KR20180058875A - The extraction method for jellyfish protein - Google Patents
The extraction method for jellyfish protein Download PDFInfo
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- KR20180058875A KR20180058875A KR1020160157018A KR20160157018A KR20180058875A KR 20180058875 A KR20180058875 A KR 20180058875A KR 1020160157018 A KR1020160157018 A KR 1020160157018A KR 20160157018 A KR20160157018 A KR 20160157018A KR 20180058875 A KR20180058875 A KR 20180058875A
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- 241000242583 Scyphozoa Species 0.000 title claims abstract description 141
- 102000004169 proteins and genes Human genes 0.000 title claims abstract description 49
- 108090000623 proteins and genes Proteins 0.000 title claims abstract description 49
- 238000000605 extraction Methods 0.000 title abstract description 10
- 102000004190 Enzymes Human genes 0.000 claims abstract description 45
- 108090000790 Enzymes Proteins 0.000 claims abstract description 45
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 27
- 239000000843 powder Substances 0.000 claims abstract description 25
- 238000001035 drying Methods 0.000 claims abstract description 17
- 239000012153 distilled water Substances 0.000 claims abstract description 10
- 238000006911 enzymatic reaction Methods 0.000 claims abstract description 10
- 238000010438 heat treatment Methods 0.000 claims abstract description 9
- 239000002245 particle Substances 0.000 claims abstract description 8
- 238000000354 decomposition reaction Methods 0.000 claims abstract description 5
- 238000001914 filtration Methods 0.000 claims abstract description 3
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- 238000002360 preparation method Methods 0.000 claims abstract 3
- 238000000034 method Methods 0.000 claims description 25
- 102000005158 Subtilisins Human genes 0.000 claims description 4
- 108010056079 Subtilisins Proteins 0.000 claims description 4
- 238000011084 recovery Methods 0.000 abstract description 10
- 102000008186 Collagen Human genes 0.000 abstract description 8
- 108010035532 Collagen Proteins 0.000 abstract description 8
- 229920001436 collagen Polymers 0.000 abstract description 8
- 238000010924 continuous production Methods 0.000 abstract description 5
- 230000018044 dehydration Effects 0.000 abstract description 5
- 238000006297 dehydration reaction Methods 0.000 abstract description 5
- 230000008901 benefit Effects 0.000 abstract description 2
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- 229940088598 enzyme Drugs 0.000 description 35
- 108091005804 Peptidases Proteins 0.000 description 12
- 102000035195 Peptidases Human genes 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 11
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- 108090001060 Lipase Proteins 0.000 description 7
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- 239000004367 Lipase Substances 0.000 description 6
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- RYMZZMVNJRMUDD-HGQWONQESA-N simvastatin Chemical compound C([C@H]1[C@@H](C)C=CC2=C[C@H](C)C[C@@H]([C@H]12)OC(=O)C(C)(C)CC)C[C@@H]1C[C@@H](O)CC(=O)O1 RYMZZMVNJRMUDD-HGQWONQESA-N 0.000 description 4
- 230000007515 enzymatic degradation Effects 0.000 description 3
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- 108091005658 Basic proteases Proteins 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
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- 230000003796 beauty Effects 0.000 description 2
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- 230000000415 inactivating effect Effects 0.000 description 2
- 239000002417 nutraceutical Substances 0.000 description 2
- 235000021436 nutraceutical agent Nutrition 0.000 description 2
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 2
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- 239000000243 solution Substances 0.000 description 2
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- 241000186361 Actinobacteria <class> Species 0.000 description 1
- 241000203578 Microbispora Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
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- 239000007864 aqueous solution Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 235000021329 brown rice Nutrition 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
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- 238000004140 cleaning Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
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- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 108010007119 flavourzyme Proteins 0.000 description 1
- 230000007407 health benefit Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 108010009355 microbial metalloproteinases Proteins 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 235000019833 protease Nutrition 0.000 description 1
- 235000004252 protein component Nutrition 0.000 description 1
- 238000000751 protein extraction Methods 0.000 description 1
- 230000017854 proteolysis Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/14—Extraction; Separation; Purification
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
- A23J1/00—Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites
- A23J1/04—Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites from fish or other sea animals
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/17—Amino acids, peptides or proteins
- A23L33/18—Peptides; Protein hydrolysates
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/12—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by hydrolysis, i.e. solvolysis in general
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/43504—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from invertebrates
- C07K14/43595—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from invertebrates from coelenteratae, e.g. medusae
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/78—Connective tissue peptides, e.g. collagen, elastin, laminin, fibronectin, vitronectin or cold insoluble globulin [CIG]
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2200/00—Function of food ingredients
- A23V2200/30—Foods, ingredients or supplements having a functional effect on health
- A23V2200/318—Foods, ingredients or supplements having a functional effect on health having an effect on skin health and hair or coat
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- General Health & Medical Sciences (AREA)
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- Gastroenterology & Hepatology (AREA)
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- Nutrition Science (AREA)
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Abstract
Description
본 발명은 해파리 단백질의 추출방법에 관한 것으로, 보다 구체적으로는 해파리의 단백질 추출 시 탈수, 건조, 분쇄, 팽창, 효소분해반응 및 회수공정으로 이루어진 일련의 연속공정을 이용하여 단백질의 추출효율을 극대화시킬 수 있는 해파리 단백질의 추출방법에 관한 것이다.The present invention relates to a method for extracting jellyfish proteins, and more particularly, to a method for extracting proteins from a jellyfish using a series of continuous processes comprising dehydration, drying, crushing, swelling, To a method for extracting a jellyfish protein that can be used as an extract.
현재 일반적으로 해파리에서 단백질을 추출하기 위해서는 대한민국특허등록번호 10-104539호와 같이 해파리에 돈 태반, 백장감, 반하 및 카제인, 전분 등의 다양한 성분을 혼합하고 마이크로비스포라 등과 같은 희소 방선균을 접종하면서 배양하여 발효시키며, 살균 및 건조단계를 거치면서 추가로 현미 등을 혼합하고 다시 발효, 살균과 혼합단계를 총 3단계를 거쳐 해파리에서 유용성분을 추출할 수 있도록 하였다.Currently, in order to extract a protein from a jellyfish, various components such as a donepane, a bacon, a bacon, a casein, and starch are mixed in a jellyfish as in Korean Patent Registration No. 10-104539, and inoculated with rare actinomycetes such as microbispora Cultured and fermented. After sterilization and drying, the brown rice was further mixed, and the fermentation, sterilization and mixing steps were repeated three times to extract the useful components from the jellyfish.
또한, 대한민국특허등록번호 제10-1536215호와 같이 해파리에 뉴트라아제를 넣고 가수분해를 실시한 후, 주석산을 추가로 혼합하여 2차로 가수분해를 실시하면서 탄산칼슘을 통해 여과하면서 해파리에서 콜라겐을 회수할 수 있도록 하였다.In addition, as described in Korean Patent Registration No. 10-1536215, after the hydrolysis of jellyfish is performed by adding Ntase, further tartaric acid is further mixed to recover the collagen from the jellyfish while being filtered through calcium carbonate while performing the second hydrolysis .
하지만, 상기와 같은 효소를 이용하여 해파리에서 콜라겐 등의 유용성분을 추출하기 위해서는 발효, 살균, 건조 등의 공정을 2회 이상 거쳐야 했으며, 각각의 공정을 수행하기 위한 장비가 대형화되면서 복잡하게 이루어져 그에 따른 경비의 증가 및 유지보수에 어려운 문제점이 발생하였다.However, in order to extract useful components such as collagen from jellyfish using the above-mentioned enzymes, fermentation, sterilization, drying, and the like have been carried out more than once, and equipment for performing each process has become larger and more complex, Resulting in increased costs and difficult maintenance.
또한, 상기와 같은 방법을 이용하여 해파리에서 콜라겐을 회수하기 위해서는 많은 공정시간이 소요되었으며, 투입된 시간과 비용에 비해 콜라겐의 회수비율은 물론, 작업효율이 좋지 못하는 문제점이 있었다.In addition, it takes a lot of time to collect the collagen in the jellyfish using the above-described method, and there is a problem that the recovery efficiency of the collagen as well as the working efficiency is poor compared to the time and cost of the injection.
본 발명은 해파리에 함유된 단백질을 간단한 연속공정으로도 회수할 수 있으면서 회수율을 향상시킬 수 있고, 우수한 경제성 및 편리성을 제공할 수 있으면서 사용자들의 건강증진과 피부미용에 유익한 효과를 제공할 수 있도록 하는데 그 목적이 있다.The present invention relates to a process for recovering proteins contained in jellyfish by a simple continuous process so as to improve the recovery rate, to provide excellent economic efficiency and convenience, and to provide users with health benefits and beneficial effects on skin beauty It has its purpose.
상기와 같은 목적을 달성하기 위한 본 발명은 해파리를 세척, 탈수시키는 준비단계와, 세척, 탈수된 해파리를 열풍건조기를 이용하여 50 ~ 80℃의 온도에서 수분함량이 10% 이내가 되도록 건조하는 건조단계와, 건조된 해파리를 100 ~ 500㎛ 크기의 분말형태로 제조하는 분쇄단계와, 분말형태의 해파리를 산도가 조정된 증류수에 첨가하고 80 ~ 100℃의 온도에서 1 ~ 3시간 가열하여, 해파리 분말 입자를 팽창시키는 팽창단계와, 상기 팽창단계 이후, 효소를 해파리 분말 중량 대비 2중량% 첨가하고, 45 ~ 60℃의 온도에서 1 ~ 3시간 반응시키는 효소반응단계와, 해파리의 효소분해반응 후, 90 ~ 100℃의 온도에서 5 ~ 20분간 가열하여 효소를 실활시키고, 해파리의 잔여물을 제거, 여과하면서 단백질 추출액을 회수하는 회수단계로 이루어진다.In order to achieve the above-mentioned object, the present invention provides a method for cleaning and dehydrating jellyfish, comprising the steps of washing and dehydrating jellyfish using a hot-air drier, drying at a temperature of 50 to 80 캜 A step of pulverizing the dried jellyfish in the form of powder having a size of 100 to 500 mu m; and a step of adding jellyfish in powder form to distilled water adjusted in acidity and heating at 80 to 100 DEG C for 1 to 3 hours, An enzyme reaction step of adding 2% by weight of the enzyme to the weight of the jellyfish powder and allowing the enzyme to react at a temperature of 45 to 60 ° C for 1 to 3 hours after the expansion step; , Heating at 90 to 100 ° C for 5 to 20 minutes to inactivate the enzyme, and removing the residue of the jellyfish, and recovering the protein extract while filtering.
본 발명은 해파리에 함유된 단백질의 추출 시 탈수, 건조, 분쇄, 팽창, 효소분해반응, 회수공정이 일련의 연속공정으로 이루어지도록 하여, 해파리에서 콜라겐을 주성분으로 하는 단백질을 우수한 회수율로 추출할 수 있어, 우수한 경제성 및 편리성을 제공할 수 있는 장점이 있다.The present invention enables extraction of proteins contained in jellyfish by a series of continuous processes such as dehydration, drying, crushing, swelling, enzymatic degradation, and recovery, thereby extracting proteins having collagen as a main component from jellyfish with excellent recovery Therefore, there is an advantage that it is possible to provide excellent economical efficiency and convenience.
그리고, 해파리로부터 콜라겐을 주성분으로 하는 단백질 성분을 간단한 공정으로 회수하여 사용자들이 편리하게 이용 및 섭취할 수 있도록 함으로써, 사용자들의 피부미용 및 건강증진에 유익한 효과를 제공할 수 있는 장점이 있다.In addition, a protein component containing collagen as a major component from the jellyfish is recovered by a simple process so that it can be conveniently used and consumed by the users, thereby providing an advantageous effect to skin beauty and health promotion of users.
도 1은 본 발명인 해파리 단백질의 추출방법을 도시한 흐름도.
도 2는 알칼라제 효소 농도에 따른 해파리 단백질의 추출량을 비교한 그래프.
도 3은 알카라제 효소 반응시간에 따른 해파리 단백질의 추출량을 비교한 그래프.1 is a flow chart showing a method for extracting jellyfish protein according to the present invention.
FIG. 2 is a graph comparing the extraction amounts of jellyfish proteins according to the concentration of the enzyme.
FIG. 3 is a graph comparing the extraction amount of jellyfish protein with the reaction time of the alkaline enzyme. FIG.
상기와 같은 목적을 달성하기 위하여 본 발명인 해파리 단백질의 추출방법에 대하여 살펴보면 다음과 같다.In order to achieve the above object, a method for extracting jellyfish protein according to the present invention will be described as follows.
<실시예 1>≪ Example 1 >
먼저, 해파리에 함유된 단백질을 회수하기 위해서는 해파리에 함유된 수분 및 염분을 제거하도록 한다.(S10)First, in order to recover the protein contained in the jellyfish, water and salt contained in the jellyfish are removed. (S10)
이를 상세히 설명하면, 일반적으로 해파리에는 99%가 넘을 정도로 수분이 함유되어 있어, 저장이 어려우면서 부패가 쉽게 일어난다.To explain this in detail, generally, jellyfish contains water in an amount exceeding 99%, which is difficult to store and corruption easily occurs.
따라서, 상술한 문제점을 해결하기 위해 해파리를 건조하는데 일반적인 건조방법을 해파리에 적용하면 99% 이상의 수분함량으로 인해 막대한 건조시간 및 비용이 발생하기 때문에, 건조시간 및 비용의 절감을 위해 건조공정 이전에 해파리를 압착 탈수시켜 상당량의 수분을 제거해야 한다.Therefore, when the general drying method for drying jellyfish is applied to the jellyfish in order to solve the above-mentioned problem, since the moisture content of 99% or more causes a considerable drying time and cost, Jellyfish must be squeezed and dewatered to remove a significant amount of water.
즉, 해파리의 수분을 제거하는데 압착식 탈수방법인 압착탈수기를 이용하여 해파리에 함유된 수분을 짜내는 것을 말하는 것이다.In other words, it refers to squeezing the water contained in the jellyfish using a crimping dehydrator, which is a compression type dehydration method, to remove moisture from the jellyfish.
특히, 압착식 탈수방법은 수분을 완벽히 제거하기는 불가능하지만 수분함량이 높은 재료로부터 다량의 수분을 쉽고 빠르게 제거하는 가장 효율적인 방법이므로, 이후에 뒤따르는 건조공정의 시간과 비용을 크게 줄일 수 있어 수분함량이 99% 이상인 해파리의 탈수에 가장 적합한 방법인 것이다.In particular, since the compression-type dewatering method is the most efficient method for easily and quickly removing a large amount of water from a material having a high water content, it is impossible to completely remove moisture, thereby greatly reducing the time and cost of the subsequent drying process, This is the most suitable method for dehydration of jellyfish having a content of 99% or more.
또한, 상기 압착탈수기를 이용하여 해파리의 수분제거 이전에 해파리에 함유된 염분을 제거하기 위해 해파리를 세척하는 것은 자명한 사항이다.It is also clear that the jellyfish is washed in order to remove the salt contained in the jellyfish before the water is removed from the jellyfish using the above-described crimping dehydrator.
<실시예 2>≪ Example 2 >
한편, 해파리의 세척, 탈수가 이루어지고 난 후, 해파리에 함유된 수분이 10% 이내가 되도록 해파리를 건조시키도록 한다.(S20)On the other hand, after the jellyfish is washed and dehydrated, the jellyfish is dried so that the water contained in the jellyfish is within 10%. (S20)
이를 상세히 설명하면, 상기와 같이 해파리를 세척하고 수분을 짜내더라도 해파리에는 일부 수분이 잔존하게 되는데, 해파리에 함유된 수분이 10% 이상일 경우 상술한 바와 같이 해파리의 저장이 어려우면서 부패가 쉽게 일어나고 제조가 어려워지게 된다.As described above, even if the jellyfish is washed and water is squeezed as described above, some moisture remains in the jellyfish. If the water content of the jellyfish is 10% or more, it is difficult to store the jellyfish and the decay easily occurs. .
따라서, 해파리에서 단백질의 원활한 회수를 위한 원료로 장기 보존할 수 있도록 하기 위해 해파리에 함유된 수분이 10% 이내가 되도록 건조를 실시하도록 한다.Therefore, in order to ensure long-term preservation as a raw material for smooth recovery of protein from jellyfish, it is necessary to dry the jellies so that the moisture contained in jellyfish is within 10%.
여기서, 상기 해파리의 건조를 실시할 때, 동결건조방식을 이용하여 해파리를 건조할 수도 있지만, 상기 동결건조방식은 설비와 운영비용이 가장 많이 발생하는 건조방식이면서 건조시간이 많이 소요되어 경제성이 좋지 못하기 때문에, 비용의 절감을 위하여 열풍건조방식으로 해파리를 건조하도록 하는데, 약 50 ~ 80℃의 온도에서 건조하는 것이 바람직하다.Here, when the jellyfish is dried, the jellyfish may be dried using the freeze-drying method. However, the freeze-drying method is a drying method in which the equipment and the operation cost are most generated, In order to reduce the cost, it is preferable to dry the jellyfish at a temperature of about 50 to 80 DEG C in order to dry the jellyfish by the hot air drying method.
즉, 열풍건조방식으로 50 ~ 80℃의 온도로 해파리에 함유된 수분이 10% 이내가 될 때까지 건조시키도록 한다.That is, it is dried by a hot air drying method at a temperature of 50 to 80 ° C until the water content in the jellyfish becomes 10% or less.
여기서, 상기 해파리는 50 ~ 80℃의 온도로 건조시킬 수도 있지만 가장 바람직하게는 60 ~ 70℃의 온도로 건조시키는 것이 좋다.Here, the jellyfish may be dried at a temperature of 50 to 80 ° C, but it is most preferable to dry the jellyfish at a temperature of 60 to 70 ° C.
<실시예 3>≪ Example 3 >
한편, 상술한 바와 같이 해파리를 건조시키고 난 후, 해파리에 함유된 단백질의 원활한 회수를 위하여 해파리를 분말형태로 파쇄한다.(S30)On the other hand, after drying the jellyfish as described above, the jellyfish is crushed in powder form for smooth recovery of proteins contained in the jellyfish. (S30)
이는, 해파리와 후술할 효소와의 반응을 통해 단백질의 추출 시 해파리와 효소와 반응을 더욱 원활하게 하면서 추출이 효율적으로 이루어질 수 있도록 해파리의 표면적을 넓히기 위해 해파리를 분말형태로 파쇄하는 것이다.This is to break down the jellyfish in powder form in order to widen the surface area of the jellyfish so that the reaction with the jellyfish and the enzyme can be more smoothly performed while extracting the protein through the reaction of the jellyfish with the enzyme to be described later.
여기서, 해파리를 분말형태로 파쇄 시 사용자의 목적이나 편의에 따라 얼마든지 다양한 크기로 파쇄할 수 있지만, 가장 좋은 효율을 위하여 해파리를 100 ~ 500㎛ 크기로 파쇄하는 것이 좋다.Here, when jellyfish are crushed in powder form, they can be crushed to various sizes according to the purpose or convenience of the user, but it is preferable to crush jellyfish to a size of 100 to 500 μm for the best efficiency.
<실시예 4><Example 4>
한편, 상기와 같이 해파리를 분말형태로 파쇄한 후, 분말형태의 해파리를 산도가 조정된 증류수(물)에 첨가하여 가열하면서 해파리 분말 입자를 팽창시키도록 한다.(S40)Meanwhile, after the jellyfish is crushed in the form of powder as described above, the jellyfish in the form of powder is added to distilled water (water) adjusted in acidity, and the jellyfish powder particles are expanded while heating. (S40)
이는, 해파리를 분말형태로 파쇄하고 바로 효소와 반응시키게 되면, 해파리 성분들이 서로 견고하게 결착되어 있어 효소와의 반응이 쉽게 일어나지 않기 때문에, 해파리 단백질의 용이한 분해 및 추출을 위하여 해파리 분말 입자를 증류수에 넣고 가열하여, 해파리 성분 간의 수소결합을 붕괴시킴으로써, 해파리 분말 입자가 팽창되도록 하는 것이다.This is because when the jellyfish is crushed in powder form and reacted with the enzyme immediately, the jellyfish components are firmly bound to each other and the reaction with the enzyme does not easily occur. Therefore, in order to easily decompose and extract the jellyfish protein, And heated to collapse the hydrogen bonds between the jellyfish components, thereby expanding the jellyfish powder particles.
또한, 낮은 온도에서는 물 분자의 에너지가 낮아 해파리 성분 간의 수소결합을 붕괴시킬 수 없기 때문에 80 ~ 100℃ 온도에서 가열하는 것이다.In addition, since the energy of water molecules is low at a low temperature, it is impossible to disrupt the hydrogen bonding between the components of jellyfish, so that it is heated at a temperature of 80 to 100 ° C.
그리고, 해파리의 추출을 위해 사용되는 증류수는 해파리의 단백질 분해에 사용되는 효소에 따라 pH가 조정되는 것은 자명한 사항이며, 본 발명에서는 해파리의 단백질을 회수하기 위해 알카라제가 사용되므로, 상기 알카라제 효소의 용이한 반응을 위해 pH가 8.0으로 조정된 증류수가 사용된다.The distilled water used for the extraction of jellyfish is a matter of course that the pH is adjusted according to the enzyme used for proteolysis of jellyfish. In the present invention, since an alkaline is used to recover the protein of jellyfish, Distilled water adjusted to pH 8.0 is used for easy reaction of enzyme.
또한, 해파리에 함유된 단백질의 효율적인 회수를 위하여 해파리는 증류수 중량 대비 1 ~ 10중량%로 투입되도록 하는 것이 좋다.In order to efficiently recover the protein contained in the jellyfish, the jellyfish is preferably added in an amount of 1 to 10% by weight based on the weight of the distilled water.
예를 들어, 해파리를 약 10 ~ 90kg을 사용할 경우 증류수는 약 900 ~ 1,000Kg으로 사용하는 것을 말하는 것이다.For example, when using about 10 ~ 90kg of jellyfish, distilled water is about 900 ~ 1,000kg.
이처럼, 해파리와 증류수의 비율을 상술한 바와 같이 혼합하는 이유는 해파리의 비율이 높을 경우 해파리의 단백질 효소분해 시 단백질에 충분한 효소분해반응이 일어나지 않아 단백질이 완전히 추출되지 못하고 일부만이 추출되어 회수율이 낮아지며, 해파리의 비율이 낮을 경우 해파리에서 추출되는 단백질의 양이 묽어지게 되면서 제대로 추출되지 않기 때문에 상술한 비율로 혼합하는 것이다.As described above, the reason why the ratio of jellyfish and distilled water is mixed as described above is that when the ratio of jellyfish is high, sufficient enzyme decomposition reaction does not occur in the protein enzyme decomposition of jellyfish, so that the protein can not be extracted completely, , And when the ratio of jellyfish is low, the amount of the protein extracted from the jellyfish is reduced, and it is not properly extracted.
즉, 분말형태의 해파리를 물 중량 대비 1 ~ 10중량%로 pH가 조정된 80 ~ 100℃의 물에 넣어 해파리 현탁액을 만든 후, 1 ~ 3시간 가열하여 해파리의 분말 입자에 물이 침투하도록 하여 분말 입자를 팽창시키는 것이다.That is, a jellyfish in the form of a powder is put into water of 80 to 100 ° C adjusted to a pH of 1 to 10% by weight with respect to the weight of water to make a jellyfish suspension, and then water is infiltrated into the jellyfish powder particles by heating for 1 to 3 hours Thereby expanding the powder particles.
<실시예 5>≪ Example 5 >
한편, 분말형태의 해파리의 입자를 팽창시키고 난 후, 효소를 첨가하여 효소분해반응이 일어나도록 한다.(S50)On the other hand, after the particles of the powdery jellyfish are expanded, an enzyme is added to cause an enzymatic degradation reaction (S50)
여기서, 해파리에 함유된 단백질을 회수(추출)하기 위해서는 단백질 분해효소와 지방 분해효소를 이용하여 단백질을 회수할 수 있는데, 단백질 분해효소는 해파리로부터 단백질을 분해 및 회수하기 위해 사용하였고, 지방 분해효소는 해파리의 세포막을 분해시켜 단백질 추출 수율을 높이기 위해 사용하였다.Here, in order to recover (extract) proteins contained in jellyfish, proteins can be recovered using proteolytic enzymes and lipolytic enzymes. Proteolytic enzymes are used for decomposing and recovering proteins from jellyfish, and lipolytic enzymes Was used to decompose the cell membrane of jellyfish and increase the protein extraction yield.
아래의 표 1에 도시된 바와 같이 해파리에 함유된 단백질을 회수하기 위해서 control(효소무첨가), 단백질 분해효소인 protamex(프로타멕스), alcalase(알카라제), flavourzyme(플라보자임), neutrase(뉴트라제) 효소반응, 지방 분해효소인 lipex(리펙스) 효소반응, 지방 분해효소와 단백질 분해효소를 혼합한 lipex + alcalase(리펙스+ 알카라제), lipex + protamex(리펙스 + 프로타멕스), lipex + flavourzyme(리펙스 + 플라보자임), lipex + neutrase(리펙스 + 뉴트라제) 효소반응을 통해 해파리 단백질 추출결과를 얻게 되었다.As shown in the following Table 1, in order to recover the proteins contained in the jellyfish, a control (no enzyme added), a protease enzyme protamex, an alcalase (alkarase), flavourzyme (flavozyme) (Lipase + protease), lipex + protease (lipase + protease), lipase + protease (lipase + protease), lipase + protease The results of extraction of jellyfish protein were obtained through enzyme reaction of lipex + flavorzyme (lipex + flavosome) and lipex + neutrase (lipase + Nutrage).
즉, 해파리에 다양한 종류의 효소를 이용하여 단백질을 분해 및 추출할 수 있게 되는데, 다양한 종류의 효소 중 알카라제를 이용한 효소반응이 가장 많은 단백질을 회수(추출)할 수 있게 되었다.In other words, it is possible to decompose and extract proteins by using various kinds of enzymes in jellyfish, and it is possible to recover (extract) the protein having the greatest enzymatic reaction using various kinds of enzymes.
따라서, 해파리의 효소 반응에 따른 단백질의 추출 시 알카라제를 이용하여 단백질을 회수하는 것이 가장 바람직하다.Therefore, it is most preferable that the protein is recovered by using an alkalase when extracting the protein according to the enzyme reaction of the jellyfish.
또한, 해파리와 알카라제를 이용한 효소 반응시 알카라제 효소는 해파리 중량 대비 약 1 ~ 3중량%가 되도록 한다.In addition, in the enzyme reaction using jellyfish and alkaline, the alkalase enzyme is about 1 to 3 wt% relative to the weight of jellyfish.
즉, 분말형태의 해파리를 1kg을 사용할 경우 효소는 약 0.01 ~ 0.03kg이 사용되도록 하는 것을 말하는 것이다.That is, when 1 kg of powdery jellyfish is used, about 0.01 ~ 0.03 kg of enzyme is used.
여기서, 상기와 같은 비율로 해파리와 알카라제 효소를 혼합하는 이유는 도 2에 도시된 바와 같이 해파리에 함유된 단백질을 가장 효율적으로 회수할 수 있기 때문이다.Herein, the reason why the jellyfish and the alkaline enzyme are mixed at the above ratio is that the proteins contained in the jellyfish can be recovered most efficiently as shown in FIG.
본 발명의 실시 예에서는 알카라제 효소가 해파리의 중량대비 0%, 1%, 2%, 3%, 4% 첨가하는 것으로 예시한다.In the examples of the present invention, it is exemplified that the alkaline enzyme is added 0%, 1%, 2%, 3% and 4% by weight of jellyfish.
즉, 도 2에 도시된 바와 같이 알카라제 효소 농도가 해파리 중량 대비 1 ~ 3 중량% 일 때, 해파리에서 효율적으로 단백질을 회수할 수 있게 되는데, 가장 바람직하게는 알카라제 효소 농도가 2중량%가 되도록 하는 것이 좋다.That is, as shown in FIG. 2, when the concentration of the alkaline enzyme is 1 to 3 wt% based on the weight of the jellyfish, the protein can be efficiently recovered from the jellyfish. Most preferably, the concentration of the alkaline enzyme is 2 wt% %.
한편, 상기와 같이 팽창과정을 거친 해파리 현탁액에 알카라제 효소를 해파리 분말 중량 대비 2중량%로 첨가한 후, 45 ~ 60℃의 온도에서 1 ~ 3시간 반응시키는 효소분해반응을 실시하도록 한다.Meanwhile, an enzymatic degradation reaction is performed in which the alcalase enzyme is added to the jellyfish suspension which has undergone the expansion process as described above in an amount of 2% by weight based on the weight of the jellyfish powder, and then the reaction is performed at a temperature of 45 to 60 ° C for 1 to 3 hours.
여기서, 해파리를 알카라제 효소에 반응시킬 때, 가장 바람직하게는 약 50℃의 온도에서 반응시키는 것이 좋다.Here, when the jellyfish is reacted with the alkaline enzyme, it is most preferable to conduct the reaction at a temperature of about 50 캜.
또한, 도 3에 도시된 바와 같이 알카라제 효소 농도를 2%가 되도록 하면서 해파리의 알카라제 효소반응을 각각 0, 1, 2, 3, 4시간 수행하여 얻어진 결과를 단백질 회수율로 나타내었다.As shown in FIG. 3, the results obtained by performing the alkaline enzyme reaction of the jellyfish for 0, 1, 2, 3, and 4 hours, respectively, while the alkaline enzyme concentration was adjusted to 2% were expressed as protein recovery rates.
즉, 해파리와 알카라제 효소가 혼합된 혼합액을 약 2시간 정도 반응시켰을 때, 가장 효율적으로 해파리에서 단백질이 추출되었다.That is, when the mixture of the jellyfish and the alkaline enzyme was reacted for about 2 hours, the protein was extracted most efficiently from the jellyfish.
따라서, 해파리의 알카라제 효소에 대한 반응은 알카라제 효소 농도를 2중량%로 하면서, 약 50℃의 온도에서 2시간 정도로 이루어질 때 가장 효율적으로 단백질이 추출되는 것이다.Therefore, the reaction of jellyfish with respect to the alkaline enzyme is most efficiently performed when the concentration of the enzyme is 2% by weight and the temperature is about 2 hours at about 50 캜.
<실시예 6>≪ Example 6 >
한편, 상기 해파리의 알카라제 효소반응 후, 생성된 반응액의 온도를 50℃에서 90 ~ 100℃의 온도로 올리고 5 ~ 20분간 가열하여 알카라제 효소를 실활시키시면서 해파리에 함유된 단백질이 추가로 추출되도록 한다.(S60)Meanwhile, after the reaction of the jellyfish with the alkaline enzyme, the temperature of the resulting reaction solution is raised from 50 to 90 DEG C to 100 DEG C and heated for 5 to 20 minutes to inactivate the alkaline protease, And further extracted (S60)
즉, 50℃의 온도에서 해파리의 알카라제 효소 분해반응을 실시한 후, 반응액을 약 90 ~ 100℃의 온도로 가열하여 알카라제 효소를 실활(활성화 상태를 잃게 되는 현상)시키고 여과하여, 해파리의 찌꺼기(잔여물)가 제거된 단백질 추출액을 획득하도록 한다.That is, after performing the enzymatic digestion reaction of jellyfish with an enzyme at a temperature of 50 캜, the reaction solution is heated to a temperature of about 90 to 100 캜 to inactivate the enzyme (phenomenon that the activated state is lost) Obtain the protein extract from which the jellyfish residue (residue) has been removed.
여기서, 알카라제 효소를 실활시킬 때, 100℃의 온도에서 10분 정도 가열함으로써, 가장 효율적으로 실활이 이루어지도록 하는 것이 바람직하다.Here, when inactivating the alkaline enzyme, it is preferable that the inactivating is performed most efficiently by heating at a temperature of 100 DEG C for about 10 minutes.
한편, 상술한 바와 같은 방법으로 회수한 해파리 단백질 추출액을 동결건조시킴으로써, 해파리 단백질의 주성분인 콜라겐이 필요한 다양한 형태(액체, 고체)의 제품에 원료로 사용하면 되는 것이다.On the other hand, by freeze-drying the recovered jellyfish protein extract by the above-described method, it can be used as a raw material for various types (liquid, solid) products requiring collagen which is a main component of jellyfish protein.
이처럼, 해파리의 건조, 분쇄, 팽창공정과 효소반응공정이 일련의 연속공정으로 이루어진 새로운 해파리 단백질의 추출방법은 단백질 분해효소인 알카라제를 이용함으로써, 해파리에 함유된 단백질을 간단한 공정으로도 높은 수율로 추출할 수 있게 되어, 해파리에서 단백질을 추출하기 위한 시간 및 비용 등의 절감으로 우수한 경제성 및 편리성을 제공할 수 있게 되는 것이다.As described above, the extraction method of a new jellyfish protein consisting of a series of continuous processes of drying, crushing, expanding and enzymatic reaction processes of jellyfish uses a proteinase, an alkaline protease, Therefore, it is possible to provide excellent economical efficiency and convenience by reducing time and cost for extracting protein from jellyfish.
또한, 해파리에서 단백질의 회수 시 분말형태의 해파리를 물에서 가열하여 먼저 입자를 팽창시킨 후 추출하도록 함은 물론, 효소처리로 해파리 조직으로부터 단백질을 잘라내어 수용액에 쉽게 용출되게 함으로써, 해파리에서 단백질이 더욱 용이하게 회수되면서 추출효율을 극대화시킬 수 있게 되는 것이다.In addition, when the protein is recovered from the jellyfish, the jellyfish in the form of powder is heated in water to expand the particles first, and then the protein is cut out from the jellyfish tissue by enzyme treatment and easily eluted into the aqueous solution. The extraction efficiency can be maximized while being easily recovered.
상술한 실시예는 본 발명의 가장 바람직한 예에 대하여 설명한 것이지만, 상기 실시예에만 한정되는 것은 아니며, 본 발명의 기술적 사상을 벗어나지 않는 범위 내에서 다양한 변형이 가능하다는 것은 본 발명이 속하는 기술분야에서 통상의 지식을 가진 자에게 있어서 명백한 것이다.Although the present invention has been described in connection with what is presently considered to be the most practical and preferred embodiment, it is to be understood that the invention is not limited to the disclosed embodiments, but, on the contrary, It is obvious to those who have knowledge of.
Claims (4)
세척, 탈수된 해파리를 열풍건조기를 이용하여 50 ~ 80℃의 온도에서 수분함량이 10% 이내가 되도록 건조하는 건조단계(S20);
건조된 해파리를 100 ~ 500㎛ 크기의 분말형태로 제조하는 분쇄단계(S30);
분말형태의 해파리를 산도가 조정된 증류수에 첨가하고 80 ~ 100℃의 온도에서 1 ~ 3시간 가열하여, 해파리 분말 입자를 팽창시키는 팽창단계(S40);
상기 팽창단계(S40) 이후, 효소를 해파리 분말 중량 대비 2중량% 첨가하고, 45 ~ 60℃의 온도에서 1 ~ 3시간 반응시키는 효소반응단계(S50);
해파리의 효소분해반응 후, 90 ~ 100℃의 온도에서 5 ~ 20분간 가열하여 효소를 실활시키고, 해파리의 잔여물을 제거, 여과하면서 단백질 추출액을 회수하는 회수단계(S60);
로 이루어진 것에 특징이 있는 해파리 단백질의 추출방법.
A preparation step (S10) of washing and dehydrating the jellyfish;
Drying (S20) drying the dehydrated jellyfish at a temperature of 50 to 80 캜 using a hot-air drier to a moisture content of 10% or less;
A pulverizing step (S30) of preparing dried jellyfish in the form of powder having a size of 100 to 500 mu m;
An expansion step (S40) of adding jellyfish in powder form to distilled water adjusted in acidity and heating the jellyfish powder particles at a temperature of 80 to 100 DEG C for 1 to 3 hours;
An enzyme reaction step (S50) of adding 2% by weight of the enzyme to the weight of jellyfish powder after the expansion step (S40) and allowing the enzyme to react at a temperature of 45 to 60 ° C for 1 to 3 hours;
A step (S60) of recovering the protein extract while filtering off the residue of jellyfish and deactivating the enzyme by heating at 90 to 100 ° C. for 5 to 20 minutes after the enzyme decomposition reaction of jellyfish;
Wherein the method comprises the steps of:
The method of claim 1, wherein the jellyfish is dehydrated in a compressed form in the preparation step (S10).
The method of extracting jellyfish protein according to claim 1, wherein the jellyfish powder is mixed in an amount of 1 to 10% by weight based on the weight of distilled water in the expansion step (S40).
The method of extracting jellyfish protein according to claim 1, wherein the enzyme used in the enzyme reaction step (S50) is an alcalase.
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CN111437242A (en) * | 2020-05-07 | 2020-07-24 | 江苏华能药业有限公司 | Crystal mask prepared from jellyfish |
WO2022097843A1 (en) * | 2020-11-05 | 2022-05-12 | 한국식품연구원 | Jellyfish pretreatment method for collagen extraction, and jellyfish collagen extraction method using same |
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CN111437242A (en) * | 2020-05-07 | 2020-07-24 | 江苏华能药业有限公司 | Crystal mask prepared from jellyfish |
WO2022097843A1 (en) * | 2020-11-05 | 2022-05-12 | 한국식품연구원 | Jellyfish pretreatment method for collagen extraction, and jellyfish collagen extraction method using same |
KR20220060743A (en) | 2020-11-05 | 2022-05-12 | 한국식품연구원 | A Jellyfish Pretreatment Method for Collagen Extraction and a Method of Extracting Jellyfish Collagen by Using the Same |
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