食品安全质量检测学报
食品安全質量檢測學報
식품안전질량검측학보
FOOD SAFETY AND QUALITY DETECTION TECHNOLOGY
2014年
4期
1045-1053
,共9页
刘妍妘%曹敏杰%李玉宝%张凌晶%杜翠红%刘光明
劉妍妘%曹敏傑%李玉寶%張凌晶%杜翠紅%劉光明
류연운%조민걸%리옥보%장릉정%두취홍%류광명
大黄鱼鱼卵%过敏原%食品加工方式%模拟胃肠液二相消化%免疫反应性
大黃魚魚卵%過敏原%食品加工方式%模擬胃腸液二相消化%免疫反應性
대황어어란%과민원%식품가공방식%모의위장액이상소화%면역반응성
the roe of large yellow croaker%food allergen%food processing%simulate gastric and intestinal fluid two phase digestion%immunoreactivity
目的:本文以大黄鱼鱼卵为原料,分析比较不同加工方式对大黄鱼鱼卵过敏原及其消化产物免疫反应性的影响。方法采用不同加工方式(美拉德反应、紫外照射、超声联合加热、高温高压)处理鱼卵,制备卵黄蛋白粗提物并进行模拟胃肠液二相消化实验,利用免疫印迹及抑制性 ELISA 方法对粗提物及消化产物中过敏原的IgG/IgE结合活性进行分析。结果分析不同加工方式处理后卵黄蛋白中过敏原的IgG结合活性,结果发现当抗体稀释倍数为4×104时,检测不到美拉德反应产物与抗体发生特异性结合,而经后三种物理加工方式处理后的粗提物均与抗体有不同程度的免疫反应。此外,分析加工处理及其消化产物中过敏原与患者血清的IgE 结合活性,结果显示经不同加工方式处理后,仅有美拉德反应产物的抑制率低于50%;经高温高压处理的粗提物抑制率为65%,但消化后其抑制率降至20%以下。结论在4种不同的加工方式中,美拉德反应能有效地降低大黄鱼鱼卵中过敏原的 IgG/IgE 结合活性,超声联合加热及高温高压处理明显减弱过敏原消化产物的IgE结合活性,紫外照射对过敏原的影响不明显。
目的:本文以大黃魚魚卵為原料,分析比較不同加工方式對大黃魚魚卵過敏原及其消化產物免疫反應性的影響。方法採用不同加工方式(美拉德反應、紫外照射、超聲聯閤加熱、高溫高壓)處理魚卵,製備卵黃蛋白粗提物併進行模擬胃腸液二相消化實驗,利用免疫印跡及抑製性 ELISA 方法對粗提物及消化產物中過敏原的IgG/IgE結閤活性進行分析。結果分析不同加工方式處理後卵黃蛋白中過敏原的IgG結閤活性,結果髮現噹抗體稀釋倍數為4×104時,檢測不到美拉德反應產物與抗體髮生特異性結閤,而經後三種物理加工方式處理後的粗提物均與抗體有不同程度的免疫反應。此外,分析加工處理及其消化產物中過敏原與患者血清的IgE 結閤活性,結果顯示經不同加工方式處理後,僅有美拉德反應產物的抑製率低于50%;經高溫高壓處理的粗提物抑製率為65%,但消化後其抑製率降至20%以下。結論在4種不同的加工方式中,美拉德反應能有效地降低大黃魚魚卵中過敏原的 IgG/IgE 結閤活性,超聲聯閤加熱及高溫高壓處理明顯減弱過敏原消化產物的IgE結閤活性,紫外照射對過敏原的影響不明顯。
목적:본문이대황어어란위원료,분석비교불동가공방식대대황어어란과민원급기소화산물면역반응성적영향。방법채용불동가공방식(미랍덕반응、자외조사、초성연합가열、고온고압)처리어란,제비란황단백조제물병진행모의위장액이상소화실험,이용면역인적급억제성 ELISA 방법대조제물급소화산물중과민원적IgG/IgE결합활성진행분석。결과분석불동가공방식처리후란황단백중과민원적IgG결합활성,결과발현당항체희석배수위4×104시,검측불도미랍덕반응산물여항체발생특이성결합,이경후삼충물리가공방식처리후적조제물균여항체유불동정도적면역반응。차외,분석가공처리급기소화산물중과민원여환자혈청적IgE 결합활성,결과현시경불동가공방식처리후,부유미랍덕반응산물적억제솔저우50%;경고온고압처리적조제물억제솔위65%,단소화후기억제솔강지20%이하。결론재4충불동적가공방식중,미랍덕반응능유효지강저대황어어란중과민원적 IgG/IgE 결합활성,초성연합가열급고온고압처리명현감약과민원소화산물적IgE결합활성,자외조사대과민원적영향불명현。
Objective To analyze and compare the effects of different processing methods on the immu-noreactivity of the roe of large yellow croaker allergen and digestion products. Methods The crude extracts of yolk protein from large yellow croaker were performed to simulate gastric and intestinal fluid two phase digesti on after extracted by 4 different processing methods (Maillard reaction, ultraviolet radiation, ultrasonic-heating, high pressure steaming). Then the IgG/IgE-binding ability of the allergen in crude extracts and digestion prod-ucts was analyzed by Western-blotting and inhibition ELISA methods. Results The IgG-binding ability of the allergen in yolk protein was analyzed after treated by different processing methods. The results showed that it could not be detected the specific binding between Maillard reaction products and antibody, when the antibody was diluted 4×104 times. However, the crude extracts could react with antibody inordinately after treated by 3 physical processing methods. In addition, analyzing the IgE-binding ability of the processed and digested al-lergen with patients’ sera found that only the inhibition ratio of Maillard reaction products was lower than 50%after treated by different processing methods, but its inhibition ratio varied inconspicuously. Nevertheless, the inhibition ratio of the crude extracts treated by high pressure steaming was 65%, while its inhibition ratio dropped to below 20% after digestion. Conclusion In the different processing methods, Maillard reaction could effectively decrease the IgG/IgE-binding ability of the allergen in the roe of large yellow croaker. Ultra-sonic-heating and high pressure steaming could decrease the IgE-binding ability of its digestion products ob-viously, although the IgG/IgE-binding ability of the allergen in large yellow croaker was not decreased. But ul-traviolet radiation had little effect on the immunoreactivity of the allergen.