Please wait a minute...

中国生物工程杂志

China Biotechnology
China Biotechnology  2011, Vol. 31 Issue (01): 61-64    DOI:
    
Detection of Allergen Mustard Components in Food by Real-time Fluorescent PCR
SHAO Juan1, CAO Ji-juan2, LIU Yang2, WANG Chang-wen2, ZHAO Tong-tong2, LI Jing-quan3
1. School of Biological Engineering, Dalian Polytechnic University, Dalian 116034, China;
2. Liaoning Entry-Exit Inspection & Quarantine Bureau, Dalian 16001, China;
3. TaKaRa Biotechnology(Dalian CO., LTD., Dalian 116600, China
Download: HTML   PDF(388KB) HTML
Export: BibTeX | EndNote (RIS)      

Abstract  

Rapid identification of mustard materials in plant raw material products and plant-based foods is essential for effective control of a potential source of Allergen pathogens. A convenient Real-Time fluorescence polymerase chain reaction (PCR)-based assay which allowed detection and identification of a mustard -specific Housekeeping gene sin AI DNA sequence in foodstuffs and food was developed. The experiment results show that: the primers and probes could specific identify three kinds of mustard with 21 kinds of samples. Sensitivities results show that: 1 mg/kg for mustard of foods could be detected. Moreover, the four commercial samples (including mustard seeds) and deep processing of mustard allergen reference material (glucose) were detected and the detection results show that mustard allergen components were detected well.



Key wordsReal-time PCR      Mustard      Allergen      Housekeeping gene     
Received: 10 September 2010      Published: 25 January 2011
ZTFLH:  Q789  
Cite this article:

SHAO Juan, CAO Ji-juan, LIU Yang, WANG Chang-wen, ZHAO Tong-tong, LI Jing-quan. Detection of Allergen Mustard Components in Food by Real-time Fluorescent PCR. China Biotechnology, 2011, 31(01): 61-64.

URL:

https://manu60.magtech.com.cn/biotech/     OR     https://manu60.magtech.com.cn/biotech/Y2011/V31/I01/61


[1] Macdougall C, Etuwewe O. How dangerous is food allergy? Current Paediatrics, 2005, 15(3):228-232.

[2] Rance F. Mustard allergy as a new food allergy. Allergy, 2003, 58(4): 287-288.

[3] Figueroa J, Blanco C, Dumpiérrez A G, et al. Mustard allergy confirmed by double-blind placebo-controlled food challenges: clinical features and cross-reactivity with mugwort pollen and plant-derived food. Allergy, 2005, 60(1):48-55.

[4] 曹际娟,郑秋月,徐扬,等. 实时荧光PCR快速检测食品中致敏原芹菜成分.生物技术通报,2009(增刊):151-153. Cao J J, Zheng Q Y, Xu Y, et al. Biotechnology Bulletin, 2009,Supplement:151-153.

[5] 麻丽丹,曹际娟,高海燕,等. 实时荧光PCR法检测食品中芝麻过敏原成分.食品科学,2009,30(12):213-214. Ma L D, Cao J J, Gao H Y, et al. Food Science, 2009, 30(12): 213-214.

[6] 董微,曹际娟,邱驰,等.实时荧光PCR法检测致敏原鱼成分的研究.安徽农业科学,2009,37(23):10911-10912. Dong W, Cao J J, Qiu C, et al. Journal of Anhui Agri Sci, 2009,37(23): 10911-10912.

[7] Niinimi A, Bjrkstén F, Puukka M, et al. Spice allergy: results of skin prick tests and RAST with spice extracts. Allergy, 1989, 44(1):60-65.

[8] Morisset M, Moneret-Vautrin D A, Maadi F. Prospective study of mustard allergy: first study with double-blind placebo-controlled food challenge trials (24 cases). Allergy, 2003, 58(4):295-299.

[9] Lee P, He?e S L, Taylor S L. Validated sandwich-type ELISA for detection of undeclared mustard residues in foods.The Journal of Allergy and Clinical Immunology, 2008,121(2):185.

[10] Mustor P S, Engdahl-Axelsson C, Svensson U, et al. Detection of celery(Apium graveolens), mustard(Sinapis alba, Brassica juncea, Brassica nigra) and sesame(Sesamum indicum) in food by real-time PCR . European Food Research and Technology, 2008, 226(4):771-778.

[1] LIU Li-yan,LIU Qi-qi,ZHANG Ying,WANG Sheng-qi. The Study of a Novel Nucleic Acid Detection Technology by Double-stranded Probe Real-time PCR[J]. China Biotechnology, 2020, 40(11): 28-34.
[2] LI Fu-wei, ZHANG Shu-ya, REN Shuo, ZHANG Rui-hao, JIANG Yu, GU Shun-zhang, GE Xin, ZHANG Lei, BAO Jian-qiang. Detection of Gadiformes by Real-time PCR Assay[J]. China Biotechnology, 2012, 32(12): 80-85.
[3] SHEN Zi-yue, LV Zhe, QIN Zong-hua, LI Ren-qiang. Applying Pull-down Technique to Study Interactional Proteins with Shrimp Allergen[J]. China Biotechnology, 2012, 32(11): 81-85.
[4] SHEN Zi-yue, LV Zhe, QIN Zong-hua, LI Ren-qiang. Applying Pull-down Technique to Study Interactional Proteins with Shrimp Allergen[J]. China Biotechnology, 2012, 32(11): 81-85.
[5] YI Hai-tao, LIU Fang, XIA Li-xin, YAN Hao, LIU Fei-yang, LI Jian-jie, LIU Zhi-gang. Hypoallergenic Derivatives of the Major Peanut Allergen Ara h 2 Obtained by Rational Sequence Reassembly[J]. China Biotechnology, 2011, 31(7): 54-59.
[6] E Guang-xin, LIU Di, ZHANG Dong-jie, CUI Yu. Cloning, Expression and Polymorphism Analysis of Porcine SRPK3 Gene[J]. China Biotechnology, 2011, 31(03): 46-54.
[7] TANG Ling-ling, SHI Yu-ling, WANG Lu-xia, LI Lin-hai, SUN Zhao-hui, CHEN Li-dan, XU Shao-shan. Clinical Application of Rapid Detection of Pathogen of Gas Gangrene[J]. China Biotechnology, 2010, 30(12): 72-75.
[8] . Development of a Real-time PCR Method to Detect Aspergillus nidulans[J]. China Biotechnology, 2008, 28(10): 95-99.
[9] . Cloning, Sequence analysis and Proeukaryotic Expression of Peroxisomal Membrane Protein Allergen Gene from Chaetomium Globosum[J]. China Biotechnology, 2006, 26(04): 40-45.