JP3110450B2 - Antibacterial agent - Google Patents

Antibacterial agent

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Publication number
JP3110450B2
JP3110450B2 JP02319270A JP31927090A JP3110450B2 JP 3110450 B2 JP3110450 B2 JP 3110450B2 JP 02319270 A JP02319270 A JP 02319270A JP 31927090 A JP31927090 A JP 31927090A JP 3110450 B2 JP3110450 B2 JP 3110450B2
Authority
JP
Japan
Prior art keywords
antibacterial agent
fumaric acid
production example
antibacterial
added
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 - Fee Related
Application number
JP02319270A
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Japanese (ja)
Other versions
JPH04187066A (en
Inventor
淳良 仁科
義孝 野崎
英治 大原
浩 木原
Original Assignee
日本油脂株式会社
第一製薬株式会社
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Priority to JP02319270A priority Critical patent/JP3110450B2/en
Publication of JPH04187066A publication Critical patent/JPH04187066A/en
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Publication of JP3110450B2 publication Critical patent/JP3110450B2/en
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  • Noodles (AREA)
  • Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
  • Cereal-Derived Products (AREA)

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、広範囲の微生物に対して発育阻止作用を示
し、特に食品への添加に適した抗菌剤に関する。
Description: TECHNICAL FIELD The present invention relates to an antibacterial agent which has a growth inhibiting effect on a wide range of microorganisms and is particularly suitable for being added to foods.

〔従来の技術〕[Conventional technology]

従来から、食品の保存性を高めるために、各種抗菌剤
が用いられてきた。これらの抗菌剤のうち合成抗菌剤に
ついては、ソルビン酸塩や安息香酸などの使用が認めら
れており、また天然抗菌剤についても、リゾチーム、プ
ロタミン、香辛料抽出物などの製剤が商品化されてき
た。
Conventionally, various antibacterial agents have been used to enhance the preservability of foods. Among these antibacterial agents, use of sorbate and benzoic acid has been approved for synthetic antibacterial agents, and preparations of lysozyme, protamine, spice extract, etc. have also been commercialized for natural antibacterial agents. .

最近になつて、合成抗菌剤は、抗菌効果は優れている
ものの、安全性に疑問が残ることが明らかになつたた
め、安全性の高い天然抗菌剤に対するニーズが高まつて
きた。しかしながら、これらの天然抗菌剤は、抗菌効果
が弱く、抗菌剤として十分満足できるものではなかつ
た。
Recently, it has become clear that synthetic antibacterial agents have excellent antibacterial effects, but their safety remains unclear, and the need for highly safe natural antibacterial agents has been increasing. However, these natural antibacterial agents have weak antibacterial effects and have not been sufficiently satisfactory as antibacterial agents.

〔発明が解決しようとする課題〕[Problems to be solved by the invention]

一般に、有機酸特にフマル酸が、抗菌性を有すること
は広く知られており、従来の抗菌剤の欠点をおぎなうも
のとして、食品用の抗菌剤としての利用が試みられてき
た。ところが、この場合もフマル酸は疎水性が強いため
水に対する溶解性が悪く、これを添加した食品に結晶が
析出したりして外観をそこねるので実用性に乏しかつ
た。
In general, it is widely known that an organic acid, particularly fumaric acid, has antibacterial properties, and attempts have been made to use it as an antibacterial agent for foods in order to overcome the drawbacks of conventional antibacterial agents. However, also in this case, fumaric acid is poor in solubility in water due to its strong hydrophobicity, and its appearance is poor due to precipitation of crystals or the like in foods to which fumaric acid is added.

これを解決するものとして、たとえば水溶性ポリマー
などを被覆剤として用い、フマル酸を被覆することによ
つてフマル酸の水に対する溶解性を向上させる方法(特
開昭60−38453号公報、特開昭60−196436号公報)など
が提案されたが、これもコストが高く、また食品添加物
として不適当なものであつた。
In order to solve this, for example, a method of improving the solubility of fumaric acid in water by coating it with fumaric acid using a water-soluble polymer or the like as a coating agent (JP-A-60-38453, JP-A-60-38453, Japanese Patent Application Laid-Open No. 60-196436) was also proposed, but this was also expensive and was unsuitable as a food additive.

〔課題を解決するための手段〕[Means for solving the problem]

本発明者らは、これらフマル酸の持つ欠点を解消し、
食品への添加に適した抗菌剤を得るため鋭意研究した結
果、粉末状のフマル酸を融点40℃以上の水溶性の粉末乳
化剤で被覆することによつて、それを添加した食品の風
味、外観などをそこなわない抗菌剤が得られることを知
り、本発明を完成するに至つた。
The present inventors have solved the disadvantages of fumaric acid,
As a result of intensive studies to obtain an antibacterial agent suitable for addition to food, the flavouric acid in powder form is coated with a water-soluble powder emulsifier having a melting point of 40 ° C or higher, and the flavor and appearance of the food to which it is added are added. The inventors have found that an antibacterial agent which does not detract from the above can be obtained, and have completed the present invention.

すなわち、本発明は、フマル酸を乳化剤により可溶化
してなることを特徴とする抗菌剤に関する。
That is, the present invention relates to an antibacterial agent obtained by solubilizing fumaric acid with an emulsifier.

そして、本発明の目的は、安全性に優れ、食品等に添
加することが可能であり、広範囲の微生物に対して発育
阻止作用を有し、かつこれを添加した食品の風味、外観
などをそこなわない抗菌剤を提供することにある。
An object of the present invention is to provide an excellent safety, which can be added to foods and the like, has a growth inhibitory action against a wide range of microorganisms, and improves the flavor, appearance, etc. of the food to which it is added. An object of the present invention is to provide an antibacterial agent.

本発明に用いるフマル酸は、通常の製造法によつて得
られる粒度200メツシユ以下のものである。また、前記
既往の技術により被覆剤を被覆したフマル酸を原料とし
て用いることにより、溶解性をさらに高めることができ
る。
The fumaric acid used in the present invention has a particle size of 200 mesh or less obtained by a usual production method. Further, by using fumaric acid coated with a coating agent by the above-mentioned conventional technique as a raw material, the solubility can be further enhanced.

本発明に用いる乳化剤としては、ポリグリセリン脂肪
酸エステル、シヨ糖脂肪酸エステル、サポニンなどの中
から水溶性で融点が40℃以上のものを粉粒体として単独
で、または適宜組み合わせて使用することができる。特
に三菱化成食品株式会社製のシヨ糖脂肪酸エステルF−
1570,P−1670などが適している。
As the emulsifier used in the present invention, water-soluble and having a melting point of 40 ° C. or more from polyglycerin fatty acid ester, sucrose fatty acid ester, saponin and the like can be used alone or in an appropriate combination as powders. . In particular, sucrose fatty acid ester F- manufactured by Mitsubishi Kasei Food Co., Ltd.
1570, P-1670, etc. are suitable.

本発明の抗菌剤には、相乗剤として他の抗菌剤、例え
ばアルコール、香辛料、フマル酸以外の有機酸、脂肪族
モノグリセリド等を、フマル酸100重量部に対して、0.1
〜1000重量部の範囲で添加することもできる。
In the antibacterial agent of the present invention, other antibacterial agents as a synergist, for example, alcohols, spices, organic acids other than fumaric acid, aliphatic monoglyceride, etc., with respect to 100 parts by weight of fumaric acid, 0.1
It can be added in the range of up to 1000 parts by weight.

本発明の抗菌剤を製造するには、芯物質である粉末状
のフマル酸と被覆剤である融点40℃以上の水溶性の乳化
剤の紛粒体とを互いに接触、衝突させてフマル酸を被覆
すればよく、その装置としては、ボールミル、電気乳
鉢、高能率粉体混合装置、高速気流の対流により粉体を
接触させる装置等を使用することができる。この際、あ
まり過激な条件で作用させると、芯物質であるフマル酸
の微粉砕が起こる危険があるため、できるだけ温和な条
件で行なうことが望ましい。また、これらの装置により
作用させるのに先駆けて、芯物質と被覆剤とを予備混合
しておくと、被覆効率をさらに高めることができる。
In order to produce the antibacterial agent of the present invention, powdery fumaric acid as a core substance and powdery particles of a water-soluble emulsifier having a melting point of 40 ° C. or higher as a coating material are brought into contact with each other and collided with each other to coat fumaric acid. As the device, a ball mill, an electric mortar, a high-efficiency powder mixing device, a device for bringing powder into contact by high-speed convection, or the like can be used. At this time, if the action is carried out under extremely extreme conditions, there is a risk that the pulverization of fumaric acid as the core substance may occur. If the core substance and the coating agent are preliminarily mixed before being operated by these devices, the coating efficiency can be further increased.

なお、この場合芯物質と被覆剤との混合比としては。
重量比で芯物質1に対して被覆剤0.1〜50の範囲で用い
ることが可能であるが、芯物質と被覆剤との粒径比との
関係でこの範囲内で適宜選定することが必要である。粒
径比が大きい場合には混合比を大きくすることができる
が、粒径比が小さい場合には混合比を4以下にすること
が望ましい。混合比は、単に小さくすれば被覆効率が高
められるわけでなく、むしろ大きい方が性能がよい場合
もある。また、同じ混合比でも、被覆剤を数回に分けて
被覆せしめることにより、被覆効率をさらに高めること
ができる。
In this case, the mixing ratio between the core substance and the coating agent is as follows.
It is possible to use the coating material in the range of 0.1 to 50 with respect to the core material 1 by weight ratio, but it is necessary to appropriately select within this range in relation to the particle size ratio between the core material and the coating material. is there. When the particle size ratio is large, the mixing ratio can be increased. However, when the particle size ratio is small, the mixing ratio is desirably 4 or less. Simply decreasing the mixing ratio does not necessarily increase the coating efficiency, but rather increasing the mixing ratio may provide better performance. Even with the same mixing ratio, the coating efficiency can be further increased by coating the coating agent several times.

本発明の抗菌剤の使用に当たつては、例えば食品等に
直接添加することなどにより、バシルス属、スタフイロ
コツカス属などのグラム陽性菌、大腸菌群、サルモネラ
属などのグラム陰性菌、サツカロマイセス属、アスペル
ギルス属などの真菌等の広範囲の微生物の発育を阻止す
ることができる。
In using the antibacterial agent of the present invention, for example, gram-positive bacteria such as Bacillus sp. It can inhibit the growth of a wide variety of microorganisms such as fungi such as genus and Aspergillus.

この際、抗菌剤の最少発育阻止濃度は、添加する対象
物質に対して1ppm以上であるが、添加量としては10〜80
00ppmであることが好ましい。添加量が10ppm未満では、
発育阻止効果が得られず、また8000ppmを超えると、添
加する食品等の味をそこねるので好ましくない。
At this time, the minimum growth inhibitory concentration of the antibacterial agent is 1 ppm or more with respect to the target substance to be added.
Preferably it is 00 ppm. If the amount added is less than 10 ppm,
If the growth inhibitory effect is not obtained, and if it exceeds 8000 ppm, the taste of the food or the like to be added is unfavorably deteriorated.

〔発明の効果〕〔The invention's effect〕

本発明の抗菌剤は、安全性が高く、しかも広範囲の微
生物に対して発育阻止作用を有するので、これを食品等
に添加することにより、強力な抗菌効果が期待できる。
Since the antibacterial agent of the present invention is highly safe and has a growth inhibitory effect on a wide range of microorganisms, a strong antibacterial effect can be expected by adding it to foods and the like.

さらに、水に対する溶解性に優れているので、食品等
への添加が容易である。
Further, since it has excellent solubility in water, it can be easily added to foods and the like.

〔実施例〕〔Example〕

以下、製造例、比較製造例、実施例および比較例によ
り、本発明をさらに詳しく説明する。
Hereinafter, the present invention will be described in more detail with reference to Production Examples, Comparative Production Examples, Examples, and Comparative Examples.

これらの例において、%は重量%を示す。 In these examples,% indicates% by weight.

製造例1 フマル酸(日本油脂株式会社製)350gとシヨ糖脂肪酸
エステルP−1670(三菱化成食品株式会社製)5gとを奈
良ハイブリタイゼーシヨンシステム(株式会社奈良機械
製作所製)にかけ、20分間処理して本発明の抗菌剤を得
た。
Production Example 1 350 g of fumaric acid (manufactured by Nippon Yushi Co., Ltd.) and 5 g of sucrose sugar fatty acid ester P-1670 (manufactured by Mitsubishi Kasei Food Co., Ltd.) were applied to Nara Hybridization System (manufactured by Nara Machinery Co., Ltd.) for 20 minutes. Treatment yielded the antimicrobial agent of the present invention.

製造例2 フマル酸(日本油脂株式会社製)をジエツト粉砕機
(日本ニユーマチツク株式会社製)により粉砕したもの
100gをシヨ糖脂肪酸エステルP−1670(三菱化成食品株
式会社製)5gと混合し、ヘンシエルキミサーにかけ、15
分間処理して本発明の抗菌剤を得た。
Production Example 2 A product obtained by crushing fumaric acid (manufactured by NOF Corporation) with a jet crusher (manufactured by Nippon New Mac Company).
100 g was mixed with 5 g of sucrose fatty acid ester P-1670 (manufactured by Mitsubishi Kasei Food Co., Ltd.) and passed through Hensiel Kimmiser to obtain 15 g
After treating for 1 minute, the antibacterial agent of the present invention was obtained.

製造例3 フマル酸(日本油脂株式会社製)100gとキラヤサポニ
ン粉末(丸善化成株式会社製)0.5gとをメカノミル(株
式会社奈良機械製作所製)に入れ、5分間処理して本発
明の抗菌剤を得た。
Production Example 3 100 g of fumaric acid (manufactured by Nippon Yushi Co., Ltd.) and 0.5 g of Kirayasaponin powder (manufactured by Maruzen Kasei Co., Ltd.) were placed in a mechanomill (manufactured by Nara Machinery Co., Ltd.) and treated for 5 minutes to treat the antibacterial agent of the present invention. I got

比較製造例1 未処理のフマル酸(日本油脂株式会社製)そのものを
比較品とした。
Comparative Production Example 1 Untreated fumaric acid (manufactured by NOF Corporation) itself was used as a comparative product.

比較製造例2 フマル酸を主原料とする一般市販の抗菌剤を比較品と
した。
Comparative Production Example 2 A commercially available antibacterial agent containing fumaric acid as a main raw material was used as a comparative product.

実施例1 製造例1〜3、比較製造例1,2で得られた本発明の抗
菌剤および比較品を、20℃の水の中に濃度0.5%となる
ように投入し、マグネチツクスターラー(約500rpm)で
撹拌し、完全に溶解するまでの時間を測定した。結果は
表1に示した。
Example 1 The antibacterial agent and the comparative product of the present invention obtained in Production Examples 1 to 3 and Comparative Production Examples 1 and 2 were charged into water at 20 ° C. so as to have a concentration of 0.5%. (About 500 rpm), and the time until complete dissolution was measured. The results are shown in Table 1.

実施例2 細菌用培地としてトリプトソイ寒天培地(栄研化学株
式会社製)、真菌用培地としてサブロー寒天培地(栄研
化学株式会社製)に、製造例1で得られた抗菌剤をそれ
ぞれ200,400,1000ppm添加し滅菌した。
Example 2 200,400,1000 ppm of the antibacterial agent obtained in Production Example 1 was added to a tryptosome agar medium (manufactured by Eiken Chemical Co., Ltd.) as a medium for bacteria and a Sabouraud agar medium (manufactured by Eiken Chemical Co., Ltd.) as a medium for fungi. It was added and sterilized.

ついで、無菌シヤーレに、この滅菌した培地を10mlず
つ流し込み、放冷して固化せしめたのち、普通ブイヨン
(栄研化学株式会社製)中で24時間培養した菌懸濁液5
μずつを滅菌培地上に接種した。接種した菌は、表2
に示した細菌4種と真菌2種で、細菌の場合は37℃で24
時間、真菌の場合は30℃で48時間培養したのち、菌の発
育を阻止するために必要な抗菌剤の最少量を判定した。
結果は表2に示した。
Then, 10 ml of this sterilized medium was poured into a sterile dish, allowed to cool and solidified, and then cultured in ordinary broth (manufactured by Eiken Chemical Co., Ltd.) for 24 hours.
Each μ was inoculated on a sterilized medium. Table 2 shows the inoculated bacteria.
4 kinds of bacteria and 2 kinds of fungi shown in the above.
After culturing at 30 ° C. for 48 hours for fungi, the minimum amount of the antibacterial agent necessary to inhibit the growth of the bacteria was determined.
The results are shown in Table 2.

実施例3 寒天培地の滅菌に用いる抗菌剤の添加量を100,200,50
0,1000ppmとする以外は、実施例2に準じて、製造例2
で得られた抗菌剤について、菌の発育を阻止するために
必要な抗菌剤の最少量を判定した。結果は表2に示し
た。
Example 3 The added amount of the antibacterial agent used for sterilizing the agar medium was 100, 200, 50
Except for 0.1 ppm, Production Example 2 was carried out in accordance with Example 2.
With respect to the antibacterial agent obtained in the above, the minimum amount of the antibacterial agent necessary for inhibiting the growth of bacteria was determined. The results are shown in Table 2.

実施例4 寒天培地の滅菌に用いる抗菌剤の添加量を100,200,10
00ppmとする以外は、実施例2に準じて、製造例3で得
られた抗菌剤について、菌の発育を阻止するために必要
な抗菌剤の最少量を判定した。結果は表2に示した。
Example 4 The added amount of the antibacterial agent used for sterilizing the agar medium was 100, 200, 10
A minimum amount of the antibacterial agent required for inhibiting the growth of bacteria was determined for the antibacterial agent obtained in Production Example 3 in the same manner as in Example 2 except that the amount was set to 00 ppm. The results are shown in Table 2.

比較例1 寒天培地の滅菌に用いる抗菌剤の添加量を2000ppmと
する以外は、実施例2に準じて、比較製造例1で得られ
た抗菌剤について、菌の発育を阻止するために必要な抗
菌剤の最少量を判定した。結果は表3に示した。
Comparative Example 1 The antibacterial agent obtained in Comparative Production Example 1 was required to inhibit the growth of bacteria according to Example 2, except that the amount of the antibacterial agent used for sterilizing the agar medium was 2000 ppm. The minimum amount of antimicrobial was determined. The results are shown in Table 3.

比較例2 寒天培地の滅菌に用いる抗菌剤の添加量を2000ppmと
する以外は、実施例2に準じて、比較製造例2で得られ
た抗菌剤について、菌の発育を阻止するために必要な抗
菌剤の最少量を判定した。結果は表3に示した。
Comparative Example 2 According to Example 2, the antibacterial agent obtained in Comparative Production Example 2 was necessary to inhibit the growth of bacteria, except that the amount of the antibacterial agent used for sterilizing the agar medium was 2000 ppm. The minimum amount of antimicrobial was determined. The results are shown in Table 3.

実施例5 製造例1および比較製造例1で得られた抗菌剤をそれ
ぞれ水に溶解し、濃度0.3%の水溶液を得た。その中に
厚さ2mmに切断したねぎを30秒間浸漬したのち、取り出
して水を切り15℃で48時間経過後の一般生菌数を測定し
た。結果は表4に示した。
Example 5 The antibacterial agents obtained in Production Example 1 and Comparative Production Example 1 were respectively dissolved in water to obtain a 0.3% aqueous solution. After the green onion cut into a thickness of 2 mm was immersed in it for 30 seconds, the green onion was taken out, drained, and the number of viable bacteria was counted after 48 hours at 15 ° C. The results are shown in Table 4.

実施例6 製造例2および比較製造例2で得られた抗菌剤をそれ
ぞれ水に溶解し、濃度0.1%の水溶液を得た。その中に3
cm角に切断したレタスを30秒間浸漬したのち、取り出し
て水を切り15℃で48時間経過後の一般生菌数の測定およ
び褐変状態の観察を行なつた。結果は表5に示した。
Example 6 The antibacterial agents obtained in Production Example 2 and Comparative Production Example 2 were each dissolved in water to obtain a 0.1% aqueous solution. 3 in it
After immersing the lettuce cut into a cm square for 30 seconds, it was taken out, drained, and the number of general viable bacteria was measured at 15 ° C. for 48 hours, and the browning state was observed. The results are shown in Table 5.

実施例7 下記配合のハンバーグ材料に、製造例3および比較製
造例2で得られた抗菌剤0.05%をそれぞれ添加し、ホバ
ートミキサーで30秒間混合してハンバーグを製造した。
Example 7 0.05% of the antibacterial agents obtained in Production Example 3 and Comparative Production Example 2 were respectively added to hamburger ingredients having the following composition, and mixed with a Hobart mixer for 30 seconds to produce hamburgers.

(ハンバーグ配合)(%) 鶏挽肉 25.0 豚挽肉 25.0 牛挽肉 18.4 玉ねぎ 20.0 パン粉 10.0 食塩 0.8 こしよう 0.1 ビーフエキス 0.5 グルタミン酸ソーダ 0.2 得られたハンバーグは20℃で24時間保存して一般生菌
数を測定した。結果は表6に示した。
(Contains hamburger) (%) Ground chicken 25.0 Ground pork 25.0 Ground beef 18.4 Onions 20.0 Bread crumbs 10.0 Salt 0.8 Pepper 0.1 Beef extract 0.5 Sodium glutamate 0.2 . The results are shown in Table 6.

実施例8 製造例1および比較製造例1で得られた抗菌剤をそれ
ぞれ水に溶解し、濃度0.3%の水溶液を得た。その中に1
cm角に切断した鶏の胸肉を30秒間浸漬したのち、取り出
して無菌シヤーレに入れ20℃で24時間経過後の一般生菌
数を測定した。結果は表7に示した。
Example 8 The antibacterial agents obtained in Production Example 1 and Comparative Production Example 1 were each dissolved in water to obtain a 0.3% aqueous solution. One in it
Chicken breast cut into cm squares was immersed for 30 seconds, taken out and placed in a sterile dish, and the number of general viable bacteria after 24 hours at 20 ° C. was measured. The results are shown in Table 7.

実施例9 原料として中力小麦粉を用い、製造例2および比較製
造例2で得られた抗菌剤0.05%をそれぞれ添加し、下記
製麺条件で製麺機(有限会社大成機械工業製)にかけ生
麺を製造した。
Example 9 Using neutral wheat flour as a raw material, 0.05% of the antibacterial agent obtained in Production Example 2 and Comparative Production Example 2 was added, and the mixture was subjected to a noodle making machine (manufactured by Taisei Machine Industry Co., Ltd.) under the following noodle making conditions. Noodles were manufactured.

(製麺条件) 捏和 12分 圧延 2.0 圧延(複合) 2.0 熟成 30分 圧延 1.3 圧延 1.6 切刃 10番 1.9 さらに、生麺を沸騰水で12分間茹でたのち、水洗いし
て茹麺とした。得られた茹麺は25℃で保存し経時的に一
般生菌数を測定した。結果は表8に示した。
(Noodle-making conditions) Kneading 12 minutes Rolling 2.0 Rolling (composite) 2.0 Aging 30 minutes Rolling 1.3 Rolling 1.6 Cutting edge No. 1.9 Further, raw noodles were boiled with boiling water for 12 minutes, and then washed with water to obtain boiled noodles. The obtained boiled noodles were stored at 25 ° C., and the number of general viable bacteria was measured over time. The results are shown in Table 8.

実施例10 白米を水洗いし、水に2時間浸漬したのち、製造例3
および比較製造例2で得られた抗菌剤1%をそれぞれ添
加して炊飯した。炊飯後室内に2時間放置して落下菌を
接種し、さらに30℃で保存して経時的に一般生菌数を測
定した。結果は表9に示した。
Example 10 After washing white rice with water and immersing it in water for 2 hours, Production Example 3
And 1% of the antibacterial agent obtained in Comparative Production Example 2 was added and cooked. After the rice was cooked, the bacteria were left in the room for 2 hours to inoculate the falling bacteria, stored at 30 ° C., and the number of general viable bacteria was measured over time. The results are shown in Table 9.

実施例11 鶏肉加工工場のまな板、包丁、コンベアのベルトに、
製造例2および比較製造例2で得られた抗菌剤の1%水
溶液をそれぞれ10秒間噴霧して一般生菌数を測定した。
結果は表10に示した。
Example 11 A cutting board of a chicken processing plant, a kitchen knife, a conveyor belt,
A 1% aqueous solution of the antibacterial agent obtained in Production Example 2 and Comparative Production Example 2 was sprayed for 10 seconds, and the number of general viable bacteria was measured.
The results are shown in Table 10.

以上の実施例および比較例の結果から、本発明の抗菌
剤が、未処理のフマル酸そのものからなる抗菌剤および
フマル酸を主原料とする一般市販の抗菌剤に比較して、
水に対する溶解性および微生物に対する抗菌効果が格段
に優れていることが分かる。
From the results of the above Examples and Comparative Examples, the antibacterial agent of the present invention is compared with an antibacterial agent consisting of untreated fumaric acid itself and a commercially available antibacterial agent containing fumaric acid as a main raw material.
It can be seen that the solubility in water and the antibacterial effect on microorganisms are remarkably excellent.

フロントページの続き (72)発明者 木原 浩 東京都武蔵野市吉祥寺東町1―25―21 (56)参考文献 特開 昭60−133863(JP,A) 特開 平1−120267(JP,A) (58)調査した分野(Int.Cl.7,DB名) A23L 3/3508 Continuation of the front page (72) Inventor Hiroshi Kihara 1-25-121 Higashicho, Kichijoji, Musashino-shi, Tokyo (56) References JP-A-60-133863 (JP, A) JP-A-1-120267 (JP, A) ( 58) Field surveyed (Int. Cl. 7 , DB name) A23L 3/3508

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】粉末状のフマル酸を融点40℃以上の水溶性
の粉末乳化剤で被覆してなる粉末状抗菌剤。
An antibacterial agent comprising a powdery fumaric acid coated with a water-soluble emulsifier having a melting point of 40 ° C. or higher.
JP02319270A 1990-11-22 1990-11-22 Antibacterial agent Expired - Fee Related JP3110450B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP02319270A JP3110450B2 (en) 1990-11-22 1990-11-22 Antibacterial agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP02319270A JP3110450B2 (en) 1990-11-22 1990-11-22 Antibacterial agent

Publications (2)

Publication Number Publication Date
JPH04187066A JPH04187066A (en) 1992-07-03
JP3110450B2 true JP3110450B2 (en) 2000-11-20

Family

ID=18108336

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Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP3110450B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5770204A (en) * 1996-06-06 1998-06-23 Nouveau Technologies, Inc. Composition for mucosa treatment with saponin

Also Published As

Publication number Publication date
JPH04187066A (en) 1992-07-03

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