用于水解小麦粉变应原蛋白的乳酸菌菌株的筛选

Selection of lactic acid bacteria strains for the hydrolysis of allergenic proteins of wheat flour.

作者信息

Stefańska Ilona, Piasecka-Jóźwiak Katarzyna, Kotyrba Danuta, Kolenda Magdalena, Stecka Krystyna M

机构信息

Prof. Wacław Dąbrowski Institute of Agricultural and Food Biotechnology, Department of Technology Fermentation, Rakowiecka 36 St, 02-532 Warsaw, Poland.

Faculty of Horticulture, Biotechnology and Landscape Architecture, Warsaw University of Life Sciences, 02-787 Warsaw, Poland.

出版信息

J Sci Food Agric. 2016 Aug;96(11):3897-905. doi: 10.1002/jsfa.7588. Epub 2016 Feb 2.

Abstract

BACKGROUND

Wheat flour is one of the most common causative agents of food allergy. The study presents the selection and characterization of lactic acid bacteria (LAB) strains capable of hydrolyzing/modifying allergenic proteins of wheat flour. Hydrolysis of wheat proteins was determined with sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblotting with sera from patients with food allergy to gluten.

RESULTS

The analysis of electrophoretic profiles of protein extracted from sourdough shows the capability of selected LAB strains for proteolytic degradation of wheat proteins that belong to two factions: albumin/globulin (hydrolysis of 13 polypeptides with a molecular weight between 103 and 22 kDa); and gliadin (seven polypeptides with a molecular weight between 39 and 24 kDa). All analyzed strains were capable of hydrolyzing some IgE-binding epitopes of wheat allergens. The lack of such changes in control samples indicates that they were induced rather by the proteolytic activity of bacterial strains than endogenous enzymes of wheat flour. The gluten proteins were susceptible to hydrolysis by sequential digestion with pepsin and trypsin.

CONCLUSION

The selected strains exhibit proteolytic activity, which leads to a reduction in allergenicity of wheat sourdoughs. These strains may be applied as specific starter cultures to prepare bakery products of special nutritional use. © 2015 Society of Chemical Industry.

摘要

背景

小麦粉是食物过敏最常见的致病因素之一。本研究介绍了能够水解/修饰小麦粉过敏原蛋白的乳酸菌(LAB)菌株的筛选与特性。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳以及用对麸质食物过敏患者的血清进行免疫印迹法来测定小麦蛋白的水解情况。

结果

对面团提取物蛋白质电泳图谱的分析表明,所选乳酸菌菌株能够对属于两个组分的小麦蛋白进行蛋白水解降解:清蛋白/球蛋白(水解13种分子量在103至22 kDa之间的多肽);以及醇溶蛋白(7种分子量在39至24 kDa之间的多肽)。所有分析菌株都能够水解小麦过敏原的一些IgE结合表位。对照样品中缺乏此类变化表明,它们是由细菌菌株的蛋白水解活性而非小麦粉的内源酶诱导产生的。麸质蛋白易被胃蛋白酶和胰蛋白酶的顺序消化作用水解。

结论

所选菌株表现出蛋白水解活性,这导致面团的过敏原性降低。这些菌株可作为特定的发酵剂用于制备具有特殊营养用途的烘焙产品。© 2015化学工业协会。

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