Effect of processing on the detectability of pecan proteins assessed by immunological and proteomic tools

The present study evaluates the effect of food processing on the antigenicity of pecan proteins as measured by enzyme-linked immunosorbent assay (ELISA). In addition, proteomic tools were used to identify potential pecan markers suitable for confirming the presence of pecan proteins in food and validating new methods developed to detect traces of the commodity. To assess the effects of processing on protein stability and antigenicity, pecan nuts were submitted to heat treatments and extracts were analysed by ELISA, sodium dodecyl sulphate polyacrylamide gel electrophoresis and Western blot. The ELISA method was able to detect pecan traces even after submitting the commodity to rigorous treatments, though these treatments affected the detectability to varying degrees. Proteomic assessment showed that the majority of pecan proteins were matched by homology to walnut proteins, which are more abundantly populated in the protein sequence databases. However, there were a few important exceptions: 7S vicilin, 11S legumin and putative allergen I1, unambiguously identified as pecan in origin. Interestingly, putative allergen I1 offered unique analytical advantages to be used as a pecan marker for validation and confirmation purposes.

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Bibliographic Details
Main Authors: Polenta, Gustavo Alberto, Weber, Dorcas, Godefroy Benrejeb, Samuel, Abbott, Michael
Format: info:ar-repo/semantics/artículo biblioteca
Language:eng
Published: Springer 2011-05-19
Subjects:Pecan, Alérgenos, Pecana, Allergens, Effect of Processing, Pecan Proteins, Immunological Tools, Proteomic Tools, Food Allergens Detection,
Online Access:https://rd.springer.com/article/10.1007/s12161-011-9255-8
http://hdl.handle.net/20.500.12123/5085
https://doi.org/10.1007/s12161-011-9255-8
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spelling oai:localhost:20.500.12123-50852019-05-09T18:36:50Z Effect of processing on the detectability of pecan proteins assessed by immunological and proteomic tools Polenta, Gustavo Alberto Weber, Dorcas Godefroy Benrejeb, Samuel Abbott, Michael Pecan Alérgenos Pecana Allergens Effect of Processing Pecan Proteins Immunological Tools Proteomic Tools Food Allergens Detection The present study evaluates the effect of food processing on the antigenicity of pecan proteins as measured by enzyme-linked immunosorbent assay (ELISA). In addition, proteomic tools were used to identify potential pecan markers suitable for confirming the presence of pecan proteins in food and validating new methods developed to detect traces of the commodity. To assess the effects of processing on protein stability and antigenicity, pecan nuts were submitted to heat treatments and extracts were analysed by ELISA, sodium dodecyl sulphate polyacrylamide gel electrophoresis and Western blot. The ELISA method was able to detect pecan traces even after submitting the commodity to rigorous treatments, though these treatments affected the detectability to varying degrees. Proteomic assessment showed that the majority of pecan proteins were matched by homology to walnut proteins, which are more abundantly populated in the protein sequence databases. However, there were a few important exceptions: 7S vicilin, 11S legumin and putative allergen I1, unambiguously identified as pecan in origin. Interestingly, putative allergen I1 offered unique analytical advantages to be used as a pecan marker for validation and confirmation purposes. Fil: Polenta, Gustavo Alberto. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Tecnología de Alimentos; Argentina. Fil: Weber, Dorcas. Health Canada. Bureau of Chemical Safety; Canada. Fil: Godefroy Benrejeb, Samuel. Health Canada. Bureau of Chemical Safety; Canada. Fil: Abbott, Michael. Health Canada. Bureau of Chemical Safety; Canada. 2019-05-09T18:22:01Z 2019-05-09T18:22:01Z 2011-05-19 info:ar-repo/semantics/artículo info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion https://rd.springer.com/article/10.1007/s12161-011-9255-8 http://hdl.handle.net/20.500.12123/5085 1936-9751 1936-976X (Online) https://doi.org/10.1007/s12161-011-9255-8 eng info:eu-repo/semantics/restrictedAccess application/pdf Springer Food analytical methods 5 (2) : 216–225. (April 2012)
institution INTA AR
collection DSpace
country Argentina
countrycode AR
component Bibliográfico
access En linea
databasecode dig-inta-ar
tag biblioteca
region America del Sur
libraryname Biblioteca Central del INTA Argentina
language eng
topic Pecan
Alérgenos
Pecana
Allergens
Effect of Processing
Pecan Proteins
Immunological Tools
Proteomic Tools
Food Allergens Detection
Pecan
Alérgenos
Pecana
Allergens
Effect of Processing
Pecan Proteins
Immunological Tools
Proteomic Tools
Food Allergens Detection
spellingShingle Pecan
Alérgenos
Pecana
Allergens
Effect of Processing
Pecan Proteins
Immunological Tools
Proteomic Tools
Food Allergens Detection
Pecan
Alérgenos
Pecana
Allergens
Effect of Processing
Pecan Proteins
Immunological Tools
Proteomic Tools
Food Allergens Detection
Polenta, Gustavo Alberto
Weber, Dorcas
Godefroy Benrejeb, Samuel
Abbott, Michael
Effect of processing on the detectability of pecan proteins assessed by immunological and proteomic tools
description The present study evaluates the effect of food processing on the antigenicity of pecan proteins as measured by enzyme-linked immunosorbent assay (ELISA). In addition, proteomic tools were used to identify potential pecan markers suitable for confirming the presence of pecan proteins in food and validating new methods developed to detect traces of the commodity. To assess the effects of processing on protein stability and antigenicity, pecan nuts were submitted to heat treatments and extracts were analysed by ELISA, sodium dodecyl sulphate polyacrylamide gel electrophoresis and Western blot. The ELISA method was able to detect pecan traces even after submitting the commodity to rigorous treatments, though these treatments affected the detectability to varying degrees. Proteomic assessment showed that the majority of pecan proteins were matched by homology to walnut proteins, which are more abundantly populated in the protein sequence databases. However, there were a few important exceptions: 7S vicilin, 11S legumin and putative allergen I1, unambiguously identified as pecan in origin. Interestingly, putative allergen I1 offered unique analytical advantages to be used as a pecan marker for validation and confirmation purposes.
format info:ar-repo/semantics/artículo
topic_facet Pecan
Alérgenos
Pecana
Allergens
Effect of Processing
Pecan Proteins
Immunological Tools
Proteomic Tools
Food Allergens Detection
author Polenta, Gustavo Alberto
Weber, Dorcas
Godefroy Benrejeb, Samuel
Abbott, Michael
author_facet Polenta, Gustavo Alberto
Weber, Dorcas
Godefroy Benrejeb, Samuel
Abbott, Michael
author_sort Polenta, Gustavo Alberto
title Effect of processing on the detectability of pecan proteins assessed by immunological and proteomic tools
title_short Effect of processing on the detectability of pecan proteins assessed by immunological and proteomic tools
title_full Effect of processing on the detectability of pecan proteins assessed by immunological and proteomic tools
title_fullStr Effect of processing on the detectability of pecan proteins assessed by immunological and proteomic tools
title_full_unstemmed Effect of processing on the detectability of pecan proteins assessed by immunological and proteomic tools
title_sort effect of processing on the detectability of pecan proteins assessed by immunological and proteomic tools
publisher Springer
publishDate 2011-05-19
url https://rd.springer.com/article/10.1007/s12161-011-9255-8
http://hdl.handle.net/20.500.12123/5085
https://doi.org/10.1007/s12161-011-9255-8
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