JPS5841824A - Inhibitory substance for rise in blood serumal cholesterol - Google Patents

Inhibitory substance for rise in blood serumal cholesterol

Info

Publication number
JPS5841824A
JPS5841824A JP56139689A JP13968981A JPS5841824A JP S5841824 A JPS5841824 A JP S5841824A JP 56139689 A JP56139689 A JP 56139689A JP 13968981 A JP13968981 A JP 13968981A JP S5841824 A JPS5841824 A JP S5841824A
Authority
JP
Japan
Prior art keywords
wheat bran
substance
cholesterol
hemicellulose
rise
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
JP56139689A
Other languages
Japanese (ja)
Other versions
JPS626691B2 (en
Inventor
Saburo Kawamura
川村 三郎
Masayasu Takeuchi
竹内 政保
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.)
Japan Maize Products Co Ltd
Nihon Shokuhin Kako Co Ltd
Original Assignee
Japan Maize Products Co Ltd
Nihon Shokuhin Kako Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Japan Maize Products Co Ltd, Nihon Shokuhin Kako Co Ltd filed Critical Japan Maize Products Co Ltd
Priority to JP56139689A priority Critical patent/JPS5841824A/en
Publication of JPS5841824A publication Critical patent/JPS5841824A/en
Publication of JPS626691B2 publication Critical patent/JPS626691B2/ja
Granted legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/20Reducing nutritive value; Dietetic products with reduced nutritive value
    • A23L33/21Addition of substantially indigestible substances, e.g. dietary fibres
    • A23L33/22Comminuted fibrous parts of plants, e.g. bagasse or pulp

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Botany (AREA)
  • Mycology (AREA)
  • Health & Medical Sciences (AREA)
  • Nutrition Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Food Science & Technology (AREA)
  • Polymers & Plastics (AREA)
  • Seeds, Soups, And Other Foods (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines Containing Plant Substances (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)

Abstract

PURPOSE:The titled substance, containing hemicellulose obtained by the extraction from wheat bran or a residue after removing starch, protein, etc. from the wheat bran on the alklaine side as a principal component, and useful as a material for health food and drink, medicine, etc. CONSTITUTION:An inhibitory substance for rise in blood serumal cholesterol containing hemicellulsoe obtained by the extraction of wheat bran (peridermal part in an amount of about 10% of wheat grains, and separated by the grinding step of the wheat flour milling) or a residue after removing impurities, e.g. starch, protien, lipid or inorganic materials, from the wheat bran on the alkaline side as a principal component. The substance consists of about 90% or more hemicellulose and a little lignin, cellulose, ash, etc. and exhibits the inhibitory action on the rise in the blood serumal cholesterol equal to or higher than that of the dietary fibers in an amount of (1/50) or less thereof.

Description

【発明の詳細な説明】 本発明は、生理活性、特に血清コレステロール上昇抑制
効果を有する新規物質に関し、詳しくは小麦ふすま又は
小麦ふすまから澱粉質、蛋白質、脂質、無機質等を除去
した残部からアルカリ側で抽出されてなるヘミセルロー
スを主成分として含有する血清コレステロール上昇抑制
物質に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a new substance that has physiological activity, particularly the effect of suppressing the increase in serum cholesterol. This invention relates to a serum cholesterol increase-inhibiting substance containing hemicellulose extracted as a main component.

近年、健康食品としてダイエタリーファイバ−(Die
tary Fiber)が注目されている。このタイエ
タリーファイバートハセルロース、ヘミセルロース、リ
グニン、ペクチン等を主成とするもので、従来のいわゆ
る粗繊維(Crude Fiber)と区別され、穀物
などに含まれている植物細胞壁(Cellwall)及
び細胞内容物に含まれる植物性の難消化性成分だとする
意見が定着しつつある。
In recent years, dietary fiber (dietary fiber) has been used as a health food.
(tary fiber) is attracting attention. This Thai fiber is mainly composed of cellulose, hemicellulose, lignin, pectin, etc., and is distinguished from conventional so-called crude fiber, and is a plant cell wall and cell contents contained in grains, etc. The opinion that it is a plant-based indigestible ingredient contained in

この様なダイエタリーファイバー源としては、広く穀類
、豆類の1ぬか“が注目され、これらが血清コレステロ
ールの増減、肥満、糖尿病の予防、虫垂炎、大腸ガン、
食品中の毒性物質の排除促進等に相互関係があることが
認められつつあるが、コーンファイバー(とうもろこし
の外皮)については生理活性、特にコレステロール上昇
抑制効果がないとの報告がなされている( Cerea
l Chemistry、56 (4)、279.19
79 )。
As a source of dietary fiber, grains and legumes (bran) are widely attracting attention, and these can increase or decrease serum cholesterol, prevent obesity, diabetes, appendicitis, colon cancer,
Although it is becoming recognized that there is a correlation between promoting the elimination of toxic substances in food, it has been reported that corn fiber (corn husk) has no physiological activity, especially no effect on cholesterol rise (Cerea)
l Chemistry, 56 (4), 279.19
79).

コーンファイバーにはセルロースのほかにヘミセルロー
ス(非セルロース性多糖類)が多量に含まれており、ダ
イエタリーファイバーとして有用であると推量されるの
に拘らず、なぜ上記報前の如く生理活性がないとされて
いるのか、この点につき本発明者らは先にコーンファイ
バーの組織構造に原因があるとの想定のもとに、コーン
ファイバーを酵素処理、化学的処理、物理的処理するこ
とによって、コーンファイバーの組織構造を弛緩させつ
つ澱粉質、蛋白質、脂質、無機質等の夾雑物を除去した
残部を動物実験に供したところ、このものが血清コレス
テロールの上昇抑制効果を発揮することを見い出した(
特願昭55−96206)。本発明者らは、さらに血清
コレステロール上昇抑制効果が前記コーンファイバーか
ら調製されたダイエタリーファイバー中のセルロース、
ヘミセルロースのいずれの物質に起因するかにつき研究
を進め、当該残部を稀酸で加水分解処理して−・ミセル
ロースの大部分を分解除去したものを動物試験に供した
ところ、血清コレステロール上昇抑制効果はほとんど認
められず、ヘミセルロースに起因するものであることを
確認し、先に、コーンファイバーからアルカリ側で抽出
したヘミセルロースを主成分とする血清コレステロール
上昇抑制物質について出願した(4!願昭55−962
07)。
Corn fiber contains a large amount of hemicellulose (non-cellulosic polysaccharide) in addition to cellulose, and although it is presumed to be useful as a dietary fiber, why is it not physiologically active as reported above? Regarding this point, the present inventors first assumed that the cause was due to the tissue structure of corn fibers, and by subjecting corn fibers to enzymatic, chemical, and physical treatments, When the tissue structure of corn fibers was relaxed and impurities such as starch, proteins, lipids, and inorganic substances were removed, the remainder was subjected to animal experiments, and it was found that this product exerted the effect of suppressing the rise in serum cholesterol (
(Patent application 1986-96206). The present inventors further found that cellulose in the dietary fiber prepared from the corn fiber has the effect of suppressing the increase in serum cholesterol.
We conducted research to find out which substance in hemicellulose is responsible, and when the remaining part was hydrolyzed with dilute acid and most of the hemicellulose was decomposed and removed, it was subjected to animal tests. was hardly observed, and confirmed that it was caused by hemicellulose, and filed an application for a serum cholesterol increase suppressing substance whose main component is hemicellulose extracted from corn fiber on the alkali side (4! 962
07).

又、最近、脱脂床ぬかよシ酵素処理及び溶媒処理し、澱
粉、蛋白を除去した残滓すなわちヘミセルロース、セル
ロース、リクニンヲ主成分とする物質が血清コレステロ
ール上昇抑制効果を有することが発表されている(特開
昭55−141415)。
In addition, it has recently been announced that the residue obtained by removing starch and proteins from defatted bed rice bran, enzyme treatment and solvent treatment, which has hemicellulose, cellulose, and licinin as its main components, has the effect of suppressing the increase in serum cholesterol. 141415 (1977).

本発明者らは、如上の知見ならびに上記従来技術に鑑み
、原料として、コーンファイバー、米ぬか以外の穀類の
ぬかについて広くもとめ、種々検討′したところ、小麦
製粉工程において多量に産出される小麦ふすまには、多
量のヘミセル0−1j存在L、コレが血清コレステロー
ル上昇抑制に顕著なる効果を発輝することを見い出し、
本発明を完成、した。
In view of the above knowledge and the prior art, the present inventors have widely sought and conducted various studies on corn fiber and grain bran other than rice bran as raw materials. found that a large amount of hemicells 0-1j present in L had a remarkable effect on suppressing the increase in serum cholesterol.
The present invention has been completed.

すなわち、本発明は小麦ふすま又は小麦ふすまから澱粉
質、蛋白質、脂質、無機質等を除去した残部からアルカ
リ側で抽出されたヘミセルロースを主成分として含有す
る血清コレステロール上昇抑制物質というにある。
That is, the present invention is directed to a serum cholesterol increase-inhibiting substance containing as a main component hemicellulose extracted from wheat bran or wheat bran after removing starch, proteins, lipids, inorganic substances, etc., on the alkaline side.

本発明によシ得られる血清コレステロール上昇、1抑制
物質は約90%以上のヘミセルロースと若干のリグニン
、セルロース、灰分等からなり、セルロース、ヘミセル
ロース、リグニン等ヲ主成分としたいわゆるダイエタリ
ーファイバーの50分の1以下の量で同等以上の血清コ
レステロール上昇抑制効果を発揮する。したがって、こ
の様な本発明物質は、飲食品に少量添加することによシ
、飲食品の風味、食感を何ら害することなく生理活性を
有効に付与することができ、健康飲食品、医薬品の素材
として広く使用することが可能であり、工業上共すると
ころ大である。
The serum cholesterol increase, 1 inhibitory substance obtained by the present invention is composed of about 90% or more hemicellulose and some lignin, cellulose, ash, etc., and contains 50% of so-called dietary fiber whose main components are cellulose, hemicellulose, lignin, etc. It exhibits the same or greater effect of suppressing the rise in serum cholesterol with less than half the amount. Therefore, by adding a small amount of the substance of the present invention to foods and drinks, it is possible to effectively impart physiological activity without impairing the flavor and texture of the food and drink, and it can be used in health foods and drinks and pharmaceuticals. It can be widely used as a material and has great industrial applications.

次に、本発明の詳細な説明する。Next, the present invention will be explained in detail.

本発明において原料とされる小麦ふすまは、小麦粒の約
10%をしめる外皮部分で、通常小麦製粉の挽砕工程で
分離されるものである。通常市販されている小麦ふすま
の組成は、粗蛋白12%、粗脂肪5%、粗繊維10%、
灰分4%及び可溶性無窒素物69%からなっている。
Wheat bran, which is used as a raw material in the present invention, is the outer skin portion of the wheat grain that accounts for about 10%, and is usually separated during the grinding process of wheat flour. The composition of commercially available wheat bran is 12% crude protein, 5% crude fat, 10% crude fiber,
It consists of 4% ash and 69% soluble nitrogen-free matter.

本発明においては、小麦ふすまから直接アルカリ側にて
ヘミセルロースを抽出することができるが、予め小麦ふ
すまから澱粉質、蛋白質、脂質、無機質等の夾雑物を除
去した方が以後の抽出精製が容易となるので好ましい。
In the present invention, hemicellulose can be extracted directly from wheat bran on the alkaline side, but subsequent extraction and purification is easier if impurities such as starch, protein, lipids, and inorganic substances are removed from wheat bran in advance. Therefore, it is preferable.

小麦ふすまから澱粉質、蛋白質、脂質、無機質iを除去
する方法としては、酵素処理、化学的処理、物理的処理
のいずれでもよく、又これらを適宜組合せて処理するこ
ともできる。酵素処理としては、例えばα−アミラーゼ
、グルコアミラーゼ等の澱粉分解酵素、プロテアーゼ等
の蛋白分解酵素、リパーゼ等の脂質分解酵素、セルラー
ゼ等の繊維素分解酵素をPH3〜9、温度30〜100
℃の条件下に添加作用させて処理することができる。化
学的処理としては、小麦ふすまに鉱酸、有機酸の水溶液
を添加し、PH−2〜5の条件下に加熱するか又は食品
用界面活性剤を添加し、 PH3〜8の条件下に熱処理
することによシ行なわれる。物理的処理としては、小麦
ふすまをホモシナイガ−、ハンマーミル等の粉砕機で粉
砕した後、篩別することによシ行なわれる。
The method for removing starch, protein, lipids, and inorganic substances i from wheat bran may be any of enzymatic treatment, chemical treatment, and physical treatment, or a suitable combination of these treatments may be used. Enzyme treatment includes, for example, starch-degrading enzymes such as α-amylase and glucoamylase, protein-degrading enzymes such as protease, lipid-degrading enzymes such as lipase, and fibrinolytic enzymes such as cellulase at pH 3-9 and temperature 30-100.
The treatment can be carried out by addition under conditions of °C. For chemical treatment, an aqueous solution of mineral acid or organic acid is added to wheat bran and heated under conditions of PH-2 to 5, or a food grade surfactant is added and heat treated under conditions of PH of 3 to 8. It is done by doing. The physical treatment is carried out by pulverizing wheat bran with a pulverizer such as a homogenizer or hammer mill, and then sieving it.

本発明の血清コレステロール上昇抑制物質は、小麦ふす
まから直接アルカリ側で抽出することによっても得られ
るが、−ミロース高含有物質を得るには、小麦ふすまか
ら酵素処理又は/及び化学的・物理的処理により、予め
澱粉質、蛋白質、脂質、無機質等を除去したものをアル
カリ側で抽出するか、又は小麦ふすまから直接アルカリ
側で抽出したものから上記と同様に処理し、澱粉質、蛋
白質、脂質、無機質等を除去する方法が採用される。
The serum cholesterol increase-inhibiting substance of the present invention can also be obtained by directly extracting it from wheat bran on the alkaline side. Either starch, proteins, lipids, inorganic substances, etc. have been removed in advance and extracted on the alkaline side, or directly extracted from wheat bran on the alkaline side and processed in the same manner as above to extract starch, proteins, lipids, etc. A method of removing inorganic substances etc. is adopted.

ここで、抽出方法については公知の方法を用いることが
できる。例えば、小麦ふすまから澱粉質、蛋白質、脂質
、無機質等を除去した残部(セルロース、ヘミセルロー
スlE成分とL若干のリグニン等を含む)100部に帆
5M水酸化す) IJウム溶液を500部加えて室温で
一夜振とりすることにより本発明物質を抽出することが
できる。
Here, a known method can be used for the extraction method. For example, to 100 parts of the residue after removing starch, proteins, lipids, inorganic substances, etc. from wheat bran (containing cellulose, hemicellulose and some lignin, etc.), add 500 parts of IJum solution (5M hydroxide). The substance of the present invention can be extracted by shaking overnight at room temperature.

上記抽出物は中和して未精製のまま、あるいは必要に応
じ精製したのち、飲食品、医薬品の素材として広く利用
することができる。
The above-mentioned extract can be widely used as a raw material for foods, drinks, and medicines, either as it is neutralized and unpurified, or after being purified if necessary.

次に、本発明物質の血清コレステロール上昇抑制効果を
確認するために行なったラットによる動物試験の結果を
以下に示す。
Next, the results of an animal test using rats conducted to confirm the inhibitory effect of the substance of the present invention on the rise in serum cholesterol are shown below.

(1)本発明物質の調製 小麦ふすまtoo+rを5を容三角フラスコに採シ、こ
れに、グルコアミラーゼ(長潮産業■製: 1 x 1
0’ 0TJN/y ) 5?を蒸留水4tに溶かし、
1紙で沢過し、f液に0.2M酢酸塩緩衝液(PH4,
8)Itを加えて調製したグルコアミラーゼ溶液5を及
びトルエン数滴を加えて、40℃で24時間保った。こ
れをガラスフィルター(151G3 )で沢過し、水で
洗滌したのち、21容三角フラスコに移し、 0.51
・N水酸化ナトリウム液1tを加え、容器内に窒素ガス
を充満させ、ゴム栓で密栓して、室温で16時間振とう
させてアルカリ可溶の非セルローズ性多糖類区分の抽出
を行なった。このものを遠心分離(3,000rpm、
19分)して液部を氷酢酸で中和し、トリクロール酢酸
を最終濃度が7%になるように添加して蛋白質を沈澱さ
せた。沈澱物を遠心分離(5,00Orpm、10分)
して除去し、得られた分離液(約650rnl)に水を
加えて約1.3tとしたのち、セロファンチューブを用
いて3日間流水中で透析した。透析内容物が中性になっ
たのを確認したのち、約4倍量のエチルアルコール(最
終濃度80%以上)を加え、−夜装置して沈澱を十分に
生成させた。この沈澱を遠心分離(4,00Orpm、
 10分)して採取し、蒸留水1tに溶解させ、凍結乾
燥して淡白の本発明物質72を得た。これを粉末とし、
実験に供した。その組成を第1表に示す。尚゛、組成の
分析はSouthgate法に従った。
(1) Preparation of the substance of the present invention Pour 50% of wheat bran too+r into an Erlenmeyer flask, add glucoamylase (manufactured by Nagashio Sangyo: 1 x 1)
0' 0TJN/y) 5? Dissolve in 4 tons of distilled water,
1 paper, and add 0.2M acetate buffer (PH4,
8) Glucoamylase solution 5 prepared by adding It and several drops of toluene were added and kept at 40°C for 24 hours. This was filtered through a glass filter (151G3), washed with water, and then transferred to a 21-volume Erlenmeyer flask.
- 1 ton of N sodium hydroxide solution was added, the container was filled with nitrogen gas, the container was sealed tightly with a rubber stopper, and the container was shaken at room temperature for 16 hours to extract the alkali-soluble non-cellulosic polysaccharide fraction. This material is centrifuged (3,000 rpm,
After 19 minutes), the liquid portion was neutralized with glacial acetic acid, and trichloroacetic acid was added to a final concentration of 7% to precipitate the protein. Centrifuge the precipitate (5,00 rpm, 10 minutes)
Water was added to the obtained separated liquid (about 650 rnl) to make about 1.3 t, and then dialyzed in running water for 3 days using a cellophane tube. After confirming that the dialyzed content had become neutral, about 4 times the amount of ethyl alcohol (final concentration 80% or more) was added, and the mixture was incubated overnight to sufficiently form a precipitate. This precipitate was centrifuged (4,00 Orpm,
10 minutes), dissolved in 1 t of distilled water, and lyophilized to obtain pale white substance 72 of the present invention. Make this into powder,
It was used for experiments. Its composition is shown in Table 1. The composition was analyzed according to the Southgate method.

(2)各実験区の飼料配合組成 各実験区の飼料配合組成(重量百分率)は第2表のとお
りである。標準区はコレステロール、コール酸ソーター
及び夫々の試験試料のいずれも無添加のもの:対照区は
コレステロール1%、コール酸ソーター 0.25%t
 添加したもの;他の区はいずれもコレステロール1%
、コール酸ソーター0.25%と夫々の試験試料とを添
加したものである。このうち小麦ふすまはNDF (中
性洗剤処理繊維)値が38.6の市販品(日東製粉■製
)、小麦フスマダイエタリーファイバーは上記市販の小
麦ふすま −を酵素処理して澱粉質、蛋白質等の夾雑物
を除去したNDF’値80.6のダイエタリーファイノ
く−であり、試験区A、B、Cは前記(1)の本発明物
質を夫々0.1%、0.5%、2.0%添加したもので
ある。尚、上記NDFとは、食品中のセルロース、ヘミ
セルロース及ヒリクニンノ含量を表わすもノテ、測定法
は、Tournal of theAss’ociat
ion of 0fficial Agricultu
ralChemists、46.P825−829.1
963  に記載されている繊維の洗剤による処理方法
による。
(2) Feed composition for each experimental group The feed composition (weight percentage) for each experimental group is shown in Table 2. The standard group has no additives of cholesterol, cholic acid sorter, or each test sample: the control group has 1% cholesterol and 0.25% cholic acid sorter.
Added: All other groups have 1% cholesterol
, 0.25% cholic acid sorter and each test sample were added. Among these, wheat bran is a commercially available product (manufactured by Nitto Seifun ■) with an NDF (neutral detergent treated fiber) value of 38.6, and wheat bran dietary fiber is the commercially available wheat bran mentioned above that is treated with enzymes to provide starch, protein, etc. It is a dietary supplement with an NDF' value of 80.6 from which impurities have been removed, and test plots A, B, and C contain 0.1%, 0.5%, and 0.5% of the inventive substance described in (1) above, respectively. 2.0% was added. Note that the above-mentioned NDF refers to the content of cellulose, hemicellulose, and hemicellulose in foods.
ion of official agriculture
ralChemists, 46. P825-829.1
According to the method for treating fibers with a detergent described in No. 963.

(以下余白) (3)実験動物及び飼育方法 体重65〜759のSpragne−Dawley系雄
ラット(日本タレア■)を標準飼料で12日間予備飼育
したのち、1群8匹ずつ7群に分け、第2表に示した各
飼料を夫々投与して8日間飼育した。飼料及び水は自由
に摂取させた。
(Margins below) (3) Experimental animals and breeding method Male Spragne-Dawley rats (Nippon Talea ■) weighing 65-759 were preliminarily bred for 12 days on a standard diet, and then divided into 7 groups of 8 rats per group. The animals were fed with each of the feeds shown in Table 2 and raised for 8 days. Feed and water were available ad libitum.

(4)血清コレステロールノ測定 実験終了したラットを一夜断食させ、常法に従い断言、
採血してデタミナーTC(協和醗酵工業■)を用いる酵
素方法により測定した。
(4) After completing the serum cholesterol measurement experiment, the rats were fasted overnight, and confirmed according to the usual method.
Blood was collected and measured by an enzyme method using Determiner TC (Kyowa Hakko Kogyo ■).

(5)実験結果 実験結果は第3表に示すとおシで、同表から明らかな如
く、対照区の血清コレステロール336〜/10圓(=
100)に対し、小麦ふすま343’f/100mg 
(102X) b小麦ふすまグイエタリーファイバー2
92WIg/AO圓(86,9%)であったが、本発明
物質を用いた試験区Aは2491100m/ (74,
1%)、同Bは242 %’l O眞−(72,0%)
、同Cは152N/10(hd (45,2X)と著し
い血パ清コレステロール上昇抑制効果を示し、有意差(
5%危険率)が認められた。
(5) Experimental results The experimental results are shown in Table 3. As is clear from the table, serum cholesterol in the control group was 336~/10 g (=
100), wheat bran 343'f/100mg
(102X) b wheat bran grainy fiber 2
It was 92WIg/AO round (86.9%), but in test area A using the substance of the present invention, it was 2491100m/(74,9%).
1%), B is 242%'l Oshin-(72,0%)
, the same C showed a remarkable effect of suppressing the increase in serum serum cholesterol with 152N/10 (hd (45,2X)), and there was a significant difference (
5% risk rate).

以上の結果から明らかな如く、小麦ふすまそのものを摂
取した場合には、血清コレステロールは若干上昇し、小
麦ふすまダイエタリーファイバーを摂取した場合には減
少の傾向を示すが本発明物質を摂取した場合には減少の
傾向がさらに著しく、ダイエタリーファイバーの50分
の1以下の量で同等以上の血清コレステロール上昇抑制
効果を発揮することが示されている。
As is clear from the above results, when wheat bran itself is ingested, serum cholesterol increases slightly, and when wheat bran dietary fiber is ingested, it tends to decrease, but when the substance of the present invention is ingested, serum cholesterol increases slightly. It has been shown that the tendency of decrease is even more remarkable, and that an amount less than 1/50th that of dietary fiber can exert the same or higher effect of suppressing the increase in serum cholesterol.

したがって、この様な本発明物質を飲食品へ添加し健へ
品とするに際しては、ごく少量の添加で目的とする効果
が発揮されるため、ダイエタリーファイバーを多量に添
加した場合の様に日中でのザラツキを感じさせることな
く、又食感、風味を損うことがなく、広く飲食品に利用
することが可能となる。
Therefore, when adding the substance of the present invention to food and drink to make it a health product, the desired effect can be achieved with a very small amount of addition, so it is difficult to add a large amount of dietary fiber. It can be widely used in foods and drinks without making the inside feel rough or deteriorating the texture or flavor.

以下に本発明を実施例をもって説明する。The present invention will be explained below with reference to examples.

実施例1゜ 市販の小麦ふすまを水に分散させ、48メツシー篩を用
いて洗滌篩別し、篩上の残渣を採取した。この残漬10
0部に飽和水酸化カルシウム溶液1000部を加え、攪
拌しながら60分間煮沸し、ついで修酸を加えて中和し
た。これを沢過し、そのr液を活性炭で脱色した後、真
空エバポレーターでBx濃度15迄濃縮し、これをドラ
ムドライヤー(蒸気圧2 Kij )で乾燥して本発明
物質を得た。本発明物質の組成は水分8.1%、ヘミセ
ルロース82.8%、セルロース0.1%、リグニン1
.5%、灰分6.1%、全窒素1.4%であった。
Example 1 Commercially available wheat bran was dispersed in water, washed and sieved using a 48 mesh sieve, and the residue on the sieve was collected. This leftover 10
1000 parts of a saturated calcium hydroxide solution was added to 0 parts, and the mixture was boiled for 60 minutes with stirring, and then oxalic acid was added to neutralize it. This was thoroughly filtered, and the r liquid was decolorized with activated carbon, concentrated to a Bx concentration of 15 using a vacuum evaporator, and dried using a drum dryer (vapor pressure: 2 Kij) to obtain the substance of the present invention. The composition of the material of the present invention is 8.1% moisture, 82.8% hemicellulose, 0.1% cellulose, and 1% lignin.
.. 5%, ash 6.1%, and total nitrogen 1.4%.

実施例2゜ 市販の小麦ふすまを16メノシー篩で篩別し、篩上の残
漬をアトマイザ−で粉砕した。この粉砕物100部に0
.5Mの水酸化ナトリウム溶液500部を加え、室温で
一夜振とうし得られた抽出物を遠心分離(4000rp
m、 10分)し、上澄液を氷酢酸で中和し、これを活
性炭処理を行なった後、さらに、これをアニオン、カチ
オン、モノベットのシリーズで精製し、Bx濃度1.5
迄濃縮し、凍結乾燥して本発明物質を得た。本発明物質
の組成id水分12.5%、ヘミセルロース82.5%
、セルロース0.1%、リグニン1.6%、灰分2.1
%、全窒素1.3%であった。
Example 2 Commercially available wheat bran was sieved using a 16-menocy sieve, and the residue on the sieve was pulverized using an atomizer. 0 parts per 100 parts of this crushed material
.. Add 500 parts of 5M sodium hydroxide solution, shake overnight at room temperature, and centrifuge the resulting extract (4000 rpm).
After neutralizing the supernatant with glacial acetic acid and treating it with activated carbon, it was further purified with an anion, cation, and monobet series to a Bx concentration of 1.5.
The substance of the present invention was obtained by concentrating and freeze-drying. Composition of the substance of the present invention: moisture 12.5%, hemicellulose 82.5%
, cellulose 0.1%, lignin 1.6%, ash 2.1
%, total nitrogen was 1.3%.

実施例6゜ 市販の小麦ふすまを32メツシユ以下に粉砕し、これを
水に懸濁させて攪拌しながら加熱処理し、常法に従い、
α−アミラーゼ、グロテアーゼ及びリパーゼを添加作用
させて澱粉、蛋白、脂肪等の夾雑物を除去してダイエタ
リーファイバー(NDF95%)を得た。このダイエタ
リーファイバー100部に0.5 M水酸化ナトリウム
溶液100部を加え、分散攪拌しながら40℃に10時
間保持して抽出した。得られた抽出物を遠心分離(40
00rpm、10分)して沈澱物を除去した稜、上澄液
を氷酢酸で中和し、活性炭で脱色した。これをセロファ
ンチューブを用いて3日間流水中で透析し、透析内容物
が中性になったのを確認したのち、約4倍量のエチルア
ルコールを加え、−夜装置して沈澱を十分に生成させた
。この沈澱を遠心分離(4000rpm 、710分)
して採取し、蒸留水に溶解させ、凍結乾燥して本発明物
質を得た。
Example 6 Commercially available wheat bran was ground to 32 meshes or less, suspended in water and heated with stirring, followed by a conventional method.
Dietary fiber (NDF 95%) was obtained by adding α-amylase, grotease and lipase to remove impurities such as starch, protein and fat. 100 parts of a 0.5 M sodium hydroxide solution was added to 100 parts of this dietary fiber, and the mixture was maintained at 40° C. for 10 hours while stirring for dispersion and extraction. The obtained extract was centrifuged (40
00 rpm, 10 minutes) to remove the precipitate, the supernatant liquid was neutralized with glacial acetic acid, and decolorized with activated carbon. This was dialyzed in flowing water for 3 days using a cellophane tube, and after confirming that the dialyzed content had become neutral, about 4 times the amount of ethyl alcohol was added, and the mixture was incubated overnight to form a sufficient amount of precipitate. I let it happen. Centrifuge this precipitate (4000 rpm, 710 minutes)
The substance of the present invention was obtained by collecting the substance, dissolving it in distilled water, and freeze-drying it.

得られた本発明物質の組成は水分9.8%、ヘミセルロ
ース86.0%、セルロース0.1%、リガニン1.4
%、灰分1.7%、全窒素1.0%であった。
The composition of the obtained substance of the present invention is 9.8% water, 86.0% hemicellulose, 0.1% cellulose, and 1.4% liganin.
%, ash content 1.7%, and total nitrogen 1.0%.

特許出願人 日本食品化工株式会社 手続補正書 昭和57年2月?日 特許庁長官 島 1)春 樹  殿 1、事件の表示 昭和56年特許願第139689号 2、発明の名称 血清コレステロ m抑制物質 3、補正をする者 事件との関係   特許出願人 4、補正の対象 明細書の発明の詳細な説明の欄 (1)  明細書第2頁第5行目のr(Cel 1wa
ll) J  をr (Cell wall)J  に
訂正する。
Patent applicant Nihon Shokuhin Kako Co., Ltd. Procedural amendment February 1982? Japan Patent Office Commissioner Shima 1) Mr. Haruki 1, Indication of the case, Patent Application No. 139689, filed in 1982, 2, Name of the invention: Serum cholesterol m inhibitory substance 3, Person making the amendment Relationship with the case Patent applicant 4, Amendment Column for detailed description of the invention in the subject specification (1) r (Cel 1wa
ll) Correct J to r (Cell wall)J.

(2)明細書第2頁第12行目の「相互関係」を「相関
関係」に訂正する。
(2) Correct "mutual relationship" in line 12 of page 2 of the specification to "correlation."

(3)明細書第2頁第16行目の「(・・・・・・、5
α4)、・・・・・・)」を「(・・・・・・、56(
4)、・・・・・・)」に訂正する。
(3) “(...,5
α4),...)" to "(......,56(
4),...)".

(4)  明細書第6頁第20行〜第7頁第1行の「ホ
モシナイガ−」を「ホモジ芙イザー」に訂正する。
(4) "Homozynaiger" on page 6, line 20 to page 7, line 1 of the specification is corrected to "homozyzizer."

(5)  明細書第7頁第18行目の「・・・・・・を
500部加えて・・・・・・」を「・・・・・・を1,
000部加えて・・・・・・」に訂正する。
(5) On page 7, line 18 of the specification, "Add 500 copies of..." to "1..."
000 copies added...'' is corrected.

(6)明細書第2頁第5粉末、同頁第6行目、同第8行
目及び第12頁の第2表中の「コール酸ソーダー」をそ
れぞれ「コール酸ソーダ」と訂正する。
(6) "Sodium cholic acid" in Powder 5, page 2, line 6, line 8 of the same page, and Table 2 on page 12 of the specification are respectively corrected to "sodium cholate."

(7)  明細書第10頁第19行目のrTourna
lJをr’Journal」に訂正する。
(7) rTourna on page 10, line 19 of the specification
Correct lJ to r'Journal.

(8)  明細書第13頁第2行目のrspragne
Jを[spragueJに訂正する。
(8) rspragne on page 13, line 2 of the specification
Correct J to [spragueJ.

(9)  明細書第13頁第8行目の「断食させ」を「
絶食させ」に訂正する。
(9) Change “to fast” on page 13, line 8 of the specification to “
I am corrected to ``Fast.''

QO明細書第13頁第10行目の「酵素方法」を「酵素
法」に、訂正する。
"Enzyme method" on page 13, line 10 of the QO specification is corrected to "enzyme method."

(lυ 明細書第14頁第1行9目の「・・・・・・示
し、有意差・・・・・・」を「・・−・・示し、対照区
に比べて有意差・・・・・・」に訂正する。
(lυ In the specification, page 14, line 1, 9, ``...shows, significant difference...'' is replaced with ``...shows, significant difference...'' compared to the control group... ...” is corrected.

@ 明細書第16頁第17行目の「水酸化ナトリウム溶
液500」を[水酸化ナトリウム溶液1,0OOJと訂
正する。
@ "Sodium hydroxide solution 500" on page 16, line 17 of the specification is corrected to [sodium hydroxide solution 1,000J].

0 明細書第17頁第2行目の「・・・・・・のシリー
ズで」を「・・・・・・のイオン交換樹脂で」と訂正す
る。
0 In the second line of page 17 of the specification, "by the series of..." is corrected to "by the ion exchange resin of...".

Q4  明細書第17頁第6行目の「1.3%」を「1
.2%−に訂正する。
Q4 Change “1.3%” on page 17, line 6 of the specification to “1.
.. Corrected to 2%-.

Oo  明細書第17頁第14行目の「水酸化ナトリウ
ム溶液100」を[水酸化ナトリウム溶液1,0OOJ
に訂正する。
Oo "Sodium hydroxide solution 100" on page 17, line 14 of the specification is [sodium hydroxide solution 1,0OOJ
Correct.

(至)明細書第18頁第6〜71行目の「リガニン」を
「リグニン」と訂正する。
(To) "Liganin" on page 18, lines 6 to 71 of the specification is corrected to "lignin."

以上that's all

Claims (1)

【特許請求の範囲】[Claims] 小麦ふすま又は小麦ふすまから澱粉質、蛋白質、脂質、
無機質等を除去した残部からアルカリ側で抽出されてな
るヘミセルロースを主成分として含有する血清コレステ
ロール上昇抑制物質。
Wheat bran or wheat bran to starch, protein, fat,
A substance that suppresses the increase in serum cholesterol and contains hemicellulose as a main component, which is extracted on the alkali side from the residue after removing inorganic substances.
JP56139689A 1981-09-07 1981-09-07 Inhibitory substance for rise in blood serumal cholesterol Granted JPS5841824A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56139689A JPS5841824A (en) 1981-09-07 1981-09-07 Inhibitory substance for rise in blood serumal cholesterol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56139689A JPS5841824A (en) 1981-09-07 1981-09-07 Inhibitory substance for rise in blood serumal cholesterol

Publications (2)

Publication Number Publication Date
JPS5841824A true JPS5841824A (en) 1983-03-11
JPS626691B2 JPS626691B2 (en) 1987-02-13

Family

ID=15251126

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56139689A Granted JPS5841824A (en) 1981-09-07 1981-09-07 Inhibitory substance for rise in blood serumal cholesterol

Country Status (1)

Country Link
JP (1) JPS5841824A (en)

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59210850A (en) * 1983-05-12 1984-11-29 Nippon Shokuhin Kako Kk Preparation of food or drink good for health
JPS60109526A (en) * 1983-11-18 1985-06-15 T Hasegawa Co Ltd Production of medicinal plant extract
JPS60146828A (en) * 1983-12-30 1985-08-02 Showa Sangyo Kk Inhibitor for rise in cholesterol and health food containing said inhibitor
JPS63185931A (en) * 1987-01-28 1988-08-01 Snow Brand Milk Prod Co Ltd Removal of blood serum cholesterol rise promoting factor from wheat bran
JPH01153701A (en) * 1987-12-10 1989-06-15 Kenichi Osa Production of biologically active hemicellulose
JPH03160973A (en) * 1989-11-17 1991-07-10 Nippon Beet Sugar Mfg Co Ltd Production of new material of food fiber
JPH03285653A (en) * 1990-03-30 1991-12-16 Snow Brand Milk Prod Co Ltd Fat metabolism improving substance and production thereof
EP0421758A3 (en) * 1989-10-05 1992-01-22 Michigan Biotechnology Institute Dietary fibres and a process for their production
AU626610B2 (en) * 1988-11-30 1992-08-06 Nisshin Seifun Group Inc. Sustained release compositions using as matrix hemicellulose extracted from wheat bran
US5174998A (en) * 1988-11-30 1992-12-29 Nisshin Flour Milling Co., Ltd. Sustained release compositions using as matrix hemicellulose extracted from wheat bran
US5622738A (en) * 1989-05-16 1997-04-22 Nihon Shokuhin Kako Co., Ltd. Method of preparing water-soluble dietary fiber
WO1998041547A1 (en) * 1997-03-20 1998-09-24 E.I. Du Pont De Nemours And Company Improvements relating to bran gels
JP2005314249A (en) * 2004-04-27 2005-11-10 Nisshin Pharma Inc epsilon-POLYLYSINE-CONTAINING SOLID PREPARATION
WO2011081488A2 (en) * 2009-12-30 2011-07-07 Lee Hai Soo Composition for treatment of obesity using wheat bran extract or active ingredient isolated therefrom
CN107691763A (en) * 2017-09-19 2018-02-16 中国科学院青岛生物能源与过程研究所 A kind of method of comprehensive utilization of wheat bran

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0424028B2 (en) * 1983-05-12 1992-04-23 Japan Maize Prod
JPS59210850A (en) * 1983-05-12 1984-11-29 Nippon Shokuhin Kako Kk Preparation of food or drink good for health
JPS60109526A (en) * 1983-11-18 1985-06-15 T Hasegawa Co Ltd Production of medicinal plant extract
JPS60146828A (en) * 1983-12-30 1985-08-02 Showa Sangyo Kk Inhibitor for rise in cholesterol and health food containing said inhibitor
JPH0434527B2 (en) * 1983-12-30 1992-06-08 Showa Sangyo Co
JPS63185931A (en) * 1987-01-28 1988-08-01 Snow Brand Milk Prod Co Ltd Removal of blood serum cholesterol rise promoting factor from wheat bran
JPH01153701A (en) * 1987-12-10 1989-06-15 Kenichi Osa Production of biologically active hemicellulose
AU626610B2 (en) * 1988-11-30 1992-08-06 Nisshin Seifun Group Inc. Sustained release compositions using as matrix hemicellulose extracted from wheat bran
US5174998A (en) * 1988-11-30 1992-12-29 Nisshin Flour Milling Co., Ltd. Sustained release compositions using as matrix hemicellulose extracted from wheat bran
US5622738A (en) * 1989-05-16 1997-04-22 Nihon Shokuhin Kako Co., Ltd. Method of preparing water-soluble dietary fiber
EP0421758A3 (en) * 1989-10-05 1992-01-22 Michigan Biotechnology Institute Dietary fibres and a process for their production
JPH03160973A (en) * 1989-11-17 1991-07-10 Nippon Beet Sugar Mfg Co Ltd Production of new material of food fiber
JPH03285653A (en) * 1990-03-30 1991-12-16 Snow Brand Milk Prod Co Ltd Fat metabolism improving substance and production thereof
WO1998041547A1 (en) * 1997-03-20 1998-09-24 E.I. Du Pont De Nemours And Company Improvements relating to bran gels
US6482430B1 (en) 1997-03-20 2002-11-19 Cambridge Biopolymers Limited Improvements Relating To Bran Gels
JP2005314249A (en) * 2004-04-27 2005-11-10 Nisshin Pharma Inc epsilon-POLYLYSINE-CONTAINING SOLID PREPARATION
WO2011081488A2 (en) * 2009-12-30 2011-07-07 Lee Hai Soo Composition for treatment of obesity using wheat bran extract or active ingredient isolated therefrom
WO2011081488A3 (en) * 2009-12-30 2011-12-01 Lee Hai Soo Composition for treatment of obesity using wheat bran extract or active ingredient isolated therefrom
CN107691763A (en) * 2017-09-19 2018-02-16 中国科学院青岛生物能源与过程研究所 A kind of method of comprehensive utilization of wheat bran

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