KR100779270B1 - The method to be microorganism of food packing coated by the alginsan - Google Patents
The method to be microorganism of food packing coated by the alginsan Download PDFInfo
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Abstract
Description
도 1,2,3은 알긴산을 이용한 코팅필름(알긴산 농도: 0.5%, 1%, 4%)1,2,3 is a coating film using alginic acid (alginic acid concentration: 0.5%, 1%, 4%)
도 4,5,6은 알긴산을 이용한 필름에서의 대장균의 생육 및 E. coli O 157: 4,5,6 shows the growth of E. coli and E. coli O 157 in a film using alginic acid:
H7 ATCC 43895의 구분(알긴산 농도: 0.5%, 1%, 1.5%, 2%) Classification of H7 ATCC 43895 (Alginate concentration: 0.5%, 1%, 1.5%, 2%)
도 7, 8은 4℃에서 보존 안정성(도 7: 4℃ 보관 지퍼백 비닐에 알긴산을 7 and 8 show storage stability at 4 ° C. (Fig. 7 shows alginic acid in 4 ° C. storage zipper bag vinyl).
코팅한 필름, 도 8: 4℃ 보관 한 달 후 식품저장용 지퍼백의 비닐) Coated film, Fig. 8: Vinyl in a food storage zipper bag after one month of storage at 4 ℃)
현재까지는 병원성 대장균 검출을 위해 배양법, 면역 분석법, 대장균독소 또는 세포기관 유전자를 근거로 한 시발 체를 이용한 PCR법 등이 이용되고 있으나 첨단 시설, 고가의 장비를 및 재료, 전문인력, 공간적 시간적 요인 등으로 인해 그 제약이 많으므로 신속하면서도 간편한 검출 방법과 기술개발이 절실히 요구되고 있다. 특히, 혈성요독증후군 등의 질병은 아직 특이한 치료약이나 백신의 개발이 아직 이루어지지 않은 실정이기 때문에 판매자 또는 소비자가 실시간으로 병원성 대장균을 검출할 수 있는 포장단위의 검출 방법의 개발이 시급한 실정으로 본 발명은 실 시간으로 식품의 부패 여부를 필름의 상태로 판단할 수 있도록 하여 식품의 안정성, 신선도 판별에 의한 효율적인 관리 및 보전체계를 제공하는 기술이다.To date, the detection of pathogenic E. coli has been carried out using a culture method, an immunoassay method, a PCR method using primers based on E. coli toxin or organelle genes, but advanced facilities, expensive equipment and materials, professional personnel, spatial and temporal factors, etc. Due to the many limitations, rapid and simple detection methods and technology development are urgently required. In particular, since diseases such as hemolytic uremic syndrome have not yet developed specific therapeutic drugs or vaccines, it is urgent to develop a method of detecting a packaging unit capable of detecting pathogenic E. coli in real time by a seller or a consumer. Is a technology that can determine whether the food corruption in real time in the state of the film to provide an efficient management and maintenance system by determining the stability of food, freshness.
본 발명은 친환경소재를 이용한 최적의 코팅 물질을 찾기 위해 친환경 코팅 물질을 검토하기 위하여 점성을 지닌 키토산, 알긴산, 키틴, 콘드로이친, 셀룰로오스, 천연 색소, starch를 각각 또는 한천과 혼합하여 굳힌 다음 점성 및 수분 유지 등 미생물 생육에 적당한 조건을 검토하여 최적의 혼합조건을 확립하였다. 특히 친환경소재 중 알긴산은 미역 다시마와 같은 갈조류의 세포벽 구성성분으로 만누론산과 글루론산을 기본단위로 하는 천연 고분자 다당체이며, 천연 식품첨가물로 사용되고 있다. 키토산과 마찬가지로 생체에 적합성이 아주 뛰어나 지혈제 및 인조장기의 구성체로 이용되고 있다. 대부분의 식물섬유처럼 음전화(-)을 띠고 있어 키토산과 응용할 경우 키토-알긴산이 형성되어 필름의 이용에 효과적으로 관찰되었다.The present invention is hardened by mixing the chitosan, alginic acid, chitin, chondroitin, cellulose, natural pigments, starch with viscous, respectively, in order to examine the eco-friendly coating material in order to find the optimal coating material using eco-friendly materials and then viscous and moisture Optimum mixing conditions were established by examining conditions suitable for the growth of microorganisms such as oils and fats. In particular, alginic acid is a natural macromolecular polysaccharide based on manuronic acid and gluronic acid as a cell wall component of brown algae, such as seaweed kelp, and is used as a natural food additive. Like chitosan, it is very suitable for living organisms and is used as a constituent of hemostatic agents and artificial organs. Like most plant fibers, it has a negative conversion (-). When applied with chitosan, chito-alginic acid is formed and effectively observed in the use of film.
본 발명은 신속하면서 간편히 소비자와 판매자가 병원성 미생물을 식품포장 단위에서 검출할 수 있는 포장 필름의 개발에 초점을 맞추어 연구를 수행하였다. 실험에 사용할 병원성 미생물인 E. coli O 157: H 7 ATCC 43895를 미국 균주은행으로부터 분양받아 생리적 특성 및 병원성을 확인하였다. 필름 형성의 재료로 사용하기 위해 생물자원 유래의 친환경소재와 고분자로써 점성을 형성하여 필름 형성에 용이한 물질인 키틴, 키토산, 알긴산, 셀룰로오스, 전분 등을 선택하였다. 이러한 친환경소재가 식품포장용 코팅필름을 형성하는지 sMAC agar와 혼합하여 그 상태를 관찰하였다. 그 결과 키틴은 수용액 상태로 형성하기가 매우 어려웠고 키토산과 셀룰로오스는 sMAC agar성분과 반응으로 침전 및 응집 현상이 나타나 코팅필름 형성이 어려웠다. 하지만, 알긴산의 경우는 적당한 점성유지 및 sMAC agar와의 조화로 코팅 필름형성이 잘 이루어졌다(도 1, 도 2). 알긴산의 성분을 4% 이상으로 높이면 키토산 및 셀룰로오스처럼 응집반응이 심하게 형성되었다(도 3). 식용색소는 병원성 미생물 또는 그 대사산 물에 의한 색 변화를 관찰하기 위해 필름형태로 위와 동일한 방법으로 만들었다. 콘드로이친은 그 성분 자체가 가지는 고분자성향이 낮아 점도의 형성이 예상한 만큼 일어나지 않아 필름 형성 소재로는 적당하지 않았다. 전분은 점도의 형성에 40% 이상의 많은 양의 시료가 필요하기 때문에 경제적 면에서 적당하지 않았다. 따라서 최종 선택 물질로 알긴산을 선택한 후 이를 필름으로 제조하였다.The present invention has focused on the development of packaging films that enable consumers and sellers to detect pathogenic microorganisms in food packaging units quickly and simply. The pathogenic microorganisms used for the experiment, E. coli O 157: H 7 ATCC 43895, were distributed from the US strain bank and confirmed their physiological characteristics and pathogenicity. In order to use it as a material for film formation, we selected chitin, chitosan, alginic acid, cellulose, starch, etc., which are easy to form films by forming viscous with environmentally friendly materials and polymers derived from biological resources. Whether these eco-friendly materials form a coating film for food packaging was observed by mixing with sMAC agar. As a result, chitin was very difficult to form in aqueous solution, and chitosan and cellulose reacted with the sMAC agar component to precipitate and aggregate, making it difficult to form a coating film. However, in the case of alginic acid, the coating film was well formed in combination with proper viscosity maintenance and sMAC agar (FIGS. 1 and 2). Increasing the component of the alginic acid to more than 4%, such as chitosan and cellulose aggregates were severely formed (Figure 3). Food coloring was made in the same manner as above in the form of a film to observe color changes caused by pathogenic microorganisms or their metabolites. Chondroitin was not suitable as a film-forming material because the formation of viscosity did not occur as expected because of its low polymer tendency. Starch was not economically suitable because a large amount of sample of 40% or more was required to form the viscosity. Therefore, after selecting alginic acid as the final selection material it was made into a film.
병원성 미생물인 E. coli O 157: H 7 ATCC 43895와 대조구 대장균인 E coli KCTC 1682, E. coli Top 10 생육 특성과 색 변화가 알긴산을 이용한 필름에 나타나는지를 확인하기 위해 각각의 미생물을 동일한 필름에 접종한 후 관찰하였다. 그 결과 도 4, 5, 6처럼 E coli O 157: H 7 ATCC 43895의 무색이 옅은 분홍색을 띄는 대조구 대장균과 구별이 되어 E coli O 157: H 7을 구분할 수 있었다. 식용색소를 이용한 실험에서는 균의 성장만 일어날 뿐 병원성 미생물을 구분할 수 있는 차이점이 발견되지 않았다. 그래서 알긴산을 이용한 필름을 실제 식품포장에 이용하는 비닐 백에 spray 분사 방법으로 코팅하였다. 이렇게 형성된 코팅 비닐 백(도 7, 8)에 병원성 대장균을 접종하고 4℃에서의 생육을 관찰하였으나 미생물성장은 이루어 지지 않았다. 코팅된 비닐 백의 안정성을 확인하기 위하여 한 달 동안 4℃에서 상태를 관찰한 결과 처음 필름 형성된 상태와 차이가 없었다. 결론적으로 친환경 소재인 알긴산을 이용한 식품 포장비닐의 코팅은 병원성 미생물인 E coli O 157: H 7 검출을 용이하게 할 뿐만 아니라 이를 통한 환경 및 식품 자체의 오염원의 검출을 용이하게 할 것으로 생각된다.The pathogenic microorganisms E. coli O 157: H 7 ATCC 43895 and the control E. coli E coli KCTC 1682, E. coli Top 10 growth characteristics and color changes were shown on the same film to see if the changes in the alginate film. Observation was made after inoculation. As a result, as shown in Figures 4, 5, 6 E coli O 157: H 7 The colorless of the ATCC 43895 was distinguished from the control E. coli with a light pink color was able to distinguish E coli O 157: H 7. In experiments with food pigments, only the growth of bacteria occurred but no difference was found to distinguish pathogenic microorganisms. Therefore, the film using alginic acid was coated on the plastic bag used for the actual food packaging by spray spraying method. The inoculated Escherichia coli was inoculated into the coated plastic bag (FIGS. 7, 8), and growth was observed at 4 ° C, but microorganism growth was not achieved. In order to confirm the stability of the coated vinyl bag, the state was observed at 4 ° C. for one month, and there was no difference from the state of the film formation. In conclusion, the coating of food packaging vinyl using alginic acid, which is an environmentally friendly material, not only facilitates the detection of pathogenic microorganisms, E coli O 157: H 7, but also facilitates the detection of environmental and food sources.
병원성 대장균 O 157: H 7은 솔비톨을 분해하지 않고 β-D-glucuronidas 효소 활성을 띠지 않고, MUG test음성이며, 44.5℃에서 생육하지 못하고, 병원성과 관련되는 장벽부착인 자(eae A)를 가지고 있고, 베로톡신을 생산한다. 이와 같은 생리활성적 특성을 신속히 검출함으로써 식품의 위생상태 안정성을 판단하고 사전에 예방조치를 취할 수 있고 질병확대를 신속 차단하는 예방효과를 가져온다. 또한, 병원균으로부터 식품오염에 따른 오염과정을 명확히 파악함으로써 축산업 및 식품 생산, 식품위생, 식품가공, 식품 유통 산업의 안전적 지속 가능성을 제시할 수 있다.Escherichia coli O 157: H 7 does not degrade sorbitol, does not have β-D-glucuronidas enzymatic activity, is MUG test negative, does not grow at 44.5 ° C, and has a barrier factor associated with pathogenicity (eae A). And produces verotoxin. By detecting such physiologically active characteristics quickly, it is possible to determine the hygiene state stability of foods and take preventive measures in advance and prevent the disease from expanding rapidly. In addition, by clearly identifying the contamination process caused by food contamination from pathogens, it is possible to suggest safe sustainability of livestock industry, food production, food hygiene, food processing and food distribution industry.
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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KR20000068573A (en) * | 1997-07-16 | 2000-11-25 | 스피겔 잭 | Food Quality Indicator Device |
KR20020066157A (en) * | 2001-02-09 | 2002-08-14 | 박찬훈 | A bio-indicator for monitoring of microbial decomposition |
US20050053640A1 (en) | 2002-09-08 | 2005-03-10 | Hettiarachchy Navam S. | Organic acids incorporated edible antimicrobial films |
WO2005059162A2 (en) | 2003-12-16 | 2005-06-30 | Kimberly-Clark Worldwide, Inc. | Microbial detection and quantification |
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Publication number | Priority date | Publication date | Assignee | Title |
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KR20000068573A (en) * | 1997-07-16 | 2000-11-25 | 스피겔 잭 | Food Quality Indicator Device |
KR20020066157A (en) * | 2001-02-09 | 2002-08-14 | 박찬훈 | A bio-indicator for monitoring of microbial decomposition |
US20050053640A1 (en) | 2002-09-08 | 2005-03-10 | Hettiarachchy Navam S. | Organic acids incorporated edible antimicrobial films |
WO2005059162A2 (en) | 2003-12-16 | 2005-06-30 | Kimberly-Clark Worldwide, Inc. | Microbial detection and quantification |
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