KR20130142697A - Method for manufacturing edible protaetia brevitarsis powder - Google Patents

Method for manufacturing edible protaetia brevitarsis powder Download PDF

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KR20130142697A
KR20130142697A KR1020120066122A KR20120066122A KR20130142697A KR 20130142697 A KR20130142697 A KR 20130142697A KR 1020120066122 A KR1020120066122 A KR 1020120066122A KR 20120066122 A KR20120066122 A KR 20120066122A KR 20130142697 A KR20130142697 A KR 20130142697A
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larvae
powder
white spotted
days
larva
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KR101359507B1 (en
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윤은영
황재삼
구태원
김미애
최영철
권은영
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대한민국(농촌진흥청장)
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    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, 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
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L3/00Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs
    • A23L3/015Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with pressure variation, shock, acceleration or shear stress or cavitation
    • A23L3/0155Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with pressure variation, shock, acceleration or shear stress or cavitation using sub- or super-atmospheric pressures, or pressure variations transmitted by a liquid or gas
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L3/00Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs
    • A23L3/16Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by heating loose unpacked materials
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L3/00Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs
    • A23L3/40Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by drying or kilning; Subsequent reconstitution
    • A23L3/44Freeze-drying
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23PSHAPING OR WORKING OF FOODSTUFFS, NOT FULLY COVERED BY A SINGLE OTHER SUBCLASS
    • A23P10/00Shaping or working of foodstuffs characterised by the products
    • A23P10/40Shaping or working of foodstuffs characterised by the products free-flowing powder or instant powder, i.e. powder which is reconstituted rapidly when liquid is added
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00Food compositions, function of food ingredients or processes for food or foodstuffs
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2300/00Processes
    • A23V2300/31Mechanical treatment

Abstract

The present invention relates to a method for manufacturing edible protaetia brevitarsis larva powder and, more specifically, to a method for manufacturing edible protaetia brevitarsis larva powder including sterilizing, freeze-drying, and crushing processes for protaetia brevitarsis larvae. If the method for manufacturing edible protaetia brevitarsis larva powder is applied to protaetia brevitarsis for food products, the method for manufacturing edible protaetia brevitarsis larva powder can be effectively used to produce food which is hygienic and popular with customers. [Reference numerals] (AA) Powder image;(BB) Sawdust sterilization;(CC) Days of fasting

Description

식용 흰점박이꽃무지 유충 분말의 제조방법{Method for manufacturing edible Protaetia brevitarsis powder}Method for manufacturing edible white spotted flower larvae powder {Method for manufacturing edible Protaetia brevitarsis powder}

본 발명은 식용 흰점박이꽃무지 유충 분말의 제조방법에 관한 것으로, 보다 상세하게는 흰점박이꽃무지 유충을 금식 후 멸균하여 동결건조 및 분쇄하는 단계를 포함하는 식용 흰점박이꽃무지 유충 분말의 제조방법에 관한 것이다.
The present invention relates to a method for preparing edible white spotted flower larvae powder, and more particularly, to a method for producing edible white spotted flower larvae powder including sterilizing and lyophilizing and pulverizing the white spotted flower larvae. It is about.

2010년 곤충산업육성법 시행 후 곤충산업의 영역확대가 필요하나 현재까지 화분매개, 학습, 정서, 천적 및 환경정화 관련 연구는 많이 진행되어 왔으나 실제로 산업을 크게 확대할 수 있는 분야인 식품, 사료, 의약, 생체모방 및 생명공학 등의 연구는 아직 미흡한 실정이다. 현재까지 식품으로 등록된 곤충은 메뚜기와 누에밖에 없으므로 메뚜기와 누에를 제외한 곤충은 식품원료로 인정되지 않아 식용으로 판매가 불가하므로 곤충을 식용으로 판매하기 위해서는 과학적이고 체계적인 연구를 통한 식약청에 식품등록이 시급히 이루어져야 한다. 식품등록이 우선적으로 이루어져야 할 곤충으로는 현재 민간요법으로 이용되고 있으며 대다수의 사육농가가 조성된 곤충을 대상으로 하는 것이 유리하다. After enacting the Insect Industry Promotion Act in 2010, it is necessary to expand the scope of the insect industry, but until now, many researches have been conducted on pollen mediation, learning, emotions, nemesis, and environmental purification. , Research on biomimetics and biotechnology is still inadequate. So far, only insects registered as food are grasshoppers and silkworms, so insects other than grasshoppers and silkworms are not recognized as food ingredients and cannot be sold for food. Should be done. As insects for which food registration should be prioritized, it is currently used as a folk remedy, and it is advantageous to target insects in which most farming farmers are established.

흰점박이꽃무지(white-spotted flower chafer, Protaetia brevitarsis seulensis)는 딱정벌레목 꽃무지과에 속하는 곤충으로써 한국, 일본, 대만, 중국, 유럽에 분포하며 7월 상순부터 출현하며 출현빈도가 가장 높은 시기는 8월 상순이고, 일부 성충으로 월동하는 개체도 있으나 대부분은 3령 유충으로 월동한다. 알, 유충, 번데기, 성충의 시기를 거치는 완전변태를 하는 곤충이며 현재 대량생산하고 있는 사육농가가 형성되어져 있으며, 딱정벌레목에 속하는 유충을 칭하는 “굼벵이”로 불리기도 한다. 흰점박이꽃무지 유충은 <동의보감>에서 “간에서 비롯되는 질병, 즉 간암, 간경화, 간염, 누적된 피로의 해소 등을 포함하여 월경불순, 시력감퇴, 백내장, 금창, 산후풍, 악성종기, 구내염, 파상풍, 중풍 등의 성인병을 치료하는데 효과가 있다”라고 보고되고 있다. 따라서 최근 흰점박이꽃무지를 대상으로 기능성 분석 등을 위한 연구가 활발히 진행되고 있다. White-spotted flower chafer, Protaetia brevitarsis seulensis ) is an insect belonging to the coleoptera of the coleoptera, distributed in Korea, Japan, Taiwan, China, and Europe. It appears from early July, and the highest frequency of emergence is early August, and some adults overwinter. Overwinters as a third-larva larva. Eggs, larvae, chrysalis and adult insects are completely metamorphic through the age of the breeding farming farms, which are now mass-produced, is also called "slugs" of larvae belonging to the coleoptera. The white spotted larvae of the larvae in the agreement agrees with, “Menstrual irregularity, decreased vision, cataracts, gold swelling, postpartum wind, malignant boils, stomatitis, including liver disease, liver cancer, cirrhosis, hepatitis, and the elimination of accumulated fatigue. It is effective in treating adult diseases such as tetanus and stroke. ” Therefore, recently, research for functional analysis on white spotted flower ignorance has been actively conducted.

그러나 곤충의 식품화는 외형적 혐오감 및 유해세균, 악취 등의 문제가 있으므로 이러한 문제를 해결할 수 있는 새로운 가공방법이 필요한 실정이다.However, since the foodization of insects has problems such as external aversion and harmful bacteria, odor, etc., a new processing method is required to solve such problems.

이에 본 발명자들은 식용 흰점박이꽃무지 유충 분말의 제조방법에 대해서 연구한 결과, 세균을 제거한 참나무 발효톱밥을 먹인 흰점박이꽃무지 유충을 금식시킨 후 고온고압 멸균을 실시하여 멸균한 후 동결건조하여 분말을 제조한 결과 미생물도 존재하지 않았고 분말의 색 및 냄새가 좋은 것을 확인하여 본 발명을 완성 하였다.
Therefore, the present inventors studied a method for preparing edible white spotted radish larvae powder, and after fasting the white spotted radish larvae fed with oak fermented sawdust removed bacteria, sterilized by high temperature and high pressure sterilization and then lyophilized to dry powder As a result of the production of microorganisms were not present, and the color and smell of the powder was confirmed to complete the present invention.

따라서, 본 발명의 목적은 식용 흰점박이꽃무지 유충 분말의 제조방법을 제공하는 것이다.
Accordingly, it is an object of the present invention to provide a method for preparing edible white spotted flower larvae powder.

본 발명의 목적을 달성하기 위하여, 본 발명은 (a) 흰점박이꽃무지 유충에게 발효톱밥을 급이하여 사육하는 단계; (b) 상기 (a)단계의 유충을 1 내지 5일간 금식시키는 단계; (c) 상기 (b)단계의 금식시킨 유충을 고온고압 멸균하는 단계 ; (d) 상기 (c)단계의 고온고압 멸균시킨 유충을 동결건조 시키는 단계 ; 및 (e) 상기 (d)단계의 건조시킨 유충을 분쇄하여 분말을 제조하는 단계를 포함하는 것을 특징으로 하는 흰점박이꽃무지 분말의 제조방법을 제공한다.
In order to achieve the object of the present invention, the present invention comprises the steps of breeding the fermented sawdust to white spotted larva larvae; (b) fasting the larva of step (a) for 1 to 5 days; (c) sterilizing the fasted larvae of step (b) at high temperature and high pressure; (d) lyophilizing the high temperature, high pressure sterilized larva of step (c); And (e) pulverizing the dried larva of step (d) to produce a powder.

이하, 본 발명을 상세히 설명한다.
Hereinafter, the present invention will be described in detail.

본 발명의 제조방법은The manufacturing method of the present invention

(a) 흰점박이꽃무지 유충에게 발효톱밥을 급이하여 사육하는 단계;(a) feeding the fermented sawdust to the white spotted radish larvae to breed;

(b) 상기 (a)단계의 유충을 1 내지 5일간 금식시키는 단계; (b) fasting the larva of step (a) for 1 to 5 days;

(c) 상기 (b)단계의 금식시킨 유충을 고온고압 멸균하는 단계; (c) sterilizing the fasting larvae of step (b) at high temperature and high pressure;

(d) 상기 (c)단계의 고온고압 멸균시킨 유충을 동결건조 시키는 단계 ; 및 (d) lyophilizing the high temperature, high pressure sterilized larva of step (c); And

(e) 상기 (d)단계의 건조시킨 유충을 분쇄하여 분말을 제조하는 단계를 포함하는 것을 특징으로 한다.
(e) pulverizing the dried larva of step (d), characterized in that it comprises the step of preparing a powder.

상기 제조방법을 단계별로 설명하면 다음과 같다.
The manufacturing method will be described step by step as follows.

(a) 단계에서는 흰점박이꽃무지 유충에게 발효톱밥을 급이하여 사육한다.In step (a), the fermented sawdust is fed to the white spotted larvae to breed.

본 발명의 흰점박이꽃무지는 딱정벌레목 꽃무지과에 속하는 곤충으로 어떠한 유충도 가능하나 바람직하게는 3령 유충을 사용할 수 있으며, 흰점박이꽃무지에게 급이하는 발효톱밥은 흰점박이꽃무지의 사료로 사용가능한 것이면 어떠한 식물의 것도 가능하나 바람직하게는 참나무를 사용할 수 있다. 또한 상기 발효톱밥은 고온의 증기로 5 내지 10분간 멸균하여 사용할 수 있다. 또한 일정기간 멸균한 발효톱밥 급이를 통하여 장내 미생물을 감소시키고, 곤충 특유의 악취를 감소시킬 수 있다. 급이 기간은 특별히 제한되지 아니하나, 바람직하게는 3 내지 5일 일 수 있다. 3일 미만으로 급이하는 경우 장내 미생물 감소효과가 떨어질 수 있으며, 5일 이상 급이하는 것은 그에 따라 상승하는 감소효과가 미비할 수 있다. 또한 사육환경은 공지의 곤충 사육 환경일 수 있으며, 흰점박이꽃무지가 생존 가능한 조건이면 특별히 제한되지 아니하며 바람직하게는 사육온도는 23 내지 27℃를 유지할 수 있다. The white spotted radish of the present invention is an insect belonging to the coleoptera flowering radish family, but any larvae can be used. Preferably, 3 larvae can be used, and the fermented sawdust fed to the white spotted radish is a feed of white spotted radish. Any plant can be used as long as it can be used, but preferably, oak can be used. In addition, the fermented sawdust may be used by sterilization for 5 to 10 minutes with high temperature steam. In addition, the fermented sawdust feed sterilized for a certain period of time can reduce the intestinal microorganisms, can reduce the odor peculiar to insects. The feeding period is not particularly limited, but may preferably be 3 to 5 days. Feeding less than 3 days may reduce the intestinal microbial reduction effect, and feeding more than 5 days may be insufficient to increase the increase accordingly. In addition, the breeding environment may be a known insect breeding environment, and if the white spotted radish is a viable condition is not particularly limited and preferably breeding temperature can be maintained at 23 to 27 ℃.

본 발명의 일실시예에서는 참나무 발효톱밥을 증기로 쪄서 멸균과정을 거친 후 미생물 존재여부를 확인한 결과 5분간만 쪄도 미생물이 완전히 제거됨을 확인 하였다.In one embodiment of the present invention was steamed oak fermented sawdust after steam sterilization process confirmed that the presence of microorganisms were confirmed that the microorganisms are completely removed even 5 minutes.

본 발명의 다른 일실시예에서는 흰점박이꽃무지는 스머프 곤충나라 영농조합법인(남양주시)에서 구매한 3령 유충을 사용하였으며, 사육온도는 25℃를 유지하였다.
In another embodiment of the present invention, the white spotted flower radish used three larvae purchased from the Smurf Insect Country Farming Corporation (Namyangju), and the breeding temperature was maintained at 25 ℃.

(b) 단계에서는 상기 (a)단계의 유충을 1 내지 5일간 금식시킨다.In step (b), the larva of step (a) is fasted for 1 to 5 days.

상기 금식시키는 과정을 통해 흰점박이꽃무지 유충의 배변을 유도하여 장내 이물질 제거가 가능하다. 상기 금식기간은 바람직하게는 1 내지 5일간 금식시킬 수 있으며, 더 바람직하게는 3 내지 5일간 금식시킬 수 있다. 금식기간이 1일 미만일 경우에는 장 내 이물질이 충분히 제거되지 않을 수 있으며, 5일 이상일 경우 유충이 사망하거나 영양상태가 나빠질 수 있다.Through the fasting process, it is possible to remove the intestinal foreign substances by inducing bowel movement of the white spotted flower larvae. The fasting period is preferably fasting for 1 to 5 days, more preferably 3 to 5 days can be fasting. If the fasting period is less than one day, the intestinal foreign matter may not be sufficiently removed, and if it is more than five days, the larvae may die or the nutrition may deteriorate.

본 발명의 일실시예에서는 흰점박이꽃무지 유충에게 물이나 먹이를 공급하지 않고 1일부터 5일간 굶기면서 배변을 유도하였고, 이 때 변은 빠지고 흰점박이꽃무지는 빠지지 않을 정도의 망을 이용하였다(실시예3 참조).
In one embodiment of the present invention induction of bowel hungry for 1 to 5 days without feeding water or food to the white spotted larva larvae, at this time the stool is missing and the white spotted blotch was used as a net (See Example 3).

(c) 단계에서는 상기 (b)단계의 금식시킨 유충을 고온고압 멸균한다.In step (c), the fasting larvae of step (b) are autoclaved at high temperature.

상기 고온고압 멸균은 가열한 포화수증기로 효소와 조직 단백질의 비가역적인 응고작용과 변성으로 미생물을 살멸시키는 멸균법으로, 온도 및 압력 범위는 일반적인 미생물 멸균을 위한 조건을 사용할 수 있으며 바람직하게는 5 내지 15분 동안 115내지 121℃, 0.9 내지 1.3kgf/㎤이상으로 고온고압 멸균할 수 있다. The high temperature and high pressure sterilization is a sterilization method for killing microorganisms by irreversible coagulation and denaturation of enzymes and tissue proteins with heated saturated steam, and temperature and pressure ranges may be used under conditions for general microorganism sterilization. High temperature and high pressure sterilization at 115-121 ° C., 0.9-1.3 kgf / cm 3 or more, for minutes.

본 발명의 일실시예에서는 유충을 3일간 굶긴 후 115℃, 0.9 kgf/㎤의 고온고압멸균을 5분간 실시하여 멸균한 후 동결건조 하여 제조한 분말이 미생물도 존재하지 않았고 분말의 색 및 냄새가 좋은 것을 확인할 수 있었다(실시예4 참조).
In one embodiment of the present invention, the larvae were starved for 3 days and then sterilized by performing high-temperature sterilization at 115 ° C. and 0.9 kgf / cm 3 for 5 minutes, and the powder prepared by freeze-drying did not contain any microorganisms. Good results could be confirmed (see Example 4).

(d) 단계에서는 상기 (c)단계의 고온고압 멸균시킨 유충을 동결건조 시킨다.In step (d), the high-temperature, high-pressure sterilized larva of step (c) is lyophilized.

상기 동결건조는 수용액이나 물을 포함하는 시료를 동결하고 그 온도의 수증기압 이하로 감압하여 물을 승화시켜 건조하는 방법으로, 온도 및 시간 범위는 일반적인 동결건조를 위한 조건을 사용할 수 있으며 바람직하게는 고온고압 멸균한 유충을 -65 내지 -85℃의 초저온 냉동고에 24 내지 36시간 냉동시킨 후 동결건조기에 약 48 내지 60시간 건조하는 방법을 사용할 수 있다.The lyophilization is a method of freezing a sample containing an aqueous solution or water and subliming the water under reduced pressure below the vapor pressure of the temperature to dry the water. The temperature and time range may be used for general lyophilization, preferably high temperature. The autoclaved larvae may be frozen in an ultra-low temperature freezer at -65 to -85 ° C. for 24 to 36 hours and then dried in a freeze dryer for about 48 to 60 hours.

본 발명의 일실시예에서는 24시간마다 5일간 무작위로 40마리씩 선발한 유충은 초저온(-80℃) 냉동고에 24시간이상 냉동시킨 후 동결건조기에 약 48~60시간 건조하였다(실시예 3참조).
In one embodiment of the present invention, larvae were randomly selected for 40 animals every 5 days for 24 hours and then frozen in an ultra-low temperature (-80 ℃) freezer for 24 hours or more and dried in a freeze dryer for about 48-60 hours (see Example 3). .

(e) 단계에서는 상기 (d)단계의 건조시킨 유충을 분쇄하여 분말을 제조한다.In step (e), the dried larvae of step (d) are ground to prepare a powder.

상기 분쇄공정은 일반적인 분쇄기를 이용한 분쇄공정을 사용할 수 있으며 바람직하게는 깨끗하게 세척이 된 분쇄기에 원형 그대로 건조된 유충을 투입하여 고운 가루분말 형태로 만드는 방법을 사용할 수 있다.The pulverization process may use a pulverization process using a general pulverizer, preferably a method of making a fine powder powder by putting the dried larvae in the original shape into a clean crusher.

본 발명의 일실시예에서는 동결건조기에 약 48~60시간 건조한 유충을 일반 분쇄기를 이용하여 분말을 제조하였다(실시 예 3참조).
In one embodiment of the present invention, the larvae dried for about 48-60 hours to prepare a powder using a general crusher (see Example 3).

본 제조방법에 의하면, 식품에 적용이 가능한 수준의, 악취가 없고 멸균된 흰점박이꽃무지 분말을 효과적으로 생산 할 수 있다.According to the present production method, it is possible to effectively produce odorless sterilized white spotted powder radish powder that can be applied to food.

본 발명의 일실시예에서는 흰점박이꽃무지 분말의 색과 향을 평가하는 관능평가를 실시한 결과 색의 밝기와 냄새의 두가지 평가에서 모두 멸균한 참나무 발효톱밥을 먹인 후 3일 동안 굶긴 샘플이 가장 좋은 평가를 받을 수 있었다.In one embodiment of the present invention, the result of performing a sensory evaluation to evaluate the color and aroma of the white spotted flower radish powder, the sample starved for 3 days after feeding the sterilized oak fermented sawdust in both evaluation of the brightness and smell of color is the best I could be evaluated.

본 발명은 흰점박이꽃무지 유충을 금식 후 멸균하여 동결건조 및 분쇄하는 단계를 포함하는 식용 흰점박이꽃무지 유충 분말의 제조방법을 제공한다. 본 발명의 식용 흰점박이꽃무지 유충 분말의 제조방법은 식품화를 위한 흰점박이꽃무지에 적용할 경우 보다 위생적이고 소비자의 선호도가 높은 식품을 제조하는데 효과적이다.The present invention provides a method for producing an edible white spotted flower larva powder comprising the step of lyophilization and pulverization after fasting white spotted larva larvae. The method of preparing the edible white spotted radish larvae powder of the present invention is effective in producing foods that are more hygienic and higher in consumer preference when applied to white spotted radish for foodization.

도 1은 먹이별 흰점박이꽃무지 유충 분말의 세포독성 측정결과 그래프이다(Cell viability: Raw 264.7 세포 생장률, 참나무발효톱밥: 미생물 배양액으로 발효시킨 참나무 발효톱밥을 급이한 흰점박이꽃무지의 현탁액을 처리한 군, 발효목초: 돈분으로 발효시킨 발효목초를 급이한 흰점박이꽃무지의 현탁액을 처리한 군, 발효볏짚: 자연 발효시킨 발효볏짚을 급이한 흰점박이꽃무지의 현탁액을 처리한 군).
도 2는 발육시기별 흰점박이꽃무지 분말의 세포독성 검정이다(Larva:3령 유충의 처리구에서의 세포독성, Pre-pupa: 용화직전 유충의 처리구에서의 세포독성, Pupa:번데기의 처리구에서의 세포독성).
도 3은 참나무 발효톱밥 멸균조건 설정을 위한 미생물 검사결과 사진이다(사진상의 숫자는 표 1의 Sample No.와 동일하다).
도 4는 흰점박이꽃무지 유충을 굶긴 후 날짜별 배변량(A), 체중(B) 및 길이(C)이다(Weight per larvae: 금식시킨 흰점박이꽃무지유충의 무게, days:흰점박이꽃무지를 굶긴 일수).
도 5는 흰점박이꽃무지 유충을 금식시킨 후 날짜별 장 이미지이다.
도 6은 흰점박이꽃무지 유충을 굶길 때 동일면적(12× 13× 5 cm3) 내 밀도별 생존 두수이다.
도 7은 굶긴 일수에 따른 흰점박이꽃무지 유충 냉동건조분말 색 및 냄새 관능평가(n=20)이다.
도 8은 흰점박이꽃무지 분말 멸균 조건이다.
1 is a graph showing the results of cytotoxicity measurement of white spotted radish larvae powder by food (Cell viability: Raw 264.7 cell growth rate, oak fermented sawdust: suspension of white spotted radish with oak fermented sawdust fermented with microbial culture) Treated group, fermented herb: group treated with suspension of white spotted radish fermented with fermented herb fermented with pig flour, fermented rice straw: group treated with suspension of white spotted radish stewed with natural fermented rice straw ).
Figure 2 is a cytotoxicity assay of white spotted radish powder according to the growth period (Larva: cytotoxicity in the treatment group of 3 larvae, Pre-pupa: cytotoxicity in the treatment group of larva just before soluble, Pupa: in the control group of pupa Cytotoxicity).
Figure 3 is a photograph of microbiological test results for setting oak fermented sawdust sterilization conditions (number in the picture is the same as Sample No. in Table 1).
Figure 4 is the variance (A), weight (B) and length (C) by date after starving white spotted larvae (Weight per larvae: weight of white spotted radish larvae fasted, days: white spotted blouse Starved days).
5 is an image of chapters by date after fasting white spotted larva larvae.
Figure 6 is the number of surviving heads by density in the same area (12 × 13 × 5 cm 3 ) when starving white spotted larvae.
7 is a white spotted larva larva freeze-dried powder color and odor sensory evaluation (n = 20) according to the number of days starved.
Figure 8 is white spotted flower solid powder sterilization conditions.

이하, 본 발명을 실시예에 의해 상세히 설명한다.Hereinafter, the present invention will be described in detail by way of examples.

단, 하기 실시예는 본 발명을 예시하는 것일 뿐, 본 발명의 내용이 하기 실시예에 한정되는 것은 아니다.
However, the following examples are illustrative of the present invention, and the present invention is not limited to the following examples.

<실시예 1>&Lt; Example 1 >

흰점박이꽃무지 사육White spotted flower breeding

흰점박이꽃무지는 스머프 곤충나라 영농조합법인(남양주시)에서 구매한 3령 유충을 사용하였으며, 사육온도는 25℃를 유지하였다. 흰점박이꽃무지 유충의 사육환경은 40 ㎝(가로) × 25 ㎝(세로) × 15 ㎝(높이) 크기의 투명한 곤충사육용기를 이용하여 용기의 2/3정도를 약60~65%의 수분이 함유된 참나무 발효톱밥을 채운 후 유충을 20마리씩 사육하였다.
White spotted radish was used as 3rd larvae purchased from Smurf Insect Country Farming Corporation (Namyangju), and the breeding temperature was maintained at 25 ℃. The breeding environment of white spotted flower larvae is about 40 cm (width) × 25 cm (length) × 15 cm (height) of transparent insect breeding container. After filling the oak fermented sawdust containing 20 larvae were reared.

<실시예 2><Example 2>

흰점박이꽃무지 유충분말의 세포독성 측정Cytotoxicity Measurement of White Spotted Flower Larva Powder

흰점박이꽃무지의 먹이로 발효볏짚을 먹인 집단, 참나무 발효톱밥을 먹인 집단, 발효목초를 먹인 집단으로 크게 3개 군으로 나누어 실험을 진행하였다. 사육방법은 상기 실시예1과 동일하였다.
The experiment was carried out by dividing into three groups: fermented straw straw, oak fermented sawdust, and fermented herb. Breeding method was the same as in Example 1.

<2-1>급이 먹이별 <2-1> star food 흰점박이꽃무지White spotted flower 유충 분말의 현탁액 제조 Preparation of suspension of larvae powder

발효볏짚을 먹인 흰점박이꽃무지 유충과 참나무 발효톱밥을 먹인 흰점박이꽃무지 유충, 발효목초를 먹인 흰점박이꽃무지 유충을 3일 동안 굶긴 후 액체질소를 부어서 급속동결한 다음 영하 80℃의 초저온 냉동고에 24시간동안 동결 시킨 후 동결건조기에서 수분이 완전히 제거될 때까지 건조 시켰다. 이 건조된 분말을 분쇄기로 파쇄하여 가루를 얻은 후 각각 D.W.(멸균수)와 DMSO에 넣은 후 초음파 분쇄기(230 Jule)로 10초간 2회 분쇄 하였다. 분쇄된 분말은 4,500 rpm에서 10분 동안 원심분리 시킨 후 상층액을 회수한 후 0.25 ㎛ 주사기 필터로 여과하였다.
White spotted larva larvae fed with fermented rice straw, white spotted larva larvae fed with oak fermented sawdust, white spotted larva larvae fed fermented herb for 3 days After freezing for 24 hours, the freeze dryer was dried until the moisture was completely removed. The dried powder was crushed with a grinder to obtain powder, and then put into DW (sterile water) and DMSO, respectively, and then pulverized twice with an ultrasonic mill (230 Jule) for 10 seconds. The pulverized powder was centrifuged at 4,500 rpm for 10 minutes and the supernatant was recovered and filtered through a 0.25 μm syringe filter.

<2-2>급이 먹이별 <2-2> star food 흰점박이꽃무지White spotted flower 유충 분말의 현탁액의 세포독성 측정 Cytotoxicity Measurement of Suspension of Larva Powder

흰점박이꽃무지의 대식세포인 Raw 264.7에 대한 독성 효과를 측정하기 위해 세포에 흰점박이꽃무지의 현탁액을 처리하고 24시간 경과시 MTS{3-(4,5-dimethylthiazol-2-yl)-5(3-carboxymethonyphenol)-2- (4-sulfophenyl)-2H-tetrazolium} 시약을 넣고 36℃에서 4시간 더 배양하였다. 배양 후 microplate reader(Beckman, USA)를 이용하여 450 nm에서 흡광도를 측정하였다. To determine the toxic effect on Raw 264.7, the macrophage of white spotted flower radish, cells were treated with suspension of white spotted radish and treated with MTS {3- (4,5-dimethylthiazol-2-yl) -5 after 24 hours. (3-carboxymethonyphenol) -2- (4-sulfophenyl) -2H-tetrazolium} reagent was added and incubated for 4 hours at 36 ° C. After incubation, the absorbance at 450 nm was measured using a microplate reader (Beckman, USA).

그 결과 발효볏짚을 먹인 유충 분말을 멸균수에 녹인 현탁액에서 경미한 독성이 검출되었고, 참나무 발효톱밥과 발효목초를 먹인 경우 세포독성은 없었으므로 가장 저렴하고 널리 사용되고 있는 참나무 발효톱밥으로 사육한 흰점박이꽃무지가 식품화하기에 적합한 것으로 판단되었다(도 1참조). As a result, a mild toxicity was detected in the suspension of larvae powder fed fermented straw and sterile water, and there was no cytotoxicity when oak fermented sawdust and fermented grass were fed. It was judged that ignorance was suitable for foodization (see Fig. 1).

다음으로 발육시기별 흰점박이꽃무지의 세포독성을 확인한 결과 최대성장단계인 3령 유충, 용화직전 유충 및 번데기의 모든 처리구에서 D.W.(멸균수) 및 DMSO를 용매로 사용하여 실험한 모든 처리구는 세포독성을 보이지 않았으며, 특히 D.W.(멸균수)를 용매로 사용하여 실험한 처리구에서는 세포생장이 촉진됨을 확인할 수 있었다. 따라서 실험에 시용한 모든 시기의 흰점박이꽃무지가 식품으로 사용하기에 문제는 없을 것으로 판단되나 용화직전 혹은 번데기 상태의 흰점박이꽃무지는 채취하기도 힘들 뿐만 아니라 판매가격도 유충에 비해 약 1.5배 정도 고가이므로 세포독성이 없고 고서에 약용으로 보고되고 있으며 가격이 저렴하고 구하기 용이한 3령 유충이 식용으로 적합한 것으로 결정하였다(도 2참조).
Next, as a result of confirming the cytotoxicity of white spotted radish according to the developmental stage, all treatments tested using DW (sterile water) and DMSO as solvents in all treatments of the 3rd larvae, larvae and pupae, which were the largest growth stages, were cells There was no toxicity, and especially in the treatment group tested using DW (sterile water) as a solvent, it was confirmed that the growth of cells was promoted. Therefore, the white spotted radish at all times used in the experiment is not a problem to use as food, but the white spotted mussel just before yonghua or chrysalis is difficult to collect and the selling price is about 1.5 times higher than the larvae. Since it is expensive, there is no cytotoxicity, it is reported as a medicinal book in ancient books, and it was determined that the third-larva larvae are cheap and easy to obtain (see FIG. 2).

<< 실시예Example 3>  3>

금식기간에 따른 유충 및 유충분말의 상태 측정Measurement of larvae and larvae powder during fasting period

<3-1> 멸균조건에 따른 <3-1> according to sterilization conditions 사료내In feed 잔류 미생물 측정 Residual Microbial Measurement

흰점박이꽃무지 유충의 장 내 이물질을 제거하기 위하여 배변을 유도하였다. 물이나 먹이를 공급하지 않고 1일부터 5일간 굶기면서 배변을 유도하였고, 이 때 변은 빠지고 흰점박이꽃무지는 빠지지 않을 정도의 망을 이용하였다. 망의 크기는 50 mm× 50 mm였다. 각 개체들은 마리당 5× 2.5× 5 cm3 크기의 공간에서 5일 동안 배변을 유도하였고, 30마리씩 3반복으로 실험을 진행하였다. 24시간마다 각 개체별 무게 및 길이를 측정하고 배변량을 확인하였다. 유충의 정확한 길이 측정을 위해 측정 전 얼음 속에서 약 15~20분 정도 방치해 두었다가 길이를 측정하였다. Bowel movement was induced to remove foreign substances in the gut of white spotted flower larvae. They did not feed the water or feed for 1 to 5 days starving to induce bowel movement. The net size was 50 mm x 50 mm. Each individual is 5 × 2.5 × 5 cm 3 per horse The bowel movement was induced for 5 days in the space of the size, and the experiment was conducted in three repetitions of 30 animals. Every 24 hours, the weight and length of each individual were measured and the bowel movement was checked. In order to measure the length of the larvae, it was left in ice for about 15 to 20 minutes before measuring the length.

한편, 배변에 앞서 흰점박이꽃무지의 먹이로 사용하고 있는 참나무 발효톱밥의 경우에도 미생물을 배합하여 발효시켰으므로 많은 종류의 미생물을 함유하고 있을 것이라 생각되어 참나무 발효톱밥을 증기로 쪄서 멸균과정을 거친 후 미생물 존재여부를 확인하였다. On the other hand, oak fermented sawdust, which is used as food for white spotted radish, was fermented by mixing microorganisms. Therefore, it is thought that it contains many kinds of microorganisms. After the presence of microorganisms was confirmed.

그 결과 표 1에서 보는바와 같이 5분이상 찌는 경우 미생물이 완전히 제거됨을 확인하였다. 따라서 식품으로 동결건조하기 전 3일 이상을 멸균한 참나무 발효톱밥을 먹여서 사육하는 것이 흰점박이꽃무지 체내에 미생물 수를 줄이는데 좋을 것으로 판단되었다(도 3참조). 도 3에 적힌 숫자는 표 1의 Sample No.와 동일하다.
As a result, it was confirmed that the microorganisms were completely removed when steaming for more than 5 minutes as shown in Table 1. Therefore, it was judged that feeding the fermented oak fermented sawdust sterilized for 3 days or more before freeze-drying would be good for reducing the number of microorganisms in the white spotted radish body (see FIG. 3). The numbers shown in FIG. 3 are the same as the Sample No. in Table 1.

<3-2> 금식기간에 따른 유충의 <3-2> Larvae of the Fasting Period 배변량Defecation 측정 Measure

5일간 24시간 간격으로 배변량을 확인한 결과 굶긴 후 1일째에 많은 양의 변을 배설하였고, 2일째부터의 배변량은 상대적으로 적은양임을 확인할 수 있었다(도 4A참조). 이 때 각각 개체의 무게나 길이에 어느 정도의 영향을 미치는지 확인한 결과 굶기는 날짜에 비례하여 무게와 길이가 줄어듬을 확인할 수 있었다(도 4B,C 참조).
As a result of checking the bowel movement at intervals of 24 hours for 5 days, a large amount of feces was excreted on the first day after starvation, and the bowel volume from the second day was confirmed to be a relatively small amount (see FIG. 4A). At this time, as a result of checking how much influence on the weight or length of each individual, it was confirmed that the weight and length decrease in proportion to the starving date (see FIGS. 4B and C).

멸균과정을 거친 후 참나무 발효톱밥 내의 잔류 미생물 측정결과Result of measuring microorganisms in oak fermented sawdust after sterilization Sample
No.
Sample
No.
찌는 시간(분)Steaming time (minutes) 미생물
(cfu/g)
microbe
(cfu / g)
1One ×× 7.5×104 7.5 × 10 4 22 55 -- 33 1010 -- 44 2020 -- 55 3030 --

<3-3> <3-3> 금식일수별Fasting Days 유충의 장내물질 변화 및 유충 행동 특성 관찰 Observation of larvae and larvae behavior

배변을 통하여 장 내 물질이 얼마나 제거가 되었는지 파악하기 위하여 5일간 24시간 마다 굶긴 유충의 장을 해부하였다. 해부 전 얼음 속에서 약 15~20분 정도 방치해 두면 기절한 상태로 몸체가 늘어지게 되는데 그때 해부를 실시하였다. 해부는 유충을 1× PBS에 담근 채 실시하였으며, 장을 적출한 후 바로 1× PBS에 담그어 마르지 않은 상태에서 유충의 장을 관찰하였다. 그 결과 굶긴 후 3일째부터 중장이 깨끗하게 비워진 것을 확인할 수 있었다(도 5참조). 참고로 굶기는 동안 카니발리즘(cannibalism) 여부를 확인하였다. 그 이유는 카니발리즘이 있으면 하나의 용기에 집단으로 흰점박이꽃무지를 넣어서 굶기기가 힘들기 때문이다. 일정면적(12× 13× 5 cm3) 내에 20∼100마리까지 넣어서 5일 동안 굶긴 결과 100마리를 넣어서 밀도가 높은 상태에서 5일 동안 굶기더라도 대부분 생존하는 것으로 보아 카니발리즘이 거의 없는 것으로 사료되어 집단으로 하나의 용기에 넣어서 굶기는 것이 가능한 것으로 판단되었다(도 6참조).
To determine how much intestinal material was removed through bowel movements, the intestines of starved larvae were dissected every 24 hours for 5 days. If left in ice for about 15 to 20 minutes before dissection, the body is stretched in a stunned state. The dissection was carried out while the larvae were soaked in 1 × PBS. After the intestines were extracted, the larvae were immersed in 1 × PBS and dried. As a result, it was confirmed that the lieutenant was emptied from the third day after starving (see Fig. 5). For reference, we checked for carnibalism during hunger. The reason is that if there is carnivalism, it is difficult to starve by putting white spotted flowers in a container. As a result of starving for 5 days in 20 ~ 100 dogs in a certain area (12 × 13 × 5 cm 3 ), 100 dogs were added, and most of them survived for 5 days in high density. It was judged that it was possible to starve in a container (see Fig. 6).

<3-4> <3-4> 금식일수별Fasting Days 유충분말의 관능평가 Sensory Evaluation of Larva Powder

흰점박이꽃무지 유충 식품화를 위하여 제조한 분말을 이용하여 사람의 후각과 시각을 이용한 관능평가를 실시하여 색과 향을 평가하였다. 관능평가의 대상은 20대부터 40대 사이의 남녀를 무작위로 20명을 선발하여 실시하였다. 유충이 지니고 있는 특유의 악취는 주로 먹이와 장 내에 존재하는 물질에서 야기되는 것으로 추정되므로 일반 참나무 발효톱밥과 이를 증기로 쪄서 멸균시킨 참나무 발효톱밥을 각각 먹이로 사용하여 3일 이상 사육한 유충들을 1∼5일간 굶겼다. 24시간마다 5일간 무작위로 40마리씩 선발한 유충은 초저온(-80℃) 냉동고에 24시간이상 냉동시킨 후 동결건조기에 약 48~60시간 건조한 후 일반 가정용 분쇄기를 이용하여 분말을 제조하였고, 이를 이용하여 색과 향을 평가하는 관능평가를 실시하였다. Using the powder prepared for food production of white spotted radish larvae, sensory evaluation using human smell and sight was carried out to evaluate color and aroma. The subjects of sensory evaluation were randomly selected 20 men and women between 20s and 40s. The odors of larvae are presumed to be mainly caused by the substances present in food and intestine. Starved for 5 days. Forty-five larvae were randomly selected for 5 days every 24 hours, frozen in an ultra-low temperature (-80 ℃) freezer for more than 24 hours, and then dried for about 48 to 60 hours in a freeze dryer. Sensory evaluation was performed to evaluate color and aroma.

그 결과 색의 밝기와 냄새의 두가지 평가에서 모두 멸균한 참나무 발효톱밥을 먹인 후 3일 동안 굶긴 샘플이 가장 좋은 평가를 받을 수 있었다. 이상의 결과를 통하여 멸균한 참나무 발효톱밥을 먹인 후 3일 동안 굶기면서 배변을 유도하는 것이 전처리 조건에 가장 적합한 것으로 판단되었다(도 7참조).
As a result, in the two evaluations of color brightness and smell, the samples starved for 3 days after sterile oak fermented sawdust received the best rating. Based on the above results, it was judged that feeding the sterilized oak fermented sawdust and then starving for 3 days was most suitable for pretreatment conditions (see FIG. 7).

<< 실시예Example 4> 4>

유충분말 멸균조건에 따른 잔류 미생물 측정Residual microbial measurement according to sterile powder sterilization conditions

식품으로 이용되는 모든 소재들은 인체에 유해한 세균들이 존재해서는 안되므로 유충이 가지고 있는 세균을 제거하기 위하여 고온고압 멸균을 실시하였다. 고온고압 하에서 유충이 가지고 있는 유효한 물질들이 파괴되는 것을 최소화하기 위하여 몇 가지 조건으로 고온고압 멸균을 수행하였다. 5분 동안 각각 115℃, 0.9 kgf/㎤ 와 121℃, 1.3 kgf/㎤ 으로 고온고압 멸균을 실시한 후 세균 및 진균의 존재여부를 표 2에 표시하였다. 세균확인용 배지로는 LB(Luria-Bertani) 고체배지를 사용하였고, 진균확인용 배지로는 PDA(Potato Dextrose Agar) 고체배지를 이용하였다. 제조한 흰점박이꽃무지 분말을 멸균수에 녹인 후 고체배지에 각각의 시료를 도말하고 세균은 37℃에서 24시간 배양하였고, 진균은 25℃에서 48시간 배양한 후 미생물 존재여부를 확인하였다. All materials used as food should not be harmful to the human body, so high temperature and high pressure sterilization was performed to remove the bacteria larvae. In order to minimize the destruction of the larvae effective substances under high temperature and high pressure, high temperature and high pressure sterilization was performed under several conditions. After high temperature and high pressure sterilization at 115 ° C, 0.9 kgf / cm 3 and 121 ° C, 1.3 kgf / cm 3 for 5 minutes, the presence of bacteria and fungi is shown in Table 2. LB (Luria-Bertani) solid medium was used as a medium for bacteria identification, and PDA (Potato Dextrose Agar) solid medium was used as a medium for fungal identification. After dissolving the prepared white spotted powdered radish powder in sterile water, each sample was smeared on a solid medium and bacteria were incubated at 37 ° C. for 24 hours, and the fungus was incubated at 25 ° C. for 48 hours to confirm the presence of microorganisms.

그 결과 115℃, 0.9 kgf/㎤ 압력을 5분간 처리하면 세균 및 진균이 제거됨을 확인할 수 있었다(도 8참조). 도 8에 적힌 숫자는 표 2의 Sample No.와 동일하다.
As a result, it was confirmed that the bacteria and fungi were removed when the 115 ° C. and 0.9 kgf / cm 3 pressure were treated for 5 minutes (see FIG. 8). The numerals shown in FIG. 8 are the same as the Sample No. in Table 2.

따라서 흰점박이꽃무지 유충을 식품화 하기 위한 전처리 조건으로써 참나무발효톱밥을 먹이로 사육한 3령 유충을 이용하는 것이 세포독성도 없을 뿐만 아니라 경제적임을 확인할 수 있었다. 그리고 분말 전처리 조건으로 증기로 5분 동안 쪄서 세균을 제거한 참나무 발효톱밥을 3일 이상 먹인 유충을 3일간 굶긴 후 115℃, 0.9 kgf/㎤의 고온고압멸균을 5분간 실시하여 멸균한 후 동결건조하여 제조한 분말이 미생물도 존재하지 않았고 분말의 색 및 냄새가 좋은 것을 확인할 수 있었다.
Therefore, it was confirmed that the use of the third-larvae larvae fed with oak fermented sawdust as a pretreatment condition for foodization of white spotted larva larvae was not cytotoxic and economical. The larvae fed with oak fermented sawdust, which had been steamed for 5 minutes with steam under powder pretreatment conditions for 3 days, were starved for 3 days, then sterilized by high temperature and high pressure sterilization at 115 ° C. and 0.9 kgf / cm 3 for 5 minutes, and then lyophilized. It was confirmed that the prepared powder did not have microorganisms and the color and smell of the powder were good.

흰점박이꽃무지White spotted flower 유충에 고온고압  High temperature and high pressure 멸균을 실시한Sterilized 후 세균 및 진균의  Of bacteria and fungi 존재여부Presence Sample
No.
Sample
No.
고온고압멸균High Temperature High Pressure Sterilization 세균
(cfu/g)
Germ
(cfu / g)
진균
(cfu/g)
Fungus
(cfu / g)
1One ×× 2.8×105 2.8 × 10 5 2.3×105 2.3 × 10 5 22 115℃, 0.9 kgf/cm3, 5min115 ° C, 0.9 kgf / cm 3 , 5min -- -- 33 115℃, 0.9 kgf/cm3, 10min115 ° C, 0.9 kgf / cm 3 , 10min -- -- 44 121℃, 1.3 kgf/cm3, 5min121 ° C, 1.3 kgf / cm 3 , 5min -- -- 55 121℃, 1.3 kgf/cm3, 10min121 ° C, 1.3 kgf / cm 3 , 10min -- --

이상 살펴본 바와 같이, 본 발명은 식용 흰점박이꽃무지 유충 분말의 제조방법을 제공한다. 본 발명의 식용 흰점박이꽃무지 유충 분말의 제조방법은 식품화를 위한 흰점박이꽃무지에 적용할 경우 보다 위생적이고 소비자의 선호도가 높은 식품을 제조하는데 효과적으로 사용할 수 있어서 산업상 이용가능성이 크다.As described above, the present invention provides a method for preparing edible white spotted flower larvae powder. The manufacturing method of the edible white spotted radish larvae powder of the present invention can be effectively used to prepare foods with higher hygiene and consumer preference when applied to the white spotted radish for foodization, and thus has high industrial applicability.

Claims (5)

(a) 흰점박이꽃무지 유충에게 발효톱밥을 급이하여 사육하는 단계;
(b) 상기 (a)단계의 유충을 1 내지 5일간 금식시키는 단계;
(c) 상기 (b)단계의 금식시킨 유충을 고온고압 멸균하는 단계;
(d) 상기 (c)단계의 고온고압 멸균시킨 유충을 동결건조 시키는 단계; 및
(e) 상기 (d)단계의 건조시킨 유충을 분쇄하여 분말을 제조하는 단계를 포함하는 것을 특징으로 하는 흰점박이꽃무지 분말의 제조방법.
(a) feeding the fermented sawdust to the white spotted radish larvae to breed;
(b) fasting the larva of step (a) for 1 to 5 days;
(c) sterilizing the fasting larvae of step (b) at high temperature and high pressure;
(d) lyophilizing the high temperature, high pressure sterilized larva of step (c); And
(e) a method of producing white spotted flower radish powder, comprising the step of preparing a powder by pulverizing the dried larva of step (d).
제1항에 있어서, 상기 발효톱밥은 멸균시킨 참나무 발효톱밥인 것을 특징으로 하는 흰점박이꽃무지 분말의 제조방법.
The method of claim 1, wherein the fermented sawdust is sterilized oak fermented sawdust manufacturing method of white spotted flower radish powder.
제1항에 있어서, 상기 사육은 3 내지 5일간 수행되는 것을 특징으로 하는 흰점박이꽃무지 분말의 제조방법.
The method according to claim 1, wherein the breeding is carried out for 3 to 5 days, characterized in that the white spotted flower radish powder.
제1항에 있어서, 상기 동결건조는 동결건조기에서 48 내지 60시간 수행되는 것을 특징으로 하는 흰점박이꽃무지 분말의 제조방법.
The method according to claim 1, wherein the freeze-drying is a method for producing white spotted flower radish powder, characterized in that performed in a freeze dryer for 48 to 60 hours.
제1항에 있어서, 상기 고온고압 멸균은 115내지 121℃, 0.9 내지 1.3kgf/㎤의 조건에서 5내지 15분 동안 수행되는 것을 특징으로 하는 흰점박이꽃무지 분말의 제조방법.The method according to claim 1, wherein the high temperature and high pressure sterilization is carried out at 115 to 121 ° C for 0.9 to 1.3 kgf / cm 3 for 5 to 15 minutes.
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