JPS6291163A - Production of ham - Google Patents

Production of ham

Info

Publication number
JPS6291163A
JPS6291163A JP60230761A JP23076185A JPS6291163A JP S6291163 A JPS6291163 A JP S6291163A JP 60230761 A JP60230761 A JP 60230761A JP 23076185 A JP23076185 A JP 23076185A JP S6291163 A JPS6291163 A JP S6291163A
Authority
JP
Japan
Prior art keywords
meat
ham
starter culture
salting
raw
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.)
Pending
Application number
JP60230761A
Other languages
Japanese (ja)
Inventor
Masao Yokoyama
横山 理雄
Hiroharu Satomi
里見 弘治
Akio Sasaki
佐々木 明男
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.)
Kureha Corp
Original Assignee
Kureha Corp
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 Kureha Corp filed Critical Kureha Corp
Priority to JP60230761A priority Critical patent/JPS6291163A/en
Publication of JPS6291163A publication Critical patent/JPS6291163A/en
Pending legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A40/00Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
    • Y02A40/90Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in food processing or handling, e.g. food conservation

Landscapes

  • Meat, Egg Or Seafood Products (AREA)

Abstract

PURPOSE:To obtain high-quality ham having improved flavor in a short time, by adding a starter culture to raw material meat, preserving the meat with salt and aging. CONSTITUTION:Raw material meat is inoculated with one or more starter cultures such as Pediococcus cervisiae, Micrococcus varians, etc., preserved with salt at 15-50 deg.C, preferably 20-45 deg.C and aged.

Description

【発明の詳細な説明】 [技術分野] 本発明は原料肉にスターターカルチャーを添加し、高温
で塩漬、熟成することにより短時間で風味の良いハムを
!!iJ造する方法に関する。
[Detailed Description of the Invention] [Technical Field] The present invention adds a starter culture to raw meat, salts it at high temperatures, and ages it to produce ham with good flavor in a short time! ! This article relates to a method for creating an iJ.

[従来技術] 従来技術によるハムのHA造においてはスターターカル
チャーを使用することはなく、塩漬の温度もほぼ10℃
以下の低温で行なわれるのが一般的である。最近の製造
においては、特に塩漬時間が短くなっており、そのため
に風味の発現に有効に作用するといわれる有用微生物が
増殖して作用する機会が失われ、ハムの風味が低下して
いる。
[Prior art] In the HA production of ham using the conventional technology, a starter culture is not used, and the salting temperature is approximately 10°C.
It is generally carried out at a low temperature of: In recent production, the salting time has become particularly short, which means that useful microorganisms that are said to have an effective effect on flavor development have no chance to grow and act, resulting in a deterioration in the flavor of ham.

[発明の目的] 従って本発明の目的は、短時間の塩漬にもかかわらず、
風味の良い高品質のハムを製造する方法を提供すること
にある。
[Object of the invention] Therefore, the object of the present invention is to
Our goal is to provide a method for producing high-quality ham with good flavor.

[発明の構成] 本発明に係るハムの製造法においては、原料肉にスター
ターカルチャーを添加し、塩漬を15℃以上50’C以
下の高温で行なうことを特徴とする。
[Structure of the Invention] The method for producing ham according to the present invention is characterized in that a starter culture is added to the raw meat, and salting is carried out at a high temperature of 15° C. or higher and 50° C. or lower.

[本発明の好ましい態様] 本発明にLr3Gノるハムとは、豚肉を原料とする0−
スハム、ボンレスハム、プレスハムの他、豚肉。
[Preferred embodiment of the present invention] In the present invention, Lr3G ham refers to 0-
Suham, boneless ham, pressed ham, and pork.

マトン肉、馬肉等を混合したプレスハムも含むものであ
る。
It also includes pressed ham made by mixing mutton meat, horse meat, etc.

これらの名称の追いは使用づる原料肉の部位の違い、あ
るいは若干の製法の違いに依るものであるが、基本的に
は大差はない。ロースハムは原料に主としてロース肉を
使用し、ボンレスハムはもも肉を使用する。プレスハム
においては色々な部分のカッ1〜肉を集めて使用する。
These names depend on the different parts of the raw meat used or slight differences in the manufacturing method, but basically there is no big difference. Roast ham mainly uses loin meat as the raw material, while boneless ham uses thigh meat. For pressed ham, various parts of the meat are collected and used.

ロースハム、ボンレスハムではスモークされることが多
く、プレスハムではスモークしないことが多い。しかし
ながら、もも肉を原料とするスモークしないクックドハ
ムやスモークするプレスハムの例もあり、これら原料肉
の部位の差やスモークの有無などは特に本発明において
意味を持つものではない。
Roast ham and boneless ham are often smoked, while pressed ham is often not smoked. However, there are also examples of unsmoked cooked hams and smoked pressed hams made from thigh meat, and differences in the parts of these raw meats and whether or not they are smoked have no particular meaning in the present invention.

次に本発明において原料肉に添加、使用するスターター
カルチャーであるが、欧米の醗酵ソーセージの製造にお
いて使用されている多くの菌株が使用可能で、特定の菌
株に限定するものではない。
Next, regarding the starter culture added to and used in the raw meat in the present invention, many strains used in the production of fermented sausages in Europe and America can be used, and the starter culture is not limited to a specific strain.

それらの菌株のいくつかを挙げると、ペディオコッカス
・セルビシエ(Pediococcus cervis
iae)。
To name a few of those strains, Pediococcus cervisiae (Pediococcus cervisiae)
iae).

ペディオコッカス・ベントサセウス(PediOcoc
cuspentosaceus)、  yクトバチルス
・ブランタルム(Lactobacillu、s p(
antarum)、ラクトバチルス・プレビス(Lac
tobacillus brevis) 、ミクロコツ
カス・パリアンス(Hicrococcus vari
ans)、スタフィロコッカス・カルノサス(5tap
hylococcus carnosus)等がある。
Pediococcus bentosaceus (PediOcoc)
cuspentosaceus), Lactobacillus blanthalum (Lactobacillus sp.
antarum), Lactobacillus plebis (Lac
tobacillus brevis), Micrococcus pariance (Hicrococcus vari)
ans), Staphylococcus carnosus (5tap
hylococcus carnosus).

これらはそれぞれ甲種で使用することも可能であるが、
それぞれの菌株の特徴を生かし、2 fi以上を組合わ
せて使用するのもよい。例えばペディオコッカス・セル
ビシエ(Pediococcus cervisiae
)は強力な乳酸産生能を有するのに対し、ミクロコツカ
ス−パリアンス(Hicrococcus varia
ns)は乳酸産生能には乏しいがフレーバーとハムの色
を良くする働きがある。両者を併用することにより、適
度な酸味があり、香りと色のよいハムを製造することが
可能である。
Each of these can be used in class A, but
It is also good to take advantage of the characteristics of each strain and use a combination of 2 fi or more. For example, Pediococcus cervisiae
) has a strong lactic acid production ability, whereas Micrococcus variance (Hicrococcus varia
ns) has a poor ability to produce lactic acid, but has the function of improving the flavor and color of ham. By using both in combination, it is possible to produce ham with moderate sourness, good aroma and color.

本発明における原料肉の塩漬、熟成温度はI!r′C以
上50℃以下、好ましくは20℃〜45℃である。一般
にスターターカルチャーとして使用される細菌の発育至
適温度が30〜40℃の場合には、塩漬、熟成温度も3
0〜40℃とした方が細菌の発育面からは好ましい。細
菌の発育至適温度をはずれた温度での塩漬では、塩漬時
間を長く設定する必要がある。
The salting and aging temperature of raw meat in the present invention is I! r'C or more and 50°C or less, preferably 20°C to 45°C. Generally, if the optimum temperature for growth of bacteria used as a starter culture is 30 to 40℃, the salting and aging temperature should also be 30℃.
A temperature of 0 to 40°C is preferable from the viewpoint of bacterial growth. When salting at a temperature outside the optimum temperature for bacterial growth, it is necessary to set the salting time longer.

従来、塩漬が10℃以下の低温で行なわれていたのは、
高温においては原料肉等に付着している腐敗原因菌など
の有害細菌が繁殖し、塩漬中に肉を腐敗させてしまうか
らである。スターターカルチャーを添加することによっ
て高温での塩漬けが可能となるのは、原料肉1gに対し
て菌数105〜107位の割合で添加されたスターター
菌が、原料肉等に付着している有害細菌よりも優勢とな
り、有害菌の発育増殖を押えることによる。鮮度が悪か
ったり、保管などが悪くて、有害m菌に高度に汚染され
ている原料肉を使用した場合は、有害細菌の方が優勢と
なり、スターターカルチャーを添加しても塩漬中に腐敗
する場合もあるから、原料肉は新鮮なものを使うのが望
ましい。また高温での塩漬、熟成は当然のことながら原
料肉の筋肉の弛緩に伴う塩漬側成分の内部への浸透を速
め、肉と塩漬側成分の相互の反応を促進する。微生物の
作用と共にこのような化学的、物理的な作用もまた塩漬
時間の短縮に有効に作用する。
Conventionally, salting was carried out at a low temperature of 10℃ or less because
This is because at high temperatures, harmful bacteria such as putrefaction-causing bacteria attached to raw meat etc. will multiply, causing the meat to rot during salting. Salting at high temperatures is possible by adding a starter culture, because the starter bacteria added at a ratio of 105 to 107 bacteria per gram of raw meat can eliminate harmful bacteria attached to raw meat, etc. This is because it becomes more dominant and suppresses the growth and proliferation of harmful bacteria. If you use raw meat that is highly contaminated with harmful bacteria due to poor freshness or poor storage, the harmful bacteria will become dominant and the meat will spoil during salting even if a starter culture is added. Therefore, it is preferable to use fresh meat as raw material. In addition, salting and aging at high temperatures naturally speed up the penetration of the salted components into the interior of the meat due to the relaxation of the muscles of the raw meat, and promote the mutual reaction between the meat and the salted components. In addition to the action of microorganisms, such chemical and physical actions also work effectively to shorten the salting time.

[実施例1 以下、水元r9Jを実施例について更に説明する。[Example 1 Hereinafter, Mizumoto r9J will be further explained with reference to Examples.

実施例1 0−スハムの本発明による製造法を記ず。Example 1 The method for producing 0-suham according to the present invention is not described.

豚のロース肉を常法に従って整形する。整形肉に対して
ピックル液を肉量に対し20%インジェクションした。
Shape the pork loin according to the usual method. Pickling liquid was injected into the shaped meat in an amount of 20% based on the amount of meat.

ピックル液の配合は次の通りである(各成分手m部、以
下間)。食Jn12.砂糖6.すん酸Jp1.8.亜硝
酸す1−リウム012.アス]ルピン酸ナトリウム0.
30.グルタミン酸ソーダ1,2゜ソルビン酸カリ09
.ブドウ糖3,0.水746及びスターターカルチャー
。なおスターターカルチャーはラクトバチルス・プラン
タルム(1゜actobacillus planta
rum)とミクロコツカス・バリ7ンス(Hicroc
occus varianslを1:1で混合したもの
を用いた。スターターカルチャーの最は肉1グラムに対
し菌数106になるように添加した。インジェクション
した肉はテンダライ畳アーで処理した。
The composition of the pickle liquid is as follows (each component is part m). Food Jn12. Sugar6. Phosphoric acid JP1.8. 1-lium nitrite 012. As] Sodium lupine 0.
30. Sodium glutamate 1,2° Potassium sorbate 09
.. Glucose 3.0. Water 746 and starter culture. The starter culture is Lactobacillus plantarum (1゜actobacillus planta).
rum) and Micrococcus vari7ns (Hicroc
A 1:1 mixture of Occus variansl was used. The starter culture was added so that the number of bacteria was 106 per gram of meat. The injected meat was processed using a tenderizer.

テンダライザー処理後の肉=Iiffiを秤ωし、元の
肉の宙吊の120%になるまで前記ピックル液を追加し
た(インジェクション後に失われたピックル液を補充、
調節する)。これら全部をタンブラ−に投入し、脱気後
雰囲気温度を35℃に調堅して、タンブラ−を毎分10
回転の速さで回転させながら3時間運転した。この操作
で添加したピックル液は完全に肉に吸収された。
Meat after tenderizer processing = Iiffi was weighed, and the pickling liquid was added until it became 120% of the original meat suspension (replenishing the pickling liquid lost after injection,
). Pour all of these into a tumbler, and after degassing, adjust the atmospheric temperature to 35°C, and turn the tumbler at 10°C per minute.
The machine was operated for 3 hours while rotating at the same speed. The pickling liquid added in this operation was completely absorbed into the meat.

タンプリング処理を終った肉を取り出し、ポリ容器に移
しで35℃の雰囲気中に20時間静静置た(この場合、
ポリ容器に移りことなくタンブラ−内で静置してもよく
、また直ちにファイブラスケーシング等に充填し、それ
を同様に放屁Jる方法をとることも可能である)。
After the tampling process, the meat was taken out, transferred to a plastic container, and left to stand still in an atmosphere of 35°C for 20 hours (in this case,
It may be allowed to stand still in a tumbler without transferring to a plastic container, or it may be immediately filled into a fibrous casing, etc., and then emptied in the same manner).

ポリ容器内に静首後、肉をファイブラスケーシングに充
填し、50℃、50%RHで50分の乾燥、65”C、
80〜85% RHr約1時間ノ燻煙、80℃F 2 
[I’1間の蒸煮を行ない1次いで冷却して製品とした
After cooling in a plastic container, the meat was packed into a fibrous casing, dried at 50°C and 50% RH for 50 minutes, and dried at 65"C.
80-85% RHr approximately 1 hour smoke, 80℃F2
[I'1] The product was steamed and then cooled to obtain a product.

実施例2 プレスハムについての実施例を記ず。Example 2 Examples regarding pressed ham are not described.

5 cm角前後の豚肉とマトン肉を原料とした。豚肉と
マトン肉の割合は30ニア0とした。この肉100部に
対し、次の配合からなるピックル液30部を加えた。
The raw materials are pork and mutton meat around 5 cm square. The ratio of pork and mutton meat was set at 30n0. To 100 parts of this meat, 30 parts of pickling liquid having the following composition was added.

(ピックル液配合) 水                    100大
豆蛋白         43 植物油          20 食  塩                 8.6り
ん酸塩         1.7 グルタミン酸ソーダ    08 コーンシロップ      2.0 アス〕ルピン酸ソーダ   034 亜硝酸ナトリウム     0.(1gさらにスタータ
ーカルチャーとしてペアイオコッカス・ベントサセウス
< Pediococcus pentO3aceus
)、ミクロコツカス・パリアンス()Iicrococ
cusvarians)、スタフィロコッカス・シミュ
ランス(5taphy+ococcus simula
ns)の3種の菌が1:1:1からなるものを肉とピッ
クル液を合わせたものに対し1グラム当り菌数107の
砧になるように加えた。
(Pickle liquid combination) Water 100 Soybean protein 43 Vegetable oil 20 Salt 8.6 Phosphate 1.7 Sodium glutamate 08 Corn syrup 2.0 Sodium arsulupate 034 Sodium nitrite 0. (1g and as a starter culture Pediococcus bentosaceus < Pediococcus pentO3aceus
), Micrococcus palliances () Iicrococ
cusvarians), Staphylococcus simulas (5taphy+ococcus simula)
A mixture of three types of bacteria (ns) was added in a 1:1:1 ratio to the meat and pickling liquid at a concentration of 107 bacteria per gram.

次にスターターカルチャーを含むピックル液と原料山を
頁空ミキサーに入れ、減圧下5〜10分ミキサーを回転
し、ピックル液を完全に肉に吸収させた。これをミキ晋
ナーから取り出して、ポリ容器に移し、(8度30℃で
20時間放置した。その後、香辛料、防腐剤、澱粉等を
混和後、ゲージングに充填し常法通り殺菌処理した。
Next, the pickling liquid containing the starter culture and the pile of raw materials were placed in an empty mixer, and the mixer was rotated under reduced pressure for 5 to 10 minutes to completely absorb the pickling liquid into the meat. This was taken out from the Miki Shinner, transferred to a plastic container, and left for 20 hours at 8°C and 30°C. After mixing with spices, preservatives, starch, etc., it was filled into a gauge and sterilized in the usual manner.

実施例1及び2のbのはいずれも風味に優れるものであ
った。
Both Examples 1 and 2 b had excellent flavor.

Claims (1)

【特許請求の範囲】[Claims] (1)原料肉にスターターカルチャーを添加し、15℃
以上50℃以下の温度で塩漬、熟成することを特徴とす
るハムの製造方法。
(1) Add starter culture to raw meat and heat to 15°C.
A method for producing ham, characterized by salting and aging at a temperature of at least 50°C.
JP60230761A 1985-10-16 1985-10-16 Production of ham Pending JPS6291163A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60230761A JPS6291163A (en) 1985-10-16 1985-10-16 Production of ham

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60230761A JPS6291163A (en) 1985-10-16 1985-10-16 Production of ham

Publications (1)

Publication Number Publication Date
JPS6291163A true JPS6291163A (en) 1987-04-25

Family

ID=16912853

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60230761A Pending JPS6291163A (en) 1985-10-16 1985-10-16 Production of ham

Country Status (1)

Country Link
JP (1) JPS6291163A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02138953A (en) * 1988-11-21 1990-05-28 Ushiwaka Shoji Kk Processing of edible meat
CN1034471C (en) * 1992-06-27 1997-04-09 云南省微生物研究所 No Mould ham salting method
EP0776611A1 (en) * 1995-12-01 1997-06-04 Unilever Plc Fermented and pre-fermented protein based products
WO2005100614A1 (en) * 2004-04-15 2005-10-27 Chr. Hansen A/S Method for reducing the content of pathogenic organisms present in food materials

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02138953A (en) * 1988-11-21 1990-05-28 Ushiwaka Shoji Kk Processing of edible meat
CN1034471C (en) * 1992-06-27 1997-04-09 云南省微生物研究所 No Mould ham salting method
EP0776611A1 (en) * 1995-12-01 1997-06-04 Unilever Plc Fermented and pre-fermented protein based products
WO2005100614A1 (en) * 2004-04-15 2005-10-27 Chr. Hansen A/S Method for reducing the content of pathogenic organisms present in food materials

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