García Teresa, Mayoral Belén, González Isabel, López-Calleja Inés, Sanz Amanda, Hernández Pablo E, Martín Rosario
Departamento de Nutrición y Bromatología y Tecnología de los Alimentos, Facultad de Veterinaria, Universidad Complutense, 28040 Madrid, Spain.
J Food Prot. 2004 Feb;67(2):357-64. doi: 10.4315/0362-028x-67.2.357.
Enzyme-linked immunosorbent assay (ELISA) and PCR techniques have been developed for the detection of spoilage yeast species in dairy products. Polyclonal antibodies against live yeast cells (AY) were raised in rabbits by inoculation of a mixture of 10 yeast species frequently associated with dairy products spoilage. AY antibodies were used for the development of two ELISA formats (indirect and double-antibody sandwich ELISA) for the detection of yeast species in milk and yogurt. A PCR assay was also developed for yeast detection in dairy products, using primers designed to amplify a conserved 250-base pair fragment of the 18S rRNA of the yeast species. The results obtained in this work show that ELISA techniques using polyclonal antibodies against viable yeast cells are of limited value for the detection and enumeration of spoilage yeast species in dairy products. On the contrary, PCR amplification of a conserved region of the 18S rRNA of the yeast species allows the homogeneous detection of all the yeast species tested and, combined with an overnight enrichment of samples, could be used for the detection of low levels of viable spoilage yeast species in dairy products.
酶联免疫吸附测定(ELISA)和聚合酶链反应(PCR)技术已被开发用于检测乳制品中的腐败酵母种类。通过接种10种经常与乳制品腐败相关的酵母菌种混合物,在兔子体内产生了针对活酵母细胞(AY)的多克隆抗体。AY抗体被用于开发两种ELISA形式(间接ELISA和双抗体夹心ELISA),以检测牛奶和酸奶中的酵母种类。还开发了一种用于检测乳制品中酵母的PCR检测方法,使用设计用于扩增酵母菌种18S rRNA保守250碱基对片段的引物。这项工作获得的结果表明,使用针对活酵母细胞的多克隆抗体的ELISA技术在检测和计数乳制品中的腐败酵母种类方面价值有限。相反,酵母菌种18S rRNA保守区域的PCR扩增能够对所有测试的酵母种类进行均匀检测,并且与样品过夜富集相结合,可用于检测乳制品中低水平的活腐败酵母种类。