JP2004180549A - Ground meat processed food - Google Patents

Ground meat processed food Download PDF

Info

Publication number
JP2004180549A
JP2004180549A JP2002349581A JP2002349581A JP2004180549A JP 2004180549 A JP2004180549 A JP 2004180549A JP 2002349581 A JP2002349581 A JP 2002349581A JP 2002349581 A JP2002349581 A JP 2002349581A JP 2004180549 A JP2004180549 A JP 2004180549A
Authority
JP
Japan
Prior art keywords
galactoxyloglucan
ground meat
processed food
producing
reversible
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
Application number
JP2002349581A
Other languages
Japanese (ja)
Other versions
JP4141238B2 (en
Inventor
Asuka Fujimori
明日香 藤森
Yoichi Terao
洋一 寺尾
Mayumi Shirakawa
真由美 白川
Hiroyuki Yamada
裕之 山田
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.)
Dainippon Pharmaceutical Co Ltd
Nitta Gelatin Inc
Original Assignee
Dainippon Pharmaceutical Co Ltd
Nitta Gelatin 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 Dainippon Pharmaceutical Co Ltd, Nitta Gelatin Inc filed Critical Dainippon Pharmaceutical Co Ltd
Priority to JP2002349581A priority Critical patent/JP4141238B2/en
Publication of JP2004180549A publication Critical patent/JP2004180549A/en
Application granted granted Critical
Publication of JP4141238B2 publication Critical patent/JP4141238B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

<P>PROBLEM TO BE SOLVED: To provide a method for producing a ground meat processed food improved in yield by suppressing dripping when cooked, maintaining soft feeling even when cooled, and not loosing its palate feeling even when frozen or defrosted. <P>SOLUTION: The method for producing a ground meat processed food such as hamburg steak comprises adding reversibly thermal-responsive galactoxyloglucan produced by enzymatically and partially eliminating side-chain galactoxyloglucan to pasted meat material. By this method, dripping when cooked is prevented so as to be improved in yield and thereby juicy palate feeling is imparted to the food and also such ground meat processed food as to maintain soft feeling even when cooled and not loosing its palate feeling even when frozen or defrosted. <P>COPYRIGHT: (C)2004,JPO&NCIPI

Description

【0001】
【発明の属する技術分野】
本発明は、挽き肉加工食品およびその製造方法に関する。
【0002】
【従来の技術および発明が解決しようとする課題】
ハンバーグ、ミートボールなどの挽き肉加工食品は、一般にミンチ肉と玉葱などの具材からなる練り肉生地に調味料で味付けし、パン粉等で生地の硬さを調節し、成型した後、焼成および蒸しにより加熱して製品化される。このような挽き肉加工食品は、加熱調理により肉汁のドリップが起こり、旨味成分が流出し、食感が固くなり、歩留まりが減少するため、全体として商品価値を低下させる。
また、調理時から時間が経過し、製品が冷えた状態では食感はさらに固くなり、また、凍結解凍により食感が損なわれ好ましくない。
【0003】
これらの問題を解決する手法として、従来大豆蛋白や乳たん白等の蛋白を生地に添加する方法、パルプを生地に添加する方法あるいは加工澱粉やカラギーナン、グァーガム等の増粘多糖類を生地に添加する方法が提案されているが、これらの方法では効果を得るだけの使用量では風味、食感が悪くなり問題の解決に十分ではなかった。例えば、蛋白を添加する方法では蛋白独特の風味が付くし、パルプを添加する方法では肉本来の食感とは異なるものとなるし、また、加工澱粉やカラギーナン、グァーガム等の増粘多糖類を添加する方法では加工澱粉や増粘多糖類独特の“ぬるみ”や“糊っぽさ”があり、また、加熱調理時にはそれらが溶出するのでその効果が十分ではない。
【0004】
【課題を解決するための手段】
本発明は、ハンバーグなどの挽き肉加工食品を製造する際、練り肉生地にガラクトキシログルカンの側鎖ガラクトースを酵素的に部分除去した可逆的熱応答性ガラクトキシログルカンを添加することにより、加熱時のドリップを防止して歩留まりを向上させ、ジューシーな食感となる。また、冷えた状態でソフト感を保ち、凍結解凍により食感を損なわない挽き肉加工食品の製造を可能とするものである。
【0005】
本明細書中では、上記「ガラクトキシログルカンの側鎖ガラクトースを酵素的に部分除去して製造される可逆的熱応答性ガラクトキシログルカン」は以下、単に「可逆的熱応答性ガラクトキシログルカン」と略称することもある。
【0006】
ガラクトキシログルカンは双子葉,単子葉植物など高等植物の細胞壁(一次壁)に存在する天然多糖である。ガラクトキシログルカンはグルコース、キシロースおよびガラクトースを構成糖とし、主鎖はグルコースがβ−1,4結合し、側鎖にキシロース、そのキシロースにさらにガラクトースが結合している。ガラクトキシログルカンは、タマリンドをはじめ、大豆、緑豆、インゲンマメ、イネ、オオムギ、リンゴなどから抽出される。ガラクトキシログルカンとしては、いかなるガラクトキシログルカンでもよいが、その含有率が高く、入手も容易なタマリンド種子由来のガラクトキシログルカン〔タマリンド種子ガム:商品名「グリロイド」大日本製薬(株)製〕が好ましい。
【0007】
ガラクトキシログルカンは単独ではゲル化しないが、糖あるいはアルコールの共存下ではゲル化することが知られている。また、ガラクトキシログルカンの側鎖ガラクトースを酵素で一定の割合で部分除去して製造されるガラクトキシログルカンは可逆的熱応答性ゲルの挙動を示すことが知られている。すなわち、当該ガラクトキシログルカンは可逆的にゾル化/ゲル化する熱相転移性を有し、特に低温側の転移温度では可逆的に加熱によりゲル化し、冷却によりゾル化する「可逆的熱ゲル化剤」である(特開平8−283305号公報)。
【0008】
本発明に用いる可逆的熱応答性ガラクトキシログルカンは特開平8−283305号公報記載の「可逆的熱ゲル化剤」と同一物であり、したがって、当該公報に記載の方法により製造することができる。すなわち、ガラクトキシログルカンの側鎖ガラクトースを酵素的に部分分解して製造することができ、より詳しくは、基質のガラクトキシログルカン水溶液に市販もしくは精製β−ガラクトシダーゼを至適の反応温度、pH、濃度などの条件下で反応させ、反応時間に応じて側鎖ガラクトースを一定の割合で部分除去して製造することができる。反応時間は基質の濃度、酵素濃度、殊にpHに依存するので、反応時間を適宜調整することができる。
【0009】
可逆的熱応答性ガラクトキシログルカンは、当該公報の記載によれば、熱によるゾル−ゲル相転移は低温側と高温側の2箇所にあり、低温側の転移温度以下および高温側の転移温度以上ではゾル化し、両転移温度間ではゲル化するという性質を有する。特に、両転移温度領域では可逆的な熱応答性を示す。例えば、基質のガラクトキシログルカンの2%水溶液を酵素反応して製造される、側鎖ガラクトースの除去率が40%の可逆的熱応答性ガラクトキシログルカンの2%水溶液は、30℃と90℃でゾル−ゲル相転移が起こり、30℃以下および90℃以上ではゾルであり、30−90℃の範囲ではゲルである。また、側鎖ガラクトースの除去率が44%の可逆的熱応答性ガラクトキシログルカンの2%水溶液は20−100℃の範囲でゲルである。
【0010】
ゾル−ゲル相転移温度は、側鎖ガラクトースの除去率および得られた可逆的熱応答性ガラクトキシログルカンの水溶液の濃度によって変化する。ガラクトース除去率が高くなるにつれて、また、得られた可逆的熱応答性ガラクトキシログルカンの水溶液の濃度が高くなるにつれて、相転移温度は低温側ではより低下し、高温側ではより高くなり、ゲル化の温度領域が拡大する。また、かかるゾル−ゲル相転移温度は塩,糖の添加によってもその影響を受け、例えば食塩の添加では上昇傾向、砂糖の添加では下降傾向が認められる。したがって、塩、糖を添加することにより転移温度を制御することもできる。
【0011】
本発明はこのような特性を有するガラクトキシログルカンの挽き肉加工食品への使用である。かかるガラクトキシログルカンは側鎖ガラクトースの除去率が30−65%であり、より好ましくは35−55%である。その使用量は挽き肉加工食品全量に対し0.05−5重量%であり、好ましくは0.1−3重量%である。0.05重量%未満であると効果が乏しく、5重量%より多いと食感が損なわれる。その使用量は食品の水分量や食感によって適宜調整することができる。
【0012】
本発明に使用される可逆的熱応答性ガラクトキシログルカンは粉末としてまたは水溶液として製造され、いずれの形態でも使用できる。また、粉末にせず反応物そのものを用いることもできる。粉末として製造されたときは、粉末をそのまま使用することもできるが、予めその粉末を水に溶解させ水溶液として用いることもできる。
【0013】
また、本発明に用いる可逆的熱応答性ガラクトキシログルカンは単独で使用することができるが、食品に汎用される他の天然多糖や食品素材、例えばキサンタンガム、タマリンド種子ガム、グアーガム、ジェランガム、カラギーナン、ローカストビーンガム、ゼラチン、乳蛋白等と併用することもできる。
【0014】
本願発明の挽き肉加工食品は、常温、冷蔵、冷凍で流通される挽き肉加工食品であり、具体的にはハンバーグ、ミートボール、ソーセージ、つくね、メンチカツ、コロッケなどであり、中華まんじゅうなどの包皮食品以外のものをいう。
【0015】
【発明の効果】
ハンバーグなどの挽き肉加工食品を製造する際、練り肉生地に可逆的熱応答性ガラクトキシログルカンを加えると、加熱時のドリップが抑えられ、そのことにより、歩留まりが向上し、さらに風味も良く、肉本来のジューシーな食感がえられる。また、冷えた状態でもソフト感を保ち、凍結解凍後の再加熱によっても食感が損なわれない。
【0016】
【実施例】
以下に参考例及び実施例を挙げ、本発明をより詳細に説明するが、本発明は以下の実施例にのみ限定されるものではなく、本発明の技術分野における通常の技術を用いる改変が可能である。また、参考例及び実施例で使用したガラクトキシログルカンはタマリンド種子ガム由来のものであり、市販品として入手することができる〔商品名「グリロイド3S」大日本製薬(株)製〕。
【0017】
参考例1 可逆的熱応答性ガラクトキシログルカンの水溶液の調製
【0018】
(1) 可逆的熱応答性ガラクトキシログルカンは、ガラクトキシログルカンを用いて、特開平8−283305号公報記載の方法に従って製造した。すなわち、基質のガラクトキシログルカンの1%水溶液に、市販のβ−ガラクトシダーゼ「ラクターゼY−AO」〔(株)ヤクルト本社製:Aspergillus oryzae由来〕を精製して得た精製酵素β−ガラクトシダーゼを用い、酵素濃度2.4×10−5重量%、pH5.6、50℃で約20時間酵素反応させた後、100℃、20分間加熱して酵素を失活させた後、室温に戻し、等容量のエタノールを加え、1時間放置した。沈殿物を吸引濾過により回収し、乾燥した後粉砕、篩過して粉末の可逆的熱応答性ガラクトキシログルカン(ガラクトースの除去率約44%)を得た。
【0019】
(2) 上記粉末の可逆的熱応答性ガラクトキシログルカン(3g)を攪拌下、水(97g)に分散させ、氷冷しながら3時間攪拌、溶解して可逆的熱応答性ガラクトキシログルカンの3重量%水溶液(100g)を調製した。以下、可逆的熱応答性ガラクトキシログルカンの3重量%水溶液を単に「参考例1の3%水溶液」と略称する。
【0020】
実施例1 ハンバーグ
【0021】
表1の処方でハンバーグを製造した。すなわち、粒状タンパクおよび可逆的熱応答性ガラクトキシログルカンを除く原材料を混合した後、戻し水に浸積した粒状タンパクおよび可逆的熱応答性ガラクトキシログルカンを順次加え混合した。次いで、成型したものを片面1分ずつ両面加熱した後10分間蒸し、歩留まりを測定した後冷凍した。次に、これをレンジで加熱した後、食感を評価し、結果を表2に示した。
【0022】
表2に示したように、発明群は対照群と比較して歩留まりが良く、ジューシーでソフトな食感であった。また、冷めてもジューシーでソフトな食感を保持していた。
【0023】
【表1】

Figure 2004180549
【0024】
【表2】
Figure 2004180549
【0025】
実施例2 ミートボール
【0026】
表3の処方でミートボールを製造した。すなわち、可逆的熱応答性ガラクトキシログルカンを除く原材料を定法に従って混合した後、可逆的熱応答性ガラクトキシログルカンを加え混合し、成型したものを10分間蒸し150℃に調整したフライヤーで2分間揚げた後、放冷、冷凍し、これをレンジで加熱して、食感を評価した。結果を表4に示した。
【0027】
表4に示したように、発明群は対照群と比較して歩留まりが良く、ジューシーでソフトな食感であった。
【0028】
【表3】
Figure 2004180549
【0029】
【表4】
Figure 2004180549
【0030】
実施例3 ソーセージ
【0031】
表5の処方で、常法に従って(乾燥:60℃20分、スモーク:65℃10分、蒸煮:75℃30分)ソーセージを試作した。結果を表6に示した。
【0032】
表6に示したように、発明群は対照群と比較して、弾力があり、ジューシーな食感であった。
【0033】
【表5】
Figure 2004180549
【0034】
【表6】
Figure 2004180549
[0001]
TECHNICAL FIELD OF THE INVENTION
The present invention relates to processed ground food and a method for producing the same.
[0002]
2. Description of the Related Art
Processed ground meat products such as hamburgers and meatballs are generally prepared by seasoning seasoned dough consisting of ingredients such as minced meat and onions with seasonings, adjusting the hardness of the dough with breadcrumbs, etc., molding, baking and steaming. To produce a product. Such ground processed meat foods cause dripping of the meat juice due to heating and cooking, and umami components flow out, the texture becomes hard, and the yield decreases, thereby lowering the commercial value as a whole.
Further, when the time has elapsed since the cooking and the product is cooled, the texture is further hardened, and the texture is impaired by freezing and thawing, which is not preferable.
[0003]
As a method of solving these problems, conventionally, a method of adding proteins such as soybean protein and milk protein to the dough, a method of adding pulp to the dough, or a method of adding a thickened polysaccharide such as processed starch, carrageenan, guar gum to the dough These methods have been proposed, but in these methods, the amount used to obtain the effect is not enough to solve the problem because the flavor and texture deteriorate. For example, the method of adding protein adds a unique flavor to the protein, the method of adding pulp results in a texture different from the original texture of the meat, and the method of adding thickened polysaccharides such as processed starch, carrageenan, and guar gum. In the method of adding, there are "slimy" and "pasteness" peculiar to the modified starch and the thickening polysaccharide, and they are not sufficiently effective because they are eluted during cooking.
[0004]
[Means for Solving the Problems]
The present invention relates to the production of processed meat products such as hamburger meat by adding a reversible thermoresponsive galactoxyloglucan obtained by partially enzymatically removing the side chain galactose of galactoxyloglucan to the dough dough, Prevents drip and improves yield, resulting in a juicy texture. Further, it is possible to produce a processed ground meat food that maintains a soft feeling in a cold state and does not impair the texture by freezing and thawing.
[0005]
In the present specification, the "reversible thermoresponsive galactoxyloglucan produced by enzymatically partially removing galactoxyloglucan side chain galactose" is hereinafter simply referred to as "reversible thermoresponsive galactoxyloglucan". Sometimes abbreviated.
[0006]
Galactoxyloglucan is a natural polysaccharide present on the cell wall (primary wall) of higher plants such as dicotyledonous and monocotyledonous plants. Galactoxyloglucan has glucose, xylose and galactose as constituent sugars, and glucose is β-1,4 linked in the main chain, xylose is linked to the side chain, and galactose is further linked to the xylose. Galactoxyloglucan is extracted from tamarind, soybean, mung bean, kidney bean, rice, barley, apple, and the like. As the galactoxyloglucan, any galactoxyloglucan may be used, but galactoxyloglucan derived from tamarind seed (having a high content thereof and easily available) (Tamarind seed gum: trade name “Glyloid” manufactured by Dainippon Pharmaceutical Co., Ltd.) is available. preferable.
[0007]
It is known that galactoxyloglucan does not gel by itself, but gels in the presence of sugar or alcohol. It is also known that galactoxyloglucan produced by partially removing galactose in the side chain of galactoxyloglucan at a certain ratio with an enzyme exhibits the behavior of a reversible thermoresponsive gel. That is, the galactoxyloglucan has a thermal phase transition property of reversibly forming a sol / gel. Particularly at a transition temperature on a low temperature side, the galactoxyloglucan gels reversibly by heating and becomes a sol by cooling. (JP-A-8-283305).
[0008]
The reversible thermoresponsive galactoxyloglucan used in the present invention is the same as the “reversible thermogelling agent” described in JP-A-8-283305, and therefore can be produced by the method described in the publication. . That is, galactoxyloglucan can be produced by enzymatically partially decomposing the side chain galactose.More specifically, commercially available or purified β-galactosidase is added to a galactoxyloglucan aqueous solution of a substrate at an optimum reaction temperature, pH, and concentration. The reaction can be carried out under such conditions as described above, and the side chain galactose can be partially removed at a certain rate depending on the reaction time to produce the product. Since the reaction time depends on the concentration of the substrate, the concentration of the enzyme, particularly the pH, the reaction time can be appropriately adjusted.
[0009]
According to the description of the publication, reversible thermoresponsive galactoxyloglucan has two sol-gel phase transitions due to heat at a low temperature side and a high temperature side, which is lower than the lower temperature transition temperature and higher than the high temperature transition temperature. Has the property of forming a sol and gelling between the two transition temperatures. In particular, it exhibits reversible thermal responsiveness in both transition temperature regions. For example, a 2% aqueous solution of a reversible thermoresponsive galactoxyloglucan with a side chain galactose removal rate of 40%, which is produced by an enzymatic reaction of a 2% aqueous solution of galactoxyloglucan as a substrate, is heated at 30 ° C. and 90 ° C. A sol-gel phase transition occurs, being sol below 30 ° C. and above 90 ° C., and gel in the range of 30-90 ° C. A 2% aqueous solution of reversible thermoresponsive galactoxyloglucan with a removal rate of side chain galactose of 44% is a gel in the range of 20-100 ° C.
[0010]
The sol-gel phase transition temperature varies depending on the side chain galactose removal rate and the concentration of the resulting aqueous solution of reversibly thermoresponsive galactoxyloglucan. As the galactose removal rate increases and as the concentration of the resulting aqueous solution of reversibly thermoresponsive galactoxyloglucan increases, the phase transition temperature decreases at lower temperatures and increases at higher temperatures, resulting in gelation. The temperature range of is expanded. The sol-gel phase transition temperature is also affected by the addition of salts and sugars. For example, the tendency is to increase when salt is added and to decrease when sugar is added. Therefore, the transition temperature can be controlled by adding salts and sugars.
[0011]
The present invention is the use of galactoxyloglucan having such properties in processed meat products. Such galactoxyloglucan has a side chain galactose removal rate of 30-65%, more preferably 35-55%. The amount used is 0.05-5% by weight, preferably 0.1-3% by weight, based on the total amount of the processed ground meat. If it is less than 0.05% by weight, the effect is poor, and if it is more than 5% by weight, the texture is impaired. The amount used can be appropriately adjusted according to the moisture content and texture of the food.
[0012]
The reversibly thermoresponsive galactoxyloglucan used in the present invention is manufactured as a powder or as an aqueous solution, and can be used in any form. Further, the reactant itself can be used instead of the powder. When manufactured as a powder, the powder can be used as it is, or the powder can be dissolved in water in advance and used as an aqueous solution.
[0013]
The reversible thermoresponsive galactoxyloglucan used in the present invention can be used alone, but other natural polysaccharides and food materials widely used in foods, such as xanthan gum, tamarind seed gum, guar gum, gellan gum, carrageenan, It can also be used in combination with locust bean gum, gelatin, milk protein and the like.
[0014]
The minced meat processed food of the present invention is a processed minced meat food which is distributed at room temperature, refrigerated, and frozen, specifically, hamburgers, meatballs, sausages, tsukune, menchikatsu, croquettes, etc., and other than foreskin foods such as Chinese steamed buns. Means
[0015]
【The invention's effect】
When manufacturing ground meat products such as hamburgers, adding reversible thermo-responsive galactoxyloglucan to the dough reduces the drip during heating, thereby improving the yield and improving the flavor and flavor. The original juicy texture can be obtained. Further, the softness is maintained even in a cold state, and the texture is not impaired by reheating after freezing and thawing.
[0016]
【Example】
Hereinafter, the present invention will be described in more detail with reference to Reference Examples and Examples, but the present invention is not limited to the following Examples, and modifications using ordinary techniques in the technical field of the present invention are possible. It is. The galactoxyloglucan used in Reference Examples and Examples is derived from tamarind seed gum and can be obtained as a commercial product [trade name "Glyloid 3S" manufactured by Dainippon Pharmaceutical Co., Ltd.].
[0017]
Reference Example 1 Preparation of an aqueous solution of reversible thermoresponsive galactoxyloglucan
(1) Reversible thermoresponsive galactoxyloglucan was produced using galactoxyloglucan according to the method described in JP-A-8-283305. That is, using a purified enzyme β-galactosidase obtained by purifying a commercially available β-galactosidase “lactase Y-AO” (manufactured by Yakult Honsha: Aspergillus oryzae ) in a 1% aqueous solution of galactoxyloglucan as a substrate, After performing an enzyme reaction at an enzyme concentration of 2.4 × 10 −5 wt%, pH 5.6, and 50 ° C. for about 20 hours, the enzyme was inactivated by heating at 100 ° C. for 20 minutes, and then returned to room temperature, and the volume was adjusted to an equal volume. Of ethanol was added and left for 1 hour. The precipitate was collected by suction filtration, dried, pulverized and sieved to obtain a reversible thermoresponsive galactoxyloglucan (galactose removal rate of about 44%) as a powder.
[0019]
(2) Disperse the reversible thermoresponsive galactoxyloglucan (3 g) in water (97 g) with stirring, stir for 3 hours while cooling with ice, and dissolve to obtain the reversible thermoresponsive galactoxyloglucan. A weight% aqueous solution (100 g) was prepared. Hereinafter, the 3% by weight aqueous solution of the reversible thermoresponsive galactoxyloglucan is simply referred to as “3% aqueous solution of Reference Example 1”.
[0020]
Example 1 Hamburger
A hamburger was manufactured according to the formulation shown in Table 1. That is, after mixing the granular protein and the raw materials except for the reversible thermoresponsive galactoxyloglucan, the granular protein soaked in the return water and the reversible thermoresponsive galactoxyloglucan were sequentially added and mixed. Next, the molded product was heated on both sides for 1 minute each side and then steamed for 10 minutes. The yield was measured and then frozen. Next, after heating this in a microwave, the texture was evaluated and the results are shown in Table 2.
[0022]
As shown in Table 2, the yield of the invention group was better than that of the control group, and the texture was juicy and soft. Also, it kept a juicy and soft texture even when cooled.
[0023]
[Table 1]
Figure 2004180549
[0024]
[Table 2]
Figure 2004180549
[0025]
Example 2 Meatball
Meatballs were manufactured according to the recipe shown in Table 3. That is, after mixing the raw materials except for the reversible thermoresponsive galactoxyloglucan according to a standard method, adding and mixing the reversible thermoresponsive galactoxyloglucan, steaming the molded product for 10 minutes, and frying for 2 minutes with a fryer adjusted to 150 ° C. After that, the mixture was allowed to cool, frozen, and heated in a microwave to evaluate the texture. The results are shown in Table 4.
[0027]
As shown in Table 4, the yield of the invention group was better than that of the control group, and the texture was juicy and soft.
[0028]
[Table 3]
Figure 2004180549
[0029]
[Table 4]
Figure 2004180549
[0030]
Example 3 Sausage
According to the formulation of Table 5, sausages were trial-produced according to a conventional method (drying: 60 ° C. for 20 minutes, smoke: 65 ° C. for 10 minutes, steaming: 75 ° C. for 30 minutes). The results are shown in Table 6.
[0032]
As shown in Table 6, the invention group had elasticity and a juicy texture as compared with the control group.
[0033]
[Table 5]
Figure 2004180549
[0034]
[Table 6]
Figure 2004180549

Claims (5)

挽き肉加工食品の製造において、ガラクトキシログルカンの側鎖ガラクトースを酵素的に部分除去して製造される可逆的熱応答性ガラクトキシログルカンを添加することを特徴とする挽き肉加工食品の製造方法。A method for producing processed ground meat, comprising adding a reversible thermoresponsive galactoxyloglucan produced by enzymatically partially removing the side chain galactose of galactoxyloglucan in the production of processed ground meat. 側鎖ガラクトースの除去率が30−65%の可逆的熱応答性ガラクトキシログルカンである請求項1記載の挽き肉加工食品の製造方法。The method for producing a processed ground meat food according to claim 1, which is a reversible thermoresponsive galactoxyloglucan having a side chain galactose removal rate of 30 to 65%. 可逆的熱応答性ガラクトキシログルカンを挽き肉加工食品の全量に対し0.05−5重量%添加する請求項1または2記載の挽き肉加工食品の製造方法。The method for producing a processed ground meat product according to claim 1 or 2, wherein the reversible thermoresponsive galactoxyloglucan is added in an amount of 0.05 to 5% by weight based on the total amount of the processed ground meat product. ガラクトキシログルカンがタマリンド種子ガム由来である請求項1−3のいずれか1項記載の挽き肉加工食品の製造方法。The method according to any one of claims 1 to 3, wherein the galactoxyloglucan is derived from tamarind seed gum. 請求項1−4のいずれか1項記載の製造方法によって製造される挽き肉加工食品。A minced processed food produced by the production method according to claim 1.
JP2002349581A 2002-12-02 2002-12-02 Ground meat processed food Expired - Fee Related JP4141238B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2002349581A JP4141238B2 (en) 2002-12-02 2002-12-02 Ground meat processed food

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2002349581A JP4141238B2 (en) 2002-12-02 2002-12-02 Ground meat processed food

Publications (2)

Publication Number Publication Date
JP2004180549A true JP2004180549A (en) 2004-07-02
JP4141238B2 JP4141238B2 (en) 2008-08-27

Family

ID=32752079

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002349581A Expired - Fee Related JP4141238B2 (en) 2002-12-02 2002-12-02 Ground meat processed food

Country Status (1)

Country Link
JP (1) JP4141238B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016193892A (en) * 2015-03-31 2016-11-17 Dsp五協フード&ケミカル株式会社 Gel composition and sheet, and method for producing the same
EP3476383A4 (en) * 2016-06-24 2020-01-01 DSP Gokyo Food & Chemical Co., Ltd. Gel composition, sheet, and production method therefor
US11021578B2 (en) 2016-06-24 2021-06-01 DSP Gokyo Food & Chemicals Co., Ltd. Gel composition and production method therefor

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4184054B2 (en) * 2002-12-02 2008-11-19 新田ゼラチン株式会社 Meat processing products
DE102004058285A1 (en) * 2004-12-02 2006-06-08 Emitec Gesellschaft Für Emissionstechnologie Mbh Connecting material for positioning of solder material, method for producing a honeycomb body and corresponding honeycomb body

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016193892A (en) * 2015-03-31 2016-11-17 Dsp五協フード&ケミカル株式会社 Gel composition and sheet, and method for producing the same
EP3476383A4 (en) * 2016-06-24 2020-01-01 DSP Gokyo Food & Chemical Co., Ltd. Gel composition, sheet, and production method therefor
US10702455B2 (en) 2016-06-24 2020-07-07 Dsp Gokyo Food & Chemical Co., Ltd. Gel composition, sheet, and production method therefor
US11021578B2 (en) 2016-06-24 2021-06-01 DSP Gokyo Food & Chemicals Co., Ltd. Gel composition and production method therefor
US11566111B2 (en) 2016-06-24 2023-01-31 Sumitomo Pharma Food & Chemical Co., Ltd. Gel composition and production method therefor

Also Published As

Publication number Publication date
JP4141238B2 (en) 2008-08-27

Similar Documents

Publication Publication Date Title
WO2017061628A1 (en) Food-improving agent
TW201127300A (en) Meat additive, pickling liquid and processed meat product
JPH02410A (en) Processed food using konjaku and production of the same food
JP2001000148A (en) Meat quality improver
JP2002281942A (en) Texture-improving agent both for processed meat article and processed fish article
WO1996015685A1 (en) Low-fat meat foods and methods for making same
JP2014100091A (en) Rare sugar-containing powder
JPH1099051A (en) Processed raw meat
JP4141238B2 (en) Ground meat processed food
EP0319987B1 (en) Process for producing processed minced meat foods
JPH0773482B2 (en) Manufacturing method of konjac food
JP2007185148A (en) Texture improver, and meat or fish meat processed food
JP4618952B2 (en) Manufacturing method of fried food
US6352735B1 (en) Process of incorporating konjac paste into a meat to provide a low calorie meat product
JP7393001B2 (en) Meat processing preparations
JP3817125B2 (en) Method for producing suspension dispersion of meat
TWI775980B (en) Composition for edible meat modification, manufacturing method of edible meat conditioner, edible meat conditioner, and edible meat modification method
JP4382534B2 (en) Pickle composition
JP4184054B2 (en) Meat processing products
JP2001252032A (en) Rice cake or dumpling and method for producing the same
JP4141237B2 (en) Foreskin food
JP2003219826A (en) Batter for oil-fried food and method for producing the oil-fried food
JP6798172B2 (en) Manufacturing method of minced meat processed food
JPH11332474A (en) Batter composition
KR20190110846A (en) Konjac gel and manufacturing method for the same

Legal Events

Date Code Title Description
RD04 Notification of resignation of power of attorney

Free format text: JAPANESE INTERMEDIATE CODE: A7424

Effective date: 20040527

RD02 Notification of acceptance of power of attorney

Free format text: JAPANESE INTERMEDIATE CODE: A7422

Effective date: 20040602

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A821

Effective date: 20040602

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20050927

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20070724

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20070807

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20071005

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20080408

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20080411

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20080513

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20080610

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110620

Year of fee payment: 3

R150 Certificate of patent or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110620

Year of fee payment: 3

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110620

Year of fee payment: 3

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120620

Year of fee payment: 4

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20140620

Year of fee payment: 6

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

LAPS Cancellation because of no payment of annual fees