KR20090026849A - Efficient Preparation of Lactic Acid Bacteria Beverage Using Eggs - Google Patents
Efficient Preparation of Lactic Acid Bacteria Beverage Using Eggs Download PDFInfo
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Preparation or treatment thereof
- A23L2/38—Other non-alcoholic beverages
- A23L2/382—Other non-alcoholic beverages fermented
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23B—PRESERVATION OF FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES; CHEMICAL RIPENING OF FRUIT OR VEGETABLES
- A23B70/00—Preservation of non-alcoholic beverages
- A23B70/30—Preservation of non-alcoholic beverages by heating
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L15/00—Egg products; Preparation or treatment thereof
- A23L15/25—Addition or treatment with microorganisms or enzymes
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Preparation or treatment thereof
- A23L2/52—Adding ingredients
- A23L2/60—Sweeteners
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Preparation or treatment thereof
- A23L2/52—Adding ingredients
- A23L2/68—Acidifying substances
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2400/00—Lactic or propionic acid bacteria
- A23V2400/11—Lactobacillus
- A23V2400/113—Acidophilus
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2400/00—Lactic or propionic acid bacteria
- A23V2400/21—Streptococcus, lactococcus
- A23V2400/249—Thermophilus
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2400/00—Lactic or propionic acid bacteria
- A23V2400/51—Bifidobacterium
- A23V2400/533—Longum
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Abstract
Description
본 발명은 유산균음료의 제조방법에 관한 것으로서, 특히 난황과 난백이 혼합된 전란액(全卵液)을 균질화하여 포도당과 과당 및 물을 첨가한 후 이에 추가적으로 유기산을 첨가하여 전란액의 수소이온농도를 조절하고 가열처리로서 살균과 유산균성장 억제효소의 열변성을 유도하며, 락토바실러스 아시도필루스(Lactobacillus acidophilus), 비피도박테리움 론검(Bifidobacterium longum) , 스트렙토코커스 써 모필루스(Streptococcus thermophilus)의 혼합유산균을 접종하여 배양, 발효시키는 계란을 이용한 유산균음료의 효율적 제조방법에 관한 것이다. 본 발명의 공정 중 주요 기술은 계란의 살균 공정 시 열 응고를 일으키지 않고 살모넬라를 비롯한 유해세균을 효과적으로 살균하는 기술과 우유의 6.7에 비해 높은 7.5의 수소이온농도를 가진 계란을 단시간에 목표 수소이온농도인 4.5 이하로 도달하게 하는 방법을 포함한다.The present invention relates to a method for producing a lactic acid bacteria beverage, in particular, homogenizing a whole egg solution mixed with egg yolk and egg white, adding glucose, fructose and water, and then adding an organic acid to the hydrogen ion concentration of the egg yolk solution. Control and heat treatment of lactic acid bacteria growth inhibitory enzyme as a heat treatment, Lactobacillus Lactobacillus acidophilus ), Bifidobacterium longum ), Streptococcus thermophilus ( Leptococcus thermophilus ) to inoculate, inoculate, culture, fermentation, and a method for the efficient production of lactic acid bacteria beverages using eggs. The main technology of the process of the present invention is a technique for effectively sterilizing harmful bacteria including Salmonella without causing heat coagulation during egg sterilization process and a target hydrogen ion concentration in a short time for eggs having a high hydrogen ion concentration of 7.5 compared to 6.7 in milk. To reach 4.5 or less.
계란의 열안정성에 대한 연구에 의하면 계란 자체에 존재하거나 혹은 2차적인 요인으로 인한 계란 내의 유해세균을 사멸시키기 위하여 열처리를 실시할 경우, 난백의 열안정성은 당이나 Fe+++, Al+++, Cu++ 같은 금속염에 의해 영향을 받으며 이러한 금속염을 첨가하고 60℃에서 5분간 가열하면 기포성이 증진된다고 알려져 있다. 또한, 1973년 발드윈(Baldwin)은 난백의 열응고성은 온도, 난백의 농도, 공존하는 염, 당 및 pH에 의해서 영향을 받는다고 보고한 바 있으며, 1985년 이사하라 로조우(石原浪三) 등은 염류는 열응고성을 촉진하지만 비전해질인 당의 첨가는 단백질 소수성기의 물에 대한 친화성을 높게 하기 때문에 염의 첨가와는 반대로 가열할 때 단백질 분자 간의 소수결합에 의한 분자 간의 회합을 억제하여 열에 의한 응고(coagulation) 억제로 난백의 열안정성을 증가시키는 것으로 추측하였다.Studies on the thermal stability of eggs have shown that when heat treatment is performed to kill harmful bacteria in eggs due to the eggs themselves or due to secondary factors, the thermal stability of egg whites is higher than sugar, Fe ++ +, and Al ++. It is known to be affected by metal salts such as + and Cu ++ and to increase the foamability by adding these metal salts and heating at 60 ° C. for 5 minutes. In 1973, Baldwin reported that egg whites' thermal coagulation was influenced by temperature, egg white concentration, coexisting salts, sugars and pH.In 1985, Isahara Rozou (石 原 浪 三) Although salts promote thermocoagulation, the addition of sugars, which are non-electrolytes, increases the affinity for water of protein hydrophobic groups to water, which, in contrast to the addition of salts, inhibits the association between molecules due to hydrophobic bonds between protein molecules when heated. Inhibition of coagulation was thought to increase the thermal stability of egg whites.
그리고 유산균을 이용한 계란발효에 대한 연구로는 주로 계란에 존재하는 소 량의 포도당을 제거하여 건조된 계란의 저장중 변색 등 품질의 변화를 억제할 목적으로 연구가 진행된 바 있다. 즉, 1974년 갈루조(Galluzzo)등은 헤테로(hetero) 발효균인 스트렙토코커스 디아세틸락티스(Streptococcus diacetilactic)와 루코노스톡 시피시스(Leuconostoc species)의 혼합균주를 이용하여, 1974년 하메드(Hamed)와 사덱(Sadek)은 페니실리움 노타툼(Penicillium notatum)에서 분리한 글루코스 옥시디아제(glucose oxidase)와 카탈라아제(catalase)복합효소를 이용하여 난백액에서 당을 제거하였고, 또한 1978년 쉬하브(Shehab)등이 스트렙토코커스 락틱스(Streptococcus lactis)와 0.2%의 효모추출물(yeast extract)를 난백에 첨가하고, pH 6.0, 30℃의 조건에서 9시간 배양으로 포도당(glucose)을 완전히 제거하였다고 보고하는 등, 분말상태의 난황, 난백단백질, 전란의 안정성 향상을 위한 연구가 1980년대 이전까지 이 분야 연구의 대부분이었다.In addition, the study on the fermentation of eggs using lactic acid bacteria has been conducted to suppress the change of quality such as discoloration during storage of dried eggs mainly by removing a small amount of glucose present in eggs. In other words, go rujo 1974 (Galluzzo) etc. heterocyclic (hetero) zymogen of diacetyl Streptococcus lactis (Streptococcus Using a mixed strain of diacetilactic and Leuconostoc species , Hamed and Sadec in 1974 were isolated from glucose oxidase isolated from Penicillium notatum . ) And catalase complexase were used to remove sugar from egg whites.In 1978, Shehab et al. Added Streptococcus lactis and 0.2% yeast extract to egg whites. This study was conducted to improve the stability of egg yolk, egg white protein and whole egg before the 1980s, including adding glucose and reporting that glucose was completely removed by incubating for 9 hours at pH 6.0 and 30 ℃. Was most of.
한편, 액상발효음료제품의 제조에 계란을 이용한 연구로는 1984년 린(Lin)과 커닝햄(Cunningham)이 난백을 이용하여 요구르트(yoghurt)형태의 제품 개발을 시도하였는데 유산균의 생육을 촉진시키기 위하여 성장배지로써 28.4%의 알칼리처리 대두유와 19.0%의 탈지유를 살균하여 혼합하고, 포도당(glucose), 설탕(sucrose), 잔산검(xanthan gum), 바닐라(vanilla) 추출물 등을 첨가하여 락토바실러스 불가리쿠스(L. bulgaricus)를 접종, 양질의 요구르트형 제품을 얻을 수 있었음을 보고하였고, 1984년 커닝햄(Cunningham)등은 저지방 균질유를 살균, 냉각시킨 후 여기에 54.4℃로 2회 살균, 냉각한 난백 알부민(albumin)을 균질화하여 미리 살균, 냉각된 저지방 균질유에 혼합 락토바실러스 불가리쿠스(Lactobacillus bulgaricus), 스트 렙토코커스 써머필루스(Streptococcus thermophilus) 혼합균주 5%를 접종하여 40℃에서 6시간 배양하여 요구르트형의 스낵식품을 제조하였는데 제조된 것이 전체적인 칼로리도 낮고 기호도 또한 높았다고 보고하였다.Meanwhile, in 1984, Lin and Cunningham attempted to develop yoghurt-type products using egg white, which were grown to promote the growth of lactic acid bacteria. As a medium, 28.4% of alkaline treated soybean oil and 19.0% of skim milk were sterilized and mixed, and glucose, sugar, xanthan gum, vanilla extract, and the like were added to Lactobacillus vulgaris. L. bulgaricus ) was inoculated and reported that a good quality yogurt-type product was obtained. In 1984, Cunningham et al. Sterilized and cooled low-fat homogeneous milk, and then sterilized and cooled twice at 54.4 ° C. Lactobacillus bulgaricus , Streptococcus thermophilus, homogenized (albumin) and mixed in pre-sterilized, cooled low-fat homogenous oil The mixture was inoculated with 5% thermophilus strain and incubated at 40 ° C. for 6 hours to prepare a yogurt-type snack food, which reported low overall calories and high preference.
또한, 1983년 김 등은 58℃, 30분의 열처리 조건으로 균질전란액에 포도당(glucose), 설탕(Sucrose), 유당(lactose)을 첨가하고, 스트렙토코커스 락티스(Streptococcus lactis ), 락토바실러스 카세이(Lactobacillus casei), 스트렙토코커스 피카리스(Streptococcus faecalis)를 접종하여 발효중 변화를 관찰하여 당의 첨가가 이들 유산균의 성장을 촉진하였고, 스트렙토코커스 피카리스(Streptococcus faecalis)의 생육이 가장 좋았음을 보고하였으며, pH를 최저 4.8까지 떨어뜨렸다고 하였다. 또한 고(1997)는 난백분말에 전지분유, 탈지분유, 유청분말, 카제인 등 4종의 유제품을 첨가하여 기질을 만들고 유산균을 접종하여 요구르트형 발효제품을 만들어 유산균의 생육, 산 생성 및 품질에 미치는 영향을 조사한 바 대조구인 우유 요구르트보다 품질이 저조했다고 보고한 바 있다.Also, in 1983, Kim et al. Added glucose (glucose), sugar (Sucrose), lactose (lactose) to the homogeneous transfer liquid under a heat treatment condition of 58 ℃, 30 minutes, Streptococcus lactis ) , Lactobacillus casei ) and Streptococcus faecalis were inoculated to observe changes during fermentation, and the addition of sugars promoted the growth of these lactic acid bacteria, and the best growth of Streptococcus faecalis was reported. Was dropped to a minimum of 4.8. In addition, Ko (1997) added four types of dairy products such as whole milk powder, skim milk powder, whey powder, and casein to egg white powder to make substrates and inoculated lactic acid bacteria to make yogurt-type fermented products. Investigations of the effects reported poor quality than the control milk yogurt.
일본 특허공고(공고번호: 소 57-54113)에는 난백에 존재하여 미생물의 생육을 억제하는 리소자임(lysozyme)을 제거한 건조멸균난백 100g을 멸균 우유 1리터에 용해하고, 포도당 60g을 첨가한 후, 락토바실러스 불가리커스(Lactobacillus bulgaricus), 스트렙토코커스 서머피루스(Streptococcus thermophilus)의 혼합균주 300㎖를 접종, 40℃에서 8시간 배양하여 최종제품의 유산함량 4.0%의 유산발효향이 강한 제품을 얻는 기술이 개시되어 있다.In Japanese Patent Publication (Notice No. 57-54113), 100 g of dried sterile egg whites, which have been removed from lysozyme, which is present in egg white and suppresses the growth of microorganisms, is dissolved in 1 liter of sterile milk, and 60 g of glucose is added, followed by lactose. Inoculate 300 ml of mixed strains of Lactobacillus bulgaricus and Streptococcus thermophilus , and incubate at 40 ° C for 8 hours to obtain a product with strong lactic acid fermentation fragrance with a lactic acid content of 4.0%. It is.
계란을 이용한 유산균음료와 관련된 국내 특허로는 특허 제115910호로서 유 와 이(1994)가 계란에 유당, 설탕, 물을 첨가하여 혼합한 후 열처리하여 살균과 난단백질의 열변성을 유도하고 혼합유산균을 접종하여 배양, 발효시킨 예가 있다. 그리고 난황액을 발효유에 첨가한 예로는 김 등(2000)이 등록특허 10-0366302호로서 특수항체가 함유된 난황액에 설탕, 고과당, 갈락토올리고당 등의 혼합당류를 첨가하고 63℃에서 6분간 열처리하여 유산균 배양액에 혼합하여 특수항체가 함유된 발효유를 생산하는 방법을 제시한바 있다. Domestic patent related to lactic acid bacteria beverage using egg is Patent No. 115910, which is combined with lactose, sugar, and water to add sugar, water and lactose to heat and sterilize and induce heat denaturation of egg protein. There is an example of inoculation, culture and fermentation. An example of adding egg yolk solution to fermented milk is that Kim et al. (2000) adds a mixed sugar such as sugar, high fructose and galactooligosaccharide to egg yolk solution containing special antibody as Patent No. 10-0366302. It has been proposed a method of producing fermented milk containing a special antibody by heat treatment for a minute mixed with lactic acid bacteria culture medium.
이상과 같이 계란발효 유산균음료의 개발을 위하여 지금까지 진행되어 온 연구들은 주원료로써 계란을 전량 이용하지 않고 난백과 같은 계란의 일부만을 이용하는 경우가 대부분이었고 더욱이 부족한 발효를 촉진시키기 위하여 당 이외에 알칼리 처리 대두유, 탈지유등을 혼합하여 발효를 유도하였으며 발효물의 물리적 안정성 즉, 층분리 현상 등을 해결하기 위하여 잔산검(xanthan gum)과 같은 안정제를 사용하여야만 하는 결점이 있었다. 다만, 특허 제115910호로서 유와 이(1994)가 계란에 유당, 설탕, 물을 첨가하여 혼합한 후 열처리하여 살균과 난단백질의 열변성을 유도하고 혼합유산균을 접종하여 배양, 발효시킨 예가 있다. 그러나 상기 특허에서 계란을 전란액의 형태로 이용하였을 경우에는 일정시간 발효 후 유산균 음료의 적정 pH인 4.5 이하를 유지하기 위하여 소요되는 유산균스타터의 첨가량이 0.001% 이하에서는 원활히 이루지 못하게 되는 문제점이 있었다. 그 이유를 추정하 면 우유의 pH는 일반적으로 6.7 내외인 데에 비해 계란의 pH는 7.3 정도로 우유의 그것에 비해 0.6정도 높아 우유에 비해 유산균으로 하여금 더 많은 산을 생성토록해야 적정 pH인 4.5 이하에 도달될 수 있으므로 상대적으로 많은 량의 유산균 접종량이 요구되는 것으로 판단되었다. 따라서 목적하는 유산균 음료의 경제적인 생산을 위한 공정개발이 필요하였다.As mentioned above, most of the studies that have been conducted to develop an egg fermented lactic acid bacteria drink mostly use only a part of eggs such as egg white without using the whole egg as the main raw material. In order to solve the physical stability of the fermentation product, that is, the delamination phenomenon, a stabilizer such as xanthan gum had to be used. However, as Patent No. 115910, there is an example in which Yu and Lee (1994) add lactose, sugar, and water to eggs, and then heat-treat them to induce sterilization and heat denaturation of egg proteins and inoculate and incubate fermented mixed lactic acid bacteria. . However, when the egg is used in the form of a whole egg in the patent, there is a problem in that the addition amount of the lactobacillus starter required to maintain the optimum pH 4.5 or less of the lactic acid bacteria beverage after fermentation for a predetermined time may not be achieved smoothly at 0.001% or less. The reason for this is that the pH of milk is generally around 6.7, whereas the pH of eggs is about 7.3, which is about 0.6 higher than that of milk. Since it could be reached, it was determined that a relatively large amount of lactic acid bacteria inoculation was required. Therefore, it was necessary to develop a process for the economic production of the desired lactic acid bacteria beverage.
본 발명은 상기한 실정을 감안하여 종래 계란 유산균음료의 제조방법이 갖는 결점 및 문제점을 해결하고자 발명한 것으로서 난황과 난백이 혼합된 전란액을 균질화하여 포도당과 과당 및 물을 첨가한 후 이에 추가적으로 구연산(citric acid) 과 아스코브산(ascorbic acid)이 함유된 혼합유기산을 첨가하여 전란액의 수소이온농도를 원래의 7.5에서 6.7로 조절함으로서 유산발효를 위한 락토바실러스 아시도필루스(Lactobacillus acidophilus), 비피도박테리움 론검(Bifidobacterium longum) , 스트렙토코커스 써모필루스(Streptococcus thermophilus)의 혼합유산균 첨가량을 최소로 할 수 있게 되었다.The present invention was invented to solve the shortcomings and problems of the conventional method for preparing a lactic acid bacteria beverage in consideration of the above-mentioned conditions, homogenizing the whole egg yolk mixed with egg yolk and egg white and adding glucose, fructose and water to the citric acid. Lactobacillus Lactobacillus for Lactic Acid Fermentation by Controlling the Hydrogen Concentration of Whole Egg Solution from 7.5 to 6.7 by Addition of Mixed Organic Acids Containing Citric Acid and Ascorbic Acid acidophilus ), Bifidobacterium longum ) and Streptococcus thermophilus can minimize the amount of mixed lactic acid bacteria added.
유기산의 첨가 여부가 접종되는 혼합유산균스타터의 접종량에 미치는 영향을 검토하기 위하여 유기산(구연산 50%와 아스코브산 50%의 혼합유기산)을 첨가하여 전란액의 pH를 6.7로 조절한 혼합유기산첨가구와 유기산 처리를 하지 않은 대조구에 대해 공히 6%의 포도당과 6%의 과당을 400% 희석 전란액에 용해 첨가하고, 80℃로 30분간 열처리 후 냉각하여 혼합유산균스타터[락토바실러스 아시도필루 스(Lactobacillus acidophilus)35%, 비피도박테리움 론검(Bifidobacterium longum) 30%,, 스트렙토코커스 써모필루스(Streptococcus thermophilus) 35% 비율의 혼합조성물]의 접종량을 변화시켜 40℃에서 7시간 배양하는 실험을 실시하고 그 효과를 검토한 결과 아래 표에서 나타난 바와 같다.In order to examine the effect of the addition of organic acid on the inoculation of mixed Lactobacillus starter inoculated, the mixed organic acid furniture with the pH of the whole egg solution adjusted to 6.7 by adding organic acid (50% citric acid and 50% ascorbic acid) 6% of glucose and 6% of fructose were dissolved in 400% diluted whole egg solution, and heat-treated at 80 ° C for 30 minutes, and then cooled and mixed with lactic acid starter [Lactobacillus adophyllus ( Lactobacillus). acidophilus ) 35%, Bifidobacterium longum ) 30%, Streptococcus thermophilus ) 35% of the mixed composition of the inoculation amount] was changed to incubation for 7 hours at 40 ℃ experiments to examine the effect is shown in the table below.
[표][table]
유기산의 첨가 여부가 접종되는 혼합유산균스타터의 접종량에 미치는 영향Effect of Addition of Organic Acid on Inoculation Volume of Mixed Lactic Acid Bacteria Starter
------------------------------------------------------------------------------------------------------------------------- ---------------------
혼합유기산첨가구 대 조 구 Mixed Organic Acid Additives
유산균접종량(%) ------------------------- ----------------------Lactobacillus inoculation amount (%) ------------------------- -------------------- -
pH 유산균수(cfu/ml) pH 유산균수(cfu/ml) pH Lactic Acid Bacteria (cfu / ml) pH Lactic Acid Bacteria (cfu / ml)
----------------------------------------------------------------------- -------------------------------------------------- ---------------------
0.0001 5.7 3.4×104 7.1 5.5×104 0.0001 5.7 3.4 × 10 4 7.1 5.5 × 10 4
0.0002 5.5 6.1×104 7.0 8.3×104 0.0002 5.5 6.1 × 10 4 7.0 8.3 × 10 4
0.0005 5.3 3.6×104 6.7 4.5×104 0.0005 5.3 3.6 × 10 4 6.7 4.5 × 10 4
0.001 5.1 7.3×105 6.5 7.5×104 0.001 5.1 7.3 × 10 5 6.5 7.5 × 10 4
0.002 4.5 8.3×107 6.5 2.8×104 0.002 4.5 8.3 × 10 7 6.5 2.8 × 10 4
0.005 4.4 5.5×108 6.1 3.4×104 0.005 4.4 5.5 × 10 8 6.1 3.4 × 10 4
0.01 4.4 2.8×108 5.7 4.7×104 0.01 4.4 2.8 × 10 8 5.7 4.7 × 10 4
0.02 4.3 6.5×108 5.3 6.1×105 0.02 4.3 6.5 × 10 8 5.3 6.1 × 10 5
0.05 4.3 3.8×108 5.2 7.5×108 0.05 4.3 3.8 × 10 8 5.2 7.5 × 10 8
0.1 4.2 4.7×109 4.5 4.2×107 0.1 4.2 4.7 × 10 9 4.5 4.2 × 10 7
0.2 4.2 6.4×109 4.4 4.7×108 0.2 4.2 6.4 × 10 9 4.4 4.7 × 10 8
0.5 4.2 6.6×109 4.4 7.4×108 0.5 4.2 6.6 × 10 9 4.4 7.4 × 10 8
1.0 4.1 7.3×109 4.3 5.8×108 1.0 4.1 7.3 × 10 9 4.3 5.8 × 10 8
------------------------------------------------------------------------------------------------------------------------- ---------------------
상기 표에 나타난 바와 같이 발효 7시간 후에 유산균의 증식에 의하여 일반적인 병원성 미생물의 성장이 억제되는 pH 4.5를 나타내는 최소 혼합유산균스타터의 접종량은 혼합유산균처리구의 경우 0.002% 이었으며 유기산을 첨가하지 않은 대조구의 경우에는 0.1% 이상임을 알 수 있었다. 따라서 혼합유산균의 처리에 의해서 유산균 스타터의 첨가량을 기존에 비해 1/10 ~ 1/50 까지 절감할 수 있다고 판단되었다.As shown in the table above, the inoculum of the mixed Lactobacillus starter exhibiting a pH of 4.5, which is inhibited by the growth of lactic acid bacteria after 7 hours of fermentation, was 0.002% in the mixed Lactobacillus treatment group and the control group without the added organic acid. It can be seen that more than 0.1%. Therefore, it was determined that the amount of lactic acid bacteria starter added by 1/10 ~ 1/50 can be reduced by the treatment of mixed lactic acid bacteria.
발명의 실시를 위한 구체적인 내용은 아래의 실시예에서 기술하기로 한다.Specific details for carrying out the invention will be described in the following examples.
[실시예 1] Example 1
계란에서 전란액을 얻어 이를 균질화하고 이에 대해 2배량에 해당하는 증류수 또는 물에 6%의 포도당과 6%의 과당을 용해한 후 전란액을 혼합 한 후 구연산과 아스코브산이 각각 1:1로 혼합된 2% 유기산 용액으로 전란액과 당 혼합액의 pH를 6.7로 맞춘 후 전체 용량이 전란액의 4배량(400%)이 되도록 증류수 또는 물로 맞춰 희석혼합용액을 만든다. 상기 혼합용액을 80℃의 온도로 30분간 열처리하여 살균 및 가열에 의한 이들 혼합용액의 적절한 열변성을 유도한 후 무균적 조건하에서 10,000r.p.m으로 기계적 균질화를 실시하고 즉시 40℃로 냉각시킨다. 이어 냉각된 혼합용액에 동결건조 혼합유산균스타터[락토바실러스 아시도필루스(Lactobacillus acidophilus)35%, 비피도박테리움 론검(Bifidobacterium longum) 30%,, 스트렙토코커스 써모필루스(Streptococcus thermophilus) 35% 비율의 혼합조성물]를 0.002% 접종한 후, 항온기에서 40℃의 온도를 유지시켜 pH가 4.5 이하가 될 때까지 약 10시간 배양하였다. 상기 배양으로 형성된 커드(curd)를 다시 무균 상태에서 10,000r.p.m으로 균질화하여 마시는 형태(drinking type)의 계란 유산균음료를 제조하였다.Obtained whole egg solution from egg, homogenize it, dissolve 6% glucose and 6% fructose in distilled water or water corresponding to 2 times, and mix the whole egg solution with citric acid and ascorbic acid 1: 1. Adjust the pH of the whole solution and the sugar mixture to 6.7 with 2% organic acid solution, and make a dilute mixture solution with distilled water or water so that the total capacity is 4 times (400%) of the whole solution. The mixed solution was heat-treated at a temperature of 80 ° C. for 30 minutes to induce proper thermal denaturation of these mixed solutions by sterilization and heating, followed by mechanical homogenization at 10,000 rpm under aseptic conditions, and immediately cooled to 40 ° C. Then, the freeze-dried mixed lactic acid bacteria starter ( Lactobacillus acidophilus ) 35%, Bifidobacterium longum ) 30%, Streptococcus thermophilus ) 35% of the mixed composition] was inoculated at 0.002%, and then incubated for about 10 hours until the pH was 4.5 or less by maintaining the temperature of 40 ℃ in a thermostat. Curd (curd) formed by the culture was homogenized at 10,000rpm again in aseptic conditions to prepare a lactic acid bacteria beverage of drinking (drinking type).
[실시예 2] Example 2
계란에서 전란액을 얻어 이를 균질화하고 이에 대해 1배량에 해당하는 증류수 또는 물에 6%의 포도당과 6%의 과당을 용해한 후 전란액을 혼합 한 후 구연산과 아스코브산이 각각 1:1로 혼합된 2% 유기산 용액으로 전란액과 당 혼합액의 pH를 6.7로 맞춘 후 전체 용량이 전란액의 3배량(300%)이 되도록 증류수 또는 물로 맞춰 희석혼합용액을 만든다. 상기 혼합용액을 80℃의 온도로 30분간 열처리하여 살균 및 가열에 의한 이들 혼합용액의 적절한 열변성을 유도한 후 무균적 조건하에서 10,000r.p.m으로 기계적 균질화를 실시하고 즉시 40℃로 냉각시킨다. 이어 냉각된 혼합용액에 동결건조 혼합유산균스타터[락토바실러스 아시도필루스(Lactobacillus acidophilus)35%, 비피도박테리움 론검(Bifidobacterium longum) 30%,, 스트렙토코커스 써모필루스(Streptococcus thermophilus) 35% 비율의 혼합조성물]를 0.002% 접종한 후, 항온기에서 40℃의 온도를 유지시켜 pH가 4.5 이하가 될 때까지 약 10시간 배양하였다. 상기 배양으로 형성된 커드(curd)를 다시 무균 상태에서 10,000r.p.m으로 균질화하여 떠먹는 형태(stirred type)의 계란 유산균음료를 제조하였다.Obtain egg solution from egg, homogenize it, dissolve 6% glucose and 6% fructose in distilled water or water corresponding to 1x, and mix the whole egg solution with citric acid and ascorbic acid 1: 1. Adjust the pH of the whole solution and sugar mixture to 6.7 with 2% organic acid solution, and then make dilute mixed solution with distilled water or water so that the total capacity is three times (300%) of the whole solution. The mixed solution was heat-treated at a temperature of 80 ° C. for 30 minutes to induce proper thermal denaturation of these mixed solutions by sterilization and heating, followed by mechanical homogenization at 10,000 rpm under aseptic conditions, and immediately cooled to 40 ° C. Then, the freeze-dried mixed lactic acid bacteria starter ( Lactobacillus acidophilus ) 35%, Bifidobacterium longum ) 30%, Streptococcus thermophilus 35% of the mixed composition] inoculated 0.002%, and incubated for about 10 hours until the pH is 4.5 or less by maintaining the temperature of 40 ℃ in a thermostat It was. The curd (curd) formed by the culture was homogenized at 10,000 rpm again in aseptic state to prepare a lactic acid bacterium beverage of stirred type.
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012020904A1 (en) * | 2010-08-11 | 2012-02-16 | Yoo Ickjong | Lactic acid-fermented egg having reduced egg protein antigenicity through addition of sodium citrate, heating treatment, and lactic acid fermentation, and method for preparing same |
| CN102726525A (en) * | 2012-07-03 | 2012-10-17 | 浙江一鸣食品股份有限公司 | A kind of egg yoghurt processing method |
| CN105124703A (en) * | 2015-09-22 | 2015-12-09 | 福建省农业科学院农业生物资源研究所 | Preparation method of soybean milk and egg liquid lactobacillus fermentation beverage |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012020904A1 (en) * | 2010-08-11 | 2012-02-16 | Yoo Ickjong | Lactic acid-fermented egg having reduced egg protein antigenicity through addition of sodium citrate, heating treatment, and lactic acid fermentation, and method for preparing same |
| CN102781261A (en) * | 2010-08-11 | 2012-11-14 | 柳益钟 | Lactic acid-fermented egg having reduced egg protein antigenicity through addition of sodium citrate, heating treatment, and lactic acid fermentation, and method for preparing same |
| CN102726525A (en) * | 2012-07-03 | 2012-10-17 | 浙江一鸣食品股份有限公司 | A kind of egg yoghurt processing method |
| CN105124703A (en) * | 2015-09-22 | 2015-12-09 | 福建省农业科学院农业生物资源研究所 | Preparation method of soybean milk and egg liquid lactobacillus fermentation beverage |
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