JPH051297A - Production of fat composition - Google Patents
Production of fat compositionInfo
- Publication number
- JPH051297A JPH051297A JP3181880A JP18188091A JPH051297A JP H051297 A JPH051297 A JP H051297A JP 3181880 A JP3181880 A JP 3181880A JP 18188091 A JP18188091 A JP 18188091A JP H051297 A JPH051297 A JP H051297A
- Authority
- JP
- Japan
- Prior art keywords
- fatty acid
- oil
- fat
- oils
- curry roux
- 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.)
- Granted
Links
Landscapes
- Edible Oils And Fats (AREA)
- Seeds, Soups, And Other Foods (AREA)
- Fats And Perfumes (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明はカレールーの製造に適し
た脂肪組成物の製造法に関する。FIELD OF THE INVENTION The present invention relates to a method for producing a fat composition suitable for producing curry roux.
【0002】[0002]
【従来の技術】本邦における固形のカレールーは、カレ
ー粉等のシーズニングと小麦粉を固形油脂にて固めた独
特のもので、固形油脂は風味の点から豚脂、牛脂を原料
とした硬化油またはそれらの調合油が使用されている。
しかしながら、近年の医学技術の発達により、動物系脂
肪による血中コレステロール上昇等の弊害が云々されて
いる。2. Description of the Related Art Solid curry roux in Japan is a unique type of seasoning such as curry powder and wheat flour solidified with solid fat and oil. The blended oil of is used.
However, with the recent development of medical technology, adverse effects such as an increase in blood cholesterol due to animal fat have been said.
【0003】[0003]
【発明が解決しようとす課題】カレールー用の固形油脂
が要求される物性は、保管中にカレールーの表面がカビ
の様に白色化するという現象を発生し難いこと、液油成
分がシミ出さないこと、使用時に適当な硬さで割れるこ
と、およびカレールー製造時の固化速度が速いこと等が
挙げられる。The physical properties required for solid fats and oils for curry roux are such that the phenomenon that the surface of curry roux whitens like mold during storage is unlikely to occur, and the liquid oil component does not stain. The fact is that it cracks with an appropriate hardness during use, and that the solidification rate during the production of curry roux is fast.
【0004】従来より使用されている豚脂、牛脂を原料
とした調合油またはそれらの硬化油を、単純に植物油の
硬化油に置き換えると、これらの油脂を使用したカレー
ルーは保管中に著しい白色化現象を発生し、短期間のう
ちに商品価値を失ってしまう。この原因としては、これ
ら植物硬化油を構成するトリグリセリドの種類が少なく
単一結晶の粗大化が発生しているためと考えられる。[0004] When the conventional blended oils made from lard, beef tallow, or their hardened oils are simply replaced with hardened oils of vegetable oils, curry roux using these fats and oils remarkably whiten during storage. A phenomenon occurs and the product value is lost in a short period of time. It is considered that this is because there are few types of triglycerides forming these hydrogenated vegetable oils and coarsening of single crystals occurs.
【0005】また、これらの硬化油は常温でのSFIが
高いためカレールーが非常に硬く、使用時に手で分割す
るのが困難であり、且つ調理中においても溶け残りがし
ばしば発生し、商品価値を低下させてしまう。Further, since these hardened oils have a high SFI at room temperature, the curry roux is very hard, it is difficult to divide by hand during use, and unmelted residue often occurs during cooking, so that the commercial value is high. Will lower it.
【0006】本発明者は天然の固体脂であるパーム油系
油脂を用い、それらの分画油を種々混合して脂肪酸組成
を調節しエステル交換することにより、カレールーとし
て適度な硬さを示す脂肪組成物が得られることに注目し
て検討を行った。The present inventor uses palm oil-based fats and oils which are natural solid fats, and mixes various fractionated oils thereof to adjust the fatty acid composition and transesterify them to obtain fats having an appropriate hardness as curry roux. The study was conducted paying attention to the fact that a composition was obtained.
【0007】しかしながら、パーム油または種々のパー
ム油系分画油を配合しエステル交換を行うことによって
適度なSFIを示す油脂は得られるが、これらのエステ
ル交換油においても粗大結晶の発生による白色化現象が
観察され、何らかの方法によりこの欠点を改善する必要
のあることがわかった。However, by mixing palm oil or various palm oil-based fractionated oils and performing transesterification, fats and oils exhibiting an appropriate SFI can be obtained, but even in these transesterified oils, whitening occurs due to the formation of coarse crystals. A phenomenon was observed and it was found that there was some need to remedy this drawback.
【0008】[0008]
【課題を解決するための手段】本発明者は、如上の点に
鑑み鋭意研究した結果、特定の脂肪酸残基を油脂のトリ
グリセリド中に結合させることにより、上記する欠点を
解決し得るという知見を得た。本発明は以上の知見に基
づいて完成されたものである。Means for Solving the Problems The inventors of the present invention have conducted extensive studies in view of the above points, and as a result, have found that the above-mentioned drawbacks can be solved by binding a specific fatty acid residue to triglyceride of fats and oils. Obtained. The present invention has been completed based on the above findings.
【0009】即ち本発明は、パーム油起源の油脂と炭素
原子数22個以上の飽和脂肪酸残基を持つ脂肪酸および
またはその誘導体とをエステル交換することを特徴とす
る、カレールー製造に適した脂肪組成物の製造法、であ
る。That is, the present invention is characterized in that fats and oils derived from palm oil are transesterified with a fatty acid having a saturated fatty acid residue having 22 or more carbon atoms and / or a derivative thereof, which is suitable for producing curry roux. It is a method of manufacturing a product.
【0010】以下、本発明について説明する。本発明に
おけるパーム油起源の油脂は、炭素原子数16個の飽和
脂肪酸(パルミチン酸)残基を35重量%以上含有する
油脂であって、パーム油自体またはそれを分画して得ら
れる分画油の何れを用いてもよい。The present invention will be described below. The oil / fat originating from palm oil in the present invention is an oil / fat containing 35% by weight or more of a saturated fatty acid (palmitic acid) residue having 16 carbon atoms, and palm oil itself or a fraction obtained by fractionating the oil. Any of the oils may be used.
【0011】炭素原子数22個以上の飽和脂肪酸残基を
持つ脂肪酸の誘導体は、エステル、トリグリセリド、ア
ルコールの何れの形態であってよい。The fatty acid derivative having a saturated fatty acid residue having 22 or more carbon atoms may be in the form of ester, triglyceride or alcohol.
【0012】本発明におけるエステル交換は、ナトリウ
ムメチラート等の金属触媒を用いる方法またはリパーゼ
を触媒とする方法の何れによっても行うことができる。The transesterification in the present invention can be carried out by either a method using a metal catalyst such as sodium methylate or a method using a lipase as a catalyst.
【0013】リパーゼを触媒とする方法は、それが1,
3位選択性を示す場合は金属触媒を用いる方法と比べ高
融点成分が少なくなる方向でトリグリセリド中の脂肪酸
残基の配列が行われるため、同一配合ではSFIが低く
なり、従ってエステル交換油の飽和酸含有量が多くなる
ように配合を調整することが好ましい。The method using a lipase as a catalyst is
When the 3-position selectivity is exhibited, the fatty acid residues in the triglyceride are arranged in the direction in which the high-melting point component is reduced as compared with the method using a metal catalyst. It is preferable to adjust the composition so that the acid content is increased.
【0014】本発明に用いるリパーゼは油脂に対しエス
テル交換活性を有するものであればどのような酵素であ
ってもよい。公知の物としては、例えば、リゾプス属リ
パーゼ、アスペルギルス属リパーゼ、ムコール属リパー
ゼ、パンクレアチツクリパーゼ、米ぬかリパーゼなどが
あげられる。The lipase used in the present invention may be any enzyme as long as it has transesterification activity for fats and oils. Known substances include, for example, Rhizopus lipase, Aspergillus lipase, Mucor lipase, Pancreatic lipase, rice bran lipase and the like.
【0015】これらの酵素は反応系で単独使用すること
も可能であるが、通常はケイソウ土、アルミナ、活性炭
等の公知の支持体に固定化させて用いるのがよい。Although these enzymes can be used alone in the reaction system, they are usually preferably immobilized on a known support such as diatomaceous earth, alumina or activated carbon before use.
【0016】[0016]
【実施例】以下、実施例を例示して本発明の効果をより
一層明瞭にするが、これは例示であって本発明の精神が
これらの例示によって制限されるものではない。なお、
例中に示す部、%は何れも重量基準を意味する。EXAMPLES Hereinafter, the effects of the present invention will be further clarified by exemplifying examples, but these are examples and the spirit of the present invention is not limited by these examples. In addition,
All parts and% shown in the examples mean weight basis.
【0017】[0017]
【実施例1】パームステアリン(沃素価33)43部、
パーム油(沃素価52)52部、ハイエルシン菜種油極
度硬化油5部の割合で混合し、ナトリウムメチラートを
触媒としてランダムエステル交換を行った後、水洗、脱
水、精製して融点45℃のエステル交換油を得た。この
エステル交換油を用いて以下の配合によりカレールーを
製造した。Example 1 Palm stearin (iodine value 33) 43 parts,
A mixture of 52 parts of palm oil (iodine value 52) and 5 parts of Hyersine rapeseed oil extremely hydrogenated oil was used, and random transesterification was carried out using sodium methylate as a catalyst, followed by washing with water, dehydration and purification, and transesterification with a melting point of 45 ° C. I got oil. Using this transesterified oil, curry roux was produced according to the following formulation.
【0018】カレールー配合 油 脂 36 部 カレー粉 29 部 粉 糖 13 部 小麦粉 11 部 食 塩 9 部 グルタミン酸ソーダ 2 部 レシチン 0.4 部Curry roux Oil and fat 36 parts 29 parts of curry powder 13 parts powdered sugar Wheat flour 11 parts 9 parts of food salt Sodium glutamate 2 parts Lecithin 0.4 parts
【0019】なお、比較のため油脂として硬化牛脂(融
点45℃)、硬化菜種油(融点45℃)を使用して同様
に実施した。For comparison, hardened beef tallow (melting point 45 ° C.) and hardened rapeseed oil (melting point 45 ° C.) were used in the same manner.
【0020】以上により製造したそれぞれのカレールー
の品質を評価した。The quality of each curry roux produced as described above was evaluated.
【0021】 (1). 20℃における白色化現象の発生状況 製造直後 10日 30日 ──────────────────────────────────── 実施例1 無し 無し 無し 硬化牛脂 無し やや発生 やや発生 硬化菜種油 無し 発生 激しく発生 ────────────────────────────────────[0021] (1). Occurrence of whitening phenomenon at 20 ℃ Immediately after production 10 days 30 days ──────────────────────────────────── Example 1 None None None No hardened beef tallow Some occurrence Somewhat occurrence Hardened rapeseed oil No ────────────────────────────────────
【0022】 (2).レオメーター(プランジャーΦ=3mm)測定による硬さ(g) 製造直後 10日 30日 ──────────────────────────────────── 実施例1 1600 1650 1680 硬化牛脂 1500 1550 1550 硬化菜種油 2300 2500 2800 ────────────────────────────────────[0022] (2). Hardness (g) measured by rheometer (plunger Φ = 3mm) Immediately after production 10 days 30 days ──────────────────────────────────── Example 1 1600 1650 1680 Hardened beef tallow 1500 1550 1550 Hydrogenated rapeseed oil 2300 2500 2800 ────────────────────────────────────
【0023】以上の結果から明らかなように、本発明の
エステル交換油を使用して製造したカレールーは硬化菜
種油に比べ遙かに良好な耐白色化性を示す。また、硬さ
においても硬化牛脂とほぼ同等の物性を示しており、固
化速度も速く、使用時の作業性も良好であった。As is clear from the above results, the curry roux produced using the transesterified oil of the present invention exhibits far better whitening resistance than hydrogenated rapeseed oil. Further, it showed almost the same physical properties as hardened beef tallow, the solidification rate was fast, and the workability during use was good.
【0024】[0024]
【実施例2】実施例1で使用したパームステアリン、パ
ーム油、ハイエルシン菜種極度硬化油、パームオレイン
(沃素価56)及びベヘン酸エステルを用いて以下の配
合にてエステル交換を行い、脱色、脱臭をして以下に示
す物性の脂肪組成物を得た。[Example 2] Using the palm stearin, the palm oil, the hyacinth rapeseed extremely hardened oil, the palm olein (iodine value 56) and the behenic acid ester used in Example 1, transesterification was carried out in the following formulation to decolorize and deodorize. Then, a fat composition having the following physical properties was obtained.
【0025】 油脂の配合 実験番号 1 2 3 4 5 6 ──────────────────────────────────── パームステアリン 43 46 35 45 ── 45 パーム油 52 54 40 50 ── 50 パームオレイン ── ── ── ── 80 ── ハイエルシン 菜種極硬油 5 ── 25 5 20 ── ベヘン酸エステル ── ── ── ── ── 5 ──────────────────────────────────── エステル交換触媒の種類 金属 金属 金属 リパーゼ 金属 金属 ──────────────────────────────────── エステル交換後の油脂の 沃素価 41.2 43.2 32.4 40.9 44.8 40.9 パルミチン酸残基含量 47.8 50.0 39.6 48.0 33.6 51.7 ベヘン酸残基含量 2.5 0 12.5 2.5 10.0 5.0 融点(℃) 45.1 46.7 46.8 44.5 38.2 44.8 ────────────────────────────────────[0025] Blending of oils and fats Experiment number 1 2 3 4 5 6 ──────────────────────────────────── Palm stearin 43 46 35 45 ── 45 Palm oil 52 54 40 50 50 Palm olein ── ── ── ── 80 ── High elsin Rapeseed extremely hard oil 5 ── 25 5 20 ── Behenate ── ── ── ── ── 5 ──────────────────────────────────── Types of transesterification catalysts Metals Metals Metals Lipases Metals Metals ──────────────────────────────────── Of oil and fat after transesterification Iodine value 41.2 43.2 32.4 40.9 44.8 40.9 Palmitic acid residue content 47.8 50.0 39.6 48.0 33.6 51.7 Behenic acid residue content 2.5 0 12.5 2.5 10.0 5.0 Melting point (℃) 45.1 46.7 46.8 44.5 38.2 44.8 ────────────────────────────────────
【0026】これらの油脂を用い実施例1と同じ方法に
よりカレールーを製造し、それらの白色化テストを行っ
た。Curry roux were produced by the same method as in Example 1 using these fats and oils, and their whitening test was conducted.
【0027】 (1).20℃における白色化現象の発生状況 実験番号 製造直後 10日 30日 ──────────────────────────────────── 1 無し 無し 無し 2 やや発生 発生 激しく発生 3 無し やや発生 発生 4 無し 無し 無し 5 無し やや発生 やや発生 6 無し 無し 無し ────────────────────────────────────[0027] (1). Occurrence of whitening phenomenon at 20 ℃ Experiment number Immediately after production 10 days 30 days ──────────────────────────────────── 1 None None None 2 Moderate Occurrence Occurs violently 3 None Occurred somewhat Occurred 4 None None 5 None Slightly Occurred Slightly Occurred 6 None None ────────────────────────────────────
【0028】以上の白色化テストの結果より、パーム油
系油脂のみのエステル交換油は結晶粗大化により激しい
白色化現象を発生したが(実験番号2)、長鎖の飽和脂
肪酸残基をトリグリセリド中に分散させる事による白色
化現象発生の抑制効果が確認された(実験番号1,4,
6)。From the results of the above whitening test, although the transesterified oil containing only palm oil-based fats and oils caused a severe whitening phenomenon due to crystal coarsening (Experiment No. 2), long-chain saturated fatty acid residues were found in triglyceride. It was confirmed that the effect of suppressing the whitening phenomenon by dispersing in water was measured (Experiment No. 1, 4,
6).
【0029】しかし長鎖の飽和脂肪酸残基の配合量は多
すぎてもその効果が減じ(実験番号3,5)、エステル
交換油の脂肪酸組成中10%までが適量である(実験番
号1,4,6)。However, even if the amount of the long-chain saturated fatty acid residue is too large, its effect is reduced (Experiment No. 3, 5), and up to 10% of the fatty acid composition of the transesterified oil is appropriate (Experiment No. 1, 1). 4, 6).
【0030】また、パーム油起源の油脂部から発生する
パルミチン酸含量は、35%より少ないと白色化現象に
対する耐性が不良となる傾向を示す(実験番号5)。こ
れは飽和酸含量が減少し、エステル交換油の液体成分が
増加するためトリグリセリドの移動が容易となり、単一
結晶の粗大化が発生しやすくなるためと考えられ、カレ
ールーの硬さ、シミ出し防止の点からもパルミチン酸含
量35%以上が必要である。When the palmitic acid content generated from the oil and fat portion derived from palm oil is less than 35%, the resistance to the whitening phenomenon tends to be poor (Experiment No. 5). It is thought that this is because the saturated acid content decreases and the liquid component of transesterified oil increases, which facilitates the transfer of triglycerides and facilitates the coarsening of single crystals. From the viewpoint of, the palmitic acid content of 35% or more is required.
【0031】[0031]
【発明の効果】本発明によるエステル交換油は、白色化
現象に対する耐性が良好で、使用時の硬さが適度であ
る、カレールー用油脂として良好な品質を示す。EFFECTS OF THE INVENTION The transesterified oil according to the present invention has good resistance to whitening phenomenon and has an appropriate hardness during use, and exhibits good quality as a fat and oil for curry roux.
Claims (3)
個の飽和脂肪酸残基を持つ脂肪酸およびまたはその誘導
体とをエステル交換することを特徴とする、カレールー
製造に適した脂肪組成物の製造法。1. A fat and oil derived from palm oil and having 22 carbon atoms
A process for producing a fat composition suitable for producing curry roux, which comprises transesterifying a fatty acid having one saturated fatty acid residue and / or a derivative thereof.
トリグリセリド、アルコールの何れかまたは混合物であ
る、請求項1に記載の方法。2. A fatty acid derivative is a fatty acid ester,
The method according to claim 1, which is any one or a mixture of triglyceride and alcohol.
素原子数16個の飽和脂肪酸残基が35〜55重量%で
あり、かつ炭素原子数22個の飽和脂肪酸残基が1〜1
0重量%である、請求項1または2に記載の方法。3. In the fatty acid composition of the fat composition, the saturated fatty acid residue having 16 carbon atoms is 35 to 55% by weight, and the saturated fatty acid residue having 22 carbon atoms is 1 to 1.
The method according to claim 1, which is 0% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3181880A JP2503811B2 (en) | 1991-06-25 | 1991-06-25 | Method for producing fat composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3181880A JP2503811B2 (en) | 1991-06-25 | 1991-06-25 | Method for producing fat composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH051297A true JPH051297A (en) | 1993-01-08 |
JP2503811B2 JP2503811B2 (en) | 1996-06-05 |
Family
ID=16108486
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3181880A Expired - Fee Related JP2503811B2 (en) | 1991-06-25 | 1991-06-25 | Method for producing fat composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2503811B2 (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0823473A1 (en) * | 1996-08-08 | 1998-02-11 | Cpc International Inc. | Rapidly crystallizing fat having a low trans-fatty acid content |
EP1249172A1 (en) * | 2001-04-12 | 2002-10-16 | Societe Des Produits Nestle S.A. | Fat |
JP2006288232A (en) * | 2005-04-07 | 2006-10-26 | Kaneka Corp | Oil-and-fat composition for roux having small amount of low trans acid |
JP2007177100A (en) * | 2005-12-28 | 2007-07-12 | Fuji Oil Co Ltd | Plastic oil-and-fat composition (hard stock) and method for producing plastic oil-and-fat food by using the same |
JP2008148670A (en) * | 2006-12-20 | 2008-07-03 | Adeka Corp | Oil and fat composition for combined confectionery |
JP2008178370A (en) * | 2007-01-26 | 2008-08-07 | Kaneka Corp | Oil and fat composition |
JP2008289404A (en) * | 2007-05-23 | 2008-12-04 | Nisshin Oillio Group Ltd | Oil and fat composition for roux |
JP5184722B1 (en) * | 2011-10-25 | 2013-04-17 | 株式会社J−オイルミルズ | Oil composition |
JP2021036828A (en) * | 2019-09-03 | 2021-03-11 | ミヨシ油脂株式会社 | Fat composition for instant precooked food and instant precooked food including the same |
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JPS58216648A (en) * | 1982-06-10 | 1983-12-16 | Kao Corp | Hard butter |
JPS6140745A (en) * | 1984-08-02 | 1986-02-27 | Asahi Denka Kogyo Kk | Oily solid ingredient |
JPH0475591A (en) * | 1990-07-17 | 1992-03-10 | Ajinomoto Co Inc | Usage for edible fatty oil |
-
1991
- 1991-06-25 JP JP3181880A patent/JP2503811B2/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58216648A (en) * | 1982-06-10 | 1983-12-16 | Kao Corp | Hard butter |
JPS6140745A (en) * | 1984-08-02 | 1986-02-27 | Asahi Denka Kogyo Kk | Oily solid ingredient |
JPH0475591A (en) * | 1990-07-17 | 1992-03-10 | Ajinomoto Co Inc | Usage for edible fatty oil |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0823473A1 (en) * | 1996-08-08 | 1998-02-11 | Cpc International Inc. | Rapidly crystallizing fat having a low trans-fatty acid content |
EP1249172A1 (en) * | 2001-04-12 | 2002-10-16 | Societe Des Produits Nestle S.A. | Fat |
JP4583225B2 (en) * | 2005-04-07 | 2010-11-17 | 株式会社カネカ | Oil composition for low transformer and roux |
JP2006288232A (en) * | 2005-04-07 | 2006-10-26 | Kaneka Corp | Oil-and-fat composition for roux having small amount of low trans acid |
JP2007177100A (en) * | 2005-12-28 | 2007-07-12 | Fuji Oil Co Ltd | Plastic oil-and-fat composition (hard stock) and method for producing plastic oil-and-fat food by using the same |
JP2008148670A (en) * | 2006-12-20 | 2008-07-03 | Adeka Corp | Oil and fat composition for combined confectionery |
JP4606406B2 (en) * | 2006-12-20 | 2011-01-05 | 株式会社Adeka | Oil composition for confectionery |
JP4697150B2 (en) * | 2007-01-26 | 2011-06-08 | 株式会社カネカ | Oil composition |
JP2008178370A (en) * | 2007-01-26 | 2008-08-07 | Kaneka Corp | Oil and fat composition |
JP2008289404A (en) * | 2007-05-23 | 2008-12-04 | Nisshin Oillio Group Ltd | Oil and fat composition for roux |
JP5184722B1 (en) * | 2011-10-25 | 2013-04-17 | 株式会社J−オイルミルズ | Oil composition |
WO2013061671A1 (en) * | 2011-10-25 | 2013-05-02 | 株式会社J-オイルミルズ | Oil or fat composition |
JP2021036828A (en) * | 2019-09-03 | 2021-03-11 | ミヨシ油脂株式会社 | Fat composition for instant precooked food and instant precooked food including the same |
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