JPS6349991B2 - - Google Patents
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- Publication number
- JPS6349991B2 JPS6349991B2 JP54085094A JP8509479A JPS6349991B2 JP S6349991 B2 JPS6349991 B2 JP S6349991B2 JP 54085094 A JP54085094 A JP 54085094A JP 8509479 A JP8509479 A JP 8509479A JP S6349991 B2 JPS6349991 B2 JP S6349991B2
- Authority
- JP
- Japan
- Prior art keywords
- water
- amount
- gel
- protein
- parts
- 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
Links
- 108090000623 proteins and genes Proteins 0.000 claims description 24
- 102000004169 proteins and genes Human genes 0.000 claims description 24
- 235000015110 jellies Nutrition 0.000 claims description 21
- 239000008274 jelly Substances 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- 230000000694 effects Effects 0.000 claims description 4
- 239000007791 liquid phase Substances 0.000 claims description 3
- 102000003505 Myosin Human genes 0.000 claims description 2
- 108060008487 Myosin Proteins 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 210000003365 myofibril Anatomy 0.000 claims description 2
- 239000000725 suspension Substances 0.000 claims 1
- 239000000499 gel Substances 0.000 description 14
- 235000002639 sodium chloride Nutrition 0.000 description 13
- 150000003839 salts Chemical class 0.000 description 11
- 235000013372 meat Nutrition 0.000 description 10
- 241000251468 Actinopterygii Species 0.000 description 9
- 235000019465 surimi Nutrition 0.000 description 8
- 241000269821 Scombridae Species 0.000 description 6
- 235000019688 fish Nutrition 0.000 description 6
- 235000020640 mackerel Nutrition 0.000 description 6
- 210000003205 muscle Anatomy 0.000 description 4
- 235000019640 taste Nutrition 0.000 description 4
- 102000008186 Collagen Human genes 0.000 description 3
- 108010035532 Collagen Proteins 0.000 description 3
- 241000442132 Lactarius lactarius Species 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- 229920001436 collagen Polymers 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 235000019512 sardine Nutrition 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- QCVGEOXPDFCNHA-UHFFFAOYSA-N 5,5-dimethyl-2,4-dioxo-1,3-oxazolidine-3-carboxamide Chemical compound CC1(C)OC(=O)N(C(N)=O)C1=O QCVGEOXPDFCNHA-UHFFFAOYSA-N 0.000 description 2
- 241000555825 Clupeidae Species 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- 102000002322 Egg Proteins Human genes 0.000 description 2
- 108010000912 Egg Proteins Proteins 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- 210000000988 bone and bone Anatomy 0.000 description 2
- 238000005119 centrifugation Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 235000014103 egg white Nutrition 0.000 description 2
- 210000000969 egg white Anatomy 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 235000011962 puddings Nutrition 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 235000019643 salty taste Nutrition 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 108010082495 Dietary Plant Proteins Proteins 0.000 description 1
- 239000004278 EU approved seasoning Substances 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 241001125046 Sardina pilchardus Species 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 235000021466 carotenoid Nutrition 0.000 description 1
- 150000001747 carotenoids Chemical class 0.000 description 1
- 235000013330 chicken meat Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000004925 denaturation Methods 0.000 description 1
- 230000036425 denaturation Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 235000011194 food seasoning agent Nutrition 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 235000008476 powdered milk Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 235000020989 red meat Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 210000001835 viscera Anatomy 0.000 description 1
Landscapes
- Meat, Egg Or Seafood Products (AREA)
- Jellies, Jams, And Syrups (AREA)
Description
【発明の詳細な説明】
本発明は蛋白ゼリーの製法に関するものであ
る。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing protein jelly.
魚肉類の利用法としては有姿の侭での利用の
他、スリ身、FPCミールなど種々の加工法が知
られており、各々保蔵性、加工適性などの特徴が
認められている。特に近年スリ身または冷凍スリ
身の加工技術は急速の進歩を逐げ巨大市場を形成
するまでに至つている。 Various processing methods are known for using fish meat, such as using it in its natural state, as well as making Surimi and FPC meal, and each method has been recognized for its characteristics such as storage stability and suitability for processing. Particularly in recent years, processing technology for surimi or frozen surimi has made rapid progress and has reached the point where it has formed a huge market.
しかしながら之等のスリ身は主に白身魚に限ら
れており血合肉の多い赤身魚などでは純白で魚種
による魚臭などの僻の無いスリ身を得ることが困
難であつて、加熱後のゲルも白身魚に比して弱
く、市場価値の高いものは得られていないのが現
状である。 However, such pickled meat is mainly limited to white fish, and it is difficult to obtain pure white fish without the fishy odor caused by the fish species, such as red meat with a lot of blood, and it is difficult to obtain the fish after cooking. The gel is also weaker than that of white fish, and the current situation is that we cannot obtain anything with high market value.
本発明者等はゲル形成力の弱い魚種の改良につ
いて、魚種によつて発生する
臭などの僻の除去
色の除去
ゲル形成力を強めること
などについて検討を行なつた結果、筋原繊維を完
全に解ぐし之を遠心分離することによつて透明に
近くて種の臭など僻や色が無く、極めて保水力の
強いゲルを作り出すことに成功し、併せてこのゲ
ルは従来法ではスリ身が出来ない様な鮮度の低い
もの、または長時間冷凍された原料でも可能であ
り、加えて従来のスリ身と比較して加工中の温度
上昇に伴なう劣化が極めて少ないため取扱いが至
極容易であること、またゲルを作るまでの操作時
間が極めて短くて済むことなどの作業性の良いこ
とも判り、更にこのゲルの呈味性が従来のスリ身
に存在していなかつた良好なものであることなど
の特徴を有する点を見出し畜肉についても確認を
行なつた。 The present inventors have investigated ways to improve fish species with weak gel-forming ability, such as removing odor and other unpleasant substances that occur depending on the fish species, removing color, and strengthening gel-forming ability. By centrifuging the completely dissolved water, we succeeded in creating a gel that is nearly transparent, has no odor of seeds, has no color, and has an extremely strong water-holding ability. It is possible to use raw fish with low freshness such that the meat cannot be made, or raw materials that have been frozen for a long time.In addition, compared to conventional surimi, there is extremely little deterioration due to temperature rise during processing, making it extremely easy to handle. It was found that the gel was easy to work with, and the operation time required to make the gel was extremely short, and the gel had a good taste that did not exist in conventional surimi. They also confirmed that meat has certain characteristics such as:
以下、更に本発明を詳細に説明する。 Hereinafter, the present invention will be explained in further detail.
(1) 生鮮魚から筋肉(肉部)を取り出す。この際
に頭部または内臓、皮を取除いた部分、即ち
肉、骨、油が混ざつていても差支えない。(1) Remove the muscle (meat) from fresh fish. At this time, there is no problem even if the head, internal organs, and parts from which the skin has been removed, ie, meat, bones, and oil, are mixed in.
(2) 次に取り出した肉に対し等量以上の加水を行
なう。加水量は等量、3倍量、5倍量、10倍
量、15倍量、20倍量、30倍量として実験した
が、加水量の多い場合程歩留が良く、等量ない
し3倍量程度では遠心分離した時の蛋白ゼリー
の純度が低く、5〜15倍量が実用的である。(2) Next, add more than the same amount of water to the removed meat. The amount of water added was the same, 3 times, 5 times, 10 times, 15 times, 20 times, and 30 times. In terms of volume, the purity of the protein jelly when centrifuged is low, so 5 to 15 times the volume is practical.
(3) 加水する際に酸素活性防止、冷凍変性防止の
目的でソルビトールなどの糖類を加える。また
カロチノイド系の魚肉の有している色素また
は、血色素、筋肉色素などをPHをアルカリ側に
調整することによつて除去することが出来る。
更に蛋白ゼリーまたはそのゲルの目的によつて
は食塩などの塩の添加によつて常法の場合と異
なつたゲルを得ることが出来る。(3) When adding water, add sugars such as sorbitol to prevent oxygen activation and freeze denaturation. In addition, carotenoid pigments, blood pigments, muscle pigments, etc. contained in fish meat can be removed by adjusting the pH to the alkaline side.
Furthermore, depending on the purpose of the protein jelly or gel, it is possible to obtain a gel different from that obtained by conventional methods by adding salt such as common salt.
(4) 次に微粉砕の程度はホモジナイザーによつて
水溶性蛋白が上記水若しくは液相に分離状態で
懸濁する程度にまで筋原繊維を解ぐすことが重
要であるが、得られる蛋白ゼリーまたはそのゲ
ルの目的によつては完全に解ぐさず適当な程度
で止めることは差支えない。実験的には軟質な
筋肉であればホモジナイザーで5〜10秒間程度
処理することによつても得られるが、畜肉など
の様に硬質な筋肉の場合には数分間ホモジナイ
ズする必要がある。(4) Next, it is important to disentangle the myofibrils using a homogenizer to the extent that the water-soluble proteins are suspended in a separated state in the water or liquid phase. Alternatively, depending on the purpose of the gel, it may not be completely dissolved, but may be stopped at an appropriate level. Experimentally, soft muscles can be obtained by treating them with a homogenizer for about 5 to 10 seconds, but hard muscles such as livestock meat require homogenization for several minutes.
(5) 微粉砕して得られる液相は骨などの未粉砕残
渣、コラーゲン質の繊維などが残つているので
蛋白ゼリーに混入させない様にするために別
を行なう。この場合、目的とする蛋白ゼリーま
たはゲルの状態により過の精度を決定すれば
よい。(5) The liquid phase obtained by pulverization contains unpulverized residues such as bones and collagen fibers, so they are separated to prevent them from being mixed into the protein jelly. In this case, the accuracy may be determined depending on the state of the target protein jelly or gel.
(6) 過された蛋白質が懸濁した溶液に遠心力を
与えて水溶性部分と沈澱とに遠心分離して蛋白
ゼリーを得る。この際に与える遠心効果は1000
〜2000程度でも若干の分離は可能であるが完全
に回収するためには3000以上、1秒間以上であ
ることが必要であるが、1分間以上を行なつて
も効果に差がなく不経済である。実用上は
10000〜12000程度の遠心効果を与えることによ
つて、より一層精度の高い蛋白ゼリーが得られ
る。(6) A centrifugal force is applied to the solution in which the filtered protein is suspended to separate the water-soluble portion and the precipitate, thereby obtaining protein jelly. The centrifugal effect given at this time is 1000
Although some separation is possible with ~2000, in order to completely recover it, it is necessary to use 3000 or more for 1 second or more, but there is no difference in effectiveness and it is uneconomical to do it for more than 1 minute. be. In practical terms
By applying a centrifugal effect of about 10,000 to 12,000, a protein jelly with even higher precision can be obtained.
(7) 遠心分離によつて得られる蛋白ゼリーはミオ
シン系蛋白を主とし透明ないし半透明のゼリー
状で温度耐性が強く、例えば8℃で2昼夜放置
してもゲル形成力の劣化は殆んど無く、極めて
安定した状態であつて、種による僻の無い蛋白
ゼリーである。(7) The protein jelly obtained by centrifugation is mainly composed of myosin proteins, is transparent or translucent jelly-like, and has strong temperature resistance; for example, even if it is left at 8°C for two days and nights, there is almost no deterioration in its gel-forming ability. It is a protein jelly that is in an extremely stable state and is not affected by seeds.
(8) 得られた蛋白ゼリーに食塩を1〜8%(以
下、総べて重量%)添加すると食塩添加量に比
例してゲル強度は強くなり水分含量が95%以上
であつても完全に保水する。この加熱ゲルはス
リ身では見られない保水力と共に透明感のある
滑らかな状態であり、更に著しく呈味性が良
く、調味料を混合しなくても旨味が充分であ
る。(8) When 1 to 8% (total by weight) of salt is added to the obtained protein jelly, the gel strength increases in proportion to the amount of salt added, and the gel strength is completely increased even when the water content is over 95%. Retains water. This heated gel has a water-holding capacity not found in Surimi, and is transparent and smooth. Furthermore, it has an extremely good taste, and has sufficient flavor even without the addition of seasonings.
(9) この蛋白ゼリーに食塩を加え撹拌すると速や
かに透明化し始め粘稠となる。この状態はこの
侭放置しても2日程度では変化が無く、従来の
スリ身に比べて作業性が極めて良く、省力化が
容易である。(9) When salt is added to this protein jelly and stirred, it quickly begins to become transparent and becomes viscous. Even if this condition is left for about two days, there is no change, and workability is extremely good compared to conventional Surimi, making it easy to save labor.
(10) 更にこの蛋白ゼリーに食塩の他の澱粉、植物
蛋白コラーゲン、卵白、粉乳などの添加剤並び
に燐酸塩などの食品改良剤を単一または複数で
加えることによつてカマボコと同様な食感から
プリンまたはゼラチンなどの食感様の軟弱な食
品に至るまで極めて多種類の食品に加えること
が出来る。(10) Furthermore, by adding single or multiple additives such as salt, starch, vegetable protein collagen, egg white, and powdered milk, and food improvers such as phosphates to this protein jelly, a texture similar to that of kamaboko can be obtained. It can be added to a wide variety of foods, from foods with a soft texture like pudding or gelatin.
実施例 1
ミンチで荒く潰ぶした鯖の骨付精肉100gを重
炭酸ソーダでPHを7.0に調整した5%濃度のソル
ビトール溶液で10倍量とし、ホモジナイズを3分
間行ない得られた溶液を5層のガーゼで過し遠
心効果を8000の場合と10000の場合とについて遠
心分離を行なつた結果、各々155g、183gの軟質
な蛋白ゼリーを得た。Example 1 100 g of bone-in mackerel meat roughly crushed with mince was made 10 times its volume with a 5% concentration sorbitol solution whose pH was adjusted to 7.0 with sodium bicarbonate, homogenized for 3 minutes, and the resulting solution was wrapped in a 5-layer gauze. As a result of centrifugation at 8,000 and 10,000, 155 g and 183 g of soft protein jelly were obtained, respectively.
この蛋白ゼリーに食塩3%を添加して撹拌した
所瞬時にして透明化し、粘稠となり、90〜95℃の
熱湯中で10分間加熱した所、カマボコ状の純白の
ゲルを得た。 When 3% salt was added to this protein jelly and stirred, it instantly became transparent and viscous, and when heated in boiling water at 90 to 95°C for 10 minutes, a pure white gel with a hollow shell shape was obtained.
実施例 2
実施例1と同様にして加水量を等量、3倍量、
5倍量、10倍量、15倍量、20倍量、30倍量として
実施した結果、等量の場合には分離性が悪く、3
倍量では原料対比57%、5倍量加水では143%、
10倍量加水では182%、15倍量加水では189%、20
倍量加水では195%、30倍量加水では196%の蛋白
ゼリーが夫々得られた。Example 2 In the same manner as in Example 1, the amount of water added was the same, three times the amount,
As a result of experimenting with 5 times the amount, 10 times the amount, 15 times the amount, 20 times the amount, and 30 times the amount, the separation was poor when the amount was the same, and 3 times the amount.
57% compared to the raw material when added with double the amount of water, 143% when added with 5 times the amount of water,
182% when adding 10 times the amount of water, 189% when adding 15 times the amount of water, 20
A protein jelly of 195% and 196% was obtained by adding double the amount of water and 30 times the amount of water, respectively.
実施例 3
得られた鯖蛋白ゼリー100重量部に対し、食塩
1〜8%を添加混合し15℃にて1時間坐らしめ、
90〜95℃にて10分間加熱して加熱ゲルの強度を対
比した処、7mmφプランジヤーにて添加食塩1%
で500g、2%で600g、3%で675g、4%で725
g、5%で775g、6%で800g、7%で825g、
8%で840g、程度の強度が認められ何れも完全
な保水状態であつた。Example 3 To 100 parts by weight of the obtained mackerel protein jelly, 1 to 8% of common salt was added and mixed, and the mixture was allowed to sit at 15°C for 1 hour.
The strength of the heated gel was compared by heating at 90 to 95℃ for 10 minutes, and the added salt was 1% using a 7mmφ plunger.
500g at 2%, 675g at 3%, 725 at 4%
g, 775g at 5%, 800g at 6%, 825g at 7%,
At 8%, the strength was approximately 840 g, and all were in a perfect water-retaining state.
スリ身と異なり4%程度の加塩においても塩味
は薄く、3%では殆んど塩味を感じない程度であ
つた。また鯖臭は全く無く、MSG、味淋を適当
量添加した時と同じ様な旨さが認められた。 Unlike surimi, the salty taste was weak even when salted at about 4%, and at 3%, the salty taste was barely noticeable. In addition, there was no mackerel odor at all, and the taste was similar to that obtained when appropriate amounts of MSG and ajirin were added.
実施例 4
実施例3と同様にして鰯、ウマズラハギなどに
ついても実施した結果、食塩3%の時に蛋白ゼリ
ーを鰯550g、ウマズラハギ750gと種による差が
認められたが魚臭、旨味は大差が認められなかつ
た。Example 4 The same procedure as in Example 3 was carried out on sardines, Japanese tuna, etc. As a result, when the salt content was 3%, protein jelly was applied to 550 g of sardines and 750 g of Japanese tang, and differences depending on the species were observed, but there were large differences in fishy odor and flavor. I couldn't help it.
実施例 5
実施例4と同様にして鯖、鰯、ウマズラハギを
鮮度を落としたものと冷凍したものとについて実
施した効果、種の差は認められるが、鮮度、冷凍
による差は認められなかつた。Example 5 In the same manner as in Example 4, mackerel, sardine, and Japanese tang were used with reduced freshness and frozen ones. Differences in effects and species were observed, but no differences due to freshness or freezing were observed.
実施例 6
前実施例と同様にして鶏の精肉について行なつ
た結果、食塩3%の時に蛋白ゼリー850gを得た。Example 6 As a result of using chicken meat in the same manner as in the previous example, 850 g of protein jelly was obtained when the salt content was 3%.
実施例 7
得られた鯖蛋白ゼリー100重量部に対し食塩3
重量部、燐酸塩0.25重量部、澱粉5重量部、コラ
ーゲン1重量部を混合し15℃で1時間坐らせた
後、90〜95℃で15分間加熱した結果、7φのプラ
ンジヤーで900gの滑らかで呈味性の良いカマボ
コを得た。Example 7 3 parts of salt per 100 parts by weight of the obtained mackerel protein jelly
Parts by weight, 0.25 parts by weight of phosphate, 5 parts by weight of starch, and 1 part by weight of collagen were mixed and allowed to sit at 15°C for 1 hour, then heated at 90-95°C for 15 minutes. We obtained kamaboko with good taste.
実施例 8
得られた鯖蛋白ゼリー100重量部に対し食塩3
重量部、澱粉3重量部、卵白3重量部、牛乳20重
量部、燐酸塩0.25重量部を混合してケーシング詰
めし15℃で2時間坐らせた後、90〜95℃で20分間
加熱した効果、歯触わりの良い魚肉臭の無いプデ
イングを得た。Example 8 3 parts of salt per 100 parts by weight of the obtained mackerel protein jelly
parts by weight, 3 parts by weight of starch, 3 parts by weight of egg white, 20 parts by weight of milk, and 0.25 parts by weight of phosphate were mixed and packed in a casing, allowed to sit at 15°C for 2 hours, and then heated at 90-95°C for 20 minutes. A pudding with good texture and no fish odor was obtained.
Claims (1)
て微粉砕し、得られた蛋白質懸濁容液に遠心効果
3000以上の遠心力を与えて得られるミオシン系蛋
白質を主成分とする蛋白ゼリーの製法。1 Animal myofibrils are pulverized in an equal or more amount of water or liquid phase, and the resulting protein suspension is subjected to a centrifugal effect.
A method for producing protein jelly whose main component is myosin protein obtained by applying a centrifugal force of 3000 or more.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8509479A JPS5611762A (en) | 1979-07-06 | 1979-07-06 | Production of protein jelly and its use |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8509479A JPS5611762A (en) | 1979-07-06 | 1979-07-06 | Production of protein jelly and its use |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5611762A JPS5611762A (en) | 1981-02-05 |
JPS6349991B2 true JPS6349991B2 (en) | 1988-10-06 |
Family
ID=13849011
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8509479A Granted JPS5611762A (en) | 1979-07-06 | 1979-07-06 | Production of protein jelly and its use |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5611762A (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57186444A (en) * | 1981-05-07 | 1982-11-16 | Amurafu Ltd | Meat protein product and production thereof |
JPS6197435A (en) * | 1984-10-15 | 1986-05-15 | 東レ株式会社 | Latent bulky yarn and its production |
FR2768308B1 (en) * | 1997-09-15 | 1999-12-03 | Pecheries Basques | PROCESS FOR PRODUCING PROTEIN GEL |
CA2616562C (en) * | 2005-07-01 | 2012-03-20 | Mpf, Inc. | Systems and methods for separating proteins from connective tissue |
CN112971112A (en) * | 2021-01-06 | 2021-06-18 | 沈阳农业大学 | Self-assembled multilayer animal-derived protein hydrogel and preparation method and application thereof |
-
1979
- 1979-07-06 JP JP8509479A patent/JPS5611762A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5611762A (en) | 1981-02-05 |
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