KR102545132B1 - Nucleoprotein powder prepared from salmon sperm and functional drinks comprising the same - Google Patents
Nucleoprotein powder prepared from salmon sperm and functional drinks comprising the same Download PDFInfo
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- KR102545132B1 KR102545132B1 KR1020230007010A KR20230007010A KR102545132B1 KR 102545132 B1 KR102545132 B1 KR 102545132B1 KR 1020230007010 A KR1020230007010 A KR 1020230007010A KR 20230007010 A KR20230007010 A KR 20230007010A KR 102545132 B1 KR102545132 B1 KR 102545132B1
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Abstract
Description
본 발명은 연어정자로부터 제조되는 핵단백질 분말과 이를 포함하는 기능성 음료, 이를 제조하는 방법에 관한 것이다.The present invention relates to a nucleoprotein powder prepared from salmon sperm, a functional beverage containing the same, and a method for preparing the same.
근년, 우리나라에서 식생활은 경제 발전과 사회구조의 변화에 따라 서구화되어 가고 있고, 이로 인하여 축산물의 소비량이 대량 증가하고 있다. 하지만, 소비자들은 국내에서 소비되고 있는 일부 국내산 및 수입산 축산물에서 조류독감, 돼지콜레라 및 광우병 등과 같은 질병의 발생 우려로 축산물의 섭취를 다소 주저하고 있어 축산물을 대체할 수 있는 새로운 단백자원의 개발이 절실하다. 이러한 일면에서 볼 때 소비자의 기호에 맞는 새로운 단백자원이 개발되는 경우 그 시장은 상당히 증가하리라 생각된다.In recent years, dietary life in Korea has been westernized in accordance with economic development and changes in social structure, and as a result, consumption of livestock products has increased significantly. However, consumers are somewhat hesitant to consume livestock products due to concerns about the occurrence of diseases such as avian flu, swine cholera, and mad cow disease in some domestic and imported livestock products consumed in Korea. Therefore, it is urgent to develop new protein resources that can replace livestock products. do. From this point of view, it is expected that the market will significantly increase if a new protein resource that meets the consumer's taste is developed.
한편, 수산가공업계는 연안 어장의 환경오염, 매립 및 모래 채취와 같은 수산물의 생태 파괴 등에 의한 자원 감소, 200해리 경제수역의 설정 등에 의한 국내외적 환경요인의 변화로 원료 확보가 어려워 궁극적인 어려움에 처하여 있다. 이러한 수산가공업계의 어려움을 타파하기 위해서는 부산물의 효율적 이용과 더불어 연어와 같이 계절에 관계없이 꾸준히 원료를 공급할 수 있는 어종을 이용하여 다양한 제품을 개발하는 것이라 할 수 있다. On the other hand, the seafood processing industry faces ultimate difficulties as it is difficult to secure raw materials due to environmental pollution of coastal fishing grounds, resource reduction due to ecological destruction of aquatic products such as landfill and sand collection, and changes in domestic and international environmental factors such as the establishment of a 200 nautical mile economic zone. are in a situation In order to overcome these difficulties in the fish processing industry, it can be said that the efficient use of by-products and the development of various products using fish species that can supply raw materials steadily regardless of the season, such as salmon.
연어(Oncorhynchus keta)는 연어과이면서 바다에서 성장하여 산란기에 민물로 돌아오는 대표적인 회귀성 어종으로, 몸이 길고 옆으로 납작하면서 입이 크며, 회귀 시 어획된 경우 전장이 일반적으로 60-80 cm에 이른다. 이와 같은 형태적 특성을 가지고 있는 연어는 eicosapentaenoic acid(EPA, 20:5) 및 docosahexaenoic acid(DHA, 22:6)와 같은 건강 기능성 고도불포화 지방산을 가지고 있어 건강 기능적으로 의미가 있고, 비린내가 적으면서 육색이 축육과 유사한 선홍색을 가지고 있어 축육을 대체할 수 있는 우수한 동물성 단백자원 중의 하나이다. 이와 같이 영양 및 건강 지향적 어종이면서 소비자들의 선호 어종인 연어는 노르웨이 및 칠레 등에서 다양한 방법으로 양식하여 다량으로 공급이 가능하고, 우리나라에서도 강원도를 중심으로 양식을 시도하여 일부 성공하고 있다. 이와 같이 수산가공학적 면에서 원료 확보에 어려움이 없으면서, 가공적성이 우수한 연어는 비린내에 대한 거부감이 강하면서 축육에 익숙한 미국 및 유럽의 소비자들은 물론이고, 서구식에 익숙한 우리나라 신세대들과 건강을 우려하는 기성세대의 경우도 선호하고 있어 소비자 선호도 면에서도 우수한 고급 어종이다. 이러한 면에서 연어는 국내에서는 단지, 훈제품 및 통조림 정도만으로 가공 및 시판되고 있을 뿐이어서, 연어를 활용한 다양한 제품의 개발이 절실하다.Salmon (Oncorhynchus keta) is a representative regressive fish that grows in the sea and returns to freshwater during the spawning season. Salmon with such morphological characteristics has health functional polyunsaturated fatty acids such as eicosapentaenoic acid (EPA, 20:5) and docosahexaenoic acid (DHA, 22:6), so it is meaningful in terms of health function and has a low fishy smell. It is one of the excellent animal protein resources that can replace livestock as it has a bright red color similar to that of livestock. Salmon, which is a nutritional and health-oriented fish species and is a fish species favored by consumers, can be farmed in various ways in Norway and Chile, etc., and can be supplied in large quantities, and in Korea, aquaculture is attempted mainly in Gangwon-do, with some success. In this way, there is no difficulty in securing raw materials in terms of fishery processing, and salmon with excellent processing aptitude has a strong reluctance to the fishy smell, and consumers in the United States and Europe who are accustomed to livestock meat, as well as new generations in Korea who are accustomed to Western food and concerned about their health. In the case of the older generation, it is also preferred, so it is an excellent high-class fish species in terms of consumer preference. In this respect, salmon is only processed and marketed in Korea as smoked products and canned products, so the development of various products using salmon is urgently needed.
연어이리 핵산 속에는 프로타민과 아데노신 성분이 많이 함유되어 있어 섭취시 체내에서 아르기닌과 오메가3 등의 불포화 지방산까지도 만들어 주게 되어 면역력 향상의 최고 영양물질로 알려져있다.Salmon milt nucleic acid contains a lot of protamine and adenosine components, so when ingested, even unsaturated fatty acids such as arginine and omega 3 are produced in the body, which is known as the best nutrient for improving immunity.
하지만, 연어를 이용한 신제품의 개발에 관한 연구는 거의 없는 실정이다.However, there is little research on the development of new products using salmon.
본 발명은 상기와 같은 문제점을 해결하기 위해 안출된 것으로서, 본 발명의 목적은 연어정자로부터 제조되는 연어정자핵단백질 분말을 제공하는 것이다.The present invention has been made to solve the above problems, and an object of the present invention is to provide salmon sperm nuclear protein powder prepared from salmon sperm.
본 발명의 과제는 이상에서 언급한 과제들로 제한되지 않으며, 언급되지 않은 또 다른 과제들은 아래의 기재로부터 당업자에게 명확하게 이해될 수 있을 것이다.The object of the present invention is not limited to the tasks mentioned above, and other tasks not mentioned will be clearly understood by those skilled in the art from the following description.
상기 목적을 달성하기 위하여 본 발명은In order to achieve the above object, the present invention
연어정자로부터 제조되는 연어정자핵단백질 분말을 제공한다.Provided is a salmon sperm nuclear protein powder prepared from salmon sperm.
또한, 본 발명은In addition, the present invention
스텐레스 탱크에 농도 0.9 중량%인 식염수를 넣고, 온도를 40℃로 유지하는 단계; 상기 식염수에 냉동된 연어정자를 투입하고, 24시간 동안 해동시키는 단계; 및 해동된 연어정자를 세척하는 단계;를 포함하는 해동 및 세척 단계;Adding saline solution having a concentration of 0.9% by weight to a stainless steel tank and maintaining the temperature at 40°C; Injecting frozen salmon sperm into the saline solution and thawing for 24 hours; and washing the thawed salmon sperm; a thawing and washing step including;
정제수 100 중량부 및 효소 15 중량부를 혼합하여 혼합액을 제조하는 단계; 상기 혼합액에 해동 및 세척된 연어정자를 투입하는 단계; 상기 혼합액을 48-52℃의 온도로 가열하고 45-75분 동안 효소반응을 수행하는 단계; 효소반응이 수행된 혼합액을 88-92℃의 온도로 가열하고 8-12분 동안 숙성하는 단계; 및 숙성된 혼합액에 촉매를 투입하여 효소반응을 멈추는 단계;를 포함하는 효소 반응 단계;Preparing a mixed solution by mixing 100 parts by weight of purified water and 15 parts by weight of an enzyme; Injecting thawed and washed salmon sperm into the mixture; heating the mixed solution to a temperature of 48-52° C. and performing an enzymatic reaction for 45-75 minutes; heating the mixture in which the enzyme reaction was performed to a temperature of 88-92° C. and aging for 8-12 minutes; Enzymatic reaction step comprising; and stopping the enzyme reaction by introducing a catalyst into the aged liquid mixture;
효소반응이 멈춘 혼합액에 구연산을 250 중량부 첨가하여 pH를 3.8-4로 조절하여 1차 멸균하는 단계; 및 1차 멸균된 혼합액을 80-85℃의 온도로 가열하고 45-75분 동안 교반하여 2차 멸균하는 단계;를 포함하는 멸균 단계;Primary sterilization by adding 250 parts by weight of citric acid to the mixture in which the enzyme reaction has stopped to adjust the pH to 3.8-4; and heating the primary sterilized mixed solution to a temperature of 80-85° C. and performing secondary sterilization by stirring for 45-75 minutes;
2차 멸균된 혼합액을 40℃의 온도로 냉각시키는 단계; 냉각된 혼합액에 농도 80 중량%의 알코올 용액 200-1000 중량부를 첨가하는 단계; 및 필터프레스를 이용하여 여과시켜 젖은 분말 상태인 연어정자핵단백질을 얻는 단계;를 포함하는 여과 단계;cooling the secondary sterilized liquid mixture to a temperature of 40°C; adding 200-1000 parts by weight of an alcohol solution having a concentration of 80% by weight to the cooled liquid mixture; and filtering using a filter press to obtain wet powdered salmon sperm nuclear protein;
젖은 분말 상태인 연어정자핵단백질에 농도 80 중량%의 알코올 용액 및 농도 50 중량%의 가성 소다를 3:2의 중량비율로 혼합한 중화용액을 가하여 중화하는 단계; 및 중화 후 1차 탈수하여 젖은 분말 상태인 연어정자핵단백질을 얻는 단계;를 포함하는 중화 단계; 및Neutralizing wet powdered salmon sperm nuclear protein by adding a neutralization solution in which an alcohol solution having a concentration of 80% by weight and caustic soda having a concentration of 50% by weight are mixed in a weight ratio of 3:2; and a step of first dehydration after neutralization to obtain wet powdered salmon sperm nuclear protein; and
젖은 분말 상태인 연어정자핵단백질과 농도 92-93 중량%의 알코올 용액을 혼합한 후, 60-90분에 걸쳐 2차 탈수하는 단계; 2차 탈수 후 원심분리기를 이용하여 젖은 분말 상태인 연어정자핵단백질을 얻는 단계; 및 젖은 분말 상태인 연어정자핵단백질을 진공건조기에 넣고 70-80℃의 온도에서 감압건조하는 단계;를 포함하는 연어정자핵단백질 분말 수득 단계;를 포함하는 연어정자핵단백질 분말의 제조방법을 제공한다.After mixing wet powdered salmon sperm nuclear protein with an alcohol solution having a concentration of 92-93% by weight, secondary dehydration for 60-90 minutes; Obtaining wet powdered salmon sperm nuclear protein using a centrifugal separator after secondary dehydration; Provides a method for producing salmon sperm nuclear protein powder comprising a step of obtaining salmon sperm nuclear protein powder, including the step of putting wet powdered salmon sperm nuclear protein in a vacuum dryer and drying under reduced pressure at a temperature of 70-80 ° C. do.
나아가, 본 발명은Furthermore, the present invention
스텐레스 탱크에 농도 0.9 중량%인 식염수를 넣고, 온도를 40℃로 유지하는 단계; 상기 식염수에 냉동된 연어정자를 투입하고, 24시간 동안 해동시키는 단계; 해동된 연어정자를 1-5℃의 온도인 농도 2-4 중량%의 천일염수를 이용하여 1차 세척하는 단계; 및 1차 세척된 연어정자를 1-5℃의 온도의 정제수를 이용하여 2차 세척하는 단계;를 포함하는 해동 및 세척 단계;Adding saline solution having a concentration of 0.9% by weight to a stainless steel tank and maintaining the temperature at 40°C; Injecting frozen salmon sperm into the saline solution and thawing for 24 hours; First washing the thawed salmon sperm with 2-4% by weight natural salt water at a temperature of 1-5°C; and secondly washing the firstly washed salmon sperm with purified water at a temperature of 1-5° C.;
정제수 100 중량부 및 판크레아틴 15 중량부를 혼합하여 혼합액을 제조하는 단계; 상기 혼합액에 해동 및 세척된 연어정자를 투입하는 단계; 상기 혼합액을 50℃의 온도로 가열하고 60분 동안 효소반응을 수행하는 단계; 효소반응이 수행된 혼합액을 90℃의 온도로 가열하고 10분 동안 숙성하는 단계; 및 숙성된 혼합액에 가성소다를 투입하여 효소반응을 멈추는 단계;를 포함하는 효소 반응 단계;preparing a mixed solution by mixing 100 parts by weight of purified water and 15 parts by weight of pancreatin; Injecting thawed and washed salmon sperm into the mixture; heating the mixed solution to a temperature of 50° C. and performing an enzymatic reaction for 60 minutes; heating the mixture in which the enzyme reaction was performed to a temperature of 90° C. and aging for 10 minutes; Enzymatic reaction step comprising; and stopping the enzyme reaction by adding caustic soda to the aged mixture;
효소반응이 멈춘 혼합액에 구연산을 250 중량부 첨가하여 pH를 3.8-4로 조절하여 1차 멸균하는 단계; 및 1차 멸균된 혼합액을 82-83℃의 온도로 가열하고 60분 동안 교반하여 2차 멸균하는 단계;를 포함하는 멸균 단계;Primary sterilization by adding 250 parts by weight of citric acid to the mixture in which the enzyme reaction has stopped to adjust the pH to 3.8-4; and heating the primary sterilized mixed solution to a temperature of 82-83° C. and performing secondary sterilization by stirring for 60 minutes;
2차 멸균된 혼합액을 40℃의 온도로 냉각시키는 단계; 냉각된 혼합액에 농도 80 중량%이고 에탄올 및 헥산올을 4:1의 중량비로 혼합한 알코올 용액 800-1000 중량부를 첨가하는 단계; 및 필터프레스를 이용하여 여과시켜 젖은 분말 상태인 연어정자핵단백질을 얻는 단계;를 포함하는 여과 단계;cooling the secondary sterilized liquid mixture to a temperature of 40°C; Adding 800-1000 parts by weight of an alcohol solution obtained by mixing ethanol and hexanol in a weight ratio of 4:1 with a concentration of 80% by weight to the cooled mixture; and filtering using a filter press to obtain wet powdered salmon sperm nuclear protein;
젖은 분말 상태인 연어정자핵단백질에 농도 80 중량%의 알코올 용액 및 농도 50 중량%의 가성 소다를 3:2의 중량비율로 혼합한 중화용액을 가하여 중화하는 단계; 및 중화 후 1차 탈수하여 젖은 분말 상태인 연어정자핵단백질을 얻는 단계;를 포함하는 중화 단계;Neutralizing wet powdered salmon sperm nuclear protein by adding a neutralization solution in which an alcohol solution having a concentration of 80% by weight and caustic soda having a concentration of 50% by weight are mixed in a weight ratio of 3:2; and a step of first dehydration after neutralization to obtain wet powdered salmon sperm nuclear protein;
젖은 분말 상태인 연어정자핵단백질과 농도 92-93 중량%의 에탄올 용액을 혼합한 후, 75분에 걸쳐 2차 탈수하는 단계; 2차 탈수 후 원심분리기를 이용하여 젖은 분말 상태인 연어정자핵단백질을 얻는 단계; 및 젖은 분말 상태인 연어정자핵단백질을 진공건조기에 넣고 70-80℃의 온도에서 감압건조하는 단계;를 포함하고, 상기 2차 탈수하는 단계, 젖은 분말 상태인 연어정자핵단백질을 얻는 단계 및 감압건조하는 단계는 5-6회 반복하여 수행하는 것을 특징으로 하는 연어정자핵단백질 분말 수득 단계;를 포함하는 연어정자핵단백질 분말 제조 단계;After mixing wet powdered salmon sperm nuclear protein with an ethanol solution having a concentration of 92-93% by weight, secondary dehydration for 75 minutes; Obtaining wet powdered salmon sperm nuclear protein using a centrifugal separator after secondary dehydration; and putting the wet powdered salmon sperm nuclear protein in a vacuum dryer and drying under reduced pressure at a temperature of 70-80° C., wherein the secondary dehydration step, obtaining wet powder salmon sperm nuclear protein and reduced pressure Salmon sperm nuclear protein powder manufacturing step comprising: obtaining salmon sperm nuclear protein powder, characterized in that the drying step is repeated 5 to 6 times;
감잎, 율무, 대추, 생강, 감초 및 계피를 2:2:2:1:2:1의 중량비율로 혼합한 한방원료를 준비하고, 액체 분사가 가능한 분사각이 60°인 노즐을 2개씩 3열로 6개 포함하는 세척기를 사용하여 식초물을 분사하여 한방원료를 1차 세척하는 단계; 1차 세척된 한방원료를 전해수로 2차 세척하는 단계; 2차 세척된 한방원료를 43-47℃의 온도에서 건조하는 단계; 건조된 한방원료를 0.095-0.105 MPa의 압력 및 230-250℃의 온도에서 80-100분 동안 증숙하고, 55-65℃의 온도에서 220-260분 동안 건조시키는 과정을 3회 수행하는 단계; 증숙 및 건조된 한방원료를 분쇄하여 한방분말을 제조하는 단계; 및 상기 한방분말 100 중량부 및 물 100 중량부를 혼합하고 78-82℃의 온도로 가열하여 1-3시간 동안 열수추출하고 여과하는 단계;를 포함하는 한방여과액을 제조하는 단계;Prepare herbal raw materials by mixing persimmon leaves, adlay, jujube, ginger, licorice, and cinnamon in a weight ratio of 2:2:2:1:2:1, and use two nozzles each with a spray angle of 60° that can spray liquid. Using a washer containing 6 heats to spray vinegar water to first wash the oriental raw materials; Secondary washing of the firstly washed herbal raw material with electrolytic water; Drying the secondary washed herbal raw material at a temperature of 43-47 ° C; Steaming the dried herbal raw material at a pressure of 0.095-0.105 MPa and a temperature of 230-250 ° C. for 80-100 minutes, and drying at a temperature of 55-65 ° C. for 220-260 minutes 3 times; Preparing herbal powder by grinding the steamed and dried herbal raw materials; Preparing an herbal filtrate containing; and mixing 100 parts by weight of the herbal powder and 100 parts by weight of water, heating at a temperature of 78-82° C., extracting hot water for 1-3 hours, and filtering;
오미자, 구기자 및 사과를 4:3:3의 중량비율로 혼합하여 과일원료를 준비하고, 상기 과일원료 100 중량부 및 물 100 중량부를 혼합하여 제1 혼합물을 제조하는 단계; 상기 제1 혼합물을 92-95℃의 온도로 가열하고, 증발하는 증기를 냉각시켜 얻은 증류액이 다시 제1 혼합물에 혼합되도록 하여 60-120분 동안 순환시키는 단계; 상기 순환이 완료된 제1 혼합물을 98-100℃의 온도로 가열하고, 60-120분 동안 증발하는 증기를 냉각시켜 1차 증류액을 얻는 단계; 상기 1차 증류액 100 중량부 및 상기 과일원료 100 중량부를 혼합하여 제2 혼합물을 제조하는 단계; 상기 제2 혼합물을 92-95℃의 온도로 가열하고, 증발하는 증기를 냉각시켜 얻은 증류액이 다시 제2 혼합물에 혼합되도록 하여 60-120분 동안 순환시키는 단계; 및 상기 순환이 완료된 제2 혼합물을 70-80℃의 온도로 가열하고, 150-210분 동안 증발하는 증기를 냉각시켜 2차 증류액을 얻는 단계;를 포함하는 과일증류액 제조 단계; 및Preparing a fruit raw material by mixing Schisandra chinensis, goji berry and apple in a weight ratio of 4: 3: 3, and preparing a first mixture by mixing 100 parts by weight of the fruit raw material and 100 parts by weight of water; Heating the first mixture to a temperature of 92-95° C. and allowing the distillate obtained by cooling the evaporating vapor to be mixed with the first mixture again and circulating for 60-120 minutes; obtaining a first distillate by heating the first mixture after completion of the circulation to a temperature of 98-100° C. and cooling the evaporating vapor for 60-120 minutes; preparing a second mixture by mixing 100 parts by weight of the primary distillate and 100 parts by weight of the fruit raw material; Heating the second mixture to a temperature of 92-95° C. and allowing the distillate obtained by cooling the evaporating vapor to be mixed with the second mixture again and circulating for 60-120 minutes; and heating the second mixture after the circulation is completed to a temperature of 70-80° C. and cooling the evaporating vapor for 150-210 minutes to obtain a secondary distillate; preparing a fruit distillate; and
상기 연어정자핵단백질 분말 48-52 중량부, 상기 한방여과액 28-32 중량부 및 상기 과일증류액 18-22 중량부를 혼합하는 단계;를 포함하는 음료 조성물의 제조방법을 제공한다.It provides a method for producing a beverage composition comprising the step of mixing 48-52 parts by weight of the salmon sperm nuclear protein powder, 28-32 parts by weight of the herbal filtrate, and 18-22 parts by weight of the fruit distillate.
본 발명에 따른 연어정자핵단백질 분말은 수용성 저분자로써 체내 흡수율이 좋은 순도 높은 핵산을 포함하는 것으로, 유전자 손상을 예방하고 손상된 유전자를 복원시켜줄 수 있어 신진대사가 좋아지게 되고 피부의 노화지연, 항산화 작용, 면역력 증가, 기억력 향상에 도움이 된다.The salmon sperm nuclear protein powder according to the present invention is a water-soluble low-molecular substance containing high-purity nucleic acid with good absorption rate in the body, which can prevent genetic damage and restore damaged genes, improving metabolism, delaying skin aging, and acting as an antioxidant. , increase immunity, help improve memory.
또한, 본 발명에 따른 연어정자핵단백질 분말의 제조방법은 연어정자로부터 연어정자핵단백질 분말을 제조함에 있어서 높은 수율의 연어정자핵단백질 분말을 얻을 수 있고 쓴맛과 비린내를 저감시켜 기호성 또한 높일 수 있다.In addition, the method for producing salmon sperm nuclear protein powder according to the present invention can obtain a high yield of salmon sperm nuclear protein powder in producing salmon sperm nuclear protein powder from salmon sperm, and can also improve palatability by reducing bitter taste and fishy smell. .
도 1은 본 발명의 일 측면에서 제공되는 연어정자핵단백질 분말의 제조방법을 순서도로 나타낸 것이고;
도 2는 본 발명의 일 실시예에 따라 제조되는 연어정자핵단백질 분말의 사진이다.1 is a flow chart showing a method for producing salmon sperm nuclear protein powder provided in one aspect of the present invention;
2 is a photograph of salmon sperm nuclear protein powder prepared according to an embodiment of the present invention.
이하에서는 첨부된 도면을 참조하여 다양한 실시예를 보다 상세하게 설명한다. 본 명세서에 기재된 실시예는 다양하게 변형될 수 있다. 특정한 실시예가 도면에서 묘사되고 상세한 설명에서 자세하게 설명될 수 있다. 그러나 첨부된 도면에 개시된 특정한 실시 예는 다양한 실시예를 쉽게 이해하도록 하기 위한 것일 뿐이다. 따라서 첨부된 도면에 개시된 특정 실시예에 의해 기술적 사상이 제한되는 것은 아니며, 발명의 사상 및 기술 범위에 포함되는 모든 균등물 또는 대체물을 포함하는 것으로 이해되어야 한다.Hereinafter, various embodiments will be described in more detail with reference to the accompanying drawings. The embodiments described in this specification may be modified in various ways. Certain embodiments may be depicted in the drawings and described in detail in the detailed description. However, specific embodiments disclosed in the accompanying drawings are only intended to facilitate understanding of various embodiments. Therefore, the technical idea is not limited by the specific embodiments disclosed in the accompanying drawings, and it should be understood to include all equivalents or substitutes included in the spirit and technical scope of the invention.
1차, 2차, 제1, 제2 등과 같이 서수를 포함하는 용어는 다양한 구성요소들을 설명하는데 사용될 수 있지만, 이러한 구성요소들은 상술한 용어에 의해 한정되지는 않는다. 상술한 용어는 하나의 구성요소를 다른 구성요소로부터 구별하는 목적으로만 사용된다.Terms including ordinal numbers such as primary, secondary, first, and second may be used to describe various elements, but these elements are not limited by the above-mentioned terms. The terminology described above is only used for the purpose of distinguishing one component from another.
본 명세서에서, '포함한다' 또는 '가지다' 등의 용어는 명세서상에 기재된 특징, 숫자, 단계, 동작, 구성요소, 부품 또는 이들을 조합한 것이 존재함을 지정하려는 것이지, 하나 또는 그 이상의 다른 특징들이나 숫자, 단계, 동작, 구성요소, 부품 또는 이들을 조합한 것들의 존재 또는 부가 가능성을 미리 배제하지 않는 것으로 이해되어야 한다. 어떤 구성요소가 다른 구성요소에 '연결되어' 있다거나 '접속되어' 있다고 언급된 때에는, 그 다른 구성요소에 직접적으로 연결되어 있거나 또는 접속되어 있을 수도 있지만, 중간에 다른 구성요소가 존재할 수도 있다고 이해되어야 할 것이다. 반면에, 어떤 구성요소가 다른 구성요소에 '직접 연결되어' 있다거나 '직접 접속되어' 있다고 언급된 때에는, 중간에 다른 구성요소가 존재하지 않는 것으로 이해되어야 할 것이다.In this specification, terms such as 'comprise' or 'having' are intended to designate that there is a feature, number, step, operation, component, part, or combination thereof described in the specification, but one or more other features It should be understood that the presence or addition of numbers, steps, operations, components, parts, or combinations thereof is not precluded. It is understood that when a component is referred to as being 'connected' or 'connected' to another component, it may be directly connected or connected to the other component, but other components may exist in the middle. It should be. On the other hand, when a component is referred to as being 'directly connected' or 'directly connected' to another component, it should be understood that no other component exists in the middle.
그 밖에도, 본 발명을 설명함에 있어서, 관련된 공지 기능 혹은 구성에 대한 구체적인 설명이 본 발명의 요지를 불필요하게 흐릴 수 있다고 판단되는 경우, 그에 대한 상세한 설명은 축약하거나 생략한다.In addition, in describing the present invention, if it is determined that a detailed description of a related known function or configuration may unnecessarily obscure the subject matter of the present invention, the detailed description thereof will be abbreviated or omitted.
본 발명은 연어정자로부터 제조되는 연어정자핵단백질 분말을 제공한다.The present invention provides salmon sperm nuclear protein powder prepared from salmon sperm.
본 발명에 따른 연어정자핵단백질 분말은 수용성 저분자로써 체내 흡수율이 좋은 순도 높은 핵산을 포함하는 것으로, 유전자 손상을 예방하고 손상된 유전자를 복원시켜줄 수 있어 신진대사가 좋아지게 되고 피부의 노화지연, 항산화 작용, 면역력 증가, 기억력 향상에 도움이 된다.The salmon sperm nuclear protein powder according to the present invention is a water-soluble low-molecular substance containing high-purity nucleic acid with good absorption rate in the body, which can prevent genetic damage and restore damaged genes, improving metabolism, delaying skin aging, and acting as an antioxidant. , increase immunity, help improve memory.
또한, 본 발명은In addition, the present invention
스텐레스 탱크에 농도 0.9 중량%인 식염수를 넣고, 온도를 40℃로 유지하는 단계; 상기 식염수에 냉동된 연어정자를 투입하고, 24시간 동안 해동시키는 단계; 및 해동된 연어정자를 세척하는 단계;를 포함하는 해동 및 세척 단계;Adding saline solution having a concentration of 0.9% by weight to a stainless steel tank and maintaining the temperature at 40°C; Injecting frozen salmon sperm into the saline solution and thawing for 24 hours; and washing the thawed salmon sperm; a thawing and washing step including;
정제수 100 중량부 및 효소 15 중량부를 혼합하여 혼합액을 제조하는 단계; 상기 혼합액에 해동 및 세척된 연어정자를 투입하는 단계; 상기 혼합액을 48-52℃의 온도로 가열하고 45-75분 동안 효소반응을 수행하는 단계; 효소반응이 수행된 혼합액을 88-92℃의 온도로 가열하고 8-12분 동안 숙성하는 단계; 및 숙성된 혼합액에 촉매를 투입하여 효소반응을 멈추는 단계;를 포함하는 효소 반응 단계;Preparing a mixed solution by mixing 100 parts by weight of purified water and 15 parts by weight of an enzyme; Injecting thawed and washed salmon sperm into the mixture; heating the mixed solution to a temperature of 48-52° C. and performing an enzymatic reaction for 45-75 minutes; heating the mixture in which the enzyme reaction was performed to a temperature of 88-92° C. and aging for 8-12 minutes; Enzymatic reaction step comprising; and stopping the enzyme reaction by introducing a catalyst into the aged liquid mixture;
효소반응이 멈춘 혼합액에 구연산을 250 중량부 첨가하여 pH를 3.8-4로 조절하여 1차 멸균하는 단계; 및 1차 멸균된 혼합액을 80-85℃의 온도로 가열하고 45-75분 동안 교반하여 2차 멸균하는 단계;를 포함하는 멸균 단계;Primary sterilization by adding 250 parts by weight of citric acid to the mixture in which the enzyme reaction has stopped to adjust the pH to 3.8-4; and heating the primary sterilized mixed solution to a temperature of 80-85° C. and performing secondary sterilization by stirring for 45-75 minutes;
2차 멸균된 혼합액을 40℃의 온도로 냉각시키는 단계; 냉각된 혼합액에 농도 80 중량%의 알코올 용액 200-1000 중량부를 첨가하는 단계; 및 필터프레스를 이용하여 여과시켜 젖은 분말 상태인 연어정자핵단백질을 얻는 단계;를 포함하는 여과 단계;cooling the secondary sterilized liquid mixture to a temperature of 40°C; adding 200-1000 parts by weight of an alcohol solution having a concentration of 80% by weight to the cooled liquid mixture; and filtering using a filter press to obtain wet powdered salmon sperm nuclear protein;
젖은 분말 상태인 연어정자핵단백질에 농도 80 중량%의 알코올 용액 및 농도 50 중량%의 가성 소다를 3:2의 중량비율로 혼합한 중화용액을 가하여 중화하는 단계; 및 중화 후 1차 탈수하여 젖은 분말 상태인 연어정자핵단백질을 얻는 단계;를 포함하는 중화 단계; 및Neutralizing wet powdered salmon sperm nuclear protein by adding a neutralization solution in which an alcohol solution having a concentration of 80% by weight and caustic soda having a concentration of 50% by weight are mixed in a weight ratio of 3:2; and a step of first dehydration after neutralization to obtain wet powdered salmon sperm nuclear protein; and
젖은 분말 상태인 연어정자핵단백질과 농도 92-93 중량%의 알코올 용액을 혼합한 후, 60-90분에 걸쳐 2차 탈수하는 단계; 2차 탈수 후 원심분리기를 이용하여 젖은 분말 상태인 연어정자핵단백질을 얻는 단계; 및 젖은 분말 상태인 연어정자핵단백질을 진공건조기에 넣고 70-80℃의 온도에서 감압건조하는 단계;를 포함하는 연어정자핵단백질 분말 수득 단계;를 포함하는 연어정자핵단백질 분말의 제조방법을 제공한다.After mixing wet powdered salmon sperm nuclear protein with an alcohol solution having a concentration of 92-93% by weight, secondary dehydration for 60-90 minutes; Obtaining wet powdered salmon sperm nuclear protein using a centrifugal separator after secondary dehydration; Provides a method for producing salmon sperm nuclear protein powder comprising a step of obtaining salmon sperm nuclear protein powder, including the step of putting wet powdered salmon sperm nuclear protein in a vacuum dryer and drying under reduced pressure at a temperature of 70-80 ° C. do.
본 발명에 따른 연어정자핵단백질 분말의 제조방법은 연어정자로부터 연어정자핵단백질 분말을 제조함에 있어서 높은 수율의 연어정자핵단백질 분말을 얻을 수 있고 쓴맛과 비린내를 저감시켜 기호성 또한 높일 수 있다.The method for producing salmon sperm nuclear protein powder according to the present invention can obtain a high yield of salmon sperm nuclear protein powder in producing salmon sperm nuclear protein powder from salmon sperm, and can improve palatability by reducing bitter taste and fishy smell.
이때, 도 1에 본 발명의 일 측면에서 제공되는 연어정자핵단백질 분말의 제조방법을 순서도로 나타내었으며, 이하, 도 1의 순서도를 참조하여 본 발명에 따른 연어정자핵단백질 분말의 제조방법을 각 단계별로 상세히 설명한다.At this time, FIG. 1 shows a flowchart of a method for producing salmon sperm nuclear protein powder provided in one aspect of the present invention. Hereinafter, referring to the flow chart of FIG. 1, the method for producing salmon sperm nuclear protein powder according to the present invention is respectively Describe in detail step by step.
먼저, 본 발명에 따른 연어정자핵단백질 분말의 제조방법은 해동 및 세척 단계를 포함한다.First, the method for producing salmon sperm nuclear protein powder according to the present invention includes thawing and washing steps.
상기 해동 및 세척 단계는, The thawing and washing steps,
스텐레스 탱크에 농도 0.9 중량%인 식염수를 넣고, 온도를 40℃로 유지하는 단계; Adding saline solution having a concentration of 0.9% by weight to a stainless steel tank and maintaining the temperature at 40°C;
상기 식염수에 냉동된 연어정자를 투입하고, 24시간 동안 해동시키는 단계; 및 Injecting frozen salmon sperm into the saline solution and thawing for 24 hours; and
해동된 연어정자를 세척하는 단계;를 포함한다.and washing the thawed salmon sperm.
먼저, 스텐레스 탱크에 농도 0.9 중량%인 식염수를 넣고, 온도를 40℃로 유지한다. 상기 식염수는 지하수 100 중량부 및 식염 0.9 중량부를 혼합한 것을 사용하는 것이 바람직하다. 또한, 상기 식염수를 40℃로 유지하여야 한다. 상기 식염수의 온도를 유지하여 후단에서 냉동된 연어정자를 해동하는 데, 이에 따라 연어정자가 물러터지지 않고 원형상태로 보존하면서 분리할 수 있다. 원형상태로 보존하면서 분리함으로써 최종 완성물에 불순물이 섞이지 않고 순도 90% 이상을 유지할 수 있다.First, saline solution having a concentration of 0.9% by weight was put into a stainless steel tank, and the temperature was maintained at 40°C. The saline solution is preferably a mixture of 100 parts by weight of ground water and 0.9 parts by weight of salt. In addition, the saline solution should be maintained at 40°C. The temperature of the saline solution is maintained to thaw frozen salmon sperm at the rear end, whereby salmon sperm can be separated while preserving them in their original state without softening. By separating while preserving in its original state, it is possible to maintain a purity of 90% or more without mixing impurities in the final product.
다음, 상기 식염수에 냉동된 연어정자를 투입하고, 24시간 동안 해동시킨다.Next, frozen salmon sperm is added to the saline solution and thawed for 24 hours.
다음, 해동된 연어정자를 세척한다. 상기 세척은, 1-5℃의 온도인 농도 2-4 중량%의 천일염수를 이용하여 연어정자를 1차 세척하는 단계; 및 1-5℃의 온도의 정제수를 이용하여 연어정자를 2차 세척하는 단계;를 수행하는 것이 바람직하다. 상기와 같이 저온의 천일염수로 1차 세척하고, 저온의 정제수로 2차 세척하여 연어정자의 세균번식을 방지하고 비린내를 저감시킬 수 있다.Next, the thawed salmon sperm is washed. The washing may include firstly washing salmon sperm using natural salt water having a concentration of 2-4% by weight at a temperature of 1-5°C; and secondarily washing the salmon sperm using purified water at a temperature of 1-5°C. As described above, first washing with low-temperature sea salt water and second washing with low-temperature purified water can prevent bacterial growth of salmon sperm and reduce fishy smell.
다음으로, 본 발명에 따른 연어정자핵단백질 분말의 제조방법은 효소 반응 단계를 포함한다.Next, the method for producing salmon sperm nuclear protein powder according to the present invention includes an enzymatic reaction step.
상기 효소 반응 단계는,The enzymatic reaction step,
정제수 100 중량부 및 효소 15 중량부를 혼합하여 혼합액을 제조하는 단계;Preparing a mixed solution by mixing 100 parts by weight of purified water and 15 parts by weight of an enzyme;
상기 혼합액에 해동 및 세척된 연어정자를 투입하는 단계; Injecting thawed and washed salmon sperm into the mixture;
상기 혼합액을 48-52℃의 온도로 가열하고 45-75분 동안 효소반응을 수행하는 단계; heating the mixed solution to a temperature of 48-52° C. and performing an enzymatic reaction for 45-75 minutes;
효소반응이 수행된 혼합액을 88-92℃의 온도로 가열하고 8-12분 동안 숙성하는 단계; 및 heating the mixture in which the enzyme reaction was performed to a temperature of 88-92° C. and aging for 8-12 minutes; and
숙성된 혼합액에 촉매를 투입하여 효소반응을 멈추는 단계;를 포함한다.Stopping the enzyme reaction by adding a catalyst to the aged mixed solution; includes.
먼저, 정제수 100 중량부 및 효소 15 중량부를 혼합하여 혼합액을 제조한다. 상기 효소는 단백질 분해효소를 사용하는 것이 바람직하고, 가장 바람직하게는 판크레F를 사용한다. 상기 효소로 판크레F를 상기 범위로 혼합한 혼합액을 사용하여 효소반응을 수행함으로써 제조되는 연어정자핵단백질의 수율을 높일 수 있다. 상기 판크레F는 판크레아틴일 수 있다.First, a mixed solution is prepared by mixing 100 parts by weight of purified water and 15 parts by weight of an enzyme. It is preferable to use a proteolytic enzyme as the enzyme, and most preferably, Pancre F is used. The yield of salmon sperm nuclear protein produced by carrying out an enzymatic reaction using a mixed solution in which Pancre F is mixed in the above range as the enzyme can be increased. The Pancre F may be Pancreatin.
다음, 상기 혼합액에 해동 및 세척된 연어정자를 투입한다.Next, the thawed and washed salmon sperm is added to the mixture.
다음, 상기 혼합액을 48-52℃의 온도로 가열하고 45-75분 동안 효소반응을 수행한다. 더욱 바람직하게는 49-51℃의 온도로 가열하고 55-65분 동안 효소반응을 수행하고, 가장 바람직하게는 50℃의 온도로 가열하고 60분 동안 효소반응을 수행한다. 상기 온도 및 시간동안 효소반응을 수행함으로써 제조되는 연어정자핵단백질의 품질 및 수율을 높일 수 있다.Next, the mixed solution is heated to a temperature of 48-52° C. and an enzyme reaction is performed for 45-75 minutes. More preferably, heating is performed at a temperature of 49-51°C and enzymatic reaction is performed for 55-65 minutes, and most preferably, heating is performed at a temperature of 50°C and enzymatic reaction is performed for 60 minutes. By carrying out the enzymatic reaction for the above temperature and time, the quality and yield of salmon sperm nuclear protein produced can be increased.
다음, 효소반응이 수행된 혼합액을 88-92℃의 온도로 가열하고 8-12분 동안 숙성한다. 더욱 바람직하게는 89-91℃의 온도로 가열하고 9-11분 동안 숙성하고, 가장 바람직하게는 90℃의 온도로 가열하고 10분 동안 숙성한다. 상기 온도 및 시간동안 숙성시킴으로써 제조되는 연어정자핵단백질의 품질 및 수율을 높일 수 있다.Next, the mixed solution in which the enzyme reaction was performed is heated to a temperature of 88-92 ° C and aged for 8-12 minutes. More preferably, it is heated to a temperature of 89-91°C and aged for 9-11 minutes, and most preferably heated to a temperature of 90°C and aged for 10 minutes. The quality and yield of salmon sperm nuclear protein prepared by aging at the above temperature and time can be improved.
다음, 숙성된 혼합액에 촉매를 투입하여 효소반응을 멈춘다. 상기 숙성 이후 혼합액에 적절한 촉매를 투입함으로써 효소반응을 멈출 수 있다. 상기 촉매는 가성소다인 것이 바람직하다.Next, a catalyst is added to the aged mixture to stop the enzyme reaction. After the aging, the enzyme reaction can be stopped by adding an appropriate catalyst to the mixed solution. The catalyst is preferably caustic soda.
다음으로, 본 발명에 따른 연어정자핵단백질 분말의 제조방법은 멸균 단계를 포함한다.Next, the method for producing salmon sperm nuclear protein powder according to the present invention includes a sterilization step.
상기 멸균 단계는,The sterilization step is
효소반응이 멈춘 혼합액에 구연산을 250 중량부 첨가하여 pH를 3.8-4로 조절하여 1차 멸균하는 단계; 및 Primary sterilization by adding 250 parts by weight of citric acid to the mixture in which the enzyme reaction has stopped to adjust the pH to 3.8-4; and
1차 멸균된 혼합액을 80-85℃의 온도로 가열하고 45-75분 동안 교반하여 2차 멸균하는 단계;를 포함한다.and secondary sterilization by heating the primary sterilized mixed solution to a temperature of 80-85° C. and stirring for 45-75 minutes.
먼저, 효소반응이 멈춘 혼합액에 구연산을 250 중량부 첨가하여 pH를 3.8-4로 조절하여 1차 멸균한다. 상기 1차 멸균에는 구연산을 사용하는 것이 바람직하고, 혼합액의 pH를 3.8-4로 조절함으로써 1차 멸균을 수행한다. 여기서 pH가 4를 초과하는 경우 알칼리성이 되어 바람직하지 않으며, pH가 3.8 미만인 경우 산성이 되어 제조되는 연어정자핵단백질에 씁쓸한 맛이 첨가되는 문제가 있다.First, 250 parts by weight of citric acid is added to the mixed solution in which the enzyme reaction has stopped, the pH is adjusted to 3.8-4, and primary sterilization is performed. It is preferable to use citric acid for the primary sterilization, and primary sterilization is performed by adjusting the pH of the mixed solution to 3.8-4. Here, when the pH exceeds 4, it becomes alkaline, which is undesirable, and when the pH is less than 3.8, it becomes acidic, and there is a problem in that a bitter taste is added to the salmon sperm nuclear protein produced.
다음, 1차 멸균된 혼합액을 80-85℃의 온도로 가열하고 45-75분 동안 교반하여 2차 멸균한다. 더욱 바람직하게는 81-84℃의 온도로 가열하고 55-65분 동안 교반하여 2차 멸균하고, 가장 바람직하게는 82-83℃의 온도로 가열하고 60분 동안 교반하여 2차 멸균한다. 상기 1차 멸균을 수행한 후, 상기 온도 및 시간동안 2차 멸균을 수행함으로써 더욱 품질 높은 연어정자핵단백질이 제조될 수 있다.Next, the primary sterilized mixture is heated to a temperature of 80-85 ° C and stirred for 45-75 minutes to perform secondary sterilization. More preferably, secondary sterilization is performed by heating at a temperature of 81-84°C and stirring for 55-65 minutes, and most preferably, secondary sterilization is performed by heating at a temperature of 82-83°C and stirring for 60 minutes. After performing the primary sterilization, secondary sterilization is performed for the above temperature and time, thereby producing higher quality salmon sperm nuclear protein.
다음으로, 본 발명에 따른 연어정자핵단백질 분말의 제조방법은 여과 단계를 포함한다.Next, the method for producing salmon sperm nuclear protein powder according to the present invention includes a filtration step.
상기 여과 단계는,The filtration step is
2차 멸균된 혼합액을 40℃의 온도로 냉각시키는 단계; cooling the secondary sterilized liquid mixture to a temperature of 40°C;
냉각된 혼합액에 농도 80 중량%의 알코올 용액 200-1000 중량부를 첨가하는 단계; 및 adding 200-1000 parts by weight of an alcohol solution having a concentration of 80% by weight to the cooled liquid mixture; and
필터프레스를 이용하여 여과시켜 젖은 분말 상태인 연어정자핵단백질을 얻는 단계;를 포함한다.Filtering using a filter press to obtain wet powdered salmon sperm nuclear protein; includes.
먼저, 2차 멸균된 혼합액을 40℃의 온도로 냉각시킨다.First, the secondary sterilized liquid mixture is cooled to a temperature of 40°C.
다음, 냉각된 혼합액에 농도 80 중량%의 알코올 용액 200-1000 중량부를 첨가한다. 더욱 바람직하게는 냉각된 혼합액에 농도 80 중량%의 알코올 용액 400-1000 중량부를 첨가하고, 가장 바람직하게는 냉각된 혼합액에 농도 80 중량%의 알코올 용액 800-1000 중량부를 첨가한다. 상기 알코올 용액은 에탄올 용액, 프로판올 용액, 부탄올 용액, 헥산올 용액일 수 있으며, 바람직하게는, 에탄올 및 헥산올을 4:1의 중량비율로 혼합한 용액이다.Next, 200-1000 parts by weight of an alcohol solution having a concentration of 80% by weight is added to the cooled mixture. More preferably, 400-1000 parts by weight of an alcohol solution having a concentration of 80% by weight is added to the cooled liquid mixture, and most preferably 800-1000 parts by weight of an alcohol solution having a concentration of 80% by weight is added to the cooled liquid mixture. The alcohol solution may be an ethanol solution, a propanol solution, a butanol solution, or a hexanol solution, and is preferably a solution in which ethanol and hexanol are mixed in a weight ratio of 4:1.
다음, 필터프레스를 이용하여 여과시켜 젖은 분말 상태인 연어정자핵단백질을 얻는다. 여과된 알코올 용액은 중화시켜 재생알코올로 생산하여 재사용 또는 다른 공정에 사용할 수 있다.Next, it is filtered using a filter press to obtain salmon sperm nuclear protein in a wet powder state. The filtered alcohol solution is neutralized and produced as regenerated alcohol, which can be reused or used in other processes.
다음으로, 본 발명에 따른 연어정자핵단백질 분말의 제조방법은 중화 단계를 포함한다.Next, the method for producing salmon sperm nuclear protein powder according to the present invention includes a neutralization step.
상기 중화 단계는,In the neutralization step,
젖은 분말 상태인 연어정자핵단백질에 농도 80 중량%의 알코올 용액 및 농도 50 중량%의 가성 소다를 3:2의 중량비율로 혼합한 중화용액을 가하여 중화하는 단계; 및 Neutralizing wet powdered salmon sperm nuclear protein by adding a neutralization solution in which an alcohol solution having a concentration of 80% by weight and caustic soda having a concentration of 50% by weight are mixed in a weight ratio of 3:2; and
중화 후 1차 탈수하여 젖은 분말 상태인 연어정자핵단백질을 얻는 단계;를 포함한다.After neutralization, primary dehydration is performed to obtain wet powdered salmon sperm nuclear protein.
먼저, 젖은 분말 상태인 연어정자핵단백질에 농도 80 중량%의 알코올 용액 및 농도 50 중량%의 가성 소다를 3:2의 중량비율로 혼합한 중화용액을 가하여 중화한다.First, a neutralization solution obtained by mixing an alcohol solution having a concentration of 80% by weight and caustic soda having a concentration of 50% by weight in a weight ratio of 3:2 is added to the wet powdered salmon sperm nuclear protein for neutralization.
다음, 중화 후 1차 탈수하여 젖은 분말 상태인 연어정자핵단백질을 얻는다.Next, after neutralization, first dehydration is performed to obtain wet powdered salmon sperm nuclear protein.
다음으로, 본 발명에 따른 연어정자핵단백질 분말의 제조방법은 연어정자핵단백질 분말 수득 단계를 포함한다.Next, the method for producing salmon sperm nuclear protein powder according to the present invention includes a step of obtaining salmon sperm nuclear protein powder.
상기 연어정자핵단백질 분말 수득 단계는,The step of obtaining salmon sperm nuclear protein powder,
젖은 분말 상태인 연어정자핵단백질과 농도 92-93 중량%의 알코올 용액을 혼합한 후, 60-90분에 걸쳐 2차 탈수하는 단계; After mixing wet powdered salmon sperm nuclear protein with an alcohol solution having a concentration of 92-93% by weight, secondary dehydration for 60-90 minutes;
2차 탈수 후 원심분리기를 이용하여 젖은 분말 상태인 연어정자핵단백질을 얻는 단계; 및 Obtaining wet powdered salmon sperm nuclear protein using a centrifugal separator after secondary dehydration; and
젖은 분말 상태인 연어정자핵단백질을 진공건조기에 넣고 70-80℃의 온도에서 감압건조하는 단계;를 포함한다.and putting the wet powdered salmon sperm nuclear protein in a vacuum dryer and drying under reduced pressure at a temperature of 70-80°C.
먼저, 젖은 분말 상태인 연어정자핵단백질과 농도 92-93 중량%의 알코올 용액을 혼합한 후, 60-90분에 걸쳐 2차 탈수한다. 상기 알코올 용액은 에탄올 용액인 것이 바람직하고, 농도 92-93 중량%의 고농도로 사용하는 것이 바람직하다. 고농도의 에탄올 용액을 전단계에서 1차 탈수된 젖은 분말 상태인 연어정자핵단백질과 혼합하고 60-90분에 걸쳐, 더욱 바람직하게는 70-80분에 걸쳐, 가장 바람직하게는 75분에 걸쳐 2차 탈수함으로써 연어정자핵단백질의 품질 및 수율을 높일 수 있다.First, wet powdered salmon sperm nuclear protein and an alcohol solution having a concentration of 92-93% by weight are mixed, followed by secondary dehydration over 60-90 minutes. The alcohol solution is preferably an ethanol solution, and is preferably used at a high concentration of 92-93% by weight. The high-concentration ethanol solution is firstly mixed with the wet powdered salmon sperm nuclear protein dehydrated in the previous step, and secondly over 60-90 minutes, more preferably over 70-80 minutes, most preferably over 75 minutes. Dehydration can improve the quality and yield of salmon sperm nucleoprotein.
다음, 2차 탈수 후 원심분리기를 이용하여 젖은 분말 상태인 연어정자핵단백질을 얻는다.Next, after secondary dehydration, a wet powdery salmon sperm nuclear protein is obtained using a centrifuge.
다음, 젖은 분말 상태인 연어정자핵단백질을 진공건조기에 넣고 70-80℃의 온도에서 감압건조한다.Next, the wet powdered salmon sperm nuclear protein is put in a vacuum dryer and dried under reduced pressure at a temperature of 70-80 ° C.
상기 2차 탈수하는 단계, 젖은 분말 상태인 연어정자핵단백질을 얻는 단계 및 감압건조하는 단계는 반복하여 수행하는 것이 바람직하고, 2-10회 반복하여 수행하는 것이 바람직하고, 5-6회 반복하여 수행하는 것이 가장 바람직하며, 이를 통해 균일한 분말 형태의 최종 연어정자핵단백질을 얻을 수 있다.The secondary dehydration step, the step of obtaining wet powdered salmon sperm nuclear protein, and the step of drying under reduced pressure are preferably repeatedly performed, preferably 2 to 10 times, and 5 to 6 times. It is most preferable to carry out, through which the final salmon sperm nuclear protein in the form of a uniform powder can be obtained.
또한, 본 발명은In addition, the present invention
스텐레스 탱크에 농도 0.9 중량%인 식염수를 넣고, 온도를 40℃로 유지하는 단계; 상기 식염수에 냉동된 연어정자를 투입하고, 24시간 동안 해동시키는 단계; 해동된 연어정자를 1-5℃의 온도인 농도 2-4 중량%의 천일염수를 이용하여 1차 세척하는 단계; 및 1차 세척된 연어정자를 1-5℃의 온도의 정제수를 이용하여 2차 세척하는 단계;를 포함하는 해동 및 세척 단계;Adding saline solution having a concentration of 0.9% by weight to a stainless steel tank and maintaining the temperature at 40°C; Injecting frozen salmon sperm into the saline solution and thawing for 24 hours; First washing the thawed salmon sperm with 2-4% by weight natural salt water at a temperature of 1-5°C; and secondly washing the firstly washed salmon sperm with purified water at a temperature of 1-5° C.;
정제수 100 중량부 및 판크레아틴 15 중량부를 혼합하여 혼합액을 제조하는 단계; 상기 혼합액에 해동 및 세척된 연어정자를 투입하는 단계; 상기 혼합액을 50℃의 온도로 가열하고 60분 동안 효소반응을 수행하는 단계; 효소반응이 수행된 혼합액을 90℃의 온도로 가열하고 10분 동안 숙성하는 단계; 및 숙성된 혼합액에 가성소다를 투입하여 효소반응을 멈추는 단계;를 포함하는 효소 반응 단계;preparing a mixed solution by mixing 100 parts by weight of purified water and 15 parts by weight of pancreatin; Injecting thawed and washed salmon sperm into the mixture; heating the mixed solution to a temperature of 50° C. and performing an enzymatic reaction for 60 minutes; heating the mixture in which the enzyme reaction was performed to a temperature of 90° C. and aging for 10 minutes; Enzymatic reaction step comprising; and stopping the enzyme reaction by adding caustic soda to the aged mixture;
효소반응이 멈춘 혼합액에 구연산을 250 중량부 첨가하여 pH를 3.8-4로 조절하여 1차 멸균하는 단계; 및 1차 멸균된 혼합액을 82-83℃의 온도로 가열하고 60분 동안 교반하여 2차 멸균하는 단계;를 포함하는 멸균 단계;Primary sterilization by adding 250 parts by weight of citric acid to the mixture in which the enzyme reaction has stopped to adjust the pH to 3.8-4; and heating the primary sterilized mixed solution to a temperature of 82-83° C. and performing secondary sterilization by stirring for 60 minutes;
2차 멸균된 혼합액을 40℃의 온도로 냉각시키는 단계; 냉각된 혼합액에 농도 80 중량%이고 에탄올 및 헥산올을 4:1의 중량비로 혼합한 알코올 용액 800-1000 중량부를 첨가하는 단계; 및 필터프레스를 이용하여 여과시켜 젖은 분말 상태인 연어정자핵단백질을 얻는 단계;를 포함하는 여과 단계;cooling the secondary sterilized liquid mixture to a temperature of 40°C; Adding 800-1000 parts by weight of an alcohol solution obtained by mixing ethanol and hexanol in a weight ratio of 4:1 with a concentration of 80% by weight to the cooled mixture; and filtering using a filter press to obtain wet powdered salmon sperm nuclear protein;
젖은 분말 상태인 연어정자핵단백질에 농도 80 중량%의 알코올 용액 및 농도 50 중량%의 가성 소다를 3:2의 중량비율로 혼합한 중화용액을 가하여 중화하는 단계; 및 중화 후 1차 탈수하여 젖은 분말 상태인 연어정자핵단백질을 얻는 단계;를 포함하는 중화 단계;Neutralizing wet powdered salmon sperm nuclear protein by adding a neutralization solution in which an alcohol solution having a concentration of 80% by weight and caustic soda having a concentration of 50% by weight are mixed in a weight ratio of 3:2; and a step of first dehydration after neutralization to obtain wet powdered salmon sperm nuclear protein;
젖은 분말 상태인 연어정자핵단백질과 농도 92-93 중량%의 에탄올 용액을 혼합한 후, 75분에 걸쳐 2차 탈수하는 단계; 2차 탈수 후 원심분리기를 이용하여 젖은 분말 상태인 연어정자핵단백질을 얻는 단계; 및 젖은 분말 상태인 연어정자핵단백질을 진공건조기에 넣고 70-80℃의 온도에서 감압건조하는 단계;를 포함하고, 상기 2차 탈수하는 단계, 젖은 분말 상태인 연어정자핵단백질을 얻는 단계 및 감압건조하는 단계는 5-6회 반복하여 수행하는 것을 특징으로 하는 연어정자핵단백질 분말 수득 단계;를 포함하는 연어정자핵단백질 분말 제조 단계;After mixing wet powdered salmon sperm nuclear protein with an ethanol solution having a concentration of 92-93% by weight, secondary dehydration for 75 minutes; Obtaining wet powdered salmon sperm nuclear protein using a centrifugal separator after secondary dehydration; and putting the wet powdered salmon sperm nuclear protein in a vacuum dryer and drying under reduced pressure at a temperature of 70-80° C., wherein the secondary dehydration step, obtaining wet powder salmon sperm nuclear protein and reduced pressure Salmon sperm nuclear protein powder manufacturing step comprising: obtaining salmon sperm nuclear protein powder, characterized in that the drying step is repeated 5 to 6 times;
감잎, 율무, 대추, 생강, 감초 및 계피를 2:2:2:1:2:1의 중량비율로 혼합한 한방원료를 준비하고, 액체 분사가 가능한 분사각이 60°인 노즐을 2개씩 3열로 6개 포함하는 세척기를 사용하여 식초물을 분사하여 한방원료를 1차 세척하는 단계; 1차 세척된 한방원료를 전해수로 2차 세척하는 단계; 2차 세척된 한방원료를 43-47℃의 온도에서 건조하는 단계; 건조된 한방원료를 0.095-0.105 MPa의 압력 및 230-250℃의 온도에서 80-100분 동안 증숙하고, 55-65℃의 온도에서 220-260분 동안 건조시키는 과정을 3회 수행하는 단계; 증숙 및 건조된 한방원료를 분쇄하여 한방분말을 제조하는 단계; 및 상기 한방분말 100 중량부 및 물 100 중량부를 혼합하고 78-82℃의 온도로 가열하여 1-3시간 동안 열수추출하고 여과하는 단계;를 포함하는 한방여과액을 제조하는 단계;Prepare herbal raw materials by mixing persimmon leaves, adlay, jujube, ginger, licorice, and cinnamon in a weight ratio of 2:2:2:1:2:1, and use two nozzles each with a spray angle of 60° that can spray liquid. Using a washer containing 6 heats to spray vinegar water to first wash the oriental raw materials; Secondary washing of the firstly washed herbal raw material with electrolytic water; Drying the secondary washed herbal raw material at a temperature of 43-47 ° C; Steaming the dried herbal raw material at a pressure of 0.095-0.105 MPa and a temperature of 230-250 ° C. for 80-100 minutes, and drying at a temperature of 55-65 ° C. for 220-260 minutes 3 times; Preparing herbal powder by grinding the steamed and dried herbal raw materials; Preparing an herbal filtrate comprising a mixture of 100 parts by weight of the herbal powder and 100 parts by weight of water, heating at a temperature of 78-82° C., followed by hot water extraction for 1-3 hours and filtering;
오미자, 구기자 및 사과를 4:3:3의 중량비율로 혼합하여 과일원료를 준비하고, 상기 과일원료 100 중량부 및 물 100 중량부를 혼합하여 제1 혼합물을 제조하는 단계; 상기 제1 혼합물을 92-95℃의 온도로 가열하고, 증발하는 증기를 냉각시켜 얻은 증류액이 다시 제1 혼합물에 혼합되도록 하여 60-120분 동안 순환시키는 단계; 상기 순환이 완료된 제1 혼합물을 98-100℃의 온도로 가열하고, 60-120분 동안 증발하는 증기를 냉각시켜 1차 증류액을 얻는 단계; 상기 1차 증류액 100 중량부 및 상기 과일원료 100 중량부를 혼합하여 제2 혼합물을 제조하는 단계; 상기 제2 혼합물을 92-95℃의 온도로 가열하고, 증발하는 증기를 냉각시켜 얻은 증류액이 다시 제2 혼합물에 혼합되도록 하여 60-120분 동안 순환시키는 단계; 및 상기 순환이 완료된 제2 혼합물을 70-80℃의 온도로 가열하고, 150-210분 동안 증발하는 증기를 냉각시켜 2차 증류액을 얻는 단계;를 포함하는 과일증류액 제조 단계; 및Preparing a fruit raw material by mixing Schisandra chinensis, goji berry and apple in a weight ratio of 4: 3: 3, and preparing a first mixture by mixing 100 parts by weight of the fruit raw material and 100 parts by weight of water; Heating the first mixture to a temperature of 92-95° C. and allowing the distillate obtained by cooling the evaporating vapor to be mixed with the first mixture again and circulating for 60-120 minutes; obtaining a first distillate by heating the first mixture after completion of the circulation to a temperature of 98-100° C. and cooling the evaporating vapor for 60-120 minutes; preparing a second mixture by mixing 100 parts by weight of the primary distillate and 100 parts by weight of the fruit raw material; Heating the second mixture to a temperature of 92-95° C. and allowing the distillate obtained by cooling the evaporating vapor to be mixed with the second mixture again and circulating for 60-120 minutes; and heating the second mixture after the circulation is completed to a temperature of 70-80° C. and cooling the evaporating vapor for 150-210 minutes to obtain a secondary distillate; preparing a fruit distillate; and
상기 연어정자핵단백질 분말 48-52 중량부, 상기 한방여과액 28-32 중량부 및 상기 과일증류액 18-22 중량부를 혼합하는 단계;를 포함하는 음료 조성물의 제조방법을 제공한다.It provides a method for producing a beverage composition comprising the step of mixing 48-52 parts by weight of the salmon sperm nuclear protein powder, 28-32 parts by weight of the herbal filtrate, and 18-22 parts by weight of the fruit distillate.
이하, 본 발명에 따른 음료 조성물의 제조방법을 각 단계별로 상세히 설명한다.Hereinafter, the manufacturing method of the beverage composition according to the present invention will be described in detail for each step.
먼저, 본 발명에 따른 음료 조성물의 제조방법은 연어정자핵단백질 분말 제조 단계를 포함한다.First, the method for producing a beverage composition according to the present invention includes a step of preparing salmon sperm nuclear protein powder.
상기 연어정자핵단백질 분말 제조 단계는 전술한 연어정자핵단백질 분말의 제조방법과 동일하게 수행할 수 있다.The step of preparing salmon sperm nuclear protein powder may be performed in the same manner as the method for preparing salmon sperm nuclear protein powder described above.
다음으로, 본 발명에 따른 음료 조성물의 제조방법은 한방여과액 제조 단계를 포함한다. 상기 한방여과액 제조 단계는, 감잎, 율무, 대추, 생강, 감초 및 계피를 2:2:2:1:2:1의 중량비율로 혼합한 한방원료를 준비하고, 액체 분사가 가능한 분사각이 60°인 노즐을 2개씩 3열로 6개 포함하는 세척기를 사용하여 식초물을 분사하여 한방원료를 1차 세척하는 단계; 1차 세척된 한방원료를 전해수로 2차 세척하는 단계; 2차 세척된 한방원료를 43-47℃의 온도에서 건조하는 단계; 건조된 한방원료를 0.095-0.105 MPa의 압력 및 230-250℃의 온도에서 80-100분 동안 증숙하고, 55-65℃의 온도에서 220-260분 동안 건조시키는 과정을 3회 수행하는 단계; 증숙 및 건조된 한방원료를 분쇄하여 한방분말을 제조하는 단계; 및 상기 한방분말 100 중량부 및 물 100 중량부를 혼합하고 78-82℃의 온도로 가열하여 1-3시간 동안 열수추출하고 여과하는 단계;를 포함한다.Next, the manufacturing method of the beverage composition according to the present invention includes the step of preparing a herbal filtrate. In the preparation of the herbal filtrate, persimmon leaves, adlay, jujube, ginger, licorice and cinnamon are prepared in a weight ratio of 2: 2: 2: 1: 2: 1, and the spray angle capable of spraying the liquid is Using a washer containing six 60° nozzles in three rows of two, spraying vinegar water to first wash the herbal raw material; Secondary washing of the firstly washed herbal raw material with electrolytic water; Drying the secondary washed herbal raw material at a temperature of 43-47 ° C; Steaming the dried herbal raw material at a pressure of 0.095-0.105 MPa and a temperature of 230-250 ° C for 80-100 minutes, and drying at a temperature of 55-65 ° C for 220-260 minutes 3 times; Preparing herbal powder by grinding the steamed and dried herbal raw materials; And mixing 100 parts by weight of the herbal powder and 100 parts by weight of water, heating to a temperature of 78-82 ° C, extracting hot water for 1-3 hours, and filtering.
먼저, 감잎, 율무, 대추, 생강, 감초 및 계피를 2:2:2:1:2:1의 중량비율로 혼합한 한방원료를 준비하고, 액체 분사가 가능한 분사각이 60°인 노즐을 2개씩 3열로 6개 포함하는 세척기를 사용하여 식초물을 분사하여 한방원료를 1차 세척한다. 상기에서는 약초를 선별하고 세척한다. First, prepare oriental raw materials mixed with persimmon leaves, adlay, jujubes, ginger, licorice, and cinnamon in a weight ratio of 2:2:2:1:2:1, and use a nozzle with a spray angle of 60 ° capable of spraying liquid 2 Wash the herbal ingredients first by spraying vinegar water using a washing machine containing 6 washing machines in 3 rows. In the above, the herbs are selected and washed.
감잎에는 탄닌을 포함한 훼놀성 화합물이 다양하게 함유되어 있어 이들 성분이 여러 경로를 거쳐 생리적 작용을 하는 것으로 알려지고 있다. 감잎에 들어있는 플라보노이드(flavonoid)는 고혈압 원인 효소를 저해하거나 탄닌 성분중 갈라이트(gallate)가 혈압상승억제 효과가 있다고 알려져 있다. 특히, 비타민 C를 과량 포함하고 있어 이를 응용하고자 한다.Persimmon leaves contain a variety of phenolic compounds, including tannins, and it is known that these components act physiologically through various pathways. It is known that flavonoids contained in persimmon leaves inhibit enzymes that cause high blood pressure or gallate among tannins has an effect of suppressing blood pressure increase. In particular, since it contains an excessive amount of vitamin C, it is intended to be applied.
율무는 전통적으로 한방에서 청폐작용, 이비작용, 치습이수작용, 건위작용 등의 약리작용을 가져, 배농, 소종, 수종각기, 이뇨, 소염, 진통, 자양, 부종, 동통, 신경통, 거친 피부, 비만, 고혈압, 당뇨억제, 환자의 손상된 기 회복 등의 효능을 발휘하는 것으로 알려져 있다. 율무에 포함된 코익스노라이드(coixnolide)는 항암작용, 면역증강작용, 중추신경계 진정작용 및 항염증 작용이 있는 것으로 알려졌으며, 율무에 포함된 다른 성분인 피토스테놀유도체는 배란유발작용이 있으며, 또 다른 성분인 그루캔과 헤테로그루캐인 CA-1과 CA-2는 황보체 활성작용, 그루캔인 코익산 A, B 및 C는 혈압강하작용을 가지고 있는 것으로 알려져 있다. 또 율무종피에는 트립신 저해제인 단백질 분리작용이 있으며, 그외에도 항동맥경화작용, 알파-아밀라제 저해작용, 항산화작용, 항혈전작용 등이 있는 것으로 알려져 있다Adlay has traditionally had pharmacological actions in oriental medicine, such as clearing and lung action, ear and nose action, chin and ear water action, and gastric action. It is known to exert effects such as suppressing obesity, high blood pressure, and diabetes, and recovering the patient's damaged energy. Coixnolide contained in adlay is known to have anti-cancer, immune-enhancing, central nervous system sedative and anti-inflammatory actions, and phytosterol derivatives, which are other components contained in adlay, have an ovulation-inducing action. , Other ingredients, grucane and heterogrucane CA-1 and CA-2, are known to have glucan activity, and coic acid A, B, and C, which are grucans, have blood pressure lowering activities. In addition, barley radish seed skin has a trypsin inhibitor, protein separation action, and other than that, it is known to have anti-arteriosclerosis, alpha-amylase inhibitory, antioxidant, and antithrombotic actions.
대추는 조(棗) 또는 목밀(木蜜)이라고도 한다. 표면은 적갈색이며 타원형이고 길이는 1.5-2.5 ㎝에 달하며 빨갛게 익으면 단맛이 있다. 과실은 생식할 뿐 아니라 채취한 후 말려 건과(乾果)로서 과자·요리 및 약용으로 쓰인다. 대추는 생활속에서 가공하여 대추술, 대추차, 대추식초, 대추죽 등으로도 활용한다. 가공품으로서의 꿀대추는 중국·일본·유럽에서도 호평을 받고 있다. 한방에서는 이뇨·강장·완화제로 쓰인다.Jujube is also called joe (棗) or mokmil (木蜜). The surface is reddish brown, oval, 1.5-2.5 cm long, and sweet when ripe. Fruits are not only raw, but also dried after being collected and used as confectionery, cooking, and medicinal purposes. Jujube is processed in daily life and used as jujube wine, jujube tea, jujube vinegar, and jujube porridge. Honey jujube as a processed product is well received in China, Japan and Europe. In oriental medicine, it is used as a diuretic, tonic, and laxative.
생강은 한방에서는 뿌리줄기 말린 것을 약재로 쓰는데, 생강은 감기로 인한 오한, 발열, 두통, 구토, 해수, 가래를 치료하며 식중독으로 인한 복통설사, 복만에도 효과가 있어 끊는 물에 생강을 달여서 차로 마시기도 한다. 약리작용으로 위액분비촉진, 소화력 증진, 심장흥분 작용, 혈액순환촉진, 억균작용 등이 보고되었다. 한자어로는 강근(姜根), 모강(母薑), 백랄운(百辣蕓), 염량소자(炎凉小子), 인지초(因地草), 자강(子薑), 자강(紫薑), 건강(乾薑)이라고도 한다. 또한, 뿌리줄기는 말려 갈아서 빵·과자·카레·소스·피클 등에 향신료로 사용하기도 하고, 껍질을 벗기고 끊인 후 시럽에 넣어 절이기도 하며 생강차와 생강주 등을 만들기도 한다.Ginger is used as a medicine for dried rhizomes in oriental medicine. Ginger treats cold-induced chills, fever, headache, vomiting, seawater, and phlegm, and is also effective for stomach pain and diarrhea caused by food poisoning. also do As pharmacological action, it has been reported that it promotes secretion of gastric juice, enhances digestive power, stimulates the heart, promotes blood circulation, and inhibits bacteria. In Chinese characters, Ganggeun(姜根), Mogang(母薑), Baekralun(百辣蕓), Yeomyangsoja(炎凉小子), Injicho(因地草), Jagang(子薑), Jagang(紫薑), It is also called health. In addition, the rhizome is dried and ground and used as a spice for bread, cookies, curry, sauce, pickles, etc., peeled and cut, and then put in syrup to pickle and make ginger tea and ginger wine.
감초는 인체의 비위(脾胃)를 건강하게 할 뿐만 아니라 오장육부의 한열사기 (寒熱邪氣)를 치료하고 근골을 튼튼하게 할 뿐만 아니라 각종 종기와 부스럼등을 치료하고 온갖 약초의 독을 해독시키는 작용을 가지며 폐의 활동을 돕고 청열해독 (淸熱解毒)의 효과가 큰 약초이다. 또한, 각종 약품의 중독 및 식물의 중독을 해독할 뿐만 아니라, 특유의 향과 맛을 갖기 때문에 감초는 고래로 한방에서 없어서는 안될 기본적인 유용한 약제로 사용되어 오고 있다. 감초의 주요 성분으로는 감미질인 글리시리진, 플라보노이드의 일종인 리키리틴, 서당, 포도당, 만니톨, 아스파라긴 등을 들 수 있다. 특히 글리시리진은 감초에 독특한 단맛을 부여하는 성분이다. 이와 같은 감초를 적용하여 헛개나무 열매 추출액의 단맛을 끌어 올린다.Licorice not only makes the spleen and stomach of the human body healthy, but also treats the heat of the five organs, strengthens the muscles and bones, treats various boils and boils, and detoxifies the poison of all kinds of herbs. It is a herb that has a great effect of helping the lungs and clearing heat and detoxifying. In addition, because it not only detoxifies the poisoning of various drugs and poisoning of plants, but also has a unique aroma and taste, licorice has been used as an indispensable basic useful medicine in oriental medicine since ancient times. The main components of licorice include glycyrrhizin, which is a sweetener, and lichiritin, which is a kind of flavonoid, sugar, glucose, mannitol, and asparagine. In particular, glycyrrhizin is a component that gives licorice its unique sweet taste. Applying such licorice enhances the sweetness of barnacle tree fruit extract.
계피는 녹나무과에 속하는 상록교목인 생달나무(天竹桂, Cinnamomum japonicum SIEB.)의 나무껍질로 만든 약재로, 약의 맛은 맵고 단맛이 나며 약성은 열성이다. 계피는 비위장의 기능을 활성화시키므로 소화기가 차서 소화장애가 있거나 복부가 차서 일어나는 복통 설사 등에 널리 이용된다. 뿐만 아니라 배가 차서 일어나는 구토에도 신속한 반응을 일으킨다. 그리고 풍습성(風濕性)으로 인한 사지마비와 동통을 그치게 하고, 허리나 무릎이 차고 시리면서 아픈 신경통과 관절 질환에도 널리 응용된다. 또한, 산후에 출혈이 계속되거나 오래된 이질과 대변시에 출혈되는 증상을 개선시키기도 한다. 이외에도 콩팥기능 감퇴증상에도 효력이 높고 하복부가 차면서 방광염이 자주 발생하는 질환에도 활용되고 있다.Cinnamon is a medicinal material made from the bark of the evergreen tree (Cinnamomum japonicum SIEB.), an evergreen tree belonging to the Lauraceae family. Cinnamon activates the function of the non-gastrointestinal tract, so it is widely used for digestive disorders due to a cold digestive tract or abdominal pain and diarrhea caused by a full stomach. In addition, it causes a rapid response to vomiting caused by a full stomach. In addition, it stops quadriplegia and pain caused by customs, and is widely applied to painful neuralgia and joint diseases as the waist or knee is cold and cold. In addition, bleeding continues after childbirth or improves symptoms of old dysentery and bleeding during stool. In addition, it is highly effective for symptoms of decreased kidney function and is also used for diseases in which cystitis often occurs due to a cold lower abdomen.
상기 감잎, 율무, 대추, 생강, 감초 및 계피를 2:2:2:1:2:1의 중량비율로 혼합한 원료를 세척, 증숙 및 건조를 수행하여 떫은 맛, 쓴맛 등의 불필요한 맛은 제거하고 단맛, 감칠맛은 끌어올리며, 동시에 원료들의 건강기능적인 부분을 부여할 수 있다.The raw materials mixed with persimmon leaves, adlay, jujube, ginger, licorice and cinnamon in a weight ratio of 2: 2: 2: 1: 2: 1 are washed, steamed and dried to remove unnecessary tastes such as astringency and bitterness It can enhance sweetness and savory taste, and at the same time, it can give health functional parts of raw materials.
상기 세척은 노즐 물 분사 세척법을 이용하여 수행되는 것이 바람직하고, 액체 분사가 가능한 분사각이 60°인 노즐을 2개씩 3열로 6개 포함하는 세척기를 사용하여 식초물을 분사하여 이루어진다. 상기 노즐 물 분사 세척법이란, 효과적인 세척을 DLN하여 고른 물 분사가 가능한 노즐을 적용하여 분무 또는 분사하는 것으로 약초에 포함된 잔여물을 확실하게 제거할 수 있다. 또한, 상기 식초물을 사용하여 살균작용을 수행한다. 동시에, 분사를 통해 한방원료 일부가 분쇄될 수 있고, 이러한 자연스러운 분쇄작업을 통해 증숙 및 건조하는 공정에서 더욱 효과적으로 영양이 날아가지 않고 숙성을 더해 더욱 깊은 맛을 끌어낼 뿐만 아니라, 최종 분쇄하는 단계에서 더욱 고르게 분쇄되어 음료 조성물 적용에 용이하다.The cleaning is preferably performed using a nozzle water spray cleaning method, and is performed by spraying vinegar water using a washer including 6 nozzles having a spray angle of 60 ° capable of spraying liquid, 2 in 3 rows. The nozzle water spray cleaning method is spraying or spraying by applying a nozzle capable of evenly spraying water by effective washing by DLN, and it is possible to reliably remove residues contained in herbs. In addition, sterilization is performed using the vinegar water. At the same time, some of the oriental raw materials can be pulverized through spraying, and through this natural pulverization, nutrients are not lost more effectively in the steaming and drying process, and a deeper taste is not only brought out by adding aging, but also more It is evenly ground and is easy to apply to a beverage composition.
다음, 1차 세척된 한방원료를 전해수로 2차 세척한다. 상기에서는 1차 세척된 한방원료를 전해수를 이용하여 2차 세척한다. 전해수는 수돗물에 일정량의 염화나트륨(NaCl)을 첨가한 후 전기분해하여 얻어지는 것으로, 바람직하게는 수돗물에 25%의 NaCl을 첨가하여 전해수 제조시스템 장치를 이용하여 제조된 것을 사용할 수 있다. 상기 전해수를 사용하여 2차 세척함으로써 한방원료의 유통기한을 더욱 늘릴 수 있다.Next, the firstly washed herbal raw materials are secondarily washed with electrolyzed water. In the above, the firstly washed herbal raw material is secondarily washed using electrolytic water. Electrolyzed water is obtained by adding a certain amount of sodium chloride (NaCl) to tap water and then electrolyzing it. The shelf life of herbal raw materials can be further extended by secondary washing using the electrolyzed water.
다음, 2차 세척된 한방원료를 43-47℃의 온도에서 건조한다. 상기 건조는 44-46℃의 온도에서 수행되는 것이 더욱 바람직하다. 일정한 중온 범위에서 건조를 수행하여 한방원료의 영양 성분을 유지시킬 수 있다.Next, the secondly washed herbal raw material is dried at a temperature of 43-47 ° C. The drying is more preferably carried out at a temperature of 44-46 °C. It is possible to maintain nutritional components of herbal raw materials by performing drying at a constant medium temperature range.
다음, 건조된 한방원료를 0.095-0.105 MPa의 압력 및 230-250℃의 온도에서 80-100분 동안 증숙하고, 55-65℃의 온도에서 220-260분 동안 건조시키는 과정을 3회 수행한다. 상기에서는 한방원료를 일정 압력 및 일정 온도 범위에서 증숙하고, 일정 온도에서 건조시키는 과정을 3회 수행한다.Next, the dried herbal raw material is steamed at a pressure of 0.095-0.105 MPa and a temperature of 230-250 ° C for 80-100 minutes, and dried at a temperature of 55-65 ° C for 220-260 minutes 3 times. In the above, the process of steaming the oriental raw material at a certain pressure and a certain temperature range and drying at a certain temperature is performed three times.
상기 한방원료를 0.098-0.102 MPa의 압력 및 235-245℃의 온도에서 85-95분 동안 증숙하고, 58-62℃의 온도에서 230-250분 동안 건조시키는 과정을 3회 수행하는 것이 더욱 바람직하다. 상기 압력 및 온도에서 상기 시간 동안 증숙 및 건조를 수행하되 이를 3회 수행함으로써 한방원료의 떫은맛, 쓴맛은 제거하고 영양 성분을 더욱 높일 수 있다.It is more preferable to perform the process of steaming the herbal raw material at a pressure of 0.098-0.102 MPa and a temperature of 235-245 ° C. for 85-95 minutes and drying at a temperature of 58-62 ° C. for 230-250 minutes three times. . Steaming and drying are performed at the pressure and temperature for the above time, but by performing this three times, the astringent taste and bitter taste of the herbal raw material can be removed and the nutritional content can be further increased.
다음, 증숙 및 건조된 한방원료를 분쇄하여 한방분말을 제조한다.Next, the steamed and dried herbal raw materials are pulverized to prepare herbal powder.
다음, 상기 한방분말 100 중량부 및 물 100 중량부를 혼합하고 78-82℃의 온도로 가열하여 1-3시간 동안 열수추출하고 여과하여 여과액을 제조한다. 바람직하게는 79-81℃의 온도로 가열하여 1.5-2.5시간 동안 열수추출한다.Next, 100 parts by weight of the herbal powder and 100 parts by weight of water are mixed, heated to a temperature of 78-82 ° C, hot water extracted for 1-3 hours, and filtered to prepare a filtrate. Preferably, hot water extraction is performed by heating to a temperature of 79-81° C. for 1.5-2.5 hours.
다음으로, 본 발명에 따른 음료 조성물의 제조방법은 과일증류액 제조 단계를 포함한다. 상기 과일증류액 제조 단계는, 오미자, 구기자 및 사과를 4:3:3의 중량비율로 혼합하여 과일원료를 준비하고, 상기 과일원료 100 중량부 및 물 100 중량부를 혼합하여 제1 혼합물을 제조하는 단계; 상기 제1 혼합물을 92-95℃의 온도로 가열하고, 증발하는 증기를 냉각시켜 얻은 증류액이 다시 제1 혼합물에 혼합되도록 하여 60-120분 동안 순환시키는 단계; 상기 순환이 완료된 제1 혼합물을 98-100℃의 온도로 가열하고, 60-120분 동안 증발하는 증기를 냉각시켜 1차 증류액을 얻는 단계; 상기 1차 증류액 100 중량부 및 상기 과일원료 100 중량부를 혼합하여 제2 혼합물을 제조하는 단계; 상기 제2 혼합물을 92-95℃의 온도로 가열하고, 증발하는 증기를 냉각시켜 얻은 증류액이 다시 제2 혼합물에 혼합되도록 하여 60-120분 동안 순환시키는 단계; 및 상기 순환이 완료된 제2 혼합물을 70-80℃의 온도로 가열하고, 150-210분 동안 증발하는 증기를 냉각시켜 2차 증류액을 얻는 단계;를 포함한다.Next, the manufacturing method of the beverage composition according to the present invention includes a fruit distillate manufacturing step. The fruit distillate preparation step is to prepare a fruit raw material by mixing Schisandra chinensis, goji berry and apple in a weight ratio of 4: 3: 3, and mixing 100 parts by weight of the fruit raw material and 100 parts by weight of water to prepare a first mixture step; Heating the first mixture to a temperature of 92-95° C. and allowing the distillate obtained by cooling the evaporating vapor to be mixed with the first mixture again and circulating for 60-120 minutes; obtaining a first distillate by heating the first mixture after completion of the circulation to a temperature of 98-100° C. and cooling the evaporating vapor for 60-120 minutes; preparing a second mixture by mixing 100 parts by weight of the primary distillate and 100 parts by weight of the fruit raw material; Heating the second mixture to a temperature of 92-95° C. and allowing the distillate obtained by cooling the evaporating vapor to be mixed with the second mixture again and circulating for 60-120 minutes; and heating the second mixture after completion of the circulation to a temperature of 70-80° C. and cooling the evaporating vapor for 150-210 minutes to obtain a secondary distillate.
먼저, 오미자, 구기자 및 사과를 4:3:3의 중량비율로 혼합하여 과일원료를 준비하고, 상기 과일원료 100 중량부 및 물 100 중량부를 혼합하여 제1 혼합물을 제조한다.First, a fruit raw material is prepared by mixing Schisandra chinensis, goji berry, and apple in a weight ratio of 4:3:3, and a first mixture is prepared by mixing 100 parts by weight of the fruit raw material and 100 parts by weight of water.
오미자는 각피로 둘러싸인 과육내에 견고한 종자가 들어있는 과실로서 과육에는 리그난류의 일군인 고미신계 물질(고미신 A-Q), 모노테르펜류, 시트랄, 사과산, 주석산, 단당류, 레신류등과 정유성분인 β2-비사볼렌, 세스키칼렌, α-이란겐등이 함유되어 있으며, 종자에는 쉬산드린, 디옥시쉬산드린, α-쉬산드린 및 고미질 물질등이 함유되어 있다. 오미자를 약용 또는 건강 식품용으로 이용할때는 통상적인 한약재와 같이 오미자 과실을 물 또는 알콜같은 용매에 침지하여 오미자에 함유된 약효성분 및 향미성분을 추출하고 이를 건강식품용 다류나 주정음료에 사용하여 왔다.Schisandra chinensis is a fruit with hard seeds in the flesh surrounded by a cuticle. It contains β2-bisabolene, sesquicalene, α-irangen, etc., and seeds contain schisandrin, deoxyssandrin, α-schisandrin and bitter substances. When Schizandra chinensis is used for medicinal or health food purposes, the fruit of Schisandra chinensis is immersed in a solvent such as water or alcohol, as in conventional herbal medicine, to extract medicinal and flavor components contained in Schisandra chinensis, and it has been used in teas for health food or alcoholic beverages. .
구기자(拘杞子)(Lycii fructus)는 국내에서 주로 사용되는 구기자는 구기자나무(Lycium chinenes Miller) 또는 기타 동속식물의 열매를 사용한다. 중국은 영하구기자(Lycium barbarum L.:寧夏拘杞子)를 사용하고 일본은 구기자나무(Lycium chinenes Miller) 또는 영하구기자(Lycium barbarum L.:寧夏拘杞子)를 사용한다.Gojija (拘杞子) (Lycii fructus), which is mainly used in Korea, uses the fruit of the Goji tree (Lycium chinenes Miller) or other plants of the same genus. China uses Lycium barbarum L.:寧夏拘杞子, and Japan uses Lycium chinenes Miller or Lycium barbarum L.:寧夏拘杞子.
상기 오미자, 구기자 및 사과를 포함하는 과일증류액을 이용하여 음료 조성물을 제조함으로써 우수한 풍미와 맛을 첨가하여 기호성을 높일 수 있다.By preparing a beverage composition using the fruit distillate containing the Schisandra chinensis, goji berry and apple, it is possible to enhance palatability by adding excellent flavor and taste.
다음, 상기 제1 혼합물을 92-95℃의 온도로 가열하고, 증발하는 증기를 냉각시켜 얻은 증류액이 다시 제1 혼합물에 혼합되도록 하여 60-120분 동안 순환시킨다. 더욱 바람직하게는 상기 제1 혼합물을 93-94℃의 온도로 가열하고, 증발하는 증기를 냉각시켜 얻은 증류액이 다시 제1 혼합물에 혼합되도록 하여 80-100분 동안 순환시키고, 가장 바람직하게는, 상기 제1 혼합물을 93℃의 온도로 가열하고, 증발하는 증기를 냉각시켜 얻은 증류액이 다시 제1 혼합물에 혼합되도록 하여 90분 동안 순환시킨다.Next, the first mixture is heated to a temperature of 92-95° C., and the distillate obtained by cooling the evaporating vapor is mixed with the first mixture again and circulated for 60-120 minutes. More preferably, the first mixture is heated to a temperature of 93-94 ° C, and the distillate obtained by cooling the evaporating vapor is mixed with the first mixture again and circulated for 80-100 minutes, most preferably, The first mixture is heated to a temperature of 93° C., and the distillate obtained by cooling the evaporating vapor is mixed with the first mixture again and circulated for 90 minutes.
다음, 상기 순환이 완료된 제1 혼합물을 98-100℃의 온도로 가열하고, 60-120분 동안 증발하는 증기를 냉각시켜 1차 증류액을 얻는다. 더욱 바람직하게는, 상기 순환이 완료된 제1 혼합물을 98-100℃의 온도로 가열하고, 80-100분 동안 증발하는 증기를 냉각시켜 1차 증류액을 얻고, 가장 바람직하게는, 상기 순환이 완료된 제1 혼합물을 98-100℃의 온도로 가열하고, 90분 동안 증발하는 증기를 냉각시켜 1차 증류액을 얻는다.Next, the first mixture after completion of the circulation is heated to a temperature of 98-100° C., and the evaporated vapor is cooled for 60-120 minutes to obtain a first distillate. More preferably, the first mixture at which the circulation is completed is heated to a temperature of 98-100 ° C, and the evaporating vapor is cooled for 80-100 minutes to obtain a first distillate, and most preferably, the circulation is completed. The first mixture is heated to a temperature of 98-100° C., and the evaporating vapor is cooled for 90 minutes to obtain a first distillate.
다음, 상기 1차 증류액 100 중량부 및 상기 과일원료 열매 100 중량부를 혼합하여 제2 혼합물을 제조한다.Next, a second mixture is prepared by mixing 100 parts by weight of the primary distillate and 100 parts by weight of the fruit raw material.
다음, 상기 제2 혼합물을 92-95℃의 온도로 가열하고, 증발하는 증기를 냉각시켜 얻은 증류액이 다시 제2 혼합물에 혼합되도록 하여 60-120분 동안 순환시킨다. 더욱 바람직하게는 상기 제2 혼합물을 93-94℃의 온도로 가열하고, 증발하는 증기를 냉각시켜 얻은 증류액이 다시 제2 혼합물에 혼합되도록 하여 80-100분 동안 순환시키고, 가장 바람직하게는, 상기 제2 혼합물을 93℃의 온도로 가열하고, 증발하는 증기를 냉각시켜 얻은 증류액이 다시 제2 혼합물에 혼합되도록 하여 90분 동안 순환시킨다.Next, the second mixture is heated to a temperature of 92-95 ° C, and the distillate obtained by cooling the evaporating vapor is mixed with the second mixture again and circulated for 60-120 minutes. More preferably, the second mixture is heated to a temperature of 93-94 ° C, and the distillate obtained by cooling the evaporating vapor is mixed with the second mixture again and circulated for 80-100 minutes, most preferably, The second mixture is heated to a temperature of 93° C., and the distillate obtained by cooling the evaporating vapor is mixed with the second mixture again and circulated for 90 minutes.
다음, 상기 순환이 완료된 제2 혼합물을 70-80℃의 온도로 가열하고, 150-210분 동안 증발하는 증기를 냉각시켜 2차 증류액을 얻는다. 더욱 바람직하게는, 상기 순환이 완료된 제2 혼합물을 74-76℃의 온도로 가열하고, 170-190분 동안 증발하는 증기를 냉각시켜 2차 증류액을 얻고, 가장 바람직하게는, 상기 순환이 완료된 제2 혼합물을 75℃의 온도로 가열하고, 180분 동안 증발하는 증기를 냉각시켜 2차 증류액을 얻는다.Next, the second mixture after completion of the circulation is heated to a temperature of 70-80° C., and the evaporated vapor is cooled for 150-210 minutes to obtain a second distillate. More preferably, the second mixture at which the circulation is completed is heated to a temperature of 74-76° C., and the evaporating vapor is cooled for 170-190 minutes to obtain a second distillate, and most preferably, the circulation is completed. The second mixture is heated to a temperature of 75° C., and the evaporating vapor is cooled for 180 minutes to obtain a second distillate.
다음으로, 본 발명에 따른 음료 조성물의 제조방법은 상기 연어정자핵단백질 분말 48-52 중량부, 상기 한방여과액 28-32 중량부 및 상기 과일증류액 18-22 중량부를 혼합하는 단계를 포함한다.Next, the method for producing a beverage composition according to the present invention includes mixing 48-52 parts by weight of the salmon sperm nuclear protein powder, 28-32 parts by weight of the herbal filtrate, and 18-22 parts by weight of the fruit distillate. .
더욱 바람직하게는, 상기 연어정자핵단백질 분말 49-51 중량부, 상기 한방여과액 29-31 중량부 및 상기 과일증류액 19-21 중량부를 혼합한다.More preferably, 49-51 parts by weight of the salmon sperm nuclear protein powder, 29-31 parts by weight of the herbal filtrate, and 19-21 parts by weight of the fruit distillate are mixed.
이하, 본 발명을 하기의 실시예에 의해 보다 상세하게 설명한다.Hereinafter, the present invention will be described in more detail by the following examples.
단, 하기 실시예는 본 발명의 내용을 예시하는 것일 뿐 발명의 범위가 실시예 및 실험예에 의해 한정되는 것은 아니다.However, the following examples are merely illustrative of the content of the present invention, but the scope of the invention is not limited by the examples and experimental examples.
<실시예 1> 연어정자핵단백질 분말의 제조<Example 1> Preparation of Salmon Sperm Nuclear Protein Powder
스텐레스 탱크에 농도 0.9 중량%인 식염수를 넣고, 온도를 40℃로 유지시킨 후, 상기 식염수에 냉동된 연어정자를 투입하고, 24시간 동안 해동시켰다. 해동된 연어정자를 1-5℃의 온도인 농도 3 중량%의 천일염수를 이용하여 1차 세척하고, 1차 세척된 연어정자를 1-5℃의 온도의 정제수를 이용하여 2차 세척하였다.Saline solution having a concentration of 0.9% by weight was put into a stainless steel tank, and the temperature was maintained at 40° C., and then frozen salmon sperm was added to the saline solution and thawed for 24 hours. The thawed salmon sperm was firstly washed with 3% by weight sun-dried salt at a temperature of 1-5°C, and the firstly washed salmon sperm was washed secondarily with purified water at a temperature of 1-5°C.
정제수 100 중량부 및 판크레아틴 15 중량부를 혼합하여 혼합액을 제조하고, 상기 혼합액에 해동 및 세척된 연어정자를 투입한 후, 상기 혼합액을 50℃의 온도로 가열하고 60분 동안 효소반응을 수행하였다. 효소반응이 수행된 혼합액을 90℃의 온도로 가열하고 10분 동안 숙성하였다. 숙성된 혼합액에 가성소다를 투입하여 효소반응을 멈추었다.A mixed solution was prepared by mixing 100 parts by weight of purified water and 15 parts by weight of pancreatin, thawed and washed salmon sperm were added to the mixed solution, and then the mixed solution was heated to a temperature of 50° C. and enzymatic reaction was performed for 60 minutes. The mixed solution in which the enzyme reaction was performed was heated to a temperature of 90° C. and aged for 10 minutes. Caustic soda was added to the aged mixture to stop the enzyme reaction.
효소반응이 멈춘 혼합액에 구연산을 250 중량부 첨가하여 pH를 3.8로 조절하여 1차 멸균하였다. 1차 멸균된 혼합액을 83℃의 온도로 가열하고 60분 동안 교반하여 2차 멸균하였다.250 parts by weight of citric acid was added to the mixed solution in which the enzyme reaction stopped to adjust the pH to 3.8, followed by primary sterilization. The primary sterilized mixed solution was heated to a temperature of 83° C. and stirred for 60 minutes to perform secondary sterilization.
2차 멸균된 혼합액을 40℃의 온도로 냉각시키고, 여기에 농도 80 중량%이고 에탄올 및 헥산올을 4:1의 중량비로 혼합한 알코올 용액 900 중량부를 첨가하였다. 이후, 필터프레스를 이용하여 여과시켜 젖은 분말 상태인 연어정자핵단백질을 얻었다.The secondary sterilized mixed solution was cooled to a temperature of 40° C., and 900 parts by weight of an alcohol solution having a concentration of 80% by weight and ethanol and hexanol mixed at a weight ratio of 4:1 was added thereto. Thereafter, it was filtered using a filter press to obtain salmon sperm nuclear protein in a wet powdery state.
젖은 분말 상태인 연어정자핵단백질에 농도 80 중량%의 알코올 용액 및 농도 50 중량%의 가성 소다를 3:2의 중량비율로 혼합한 중화용액을 가하여 중화하였다. 이후, 1차 탈수하여 젖은 분말 상태인 연어정자핵단백질을 얻었다.The wet powdered salmon sperm nuclear protein was neutralized by adding a neutralization solution in which an alcohol solution having a concentration of 80% by weight and caustic soda having a concentration of 50% by weight were mixed in a weight ratio of 3:2. Thereafter, the first dehydration was performed to obtain salmon sperm nuclear protein in a wet powder state.
젖은 분말 상태인 연어정자핵단백질과 농도 92-93 중량%의 에탄올 용액을 혼합한 후, 75분에 걸쳐 2차 탈수하고, 2차 탈수 후 원심분리기를 이용하여 젖은 분말 상태인 연어정자핵단백질을 얻은 후, 젖은 분말 상태인 연어정자핵단백질을 진공건조기에 넣고 75℃의 온도에서 감압건조하여 분말을 얻고, 이를 다시 농도 92-93 중량%의 에탄올 용액을 혼합한 후, 75분에 걸쳐 2차 탈수하고, 2차 탈수 후 원심분리기를 이용하여 젖은 분말 상태인 연어정자핵단백질을 얻은 후, 젖은 분말 상태인 연어정자핵단백질을 진공건조기에 넣고 75℃의 온도에서 감압건조하는 것을 5회 반복수행하여 연어정자핵단백질 분말을 제조하였다.After mixing wet powdered salmon sperm nuclear protein and 92-93% by weight ethanol solution, secondary dehydration over 75 minutes, and after secondary dehydration, use a centrifuge to obtain wet powder salmon sperm nuclear protein After obtaining, the wet powdered salmon sperm nuclear protein was placed in a vacuum dryer and dried under reduced pressure at a temperature of 75 ° C to obtain a powder, which was mixed with an ethanol solution having a concentration of 92-93% by weight again, followed by a second process over 75 minutes. After dehydration, and after secondary dehydration, a centrifugal separator is used to obtain salmon sperm nuclear protein in a wet powder state, and then putting the wet powder salmon sperm nuclear protein in a vacuum dryer and drying under reduced pressure at a temperature of 75 ° C. Repeated 5 times Thus, salmon sperm nuclear protein powder was prepared.
<실시예 2> 음료 조성물의 제조<Example 2> Preparation of beverage composition
감잎, 율무, 대추, 생강, 감초 및 계피를 2:2:2:1:2:1의 중량비율로 혼합한 한방원료를 준비하고, 액체 분사가 가능한 분사각이 60°인 노즐을 2개씩 3열로 6개 포함하는 세척기를 사용하여 식초물을 분사하여 한방원료를 1차 세척하였다. 1차 세척된 한방원료를 전해수로 2차 세척하였다. 2차 세척된 한방원료를 45℃의 온도에서 건조한 후, 건조된 한방원료를 0.1 MPa의 압력 및 240℃의 온도에서 90분 동안 증숙하고, 60℃의 온도에서 240분 동안 건조시키는 과정을 3회 수행하였다. 증숙 및 건조된 한방원료를 분쇄하여 한방분말을 제조하고, 상기 한방분말 100 중량부 및 물 100 중량부를 혼합하고 80℃의 온도로 가열하여 2시간 동안 열수추출하고 여과하여 잔여물은 버림으로써 한방여과액을 제조하였다.Prepare herbal raw materials by mixing persimmon leaves, adlay, jujube, ginger, licorice, and cinnamon in a weight ratio of 2:2:2:1:2:1, and use two nozzles each with a spray angle of 60° that can spray liquid. Herbal raw materials were first washed by spraying vinegar water using a washer containing 6 heats. The firstly washed herbal raw materials were secondly washed with electrolyzed water. After drying the secondary washed herbal raw materials at a temperature of 45 ° C, the dried herbal raw materials were steamed at a pressure of 0.1 MPa and a temperature of 240 ° C for 90 minutes, and dried at a temperature of 60 ° C for 240 minutes 3 times. performed. The steamed and dried herbal raw materials are pulverized to prepare herbal powder, 100 parts by weight of the herbal powder and 100 parts by weight of water are mixed, heated to a temperature of 80 ° C. liquid was prepared.
오미자, 구기자 및 사과를 4:3:3의 중량비율로 혼합하여 과일원료를 준비하고, 상기 과일원료 100 중량부 및 물 100 중량부를 혼합하여 제1 혼합물을 제조하였다. 상기 제1 혼합물을 93℃의 온도로 가열하고, 증발하는 증기를 냉각시켜 얻은 증류액이 다시 제1 혼합물에 혼합되도록 하여 90분 동안 순환시켰다. 상기 순환이 완료된 제1 혼합물을 100℃의 온도로 가열하고, 90분 동안 증발하는 증기를 냉각시켜 1차 증류액을 얻었다. 상기 1차 증류액 100 중량부 및 상기 과일원료 100 중량부를 혼합하여 제2 혼합물을 제조하였다. 상기 제2 혼합물을 93℃의 온도로 가열하고, 증발하는 증기를 냉각시켜 얻은 증류액이 다시 제2 혼합물에 혼합되도록 하여 90분 동안 순환시키고, 상기 순환이 완료된 제2 혼합물을 75℃의 온도로 가열하고, 180분 동안 증발하는 증기를 냉각시켜 2차 증류액을 얻어 과일증류액 제조하였다.Fruit raw materials were prepared by mixing Schisandra chinensis, goji berry, and apples in a weight ratio of 4:3:3, and a first mixture was prepared by mixing 100 parts by weight of the fruit raw materials and 100 parts by weight of water. The first mixture was heated to a temperature of 93° C., and the distillate obtained by cooling the evaporating vapor was mixed with the first mixture again and circulated for 90 minutes. The first mixture after completion of the circulation was heated to a temperature of 100° C., and the evaporating vapor was cooled for 90 minutes to obtain a first distillate. A second mixture was prepared by mixing 100 parts by weight of the primary distillate and 100 parts by weight of the fruit raw material. The second mixture is heated to a temperature of 93 ° C., and the distillate obtained by cooling the evaporating vapor is mixed with the second mixture again and circulated for 90 minutes, and the second mixture after the circulation is completed is heated to a temperature of 75 ° C. After heating and cooling the evaporating vapor for 180 minutes, a second distillate was obtained and a fruit distillate was prepared.
상기 실시예 1에서 제조된 연어정자핵단백질 분말 50 중량부, 상기 한방여과액 30 중량부 및 상기 과일증류액 20 중량부를 혼합하여 음료 조성물을 제조하였다.A beverage composition was prepared by mixing 50 parts by weight of the salmon sperm nuclear protein powder prepared in Example 1, 30 parts by weight of the herbal filtrate, and 20 parts by weight of the fruit distillate.
<비교예 1> <Comparative Example 1>
스텐레스 탱크에 증류수를 넣고 냉동된 연어정자를 투입하고, 24시간 동안 해동시켰다. 해동된 연어정자를 정제수를 이용하여 세척하였다.Distilled water was put into a stainless steel tank, and frozen salmon sperm was added and thawed for 24 hours. The thawed salmon sperm was washed with purified water.
정제수 100 중량부 및 프로테아제 15 중량부를 혼합하여 혼합액을 제조하고, 상기 혼합액에 해동 및 세척된 연어정자를 투입한 후, 상기 혼합액을 50℃의 온도로 가열하고 60분 동안 효소반응을 수행하였다. 효소반응이 수행된 혼합액을 70℃의 온도로 가열하고 10분 동안 숙성하였다. 숙성된 혼합액에 가성소다를 투입하여 효소반응을 멈추었다.A mixed solution was prepared by mixing 100 parts by weight of purified water and 15 parts by weight of protease, and thawed and washed salmon sperm were added to the mixed solution, and then the mixture was heated to a temperature of 50° C. and enzymatic reaction was performed for 60 minutes. The mixed solution in which the enzyme reaction was performed was heated to a temperature of 70° C. and aged for 10 minutes. Caustic soda was added to the aged mixture to stop the enzyme reaction.
효소반응이 멈춘 혼합액에 구연산을 250 중량부 첨가하여 pH를 3.8로 조절하여 1차 멸균하였다. 1차 멸균된 혼합액을 83℃의 온도로 가열하고 60분 동안 교반하여 2차 멸균하였다.250 parts by weight of citric acid was added to the mixed solution in which the enzyme reaction stopped to adjust the pH to 3.8, followed by primary sterilization. The primary sterilized mixed solution was heated to a temperature of 83° C. and stirred for 60 minutes to perform secondary sterilization.
2차 멸균된 혼합액을 40℃의 온도로 냉각시키고, 여기에 농도 80 중량%이고 에탄올 및 헥산올을 4:1의 중량비로 혼합한 알코올 용액 900 중량부를 첨가하였다. 이후, 필터프레스를 이용하여 여과시켜 젖은 분말 상태인 연어정자핵단백질을 얻었다.The secondary sterilized mixed solution was cooled to a temperature of 40° C., and 900 parts by weight of an alcohol solution having a concentration of 80% by weight and ethanol and hexanol mixed at a weight ratio of 4:1 was added thereto. Thereafter, it was filtered using a filter press to obtain salmon sperm nuclear protein in a wet powdery state.
젖은 분말 상태인 연어정자핵단백질에 농도 80 중량%의 알코올 용액 및 농도 50 중량%의 가성 소다를 3:2의 중량비율로 혼합한 중화용액을 가하여 중화하였다. 이후, 1차 탈수하여 젖은 분말 상태인 연어정자핵단백질을 얻었다.The wet powdered salmon sperm nuclear protein was neutralized by adding a neutralization solution in which an alcohol solution having a concentration of 80% by weight and caustic soda having a concentration of 50% by weight were mixed in a weight ratio of 3:2. Thereafter, the first dehydration was performed to obtain salmon sperm nuclear protein in a wet powder state.
젖은 분말 상태인 연어정자핵단백질과 농도 92-93 중량%의 에탄올 용액을 혼합한 후, 75분에 걸쳐 2차 탈수하고, 2차 탈수 후 원심분리기를 이용하여 젖은 분말 상태인 연어정자핵단백질을 얻은 후, 젖은 분말 상태인 연어정자핵단백질을 진공건조기에 넣고 75℃의 온도에서 감압건조하여 분말을 얻고, 이를 다시 농도 92-93 중량%의 에탄올 용액을 혼합한 후, 75분에 걸쳐 2차 탈수하고, 2차 탈수 후 원심분리기를 이용하여 젖은 분말 상태인 연어정자핵단백질을 얻은 후, 젖은 분말 상태인 연어정자핵단백질을 진공건조기에 넣고 75℃의 온도에서 감압건조하는 것을 5회 반복수행하여 연어정자핵단백질 분말을 제조하였다.After mixing wet powdered salmon sperm nuclear protein and 92-93% by weight ethanol solution, secondary dehydration over 75 minutes, and after secondary dehydration, use a centrifuge to obtain wet powder salmon sperm nuclear protein After obtaining, the wet powdered salmon sperm nuclear protein was placed in a vacuum dryer and dried under reduced pressure at a temperature of 75 ° C to obtain a powder, which was mixed with an ethanol solution having a concentration of 92-93% by weight again, followed by a second process over 75 minutes. After dehydration, and after secondary dehydration, a centrifugal separator is used to obtain salmon sperm nuclear protein in a wet powder state, and then putting the wet powder salmon sperm nuclear protein in a vacuum dryer and drying under reduced pressure at a temperature of 75 ° C. Repeated 5 times Thus, salmon sperm nuclear protein powder was prepared.
<비교예 2><Comparative Example 2>
스텐레스 탱크에 농도 0.9 중량%인 식염수를 넣고, 온도를 40℃로 유지시킨 후, 상기 식염수에 냉동된 연어정자를 투입하고, 24시간 동안 해동시켰다. 해동된 연어정자를 1-5℃의 온도인 농도 3 중량%의 천일염수를 이용하여 1차 세척하고, 1차 세척된 연어정자를 1-5℃의 온도의 정제수를 이용하여 2차 세척하였다.Saline solution having a concentration of 0.9% by weight was put into a stainless steel tank, and the temperature was maintained at 40° C., and then frozen salmon sperm was added to the saline solution and thawed for 24 hours. The thawed salmon sperm was firstly washed with 3% by weight sun-dried salt at a temperature of 1-5°C, and the firstly washed salmon sperm was washed secondarily with purified water at a temperature of 1-5°C.
정제수 100 중량부 및 판크레아틴 15 중량부를 혼합하여 혼합액을 제조하고, 상기 혼합액에 해동 및 세척된 연어정자를 투입한 후, 상기 혼합액을 50℃의 온도로 가열하고 60분 동안 효소반응을 수행하였다. 효소반응이 수행된 혼합액을 90℃의 온도로 가열하고 10분 동안 숙성하였다. 숙성된 혼합액에 가성소다를 투입하여 효소반응을 멈추었다.A mixed solution was prepared by mixing 100 parts by weight of purified water and 15 parts by weight of pancreatin, thawed and washed salmon sperm were added to the mixed solution, and then the mixed solution was heated to a temperature of 50° C. and enzymatic reaction was performed for 60 minutes. The mixed solution in which the enzyme reaction was performed was heated to a temperature of 90° C. and aged for 10 minutes. Caustic soda was added to the aged mixture to stop the enzyme reaction.
효소반응이 멈춘 혼합액을 40℃의 온도로 냉각시키고, 여기에 농도 80 중량%이고 에탄올 및 헥산올을 4:1의 중량비로 혼합한 알코올 용액 900 중량부를 첨가하였다. 이후, 필터프레스를 이용하여 여과시켜 젖은 분말 상태인 연어정자핵단백질을 얻었다.The mixed solution in which the enzyme reaction stopped was cooled to a temperature of 40° C., and 900 parts by weight of an alcohol solution having a concentration of 80% by weight and a mixture of ethanol and hexanol at a weight ratio of 4:1 was added thereto. Thereafter, it was filtered using a filter press to obtain salmon sperm nuclear protein in a wet powdery state.
젖은 분말 상태인 연어정자핵단백질에 농도 80 중량%의 알코올 용액 및 농도 50 중량%의 가성 소다를 3:2의 중량비율로 혼합한 중화용액을 가하여 중화하였다. 이후, 1차 탈수하여 젖은 분말 상태인 연어정자핵단백질을 얻었다.The wet powdered salmon sperm nuclear protein was neutralized by adding a neutralization solution in which an alcohol solution having a concentration of 80% by weight and caustic soda having a concentration of 50% by weight were mixed in a weight ratio of 3:2. Thereafter, the first dehydration was performed to obtain salmon sperm nuclear protein in a wet powder state.
젖은 분말 상태인 연어정자핵단백질과 농도 92-93 중량%의 에탄올 용액을 혼합한 후, 75분에 걸쳐 2차 탈수하고, 2차 탈수 후 원심분리기를 이용하여 젖은 분말 상태인 연어정자핵단백질을 얻은 후, 젖은 분말 상태인 연어정자핵단백질을 진공건조기에 넣고 75℃의 온도에서 감압건조하여 분말을 얻고, 이를 다시 농도 92-93 중량%의 에탄올 용액을 혼합한 후, 75분에 걸쳐 2차 탈수하고, 2차 탈수 후 원심분리기를 이용하여 젖은 분말 상태인 연어정자핵단백질을 얻은 후, 젖은 분말 상태인 연어정자핵단백질을 진공건조기에 넣고 75℃의 온도에서 감압건조하는 것을 5회 반복수행하여 연어정자핵단백질 분말을 제조하였다.After mixing wet powdered salmon sperm nuclear protein and 92-93% by weight ethanol solution, secondary dehydration over 75 minutes, and after secondary dehydration, use a centrifuge to obtain wet powder salmon sperm nuclear protein After obtaining, the wet powdered salmon sperm nuclear protein was placed in a vacuum dryer and dried under reduced pressure at a temperature of 75 ° C to obtain a powder, which was mixed with an ethanol solution having a concentration of 92-93% by weight again, followed by a second process over 75 minutes. After dehydration, and after secondary dehydration, a centrifugal separator is used to obtain salmon sperm nuclear protein in a wet powder state, and then putting the wet powder salmon sperm nuclear protein in a vacuum dryer and drying under reduced pressure at a temperature of 75 ° C. Repeated 5 times Thus, salmon sperm nuclear protein powder was prepared.
<실험예 1> 연어정자핵단백질 분말<Experimental Example 1> Salmon Sperm Nuclear Protein Powder
상기 실시예 1에서 제조된 연어정자핵단백질 분말을 도 2의 사진으로 나타내었고, 외관, 액체시 상태의 적합여부, 건조감량, 일반생균수, 대장균 적합여부, 중금속 함량, 비소 함량, DNA 함량, 인 함량을 분석하여 하기 표 1에 나타내었다.The salmon sperm nuclear protein powder prepared in Example 1 is shown in the photograph of FIG. Phosphorus content was analyzed and shown in Table 1 below.
도 2에 나타낸 바와 같이, 연어정자핵단백질 분말이 분말화가 정상적으로 수행되어 고르게 분말화된 것을 살펴볼 수 있으며, 상기 표 1에 나타낸 바와 같이 성분을 확인할 수 있다.As shown in FIG. 2, it can be seen that the salmon sperm nuclear protein powder was powdered normally and evenly powdered, and the components can be confirmed as shown in Table 1 above.
또한, 연어정자 투입량 대비 연어정자핵단백질 분말 제조에 따른 수율을 분석하였으며, 실시예 1의 경우 연어정자 1200 kg을 적용하여 연어정자핵단백질 분말을 300 kg 제조할 수 있어 약 25%의 수율을 나타내었고, 비교예 1의 경우 약 18%의 수율을 나타내었고, 비교예 2의 경우 약 23%의 수율을 나타내었다.In addition, the yield according to the production of salmon sperm nuclear protein powder was analyzed compared to the amount of salmon sperm input. In the case of Example 1, 300 kg of salmon sperm nuclear protein powder could be produced by applying 1200 kg of salmon sperm, showing a yield of about 25% In the case of Comparative Example 1, the yield was about 18%, and in the case of Comparative Example 2, the yield was about 23%.
비교예 1의 경우, 세척 단계를 단순 수세만 하여 연어정자 자체가 물러터지는 문제가 발생하고, 이에 따라 수율이 저하되는 것이고, 더불어 멀균 단계를 수행하지 않아 품질이 저하된 것으로 판단된다.In the case of Comparative Example 1, the washing step was performed only by simple water washing, resulting in the problem of softening the salmon sperm itself, resulting in a decrease in yield, and it was determined that the quality was reduced because the sterilization step was not performed.
<실험예 2> 관능검사<Experimental Example 2> Sensory test
상기 실시예 1 및 비교예 1-2에서 제조된 연어정자핵단백질 분말 및 실시예 2에서 제조된 음료 조성물을 사용하여 남녀노소 패널 40명을 대상으로 하여 맛, 향, 전체적인 기호도를 분석하였으며, 9점 척도법을 사용하여 조사하고 그 결과를 하기 표 1에 나타내었다.Using the salmon sperm nuclear protein powder prepared in Example 1 and Comparative Example 1-2 and the beverage composition prepared in Example 2, 40 male and female panels were analyzed for taste, aroma, and overall acceptability. It was investigated using a point scale method, and the results are shown in Table 1 below.
상기 표 1에 나타낸 바와 같이, 본 발명에 따른 연어정자핵단백질 분말은 맛과 향이 높고 전체적인 기호도가 우수하다. 반면, 비교예 1 및 비교예 2에서 제조된 연어정자핵단백질 분말은 비린맛과 향이 남아있고 떫은맛이 남아있어 문제가 된다.As shown in Table 1, the salmon sperm nuclear protein powder according to the present invention has high taste and aroma and excellent overall acceptability. On the other hand, the salmon sperm nuclear protein powders prepared in Comparative Examples 1 and 2 have a fishy taste and aroma and an astringent taste, which is a problem.
나아가서는, 본 발명에 따른 음료 조성물은 맛과, 향, 전체적인 기호도가 매우 우수한 것을 확인할 수 있다.Furthermore, it can be confirmed that the beverage composition according to the present invention has very excellent taste, aroma, and overall preference.
Claims (3)
정제수 100 중량부 및 판크레아틴 15 중량부를 혼합하여 혼합액을 제조하는 단계; 상기 혼합액에 해동 및 세척된 연어정자 120 중량부를 투입하는 단계; 상기 혼합액을 50℃의 온도로 가열하고 60분 동안 효소반응을 수행하는 단계; 효소반응이 수행된 혼합액을 90℃의 온도로 가열하고 10분 동안 숙성하는 단계; 및 숙성된 혼합액에 가성소다를 투입하여 효소반응을 멈추는 단계;를 포함하는 효소 반응 단계;
효소반응이 멈춘 혼합액에 구연산을 250 중량부 첨가하여 pH를 3.8-4로 조절하여 1차 멸균하는 단계; 및 1차 멸균된 혼합액을 82-83℃의 온도로 가열하고 60분 동안 교반하여 2차 멸균하는 단계;를 포함하는 멸균 단계;
2차 멸균된 혼합액을 40℃의 온도로 냉각시키는 단계; 냉각된 혼합액에 농도 80 중량%이고 에탄올 및 헥산올을 4:1의 중량비로 혼합한 알코올 용액 800-1000 중량부를 첨가하는 단계; 및 필터프레스를 이용하여 여과시켜 젖은 분말 상태인 연어정자핵단백질을 얻는 단계;를 포함하는 여과 단계;
젖은 분말 상태인 연어정자핵단백질에 농도 80 중량%의 알코올 용액 및 농도 50 중량%의 가성 소다를 3:2의 중량비율로 혼합한 중화용액을 가하여 중화하는 단계; 및 중화 후 1차 탈수하여 젖은 분말 상태인 연어정자핵단백질을 얻는 단계;를 포함하는 중화 단계;
젖은 분말 상태인 연어정자핵단백질과 농도 92-93 중량%의 에탄올 용액을 혼합한 후, 75분에 걸쳐 2차 탈수하는 단계; 2차 탈수 후 원심분리기를 이용하여 젖은 분말 상태인 연어정자핵단백질을 얻는 단계; 및 젖은 분말 상태인 연어정자핵단백질을 진공건조기에 넣고 70-80℃의 온도에서 감압건조하는 단계;를 포함하고, 상기 2차 탈수하는 단계, 젖은 분말 상태인 연어정자핵단백질을 얻는 단계 및 감압건조하는 단계는 5-6회 반복하여 수행하는 것을 특징으로 하는 연어정자핵단백질 분말 수득 단계;를 포함하는 연어정자핵단백질 분말 제조 단계;
감잎, 율무, 대추, 생강, 감초 및 계피를 2:2:2:1:2:1의 중량비율로 혼합한 한방원료를 준비하고, 액체 분사가 가능한 분사각이 60°인 노즐을 2개씩 3열로 6개 포함하는 세척기를 사용하여 식초물을 분사하여 한방원료를 1차 세척하는 단계; 1차 세척된 한방원료를 전해수로 2차 세척하는 단계; 2차 세척된 한방원료를 43-47℃의 온도에서 건조하는 단계; 건조된 한방원료를 0.095-0.105 MPa의 압력 및 230-250℃의 온도에서 80-100분 동안 증숙하고, 55-65℃의 온도에서 220-260분 동안 건조시키는 과정을 3회 수행하는 단계; 증숙 및 건조된 한방원료를 분쇄하여 한방분말을 제조하는 단계; 및 상기 한방분말 100 중량부 및 물 100 중량부를 혼합하고 78-82℃의 온도로 가열하여 1-3시간 동안 열수추출하고 여과하는 단계;를 포함하는 한방여과액을 제조하는 단계;
오미자, 구기자 및 사과를 4:3:3의 중량비율로 혼합하여 과일원료를 준비하고, 상기 과일원료 100 중량부 및 물 100 중량부를 혼합하여 제1 혼합물을 제조하는 단계; 상기 제1 혼합물을 92-95℃의 온도로 가열하고, 증발하는 증기를 냉각시켜 얻은 증류액이 다시 제1 혼합물에 혼합되도록 하여 60-120분 동안 순환시키는 단계; 상기 순환이 완료된 제1 혼합물을 98-100℃의 온도로 가열하고, 60-120분 동안 증발하는 증기를 냉각시켜 1차 증류액을 얻는 단계; 상기 1차 증류액 100 중량부 및 상기 과일원료 100 중량부를 혼합하여 제2 혼합물을 제조하는 단계; 상기 제2 혼합물을 92-95℃의 온도로 가열하고, 증발하는 증기를 냉각시켜 얻은 증류액이 다시 제2 혼합물에 혼합되도록 하여 60-120분 동안 순환시키는 단계; 및 상기 순환이 완료된 제2 혼합물을 70-80℃의 온도로 가열하고, 150-210분 동안 증발하는 증기를 냉각시켜 2차 증류액을 얻는 단계;를 포함하는 과일증류액 제조 단계; 및
상기 연어정자핵단백질 분말 48-52 중량부, 상기 한방여과액 28-32 중량부 및 상기 과일증류액 18-22 중량부를 혼합하는 단계;를 포함하는 음료 조성물의 제조방법.Adding saline solution having a concentration of 0.9% by weight to a stainless steel tank and maintaining the temperature at 40°C; Injecting frozen salmon sperm into the saline solution and thawing for 24 hours; First washing the thawed salmon sperm with 2-4% by weight natural salt water at a temperature of 1-5°C; and secondly washing the firstly washed salmon sperm with purified water at a temperature of 1-5° C.;
preparing a mixed solution by mixing 100 parts by weight of purified water and 15 parts by weight of pancreatin; adding 120 parts by weight of thawed and washed salmon sperm to the mixture; heating the mixed solution to a temperature of 50° C. and performing an enzymatic reaction for 60 minutes; heating the mixture in which the enzyme reaction was performed to a temperature of 90° C. and aging for 10 minutes; Enzymatic reaction step comprising; and stopping the enzyme reaction by adding caustic soda to the aged mixture;
Primary sterilization by adding 250 parts by weight of citric acid to the mixture in which the enzyme reaction has stopped to adjust the pH to 3.8-4; and heating the primary sterilized mixed solution to a temperature of 82-83° C. and performing secondary sterilization by stirring for 60 minutes;
cooling the secondary sterilized liquid mixture to a temperature of 40°C; Adding 800-1000 parts by weight of an alcohol solution obtained by mixing ethanol and hexanol in a weight ratio of 4:1 with a concentration of 80% by weight to the cooled mixture; and filtering using a filter press to obtain wet powdered salmon sperm nuclear protein;
Neutralizing wet powdered salmon sperm nuclear protein by adding a neutralization solution in which an alcohol solution having a concentration of 80% by weight and caustic soda having a concentration of 50% by weight are mixed in a weight ratio of 3:2; and a step of first dehydration after neutralization to obtain wet powdered salmon sperm nuclear protein;
After mixing wet powdered salmon sperm nuclear protein with an ethanol solution having a concentration of 92-93% by weight, secondary dehydration for 75 minutes; Obtaining wet powdered salmon sperm nuclear protein using a centrifugal separator after secondary dehydration; and putting the wet powdered salmon sperm nuclear protein in a vacuum dryer and drying under reduced pressure at a temperature of 70-80° C., wherein the secondary dehydration step, obtaining wet powder salmon sperm nuclear protein and reduced pressure Salmon sperm nuclear protein powder manufacturing step comprising: obtaining salmon sperm nuclear protein powder, characterized in that the drying step is repeated 5 to 6 times;
Prepare herbal raw materials by mixing persimmon leaves, adlay, jujube, ginger, licorice, and cinnamon in a weight ratio of 2:2:2:1:2:1, and use two nozzles each with a spray angle of 60° that can spray liquid. Using a washer containing 6 heats to spray vinegar water to first wash the oriental raw materials; Secondary washing of the firstly washed herbal raw material with electrolytic water; Drying the secondary washed herbal raw material at a temperature of 43-47 ° C; Steaming the dried herbal raw material at a pressure of 0.095-0.105 MPa and a temperature of 230-250 ° C. for 80-100 minutes, and drying at a temperature of 55-65 ° C. for 220-260 minutes 3 times; Preparing herbal powder by grinding the steamed and dried herbal raw materials; Preparing an herbal filtrate containing; and mixing 100 parts by weight of the herbal powder and 100 parts by weight of water, heating at a temperature of 78-82° C., extracting hot water for 1-3 hours, and filtering;
Preparing a fruit raw material by mixing Schisandra chinensis, goji berry and apple in a weight ratio of 4: 3: 3, and preparing a first mixture by mixing 100 parts by weight of the fruit raw material and 100 parts by weight of water; Heating the first mixture to a temperature of 92-95° C. and allowing the distillate obtained by cooling the evaporating vapor to be mixed with the first mixture again and circulating for 60-120 minutes; obtaining a first distillate by heating the first mixture after completion of the circulation to a temperature of 98-100° C. and cooling the evaporating vapor for 60-120 minutes; preparing a second mixture by mixing 100 parts by weight of the primary distillate and 100 parts by weight of the fruit raw material; Heating the second mixture to a temperature of 92-95° C. and allowing the distillate obtained by cooling the evaporating vapor to be mixed with the second mixture again and circulating for 60-120 minutes; and heating the second mixture after the circulation is completed to a temperature of 70-80° C. and cooling the evaporating vapor for 150-210 minutes to obtain a secondary distillate; preparing a fruit distillate; and
Mixing 48-52 parts by weight of the salmon sperm nuclear protein powder, 28-32 parts by weight of the herbal filtrate, and 18-22 parts by weight of the fruit distillate;
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Citations (3)
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---|---|---|---|---|
JP2004016143A (en) * | 2002-06-18 | 2004-01-22 | Ls Corporation:Kk | Method for producing water soluble decomposed product of nucleoprotein |
CN102084994A (en) * | 2009-12-04 | 2011-06-08 | 东港市慧海海洋生物科技开发有限公司 | Protamine and preparation method thereof |
KR101182023B1 (en) | 2003-07-04 | 2012-09-11 | 아틀란틱 가든 아에스 | Fish protein hydrolyzate |
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JP2004016143A (en) * | 2002-06-18 | 2004-01-22 | Ls Corporation:Kk | Method for producing water soluble decomposed product of nucleoprotein |
KR101182023B1 (en) | 2003-07-04 | 2012-09-11 | 아틀란틱 가든 아에스 | Fish protein hydrolyzate |
CN102084994A (en) * | 2009-12-04 | 2011-06-08 | 东港市慧海海洋生物科技开发有限公司 | Protamine and preparation method thereof |
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