KR20230045760A - Food preservatives made from natural ingredients - Google Patents
Food preservatives made from natural ingredients Download PDFInfo
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- KR20230045760A KR20230045760A KR1020210128413A KR20210128413A KR20230045760A KR 20230045760 A KR20230045760 A KR 20230045760A KR 1020210128413 A KR1020210128413 A KR 1020210128413A KR 20210128413 A KR20210128413 A KR 20210128413A KR 20230045760 A KR20230045760 A KR 20230045760A
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- unripe
- raspberry
- extract
- food
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- ALABRVAAKCSLSC-UHFFFAOYSA-N rutin Natural products CC1OC(OCC2OC(O)C(O)C(O)C2O)C(O)C(O)C1OC3=C(Oc4cc(O)cc(O)c4C3=O)c5ccc(O)c(O)c5 ALABRVAAKCSLSC-UHFFFAOYSA-N 0.000 description 1
- 235000005493 rutin Nutrition 0.000 description 1
- 229960004555 rutoside Drugs 0.000 description 1
- ZWRRJEICIPUPHZ-UHFFFAOYSA-N schisandrol B Natural products COC1=C2C=3C(OC)=C(OC)C(OC)=CC=3CC(C)(O)C(C)CC2=CC2=C1OCO2 ZWRRJEICIPUPHZ-UHFFFAOYSA-N 0.000 description 1
- 229930193195 schizandrin Natural products 0.000 description 1
- KZJWDPNRJALLNS-VJSFXXLFSA-N sitosterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CC[C@@H](CC)C(C)C)[C@@]1(C)CC2 KZJWDPNRJALLNS-VJSFXXLFSA-N 0.000 description 1
- 229950005143 sitosterol Drugs 0.000 description 1
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- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
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- 239000001648 tannin Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
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- 235000019156 vitamin B Nutrition 0.000 description 1
- 239000011720 vitamin B Substances 0.000 description 1
- 235000008979 vitamin B4 Nutrition 0.000 description 1
- 239000011579 vitamin B4 Substances 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 239000000341 volatile oil 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
- A23L3/3454—Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals in the form of liquids or solids
- A23L3/3463—Organic compounds; Microorganisms; Enzymes
- A23L3/3472—Compounds of undetermined constitution obtained from animals or plants
-
- 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
- A23L3/40—Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by drying or kilning; Subsequent reconstitution
- A23L3/44—Freeze-drying
-
- 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
- A23V2250/00—Food ingredients
- A23V2250/20—Natural extracts
- A23V2250/21—Plant extracts
-
- 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
- A23V2300/14—Extraction
-
- 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
- A23V2300/31—Mechanical 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
- A23V2300/00—Processes
- A23V2300/50—Concentrating, enriching or enhancing in functional factors
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Botany (AREA)
- Microbiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
Abstract
Description
본 발명은 인체에 무해한 천연성분을 최적의 배합비율로 조성하여 식품에 첨가하면서 미생물 성장을 억제하여 식품의 저장성과 안전성을 연장시키면서 식중독 사고등의 질병의 원인이 되는 병원성 세균으로부터 인체를 보호할 수 있는 것을 특징으로 하는 천연성분으로 제조된 식품보존료 및 이의 제조방법에 관한 것이다. The present invention is able to protect the human body from pathogenic bacteria that cause diseases such as food poisoning accidents while extending the shelf life and safety of food by suppressing the growth of microorganisms while adding natural ingredients harmless to the human body in an optimal mixing ratio and adding them to food. It relates to a food preservative made of natural ingredients and a method for producing the same.
일반적으로 식품의 미생물 성장을 억제하여 저장성 및 안전성을 연장시키기 위한 방법으로 인공 합성보존료가 사용되고 있으나, 합성 물질의 독성 및 돌연변이 유발 등의 위험성 때문에 안전한 천연 보존료의 대한 관심이 증가하고 있고, 더불어, 최근 다양한 식중독 사고와 신종 코로나바이러스 감염증(COVID-19)의 확산으로 각종 질병의 원인이 되는 병원성 세균으로부터 인체를 보호하기 위한 다양한 항균제품에 대한 수요가 늘어가고 있다.In general, artificial synthetic preservatives are used as a way to prolong shelf life and safety by inhibiting the growth of microorganisms in food, but interest in safe natural preservatives is increasing due to the toxicity and mutagenicity of synthetic materials. Demand for various antibacterial products to protect the human body from pathogenic bacteria that cause various diseases is increasing due to various food poisoning accidents and the spread of new coronavirus infection (COVID-19).
각종 식물에는 페놀류와 플라보노이드류 등의 항산화를 비롯한 항균에 유용한 생리활성 성분이 다량 함유된 것으로 알려져 있다. It is known that various plants contain a large amount of physiologically active components useful for antibacterial activity including antioxidants such as phenols and flavonoids.
특히, 식물 중 복분자는 엘라그산(ellagic acid), 갈산(gallic acid), 안토시아닌(anthocyanin), 플라보노이드(flavonoid), 폴리페놀(polyphenol)등의 기능성 화합물이 존재하며, 항균 활성의 효과가 보고되고 있는데, 이와 같은 생리활성은 품종이나 성숙도, 추출 방법에 따라 차이가 있다. 따라서, 본 발명자는 복분자를 활용하되, 최적의 성숙도, 추출 방법을 통해 세균 8종에 대한 항균 활성을 기능을 갖도록 하는 식품보존료를 제공하고 자 한다. In particular, bokbunja among plants has functional compounds such as ellagic acid, gallic acid, anthocyanin, flavonoid, and polyphenol, and the effect of antibacterial activity has been reported. However, these physiological activities differ depending on the variety, degree of maturity, and extraction method. Therefore, the inventors of the present invention intend to provide a food preservative that utilizes bokbunja but has an antibacterial activity against 8 types of bacteria through an optimal maturity and extraction method.
본 발명은 상기 문제를 해결하기 위해,In order to solve the above problem, the present invention
인체에 무해한 천연성분으로 제조하면서 최적의 배합비율로 조성하여 식품에 첨가하고, 미생물 성장을 억제하여 식품의 저장성과 안전성을 연장시키면서 식중독 사고등의 질병의 원인이 되는 병원성 세균으로부터 인체를 보호할 수 있도록 하는 것을 특징으로 하는 천연성분으로 제조된 식품보존료 및 이의 제조방법을 제공하는 것을 발명의 목적으로 한다. Manufactured with natural ingredients that are harmless to the human body, formulated in an optimal blending ratio, added to food, and inhibited microbial growth to extend food shelf life and safety while protecting the human body from pathogenic bacteria that cause diseases such as food poisoning accidents. It is an object of the invention to provide a food preservative made of natural ingredients and a method for producing the same, characterized in that so as to be.
상기 목적을 달성하기 위해, To achieve the above purpose,
본 발명은 복분자 미숙과추출액을 포함하는 것을 특징으로 하는 천연 식품 보존료를 제공한다. The present invention provides a natural food preservative comprising an unripe raspberry fruit extract.
또한, 본 발명은 상기 목적을 달성하기 위해, In addition, the present invention to achieve the above object,
복분자 미숙과를 준비하는 단계(S1)와, Step (S1) of preparing unripe bokbunja,
에탄올(EtOH) 또는 물 중 선택되는 어느 1종 또는 2종을 혼합하여 추출용매를 조성하는 단계(S2)와, Forming an extraction solvent by mixing one or two selected from ethanol (EtOH) or water (S2);
상기 복분자 미숙과를 추출용매에 투입하고 50 ~ 130 ℃에서 열수추출하여 복분자미숙과추출액을 제조하는 단계(S3)와,A step (S3) of preparing an extract of unripe raspberries by adding the unripe raspberries to an extraction solvent and extracting with hot water at 50 to 130 ° C;
상기 복분자미숙과추출액을 여과하여 수득한 여액을 50 ~ 60 ℃, 0.2 ~ 0.4 mPA의 조건에서 3 ~ 5 시간 동안 감압농축하여 복분자미숙과농축액을 제조하는 단계(S4)와, Preparing an unripe raspberry fruit concentrate by concentrating the filtrate obtained by filtering the unripe raspberry extract under reduced pressure at 50 to 60 ° C. and 0.2 to 0.4 mPA for 3 to 5 hours (S4);
상기 복분자미숙과농축액을 0 ~ -40 ℃에서 10 ~ 60분 급속동결시키고, 품온 30 ~ 49℃, 진공도 0.1 ~ 0.4 Torr에서 동결건조시키고, 상기 건조물을 분쇄하여 300 ~ 700 mesh의 분말 형태의 식품보존료를 제조하는 단계(S5)를 포함하는 것을 특징으로 하는 복분자 미숙과추출액을 포함하는 식품보존료 제조방법을 제공한다.The raspberry unripe fruit concentrate was rapidly frozen at 0 to -40 ° C for 10 to 60 minutes, freeze-dried at a temperature of 30 to 49 ° C and a vacuum of 0.1 to 0.4 Torr, and the dried product was pulverized to form a powdered food of 300 to 700 mesh. It provides a food preservative manufacturing method comprising an unripe fruit extract of raspberry, characterized in that it comprises a step (S5) of preparing a preservative.
또한, 본 발명은 상기 목적을 달성하기 위해, In addition, the present invention to achieve the above object,
복분자, 오미자, 치자, 구기자, 육두구, 산사자, 금앵자 및 소목을 혼합한 항균혼합물을 제조하고, An antibacterial mixture is prepared by mixing bokbunja, omija, gardenia, goji, nutmeg, mountain lion, golden apricot and somok,
상기 항균혼합물을 물 또는 에탄올(EtOH) 중 선택되는 어느 1종 또는 2종을 혼합한 추출용매에 투입하고 50 ~ 130 ℃에서 2 ~ 4 시간 2 ~ 4회 반복 추출하여 항균혼합물 추출액을 제조하고, The antibacterial mixture was added to an extraction solvent in which one or two selected from water or ethanol (EtOH) was mixed, and extracted 2 to 4 times for 2 to 4 hours at 50 to 130 ° C. to prepare an extract of the antibacterial mixture,
상기 항균혼합물 추출액을 여과하여 수득한 여액을 50 ~ 60 ℃, 0.2 ~ 0.4 mPA의 조건에서 3 ~ 5 시간 동안 감압농축하여 항균혼합물 농축액을 제조하고, The filtrate obtained by filtering the antibacterial mixture extract was concentrated under reduced pressure for 3 to 5 hours at 50 to 60 ° C. and 0.2 to 0.4 mPA to prepare an antibacterial mixture concentrate,
상기 항균혼합물 농축액을 0 ~ -40 ℃에서 10 ~ 60분 급속동결시키고, 품온 30 ~ 49 ℃, 진공도 0.1 ~ 0.4 Torr에서 동결건조시키고, 그 건조물을 분쇄하여 분말 형태로 제조한 식품보존료인 것을 특징으로 하는 복분자 미숙과추출액을 포함하는 식품보존료 제조방법을 제공한다. Characterized in that the antibacterial mixture concentrate is quickly frozen at 0 ~ -40 ℃ for 10 ~ 60 minutes, freeze-dried at a temperature of 30 ~ 49 ℃, vacuum degree 0.1 ~ 0.4 Torr, and the dried product is pulverized to produce a food preservative in powder form. It provides a method for producing a food preservative containing an unripe raspberry extract.
본 발명은 인체에 무해한 천연항균성분을 활용하여 식품에 첨가하면서 미생물 성장을 억제하여 저장성 및 안전성을 연장시킬 수 있고, 식중독 사고 등의 질병의 원인이 되는 병원성 세균으로부터 인체를 보호할 수 있는 효과를 갖는다.The present invention utilizes a natural antibacterial component harmless to the human body and adds it to food while suppressing the growth of microorganisms to extend storage and safety, and to protect the human body from pathogenic bacteria that cause diseases such as food poisoning accidents. have
이하 구체적인 내용을 살펴보도록 한다. Let's take a look at the specific details below.
실시예1의 식품보존료에 관한 것으로서, As for the food preservative of Example 1,
복분자 미숙과를 준비하는 단계(S1)와, Step (S1) of preparing unripe bokbunja,
에탄올(EtOH) 또는 물 중 선택되는 어느 1종 또는 2종을 혼합하여 조성된 추출용매를 혼합하여 추출용매를 조성하는 단계(S2)와, A step (S2) of forming an extraction solvent by mixing an extraction solvent prepared by mixing any one or two selected from ethanol (EtOH) or water;
상기 복분자 미숙과를 추출용매에 투입하고 50 ~ 130 ℃에서 열수추출하여 복분자미숙과추출액을 제조하는 단계(S3)와,A step (S3) of preparing an extract of unripe raspberries by adding the unripe raspberries to an extraction solvent and extracting with hot water at 50 to 130 ° C;
상기 복분자미숙과추출액을 여과하여 수득한 여액을 50 ~ 60 ℃, 0.2 ~ 0.4 mPA의 조건에서 3 ~ 5 시간 동안 감압농축하여 복분자미숙과농축액을 제조하는 단계(S4)와, Preparing an unripe raspberry fruit concentrate by concentrating the filtrate obtained by filtering the unripe raspberry extract under reduced pressure at 50 to 60 ° C. and 0.2 to 0.4 mPA for 3 to 5 hours (S4);
상기 복분자미숙과농축액을 0 ~ -40 ℃에서 10 ~ 60분 급속동결시키고, 품온 30 ~ 49℃, 진공도 0.1 ~ 0.4 Torr에서 동결건조시키고, 상기 건조물을 분쇄하여 300 ~ 700 mesh의 분말 형태의 식품보존료를 제조하는 단계(S5)를 포함한다.The raspberry unripe fruit concentrate was rapidly frozen at 0 to -40 ° C for 10 to 60 minutes, freeze-dried at a temperature of 30 to 49 ° C and a vacuum of 0.1 to 0.4 Torr, and the dried product was pulverized to form a powdered food of 300 to 700 mesh. and preparing a preservative (S5).
이하, 실시예 1의 식품보존료의 더욱 구체적인 내용을 살펴보도록 한다. Hereinafter, more specific details of the food preservative of Example 1 will be described.
[복분자 미숙과를 준비하는 단계(S1)][Step of preparing unripe raspberries (S1)]
본 발명의 복분자(R. occidentalis)는 색이 녹색인 것을 미숙과를 사용하는 것이다. Bokbunja ( R. occidentalis ) of the present invention is to use unripe fruits that are green in color.
상기 복분자에 대해 간략하게 살펴보도록 한다. Let's briefly look at the bokbunja.
상기 복분자는 안토시아닌은 강력한 항산화 효과로 노화 방지에 좋고, 폴리페놀 성분이 풍부하고 퀘르세틴, 엘라그산, 탄닌 및 캠페롤등 생리활성 물질도 들어 있어 기운을 샘솟게 한다. The raspberry anthocyanin is good for anti-aging with a strong antioxidant effect, is rich in polyphenols, and also contains physiologically active substances such as quercetin, ellagic acid, tannins and kaempferol, so as to energize.
더불어, 복분자는 헬리코박터 파일로리균 및 장내유해균의 억제효과를 가지고 있으며, 요도관의 감염등의 도움을 주는 강력한 천연 항균 식품이다. In addition, bokbunja has an inhibitory effect on Helicobacter pylori and intestinal harmful bacteria, and is a powerful natural antibacterial food that helps with infections of the urinary tract.
또한, 본 발명은 색이 녹색인 복분자 미숙과를 사용하는 것으로, 복분자 완숙과 보다 항산화 효과 및 항균 효과가 뛰어나 식품의 미생물 성장을 억제하여 저장성 및 안전성을 효과적으로 연장시킬 수 있다. In addition, the present invention is to use unripe raspberry green in color, and has excellent antioxidant and antibacterial effects than mature raspberry fruit, thereby inhibiting the growth of microorganisms in food, thereby effectively extending shelf life and safety.
[추출용매를 조성하는 단계(S2)] [Step of forming an extraction solvent (S2)]
에탄올(EtOH) 또는 물 중 선택되는 어느 1종 또는 2종을 혼합하여 조성된 추출용매를 혼합하여 추출용매를 조성한다.An extraction solvent is formed by mixing an extraction solvent prepared by mixing any one or two selected from ethanol (EtOH) or water.
더욱 바람직하게는, 농도 90% 이하의 에탄올(EtOH)을 추출용매로 사용하고, 더욱 더 바람직하게는, 농도 75%의 에탄올(EtOH)을 혼합하여 추출용매를 조성하여 사용하는 것이 더 높은 항균 효과를 나타낼 수 있다.More preferably, ethanol (EtOH) with a concentration of 90% or less is used as an extraction solvent, and even more preferably, ethanol (EtOH) with a concentration of 75% is mixed to form an extraction solvent for higher antibacterial effect. can represent
[복분자미숙과추출액을 제조하는 단계(S3)][Step of preparing unripe raspberry fruit extract (S3)]
복분자미숙과추출액은 추출용매를 물 단독으로 사용하거나, 에탄올(EtOH)과 물을 혼합하여 사용할 수 있다. The extract of unripe raspberry fruit can be used as an extraction solvent by using water alone or by mixing ethanol (EtOH) and water.
물 단독으로 사용할 경우, 상기 복분자 미숙과를 추출용매인 물에 투입하고 100 ~ 130℃ 에서 열수추출하여 복분자미숙과추출액을 제조한다. When water is used alone, the unripe raspberry fruit is added to water as an extraction solvent and hot water extraction is performed at 100 to 130 ° C to prepare an extract of unripe raspberry fruit.
더욱 바람직하게는, 농도 95% 이하의 에탄올(EtOH) 추출용매 80 ~ 90 wt%에 상기 복분자 미숙과 10 ~ 20 wt%를 투입하고 60 ~ 90 ℃에서 2 ~ 4 시간 2 ~ 4 회 열수추출하여 복분자미숙과추출액을 제조한다. More preferably, 80 to 90 wt% of an ethanol (EtOH) extraction solvent having a concentration of 95% or less was added with 10 to 20 wt% of the unripe raspberry fruit, followed by hot water extraction at 60 to 90 ° C. for 2 to 4 hours 2 to 4 times. Prepare an extract of unripe raspberry fruit.
더욱 더 바람직하게는, 농도 75%의 에탄올(EtOH) 추출용매 80 ~ 90 wt%에 상기 복분자 미숙과 10 ~ 20 wt%를 투입하고 80 ℃에서 2 시간 2 회 열수추출하여 복분자미숙과추출액을 제조한다. Even more preferably, 10 to 20 wt% of the unripe raspberry fruit was added to 80 to 90 wt% of an ethanol (EtOH) extraction solvent having a concentration of 75%, and hot water extraction was performed twice for 2 hours at 80 ° C to prepare an extract of unripe raspberry fruit. do.
[감압농축하여 농축액을 제조하는 단계(S4)][Concentrate under reduced pressure to prepare a concentrate (S4)]
상기 복분자미숙과추출액을 여과하고, 상기 수득한 여액을 50 ~ 60 ℃, 0.2 ~ 0.4 mPA의 조건에서 3 ~ 5 시간 동안 감압농축하여 복분자미숙과 농축액을 제조한다. The unripe raspberry fruit extract is filtered, and the obtained filtrate is concentrated under reduced pressure for 3 to 5 hours at 50 to 60 ° C. and 0.2 to 0.4 mPA to prepare an unripe raspberry fruit concentrate.
더욱 바람직하게는, 상기 복분자미숙과추출액을 여과하고, 상기 수득한 여액을 50 ℃, 0.4 mPA의 조건에서 4 시간 동안 감압농축하여 복분자미숙과농축액을 제조한다. More preferably, the unripe raspberry fruit extract is filtered, and the obtained filtrate is concentrated under reduced pressure at 50° C. and 0.4 mPA for 4 hours to prepare an unripe raspberry fruit concentrate.
[식품보존료를 제조하는 단계(S5)] [Step of preparing food preservatives (S5)]
상기 복분자미숙과농축액을 0 ~ -40 ℃에서 10 ~ 60분 급속동결시키고, 품온 30 ~ 49 ℃, 진공도 0.1 ~ 0.4 Torr에서 동결건조시키고, 상기 건조물을 분쇄하여 300 ~ 700 mesh의 분말 형태의 식품보존료를 제조한다. The raspberry unripe fruit concentrate was rapidly frozen at 0 to -40 ° C for 10 to 60 minutes, freeze-dried at a temperature of 30 to 49 ° C and a vacuum degree of 0.1 to 0.4 Torr, and the dried product was pulverized to form a powdered food of 300 to 700 mesh. make preservatives.
더욱 더 바람직하게는, 복분자미숙과농축액을 -40 ℃에서 10분 급속동결시키고, 품온 38.3℃, 진공도 0.4 Torr에서 동결건조시키고, 상기 건조물을 분쇄하여 300 mesh의 분말 형태의 식품보존료를 제조한다. Even more preferably, the raspberry unripe fruit concentrate is rapidly frozen at -40 ° C for 10 minutes, freeze-dried at a temperature of 38.3 ° C and a vacuum of 0.4 Torr, and the dried product is pulverized to prepare a food preservative in the form of a 300 mesh powder.
이하, 배합예1과 배합예2에 따른 비교예를 살펴보도록 한다. Hereinafter, a comparative example according to Blending Example 1 and Blending Example 2 will be reviewed.
하기, 배합예1과 배합예2는 복분자(R. occidentalis)는 2020년에 전라북도 고창군에서 수확한 것으로 색이 녹색인 것을 본 발명의 미숙과(배합예1), 검붉은색을 완숙과(배합예2)로 구분하여 -40 ℃에서 냉동 보관하여 사용하였다.In the following, Blending Example 1 and Blending Example 2, Bokbunja ( R. occidentalis ) was harvested in Gochang-gun, Jeollabuk-do in 2020, and the green color is the immature fruit of the present invention (Formulation Example 1), and the dark red color is ripe (mixing) Example 2) was used after being frozen at -40 ° C.
배합예 1Combination example 1
상기 복분자 미숙과를 100 g을 정량하여 10배의 물 단독 또는 농도 25, 50, 75%의 에탄올(EtOH)을 넣고 상기 물은 100 ℃ 에서 상기 에탄올(EtOH)은 80 ℃ 에서 2 시간 2 회 반복 추출하여 여과한 후, 감압농축기(Buchi R210, Flawil, Swizerland)로 50 ℃, 0.4 mPA의 조건에서 4 시간 동안 감압농축하여 농축한 후, 상기 농축액을 -40 ℃에서 10 분 급속동결시킨 후, 품온 38.3℃, 진공도 0.4 Torr에서 동결건조하고, 300 mesh로 분쇄한 분말형태의 본 발명의 복분자미숙과를 사용한 식품보존료를 DMSO 1%로 최종농도가 10 mg/mL이 되도록 용해시킨 후 0.20 μm syringe filter(Sartorius, Germany)로 제균한 후 사용하였다. Quantify 100 g of the unripe raspberry fruit, add 10 times as much water alone or 25, 50, or 75% ethanol (EtOH), and repeat the water at 100 ° C and the ethanol (EtOH) at 80 ° C for 2 hours twice. After extraction and filtration, the concentrate was concentrated under reduced pressure with a vacuum concentrator (Buchi R210, Flawil, Switzerland) at 50 ° C. and 0.4 mPA for 4 hours, and the concentrate was rapidly frozen at -40 ° C. for 10 minutes. After dissolving the food preservative using the unripe raspberry fruit of the present invention in powder form freeze-dried at 38.3 ℃ and vacuum degree 0.4 Torr and pulverized with 300 mesh in DMSO 1% to a final concentration of 10 mg / mL, 0.20 μm syringe filter (Sartorius, Germany) was used after eradication.
배합예 2Combination example 2
상기 복분자 완숙과를 100 g을 정량하여 10 배의 물 단독 또는 농도 25, 50, 75%의 에탄올(EtOH)을 넣고 상기 물은 100 ℃ 에서 상기 에탄올(EtOH)은 80 ℃ 에서 2 시간 2 회 반복 추출하여 여과한 후 감압농축기(Buchi R210, Flawil, Swizerland)로 50 ℃, 0.4 mPA의 조건에서 4 시간 동안 감압농축하여 농축한 후, 상기 농축액을 -40 ℃에서 10 분 급속동결시킨 후, 품온 38.3 ℃, 진공도 0.4 Torr에서 동결건조하고, 300 mesh로 분쇄한 분말형태의 복분자완숙과를 사용한 식품보존료를 DMSO 1%로 최종농도가 10 mg/mL이 되도록 용해시킨 후 0.20 μm syringe filter(Sartorius, Germany)로 제균한 후 사용하였다100 g of the ripe raspberry fruit was quantified, and 10 times water alone or 25, 50, and 75% ethanol (EtOH) was added, and the water was 100 ° C and the ethanol (EtOH) was 80 ° C for 2 hours twice. After extraction and filtration, the concentrate was concentrated under reduced pressure using a vacuum concentrator (Buchi R210, Flawil, Switzerland) at 50 ° C and 0.4 mPA for 4 hours, and the concentrate was rapidly frozen at -40 ° C for 10 minutes, and the product temperature was 38.3 After dissolving the food preservative using ripe raspberry fruit in powder form freeze-dried at 0.4 Torr and vacuum degree 0.4 Torr and pulverized with 300 mesh in DMSO 1% to a final concentration of 10 mg/mL, apply a 0.20 μm syringe filter (Sartorius, Germany). ) and used after disinfection
이하, 미숙과(배합예1), 검붉은색을 완숙과(배합예2)로 구분하여 항균활성에 대한 비교분석 해보도록 한다. Hereinafter, comparative analysis of antibacterial activity will be conducted by dividing immature fruits (mixing example 1) and dark red ripe fruits (mixing example 2).
비교예 1Comparative Example 1
항균활성에 사용된 미생물은 총 8개의 균주를 이용하였으며, 실험에 사용된 균주와 배지 및 배양온도는 표1과 같다. 병원성 미생물 균주 5종은 한국미생물보존센터(Korean Culture Center of Microorganisms, KCCM)에서 분양받았으며, 호흡기 질환의 원인 세균 3종은 한국생명공학연구원 생물자원센터(Korean Collection for Type Cultures, KCTC)로부터 분양받아 사용하였다. A total of eight strains were used as microorganisms used for antibacterial activity, and the strains, media, and culture temperatures used in the experiment are shown in Table 1. Five strains of pathogenic microorganisms were distributed from the Korean Culture Center of Microorganisms (KCCM), and three strains of bacteria causing respiratory diseases were distributed from the Korean Collection for Type Cultures (KCTC) of the Korea Research Institute of Bioscience and Biotechnology. used
항균 실험의 균주 배양을 위한 nutrient broth, brain heart infusion broth 및 trypticase soy broth는 Difco Laboratories (Detroit, MI, USA)에서 구입하였으며, 각각의 고체배지는 기산바이오텍(Seoul, Korea)에서 구입하여 사용하였다. 배합예1과 배합예2의 항균력 측정은 disc diffusion method를 이용하여 확인하였다. 하기 표 1의 각 균주를 액체배지에서 계대 배양한 후, UV/VIS 분광광도계(Shimadzu)를 이용하여 600 nm에서 흡광도가 0.08 ~ 0.1이 되도록 희석한 후 100 μL를 도말 하였다. 균이 도말된 평판배지위에 멸균된 paper disc(8.0 mm, Advantec, Tokyo, Japan)를 올린 후 배합예1와 배합예2 각각 50 μL씩 점적한 후 건조과정을 거쳐 용매를 휘발시킨 후 각 균주의 조건에 맞추어 배양하였다. 그 후 disc 주변에 생성된 inhibition zone의 직경(mm)을 측정하여 항균활성을 비교하였다. Nutrient broth, brain heart infusion broth and trypticase soy broth for culturing strains of antibacterial experiments were purchased from Difco Laboratories (Detroit, MI, USA), and each solid medium was purchased from Kisan Biotech (Seoul, Korea) and used. The antimicrobial activity of Blending Example 1 and Blending Example 2 was measured using the disc diffusion method. After subculturing each strain of Table 1 in liquid medium, using a UV / VIS spectrophotometer (Shimadzu), the absorbance at 600 nm was diluted to 0.08 ~ 0.1, and then 100 μL was smeared. After placing a sterilized paper disc (8.0 mm, Advantec, Tokyo, Japan) on a plate medium smeared with bacteria, 50 μL each of Blending Example 1 and Blending Example 2 were added, dried, and the solvent was evaporated. Cultivated according to conditions. Then, the antibacterial activity was compared by measuring the diameter (mm) of the inhibition zone created around the disc.
배합예 1와 배합예 2의 병원성 미생물 균주 및 호흡기 질환 원인균에 대한 항균 활성 결과는 하기 표 2 및 표 3와 같다. The antibacterial activity results for pathogenic microbial strains and respiratory disease causative bacteria of Combination Example 1 and Combination Example 2 are shown in Tables 2 and 3 below.
배합예 1의 경우 물 단독의 열수추출방법과 에탄올(EtOH)을 활용한 추출방법 모두 균주에서 항균 활성을 나타내었으며, 물 단독 추출보다 에탄올(EtOH) 추출의 항균 활성이 더 높은 것으로 나타났다. In the case of Blending Example 1, both the hot water extraction method using water alone and the extraction method using ethanol (EtOH) showed antibacterial activity in the strain, and the antibacterial activity of ethanol (EtOH) extraction was higher than that of water alone extraction.
균주에 따라 동일한 추출 용매 및 농도에서도 각기 다른 크기의 생육저해환을 나타내었으며, 배합예 1의 물 단독의 열수추출은 C. diptheriae KCTC 3075에 대한 생육저해환이 16.26 mm로 가장 크게 나타났으며, 25 % 에탄올(EtOH) 추출물은 C. diptheriae KCTC 3075 (16.41 mm)와 S. aureus KCCM 12103 (16.26 mm)의 항균 활성이 가장 높은 것으로 나타났다.Depending on the strain, even in the same extraction solvent and concentration, growth-inhibiting rings of different sizes were exhibited, and the hot water extraction of water alone in Formulation Example 1 was C . The growth inhibition ring for diptheriae KCTC 3075 was the largest at 16.26 mm, and the 25% ethanol (EtOH) extract showed C . diptheriae KCTC 3075 (16.41 mm) and S. aureus KCCM 12103 (16.26 mm) showed the highest antibacterial activity.
50 % 에탄올(EtOH) 추출물에 대한 항균 활성 또한 C. diptheriae KCTC 3075에 대한 생육저해환의 크기가 다른 균에 비해 가장 큰 것으로 나타났으며, Antibacterial activity against 50% ethanol (EtOH) extract also showed C. It was found that the size of the growth inhibition ring for diptheriae KCTC 3075 was the largest compared to other bacteria.
75 % 에탄올(EtOH) 추출물의 경우 모든 균주에 대한 항균 활성이 가장 높은 것으로 나타났다. The 75% ethanol (EtOH) extract showed the highest antibacterial activity against all strains.
배합예 2의 경우 미숙과와 마찬가지로 물 또는 25 %, 50 % 에탄올(EtOH) 추출물에서 모두 일정 수준 이상의 항균력을 나타내었으나 75 % 에탄올(EtOH) 추출물의 경우 S. aureus KCCM 12103과 E. coli O157:H7 KCCM 40406에서는 항균 활성이 없는 것으로 나타났다. In the case of Formulation Example 2, as in the case of immature fruits, water or 25%, 50% ethanol (EtOH) extracts all showed a certain level of antibacterial activity, but in the case of 75% ethanol (EtOH) extracts, S. aureus KCCM 12103 and E. coli O157:H7 KCCM 40406 showed no antibacterial activity.
또한, 배합예 2는 8종의 균주 모두 50 % 에탄올(EtOH) 추출물이 다른 추출물에 비해 높은 항균 활성을 나타내었으며, 특히 B. cereus KCCM 40935 균주에 대해서는 모든 추출물에서 다른 균주보다 높은 항균 효과를 보였다. In addition, in Combination Example 2, the 50% ethanol (EtOH) extract of all 8 strains exhibited higher antibacterial activity than other extracts, especially B. cereus KCCM 40935 showed a higher antibacterial effect than other strains in all extracts.
한편, 배합예 1과 배합예 2의 항균 활성을 비교한 결과 k.pneumoniae KCTC 2245 균주에 대한 물 단독 추출을 제외하고 배합예 1이 배합예 2에 비해 상대적으로 높은 항균 효과를 갖고 있음을 확인하였다.On the other hand, as a result of comparing the antibacterial activity of Formulation Example 1 and Formulation Example 2 k. pneumoniae KCTC 2245 was confirmed to have a relatively high antibacterial effect compared to Formulation Example 2, except for water alone extraction.
복분자
Bokbunja
Extraction Solvent
Extraction Solvent
Diameter of inhibition zone (mm)
Diameter of inhibition zone (mm)
KCCM 12119 E. coli
KCCM 12119
배합예1
Formulation example 1
배합예2
Combination example 2
복분자
Bokbunja
Extraction Solvent
Extraction Solvent
Diameter of inhibition zone (mm)
Diameter of inhibition zone (mm)
aureus KCTC 1928 S.
aureus KCTC 1928
배합예1
Formulation example 1
0.559.37±
0.55
배합예2
Combination example 2
-
-
0.459.02±
0.45
또한, 항균 활성은 페놀성 물질과 상관관계가 있으며, 플라보노이드, 같은 물질은 항산화 작용 뿐만 아니라 세균의 DNA gyrase와 같은 효소활성을 억제하고 증식을 차단하여 항균 활성을 가진다. In addition, antibacterial activity is correlated with phenolic substances, and substances such as flavonoids have antibacterial activity by inhibiting the activity of enzymes such as DNA gyrase and blocking the proliferation of bacteria as well as antioxidant activity.
이하, 배합예 1과 배합예 2의 총 폴리페놀, 총 플라보노이드을 비교예2를 통해 살펴보도록 한다. Hereinafter, total polyphenols and total flavonoids of Blending Example 1 and Blending Example 2 will be examined through Comparative Example 2.
비교예 2Comparative Example 2
건강기능식품공전 방법을 응용하여 측정하였다. 배합예 1 또는 배합예 2로 제조한 식품보존료을 각각 1 mL에 증류수 7.5 mL와 Folin-Ciocalteau’s phenol regent(Sigma-Aldrich, St. Louis, MO, USA) 0.5 mL, 35% sodium carbonate(Sigma-Aldrich) 1 mL를 가한 후 실온 암 조건에서 1시간 동안 정치하고 UV/VIS 분광광도계(UV-2450, Shimadzu Co., Kyoto, Japan)를 사용하여 760 nm에서 흡광도를 측정하였다. It was measured by applying the health functional food code method. 7.5 mL of distilled water and 0.5 mL of Folin-Ciocalteau's phenol regent (Sigma-Aldrich, St. Louis, MO, USA), 35% sodium carbonate (Sigma-Aldrich) for each 1 mL of the food preservative prepared in Formulation Example 1 or Formulation Example 2 After adding 1 mL, the mixture was allowed to stand for 1 hour at room temperature and the absorbance was measured at 760 nm using a UV/VIS spectrophotometer (UV-2450, Shimadzu Co., Kyoto, Japan).
이때, tannic acid(Sigma-Aldrich)를 표준물질로 사용하여 검량곡선을 작성하고 이로부터 총 폴리페놀 함량을 구하였고, 총 플라보노이드 함량 또한 건강기능식품공전 방법을 응용하여 측정하였고, 총 안토시아닌 함량은 Kim YD 등의 방법을 응용하여 측정하였다. At this time, a calibration curve was prepared using tannic acid (Sigma-Aldrich) as a standard material, and the total polyphenol content was obtained from it, and the total flavonoid content was also measured by applying the method of the Health Functional Food Code, and the total anthocyanin content It was measured by applying the method of YD et al.
배합예 1와 배합예 2의 총 폴리페놀, 총 플라보노이드 및 총 안토시아닌 함량을 분석한 결과는 표 4와 같다. Table 4 shows the results of analyzing total polyphenols, total flavonoids, and total anthocyanin contents of Blending Example 1 and Blending Example 2.
총 폴리페놀 함량의 경우 배합예 1은 75 % 에탄올(EtOH) 추출물에서 106.12 TAE mg/mL로 가장 높았으며, 50 % 에탄올(EtOH) 추출물(101.40 TAE mg/mL), 25 % 에탄올(EtOH) 추출물(84.00 TAE mg/mL), 물 단독 (78.21 TAE mg/mL)순으로 나타났다. In the case of total polyphenol content, Blending Example 1 was the highest with 106.12 TAE mg/mL in the 75% ethanol (EtOH) extract, and 50% ethanol (EtOH) extract (101.40 TAE mg/mL) and 25% ethanol (EtOH) extract. (84.00 TAE mg/mL), followed by water alone (78.21 TAE mg/mL).
배합예 2의 총 폴리페놀 함량은 38.25 ~ 53.41 TAE mg/mL 범위로 나타났으며 이는 배합예 2와 마찬가지로 에탄올(EtOH) 농도 의존적으로 총 폴리페놀 함량 또한 증가하는 것으로 나타났으나, 배합예1이 배합예2 보다 2 배 이상 높은 함량을 나타내었다.The total polyphenol content of Blending Example 2 was found to be in the range of 38.25 to 53.41 TAE mg/mL, which was found to increase in ethanol (EtOH) concentration-dependent manner, as in Blending Example 2, but Blending Example 1 It showed a content more than twice as high as that of Blending Example 2.
총 플라보노이드 함량의 경우, 배합예 1와 배합예 2 각각 농도 75 %의 에탄올(EtOH) 추출물에서 19.09 RUE mg/mL, 14.73 RUE mg/mL로 가장 높은 함량을 나타내었다. 배합예 1와 배합예 2 모두 에탄올(EtOH) 농도가 증가할수록 총 플라보노이드 함량이 증가함을 확인할 수 있었다. 배합예 1와 배합예 2의 총 플라보노이드 함량을 비교하면 배합예 1이 배합예 2 보다 유의적으로 높게 나타났다. In the case of total flavonoid content, 19.09 RUE mg/mL and 14.73 RUE mg/mL were the highest in the 75% ethanol (EtOH) extract of Blending Example 1 and Blending Example 2, respectively. It was confirmed that the total flavonoid content increased as the ethanol (EtOH) concentration increased in both Blending Example 1 and Blending Example 2. Comparing the total flavonoid contents of Blending Example 1 and Blending Example 2, Blending Example 1 was significantly higher than Blending Example 2.
또한, 배합예 1와 배합예 2 모두 75 % 에탄올(EtOH) 추출물에서 가장 높은 함량을 나타나 75 %의 에탄올(EtOH)을 활용하는 것이 증식을 차단하여 더 높은 항균 활성을 갖는 것을 알 수 있다. 또한, 배합예 1이 배합예 2 보다 세균의 DNA gyrase와 같은 효소활성에 대한 더 높은 효과가 있다는 것을 알 수 있다. In addition, both Blending Example 1 and Blending Example 2 showed the highest content in the 75% ethanol (EtOH) extract, and it can be seen that using 75% ethanol (EtOH) blocks proliferation and has higher antibacterial activity. In addition, it can be seen that Blending Example 1 has a higher effect on enzyme activity such as bacterial DNA gyrase than Blending Example 2.
복분자
Bokbunja
Extraction Solvent
Extraction Solvent
(TAE1) mg/mL)Total polyphenol contents
(TAE 1) mg/mL)
(RUE2) mg/mL)Total flavonoid contents
(RUE 2 mg/mL)
배합예 1
Combination example 1
Water
Water
78.21±0.40
78.21±0.40
16.78±0.85
16.78±0.85
25% EtOH
25% EtOH
84.00±0.83
84.00±0.83
18.01±0.44
18.01±0.44
50% EtOH
50% EtOH
101.40±0.29
101.40±0.29
18.57±0.24
18.57±0.24
75% EtOH
75% EtOH
106.12±0.50
106.12±0.50
19.09±0.39
19.09±0.39
배합예 2
Combination example 2
Water
Water
12.01±0.39
12.01±0.39
65.35±0.02
65.35±0.02
25% EtOH
25% EtOH
12.22±0.27
12.22±0.27
78.66±0.04
78.66±0.04
50% EtOH
50% EtOH
13.81±0.18
13.81±0.18
80.05±0.02
80.05±0.02
75% EtOH
75% EtOH
14.73±0.18
14.73±0.18
91.96±0.06
91.96±0.06
실시예2의 식품보존료로서, 복분자, 오미자, 치자, 구기자, 육두구, 산사자, 가자육 금앵자, 소목 및 오미자를 혼합한 항균혼합물을 제조하고, As a food preservative of Example 2, an antibacterial mixture was prepared by mixing bokbunja, omija, gardenia, wolfberry, nutmeg, hawthorn japonica, hawthorn japonica, somok and omija,
상기 항균혼합물을 에탄올(EtOH)에 투입하고 50 ~ 130 ℃에서 2 ~ 4 시간 2 ~ 4 회 반복 추출하여 항균혼합물 추출액을 제조하고, The antibacterial mixture was added to ethanol (EtOH) and extracted 2 to 4 times for 2 to 4 hours at 50 to 130 ° C. to prepare an extract of the antibacterial mixture,
상기 항균혼합물 추출액을 여과하여 수득한 여액을 50 ~ 60 ℃, 0.2 ~ 0.4 mPA의 조건에서 3 ~ 5 시간 동안 감압농축하여 항균혼합물 농축액을 제조하고, The filtrate obtained by filtering the antibacterial mixture extract was concentrated under reduced pressure for 3 to 5 hours at 50 to 60 ° C. and 0.2 to 0.4 mPA to prepare an antibacterial mixture concentrate,
상기 항균혼합물 농축액을 0 ~ -40 ℃에서 10 ~ 60분 급속동결시키고, 품온 30 ~ 49 ℃, 진공도 0.1 ~ 0.4 Torr에서 동결건조시키고, 그 건조물을 분쇄하여 300 ~ 700 mesh의 분말 형태로 제조한 식품보존료인 것을 특징으로 한다. The antibacterial mixture concentrate was rapidly frozen at 0 ~ -40 ℃ for 10 ~ 60 minutes, freeze-dried at a temperature of 30 ~ 49 ℃, vacuum degree 0.1 ~ 0.4 Torr, and the dried product was pulverized to prepare a powder form of 300 ~ 700 mesh Characterized in that it is a food preservative.
이하, 실시예 2의 식품보존료의 더욱 구체적인 내용을 살펴보도록 한다. Hereinafter, more specific details of the food preservative of Example 2 will be described.
먼저, 복분자 미숙과, 오미자, 치자, 구기자, 육두구, 산사자, 금앵자 및 소목을 혼합한 항균혼합물을 조성한다. First, an antibacterial mixture is prepared by mixing unripe raspberry fruit, Schisandra chinensis, gardenia, goji berry, nutmeg, mountain lion, golden apricot, and somok.
이하, 상기 항균혼합물을 구성하는 성분들을 간략하게 살펴보록 한다. Hereinafter, the components constituting the antibacterial mixture will be briefly reviewed.
상기 오미자는 목련과에 속한 갈잎 덩굴나무이면서 잎은 어긋 나고 타원형이며, 길이 7 ~ 10 cm, 너비 3 ~ 5 cm 이고. 꽃은 암수딴그루로 붉은빛이 도는 황백색이다. 6 ~ 7월에 피고 지름 15 mm 가량이다. 구성 성분으로는 gomisin A, B, C, D, E, F, G, schizandrin, deoxyschizandrin 등이 함유되어 있다. The Schizandra chinensis is a cedar vine belonging to the Magnolia family, and the leaves are alternate and oval, 7 to 10 cm in length and 3 to 5 cm in width. The flowers are dioecious, reddish yellowish white. It blooms in June-July and is about 15 mm in diameter. Components include gomisin A, B, C, D, E, F, G, schizandrin, deoxyschizandrin, etc.
특히, 오미자의 방향족 성분인 플라보노이드류 중 cirsimaritin, 페놀류인 magnolia와 honokinol, 그리고 테르펜류인 a-pinene, menthol, camphor, geraniol 등은 미생물억제 작용에 강한 생리활성있어 폐렴균, 포도상구균, 녹농간균, 티푸스균 등에 대하여 항균 작용이 우수하다.In particular, among flavonoids, which are aromatic components of Schisandra chinensis, cirsimaritin, phenols magnolia and honokinol, and terpenes a-pinene, menthol, camphor, geraniol, etc. It has excellent antibacterial activity against germs and the like.
상기 치자는 꼭두서니과에 속하는 상록관목인 치자나무의 열매를 말하고, 흰 꽃이 피며 달콤한 향기가 난다. 열매인 치자는 헝겊이나 단무지 등을 노랗게 물들일 때 쓰고 한약재로 주로 사용한다. 또한, 구성 성분으로 플로보노이드, 게니포사이드 성분이 풍부하게 들어가 천연항균 성분으로 세균에 대하여 증식억제 효과가 있다. The gardenia refers to the fruit of the gardenia tree, an evergreen shrub belonging to the madder family, and has white flowers and a sweet scent. Gardenia, a fruit, is used to dye cloth or pickled radish yellow and is mainly used as a herbal medicine. In addition, flavonoids and geniposide components are abundant in the composition and have a growth inhibitory effect against bacteria as a natural antibacterial component.
구기자는 가짓과에 속하는 구기자나무의 열매이고, 구기자나무는 낙엽성 활엽관목(闊葉灌木: 넓은 잎의 떨기나무)으로 줄이 처져 있는 줄기는 보통 1∼1.5m 정도이고, 작은 가지가 변한 가시가 있는데, 없는 것도 있다. Gojija is the fruit of the Gojija tree belonging to the Solanaceae family. Gojija tree is a deciduous broad-leaved shrub (wide-leaved shrub) with drooping stems of usually 1 to 1.5m, and small branches with changed thorns. There is, and there is also not.
또한. betaine, cholin,physalien, rutin, β-sitosterol, zeazanthin등 다양한 기능성성분을 함유하고 있으며 항균효과가 우수하다. also. It contains various functional ingredients such as betaine, cholin, physalien, rutin, β-sitosterol, and zeazanthin, and has excellent antibacterial effect.
육두구는 쌍떡잎식물 미나리아재비목 육두구과의 상록활엽 교목. 인도네시아 몰루카제도 원산이다. 높이 약 20m이다. 잎은 어긋나고 긴 타원형이며 가장자리가 밋밋하고 두껍고, 2 ~ 9 %의 정유성분이 들어있으며, d-camphene, a-pinene등이 함유된다. 또한, 지방중에는 myristic acid가 70 ~ 80%를 차지하며 육도구는 기름에는 방향성 물질이외에 현저한 마취기능도 있다. 또한, 육두구가 함유하고 있는 terpene 성분은 항균작용을 한다. Nutmeg is an evergreen broad-leaved tree of the dicotyledonous buttercup family Nutmegaceae. It is native to the Moluccas Islands of Indonesia. It is about 20m high. The leaves are alternate, long oval, with flat and thick edges, and contain 2 to 9% of essential oil, including d-camphene and a-pinene. In addition, myristic acid occupies 70 to 80% of fat, and meat tools have a remarkable anesthetic function in addition to aromatic substances in oil. In addition, the terpene component contained in nutmeg has an antibacterial effect.
산사자는 산사나무의 열매이고, 둥글고 작은 사과 모양이며, 9 ~ 10월에 붉은색으로 익는데 겉면에는 흰 점들이 있다. 열매에는 amygdalin, citric acid, tartaric acid을 비롯한 유기산, flavonoid등을 함유한다. Hawthorn is the fruit of the hawthorn tree, round and small apple-shaped, ripens in red in September-October, and has white dots on the outside. The fruit contains organic acids including amygdalin, citric acid and tartaric acid, and flavonoids.
또한, 산사자는 산사는 이질간균, 황색포도상구균, B형 연쇄구균, 대장간균, 변형간균, 탄저간균, 백후간균, 상한간균, 녹농간균 등에 대해 항균활성이 있다 In addition, hawthorn has antibacterial activity against bacillus dysentery, Staphylococcus aureus, streptococcus type B, coliform bacillus, modified bacillus, bacillus anthracis, baekho bacillus, upper limit bacillus, Pseudomonas aeruginosa, etc.
금앵자는 장미과에 속한 금앵자나무 꽃은 6 ∼ 7월에 작은가지 끝에 백색으로 피며, 꽃자루와 꽃받침통에 가시가 밀생하고 그 과실을 금앵자라하여 황색 포도상 구균과 대장균에 대해 아주 높은 항균효과를 나타내고, vitamin C, vitamin B, vitamin P, flavonoid, carotene, tannic acid, 유기산등을 함유한다. Golden cherry blossoms belonging to the Rosaceae family bloom in white at the tip of small branches in June-July, and thorns grow densely on the peduncle and calyx tube, and the fruits are called gold cherry blossoms, showing a very high antibacterial effect against Staphylococcus aureus and Escherichia coli. , vitamin C, vitamin B, vitamin P, flavonoid, carotene, tannic acid, and organic acid.
소목은 소목(蘇木) Caesalpinia sappan Linne (콩과 Leguminosae)의 심재이다. 일명 Sappan Wood 라고 한다. 심재 조각으로 긴 원기둥 모양, 반으로 자른 원주형 또는 막대모양이다. 소목의 주성분 가운데 약 2 %를 차지하는 염료성 화합물은 무색의 flavonoid 구조를 갖는 brazilin이며, 이는 공기 중에 산화되어 brazilein이 된다상기 brazilin은 식중독의 주된 원인균에 대해 높은 항균효과가 있다. Somok is the heartwood of Caesalpinia sappan Linne (leguminosae). It is also called Sappan Wood. A piece of heartwood in the shape of a long cylinder, a cylinder cut in half, or a rod. The dye compound, which accounts for about 2% of the main components of somok, is brazilin having a colorless flavonoid structure, which is oxidized in the air to become brazilein. The brazilin has a high antimicrobial effect against the main causative bacteria of food poisoning.
더욱 구체적으로는, 복분자 미숙과 10 ~ 20 wt% , 오미자 10 ~ 20 wt%, 치자 10 ~ 20 wt%, 구기자 10 ~ 20 wt%, 육두구 10 ~ 20 wt%, 산사자 10 ~ 20 wt%, 금앵자 10 ~ 20 wt% 및 소목 10 ~ 20 wt%을 혼합하여 항균혼합물을 조성한다. More specifically, 10 to 20 wt% of unripe raspberry fruit, 10 to 20 wt% of Schisandra chinensis, 10 to 20 wt% of gardenia, 10 to 20 wt% of goji berry, 10 to 20 wt% of nutmeg, 10 to 20 wt% of hawthorn, gold An antibacterial mixture is prepared by mixing 10 to 20 wt% of Aengja and 10 to 20 wt% of Somok.
더욱 구체적으로는, 복분자 미숙과 12.5 wt%, 오미자 12.5 wt%, 치자 12.5 wt% 구기자 12.5 wt%, 육두구 12.5 wt%, 산사자 12.5 wt%, 금앵자 12.5 wt% 및 소목 12.5 wt%을 혼합하여 항균혼합물을 조성한다.More specifically, 12.5 wt% of unripe Bokbunja, 12.5 wt% of Schisandra chinensis, 12.5 wt% of Gardenia, 12.5 wt% of Gojija, 12.5 wt% of nutmeg, 12.5 wt% of hawthorn, 12.5 wt% of Golden Angel, and 12.5 wt% of Somok were mixed to antibacterial effect. make up the mixture
그 후, 상기 항균혼합물을 에탄올(EtOH)에 투입하고 50 ~ 130 ℃에서 2 ~ 4 시간 2 ~ 4 회 반복 추출하여 항균혼합물 추출액을 제조한다.Then, the antibacterial mixture is put into ethanol (EtOH) and extracted repeatedly 2 to 4 times for 2 to 4 hours at 50 to 130 ° C. to prepare an antibacterial mixture extract.
그 후, 상기 항균혼합물 추출액을 여과하여 수득한 여액을 50 ~ 60 ℃, 0.2 ~ 0.4 mPA의 조건에서 3 ~ 5 시간 동안 감압농축하여 항균혼합물 농축액을 제조한다. Thereafter, the filtrate obtained by filtering the antibacterial mixture extract is concentrated under reduced pressure for 3 to 5 hours at 50 to 60 °C and 0.2 to 0.4 mPA to prepare an antimicrobial mixture concentrate.
상기 항균혼합물 농축액을 0 ~ -40 ℃에서 10 ~ 60분 급속동결시키고, 품온 30 ~ 49 ℃, 진공도 0.1 ~ 0.4 Torr에서 동결건조시키고, 그 건조물을 분쇄하여 300 ~ 700 mesh의 분말 형태인 식품보존료를 제조한다. The antibacterial mixture concentrate was rapidly frozen at 0 to -40 ° C for 10 to 60 minutes, freeze-dried at a temperature of 30 to 49 ° C and a vacuum degree of 0.1 to 0.4 Torr, and the dried product was pulverized to form a food preservative in the form of a powder of 300 to 700 mesh. to manufacture
이하, 실시예 2의 식품보존료의 항균활성을 배합예 3을 통한 시험예 1를 통해 알아보도록 한다. Hereinafter, the antibacterial activity of the food preservative of Example 2 will be examined through Test Example 1 through Formulation Example 3.
배합예 3 Combination example 3
항균혼합물 100 g을 정량하여 10 배의 농도 70%의 에탄올(EtOH)에 넣고 80 ℃ 에서 2 시간 2 회 반복 추출하여 여과한 후 감압농축기(Buchi R210, Flawil, Swizerland)로 50 ℃, 0.4 mPA의 조건에서 4 시간 동안 감압농축하여 농축한 후, 상기 농축액을 -40 ℃에서 10 분 급속동결시킨 후, 품온 38.3 ℃, 진공도 0.4 Torr에서 동결건조하고, 300 mesh로 분쇄한 분말형태의 복분자완숙과를 사용한 제1식품보존료를 DMSO 1%로 최종농도가 10 mg/mL이 되도록 용해시킨 후 0.20 μm syringe filter(Sartorius, Germany)로 제균한 후 사용하였다100 g of the antibacterial mixture was quantified, put in 70% ethanol (EtOH) at a concentration 10 times higher, extracted twice for 2 hours at 80 ° C, filtered, and then vacuum concentrator (Buchi R210, Flawil, Switzerland) at 50 ° C and 0.4 mPA. After concentrating under reduced pressure for 4 hours under the conditions, the concentrate was rapidly frozen at -40 ° C for 10 minutes, lyophilized at a temperature of 38.3 ° C and a vacuum of 0.4 Torr, and then pulverized with 300 mesh. The first food preservative used was dissolved in DMSO 1% to a final concentration of 10 mg/mL, and then sterilized with a 0.20 μm syringe filter (Sartorius, Germany) before use.
시험예 1Test Example 1
항균활성에 사용된 미생물은 총 8개의 균주를 이용하였으며, 실험에 사용된 균주와 배지 및 배양온도는 표 5과 같다. 병원성 미생물 균주 5종은 한국미생물보존센터(Korean Culture Center of Microorganisms, KCCM)에서 분양받았으며, 호흡기 질환의 원인 세균 3종은 한국생명공학연구원 생물자원센터(Korean Collection for Type Cultures, KCTC)로부터 분양받아 사용하였다. A total of eight strains were used as microorganisms used for antibacterial activity, and the strains, media, and culture temperatures used in the experiment are shown in Table 5. Five strains of pathogenic microorganisms were distributed from the Korean Culture Center of Microorganisms (KCCM), and three strains of bacteria causing respiratory diseases were distributed from the Korean Collection for Type Cultures (KCTC) of the Korea Research Institute of Bioscience and Biotechnology. used
항균 실험의 균주 배양을 위한 nutrient broth, brain heart infusion broth 및 trypticase soy broth는 Difco Laboratories (Detroit, MI, USA)에서 구입하였으며, 고체배지는 기산바이오텍(Seoul, Korea)에서 구입하여 사용하였다. 배합예3의 항균력 측정은 disc diffusion method를 이용하여 확인하였다. 하기 표 5의 각 균주를 액체배지에서 계대 배양한 후, UV/VIS 분광광도계(Shimadzu)를 이용하여 600 nm에서 흡광도가 0.08 ~ 0.1이 되도록 희석한 후 100 μL를 도말 하였다. 균이 도말된 평판배지위에 멸균된 paper disc(8.0 mm, Advantec, Tokyo, Japan)를 올린 후 , 배합예 3을 50 μL 점적한 후 건조과정을 거쳐 용매를 휘발시킨 후 각 균주의 조건에 맞추어 배양하였다. 그 후 disc 주변에 생성된 inhibition zone의 직경(mm)을 측정하여 항균활성을 비교하였다. Nutrient broth, brain heart infusion broth and trypticase soy broth for culturing strains of antibacterial experiments were purchased from Difco Laboratories (Detroit, MI, USA), and solid medium was purchased from Kisan Biotech (Seoul, Korea). The antibacterial activity of Formulation Example 3 was measured using the disc diffusion method. After subculturing each of the strains in Table 5 below in liquid medium, using a UV/VIS spectrophotometer (Shimadzu), the absorbance at 600 nm was diluted to 0.08 to 0.1, and then 100 μL was smeared. After placing a sterilized paper disc (8.0 mm, Advantec, Tokyo, Japan) on a plate medium smeared with bacteria, 50 μL of Formulation Example 3 was dropped, and the solvent was evaporated through a drying process, followed by culturing according to the conditions of each strain did Then, the antibacterial activity was compared by measuring the diameter (mm) of the inhibition zone created around the disc.
배합예 3의 병원성 미생물 균주 및 호흡기 질환 원인균에 대한 항균 활성 결과는 하기 표 6 및 표 7와 같다. The results of antibacterial activity against pathogenic microbial strains and respiratory disease causative bacteria of Combination Example 3 are shown in Tables 6 and 7 below.
배합예 3은 S. aureus KCCM 12103에 대한 생육저해환이 19.9 mm로 가장 크게 나타났으며, C. diptheriae KCTC 3075 (18.52 mm)와 S. aureus KCTC 1928 (18.37 mm)의 항균 활성이 가장 높은 것으로 나타났다.In Combination Example 3, the growth inhibition ring for S. aureus KCCM 12103 was the largest at 19.9 mm, and C. diptheriae KCTC 3075 (18.52 mm) and S. aureus KCTC 1928 (18.37 mm) showed the highest antibacterial activity.
복분자
Bokbunja
Extraction Solvent
Extraction Solvent
Diameter of inhibition zone (mm)
Diameter of inhibition zone (mm)
KCCM 12119 E. coli
KCCM 12119
복분자
Bokbunja
Extraction Solvent
Extraction Solvent
Diameter of inhibition zone (mm)
Diameter of inhibition zone (mm)
aureus KCTC 1928 S.
aureus KCTC 1928
실시예1의 식품보존료 또는 실시예 2의 식품보존료를 식품에 첨가하여, 쳔연성분으로 인체에 무해하면서, 식품의 미생물 성장을 억제하여 저장성 및 안전성을 연장시킬 수 있고, 식중독 사고등의 질병의 원인이 되는 병원성 세균으로부터 인체를 보호할 수 있다. By adding the food preservative of Example 1 or the food preservative of Example 2 to food, it is harmless to the human body as a natural ingredient, inhibits the growth of microorganisms in food, prolongs shelf life and safety, and causes diseases such as food poisoning accidents It can protect the human body from pathogenic bacteria.
본 발명은 천연성분을 활용하여 인체에 무해하면서 식품의 변질, 부패를 방지할 수 있어 산업상 이용 가능성이 매우 크다. The present invention utilizes natural ingredients to prevent deterioration and spoilage of food while being harmless to the human body, and thus has great industrial applicability.
Claims (7)
A food preservative containing an unripe raspberry fruit extract, characterized in that it is a food preservative containing an unripe raspberry fruit extract.
복분자 미숙과추출액은,
복분자 미숙과를 추출하여 제조하되,
상기 추출은 에탄올(EtOH) 또는 물 중 선택되는 어느 1종 또는 2종을 혼합하여 조성된 추출용매를 통해 추출하는 것을 특징으로 하는 복분자 미숙과추출액을 포함하는 식품보존료.
The method of claim 1,
Unripe raspberry fruit extract,
It is prepared by extracting unripe raspberry fruit,
The extraction is a food preservative comprising an unripe raspberry fruit extract, characterized in that the extraction is performed through an extraction solvent composed by mixing any one or two selected from ethanol (EtOH) or water.
식품보존료는,
복분자 미숙과추출액을 농축 및 동결건조하고, 상기 건조된 건조물을 분쇄화하여 300 ~ 700 mesh의 분말형태로 제조되는 것을 특징으로 하는 복분자 미숙과추출액을 포함하는 식품보존료.
The method of claim 1,
food preservatives,
A food preservative comprising an unripe raspberry extract, characterized in that it is prepared in the form of a powder of 300 to 700 mesh by concentrating and freeze-drying the unripe raspberry extract, and pulverizing the dried product.
에탄올(EtOH) 또는 물 중 선택되는 어느 1종 또는 2종을 혼합하여 추출용매를 조성하는 단계(S2)와,
상기 복분자 미숙과를 추출용매에 투입하고 50 ~ 130 ℃에서 열수추출하여 복분자미숙과추출액을 제조하는 단계(S3)와,
상기 복분자미숙과추출액을 여과하여 수득한 여액을 50 ~ 60 ℃, 0.2 ~ 0.4 mPA의 조건에서 3 ~ 5 시간 동안 감압농축하여 복분자미숙과농축액을 제조하는 단계(S4)와,
상기 복분자미숙과농축액을 0 ~ -40 ℃에서 10 ~ 60분 급속동결시키고, 품온 30 ~ 49℃, 진공도 0.1 ~ 0.4 Torr에서 동결건조시키고, 상기 건조물을 분쇄하여 300 ~ 700 mesh의 분말 형태의 식품보존료를 제조하는 단계(S5)를 포함하는 것을 특징으로 하는 복분자 미숙과추출액을 포함하는 식품보존료 제조방법.
Step (S1) of preparing unripe bokbunja,
Forming an extraction solvent by mixing one or two selected from ethanol (EtOH) or water (S2);
A step (S3) of preparing an extract of unripe raspberries by adding the unripe raspberries to an extraction solvent and extracting with hot water at 50 to 130 ° C;
Preparing an unripe raspberry fruit concentrate by concentrating the filtrate obtained by filtering the unripe raspberry extract under reduced pressure at 50 to 60 ° C. and 0.2 to 0.4 mPA for 3 to 5 hours (S4);
The raspberry unripe fruit concentrate was rapidly frozen at 0 to -40 ° C for 10 to 60 minutes, freeze-dried at a temperature of 30 to 49 ° C and a vacuum of 0.1 to 0.4 Torr, and the dried product was pulverized to form a powdered food of 300 to 700 mesh. A food preservative manufacturing method comprising a raspberry unripe fruit extract comprising the step (S5) of preparing a preservative.
에탄올(EtOH)은,
농도 25 ~ 75%의 에탄올(EtOH)인 것을 특징으로 하는 복분자 미숙과추출액을 포함하는 식품보존료 제조방법.
The method of claim 4,
Ethanol (EtOH) is
A method for producing a food preservative comprising an unripe raspberry fruit extract, characterized in that the concentration is 25 to 75% ethanol (EtOH).
상기 항균혼합물을 물 또는 에탄올(EtOH) 중 선택되는 어느 1종 또는 2종을 혼합한 추출용매에 투입하고 50 ~ 130 ℃에서 2 ~ 4 시간 2 ~ 4회 반복 추출하여 항균혼합물 추출액을 제조하고,
상기 항균혼합물 추출액을 여과하여 수득한 여액을 50 ~ 60 ℃, 0.2 ~ 0.4 mPA의 조건에서 3 ~ 5 시간 동안 감압농축하여 항균혼합물 농축액을 제조하고,
상기 항균혼합물 농축액을 0 ~ -40 ℃에서 10 ~ 60분 급속동결시키고, 품온 30 ~ 49 ℃, 진공도 0.1 ~ 0.4 Torr에서 동결건조시키고, 그 건조물을 분쇄하여 분말 형태로 제조한 식품보존료인 것을 특징으로 하는 복분자 미숙과추출액을 포함하는 식품보존료 제조방법.
An antibacterial mixture is prepared by mixing bokbunja, omija, gardenia, goji, nutmeg, mountain lion, golden apricot and somok,
The antibacterial mixture was added to an extraction solvent in which one or two selected from water or ethanol (EtOH) was mixed, and extracted 2 to 4 times for 2 to 4 hours at 50 to 130 ° C. to prepare an extract of the antibacterial mixture,
The filtrate obtained by filtering the antibacterial mixture extract was concentrated under reduced pressure for 3 to 5 hours at 50 to 60 ° C. and 0.2 to 0.4 mPA to prepare an antibacterial mixture concentrate,
Characterized in that the antibacterial mixture concentrate is quickly frozen at 0 ~ -40 ℃ for 10 ~ 60 minutes, freeze-dried at a temperature of 30 ~ 49 ℃, vacuum degree 0.1 ~ 0.4 Torr, and the dried product is pulverized to produce a food preservative in powder form. A method for producing a food preservative comprising an unripe raspberry fruit extract.
식품보존료는 300 ~ 700 mesh의 분말 형태로 이루어진 것을 특징으로 하는 복분자 미숙과추출액을 포함하는 식품보존료 제조방법.The method of claim 6,
The food preservative is a food preservative manufacturing method comprising an unripe raspberry fruit extract, characterized in that consisting of a powder form of 300 ~ 700 mesh.
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