JPS6037965A - Food preservative - Google Patents
Food preservativeInfo
- Publication number
- JPS6037965A JPS6037965A JP14599283A JP14599283A JPS6037965A JP S6037965 A JPS6037965 A JP S6037965A JP 14599283 A JP14599283 A JP 14599283A JP 14599283 A JP14599283 A JP 14599283A JP S6037965 A JPS6037965 A JP S6037965A
- Authority
- JP
- Japan
- Prior art keywords
- food
- lysozyme
- preservative
- bacteria
- fatty 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
Links
Landscapes
- Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
Abstract
Description
【発明の詳細な説明】 本・尾側は新規な食品用保存剤に関するものである。[Detailed description of the invention] The tail of this book is about a new food preservative.
従来から各抽食品を最期間保存するために、その食品に
イチ在する大腸菌、乳酸菌等各種の菌に対し静菌作用の
ある、即ちそれらの面の発育を停止する作用を有する食
品用保存剤が種々提供され、使用されている。たとえば
、エタノール、有機酸又はその塩類、低級脂肪酸モノグ
リセライド、リゾチーム等があげられ、これらは単独で
使用されるか、又は数種併用して用いられているが、夫
々に利点とともに難点を有し、十分満足すべきものは見
出されていない。Conventionally, in order to preserve each extracted food for the maximum period of time, food preservatives have been developed that have a bacteriostatic effect on various bacteria such as Escherichia coli and lactic acid bacteria that are present in the food, that is, they have the effect of stopping the growth of these bacteria. are provided and used in various ways. For example, ethanol, organic acids or their salts, lower fatty acid monoglycerides, lysozyme, etc. are used alone or in combination, but each has advantages and disadvantages. Nothing has been found that is fully satisfactory.
酵素の一種であり、卵白リゾチームとして容易に入手し
うるリゾチームを例にとれば、このリゾチームは静菌作
用は有するが、静菌しうる細菌が限られ、しかも静菌作
用が鈍いため単独では汎用性のある食品用保有剤とはな
らない。そのため卵白リソチームにIリシン、シスチン
、システィン、カプリル酸モノグリセリド等を組合わせ
て用いる飲食品の保存、改良法(特開昭48−8822
5号公報)、卵白リゾチームにフィチン酸やグルコノデ
ルタラクトンを組合わせ用いて食品の保存性の高揚をは
かる方法(%開昭50−19950号公報)等が提案さ
れ、これらの外、他の櫨々の化合物を組合わせた保存料
、たとえば酢酸、酢酸ナトリウムにフイチン酸とアルコ
ールを組合わせてなる食品の保存料(特開昭56413
285号公報)なども提案されている。For example, lysozyme, which is a type of enzyme and is easily available as egg white lysozyme, has a bacteriostatic effect, but only a limited number of bacteria can be bacteriostatic, and its bacteriostatic effect is weak, so it cannot be used alone for general purpose. It is not a food-grade retention agent. Therefore, a method for preserving and improving foods and drinks using egg white lysozyme in combination with I-lysine, cystine, cysteine, caprylic acid monoglyceride, etc.
5), a method of increasing the preservability of foods by using egg white lysozyme in combination with phytic acid and glucono delta-lactone (% 1995-19950), and in addition to these, other methods have been proposed. A food preservative containing a combination of compounds such as acetic acid, sodium acetate, phytic acid, and alcohol (Japanese Patent Application Laid-open No. 56413
No. 285) have also been proposed.
周矧のように食品にはhJhk雑多の細菌が付着し、繁
殖している。そして食品の種類、製造条件、保存条件な
どにより繁殖する#1菌が異なる。上記の例を倉む食品
用保存剤は夫々特定の菌に対しては静菌効果を有するが
限られたものであって、食品に付着、諮殖する可能性の
あるすべての菌には力・かる効果は示さない。たとえば
前記特開昭48−88225号公報には大腸]!i、ズ
ドー状球菌、一般細菌等について有効なことが記載され
ているのみであり、特開昭50−19950号公報でも
同様に食品にイ」着する可能性のあるあらゆる菌に対し
て静菌作用を有することは何ら示されていない。Just like in the world, various types of hJhk bacteria are attached to food and are multiplying. The #1 bacteria that proliferate differs depending on the type of food, manufacturing conditions, storage conditions, etc. Food preservatives such as those mentioned above each have a bacteriostatic effect against specific bacteria, but these are limited and have no effect on all bacteria that may adhere to or colonize food.・No effect is shown. For example, in the above-mentioned Japanese Patent Application Laid-open No. 48-88225, large intestine]! It is only stated that it is effective against i, cocci, general bacteria, etc., and JP-A-19950 also states that it is bacteriostatic against all kinds of bacteria that may attach to food. It has not been shown to have any effect.
かくて本発明は食品に付着する可能性のある種々の白に
対して静菌効果を示す食品用保存剤を提供することを目
的とするものである。Thus, an object of the present invention is to provide a food preservative that exhibits a bacteriostatic effect on various types of white matter that may adhere to foods.
本発明名らはかかる目的を達成するために多数の食品用
保存剤について組合わせを変えるなど種々研究、実験を
重ねた結果、リゾチームと低級脂肪酸モノグリセライド
に更にフィチン酸或は酢酸ナトリウム或はこれらの両者
を絹合わ、(1)れば、これら3種又は4棟の物質が相
乗効果を発揮して、食品に付着しうる種々の菌に対して
静閑作用を有し汎用性のある食品用保存剤を提供しうろ
ことが見出されたのである。In order to achieve this objective, the inventors of the present invention have conducted various studies and experiments, including changing the combination of many food preservatives. If the two are combined (1), these three or four substances will exhibit a synergistic effect, resulting in a versatile food product that has a calming effect on various bacteria that may attach to food. It was discovered that it could provide a preservative.
かくて、本発明は第1にリゾチーム、低級脂肪酸モノグ
リセライP及びフィチンM’x有効成分とする食品用保
存剤、第2にリゾチーム、低級)脂肪酸モノグリセライ
ド及び酢酸ナトリウムを有効成分とする食品用保存剤、
第3にリゾチーム、低級脂肪酸モノプリセライト、フィ
チン酸及び酢酸ナトリウムを有効成分とする食品用保存
剤を提供するものである。尚上記3種の食品用保存剤を
本明細書において以下類に保存剤1.2.3と称するこ
ととする。Thus, the present invention provides, firstly, a food preservative containing lysozyme, lower fatty acid monoglyceride P, and phytin M'x as active ingredients, and secondly, a food preservative containing lysozyme, lower fatty acid monoglyceride, and sodium acetate as active ingredients. ,
Thirdly, the present invention provides a food preservative containing lysozyme, lower fatty acid monopricerite, phytic acid, and sodium acetate as active ingredients. In this specification, the above three types of food preservatives will be referred to as preservatives 1.2.3 in the following categories.
本発明について以下拝眉1に説明する。The present invention will be explained below.
まず本発明において有効成分として用いられる各化合物
について云えば、リゾチームは卵白やイチジク乳液中等
から常法によシ抽出してえられる酵素であり、等電点リ
ゾチームのみでなく塩化リゾチーム等のりゾチーム塩類
も含む。通常卵白中のりゾチームを抽出し、結晶化して
見られる結晶状の卵白リゾチームの外結晶状の卵白リゾ
チームを微粉末化した粉末状リゾチーム等卵白起源のり
ゾチームが用いられる。First, regarding each compound used as an active ingredient in the present invention, lysozyme is an enzyme obtained by extraction from egg white, fig milk, etc. by a conventional method, and not only isoelectric point lysozyme but also lysozyme salts such as lysozyme chloride. Also included. Normally, egg white-derived glysozyme is used, such as powdered lysozyme, which is obtained by extracting the glysozyme from the egg white and pulverizing the outer crystalline egg white lysozyme that is found by crystallization.
つぎに本発明における低級脂肪酸モノグリセライPは炭
素数4〜12の範囲の低級脂肪酸とグリセリンのモノエ
ステルでアム このうちカシロン酸、カプリル酸、カプ
リン酸(夫々順に炭素数6,8゜10)のモノグリセラ
イドが好ましい。この低級脂肪酸モノグリセライPは分
子蒸留法等によジえられた純度80%以上のものを用い
るのが望ましいが、純度50チ程度のものを用いること
もできる。風味の而からみると純度の高いのが好ましい
。種類によって常温で液状、結晶状、ろう状等をなして
おり、ろう状の場合は加熱して溶かして用いる。Next, lower fatty acid monoglyceride P in the present invention is a monoester of a lower fatty acid having 4 to 12 carbon atoms and glycerin.Among these, monoglyceride of casillonic acid, caprylic acid, and capric acid (each having 6.8 to 10 carbon atoms) is preferred. It is desirable to use lower fatty acid monoglycerai P with a purity of 80% or more obtained by molecular distillation or the like, but one with a purity of about 50% can also be used. From the viewpoint of flavor, high purity is preferable. Depending on the type, it is liquid, crystalline, waxy, etc. at room temperature, and if waxy, it is heated and melted before use.
次にフィチン酸は植物種子等植物体中にカルシウムマグ
ネシウム複塩として広く存在するフィチンを常法により
抽出して酸処理してえられるイノジットのヘキサリン酸
エステルと称される化合物である。常温では黄色を帯び
た粘供な液体として存在するが、通常賦形剤を加えて乾
燥して純度約30%の粉末としたものが用いられる。Next, phytic acid is a compound called hexaphosphoric acid ester of Inosit, which is obtained by extracting phytin, which is widely present as a calcium magnesium double salt in plants such as plant seeds, by a conventional method and treating it with acid. It exists as a yellowish viscous liquid at room temperature, but it is usually used as a powder with a purity of about 30% by adding excipients and drying it.
酢酸ナトリウムは酢酸を水酸化ナトリウムなどで中和し
てえられる結晶の形で用いられる。Sodium acetate is used in the form of crystals obtained by neutralizing acetic acid with sodium hydroxide.
これら化合物全有効成分とする本発明の食品用保存剤は
保存中の吸湿や変性を防止するため、また、食品にとけ
やすくするために通常デキストリン等の賦形剤を加えて
粉末又は顆粒状にして用いられる。The food preservative of the present invention, which contains all of these compounds as active ingredients, is usually made into powder or granules by adding an excipient such as dextrin to prevent moisture absorption and denaturation during storage and to make it easier to dissolve in food. It is used as
これら各有効成分及びこれに加えうる賦形剤の配合割合
について云えば、食品に用いてそこに付着しうる細菌す
べてに対し静菌効果をウラ揮させるために至適な配合割
合があり、保存剤1.2.3において有効成分の比をあ
げれば次のとおりである。ただし、使用するリゾチーム
の純度は80チ、低級脂肪酸モノグリセライドの純度は
80%、フィチン酸の純度は30%、酢酸ナトリウムの
純度は100チとする。Regarding the blending ratio of each of these active ingredients and the excipients that can be added to them, there is an optimal blending ratio in order to exert a bacteriostatic effect against all bacteria that may attach to food when used in food. The ratio of active ingredients in Agent 1.2.3 is as follows. However, the purity of the lysozyme used is 80%, the purity of lower fatty acid monoglyceride is 80%, the purity of phytic acid is 30%, and the purity of sodium acetate is 100%.
保存剤1においては、リゾチーム5〜lO%、イ氏級脂
肪酸モノグリセライド24〜35係、フィチン酸55〜
71%であり、保存剤2においては、1ノゾチ一ム1〜
2%、低級脂肪酸モノグリセライ)′5〜15%、酢酸
ナトリウム83〜94%である。保存斉IJ3において
はりゾチーム1〜2チ、イ氏級月旨1辺酸モノグリセラ
イド4〜7チ、フィチン2s〜16チ、酢酸ナトリウム
75〜87係である。Preservative 1 contains 5 to 10% lysozyme, 24 to 35 percent of A grade fatty acid monoglyceride, and 55 to 10 percent of phytic acid.
71%, and in preservative 2, 1-nozotyme 1-
2%, lower fatty acid monoglyceride)' 5-15%, and sodium acetate 83-94%. In the preservation ratio IJ3, there are 1 to 2 parts of harizozyme, 4 to 7 parts of I-class unilateral acid monoglyceride, 2s to 16 parts of phytin, and 75 to 87 parts of sodium acetate.
実際に提供される純度80%の低級脂肪酸モノグリセン
イド、純度30チのフィチン酸、その…籾純度100襲
のリゾチーム、酢酸ナトリウムを用い賦51剤(デキス
トリン)によって粉末又は顆粒状にノ杉成される場合の
各保存剤の好ましい自己上・害u合を示せば次のとおり
である。The actually provided lower fatty acid monoglycenide with a purity of 80%, phytic acid with a purity of 30%, lysozyme with a purity of 100% from rice, sodium acetate, and Nosugi is made into powder or granules with an excipient (dextrin). The preferable self-harm and harmful effects of each preservative in this case are as follows.
保存剤1
リゾチーム 0.5〜2係
低級脂肪酸モノグリセライド 3〜5チフィチン酸 5
〜6チ
賦形剤 91.5〜83チ
保存剤2
リゾチーム 0.5−2係
低級脂肪酸モノグリセライド 3〜5%酢酸ナトリウム
40 〜60%
賦形剤 56.5〜33 efb
保存剤3
リゾチーム 0.5〜2%
低級脂肪酸モノグリセライド 3〜5条フィチン酸 5
〜10チ
酢酸ナトリウム 40〜60チ
賦形剤 51.5〜23チ
上述のように本発明に係る食品用保存剤においては低級
脂肪酸モノグリセライPが用いられるが、この物質は静
菌には欠かせない成分である反面、特有の臭気を有する
ためあまり多喰に使用すると食品の風味を害する慣れが
あるため、賦形剤を含めた保存剤全原料に対しての使用
割きを、純度80チの場合上記のように5チ以下に留め
るのが好ましい。Preservative 1 Lysozyme 0.5-2 lower fatty acid monoglyceride 3-5 Typhytic acid 5
-6 Excipients 91.5-83 Preservatives 2 Lysozyme 0.5-2 Lower fatty acid monoglyceride 3-5% Sodium acetate 40 -60% Excipients 56.5-33 efb Preservatives 3 Lysozyme 0. 5-2% lower fatty acid monoglyceride 3-5 phytic acid 5
-10 Sodium thiacetate 40-60 Excipients 51.5-23 As mentioned above, lower fatty acid monoglycerai P is used in the food preservative of the present invention, and this substance is essential for bacteriostasis. On the other hand, since it has a characteristic odor and is used in large quantities, it can harm the flavor of food. In this case, as mentioned above, it is preferable to keep it to 5 inches or less.
上記の如き配合割合の成分から粉末又は顆粒に形成して
本発明に係る保存剤を製造する方法の一例を示すと、ま
ず卵白リゾチームの如きリゾチームと、カプリン酸モノ
グリセライドの如き低級脂肪酸モノグリセライPとデキ
ストリンの如き賦形剤をよく混合し、これを、60℃に
加温されたこの混合物の2倍量の温水中に投入して攪拌
混合し、當法によりスプレードライして粉末状とする。An example of a method for manufacturing the preservative according to the present invention by forming powder or granules from the ingredients in the above-mentioned proportions is as follows: lysozyme such as egg white lysozyme, lower fatty acid monoglyceride P such as capric acid monoglyceride, and dextrin. The following excipients are thoroughly mixed, the mixture is poured into twice the amount of warm water heated to 60° C., stirred and mixed, and the mixture is spray-dried to form a powder.
その後所要量のフィチン酸或は酢酸ナトリウム、或はフ
ィチン酸と酢酸ナトリウムを添加混合して本発明に係る
食品用保存剤とする。Thereafter, a required amount of phytic acid or sodium acetate, or phytic acid and sodium acetate, is added and mixed to obtain a food preservative according to the present invention.
本発明に係る食品用保存剤によれば上記の如き3種乃至
44!Aの有効成分を用いることによって相乗された静
菌効果が生じ、食品中に存在しうる各S細菌の殆どを静
菌する効果を発揮する。これは従来公知のこの種保存剤
には見られなかった効果であり、誠に顕著である。又本
発明の食品用保存剤は加熱してもリゾチームの活性は失
なわれず有効に働く。According to the food preservative according to the present invention, there are 3 to 44 types as described above! By using the active ingredients of A, a synergistic bacteriostatic effect is produced, and the effect of bacteriostasis on most of the S bacteria that may exist in foods is exhibited. This is an effect that has not been seen in conventionally known preservatives of this type, and is truly remarkable. In addition, the food preservative of the present invention does not lose its lysozyme activity even when heated and remains effective.
本発明に係る食品用保存剤は種々の食品に広く使用する
ことができる。例えばクリーム、ケーキ、パ/、カマポ
コ、ソーセージ、ヨーグルト、ジュース等の各種食料品
或は飲料品に有効に利用しうるが、とくにカマポコ、ソ
ーセー−)等加熱が必要な食品の保存剤として用いると
有効である。The food preservative according to the present invention can be widely used in various foods. For example, it can be effectively used in various foods and beverages such as cream, cake, pastry, kamapoko, sausage, yogurt, and juice, but it is especially useful as a preservative for foods that require heating, such as kamapoko, sauce, etc. It is valid.
以下に試験例をあげて本発明について更に説明する。尚
この例を含む明細I11.においてチ又は部は重愉チ又
は重量部を意味する。The present invention will be further explained with reference to test examples below. Note that specification I11. including this example. In the above, "chi" or "part" means "weight part" or "part by weight".
試験例1
次の如き5つの保存剤試料(A−E)を調製した。同試
料C−Eは順に本発明に係る上記保存剤1〜3に相当し
、これケチスト1〜3と表示する。Test Example 1 Five preservative samples (A-E) were prepared as follows. Samples C to E correspond to the above preservatives 1 to 3 according to the present invention, and are designated as Kechist 1 to 3.
又比較対照のため保存剤無添加のものを試料A(対照1
)とし、本発明にて有効成分として用いる物質の中2種
頬のみを含有するものを試料B(対照2)とする。For comparison, sample A (control 1) with no preservative added was used.
), and a sample containing only two of the substances used as active ingredients in the present invention is designated as Sample B (Control 2).
保存剤試料
A、対照1 保存剤無添加
B、対照2 卵白リゾチーム2部、カプリン酸モノグリ
セライド3部、デキス
トリン93部
C,テスト1 卵白リゾチーム1部、カプリン酸モノグ
リセライド、 フィチン酸
5部、デキストリン91部
り、テスト2 卵白リゾチーム1部、カプリン酸モノグ
リセライド3部、酢酸ナ
トリウム刃部、デキストリン46部
E、テスト3 卵白リゾチーム1部、カプリン酸モノグ
リセライド3部、フィチ
ン散lO部、酢酸ナトリウム(資)部、デキストリン3
6部
ここに用いられたカプリン酸モノグリセライドは純度8
0φのもの、フィチン酸は純度30%のものであり、卵
白リゾチーム及び酢酸ナトリウムは純度100多のもの
でおった。Preservative Sample A, Control 1 Preservative-free B, Control 2 2 parts of egg white lysozyme, 3 parts of capric acid monoglyceride, 93 parts of dextrin C, Test 1 1 part of egg white lysozyme, capric acid monoglyceride, 5 parts of phytic acid, 91 parts of dextrin Test 2: 1 part of egg white lysozyme, 3 parts of capric acid monoglyceride, sodium acetate, 46 parts of dextrin E, Test 3: 1 part of egg white lysozyme, 3 parts of capric acid monoglyceride, 1 part of phytin powder, 1 part of sodium acetate, dextrin 3
6 parts The capric acid monoglyceride used here has a purity of 8
The purity of phytic acid was 30%, and the purity of egg white lysozyme and sodium acetate was 100%.
上記保存剤試料A−Eについて次の如き試験方法により
代表的な細菌に対する静菌作用のテストを行なった。The above preservative samples A to E were tested for bacteriostatic activity against typical bacteria using the following test method.
試験方法: まず次の如き成分により液状の培地をつくった。Test method: First, a liquid medium was prepared using the following ingredients.
牛肉エキス 5g
ペゾト7 10g
グルコース 5g
Mail 5 g
これに水10100Of加えpH6,8としこれを大試
験管に20m1づつ分注し、次いで121℃に15分間
加熱して滅菌した。Beef extract 5 g Pezoto 7 10 g Glucose 5 g Mail 5 g To this was added 10,100 Of water to adjust the pH to 6.8, which was dispensed into large test tubes in 20 ml portions and then heated to 121° C. for 15 minutes to sterilize.
このようにしてつくられた培地に上述の如き成分の保存
剤試料を七の培地の1%量亦加し無添加のものとともに
保存剤試料A−Eに相当する5種の培地をつくった。To the medium prepared in this manner, preservative samples having the above-mentioned components were added in an amount of 1% of the seven mediums, and five types of culture medium corresponding to preservative samples A to E were prepared as well as those without additives.
一方次の如き菌株を用いて菌敢忙つくった。On the other hand, the following bacterial strains were used to create a bacterial strain.
a、 E、coli (大腸函)
b、L、plantarum (乳酸菌)c、 B、c
ereus (セレウス菌)d、 Sta、aureu
g (黄色ブドウ球菌)e、 Sac、cerevis
iae (lap母)これら各菌株それぞれを約1白金
耳量とりこれを生理食塩水9mlに添加踵 よ<&拌し
て菌液とする。a, E, coli (colon box) b, L, plantarum (lactic acid bacteria) c, B, c
ereus (Bacillus cereus) d, Sta, aureu
g (Staphylococcus aureus) e, Sac, cerevis
iae (lap mother) Take about 1 platinum loopful of each of these bacterial strains and add it to 9 ml of physiological saline and stir to obtain a bacterial solution.
上記のようにしてつくられた5f!r+の保存剤試料A
−Eを添加した5種の培地を含む試験管各5本に上記の
如き菌液5種を夫々0.4mlづつ分注、添加し、別に
1本菌液無添加のものをつくった。5f made as above! r+ preservative sample A
0.4 ml of each of the five bacterial solutions described above was added to five test tubes each containing the five types of culture medium supplemented with -E, and one tube without any bacterial solution was prepared.
これらを加℃の恒温器中に保存しU時間後の菌数を測定
した。菌数はSPC培地を使用し35℃で冴〜路時間培
養後測定した。These were stored in an incubator at a temperature of 0.degree. C., and the number of bacteria was measured after U hours. The number of bacteria was measured after culturing at 35° C. for a certain period of time using SPC medium.
菌数を測定した結果は図面第1〜5図に示すグラフのと
おりである。第1〜5図は順に大腸菌、乳酸菌、セレウ
ス囚、黄色ブドウ球菌、酵母の菌数変化を示すものであ
る。The results of measuring the number of bacteria are shown in the graphs shown in Figures 1 to 5 of the drawings. Figures 1 to 5 show, in order, changes in the numbers of Escherichia coli, lactic acid bacteria, P. cereus, Staphylococcus aureus, and yeast.
このグラフから明らかなように、リゾチームと低級脂肪
酸モノグリセライドの2種の有効成分からなる保存剤試
料Bの場合は保存剤試料A即ち保存剤鳳添加の場合と同
様に、u時間後いづれの菌の菌数も増加して、各面に対
して何ら静菌作用を示していないが、これに対して本発
明の保存剤1〜3に相当する保存剤試料C−Eを添加し
た場合はU時間後にm数はかなシ減少して、6菌に対し
いづれも著しい静菌作用を示していることが明らかであ
る。殊にリゾチーム、低級脂肪酸モノグリセライド、フ
ィチン酸、酢酸ナトリウムの4種の有効成分を有する保
存剤試料Eの場合は6菌に対して等しく著しい静菌作用
を示しこれら各有効成分が相乗効果を発揮しているのが
見出される。As is clear from this graph, in the case of preservative sample B consisting of two active ingredients, lysozyme and lower fatty acid monoglyceride, as in the case of preservative sample A, i.e., with the addition of preservative, the growth of bacteria after u hours. The number of bacteria also increased and did not show any bacteriostatic effect on each surface, but on the other hand, when preservative samples C-E corresponding to preservatives 1 to 3 of the present invention were added, U time Afterwards, the number of m decreased slightly, and it is clear that all of them exhibited a remarkable bacteriostatic effect against the six bacteria. In particular, in the case of preservative sample E, which has four types of active ingredients: lysozyme, lower fatty acid monoglyceride, phytic acid, and sodium acetate, it showed an equally remarkable bacteriostatic effect against six bacteria, indicating that each of these active ingredients exerts a synergistic effect. It is found that
かくて本発明に係る食品用保存剤は保存剤1〜3ともに
いずれも食品に付着しうる各挿細菌に対してすぐれた静
菌効果を有することが明らかである。Thus, it is clear that all of the food preservatives according to the present invention, Preservatives 1 to 3, have an excellent bacteriostatic effect against various bacterial inoculations that may adhere to foods.
試験例2
次の原料を用いて常法によシカスタートクリームを試作
した。Test Example 2 Deer start cream was experimentally produced using the following raw materials in a conventional manner.
牛乳 250g
砂糖 75g
小麦粉 10g
コーンスターチ 9g
卵黄 25g
計 369g
試作に当9ペースト状のこの原料混合物に試験例1にお
いて用いられた保存剤試料A−Eを混合物取量に対して
1%の量各別に添加し、この混合物を85℃で5分間加
熱した後冷却し、5種のカスター1クリーム試料をつく
った。Milk 250g Sugar 75g Flour 10g Cornstarch 9g Egg yolk 25g Total 369g For trial production 9 To this paste-like raw material mixture, preservative samples A-E used in Test Example 1 were added in an amount of 1% of the amount of the mixture. The mixture was heated at 85° C. for 5 minutes and then cooled to prepare five types of Castor 1 cream samples.
これらの試料を15℃の温度に4日乃至8日間保存して
各日毎に菌数とpHと外観をしらべてfJ′p菌効果全
効果した。その結果は下記の表に示すとおρである。These samples were stored at a temperature of 15° C. for 4 to 8 days, and the number of bacteria, pH, and appearance were checked every day to determine the full effect of the fJ'p bacteria. The results are shown in the table below.
この表から明らかなように保存剤無添加のへの場合は4
日目にして腐敗臭を発生し菌数が108台に達し、有効
成分二つケ含む保存剤試料(n)の場合は6日目にして
腐敗臭を発生し、菌数は+Tl1I定しえぬ程増大した
のに対し、本発明の保存剤1〜3に相当する保存剤試料
C−Eの場合は8日間保存後もいづれも外観に変化なく
菌数も未だ10 〜10の範囲ですぐれた静閑効果を示
していた。As is clear from this table, in the case of no preservatives, 4
On the 6th day, a putrid odor was generated and the number of bacteria reached 108, and in the case of the preservative sample (n) containing two active ingredients, a putrid odor was generated on the 6th day, and the number of bacteria reached +Tl1I. In contrast, in the case of preservative samples C-E, which correspond to preservatives 1 to 3 of the present invention, there was no change in appearance after 8 days of storage, and the number of bacteria was still excellent in the range of 10 to 10. It had a calming effect.
かくてこの試験例2はさきの試験例1とともに本発明に
かかる保存剤1−3がいづれも食品に使用して6菌に対
してすぐれた静菌効果を有する汎用性食品用保存剤であ
ること全庁している。Thus, this Test Example 2, as well as the previous Test Example 1, and Preservatives 1-3 according to the present invention are all general-purpose food preservatives that have excellent bacteriostatic effects against 6 bacteria when used in foods. The entire agency is doing this.
しかも本発明においては3種乃至4種物質を有効成分と
する食品用保存剤1〜3がその中の2種の物質を有効成
分とする保存剤に比べて顕著な静菌効果を示すことから
みてこれら3種乃至4種の物質により相乗された静菌効
果かえられることが明らかである。Moreover, in the present invention, food preservatives 1 to 3 containing three to four kinds of substances as active ingredients exhibit a remarkable bacteriostatic effect compared to preservatives containing two of them as active ingredients. It is clear that a synergistic bacteriostatic effect can be achieved by these three or four types of substances.
かくて本発明は誠にすぐれた食品用保存剤を提供するも
のである。Thus, the present invention provides a truly excellent food preservative.
図面第1〜5図は試験例1に従って各保存剤試料(A−
E)の6菌に対する静菌幼果を示すグラフであって、植
に大腸菌、乳酸菌、セレウス菌、黄色ブドウ球菌及び酵
母に対する場合を示す。
出願人代理人 猪 股 清
第 1 図
第2図Figures 1 to 5 show each preservative sample (A-
It is a graph showing the bacteriostatic seedlings against the six bacteria of E), and shows the case where the inoculations are Escherichia coli, lactic acid bacteria, Bacillus cereus, Staphylococcus aureus, and yeast. Applicant's agent Kiyoshi Inomata 1 Figure 2
Claims (1)
チン酸を有効成分とする食品用保存剤。 2、リゾチーム、低級脂肪酸モノグリセライド及び酢酸
ナトリウムを有効成分とする食品用保存剤。 3、リゾチーム、低級脂肪酸モノグリセライド、フィチ
ン酸及び酢酸ナトリウムを有効成分とする食品用保存剤
。[Claims] 1. A food preservative containing lysozyme, lower fatty acid monoglyceride, and phytic acid as active ingredients. 2. A food preservative containing lysozyme, lower fatty acid monoglyceride, and sodium acetate as active ingredients. 3. A food preservative containing lysozyme, lower fatty acid monoglyceride, phytic acid, and sodium acetate as active ingredients.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14599283A JPS6037965A (en) | 1983-08-10 | 1983-08-10 | Food preservative |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14599283A JPS6037965A (en) | 1983-08-10 | 1983-08-10 | Food preservative |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6037965A true JPS6037965A (en) | 1985-02-27 |
JPS6134793B2 JPS6134793B2 (en) | 1986-08-09 |
Family
ID=15397665
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14599283A Granted JPS6037965A (en) | 1983-08-10 | 1983-08-10 | Food preservative |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6037965A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4814193A (en) * | 1988-04-06 | 1989-03-21 | General Foods Corporation | Reduction of microbial population on surface of food materials |
CN102687841A (en) * | 2011-03-25 | 2012-09-26 | 小川博卫 | Stable powder phytic acid composition and manufacture method thereof |
JP2012213380A (en) * | 2011-03-25 | 2012-11-08 | Hiroe Ogawa | Stabilized powdery phytic acid composition, its production method and food taste quality improver using the composition |
JP2020037543A (en) * | 2018-09-05 | 2020-03-12 | 株式会社日清製粉グループ本社 | Liquid composition for sterilization or bacteriostasis |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994024890A1 (en) * | 1993-04-26 | 1994-11-10 | Eisai Co., Ltd. | Food preservative and food preservation |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4888225A (en) * | 1972-03-02 | 1973-11-19 | ||
JPS5167741A (en) * | 1974-12-09 | 1976-06-11 | Freunt Ind Co Ltd | Shokuhinno hozonhoho |
JPS5231848A (en) * | 1975-09-04 | 1977-03-10 | Sanei Kagaku Kogyo Kk | Method of protecting noodles from deterioration |
-
1983
- 1983-08-10 JP JP14599283A patent/JPS6037965A/en active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4888225A (en) * | 1972-03-02 | 1973-11-19 | ||
JPS5167741A (en) * | 1974-12-09 | 1976-06-11 | Freunt Ind Co Ltd | Shokuhinno hozonhoho |
JPS5231848A (en) * | 1975-09-04 | 1977-03-10 | Sanei Kagaku Kogyo Kk | Method of protecting noodles from deterioration |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4814193A (en) * | 1988-04-06 | 1989-03-21 | General Foods Corporation | Reduction of microbial population on surface of food materials |
CN102687841A (en) * | 2011-03-25 | 2012-09-26 | 小川博卫 | Stable powder phytic acid composition and manufacture method thereof |
JP2012213380A (en) * | 2011-03-25 | 2012-11-08 | Hiroe Ogawa | Stabilized powdery phytic acid composition, its production method and food taste quality improver using the composition |
JP2015211697A (en) * | 2011-03-25 | 2015-11-26 | 博衛 小川 | Stable powder phytic acid composition, method for producing the same, and flavor quality improver for food using the same |
CN102687841B (en) * | 2011-03-25 | 2016-06-22 | 小川博卫 | Stable powdered vegetable acid composition and preparation method thereof |
JP2020037543A (en) * | 2018-09-05 | 2020-03-12 | 株式会社日清製粉グループ本社 | Liquid composition for sterilization or bacteriostasis |
Also Published As
Publication number | Publication date |
---|---|
JPS6134793B2 (en) | 1986-08-09 |
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