[go: up one dir, main page]

JPH0475591A - Usage for edible fatty oil - Google Patents

Usage for edible fatty oil

Info

Publication number
JPH0475591A
JPH0475591A JP2188213A JP18821390A JPH0475591A JP H0475591 A JPH0475591 A JP H0475591A JP 2188213 A JP2188213 A JP 2188213A JP 18821390 A JP18821390 A JP 18821390A JP H0475591 A JPH0475591 A JP H0475591A
Authority
JP
Japan
Prior art keywords
oil
fat
fats
oils
reaction
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2188213A
Other languages
Japanese (ja)
Inventor
Fumino Nishiuchi
西内 文野
Hironori Takahashi
高橋 弘憲
Hisao Miyagawa
宮川 久雄
Chihiro Katou
加藤 千潯
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ajinomoto Co Inc
Original Assignee
Ajinomoto Co Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ajinomoto Co Inc filed Critical Ajinomoto Co Inc
Priority to JP2188213A priority Critical patent/JPH0475591A/en
Publication of JPH0475591A publication Critical patent/JPH0475591A/en
Pending legal-status Critical Current

Links

Landscapes

  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Fats And Perfumes (AREA)

Abstract

PURPOSE:To obtain a stable, low-melting fatty oil giving relatively low level of oily flavor to foods by selective ester interchange reaction of a fatty oil mixture using a 1,3-site-specific lipase. CONSTITUTION:Firstly, a 1,3-site-specific lipase of Rhizopus origin to be used in the reaction, together with an enzyme activator such as lecithin, is dissolved in water and then immobilized on a carrier such as an ion exchange resin followed by drying, thus preparing an immobilized enzyme. Thence, a column is packed with this immobilized enzyme, and continuously charged with a mixed fatty oil (substrate) such as (A) a liquid oil dried to a moisture content of ca. <=200ppm (fractionated oil, vegetable oil such as coconut oil, or animal oil) and another liquid oil, (B) a solid fat (hydrogenated oil, animal fat such as tallow, or vegetable fat) and another solid fat or (C) a liquid oil and a solid oil, to carry out a selective ion exchange reaction, and from a reaction product, the objective low-melting, purified fatty oil excellent in storage stability can be obtained. For the present fatty oil, as its oily flavor is plain, it is possible to make the most of the taste inherent in food materials to be used.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は酵素で改質した油脂のフライ・天ぷら・炒め物
・揚げ菓子・揚げスナック用油脂、ルー・惣菜・真空調
理等の煮込み用油脂、米菓・スナック・麺・調味料・冷
凍食品等のかけ・スプレー等の被覆用油脂、また香料・
天板油・離型油・賦昧油等のベース用油脂、スープ用油
脂等の利用に[従来技術及び問題点] 常温固体脂等融点の高い油脂を用いる場合、安定性は良
いが溶解作業が必要で操作が煩雑になる欠点がある。安
定性が良く融点の低い油脂を得るために行われる分別も
コスト高になるという欠点がある。
[Detailed Description of the Invention] [Industrial Application Field] The present invention is directed to enzyme-modified fats and oils for frying, tempura, stir-fried foods, fried sweets, and fried snacks, and fats and oils for stewing in roux, side dishes, vacuum cooking, etc. , oils and fats for coating rice crackers, snacks, noodles, seasonings, frozen foods, etc., and for flavorings and sprays.
For use as base oils such as baking oil, mold release oil, dipping oil, soup oils, etc. [Prior art and problems] When using oils with a high melting point such as solid fats at room temperature, stability is good, but the dissolution work is difficult. This has the disadvantage that it is necessary and the operation is complicated. Fractionation, which is performed to obtain oils and fats with good stability and a low melting point, also has the drawback of being costly.

また、例えば水添脂を用いた場合は特有の臭気が残るた
め、食品の風味を生かしきることができない。
Furthermore, for example, when hydrogenated fat is used, a characteristic odor remains, making it impossible to bring out the full flavor of the food.

[発明が解決しようとする課題〕 本発明の課題は安定性を持ちかつ融点が低く作業性の良
い油脂、食品に与える油虱昧をできるだけ少なくし、素
材の持つ本来の風味を生かすことのできる油脂を得るこ
とである。
[Problems to be Solved by the Invention] The problem of the present invention is to develop oils and fats that are stable, have a low melting point, and are easy to work with, which can minimize the amount of oil added to foods and make the most of the original flavor of the ingredients. It is to obtain fats and oils.

[課題を解決するための手段〕 上記課題を達成するために液体油(分別油、植物油、動
物油)と液体油、固体脂(水添油、動物脂、植物油)と
固体脂、液体油と固体脂の混合物を1゜3−位置特異性
リパーゼを用いるエステル交換法による油脂改質により
得ることができた。すなわち、油脂中の水分が2oop
pm以下の微水分系で1,3−位置特異性リパーゼを用
いて、選択的エステル交換反応を行うことによって、原
料混合物よりも優れた物性を有する食用油脂を得ること
ができた。
[Means for solving the problem] In order to achieve the above problem, liquid oil (fractionated oil, vegetable oil, animal oil), liquid oil, solid fat (hydrogenated oil, animal fat, vegetable oil) and solid fat, liquid oil and solid A mixture of fats could be obtained by modifying fats and oils by transesterification using a 1°3-regiospecific lipase. In other words, the water content in fats and oils is 2oop
By carrying out a selective transesterification reaction using a 1,3-regiospecific lipase in a microhydric system with a water content below pm, it was possible to obtain an edible fat and oil having physical properties superior to those of the raw material mixture.

原料の油脂の種類や配合比率を種々変更することによっ
て、目的にあった融点や、物性を持つ風味良好な油脂を
得ることができ方。
By changing the type and blending ratio of the raw material oils and fats, it is possible to obtain oils and fats with good flavor and melting points and physical properties that suit the purpose.

本発明で用いるリパーゼとして、リゾーブス属(Rhi
zopus) 、アスペルギルス(Aspergill
us)、ムコール属(Mucor) 、フミコーラ属(
Humicola) 、ペニシリウム属(P enic
Hlitv)由来のリパーゼなどを用いることができる
具体的には、天野製薬(株)が販売している次のリパー
ゼを用いることができる。すなわち、Rhizopus
  delemer由来の「リパーゼDJ (商品名、
以下同じ)Rhizopus  javanicus由
来の「リパーゼF−AP15 J 、Rhizopus
niger由来の「リパーゼAPJ、M ucOr  
jaVanictls由来の「リパーゼ゛M−APJ、
Hua+1cola  lanugfnosa由来の「
リパーゼCEJ、P enicillium  roq
ueforti由来の「リパーゼR−20」などである
As the lipase used in the present invention, Rhizobus sp.
zopus), Aspergillus
us), Mucor, Humicola (
Humicola), Penicillium (P enic
Specifically, the following lipases sold by Amano Pharmaceutical Co., Ltd. can be used. Namely, Rhizopus
"Lipase DJ" (product name,
Same hereafter) "Lipase F-AP15 J" derived from Rhizopus javanicus, Rhizopus javanicus
"Lipase APJ, MucOr" derived from niger
"Lipase M-APJ," derived from jaVanicls.
Hua+1cola lanugfnosa derived from “
Lipase CEJ, P enicillium roq
ueforti-derived "Lipase R-20" and the like.

また、本発明で用いることのできる油脂としては、ヘッ
ド、ラードなどの動物脂、ヤシ油、パーム油、パーム核
油、大豆油、なたね油、米油、綿実油などあらゆる植物
油脂またはそれら種々の油脂の水添脂、分別油脂、これ
らを配合した混合脂などを用いることができる。
In addition, the oils and fats that can be used in the present invention include animal fats such as head and lard, all kinds of vegetable oils and fats such as coconut oil, palm oil, palm kernel oil, soybean oil, rapeseed oil, rice oil, and cottonseed oil, and various oils and fats such as these. Hydrogenated fats, fractionated fats, mixed fats containing these, etc. can be used.

本発明の選択的エステル交換反応は次の様に行う。反応
に使用するリパーゼをレシチンなどの酵素活性化剤と共
に水にとかしてセライトやイオン交換樹脂などの担体に
固定化し・乾燥し、固定化酵素を精製する。この固定化
酵素剤をカラムに充填し、油脂中の水分200ppm以
下、好ましくは1100pp以下に乾燥した混合油脂(
基質)を30〜60°Cで連続的にカラムに流して反応
を行う。なお、この反応は連続式でなく、パッチ方式で
行ってもよい。
The selective transesterification reaction of the present invention is carried out as follows. The lipase used in the reaction is dissolved in water together with an enzyme activator such as lecithin, immobilized on a carrier such as Celite or ion exchange resin, and dried to purify the immobilized enzyme. This immobilized enzyme agent is packed into a column, and the mixed fat and oil is dried to a moisture content of 200 ppm or less, preferably 1100 ppm or less (
The reaction is carried out by continuously flowing the substrate (substrate) through the column at 30-60°C. Note that this reaction may be carried out not in a continuous manner but in a patch manner.

実施例1 通過した反応生成物に2重量%の活性白土を加えて80
°Cl2O分間20 mmHg、吹き込み水蒸気蒸留2
.6重量%で真空水蒸気蒸留(脱臭)を行って精製油を
得た。
Example 1 2% by weight of activated clay was added to the passed reaction product to
°Cl2O min 20 mmHg, blown steam distillation 2
.. Refined oil was obtained by vacuum steam distillation (deodorization) at 6% by weight.

Rhizopus  delemer由来のリパーゼ(
天野製薬(株)商品名「リパーゼDJ266gと精製粉
末大豆レシチン80gを水600m1に溶かし、担体と
して9000gの陽イオン交換樹脂rWK−13J(三
菱化成(株)製)に加え、約30分間よく撹拌し、担体
の表面にリパーゼが均一にコーティングされた樹脂を乾
燥せずに固定化リパーゼとして用いた。この固定化リパ
ーゼには水分を約6.6%含んでいた。反応基質として
、パーム油となたね油を1:3の比率で混合したものを
減圧乾燥し、水分を50ppmに調製した。固定化リパ
ーゼ3oogを内径10cm、長さ50cmのカラム全
体を60°Cに保った。上記の混合原料油脂を60°C
に加温し、ポンプで毎分5gを定量的にカラムに流し、
60°C連続的に酵素反応を行った。カラムを比較例1 パーム油となたね油を実施例1の原料と同じ油脂比率(
1:3)で混合した油脂を得た。
Lipase from Rhizopus delemer (
Amano Pharmaceutical Co., Ltd. trade name: 266 g of Lipase DJ and 80 g of purified powdered soybean lecithin were dissolved in 600 ml of water, added to 9000 g of cation exchange resin rWK-13J (manufactured by Mitsubishi Kasei Corporation) as a carrier, and stirred well for about 30 minutes. , a resin with lipase uniformly coated on the surface of the carrier was used as immobilized lipase without drying.This immobilized lipase contained approximately 6.6% water.Palm oil and rapeseed oil were used as reaction substrates. were mixed at a ratio of 1:3 and dried under reduced pressure to adjust the water content to 50 ppm.The entire column with an inner diameter of 10 cm and a length of 50 cm containing 300 grams of immobilized lipase was kept at 60 °C.The above mixed raw material fats and oils were 60°C
5 g per minute was quantitatively poured into the column using a pump.
Enzyme reactions were performed continuously at 60°C. Comparative Example 1 The column was mixed with palm oil and rapeseed oil in the same oil and fat ratio as the raw materials in Example 1 (
Oils and fats mixed at a ratio of 1:3) were obtained.

試験例1 実施例1と、比較例1でrA製した油脂を用いて常法に
てえびの天ぷらを試作し、味覚試験を行なった。試験結
果を表−1に示す。
Test Example 1 Using the rA-produced fats and oils in Example 1 and Comparative Example 1, shrimp tempura was prototyped in a conventional manner, and a taste test was conducted. The test results are shown in Table-1.

表−1から明らかなように実施例1は風味の点で評価が
高く、タネの持つ本来の風味・うま味の感じられ方に最
も違いがみられると思われ、時間がたって冷めても食感
(口ざわり)が良いという結果が得られた。
As is clear from Table 1, Example 1 was highly evaluated in terms of flavor, and it seems that the most difference is seen in how the original flavor and umami of the seeds are perceived, and the texture even after cooling down over time. The result was that the texture was good.

本発明により作業性がサラダ油と同等でかつ風味がよく
、安定性の寓い油脂かえられた。
The present invention provides a substitute for oils and fats that have workability equivalent to that of salad oil, good flavor, and stability.

表−1 表1−1 えび天プラの味覚評価結果 揚げ直後 味覚評価方法 各項目の評点は0を普通とし、±2の範囲でよい・わる
いの相対評価を行ったものであり、評点の平均値をとっ
た。総合評価は10点法で行ない、平均点をとった。パ
ネラ−の人数は18名であった。
Table 1 Table 1-1 Taste evaluation results of shrimp tempura Immediately after frying Taste evaluation method The scores for each item are 0 as normal, and a relative evaluation of good or bad within the range of ±2, and the average of the scores. took the value. Comprehensive evaluation was performed on a 10-point scale, and the average score was taken. The number of panelists was 18.

表1−2 揚げ後5時間 実施例2 パームオレインとなたね油を1:1の比率で配合し、実
施例1と同様に改質を行い、精製油脂を得た。
Table 1-2 5 hours after frying Example 2 Palm olein and rapeseed oil were blended at a ratio of 1:1 and modified in the same manner as in Example 1 to obtain a refined fat or oil.

比較例2 パームオレインとなたね油を1:1の比率で配合した配
合油脂を得た。
Comparative Example 2 A blended fat and oil containing palm olein and rapeseed oil in a ratio of 1:1 was obtained.

試験例2 実施例2と比較例2を用いて、冷凍コロッケを常法にて
フライし味覚評価を行った。フライ温度、時間は表2と
同様。結果を表2−1に示す。また同様に試作したコロ
ッケをウオーマ−内で5時間保存し、味覚評価を行った
。結果を表2−2に示す。
Test Example 2 Using Example 2 and Comparative Example 2, frozen croquettes were fried in a conventional manner and taste evaluation was performed. Frying temperature and time are the same as in Table 2. The results are shown in Table 2-1. Croquettes prepared in the same manner were stored in a warmer for 5 hours, and the taste was evaluated. The results are shown in Table 2-2.

表2−1より実施例2は油風味が少ないため、フライ直
後の香りは好まれないが、風味は優っていた。ウオーマ
−内で保存後、総合・食感・風味は明らかに実施例2の
油脂でフライしたものが良いという評価が得られた。
From Table 2-1, Example 2 had less oily flavor, so the aroma immediately after frying was not pleasant, but the flavor was excellent. After being stored in a warmer, the overall quality, texture, and flavor of the fried food using the oil and fat of Example 2 were clearly evaluated as being better.

店舗・給食・産業・業務用等と同レベルの大きな規模で
フライ試験をした場合の酸価と粘度上昇率・泡高・色の
測定を行った。フライ条件は表2に示す。結果を表2−
3に示す。
We measured the acid value, viscosity increase rate, foam height, and color when frying tests were conducted on a large scale similar to those used in stores, school lunches, industry, and commercial use. The frying conditions are shown in Table 2. The results are shown in Table 2-
Shown in 3.

表2−1〜3から、実施例2で保存しても風味が良く同
時に安定性の優れた油脂を得られたことがわかる。
Tables 2-1 to 2-3 show that even when stored in Example 2, oils and fats with good flavor and stability were obtained.

コロッケの味覚評価結果 表2−1 フライ直後 表2−2 フライ後5時間 表2−3  フライテスト後の油脂分析方法兼2−3(
薮ヤ) 油脂分析方法 酸価(AV);基準油脂分析法による 粘度  ;E型粘度計(40°C1100rpIIl)
泡高  ;当社の方法による。2.5cm径の試験管を
使用1xlx1.5cm角に切ったじゃがいもを冷水に
つけておく。軽く水気をきったもの1個を150°Cの
油の中にいれたときの泡の高さを測定した。
Croquette taste evaluation results Table 2-1 Immediately after frying Table 2-2 5 hours after frying Table 2-3 Fat and oil analysis method after frying test 2-3 (
Yabuya) Oil and fat analysis method Acid value (AV); Viscosity according to standard oil and fat analysis method; E-type viscometer (40°C 1100rpIIl)
Foam height: Based on our method. Using a 2.5cm diameter test tube, soak potatoes cut into 1x1.5cm cubes in cold water. The height of bubbles was measured when one lightly drained piece was placed in oil at 150°C.

色 ;ロビボンド 1インチセル使用 フライ条件 フライヤー− フライ温度; フライ時間; 油量; フライ量 ; 実施例3 3kg電気フライヤー使用 185〜195℃ 5分間 kg 冷凍コロッケ 5個/回 パームオレインとなたね油を3:1の比率で配合し実施
例1と同様に改質を行い、精製油脂を得た。
Color: Frying conditions using Lovibond 1-inch cell - Frying temperature; Frying time; Oil amount; Frying amount; Example 3 Using a 3kg electric fryer 185-195℃ for 5 minutes kg Frozen croquettes 5 pieces/time Palm olein and rapeseed oil at 3:1 The oils and fats were blended in the same ratio as in Example 1 and modified in the same manner as in Example 1 to obtain purified fats and oils.

比較例3 バームオレインとなたね油を3=1の比率で混合し配合
油脂を得た。
Comparative Example 3 Balm olein and rapeseed oil were mixed at a ratio of 3=1 to obtain a blended fat and oil.

試験例3 実施例3と比較例3の油脂をフライ油として用い、ポテ
トチップスを試作した。試作直後のポテトチップスをO
とし、0.75力月、1.5力月、3力月間30°Cに
て保存を行ない味覚評価・AV・povの測定を行った
Test Example 3 Using the fats and oils of Example 3 and Comparative Example 3 as frying oil, potato chips were experimentally produced. Potato chips immediately after trial production
The samples were stored at 30°C for 0.75 months, 1.5 months, and 3 months, and taste evaluation and AV and pov measurements were performed.

結果を表3に示す。The results are shown in Table 3.

結果より、試作直後の段階から風味には明らかに差があ
ることがわかる。保存を行なうことによりさらに差がは
っきりしてくる結果となった。泣きがなく、油脂の劣化
速度が遅く、かつ風味に優れたスナック用油脂が本発明
によってえられた。
The results show that there is a clear difference in flavor from the stage immediately after trial production. The difference became even clearer after storage. The present invention has provided an oil and fat for snacks that does not runny, has a slow deterioration rate, and has excellent flavor.

油脂分析法 過酸化物価(P○■) ;基準油脂分析法による 実施例4 パーム油とコーン油を1=3の比率で混合したものを実
施例1と同様に改質し、精製油脂を得た。
Fat and oil analysis method Peroxide value (P○■); Based on standard fat and oil analysis method Example 4 A mixture of palm oil and corn oil at a ratio of 1=3 was modified in the same manner as in Example 1 to obtain a refined oil and fat. Ta.

比較例4 パーム油とコーン油を1:3の比率で混合し油脂を得た
Comparative Example 4 Palm oil and corn oil were mixed at a ratio of 1:3 to obtain fats and oils.

試験例4 実施例4と比較例4で得た油脂を用いて常法番こてホワ
イトソースを試作した。
Test Example 4 Using the oils and fats obtained in Example 4 and Comparative Example 4, a standard white sauce was prepared as a prototype.

レシピ−は以下に示す。(今回は生クリームで番よなく
牛乳だけを用いた) ホワイトソースそれぞれについて味覚試験を行った。結
果を表4に示す。
The recipe is shown below. (This time, I used only milk instead of fresh cream.) Taste tests were conducted for each of the white sauces. The results are shown in Table 4.

表4 ホワイトソースの味覚評価 コメント 実施例4;サラパリしたミルク風味 自然なうまみがある また、給食産業用・業羨用等でルーやソースをつくる場
合には、バターではなくサラダ油やマーガリンが使われ
ることが多い。その場合、コスト面・作業面ではバター
よりも優れているものの、牛乳または生クリームの風味
をいかしきれず、こげつきやすいという欠点がある。一
方、最近は嗜好の変化からバターのみで作られたホワイ
トソースはこくはあるが、くどく感じられ好まれない傾
向にあり、かつ動物脂だけであるため油のバランスも良
いとは言えない。実施例4では、牛乳または生クリーム
の自然な風味とこく、加熱による酸価安定性がよくコス
トを削減することもできる低融点の油脂が得られた。
Table 4 Taste evaluation comments for white sauce Example 4: It has a smooth, milky flavor and a natural flavor.Also, when making roux or sauce for the school lunch industry or industry, salad oil or margarine is used instead of butter. There are many things. In that case, although it is superior to butter in terms of cost and workability, it has the disadvantage that it cannot retain the flavor of milk or fresh cream and tends to burn. On the other hand, due to recent changes in tastes, white sauces made only with butter tend to be rich, but tend not to be liked because they taste too strong.Also, since they are made only from animal fat, the balance of oil cannot be said to be good. In Example 4, a low melting point fat and oil was obtained that had the natural flavor and richness of milk or fresh cream, had good acid value stability upon heating, and could also reduce costs.

ホワイトソースレシピ−(4人分) 実施例4   比較例4 バター(大さじ) 植物油(大さじ) 牛乳 (カップ) ブイヨン(カップ) 小麦粉 (カップ) 実施例5 パームオレインとなたね油を1:3の比率で配合し、実
施例1と同様に改質をおこない精製油脂として得た。
White sauce recipe - (serves 4) Example 4 Comparative example 4 Butter (tablespoon) Vegetable oil (tablespoon) Milk (cup) Bouillon (cup) Flour (cup) Example 5 Palm olein and rapeseed oil in a ratio of 1:3 Then, it was modified in the same manner as in Example 1 to obtain a refined oil or fat.

比較例5 パームオレインとなたね油を1:3の比率で混合して油
脂を得た。
Comparative Example 5 Oil and fat were obtained by mixing palm olein and rapeseed oil at a ratio of 1:3.

試験例5 実施例6(レシチン0.5%権加)、比較例5(レシチ
ン1%添加)の油脂をかけ油として用いて米菓を試作し
、保存評価を行った。
Test Example 5 Rice crackers were prepared using the fats and oils of Example 6 (0.5% lecithin added) and Comparative Example 5 (1% lecithin added) as pouring oil, and storage evaluation was performed.

油脂を抽出し、その酸価・POvの測定を行った。結果
は表5に示す。
Fats and oils were extracted and their acid value and POv were measured. The results are shown in Table 5.

結果より、実施例6は比較例5と風味の点で違いがみら
れた。
The results showed that Example 6 was different from Comparative Example 5 in terms of flavor.

実施例5の保存後のPOvは、レシチン添加量が少ない
こと、比較例5よりも測定値がやや高めであるにもかか
わらず風味の点では優っている。油の風味にくせがなく
、保存安定性がよい作業性に優れた油脂を実施例5でえ
られた。
The POv after storage of Example 5 is superior in terms of flavor despite the fact that the amount of lecithin added is small and the measured value is slightly higher than that of Comparative Example 5. In Example 5, an oil or fat with no peculiar flavor, good storage stability, and excellent workability was obtained.

本発明により作業性・剥離性はもちろんのこと、食品の
風味に悪影響のでない風味のない安定性のよい油脂がえ
られた。
According to the present invention, not only workability and peelability but also flavorless and stable fats and oils which do not adversely affect the flavor of foods can be obtained.

実施例 6 パームオレインとコーン油を1:3の比率で配合し、実
施例1と同様に改質し精製油脂を得た。
Example 6 Palm olein and corn oil were blended at a ratio of 1:3 and modified in the same manner as in Example 1 to obtain a refined fat or oil.

実施例7 パーム油と大豆油を1=3の比率で配合し実施例1と同
様に改質しn製油脂を得た。
Example 7 Palm oil and soybean oil were blended at a ratio of 1=3 and modified in the same manner as in Example 1 to obtain n-made oil and fat.

比較例 6 パームオレインとコーン油を1:3の比率で混合油脂を
得た。
Comparative Example 6 A mixed fat and oil was obtained using palm olein and corn oil in a ratio of 1:3.

比較例7 パーム油と大豆油を1=3の比率で混合し、精製油脂を
得た。
Comparative Example 7 Palm oil and soybean oil were mixed at a ratio of 1=3 to obtain a refined fat or oil.

試験例 6 実施例6と比較例6で得た油脂を離型油としてもちいて
カップケーキを常法にて試作し、味覚試験をおこなった
。表6に結果を示す。
Test Example 6 Using the oils and fats obtained in Example 6 and Comparative Example 6 as mold release oils, cupcakes were prepared in a conventional manner and a taste test was conducted. Table 6 shows the results.

試験例7 実施例7と比較例7で得た油脂を用い、常法にてガーリ
ックローストオイルを試作した。無色透明瓶(300m
l)34°C1蛍光灯1000ルクスにて明所保存安定
テストを行った。コントロールとしてなたね油も同時に
保存試験をおこなった。
Test Example 7 Using the fats and oils obtained in Example 7 and Comparative Example 7, garlic roast oil was experimentally produced in a conventional manner. Colorless transparent bottle (300m
l) A light storage stability test was conducted under a fluorescent lamp of 1000 lux at 34°C. As a control, rapeseed oil was also subjected to a storage test at the same time.

結果は表7−1に示す。The results are shown in Table 7-1.

褐色瓶(300ml)常温にて2力月・4カ月間表6 カップケーキの評価 表7−1 ガーリックオイルの保存評価 保存を行ったものを用いて海の幸スパゲツティを試作し
、味覚評価を行った。
Amber bottle (300 ml) at room temperature for 2 months and 4 months Table 6 Cupcake evaluation table 7-1 Garlic oil preservation evaluation We made a prototype of seafood spaghetti using the preserved product and conducted a taste evaluation. Ta.

あさり水・いか・えびをガーリックローストオイルで炒
めたあと、塩・こしようで味付けをし、ゆでたパスタに
からめた。結果を表7−2に示す。
After sautéing clam water, squid, and shrimp in garlic roasted oil, season with salt and pepper, and toss with boiled pasta. The results are shown in Table 7-2.

表7−1に示されるように保存安定性良好、表7−2よ
り風味の優れた油脂を実施例7で得られえたことがわか
る。
As shown in Table 7-1, it can be seen that Example 7 was able to obtain an oil with good storage stability and an excellent flavor from Table 7-2.

[発明の効果] 本発明によって得られる油脂は、酸化安定性と加熱安定
性に優れているため、保存安定性または泡立ち性におい
ても優れており、融点の低い作業性の良好な油脂である
。また、油風味はさっばりしているため食用にした場合
、素材の持ち味を十分に生かすことのできる優れた特性
を有している。
[Effects of the Invention] The fats and oils obtained by the present invention are excellent in oxidation stability and heating stability, and therefore are also excellent in storage stability and foaming properties, and are oils and fats with a low melting point and good workability. In addition, since the oil has a light flavor, it has excellent properties that allow the natural flavor of the material to be fully utilized when eaten.

比願人 昧の素株式会社Higanjin Majinomoto Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] (1)液体油と液体油、固体脂(水添脂・動物脂・植物
脂)と固体脂、液体油と固体脂の混合物を1,3−位置
特異性リパーゼを用い、選択的エステル交換反応によっ
て得られる食用油脂の利用方法。
(1) Selective transesterification of mixtures of liquid oils, liquid oils, solid fats (hydrogenated fats, animal fats, vegetable fats) and solid fats, and liquid oils and solid fats using 1,3-regiospecific lipase. How to use the edible fats and oils obtained by
JP2188213A 1990-07-17 1990-07-17 Usage for edible fatty oil Pending JPH0475591A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2188213A JPH0475591A (en) 1990-07-17 1990-07-17 Usage for edible fatty oil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2188213A JPH0475591A (en) 1990-07-17 1990-07-17 Usage for edible fatty oil

Publications (1)

Publication Number Publication Date
JPH0475591A true JPH0475591A (en) 1992-03-10

Family

ID=16219750

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2188213A Pending JPH0475591A (en) 1990-07-17 1990-07-17 Usage for edible fatty oil

Country Status (1)

Country Link
JP (1) JPH0475591A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH051297A (en) * 1991-06-25 1993-01-08 Fuji Oil Co Ltd Production of fat composition
WO1994026855A1 (en) * 1993-05-13 1994-11-24 Loders-Croklaan Human milk fat replacers from interesterified blends of triglycerides
JP2012249617A (en) * 2011-06-07 2012-12-20 Nisshin Oillio Group Ltd Oil-and-fat composition and bubble-containing chocolate using the oil-and-fat composition

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH051297A (en) * 1991-06-25 1993-01-08 Fuji Oil Co Ltd Production of fat composition
WO1994026855A1 (en) * 1993-05-13 1994-11-24 Loders-Croklaan Human milk fat replacers from interesterified blends of triglycerides
JP2012249617A (en) * 2011-06-07 2012-12-20 Nisshin Oillio Group Ltd Oil-and-fat composition and bubble-containing chocolate using the oil-and-fat composition

Similar Documents

Publication Publication Date Title
KR101437662B1 (en) Oil and fat composition for improving texture
JPH0738771B2 (en) Liquid edible oil composition
JP2009089684A (en) Low trans-fatty acid oil and fat composition
JPH02291228A (en) Edible fat and oil composition
JP5072236B2 (en) Salty taste enhancing method and salt reducing method, salt reduced food and method for producing the same
CN109600984A (en) Cheese flavor assign enhancing composition, the imparting preparation method of enhancing composition of cheese flavor, food cheese flavor impartings Enhancement Method and cheese flavor through assigning the manufacturing method of the food enhanced
JP2018130052A (en) Method for producing flavor-enhancing oil/fat
JP4171136B2 (en) Ingredients for fried cooked food and fried food
JP2006246857A (en) Oil and fat composition and food
CA2192749A1 (en) Oils or fats composition for fried food
JP2019041633A (en) Composition for fried jiaozi blade
JPH0475591A (en) Usage for edible fatty oil
JP2002253118A (en) Formulated food oil and utilization thereof
JPH08131071A (en) Oil and fat composition for cooking
JP2000270770A (en) Oil and fat for fry and fried food
JP2021166479A (en) Fat and oil composition
JPH08298928A (en) Oil and fat composition for preparing fried frozen food and food fried with the same
JPS62181738A (en) Oil for meat roasted on hot plate
US20080206435A1 (en) Edible Oil Composition Suitable For Frying Food
TWI837250B (en) Oil and fat composition for heating and cooking
JP2005160453A (en) Oil and fat composition for frying and fried food
TW202404473A (en) Hydrogenated odor imparting agent,oil and fat composition,method for producing oll and fat composition,method for imparting hydrogenated odor to food,and method for producing fried food
JPH0994064A (en) Oil and fat composition for food improved in waterwetting property
TW202444258A (en) Oil and fat composition with enhanced beef tallow feel, beef tallow feel enhancer, method for producing the oil and fat composition with enhanced beef tallow feel, method for producing fried food, and method for enhancing fee tallow feel
JP2024097287A (en) Method for producing flavor oil, method for producing flavor oil mixture, method for imparting flavor to food, and use of microalgae for producing flavor oil