JPS6136897B2 - - Google Patents

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Publication number
JPS6136897B2
JPS6136897B2 JP57140364A JP14036482A JPS6136897B2 JP S6136897 B2 JPS6136897 B2 JP S6136897B2 JP 57140364 A JP57140364 A JP 57140364A JP 14036482 A JP14036482 A JP 14036482A JP S6136897 B2 JPS6136897 B2 JP S6136897B2
Authority
JP
Japan
Prior art keywords
starch
fish
esterified
kamaboko
water
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.)
Expired
Application number
JP57140364A
Other languages
Japanese (ja)
Other versions
JPS5931672A (en
Inventor
Naoyuki Yago
Ichiro Iida
Norishige Ogura
Yasuo Endo
Tooru Nakajima
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.)
Nippon Starch Chemical Co Ltd
Original Assignee
Nippon Starch Chemical Co Ltd
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 Nippon Starch Chemical Co Ltd filed Critical Nippon Starch Chemical Co Ltd
Priority to JP57140364A priority Critical patent/JPS5931672A/en
Publication of JPS5931672A publication Critical patent/JPS5931672A/en
Publication of JPS6136897B2 publication Critical patent/JPS6136897B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は置換度(D.S.)が0.005〜0.3好ましく
は0.01〜0.2の澱粉リン酸エステル、澱粉オクテ
ニルコハク酸ナトリウムおよび澱粉オクテニルコ
ハク酸アンモニウムの少なくとも1種を添加する
ことを特徴とする水産練製品の製造方法に関し、
その目的とするところは優れた弾力性、保水性お
よび耐老化性を有する水産練製品を工業的に有利
に製造することにある。 従来、水産練製品の製造においては、小麦澱
粉、馬鈴薯澱粉、甘藷澱粉などを5〜20%添加す
ることが一般に行なわれている。その目的とする
ところは練製品の“あし”を強くして食感を改善
することにあり、増量剤としての効果もある。 水産練製品の原料となる魚肉には強足魚、弱足
魚があるが、弱足魚を使用する際には澱粉の“あ
し”の補強効果が特に重要になる。 澱粉が水産練製品の“あし”の補強効果を現わ
すのは、魚肉中に粒子のまま混和された澱粉が糊
化温度以上に加熱されると、周囲の魚肉から水を
吸収し弾力に富む粒子となり魚肉から吸収した水
は澱粉粒子中に固定される。この糊化した澱粉粒
子の弾力性、機械的強度が周囲の魚肉部分よりも
優れているため補強効果を現わす。 また、強足魚、弱足魚いずれを原料とする場合
においても、澱粉を添加することにより、その添
加量の2〜3倍の水を添加することができるので
増量剤としても有用である。 しかし、このように“あし”の補強剤、増量剤
として有用な未変性澱粉も糊化後、時間の経過と
共に老化を起こし、吸収固定した水を再放出(離
水)してしまう。そうなると澱粉粒子間の水が増
加し、組識中の自由水が増大してもろくなり、食
感を著しく損ない商品価値を低下させてしまう。
このような未変性澱粉の中で比較的優れた性質を
持つものとして小麦澱粉が挙げられるが、これも
老化を比較的起こしにくい程度のものであり、ゲ
ル強度が弱いので弾力、食感なども劣つたものと
なり優れた性質を持つものとは言いがたい。 本発明者らは、水産練製品のこれらの問題点を
解消すべく、弾力性、ゲル強度、食感などが優れ
経時変化が小さい澱粉を求めて鋭意研究を重ねた
結果、一定の範囲の置換度を有する澱粉リン酸エ
ステル、澱粉オクテニルコハク酸ナトリウムおよ
び澱粉オクテニルコハク酸アンモニウム等のエス
テル化澱粉がこの目的に適することを見い出し、
本発明を完成するに至つた。 本発明の要旨は、置換度(D.S.)が0.005〜0.3
好ましくは0.01〜0.2の澱粉リン酸エステル、澱
粉オクテニルコハク酸ナトリウムおよび澱粉オク
テニルコハク酸アンモニウムの少なくとも1種を
添加することを特徴とする水産練製品の製造方法
に存する。 かかるエステル化澱粉は、未変性(原料)澱粉
例えば、小麦澱粉、馬鈴薯澱粉、コーンスター
チ、ワキシコーンスターチ、甘藷澱粉、タピオカ
澱粉、サゴ澱粉、米澱粉などの天然澱粉やこれら
の分解物、アミロースやアミロペクチン分画物、
小麦粉、トウモロコシ粉、切干甘藷、切干タピオ
カなどの澱粉含有物が挙げられ好ましくは粒状澱
粉にエステル化剤を作用させることにより得られ
る。エステル化剤としては、メタリン酸、リン酸
ナトリウム、リン酸カルシウム、1−オクテニル
無水コハク酸などが挙げられる。 このようにして得られるエステル化澱粉のエス
テル化度は置換度として表し(無水グルコース残
基1モル当りの置換基D.S.モル)D.S.=0.005〜
0.3好ましくは0.01〜0.2のとき好適な性質を示
し、そのときの糊化開始温度はそれぞれ70〜30℃
および60〜40℃を示す。 なお、糊化開始温度は2.7%食塩水溶液で5%
澱粉スラリーを調整して加熱し、ブラベンダーア
ミログラフにおいて粘度増加開始時の温度を示
す。 本発明のエステル化澱粉のうち少なくとも1種
を魚肉に添加して常法により肉類練製品を製造す
れば、澱粉粒子は十分に膨潤し、周囲の魚肉から
一定の水分を澱粉粒子中に保持するので優れた弾
力性、ゲル強度、食感を示す。 また、本発明のエステル化澱粉を用いると経時
変化が小さく、すなわち圧出水分の増加が少なく
軟らかさを失なわず食感の経時変化がほとんどな
い。またカマボコなどの切り口に透明感があり、
つやのあるものとなり、著しく商品価値の高いも
のとなることを見い出した。 また、水産練製品中には“あし”の強化を目的
とし、食塩2.0〜3.0%が添加されている。これに
より、澱粉の糊化開始温度は、10〜15℃蒸留水中
よりも上昇し、馬鈴薯澱粉では70〜80℃、コーン
スターチにいたつては80〜90℃にもなつてしま
う。特にコーンスターチにおいては通常の加熱に
より、十分に澱粉粒子を膨潤させることが困難と
なり、不十分な膨潤のために老化を早める結果と
なる。これに対し、本発明のエステル化澱粉は原
料澱粉より糊化開始温度がかなり低いものとな
り、コーンスターチを原料としたエステル化澱粉
であつても、通常の加熱で十分に膨潤した状態と
なりより強いゲル強度を持つた“あし”の強い製
品となる。しかるに、これまで使用困難であつた
安価なコーンスターチをも原料として使用可能な
ものとして、安価で優れた水産練製品を製造し得
ることをも見い出した。 なお、特公昭45−31347号公報において水産練
製品の品質改良のために、オキシアルキルエーテ
ル化澱粉を使用する方法が開示されているが、こ
のオキシアルキルエーテル化澱粉を得るには、エ
ーエル化剤としてエチレンオキシド(沸点10.7
℃)、プロピレンオキシド(沸点34.2℃)を使用
し完全密閉容器内で、反応温度を厳密に長時間管
理しなければならない。(例えば、プロピレンオ
キシドの場合37〜39℃で24時間程度の反応時間を
要する。) また、既存の反応容器を使用した場合、大量の
エーテル化剤が必要となるがこれは揮発性、引火
性が高いので爆発の危険性が大きく安全性の面か
らは望ましいものではないし、コスト的にも高価
なものになる。 一方、本発明のエステル化澱粉を得るには、常
温反応が可能で、温度管理を厳密に行なう必要は
ない。またエステル化剤は上記のエーテル化剤よ
りも揮発性、引火性が低いので、安全性の面でも
より好ましいものと言える。 また、本発明のエステル化澱粉は、馬鈴薯澱
粉、小麦澱粉、コーンスターチ、甘藷澱粉などの
未変性の原料澱粉との併用が可能である。特に高
置換度のエステル化澱粉は多少曵糸性があるの
で、必要があれば原料澱粉を併用することによつ
て曵糸性を押えることができる。そして未変性の
原料澱粉を併用してもその効果は十分に現われ
る。 本発明のエステル化澱粉は、かまぼこ、ちく
わ、さつまあげ、魚肉ソーセージ、魚肉ハムなど
の魚肉を用いる水産練製品の製造において好適に
使用されるが、かまぼこ、ちくわにおける使用を
次の参考例、実施例、比較例によつてさらに詳細
に説明する。 参考例 1 水120部にリン酸二水素ナトリウム0.3〜10部及
びりん酸一水素ナトリウム0.3〜10部を溶解し、
これにコーンスターチ100部を撹拌下に分散させ
た後、乾燥する。これを回転釜内で130℃にて3
時間反応させ、水洗、乾燥し澱粉リン酸モノエス
テルナトリウムを得た。 実施例 1 冷凍助宗1000部を解凍後、空摺5分後、食塩30
部を添加し、塩摺を10分間行なう。ついでM.S.
G.15部、砂糖25部等調味料を加え、さらに参考
例1で得た澱粉リン酸モノエステルナトリウム
100部、氷水200部を添加して本摺を10分間行なつ
た後ケーシングを行ない、90℃で40分間蒸煮を行
ないかまぼこを得た。 実施例 2 澱粉リン酸モノエステルナトリウムの添加量の
内、半分を小麦澱粉に置き換える以外は実施例1
と同様にしてかまぼこを得た。 比較例 1 澱粉リン酸モノエステルナトリウムの代りに未
変性の馬鈴薯澱粉、コーンスターチ、小麦澱粉を
用いる以外は実施例1と同様にしてかまぼこを得
た。 実施例 3 魚肉(冷凍助宗)1000部に調味料等を加え混合
を行ない、参考例1で得た澱粉リン酸エステルナ
トリウム300部および氷水200部と共に5分間混合
した摺身を自動成型機で成型後、加熱温度170〜
180℃、通過時間3分間で焼ちくわを得た。 比較例 2 澱粉リン酸モノエステルナトリウムの代りに未
変性の馬鈴薯澱粉、コーンスターチ、小麦澱粉を
用いる以外は実施例5と同様にして焼ちくわを得
た。 次に実施例および比較例で使用した澱粉および
それらで得られたかまぼこおよびちくわについ
て、その物性を測定して結果を表に示す。 第1表には使用した澱粉の置換度、糊化開始温
度および膨潤率が示されている。ここで膨潤率と
は2.7%食塩水溶液に澱粉1gを懸濁させ、75℃
で30分間加熱した後、30℃に冷却し20分間遠心分
離(4000r.p.m.)して上澄液を除去した後の残渣
の重量値(g)である。 第2表には第1表の澱粉を使用して作られたか
まぼこの物性が示されており、ゼリー強度および
軟らかさは岡田式カードメーターを用いて試料か
まぼこ片(縦5cm×横5cm×厚さ2.5cm)を測定
した値より算出した数値である。 弾力性および食感は馬鈴薯澱粉を使用したかま
ぼこの1日後を10.0とし、同様にコーンスターチ
を使用したものを5.0とした官能値である。 また、圧出水分は、かまぼこ断面2.25cm2、重量
0.6gの試験片の全断面に10Kgの荷重をかけ1分
間経過後に、にじみ出した水分の量である。 未変性の原料澱粉を添加した通常の場合に比較
し、本発明のエステル化澱粉を使用した場合の方
が圧出水分は、はるかに少なく軟らかさ、弾力
性、食感においてすべて優れていること明白であ
る。また、未変性の原料澱粉との混合使用に際し
ても、十分に効果があることが認められる。 一方、置換度0.3以上のエステル化澱粉を使用
した場合、圧出水分が多くなり、また、弾力性、
食感等いわゆる“あし”の悪化が起つていること
がわかる。このことより本発明のエステル化澱粉
の置換度は0.005〜0.3が好ましいことがわかる。 第3表には、第1表の澱粉を使用して作られた
焼ちくわの物性をかまぼこの場合と同様に求め
た。 焼ちくわにおいても、本発明のエステル化澱粉
は未変性の原料澱粉を使用したものに比較し、弾
力性、食感、圧出水分のいずれも優れていること
が明白であり、原料澱粉との混合使用においても
十分な効果が認められる。また、焼ちくわにおい
ても本発明のエステル化澱粉の置換度は0.005〜
0.3が好ましいことがわかる。
The present invention is a method for producing a seafood paste product, which is characterized in that at least one of starch phosphate ester, sodium starch octenyl succinate, and ammonium starch octenyl succinate having a degree of substitution (DS) of 0.005 to 0.3, preferably 0.01 to 0.2 is added. Regarding
The purpose is to industrially advantageously produce fish paste products having excellent elasticity, water retention and aging resistance. Conventionally, in the production of fish paste products, it has been common practice to add 5 to 20% of wheat starch, potato starch, sweet potato starch, etc. Its purpose is to strengthen the "legs" of the paste product and improve its texture, and it also has the effect of acting as a bulking agent. There are two types of fish meat that are used as raw materials for fish paste products: strong-legged fish and weak-legged fish.When using weak-legged fish, the reinforcing effect of starch on the legs is particularly important. Starch has the effect of reinforcing the legs in fish paste products because when starch is mixed into fish meat as particles and heated above the gelatinization temperature, it absorbs water from the surrounding fish meat and becomes elastic. The water absorbed from the fish meat becomes particles and is fixed in the starch particles. These gelatinized starch particles exhibit a reinforcing effect because they have better elasticity and mechanical strength than the surrounding fish meat. In addition, when using either strong-legged fish or weak-legged fish as a raw material, by adding starch, 2 to 3 times the amount of water added can be added, so it is useful as a filler. However, even unmodified starch, which is useful as a leg reinforcing agent and filler, ages over time after gelatinization and re-releases absorbed and fixed water (hydrosyneresis). In this case, the amount of water between starch particles increases, and the amount of free water in the structure increases, resulting in brittleness, which significantly impairs the texture and lowers the commercial value.
Among these unmodified starches, wheat starch has relatively excellent properties, but it is also relatively resistant to aging, and its gel strength is weak, resulting in poor elasticity and texture. It becomes inferior and cannot be said to have superior qualities. In order to solve these problems with fish paste products, the present inventors have conducted extensive research in search of a starch that has excellent elasticity, gel strength, texture, etc. and has little change over time. We have found that esterified starches such as starch phosphate ester, sodium starch octenyl succinate and ammonium starch octenyl succinate having a certain degree of
The present invention has now been completed. The gist of the present invention is that the degree of substitution (DS) is between 0.005 and 0.3.
Preferably, there is provided a method for producing a fish paste product characterized in that 0.01 to 0.2 of at least one of starch phosphate ester, sodium starch octenyl succinate, and ammonium starch octenyl succinate is added. Such esterified starches include unmodified (raw material) starches, such as natural starches such as wheat starch, potato starch, corn starch, waxy corn starch, sweet potato starch, tapioca starch, sago starch, and rice starch, and their decomposed products, amylose and amylopectin. fraction,
Examples include starch-containing materials such as wheat flour, corn flour, dried sweet potato, and dried tapioca, and are preferably obtained by treating granular starch with an esterifying agent. Examples of the esterifying agent include metaphosphoric acid, sodium phosphate, calcium phosphate, and 1-octenylsuccinic anhydride. The degree of esterification of the esterified starch thus obtained is expressed as the degree of substitution (DS mole of substituent per mole of anhydroglucose residue) DS = 0.005 to
0.3, preferably 0.01 to 0.2, exhibits suitable properties, and the gelatinization initiation temperature at that time is 70 to 30°C, respectively.
and 60-40℃. In addition, the gelatinization start temperature is 2.7% saline solution and 5%
The starch slurry is prepared and heated to indicate the temperature at which the viscosity begins to increase in the Brabender amylograph. If at least one of the esterified starches of the present invention is added to fish meat and a meat paste product is produced by a conventional method, the starch particles will sufficiently swell, and a certain amount of moisture from the surrounding fish meat will be retained in the starch particles. It exhibits excellent elasticity, gel strength, and texture. Further, when the esterified starch of the present invention is used, the change over time is small, that is, the increase in extruded water is small, the softness is not lost, and the texture hardly changes over time. In addition, there is a sense of transparency in the cut parts such as kamaboko,
It has been found that the product becomes glossy and has an extremely high commercial value. In addition, 2.0 to 3.0% salt is added to fish paste products for the purpose of strengthening the legs. As a result, the gelatinization start temperature of starch is 10 to 15 degrees Celsius higher than that of distilled water, reaching 70 to 80 degrees Celsius for potato starch and 80 to 90 degrees Celsius for corn starch. Particularly in the case of corn starch, it is difficult to sufficiently swell the starch particles by ordinary heating, and insufficient swelling results in premature aging. On the other hand, the esterified starch of the present invention has a gelatinization initiation temperature much lower than that of the raw material starch, and even if it is an esterified starch made from cornstarch, it will be sufficiently swollen by normal heating and will have a stronger gelatinization temperature. The product is strong and has strong legs. However, it has been discovered that inexpensive cornstarch, which has been difficult to use up to now, can be used as a raw material to produce excellent seafood paste products at low cost. Note that Japanese Patent Publication No. 45-31347 discloses a method of using oxyalkyl etherified starch to improve the quality of fish paste products, but in order to obtain this oxyalkyl etherified starch, it is necessary to as ethylene oxide (boiling point 10.7
℃), propylene oxide (boiling point 34.2℃) is used, and the reaction temperature must be strictly controlled for a long time in a completely sealed container. (For example, in the case of propylene oxide, the reaction time is about 24 hours at 37 to 39°C.) In addition, if an existing reaction vessel is used, a large amount of etherification agent is required, but this is volatile and flammable. This is not desirable from a safety point of view since it has a high risk of explosion, and it is also expensive in terms of cost. On the other hand, in order to obtain the esterified starch of the present invention, the reaction can be carried out at room temperature and there is no need to strictly control the temperature. Furthermore, since the esterification agent has lower volatility and flammability than the above-mentioned etherification agents, it can be said to be more preferable from the viewpoint of safety. Furthermore, the esterified starch of the present invention can be used in combination with unmodified raw material starches such as potato starch, wheat starch, corn starch, and sweet potato starch. In particular, since esterified starch with a high degree of substitution has some spinnability, if necessary, the spinnability can be suppressed by using raw starch in combination. Even if unmodified raw starch is used in combination, the effect will be fully manifested. The esterified starch of the present invention is suitably used in the production of fish paste products using fish meat, such as kamaboko, chikuwa, fish cakes, fish sausage, and fish ham. , will be explained in more detail with reference to a comparative example. Reference example 1 Dissolve 0.3 to 10 parts of sodium dihydrogen phosphate and 0.3 to 10 parts of sodium monohydrogen phosphate in 120 parts of water,
100 parts of cornstarch is dispersed into this while stirring, and then dried. This was heated to 130℃ in a rotary pot.
The mixture was reacted for a period of time, washed with water, and dried to obtain starch sodium phosphate monoester. Example 1 After thawing 1000 copies of frozen Sukemune, after 5 minutes of drying, add 30% salt.
Add 50% of the total amount of salt, and perform salting for 10 minutes. Then MS
Add 15 parts of G., 25 parts of sugar, and other seasonings, and further add starch sodium phosphate monoester obtained in Reference Example 1.
After adding 100 parts and 200 parts of ice water and carrying out the final printing for 10 minutes, casing was carried out and steaming was carried out at 90°C for 40 minutes to obtain kamaboko. Example 2 Example 1 except that half of the amount of sodium starch phosphate monoester added was replaced with wheat starch
I obtained kamaboko in the same way. Comparative Example 1 Kamaboko was obtained in the same manner as in Example 1, except that unmodified potato starch, corn starch, and wheat starch were used instead of starch monoester sodium phosphate. Example 3 Seasonings, etc. were added to 1000 parts of fish meat (frozen Sukemune), mixed, and mixed with 300 parts of sodium starch phosphate obtained in Reference Example 1 and 200 parts of ice water for 5 minutes.The resulting surimi was molded using an automatic molding machine. After that, heating temperature 170 ~
Baked chikuwa was obtained at 180°C for 3 minutes. Comparative Example 2 Baked chili peppers were obtained in the same manner as in Example 5, except that unmodified potato starch, corn starch, and wheat starch were used instead of starch monoester sodium phosphate. Next, the physical properties of the starches used in the Examples and Comparative Examples and the kamaboko and chikuwa obtained using them were measured and the results are shown in the table. Table 1 shows the degree of substitution, gelatinization onset temperature and swelling rate of the starch used. Here, the swelling rate is defined as 1 g of starch suspended in a 2.7% saline solution at 75°C.
This is the weight value (g) of the residue after heating for 30 minutes, cooling to 30°C, centrifuging (4000 rpm) for 20 minutes, and removing the supernatant. Table 2 shows the physical properties of the kamaboko made using the starch in Table 1, and the jelly strength and softness were measured using a sample kamaboko piece (length 5 cm x width 5 cm x thickness) using an Okada card meter. This is a value calculated from the measured value of 2.5 cm). Elasticity and texture are organoleptic values with kamaboko made with potato starch after 1 day being 10.0 and kamaboko made with corn starch being 5.0. In addition, the extruded water is calculated based on the kamaboko cross section of 2.25 cm 2 and the weight of the kamaboko.
This is the amount of water that oozed out after 1 minute of applying a load of 10 kg to the entire cross section of a 0.6 g test piece. Compared to the usual case where unmodified raw starch is added, when the esterified starch of the present invention is used, the extruded moisture is much lower and the softness, elasticity, and texture are all superior. It's obvious. Furthermore, it is recognized that it is sufficiently effective even when used in combination with unmodified raw material starch. On the other hand, when using esterified starch with a degree of substitution of 0.3 or more, the extruded water content increases, and the elasticity and
It can be seen that the so-called "legs", such as the texture, have deteriorated. This shows that the degree of substitution of the esterified starch of the present invention is preferably 0.005 to 0.3. In Table 3, the physical properties of baked chikuwa made using the starches in Table 1 were determined in the same manner as for kamaboko. Even in baked chikuwa, it is clear that the esterified starch of the present invention is superior to those using unmodified raw material starch in terms of elasticity, texture, and extruded moisture. Sufficient effects are observed even when used in combination. In addition, even in baked chikuwa, the degree of substitution of the esterified starch of the present invention is from 0.005 to
It can be seen that 0.3 is preferable.

【表】【table】

【表】【table】

【表】【table】

Claims (1)

【特許請求の範囲】[Claims] 1 置換度(D.S.)が0.005〜0.3好ましくは0.01
〜0.2の澱粉リン酸エステル、澱粉オクテニルコ
ハク酸ナトリウムおよび澱粉オクテニルコハク酸
アンモニウムの少なくとも1種を添加することを
特徴とする水産練製品の製造方法。
1 Degree of substitution (DS) is 0.005 to 0.3, preferably 0.01
A method for producing a fish paste product, which comprises adding at least one of starch phosphate ester, sodium starch octenyl succinate, and ammonium starch octenyl succinate in an amount of ~0.2.
JP57140364A 1982-08-12 1982-08-12 Preparation of fish paste product Granted JPS5931672A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57140364A JPS5931672A (en) 1982-08-12 1982-08-12 Preparation of fish paste product

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57140364A JPS5931672A (en) 1982-08-12 1982-08-12 Preparation of fish paste product

Publications (2)

Publication Number Publication Date
JPS5931672A JPS5931672A (en) 1984-02-20
JPS6136897B2 true JPS6136897B2 (en) 1986-08-21

Family

ID=15267100

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57140364A Granted JPS5931672A (en) 1982-08-12 1982-08-12 Preparation of fish paste product

Country Status (1)

Country Link
JP (1) JPS5931672A (en)

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JP2012246374A (en) * 2011-05-26 2012-12-13 Nihon Cornstarch Corp Process for manufacturing modified starch

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Publication number Priority date Publication date Assignee Title
EP2716166A4 (en) * 2011-06-01 2015-02-18 J Oil Mills Inc Starch processed with oil or fat and method for producing same
JP4942855B1 (en) * 2011-11-15 2012-05-30 日本食品化工株式会社 Fishery paste product improver and fish paste product
CN103734249A (en) * 2013-12-25 2014-04-23 广西科技大学 Fish freezing denaturation inhibitor
JP6651272B1 (en) 2019-03-29 2020-02-19 日本食品化工株式会社 Aquatic meat product improver and aquatic meat products
CN113662159B (en) * 2021-08-02 2022-08-23 浙江顶味食品有限公司 Compound seasoning and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012246374A (en) * 2011-05-26 2012-12-13 Nihon Cornstarch Corp Process for manufacturing modified starch

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