrochloric acid.
500 kg of commercially available high maltose syrup (MC-75, manufactured by Nippon Shokuhin Kako Co., Ltd.) adjusted to a concentration of 0.02.50% was sprayed using pressurized air, mixed for 1 hour, passed through a pulverizer to make it uniform, and then further processed into a ribbon mixer. It was aged for 12 hours inside. This mixture was dried with a flash dryer to reduce the moisture content to 3.5%.
After pre-drying, the mixture was continuously put into a rotary kiln roaster and roasted at 175°C for 1.5 hours. The DE of the obtained roasted dextrin is 9.
It had a viscosity of 200 cps (50%, 30°C) at 0 and an M content of indigestible dextrin of 45%.

上記の方法で調製した焙焼デキストリン2000kgに
4000 ffiの熱水を加え溶解し20%水酸化ナト
リウムでpus、oに調整し、α−アミラーゼ(ターマ
ミル60L、ノボ社製)0.3%を添加し95°Cで反
応、1時間後115°Cまで昇温しで反応を終了させて
55%濃度に調製し、β−アミラーゼ(天野製薬製)0
.2%、トランスグルコシダーゼ(天野製薬製)0.1
%を添加し、48時間反応させ次のような糖組成のデキ
ストリンを得た。
2,000 kg of roasted dextrin prepared by the above method was dissolved in 4,000 ffi of hot water, adjusted to pus and o with 20% sodium hydroxide, and 0.3% of α-amylase (Termamyl 60L, manufactured by Novo) was added. The reaction was carried out at 95°C, and after 1 hour, the temperature was raised to 115°C to complete the reaction and the concentration was adjusted to 55%.
.. 2%, transglucosidase (manufactured by Amano Pharmaceutical) 0.1
% and reacted for 48 hours to obtain dextrin with the following sugar composition.

DPI   7.4%、DP2  8.7%(マルトー
ス1、l、コージビオース0.6%、イソマルトース7
.0%)、DP3  6.3% (マルトトリオース0
.7% パノース2.7%、イソマルトトリオース2.
9%)DP4以上77.6% 粘度70cps(50%
、30°C)、難消化性デキストリン含量60%。
DPI 7.4%, DP2 8.7% (maltose 1,1, cordibiose 0.6%, isomaltose 7
.. 0%), DP3 6.3% (maltotriose 0
.. 7% Panose 2.7%, Isomaltotriose 2.
9%) DP4 or higher 77.6% Viscosity 70cps (50%
, 30°C), 60% indigestible dextrin content.

但し、上記参考例1及び2の難消化性デキストリン含有
の測定は次の方法で行った。
However, the content of indigestible dextrin in Reference Examples 1 and 2 was determined by the following method.

−゛キス !ンの  の サンプル1gを精秤し、水50m1を加えpH5,8と
なした後、α−アミラーゼ(ラーマミル120L1ノボ
社製)  0.1mftを添加し、95°C130分間
反応させる。つぎに冷却後、pH4,5に調整しアミロ
グルコシダーゼ(シグマ社製)0.1dを添加し60°
C530分間反応させた後、90’Cまで昇温し反応を
終了させた。終了液は濾過後、5%まで濃縮してHP 
L Cに供し、糖組成より生成したグルコース量を測定
した。そして、次の式より難消化デキストリンの含量を
求めた。
−゛Kiss! After accurately weighing 1 g of a sample of water and adjusting the pH to 5.8 by adding 50 ml of water, 0.1 mft of α-amylase (Ramamil 120L1 manufactured by Novo) was added and reacted at 95° C. for 130 minutes. Next, after cooling, adjust the pH to 4.5, add 0.1 d of amyloglucosidase (manufactured by Sigma), and hold the mixture at 60°C.
C5 After reacting for 30 minutes, the temperature was raised to 90'C to terminate the reaction. After filtration, the finished liquid is concentrated to 5% and HP
The sample was subjected to LC, and the amount of glucose produced was measured based on the sugar composition. Then, the content of indigestible dextrin was determined from the following formula.

難消化性デキストリン含量% =100−生成グルコース% 参考例3 市販の馬鈴薯澱粉5000kgをリボン式ミキサーに入
れ、撹拌しながら160%塩酸1501をスプレ、続い
て粉砕機を通し均一にした後、更にリボン式ミキサー中
で5時間熟成した。この混合物をフラッシュドライヤー
で水分3%に予備乾燥した後、ロータリーキルン式焙焼
機に連続投入し、180℃で2時間焙焼した。
Indigestible dextrin content % = 100 - produced glucose % Reference example 3 5000 kg of commercially available potato starch was put into a ribbon mixer, sprayed with 160% hydrochloric acid 1501 while stirring, then passed through a pulverizer to make it uniform, and then further mixed into ribbons. Aged for 5 hours in a mixer. This mixture was pre-dried to a moisture content of 3% using a flash dryer, and then continuously fed into a rotary kiln roaster and roasted at 180°C for 2 hours.

次に、上記方法で得た焙焼デキストリン2000kgに
水40001を添加し、pHを6.0に調整し、α−ア
ミラーゼ(ターフミル60L1ノボ社)0.2%を添加
し95℃で1時間加水分解し、この反応終了液を脱色、
脱塩等の精製を行い、スプレードライヤーで乾燥し、1
700kgの粉末品を得た。このようにして得られた焙
焼デキストリン精製物の食物繊維含量はプロスキーAO
AC法で定量した時35%であった。
Next, 40,001 kg of water was added to 2,000 kg of roasted dextrin obtained by the above method, the pH was adjusted to 6.0, 0.2% of α-amylase (Turfmill 60L1 Novo) was added, and water was added at 95°C for 1 hour. Decompose and decolorize this reaction-finished liquid.
Perform purification such as desalting, dry with a spray dryer,
700 kg of powder product was obtained. The dietary fiber content of the roasted dextrin purified product obtained in this way was determined by Proski AO.
When quantified by AC method, it was 35%.

参考例4 参考例3で得られた食物繊維含有デキストリンを40%
濃度に再調製し、液に対して0.4%相当の8%第ユニ
リン酸ナトリウム液加え、更に20%水酸化ナトリウム
液を加えpH9,5とした。この溶液をオートクレーブ
に入れ、液に対して1%のラネーニッケル(0興理化製
R−100)を添加し、温度21’C,水素ガスゲージ
圧95kg/Cl1lまで充填した後オートクレーブを
振とうさせなから130 ’Cまで加熱し120分間保
持し還元反応を終了させた。放冷後、反応液に活性炭を
加え触媒も同時にろ過した。ろ液はイオン交換樹脂によ
り脱塩し、?a縮し75%溶液を得た。
Reference Example 4 40% dietary fiber-containing dextrin obtained in Reference Example 3
The concentration was readjusted, and an 8% sodium uniphosphate solution equivalent to 0.4% was added to the solution, followed by a 20% sodium hydroxide solution to adjust the pH to 9.5. Put this solution into an autoclave, add 1% Raney nickel (R-100 made by Ko Rika Co., Ltd.) to the solution, and fill the autoclave to a temperature of 21'C and a hydrogen gas gauge pressure of 95 kg/1 liter of Cl. Do not shake the autoclave. It was heated to 130'C and held for 120 minutes to complete the reduction reaction. After cooling, activated carbon was added to the reaction solution, and the catalyst was also filtered at the same time. The filtrate is desalted using an ion exchange resin. A 75% solution was obtained by condensation.

この濃縮液は無色透明な粘稠液で食物繊維27%(プロ
スキー−AOAC法により)含んでいた。
This concentrate was a colorless and transparent viscous liquid containing 27% dietary fiber (according to the Prosky-AOAC method).

裏施■土 全卵              140g上白糖  
             66g参考例1の難消化性
デキストリン  44gガラクトオリゴ$1!    
       10 g(rカップオリゴ」 日新製糖
社製) ラード               35g薄刃粉 
             100gベーキングパウダ
ー          1g水           
           10g上記、処方でスポンジケ
ーキを常法に従って作り、比容積 326a!1!/1
00g、硬度154gでしっとりとした感触のあるスポ
ンジケーキを得た。
Urasedo whole egg 140g caster sugar
66g Indigestible dextrin of Reference Example 1 44g Galacto-oligo $1!
10 g (R Cup Oligo) manufactured by Nisshin Sugar Co., Ltd. Lard 35 g thin blade powder
100g baking powder 1g water
10gMake a sponge cake according to the above recipe according to the usual method, and the specific volume will be 326a! 1! /1
A sponge cake with a moist feel and a hardness of 154 g was obtained.

1講114 すりみ            100部食塩    
            3部馬鈴薯澱粉      
       5部参考例3の難消化性デキストリン 
  5部異性化乳I!(ウェルミー)       5
部氷水               20部(但し部
はすべて重量部) 予め澱粉、難消化性デキストリン、ウェルミーを食塩水
に溶解し、常法により蒲鉾を製造した。
1 Lecture 114 Surimi 100 parts Salt
3 parts potato starch
5 parts Indigestible dextrin of Reference Example 3
Part 5 isomerized breasts I! (Welcome) 5
Part ice water 20 parts (all parts are parts by weight) Starch, indigestible dextrin, and Wellme were dissolved in saline in advance, and kamaboko was produced by a conventional method.

但し荒ずり、本ずり後10’Cでケーシングに詰め、9
0℃30分加熱し、冷却し製造した。得られた謂鉾は破
断強度712g、ゼリー強度1047gの食感に優れた
製品となっていた。
However, after rough shearing and final shearing, it is packed in the casing at 10'C.
The product was produced by heating at 0°C for 30 minutes and cooling. The obtained so-called hoko had a breaking strength of 712 g and a jelly strength of 1047 g, making it a product with excellent texture.

1韮−例J− 寒天                4g水    
                350g砂tJ! 
              125 gオレンジ果汁
          150g参考例2の難消化性デキ
ストリン  25gフラクトオリゴ$7!      
    25 gシラツブ(明治製菓製、メイオリゴ) 上記処方でゼリーを常法に従って製造したとき風味、食
感とも通常のオレンジゼリーと遜色のないものであった
1 fish - Example J - Agar 4g water
350g sand tJ!
125 g Orange juice 150 g Indigestible dextrin of Reference Example 2 25 g Fructooligo $7!
25 g Shiratsubu (Meiji Seika Co., Ltd., Mayoligo) When a jelly was produced according to the conventional method using the above recipe, the flavor and texture were comparable to ordinary orange jelly.

尖胤阻土 牛乳              200gパター  
             60g加糖脱脂練乳   
       150g脱脂粉乳          
   40gフラクトオリゴ糖シラツブ     90
g(日本オリゴ社製、「β−オリゴ」) 参考例4の難消化性デキストリン  30gステビア 
             0.1g安定剤     
          3g乳化剤          
     3g水                 
   420g上記処方でアイスミルク(乳脂肪5.5
%)を常法により製造し、風味、テクスチャーともに通
常品と異なる事のないものを得た。
Tsunetane Edo milk 200g putter
60g sweetened skimmed condensed milk
150g skim milk powder
40g fructooligosaccharide 90
g (manufactured by Nippon Oligo Co., Ltd., "β-Oligo") Indigestible dextrin of Reference Example 4 30g Stevia
0.1g stabilizer
3g emulsifier
3g water
420g Ice milk with the above formula (milk fat 5.5
%) was produced using a conventional method to obtain a product that had the same flavor and texture as ordinary products.

実Jfll引i二1− 下記第1表に示す所定の組成配合によりオリゴ糖シラツ
ブと難消化性デキストリンを使用して次の処方で約40
%の溶液を作り、これをスプレードライヤーを使用して
粉末とした。熱風温度160℃、俳風95℃で乾燥して
、製品の水分はいずれも約4%であった。これらの粉末
は吸湿性あり、水溶性は良好であったが更にこれらの流
動性をよくするため流動層造粒機でサラサラの粉末にす
ることも出来た。
The following formulation uses oligosaccharide silica and indigestible dextrin according to the prescribed composition shown in Table 1 below.
% solution was prepared and powdered using a spray dryer. The products were dried at a hot air temperature of 160°C and a haiku air temperature of 95°C, and the moisture content of each product was approximately 4%. These powders were hygroscopic and had good water solubility, but in order to further improve their fluidity, they could be made into smooth powders using a fluidized bed granulator.

(以 上)(that's all)

Claims (9)

【特許請求の範囲】[Claims] (1)焙焼デキストリンの水溶液にα−アミラーゼを作
用させて得られる食物繊維分含有デキストリンとオリゴ
糖とを主成分として成ることを特徴とする食物繊維成分
含有食品用組成物乃至食品。
(1) A dietary fiber component-containing food composition or food product, characterized in that the main components are a dietary fiber-containing dextrin obtained by treating an aqueous solution of roasted dextrin with α-amylase and an oligosaccharide.
(2)α−アミラーゼ作用後、トランスグルコシダーゼ
または(及び)β−アミラーゼを作用させて得られる食
物繊維含有デキストリンである請求項1に記載の食品用
組成物乃至食品。
(2) The food composition or food according to claim 1, which is a dietary fiber-containing dextrin obtained by acting with transglucosidase or (and) β-amylase after the action of α-amylase.
(3)α−アミラーゼを作用させた後或いは更にトラン
スグルコシダーゼを作用させた後、更に水素添加処理を
施こした食物繊維含有デキストリンを使用することを特
徴とする請求項1に記載の食品用組成物乃至食品。
(3) The composition for food according to claim 1, characterized in that the dietary fiber-containing dextrin is used which has been subjected to a hydrogenation treatment after being treated with α-amylase or further with transglucosidase. Things or food.
(4)焙焼デキストリンとして澱粉単独、或いはこれに
単糖類及びオリゴ糖の少なくとも1種を混合したものを
常法で焙焼して製造したものを使用する請求項(1)乃
至(3)のいずれかに記載の食品用組成物乃至食品。
(4) The roasted dextrin of claims (1) to (3) is prepared by roasting starch alone or a mixture thereof with at least one of monosaccharides and oligosaccharides in a conventional manner. The food composition or food according to any one of the above.
(5)オリゴ糖が難消化性で且つ易発酵性のオリゴ糖で
ある請求項(1)乃至(4)のいずれかに記載の食品用
組成物乃至食品。
(5) The food composition or food according to any one of claims (1) to (4), wherein the oligosaccharide is an indigestible and easily fermentable oligosaccharide.
(6)難消化性かつ易発酵性のオリゴ糖がラフィノース
系のものである請求項(5)に記載の食品用組成物乃至
食品。
(6) The food composition or food according to claim (5), wherein the indigestible and easily fermentable oligosaccharide is a raffinose-based oligosaccharide.
(7)難消化性且つ易発酵性のオリゴ糖が乳糖由来のガ
ラクトース系のものである請求項(5)に記載の食品用
組成物乃至食品。
(7) The food composition or food according to claim (5), wherein the indigestible and easily fermentable oligosaccharide is a galactose-based oligosaccharide derived from lactose.
(8)難消化性且つ易発酵性のオリゴ糖がフラクトース
系のものである請求項(5)に記載の食品用組成物乃至
食品。
(8) The food composition or food according to claim (5), wherein the indigestible and easily fermentable oligosaccharide is fructose-based.
(9)粉末状である請求項(1)乃至(8)のいずれか
に記載の食品用組成物乃至食品。
(9) The food composition or food according to any one of claims (1) to (8), which is in powder form.
JP1200828A 1989-01-24 1989-08-02 Composition for food containing edible fiber component and food prepared therefrom Granted JPH02276556A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP1574489 1989-01-24
JP1-15744 1989-01-24

Publications (2)

Publication Number Publication Date
JPH02276556A true JPH02276556A (en) 1990-11-13
JPH0473986B2 JPH0473986B2 (en) 1992-11-25

Family

ID=11897273

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1200828A Granted JPH02276556A (en) 1989-01-24 1989-08-02 Composition for food containing edible fiber component and food prepared therefrom

Country Status (1)

Country Link
JP (1) JPH02276556A (en)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03151854A (en) * 1989-11-10 1991-06-28 Calpis Food Ind Co Ltd:The Composition for improving intestinal environment
JPH03244364A (en) * 1990-02-20 1991-10-31 Matsutani Kagaku Kogyo Kk Food composition effective in suppressing secretion of insulin
EP0605632A1 (en) 1991-09-27 1994-07-13 Wm. Wrigley Jr. Company Chewing gum and other comestibles containing indigestible dextrin
US5380717A (en) * 1990-02-22 1995-01-10 Matsutani Chemical Industries Co., Ltd. Food composite for performing function of large bowel regulation
US5505981A (en) * 1992-08-07 1996-04-09 Matsutani Chemical Industries Co., Ltd. Method for imparting ability of preventing obesity and impaired glucose tolerance to foods and foods and sugar preparations exhibiting such preventive effects
JP2007197331A (en) * 2006-01-24 2007-08-09 Nisshin Sugar Mfg Co Ltd Composition for ameliorating allergic physical constitution
US7387803B2 (en) 1995-12-26 2008-06-17 Cns, Inc. Dietary fiber delivery system
US7473776B2 (en) * 2001-10-30 2009-01-06 Roquette Freres Soluble hydrogenated starch derivatives containing nondigestible dietary fibres
US8187624B1 (en) 2000-06-14 2012-05-29 Kao Corporation Compositions for taking dietary fibers
JP2012192339A (en) * 2011-03-16 2012-10-11 Denso Corp Method and apparatus for treating wastewater containing organic matter
JP2013506405A (en) * 2009-10-01 2013-02-28 ロケット フレール Carbohydrate compositions having a greater impact on insulin response than on blood glucose response
JP2016149981A (en) * 2015-02-18 2016-08-22 株式会社シーキューブ・アイ Processed raw meat containing indigestible dextrin and production method thereof

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03151854A (en) * 1989-11-10 1991-06-28 Calpis Food Ind Co Ltd:The Composition for improving intestinal environment
JPH03244364A (en) * 1990-02-20 1991-10-31 Matsutani Kagaku Kogyo Kk Food composition effective in suppressing secretion of insulin
US5380717A (en) * 1990-02-22 1995-01-10 Matsutani Chemical Industries Co., Ltd. Food composite for performing function of large bowel regulation
EP0605632B2 (en) 1991-09-27 2007-08-22 Wm. Wrigley Jr. Company Chewing gum containing indigestible dextrin
EP0605632A1 (en) 1991-09-27 1994-07-13 Wm. Wrigley Jr. Company Chewing gum and other comestibles containing indigestible dextrin
US5505981A (en) * 1992-08-07 1996-04-09 Matsutani Chemical Industries Co., Ltd. Method for imparting ability of preventing obesity and impaired glucose tolerance to foods and foods and sugar preparations exhibiting such preventive effects
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