Abstract
Among food allergens, celery is a frequent cause for adverse food reactions in allergic patients. In this study, the celery allergen protein Api g 1.01 RNA was amplified by RT-PCR and cloned into the pET-32a expression vector. The recombinant plasmid was transformed into E.coli BL21(DE3) pLys for the expression of protein Api g 1.01. Monoclonal antibodies were prepared against the expressed purified Api g 1.01 protein. A sandwich enzyme-linked immunosorbent assay (ELISA) for the detection and quantification of celery soluble proteins in processed foods was developed using the prepared monoclonal antibodies. The developed ELISA had a high specificity, although it showed slight cross-reactivity to carrot. The limit of quantification (LOQ) was 0.28 μg/mL (equivalent to 5.6 μg whole celery protein/g food sample). The recovery ranged from 83 to 115%, whereas coefficients of variation were 6.7–8.9%.
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Acknowledgments
This work was supported by National Natural Science Foundation of P. R. of China (31071552), National Key Technologies R&D Program of Ministry of Science and Technology of P. R. of China (2009BADB9B03, 2011BAK10B03) and Special Fund for Quality Inspection Research in the Public Interest (10-46).
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Wang, H., Li, G., Yuan, F. et al. Detection of the allergenic celery protein component (Api g 1.01) in foods by immunoassay. Eur Food Res Technol 233, 1023–1028 (2011). https://doi.org/10.1007/s00217-011-1597-3
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DOI: https://doi.org/10.1007/s00217-011-1597-3