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JPS5910787B2 - Sausage manufacturing method - Google Patents
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JPS5910787B2 - Sausage manufacturing method - Google Patents

Sausage manufacturing method

Info

Publication number
JPS5910787B2
JPS5910787B2 JP52086545A JP8654577A JPS5910787B2 JP S5910787 B2 JPS5910787 B2 JP S5910787B2 JP 52086545 A JP52086545 A JP 52086545A JP 8654577 A JP8654577 A JP 8654577A JP S5910787 B2 JPS5910787 B2 JP S5910787B2
Authority
JP
Japan
Prior art keywords
lactic acid
acid bacteria
hours
sausage
add
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
JP52086545A
Other languages
Japanese (ja)
Other versions
JPS5423162A (en
Inventor
保美 浅野
照雄 古畑
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.)
NITSUKEN FUUDO KK
Original Assignee
NITSUKEN FUUDO KK
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 NITSUKEN FUUDO KK filed Critical NITSUKEN FUUDO KK
Priority to JP52086545A priority Critical patent/JPS5910787B2/en
Publication of JPS5423162A publication Critical patent/JPS5423162A/en
Publication of JPS5910787B2 publication Critical patent/JPS5910787B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は、ソーセージの製造方法に係るものである。[Detailed description of the invention] The present invention relates to a method for producing sausage.

従来、ソーセージの製造方法としては、原料肉の結着性
をよくするため、安価で経済的な粉末牛乳カゼインをそ
のまま原料肉に添加することが行なわれて(・る。
Conventionally, the method for producing sausages has been to add cheap and economical powdered milk casein to the raw meat as it is in order to improve the binding properties of the raw meat.

しかしこの場合にあっては、製品としてのソーセージに
残る原料肉に特有の臭気、例えば魚肉を用(・た場合の
魚肉臭などを完全に除《ことができな(・し、また、一
般生菌の増殖を抑制するために亜硝酸ソーダ等の化学薬
品を用(・るから、製品の保存期間にも自ずと限界があ
り、長期の保存は不可能であった。
However, in this case, it is not possible to completely eliminate the odor peculiar to the raw meat that remains in the sausage product, such as the fish odor when using fish meat. Because chemicals such as sodium nitrite are used to suppress the growth of bacteria, there is a natural limit to the product's shelf life, and long-term storage was impossible.

また、牛乳又は脱脂乳に乳酸菌を加えて醗酵させ、カー
ド状になったものから乳清を除去したし・わゆるナチュ
ラルチーズを原料肉に添加する製法もあるが、乳清の前
記分離過程におし・て、乳酸、乳糖、乳酸菌、乳脂肪及
び乳蛋白の一部が同時に除去されてしまうため、製品と
してのソーセージには味の濃密性がなく、(・わゆるコ
クのな(・ものとなる欠点がある。
There is also a manufacturing method in which lactic acid bacteria are added to milk or skim milk and fermented, and the whey is removed from the curd-like product.So-called natural cheese is added to the raw meat, but the whey separation process is During cooking, lactic acid, lactose, lactic acid bacteria, milk fat, and part of the milk protein are removed at the same time, so the sausage product lacks a rich flavor (so-called full-bodied). There is a drawback.

さらに、例えば特公昭50−7142号の製法のように
、脱脂粉乳に乳酸菌を添加して醗酵させた培養物を肉混
合物に少なくとも0.1重量係混合し、これを45.5
〜51.6℃で8〜15時間曝露させpH 4.4〜5
,4程度にすることにより、一般生菌の生育を抑制し保
存性を高める製法も提供されて℃・る。
Furthermore, for example, as in the method disclosed in Japanese Patent Publication No. 50-7142, a culture obtained by adding lactic acid bacteria to skim milk powder and fermenting it is mixed with the meat mixture by at least 0.1% by weight, and this is added to 45.5%
Exposure for 8-15 hours at ~51.6°C and pH 4.4-5
A manufacturing method is also provided that suppresses the growth of general viable bacteria and improves storage stability by increasing the temperature to about 4°C.

しかしこの製法では、肉混合物に加えられる乳酸菌培養
物はその重量に対して少なくとも0.1%程度であるか
ら、前記条件下の曝露中に一般生菌は乳酸菌の生育な上
廻って生育増殖してしまうのであり、このため、それ程
保存性を高められなかった。
However, in this production method, the lactic acid bacteria culture added to the meat mixture accounts for at least 0.1% of its weight, so during exposure under the above conditions, general viable bacteria grow and proliferate by outpacing the growth of lactic acid bacteria. For this reason, it was not possible to improve the shelf life that much.

本発明は従来の製法における上記の諸点を解決するもの
であり、ここに原料肉とは、牛肉、馬肉、豚肉、羊肉な
どの獣肉類、鳥肉、魚肉などの1種か又は数種を適当に
混合して細切りしたもので、以下、本製法を詳細に説明
する。
The present invention solves the above-mentioned problems in the conventional production method, and the raw meat here refers to one or more of animal meat such as beef, horse meat, pork, and mutton, poultry, and fish. This manufacturing method will be explained in detail below.

本製法にお(・ては、まづ、原料肉に添加する凝固乳蛋
白をあらかじめ作り出す。
In this manufacturing method, the coagulated milk protein to be added to the raw meat is prepared in advance.

すなわち、粉末牛乳カゼインに水を加えて浸漬しよく攪
拌して牛乳還元した後、無菌沢布を用℃・て水分量10
〜50チ程度に脱水し、これに乳糖又は脱脂粉乳3係を
加えて約63℃でほぼ30分間加熱し殺菌する。
That is, after adding water to powdered milk casein and soaking it and stirring well to reduce the milk, use a sterile cotton cloth to reduce the moisture content to 10°C.
Dehydrate to about 50 g, add 3 parts of lactose or skim milk powder, and heat at about 63° C. for about 30 minutes to sterilize.

次(・で35℃附近に冷却して純粋培養された乳酸菌ス
ターター3%を加え、18〜20時間醗酵させて乳酸度
0.6〜0.7係の凝固乳蛋白を作る。
Next, cool to around 35°C, add 3% pure cultured lactic acid bacteria starter, and ferment for 18 to 20 hours to produce coagulated milk protein with lactic acidity of 0.6 to 0.7.

次に、通常の製法で用(・られるよく細切りした原料肉
に対して前記の凝固乳蛋白を約10係加え、チョツパー
にかげてさらに細切りし均一に混和する。
Next, about 10 parts of the above-mentioned coagulated milk protein is added to the well-sliced raw meat used in the usual manufacturing method, and the mixture is further shredded using a chopper and mixed uniformly.

これは、乳酸菌が活性状態を保ってその発育増殖を可能
にする適応環境を与えるためであるから、できるだけ均
一に混和させる。
This is to provide an adapted environment for the lactic acid bacteria to maintain their active state and allow them to grow and multiply, so mix as uniformly as possible.

さらに、香辛料、調味料、硝酸ソーダその他の添加物を
加えた後、再び脱脂粉乳3チと純粋培養された乳酸菌ス
ターター2係とを添加し、サイレントカッター等の機械
的手段によってよく攪拌混合してエマルジョン化させる
Furthermore, after adding spices, seasonings, sodium nitrate, and other additives, 3 parts of skim milk powder and 2 parts of pure cultured lactic acid bacteria starter were added again, and the mixture was thoroughly stirred and mixed using a mechanical means such as a silent cutter. Make it into an emulsion.

この場合の温度は乳酸菌の生育至適温度である35℃前
後に氷を用(・て調節する。
In this case, the temperature is adjusted using ice to around 35°C, which is the optimum temperature for the growth of lactic acid bacteria.

このように脱脂粉乳と乳酸菌とを、追加してエマルジョ
ン化させたソーセージ原料は、乳酸菌の発育増殖に至適
の環境となる。
The sausage raw material obtained by adding and emulsifying skim milk powder and lactic acid bacteria in this way provides an optimal environment for the growth and proliferation of lactic acid bacteria.

このソーセージ原料は、次に通常法と同じく充填スタッ
ファ−に入れてケーシングに充填し、結縛後乾燥し燻煙
する。
This sausage material is then placed in a filling stuffer and filled into a casing in the same manner as in the conventional method, tied, dried and smoked.

乾燥及び燻煙は、通常法では一般的に60〜75℃で2
〜3時間行なわれて℃・るが、本製法では35℃前後で
20〜24時間行なう。
Drying and smoking are generally carried out at 60-75°C for 2
The process is carried out at 35°C for 20 to 24 hours at around 35°C.

このように乳酸菌の生育至適温度で前記時間をかけるこ
とにより、ほぼpH4.0〜4.8の目的酸度がソーセ
ージに得られ、また、通常法より低温であるが時間を長
くするため、ソーセージに必要な乾燥●燻煙効果が充分
に得られるのである。
By taking the above-mentioned time at the optimum growth temperature for lactic acid bacteria, the desired acidity of approximately pH 4.0 to 4.8 can be obtained in the sausage. The necessary drying and smoking effects can be obtained.

この工程を経たソーセージは、通常法のごとく、中心部
の温度が63℃以上となるように湯煮又は蒸煮して製品
とする。
The sausages that have gone through this process are boiled or steamed in the usual manner so that the temperature at the center reaches 63°C or higher to produce a product.

上記のごとく、本製法にお(・て原料肉に加える凝固乳
蛋白は、粉末牛乳カゼインを乳酸醗酵させたものである
から、牛乳又は脱脂乳を乳酸醗酵させて脱水したナチュ
ラルチーズを添加する従来の製法のように乳清を分離す
る必要がなし・。
As mentioned above, the coagulated milk protein added to the raw meat in this manufacturing method is obtained by lactic acid fermentation of powdered milk casein. There is no need to separate the whey as in the manufacturing method.

このため、乳酸菌、乳酸、乳糖、乳脂肪及び乳蛋白など
は少しも凝固乳蛋白中から失なわれな(・ので、味が濃
密でコクのあるンーセージを安価に製造できる効果があ
る。
For this reason, lactic acid bacteria, lactic acid, lactose, milk fat, and milk protein are not lost in the coagulated milk protein (-), so it is effective to produce rich and rich flavor at a low cost.

また、凝固乳蛋白における香気成分のフレーバ画分とし
ては、ジアセチル、アセトアルデヒド、メチルチトン、
脂肪酸のメチル、エチルエステル、アルコール等を含む
多種多様のものがあるが、本製法ではこの凝固乳蛋白を
原料肉に加え、前記の乾燥、燻煙時間を与えて乳酸醗酵
させるので、例えば馬肉等の青く生臭い臭気に関係する
アセトアルデヒド、あるいは魚肉特有の臭気に関係する
トリメチルアミン類が、好ましい酪臭に関するジアセチ
ルその他の上記フレーバによって相乗的に中和融合され
、香ばしい酪酸香臭のソーセージを製し得るのである。
In addition, the flavor fractions of aroma components in coagulated milk protein include diacetyl, acetaldehyde, methyltiton,
There are a wide variety of products containing fatty acid methyl, ethyl ester, alcohol, etc., but in this production method, this coagulated milk protein is added to the raw meat, and the drying and smoking time described above is given for lactic acid fermentation. Acetaldehyde, which is associated with the blue, fishy odor of fish meat, or trimethylamines, which are associated with the odor characteristic of fish meat, are synergistically neutralized and fused with diacetyl and other flavors associated with the desirable dairy odor, making it possible to produce sausages with a fragrant butyric acid aroma. be.

さらに、前記の凝固乳蛋白には1 mlあたり1.4×
109の乳酸菌が認められ、これを原料肉に対して約1
0受加えるのであるから、一般生菌に対してほぼ対抗的
な数の乳酸菌が発育増殖の可能な環境におかれている。
Furthermore, the above-mentioned coagulated milk protein contains 1.4x per ml.
109 lactic acid bacteria were observed, which was approximately 1% per raw meat.
Therefore, lactic acid bacteria are placed in an environment where they can grow and multiply in numbers that are almost competitive with general viable bacteria.

さらに、本製法ではこれに対して再び脱脂粉乳と乳酸菌
とを追加してソーセージ原料をエマルジョン化させるの
で、一般生菌に対する乳酸菌の対数が多くなり、2種以
上の異なった微生物間の生息バランスを崩l7、一般生
菌の発育増殖をある程度までそれ自体によって抑制させ
ることが可能となって(・る。
Furthermore, in this manufacturing method, skim milk powder and lactic acid bacteria are added again to emulsify the sausage raw material, so the logarithm of lactic acid bacteria compared to general viable bacteria is increased, and the balance between two or more different microorganisms is improved. It has become possible to suppress the growth and proliferation of common viable bacteria to a certain extent by itself.

そして、このようにしたソーセージ原料を35℃前後で
20〜24時間乾燥し燻煙する工程中に乳酸醗酵を促進
させるから、一般生菌に対する乳酸菌の数は圧倒的に多
数となり、一般生菌の増殖を充分に抑制できる目的酸度
pH4.0〜4.8が得られ、保存性のきわめて高し・
ソーセージが製造されるのである。
Since lactic acid fermentation is promoted during the process of drying and smoking sausage ingredients at around 35°C for 20 to 24 hours, the number of lactic acid bacteria is overwhelmingly larger than that of general viable bacteria. Achieves the target acidity pH 4.0 to 4.8 that can sufficiently inhibit proliferation, and has an extremely high shelf life.
Sausage is produced.

比較実験表のグラフは、前記の工程中における乳酸菌及
び一般生菌の増殖数を本製法と従来法(特公昭50−7
142号の製法)とにリし・て、比較試験した結果を示
す。
The graph in the comparative experiment table shows the growth numbers of lactic acid bacteria and general viable bacteria during the above process between this production method and the conventional method (Special Publication Publication No. 50-7).
The results of a comparative test are shown below.

すなわち、本製法ではソーセージ原料を前記のようにす
る結果、乾燥・燻煙の開始後約6時間で乳酸菌の急速な
増殖がみられ、一般生菌はわずかに増殖するのみで、約
24時間後にpH4.0となる。
In other words, in this production method, as a result of using the sausage raw material as described above, rapid growth of lactic acid bacteria was observed approximately 6 hours after the start of drying and smoking, and only a slight growth of general viable bacteria was observed after approximately 24 hours. The pH becomes 4.0.

他方、従来法では0.1重量係の乳酸菌培養物を添加し
た場合、一般生菌は乳酸菌の増殖を上廻って発育増殖し
てしまうのであり、15時間後にpH5.4程度になっ
たとしても一般生菌の数は乳酸菌より多(・のであって
、保存性が本製法よりも劣ることは明らかである。
On the other hand, in the conventional method, when 0.1 weight of lactic acid bacteria culture is added, general viable bacteria grow and proliferate faster than lactic acid bacteria, even if the pH reaches about 5.4 after 15 hours. The number of general viable bacteria is greater than that of lactic acid bacteria, and it is clear that the storage stability is inferior to that of this production method.

なお、この比較実験は、本製法にお(・ては後述する実
施例1,2により、また、従来法は特公昭50−714
2号公報に記載された実施例により行なった。
This comparative experiment was carried out using the present manufacturing method (as described in Examples 1 and 2 below), and the conventional method as described in Japanese Patent Publication No. 50-714.
This was carried out according to the example described in Publication No. 2.

さらに、従来法の菌種は、ペテイオコツカスセレビシー
をあらかじめ培養濃縮したもので、1 1’fllあた
り約109の細胞数を有し、東京大学応用微生物研究所
有用菌保存施設受付の凍結乾燥菌ケ復元し、本製法のス
トレプトコツカス・ラクテイス菌及びストレプトコツカ
ス・クレモリス菌は、財団法人日本乳業技術協会受付の
純粋培養した1 mlあたり約109対数の乳酸菌を用
℃゛た。
Furthermore, the bacterial species used in the conventional method is P. cerevisiae that has been cultured and concentrated in advance, and has a cell count of approximately 109 per 11'fll. The dried bacteria were reconstituted, and the Streptococcus lacteis and Streptococcus cremoris bacteria used in this production method were obtained using approximately 109 logarithm of lactic acid bacteria per ml of pure culture received from the Japan Dairy Technology Association.

また、乳酸菌数の測定は、滅菌ペトリ氏皿に試料1CE
を採り、あらかじめ加温溶融したプレカウント寒天培地
15Crを44℃に保って加え、回転混合、冷却凝固し
、35〜37℃の温度で約72時間培養し、発生集落中
の黄変してし・るところを乳酸菌集落として稀釈倍率に
より行なった。
To measure the number of lactic acid bacteria, place 1 CE sample in a sterile Petri dish.
A pre-count agar medium 15Cr that had been heated and melted in advance was added at 44°C, mixed by rotation, cooled and solidified, and cultured at a temperature of 35 to 37°C for about 72 hours to remove yellowing in the infected colonies.・Lactic acid bacteria colonies were harvested and dilution ratios were determined.

一般生菌数の測定は、滅菌ペトリ氏皿に試料1 cr:
を採り、滅菌普通寒天培地を43〜45℃で溶融させて
15cr:加え、回転、冷却凝固し、35〜37℃で4
8時間培養し、発生した集落を測定したものである。
To measure the general number of viable bacteria, place 1 sample in a sterile Petri dish:
Melt a sterilized ordinary agar medium at 43-45°C, add 15 cr:, rotate, cool and solidify, and melt at 35-37°C for 15 cr.
The cells were cultured for 8 hours and the colonies that formed were measured.

なお、本発明にお(・ても硝酸ソーダを添加するが、一
般生菌の生化学的硝酸還元現象(NO3−NO2 )に
より自ら発育を抑制させるものであって、本製法の乳酸
菌スターターには硝酸還元酵素を有しないものを用(・
るから、その発育が抑制されることはな℃゛。
In addition, although sodium nitrate is added to the present invention, it suppresses its own growth due to the biochemical nitrate reduction phenomenon (NO3-NO2) of general living bacteria, and the lactic acid bacteria starter of this production method does not contain sodium nitrate. Use one that does not have nitrate reductase (・
Therefore, its growth is not inhibited.

次に、本発明の製法の実施例を示す。Next, examples of the manufacturing method of the present invention will be shown.

実施例 1 (凝固乳蛋白) 粉末牛乳カゼイン1 1(qに水9k7を加え、1時間
浸漬した後よく攪拌し、無菌r布を用(・て水分量ほぼ
50%程度に脱水した。
Example 1 (Coagulated milk protein) Powdered milk casein 1 1 (9 k7) of water was added to 1 q, soaked for 1 hour, stirred well, and dehydrated to approximately 50% water content using a sterile cloth.

次に乳糖,(脱脂粉乳でもよ’−)3%を加えて63℃
で30分間加熱殺菌し、35℃に冷却した後、純粋培養
されたラクテイス( ,S tr.Lactis )菌
を2.5係、クレモリス( Str .Cremori
s )菌をQ.5%、計3係加え、35℃で18〜20
時間醗酵させ、乳酸度0.6〜0.7’%、水分量約5
0係の凝固乳蛋白5.0kqを得た。
Next, add 3% lactose (you can also use skim milk powder) and heat to 63°C.
After heat sterilizing for 30 minutes at 35°C and cooling to 35°C, 2.5 parts of pure cultured Str.
s) Bacteria Q. 5%, total of 3 parts added, 18-20 at 35℃
Fermented for hours, lactic acidity 0.6-0.7'%, water content approximately 5
5.0 kq of coagulated milk protein of ratio 0 was obtained.

実施例 2 (エマルジョンタイプソーセージ) 豚肉トリミング(赤肉80%) 15府牛肉トリ
ミング(赤肉)7k9 バックファット(豚脂肪)5k7 凝固乳蛋白 3 kq塩
720グ砂糖
1001ガリツク粉
21ホワイトペッパー
100グコリアンダ
20ググルタミン酸ナトリウム 1
001硝酸ナトリウム 3グ乳
酸菌スターター x,ooomg脱脂粉
乳 1k7氷
6&7上記の配合割合
で本文に詳記した通りの工程を行なうが、追添加する乳
酸菌スターターは凝固乳蛋白と同じ菌種のものを用(・
、サイレントカッターによる攪拌混合はエマルジョン化
するまで約15分間行なし・、氷は温度の調節に用(・
た。
Example 2 (emulsion type sausage) Pork trimmings (80% red meat) 15 prefecture beef trimmings (red meat) 7k9 Back fat (pork fat) 5k7 Coagulated milk protein 3 kq salt
720g sugar
1001 Garitsuku powder
21 white pepper
100 grams of coriander
20 Sodium Gglutamate 1
001 Sodium nitrate 3g Lactic acid bacteria starter x,oomg Skim milk powder 1k7 ice
6 & 7 Carry out the process as detailed in the text with the above mixing ratio, but use the same type of lactic acid bacteria starter as the coagulated milk protein (・
・Do not stir or mix with a silent cutter for about 15 minutes until it becomes an emulsion. ・Ice is used to adjust the temperature (・
Ta.

なお、ケーシングに充填後、室温中に約2時間吊し置き
、燻煙室に入れて33℃で14時間放置し、その後10
時間の燻煙を行な(・、常法によって湯煮して製品を得
たが、そのpHの平均値は4.6であった。
After filling the casing, leave it hanging at room temperature for about 2 hours, put it in a smoking room and leave it at 33℃ for 14 hours, and then leave it for about 10 hours.
A product was obtained by boiling in boiling water by the usual method, and the average pH value was 4.6.

実施例3 (ドライ・セミドライタイプソーセージ)豚肉トリミン
グ(赤肉80チ)9k7 牛肉トリミング(赤肉) 1 5 @
凝固乳蛋白 3kg塩
6501砂糖
9CI’ガリツク粉
2L?ブラックペッパー
1007グルタミン酸ナトリウム
1002硝酸ナトリウム
3L?乳酸菌スターター 1.00
0772g脱脂粉乳 I
J(q氷
2ktj上記の配合割合で前記実施例2と同じように
して製造する。
Example 3 (Dry/semi-dry type sausage) Pork trimmings (80 inches of red meat) 9k7 Beef trimmings (red meat) 1 5 @
Coagulated milk protein 3kg salt
6501 sugar
9CI'garic powder
2L? black pepper
1007 Monosodium glutamate
1002 Sodium nitrate
3L? Lactic acid bacteria starter 1.00
0772g skimmed milk powder I
J (q ice
2ktj Produced in the same manner as in Example 2 at the above blending ratio.

なお、ドライソーセージの場合は常法による最後の湯煮
又は蒸煮を省略し、20℃で相対湿度が60%の室中に
3日間放置し、さらに12℃、相対湿度60チの乾燥室
に30日間収蔵して水分量が35q/)以下、pH4.
0〜4.2の範囲内の製品が得られた。
In addition, in the case of dry sausages, the final boiling or steaming in the conventional method is omitted, and the sausages are left in a room at 20°C and a relative humidity of 60% for 3 days, and then placed in a drying room at 12°C and a relative humidity of 60% for 30 days. After storage for several days, the moisture content should be 35q/) or less, and the pH should be 4.
Products within the range of 0 to 4.2 were obtained.

また、セミドライソーセージの場合は、常法によって湯
煮したのち、12℃の乾燥室に入れて15日間乾燥し、
水分量がほぼ55チ以下でpH4.3〜4.6の範囲内
の製品が得られた。
In addition, in the case of semi-dry sausages, after boiling them in hot water using the usual method, they are placed in a drying room at 12°C and dried for 15 days.
A product with a water content of approximately 55 inches or less and a pH within the range of 4.3 to 4.6 was obtained.

Claims (1)

【特許請求の範囲】[Claims] 1 粉末牛乳カゼインに水を加えて牛乳還元し、その脱
水後、乳糖又は脱脂粉乳を加えて殺菌し乳酸菌スタータ
ー3係を接種して35℃附近で18〜20時間醗酵させ
て凝固乳蛋白を作り、これを原料肉に約10係加えて均
一に混合し、再び脱脂粉乳と乳酸菌2%とを添加し攪拌
混合してソーセージ原料をエマルジョン化させ、これを
ケーシングに充填結縛した後35℃前後で20〜24時
間乾燥及び燻煙し、以下常法によって湯煮又は蒸煮する
ことを特徴とするソーセージの製造方法。
1 Add water to powdered milk casein to reconstitute milk, and after dehydration, add lactose or skim milk powder to sterilize it, inoculate it with lactic acid bacteria starter 3, and ferment it at around 35℃ for 18 to 20 hours to make coagulated milk protein. Add about 10 parts of this to the raw meat and mix uniformly, add skim milk powder and 2% lactic acid bacteria again, stir and mix to emulsify the sausage raw material, fill it into a casing and tie it up, then heat to around 35°C. A method for producing sausage, which comprises drying and smoking for 20 to 24 hours, followed by boiling or steaming in a conventional manner.
JP52086545A 1977-07-19 1977-07-19 Sausage manufacturing method Expired JPS5910787B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP52086545A JPS5910787B2 (en) 1977-07-19 1977-07-19 Sausage manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP52086545A JPS5910787B2 (en) 1977-07-19 1977-07-19 Sausage manufacturing method

Publications (2)

Publication Number Publication Date
JPS5423162A JPS5423162A (en) 1979-02-21
JPS5910787B2 true JPS5910787B2 (en) 1984-03-12

Family

ID=13889969

Family Applications (1)

Application Number Title Priority Date Filing Date
JP52086545A Expired JPS5910787B2 (en) 1977-07-19 1977-07-19 Sausage manufacturing method

Country Status (1)

Country Link
JP (1) JPS5910787B2 (en)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5139708B2 (en) * 1972-08-11 1976-10-29
JPS5127500B2 (en) * 1973-05-24 1976-08-13

Also Published As

Publication number Publication date
JPS5423162A (en) 1979-02-21

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