发酵
面筋
食品科学
开胃菜
发酵剂
化学
多路复用
谷蛋白
再现性
醇溶蛋白
蛋白质水解
生物化学
色谱法
生物
细菌
酶
乳酸
基因
蛋白质亚单位
生物信息学
遗传学
作者
Rakhi Panda,Chung Y. Cho,Katherine O. Ivens,Lauren S. Jackson,Marc Boyer,Eric A. E. Garber
标识
DOI:10.1021/acs.jafc.1c02124
摘要
The protein/peptide profiles of gluten during yogurt fermentation were evaluated using an optimized multiplex-competitive ELISA by preparing yogurts incurred with gluten at different concentrations and by varying certain fermentation conditions. Analysis indicated that epitope-specific responses with antibody binding to glutenin epitopes decreased less during longer fermentation times or at higher starter culture concentrations relative to gliadins. Incomplete proteolysis was observed after 24 h of fermentation, which became more efficient as fermentation time was increased. Western blot confirmed the results of ELISA. Cluster analysis indicated that out of the investigated parameters, fermentation time is the only parameter that could affect the overall gluten protein/peptide profiles during yogurt fermentation. This parameter needs consideration in evaluating the suitability of calibrant(s) to be used with the multiplex-competitive ELISA or any other methods to ensure accurate quantitation of gluten in yogurts and potentially in other foods with similar fermentation chemistry. A small-scale multilaboratory evaluation indicated that the multiplex-competitive ELISA has good analytical reproducibility (average interlaboratory % CV of 28-41%).
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