낫또(natto)는 일본의 전통 콩 발효식품으로 혈전용해, 면역증강, 항고혈압, 항비만, 항균, 항산화, 항당뇨등의 다양한 효과를 가지고 있어 소비가 점차 증가하고 있다. 그러나, 낫또용으로 이용되는 콩 품종의 성숙 종실에는 소화 불량, 알러지 유발 및 가공 적성을 저하시키는 P34, lectin, Kunitz Trypsin Inhibitor (KTI), 7S α′subunit 및 lipoxygenase 단백질과 같은 항영양성분도 포함되어져 있다. 따라서, 본 연구는 이러한 성분에 대하여 penta null 유전자형(p34leticgy1lox1lox2lox3)을 가지면서 종자 크기가 중소립이고 노란색 종피와 제색이 노란 또는 옅은 갈색을 가진 낫또용 콩 계통을 육성하기 위하여 진행되었다. 64 및 22C1 모본과의 교배를 통하여 제색이 노란 및 옅은 갈색이면서 종자 크기가 소립인 81개의 F2 종자가 선발되었고 그 중에서, P34 단백질 함량이 매우 낮은 18개의 F2 종자가 선발되었다. 18개의 F2 종자로부터 초형, 성숙기, 종피색, 제색 및 백립중이 양호한 2개의 F2 개체(BL1 및 BL2)가 최종 선발되었다. BL1 선발 개체의 성숙기는 중간이었고 종피색은 노란색이며 제색은 연한 갈색을 보였고 백립중은 12.4g으로 소립이었다. BL2 선발 개체는 성숙기가 조생이었고 종피색과 제색은 모두 노란색은 보였으며 백립중은 12.6g으로 소립이었다. 선발된 두 개체는 모두 대표적인 항영양성분인 P34, lectin, KTI, 7S α′subunit 및 lipoxygenase 단백질에 대하여 모두 열성인 penta null 유전자형(p34leticgy1lox1lox2lox3)을 가진 것으로 확인되었다. 선발 개체는 낫또용 콩 품종으로 육성될 수 있을 것으로 사료되었다.

콩 종실에는 레시틴, 아이소플라본, 사포닌, 루테인, 안토시아닌 및 플라보노이드와 같은 생리활성 성분과 약 40%의 단백질이 들어 있어 최근 식물성 대체 단백질의 주요 재료로 이용성이 점차 증가되고 있다. 그러나 lipoxygenase, Kunitz Trypsin Inhibitor (KTI), lectin, 7Sα′subunit 단백질 및 stachyose와 같은 알레르기를 유발시키고 품질 및 기능성을 저하시키는 성분들도 존재한다. 본 연구는 갈색 종피와 penta null 유전자형 (lox1lox2lox3tilecgy1rs2)을 가져 성숙 종실에서 lipoxygenase, KTI, lectin 및 7Sα′subunit의 4가지 단백질이 모두 없으면서 stachyose의 함량이 매우 낮은 콩 계통을 육성하기 위하여 진행되었다. 5개의 자원을 이용하여 창성된 육종집단으로부터 갈색 종피와 penta null 유전자형을 가진 6개의 F2 종자가 선발되었다. 농업형질이 양호한 계통을 선발하여 F7 계통에서 lipoxygenase, KTI, lectin 및 7Sα' subunit의 4가지 단백질에 대한 부재를 확인하였다. 선발계통은 갈색종피와 자주색 꽃 및 유한신육형이며 배꼽색은 흰색이고 성숙 자엽색은 노란색이었다. 선발계통의 경장은 68cm 정도이며 백립중은 29.2g으로 대립이었고 stachyose의 함량은 3.8g/kg으로 매우 낮았으며 수량은 2.75ton/ha 정도였다. 선발된 계통은 성숙 콩 종실에서 콩 가공적성과 품질 및 기능성을 저하시키는 lipoxygenase, KTI, lectin 및 7Sα′subunit의 4가지 단백질이 모두 없으면서 난소화성 당으로 알려진 stachyose의 함량이 매우 낮은 유색콩 품종 및 중간모본으로 이용될 수 있을 것으로 사료되었다.

Food allergy is a chronic disease that is increasing all over the world, and it can even lead to a loss of life. To prevent any incidents resulting from food allergies, most countries keep strengthening their food allergen labeling requirements domestically and internationally, with a constant monitoring system against undeclared allergens and recall of offending products. In order to avoid economic losses to industry and damages to international relations from undeclared allergens, it is necessary to confirm each country’s regulatory policy on food allergen labeling prior to exportation. Another required action is to try for a reduction of the cross-contamination risk of the allergens during manufacturing and storage, which should be verified by using an accurate and reliable analysis of food allergens. This paper is intended to provide an introduction to the regulation of food allergen labeling by country, allergen management methods to avoid cross-contamination, and allergen detection methods using ELISA, PCR, and LC/ MS. Changes of allergenicity during thermal or nonthermal processing also will be investigated in our review. This review will be helpful for the food industry to better understand patients suffering from food allergies and to manage food allergens in food manufacturing.

The purpose of this study was to develop an indirect enzyme-linked immunosorbent assay (indirect ELISA) based on a monoclonal antibody (MAb) that is specific to mackerel thermal stable-soluble protein (TSSP), that can be used for the rapid detection of mackerel in processed marine foods. Among the four MAbs (3A5-1, 2, 9, and 12) developed in previous studies, the 3A5-2 MAb that showed high specificity and sensitivity were selected and used to develop the indirect ELISA method. The detection range of the indirect ELISA was 0.02%-0.001% and the detection limit of 0.001% was shown. No cross-reaction to other marine products and food ingredients was observed by the indirect ELISA. Processed marine foods containing mackerel with ≥ 0.3 O.D. value at 405 nm were estimated as positive samples by the indirect ELISA. Therefore, the indirect ELISA can be used as a rapid and sensitive method to identify mackerel authenticity and adulteration in processed marine foods.

An importance of food allergen detection has been growing in food industry. Here, we developed a rapid and easy-to-use detection system for Ara h1, a major allergen in peanut, using gold nanoparticles and switchable linkers. The detection system was performed by two steps. In the first step, Ara h1 was mixed with various concentrations (0.2 - 1.0μg/mL) of biotinylated anti-Ara h1 antibody (i.e., switchable linker, SLs) solutions for 20 min. After mixing, streptavidin coated gold nanoparticle (Abs. 4.0) was added to the mixture solutions with agitation for10 min. Without Ara h1(control), the region of aggregation caused by quantitative relationship between SLs and gold nanoparticle was observed at more than 0.4 μg/mL of SLs. However, under presence of Ara h1, SLs covered with Ara h1 had less ability to react with gold nanoparticles than naked SLs. This resulted in a change of the quantitative relationship mentioned above, which led to shift of the aggregation region. When 10 nM and 40 nM of Ara h1 were added, the aggregation region was appeared from 0.5and 0.8 μg/mLof switchable linkers, respectively. Ara h1 in peanut sample was also detected with this system. 0.4 μg/mL of switchable linkers are mixed with serially diluted peanut extract solutions. As a result, the shift of the aggregation region was observed from undiluted extract to 10 -2 diluted solution. This system could be adapted to detect other harmful/useful bio materials in food.

Canine atopic dermatitis (CAD) is an allergic skin disease with characteristic clinical features associated with immunoglobulin E (IgE) antibodies. Identification of the causative allergens is the diagnostic goal, which is essential to treat and manage CAD patients. CAD is commonly associated with environmental allergens surrounding the patients. For this reason, it is important for diagnostic tests to select allergens that are related to the environment of each country and each province. There are two main allergen-specific tests, serological IgE test (SAT) and intradermal skin test (IDT). SAT did not show direct cutaneous reaction but did show serological reaction against allergens. However, SAT is simpler and more convenient than IDT in small animal practice. In this study, we selected domestically prevalent allergens for SAT, including 60 food allergens and 60 inhalant allergens, and tested eight dogs tentatively diagnosed with CAD based on Favrot’s criteria. Furthermore, IDT was performed on four dogs from the SAT group for comparison of SAT and IDT, and the results were very similar. In SAT, four types of mites (Bloomia tropicalis, Glycophagus domesticus, Euroglyphus maynei, and mite mixture 1 Korea; house dust mites), four types of molds (Botrytis cinerea, Alternaria alternata, mold fungi mixture 11, mold fungi mixture), and one type of pollen (tree pollen mix 3 Korea) induced a reaction in more than half of dogs tested. In IDT, all four dogs reacted positively to Dermatophagoides farinae, and three reacted positively to Dermatophagoides pteronyssinus and house dust. The mean agreement rate between SAT and IDT in this study was 76.3%. This is the first trial to apply local allergens for SAT in Korean veterinary medicine, and it might play an important role for diagnoses and management of animal allergic diseases.

This study was conducted to analyze dust mite allergen and bacterial endotoxin concentrations in the subwaycabins. For this aim, we sampled dust using a vacuum cleaner on cabin seats of subway trains operating in threeSeoul Metro Lines from April to May in 2011. The concentration of dust mite allergen and endotoxin were1,137.51±806.26ng/g and 5,742.1(4.68)EU/g, respectively. While, the concentration of dust mite allergen washigher on cabin seats of subway trains in Line B(1,487.61±930.59ng/g) than on those of trains in Lines A andC(641.9±398.3 and 1,344.9±822.4ng/g). All measurements did not exceed the National Workshop Guidelineof 2,000ng/g. While, bacterial endotoxin concentration [GM (GSD)] was higher on cabin seats of subway trainsin Line A [12,373.21(4.97EU/g)] than on those of trains in Line B and C8,520.77(3.98) and 1,631.43(1.88)EU/g. Dust mite allergen concentrations were strongly influenced by the portion of underground (on the subway line)and endotoxin concentrations were significantly correlated with the number of passengers using the subway lines.Seats for seniors and the week showed relatively higher concentrations compared to seats for general passengers.But, no significant difference of dust mite allergen and endotoxin concentrations in the subway cabins was foundrelating to seat type (p=0.451, p=0.564). There was no correlation between the dust mite allergen levels andendotoxin levels in the subway cabins (p=0.439).

본 연구에서는 분자생물학적 방법을 통한 알레르기 유발 원재료 확인을 위해 PCR방법의 최적 조건을 구축하였 다. 가공식품에서 알레르기 원료성분 확인을 위하여 200bp 내외의 PCR 산물을 생성할 수 있는 종특이 프라이머를 설계하거나 선행연구사업 결과를 활용하였다. 대상 원료로는 국내 식품알레르기 표시대상인 난류, 우유, 메밀, 땅 콩, 대두, 밀, 고등어, 게, 새우, 돼지고기, 복숭아 및 토마 토와 제외국에서 알레르기 유발 성분으로 규정하고있는 아몬드, 참깨를 포함하여 총 14종을 대상으로 하였다. 특이 프라이머를 사용하여 PCR 한 결과 난류, 우유, 메밀, 땅콩, 대두, 밀, 고등어, 게, 새우, 돼지고기, 복숭아, 토마토, 아몬드 및 참깨로부터 각각 281, 131, 138, 120, 118, 127, 211, 174, 231, 138, 174, 132, 103 및 220bp의 특이 밴드를 확인하였으며 상호간의 비특이적 밴드는 검출되 지 않았다. 본 연구에서 확립한 알레르기 유발 원재료 검출법은 식품의 부정확한 표시나 가공식품의 제조과정 중 알레르기 유발물질의 비의도적 혼입 등으로부터 소비자를 보호하고 향후 수출 제품에 있어서 정확한 알레르기 유발 원재료 표기에 활용이 가능할 것으로 판단된다.

Buckwheat (Fagopyrum esculentum) is one of the traditional crops and there is a growing global attention as a healthy food because of its rich nutrition. Buckwheat allergy is an IgE mediated immediate-type reaction and it is considered to be a critical allergen because it causes severe allergic reactions by small amount of intake particularly in children. In this issue of Buckwheat allergy, research papers about various topics - major allergens of buckwheat, clinical reports, detection methods and methods to reduce allergenic reaction - were reviewed. Major buckwheat allergens reported and listed on IUIS are Fag e 1 with molecular weight 24 kDa, Fag e 2 with molecular weight 16 kDa and Fag e 3 with molecular weight 19 kDa. PCR and ELISA methods have been used to detect buckwheat allergens. Recently, the LC/MS method has been developed to apply to detect buckwheat allergens. In addition to detection methods development, there have been efforts to reduce buckwheat allergens using chemical and/or physical methods, but not commercialized yet.

Venom allergen-like protein 2 (Vap2) was characterized from the pinewood nematode, Bursaphelenchus xylophilus, which is a destructive pathogen in several countries including Japan, China and Korea. Among three vaps of B. xylophilus (Bx-vap)reported in GenBank, Bx-vap2 showed the highest transcript level in both pine-grown propagative stage (PGPS) and media-grown propagative stage (MGPS). Bx-vap2 also was revealed that its transcript level over 10-fold increased in PGPS. In addition, western blot using BxVap2-polyclonal antibody showed that expression level of BxVap2 was significantly increased in PGPS. In immunohistochemistry, moreover, strong signals were detected around putative subventral gland in PGPS, whereas weak signals were observed in MGPS. These experimental results suppose pathogenic function of BxVap2 and migration assay using Bx-vap2 knock-down worms by RNA interference supports this postulation.

The American house dust mite, Dermatophagoides farinae Hughes, is the most important factor of allergic diseases, such as atopic dermatitis, rhinitis, and asthma. The protein-denaturing activity of nerolidol (1), chrysin (2), and spathulenol (3) identified in the Brazilian propolis against D. farinae was evaluated using SDS-PAGE and dot-blot immunoassay. Results were compared with those of the currently available dust mite protein-denaturing agent tannic acid. SDS-PAGE showed that application of test compounds and tannic acid (100 μg each) caused complete disappearance of D. farinae protein bands. In a dot-blot immunoassay, test compounds and tannic acid (100 μg each) strongly inhibited the IgE-binding reactivity to D. farinae protein of a highly mite-sensitive asthmatic patient. The Brazilian propolis constituents described merit further study as potential dust mite-allergen denaturants for protection from humans from various diseases caused by house dust mites.

House dust mites (HDMs) play an important role in the occurrence of allergic diseases such as asthma and atopic dermatitis. Dermatophagoides pteronyssinus (Der p) is one of the most prevalent HDMs. It mediates the activation of T cells and monocytes, and induces the elevation of immunoglobulin E levels in allergic diseases. However, the effects of Der p on human monocytes have not been fully understood. In the present study, we investigated whether or not Der p has a great effect on the chemotactic activity of the human monocytic cell line, THP-1 cells, as induced by CC chemokines. We also show that the Der p extract (DpE) increased the chemotactic activity of THP-1 cells in response to MCP-1, RANTES, MIP-1α, and TARC, but has no effect on the expressions of CC chemokine receptors (CCRs) binding to CC chemokines in THP-1 cells. Protease inhibitors, such as aprotinin and E64, blocked the increased chemotaxis, while cytoplasmic Ca2+ influx mediated by these chemokines was inhibited by DpE. These results indicate that DpE increases the chemotactic activity of THP-1 cells in response to CC chemokines by regulating the cells’ protease-dependent mechanism. This finding may be useful in identifying the pathogenesis of allergic diseases induced by Der p.

This study was followed up asthma incidence rate in primary schools indoor air quality. To investigate the history and prevalence rate of allergic diseases(asthma, atopy dermatitis, allergic rhinitis and conjunctivitis), the standardized and generally used International Study of Asthma and Allergies in Childhood(ISAAC) questionnaire was used to conduct the symptom survey for all participating subjects. The concentrations of major indoor air pollutants(dust mite allergen, aldehydes , VOCs, TBC, phthalate) were observed from April to May 2007. Sampling was undertaken at 19 primary schools. The sampling sites of air pollutants are classroom’s indoor and hallway. Dust mite allergen part it was detected from the case classroom and infirmary. The exposure quality of aldehyde and the place pollution level was indoor>outdoor>hallway, which whole is disease incidence rate high group appears more highly the low group than. The partially result of formaldehy and VOCs, the concentration of high environmental disease incidence rate showed also high. However, house dust allergen, TBC and phthalate measurement school was not the effect where the comparison of difference.

This study was performed to investigate airborne volatile organic compounds(VOCs), formaldehyde, respiratory particulate for concentration in primary schools. The concentrations of major indoor air pollutants(VOCs , benzene, toluene, ethylbenzene, xylene, styrene, formaldehyde, PM-10) were observed from November to December 2006. Sampling was undertaken at 81 primary schools. The sampling sites of air pollutants are classroom and hallway. VOCs with distribution of most of general environmental contamination material will be able to confirm that it shows the log-normal distribution which is similar exposure distribution. The exposure quality of VOCs and the place pollution level was indoor> hallway>outdoor, which whole is located in the metropolis and the industrial areas is higher than farm village area. It tried to observe the I/O ratio, it appeared highly from the interior of the material of most. The mean concentrations of formaldehyde, respiratory particulate were 22.07㎍/㎥, 88.06㎍/㎥ respectively. Indoor and outdoor ratios(I/O) of formaldehyde and respiratory particulate were 3.6 and 1.4, respectively. The concentration of respiratory particulate is 27.2% higher than guideline for school hygiene(100㎍/㎥). From the comparison in the construction year, the highest concentration of formaldehyde is showed under one year. However, as time passed by the concentrations of formaldehyde become lower.

Increased total IgE and eosinophil count levels are thought to provoke the occurrence of urticaria. The purpose of this study is to measure serum total IgE levels, specific IgE sensitization rates, and blood eosinophil count and to investigate the relationship between those factors. Among children who visited the Department of Pediatrics at Chosun University Hospital from January 2011 to December 2013, we retrospectively analyzed 63 patients with acute urticaria. Positive rates of the total serum IgE level, specific IgE, and blood eosinophil count were analyzed in patients with acute urticaria. A total of 63 patients were included in the study and the rate of males to females was 1: 0.8. Mean age of patients was 6.41±4.97 years (range 0-17 years). Among the subjects, 42.9% of patients showed an elevated serum total IgE and 63.5% of patients showed at least more than one allergen-specific IgE by MAST (multiple allergosorbent test). The mean number of allergens detected in positive patients was 2.42±2.56/patient. The serum total IgE and allergen specific IgE showed significant positive correlation (OR = 0.290, p=0.02). This study is meaningful as it revealed a positive correlation between serum total IgE and allergen specific IgE in urticaria patients.

Soybean proteins are widely used for human and animal feeds worldwide. The use of soybean protein has been expanded in the food industry due to their excellent nutritional benefits. But, antinutritional and allergenic factors are present in the raw mature soybean. P34 protein, referred as Gly m Bd 30K, has been identified as a predominant immunodominant allergen. The objective of this research is to identify the genetic mode of P34 protein for the improvement of soybean cultivar with a very low level of P34 protein. Two F2 populations were developed from the cross of "Pungsannamulkong" x PI567476 and "Gaechuck2ho" x PI567476 (very low level of P34 protein). Relative amount of P34 protein was observed by Western blot analysis. The observed data for the progeny of "Pungsannamulkong" and PI567476 were 133 seeds with normal content of P34 protein and 35 seeds with very low level of P34 protein (X2=1.157, P=0.20-0.30). For the progeny of "Gaechuck#1" and PI567476, the observed data were 177 seeds with normal content of P34 protein and 73 seeds with very low level of P34 protein (X2=2.353, P=0.10-0.20). From pooled data, observed data were 310 seeds with normal content of P34 protein and 108 seeds with very low level of P34 protein (X2=0.156, P=0.50-0.70). The segregation ratio (3:1) and the Chi-square value obtained from the two populations suggested that P34 protein in mature soybean seed is controlled by a single major gene. Single gene inheritance of P34 protein was confirmed in 32 F2 derived lines in F3 seeds, which were germinated from the low level of P34 protein obtained from the cross of "Pungsannamulkong" and PI567476. These results may provide valuable information to breed for new soybean line with low level of P34 protein and identification of molecular markers linked to P34 locus.