KR20230038075A - Manufacturing method of marshmallow maximizing the content of lactic acid bacteria using lactic acid bacteria instantaneous deposition technique and marshmallow manufactured using the same - Google Patents
Manufacturing method of marshmallow maximizing the content of lactic acid bacteria using lactic acid bacteria instantaneous deposition technique and marshmallow manufactured using the same Download PDFInfo
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- KR20230038075A KR20230038075A KR1020220020272A KR20220020272A KR20230038075A KR 20230038075 A KR20230038075 A KR 20230038075A KR 1020220020272 A KR1020220020272 A KR 1020220020272A KR 20220020272 A KR20220020272 A KR 20220020272A KR 20230038075 A KR20230038075 A KR 20230038075A
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- lactic acid
- acid bacteria
- marshmallow
- weight
- dried
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- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 title claims abstract description 422
- 235000014655 lactic acid Nutrition 0.000 title claims abstract description 211
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Images
Classifications
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G3/00—Sweetmeats; Confectionery; Marzipan; Coated or filled products
- A23G3/34—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof
- A23G3/36—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds
- A23G3/364—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds containing microorganisms or enzymes; containing paramedical or dietetical agents, e.g. vitamins
- A23G3/366—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds containing microorganisms or enzymes; containing paramedical or dietetical agents, e.g. vitamins containing microorganisms, enzymes
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G3/00—Sweetmeats; Confectionery; Marzipan; Coated or filled products
- A23G3/34—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof
- A23G3/36—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds
- A23G3/42—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds characterised by the carbohydrates used, e.g. polysaccharides
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G3/00—Sweetmeats; Confectionery; Marzipan; Coated or filled products
- A23G3/34—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof
- A23G3/36—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds
- A23G3/44—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds containing peptides or proteins
-
- 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
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- 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
- A23V2300/00—Processes
- A23V2300/10—Drying, dehydrating
-
- 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
- A23V2300/00—Processes
- A23V2300/24—Heat, thermal treatment
-
- 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
-
- 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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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
- C12R2001/01—Bacteria or Actinomycetales ; using bacteria or Actinomycetales
- C12R2001/225—Lactobacillus
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
- C12R2001/01—Bacteria or Actinomycetales ; using bacteria or Actinomycetales
- C12R2001/225—Lactobacillus
- C12R2001/23—Lactobacillus acidophilus
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
- C12R2001/01—Bacteria or Actinomycetales ; using bacteria or Actinomycetales
- C12R2001/225—Lactobacillus
- C12R2001/245—Lactobacillus casei
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
- C12R2001/01—Bacteria or Actinomycetales ; using bacteria or Actinomycetales
- C12R2001/225—Lactobacillus
- C12R2001/25—Lactobacillus plantarum
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
- C12R2001/01—Bacteria or Actinomycetales ; using bacteria or Actinomycetales
- C12R2001/46—Streptococcus ; Enterococcus; Lactococcus
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- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Microbiology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Dairy Products (AREA)
Abstract
Description
본 발명은 유산균 함유량을 극대화하는 마쉬멜로의 제조방법 및 이를 이용하여 제조된 마쉬멜로에 관한 것이다.The present invention relates to a method for producing marshmallows maximizing the content of lactic acid bacteria and a marshmallow prepared using the same.
인간의 장내에 서식하는 미생물 중 유산균은 각종 유기산을 생성하여 장내 pH를 저하시키고 장내 유해 미생물의 생육을 억제하고 장관 벽을 자극하여 연동운동을 촉진시켜 소화 및 흡수를 돕고 생성된 산은 암모니아와 아민을 이온 형태로 전환시킴으로써 유해 물질의 장내 흡수를 억제시키는 등의 역할을 하는 유익한 균이다.Among the microorganisms living in the human intestine, lactic acid bacteria produce various organic acids to lower the pH of the intestine, inhibit the growth of harmful microorganisms in the intestine, and stimulate the intestinal wall to promote peristalsis, thereby helping digestion and absorption, and the produced acid is ammonia and amine. It is a beneficial bacteria that plays a role such as inhibiting intestinal absorption of harmful substances by converting them into ionic forms.
최근 유산균이 미치는 건강증진효과에 대한 많은 연구가 진행되고 있으며, 유산균이 장내 균총의 개선, 정장작용으로 설사와 변비의 개선, 혈중 콜레스테롤의 저하효과, 세균성 식중독 억제효과 등의 기능을 나타낼 수 있음이 밝혀졌다. 이러한 점에 따라 국내에서는 물론 전 세계적으로 유산균 제품의 섭취량이 증대되고 있다.Recently, many studies have been conducted on the health promotion effects of lactic acid bacteria, and it is known that lactic acid bacteria can exhibit functions such as improvement of intestinal flora, improvement of diarrhea and constipation through intestinal action, lowering of blood cholesterol, and inhibitory effect of bacterial food poisoning. Turns out. Accordingly, the intake of lactic acid bacteria products is increasing both domestically and globally.
유산균 제품의 섭취방법으로는 요구르트나 김치 등의 유산균 발효 제품 섭취에 의한 간접적 섭취방법과 동결 건조 분말 제품 섭취에 의한 직접적 섭취방법이 있다. 그러나 상기 두 제품군의 경우 여러 문제점이 있다. 먼저, 간접적 섭취방법은 발효 제품에 포함된 유산균 외의 다른 구성성분에 의해 인체에 좋지 않은 영향이 미칠 수 있다. 예컨대, 김치와 같은 발효제품은 염도가 높아 고혈압 및 당뇨병을 유발할 수 있다. 또한, 유산균 함량을 조절하는데 어려움이 있으며, 제품 내 대부분의 유산균이 위를 통과하면서 사멸하게 되어 장내 정착 효과가 낮다. 또한 요구르트와 같은 발효제품은 국내에서 가장 선호되는 유산균 제품 형태로서 가장 많이 음용되나, 제품 특성상 고농도의 유산균을 포함하기에 부적합한 면이 있다. 설령 고농도로 유산균을 포함한다 하더라도 유통기간 중 발효가 급격히 진행되어 맛이 변질되고, pH 저하로 인해 유산균 생존율이 급격히 감소되는 문제점이 있다. 또한 섭취시 포만감이 있어 일일 섭취량이 제한된다. 한편, 직접적 섭취방법으로 섭취되는 건조분말 형태의 유산균 제제는 유산균 특유의 냄새로 인해 단독 섭취가 어려우며, 복용 방법이 번거로울 뿐만 아니라 일반 소비자에게 식품 보다는 약품으로서의 인식이 강하여 선호도가 낮다고 할 수 있다. 이에 소비자에게 수요도가 높고 유산균이 고농도로 함유된 유산균 제품을 제조할 필요성이 있다.Intake methods of lactic acid bacteria products include an indirect intake method by ingestion of lactic acid bacteria fermented products such as yogurt or kimchi, and a direct intake method by ingestion of freeze-dried powder products. However, there are several problems in the case of the above two product groups. First, the indirect intake method may adversely affect the human body due to components other than lactic acid bacteria included in the fermented product. For example, fermented products such as kimchi may cause high blood pressure and diabetes due to their high salt content. In addition, it is difficult to control the content of lactic acid bacteria, and most of the lactic acid bacteria in the product die while passing through the stomach, so the intestinal fixation effect is low. In addition, fermented products such as yogurt are most commonly consumed as the most preferred form of lactic acid bacteria in Korea, but due to the nature of the product, they are inappropriate to contain high concentrations of lactic acid bacteria. Even if it contains lactic acid bacteria at a high concentration, there is a problem that fermentation rapidly progresses during the distribution period, and the taste is deteriorated, and the survival rate of lactic acid bacteria is rapidly reduced due to a decrease in pH. In addition, there is a feeling of satiety when ingested, so the daily intake is limited. On the other hand, lactic acid bacteria preparations in the form of dry powder consumed by direct intake method are difficult to consume alone due to the unique smell of lactic acid bacteria, and the dosage method is cumbersome, and preference is low because general consumers perceive it as a drug rather than food. Accordingly, there is a need to manufacture lactic acid bacteria products that are in high demand from consumers and contain high concentrations of lactic acid bacteria.
본 발명은 유산균의 증착률을 극대화하는 마쉬멜로의 제조방법을 제공하는 것을 목적으로 한다.An object of the present invention is to provide a method for producing a marshmallow that maximizes the deposition rate of lactic acid bacteria.
본 발명은 유산균의 증착률이 극대화된 마쉬멜로를 제공하는 것을 목적으로 한다.An object of the present invention is to provide a marshmallow with a maximized deposition rate of lactic acid bacteria.
1. 원료 마쉬멜로를 건조기에서 1차 건조한 후 냉각하고, 1차 건조된 마쉬멜로를 60℃ 내지 150℃에서 1차 가열한 후 냉각하고, 1차 가열된 마쉬멜로를 60℃ 내지 150℃에서 2차 가열한 후 냉각하고, 2차 가열된 마쉬멜로를 건조기에서 2차 건조한 후 냉각하여 건조 마쉬멜로를 제조하는 단계(S100);1. The raw material marshmallow is firstly dried in a dryer and then cooled, the firstly dried marshmallow is firstly heated at 60 ° C to 150 ° C and then cooled, and the firstly heated marshmallow is secondarily heated at 60 ° C to 150 ° C After cooling, and secondarily drying the secondarily heated marshmallow in a dryer and then cooling to prepare a dried marshmallow (S100);
상기 건조 마쉬멜로에 유산균을 첨가하고 교반하는 단계(S200);Adding lactic acid bacteria to the dried marshmallow and stirring (S200);
상기 교반된 건조 마쉬멜로의 표면을 30℃ 내지 37℃로 가열하는 유산균 증착 단계(S300); 및Lactic acid bacteria deposition step (S300) of heating the surface of the stirred dry marshmallow to 30 ° C to 37 ° C; and
상기 유산균 증착 단계(S300)에서 수득한 마쉬멜로를 건조한 후 냉각하는 단계;를 포함하고,Including; drying the marshmallow obtained in the lactic acid bacteria deposition step (S300) and then cooling it;
상기 원료 마쉬멜로는 설탕 40 내지 50 중량부, 산화전분 16 내지 18 중량부, 옥수수시럽 15 내지 17 중량부, 포도당 13 내지 15 중량부, 젤라틴 1.4 내지 1.6 중량부, 향료 2.8 내지 3.2 중량부, 메타인산나트륨 0.45 내지 0.55 중량부 및 식용색소 0.015 내지 0.025 중량부를 포함하며,The raw material marshmallow contains 40 to 50 parts by weight of sugar, 16 to 18 parts by weight of oxidized starch, 15 to 17 parts by weight of corn syrup, 13 to 15 parts by weight of glucose, 1.4 to 1.6 parts by weight of gelatin, 2.8 to 3.2 parts by weight of flavoring agent, metaphosphoric acid 0.45 to 0.55 parts by weight of sodium and 0.015 to 0.025 parts by weight of food coloring,
상기 유산균을 첨가하고 교반하는 단계(S200)에서 첨가되는 유산균은 108 내지 109CFU/g인 유산균이 증착된 마쉬멜로의 제조방법.The lactic acid bacteria added in the step of adding and stirring the lactic acid bacteria (S200) is 10 8 to 10 9 CFU / g. Method for producing a marshmallow deposited with lactic acid bacteria.
2. 위 1에 있어서, 상기 유산균을 첨가하고 교반하는 단계(S200)를 수행하기 전에 상기 건조 마쉬멜로의 표면을 20℃ 내지 25℃로 가열하는 단계를 더 포함하는 유산균이 증착된 마쉬멜로의 제조방법.2. The method of producing marshmallows deposited with lactic acid bacteria in the above 1, further comprising heating the surface of the dried marshmallow to 20 ° C to 25 ° C before performing the step (S200) of adding and stirring the lactic acid bacteria.
3. 위 1에 있어서, 상기 유산균을 첨가하고 교반하는 단계(S200)에서 첨가되는 유산균은 유산균 생균; 유산균 사균; 또는 유산균 생균 및 유산균 사균의 혼합물인 유산균이 증착된 마쉬멜로의 제조방법.3. In the above 1, the lactic acid bacteria added in the step of adding and stirring the lactic acid bacteria (S200) is lactic acid bacteria live bacteria; dead lactic acid bacteria; Or a method for producing a marshmallow deposited with lactic acid bacteria, which is a mixture of live lactic acid bacteria and dead lactic acid bacteria.
4. 위 1에 있어서, 상기 유산균은 락토바실러스 플란타럼(Lactobacillus plantarum), 락포바실러스 람노서스(Lactobacillus rhamnosus), 스트렙토코커스 써모필러스(Streptococcus thermophilus), 비피도박테리움 롱검(Bifidobacterium longum), 락토바실러스 애시도필러스(Lactobacillus acidophilus), 락토바실러스 카제이(Lactobacillus casei) 및 락토바실러스 퍼멘텀(Lactobacillus fermentum)으로 이루어진 군에서 선택된 적어도 하나인 유산균이 증착된 마쉬멜로의 제조방법.4. The method of 1 above, wherein the lactic acid bacteria are Lactobacillus plantarum , Lactobacillus rhamnosus, Streptococcus thermophilus, Bifidobacterium longum , lacto Bacillus acidophilus ( Lactobacillus acidophilus ), Lactobacillus casei ( Lactobacillus casei ) and Lactobacillus fermentum ( Lactobacillus fermentum ) A method for producing a marshmallow deposited with at least one lactic acid bacteria selected from the group consisting of.
5. 위 1에 있어서, 상기 건조 마쉬멜로의 부피는 0.1 내지 5mm3인 유산균이 증착된 마쉬멜로의 제조방법.5. The method of producing a marshmallow deposited with lactic acid bacteria according to 1 above, wherein the dry marshmallow has a volume of 0.1 to 5 mm 3 .
6. 위 1에 있어서, 상기 유산균 증착 단계(S300)는 상기 교반된 건조 마쉬멜로를 컨베이어 벨트에 위치시키고, 상기 컨베이어 벨트의 상부 및 하부에 배치된 전열기로 상기 교반된 건조 마쉬멜로의 표면을 30℃ 내지 37℃로 가열하는 것인 유산균이 증착된 마쉬멜로의 제조방법.6. In the above 1, in the lactic acid bacteria deposition step (S300), the agitated dry marshmallow is placed on a conveyor belt, and the surface of the agitated dried marshmallow is heated with electric heaters disposed above and below the conveyor belt at 30 ° C. Method for producing a marshmallow deposited with lactic acid bacteria, which is heated to 37 ° C.
7. 위 1에 있어서, 상기 유산균 증착 단계(S300)는 상기 교반된 건조 마쉬멜로의 표면을 30℃ 내지 37℃로 1.5 내지 3.5초 가열하는 것인 유산균이 증착된 마쉬멜로의 제조방법.7. The method of producing marshmallows deposited with lactic acid bacteria in the above 1, wherein the lactic acid bacteria deposition step (S300) is to heat the surface of the stirred dry marshmallow to 30 ° C to 37 ° C for 1.5 to 3.5 seconds.
8. 위 1 내지 7 중 어느 한 항목의 제조방법으로 제조된 유산균이 증착된 마쉬멜로.8. Marshmallow deposited with lactic acid bacteria prepared by any one of the above 1 to 7 manufacturing methods.
9. 위 8에 있어서, 상기 마쉬멜로는 수분함량이 0.0001 내지 10 중량%인 유산균이 증착된 마쉬멜로.9. The marshmallow according to 8 above, wherein the marshmallow has a moisture content of 0.0001 to 10% by weight and is deposited with lactic acid bacteria.
본 발명의 제조방법은 마쉬멜로에 유산균을 투입하여 최적 온도로 마쉬멜로의 표면을 가열함으로써 마쉬멜로의 표면에 높은 농도로 유산균을 증착시킬 수 있다.In the manufacturing method of the present invention, lactic acid bacteria can be deposited at a high concentration on the surface of the marshmallow by adding lactic acid bacteria to the marshmallow and heating the surface of the marshmallow to an optimum temperature.
또한, 본 발명의 제조방법으로 제조된 마쉬멜로는 장기간 보존에도 높은 유산균 보존율을 나타내며, 장내에서 우수한 보존력을 나타낼 수 있다.In addition, the marshmallow produced by the manufacturing method of the present invention shows a high lactic acid bacteria preservation rate even after long-term storage, and can exhibit excellent preservation power in the intestine.
도 1은 일 실시예에 따른 유산균이 증착된 마쉬멜로를 제조하는 방법을 도식화한 것이다.
도 2는 잘게 분쇄된 형태의 건조 마쉬멜로의 사진이다.1 is a schematic diagram of a method for producing a marshmallow deposited with lactic acid bacteria according to an embodiment.
Figure 2 is a photograph of dried marshmallows in finely ground form.
이하, 본 발명을 상세하게 설명한다.Hereinafter, the present invention will be described in detail.
본 발명은 건조 마쉬멜로에 유산균을 첨가하고 교반하는 단계(S200);The present invention includes the steps of adding lactic acid bacteria to dry marshmallow and stirring (S200);
상기 교반된 건조 마쉬멜로의 표면을 가열하는 유산균 증착 단계(S300); 및Lactic acid bacteria deposition step of heating the surface of the stirred dry marshmallow (S300); and
상기 유산균 증착 단계(S300)에서 수득한 마쉬멜로를 건조한 후 냉각하는 단계(S400)를 포함하는 유산균이 증착된 마쉬멜로의 제조방법을 제공한다.It provides a method for producing a marshmallow deposited with lactic acid bacteria, comprising drying and cooling the marshmallow obtained in the lactic acid bacteria deposition step (S300) (S400).
본 발명의 방법은 유산균을 첨가하고 교반하는 단계(S200)를 수행하기 전에 건조 마쉬멜로를 제조하는 단계(S100)를 더 포함할 수 있다(도 1 참조).The method of the present invention may further include a step of preparing a dried marshmallow (S100) before adding lactic acid bacteria and stirring (S200) (see FIG. 1).
건조 마쉬멜로는 수분 함량이 일정 수준 이하로 건조된 마쉬멜로를 의미한다(도 2 참조). 건조 마쉬멜로는 원료 마쉬멜로를 건조기에서 건조한 후 냉각하는 방법, 고온에서 가열한 후 냉각하는 방법, 또는 이들 조합으로 제조될 수 있다. 건조 마쉬멜로는 상용화된 제품일 수 있다.Dried marshmallow means a marshmallow that has been dried to a moisture content below a certain level (see FIG. 2). Dried marshmallows may be prepared by drying raw marshmallows in a dryer and then cooling them, heating them at a high temperature and then cooling them, or a combination thereof. Dried marshmallows may be commercially available products.
원료 마쉬멜로는 당업계에 알려진 스펀지 형태의 사탕류 식품을 의미하며, 설탕이나 콘 시럽, 물, 젤라틴, 포도당, 조미료 등으로 거품을 낸 후 굳혀서 제조될 수 있다. 원료 마쉬멜로는 상용화된 제품일 수 있다.Raw marshmallow refers to a sponge-type candy food known in the art, and can be prepared by foaming with sugar, corn syrup, water, gelatin, glucose, seasoning, etc. and then hardening. The raw material marshmallow may be a commercially available product.
원료 마쉬멜로는 설탕, 산화전분, 옥수수시럽, 포도당, 젤라틴, 향료, 메타인산나트륨 및 식용색소를 포함할 수 있다.Raw marshmallow may contain sugar, oxidized starch, corn syrup, glucose, gelatin, flavoring, sodium metaphosphate and food coloring.
향료는 천연향료 또는 합성향료일 수 있고, 예컨대, 천연 바닐라향료, 합성 바닐라향료, 천연 카카오향료, 합성 카카오향료, 천연 딸기향료, 또는 합성 딸기향료일 수 있다.The flavor may be a natural flavor or a synthetic flavor, for example, natural vanilla flavor, synthetic vanilla flavor, natural cacao flavor, synthetic cacao flavor, natural strawberry flavor, or synthetic strawberry flavor.
원료 마쉬멜로는 설탕 40 내지 50 중량부, 산화전분 16 내지 18 중량부, 옥수수시럽 15 내지 17 중량부, 포도당 13 내지 15 중량부, 젤라틴 1.4 내지 1.6 중량부, 향료 2.8 내지 3.2 중량부, 메타인산나트륨 0.45 내지 0.55 중량부 및 식용색소 0.015 내지 0.025 중량부를 포함할 수 있다.Raw marshmallow contains 40 to 50 parts by weight of sugar, 16 to 18 parts by weight of oxidized starch, 15 to 17 parts by weight of corn syrup, 13 to 15 parts by weight of glucose, 1.4 to 1.6 parts by weight of gelatin, 2.8 to 3.2 parts by weight of flavoring, sodium metaphosphate It may include 0.45 to 0.55 parts by weight and food coloring 0.015 to 0.025 parts by weight.
일 구현예에 따르면, 원료 마쉬멜로는 설탕 48 중량부, 산화전분 17 중량부, 옥수수시럽 16 중량부, 포도당 14 중량부, 젤라틴 1.5 중량부, 향료 2.99 중량부, 메타인산나트륨 0.490 중량부 및 식용색소 0.02 중량부를 포함할 수 있다.According to one embodiment, raw marshmallow contains 48 parts by weight of sugar, 17 parts by weight of oxidized starch, 16 parts by weight of corn syrup, 14 parts by weight of glucose, 1.5 parts by weight of gelatin, 2.99 parts by weight of flavoring, 0.490 parts by weight of sodium metaphosphate, and food coloring. It may contain 0.02 parts by weight.
건조 마쉬멜로를 제조하는 단계(S100)는 원료 마쉬멜로를 건조기에서 1차 건조한 후 냉각하고, 1차 건조된 마쉬멜로를 60℃내지 150℃에서 1차 가열한 후 냉각하는 것을 포함할 수 있다.The step of preparing a dried marshmallow (S100) may include firstly drying the raw marshmallow in a dryer and then cooling it, and firstly heating the firstly dried marshmallow at 60 ° C to 150 ° C and then cooling it.
건조 마쉬멜로를 제조하는 단계(S100)는 원료 마쉬멜로를 건조기에서 1차 건조한 후 냉각하고, 1차 건조된 마쉬멜로를 60℃내지 150℃에서 1차 가열한 후 냉각하고, 1차 가열된 마쉬멜로를 60℃내지 150℃에서 2차 가열한 후 냉각하고, 2차 가열된 마쉬멜로를 건조기에서 2차 건조한 후 냉각하는 것을 포함할 수 있다.In the step of preparing a dried marshmallow (S100), the raw material marshmallow is firstly dried in a dryer and then cooled, the firstly dried marshmallow is firstly heated at 60 ° C to 150 ° C and then cooled, and the firstly heated marshmallow is cooled at 60 ° C It may include cooling after secondary heating at 150 ° C., secondary drying of the secondary heated marshmallow in a dryer, and then cooling.
건조 마쉬멜로는 수분함량이 10 중량% 이하, 8 중량% 이하, 7 중량% 이하, 6 중량% 이하, 5 중량% 이하, 4 중량% 이하 또는 3 중량% 이하일 수 있다. 건조 마쉬멜로는 전체 중량 대비 수분함량이 0.0001 내지 10 중량%, 0.0001 내지 9 중량%, 0.0001 내지 8 중량%, 0.0001 내지 7 중량%, 0.0001 내지 6 중량%, 0.0001 내지 5 중량%, 0.001 내지 4 중량%, 0.001 내지 3 중량%, 0.0001 내지 2 중량%, 또는 0.001 내지 1 중량%일 수 있다.The dried marshmallow may have a moisture content of 10% or less, 8% or less, 7% or less, 6% or less, 5% or less, 4% or less, or 3% or less by weight. The moisture content of the dried marshmallow is 0.0001 to 10% by weight, 0.0001 to 9% by weight, 0.0001 to 8% by weight, 0.0001 to 7% by weight, 0.0001 to 6% by weight, 0.0001 to 5% by weight, and 0.001 to 4% by weight relative to the total weight. , 0.001 to 3 wt%, 0.0001 to 2 wt%, or 0.001 to 1 wt%.
건조 마쉬멜로는 설탕, 산화전분, 옥수수시럽, 포도당, 젤라틴, 향료, 메타인산나트륨 및 식용색소를 포함할 수 있다.Dried marshmallows may contain sugar, oxidized starch, corn syrup, glucose, gelatin, flavoring, sodium metaphosphate and food coloring.
건조 마쉬멜로는 교반 및 취식이 용이한 크기로 분쇄된 것일 수 있다(도 2 참조).Dried marshmallows may be pulverized to a size that is easy to stir and eat (see FIG. 2).
건조 마쉬멜로의 부피는 0.1 내지 50 mm3, 0.1 내지 45mm3, 0.1 내지 40mm3, 0.1 내지 35mm3, 0.1 내지 30 mm3, 0.1 내지 25mm3, 0.1 내지 20mm3, 0.1 내지 15mm3, 0.1 내지 10 mm3, 또는 0.1 내지 5mm3일 수 있다.The volume of dry marshmallow is 0.1 to 50 mm 3 , 0.1 to 45 mm 3 , 0.1 to 40 mm 3 , 0.1 to 35 mm 3 , 0.1 to 30 mm 3 , 0.1 to 25 mm 3 , 0.1 to 20 mm 3 , 0.1 to 15 mm 3 , 0.1 to 10 mm 3 , or 0.1 to 5 mm 3 .
본 발명의 방법은 유산균을 첨가하고 교반하는 단계(S200)를 수행하기 전에 건조 마쉬멜로를 제조하는 단계(S100)에서 제조된 건조 마쉬멜로를 분쇄하는 단계를 더 포함할 수 있다. 분쇄 방법은 한정되지 않고 공지된 방법을 이용하여 수행될 수 있다.The method of the present invention may further include a step of pulverizing the dried marshmallow prepared in the step of preparing a dry marshmallow (S100) before performing the step of adding and stirring the lactic acid bacteria (S200). The grinding method is not limited and may be performed using a known method.
건조 마쉬멜로를 분쇄하는 단계는 건조 마쉬멜로를 0.1 내지 50 mm3, 0.1 내지 45mm3, 0.1 내지 40mm3, 0.1 내지 35mm3, 0.1 내지 30 mm3, 0.1 내지 25mm3, 0.1 내지 20mm3, 0.1 내지 15mm3, 0.1 내지 10 mm3, 또는 0.1 내지 5mm3부피로 분쇄하는 것일 수 있다.The step of crushing the dry marshmallow is to grind the dried marshmallow into 0.1 to 50 mm 3 , 0.1 to 45 mm 3 , 0.1 to 40 mm 3 , 0.1 to 35 mm 3 , 0.1 to 30 mm 3 , 0.1 to 25 mm 3 , 0.1 to 20 mm 3 , 0.1 to 15 mm 3 , 0.1 to 10 mm 3 , or 0.1 to 5 mm 3 may be ground to a volume.
건조 마쉬멜로가 분쇄됨으로써 후속 유산균을 첨가하고 교반하는 단계(S200)에서 교반이 용이해질 수 있고, 취식이 용이해질 수 있는 장점이 있다.The grinding of the dried marshmallow has the advantage of facilitating stirring and facilitating eating in the step of adding and stirring the subsequent lactic acid bacteria (S200).
본 발명의 방법은 유산균을 첨가하고 교반하는 단계(S200)를 수행하기 전에 건조 마쉬멜로의 표면을 가열하는 표면 가열 단계(S500)를 더 포함할 수 있다.The method of the present invention may further include a surface heating step (S500) of heating the surface of the dried marshmallow before performing the step (S200) of adding and stirring the lactic acid bacteria.
유산균을 첨가하기 전에 건조 마쉬멜로 표면을 가열하는 경우 건조 마쉬멜로의 표면의 점성이 다소 높아져 후속 단계에서 첨가되는 유산균 생균이 마쉬멜로 표면에 용이하게 접착될 수 있고, 표면 가열시 증착 효율이 높아질 수 있다.When the surface of the dry marshmallow is heated before adding the lactic acid bacteria, the viscosity of the surface of the dry marshmallow is slightly increased, so that the lactic acid bacteria added in the subsequent step can be easily adhered to the surface of the marshmallow, and the deposition efficiency when the surface is heated can be increased.
표면 가열 단계(S500)는 건조 마쉬멜로의 점성이 표면 가열 전 점성 대비 미리 결정된 값 이상이 될 때까지 수행될 수 있다.The surface heating step (S500) may be performed until the viscosity of the dried marshmallow becomes equal to or greater than a predetermined value compared to the viscosity before surface heating.
표면 가열 단계(S500)는 건조 마쉬멜로의 표면을 29℃이하로 가열하는 것일 수 있고, 예컨대 15℃ 내지 29℃, 20℃ 내지 25℃로 가열하는 것일 수 있다.The surface heating step (S500) may be heating the surface of the dried marshmallow to 29 ° C or lower, for example, heating to 15 ° C to 29 ° C, 20 ° C to 25 ° C.
유산균을 첨가하고 교반하는 단계(S200)에서 첨가되는 유산균은 108 내지 109CFU/g 예컨대, 1Х108 내지 9Х108CFU/g, 2Х108 내지 8Х108CFU/g, 3Х108 내지 7Х108CFU/g, 4Х108 내지 6Х108CFU/g 일 수 있다.The lactic acid bacteria added in the step of adding and stirring the lactic acid bacteria (S200) is 10 8 to 10 9 CFU / g, for example, 1Х10 8 to 9Х10 8 CFU / g, 2Х10 8 to 8Х10 8 CFU / g, 3Х10 8 to 7Х10 8 CFU / g, 4Х10 8 to 6Х10 8 CFU/g.
유산균을 첨가하고 교반하는 단계(S200)에서 첨가되는 유산균은 유산균 생균; 유산균 사균; 또는 유산균 생균 및 유산균 사균의 혼합물일 수 있다.The lactic acid bacteria added in the step of adding and stirring the lactic acid bacteria (S200) include live bacteria of lactic acid bacteria; dead lactic acid bacteria; Or it may be a mixture of live lactic acid bacteria and dead lactic acid bacteria.
유산균 생균 및 유산균 사균의 혼합물을 첨가하는 경우 유산균 생균만 추가하는 경우에 비해 유산균을 첨가하고 교반하는 단계(S200)에서 높은 온도로 표면을 가열하더라도 첨가된 유산균의 생존이나 활성에 부정적인 영향을 적게 미칠 수 있다는 장점이 있다.In the case of adding a mixture of live lactic acid bacteria and dead lactic acid bacteria, compared to the case of adding only live lactic acid bacteria, even if the surface is heated to a high temperature in the step of adding and stirring lactic acid bacteria (S200), the negative effect on the survival or activity of the added lactic acid bacteria is less. There are advantages to being able to.
일 구현예에 따르면, 유산균을 첨가하고 교반하는 단계(S200)에서 첨가되는 유산균은 유산균 생균일 수 있다.According to one embodiment, the lactic acid bacteria added in the step of adding and stirring the lactic acid bacteria (S200) may be live lactic acid bacteria.
유산균은 락토바실러스속 (Lactobacillus spp.), 락토코커스속 (Lactococcus spp.), 엔테로코커스속(Enterococcus spp.), 스트렙토코커스속(Streptococcus spp.) 및 비피도박테리움속 (Bififobacterium spp.)으로 이루어진 군에서 선택된 것일 수 있다.Lactobacillus is composed of Lactobacillus spp. , Lactococcus spp. , Enterococcus spp. , Streptococcus spp. and Bifidobacterium spp. It may be selected from the group.
유산균은 락토바실러스 플란타럼(Lactobacillus plantarum), 락포바실러스 람노서스(Lactobacillus rhamnosus), 스트렙토코커스 써모필러스(Streptococcus thermophilus), 비피도박테리움 롱검(Bifidobacterium longum), 락토바실러스 애시도필러스(Lactobacillus acidophilus), 락토바실러스 카제이(Lactobacillus casei), 락토바실러스 퍼멘텀(Lactobacillus fermentum), 락토바실러스 가세리(Lactobacillus gasseri), 락토바실러스 불가리쿠스(Lactobacillus delbrueckii subsp. Bulgaricus), 락토바실러스 헬베티쿠스(Lactobacillus helveticus), 락토바실러스 파라카제이(Lactobacillus paracasei), 락토바실러스 루테리(Lactobacillus reuteri) 및 락토바실러스 살리바리우스(Lactobacillus salivarius)로 이루어진 군에서 선택되는 것일 수 있으며, 이에 제한되는 것은 아니다.Lactic acid bacteria are Lactobacillus plantarum , Lactobacillus rhamnosus , Streptococcus thermophilus, Bifidobacterium longum , Lactobacillus acidophilus ), Lactobacillus casei , Lactobacillus fermentum , Lactobacillus gasseri, Lactobacillus delbrueckii subsp. Bulgaricus , Lactobacillus helveticus , Lactobacillus paracasei , Lactobacillus reuteri , and Lactobacillus salivarius. It may be selected from the group consisting of, but is not limited thereto.
유산균 증착 단계(S300)는 유산균과 교반된 건조 마쉬멜로의 표면을 특정 범위의 온도로 가열하는 것을 포함한다.The lactic acid bacteria deposition step (S300) includes heating the surface of the lactic acid bacteria and the stirred dried marshmallow to a temperature within a specific range.
건조 마쉬멜로와 유산균을 교반하기만 하는 경우에 비해, 유산균 교반 후 표면을 가열하는 유산균 증착 단계(S300)를 수행하는 경우 적은 양의 유산균으로도 건조 마쉬멜로 표면의 상당 부분을 유산균으로 코팅할 수 있다. 즉, 유산균을 교반한 후 표면 가열을 수행함으로써 건조 마쉬멜로 표면에 대한 유산균의 증착 효율을 높일 수 있다. 한편, 건조 마쉬멜로가 아닌 통상적인 마쉬멜로(예컨대 수분함량이 12 내지 25 중량%인 마쉬멜로)의 경우 건조 마쉬멜로에 비해 점성이 높아 유산균 첨가 만으로도 증착 효율이 우수할 수 있으나, 장기간 보존 시 유산균의 생존율이 낮아지고 최종 생산품 자체에서 부패가 쉽게 발생할 수 있는 문제가 있다.Compared to the case of just stirring the dry marshmallow and lactic acid bacteria, when the lactic acid bacteria deposition step (S300) of heating the surface after stirring the lactic acid bacteria is performed, a significant portion of the surface of the dry marshmallow can be coated with lactic acid bacteria even with a small amount of lactic acid bacteria. That is, by performing surface heating after stirring the lactic acid bacteria, the deposition efficiency of the lactic acid bacteria on the dry marshmallow surface can be increased. On the other hand, in the case of normal marshmallows (eg, marshmallows having a moisture content of 12 to 25% by weight), rather than dry marshmallows, the viscosity is higher than that of dry marshmallows, so the deposition efficiency may be excellent even with the addition of lactic acid bacteria, but the survival rate of lactic acid bacteria is low during long-term storage. However, there is a problem that corruption can easily occur in the final product itself.
유산균의 증착 효율을 높이게 되면 건조 마쉬멜로 한 개 당 더 많은 양의 유산균이 포함될 수 있어, 수요자가 적은 양의 마쉬멜로로부터 높은 함량의 유산균을 섭취할 수 있게 된다.If the deposition efficiency of lactic acid bacteria is increased, a larger amount of lactic acid bacteria can be included per dry marshmallow, so that consumers can consume a high content of lactic acid bacteria from a small amount of marshmallow.
한편, 유산균의 증착 효율이 낮은 경우 동일 함량의 유산균이 증착된 마쉬멜로를 제조하기 위해 더 많은 양의 유산균이 필요하여 비용적, 시간적인 단점이 있다. 또한, 유산균이 마쉬멜로 표면에 효과적으로 증착되지 않는 경우 최종적으로 얻어진 마쉬멜로 제품을 포장할 때 포장지 내부 바닥으로 유산균이 흘러내려 제품의 품질이 낮아지며, 보관이 어려운 단점이 있다.On the other hand, when the deposition efficiency of lactic acid bacteria is low, a larger amount of lactic acid bacteria is required to produce a marshmallow having the same amount of lactic acid bacteria deposited, which has disadvantages in terms of cost and time. In addition, when the lactic acid bacteria are not effectively deposited on the surface of the marshmallow, when the finally obtained marshmallow product is packaged, the lactic acid bacteria flow down to the inner bottom of the wrapping paper, reducing the quality of the product and making it difficult to store.
유산균 증착 단계(S300)의 가열 온도는 유산균의 증착 효율을 높일 수 있는 동시에, 증착된 유산균이 우수한 활성을 유지하면서 장기간 보존될 수 있는 범위에서 선택되는 것이 중요하다.It is important that the heating temperature of the lactic acid bacteria deposition step (S300) be selected within a range that can increase the deposition efficiency of lactic acid bacteria and preserve the deposited lactic acid bacteria for a long period of time while maintaining excellent activity.
유산균 증착 단계(S300)의 가열 온도는 30℃이상일 수 있다. 상기 온도범위는 유산균이 증착되지 않은 일반적인 건조 마쉬멜로의 최적 저장온도 보다 다소 높은 온도이며, 상기 최적 저장온도 보다 높은 온도로 가열하게 되면 마쉬멜로의 표면의 점성이 높아져 유산균의 증착률이 높아질 수 있다.The heating temperature of the lactic acid bacteria deposition step (S300) may be 30° C. or higher. The temperature range is a temperature slightly higher than the optimum storage temperature of general dry marshmallows in which lactic acid bacteria are not deposited, and when heated to a temperature higher than the optimum storage temperature, the viscosity of the surface of the marshmallow increases, thereby increasing the deposition rate of lactic acid bacteria.
또한, 유산균 증착 단계(S300)의 가열 온도는 40℃미만, 39℃이하, 38℃이하, 또는 37℃이하일 수 있다. 상기 온도 범위는 유산균 내 단백질이 변형되지 않을 수 있는 온도로, 해당 온도 범위 내에서 마쉬멜로 표면에 증착된 유산균의 활성이 높게 유지될 수 있다.In addition, the heating temperature of the lactic acid bacteria deposition step (S300) may be less than 40 °C, 39 °C or less, 38 °C or less, or 37 °C or less. The temperature range is a temperature at which proteins in the lactic acid bacteria may not be transformed, and the activity of the lactic acid bacteria deposited on the surface of the marshmallow can be maintained high within the temperature range.
일 구현예에 따르면, 유산균 증착 단계(S300)는 유산균과 교반된 건조 마쉬멜로의 표면을 30℃ 내지 37℃로 가열하는 것일 수 있다.According to one embodiment, the lactic acid bacteria deposition step (S300) may be to heat the surface of the lactic acid bacteria and the stirred dry marshmallow to 30 ° C to 37 ° C.
상기 온도 범위로 가열하게 되면 유산균의 높은 증착률을 나타냄과 동시에 유산균의 활성 및 보존성이 높은 효과가 나타날 수 있다. 이러한 효과는 8℃이상에서 서서히 활동을 시작하고, 체온과 유사한 37℃에서 가장 높은 활성을 나타내며, 45℃가 넘어가면 생육을 정지하고 60℃가 넘어가면 사멸하는 유산균의 성질과도 관련이 있을 것으로 예상된다.When heated to the above temperature range, a high deposition rate of lactic acid bacteria may be exhibited, and at the same time, the effect of high activity and preservation of lactic acid bacteria may be exhibited. These effects are thought to be related to the nature of lactic acid bacteria, which start their activity slowly at 8℃ or higher, show the highest activity at 37℃, which is similar to body temperature, stop growing at 45℃, and die at 60℃. expected
유산균 증착 단계(S300)의 가열 시간은 유산균이 충분히 증착될 수 있을 정도로 충분한 시간 동안 수행될 수 있다.The heating time of the lactic acid bacteria deposition step (S300) may be performed for a sufficient time to sufficiently deposit the lactic acid bacteria.
구체적으로, 유산균 증착 단계(S300)는 상기 교반된 건조 마쉬멜로의 표면을 1 내지 5초, 1 내지 4초, 또는 1.5 내지 3.5초 가열하는 것일 수 있다. 유산균 증착 단계(S300)는 상기 교반된 건조 마쉬멜로의 표면을 30℃ 내지 37℃로 1.5 내지 3.5초 가열하는 것일 수 있다.Specifically, the lactic acid bacteria deposition step (S300) may be to heat the surface of the stirred dry marshmallow for 1 to 5 seconds, 1 to 4 seconds, or 1.5 to 3.5 seconds. The lactic acid bacteria deposition step (S300) may be to heat the surface of the stirred dry marshmallow to 30 ° C to 37 ° C for 1.5 to 3.5 seconds.
유산균 증착 단계(S300)에서 가열 방식은 히터를 이용해 마쉬멜로의 표면을 가열하는 것일 수 있다. 히터는 전열기일 수 있다.In the lactic acid bacteria deposition step (S300), the heating method may be to heat the surface of the marshmallow using a heater. The heater may be an electric heater.
유산균 증착 단계(S300)에서 가열 방식은 상부 및/또는 하부에 히터가 배치된 컨베이어 벨트 상에 교반된 건조 마쉬멜로를 위치시켜 이동시키면서 가열하는 것일 수 있다. 컨베이어 벨트의 이동 속도에 따라 교반된 건조 마쉬멜로에 대한 가열 시간이 변경될 수 있다.In the lactic acid bacteria deposition step (S300), the heating method may be to place the stirred dry marshmallow on a conveyor belt having a heater disposed thereon and/or below it and heat it while moving it. Depending on the moving speed of the conveyor belt, the heating time for the stirred dry marshmallows can be changed.
예를 들어, 유산균 증착 단계(S300)는 상기 교반된 건조 마쉬멜로를 컨베이어 벨트 상에 위치시키고, 상기 컨베이어 벨트의 상부 및 하부에 배치된 전열기로 상기 교반된 건조 마쉬멜로의 표면을 가열하는 것일 수 있다. 이 경우, 컨베이어 벨트 상부 및 하부에 배치된 전열기에 의해 건조 마쉬멜로의 상부 및 하부에 고르게 열을 전달시킬 수 있고, 궁극적으로 마쉬멜로의 상하부에 유산균을 동시 증착시킬 수 있다.For example, in the lactic acid bacteria deposition step (S300), the stirred dry marshmallow is placed on a conveyor belt, and the surface of the stirred dried marshmallow is heated with electric heaters disposed above and below the conveyor belt. In this case, heat can be evenly transferred to the upper and lower portions of the dried marshmallows by electric heaters disposed above and below the conveyor belt, and ultimately, lactic acid bacteria can be simultaneously deposited on the upper and lower portions of the marshmallows.
건조한 후 냉각하는 단계(S400)는 유산균 증착 단계(S300)에서 수득한 마쉬멜로를 건조한 후 냉각하는 것을 포함할 수 있다.The step of drying and then cooling (S400) may include drying and then cooling the marshmallow obtained in the lactic acid bacteria deposition step (S300).
유산균 증착 단계(S300)를 수행한 후 상기 건조한 후 냉각하는 단계(S400)를 수행함으로써 유산균이 증착된 마쉬멜로가 수분을 흡수하는 것을 억제할 수 있다. 건조한 후 냉각하는 단계(S400)를 수행하는 경우 최종 생성물의 수분함량이 낮아질 수 있어 건조한 후 냉각하는 단계(S400)를 수행하지 않는 경우에 비해 유산균이 증착된 마쉬멜로의 부패 정도가 억제될 수 있고, 생성물의 부피가 작아져 보관 및 이동이 용이한 장점이 있다.After the lactic acid bacteria deposition step (S300) is performed, the drying and then cooling step (S400) is performed to prevent the marshmallow on which the lactic acid bacteria are deposited from absorbing moisture. When the drying and cooling step (S400) is performed, the moisture content of the final product can be lowered, so that the degree of decay of the marshmallow deposited with lactic acid bacteria can be suppressed compared to the case where the drying and cooling step (S400) is not performed, The volume of the product is small, so it has the advantage of being easy to store and move.
또한, 본 발명은 전술한 제조방법으로 제조된 유산균이 증착된 마쉬멜로를 제공한다.In addition, the present invention provides a marshmallow deposited with lactic acid bacteria prepared by the above-described manufacturing method.
유산균이 증착된 마쉬멜로는 전체 중량 대비 수분함량이 10 중량% 이하, 8 중량% 이하, 7 중량% 이하, 6 중량% 이하, 5 중량% 이하, 4 중량% 이하 또는 3 중량% 이하일 수 있다. 유산균이 증착된 마쉬멜로는 전체 중량 대비 수분함량이 0.0001 내지 10 중량%, 0.0001 내지 9 중량%, 0.0001 내지 8 중량%, 0.0001 내지 7 중량%, 0.0001 내지 6 중량%, 0.0001 내지 5 중량%, 0.001 내지 4 중량%, 0.001 내지 3 중량%, 0.0001 내지 2 중량%, 또는 0.001 내지 1 중량%일 수 있다.The marshmallow deposited with lactic acid bacteria may have a moisture content of 10% by weight or less, 8% by weight or less, 7% by weight or less, 6% by weight or less, 5% by weight or less, 4% by weight or less, or 3% by weight or less, based on the total weight. The marshmallow deposited with lactic acid bacteria has a water content of 0.0001 to 10% by weight, 0.0001 to 9% by weight, 0.0001 to 8% by weight, 0.0001 to 7% by weight, 0.0001 to 6% by weight, 0.0001 to 5% by weight, and 0.001 to 6% by weight relative to the total weight. 4 wt%, 0.001 to 3 wt%, 0.0001 to 2 wt%, or 0.001 to 1 wt%.
본 발명의 방법으로 제조된 마쉬멜로는 통상적으로 알려진 마쉬멜로의 수분함량(약 12-25 중량%)에 비해 낮은 수분함량(약 10 중량% 이하)을 가짐으로써 장기간 보존 시에도 쉽게 변질되지 않는 장점이 있다. 또한, 본 발명의 방법으로 제조된 마쉬멜로는 낮은 수분함량으로 인해 상대적으로 부피가 작아 보관성 및 휴대성이 우수하다.The marshmallows prepared by the method of the present invention have a low moisture content (about 10% by weight or less) compared to the commonly known moisture content (about 12-25% by weight) of marshmallows, and thus have the advantage of not easily deteriorating even when stored for a long time. . In addition, the marshmallow prepared by the method of the present invention has a relatively small volume due to its low moisture content, and thus has excellent storage and portability.
본 발명의 제조방법은 우수한 효율로 건조 마쉬멜로에 유산균을 증착시킬 수 있다. 본 발명의 제조방법으로 제조된 유산균이 증착된 마쉬멜로는 장기간 보존 시에도 높은 유산균 생존율을 나타내며, 위액 및 장액의 환경에서도 유산균이 보존될 수 있다.The manufacturing method of the present invention can deposit lactic acid bacteria on dry marshmallows with excellent efficiency. Marshmallow deposited with lactic acid bacteria prepared by the manufacturing method of the present invention shows a high lactic acid bacteria survival rate even when stored for a long time, and lactic acid bacteria can be preserved in the environment of gastric juice and intestinal juice.
이하, 본 발명을 구체적으로 설명하기 위해 실시예를 들어 상세하게 설명하기로 한다.Hereinafter, examples will be described in detail to explain the present invention in detail.
유산균이 증착된 마쉬멜로 제조Production of marshmallow deposited with lactic acid bacteria
실시예 1Example 1
설탕 48 중량부, 산화전분 17 중량부, 옥수수시럽 16 중량부, 포도당 14 중량부, 젤라틴 1.5 중량부, 향료 2.99 중량부, 메타인산나트륨 0.490 중량부 및 식용색소 0.02 중량부를 포함하는 마쉬멜로를 준비하였다. 식품 건조기를 이용해 약 100-120℃에서 마쉬멜로를 건조한 후 냉각하고, 약 100-120℃에서 가열하고 냉각하는 것을 2회 반복하고, 다시 약 100-120℃에서 건조하고 냉각하여 수분함량이 2.5 중량%인 건조 마쉬멜로를 제조하였다(S100에 대응). 제조된 건조 마쉬멜로가 담긴 용기에 락토바실러스 플란타럼 균주(KCTC3108)를 5ⅹ108CFU/g의 생균수가 포함된 건조 분말 형태로 첨가하였다. 건조 마쉬멜로와 균주를 일정 시간동안 충분히 교반하였다(S200에 대응). 그 후 건조 마쉬멜로의 표면을 30℃로 가열하였다(S300에 대응). 표면이 가열된 건조 마쉬멜로를 식품 건조기에서 건조한 후 냉각하였다(S400에 대응).A marshmallow containing 48 parts by weight of sugar, 17 parts by weight of oxidized starch, 16 parts by weight of corn syrup, 14 parts by weight of glucose, 1.5 parts by weight of gelatin, 2.99 parts by weight of flavoring, 0.490 parts by weight of sodium metaphosphate and 0.02 parts by weight of food coloring was prepared. . After drying the marshmallows at about 100-120 ° C using a food dryer, cooling them, repeating the heating and cooling at about 100-120 ° C twice, and drying and cooling again at about 100-120 ° C to reduce the moisture content to 2.5% by weight. Phosphorus dried marshmallows were prepared (corresponding to S100). Lactobacillus plantarum strain (KCTC3108) was added in the form of dry powder containing 5×10 8 CFU/g viable cell count to a container containing the prepared dry marshmallow. The dry marshmallow and the strain were sufficiently stirred for a certain period of time (corresponding to S200). After that, the surface of the dried marshmallow was heated to 30 ° C. (corresponding to S300). The dried marshmallows with heated surfaces were dried in a food dryer and then cooled (corresponding to S400).
실시예 2Example 2
실시예 1과 동일하되, 균주와 교반된 건조 마쉬멜로의 표면을 35℃로 가열하였다.Same as Example 1, but the surface of the dry marshmallow stirred with the strain was heated to 35 ° C.
실시예 3Example 3
실시예 1과 동일하되, 균주와 교반된 건조 마쉬멜로의 표면을 37℃로 가열하였다.Same as in Example 1, but the surface of the dried marshmallow stirred with the strain was heated to 37 ° C.
실시예 4Example 4
실시예 1과 동일하되, 락토바실러스 플란타럼 균주 대신 락토바실러스 람노서스 균주(ATCC7469)를 첨가하였다.Same as Example 1, except that Lactobacillus rhamnosus strain (ATCC7469) was added instead of Lactobacillus plantarum strain.
실시예 5Example 5
실시예 1과 동일하되, 락토바실러스 플란타럼 균주 대신 락토바실러스 애씨도필러스 균주(ATCC-4356L)를 첨가하였다.Same as Example 1, except that Lactobacillus acidophilus strain (ATCC-4356L) was added instead of Lactobacillus plantarum strain.
실시예 6Example 6
실시예 1과 동일하되, 락토바실러스 플란타럼 균주 대신 비피도박테리움 롱검(ATCC 15707) 균주를 첨가하였다.Same as in Example 1, except that the Bifidobacterium longum (ATCC 15707) strain was added instead of the Lactobacillus plantarum strain.
실시예 7Example 7
실시예 1과 동일하되, 균주를 첨가하기 전 건조 마쉬멜로의 표면을 20℃로 가열하였다(S500에 대응).Same as Example 1, but before adding the strain, the surface of the dried marshmallow was heated to 20 ° C (corresponding to S500).
실시예 8Example 8
실시예 1과 동일하되, 균주를 첨가하기 전 건조 마쉬멜로의 표면을 25℃로 가열하였다.Same as Example 1, but the surface of the dried marshmallow was heated to 25 ° C. before adding the strain.
비교예 1Comparative Example 1
실시예 1과 동일하되, 균주와 교반된 건조 마쉬멜로의 표면을 가열하지 않았다.Same as Example 1, but the surface of the dry marshmallow stirred with the strain was not heated.
비교예 2Comparative Example 2
실시예 1과 동일하되, 균주와 교반된 건조 마쉬멜로의 표면을 20℃로 가열하였다.Same as in Example 1, but the surface of the dried marshmallow stirred with the strain was heated to 20 ° C.
비교예 3Comparative Example 3
실시예 1과 동일하되, 균주와 교반된 건조 마쉬멜로의 표면을 25℃로 가열하였다.Same as Example 1, but the surface of the dry marshmallow stirred with the strain was heated to 25 ° C.
비교예 4Comparative Example 4
실시예 1과 동일하되, 균주와 교반된 건조 마쉬멜로의 표면을 45℃로 가열하였다.Same as in Example 1, but the surface of the dried marshmallow stirred with the strain was heated to 45 ° C.
비교예 5Comparative Example 5
실시예 1과 동일하되, 표면이 가열된 건조 마쉬멜로를 식품 건조기에서 건조하고 냉각하는 단계를 수행하지 않았다.Same as Example 1, but drying and cooling the dried marshmallow with a heated surface in a food dryer was not performed.
비교예 6Comparative Example 6
설탕 48 중량부, 산화전분 17 중량부, 옥수수시럽 16 중량부, 포도당 14 중량부, 젤라틴 1.5 중량부, 향료 2.99 중량부, 메타인산나트륨 0.490 중량부 및 식용색소 0.02 중량부를 포함하는 마쉬멜로를 준비하였다. 마쉬멜로가 담긴 용기에 락토바실러스 플란타럼 균주를 5ⅹ108CFU/g의 생균수가 포함된 건조 분말 형태로 첨가하였다. 마쉬멜로와 균주를 일정 시간동안 충분히 교반하였다. 균주와 교반된 마쉬멜로의 표면을 25℃로 가열하였다.A marshmallow containing 48 parts by weight of sugar, 17 parts by weight of oxidized starch, 16 parts by weight of corn syrup, 14 parts by weight of glucose, 1.5 parts by weight of gelatin, 2.99 parts by weight of flavoring, 0.490 parts by weight of sodium metaphosphate and 0.02 parts by weight of food coloring was prepared. . Lactobacillus plantarum strain was added to the container containing the marshmallow in the form of a dry powder containing 5ⅹ10 8 CFU/g viable cell count. The marshmallow and the strain were sufficiently stirred for a certain period of time. The surface of the strain and stirred marshmallow was heated to 25 ° C.
비교예 7Comparative Example 7
비교예 6과 동일하되, 균주와 교반된 마쉬멜로의 표면을 30℃로 가열하였다.Same as Comparative Example 6, but the surface of the strain and the stirred marshmallow was heated to 30 ° C.
비교예 8Comparative Example 8
비교예 6과 동일하되, 균주와 교반된 마쉬멜로의 표면을 가열하지 않았다.Same as Comparative Example 6, but the surface of the strain and stirred marshmallow was not heated.
표 1에 실시예 1 내지 8 및 비교예 1 내지 8의 제조조건 및 최종 생성물의 수분함량을 정리하였다. 수분함량은 생성물의 전체 중량 대비 수분의 중량%를 나타낸 것이다.Table 1 summarizes the manufacturing conditions of Examples 1 to 8 and Comparative Examples 1 to 8 and the moisture content of the final product. Moisture content represents the weight percent of moisture relative to the total weight of the product.
실험예 1: 제조방법에 따른 유산균 함유량Experimental Example 1: Lactic acid bacteria content according to manufacturing method
상기 방법으로 제조된 직후에 마쉬멜로 내 유산균수를 확인하여 제조방법에 따른 유산균 증착 효율을 확인하였다. 마쉬멜로 내 유산균수를 측정하기 위해 마쉬멜로를 식품용 분쇄기(BagMixer 400, 인터사이언스, 프랑스)를 사용하여 마쉬멜로 1g 당 4 ㎖ 의 멸균 생리 식염수를 첨가하여 10분간 분쇄하였다. 유산균 생균 수의 측정은 멸균 생리 식염수로 적정량 십진 희석하여 MRS 한천 배지에 도말한 후 37 ℃에 서 24시간 배양 후 측정하였다. 표 2에 마쉬멜로 1g 당 유산균수를 나타내었다(단위: CFU/g). 유산균 함유량은 최초 투입된 유산균수 대비 마쉬멜로에 남아있는 유산균수의 비율로 나타내었다. Immediately after manufacturing by the above method, the number of lactic acid bacteria in the marshmallow was confirmed to confirm the lactic acid bacteria deposition efficiency according to the manufacturing method. To measure the number of lactic acid bacteria in the marshmallow, the marshmallow was ground using a food grinder (BagMixer 400, Interscience, France) for 10 minutes by adding 4 ml of sterile physiological saline per 1 g of marshmallow. The number of viable lactic acid bacteria was measured after 24 hours of culture at 37 ° C. after smearing on MRS agar medium after diluting an appropriate amount with sterile physiological saline in decimal. Table 2 shows the number of lactic acid bacteria per 1 g of marshmallow (unit: CFU / g). The content of lactic acid bacteria was expressed as the ratio of the number of lactic acid bacteria remaining in the marshmallow to the number of lactic acid bacteria initially added.
유산균수를 측정한 결과 유산균을 교반한 후 건조 마쉬멜로의 표면을 30-37℃로 가열한 경우 유산균 함유량이 약 80-85%였다 (실시예 1 내지 6). 반면 유산균을 교반한 후 표면 가열을 수행하지 않은 경우 유산균 함유량이 약 20%로 현저히 낮았다(비교예 1). 또한 유산균과 교반된 마쉬멜로의 표면을 30℃보다 낮은 온도인 20-25℃로 가열한 경우 유산균 함유량이 약 55%로 높지 않았다(비교예 2 및 3). 한편 전술한 것처럼 건조 마쉬멜로는 유산균을 교반한 후 표면을 25℃로 가열한 경우 유산균 함유량이 약 58%로 높지 않았으나(비교예 3), 비건조 마쉬멜로의 경우 유산균을 교반한 후 표면을 가열하지 않더라도 유산균 함유량이 약 70%였고(비교예 8), 표면을 25℃로 가열한 경우 유산균 함유량이 약 80%였다(비교예 6). 이는 마쉬멜로의 물성(건조 또는 비건조)에 따라 유산균을 효과적으로 증착시키기 위한 표면 가열 온도가 상이하다는 것을 의미한다. 또한, 유산균을 투입하기 전에 건조 마쉬멜로의 표면을 먼저 가열한 경우의 유산균 함유량은 약 85% 였다(실시예 7 및 8). 실시예 7 및 8은 유산균과 교반하기 전 건조 마쉬멜로의 표면을 먼저 가열하는 단계를 수행하지 않은 실시예 1에 비해 높은 증착률을 나타내었다.As a result of measuring the number of lactic acid bacteria, when the surface of the dried marshmallow was heated to 30-37 ° C. after stirring the lactic acid bacteria, the lactic acid bacteria content was about 80-85% (Examples 1 to 6). On the other hand, when surface heating was not performed after stirring the lactic acid bacteria, the content of lactic acid bacteria was significantly low at about 20% (Comparative Example 1). In addition, when the surface of the marshmallow stirred with lactic acid bacteria was heated to 20-25 ° C, which is lower than 30 ° C, the lactic acid bacteria content was not as high as about 55% (Comparative Examples 2 and 3). On the other hand, as described above, when the surface of the dried marshmallow was stirred at 25 ° C. after stirring the lactic acid bacteria, the content of lactic acid bacteria was not as high as about 58% (Comparative Example 3), but in the case of non-dried marshmallows, even if the surface was not heated after stirring the lactic acid bacteria The lactic acid bacteria content was about 70% (Comparative Example 8), and the lactic acid bacteria content was about 80% when the surface was heated to 25 ° C (Comparative Example 6). This means that the surface heating temperature for effectively depositing lactic acid bacteria is different depending on the physical properties (dried or non-dried) of the marshmallow. In addition, when the surface of the dried marshmallow was first heated before adding the lactic acid bacteria, the lactic acid bacteria content was about 85% (Examples 7 and 8). Examples 7 and 8 showed a higher deposition rate than Example 1 in which the step of first heating the surface of the dried marshmallow before stirring with lactic acid bacteria was not performed.
실험예 2: 장기 보존시 유산균 수 변화 측정Experimental Example 2: Measurement of change in the number of lactic acid bacteria during long-term storage
상기 방법으로 제조된 마쉬멜로를 상온, 상대습도 40% 조건에서 3개월 보존한 후 유산균수의 변화를 측정하였다. 마쉬멜로의 분쇄 방법 및 유산균수의 측정 방법은 위 실험예 1과 동일하게 적용하였다. 보존기간의 경과에 따른 생균수의 변화를 아래 표 3에 나타내었다. 표 3에서 생존율은 최초 유산균이 증착된 마쉬멜로 제조 시 측정한 유산균 수에 대한 3개월 경과 후 마쉬멜로에 포함된 유산균 수를 대비하여 산출하였다.After storing the marshmallows prepared by the above method for 3 months at room temperature and 40% relative humidity, the change in the number of lactic acid bacteria was measured. The method of crushing the marshmallow and measuring the number of lactic acid bacteria was applied in the same manner as in Experimental Example 1 above. Changes in the number of viable cells over the storage period are shown in Table 3 below. In Table 3, the survival rate was calculated by comparing the number of lactic acid bacteria contained in the marshmallow after 3 months to the number of lactic acid bacteria measured during production of the marshmallow on which the lactic acid bacteria were initially deposited.
높은 온도에서 표면가열을 수행한 비교예 4의 마쉬멜로는 상온, 40% 습도 조건에서 장기보관 시 유산균 생존율이 약 85% 였으나, 실시예들의 유산균 생존율은 약 95% 로 상대적으로 높았다.또한, 유산균을 교반하고 표면 가열시킨 후 추가 건조 및 냉각 단계를 수행하지 않은 비교예 5의 마쉬멜로는 추가 건조 및 냉각 단계를 수행한 실시예 1에 비해 상온, 40% 습도 조건에서 장기보관 시 유산균 생존율이 현저히 낮았다. 추가로, 건조 마쉬멜로가 아닌 일반 마쉬멜로에 유산균을 증착시킨 비교예 6 내지 8은 건조 마쉬멜로에 유산균을 증착시킨 경우에 비해 상온, 40% 습도 조건에서 장기보관 시 유산균 생존율이 현저히 낮았다.The marshmallow of Comparative Example 4, which was subjected to surface heating at a high temperature, had a lactic acid bacteria survival rate of about 85% when stored for a long time at room temperature and 40% humidity conditions, but the lactic acid bacteria survival rate of the examples was relatively high at about 95%. In addition, the lactic acid bacteria The marshmallow of Comparative Example 5, which was not subjected to additional drying and cooling steps after stirring and surface heating, showed significantly lower lactic acid bacteria survival rate during long-term storage at room temperature and 40% humidity conditions compared to Example 1 in which additional drying and cooling steps were performed. In addition, in Comparative Examples 6 to 8, in which lactic acid bacteria were deposited on normal marshmallows rather than dry marshmallows, the survival rate of lactic acid bacteria during long-term storage at room temperature and 40% humidity was significantly lower than when lactic acid bacteria were deposited on dry marshmallows.
실험예 3: 인공위액 및 인공장액 내 유산균 생존율 측정Experimental Example 3: Measurement of lactic acid bacteria survival rate in artificial gastric juice and artificial intestinal fluid
마쉬멜로에 증착된 유산균이 인체의 위 및 장의 환경에서 보호될 수 있는지 확인하기 위해, 인공적으로 조성된 위액 및 장액 배지를 제조하고 인공위액 및 인공장액 연속 처리 시 유산균의 생존율을 측정하였다.In order to confirm whether the lactic acid bacteria deposited on the marshmallow can be protected in the human stomach and intestinal environment, artificially prepared gastric and intestinal media were prepared and the survival rate of the lactic acid bacteria was measured during continuous treatment of artificial gastric and intestinal fluids.
NaCl 8.5g/L가 첨가된 생리식염수에 pepsin (Pepsin from porcine gastric mucosa, 1000 units/mg protein, Sigma USA) 0.4g/L를 투입하고, 10% HCl을 이용하여 pH 2.5로 조정하여 인공위액을 제조하였다. 인공위액 90ml에 유산균이 증착된 마쉬멜로를 적정량 넣고 30초간 교반(stirring)한 다음, 37, 150 rpm로 유지되는 워터 배스(water bath)에서 2시간 동안 반응시켜 주었다. 반응 후 3.0%의 Ox-gall solution을 10ml 첨가하여 담즙 농도를 0.3%로 조정하였으며, 4N NaOH 1ml 첨가하여 최종 pH 6.8 되게 조정하여 주었다. 인공장액 조건 조성 후 37, 150 rpm으로 유지되는 워터 배스(water bath)에서 2시간 동안 반응시켰다. 반응 후의 생균수를 MRS agar를 이용하여 측정하였다. 유산균이 증착된 마쉬멜로의 인공위액과 인공장액 연속적 측정 실험 결과는 하기 표 4에 나타내었다. 아래 표 4처럼 건조 마쉬멜로에 증착된 유산균은 위액 및 장액의 환경에서 보존되는 것을 확인하였다.0.4 g/L of pepsin (Pepsin from porcine gastric mucosa, 1000 units/mg protein, Sigma USA) was added to physiological saline with 8.5 g/L of NaCl, and the pH was adjusted to 2.5 with 10% HCl to simulate gastric juice. manufactured. An appropriate amount of lactic acid bacteria-deposited marshmallow was added to 90 ml of artificial gastric juice, stirred for 30 seconds, and then reacted for 2 hours in a water bath maintained at 37 and 150 rpm. After the reaction, the bile concentration was adjusted to 0.3% by adding 10ml of 3.0% Ox-gall solution, and the final pH was adjusted to 6.8 by adding 1ml of 4N NaOH. After creating artificial intestinal fluid conditions, it was reacted for 2 hours in a water bath maintained at 37 and 150 rpm. The number of viable cells after the reaction was measured using MRS agar. The experimental results of continuous measurement of artificial gastric juice and artificial intestinal fluid of marshmallow deposited with lactic acid bacteria are shown in Table 4 below. As shown in Table 4 below, it was confirmed that the lactic acid bacteria deposited on the dried marshmallow were preserved in the environment of gastric juice and intestinal juice.
전술한 본 발명의 설명은 예시를 위한 것이며, 본 발명이 속하는 기술분야의 통상의 지식을 가진 자는 본 발명의 기술적 사상이나 필수적인 특징을 변경하지 않고서 다른 구체적인 형태로 쉽게 변형이 가능하다는 것을 이해할 수 있을 것이다. 그러므로 이상에서 기술한 실시예들은 모든 면에서 예시적인 것이며 한정적이 아닌 것으로 이해해야만 한다.The above description of the present invention is for illustrative purposes, and those skilled in the art can understand that it can be easily modified into other specific forms without changing the technical spirit or essential features of the present invention. will be. Therefore, the embodiments described above should be understood as illustrative in all respects and not limiting.
Claims (10)
상기 건조 마쉬멜로에 유산균을 첨가하고 교반하는 단계;
상기 교반된 건조 마쉬멜로의 표면을 30℃ 내지 37℃로 가열하는 유산균 증착 단계; 및
상기 유산균 증착 단계에서 수득한 마쉬멜로를 건조한 후 냉각하는 단계;를 포함하고,
상기 원료 마쉬멜로는 설탕 40 내지 50 중량부, 산화전분 16 내지 18 중량부, 옥수수시럽 15 내지 17 중량부, 포도당 13 내지 15 중량부, 젤라틴 1.4 내지 1.6 중량부, 향료 2.8 내지 3.2 중량부, 메타인산나트륨 0.45 내지 0.55 중량부 및 식용색소 0.015 내지 0.025 중량부를 포함하며,
상기 유산균을 첨가하고 교반하는 단계에서 첨가되는 유산균은 108 내지 109CFU/g인 유산균이고,
상기 유산균 증착 단계에서는
상기 교반된 건조 마쉬멜로를 컨베이어 벨트에 위치시켜 상기 컨베이어 벨트의 상부 및 하부에 배치된 전열기로 상기 교반된 건조 마쉬멜로의 표면을 30℃ 내지 37℃로 1.5 내지 3.5초 가열하는 것인 유산균이 증착된 마쉬멜로의 제조방법.
The raw material marshmallow is firstly dried in a dryer and then cooled, the firstly dried marshmallow is firstly heated at 60 ° C to 150 ° C and then cooled, and the firstly heated marshmallow is secondarily heated at 60 ° C to 150 ° C and then cooled and drying the secondarily heated marshmallow in a dryer and then cooling it to prepare a dried marshmallow having a volume of 0.1 to 5 mm 3 ;
Adding lactic acid bacteria to the dried marshmallow and stirring;
Lactic acid bacteria deposition step of heating the surface of the stirred dry marshmallow to 30 ° C to 37 ° C; and
Including; drying and cooling the marshmallow obtained in the lactic acid bacteria deposition step;
The raw material marshmallow contains 40 to 50 parts by weight of sugar, 16 to 18 parts by weight of oxidized starch, 15 to 17 parts by weight of corn syrup, 13 to 15 parts by weight of glucose, 1.4 to 1.6 parts by weight of gelatin, 2.8 to 3.2 parts by weight of flavoring agent, metaphosphoric acid 0.45 to 0.55 parts by weight of sodium and 0.015 to 0.025 parts by weight of food coloring,
The lactic acid bacteria added in the step of adding and stirring the lactic acid bacteria is 10 8 to 10 9 CFU / g of lactic acid bacteria,
In the lactic acid bacteria deposition step,
A marshmallow deposited with lactic acid bacteria, wherein the agitated dry marshmallow is placed on a conveyor belt and the surface of the agitated dried marshmallow is heated to 30 ° C to 37 ° C for 1.5 to 3.5 seconds with electric heaters disposed at the top and bottom of the conveyor belt. Manufacturing method of.
The method of claim 1 , further comprising heating the surface of the dried marshmallow to 20° C. to 25° C. before adding and stirring the lactic acid bacteria.
The method of claim 1, wherein the lactic acid bacteria added in the step of adding and stirring the lactic acid bacteria are live lactic acid bacteria.
The method of claim 1, wherein the lactic acid bacteria added in the step of adding and stirring the lactic acid bacteria are dead lactic acid bacteria.
The method of claim 1, wherein the lactic acid bacteria added in the step of adding and stirring the lactic acid bacteria is a mixture of live lactic acid bacteria and dead lactic acid bacteria.
The method according to claim 1, wherein the lactic acid bacteria are Lactobacillus plantarum , Lactobacillus rhamnosus, Streptococcus thermophilus, Bifidobacterium longum , Lactobacillus ash Dophilus ( Lactobacillus acidophilus ), Lactobacillus casei ( Lactobacillus casei ) and Lactobacillus fermentum ( Lactobacillus fermentum ) A method for producing a marshmallow deposited with at least one lactic acid bacteria selected from the group consisting of.
A marshmallow deposited with lactic acid bacteria prepared by the method of any one of claims 1 to 6.
The marshmallow of claim 7, wherein the marshmallow has a moisture content of 0.0001 to 10% by weight.
An apparatus for producing marshmallows deposited with lactic acid bacteria prepared by the manufacturing method of claim 1.
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