JP6884066B2 - Powdered fats and oils - Google Patents

Powdered fats and oils Download PDF

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JP6884066B2
JP6884066B2 JP2017149152A JP2017149152A JP6884066B2 JP 6884066 B2 JP6884066 B2 JP 6884066B2 JP 2017149152 A JP2017149152 A JP 2017149152A JP 2017149152 A JP2017149152 A JP 2017149152A JP 6884066 B2 JP6884066 B2 JP 6884066B2
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starch decomposition
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JP2019024432A (en
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敦 寺田
敦 寺田
政泰 樋口
政泰 樋口
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Showa Sangyo Co Ltd
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Description

本発明は、粉末油脂に関する。より詳しくは、所定の特性を満たす澱粉分解物を含有する粉末油脂に関する。 The present invention relates to powdered fats and oils. More specifically, the present invention relates to powdered fats and oils containing a starch decomposition product satisfying predetermined properties.

粉末油脂は、その作業性・保存安定性の良さや、水溶性の物性等から、近年、様々な食品に用いられている。例えば、粉末スープ、粉末調味料、粉末飲料等の粉末食品、ホットケーキミックス、お好み焼粉、たこ焼粉、天ぷら粉、から揚げ粉等のプレミックス製品、パン類、菓子類、麺類、水練り製品、畜肉製品、お好み焼、たこ焼、揚げ物などの加工食品等に、粉末油脂が用いられている。このように、様々な食品への用途が期待できる粉末油脂について、種々の特性を有する粉末油脂を製造する技術が開発されつつある。 Powdered fats and oils have been used in various foods in recent years because of their good workability and storage stability, and their water-soluble physical characteristics. For example, powdered foods such as powdered soups, powdered seasonings, powdered beverages, premixed products such as hot cake mix, okonomiyaki powder, takoyaki powder, tempura powder, fried chicken, breads, confectionery, noodles, water. Powdered fats and oils are used in processed foods such as paste products, livestock meat products, okonomiyaki, takoyaki, and fried foods. As described above, with respect to powdered fats and oils that can be expected to be used in various foods, techniques for producing powdered fats and oils having various characteristics are being developed.

例えば、特許文献1では、澱粉分解物及び還元澱粉分解物からなる群から選択される少なくとも1種を含む溶液を乾燥面に吹き付け液滴状態で乾燥し、剥離することで、中空球状物を形成された、油の吸着性及び保持能に優れた吸油性組成物を製造する技術が開示されている。 For example, in Patent Document 1, a hollow sphere is formed by spraying a solution containing at least one selected from the group consisting of a starch decomposition product and a reduced starch decomposition product onto a dry surface, drying the solution in a droplet state, and peeling the solution. A technique for producing an oil-absorbing composition having excellent oil adsorptivity and retention ability is disclosed.

特許文献2では、食用油脂100重量部に対して、ヘミセルロース6.6〜10重量部および高度分岐環状デキストリン34〜60重量部を含有させることで、保存安定性が高く、水に対する溶解性の良好な粉末油脂組成物を製造する技術が開示されている。 In Patent Document 2, by containing 6.6 to 10 parts by weight of hemicellulose and 34 to 60 parts by weight of highly branched cyclic dextrin with respect to 100 parts by weight of edible oil and fat, storage stability is high and solubility in water is good. A technique for producing a powdered oil / fat composition is disclosed.

ここで、粉末油脂は、油脂にタンパク質や糖、乳化剤などを加えて乾燥して粉末にしたもので、その製造工程で、水相と油相とを混合して乳化させる必要があるため、一般的に乳化剤の使用が必須である。しかし、乳化剤によっては、特有の不快な風味があるため、飲食品の風味に悪影響を与えることがあり、添加できる量に限りがある等というデメリットがある。また、乳化剤は、添加コストが高いことや食品添加物であることにより、近年、消費者から敬遠される傾向がある。 Here, powdered fats and oils are made by adding proteins, sugars, emulsifiers, etc. to fats and oils and drying them into powder. In the manufacturing process, it is necessary to mix the aqueous phase and the oil phase and emulsify them. The use of emulsifiers is essential. However, some emulsifiers have a peculiar unpleasant flavor, which may adversely affect the flavor of foods and drinks, and have a demerit that the amount that can be added is limited. In addition, emulsifiers tend to be shunned by consumers in recent years due to their high addition cost and food additives.

そこで、乳化剤等の添加剤を用いないで、粉末油脂を製造する技術も開発されている。例えば、特許文献3では、XXX型トリグリセリドを65〜99質量%と、X2Y型トリグリセリドを35〜1質量%とを含有させることにより、乳化剤、賦形剤等の添加剤を含めることなく粉末状の油脂組成物を製造する技術が開示されている。 Therefore, a technique for producing powdered fats and oils without using additives such as emulsifiers has also been developed. For example, in Patent Document 3, by containing 65 to 99% by mass of XXX type triglyceride and 35 to 1% by mass of X2Y type triglyceride, it is in powder form without including additives such as emulsifiers and excipients. A technique for producing an oil / fat composition is disclosed.

特開2012−96226号公報Japanese Unexamined Patent Publication No. 2012-96226 特開2006−14629号公報Japanese Unexamined Patent Publication No. 2006-14629 WO2016/013582A1WO2016 / 013582A1

前述の通り、粉末油脂の製造技術については様々な提案がされているが、消費者の嗜好性の変化や、より高品質な製品が好まれるようになり、その技術はまだまだ発展途上にあるのが実情である。 As mentioned above, various proposals have been made for manufacturing technology for powdered fats and oils, but the technology is still developing due to changes in consumer tastes and the preference for higher quality products. Is the reality.

特に、前述したように、粉末油脂に必須とされていた乳化剤については、消費者の健康志向の高まり等によって、その使用量を減らす技術が期待されている。 In particular, as described above, with respect to emulsifiers that have been essential for powdered fats and oils, a technique for reducing the amount of emulsifiers used is expected due to the growing health consciousness of consumers.

そこで、本発明では、乳化剤の添加量を減らすことが可能な粉末油脂の製造技術を提供することを主目的とする。 Therefore, it is a main object of the present invention to provide a technique for producing powdered fats and oils capable of reducing the amount of emulsifier added.

本願発明者らは、粉末油脂の製造技術について鋭意研究を行った結果、特定の構造を有する澱粉分解物を基材として用いることにより、乳化剤の添加量が少なくても、既存の粉末油脂と同等の品質の粉末油脂を製造できることを見出した。また、この澱粉分解物の配合割合を高めることで、他の乳化安定剤を使用しなくても乾燥前の乳化液の乳化安定性を高めることにも成功した。即ち、乳化剤フリーの粉末油脂を製造することも可能にし、本発明を完成させるに至った。 As a result of diligent research on the manufacturing technology of powdered fats and oils, the inventors of the present application use a starch decomposition product having a specific structure as a base material, so that even if the amount of emulsifier added is small, it is equivalent to existing powdered fats and oils. It was found that it is possible to produce powdered fats and oils of the same quality. In addition, by increasing the blending ratio of this starch decomposition product, we succeeded in increasing the emulsion stability of the emulsion before drying without using other emulsion stabilizers. That is, it has also made it possible to produce emulsifier-free powdered fats and oils, which has led to the completion of the present invention.

即ち、本発明では、下記(1)及び(2)を満たす主鎖と分岐鎖とからなる分岐糖質を含む澱粉分解物を含む粉末油脂を提供する。
(1)7≦x;但し、xは、グルコース重合度(DP)が8〜9である分岐鎖の澱粉分解物中の含有量(質量%)である。
(2)31≦y≦60;但し、yは、分子量が14000〜80000である画分の澱粉分解物中の含有量(質量%)である。
本発明に係る粉末油脂において、前記xは、下記(1’)を満たしていてもよい。
(1’)8≦x
本発明に係る粉末油脂において、前記yは、下記(2’)を満たしていてもよい。
(2’)35≦y≦60
本発明に係る粉末油脂に用いる前記澱粉分解物において、分子量が14000〜80000である画分には、グルコース重合度(DP)が8〜9である分岐鎖を有する分岐糖質の少なくとも一部が含まれていてもよい。
That is, the present invention provides a powdered fat or oil containing a starch decomposition product containing a branched sugar composed of a main chain and a branched chain satisfying the following (1) and (2).
(1) 7 ≦ x; However, x is the content (mass%) of the branched chain having a glucose polymerization degree (DP) of 8 to 9 in the starch decomposition product.
(2) 31 ≦ y ≦ 60; However, y is the content (mass%) in the starch decomposition product of the fraction having a molecular weight of 14,000 to 80,000.
In the powdered oil and fat according to the present invention, the x may satisfy the following (1').
(1') 8 ≤ x
In the powdered oil and fat according to the present invention, the y may satisfy the following (2').
(2') 35 ≤ y ≤ 60
In the starch decomposition product used for the powdered fats and oils according to the present invention, at least a part of the branched sugar having a branched chain having a glucose polymerization degree (DP) of 8 to 9 is contained in the fraction having a molecular weight of 14,000 to 80,000. It may be included.

本発明によれば、乳化剤の添加量が少ない粉末油脂や、乳化剤フリーの粉末油脂を提供することができる。 According to the present invention, it is possible to provide powdered fats and oils with a small amount of emulsifier added and emulsifier-free powdered fats and oils.

以下、本発明を実施するための好適な形態について説明する。なお、以下に説明する実施形態は、本発明の代表的な実施形態の一例を示したものであり、これにより本発明の範囲が狭く解釈されることはない。 Hereinafter, suitable embodiments for carrying out the present invention will be described. It should be noted that the embodiments described below show an example of typical embodiments of the present invention, and the scope of the present invention is not narrowly interpreted by this.

<澱粉分解物>
まず、本発明に用いる澱粉分解物について説明する。本発明に係る粉末油脂は、以下に説明する澱粉分解物を含有する。
<Starch decomposition product>
First, the starch decomposition product used in the present invention will be described. The powdered fats and oils according to the present invention contain the starch decomposition products described below.

粉末油脂の製造において、以下に説明する澱粉分解物を用いることで、粉末油脂の製造過程で調製する乳化液(噴霧原液等)の粘度が上昇しすぎるのを防止し、また、乳化液の乳化安定性を良好にすることができる。また、粉末油脂の製造過程(例えば、噴霧乾燥工程等)において、その作業性を良好にすることができる。また、以下に説明する澱粉分解物を粉末油脂に用いれば、乳化剤の添加量を低減させることができる。更に、以下に説明する澱粉分解物は、粉末油脂の基材として用いるとともに、乳化液中の配合割合を高めることで、乳化剤フリーの粉末油脂を製造することも可能である。また、以下に説明する澱粉分解物を粉末油脂に用いれば、外観、保存安定性、溶解性、食味等が良好な粉末油脂を得ることができる。加えて、以下に説明する澱粉分解物は、従来の澱粉分解物に比べて、所謂、澱粉臭が低減されているため、これを、粉末油脂に用いた場合に、風味への悪影響がほとんどない。 By using the starch decomposition products described below in the production of powdered fats and oils, it is possible to prevent the viscosity of the emulsion (spray stock solution, etc.) prepared in the manufacturing process of the powdered fats and oils from increasing too much, and to emulsify the emulsion. Stability can be improved. Further, in the manufacturing process of powdered fats and oils (for example, spray drying step, etc.), the workability can be improved. Further, if the starch decomposition product described below is used for powdered fats and oils, the amount of emulsifier added can be reduced. Further, the starch decomposition product described below can be used as a base material for powdered fats and oils, and an emulsifier-free powdered fats and oils can be produced by increasing the blending ratio in the emulsion. Further, when the starch decomposition product described below is used for the powdered fat or oil, the powdered fat or oil having good appearance, storage stability, solubility, taste and the like can be obtained. In addition, the starch decomposition product described below has a reduced so-called starch odor as compared with the conventional starch decomposition product, and therefore, when it is used for powdered fats and oils, there is almost no adverse effect on the flavor. ..

本発明で用いる澱粉分解物は、主鎖と分岐鎖とからなる分岐糖質を含む。そして、この澱粉分解物中のグルコース重合度(DP)が8〜9である分岐鎖の含有量(質量%)xが、下記(1)を満たすことを特徴とする。
(1)7≦x
The starch decomposition product used in the present invention contains a branched sugar composed of a main chain and a branched chain. The content (mass%) x of the branched chain having a glucose polymerization degree (DP) of 8 to 9 in the starch decomposition product is characterized by satisfying the following (1).
(1) 7 ≦ x

なお、グルコース重合度(DP)が8〜9である分岐鎖の澱粉分解物中の含有量(質量%)xは、澱粉分解物中に含まれるDP8〜9である糖鎖の含有量と、澱粉分解物をイソアミラーゼやプルラナーゼ等の枝切り酵素で処理することにより分岐鎖が切られた状態でのDP8〜9である糖鎖の含有量とを測定し、枝切り酵素処理によって増加したDP8〜9である糖鎖の量を算出することにより求めることができる。 The content (% by mass) x of the branched chain having a glucose polymerization degree (DP) of 8 to 9 in the starch decomposition product is the content of the sugar chain having DP 8 to 9 contained in the starch decomposition product. By treating the starch decomposition product with a debranching enzyme such as isoamylase or pullulanase, the sugar chain content, which is DP8 to 9 in the state where the branched chain was cut, was measured, and the DP8 increased by the debranching enzyme treatment. It can be obtained by calculating the amount of sugar chains of ~ 9.

また、本発明で用いる澱粉分解物は、分子量が14000〜80000である画分の含有量(質量%)yが、下記(2)を満たすことを特徴とする。
(2)31≦y≦60
Further, the starch decomposition product used in the present invention is characterized in that the content (mass%) y of the fraction having a molecular weight of 14,000 to 80,000 satisfies the following (2).
(2) 31 ≤ y ≤ 60

本発明で用いる澱粉分解物は、グルコース重合度(DP)が8〜9である分岐鎖の澱粉分解物中の含有量(質量%)xと、分子量が14000〜80000である画分の澱粉分解物中の含有量(質量%)yとが、前記(1)及び(2)の両方を満たすことを特徴とする。 The starch decomposition product used in the present invention has a content (mass%) x in the starch decomposition product of a branched chain having a glucose polymerization degree (DP) of 8 to 9, and starch decomposition of a fraction having a molecular weight of 14,000 to 80,000. The content (% by mass) y in the product is characterized by satisfying both (1) and (2) above.

本発明で用いる澱粉分解物は、前記(1)及び(2)を満たしていればよいが、前記xは、下記(1’)を満たすことが好ましい。前記xが、下記(1’)を満たすと、粉末油脂の製造過程で調製する乳化液(噴霧原液等)の乳化安定性が更に良好となり、また、粉末油脂の製造工程における作業性を良好にすることができる。更に、外観、保存安定性、溶解性、食味等が更に良好な粉末油脂を得ることができる。
(1’)8≦x
The starch decomposition product used in the present invention may satisfy the above (1) and (2), but it is preferable that the x satisfies the following (1'). When the x satisfies the following (1'), the emulsification stability of the emulsified liquid (spray stock solution, etc.) prepared in the powdered fats and oils manufacturing process becomes further good, and the workability in the powdered fats and oils manufacturing process is improved. can do. Further, powdered fats and oils having better appearance, storage stability, solubility, taste and the like can be obtained.
(1') 8 ≤ x

また、前記yは、下記(2’)を満たすことが好ましい。前記yが、下記(2’)を満たすと、粉末油脂の製造過程で調製する乳化液(噴霧原液等)の乳化安定性が更に良好となり、また、粉末油脂の製造工程における作業性を良好にすることができる。更に、外観、保存安定性、溶解性、食味等が良好な粉末油脂を得ることができる。
(2’)35≦y≦60
Further, it is preferable that the y satisfies the following (2'). When the y satisfies the following (2'), the emulsification stability of the emulsion (spray stock solution, etc.) prepared in the powder fat and oil production process becomes further good, and the workability in the powder fat and oil production process becomes good. can do. Further, powdered fats and oils having good appearance, storage stability, solubility, taste and the like can be obtained.
(2') 35 ≤ y ≤ 60

本発明で用いる澱粉分解物において、分子量が14000〜80000である画分には、グルコース重合度(DP)が8〜9である分岐鎖を有する分岐糖質の少なくとも一部が含まれていてもよい。即ち、グルコース重合度(DP)が8〜9である分岐鎖を有する分岐糖質の一部又は全部が、分子量が14000〜80000である画分に含まれていてもよく、グルコース重合度(DP)が8〜9である分岐鎖を有する分岐糖質の一部が、分子量が14000〜80000である画分以外の画分に含まれていてもよい。 In the starch decomposition product used in the present invention, even if the fraction having a molecular weight of 14,000 to 80,000 contains at least a part of branched sugar having a branched chain having a glucose polymerization degree (DP) of 8 to 9. Good. That is, a part or all of the branched sugar having a branched chain having a glucose polymerization degree (DP) of 8 to 9 may be contained in the fraction having a molecular weight of 14,000 to 80,000, and the glucose polymerization degree (DP) may be contained. ) May be contained in a fraction other than the fraction having a molecular weight of 14,000 to 80,000.

更に、本発明に用いる澱粉分解物において、グルコース重合度(DP)が3〜7である分岐鎖の澱粉分解物中の含有量(質量%)zは、下記(3)を満たすことが好ましい。
(3)z≦15
Further, in the starch decomposition product used in the present invention, the content (mass%) z of the branched chain in the starch decomposition product having a glucose polymerization degree (DP) of 3 to 7 preferably satisfies the following (3).
(3) z ≦ 15

グルコース重合度(DP)が3〜7である分岐鎖の澱粉分解物中の含有量(質量%)を15質量%以下とすることにより、粉末油脂の製造過程で調製する乳化液(噴霧原液等)の乳化安定性が更に良好となり、また、粉末油脂の製造工程における作業性を良好にすることができる。更に、外観、保存安定性、溶解性、食味等が良好な粉末油脂を得ることができる。 An emulsion (spray stock solution, etc.) prepared in the process of producing powdered fats and oils by setting the content (% by mass) of the branched chain having a glucose polymerization degree (DP) of 3 to 7 in the starch decomposition product to 15% by mass or less. ) Can be further improved in emulsion stability, and workability in the manufacturing process of powdered fats and oils can be improved. Further, powdered fats and oils having good appearance, storage stability, solubility, taste and the like can be obtained.

なお、グルコース重合度(DP)が3〜7である分岐鎖の澱粉分解物中の含有量(質量%)zは、グルコース重合度(DP)が8〜9である分岐鎖の澱粉分解物中の含有量(質量%)xと同様に、澱粉分解物中に含まれるDP3〜7である糖鎖の含有量と、澱粉分解物をイソアミラーゼやプルラナーゼ等の枝切り酵素で処理することにより分岐鎖が切られた状態でのDP3〜7である糖鎖の含有量とを測定し、枝切り酵素処理によって増加したDP3〜7である糖鎖の量を算出することにより求めることができる。 The content (% by mass) z in the starch decomposition product of the branched chain having a glucose polymerization degree (DP) of 3 to 7 is the content (mass%) z in the starch decomposition product of the branched chain having a glucose polymerization degree (DP) of 8 to 9. Content (% by mass) x, the content of sugar chains that are DP3 to 7 contained in the starch decomposition product, and the starch decomposition product are branched by treating with a debranching enzyme such as isoamylase or pullulanase. It can be obtained by measuring the content of sugar chains having DP3 to 7 in a broken chain state and calculating the amount of sugar chains having DP3 to 7 increased by pullulanase treatment.

<澱粉分解物の製造方法>
本発明で用いる澱粉分解物は、その組成自体が新規であって、その収得の方法については特に限定されることはない。例えば、澱粉原料を、一般的な酸や酵素を用いた処理や、各種クロマトグラフィー、膜分離、エタノール沈殿等の所定操作を適宜、組み合わせて行うことによって得ることができる。
<Manufacturing method of starch decomposition products>
The starch decomposition product used in the present invention has a novel composition itself, and the method for obtaining the starch decomposition product is not particularly limited. For example, the starch raw material can be obtained by appropriately combining predetermined operations such as treatment with a general acid or enzyme, various chromatographys, membrane separation, ethanol precipitation and the like.

本発明で用いる澱粉分解物を得るために原料となり得る澱粉原料としては、公知の澱粉分解物の原料となり得る澱粉原料を1種又は2種以上自由に選択して用いることができる。例えば、コーンスターチ、米澱粉、小麦澱粉等の澱粉(地上系澱粉)、馬鈴薯、キャッサバ、甘藷等のような地下茎又は根由来の澱粉(地下系澱粉)を挙げることができる。 As the starch raw material that can be used as a raw material for obtaining the starch decomposition product used in the present invention, one or more starch raw materials that can be a known raw material for the starch decomposition product can be freely selected and used. Examples thereof include starches such as cornstarch, rice starch and wheat starch (aboveground starch), and starches derived from underground stems or roots such as potatoes, cassava and sweet potatoes (underground starch).

本発明で用いる澱粉分解物を効率的に得る方法として、澱粉原料を、酸又はαアミラーゼを用いて液化した後、枝作り酵素を作用させる方法がある。酸を用いて液化する場合、本発明で用いる澱粉分解物の製造に用いることができる酸の種類は特に限定されず、澱粉の酸液化が可能な酸であれば、公知の酸を1種又は2種以上、自由に選択して用いることができる。例えば、塩酸、シュウ酸等を用いることができる。 As a method for efficiently obtaining the starch decomposition product used in the present invention, there is a method in which a starch raw material is liquefied with an acid or α-amylase and then a branching enzyme is allowed to act on it. When liquefied with an acid, the type of acid that can be used for producing the starch decomposition product used in the present invention is not particularly limited, and if the acid is capable of acid liquefying starch, one known acid or one is used. Two or more types can be freely selected and used. For example, hydrochloric acid, oxalic acid and the like can be used.

また、澱粉原料の酸液化の前後や、枝作り酵素を作用させる前後に、他の分解酵素(例えば、αアミラーゼ等)による処理を自由に組み合わせることも可能である。例えば、澱粉原料を、酸を用いて液化した後、枝作り酵素を作用させ、更に、他の分解酵素(例えば、αアミラーゼ等)による処理を行う方法を採用することも可能である。このように、酸液化、枝作り酵素による作用の後に、分解酵素を作用させることで、澱粉分解物の分解度を所望の範囲に調整することが容易になる。 It is also possible to freely combine treatments with other degrading enzymes (for example, α-amylase) before and after acid liquefaction of the starch raw material and before and after the action of the branching enzyme. For example, it is also possible to adopt a method in which a starch raw material is liquefied with an acid, then a branching enzyme is allowed to act on the starch raw material, and then the starch raw material is further treated with another degrading enzyme (for example, α-amylase). As described above, by allowing the decomposing enzyme to act after the action by the acid liquefaction and the branching enzyme, it becomes easy to adjust the degree of decomposition of the starch decomposition product to a desired range.

また、本発明で用いる澱粉分解物は、澱粉原料の酸液化を行わず、澱粉原料をαアミラーゼ等の分解酵素を用いて液化し、次いで、枝作り酵素を用いた処理を行った後、更に、αアミラーゼ等の分解酵素を用いて分解することによっても、製造することができる。 Further, in the starch decomposition product used in the present invention, the starch raw material is not acidified, but the starch raw material is liquefied using a decomposing enzyme such as α-amylase, and then treated with a branching enzyme, and then further. It can also be produced by degrading with a degrading enzyme such as α-amylase.

ここで、枝作り酵素(branching enzyme)とは、α−1,4−グルコシド結合でつながった直鎖グルカンに作用し、α−1,4−グルコシド結合を切断してα−1,6−グルコシド結合による枝分かれを形成させる働きを持った酵素の総称である。本発明で用いる澱粉分解物の製造で枝作り酵素を用いる場合、その種類は特に限定されず、公知の枝作り酵素を1種又は2種以上、自由に選択して用いることができる。例えば、動物や細菌等から精製したもの、又は、馬鈴薯、イネ種実、トウモロコシ種実等の植物から精製したもの等を用いることができる。 Here, the branching enzyme acts on a linear glucan linked by an α-1,4-glucoside bond, cleaves the α-1,4-glucoside bond, and α-1,6-glucoside. It is a general term for enzymes that have the function of forming branches by binding. When a branching enzyme is used in the production of the starch decomposition product used in the present invention, the type thereof is not particularly limited, and one or more known branching enzymes can be freely selected and used. For example, those purified from animals, bacteria and the like, or those purified from plants such as potatoes, rice seeds and corn seeds can be used.

以上のように、本発明で用いる澱粉分解物を製造する方法は特に限定されないが、澱粉原料を酸又は酵素で液化した後、枝作り酵素処理を行う方法が好ましい。この方法を用いれば、グルコース重合度(DP)8〜9の分岐鎖の含有量を所望の範囲に調整しやすいため、本発明で用いる澱粉分解物を安価にかつ、工業的に製造する場合に好適である。更に、澱粉原料の液化の前後や、枝作り酵素を作用させる前後に、αアミラーゼ処理を行う方法が好ましい。この方法を用いれば、澱粉分解物の分解度を所望の範囲に調整することが容易になる。 As described above, the method for producing the starch decomposition product used in the present invention is not particularly limited, but a method in which the starch raw material is liquefied with an acid or an enzyme and then subjected to a branching enzyme treatment is preferable. By using this method, the content of branched chains having a glucose polymerization degree (DP) of 8 to 9 can be easily adjusted to a desired range. Therefore, when the starch decomposition product used in the present invention is inexpensively and industrially produced. Suitable. Further, a method of performing α-amylase treatment before and after liquefaction of the starch raw material and before and after the action of the branching enzyme is preferable. By using this method, it becomes easy to adjust the degree of decomposition of the starch decomposition product to a desired range.

また、本発明では、目的の澱粉分解物となるように各種処理を行った後に、活性炭脱色、イオン精製等を行い、不純物を除去することも可能であり、不純物を除去することが好ましい。 Further, in the present invention, it is possible to remove impurities by performing various treatments so as to obtain the desired starch decomposition product, and then performing activated carbon decolorization, ion purification and the like, and it is preferable to remove impurities.

そして、真空乾燥や噴霧乾燥により脱水乾燥することで粉末化した状態で粉末油脂に用いることができる。 Then, it can be used for powdered fats and oils in a powdered state by dehydration drying by vacuum drying or spray drying.

<粉末油脂>
本発明に係る粉末油脂は、前述した澱粉分解物を含有することを特徴とする。また、本発明に係る粉末油脂は、澱粉分解物特有の不快な風味が非常に少ないため、食品の風味への悪影響がほとんどなく、様々な食品への応用が可能である。
<Powdered fats and oils>
The powdered oil and fat according to the present invention is characterized by containing the above-mentioned starch decomposition product. Further, since the powdered oil and fat according to the present invention has very little unpleasant flavor peculiar to starch decomposition products, it has almost no adverse effect on the flavor of foods and can be applied to various foods.

本発明に係る粉末油脂は、前述した澱粉分解物を含んでいれば、他の組成は特に限定されない。例えば、前述した澱粉分解物を単独で基材として用いてもよいし、公知の粉末油脂に用いられている基材と、前述した澱粉分解物とを併用して用いることもできる。そして、いずれの場合も、従来の粉末油脂には必須と考えられていた乳化剤の添加量を低減したり、乳化剤を全く用いない、所謂、乳化剤フリーの粉末油脂を製造することも可能である。 The powdered fats and oils according to the present invention are not particularly limited in composition as long as they contain the above-mentioned starch decomposition products. For example, the above-mentioned starch decomposition product may be used alone as a base material, or the base material used for known powdered fats and oils and the above-mentioned starch decomposition product may be used in combination. In either case, it is possible to reduce the amount of emulsifier added, which was considered to be essential for conventional powdered fats and oils, and to produce so-called emulsifier-free powdered fats and oils that do not use emulsifiers at all.

本発明に係る粉末油脂に用いる食用油脂としては、本発明の効果を損なわない限り、公知の食用油脂を1種又は2種以上、自由に選択して用いることができる。例えば、大豆油、菜種油、キャノーラ油、コーン油、ひまわり油、紅花油、とうもろこし油、綿実油、ゴマ油、シソ油、亜麻仁油、落花生油、オリーブ油、アボカド油、チアシード油、ブドウ種子油、マカデミアナッツ油、ヘーゼルナッツ油、カボチャ種子油、クルミ油、椿油、茶実油、エゴマ油、ボラージ油、米糠油、小麦胚芽油、パーム油、パーム核油、ヤシ油、カカオ脂、牛脂、豚脂、鶏脂、乳脂、魚脂、アザラシ脂、藻類脂等を挙げることができる。また、品質改良によって低飽和化された油脂、水素添加油脂、グリセリンと脂肪酸のエステル化油、エステル交換油、分別油脂なども適宜使用することができる。さらに、遺伝子組換えの技術を用いて品種改良した植物から抽出したものであってもよい。 As the edible fats and oils used for the powdered fats and oils according to the present invention, one or more known edible fats and oils can be freely selected and used as long as the effects of the present invention are not impaired. For example, soybean oil, rapeseed oil, canola oil, corn oil, sunflower oil, red flower oil, corn oil, cottonseed oil, sesame oil, perilla oil, flaxseed oil, peanut oil, olive oil, avocado oil, chia seed oil, grape seed oil, macadamia nut oil, Hazelnut oil, pumpkin seed oil, walnut oil, camellia oil, tea seed oil, egoma oil, borage oil, rice bran oil, wheat germ oil, palm oil, palm kernel oil, palm oil, cacao butter, beef fat, pork fat, chicken fat, Milk fat, fish fat, corn oil, algae fat and the like can be mentioned. Further, fats and oils saturated by quality improvement, hydrogenated fats and oils, esterified oils of glycerin and fatty acids, transesterified oils, fractionated fats and oils and the like can also be appropriately used. Further, it may be extracted from a plant whose variety has been improved by using a gene recombination technique.

本発明に係る粉末油脂では、前述した澱粉分解物を単独で基材として用いることができるが、必要に応じて、公知の基材を用いることも可能である。公知の基材を用いる場合、本発明の効果を損なわない限りその種類は特に限定されず、粉末油脂に用いることができる公知の基材を1種又は2種以上、自由に選択して用いることができる。例えば、乳蛋白、大豆蛋白、小麦蛋白、全脂粉乳、脱脂粉乳、小麦粉、澱粉、糖類、ゼラチン、ガム質、前述した澱粉分解物以外の澱粉分解物、デキストリン、及びこれらの加工品等が挙げられる。 In the powdered fats and oils according to the present invention, the above-mentioned starch decomposition product can be used alone as a base material, but a known base material can also be used if necessary. When a known base material is used, the type is not particularly limited as long as the effect of the present invention is not impaired, and one or more known base materials that can be used for powdered fats and oils can be freely selected and used. Can be done. For example, milk protein, soy protein, wheat protein, whole fat powder milk, defatted milk powder, wheat flour, starch, sugar, gelatin, gum, starch decomposition products other than the above-mentioned starch decomposition products, dextrin, processed products thereof and the like can be mentioned. Be done.

本発明に係る粉末油脂において、前述した澱粉分解物と油脂との質量割合は、本発明の効果を損なわない限り、その配合量は特に限定されず、自由に設定することができる。本発明では特に、前述した澱粉分解物を単独で基材として用いる場合、前記澱粉分解物と前記食用油脂との質量割合を、5:1〜1:30に設定することが好ましく、2:1〜1:20がより好ましく、1:1〜1:10がさらにより好ましい。この範囲に設定することで、乳化剤フリーでありながら、又は、乳化剤の添加量を低減させつつ、外観、保存安定性、溶解性、食味等が良好な粉末油脂を提供することができる。また、前述した澱粉分解物と公知の基材とを併用する場合は、基材中における前述した澱粉分解物の割合が、55.0〜99.9質量%とするのが好ましく、60.0〜99.5質量%とするのがより好ましく、70.0〜99.0質量%とするのが更に好ましい。この範囲に設定することで、乳化剤フリーでありながら、又は、乳化剤の添加量を低減させつつ、外観、保存安定性、溶解性、食味等が良好な粉末油脂を提供することができる。 In the powdered fats and oils according to the present invention, the mass ratio of the starch decomposition product and the fats and oils described above is not particularly limited and can be freely set as long as the effect of the present invention is not impaired. In the present invention, particularly when the above-mentioned starch decomposition product is used alone as a base material, the mass ratio of the starch decomposition product to the edible oil / fat is preferably set to 5: 1 to 1:30, 2: 1. ~ 1:20 is more preferable, and 1: 1 to 1:10 is even more preferable. By setting this range, it is possible to provide powdered fats and oils that are emulsifier-free or have good appearance, storage stability, solubility, taste, etc. while reducing the amount of emulsifier added. When the above-mentioned starch decomposition product and a known base material are used in combination, the ratio of the above-mentioned starch decomposition product in the base material is preferably 55.0 to 99.9% by mass, preferably 60.0. It is more preferably to 99.5% by mass, and further preferably 70.0 to 99.0% by mass. By setting this range, it is possible to provide powdered fats and oils that are emulsifier-free or have good appearance, storage stability, solubility, taste, etc. while reducing the amount of emulsifier added.

本発明に係る粉末油脂には、本発明の効果を損なわない限り、他の成分を1種又は2種以上、自由に選択して含有させることもできる。他の成分としては、例えば、通常粉末油脂に用いられている乳化剤、pH調整剤、着色剤、矯味剤、安定剤等の成分を用いることができる。更に、公知の又は将来的に見出される機能を有する成分を、適宜目的に応じて併用することも可能である。前述した澱粉分解物は、食品に分類されるため、当該澱粉分解物以外の成分の選択次第では、本発明に係る粉末油脂を、添加剤フリーの食品として取り扱うことも可能である。 The powdered fats and oils according to the present invention may contain one or more other components freely selected as long as the effects of the present invention are not impaired. As other components, for example, components such as emulsifiers, pH adjusters, colorants, flavoring agents, and stabilizers usually used for powdered fats and oils can be used. Furthermore, components having known or future functions can be used in combination as appropriate according to the purpose. Since the starch decomposition products described above are classified as foods, the powdered fats and oils according to the present invention can be treated as additive-free foods depending on the selection of components other than the starch decomposition products.

本発明に係る粉末油脂は、公知の粉末油脂と同等又はそれ以上の品質を有するため、公知の粉末油脂の用途に、好適に用いることができる。例えば、粉末スープ、粉末調味料、粉末飲料等の粉末食品、ホットケーキミックス、お好み焼粉、たこ焼粉、天ぷら粉、から揚げ粉等のプレミックス製品、パン類、菓子類、麺類、水練り製品、畜肉製品、お好み焼、たこ焼、揚げ物などの加工食品等に用いることができる。 Since the powdered fats and oils according to the present invention have a quality equal to or higher than that of known powdered fats and oils, they can be suitably used for known powdered fats and oils. For example, powdered foods such as powdered soups, powdered seasonings, powdered beverages, premixed products such as hot cake mix, okonomiyaki flour, takoyaki flour, tempura flour, and fried flour, breads, confectionery, noodles, and water. It can be used for paste products, livestock meat products, okonomiyaki, takoyaki, processed foods such as fried foods, and the like.

<粉末油脂の製造方法>
本発明に係る粉末油脂は、前述した澱粉分解物を用いていれば、その製造方法については特に限定されず、公知の粉末油脂の製造方法を自由に採用することができる。例えば、前述した澱粉分解物を含有する水相と、食用油脂を含有する油相とをそれぞれ調製した上で、これらの水相及び油相を混合して乳化液を調製し、この乳化液を真空乾燥、噴霧乾燥、凍結乾燥、ドラムドライヤーを用いた乾燥等により乾燥することで、粉末油脂を製造することができる。
<Manufacturing method of powdered fats and oils>
As long as the above-mentioned starch decomposition product is used, the powdered fat or oil according to the present invention is not particularly limited in its production method, and a known method for producing powdered fat or oil can be freely adopted. For example, after preparing the aqueous phase containing the above-mentioned starch decomposition product and the oil phase containing edible oil and fat, these aqueous phases and the oil phase are mixed to prepare an emulsion, and the emulsion is prepared. Powdered oils and fats can be produced by drying by vacuum drying, spray drying, freeze drying, drying using a drum dryer, or the like.

以下、実施例に基づいて本発明を更に詳細に説明する。なお、以下に説明する実施例は、本発明の代表的な実施例の一例を示したものであり、これにより本発明の範囲が狭く解釈されることはない。 Hereinafter, the present invention will be described in more detail based on Examples. It should be noted that the examples described below show an example of a typical example of the present invention, and the scope of the present invention is not narrowly interpreted by this.

(1)試験方法
[枝作り酵素]
本実験例では、枝作り酵素の一例として、WO00/58445の方法に則って、精製したRhodothermus obamensis由来の酵素(以下「枝作り酵素」とする)を用いた。
(1) Test method [branch-making enzyme]
In this experimental example, an enzyme derived from Rhodothermus obamensis (hereinafter referred to as "branching enzyme") purified according to the method of WO00 / 58445 was used as an example of the branching enzyme.

なお、枝作り酵素の活性測定は、以下の方法で行った。
基質溶液として、0.1M酢酸緩衝液(pH5.2)にアミロース(Sigma社製,A0512)を0.1質量%溶解したアミロース溶液を用いた。
50μLの基質液に50μLの酵素液を添加し、30℃で30分間反応させた後、ヨウ素-ヨウ化カリウム溶液(0.39mMヨウ素−6mMヨウ化カリウム−3.8mM塩酸混合用液)を2mL加え反応を停止させた。ブランク溶液として、酵素液の代わりに水を添加したものを調製した。反応停止から15分後に660nmの吸光度を測定した。枝作り酵素の酵素活性量1単位は、上記の条件で試験する時、660nmの吸光度を1分間に1%低下させる酵素活性量とした。
The activity of the branching enzyme was measured by the following method.
As the substrate solution, an amylose solution in which 0.1% by mass of amylose (manufactured by Sigma, A0512) was dissolved in 0.1 M acetate buffer (pH 5.2) was used.
Add 50 μL of enzyme solution to 50 μL of substrate solution, react at 30 ° C. for 30 minutes, and then add 2 mL of iodine-potassium iodide solution (0.39 mM iodine-6 mM potassium iodide-3.8 mM hydrochloric acid mixing solution). In addition, the reaction was stopped. As a blank solution, a solution to which water was added instead of the enzyme solution was prepared. The absorbance at 660 nm was measured 15 minutes after the reaction was stopped. The enzyme activity amount of 1 unit of the branching enzyme was defined as the enzyme activity amount that reduces the absorbance at 660 nm by 1% per minute when tested under the above conditions.

[DE]
「澱粉糖関連工業分析法」(澱粉糖技術部会編)のレインエイノン法に従って算出した。
[DE]
It was calculated according to the Raineinon method of "Starch sugar-related industrial analysis method" (edited by the Starch Sugar Technology Subcommittee).

[澱粉分解物の分子量14000〜80000の画分の含有量]
下記の表1に示す条件で、ゲルろ過クロマトグラフィーにて分析を行った。分子量スタンダードとして、ShodexスタンダードGFC(水系GPC)カラム用Standard P-82(昭和電工株式会社製)を使用し、分子量スタンダードの溶出時間と分子量の相関から算出される検量線に基づいて、澱粉分解物中の分子量14000〜80000の画分の含有量を算出した。
[Contents of fractions having a molecular weight of 14,000 to 80,000 of starch decomposition products]
The analysis was performed by gel filtration chromatography under the conditions shown in Table 1 below. Standard P-82 (manufactured by Showa Denko Co., Ltd.) for Shodex standard GFC (water-based GPC) columns is used as the molecular weight standard, and the decomposition product of starch is based on the calibration curve calculated from the correlation between the elution time of the molecular weight standard and the molecular weight. The content of the fraction having a molecular weight of 14,000 to 80,000 was calculated.

Figure 0006884066
Figure 0006884066

[澱粉分解物中のDP8〜9である分岐鎖又はDP3〜7である分岐鎖の含有量]
a.未処理の澱粉分解物中のDP8〜9又はDP3〜7である糖鎖の含有量の測定
Brix1%に調整した澱粉分解物溶液について、下記表2に示す条件で液体クロマトグラフィーにて分析を行い、保持時間に基づいて、DP8〜9又はDP3〜7の含量を測定した。
[Content of branched chain having DP8-9 or branched chain having DP3-7 in starch decomposition product]
a. Measurement of sugar chain content of DP8-9 or DP3-7 in untreated starch decomposition product The starch decomposition product solution adjusted to Brix 1% was analyzed by liquid chromatography under the conditions shown in Table 2 below. , The content of DP8-9 or DP3-7 was measured based on the retention time.

Figure 0006884066
Figure 0006884066

b.分岐鎖が切られた状態の澱粉分解物の枝切り酵素処理物中のDP8〜9又はDP3〜7である糖鎖の含有量の測定
Brix5%に調整した澱粉分解物溶液200μLに、1M酢酸緩衝液(pH5.0)を2μL、イソアミラーゼ(Pseudomonas sp.由来、Megazyme製)を固形分(g)当たり125ユニット、プルラナーゼ(Klebsiella planticola由来、Megazyme製)を固形分(g)当たり800ユニット添加し、水で全量400μLになるように調整した。これを40℃で24時間酵素反応させた後、煮沸により反応を停止した。これに600μLの水を加え、12000rpmにて5分間遠心分離を行った。上清900μLを脱塩、フィルター処理後、表2に示す条件で液体クロマトグラフィーにて分析を行い、保持時間に基づいて、DP8〜9又はDP3〜7の含量を測定した。
b. Measurement of sugar chain content of DP8-9 or DP3-7 in the debranched enzyme-treated product of starch decomposition product with branched chains 1M acetate buffer in 200 μL of starch decomposition product solution adjusted to Brix 5% Add 2 μL of solution (pH 5.0), 125 units of isoamylase (derived from Pseudomonas sp., Made by Megazyme) per solid content (g), and 800 units of plulanase (derived from Klebsiella starchicola, manufactured by Megazyme) per solid content (g). , The total amount was adjusted to 400 μL with water. This was enzymatically reacted at 40 ° C. for 24 hours, and then the reaction was stopped by boiling. 600 μL of water was added thereto, and centrifugation was performed at 12000 rpm for 5 minutes. After desalting and filtering 900 μL of the supernatant, analysis was performed by liquid chromatography under the conditions shown in Table 2, and the content of DP8-9 or DP3-7 was measured based on the retention time.

c.澱粉分解物中のDP8〜9又はDP3〜7である分岐鎖の含有量の算出
前記bで求めたDP8〜9の含量から、前記aで求めたDP8〜9の含量を引くことにより、澱粉分解物中のDP8〜9である分岐鎖の含有量を算出した。同様に、前記bで求めたDP3〜7の含量から、前記aで求めたDP3〜7の含量を引くことにより、澱粉分解物中のDP3〜7である分岐鎖の含有量を算出した。
c. Calculation of the content of branched chains that are DP8-9 or DP3-7 in the starch decomposition product Starch decomposition by subtracting the content of DP8-9 determined in a from the content of DP8-9 determined in b above. The content of branched chains with DP8-9 in the substance was calculated. Similarly, the content of the branched chain which is DP3 to 7 in the starch decomposition product was calculated by subtracting the content of DP3 to 7 determined in a from the content of DP3 to 7 determined in b.

[評価方法]
a.乳化液(噴霧原液)の粘度
後述する実施例及び比較例に係る乳化液(噴霧原液)について、B型粘度計(東京計器株式会社製)を用いて、その粘度を測定した。測定温度は30℃とし、ローターは、粘度が50〜10,000cpの場合はHM−1ローターを、10,000cp以上の場合はHM−3ローターを用いて、各粘度に適したローターの回転速度で測定を行った。
[Evaluation method]
a. Viscosity of Emulsion Solution (Spray Stock Solution) The viscosity of the emulsion solution (spray stock solution) according to Examples and Comparative Examples described later was measured using a B-type viscometer (manufactured by Tokyo Keiki Co., Ltd.). The measurement temperature is 30 ° C., and the rotor uses an HM-1 rotor when the viscosity is 50 to 10,000 cp and an HM-3 rotor when the viscosity is 10,000 cp or more, and the rotation speed of the rotor suitable for each viscosity is used. The measurement was performed at.

b.乳化液(噴霧原液)の乳化安定性
後述する実施例及び比較例に係る乳化液(噴霧原液)400gを、ガラス瓶(容量500mL)に移したのち、70℃(噴霧原液の貯留温度)で保管して、6時間後の状態を観察し、下記の評価に従って、油相の分離状況を評価した。
◎:油相の分離は認められない。
○:注意して観察すれば、僅かに油相の分離が確認できる。
△:油相の分離が認められる。
×:油相の半分程度が分離していると認められる。
××:油相の大部分〜全部が分離していると認められる。
b. Emulsification stability of emulsion (spray stock solution) 400 g of the emulsion (spray stock solution) according to Examples and Comparative Examples described later is transferred to a glass bottle (capacity 500 mL) and then stored at 70 ° C. (storage temperature of the spray stock solution). Then, the state after 6 hours was observed, and the separation state of the oil phase was evaluated according to the following evaluation.
⊚: Oil phase separation is not observed.
◯: If observed carefully, the separation of the oil phase can be confirmed slightly.
Δ: Separation of oil phase is observed.
X: It is recognized that about half of the oil phase is separated.
XX: It is recognized that most to all of the oil phase is separated.

c.噴霧乾燥工程における作業性
後述する実施例及び比較例に係る乳化液(噴霧原液)を噴霧乾燥する工程における作業性について、下記の評価基準に基づいて評価した。
〇:不具合無く、噴霧乾燥ができた。
△:噴霧乾燥はできたが、何らかの不具合を生じた。
×:噴霧乾燥ができなかった。
c. Workability in the spray drying step The workability in the step of spray drying the emulsion (spray stock solution) according to Examples and Comparative Examples described later was evaluated based on the following evaluation criteria.
〇: Spray drying was possible without any problems.
Δ: Spray drying was possible, but some trouble occurred.
X: Spray drying was not possible.

d.粉末油脂の製造直後の外観評価
後述する実施例及び比較例に係る粉末油脂の製造直後の外観について、下記の評価基準に基づいて評価した。
〇:良好
×:不良(油の分離が認められる等)
d. Appearance evaluation immediately after production of powdered fats and oils The appearance of powdered fats and oils immediately after production according to Examples and Comparative Examples described later was evaluated based on the following evaluation criteria.
〇: Good ×: Defective (oil separation is recognized, etc.)

e.粉末油脂の保存安定性評価
後述する実施例及び比較例に係る粉末油脂を、40℃、湿度75%の条件で5日間保存した後に、油の浸み出し、ケーキング等の有無を外観観察し、下記の評価基準に基づいて評価した。
〇:良好
×:不良(油の浸み出しやケーキングがあり、粉末とは言えない状態等)
e. Evaluation of storage stability of powdered fats and oils After storing the powdered fats and oils according to Examples and Comparative Examples described later for 5 days under the conditions of 40 ° C. and 75% humidity, the appearance of oil seepage, caking, etc. was observed. Evaluation was made based on the following evaluation criteria.
〇: Good ×: Poor (oil oozes and caking, so it cannot be said to be powder, etc.)

f.粉末油脂の溶解性評価
300mLビーカーに後述する実施例及び比較例に係る粉末油脂を10g量りとり、水を100mL注いだ。次に撹拌を行ったのち、溶解するかどうかを観察し、下記の評価基準に基づいて評価した。
〇:全て溶解した。
×:未溶解の粉末油脂があった。
f. Evaluation of Solubility of Powdered Oils and Fats 10 g of powdered oils and fats according to Examples and Comparative Examples described later was weighed in a 300 mL beaker, and 100 mL of water was poured. Next, after stirring, it was observed whether or not it was dissolved, and evaluation was made based on the following evaluation criteria.
〇: All dissolved.
X: There was undissolved powdered fat.

g.粉末油脂の食味
後述する実施例及び比較例に係る粉末油脂を、専門パネラーがさじにて舌先に載せて、その味について、下記の評価基準に基づいて評価した。
◎:非常に良好
○:良好
×:不良
g. Taste of powdered fats and oils Powdered fats and oils according to Examples and Comparative Examples described later were placed on the tip of the tongue by a specialized panelist, and the taste was evaluated based on the following evaluation criteria.
◎: Very good ○: Good ×: Bad

(2)澱粉分解物の製造
[澱粉分解物A]
10質量%消石灰にてpH5.8に調整した30質量%のコーンスターチスラリーに、αアミラーゼ(クライスターゼT10S、天野エンザイム株式会社製)を、固形分(g)当たり0.2質量%添加し、ジェットクッカー(温度110℃)で液化して、この液化液を95℃で保温して、継時的にDEを測定して、DE7になった時点で、10%塩酸でpH4.0に調整し、煮沸により反応を停止した。反応を停止した糖液のpHを6.0に調整した後、枝作り酵素を固形分(g)当たり600ユニット添加し、65℃で60時間反応させた。更にαアミラーゼ(クライスターゼT10S、天野エンザイム株式会社製)を、固形分(g)当たり0.02質量%添加し、80℃で反応を行い、経時的にDEを測定して、DEが10になった時点で、10%塩酸でpH4.0に調整し、煮沸により反応を停止した。この澱粉分解物の溶液を、活性炭脱色、イオン精製し、固形分濃度50質量%に濃縮した。更に濃縮液をスプレードライヤーで粉末化し、澱粉分解物Aを得た。
(2) Production of starch decomposition product [Starch decomposition product A]
Α-amylase (Crystase T10S, manufactured by Amano Enzyme Co., Ltd.) was added in an amount of 0.2% by mass per solid content (g) to a 30% by mass cornstarch slurry adjusted to pH 5.8 with 10% by mass of slaked lime, and jetted. It was liquefied with a cooker (temperature 110 ° C.), the liquefied liquid was kept warm at 95 ° C., DE was measured over time, and when DE7 was reached, the pH was adjusted to 4.0 with 10% hydrochloric acid. The reaction was stopped by boiling. After adjusting the pH of the sugar solution in which the reaction was stopped to 6.0, 600 units of branching enzyme was added per solid content (g), and the reaction was carried out at 65 ° C. for 60 hours. Further, α-amylase (Crystase T10S, manufactured by Amano Enzyme Co., Ltd.) was added in an amount of 0.02% by mass per solid content (g), the reaction was carried out at 80 ° C., and DE was measured over time to bring DE to 10. At that time, the pH was adjusted to 4.0 with 10% hydrochloric acid, and the reaction was stopped by boiling. The solution of this starch decomposition product was decolorized with activated carbon, ion-purified, and concentrated to a solid content concentration of 50% by mass. Further, the concentrated solution was pulverized with a spray dryer to obtain a starch decomposition product A.

[澱粉分解物B]
10質量%消石灰にてpH5.8に調整した30質量%のコーンスターチスラリーに、αアミラーゼ(スピターゼHK、ナガセケムテックス株式会社製)を、固形分(g)当たり0.2質量%添加し、ジェットクッカー(温度110℃)で液化して、この液化液を95℃で保温して、継時的にDEを測定して、DE7になった時点で、10%塩酸でpH4.0に調整し、煮沸により反応を停止した。反応を停止した糖液のpHを6.0に調整した後、枝作り酵素を固形分(g)当たり400ユニット添加し、65℃で60時間反応させた。この澱粉分解物の溶液を、活性炭脱色、イオン精製し、固形分濃度45質量%に濃縮した。更に濃縮液をスプレードライヤーで粉末化し、澱粉分解物Bを得た。
[Starch decomposition product B]
To 30% by mass of cornstarch slurry adjusted to pH 5.8 with 10% by mass of slaked lime, α-amylase (Spitzase HK, manufactured by Nagase ChemteX Corporation) was added in an amount of 0.2% by mass per solid content (g), and jetted. It was liquefied with a cooker (temperature 110 ° C.), the liquefied liquid was kept warm at 95 ° C., DE was measured over time, and when DE7 was reached, the pH was adjusted to 4.0 with 10% hydrochloric acid. The reaction was stopped by boiling. After adjusting the pH of the sugar solution in which the reaction was stopped to 6.0, 400 units of branching enzyme was added per solid content (g), and the reaction was carried out at 65 ° C. for 60 hours. The solution of this starch decomposition product was decolorized with activated carbon, ion-purified, and concentrated to a solid content concentration of 45% by mass. Further, the concentrated solution was pulverized with a spray dryer to obtain a starch decomposition product B.

[澱粉分解物C]
10%塩酸にてpH2.5に調整した30質量%のコーンスターチスラリーを、140℃の温度条件でDE4まで分解した。常圧に戻した後、消石灰を用いて中和することにより反応を停止した糖液のpHを5.8に調整した後、αアミラーゼ(ターマミル120L、ノボザイムズ社製)を、固形分(g)当たり0.02質量%添加し、95℃で反応を行い、経時的にDEを測定して、DEが8になった時点で、10%塩酸でpH4.0に調整し、煮沸により反応を停止した。反応を停止した糖液のpHを6.0に調整した後、枝作り酵素を固形分(g)当たり500ユニット添加し、65℃で45時間反応させた。更にαアミラーゼ(ターマミル120L、ノボザイムズ社製)を、固形分(g)当たり0.02質量%添加し、80℃で反応を行い、経時的にDEを測定して、DEが9になった時点で、10%塩酸でpH4.0に調整し、煮沸により反応を停止した。この澱粉分解物の溶液を、活性炭脱色、イオン精製し、固形分濃度50質量%に濃縮した。更に濃縮液をスプレードライヤーで粉末化し、澱粉分解物Cを得た。
[Starch decomposition product C]
A 30% by mass cornstarch slurry adjusted to pH 2.5 with 10% hydrochloric acid was decomposed to DE4 under a temperature condition of 140 ° C. After returning to normal pressure, the pH of the sugar solution whose reaction was stopped by neutralizing with slaked lime was adjusted to 5.8, and then α-amylase (Termamil 120L, manufactured by Novozymes) was added to the solid content (g). 0.02% by mass was added per unit, the reaction was carried out at 95 ° C., DE was measured over time, and when DE reached 8, the pH was adjusted to 4.0 with 10% hydrochloric acid, and the reaction was stopped by boiling. did. After adjusting the pH of the sugar solution in which the reaction was stopped to 6.0, 500 units of branching enzyme was added per solid content (g), and the reaction was carried out at 65 ° C. for 45 hours. Further, α-amylase (Termamil 120L, manufactured by Novozymes) was added in an amount of 0.02% by mass per solid content (g), the reaction was carried out at 80 ° C., and DE was measured over time. Then, the pH was adjusted to 4.0 with 10% hydrochloric acid, and the reaction was stopped by boiling. The solution of this starch decomposition product was decolorized with activated carbon, ion-purified, and concentrated to a solid content concentration of 50% by mass. Further, the concentrated solution was pulverized with a spray dryer to obtain a starch decomposition product C.

[澱粉分解物D]
10質量%消石灰にてpH5.8に調整した30質量%のタピオカスターチスラリーに、αアミラーゼ(ターマミル120L、ノボザイムズ社製)を、固形分(g)当たり0.2質量%添加し、ジェットクッカー(温度110℃)で液化して、この液化液を95℃で保温して、継時的にDEを測定して、DE10になった時点で、10%塩酸でpH4.0に調整し、煮沸により反応を停止した。この澱粉分解物の溶液を、活性炭脱色、イオン精製し、固形分濃度40質量%に濃縮した。更に濃縮液をスプレードライヤーで粉末化し、澱粉分解物Dを得た。
[Starch decomposition product D]
Α-Amylase (Termamil 120L, manufactured by Novozymes) was added to 30% by mass of tapioca starch slurry adjusted to pH 5.8 with 10% by mass of slaked lime, and 0.2% by mass per solid content (g) was added to a jet cooker (jet cooker). It is liquefied at a temperature of 110 ° C.), the liquefied solution is kept warm at 95 ° C., DE is measured over time, and when DE10 is reached, the pH is adjusted to 4.0 with 10% hydrochloric acid and boiled. The reaction was stopped. The solution of this starch decomposition product was decolorized with activated carbon, ion-purified, and concentrated to a solid content concentration of 40% by mass. Further, the concentrated solution was pulverized with a spray dryer to obtain a starch decomposition product D.

[澱粉分解物E]
10質量%消石灰にてpH5.8に調整した20質量%のワキシーコーンスターチスラリーに、αアミラーゼ(クライスターゼT10S、天野エンザイム株式会社製)を、固形分(g)当たり0.2質量%添加し、ジェットクッカー(温度110℃)で液化して、この液化液を95℃で保温して、継時的にDEを測定して、DE3になった時点で、10%塩酸でpH4.0に調整し、煮沸により反応を停止した。反応を停止した糖液のpHを6.0に調整した後、枝作り酵素を固形分(g)当たり100ユニット添加し、65℃で5時間反応させた。この澱粉分解物の溶液を、活性炭脱色、イオン精製し、固形分濃度30質量%に濃縮した。更に濃縮液をスプレードライヤーで粉末化し、澱粉分解物Eを得た。
[Starch decomposition product E]
Α-amylase (Crystase T10S, manufactured by Amano Enzyme Co., Ltd.) was added in an amount of 0.2% by mass per solid content (g) to 20% by mass of waxy cornstarch slurry adjusted to pH 5.8 with 10% by mass of slaked lime. It was liquefied with a jet cooker (temperature 110 ° C.), the liquefied liquid was kept warm at 95 ° C., DE was measured over time, and when it reached DE3, the pH was adjusted to 4.0 with 10% hydrochloric acid. , The reaction was stopped by boiling. After adjusting the pH of the sugar solution in which the reaction was stopped to 6.0, 100 units of branching enzyme was added per solid content (g), and the reaction was carried out at 65 ° C. for 5 hours. The solution of this starch decomposition product was decolorized with activated carbon, ion-purified, and concentrated to a solid content concentration of 30% by mass. Further, the concentrated solution was pulverized with a spray dryer to obtain a starch decomposition product E.

[澱粉分解物F]
10質量%消石灰にてpH5.8に調整した30質量%のコーンスターチスラリーに、αアミラーゼ(スピターゼHK、ナガセケムテックス株式会社製)を、固形分(g)当たり0.2質量%添加し、ジェットクッカー(温度110℃)で液化して、この液化液を95℃で保温して、継時的にDEを測定して、DE17になった時点で、10%塩酸でpH4.0に調整し、煮沸により反応を停止した。この澱粉分解物の溶液を、活性炭脱色、イオン精製し、固形分濃度50質量%に濃縮した。更に濃縮液をスプレードライヤーで粉末化し、澱粉分解物Fを得た。
[Starch decomposition product F]
To 30% by mass of cornstarch slurry adjusted to pH 5.8 with 10% by mass of slaked lime, α-amylase (Spitzase HK, manufactured by Nagase ChemteX Corporation) was added in an amount of 0.2% by mass per solid content (g), and jetted. It was liquefied with a cooker (temperature 110 ° C.), the liquefied liquid was kept warm at 95 ° C., DE was measured over time, and when DE17 was reached, the pH was adjusted to 4.0 with 10% hydrochloric acid. The reaction was stopped by boiling. The solution of this starch decomposition product was decolorized with activated carbon, ion-purified, and concentrated to a solid content concentration of 50% by mass. Further, the concentrated solution was pulverized with a spray dryer to obtain a starch decomposition product F.

[澱粉分解物G]
クラスターデキストリン(グリコ栄養食品株式会社製)を澱粉分解物Gとした。
[Starch decomposition product G]
Cluster dextrin (manufactured by Glico Foods Co., Ltd.) was designated as starch decomposition product G.

(3)測定
前記で得られた澱粉分解物A〜Gについて、それぞれ、澱粉分解物中のDE、DP8〜9である分岐鎖の含有量、分子量14000〜80000の画分の含有量、DP3〜7の分岐鎖の含有量を、前述した方法で測定した。結果を下記表3に示す。
(3) Measurement For the starch decomposition products A to G obtained above, the content of the branched chains having DE and DP8 to 9 in the starch decomposition product, the content of the fraction having a molecular weight of 14,000 to 80,000, and DP3 to DP3, respectively. The content of the branched chain of 7 was measured by the method described above. The results are shown in Table 3 below.

Figure 0006884066
Figure 0006884066

(4)乳化剤を用いた粉末油脂の製造及び各種評価
[実施例1〜3、比較例1、参考例1]
下記表4に示す量の澱粉分解物A〜D及びFとカゼインナトリウム(「カゼインナトリウムCW」日本新薬株式会社製)を、70℃の水350質量部に溶解して、水相を調製した。油相は、70℃で完全に溶解した精製パーム油(「日清デリカプレミアP」日清オイリオグループ株式会社製、以下同じ)に、下記表4に示す量の乳化剤(「サンソフトNo.8000V」太陽化学株式会社製)を溶解して油相を調製した。調製した水相と油相を混合し、ホモミキサー(ホモミクサーMARKII、プライミクス株式会社製、以下同じ)で12,000rpm、20分間撹拌して乳化液(噴霧原液)を調製した。この乳化液(噴霧原液)について、前記の方法にて粘度と乳化安定性の評価を行った。
(4) Production of powdered fats and oils using an emulsifier and various evaluations [Examples 1 to 3, Comparative Example 1, Reference Example 1]
The amounts of the decomposition products A to D and F shown in Table 4 below and sodium casein (“casein sodium CW” manufactured by Nippon Shinyaku Co., Ltd.) were dissolved in 350 parts by mass of water at 70 ° C. to prepare an aqueous phase. The oil phase is prepared by adding an emulsifier (“Sunsoft No. 8000V”) in the amount shown in Table 4 below to refined palm oil (“Nisshin Delica Premier P” manufactured by Nisshin Oillio Group Co., Ltd., the same applies hereinafter) completely dissolved at 70 ° C. The oil phase was prepared by dissolving (manufactured by Taiyo Kagaku Co., Ltd.). The prepared aqueous phase and oil phase were mixed and stirred with a homomixer (Homomixer MARKII, manufactured by Primix Corporation, the same applies hereinafter) at 12,000 rpm for 20 minutes to prepare an emulsion (spray stock solution). The viscosity and emulsion stability of this emulsion (spray stock solution) were evaluated by the above method.

調製した乳化液を貯留槽に移して70℃に保温し、スプレードライヤーで噴霧乾燥しながら、前記の方法で作業性を評価しつつ、実施例1〜3、比較例1、参考例1の粉末油脂を製造した。なお、参考例1の粉末油脂は、一般的な配合割合で製造した粉末油脂である。製造した各粉末油脂について、前記の方法にて、製造直後の外観、保存安定性、溶解性、及び食味の評価を行った。 The powders of Examples 1 to 3, Comparative Example 1 and Reference Example 1 were transferred to a storage tank, kept at 70 ° C., spray-dried with a spray dryer, and evaluated for workability by the above method. Manufactured fats and oils. The powdered fats and oils of Reference Example 1 are powdered fats and oils produced in a general blending ratio. The appearance, storage stability, solubility, and taste of each of the produced powdered fats and oils immediately after production were evaluated by the above method.

(5)乳化剤を用いた粉末油脂の評価結果
結果を下記表4に示す。
(5) Evaluation results of powdered fats and oils using an emulsifier The results are shown in Table 4 below.

Figure 0006884066
Figure 0006884066

(6)乳化剤フリーの粉末油脂の製造及び各種評価
[実施例4〜6、比較例2〜5]
澱粉分解物A〜G150.0質量部を水350.0質量部に溶解した水溶液(70℃)に、70℃で完全に溶解した精製パーム油190.0質量部を加えて、ホモミキサーで12,000rpm、20分間撹拌して乳化液(噴霧原液)を調製した。この乳化液(噴霧原液)について、前記の方法にて粘度と乳化安定性の評価を行った。なお、比較例2及び4の乳化液(噴霧原液)の粘度測定では、ローターを回転させた直後に、油が分離してきたため、正確な測定ができなかった。
(6) Production of emulsifier-free powdered fats and oils and various evaluations [Examples 4 to 6, Comparative Examples 2 to 5]
Add 190.0 parts by mass of refined palm oil completely dissolved at 70 ° C to an aqueous solution (70 ° C) in which 150.0 parts by mass of starch decomposition products A to G are dissolved in 350.0 parts by mass of water, and use a homomixer to add 120.0 parts by mass. An emulsion (spray stock solution) was prepared by stirring at 000 rpm for 20 minutes. The viscosity and emulsion stability of this emulsion (spray stock solution) were evaluated by the above method. In the viscosity measurement of the emulsions (spray stock solution) of Comparative Examples 2 and 4, the oil was separated immediately after the rotor was rotated, so that accurate measurement could not be performed.

次いで、調製した乳化液を貯留槽に移して70℃に保温し、スプレードライヤーで噴霧乾燥しながら、前記の方法で作業性を評価しつつ、実施例4〜6、比較例2〜5の粉末油脂を製造した。製造した各粉末油脂について、前記の方法にて、製造直後の外観、保存安定性、溶解性、及び食味の評価を行った。なお、比較例2及び4については、乳化液(噴霧原液)を貯留槽に移した段階で油相の分離が発生し、比較例3及び5については、噴霧乾燥工程中に、貯留槽内の乳化液(噴霧原液)に油の分離が認められた。 Next, the prepared emulsion was transferred to a storage tank, kept at 70 ° C., spray-dried with a spray dryer, and while evaluating workability by the above method, the powders of Examples 4 to 6 and Comparative Examples 2 to 5 were used. Manufactured fats and oils. The appearance, storage stability, solubility, and taste of each of the produced powdered fats and oils immediately after production were evaluated by the above method. In Comparative Examples 2 and 4, the oil phase was separated when the emulsion (spray stock solution) was transferred to the storage tank, and in Comparative Examples 3 and 5, the inside of the storage tank was in the spray drying step. Oil separation was observed in the emulsion (spray stock solution).

[比較例6]
澱粉分解物G170.0質量部及びヘミセルロース(「セルエース#80」日本食品化工株式会社製)30.0質量部を水500.0質量部に溶解した水溶液(70℃)に、70℃で完全に溶解した精製パーム油300.0質量部を加えて、ホモミキサーで12,000rpm、20分間撹拌して乳化液(噴霧原液)を調製した。この乳化液(噴霧原液)について、前記の方法にて粘度と乳化安定性の評価を行ったが、粘度については、装置の測定上限(200,000cP)を超過したため、測定できなかった。
[Comparative Example 6]
Completely at 70 ° C. in an aqueous solution (70 ° C.) in which 170.0 parts by mass of starch decomposition product G and hemicellulose (“Cell Ace # 80” manufactured by Nippon Shokuhin Kako Co., Ltd.) were dissolved in 500.0 parts by mass of water. 300.0 parts by mass of dissolved refined palm oil was added, and the mixture was stirred with a homomixer at 12,000 rpm for 20 minutes to prepare an emulsion (spray stock solution). The viscosity and emulsion stability of this emulsion (spray stock solution) were evaluated by the above method, but the viscosity could not be measured because it exceeded the measurement upper limit (200,000 cP) of the apparatus.

次いで、調製した乳化液を貯留槽に移して70℃に保温し、スプレードライヤーで噴霧乾燥しようとしたが、噴霧原液の粘度が高く、噴霧乾燥することができなかった。 Next, the prepared emulsion was transferred to a storage tank, kept at 70 ° C., and attempted to be spray-dried with a spray dryer, but the viscosity of the spray stock solution was high and spray-drying was not possible.

(7)乳化剤フリーの粉末油脂の評価結果
結果を下記表5に示す。
(7) Evaluation results of emulsifier-free powdered fats and oils The results are shown in Table 5 below.

Figure 0006884066
Figure 0006884066

(8)考察
表4に示す通り、DP8〜9の分岐鎖の含有量が7質量%以上、かつ、分子量14000〜80000の画分の含有量が31〜60質量%範囲内の実施例1〜3は、比較例1に比べて、全ての評価において良好であった。また、参考例1と比べても、実施例1〜3は、乳化剤の添加量が少ないにも関わらず、全ての評価において、同等の評価結果を得ることができた。この結果から、前述した澱粉分解物を用いれば、粉末油脂の製造において、乳化剤の添加量を低減させることが可能であることが証明された。
(8) Discussion As shown in Table 4, Examples 1 to 1 in which the content of the branched chain of DP8 to 9 is 7% by mass or more and the content of the fraction having a molecular weight of 14,000 to 80000 is in the range of 31 to 60% by mass. 3 was better in all evaluations than in Comparative Example 1. Further, as compared with Reference Example 1, in Examples 1 to 3, although the amount of the emulsifier added was small, the same evaluation results could be obtained in all the evaluations. From this result, it was proved that the amount of emulsifier added can be reduced in the production of powdered fats and oils by using the above-mentioned starch decomposition product.

表5に示す通り、DP8〜9の分岐鎖の含有量が7質量%以上、かつ、分子量14000〜80000の画分の含有量が31〜60質量%範囲内の実施例4〜6は、比較例2〜6に比べて、全ての評価において良好であった。即ち、前述した澱粉分解物は、乳化液中の配合割合を高めることで、乳化剤フリーの粉末油脂を製造することができることが証明された。 As shown in Table 5, Examples 4 to 6 in which the content of the branched chain of DP8 to 9 is 7% by mass or more and the content of the fraction having a molecular weight of 14,000 to 80000 is in the range of 31 to 60% by mass are compared. Compared with Examples 2 to 6, all evaluations were good. That is, it was proved that the above-mentioned starch decomposition product can produce emulsifier-free powdered fats and oils by increasing the blending ratio in the emulsion.

(9)粉末油脂の食品への利用
[コーンスープ]
スイートコーン缶詰100g、牛乳300g、実施例1、実施例4または参考例1の粉末油脂50gを鍋に入れて、撹拌しながら加熱した。これに食塩およびコショウを少々加えて、コーンスープを製造した。
(9) Use of powdered fats and oils for food [corn soup]
100 g of canned sweet corn, 300 g of milk, and 50 g of powdered fats and oils of Example 1, Example 4 or Reference Example 1 were placed in a pan and heated with stirring. A little salt and pepper were added to this to make corn soup.

実施例1及び4の粉末油脂は、参考例1の粉末油脂と同様に、油浮きや溶け残り等がなく、食味ともに良好なコーンスープを製造できた。 Similar to the powdered fats and oils of Reference Example 1, the powdered fats and oils of Examples 1 and 4 did not have oil floating or undissolved residue, and corn soup having a good taste could be produced.

[食パン]
強力粉250g、ドライイースト3g、グラニュー糖17g、食塩5g、脱脂粉乳6g、実施例3、実施例6または参考例1の粉末油脂8g、水180gの原料配合で、ホームベーカリー(「SD−BT113」パナソニック株式会社製)にて、食パンを製造した。
[Plain bread]
Home bakery ("SD-BT113" Panasonic stock Bread was manufactured at (manufactured by the company).

実施例3及び6の粉末油脂は、参考例1の粉末油脂と同様に、外観・食感ともに良好な食パンを製造できた。
The powdered fats and oils of Examples 3 and 6 were able to produce bread having a good appearance and texture, similarly to the powdered fats and oils of Reference Example 1.

Claims (4)

酸及び/又はαアミラーゼで液化されたコーンスターチを、α−1,4−グルコシド結合を切断してα−1,6−グルコシド結合による枝分かれを形成させる枝作り酵素により処理することで得られる、下記(1)及び(2)を満たす主鎖と分岐鎖とからなる分岐糖質を含む澱粉分解物を含み、
該澱粉分解物:食用油脂=1:1〜10である、粉末油脂。
(1)7≦x;但し、xは、グルコース重合度(DP)が8〜9である分岐鎖の澱粉分解物中の含有量(質量%)である。
(2)31≦y≦60;但し、yは、分子量が14000〜80000である画分の澱粉分解物中の含有量(質量%)である。
Obtained by treating cornstarch liquefied with acid and / or α-amylase with a branching enzyme that cleaves the α-1,4-glucoside bond to form a branch by the α-1,6-glucoside bond, as described below. (1) and viewed including the starch hydrolyzate comprising a branched carbohydrate consisting of a branched main chain satisfying (2),
The starch decomposition product: edible oil and fat = 1: 1 to 10, powdered oil and fat.
(1) 7 ≦ x; However, x is the content (mass%) of the branched chain having a glucose polymerization degree (DP) of 8 to 9 in the starch decomposition product.
(2) 31 ≦ y ≦ 60; However, y is the content (mass%) in the starch decomposition product of the fraction having a molecular weight of 14,000 to 80,000.
前記xが、下記(1’)を満たす請求項1に記載の粉末油脂。
(1’)8≦x
The powdered fat or oil according to claim 1, wherein x satisfies the following (1').
(1') 8 ≤ x
前記yが、下記(2’)を満たす請求項1又は2に記載の粉末油脂。
(2’)35≦y≦60
The powdered fat or oil according to claim 1 or 2, wherein y satisfies the following (2').
(2') 35 ≤ y ≤ 60
前記澱粉分解物の分子量が14000〜80000である画分に、グルコース重合度(DP)が8〜9である前記分岐鎖を有する分岐糖質の少なくとも一部が含まれる請求項1から3のいずれか一項に記載の粉末油脂。 Any of claims 1 to 3, wherein the fraction having a molecular weight of 14,000 to 80,000 of the starch decomposition product contains at least a part of the branched sugar having a branched chain having a glucose polymerization degree (DP) of 8 to 9. The powdered fats and oils according to item 1.
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