JP2008029231A - Egg processed product and method for producing the same - Google Patents
Egg processed product and method for producing the same Download PDFInfo
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- JP2008029231A JP2008029231A JP2006204733A JP2006204733A JP2008029231A JP 2008029231 A JP2008029231 A JP 2008029231A JP 2006204733 A JP2006204733 A JP 2006204733A JP 2006204733 A JP2006204733 A JP 2006204733A JP 2008029231 A JP2008029231 A JP 2008029231A
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- 102000002322 Egg Proteins Human genes 0.000 claims abstract description 64
- 108010000912 Egg Proteins Proteins 0.000 claims abstract description 64
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- 235000013601 eggs Nutrition 0.000 claims abstract description 48
- 230000003647 oxidation Effects 0.000 claims abstract description 35
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 35
- 238000006243 chemical reaction Methods 0.000 claims abstract description 30
- 150000001720 carbohydrates Chemical class 0.000 claims abstract description 26
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- QCVGEOXPDFCNHA-UHFFFAOYSA-N 5,5-dimethyl-2,4-dioxo-1,3-oxazolidine-3-carboxamide Chemical compound CC1(C)OC(=O)N(C(N)=O)C1=O QCVGEOXPDFCNHA-UHFFFAOYSA-N 0.000 description 2
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- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Natural products OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
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- AANLCWYVVNBGEE-IDIVVRGQSA-L Disodium inosinate Chemical compound [Na+].[Na+].O[C@@H]1[C@H](O)[C@@H](COP([O-])([O-])=O)O[C@H]1N1C(NC=NC2=O)=C2N=C1 AANLCWYVVNBGEE-IDIVVRGQSA-L 0.000 description 1
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- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
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- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 1
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- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 description 1
- 235000019463 artificial additive Nutrition 0.000 description 1
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- 235000010323 ascorbic acid Nutrition 0.000 description 1
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- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000006701 autoxidation reaction Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
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- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
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- PXEDJBXQKAGXNJ-QTNFYWBSSA-L disodium L-glutamate Chemical compound [Na+].[Na+].[O-]C(=O)[C@@H](N)CCC([O-])=O PXEDJBXQKAGXNJ-QTNFYWBSSA-L 0.000 description 1
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- 239000008103 glucose Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 235000013923 monosodium glutamate Nutrition 0.000 description 1
- 230000000050 nutritive effect Effects 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 238000003506 protein modification method Methods 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
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- 230000000007 visual effect Effects 0.000 description 1
Landscapes
- Seasonings (AREA)
- Edible Oils And Fats (AREA)
- Meat, Egg Or Seafood Products (AREA)
Abstract
Description
本発明は、卵加工品とその製造方法に関し、詳しくは卵加工品とその製造方法、並びに該卵加工品を用いた、酸化安定性に優れた水中油型乳化食品とその製造方法に関する。さらに詳しくは、本発明は、マヨネーズやドレッシング等の水中油型乳化食品に使用された場合に、強い酸化安定性を付与することのできる卵加工品とその製造方法、並びに該卵加工品を用いた、酸化安定性に優れた水中油型乳化食品とその製造方法に関する。 The present invention relates to an egg processed product and a method for producing the same, and more particularly to an egg processed product and a method for producing the same, an oil-in-water emulsified food excellent in oxidation stability using the egg processed product, and a method for producing the same. More specifically, the present invention relates to an egg processed product capable of imparting strong oxidative stability when used in an oil-in-water emulsified food such as mayonnaise or dressing, a method for producing the same, and the processed egg product. The present invention relates to an oil-in-water emulsified food excellent in oxidation stability and a method for producing the same.
食品中に含まれる油脂は、保存期間中に徐々に酸素を吸収し、それらがある段階に達すると急速に酸化が進む結果、食品の変質、変色などの劣化をもたらす。 Oils and fats contained in foods gradually absorb oxygen during the storage period, and when they reach a certain stage, they rapidly oxidize, resulting in deterioration of foods such as alteration and discoloration.
ところで水相原料と油相原料とが水中油型に乳化され、エマルジョン状とされた水中油型乳化食品の代表的なものとして、マヨネーズやドレッシング類等がよく知られている。これらは、水相原料と油相原料とが水中油型に乳化された、美味しく、且つ、栄養価の高い食品となっている。
ここで、油相原料としては、大豆油、菜種油等の食用植物油が一般的に使用されており、乳化剤としては、通常、呈味、色調及び乳化安定性の観点から、卵黄が主に用いられている。
Incidentally, mayonnaise and dressings are well known as representative examples of oil-in-water emulsified foods in which an aqueous phase raw material and an oil phase raw material are emulsified in an oil-in-water type. These are delicious and high nutritive foods in which an aqueous phase raw material and an oil phase raw material are emulsified in an oil-in-water type.
Here, edible vegetable oils such as soybean oil and rapeseed oil are generally used as the oil phase material, and egg yolk is usually used as the emulsifier from the viewpoints of taste, color tone and emulsion stability. ing.
しかしながら、卵黄を使用した、これらマヨネーズやドレッシング類等は酸化に弱く、長期間酸化条件に置かれると変色を生じたり、更には乳化が破壊され、油相が分離するなどの欠点があった。また、過酸化物から生ずる二次生成物の中には、人体に対して有害な物質も検出されている。 However, these mayonnaises, dressings and the like using egg yolk are vulnerable to oxidation, and suffer from such problems as discoloration when subjected to oxidation conditions for a long period of time, and further, the emulsion is broken and the oil phase is separated. In addition, substances that are harmful to the human body are also detected in secondary products produced from peroxides.
上記のような酸化による劣化を防止するためには、抗酸化作用を有する化学物質からなる化学抗酸化剤を油脂食品に添加するのが一般的である。
例えば、アスコルビン酸脂肪酸エステルを含有していることを特徴とする酸性調味料に関する発明が提案されている(例えば、特許文献1参照)。この発明によれば、製造直後の風味がほぼ維持された風味安定性に優れた酸性調味料が得られるとされている。
しかしながら、近年、化学物質の生体機能への悪影響が問題となっており、消費者は一般的にこのような人工添加物を避ける傾向にある。
In order to prevent deterioration due to oxidation as described above, it is common to add a chemical antioxidant comprising a chemical substance having an antioxidant action to fat and oil foods.
For example, the invention regarding the acidic seasoning characterized by containing ascorbic acid fatty acid ester is proposed (for example, refer patent document 1). According to this invention, it is said that an acidic seasoning excellent in flavor stability in which the flavor immediately after production is substantially maintained is obtained.
However, in recent years, adverse effects on the biological function of chemical substances have become a problem, and consumers generally tend to avoid such artificial additives.
そのほか、炭素数2〜10の脂肪酸及び炭素数10の脂肪酸より構成されるジグリセリドを含むことによる、酸化安定性に優れたマヨネーズやドレッシング類等に関する技術が提案されている(例えば、特許文献2参照)。
しかしながら、この技術で使用されるジグリセリドは乳化剤そのものであり、食品添加物である乳化剤を主成分とする食品に対して、消費者は一般的に敬遠する傾向にある。
In addition, techniques relating to mayonnaise, dressings and the like excellent in oxidative stability by including diglycerides composed of fatty acids having 2 to 10 carbon atoms and fatty acids having 10 carbon atoms have been proposed (see, for example, Patent Document 2). ).
However, the diglyceride used in this technique is an emulsifier itself, and consumers generally tend to avoid foods based on an emulsifier which is a food additive.
また、食品蛋白の機能性を改質する方法として、メイラード反応を利用して蛋白の側鎖を修飾する方法が知られている。メイラード反応とは、非酵素的な褐変反応を意味し、アミノ−カルボニル反応とも呼ばれている反応である。カルボニル基としては、アルデヒド類やケトン類の代表的なものとしての糖類等が、一方、アミノ基としては、アミノ酸類、ペプタイドや蛋白類が反応に関与する。 As a method for modifying the functionality of food protein, a method of modifying the side chain of a protein using the Maillard reaction is known. The Maillard reaction means a non-enzymatic browning reaction and is also called an amino-carbonyl reaction. Examples of the carbonyl group include saccharides as typical aldehydes and ketones, and examples of the amino group include amino acids, peptides, and proteins.
このようなメイラード反応を利用した蛋白の改質方法として、蛋白質とキトサンとの複合体を形成させる技術(例えば、特許文献3参照)や、蛋白質とキシログルカンとの複合体を形成させる技術(例えば、特許文献4参照)が提案されている。
しかしながら、これらの技術では、メイラード反応を約50℃付近での乾燥系で行なっている為、長時間(数日間)を要し、更に、風味が消失し易いといった欠点があった。
As a protein modification method using such a Maillard reaction, a technique for forming a complex of protein and chitosan (for example, see Patent Document 3), or a technique for forming a complex of protein and xyloglucan (for example, , See Patent Document 4).
However, in these techniques, since the Maillard reaction is performed in a dry system at about 50 ° C., it takes a long time (several days), and further, there is a drawback that the flavor is easily lost.
本発明は、化学物質からなる化学抗酸化剤やジグリセリドのような乳化剤を主成分として使用することなく、長期間保存しても酸化安定性が損なわれることなく、消費者にとって好ましく受け入れられる、水中油型乳化食品を提供することを目的とするものである。 The present invention is a water solution that is preferably accepted by consumers without using a chemical antioxidant consisting of a chemical substance or an emulsifier such as diglyceride as a main component, without losing oxidation stability even when stored for a long period of time. An object of the present invention is to provide an oil-type emulsified food.
本発明者は、上記課題を解決すべく鋭意検討を重ねた結果、驚くべきことに、卵黄と糖類とを水系でメイラード反応させて得られる卵加工品を添加して得られる水中油型乳化食品が、優れた酸化安定性を有することを見出し、この知見に基づいて本発明を完成するに至った。
なお、蛋白質と糖類とのメイラード反応は、食品の製造過程で通常見られる反応であるが、卵黄と糖類とを水系でメイラード反応させて得られる卵加工品を添加して得られる水中油型乳化食品が優れた酸化安定性を有することは、これまで全く知られていなかった。
As a result of intensive studies to solve the above problems, the present inventors have surprisingly found that an oil-in-water emulsified food obtained by adding an egg processed product obtained by subjecting egg yolk and saccharide to an aqueous Maillard reaction in an aqueous system. However, it has been found that it has excellent oxidative stability, and the present invention has been completed based on this finding.
The Maillard reaction between protein and saccharide is a reaction usually seen in the production process of food, but it is an oil-in-water emulsification obtained by adding egg processed product obtained by Maillard reaction of egg yolk and saccharide in an aqueous system. It has never been known until now that foods have excellent oxidative stability.
即ち、請求項1に係る本発明は、卵黄と糖類とを水系でメイラード反応させることを特徴とする卵加工品の製造方法を提供するものである。
請求項2に係る本発明は、糖類が5炭糖類である請求項1記載の卵加工品の製造方法を提供するものである。
請求項3に係る本発明は、請求項1又は2記載の方法により得られる卵加工品を提供するものである。
請求項4に係る本発明は、油相と水相とが乳化されてなる水中油型乳化食品を製造するにあたり、乳化剤として、請求項3記載の卵加工品を用いることを特徴とする、酸化安定性に優れた水中油型乳化食品の製造方法を提供するものである。
請求項5に係る本発明は、請求項4記載の方法により得られる、酸化安定性に優れた水中油型乳化食品を提供するものである。
That is, this invention which concerns on Claim 1 provides the manufacturing method of the egg processed product characterized by making an egg yolk and saccharides Maillard react in aqueous system.
The present invention according to claim 2 provides the method for producing a processed egg product according to claim 1, wherein the saccharide is pentose.
The present invention according to claim 3 provides a processed egg product obtained by the method according to claim 1 or 2.
The present invention according to claim 4 is characterized in that the processed egg product according to claim 3 is used as an emulsifier in producing an oil-in-water-type emulsified food in which an oil phase and an aqueous phase are emulsified. The present invention provides a method for producing an oil-in-water emulsified food having excellent stability.
The present invention according to claim 5 provides an oil-in-water emulsified food product obtained by the method of claim 4 and having excellent oxidation stability.
本発明によれば、従来のように化学物質からなる化学抗酸化剤や炭素数2〜10の脂肪酸及び炭素数10の脂肪酸より構成されるジグリセリドのような乳化剤を使用することなく、マヨネーズやドレッシング等の水中油型乳化食品に添加することにより、該水中油型乳化食品に優れた酸化安定性を付与することのできる、卵加工品が提供される。
さらに、本発明によれば、該卵加工品を乳化剤として用いることにより、酸化性安定に優れており、長期間保存可能な水中油型乳化食品及びその製造方法が提供される。
該卵加工品を用いて製造されたマヨネーズやドレッシング等の水中油型乳化食品は、生体への影響が懸念される化学物質やジグリセリドのような乳化剤を含有しないため、消費者が敬遠することなく、安心して食することができ、長期間酸化安定性に優れたものである。
According to the present invention, mayonnaise and dressing can be used without using chemical antioxidants made of chemical substances and emulsifiers such as diglycerides composed of fatty acids having 2 to 10 carbon atoms and fatty acids having 10 carbon atoms as in the past. By adding to an oil-in-water emulsified food such as the above, an egg processed product that can impart excellent oxidation stability to the oil-in-water emulsified food is provided.
Furthermore, according to the present invention, by using the processed egg product as an emulsifier, an oil-in-water emulsified food that is excellent in oxidative stability and can be stored for a long period of time is provided.
Oil-in-water emulsified foods such as mayonnaise and dressings produced using the processed egg products do not contain chemical substances that may be affected by the body or emulsifiers such as diglycerides, so consumers are not shy away It is safe to eat and has excellent long-term oxidation stability.
以下、本発明を詳しく説明する。
請求項1に係る本発明は、卵加工品の製造方法に関し、卵黄と糖類とを水系でメイラード反応させることを特徴とするものである。
The present invention will be described in detail below.
The present invention according to claim 1 relates to a method for producing a processed egg product, characterized in that egg yolk and saccharide are subjected to a Maillard reaction in an aqueous system.
請求項1に係る本発明において用いる卵黄としては、全卵であってもよいし、或いは卵液から卵白を分離して得られる生卵黄であってもよい。また、生卵黄であってもよいし、或いは乾燥卵黄を水戻しした卵黄液であってもよい。さらには、卵黄の他に卵白等が少量加わっているものであってもよい。
また、卵黄としては、鶏卵の卵黄に限定されるのもではなく、広く家禽、その他の鳥類の卵の卵黄も使用することができる。
The egg yolk used in the present invention according to claim 1 may be whole egg or raw egg yolk obtained by separating egg white from egg liquid. Moreover, raw egg yolk may be sufficient, or the egg yolk liquid which dried water yolk rehydrated may be sufficient. Furthermore, in addition to egg yolk, a small amount of egg white may be added.
Further, the egg yolk is not limited to the egg yolk of a chicken egg, and the egg yolk of eggs of poultry and other birds can be widely used.
次に、請求項1に係る本発明において用いる糖類としては、4炭糖類であるトレオロース等、5炭糖類であるキシロース、リボースやアラビノース等、6炭糖類であるグルコース、フラクトース、マンノースやガラクトース等、及び澱粉の加水分解物等の1種もしくは2種以上のものが挙げられる。
これらの糖類では、前記した卵黄とのメイラード反応を起こすために、還元性を持つことが必要である。特に澱粉の加水分解物では、DE(Dextrose Equivalent)として、25以上が必要であるが、好ましくは30以上が好適に用いられる。
これら糖類の種類として、実用性や経済性を考慮すると、請求項2に記載したように、還元性を有する5炭糖類である、キシロースやリボース等が好適に用いられる。
Next, as saccharides used in the present invention according to claim 1, throse, which is a 4-carbon sugar, xylose, which is a 5-carbon sugar, ribose, arabinose, etc., glucose, fructose, mannose, galactose, etc., which are 6-carbon sugars, And one or more of hydrolysates of starch and the like.
These sugars need to have reducing properties in order to cause the Maillard reaction with the above-mentioned egg yolk. In particular, starch hydrolyzate requires 25 or more as DE (Dextrose Equivalent), and preferably 30 or more is preferably used.
In consideration of practicality and economical efficiency, xylose, ribose and the like, which are pentoses having reducing properties, are preferably used as the types of these saccharides.
請求項1に係る本発明における卵黄と糖類との使用割合については、卵黄と糖類との混合物中における糖類の濃度が1質量%以上であることが望ましく、特に3〜10質量%であることがより望ましい。
ここで、卵黄と糖類との混合物中における糖類の濃度が1質量%未満では、メイラード反応後の卵加工品に酸化安定性を充分に付与させることができない。また、卵黄と糖類との混合物中における糖類の濃度が10質量%を超えても、メイラード反応後の卵加工品の酸化安定性が向上せず、添加量に見合う効果が得られないため、好ましくない。
About the usage-amount of the egg yolk and saccharides in this invention which concerns on Claim 1, it is desirable that the density | concentration of the saccharide | sugar in the mixture of an egg yolk and saccharides is 1 mass% or more, and it is especially 3-10 mass%. More desirable.
Here, if the concentration of the saccharide in the mixture of egg yolk and saccharide is less than 1% by mass, it is not possible to sufficiently impart oxidation stability to the processed egg product after the Maillard reaction. Moreover, even if the concentration of the saccharide in the mixture of egg yolk and saccharide exceeds 10% by mass, the oxidation stability of the processed egg product after the Maillard reaction is not improved, and an effect commensurate with the amount added cannot be obtained. Absent.
請求項1に係る本発明は、上記した如き卵黄と糖類とを水系でメイラード反応させることを特徴としている。
乾燥系でのメイラード反応に比べて、水系でのメイラード反応が有利な点としては、卵液を乾燥する操作などの煩雑さがないこと、処理時間が比較的短時間であること、更に卵風味が比較的、消失し難い、といった利点がある。
The present invention according to claim 1 is characterized in that the above-described egg yolk and saccharide are subjected to a Maillard reaction in an aqueous system.
Compared with the Maillard reaction in the dry system, the Maillard reaction in the aqueous system is advantageous in that there is no trouble such as an operation of drying the egg liquid, the processing time is relatively short, and the egg flavor. Has the advantage that it is relatively difficult to disappear.
卵黄と糖類とを水系でメイラード反応させるにあたっては、まず糖濃度が1〜10質量%の卵黄液を調製し、pHを6.0〜9.5の範囲に調整する。
ここで、pHが6.0未満であると、得られるメイラード反応物は、水中油型乳化食品に充分な酸化安定性を付与することができない。一方、pHが9.5を超えると、卵黄がゲル化するため、ハンドリング性が極端に低下することから好ましくない。
In the Maillard reaction of egg yolk and saccharide in an aqueous system, first, an egg yolk solution having a sugar concentration of 1 to 10% by mass is prepared, and the pH is adjusted to a range of 6.0 to 9.5.
Here, when the pH is less than 6.0, the Maillard reaction product obtained cannot impart sufficient oxidation stability to the oil-in-water emulsion food. On the other hand, if the pH exceeds 9.5, the yolk becomes gelled, which is not preferable because handling properties are extremely lowered.
次いで、糖類を溶解した卵黄液を、温度50〜65℃及び0.5〜5時間の条件で熱処理を施す。この熱処理により、メイラード反応させる。通常、メイラード反応では、温度が低いほど長い処理時間を要し、温度が高いほど短時間の処理で効果が得られる。 Subsequently, the egg yolk liquid which melt | dissolved saccharides is heat-processed on the conditions of temperature 50-65 degreeC and 0.5 to 5 hours. A Maillard reaction is caused by this heat treatment. Usually, in the Maillard reaction, the lower the temperature, the longer the treatment time is required, and the higher the temperature, the shorter the treatment, the more effective.
ここで熱処理の温度が50℃未満である場合、得られるメイラード反応物は、水中油型乳化食品に充分な酸化安定性を付与することができない。一方、熱処理の温度が65℃を超える場合では、卵黄がゲル化し、ハンドリング性が極端に低下するため、いずれも好ましくない。
従って、メイラード反応させる際の熱処理温度としては、通常、55〜60℃の温度領域が好適に用いられる。
Here, when the temperature of the heat treatment is less than 50 ° C., the obtained Maillard reaction product cannot give sufficient oxidation stability to the oil-in-water emulsion food. On the other hand, when the temperature of the heat treatment exceeds 65 ° C., the egg yolk is gelled, and handling properties are extremely lowered.
Therefore, as a heat treatment temperature for the Maillard reaction, a temperature range of 55 to 60 ° C. is usually preferably used.
次に、メイラード反応させる際の熱処理時間が0.5時間未満では、得られるメイラード反応物は、水中油型乳化食品に充分な酸化安定性を付与することができない。一方、処理時間が5時間を超えても、効果が向上しないため、いずれも好ましくない。
従って、メイラード反応させる際の熱処理時間としては、通常、1〜4時間の時間領域が好適に用いられる。
Next, if the heat treatment time for Maillard reaction is less than 0.5 hours, the Maillard reaction product obtained cannot give sufficient oxidation stability to the oil-in-water emulsion food. On the other hand, even if the treatment time exceeds 5 hours, the effect is not improved, so that neither is preferable.
Therefore, a time region of 1 to 4 hours is usually suitably used as the heat treatment time for the Maillard reaction.
卵黄がどの程度、メイラード反応にあずかっているかについては、SDS−ポリアクリルアミド・ゲル電気泳動(SDS−PAGE)により分析することができる。
即ち、アミノ−カルボニル反応により、糖類が卵黄蛋白の側鎖に結合した、請求項1に係る本発明の卵加工品では、分子量が増加するため、未反応の卵黄蛋白と比べて、蛋白バンドが高分子側にシフトすることが把握される(J. Food Sci., Vol51, p11151117, 1986)。
The degree to which the yolk participates in the Maillard reaction can be analyzed by SDS-polyacrylamide gel electrophoresis (SDS-PAGE).
That is, in the processed egg product of the present invention according to claim 1 in which a saccharide is bound to the side chain of egg yolk protein by an amino-carbonyl reaction, the molecular weight increases, so that the protein band is higher than that of unreacted egg yolk protein. It is understood that it shifts to the polymer side (J. Food Sci., Vol51, p11151117, 1986).
このようにして得られたメイラード反応物が、請求項3に係る本発明の卵加工品であり、マヨネーズやドレッシング類等の調製時に乳化剤として使用することにより、酸化安定性に優れたマヨネーズやドレシング類等のような水中油型乳化食品を得ることができる。 The Maillard reaction product obtained in this way is the processed egg product of the present invention according to claim 3 and may be used as an emulsifier in the preparation of mayonnaise, dressings, etc., and mayonnaise and dressing having excellent oxidation stability. An oil-in-water emulsified food product such as sucrose can be obtained.
次に、水中油型乳化食品を製造するにあたり、このようにして得られる卵加工品を用いるのが、請求項4に係る本発明である。
即ち、請求項4に係る本発明は、酸化安定性に優れた水中油型乳化食品の製造方法に関し、油相と水相とが乳化されてなる水中油型乳化食品を製造するにあたり、乳化剤として、請求項3記載の卵加工品を用いることを特徴とするものである。
Next, in producing the oil-in-water type emulsified food, the processed egg product thus obtained is the present invention according to claim 4.
That is, the present invention according to claim 4 relates to a method for producing an oil-in-water emulsified food excellent in oxidation stability. In producing an oil-in-water emulsified food in which an oil phase and an aqueous phase are emulsified, The processed egg product according to claim 3 is used.
ここで水中油型乳化食品の水相を構成する原料(水相原料)としては、乳化剤として請求項3に係る本発明の卵加工品を用いる以外には、マヨネーズやドレッシング類の製造に際して使用される原料や、その配合割合に準じて決定すればよく、特に制限されない。
通常、用いられる水相原料の例としては、水の他に、食塩,食酢,グルタミン酸ナトリウム,イノシン酸ナトリウム等の調味料、乳化剤、糖類、澱粉、ガム類、香辛料、着色料、着香料などがある。
なお、乳化剤としては、上記したように請求項3に係る本発明の卵加工品が用いられ、上記水相原料と一緒に混合・溶解して水相が調製される
Here, the raw material constituting the aqueous phase of the oil-in-water emulsified food (aqueous phase raw material) is used in the production of mayonnaise and dressings other than using the processed egg product of the present invention according to claim 3 as an emulsifier. It may be determined according to the raw material to be used and the blending ratio thereof, and is not particularly limited.
Examples of water phase materials that are usually used include, in addition to water, seasonings such as salt, vinegar, sodium glutamate, sodium inosinate, emulsifiers, sugars, starches, gums, spices, coloring agents, flavoring agents, and the like. is there.
As described above, the processed egg product of the present invention according to claim 3 is used as the emulsifier, and the aqueous phase is prepared by mixing and dissolving together with the aqueous phase raw material.
一方、水中油型乳化食品の油相を構成する原料(油相原料)としては、通常、食品に添加可能な親油性の物質であれば、特に制限がなく、例えば、食用植物油脂や、親油性のある香辛料や着香料等が挙げられる。
食用植物油としては、常温で液体の菜種油、大豆油、サフラワー油、コーン油、ヒマワリ油等が挙げられ、これらを単独で、又は2種以上を混合して使用することができる。
On the other hand, the raw material constituting the oil phase of the oil-in-water emulsion food (oil phase raw material) is not particularly limited as long as it is a lipophilic substance that can be added to food. For example, edible vegetable oils and fats, Examples include oily spices and flavorings.
Examples of edible vegetable oils include rapeseed oil, soybean oil, safflower oil, corn oil, sunflower oil and the like that are liquid at room temperature, and these can be used alone or in admixture of two or more.
請求項4に係る本発明における油相と水相との割合については、特に制限はないが、通常は、油相10〜90質量%に対して、水相90〜10質量%、好ましくは油相30〜80質量%に対して、水相70〜20質量%とする。
ここで、油相の比率が10質量%未満であると、調製された水中油型乳化食品が美味しくなく、一方、油相の比率が90質量%を超えると転相を起こし易くなることから、いずれも好ましくない。
Although there is no restriction | limiting in particular about the ratio of the oil phase in this invention which concerns on Claim 4, A water phase 90-10 mass% with respect to 10-90 mass% of an oil phase, Preferably it is an oil. It is set as 70-20 mass% of water phases with respect to 30-80 mass% of phases.
Here, when the ratio of the oil phase is less than 10% by mass, the prepared oil-in-water emulsified food is not delicious, whereas when the ratio of the oil phase exceeds 90% by mass, phase inversion is likely to occur. Neither is preferred.
また、請求項4に係る本発明において、水中油型乳化食品の製造は、既知の手法により行なえばよく、特に制限されない。
例えば、水以外の水相原料を水等に分散・溶解し、これらに油相原料を加えて、一般的な攪拌機、例えば市販の万能攪拌機を用いて予備乳化する。
次いで、コロイドミル等の乳化機を用いて、仕上げ乳化を行なうことによって、水中油型乳化食品を製造することができる。
Moreover, in this invention which concerns on Claim 4, the manufacture of an oil-in-water type emulsified food should just be performed by a known method, and is not restrict | limited in particular.
For example, an aqueous phase raw material other than water is dispersed and dissolved in water or the like, and an oil phase raw material is added thereto, followed by preliminary emulsification using a general stirrer, for example, a commercially available universal stirrer.
Subsequently, an oil-in-water type emulsified food can be produced by performing final emulsification using an emulsifier such as a colloid mill.
このようにして得られたものが、請求項5に係る本発明の水中油型乳化食品である。
このようにして製造された水中油型乳化食品は、乳化剤として、卵黄と糖類とを水系でメイラード反応させて得られる卵加工品を用いていることから、エマルジョンの破壊が防止されており、長期間酸化安定性に優れたものとなっている。
What was obtained in this way is the oil-in-water emulsified food of the present invention according to claim 5.
The oil-in-water emulsified food produced in this way uses a processed egg product obtained by subjecting egg yolk and sugar to a Maillard reaction in an aqueous system as an emulsifier. It has excellent period oxidation stability.
なお、卵黄と糖類とのメイラード反応物である卵加工品を乳化剤として使用することにより、水中油型食品に酸化安定性が付与される理由については、必ずしも明らかではないが、卵黄蛋白の側鎖と糖類との間で生じるアミノ−カルボニル反応基が、酸化のスタート物質であるラジカルを形成する際の触媒となる鉄等の金属イオンの封鎖や、油脂の自動酸化で生じるラジカルの消去等に関与しているものと考えられる。 The reason why oxidative stability is imparted to oil-in-water foods by using processed egg products that are Maillard reaction products of egg yolk and saccharides as an emulsifier is not always clear, but the side chain of egg yolk protein The amino-carbonyl reactive group generated between the saccharide and the saccharide is involved in the sequestration of radicals generated by the sequestration of metal ions such as iron and the autoxidation of fats and oils as catalysts for the formation of radicals that are the starting materials for oxidation It is thought that.
次に、本発明を実施例等により詳しく説明するが、本発明の範囲をこれらにより何ら限定されるものではない。 EXAMPLES Next, although an Example etc. demonstrate this invention in detail, the scope of the present invention is not limited at all by these.
製造例1(本発明品1の製造)
卵黄1980gに、和光純薬工業(株)製のD−キシロース20gを加えた後、十分に混合・溶解し、D−キシロース濃度1質量%の卵黄液を得た。得られた卵黄液のpHは6.3であるが、10質量%の水酸化ナトリウム水溶液を用いて、pH8.5に調整した。
次いで、得られた卵黄液を3L容攪拌槽に充填し、56℃の品温で3時間、熱処理を行って、本発明の卵加工品(本発明品1)を得た。
Production Example 1 (Production of Invention Product 1)
After adding 20 g of D-xylose manufactured by Wako Pure Chemical Industries, Ltd. to 1980 g of egg yolk, it was sufficiently mixed and dissolved to obtain an egg yolk solution having a D-xylose concentration of 1% by mass. Although the pH of the obtained egg yolk liquid was 6.3, it was adjusted to pH 8.5 using a 10% by mass aqueous sodium hydroxide solution.
Next, the obtained egg yolk liquid was filled in a 3 L stirring tank and heat-treated at a product temperature of 56 ° C. for 3 hours to obtain an egg processed product of the present invention (Product 1 of the present invention).
製造例2(本発明品2の製造)
卵黄1940gに、和光純薬工業(株)製のD−キシロース60gを加えた後、十分に混合・溶解し、D−キシロース濃度3質量%の卵黄液を得た。得られた卵黄液のpHは6.3であり、これをpH未調整のまま3L容攪拌槽に充填し、56℃の品温で3時間、熱処理を行なって、本発明の卵加工品(本発明品2)を得た。
Production Example 2 (Production of Invention Product 2)
After adding 60 g of D-xylose manufactured by Wako Pure Chemical Industries, Ltd. to 1940 g of egg yolk, the mixture was sufficiently mixed and dissolved to obtain an egg yolk solution having a D-xylose concentration of 3 mass%. The obtained egg yolk liquid has a pH of 6.3, and this is filled in a 3 L stirring tank with the pH not adjusted, and subjected to heat treatment at a product temperature of 56 ° C. for 3 hours. An inventive product 2) was obtained.
製造例3(本発明品3の製造)
卵黄1900gに、和光純薬工業(株)製のD−キシロース100gを加えた後、十分に混合・溶解し、D−キシロース濃度5質量%の卵黄液を得た。得られた卵黄液のpHは6.3であり、これをpH未調整のまま3L容攪拌槽に充填し、56℃の品温で3時間、熱処理を行って、本発明の卵加工品(本発明品3)を得た。
Production Example 3 (Production of Invention Product 3)
After adding 100 g of D-xylose manufactured by Wako Pure Chemical Industries, Ltd. to 1900 g of egg yolk, it was sufficiently mixed and dissolved to obtain an egg yolk solution having a D-xylose concentration of 5 mass%. The obtained egg yolk liquid has a pH of 6.3, and this is filled in a 3 L stirring tank with the pH not adjusted, and subjected to heat treatment at a product temperature of 56 ° C. for 3 hours. An inventive product 3) was obtained.
製造例4(本発明品4の製造)
卵黄1980gに、和光純薬工業(株)製のD−リボース20gを加えた後、十分に混合・溶解し、リボース濃度1質量%の卵黄液を得た。得られた卵黄液のpHは6.3であるが、10質量%の水酸化ナトリウムの水溶液を用いて、pH8.5に調整した。
次いで、卵黄液を3L容攪拌槽に充填し、56℃の品温で3時間、熱処理を行って、本発明の卵加工品(本発明品4)を得た。
Production Example 4 (Production of Invention Product 4)
After adding 20 g of D-ribose manufactured by Wako Pure Chemical Industries, Ltd. to 1980 g of egg yolk, the mixture was sufficiently mixed and dissolved to obtain an egg yolk liquid having a ribose concentration of 1% by mass. Although the pH of the obtained egg yolk was 6.3, it was adjusted to pH 8.5 using an aqueous solution of 10% by mass sodium hydroxide.
Next, the egg yolk liquid was filled into a 3 L stirring tank and heat treated at a product temperature of 56 ° C. for 3 hours to obtain an egg processed product of the present invention (Product 4 of the present invention).
製造例5(本発明品5の製造)
卵黄1940gに、和光純薬工業(株)製のD−リボース60gを加えた後、十分に混合・溶解し、リボース濃度3質量%の卵黄液を得た。得られた卵黄液のpHは6.3であり、これをpH未調整のまま、3L容攪拌槽に充填し、56℃の品温で3時間、熱処理を行って、本発明の卵加工品(本発明品5)を得た。
Production Example 5 (Production of Invention Product 5)
After adding 60 g of D-ribose manufactured by Wako Pure Chemical Industries, Ltd. to 1940 g of egg yolk, the mixture was sufficiently mixed and dissolved to obtain an egg yolk liquid having a ribose concentration of 3 mass%. The obtained egg yolk liquid has a pH of 6.3, and this is filled in a 3 L stirring tank with the pH not adjusted, and subjected to heat treatment at a product temperature of 56 ° C. for 3 hours to obtain the processed egg product of the present invention. (Invention product 5) was obtained.
製造例6(本発明品6の製造)
卵黄1900gに、和光純薬工業(株)製のD−リボース100gを加えた後、十分に混合・溶解し、リボース濃度5質量%の卵黄液を得た。得られた卵黄液のpHは6.3であり、これをpH未調整のまま、3L容攪拌槽に充填し、56℃の品温で3時間、熱処理を行って、本発明の卵加工品(本発明品6)を得た。
Production Example 6 (Production of Invention Product 6)
After adding 100 g of D-ribose manufactured by Wako Pure Chemical Industries, Ltd. to 1900 g of egg yolk, it was sufficiently mixed and dissolved to obtain an egg yolk liquid having a ribose concentration of 5 mass%. The obtained egg yolk liquid has a pH of 6.3, and this is filled in a 3 L stirring tank with the pH not adjusted, and subjected to heat treatment at a product temperature of 56 ° C. for 3 hours to obtain the processed egg product of the present invention. (Invention product 6) was obtained.
比較製造例1(比較品1の製造)
pH未調整の卵黄(pH6.3)2000gを、10質量%の水酸化ナトリウム水溶液を用いてpHを8.5に調整し、次いで3L容攪拌槽に充填し、56℃の品温で3時間、熱処理を行って、卵黄液(比較品1)を得た。
Comparative Production Example 1 (Production of Comparative Product 1)
The pH of egg yolk (pH 6.3) of 2000 g not adjusted was adjusted to 8.5 using a 10% by mass aqueous sodium hydroxide solution, and then charged into a 3 L stirring tank, and the product temperature at 56 ° C. was maintained for 3 hours. The egg yolk liquid (Comparative product 1) was obtained by heat treatment.
比較製造例2(比較品2の製造)
製造例3において、熱処理を行わないこと以外は製造例3と同様にして卵黄液(比較品2)を得た。
Comparative Production Example 2 (Production of Comparative Product 2)
In Production Example 3, an egg yolk liquid (Comparative Product 2) was obtained in the same manner as in Production Example 3 except that no heat treatment was performed.
比較製造例3(比較品3の製造)
製造例6において、熱処理を行わないこと以外は製造例6と同様にして卵黄液(比較品3)を得た。
Comparative Production Example 3 (Production of Comparative Product 3)
In Production Example 6, an egg yolk liquid (Comparative Product 3) was obtained in the same manner as in Production Example 6 except that no heat treatment was performed.
実施例1〜6
(1)水中油型乳化食品(マヨネーズ)の調製
下記表1に示す処方に従い、製造例1〜6で得られた卵加工品(本発明品1〜6)を用いて、6種類の水中油型乳化食品(マヨネーズ)2kgをコロイドミルにてそれぞれ調製した。なお、実施例1〜6の水中油型乳化食品(マヨネーズ)の配合割合において、卵加工品中の卵黄量は5質量%とし、全体が100質量%となるように水により調整した。
Examples 1-6
(1) Preparation of oil-in-water emulsified food (mayonnaise) In accordance with the prescription shown in Table 1 below, six kinds of oil-in-water using processed egg products (Products 1 to 6 of the present invention) obtained in Production Examples 1 to 6 2 kg of each type of emulsified food (mayonnaise) was prepared in a colloid mill. In addition, in the mixture ratio of the oil-in-water type emulsified food (mayonnaise) of Examples 1-6, the amount of egg yolk in processed egg products was 5 mass%, and it adjusted with water so that the whole might be 100 mass%.
(2)酸化安定性の評価
上記(1)にて得られた各水中油型乳化食品(マヨネーズ)の酸化安定性を、以下の方法で評価した。
約200g容のガラス瓶に、得られた水中油型乳化食品(マヨネーズ)の約100gを充填し、一重のサランラップで瓶の口を密封し、34℃暗所の条件下に保管した。5週間及び7週間後、水中油型乳化食品(マヨネーズ)表層の分離状態により、酸化安定性を次の4段階で評価した。
ここで、「安定」及び「やや安定」であれば、酸化安定性に優れていると言うことができる。なお、評価は、経験豊かな5名のパネラーによる視覚観察の平均値で示した。結果を表1に示す。
(2) Evaluation of oxidation stability The oxidation stability of each oil-in-water emulsified food (mayonnaise) obtained in (1) above was evaluated by the following method.
About 200 g of a glass bottle was filled with about 100 g of the obtained oil-in-water emulsified food (mayonnaise), and the mouth of the bottle was sealed with a single Saran wrap and stored at 34 ° C. in a dark place. After 5 weeks and 7 weeks, the oxidation stability was evaluated in the following four stages according to the separation state of the oil-in-water emulsified food (mayonnaise) surface layer.
Here, if it is “stable” and “somewhat stable”, it can be said that the oxidation stability is excellent. In addition, evaluation was shown by the average value of visual observation by five experienced panelists. The results are shown in Table 1.
[酸化安定性の評価]
・安定 :油分離していない。
・やや安定 :表層は強く褐変しているが、油分離していない。
・やや不安定 :表層がやや油分離している。
・不安定 :表層がひどく油分離している。
[Evaluation of oxidation stability]
・ Stable: No oil separation.
・ Slightly stable: The surface layer is strongly browned, but the oil is not separated.
・ Slightly unstable: The surface layer is somewhat oil-separated.
・ Unstable: The surface layer is severely oil-separated.
比較例1〜3
(1)水中油型乳化食品(マヨネーズ)の調製
比較製造例1〜3で得られた卵黄液(比較品1〜3)を下記表2に示す所定量用い、下記表2に示す配合割合の水中油型乳化食品(マヨネーズ)2kgを、実施例1〜6と同様にして調製した。
Comparative Examples 1-3
(1) Preparation of oil-in-water emulsified food (mayonnaise) The egg yolk liquid (comparative products 1 to 3) obtained in Comparative Production Examples 1 to 3 was used in a predetermined amount shown in Table 2 below, and the mixing ratio shown in Table 2 below was used. 2 kg of oil-in-water emulsified food (mayonnaise) was prepared in the same manner as in Examples 1-6.
(2)酸化安定性の評価
上記(1)にて得られた各水中油型乳化食品(マヨネーズ)の酸化安定性を、実施例1〜6と同様にして評価した。結果を表2に示す。
(2) Evaluation of oxidation stability The oxidation stability of each oil-in-water emulsified food (mayonnaise) obtained in (1) above was evaluated in the same manner as in Examples 1-6. The results are shown in Table 2.
表1の結果から明らかなように、卵黄中に5炭糖類であるD−キシロース又はD−リボースを1〜5質量%添加し、熱処理を施して得られた本発明品1〜6を使用した水中油型乳化食品(マヨネーズ)は、34℃保存後でも表層が分離することなく、長期間の優れた酸化安定性を示した。
特に、実施例1〜3及び実施例4〜6の結果から明らかなように、D−キシロース及びD−リボース共に、卵黄中の添加量の増加に従って、酸化安定性が向上することが認められた。
As is apparent from the results in Table 1, 1 to 5% by mass of D-xylose or D-ribose, which is a pentose, was added to egg yolk, and the products 1 to 6 of the present invention obtained by heat treatment were used. The oil-in-water emulsified food (mayonnaise) showed excellent oxidative stability over a long period without separation of the surface layer even after storage at 34 ° C.
In particular, as is apparent from the results of Examples 1 to 3 and Examples 4 to 6, it was observed that both D-xylose and D-ribose improved in oxidative stability as the amount added in egg yolk increased. .
これに対して、表2の比較例1に示されるように、5炭糖類を添加せずに、熱処理のみを施した卵黄液(比較品1)を使用した水中油型乳化食品(マヨネーズ)では、34℃保存後の酸化安定性は著しく低かった。
また、比較例2及び3に示されるように、D−キシロース又はD−リボースを卵黄中に5質量%添加しているものの、熱処理を施さずメイラード反応を起こしていない卵黄液(比較品2及び3)を用いた水中油型乳化食品(マヨネーズ)においても、比較例1と同様に、34℃保存後の酸化安定性は著しく低いことが分った。
On the other hand, as shown in Comparative Example 1 of Table 2, in the oil-in-water emulsified food (mayonnaise) using egg yolk liquid (comparative product 1) subjected to only heat treatment without adding pentose. The oxidation stability after storage at 34 ° C. was remarkably low.
In addition, as shown in Comparative Examples 2 and 3, although 5% by mass of D-xylose or D-ribose was added to the yolk, it was not subjected to heat treatment and did not cause a Maillard reaction (Comparative products 2 and Also in the oil-in-water emulsified food (mayonnaise) using 3), it was found that the oxidation stability after storage at 34 ° C. was remarkably low as in Comparative Example 1.
以上の結果より、卵黄に糖類を添加し、且つ熱処理を施すことにより引き起こされるメイラード反応によって得られた卵加工品を用いた場合、長期間酸化安定性の優れた水中油型乳化食品(マヨネーズ)を調製できることが明らかである。 From the above results, when using processed egg products obtained by Maillard reaction caused by adding saccharides to egg yolk and applying heat treatment, oil-in-water emulsified food with long-term oxidation stability (mayonnaise) It is clear that can be prepared.
本発明によれば、従来のように化学物質からなる化学抗酸化剤や炭素数2〜10の脂肪酸及び炭素数10の脂肪酸より構成されるジグリセリドのような乳化剤を使用することなく、マヨネーズやドレッシング等の水中油型乳化食品に添加することにより、該水中油型乳化食品に優れた酸化安定性を付与することのできる、卵加工品が提供される。
さらに、本発明によれば、該卵加工品を乳化剤として用いることにより、酸化性安定に優れており、長期間保存可能な水中油型乳化食品及びその製造方法が提供される。
該卵加工品を用いて製造されたマヨネーズやドレッシング等の水中油型乳化食品は、生体への影響が懸念される化学物質やジグリセリドのような乳化剤を含有しないため、消費者が敬遠することなく、安心して食することができ、長期間酸化安定性に優れたものである。
従って、本発明は食品産業分野において有効に利用することができる。
According to the present invention, mayonnaise and dressing can be used without using chemical antioxidants made of chemical substances and emulsifiers such as diglycerides composed of fatty acids having 2 to 10 carbon atoms and fatty acids having 10 carbon atoms as in the past. By adding to an oil-in-water emulsified food such as the above, an egg processed product that can impart excellent oxidation stability to the oil-in-water emulsified food is provided.
Furthermore, according to the present invention, by using the processed egg product as an emulsifier, an oil-in-water emulsified food that is excellent in oxidative stability and can be stored for a long period of time is provided.
Oil-in-water emulsified foods such as mayonnaise and dressings produced using the processed egg products do not contain chemical substances that may be affected by the body or emulsifiers such as diglycerides, so consumers are not shy away It is safe to eat and has excellent long-term oxidation stability.
Therefore, the present invention can be effectively used in the food industry field.
Claims (5)
An oil-in-water emulsified food excellent in oxidation stability, obtained by the method according to claim 4.
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Publication number | Priority date | Publication date | Assignee | Title |
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WO2010110269A1 (en) * | 2009-03-26 | 2010-09-30 | キッコーマン株式会社 | Browning reaction product and fat-based food |
CN108013319A (en) * | 2017-11-22 | 2018-05-11 | 恒枫食品科技有限公司 | Antioxidation activity lotion and preparation method thereof |
CN115736150A (en) * | 2022-11-28 | 2023-03-07 | 成都鸾翔凤集食品有限公司 | Yolk liquid instant drink and preparation method thereof |
CN116076675A (en) * | 2022-11-28 | 2023-05-09 | 成都鸾翔凤集食品有限公司 | A kind of low-gelling egg yolk liquid, preparation method and application |
JP7510784B2 (en) | 2020-04-28 | 2024-07-04 | キユーピー株式会社 | Acidic oil-in-water emulsified food and method for improving the browning of the food when baked |
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2006
- 2006-07-27 JP JP2006204733A patent/JP2008029231A/en not_active Withdrawn
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2010110269A1 (en) * | 2009-03-26 | 2010-09-30 | キッコーマン株式会社 | Browning reaction product and fat-based food |
JPWO2010110269A1 (en) * | 2009-03-26 | 2012-09-27 | キッコーマン株式会社 | Browning reaction product and oil and fat food |
CN108013319A (en) * | 2017-11-22 | 2018-05-11 | 恒枫食品科技有限公司 | Antioxidation activity lotion and preparation method thereof |
JP7510784B2 (en) | 2020-04-28 | 2024-07-04 | キユーピー株式会社 | Acidic oil-in-water emulsified food and method for improving the browning of the food when baked |
CN115736150A (en) * | 2022-11-28 | 2023-03-07 | 成都鸾翔凤集食品有限公司 | Yolk liquid instant drink and preparation method thereof |
CN116076675A (en) * | 2022-11-28 | 2023-05-09 | 成都鸾翔凤集食品有限公司 | A kind of low-gelling egg yolk liquid, preparation method and application |
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