JPH05239106A - Production of purified galactomannan - Google Patents

Production of purified galactomannan

Info

Publication number
JPH05239106A
JPH05239106A JP7880992A JP7880992A JPH05239106A JP H05239106 A JPH05239106 A JP H05239106A JP 7880992 A JP7880992 A JP 7880992A JP 7880992 A JP7880992 A JP 7880992A JP H05239106 A JPH05239106 A JP H05239106A
Authority
JP
Japan
Prior art keywords
galactomannan
solution
viscosity
aqueous solution
purified
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
JP7880992A
Other languages
Japanese (ja)
Other versions
JP2729722B2 (en
Inventor
Mitsuo Morikawa
光雄 森川
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.)
Mitsubishi Rayon Co Ltd
Original Assignee
Mitsubishi Rayon 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 Mitsubishi Rayon Co Ltd filed Critical Mitsubishi Rayon Co Ltd
Priority to JP7880992A priority Critical patent/JP2729722B2/en
Publication of JPH05239106A publication Critical patent/JPH05239106A/en
Application granted granted Critical
Publication of JP2729722B2 publication Critical patent/JP2729722B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Polysaccharides And Polysaccharide Derivatives (AREA)

Abstract

PURPOSE:To obtain a purified galactomannan capable of providing its aqueous solution having excellent transparency and viscosity stability, in production of purified galactomannan. CONSTITUTION:An aqueous solution of crude galactomannan and a monosaccharide is adjusted to proper pH and filtered and purified galactomannan is recovered from the filtrate to produce purified galactomannan. By this method, purified galactomannan providing an aqueous solution of galactomannan showing characteristics of high transparency and excellent viscosity stability is obtained.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は精製ガラクトマンナンの
製法に関する。ガラクトマンナンはマンノースを構成単
位とする主鎖にガラクトース単位が側鎖として構成され
る中性多糖類であり、主として豆科植物の種子の胚乳部
に多く含有されている。グア豆を原料とするグアガム、
タラ豆を原料とするタラガムおよびローカストビーンを
原料とするローカストビーンガムは代表的なガラクトマ
ンナンを主成分とする植物ガム質である。
FIELD OF THE INVENTION The present invention relates to a method for producing purified galactomannan. Galactomannan is a neutral polysaccharide in which a galactose unit is a side chain in a main chain having mannose as a constituent unit, and is mainly contained in the endosperm portion of seeds of legumes in large amounts. Gua gum made from gua beans,
Cod gum made from cod beans and locust bean gum made from locust beans are typical plant gums containing galactomannan as a main component.

【0002】ガラクトマンナンは水に溶解したときに、
極めて高い粘性を示し、その水溶液は巾広いpH領域にお
いて安定であり、かつ、塩類が共存する水溶液の安定性
も優れており、食品分野の他、捺染、糊料等の諸工業に
も広く利用されている。しかし、通常のガラクトマンナ
ンは、種子胚乳部よりの摘出に際して種皮や胚芽部に含
まれる蛋白質、油分、繊維質等の不純物が混入するの
で、その水溶液はその透明性および品質安定性が劣った
ものになる。そのため高純度で、その水溶液の透明性が
高いことなどの品質を要求されるガラクトマンナンの用
途においては、これらの要求を満たした精製ガラクトマ
ンナンを提供することが要望されている。
Galactomannan, when dissolved in water,
It has an extremely high viscosity, its aqueous solution is stable in a wide pH range, and the stability of the aqueous solution in which salts coexist is also excellent, and it is widely used in various industries such as printing, paste, etc. in addition to the food field. Has been done. However, ordinary galactomannan is contaminated with impurities such as proteins, oils, and fibers contained in the seed coat and germ when extracting from the seed endosperm, so that its aqueous solution is inferior in transparency and quality stability. become. Therefore, in the application of galactomannan that is required to have high purity and high quality such as high transparency of the aqueous solution, it is desired to provide a purified galactomannan satisfying these requirements.

【0003】[0003]

【従来の技術】ガラクトマンナンの精製方法としては、
ガラクトマンナンを熱水に溶解した後、蛋白質、繊維質
等の不溶解物質を濾過除去し、濾液にメタノール、イソ
プロピルアルコール、アセトン等の水親和性有機溶剤を
加えてガム質を析出させ、圧搾脱水し、さらにこの脱水
物を乾燥、粉砕して精製ガラクトマンナンとする方法が
知られている。
2. Description of the Related Art As a method for purifying galactomannan,
After dissolving galactomannan in hot water, insoluble substances such as proteins and fibers are removed by filtration, and water-affinity organic solvents such as methanol, isopropyl alcohol, and acetone are added to the filtrate to precipitate gums, which are squeezed and dehydrated. Then, a method is known in which the dehydrated product is dried and pulverized to obtain purified galactomannan.

【0004】[0004]

【発明が解決しようとする課題】しかし、ガラクトマン
ナンの精製工程では、工程中にガラクトマンナンが水溶
液の状態で1〜2日程度滞留することがあるが、ガラク
トマンナンは水溶液の状態で放置すると経時的に水溶液
粘度が低下してくるという現象があり、高粘度タイプの
精製ガラクトマンナンを工業的に安定に生産するのが困
難であった。
However, in the galactomannan purification step, the galactomannan sometimes stays in the state of an aqueous solution for about 1 to 2 days during the purification step. There is a phenomenon that the viscosity of the aqueous solution is reduced, and it is difficult to industrially produce a highly viscous type purified galactomannan.

【0005】また、粘度の低下したガラクトマンナンが
共存する水溶液に、新たにガラクトマンナンを溶解する
と、この新規に溶解したガラクトマンナンの粘度低下が
急速に進むことが知られており、ガラクトマンナンの粘
度低下防止のため、現在用いられているガラクトマンナ
ンの連続精製装置等では、1回/日以上の頻度で装置内
を完全に洗浄する必要があり、その生産性が低いことお
よびその生産に過度の労力を必要とする原因になってお
り、より効率的で粘度低下をきたさない精製ガラクトマ
ンナンの製造方法の出現が待たれている。
It is known that when galactomannan is newly dissolved in an aqueous solution in which galactomannan of reduced viscosity coexists, the viscosity of the newly dissolved galactomannan rapidly decreases. In order to prevent deterioration, it is necessary to completely clean the inside of the galactomannan continuous purification device currently used at a frequency of once or more per day, which is low in productivity and excessive in its production. It is a cause of requiring labor, and the advent of a more efficient method for producing purified galactomannan without causing a decrease in viscosity is awaited.

【0006】[0006]

【課題を解決するための手段】本発明者等はこのような
状況に鑑み、精製ガラクトマンナンの製造法につき鋭意
検討した結果、粗製ガラクトマンナンに単糖類を添加し
て精製することにより粘度低下をきたさないガラクトマ
ンナンが得られることを見出し、本発明に至ったもので
あり、その要旨とするところは、粗製ガラクトマンナン
に単糖類を添加した水溶液から不溶解物質を濾過、除去
し、この濾液からガラクトマンナンを回収することを特
徴とするガラクトマンナンの精製方法にある。
In view of such circumstances, the inventors of the present invention have diligently studied a method for producing purified galactomannan, and as a result, the viscosity reduction is caused by adding a monosaccharide to crude galactomannan for purification. It has been found that a galactomannan which does not cause trouble can be obtained, which has led to the present invention. The gist of the invention is to remove an insoluble substance from an aqueous solution obtained by adding a monosaccharide to crude galactomannan, and remove the insoluble substance from the filtrate. A method for purifying galactomannan is characterized by recovering galactomannan.

【0007】本発明を実施するに際して用いられる粗製
ガラクトマンナンとしては、ガラクトマンナン含有種子
から種皮や胚芽部をおおまかに除去して粉砕したもので
もよく、あるいは不純物をある程度除去し粗精製した粉
砕品でもよい。グアガム、タラガム、ローカストビーン
ガム等の市販品を用いることもできる。
The crude galactomannan used in the practice of the present invention may be a galactomannan-containing seed obtained by roughly removing the seed coat and the germ part and crushing it, or a crushed product roughly purified by removing impurities to some extent. Good. Commercially available products such as guar gum, tara gum and locust bean gum can also be used.

【0008】本発明を実施するに際しては、まず、単糖
類を含有する粗製ガラクトマンナンの水溶液を調製す
る。粗製ガラクトマンナンを溶解させる水としては、70
〜 100℃の熱水が用いられる。熱水の使用量は粗製ガラ
クトマンナン1部に対して70〜125 部である。熱水に粗
製ガラクトマンナンを溶解させる方法としては、まず粗
製ガラクトマンナン粉体を20℃前後の冷水中に充分に攪
拌して分散させ、攪拌を継続しながら所定の温度まで加
温して溶解する方法、または所定の温度に保持した熱水
を攪拌しながら徐々に粗製ガラクトマンナン粉体を添加
して溶解させる方法があげられる。
In carrying out the present invention, first, an aqueous solution of crude galactomannan containing a monosaccharide is prepared. As water for dissolving the crude galactomannan, 70
Hot water at ~ 100 ° C is used. The amount of hot water used is 70 to 125 parts per 1 part of crude galactomannan. As a method for dissolving the crude galactomannan in hot water, first, the crude galactomannan powder is sufficiently stirred and dispersed in cold water at about 20 ° C., and the mixture is heated to a predetermined temperature and dissolved while continuing stirring. The method is, or a method of gradually adding and dissolving the crude galactomannan powder while stirring hot water held at a predetermined temperature.

【0009】本発明を実施するに際して用いられる単糖
類としては、アラビノース、キシロース、フルクトー
ス、ガラクトース、グルコース、マンノースなどが好ま
しい。これら単糖類は単独で用いてもよく、2種以上を
併用してもよい。単糖類の添加量は粗製ガラクトマンナ
ンに対し1〜20重量%が好ましい。添加量をこれより多
くしても格別の効果はなく、また添加量がこれより少な
いとガラクトマンナンの粘度低下を生ずる。単糖類は粗
製ガラクトマンナンと一緒に水に溶解してもよく、粗製
ガラクトマンナンの溶解前または溶解後に加えてもよ
い。
As the monosaccharide used for carrying out the present invention, arabinose, xylose, fructose, galactose, glucose, mannose and the like are preferable. These monosaccharides may be used alone or in combination of two or more. The addition amount of the monosaccharide is preferably 1 to 20% by weight based on the crude galactomannan. If the amount added is larger than this, there is no particular effect, and if the amount added is smaller than this, the viscosity of galactomannan decreases. The monosaccharide may be dissolved in water together with the crude galactomannan, or may be added before or after the dissolution of the crude galactomannan.

【0010】粗製ガラクトマンナン溶液の濾過は、特公
平2−7962号公報に示されるごとく、溶解液のpHを
4.5〜6.3 に調整し、単糖類を含有するガラクトマンナ
ン水溶液として濾過する。濾過は70℃以上の温度で行う
ことが好ましい。温度が下がるとガラクトマンナン水溶
液の粘度が高くなり、濾過性が悪化し濾過速度が低下す
るので好ましくない。濾過する際には濾過助剤、例えば
パーライトをガラクトマンナン水溶液に対して 0.5〜
1.5%添加し、フィルタープレスでケーキ層を充分に形
成した後、濾液を取り出す方法を用いることもできる。
Filtration of the crude galactomannan solution is carried out by adjusting the pH of the solution as disclosed in Japanese Patent Publication No. 2-7962.
Adjust to 4.5-6.3 and filter as an aqueous galactomannan solution containing monosaccharides. The filtration is preferably performed at a temperature of 70 ° C or higher. When the temperature is lowered, the viscosity of the galactomannan aqueous solution is increased, the filterability is deteriorated and the filtration rate is decreased, which is not preferable. When filtering, a filter aid such as perlite is added to the galactomannan aqueous solution in an amount of 0.5 to
A method may also be used in which 1.5% is added, a filter layer is sufficiently formed to form a cake layer, and then the filtrate is taken out.

【0011】こうして得られた不純物を濾別した水溶液
からガラクトマンナンを回収する方法としては、メタノ
ール、イソプロピルアルコール、アセトン等の水親和性
有機溶剤を添加して沈殿を形成させ、これを回収する方
法が用いられる。
As a method for recovering galactomannan from the aqueous solution obtained by filtering off the impurities thus obtained, a method is used in which a water-affinitive organic solvent such as methanol, isopropyl alcohol, or acetone is added to form a precipitate and the precipitate is recovered. Is used.

【0012】[0012]

【実施例】以下、実施例を用いて本発明をさらに詳しく
説明する。なお、実施例において水溶液粘度は精製ガラ
クトマンナン4.0gをイオン交換水400ml 中に冷水分散し
た後、85℃で1時間攪拌して溶解させた後、水分補正し
て正確に全量400gとし、この溶液をB型粘度計20rpm で
の測定値(cps) として示した。
EXAMPLES The present invention will be described in more detail below with reference to examples. In the examples, the viscosity of the aqueous solution was such that 4.0 g of purified galactomannan was dispersed in 400 ml of deionized water in cold water, and the mixture was stirred at 85 ° C. for 1 hour to dissolve, and the total amount was accurately corrected to 400 g. Is shown as a measured value (cps) at 20 rpm of B type viscometer.

【0013】[0013]

【実施例1】粗製ローカストビーンガム240gおよびアラ
ビノース20gを水20リットルに分散し、85℃で1時間攪
拌して溶解した。次に溶解液にクエン酸とリン酸第2水
素ナトリウムを加えて溶液のpHを 5.8に調整した。この
溶液を40℃で放置したときの溶液の粘度変化を表1に示
した。次にpH調整後の溶液に濾過助剤のパーライト240g
を添加混合し、フィルタープレスで加圧濾過した。次に
濾液に同容量のイソプロピルアルコールを添加して生成
した沈殿を圧搾脱水し、乾燥、粉砕して精製ローカスト
ビーンガムを得た。得られた精製ローカストビーンガム
の水溶液粘度(25℃)は3500cps であった。得られた精
製ローカストビーンガムの40℃放置下での水溶液粘度
(40℃)の経時変化を表1に示した。
Example 1 240 g of crude locust bean gum and 20 g of arabinose were dispersed in 20 liters of water and dissolved by stirring at 85 ° C. for 1 hour. Next, citric acid and sodium dihydrogen phosphate were added to the solution to adjust the pH of the solution to 5.8. Table 1 shows the change in viscosity of the solution when the solution was allowed to stand at 40 ° C. Next, 240g of filter aid perlite was added to the solution after pH adjustment.
Was added and mixed, and pressure filtration was performed with a filter press. Next, the same volume of isopropyl alcohol was added to the filtrate, and the resulting precipitate was squeezed and dehydrated, dried and pulverized to obtain purified locust bean gum. The aqueous solution viscosity (25 ° C) of the obtained purified locust bean gum was 3500 cps. Table 1 shows the time-dependent changes in aqueous solution viscosity (40 ° C.) of the obtained purified locust bean gum when allowed to stand at 40 ° C.

【0014】[0014]

【実施例2】粗製ローカストビーン240gおよびキシロー
ス20gを水20リットルに分散し、85℃で1時間攪拌して
溶解した。次にこの溶液を実施例1と同様に処理して溶
液のpHを5.8 に調整した。この溶液を40℃で放置したと
きの粘度変化を表1に示した。次にこの溶液を実施例1
と同様に処理して精製ローカストビーンガムを得た。得
られた精製ローカストビーンガムの水溶液粘度(25℃)
は3550cps であった。得られた精製ローカストビーンガ
ムの40℃放置下での水溶液(40℃)の経時変化を表1に
示した。
Example 2 240 g of crude locust bean and 20 g of xylose were dispersed in 20 liters of water and dissolved by stirring at 85 ° C. for 1 hour. Next, this solution was treated in the same manner as in Example 1 to adjust the pH of the solution to 5.8. Table 1 shows the change in viscosity when the solution was left at 40 ° C. This solution was then added to Example 1
The same procedure was followed to obtain a purified locust bean gum. Aqueous solution viscosity of the obtained refined locust bean gum (25 ℃)
Was 3550 cps. Table 1 shows the time-dependent changes in the aqueous solution (40 ° C.) of the obtained purified locust bean gum left at 40 ° C.

【0015】[0015]

【実施例3】粗製ローカストビーンガム240gおよびフル
クトース20gを水20リットルに分散し、85℃で1時間攪
拌して溶解した。次にこの溶液を実施例1と同様にして
溶液のpHを5.8 に調整した。この溶液を40℃で放置した
ときの粘度変化を表1に示した。次にこの溶液を実施例
1と同様に処理して精製ローカストビーンガムを得た。
得られた精製ローカストビーンガムの水溶液粘度(25
℃)は3400cps であった。得られた精製ローカストビー
ンガムの40℃放置下での水溶液粘度(40℃)の経時変化
を表1に示した。
Example 3 240 g of crude locust bean gum and 20 g of fructose were dispersed in 20 liters of water and dissolved by stirring at 85 ° C. for 1 hour. Next, the pH of this solution was adjusted to 5.8 in the same manner as in Example 1. Table 1 shows the change in viscosity when the solution was left at 40 ° C. Next, this solution was treated in the same manner as in Example 1 to obtain purified locust bean gum.
Aqueous solution viscosity of the obtained purified locust bean gum (25
C) was 3400 cps. Table 1 shows the time-dependent changes in aqueous solution viscosity (40 ° C.) of the obtained purified locust bean gum when allowed to stand at 40 ° C.

【0016】[0016]

【実施例4】粗製タラガム240gおよびアラビノース20g
を水20リットルに分散し、85℃で1時間攪拌して溶解し
た。次に、この溶液を実施例1と同様に処理して溶液の
pHを5.8 に調整した。この溶液を40℃で放置したときの
粘度変化を表1に示した。次に実施例1と同様にこの溶
液を処理して精製タラガムを得た。得られた精製タラガ
ムの水溶液粘度(25℃)は2900cps であった。得られた
精製タラガムの40℃放置下での水溶液粘度(40℃)の経
時変化を表1に示した。
Example 4 240 g of crude tara gum and 20 g of arabinose
Was dispersed in 20 liters of water and dissolved by stirring at 85 ° C. for 1 hour. Next, this solution was treated in the same manner as in Example 1 to prepare a solution.
The pH was adjusted to 5.8. Table 1 shows the change in viscosity when the solution was left at 40 ° C. Next, this solution was treated in the same manner as in Example 1 to obtain purified tara gum. The purified cod gum obtained had an aqueous solution viscosity (25 ° C) of 2900 cps. Table 1 shows the time-dependent changes in aqueous solution viscosity (40 ° C.) of the obtained purified tara gum left at 40 ° C.

【0017】[0017]

【比較例1】粗製ローカストビーンガム240gを水20リッ
トルに分散し、85℃で1時間攪拌して溶解した。次にこ
の溶解液にクエン酸とリン酸第2水素ナトリウムを加え
て溶液のpHを5.8 に調整した。この溶液の40℃放置での
粘度変化を表1に示した。次にこの溶液を実施例1と同
様に処理して精製ローカストビーンガムを得た。得られ
た精製ローカストビーンガムの水溶液粘度(25℃)は33
00cps であった。得られた精製ローカストビーンガムの
40℃放置下での水溶液粘度(40℃)の経時変化を表1に
示した。
Comparative Example 1 240 g of crude locust bean gum was dispersed in 20 liters of water and dissolved by stirring at 85 ° C. for 1 hour. Next, citric acid and sodium dihydrogen phosphate were added to this solution to adjust the pH of the solution to 5.8. Table 1 shows the change in viscosity of this solution when allowed to stand at 40 ° C. Next, this solution was treated in the same manner as in Example 1 to obtain purified locust bean gum. The obtained purified locust bean gum has an aqueous solution viscosity (25 ° C) of 33.
It was 00 cps. Of the resulting refined locust bean gum
Table 1 shows the changes over time in the viscosity of the aqueous solution (40 ° C.) when allowed to stand at 40 ° C.

【0018】[0018]

【比較例2】粗製タラガム240gを水20リットルに分散
し、85℃で1時間攪拌して溶解した。次にこの溶液を実
施例1と同様に処理して溶液のpHを5.8 に調整した。こ
の溶液の40℃放置での粘度変化を表1に示した。次にこ
の溶液を実施例1と同様に処理して精製タラガムを得
た。得られた精製タラガムの水溶液粘度(25℃)は2700
cps であった。得られた精製タラガムの40℃放置下での
水溶液粘度(40℃)の経時変化を表1に示した。
Comparative Example 2 240 g of crude tara gum was dispersed in 20 liters of water and dissolved by stirring at 85 ° C. for 1 hour. Next, this solution was treated in the same manner as in Example 1 to adjust the pH of the solution to 5.8. Table 1 shows the change in viscosity of this solution when allowed to stand at 40 ° C. Next, this solution was treated in the same manner as in Example 1 to obtain purified tara gum. The obtained purified cod gum has an aqueous solution viscosity (25 ° C) of 2700.
It was cps. Table 1 shows the time-dependent changes in aqueous solution viscosity (40 ° C.) of the obtained purified tara gum left at 40 ° C.

【0019】[0019]

【表1】[Table 1]

【0020】[0020]

【発明の効果】本発明の製造方法では、単糖類の添加に
よりガラクトマンナンの水溶液状態での粘度安定性に優
れ、透明性の高い、高品質の精製ガラクトマンナンを安
定して生産できるものである。
INDUSTRIAL APPLICABILITY According to the production method of the present invention, by adding a monosaccharide, it is possible to stably produce high-quality purified galactomannan having excellent viscosity stability in the aqueous solution state of galactomannan, high transparency. ..

【手続補正書】[Procedure amendment]

【提出日】平成4年5月28日[Submission date] May 28, 1992

【手続補正1】[Procedure Amendment 1]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0013[Correction target item name] 0013

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0013】[0013]

【実施例1】粗製ローカストビーンガム240gおよび
アラビノース20gを水20リットルに分散し、85℃
で1時間撹拌して溶解した。次に溶解液にクエン酸とリ
ン酸第2水素ナトリウムを加えて溶液のpHを5.8に
調整した。この溶液を40℃で放置したときの溶液の粘
度変化を表1に示した。次にpH調整後の溶液に濾過助
剤のパーライト240gを添加混合し、フィルタープレ
スで加圧濾過した。次に濾液に同容量のイソプロピルア
ルコールを添加して生成した沈殿を圧搾脱水し、乾燥、
粉砕して精製ローカストビーンガムを得た。得られた精
製ローカストビーンガムの水溶液粘度(25℃)は35
00cpsであった。
Example 1 240 g of crude locust bean gum and 20 g of arabinose were dispersed in 20 liters of water and the mixture was heated to 85 ° C.
It was dissolved by stirring for 1 hour. Next, citric acid and sodium dihydrogen phosphate were added to the solution to adjust the pH of the solution to 5.8. Table 1 shows the change in viscosity of the solution when the solution was allowed to stand at 40 ° C. Next, 240 g of perlite as a filter aid was added to and mixed with the solution after pH adjustment, and pressure filtration was performed with a filter press. Next, the same volume of isopropyl alcohol was added to the filtrate, the precipitate formed was squeezed and dehydrated, and dried,
It was crushed to obtain purified locust bean gum. The purified locust bean gum obtained had an aqueous solution viscosity (25 ° C.) of 35.
It was 00 cps.

【手続補正2】[Procedure Amendment 2]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0014[Correction target item name] 0014

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0014】[0014]

【実施例2】粗製ローカストビーン240gおよびキシ
ロース20gを水20リットルに分散し、85℃で1時
間撹拌して溶解した。次にこの溶液を実施例1と同様に
処理して溶液のpHを5.8に調整した。この溶液を4
0℃で放置したときの粘度変化を表1に示した。次にこ
の溶液を実施例1と同様に処理して精製ローカストビー
ンガムを得た。得られた精製ローカストビーンガムの水
溶液粘度(25℃)は3550cpsであった。
Example 2 240 g of crude locust bean and 20 g of xylose were dispersed in 20 liters of water and dissolved by stirring at 85 ° C. for 1 hour. Next, this solution was treated in the same manner as in Example 1 to adjust the pH of the solution to 5.8. Add this solution to 4
Table 1 shows the change in viscosity when left at 0 ° C. Next, this solution was treated in the same manner as in Example 1 to obtain purified locust bean gum. The aqueous solution viscosity (25 ° C.) of the obtained purified locust bean gum was 3550 cps.

【手続補正3】[Procedure 3]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0015[Correction target item name] 0015

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0015】[0015]

【実施例3】粗製ローカストビーンガム240gおよび
フルクトース20gを水20リットルに分散し、85℃
で1時間撹拌して溶解した。次にこの溶液を実施例1と
同様にして溶液のpHを5.8に調整した。この溶液を
40℃で放置したときの粘度変化を表1に示した。次に
この溶液を実施例1と同様に処理して精製ローカストビ
ーンガムを得た。得られた精製ローカストビーンガムの
水溶液粘度(25℃)は3400cpsであった。
[Example 3] 240 g of crude locust bean gum and 20 g of fructose were dispersed in 20 liters of water, and the mixture was heated to 85 ° C.
It was dissolved by stirring for 1 hour. Next, this solution was adjusted to pH 5.8 in the same manner as in Example 1. Table 1 shows the change in viscosity when the solution was left at 40 ° C. Next, this solution was treated in the same manner as in Example 1 to obtain purified locust bean gum. The aqueous solution viscosity (25 ° C.) of the obtained purified locust bean gum was 3400 cps.

【手続補正4】[Procedure amendment 4]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0016[Correction target item name] 0016

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0016】[0016]

【実施例4】粗製タラガム240gおよびアラビノース
20gを水20リットルに分散し、85℃で1時間撹拌
して溶解した。次に、この溶液を実施例1と同様に処理
して溶液のpHを5.8に調整した。この溶液を40℃
で放置したときの粘度変化を表1に示した。次に実施例
1と同様にこの溶液を処理して精製タラガムを得た。得
られた精製タラガムの水溶液粘度(25℃)は2900
cpsであった。
Example 4 240 g of crude tara gum and 20 g of arabinose were dispersed in 20 liters of water and dissolved by stirring at 85 ° C. for 1 hour. Next, this solution was treated in the same manner as in Example 1 to adjust the pH of the solution to 5.8. This solution at 40 ℃
Table 1 shows the change in viscosity when left to stand. Next, this solution was treated in the same manner as in Example 1 to obtain purified tara gum. The obtained purified cod gum has an aqueous solution viscosity (25 ° C.) of 2900.
It was cps.

【手続補正5】[Procedure Amendment 5]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0017[Correction target item name] 0017

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0017】[0017]

【比較例1】粗製ローカストビーンガム240gを水2
0リットルに分散し、85℃で1時間撹拌して溶解し
た。次にこの溶解液にクエン酸とリン酸第2水素ナトリ
ウムを加えて溶液のpHを5.8に調整した。この溶液
の40℃放置での粘度変化を表1に示した。次にこの溶
液を実施例1と同様に処理して精製ローカストビーンガ
ムを得た。得られた精製ローカストビーンガムの水溶液
粘度(25℃)は3300cpsであった。
Comparative Example 1 240 g of crude locust bean gum was added to 2 parts of water.
It was dispersed in 0 liter and dissolved by stirring at 85 ° C. for 1 hour. Next, citric acid and sodium dihydrogen phosphate were added to this solution to adjust the pH of the solution to 5.8. Table 1 shows the change in viscosity of this solution when allowed to stand at 40 ° C. Next, this solution was treated in the same manner as in Example 1 to obtain purified locust bean gum. The aqueous solution viscosity (25 ° C.) of the obtained purified locust bean gum was 3300 cps.

【手続補正6】[Procedure correction 6]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0018[Correction target item name] 0018

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0018】[0018]

【比較例2】粗製タラガム240gを水20リットルに
分散し、85℃で1時間撹拌して溶解した。次にこの溶
液を実施例1と同様に処理して溶液のpHを5.8に調
整した。この溶液の40℃放置での粘度変化を表1に示
した。次にこの溶液を実施例1と同様に処理して精製タ
ラガムを得た。得られた精製タラガムの水溶液粘度(2
5℃)は2700cpsであった。
Comparative Example 2 240 g of crude tara gum was dispersed in 20 liters of water and dissolved by stirring at 85 ° C. for 1 hour. Next, this solution was treated in the same manner as in Example 1 to adjust the pH of the solution to 5.8. Table 1 shows the change in viscosity of this solution when allowed to stand at 40 ° C. Next, this solution was treated in the same manner as in Example 1 to obtain purified tara gum. Aqueous solution viscosity (2
5 ° C.) was 2700 cps.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 粗製ガラクトマンナンに単糖類を添加し
た水溶液から、不溶解物質を濾過除去し、該濾液からガ
ラクトマンナンを回収することを特徴とする精製ガラク
トマンナンの製造方法。
1. A method for producing purified galactomannan, which comprises removing insoluble substances by filtration from an aqueous solution obtained by adding a monosaccharide to crude galactomannan, and recovering galactomannan from the filtrate.
【請求項2】 単糖類がアラビノース、キシロース、フ
ルクトース、ガラクトース、グルコース、マンノースか
ら選ばれた少なくとも1種のものであることを特徴とす
る請求項1記載の精製ガラクトマンナンの製造方法。
2. The method for producing purified galactomannan according to claim 1, wherein the monosaccharide is at least one selected from arabinose, xylose, fructose, galactose, glucose and mannose.
JP7880992A 1992-03-02 1992-03-02 Method for producing purified galactomannan Expired - Fee Related JP2729722B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7880992A JP2729722B2 (en) 1992-03-02 1992-03-02 Method for producing purified galactomannan

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7880992A JP2729722B2 (en) 1992-03-02 1992-03-02 Method for producing purified galactomannan

Publications (2)

Publication Number Publication Date
JPH05239106A true JPH05239106A (en) 1993-09-17
JP2729722B2 JP2729722B2 (en) 1998-03-18

Family

ID=13672176

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7880992A Expired - Fee Related JP2729722B2 (en) 1992-03-02 1992-03-02 Method for producing purified galactomannan

Country Status (1)

Country Link
JP (1) JP2729722B2 (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11308973A (en) * 1998-04-27 1999-11-09 Nisshin Oil Mills Ltd:The Locust bean gum having high viscosity and its production
WO2005073255A1 (en) * 2004-01-30 2005-08-11 Toho Chemical Industry Co., Ltd. Cation-modified purified galactomannan polysaccharide and cosmetic composition containing the substance
JP2008109941A (en) * 2008-01-23 2008-05-15 Nisshin Oillio Group Ltd High viscosity locust bean gum and method for producing the same
US7408057B2 (en) 2000-07-03 2008-08-05 Marine Bioproducts Intenational Clarified hydrocolloids of undiminished properties and method of producing same
US8536325B2 (en) 2009-02-05 2013-09-17 Alcon Research, Ltd. Process for purifying guar
US9175249B2 (en) 2009-07-07 2015-11-03 Alcon Research, Ltd. Ethyleneoxide butyleneoxide block copolymer compositions

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11308973A (en) * 1998-04-27 1999-11-09 Nisshin Oil Mills Ltd:The Locust bean gum having high viscosity and its production
US7408057B2 (en) 2000-07-03 2008-08-05 Marine Bioproducts Intenational Clarified hydrocolloids of undiminished properties and method of producing same
WO2005073255A1 (en) * 2004-01-30 2005-08-11 Toho Chemical Industry Co., Ltd. Cation-modified purified galactomannan polysaccharide and cosmetic composition containing the substance
JP2008109941A (en) * 2008-01-23 2008-05-15 Nisshin Oillio Group Ltd High viscosity locust bean gum and method for producing the same
US8536325B2 (en) 2009-02-05 2013-09-17 Alcon Research, Ltd. Process for purifying guar
US9175249B2 (en) 2009-07-07 2015-11-03 Alcon Research, Ltd. Ethyleneoxide butyleneoxide block copolymer compositions

Also Published As

Publication number Publication date
JP2729722B2 (en) 1998-03-18

Similar Documents

Publication Publication Date Title
DE69617088T2 (en) Process for the preparation of crystallized maltitol and crystallines containing it.
AU2001282708B2 (en) Cold water soluble beta-glucan product and process for preparing the same
CN105418783A (en) Bletilla striata polysaccharide extraction and purification method
DE69227621T2 (en) Process for refining zein
JP2003201497A (en) Method of production for concentrated lutein fatty acid ester
JPH05239106A (en) Production of purified galactomannan
CH496093A (en) Cyclodextrins complexing agents for foodstuffs tobacco
JPH05239105A (en) Production of purified galactomannan
US2520161A (en) Carboxyalkyl ethers of carbohydrate gums
JP3055565B2 (en) Cyclodextrin purification process
JPS6335606A (en) Purification of galactomannan
EP0747344B1 (en) Process for the purification and crystallisation of iopamidol
JPS62247802A (en) Crystallization method
CN113004366A (en) Novel method for producing diammonium glycyrrhizinate
JPH05401B2 (en)
JPH0615563B2 (en) Pectin purification method
KR950004899B1 (en) Process for preparing moranoline derivatives
JP2017088804A (en) Manufacturing method of purified water soluble seed-based polysaccharide
JPS63105004A (en) Purification of locust beam gum
JP4548764B2 (en) Method for producing low viscosity galactomannan
JPS6176502A (en) Production of partially amidated pectin
CN110214932B (en) High-temperature-resistant sodium carboxymethyl cellulose and preparation method thereof
JP3120155B2 (en) Processing method of raw fried soy sauce without burning
JPH04131051A (en) Production of thick malt syrup
JPH0689044B2 (en) How to clarify gum arabic

Legal Events

Date Code Title Description
FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20071219

Year of fee payment: 10

FPAY Renewal fee payment (prs date is renewal date of database)

Year of fee payment: 11

Free format text: PAYMENT UNTIL: 20081219

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20091219

Year of fee payment: 12

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20091219

Year of fee payment: 12

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20101219

Year of fee payment: 13

FPAY Renewal fee payment (prs date is renewal date of database)

Year of fee payment: 13

Free format text: PAYMENT UNTIL: 20101219

FPAY Renewal fee payment (prs date is renewal date of database)

Year of fee payment: 14

Free format text: PAYMENT UNTIL: 20111219

FPAY Renewal fee payment (prs date is renewal date of database)

Year of fee payment: 14

Free format text: PAYMENT UNTIL: 20111219

LAPS Cancellation because of no payment of annual fees