JPS62186756A - Method for preservation of rice cake from decay - Google Patents
Method for preservation of rice cake from decayInfo
- Publication number
- JPS62186756A JPS62186756A JP61027607A JP2760786A JPS62186756A JP S62186756 A JPS62186756 A JP S62186756A JP 61027607 A JP61027607 A JP 61027607A JP 2760786 A JP2760786 A JP 2760786A JP S62186756 A JPS62186756 A JP S62186756A
- Authority
- JP
- Japan
- Prior art keywords
- rice cake
- lactic acid
- bacillus
- acid bacteria
- rice
- 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
- 235000007164 Oryza sativa Nutrition 0.000 title claims abstract description 36
- 235000009566 rice Nutrition 0.000 title claims abstract description 36
- 238000000034 method Methods 0.000 title claims description 10
- 240000007594 Oryza sativa Species 0.000 title claims 2
- 238000004321 preservation Methods 0.000 title 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims abstract description 42
- 241000894006 Bacteria Species 0.000 claims abstract description 30
- 239000004310 lactic acid Substances 0.000 claims abstract description 21
- 235000014655 lactic acid Nutrition 0.000 claims abstract description 21
- 241000209094 Oryza Species 0.000 abstract description 34
- 240000006024 Lactobacillus plantarum Species 0.000 abstract description 5
- 235000013965 Lactobacillus plantarum Nutrition 0.000 abstract description 5
- 229940072205 lactobacillus plantarum Drugs 0.000 abstract description 5
- 241000194020 Streptococcus thermophilus Species 0.000 abstract description 4
- 230000006866 deterioration Effects 0.000 abstract description 2
- 238000000354 decomposition reaction Methods 0.000 abstract 1
- 238000000855 fermentation Methods 0.000 abstract 1
- 230000004151 fermentation Effects 0.000 abstract 1
- 241000204117 Sporolactobacillus Species 0.000 description 15
- 244000063299 Bacillus subtilis Species 0.000 description 12
- 235000014469 Bacillus subtilis Nutrition 0.000 description 12
- 241000194108 Bacillus licheniformis Species 0.000 description 10
- 241000519695 Ilex integra Species 0.000 description 9
- 241000193755 Bacillus cereus Species 0.000 description 8
- 241000193830 Bacillus <bacterium> Species 0.000 description 7
- 241000519995 Stachys sylvatica Species 0.000 description 7
- 239000003381 stabilizer Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 4
- 241000186660 Lactobacillus Species 0.000 description 4
- 230000001580 bacterial effect Effects 0.000 description 4
- 229940039696 lactobacillus Drugs 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 229920001817 Agar Polymers 0.000 description 3
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 3
- 239000008272 agar Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000013065 commercial product Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000012258 culturing Methods 0.000 description 3
- 239000008101 lactose Substances 0.000 description 3
- 230000000813 microbial effect Effects 0.000 description 3
- 244000005706 microflora Species 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 239000005022 packaging material Substances 0.000 description 3
- 239000008223 sterile water Substances 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 239000004471 Glycine Substances 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 230000003042 antagnostic effect Effects 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 235000013373 food additive Nutrition 0.000 description 2
- 239000002778 food additive Substances 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 230000002335 preservative effect Effects 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241001660259 Cereus <cactus> Species 0.000 description 1
- 229940123973 Oxygen scavenger Drugs 0.000 description 1
- 241000227425 Pieris rapae crucivora Species 0.000 description 1
- 241000270295 Serpentes Species 0.000 description 1
- 241000212749 Zesius chrysomallus Species 0.000 description 1
- JAWMENYCRQKKJY-UHFFFAOYSA-N [3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-ylmethyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-en-8-yl]-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]methanone Chemical compound N1N=NC=2CN(CCC=21)CC1=NOC2(C1)CCN(CC2)C(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F JAWMENYCRQKKJY-UHFFFAOYSA-N 0.000 description 1
- 230000001028 anti-proliverative effect Effects 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L3/00—Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs
- A23L3/34—Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、餅の変改及び腐敗を防止する技術に関するも
のである。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a technique for preventing tampering and spoilage of rice cakes.
(従来の技術)
餅は餅米を蒸竜しこれを捏和して生成する我国ではよく
知られた繁用食品である。餅の変改及び腐敗を防止しそ
の品質を安定させることは、流通機構を整備する上から
もまた腐敗に起因する疫痛の発生を防止する上からも重
要なことである。(Prior Art) Mochi is a well-known and commonly used food in Japan, which is produced by steaming sticky rice and kneading the rice. Preventing mochi from being tampered with and spoiled, and stabilizing its quality, is important from the perspective of improving the distribution system and preventing the outbreak of epidemics caused by spoilage.
餅の防腐方法はこれまで食品添加物からなる品質安定剤
等を生餅に添加し、これによるカビや細菌の発生を防止
する方法が多用されて来ていた。Up until now, the most commonly used method for preserving rice cakes has been to add quality stabilizers made of food additives to raw rice cakes to prevent the growth of mold and bacteria.
包装餅の変改防止は、製造環境のクリーン化又は食品添
加物、脱酸素剤、若しくは包材等の使用によってシステ
ム化されているが、食品添加物による変改防止はグリシ
ン(特公昭50−11969号公報)、クエン酸を中心
とする有機酸(特公昭57−1215号公報)と甘味料
の併用が開示され°ζいる。Preventing tampering with packaged rice cakes has been systematized by cleaning the manufacturing environment or using food additives, oxygen absorbers, or packaging materials. Japanese Patent Publication No. 11969), and the combined use of an organic acid, mainly citric acid (Japanese Patent Publication No. 1215/1983), and a sweetener have been disclosed.
ガスバリアー性能の高い密封包材中に餅を保持し、鉄系
の胸酸素剤(特開昭55−104867号公報)や脱酸
素剤と炭酸ガス吸収剤の併用(特開昭56−11326
4号公報)等によって、包材内を無酸素又は無炭酸ガス
状態にして変敗菌の増殖を抑制する方法が開示されてい
る。The rice cakes are held in a sealed packaging material with high gas barrier performance, and iron-based chest oxygen agents (Japanese Patent Application Laid-Open No. 104867/1982) or a combination of oxygen scavengers and carbon dioxide absorbers (Japanese Patent Application Laid-Open No. 11326/1982) are used.
Publication No. 4) and others disclose a method of suppressing the growth of spoilage bacteria by creating an oxygen-free or carbon dioxide-free state within the packaging material.
(発明が解決しようとする問題点)
ところがこれらの方法では、添加すべき品質安定剤を増
やせばそれだけ防腐効果は高まるものの、餅の品質を劣
化させ若しくは人体に悪い影響をもらたず等の好ましか
らざる結果を招来することとなっていた。そこで、本発
明者らは上記品質安定剤等を使用せずにしかも一定以上
の防腐効果をあげることができる方法を摸索することと
なった。(Problems to be Solved by the Invention) However, in these methods, although the preservative effect increases as the amount of quality stabilizers to be added increases, it does not deteriorate the quality of the rice cake or has a negative effect on the human body, etc. This would have led to negative results. Therefore, the present inventors searched for a method that could achieve a preservative effect above a certain level without using the above-mentioned quality stabilizers.
(問題点を解決するための手段)
本発明者らは上記視点から種々の検討を行った結果、餅
腐敗時に腐敗菌とともに同時に発生ずる乳酸菌が<シフ
も腐敗菌の増殖を阻害していることを発見するに至り、
当該乳酸菌そのものが腐敗現象を防止する効果があるこ
とを突き止めた。そごで更に研究を続行するうち、乳酸
菌を添加した餅は品質安定剤を添加した餅よりもその安
定性が優れかつ腐敗がもののみごとに防止されることを
発見した。そして乳酸菌の増殖によって餅のpl+も若
干は低下するものの酸味は全く感じることがなく食味の
点でも問題のないことを確認し本発明を完成するに至っ
た。(Means for Solving the Problems) As a result of various studies from the above viewpoint, the present inventors found that lactic acid bacteria, which are generated simultaneously with putrefaction bacteria when rice cakes rot, also inhibit the growth of putrefaction bacteria. I came to discover that
It was discovered that the lactic acid bacteria themselves are effective in preventing spoilage. As Sogo continued his research, he discovered that mochi to which lactic acid bacteria had been added had better stability than mochi to which quality stabilizers had been added, and was better able to prevent spoilage. Although the pl+ of the rice cake decreased slightly due to the proliferation of lactic acid bacteria, it was confirmed that no sourness was felt at all and there was no problem in terms of taste, leading to the completion of the present invention.
本発明の要旨は、餅に乳酸菌を添加することにある。The gist of the present invention is to add lactic acid bacteria to rice cake.
乳酸菌としては、本発明の効果を表わすものであればい
ずれの種頬のものでも使用することができる。本発明に
係る乳酸菌としては、例えば、ラクトバチルス・ブラン
フルム(Lactobacillus plnnLnr
llm ) 、ストレプトコッカス・テルモフィルス(
SLrepLococcus tbermophilu
s) 、スポロラクトバチルス(Sporolacto
bacillus)等を挙げることができる。本発明の
実施にあたっては、乳f’rJ 1.¥iのうちこれら
ホモ醗酵型乳酸菌が好ましい。As the lactic acid bacteria, any type of lactic acid bacteria can be used as long as it exhibits the effects of the present invention. As the lactic acid bacteria according to the present invention, for example, Lactobacillus plnnLnr
llm), Streptococcus thermophilus (
SLrepLococcus tbermophilu
s), Sporolactobacillus
bacillus), etc. In carrying out the present invention, milk f'rJ 1. Of these, these homofermentative lactic acid bacteria are preferred.
これらの乳酸菌を餅に添力1目°る場合には、Illを
1島き上げる前に練り込んで添加する方法のばか、餅1
rj+き上げ後冷却後に噴7i等の方法で餅の表面に添
加する方法をとることができる。If you want to add these lactic acid bacteria to mochi, you should knead it into the rice cake before adding it to the rice cake.
After rj+ raising and cooling, it can be added to the surface of the rice cake using a method such as injection 7i.
また生切餅の場合には、包装前に乳酸菌の培養液を噴霧
又は浸漬する方法等によって本発明を実施することがで
きる。In the case of raw cut rice cakes, the present invention can be carried out by spraying or dipping them in a culture solution of lactic acid bacteria before packaging.
(実施例)
以下に実施例を掲げ°C1本発明を更に詳しく説明する
。(Example) The present invention will be described in more detail with reference to Examples below.
実施例1
餅米8kgを、24時間水浸しく水浸後9.6kr)、
吸水米1.2kg(10フト分)を、底部ボイラーに水
310m1を入れた自動餅搗き機(東芝へFC153型
)を使用して蒸し上げた。この蒸し米に乳酸閉未(5x
109 ccll/g ) 1.5gとバチJLtス
ーズブ−f−IJス芽胞液(Bacillus sub
目1is PCI−219株を1tri lず5寒天斜
面培地で30℃で48時間培養後、室温で2週間放置し
て芽胞を形成させ、その芽胞を滅菌水に’、73調(1
,6X107spores/ml)させたもの)1ml
と乳糖15gを添加し、9分間で搗き上げた。仕上がり
OJf、 (約1.5kg)を折径10cmのタレハロ
ンケーシングに充填し、85℃で1分間加熱後、冷却し
て仕上がりとした。Example 1 8 kg of sticky rice was soaked in water for 24 hours (9.6 kr),
1.2 kg (10 feet) of water-absorbed rice was steamed using an automatic rice cake pounder (Model FC153 to Toshiba) with 310 ml of water in the bottom boiler. This steamed rice contains lactic acid (5x
109 ccll/g) 1.5g and Bacillus sub
After culturing 1 is PCI-219 strain in 1 trial 5 agar slant medium at 30°C for 48 hours, leave it at room temperature for 2 weeks to form spores, and incubate the spores in sterile water with 73 samples (1
,6X107spores/ml)) 1ml
and 15 g of lactose were added and stirred up for 9 minutes. Finished OJf (approximately 1.5 kg) was filled into a Talehalon casing with a folded diameter of 10 cm, heated at 85° C. for 1 minute, and then cooled to give a finished product.
上記ケーシング餅を、30℃で保存し、pH、細菌数、
微生物置の変化を試験した。The above casing mochi was stored at 30°C, and the pH, bacterial count,
Changes in microbial location were tested.
更に無菌的にケーシングを剥ぎ、縦に切断して無菌シャ
ーレに入れ、室温及び30℃で保存して白斑点や赤斑点
の発生状況を観察した。Furthermore, the casing was removed aseptically, cut lengthwise, placed in a sterile petri dish, and stored at room temperature and 30°C to observe the occurrence of white spots and red spots.
ケーシング餅検体内容は下記の通りである。The contents of the casing mochi sample are as follows.
各検体とも、バチルス・ズブチリス芽胞は、1.1X1
0’ cell/g 、乳糖は1 、0 %6を含む。For each sample, Bacillus subtilis spores were 1.1×1
0' cell/g, lactose contains 1,0%6.
また市販品Nは品質安定剤であっ°ζ、グリシンと有機
酸とを組合せた製品である。Commercially available product N is a quality stabilizer °ζ, which is a product that combines glycine and an organic acid.
■はラクトバチルス・ブランフルム
(Lactobacillus plantarum
) (IlanSOn社II<J 。■ is Lactobacillus plantarum
) (IlanSOn Company II<J.
LACTO−START 03゜以下同様)を、■はス
トレプトコッカス・テルモフィルス(S Lrep L
ococcusLhcrmopl+1lus)を、また
■はスポロラクトバチルス(Sporolactoba
cillus) (三共株式会社製、ラフリスS。以
下同様)を、それぞれ表わす。LACTO-START 03° and below), ■ is Streptococcus thermophilus (S Lrep L
ococcus Lhcrmopl+1lus), and ■ is Sporolactobacillus (Sporolactobacillus).
cillus) (manufactured by Sankyo Co., Ltd., Lafrys S. The same applies hereinafter), respectively.
保存中のpH、生菌数、微生物広の変化は第1表に示し
た。また、室温(20〜25℃)でのωを保存中の外観
の観察結果(シャーレ中)は第2表に示した。Changes in pH, number of viable bacteria, and microbial prevalence during storage are shown in Table 1. In addition, the observation results of the external appearance (in a petri dish) during storage of ω at room temperature (20 to 25°C) are shown in Table 2.
(以下次頁)
第1表中、生菌数の単位は、XIO’ CPU/g、
微生物叢中■はバチルス・ズブチルス、■はスポロラク
トバチルスを表わす。(See next page) In Table 1, the units of viable bacteria count are XIO' CPU/g,
In the microflora, ■ represents Bacillus subtilis, and ■ represents Sporolactobacillus.
第2表は斑点発生状況を表わすものである(−:発生を
認めず。±:わずかに発生。+:発生を認む。+1−:
発生大)。表中数字は経過日数を表わす。Δ、B、Dは
白斑点で、餅全体が赤みを帯びてきた。また、C,Eで
は黒斑点であった。Table 2 shows the status of spot occurrence (-: No occurrence observed. ±: Slight occurrence. +: Occurrence observed. +1-:
large outbreak). The numbers in the table represent the number of days that have passed. Δ, B, and D have white spots, and the entire mochi has become reddish. In addition, black spots were observed in C and E.
検体へ〜Eは、pHの変動も少なく、微生物叢もバチル
ス・ズブチリス以外には認められなかった。In sample E, there was little variation in pH, and no microflora other than Bacillus subtilis was observed.
これは耐熱性の比較的強い、ラクトバチルス・プランタ
ルム、ストレプトコッカス・テルモフィルスを選定した
が、やはり餅仕上がり温度に耐えられず、死滅してしま
ったものと考えられる。Lactobacillus plantarum and Streptococcus thermophilus, which have relatively strong heat resistance, were selected, but it is thought that they could not withstand the temperature at which the rice cake was finished and died.
また、Δ、B、DとC,Eとの比較により、市販品Nの
バチルス・ズブチリス抑制効果は、余り認められないこ
とがわかる。Furthermore, by comparing Δ, B, and D with C and E, it can be seen that the Bacillus subtilis inhibiting effect of commercial product N is not so recognized.
バチルス・ズブチリスの餅表面の変改形態は、市販品N
の有無で若干具なり、市販品N無添加の場合は通常よく
みられる白斑点として観察されるが、市販品N添加検体
は黒褐色の斑点として出現している。The modified form of the rice cake surface of Bacillus subtilis is commercially available product N.
In the case of the commercially available N-free sample, it is observed as a common white spot, but in the sample with the commercially available N added, it appears as a blackish brown spot.
スポロラクトバチルス単独添加の場合、T、Q生物恣に
しめるスポロラクトバチルス
間とともに増加し、それに伴い餅のpl+も低下して最
終的にはスポロラクトバチルスのみとなった。When sporolactobacillus was added alone, the number of sporolactobacilli that were detected by T and Q organisms increased, and the pl+ of the rice cake decreased accordingly, and eventually only sporolactobacillus remained.
乳酸菌の拮抗作用によりバチルス・ズブチリスの増η(
1が抑制され、斑点発生を抑制したごとが明白である。Increase in Bacillus subtilis due to the antagonistic action of lactic acid bacteria (
1 was suppressed, and it was clear that the occurrence of spots was suppressed.
検体Gの結果をみてみると、市販品NはスボI−1ラク
トバチルス及びバチルス・ズブチリスの両方の菌の生育
を抑制するためか、スポロラクトバチルスの生育に対す
る拮抗作用が充分には発叩されず、スポロラクトバチル
スと市販品Nの併用は却って良くない結果をもたらして
いる。スポロラクトバチルス単独添加の方が保存性が良
いことが判った。Looking at the results for sample G, it appears that commercial product N suppresses the growth of both Lactobacillus subI-1 and Bacillus subtilis, but its antagonistic effect on the growth of Sporolactobacillus is not sufficiently strong. However, the combined use of Sporolactobacillus and commercial product N has produced rather poor results. It was found that the addition of Sporolactobacillus alone had better storage stability.
ラクトバチルス・プランタルレム、ストレブト二1ッカ
ス・テルモフィルス等を添加する場合には、その耐熱性
を考慮して、餅の冷却後に菌液を表面噴霧する等の方法
を採ることができる。When adding Lactobacillus plantarum, Strebuticus thermophilus, etc., a method such as spraying a bacterial solution on the surface of the rice cake after cooling may be adopted, taking into account its heat resistance.
実施例2
実施例1と同様の方法によってケーシング餅を、 製
造した。変敗菌として実施例1のバチルス・ズブチリス
の代わりに、バチルス・リケニフォルミス(Bacjl
lus !icl+eniformis) IFO−1
2107及び、バチルス・セレウス(Bacillus
cereus ) OUT−8032を使用した。芽
胞液は、同株を標準寒天斜面培地で30℃で48時間培
養後、室温で2週間放置し、芽胞を形成させてその芽胞
を滅菌水に)U濁させ(バチルス・リケニフォルミス3
.I X 10’ spores/m1、バチルス・セ
レウス2.2X106spores/ml)°ζ151
すl した。Example 2 A casing rice cake was produced in the same manner as in Example 1. Instead of Bacillus subtilis in Example 1, Bacillus licheniformis was used as the spoilage bacterium.
Lus! icl+eniformis) IFO-1
2107 and Bacillus cereus
cereus) OUT-8032 was used. The spore solution was prepared by culturing the same strain on a standard agar slant medium at 30°C for 48 hours, leaving it at room temperature for 2 weeks to form spores, and making the spores turbid (Bacillus licheniformis 3) in sterile water.
.. I X 10' spores/ml, Bacillus cereus 2.2
I was bored.
芽胞液の■はバチルス・リケニフォルミス、■はバチル
ス・セレウスを表わす。iQ位はcell/gである。■ in the spore fluid represents Bacillus licheniformis, and ■ represents Bacillus cereus. iQ rank is cell/g.
乳酸菌の■はスポロラクトバチルスを表わす。単位はc
ell/gである。安定剤はグリシンと有機酸と組合せ
たものである。■ of lactic acid bacteria represents Sporolactobacillus. The unit is c
ell/g. The stabilizer is a combination of glycine and an organic acid.
ケーシング餅を30℃で保存しpl+、細菌数、微生物
叢の変化を第3表に示した。また、無菌的にゲージング
を剥ぎ、縦に切断して無菌シャーレに入れ、室温及び3
0℃で保存してバチルスによる斑点発生状況を観察し第
4表に示した。The casing rice cakes were stored at 30°C, and changes in pl+, bacterial count, and microflora are shown in Table 3. In addition, aseptically remove the gauging, cut it lengthwise, place it in a sterile petri dish, and keep it at room temperature for 30 minutes.
The samples were stored at 0°C and the appearance of bacillus spots was observed, and the results are shown in Table 4.
(以下次頁)
第3表中、生菌数の単位は、X104 C同/g、微
生物叢中■はスポロラクトバチルス、■はバチルス・リ
ケニフォルミス、■はバチルス・セレウスを表わす。(See next page below) In Table 3, the unit of the number of viable bacteria is X104C/g, and in the microbial flora, ■ represents Sporolactobacillus, ■ represents Bacillus licheniformis, and ■ represents Bacillus cereus.
第4表は白斑点発生状況を表わすものである。Table 4 shows the occurrence of white spots.
表中数字は経過日数を表わす、いずれも30℃で保存し
た。巳は実験に供していない。The numbers in the table represent the number of days that have passed. All samples were stored at 30°C. The snake was not used for experiments.
バチルス・リケニフォルミス単独添加の場合には、9[
1目あたりから斑点が発生した。しかし、バチルス・リ
ケニフォルミスとスポロラクトバチルスを併用添加した
場合、検出されるバチルス・リケニフォルミス菌はほと
んどなく、斑点も全く発生しなかった。When Bacillus licheniformis is added alone, 9[
Spots appeared from around the first eye. However, when Bacillus licheniformis and Sporolactobacillus were added together, very few Bacillus licheniformis bacteria were detected and no spots were observed.
スポロラクトバチルスのバチルス・リケニフォルミスに
対する増殖阻止作用が明白である。The antiproliferative effect of Sporolactobacillus on Bacillus licheniformis is evident.
また、バチルス・セレウスの場合も、バチルス・リゲニ
フォルミスの場合と全く同様の結果となったことが判っ
た。It was also found that the results for Bacillus cereus were exactly the same as for Bacillus ligeniformis.
スポロラクトバチルスのみが添加された餅の場合には、
生菌数そのものは保存とともに漸減してゆくが、pHは
順調に低下してゆく。スポロラクトバチルスの活発な代
謝による乳酸生成が起こっていることが明白である。こ
の乳酸やその他の生成過酸化物(1202など)等によ
りバチルスの増殖を抑制していると考えることができる
。In the case of rice cakes containing only Sporolactobacillus,
Although the number of viable bacteria itself gradually decreases with storage, the pH steadily decreases. It is clear that lactic acid production is occurring due to the active metabolism of Sporolactobacillus. It can be considered that the growth of Bacillus is suppressed by this lactic acid and other produced peroxides (1202, etc.).
実施例3
実施例1と同様の方法によってケーシング餅を製造した
。変敗菌としてバチルス・スブチリスl)CI −21
9、バチルス・リケニオルミスIFO−12107、及
びバチルス・セレウスOU i’ −8032を使用し
た。Example 3 A casing rice cake was produced in the same manner as in Example 1. Bacillus subtilis as a spoilage bacterium CI-21
9, Bacillus licheniormis IFO-12107, and Bacillus cereus OU i'-8032.
1211. 芽胞液は同株を標準寒天斜面
培地で30’C148時間培養後、室温で2週間放置し
芽胞を形成さ−l°ζ、その芽胞を滅菌水に懸濁させ(
バチルス・ズブチリス2.5X10’ 5pores/
ml、バチルス・りう゛ニブオルミス2.3X10フs
poresフウス1.2XlO’ 5pores/ml
)で1周j醐した。1211. The spore solution was prepared by culturing the same strain on a standard agar slant medium for 30°C for 148 hours, leaving it at room temperature for 2 weeks to form spores, and suspending the spores in sterile water (
Bacillus subtilis 2.5X10' 5pores/
ml, Bacillus riunibuormis 2.3X10fus
pores 1.2XlO' 5pores/ml
), I was very happy with it for one lap.
各検体別に所定の変敗菌と乳糖を添加してケーシング餅
をiJi!Ii!!L、冷却、硬化後、無菌的にスライ
スして切餅とした。次に検体13,l)、Fの切βノ1
をラクトバチルス・ブランフルム(Lac tobac
i l I usplanLarum)の菌懸濁液(
e.oxiov ccll/ml)に30秒間浸漬後
、無菌的に風乾した。iJi! Add the designated spoilage bacteria and lactose to each sample and make casing mochi! Ii! ! L: After cooling and hardening, it was sliced aseptically into cut rice cakes. Next, sample 13, l), cut β of F
Lactobacillus branfrum (Lac tobac
I l I usplanLarum) bacterial suspension (
e. oxiov ccll/ml) for 30 seconds, and then air-dried aseptically.
芽胞液の■はバチルス・ズブチリス、■はバチルス・リ
ケニフォルミス、■はバチルス・セレウスを表わす。単
位はcell/gである。乳酸菌■はラクトバチルス・
ブランフルムを表わす。■ in the spore fluid represents Bacillus subtilis, ■ represents Bacillus licheniformis, and ■ represents Bacillus cereus. The unit is cell/g. Lactic acid bacteria■ is Lactobacillus
Represents Branflum.
検体切餅は、無菌シャーレに入れ、30℃で保存して白
斑点の発生状況を観察し第5表に示した。The sample cut rice cakes were placed in a sterile petri dish and stored at 30° C., and the occurrence of white spots was observed as shown in Table 5.
(以下次頁) 第5表 第5表は白斑点発生状況を表わすものである。(Next page below) Table 5 Table 5 shows the occurrence of white spots.
表中数字は経過時間を表わす。ラクトバチルス・プラン
タルム菌液浸漬処理を行っていない検体A、C,Eはそ
の各々の変敗菌バチルス・ズブチリス、バチルス・リケ
ニフオルミス、バチルス・セレウスによる白斑点が発生
した。これに対して浸漬処理を行った検体B,D,Fは
全く白斑点は発生せず、食味は長期に亘って正常に維持
された。このような浸漬処理法によっても餅の変改を防
止できることが1男白である。The numbers in the table represent elapsed time. Specimens A, C, and E, which were not subjected to the Lactobacillus plantarum solution immersion treatment, developed white spots due to their respective decomposing bacteria, Bacillus subtilis, Bacillus licheniformis, and Bacillus cereus. On the other hand, samples B, D, and F, which were subjected to the immersion treatment, had no white spots at all, and the taste remained normal over a long period of time. It is a fact that such a soaking treatment method can also prevent deterioration of the rice cake.
Claims (1)
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61027607A JPS62186756A (en) | 1986-02-10 | 1986-02-10 | Method for preservation of rice cake from decay |
KR870001053A KR870007667A (en) | 1986-02-10 | 1987-02-10 | Prevention of Rice Cake Decay |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61027607A JPS62186756A (en) | 1986-02-10 | 1986-02-10 | Method for preservation of rice cake from decay |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62186756A true JPS62186756A (en) | 1987-08-15 |
JPS6359667B2 JPS6359667B2 (en) | 1988-11-21 |
Family
ID=12225612
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61027607A Granted JPS62186756A (en) | 1986-02-10 | 1986-02-10 | Method for preservation of rice cake from decay |
Country Status (2)
Country | Link |
---|---|
JP (1) | JPS62186756A (en) |
KR (1) | KR870007667A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100297521B1 (en) * | 1999-01-09 | 2001-09-13 | 이상윤 | A method for the preparation of ddugboggi with a long shelf-life at room temperature |
KR100345185B1 (en) * | 1999-11-11 | 2002-07-24 | 조남지 | Rice cake and producing method thereof |
KR100645089B1 (en) * | 2004-07-08 | 2006-11-10 | 주식회사 바이오리더스 | Food Preservatives Comprising Culture broth of Lactic Acid Bacteria and Poly-?-glutamic Acid |
KR101030117B1 (en) * | 2008-09-10 | 2011-04-20 | 김순기 | Manufacturing method of rice cake composition and rice cake |
-
1986
- 1986-02-10 JP JP61027607A patent/JPS62186756A/en active Granted
-
1987
- 1987-02-10 KR KR870001053A patent/KR870007667A/en not_active Application Discontinuation
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100297521B1 (en) * | 1999-01-09 | 2001-09-13 | 이상윤 | A method for the preparation of ddugboggi with a long shelf-life at room temperature |
KR100345185B1 (en) * | 1999-11-11 | 2002-07-24 | 조남지 | Rice cake and producing method thereof |
KR100645089B1 (en) * | 2004-07-08 | 2006-11-10 | 주식회사 바이오리더스 | Food Preservatives Comprising Culture broth of Lactic Acid Bacteria and Poly-?-glutamic Acid |
KR101030117B1 (en) * | 2008-09-10 | 2011-04-20 | 김순기 | Manufacturing method of rice cake composition and rice cake |
Also Published As
Publication number | Publication date |
---|---|
JPS6359667B2 (en) | 1988-11-21 |
KR870007667A (en) | 1987-09-21 |
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