JPH025842A - Production of purified beverage or raw material thereof - Google Patents
Production of purified beverage or raw material thereofInfo
- Publication number
- JPH025842A JPH025842A JP63151739A JP15173988A JPH025842A JP H025842 A JPH025842 A JP H025842A JP 63151739 A JP63151739 A JP 63151739A JP 15173988 A JP15173988 A JP 15173988A JP H025842 A JPH025842 A JP H025842A
- Authority
- JP
- Japan
- Prior art keywords
- hydrolyzed
- protein
- molecular weight
- ultrafiltration membrane
- proteins
- 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.)
- Pending
Links
- 235000013361 beverage Nutrition 0.000 title claims abstract description 17
- 239000002994 raw material Substances 0.000 title claims abstract description 10
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 102000004169 proteins and genes Human genes 0.000 claims abstract description 27
- 108090000623 proteins and genes Proteins 0.000 claims abstract description 27
- 238000000108 ultra-filtration Methods 0.000 claims abstract description 14
- 239000012528 membrane Substances 0.000 claims abstract description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000002904 solvent Substances 0.000 claims abstract 2
- 239000007864 aqueous solution Substances 0.000 abstract description 10
- 239000000243 solution Substances 0.000 abstract description 5
- 102000008186 Collagen Human genes 0.000 abstract description 4
- 108010035532 Collagen Proteins 0.000 abstract description 4
- 229920001436 collagen Polymers 0.000 abstract description 4
- 239000002244 precipitate Substances 0.000 abstract description 4
- 235000010469 Glycine max Nutrition 0.000 abstract description 3
- 244000068988 Glycine max Species 0.000 abstract description 3
- 241000209140 Triticum Species 0.000 abstract description 3
- 235000021307 Triticum Nutrition 0.000 abstract description 3
- 235000013336 milk Nutrition 0.000 abstract description 2
- 239000008267 milk Substances 0.000 abstract description 2
- 210000004080 milk Anatomy 0.000 abstract description 2
- 239000003531 protein hydrolysate Substances 0.000 abstract description 2
- 235000018102 proteins Nutrition 0.000 description 25
- 238000000034 method Methods 0.000 description 12
- 238000001556 precipitation Methods 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 5
- 108010082495 Dietary Plant Proteins Proteins 0.000 description 4
- 241001465754 Metazoa Species 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000012460 protein solution Substances 0.000 description 4
- 238000001914 filtration Methods 0.000 description 3
- 230000003301 hydrolyzing effect Effects 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 244000144725 Amygdalus communis Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 108091005804 Peptidases Proteins 0.000 description 2
- 102000035195 Peptidases Human genes 0.000 description 2
- 108010073771 Soybean Proteins Proteins 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 235000020224 almond Nutrition 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 230000002335 preservative effect Effects 0.000 description 2
- 235000011437 Amygdalus communis Nutrition 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 108090000526 Papain Proteins 0.000 description 1
- 102000057297 Pepsin A Human genes 0.000 description 1
- 108090000284 Pepsin A Proteins 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 102000004142 Trypsin Human genes 0.000 description 1
- 108090000631 Trypsin Proteins 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 229940088598 enzyme Drugs 0.000 description 1
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 235000013402 health food Nutrition 0.000 description 1
- 239000012510 hollow fiber Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 229940055729 papain Drugs 0.000 description 1
- 235000019834 papain Nutrition 0.000 description 1
- 229940111202 pepsin Drugs 0.000 description 1
- 235000021118 plant-derived protein Nutrition 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 229940001941 soy protein Drugs 0.000 description 1
- 235000019710 soybean protein Nutrition 0.000 description 1
- 239000012588 trypsin Substances 0.000 description 1
- 229960001322 trypsin Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Landscapes
- Non-Alcoholic Beverages (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は透明飲料又はその原料の加水分解蛋白質であっ
て、潜在的不溶化成分を除去したものの製法に間する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention is directed to a process for producing a transparent beverage or a hydrolyzed protein from its raw material, from which potentially insolubilized components have been removed.
[従来の技術・発明が解決しようとする問題点]飲料又
はその原料である加水分解蛋白質とじて、動物起源のも
のおよび植物起源のものが使用されている。[Prior Art/Problems to be Solved by the Invention] As beverages or hydrolyzed proteins as raw materials thereof, those of animal origin and those of plant origin are used.
前記動物起源のものの具体例としては、コラーゲン、牛
乳、鶏卵などの蛋白質の加水分解物、また植物起源のも
のの具体例としては、大豆、小麦、トウモロコシ、アー
モンドなどの蛋白質の加水分解物が知られている。叉、
植物油脂のしぼり粕は一般に蛋白質から見れば濃縮され
た形になっているので本願の加水分解原料になるものが
ある。Specific examples of the animal-derived proteins include hydrolysates of proteins such as collagen, milk, and chicken eggs, and specific examples of plant-derived proteins include hydrolysates of proteins such as soybean, wheat, corn, and almonds. ing. Fork,
Since the squeezed lees of vegetable oils and fats are generally concentrated in terms of protein, some of them can be used as raw materials for hydrolysis in the present application.
これら飲料配合用の加水分解蛋白質は、通常、水を主体
とする溶液(以下、水性溶液という)または乾燥個体(
粉末)として市場に供給されているが、固体のばあいで
も飲料に配合されるときには水性溶液として使用される
。これらの水性溶液は飲料の均一性を維持し、また商品
価値を高めるため、長間間保存しても透明で、曇リ、に
ごり、沈澱なとの生しないことが必要である。さらにこ
れを配合した飲料においても、とくにその飲料が透明な
製品であるばあいには、長期間透明であることが要求さ
れる。These hydrolyzed proteins for beverage formulation are usually prepared in solutions mainly composed of water (hereinafter referred to as aqueous solutions) or dried solids (
It is supplied on the market as a powder (powder), but even in solid form it is used as an aqueous solution when added to drinks. In order to maintain the uniformity of the beverage and increase its commercial value, these aqueous solutions must be transparent and free from cloudiness, turbidity, and sedimentation even after long-term storage. Furthermore, even in beverages containing this, especially if the beverage is a transparent product, it is required to remain transparent for a long period of time.
しかし、従来市場に供給されている加水分解蛋白質また
はその誘導体は、製造時に濾過された際には透明なもの
でも、1〜6力月程度保存すれば沈澱が生じるものが多
く、飲料原料としての商品価値も下がり、飲料に配合す
るにも制限のあるものである。However, even if the hydrolyzed proteins or their derivatives conventionally supplied on the market are transparent when filtered during production, they tend to form precipitates after being stored for 1 to 6 months, making them difficult to use as beverage ingredients. The product value has also decreased, and there are restrictions on its inclusion in beverages.
このようなにごり、沈澱などが生じる規1象は、一般に
加水分解蛋白質の平均外資料が大きい程著しく、また植
物性蛋白質起源のものがコラーゲンなとを起源とするも
のより著しいことが知られている。It is known that the phenomenon of cloudiness, precipitation, etc., is generally more pronounced as the average deviation of the hydrolyzed protein is larger, and it is known that it is more pronounced when the hydrolyzed protein is derived from vegetable protein than when it is derived from collagen. There is.
このにごり、沈澱などは濾過すればその時点では透明に
なるが、1〜6力月経過すれはまた発生し、再び濾過し
てもまた発生し、際限がなく、根本的に長期間透明を維
持しうる加水分解蛋白質を製造することは非常に困難で
ある。This cloudiness and precipitate will become transparent when filtered, but they will appear again after 1 to 6 months have passed, and even if you filter them again, they will appear again.There is no limit to this, and fundamentally they remain transparent for a long time. It is very difficult to produce hydrolyzed proteins that can be used.
なお、天然の蛋白質を加水分解させろ方法としては、酸
、アルカリまたは蛋白分解酵素により加水分解する方法
が知られている。Note that as a method for hydrolyzing natural proteins, methods of hydrolyzing with acid, alkali, or proteolytic enzyme are known.
[問題点を解決するための手段]
本発明は前記のごとき加水分解蛋白質を水性溶液として
保存したばあいに生じる頑固なにごり、沈澱などの問題
を解決するためになされたちのでてあり、加水分解蛋白
質を分画分子量2000〜200.000の限外濾過膜
で濾過し、潜在的不溶化成分を除去することを特徴とす
るM製された飲料又はその原料の製法に閏ずろ。[Means for Solving the Problems] The present invention has been made in order to solve the problems such as stubborn cloudiness and precipitation that occur when hydrolyzed proteins as described above are stored as an aqueous solution. A method for producing M-made beverages or raw materials thereof, characterized in that proteins are filtered through an ultrafiltration membrane with a molecular weight cutoff of 2000-200.000 to remove potential insolubilized components.
本発明における加水分解蛋白質溶液とは、従来より飲料
及びその原料として使用されている加水分解蛋白質のこ
とであり、飲料又はその原料として使用しろるものであ
る限りとくに限定はない。The hydrolyzed protein solution in the present invention refers to a hydrolyzed protein that has conventionally been used as a beverage or its raw material, and is not particularly limited as long as it can be used as a beverage or its raw material.
このような加水分解蛋白質溶液の具体例としては、 [
従来の技術・発明が解決しようとする問題点]の項に記
載したような動物性や植物性の蛋白質の加水分解物の溶
液があげられる。Specific examples of such hydrolyzed protein solutions include [
Examples include solutions of animal or vegetable protein hydrolysates as described in the section ``Prior Art/Problems to be Solved by the Invention''.
上記のごとき加水分解蛋白質は、通常、酸やアルカリ、
さらにはペプシン、パパイン、トリプシンなど及び各種
菌起源の蛋白分解酵素により動物性や植物性の蛋白質を
常法により加水分解することにより、えられる。Hydrolyzed proteins such as those mentioned above are usually treated with acids, alkalis,
Furthermore, it can be obtained by hydrolyzing animal or vegetable proteins in a conventional manner using pepsin, papain, trypsin, or other proteolytic enzymes derived from various bacteria.
本明細書にいう潜在的な不溶化成分とは、加水分解蛋白
質を一度濾過したものを、そのまままたは飲料に配合し
て透明な飲料を製造して保存しておくと、経時的に不溶
化して曇りや沈澱などの原因になる成分のことである。In this specification, potential insolubilized components refer to hydrolyzed proteins that have been filtered and are stored as they are or added to a drink to produce a clear drink, which becomes insolubilized over time and becomes cloudy. It is a component that causes precipitation, etc.
本発明者らの研究の結果、この成分は主として加水分解
によって充分分解しなかった分子量の高い成分からなり
、−時的に水を主体とする溶媒に溶解しても会合などに
より経時的に不溶イヒする成分であることが判明してい
る。又、植物性蛋白質を原料とするものでは精製で除去
できなかった少量の多糖類も沈澱に影響する。この不溶
化現象は、保存の時間、温度、PH5平均分子量、他成
分の存在などによって影響され、そのしくみはmlで充
分解明されていないが、いずれにしても加水分解蛋白質
溶液を限外濾過することにより潜在的不溶化成分を除去
しろろ。もちろん、この限外濾過によって顕在不溶成分
(曇り、沈澱などとして目に見える成分)も同時に除去
しろるが、これは通常の濾過(たとえば濾過助剤と濾紙
による濾過)によっても除去できる。As a result of the research conducted by the present inventors, this component mainly consists of high molecular weight components that were not sufficiently decomposed by hydrolysis; It has been found that it is an irritating ingredient. In addition, in products made from vegetable proteins, small amounts of polysaccharides that cannot be removed by purification also affect precipitation. This insolubilization phenomenon is affected by storage time, temperature, PH5 average molecular weight, presence of other components, etc., and its mechanism has not been fully elucidated in terms of ml, but in any case, it is important to ultrafiltrate a hydrolyzed protein solution. Remove potentially insolubilized components. Of course, this ultrafiltration also removes visible insoluble components (components visible as cloudiness, precipitate, etc.), but these can also be removed by conventional filtration (for example, filtration with a filter aid and filter paper).
本発明に使用する限外濾過膜の分画分子量(排除限界分
子りは2.000〜200.000ものであり、+0,
000〜too、ooo程度のものがとくに好ましい。The molecular weight cutoff (exclusion limit molecular weight is 2.000 to 200.000, +0,
Particularly preferred are those of the order of 000 to too or ooo.
なお、限外濾過膜と称していなくても上記分画分子量を
有する膜は本発明における限外濾過膜の概念に含まれろ
ものである。Incidentally, even if not called an ultrafiltration membrane, a membrane having the above molecular weight cut-off is included in the concept of an ultrafiltration membrane in the present invention.
前記分画分子量が2000未満のように小さくなり過ぎ
ると、通過時間が長く収率が低下するとともに、限外濾
過物の感触がねばりの小さいものになる。また分画分子
量が200.000をこえると、潜在不溶成分の除去が
充分でなくなる。実際には個々の加水分解蛋白質につい
て、ilを過速度、収率、限外濾過液の不溶物析出安定
性などを見て適した限外′IIl過膜を選んで使用する
のが好ましい。If the molecular weight cut-off is too small, such as less than 2,000, the passage time will be long, the yield will be low, and the ultrafiltrate will have a sticky feel. Furthermore, if the molecular weight cutoff exceeds 200,000, the removal of latent insoluble components will not be sufficient. In practice, it is preferable to select and use a suitable ultra'II filtration membrane for each hydrolyzed protein, taking into account the IL overrate, yield, stability of insoluble matter precipitation in the ultrafiltrate, etc.
限外濾過膜を構成する材質にはとくに限定はなく、たと
えばポリスルホン、ポリアクリロニトル、ボ+7エチレ
ン系ポリマー 親水性ポリオレフィン、セルローズ、酢
酸セルローズなと、通常限外濾過膜を形成するのに使用
される材質であれば限定なく使用しうるが、水系の溶媒
を使用するので親水性の材質であるのが好ましい。There are no particular limitations on the materials that make up the ultrafiltration membrane, and examples of materials that are commonly used to make the ultrafiltration membrane include polysulfone, polyacrylonitrile, polyethylene polymer, hydrophilic polyolefin, cellulose, and cellulose acetate. Any material can be used without limitation, but since an aqueous solvent is used, a hydrophilic material is preferable.
限外濾過膜の形状にもとくに限定はなく、たとえば平瞑
、プリーツ、スパイラル、チューブ中空糸など、各種形
状のものが使用されうる。There is no particular limitation on the shape of the ultrafiltration membrane, and various shapes such as flat, pleated, spiral, and hollow fiber tubes can be used.
限外濾過の条件にはとくに限定はなく、通常の条件、た
とえば40%(重量%、以下同様)以下、好ましくは3
〜30%の濃度の加水分解蛋白質溶液を50〜80°C
以下の温度、1〜5にz/Cm2のごとき条件が採用さ
れる。There are no particular limitations on the conditions for ultrafiltration, and the usual conditions, for example, 40% (wt%, same hereinafter) or less, preferably 3%
~30% concentration hydrolyzed protein solution at 50-80°C
Conditions such as z/Cm2 are adopted for temperatures 1 to 5 below.
飲料に配合するための加水分解蛋白質が市場に供給され
るばあい、乾燥固体(粉末)の形状のものも多いが、こ
のばあいには乾燥固形化する前の溶液状態で本発明の方
法を実施しておけば、乾燥固体を溶液にする際に溶解さ
せやすく、不溶分が生し難くなり有効で、あるが、限外
濾過していない乾燥固体を溶解させ濃縮液又は飲料製品
にしてから限外濾過した方が有効性は高い。When hydrolyzed proteins for blending into beverages are supplied on the market, they are often in the form of dry solids (powders), but in this case, the method of the present invention can be carried out in a solution state before drying and solidifying. If you do this, it will be easier to dissolve the dry solids when making them into a solution, and it will be less likely to produce insoluble matter, which is effective. Ultrafiltration is more effective.
本発明における飲料は通常の補水のための飲料、嗜好品
としての飲料、(3*康食品、医薬部外品、及び医薬等
、飲用できるものすべてを含む。Beverages in the present invention include all drinks that can be drunk, such as ordinary drinks for rehydration, drinks for luxury foods, (3* health foods, quasi-drugs, and medicines).
つぎに本発明の方法を実施例に基づき、さらに詳細に説
明する。Next, the method of the present invention will be explained in more detail based on Examples.
実施例1〜5および比較例1〜2
脱脂大豆粉を水中で酵素によって加水分解したのち濾過
助剤(珪藻土)と濾紙とを使用して濾過し、平均分子竜
約4000の透明な加水分解蛋白質の水溶液(濃度20
%)を得た(比較例1)。Examples 1 to 5 and Comparative Examples 1 to 2 Defatted soybean flour was hydrolyzed in water with an enzyme and then filtered using a filter aid (diatomaceous earth) and filter paper to obtain a transparent hydrolyzed protein with an average molecular weight of about 4000. aqueous solution (concentration 20
%) (Comparative Example 1).
得られた水溶液を温度30°C1圧力3にg/cm2で
第1表に示す6種の限外濾過膜を用いて限外濾過し、6
種の限外濾過液を得た〈実施例1−5及び比較例2)。The obtained aqueous solution was ultrafiltered at a temperature of 30°C and a pressure of 3g/cm2 using six types of ultrafiltration membranes shown in Table 1.
A seed ultrafiltrate was obtained (Examples 1-5 and Comparative Example 2).
得られた水溶液および限外濾過液それぞれの濃度、製造
直後、1力月後および6力月後の色調(ガードナーナン
バー)、ならびに透明性(目視観察)を調べた。結果を
第1表に示す。The resulting aqueous solution and ultrafiltrate were examined for their respective concentrations, color tone (Gardner number) immediately after production, one month later, and six months later, and transparency (visual observation). The results are shown in Table 1.
なお、ガードナーナンバーは、日本油化学協会制定の色
(ガードナー法)に記載された方法て測定した。The Gardner number was measured by the method described in the color (Gardner method) established by the Japan Oil Chemists' Association.
第1表の結果から、本発明の方法により製造したものは
6力月間保存後も曇りや沈澱が生じず、色調も淡く、優
れていることがわかる。又、比較例2から分画分子量2
00.000を越える膜では効果が劣ることがわかる。From the results in Table 1, it can be seen that the products produced by the method of the present invention do not develop cloudiness or precipitation even after storage for 6 months, and have a light color tone, which is excellent. Also, from Comparative Example 2, molecular weight cutoff 2
It can be seen that the effect is poor in films exceeding 00.000.
実施例6および比較例3
下記A、 B、 Cの加水分解蛋白質の15%水性
溶液のそれぞれの通常濾過物を、実施例3で用いた限外
濾過膜(分画分子f150.0oo)を使用1−。Example 6 and Comparative Example 3 The normal filtrate of each of the following 15% aqueous solutions of hydrolyzed proteins A, B, and C was filtered using the ultrafiltration membrane (fraction molecule f150.0oo) used in Example 3. 1-.
て、温度25°C1圧力3.’5Kj!/cm2で限外
濾過した。temperature 25°C1 pressure 3. '5Kj! /cm2.
えられた限外濾過後(実施例6)および通常濾過物(比
較例3)それぞれの製造直後、1力月後および6力月後
の透明性を比較した。結果を第2表に示す。なお全サン
プルに防腐剤としてソルビン酸r4@を添加した。The transparency of the resulting ultrafiltrated product (Example 6) and normal filtrate (Comparative Example 3) immediately after production, 1 month, and 6 months after production were compared. The results are shown in Table 2. In addition, sorbic acid r4@ was added to all samples as a preservative.
A:加水分解コラーゲン(平均分+ t 10.000
)B:加水分解小麦蛋白質(平均分子@I 、!’1o
O)C:加水分解アーモンド蛋白質
(平均分子量2.000)
第2表の結果からも本発明の方法が有効であることがわ
かる。A: Hydrolyzed collagen (average + t 10.000
) B: Hydrolyzed wheat protein (average molecule @I,!'1o
O) C: Hydrolyzed almond protein (average molecular weight 2.000) The results in Table 2 also show that the method of the present invention is effective.
実施例7
実施例2て得られた加水分解大豆蛋白を使用して次の処
方で健康飲料を作った。Example 7 A health drink was prepared using the hydrolyzed soybean protein obtained in Example 2 according to the following formulation.
加水分解大豆蛋白(固形分として)10(@f1%)エ
タノール ・ 0.5砂糖
5
ヒタミンC(Na基塩12を含む)0.1食添用防腐剤
微竜
精製水を加えた全型 100この製品は透
明であり製造から6力月後も透明性に変化はなかった。Hydrolyzed soy protein (as solid content) 10 (@f1%) Ethanol / 0.5 sugar
5 Hitamine C (contains 12 Na base salts) 0.1 Preservative for food additives All types with Weilong purified water added 100 This product is transparent and there was no change in transparency 6 months after manufacture.
父、飲料としての味にも殆ど変化がなく良好であった。The taste as a drink was also good with almost no change.
[発明の効果]
本発明の方法によらない加水分解蛋白質の水性溶液は、
初め透明であってもほとんどのばあい1週間から6力月
の間に、わずかな曇りを生じるものから明らかな沈澱を
生じるものまで程度の差こそあれ透明性が失われる。[Effect of the invention] An aqueous solution of a hydrolyzed protein that is not produced by the method of the present invention has the following properties:
Even if it is initially transparent, in most cases it will lose its transparency to varying degrees between a week and six months, ranging from slight clouding to obvious precipitation.
しかし、加水分解蛋白質から本発明の方法により潜在的
不溶化成分を除去した飲料又はその原料は、長時間(た
とえば6力月)経過後も曇り、沈澱などを生じることな
く透明である。そのうえ、その色調も本発明の方法を適
用しないものと比べて明らかに淡色であり優れている。However, beverages or their raw materials from which potentially insolubilized components have been removed from hydrolyzed proteins by the method of the present invention remain transparent without clouding or precipitation even after a long period of time (for example, 6 months). Furthermore, the color tone is clearly lighter and superior than that of a sample to which the method of the present invention is not applied.
Claims (1)
を分画分子量2000〜200,000の限外濾過膜で
濾過し、潜在的不溶化成分を除去することを特徴とする
精製された透明飲料又はその原料の製造法。1. A purified transparent beverage characterized in that a solution of hydrolyzed protein dissolved in a solvent mainly composed of water is filtered through an ultrafiltration membrane with a molecular weight cutoff of 2000 to 200,000 to remove potential insolubilized components. or the manufacturing method of its raw materials.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63151739A JPH025842A (en) | 1988-06-20 | 1988-06-20 | Production of purified beverage or raw material thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63151739A JPH025842A (en) | 1988-06-20 | 1988-06-20 | Production of purified beverage or raw material thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH025842A true JPH025842A (en) | 1990-01-10 |
Family
ID=15525228
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63151739A Pending JPH025842A (en) | 1988-06-20 | 1988-06-20 | Production of purified beverage or raw material thereof |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH025842A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04267865A (en) * | 1991-02-21 | 1992-09-24 | Asahi Breweries Ltd | Soft drink |
JP2017216890A (en) * | 2016-06-03 | 2017-12-14 | アサヒ飲料株式会社 | Acidic milk-containing highly refined beverage and method for preventing white turbidness of acidic milk-containing highly refined beverage |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59205966A (en) * | 1983-04-21 | 1984-11-21 | ヘキスト・アクチエンゲゼルシヤフト | Protein fortified beverage |
-
1988
- 1988-06-20 JP JP63151739A patent/JPH025842A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59205966A (en) * | 1983-04-21 | 1984-11-21 | ヘキスト・アクチエンゲゼルシヤフト | Protein fortified beverage |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04267865A (en) * | 1991-02-21 | 1992-09-24 | Asahi Breweries Ltd | Soft drink |
JP2017216890A (en) * | 2016-06-03 | 2017-12-14 | アサヒ飲料株式会社 | Acidic milk-containing highly refined beverage and method for preventing white turbidness of acidic milk-containing highly refined beverage |
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