JP2545074B2 - Method of manufacturing emulsified material - Google Patents

Method of manufacturing emulsified material

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Publication number
JP2545074B2
JP2545074B2 JP62041510A JP4151087A JP2545074B2 JP 2545074 B2 JP2545074 B2 JP 2545074B2 JP 62041510 A JP62041510 A JP 62041510A JP 4151087 A JP4151087 A JP 4151087A JP 2545074 B2 JP2545074 B2 JP 2545074B2
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JP
Japan
Prior art keywords
phospholipids
phospholipase
phospholipid
present
protein
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.)
Expired - Lifetime
Application number
JP62041510A
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Japanese (ja)
Other versions
JPS63209742A (en
Inventor
一夫 押田
圭子 高橋
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QP Corp
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QP Corp
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Publication of JPS63209742A publication Critical patent/JPS63209742A/en
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  • Seasonings (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
  • General Preparation And Processing Of Foods (AREA)

Description

【発明の詳細な説明】 <産業上の利用分野> 本発明は乳化材の製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION <Field of Industrial Application> The present invention relates to a method for producing an emulsified material.

<従来の技術> 従来から、乳化材としてリン脂質をホスフォリパーゼ
A2で処理して得られるリゾ型リン脂質をかなりの割合で
含んだリン脂質、つまりリゾ型含有リン脂質が知られて
いる。このリゾ型含有リン脂質はリゾ型を含まないリン
脂質そのものよりは一段と乳化力が高いとされている。
<Prior art> Phospholipase has been used as an emulsifying agent for the past time.
Phospholipids containing lyso-type phospholipids obtained by treating with A2 in a considerable proportion, that is, lyso-type phospholipids are known. This lyso-type phospholipid is said to have much higher emulsifying power than the phospholipid itself which does not contain the lyso type.

<発明が解決しようとする問題点> しかし、前記従来のリゾ型含有リン脂質は、その乳化
力が必ずしも満足なものとは云えなかった。
<Problems to be Solved by the Invention> However, it cannot be said that the conventional lyso-type phospholipids have satisfactory emulsifying power.

本発明は前記従来技術の問題点を解決するものであ
り、リゾ型含有リン脂質を含むが、従来のリゾ型含有リ
ン脂質そのものより一段と高い乳化力をもつ乳化材の製
造方法を提供することを目的とする。
The present invention is to solve the above-mentioned problems of the prior art, and includes a lyso-type phospholipid, but to provide a method for producing an emulsifying material having a much higher emulsifying power than the conventional lyso-type phospholipid itself. To aim.

<問題点を解決するための手段> 本発明者らは前記目的を達成するために種々検討を重
ねた結果、リン脂質を蛋白質存在下でホスフォリパーゼ
A2で処理し、さらに乾燥することで得られたものは蛋白
質を共存させないでリン脂質をホスフォリパーゼA2で処
理して得られたものに比べて乳化力が一段と高くなるこ
とを知見した。かかる知見に基づく本発明の乳化材の製
造方法は、リン脂質の水懸濁液を食用蛋白質(但し、グ
ルテンおよび卵黄蛋白は除く。)存在下でホスフォリパ
ーゼA2で処理し、さらに乾燥することを特徴とするもの
である。
<Means for Solving Problems> As a result of various studies to achieve the above-mentioned object, the present inventors have found that phospholipids are added to phospholipase in the presence of protein.
It was found that the one obtained by treating with A2 and further drying has a much higher emulsifying power than the one obtained by treating phospholipids with phospholipase A2 in the absence of protein. According to the method for producing an emulsifying material of the present invention based on such findings, an aqueous suspension of phospholipids is treated with phospholipase A2 in the presence of edible proteins (excluding gluten and egg yolk proteins), and further dried. It is characterized by.

以下、本発明を詳細に説明する。 Hereinafter, the present invention will be described in detail.

本発明でリン脂質とは、その給源は問わず、例えば大
豆リン脂質、卵黄リン脂質あるいは動物(牛、ヒツジ、
ブタ、ニワトリなど)の脳のリン脂質などをいい、その
形態は固形状、粉末状、あるいは液状などいずれでもよ
い。なお、上述したリン脂質の中では大豆リン脂質が安
価で使用しやすい。
The phospholipid in the present invention may be any source, for example, soybean phospholipid, egg yolk phospholipid or animal (cow, sheep,
Phospholipids of the brain of pigs, chickens, etc.), which may be in the form of solid, powder or liquid. Among the above-mentioned phospholipids, soybean phospholipid is inexpensive and easy to use.

また本発明でリン脂質の水懸濁液とは、リン脂質が水
に懸濁した液をいい、ここでの懸濁の意味はリン脂質の
粒子が水に分散している状態の他にリン脂質が水に溶解
している場合も含むものである。水懸濁液中のリン脂質
の割合は、普通には固形分として5〜20%ぐらいが適当
である。すなわち、固形リン脂質の場合、その1重量部
を5〜20倍重量部の水に分散または溶解すればよい。
In the present invention, the aqueous suspension of phospholipids refers to a liquid in which phospholipids are suspended in water. It also includes the case where the lipid is dissolved in water. The proportion of phospholipid in the water suspension is usually about 5 to 20% as solid content. That is, in the case of solid phospholipid, 1 part by weight thereof may be dispersed or dissolved in 5 to 20 parts by weight of water.

本発明では、このようなリン脂質の水懸濁液を蛋白質
存在下でホスフォリパーゼA2で処理する。つまり、リン
脂質の水懸濁液に蛋白質を混和してホスフォリパーゼA2
で処理する。
In the present invention, such an aqueous suspension of phospholipid is treated with phospholipase A2 in the presence of protein. In other words, phospholipase A2 was obtained by mixing proteins with an aqueous suspension of phospholipids.
To process.

ここで用いることができる食用蛋白質としては、アル
ブミン、グロブリン、ゼラチン、カゼイン、グリアジ
ン、これらの混合物あるいは、卵蛋白(アルブミン52
%、グロブリン8〜10%)、大豆蛋白(グロブリン84
%、アルブミン5.3%)、小麦タンパク(グリアジンな
どからなる)などがあげられる。また、この蛋白質は液
状原料の他に粉末原料を用いてもよい。
Examples of the edible protein that can be used here include albumin, globulin, gelatin, casein, gliadin, a mixture thereof, or egg protein (albumin 52
%, Globulin 8-10%), soy protein (globulin 84
%, Albumin 5.3%), wheat protein (consisting of gliadin, etc.) and the like. In addition to liquid raw materials, powder raw materials may be used for this protein.

またリン脂質の水懸濁液中に蛋白質を存在させる割合
は、一般的に、水懸濁液のリン脂質(固形分)と蛋白質
(固形分)とを1:0.5〜2ぐらいにすればよい。
In addition, the ratio of the protein to be present in the phospholipid aqueous suspension may generally be about 1: 0.5 to 2 between the phospholipid (solid content) and the protein (solid content) of the aqueous suspension. .

またリン脂質の水懸濁液への混和の際、蛋白質は、固
定分濃度8〜15%ぐらいの水溶液としておくと混和がさ
せ易いので好ましい。この混和の方法はミキサー、コロ
イドミル、ホモゲナイザー等で均一になるようにすれば
よい。
Further, when the phospholipid is mixed in the aqueous suspension, it is preferable that the protein is an aqueous solution having a fixed concentration of about 8 to 15% because mixing is easy. This mixing method may be carried out by using a mixer, a colloid mill, a homogenizer or the like so as to make the mixture uniform.

また本発明でホスフォリパーゼA2とは、リン脂質を構
成するグリセライドの、中央の脂肪酸エステル部分を加
水分解する酵素をいい、ホスフォリパーゼA2を含むパン
クレアチンのような形で用いてもよい。
In the present invention, phospholipase A2 refers to an enzyme that hydrolyzes the central fatty acid ester portion of glyceride that constitutes phospholipid, and may be used in a form such as pancreatin containing phospholipase A2.

なお、ホスフォリパーゼA2はデンマークのノボ社、パ
ンクレアチンは米国のシグマ社などより販売されている
ので、これを購入して使用すればよい。この場合、前者
は通常液状であり、後者は通常粉末状である。
Since phospholipase A2 is sold by Novo Co. of Denmark and pancreatin is sold by Sigma of the United States, etc., it can be purchased and used. In this case, the former is usually liquid and the latter is usually powder.

本発明では、前記リン脂質の水懸濁液を前記ホスフォ
リパーゼA2で処理するものであり、ノボ社のホスフォリ
パーゼA2あるいはシグマ社のパンクレアチンを使用する
場合には、その使用量は、リン脂質(固形分)の重量に
対していずれも0.1〜5%ぐらいとすればよい。また処
理の目安としての条件は、加水分解を受けた結果リン脂
質の少なくとも2%がリゾ型になるぐらい、好ましくは
20%ぐらい、より好ましくは25%以上がリゾ型になるぐ
らいを目安にすればよく、ちなみに処理温度を約40℃と
すると、1時間、4時間、15時間の処理時間の経過とと
もにリゾ型の変換率は各々約20%、50%、90%となる。
In the present invention, the aqueous suspension of the phospholipid is treated with the phospholipase A2, when using the phospholipase A2 of Novo Co. or pancreatin of Sigma Co., the amount used, It may be about 0.1 to 5% with respect to the weight of the phospholipid (solid content). The conditions for the treatment are preferably such that at least 2% of the phospholipids are hydrolyzed as a result of hydrolysis.
About 20%, more preferably 25% or more should be litho type as a guide. By the way, if the treatment temperature is about 40 ° C., the litho type will change with the lapse of treatment time of 1 hour, 4 hours, 15 hours. The conversion rates are about 20%, 50% and 90%, respectively.

なお、処理時のリン脂質の水懸濁液のpHは、一般的に
ホスフォリパーゼA2の至適pHを含む6〜9ぐらいにすれ
ばよく、pH調整剤として、塩酸、酢酸、リン酸などの酸
剤ないしはカセイソーダ、第二リン酸カリウム、第三リ
ン酸カリウム、酢酸ナトリウムなどのアルカリ剤、その
他任意のpHに調整したリン酸バッファ液等を使用すれば
よい。
The pH of the aqueous suspension of phospholipids at the time of treatment should generally be around 6 to 9, which includes the optimum pH of phospholipase A2. As pH adjusters, hydrochloric acid, acetic acid, phosphoric acid, etc. The above-mentioned acid agent or caustic soda, potassium diphosphate, potassium phosphate tribasic, an alkali agent such as sodium acetate, or a phosphate buffer solution adjusted to an arbitrary pH may be used.

乾燥する方法としては、あまり熱がかからない方が好
ましく、そのような方法には代表例として凍結乾燥及び
噴霧乾燥があるが一般的には凍結乾燥が無難である。凍
結乾燥の具体的方法は、処理量により条件が異なるので
一概にはいえないが、−30〜−40℃で凍結させて0.05〜
0.25トールの真空下で20〜30時間ぐらいかけて乾燥させ
ればよい。なお、噴霧乾燥は加温による方法より常温に
よる方法がよい。
As a method for drying, it is preferable that heat is not applied so much, and typical examples of such a method include freeze-drying and spray-drying, but freeze-drying is generally safe. The specific method of freeze-drying cannot be said to be unequivocal because the conditions vary depending on the amount of treatment, but 0.05-
Dry under a vacuum of 0.25 torr for 20-30 hours. The spray drying is preferably performed at room temperature rather than by heating.

上述のようにリン脂質の水懸濁液をホスフォリパーゼ
A2で処理し、さらに乾燥することにより本発明の乳化材
が製造される。
Aqueous suspensions of phospholipids were treated with phospholipase as described above.
The emulsified material of the present invention is produced by treating with A2 and further drying.

なお、本発明の乳化材の製造工程において、本発明の
目的を損わない範囲で、他の副原料を添加することは任
意である。この一例として、必要によりホスフォリパー
ゼA2の作用を促進するためリン脂質の水懸濁液に2価の
カルシウムを添加することがあげられる。
In addition, in the manufacturing process of the emulsified material of the present invention, it is optional to add other auxiliary raw materials within a range not impairing the object of the present invention. An example of this is the addition of divalent calcium to an aqueous suspension of phospholipids in order to accelerate the action of phospholipase A2, if necessary.

<作用> 本発明の作用は必ずしも明らかではない。しかし、リ
ン脂質が食用蛋白質(但し、グルテンおよび卵黄蛋白は
除く。)の存在下でホスフォリパーゼA2の作用を受ける
ことによりその一部がリゾ型に加水分解され、この際
に、部分的に加水分解されたリン脂質及び遊離脂肪酸が
食用蛋白質(但し、グルテンおよび卵黄蛋白は除く。)
と一定の結合関係を生じ、乾燥することでさらに強固な
結合状態となり、そのことが水と油への親和性を高める
結果になっているのではないかと推察される。
<Action> The action of the present invention is not always clear. However, phospholipids are partially hydrolyzed to the lyso form by the action of phospholipase A2 in the presence of edible proteins (excluding gluten and egg yolk protein), and at this time, Hydrolyzed phospholipids and free fatty acids are edible proteins (excluding gluten and egg yolk proteins)
It is presumed that a certain binding relationship is generated, and when it is dried, it becomes a stronger binding state, which results in an increase in the affinity for water and oil.

<実 施 例> 以下、本発明の実施例を説明する。なお、実施例1
は、本発明の効果も示すものである。
<Examples> Examples of the present invention will be described below. In addition, Example 1
Shows the effect of the present invention.

実施例1 大豆リン脂質200g、デンマークのノボ社製ホスフォリ
パーゼA2製剤(液状)4g、清水700g及び卵白液1000g
(固形分の重量は約100gでほとんどアルブミンからな
る)を混和し、塩酸で液のpHを8.0に調整したのち、40
℃に加温し、その温度で4時間放置することにより乳化
材(比較品1)を得た(このときのリン脂質のリゾ型へ
の変換率は約50%であった)。そして、この混和液を−
40℃の極低温下で凍結させたのち、0.1トールの真空下
で25時間処理して乾燥した乳化材(本発明品)を製造し
た。
Example 1 200 g of soybean phospholipid, 4 g of phospholipase A2 formulation (liquid form) manufactured by Novo Danish (liquid), 700 g of clear water and 1000 g of egg white liquor
(The solid content weighs about 100 g and consists mostly of albumin.) After adjusting the pH of the solution to 8.0 with hydrochloric acid, add 40
The emulsified material (comparative product 1) was obtained by warming to 0 ° C. and allowing it to stand at that temperature for 4 hours (the conversion rate of phospholipid to lyso form was about 50%). Then add this mixture-
After freezing at a very low temperature of 40 ° C., it was treated under a vacuum of 0.1 Torr for 25 hours to produce a dried emulsified material (product of the present invention).

これら非乾燥品の乳化材(比較品1)及び乾燥品の乳
化材(本発明品)をそれぞれ使用して本発明品の水中油
型乳化食品を製した。
The non-dry emulsified material (Comparative Product 1) and the dry emulsified material (Invention Product) were used to produce an oil-in-water emulsified food product of the Invention.

併せてこの乳化材に代えて、さらに比較のため、大豆
リン脂質のみをホスフォリパーゼA2で同条件で処理した
乳化材(比較品2)に後で卵白液を加えたものを使用し
て同様に水中油型乳化食品を製した。
Also, instead of this emulsified material, for comparison, an emulsified material obtained by treating only soybean phospholipids with phospholipase A2 under the same conditions (comparative product 2) to which egg white liquor was added later was used. An oil-in-water emulsion food was produced.

これら本発明品及び比較品1,2の各乳化食品について
粘度、粒子、2ヶ月保存後の分離状況を測定・観察した
ところ下表に示すとおりとなった。
The emulsified foods of the present invention product and the comparative products 1 and 2 were measured and observed for viscosity, particles, and separation state after storage for 2 months.

註 1) 水中油型乳化食品の製造方法 ミキサー内にて、水相原料の混合5分、油相原料の添
加10分、仕上撹拌5分の工程を経て製造した。
Note 1) Method for producing oil-in-water emulsified food product was produced in a mixer through steps of mixing the aqueous phase raw material for 5 minutes, adding the oil phase raw material for 10 minutes, and finishing stirring for 5 minutes.

2) 粘度の測定法 米国ブルックフィールド社の回転粘度計で測定した。
使用ローター型:T−E、回転数2.5rpmで測定した。
2) Viscosity measuring method The viscosity was measured with a rotational viscometer manufactured by Brookfield, USA.
Rotor type used: TE, rotation speed was measured at 2.5 rpm.

3) 粒 子 油滴粒子の大きさの範囲を示す。3) Particle Indicates the size range of oil droplet particles.

4) 分離状況 ○印:分離認められず ×印:油浮上による分離あり 上表のとおり、本発明の乳化材を使用して製造した水
中油型乳化食品は、前記比較とする乳化材を使用して製
造した比較乳化食品に比べて、粘度が一段と大きく(比
較品1の2.9倍、比較品2の3.2倍)、油滴粒子の大きさ
が一段と小さく、また2ヶ月保存後の分離も認められな
かった。このことから、本発明の乳化材の乳化力が比較
とした非乾燥品の乳化材のそれに比し一段と優れること
が理解される。
4) Separation status ○: Separation is not recognized ×: Separation due to oil levitation As shown in the above table, the oil-in-water emulsified food produced using the emulsifying agent of the present invention uses the emulsifying agent for comparison. Compared with the comparatively emulsified food produced in this way, the viscosity is much higher (2.9 times that of comparative product 1 and 3.2 times that of comparative product 2), the size of the oil droplet particles is much smaller, and separation after storage for 2 months is also recognized. I couldn't do it. From this, it is understood that the emulsifying power of the emulsifying material of the present invention is far superior to that of the non-dried emulsifying material for comparison.

実施例2 大豆リン脂質200g、卵白液1000g(固形分は約100gで
ほとんどアルブミンからなる)、シグマ社のパンクレア
チン(粉末)2g及び清水700gとを混和し、酢酸で液のpH
を8.0に調整したのち、40℃に加温し、その温度で4時
間放置した(このときのリン脂質のリゾ型への変換率は
約50%であった)。そして、この処理液を−40℃の極低
温下で凍結させたのち、0.1トールの真空下で25時間処
理して乾燥させて本発明の乳化材を製造した。
Example 2 200 g of soybean phospholipids, 1000 g of egg white liquor (solid content is about 100 g, consisting mostly of albumin), 2 g of pancreatin (powder) from Sigma Co., and 700 g of fresh water were mixed, and the pH of the liquor was adjusted with acetic acid.
Was adjusted to 8.0, heated to 40 ° C., and allowed to stand at that temperature for 4 hours (the conversion rate of phospholipid to lyso form was about 50%). Then, this treatment liquid was frozen at an extremely low temperature of -40 ° C, then treated under a vacuum of 0.1 Torr for 25 hours and dried to produce the emulsified material of the present invention.

実施例3 大豆リン脂質200g、分離大豆蛋白の水溶液1000g(固
形分は約100gでその約84%がグロブリン約5%がアルブ
ミンからなる)、デンマークのノボ社製ホスフォリパー
ゼA2製剤(液状)2g及び清水700gとを混和し、カセイソ
ーダで液のpHを8.0に調整したのち、40℃に加温し、そ
の温度で1時間放置した(このときのリン脂質のリゾ型
への変換率は約20%であった)。そして、この処理液を
−40℃の極低温下で凍結さ化材を製造した。
Example 3 200 g of soybean phospholipids, 1000 g of an isolated soybean protein aqueous solution (solid content is about 100 g, about 84% of which is about 5% globulin consisting of albumin), 2 g of phospholipase A2 preparation (liquid form) made by Novo, Denmark After mixing with 700 g of clear water and adjusting the pH of the solution to 8.0 with caustic soda, the mixture was heated to 40 ° C and left at that temperature for 1 hour (the conversion rate of phospholipids to lyso form was about 20 at this time). %Met). Then, a frozen material was produced from this treated liquid at an extremely low temperature of -40 ° C.

実施例4 大豆リン脂質200g、ラクトアルブミン(粉末)100gと
水900gとの混合液、デンマークのノボ社製ホスフォリパ
ーゼA2製剤(液状)2g及び清水600gとを混和し、第三リ
ン酸ソーダで液のpHを7.8に調整したのち、40℃に加温
し、その温度で4時間放置した(このときのリン脂質の
リゾ型への変換率は約50%であった)。そして、この処
理液を−40℃の極低温下で凍結させたのち、0.1トール
の真空下で25時間処理して乾燥させて本発明の乳化材を
製造した。
Example 4 200 g of soybean phospholipids, a mixed solution of 100 g of lactalbumin (powder) and 900 g of water, 2 g of phospholipase A2 preparation (liquid) made by Novo Ltd. of Denmark (liquid) and 600 g of clear water were mixed, and tribasic sodium phosphate was added. After adjusting the pH of the liquid to 7.8, it was heated to 40 ° C. and left at that temperature for 4 hours (the conversion rate of phospholipids to lyso form was about 50%). Then, this treated liquid was frozen at an extremely low temperature of -40 ° C, then treated under a vacuum of 0.1 Torr for 25 hours and dried to produce the emulsified material of the present invention.

<発明の効果> 以上説明したようにリン脂質の水懸濁液を食用蛋白質
(但し、グルテンおよび卵黄蛋白を除く。)存在下でホ
スフォリパーゼA2で処理し、さらに乾燥することで、従
来のリゾ型含有リン脂質より一段と乳化力に優れた乳化
材を得ることができる。
<Effects of the Invention> As described above, an aqueous suspension of phospholipids is treated with phospholipase A2 in the presence of edible proteins (excluding gluten and egg yolk proteins), and then dried, It is possible to obtain an emulsifying agent having a much higher emulsifying power than the lyso-type phospholipid.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】リン脂質の水懸濁液を食用蛋白質(但し、
グルテンおよび卵黄蛋白は除く。)の存在下でホスフォ
リパーゼA2で処理し、該ホスフォリパーゼA2処理液を乾
燥することを特徴とする乳化材の製造方法。
1. An aqueous suspension of phospholipids containing an edible protein (however,
Excludes gluten and yolk proteins. ) Is present in the presence of phospholipase A2, and the phospholipase A2 treatment liquid is dried.
JP62041510A 1987-02-26 1987-02-26 Method of manufacturing emulsified material Expired - Lifetime JP2545074B2 (en)

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Application Number Priority Date Filing Date Title
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JPS63209742A JPS63209742A (en) 1988-08-31
JP2545074B2 true JP2545074B2 (en) 1996-10-16

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Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK0426211T3 (en) * 1989-09-29 1994-01-31 Unilever Plc Nutrient product containing dried lysophospholipoprotein
JP2618540B2 (en) * 1991-03-26 1997-06-11 キユーピー株式会社 Protein complex
JP2618551B2 (en) * 1991-08-31 1997-06-11 キユーピー株式会社 Protein complex
NL9400757A (en) * 1994-05-06 1995-12-01 Campina Melkunie Bv Heat-stable oil-in-water emulsions stabilized by hydrolysates.
US6773731B2 (en) 2002-10-18 2004-08-10 James S. Campbell Liquid egg yolk product comprising lysophospholipoprotein

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6030644A (en) * 1983-07-13 1985-02-16 Kyowa Hakko Kogyo Co Ltd Active gluten
JPS6156037A (en) * 1984-08-23 1986-03-20 協和醗酵工業株式会社 Food quality modifier
JPS6214790A (en) * 1985-07-11 1987-01-23 Nisshin Oil Mills Ltd:The Modification of lecithin
JPH0622461B2 (en) * 1985-07-31 1994-03-30 キユーピー株式会社 Method for producing oil-in-water emulsified food

Also Published As

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