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Effects of enzymatic hydrolysis of buckwheat protein on antigenicity and allergenicity

BACKGROUND/OBJECTIVES: Due to its beneficial health effects, use of buckwheat has shown a continuous increase, and concerns regarding the allergic property of buckwheat have also increased. This study was conducted for evaluation of the hydrolytic effects of seven commercial proteases on buckwheat a...

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Autores principales: Sung, Dong-Eun, Lee, Jeongok, Han, Youngshin, Shon, Dong-Hwa, Ahn, Kangmo, Oh, Sangsuk, Do, Jeong-Ryong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Nutrition Society and the Korean Society of Community Nutrition 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058561/
https://www.ncbi.nlm.nih.gov/pubmed/24944772
http://dx.doi.org/10.4162/nrp.2014.8.3.278
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author Sung, Dong-Eun
Lee, Jeongok
Han, Youngshin
Shon, Dong-Hwa
Ahn, Kangmo
Oh, Sangsuk
Do, Jeong-Ryong
author_facet Sung, Dong-Eun
Lee, Jeongok
Han, Youngshin
Shon, Dong-Hwa
Ahn, Kangmo
Oh, Sangsuk
Do, Jeong-Ryong
author_sort Sung, Dong-Eun
collection PubMed
description BACKGROUND/OBJECTIVES: Due to its beneficial health effects, use of buckwheat has shown a continuous increase, and concerns regarding the allergic property of buckwheat have also increased. This study was conducted for evaluation of the hydrolytic effects of seven commercial proteases on buckwheat allergens and its allergenicity. MATERIALS/METHODS: Extracted buckwheat protein was hydrolyzed by seven proteolytic enzymes at individual optimum temperature and pH for four hours. Analysis was then performed using SDS-PAGE, immunoblotting, and competitive inhibition ELISA (ciELISA) with rabbit antiserum to buckwheat protein, and direct ELISA with pooled serum of 21 buckwheat-sensitive patients. RESULTS: Alkaline protease, classified as serine peptidase, was most effective in reducing allergenicity of buckwheat protein. It caused decomposition of the whole buckwheat protein, as shown on SDS-PAGE, and results of immunoblotting showed that the rabbit antiserum to buckwheat protein no longer recognized it as an antigen. Allergenicity showed a decrease of more than 50% when pooled serum of patients was used in ELISA. Two proteolytic enzymes from Aspergillus sp. could not hydrolyze buckwheat allergens effectively, and the allergenicity even appeared to increase. CONCLUSIONS: Serine-type peptidases appeared to show a relatively effective reduction of buckwheat allergenicity. However, the antigenicity measured using rabbit antiserum did not correspond to the allergenicity measured using sera from human patients. Production of less allergenic buckwheat protein may be possible using enzymatic hydrolysis.
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spelling pubmed-40585612014-06-18 Effects of enzymatic hydrolysis of buckwheat protein on antigenicity and allergenicity Sung, Dong-Eun Lee, Jeongok Han, Youngshin Shon, Dong-Hwa Ahn, Kangmo Oh, Sangsuk Do, Jeong-Ryong Nutr Res Pract Original Research BACKGROUND/OBJECTIVES: Due to its beneficial health effects, use of buckwheat has shown a continuous increase, and concerns regarding the allergic property of buckwheat have also increased. This study was conducted for evaluation of the hydrolytic effects of seven commercial proteases on buckwheat allergens and its allergenicity. MATERIALS/METHODS: Extracted buckwheat protein was hydrolyzed by seven proteolytic enzymes at individual optimum temperature and pH for four hours. Analysis was then performed using SDS-PAGE, immunoblotting, and competitive inhibition ELISA (ciELISA) with rabbit antiserum to buckwheat protein, and direct ELISA with pooled serum of 21 buckwheat-sensitive patients. RESULTS: Alkaline protease, classified as serine peptidase, was most effective in reducing allergenicity of buckwheat protein. It caused decomposition of the whole buckwheat protein, as shown on SDS-PAGE, and results of immunoblotting showed that the rabbit antiserum to buckwheat protein no longer recognized it as an antigen. Allergenicity showed a decrease of more than 50% when pooled serum of patients was used in ELISA. Two proteolytic enzymes from Aspergillus sp. could not hydrolyze buckwheat allergens effectively, and the allergenicity even appeared to increase. CONCLUSIONS: Serine-type peptidases appeared to show a relatively effective reduction of buckwheat allergenicity. However, the antigenicity measured using rabbit antiserum did not correspond to the allergenicity measured using sera from human patients. Production of less allergenic buckwheat protein may be possible using enzymatic hydrolysis. The Korean Nutrition Society and the Korean Society of Community Nutrition 2014-06 2014-05-15 /pmc/articles/PMC4058561/ /pubmed/24944772 http://dx.doi.org/10.4162/nrp.2014.8.3.278 Text en ©2014 The Korean Nutrition Society and the Korean Society of Community Nutrition http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Sung, Dong-Eun
Lee, Jeongok
Han, Youngshin
Shon, Dong-Hwa
Ahn, Kangmo
Oh, Sangsuk
Do, Jeong-Ryong
Effects of enzymatic hydrolysis of buckwheat protein on antigenicity and allergenicity
title Effects of enzymatic hydrolysis of buckwheat protein on antigenicity and allergenicity
title_full Effects of enzymatic hydrolysis of buckwheat protein on antigenicity and allergenicity
title_fullStr Effects of enzymatic hydrolysis of buckwheat protein on antigenicity and allergenicity
title_full_unstemmed Effects of enzymatic hydrolysis of buckwheat protein on antigenicity and allergenicity
title_short Effects of enzymatic hydrolysis of buckwheat protein on antigenicity and allergenicity
title_sort effects of enzymatic hydrolysis of buckwheat protein on antigenicity and allergenicity
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058561/
https://www.ncbi.nlm.nih.gov/pubmed/24944772
http://dx.doi.org/10.4162/nrp.2014.8.3.278
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