JPH0751038A - Antimicrobial agent for preserving food - Google Patents

Antimicrobial agent for preserving food

Info

Publication number
JPH0751038A
JPH0751038A JP5197522A JP19752293A JPH0751038A JP H0751038 A JPH0751038 A JP H0751038A JP 5197522 A JP5197522 A JP 5197522A JP 19752293 A JP19752293 A JP 19752293A JP H0751038 A JPH0751038 A JP H0751038A
Authority
JP
Japan
Prior art keywords
bifidobacterium
food
propionic acid
lactic acid
acetic acid
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
JP5197522A
Other languages
Japanese (ja)
Other versions
JP3241500B2 (en
Inventor
Masayuki Taniguchi
正之 谷口
Tsutomu Kaneko
勉 金子
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.)
Meiji Dairies Corp
Original Assignee
Meiji Milk Products 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 Meiji Milk Products Co Ltd filed Critical Meiji Milk Products Co Ltd
Priority to JP19752293A priority Critical patent/JP3241500B2/en
Publication of JPH0751038A publication Critical patent/JPH0751038A/en
Application granted granted Critical
Publication of JP3241500B2 publication Critical patent/JP3241500B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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

  • Food Preservation Except Freezing, Refrigeration, And Drying (AREA)

Abstract

PURPOSE:To obtain an antimicrobial agent for preserving food, containing a fermentative preparation obtained by carrying out the mixed culturing of a bifidus bacterium with a propionibacterium and thereby having high antimicrobial activities. CONSTITUTION:This antimicrobial agent contains a fermentative preparation obtained by carrying out the mixed culturing of a bifidus bacterium with a propionibacterium at preferably (1:5) to (1:2) ratio as an active ingredient. The proliferation of the bifidus bacterium is promoted by a proliferation promoter produced by the propionibacterium to increase the amounts of produced lactic acid and acetic acid. The lactic acid is converted into propionic acid and acetic acid to improve antimicrobial activities.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は食品に添加することによ
り、当該食品の保存中に起こる微生物の増殖を抑制し、
その結果優れた保存性を食品に付与することのできる食
品保存用抗菌剤に関するものである。
TECHNICAL FIELD The present invention suppresses the growth of microorganisms during storage of food by adding it to food,
As a result, the present invention relates to an antibacterial agent for preserving foods, which can impart excellent preservability to foods.

【0002】[0002]

【従来の技術】食品の微生物による変質、変敗を防止す
る方法としては、1)物理的方法(加熱処理、低温保
存、水分除去、包装等)、2)化学的方法(殺菌剤、保
存料などの添加等)、3)生物学的方法(アルコール発
酵、酢酸発酵、乳酸発酵等を行う微生物またはその発酵
調製物の添加等)等があるが、このなかで、3)の生物
学的方法による食品の保存性の改善法は、消費者の健康
指向又は天然物指向と相俟って、近年、ますます注目さ
れている。例えば、Lactobacillus やPediococcusなど
の乳酸菌をスターターとして利用することによる食肉加
工品(例えば、発酵ソーセージ)の風味および保存性の
改善例(J. Food Protect., 49, 280 (1986)、J. Food
Protect., 46, 997 (1983)、Food Technol., Jan., 74
(1981)) 、乳酸菌の産生する抗菌性物質であるナイシン
を添加することによる食肉の保存性の改善例(J. Food
Protect., 48, 330 (1985)) 、ビフィズス菌の発酵調製
物もしくはその乾燥物を添加することによる生ソーセー
ジの保存性の改善例(フードケミカル、(10), 98, (198
9)、特開昭63-14656、特開昭64-30565)等が報告されて
いる。
2. Description of the Related Art 1) Physical methods (heat treatment, low temperature preservation, moisture removal, packaging, etc.), 2) Chemical methods (bactericides, preservatives) as methods for preventing deterioration and deterioration of foods by microorganisms. Etc.), and 3) biological methods (addition of microorganisms that carry out alcoholic fermentation, acetic acid fermentation, lactic acid fermentation, or fermentation preparations thereof), etc., among which the biological method of 3) In recent years, the method for improving the storability of foods has been attracting more and more attention in combination with consumer-oriented or natural product-oriented methods. For example, examples of improving the flavor and preservability of processed meat products (eg, fermented sausage) by using lactic acid bacteria such as Lactobacillus and Pediococcus as a starter (J. Food Protect., 49, 280 (1986), J. Food.
Protect., 46, 997 (1983), Food Technol., Jan., 74
(1981)), an example of improving the preservability of meat by adding nisin, which is an antibacterial substance produced by lactic acid bacteria (J. Food.
Protect., 48, 330 (1985)), an example of improving the preservability of raw sausage by adding a fermented preparation of Bifidobacterium or a dried product thereof (Food Chemical, (10), 98, (198
9), JP-A-63-14656, JP-A-64-30565) and the like.

【0003】前述した従来の技術のなかで、乳酸菌の生
菌をスターターとして直接食品に接種する方法は乳酸菌
の発酵によりpHが低下することから、中性の食品素材に
適用することはできない。また、乳酸菌の産生する抗菌
性物質であるナイシン添加による食品の保存性改善法
は、タンパク質分解酵素によりナイシンが分解失活する
ことから、該酵素を含む食品への利用は好ましくない。
さらに、ビフィズス菌の発酵調製物もしくはその乾燥物
を添加する方法は、該発酵調製物もしくはその乾燥物が
抗菌活性を有する有機酸(乳酸、酢酸)を含んでいるの
に加え、ビフィズス菌は嫌気性菌であるために食品素材
のpHを低下させる程増殖するおそれがないことから、食
品の保存性改善法として極めて有効な方法と言えるが、
広汎な食品に応用するためには更に抗菌活性を高くする
ことが求められていた。
Among the above-mentioned conventional techniques, the method of directly inoculating food with live lactic acid bacteria as a starter cannot be applied to neutral food materials because the pH is lowered by fermentation of lactic acid bacteria. In addition, the method for improving the preservability of foods by adding nisin, which is an antibacterial substance produced by lactic acid bacteria, is not preferable for use in foods containing the enzyme because nisin is decomposed and inactivated by proteolytic enzymes.
Furthermore, the method for adding a fermented preparation of Bifidobacterium or a dried product thereof is such that, in addition to the fact that the fermented preparation or a dried product thereof contains an organic acid (lactic acid, acetic acid) having antibacterial activity, Bifidobacterium is anaerobic. Since it is a virulent bacterium, there is no danger of growing enough to lower the pH of the food material, so it can be said that it is an extremely effective method as a method for improving the preservability of food.
In order to apply it to a wide range of foods, it has been required to further enhance the antibacterial activity.

【0004】[0004]

【発明が解決しようとする課題】従って、本発明の目的
は、微生物の発酵調製物を利用した、高い抗菌活性を有
する食品保存用抗菌剤を提供することである。
SUMMARY OF THE INVENTION Therefore, an object of the present invention is to provide an antibacterial agent for food preservation which has a high antibacterial activity and utilizes a fermented preparation of microorganisms.

【0005】[0005]

【課題を解決するための手段】本発明者らは、鋭意研究
を重ね、ビフィズス菌とプロピオン酸菌を混合培養して
得られた発酵調製物が高い抗菌活性を有することを見出
し、本発明を完成させるに至った。すなわち、本発明
は、ビフィズス菌およびプロピオン酸菌を混合培養して
得られた発酵調製物を有効成分として含む食品保存用抗
菌剤を提供するものである。
Means for Solving the Problems The present inventors have conducted extensive studies and found that a fermented preparation obtained by mixed culture of bifidobacteria and propionic acid bacteria has high antibacterial activity, and It came to completion. That is, the present invention provides an antibacterial agent for food preservation, which comprises, as an active ingredient, a fermentation preparation obtained by mixing and culturing bifidobacteria and propionic acid bacteria.

【0006】一般に、プロピオン酸と酢酸は乳酸に比較
して抗菌活性が高いことが知られている(フードケミカ
ル、(10), 98, (1989)、日本食品工業学会誌、31, 525
(1984)) 。また、ビフィズス菌はグルコースまたはラク
トースを乳酸と酢酸に変換するのに対し、プロピオン酸
菌は糖または乳酸を代謝して、酢酸とプロピオン酸に変
換する。さらに、プロピオン酸菌は菌体内外にビフィズ
ス菌の増殖促進物質を産生することが本願発明者らによ
り見い出された(日本農芸化学会、1993年度大会講演要
旨集、300 (1993)) 。従って、プロピオン酸菌とビフィ
ズス菌を混合培養すると、プロピオン酸菌の産生する増
殖促進物質によりビフィズス菌の増殖が促進され、乳酸
および酢酸生成量が著しく高くなるとともに、生成した
乳酸はプロピオン酸菌によって抗菌活性のより高いプロ
ピオン酸と酢酸に変換され得るのである。
It is generally known that propionic acid and acetic acid have higher antibacterial activity than lactic acid (Food Chemical, (10), 98, (1989), Journal of Japan Food Industry Society, 31, 525).
(1984)). Bifidobacteria convert glucose or lactose to lactic acid and acetic acid, whereas propionic acid bacteria metabolize sugar or lactic acid to convert acetic acid and propionic acid. Furthermore, it was found by the present inventors that propionic acid bacteria produce a growth-promoting substance for bifidobacteria inside and outside the cells (Agricultural Chemical Society of Japan, 1993 Annual Meeting Abstracts, 300 (1993)). Therefore, when mixed culture of propionic acid bacteria and bifidobacteria, the growth of bifidobacteria is promoted by the growth-promoting substance produced by propionic acid bacteria, and the amount of lactic acid and acetic acid produced is significantly increased, and the produced lactic acid is produced by propionic acid bacteria. It can be converted to propionic acid and acetic acid, which have higher antibacterial activity.

【0007】本発明において、ビフィズス菌としてはい
ずれの菌種も使用が可能であるが、例えば、ヒト由来菌
のビフィドバクテリウム・ロングム、ビフィドバクテリ
ウム・インファンティス、ビフィドバクテリウム・ブレ
ベ、ビフィドバクテリウム・アドレセンティス、および
ビフィドバクテリウム・ビフィダムより成る群から選択
されたものが好ましい。ビヒィズス菌は一種でも、二種
以上の組み合わせでもよい。
In the present invention, any species of Bifidobacterium can be used. For example, human-derived bacterium Bifidobacterium longum, Bifidobacterium infantis, Bifidobacterium Preference is given to those selected from the group consisting of Brevet, Bifidobacterium adrescentis, and Bifidobacterium bifidum. The Behizus bacterium may be one kind or a combination of two or more kinds.

【0008】プロピオン酸菌としては、公知のいかなる
菌も使用可能であるが、ビフィズス菌に対する増殖促進
物質を産生することから、プロピオニバクテリウム・フ
ロイデンライヒ(Propionibacterium freudenreichi
i)、プロピオニバクテリウム・ゼェンセニ(Propionib
acterium jensenii)、プロピオニバクテリウム・アシ
デプロピオニ(Propionibacterium acidipropionici
等が好ましく、このうち、プロピオニバクテリウム・フ
ロイデンライヒがより好ましい。
As the propionic acid bacterium, any known bacterium can be used. However, since it produces a growth promoting substance for bifidobacteria, it can be used for Propionibacterium freudenreichi.
i ), Propionibium senseni ( Propionib
acterium jensenii ), Propionibacterium acidipropionici
Etc. are preferred, and of these, Propionibacterium freudenreich is more preferred.

【0009】ビフィズス菌とプロピオン酸菌の比率は特
に限定されないが、1:5〜1:20の範囲で使用するこ
とが好ましい。ビフィズス菌およびプロピオン酸菌を以
下のように混合培養して発酵調製物を得ることができ
る。まず、ビフィズス菌を例えばTPY培地のような糖
を含む適当な培地中で、例えば窒素ガスと炭酸ガスの混
合ガスを通気しながら嫌気的条件下で、30〜40℃の温度
で、12〜20時間培養する。一方、プロピオン酸菌は、例
えばTPY培地のような適当な培地中で、好気的乃至嫌
気的条件下で、30〜40℃の温度で、48〜120 時間培養す
る。その後、両培養液を適当な比率で混合し、嫌気的条
件下で、30〜40℃の温度で、48〜120 時間混合培養して
発酵させる。
The ratio of bifidobacteria to propionic acid bacteria is not particularly limited, but it is preferably used in the range of 1: 5 to 1:20. Bifidobacteria and propionic acid bacteria can be mixed and cultured as described below to obtain a fermentation preparation. First, Bifidobacteria in a suitable medium containing sugar such as TPY medium, for example, while aeration of a mixed gas of nitrogen gas and carbon dioxide under anaerobic conditions at a temperature of 30 to 40 ° C. for 12 to 20 ° C. Incubate for hours. On the other hand, the propionic acid bacterium is cultured in an appropriate medium such as TPY medium under aerobic or anaerobic conditions at a temperature of 30 to 40 ° C. for 48 to 120 hours. After that, both cultures are mixed at an appropriate ratio, and mixed and cultured under anaerobic conditions at a temperature of 30 to 40 ° C. for 48 to 120 hours to ferment.

【0010】上記のようにして得られた発酵調製物をそ
のまま、あるいは乾燥して、あるいはまた、乾燥したも
のを製剤化して、食品に添加し、該食品の保存性を改善
することができる。発酵調製物は、所望により濃縮した
後に、噴霧乾燥、凍結乾燥、真空乾燥、ドラム乾燥等の
手段で乾燥することができる。さらに、この乾燥物を常
法により製剤化することができ、例えば、溶液、懸濁
液、粉末、顆粒、カプセル、錠剤等のいずれの形態にす
ることもできる。また、結合剤、滑沢剤、分散剤、懸濁
剤、乳化剤、希釈剤、緩衝剤、抗酸化剤、細菌抑制剤等
の添加剤を適宜使用してもよい。
The fermented preparation obtained as described above may be used as it is, or after being dried, or alternatively, a dried product may be formulated into a food product and added to a food product to improve the storage stability of the food product. The fermentation preparation can be dried by means of spray drying, freeze drying, vacuum drying, drum drying, etc., after being optionally concentrated. Furthermore, this dried product can be formulated by a conventional method, and can be in any form such as solution, suspension, powder, granules, capsules, tablets and the like. Further, additives such as binders, lubricants, dispersants, suspending agents, emulsifiers, diluents, buffers, antioxidants, and bacterial inhibitors may be appropriately used.

【0011】本発明の食品保存用抗菌剤は、ハム、ソー
セージなどの食肉製品の他、シュウマイ、ギョウザなど
の惣菜、カマボコなどの練り製品、カスタードクリーム
などの洋菓子等の各種食品に添加使用することができ、
当該食品の微生物学的保存性を著しく改善することがで
きる。本発明の食品保存用抗菌剤の添加量は、特に限定
されるものではないが、食品100g当たり0.1〜2.0gが
好ましい。
The antibacterial agent for preserving foods of the present invention can be used in addition to meat products such as ham and sausage, as well as prepared foods such as maimai and gyoza, paste products such as kamaboko, and Western foods such as custard cream. You can
It is possible to significantly improve the microbiological preservation of the food. The amount of the antimicrobial agent for food preservation of the present invention to be added is not particularly limited, but is preferably 0.1 to 2.0 g per 100 g of food.

【0012】ビフィズス菌は、ヒトの腸内細菌の一種で
あり、またプロピオン酸菌は、古来よりエメンタールチ
ーズ等のスターターとして利用されている安全性の確認
されている菌であるから、本発明の食品保存用抗菌剤は
極めて毒性の低いものである。以下、本発明を実施例に
より具体的に説明するが、本発明の範囲はこれに限定さ
れることはない。
Bifidobacteria are a kind of human intestinal bacteria, and propionic acid bacteria have been used as starters for Emmental cheese and the like since their safety has been confirmed. Antibacterial agents for food preservation have extremely low toxicity. Hereinafter, the present invention will be specifically described with reference to Examples, but the scope of the present invention is not limited thereto.

【0013】[0013]

【実施例】【Example】

〔実施例1〕工業技術院生命工学工業技術研究所に平成
5年4月20日付で寄託されたBifidobacterium longum N
o.7 (微生物受託番号 FERM P-13610)を、TPY培地
(トリプチケース(BBL)8g、フィトンペプトン
(BBL)3g、グルコース20g、酵母エキス5g、L
−システイン塩酸塩0.5g、K2HPO42g、KH2PO43g、M
gCl2・6H2O 0.5g、FeSO4・7H2O 10mg、H2O 1000ml、
pH 6.5)中で、37℃で、窒素ガス90%及び炭酸ガス10%
の混合ガスを通気しながら嫌気培養した。経時的に、酢
酸および乳酸生成量、グルコース消費量、濁度(OD
660)を測定するとともに、Micrococcus flavus IFO 13
867 を検定菌として、抗菌力価をペーパーディスク寒天
平板拡散法により測定した。抗菌力価は培養24時間後の
生育阻止円径により求め、pH 3.5における酢酸相当量
(g/l)として示した。グルコース濃度は酵素法によ
り、酢酸および乳酸濃度は高速液体クロマトグラフィー
によりそれぞれ測定した。結果を図1に示す。図1中、
△は酢酸濃度(g/l)、▲は乳酸濃度(g/l)、□
はグルコース濃度(g/l)、○は濁度、◎は抗菌力価
を示す。
[Example 1] Bifidobacterium longum N deposited on April 20, 1993 at the Institute of Biotechnology, Institute of Biotechnology, AIST.
o.7 (Microbial Accession No. FERM P-13610), TPY medium (trypticase (BBL) 8g, phytonpeptone (BBL) 3g, glucose 20g, yeast extract 5g, L
-Cysteine hydrochloride 0.5 g, K 2 HPO 4 2 g, KH 2 PO 4 3 g, M
gCl 2 · 6H 2 O 0.5g, FeSO 4 · 7H 2 O 10mg, H 2 O 1000ml,
90% nitrogen gas and 10% carbon dioxide at 37 ° C in pH 6.5)
Anaerobically culturing was carried out while aerating the mixed gas. Acetic acid and lactic acid production, glucose consumption, turbidity (OD
660 ) and the Micrococcus flavus IFO 13
The antibacterial titer was measured by the paper disk agar plate diffusion method using 867 as a test bacterium. The antibacterial titer was determined by the diameter of the growth inhibition circle after 24 hours of culture, and shown as the acetic acid equivalent amount (g / l) at pH 3.5. The glucose concentration was measured by the enzymatic method, and the acetic acid and lactic acid concentrations were measured by high performance liquid chromatography. The results are shown in Fig. 1. In Figure 1,
△ is acetic acid concentration (g / l), ▲ is lactic acid concentration (g / l), □
Indicates glucose concentration (g / l), O indicates turbidity, and O indicates antibacterial titer.

【0014】一方、Bifidobacterium longum No.7 を上
記と同様に単独で10時間培養した後、TPY培地中で嫌
気的条件下で37℃で72時間培養したPropionibacterium
freudenreichii IFO 12424の培養液を濁度が1.00となる
ように接種し、Bifidobacterium longum No.7 の単独培
養の培養条件と同じ条件下で混合培養を行なった。経時
的に、酢酸および乳酸生成量、グルコース消費量、濁度
(OD660)ならびに抗菌力価を上記と同様に測定し
た。結果を図2に示す。図2中の各記号は、図1中のそ
れと同じものを示す。
On the other hand, Bifidobacterium longum No. 7 was independently cultivated in the same manner as above for 10 hours and then cultured in TPY medium under anaerobic conditions at 37 ° C. for 72 hours to produce Propionibacterium.
A culture solution of freudenreichii IFO 12424 was inoculated so that the turbidity was 1.00, and mixed culture was carried out under the same conditions as the culture conditions for the single culture of Bifidobacterium longum No. 7. Over time, acetic acid and lactic acid production, glucose consumption, turbidity (OD 660 ) and antibacterial titer were measured as above. The results are shown in Figure 2. Each symbol in FIG. 2 is the same as that in FIG.

【0015】図2は、培養液中のグルコース濃度が0と
なった後に、乳酸の濃度が低下するとともにプロピオン
酸と酢酸の濃度が上昇したことを示している。このこと
から、ビフィズス菌とプロピオン酸菌を混合培養するこ
とにより、ビフィズス菌が産生した乳酸は、グルコース
が完全に消費された後、プロピオン酸菌によりプロピオ
ン酸と酢酸に変換されることがわかる。また、図1と2
を比較することにより、ビフィズス菌とプロピオン酸菌
を混合培養した培養液のMicrococcus flavus IFO 13867
に対する抗菌力価はビフィズス菌を単独培養した培養液
のそれよりも高いことが明らかとなった。
FIG. 2 shows that after the glucose concentration in the culture medium became 0, the concentration of lactic acid decreased and the concentrations of propionic acid and acetic acid increased. From this, it can be seen that by mixing and culturing Bifidobacteria and propionic acid bacteria, the lactic acid produced by Bifidobacterium is converted into propionic acid and acetic acid by the propionic acid bacteria after glucose is completely consumed. 1 and 2
By comparing the two, Micrococcus flavus IFO 13867 of the culture solution in which bifidobacteria and propionic acid bacteria were mixed and cultured
It was clarified that the antibacterial titer against B. pylori was higher than that of the culture solution in which Bifidobacterium was cultivated alone.

【0016】[0016]

【発明の効果】本発明により、極めて毒性が低く、ま
た、ビフィズス菌を単独培養して得られる発酵調製物よ
りも高い抗菌活性を有する食品保存用抗菌剤が得られ
た。
INDUSTRIAL APPLICABILITY According to the present invention, an antibacterial agent for food preservation having extremely low toxicity and having higher antibacterial activity than the fermented preparation obtained by culturing bifidobacteria alone was obtained.

【図面の簡単な説明】[Brief description of drawings]

【図1】図1は、ビフィズス菌を単独培養したときの、
酢酸濃度、乳酸濃度、グルコース濃度、濁度、および抗
菌力価の経時変化を示す図である。
FIG. 1 shows the results of culturing Bifidobacterium alone,
It is a figure which shows a time-dependent change of acetic acid concentration, lactic acid concentration, glucose concentration, turbidity, and antibacterial titer.

【図2】図2は、ビフィズス菌およびプロピオン酸菌を
混合培養したときの、酢酸濃度、乳酸濃度、グルコース
濃度、濁度、および抗菌力価の経時変化を示す図であ
る。
FIG. 2 is a diagram showing changes with time of acetic acid concentration, lactic acid concentration, glucose concentration, turbidity, and antibacterial titer when bifidobacteria and propionic acid bacteria were mixed and cultured.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 ビフィズス菌およびプロピオン酸菌を混
合培養して得られた発酵調製物を有効成分として含む食
品保存用抗菌剤。
1. An antibacterial agent for food preservation, which comprises, as an active ingredient, a fermentation preparation obtained by mixing and culturing Bifidobacteria and propionic acid bacteria.
【請求項2】 ビフィズス菌が、ビフィドバクテリウム
・ロングム、ビフィドバクテリウム・インファンティ
ス、ビフィドバクテリウム・ブレベ、ビフィドバクテリ
ウム・アドレセンティス、およびビフィドバクテリウム
・ビフィダムより成る群から選択される少なくとも一種
の菌である請求項1記載の食品保存用抗菌剤。
2. A group of Bifidobacterium consisting of Bifidobacterium longum, Bifidobacterium infantis, Bifidobacterium breve, Bifidobacterium adrescentis, and Bifidobacterium bifidum. The antibacterial agent for food preservation according to claim 1, which is at least one bacterium selected from the group consisting of:
【請求項3】 プロピオン酸菌が、プロピオニバクテリ
ウム・フロイデンライヒである請求項1記載の食品保存
用抗菌剤。
3. The antibacterial agent for food preservation according to claim 1, wherein the propionic acid bacterium is Propionibacterium freudenreich.
JP19752293A 1993-08-09 1993-08-09 Antimicrobial agent for food preservation Expired - Lifetime JP3241500B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19752293A JP3241500B2 (en) 1993-08-09 1993-08-09 Antimicrobial agent for food preservation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19752293A JP3241500B2 (en) 1993-08-09 1993-08-09 Antimicrobial agent for food preservation

Publications (2)

Publication Number Publication Date
JPH0751038A true JPH0751038A (en) 1995-02-28
JP3241500B2 JP3241500B2 (en) 2001-12-25

Family

ID=16375871

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19752293A Expired - Lifetime JP3241500B2 (en) 1993-08-09 1993-08-09 Antimicrobial agent for food preservation

Country Status (1)

Country Link
JP (1) JP3241500B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100399362B1 (en) * 1996-12-24 2003-09-26 라보라토이레스 스탄다 에스. 에이. Absorbable composition containing propionic bacteria capable of releasing nitric oxide in the human or animal alimentary canal
JP2013544528A (en) * 2010-12-07 2013-12-19 ピュラック バイオケム ビー. ブイ. Fruit fermented product containing propionate and use thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100399362B1 (en) * 1996-12-24 2003-09-26 라보라토이레스 스탄다 에스. 에이. Absorbable composition containing propionic bacteria capable of releasing nitric oxide in the human or animal alimentary canal
JP2013544528A (en) * 2010-12-07 2013-12-19 ピュラック バイオケム ビー. ブイ. Fruit fermented product containing propionate and use thereof
CN108936160A (en) * 2010-12-07 2018-12-07 普拉克生化公司 Fruit ferment and application thereof comprising propionate
US11337433B2 (en) 2010-12-07 2022-05-24 Purac Biochem Bv Fruit ferments containing propionate and use thereof

Also Published As

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