Röder Christoph, König Helmut, Fröhlich Jürgen
Institute of Microbiology and Wine Research, Johannes Gutenberg University, Mainz, Germany.
FEMS Yeast Res. 2007 Sep;7(6):1013-26. doi: 10.1111/j.1567-1364.2007.00267.x. Epub 2007 Jun 27.
Sequencing of the complete 26S rRNA genes of all Dekkera/Brettanomyces species colonizing different beverages revealed the potential for a specific primer and probe design to support diagnostic PCR approaches and FISH. By analysis of the complete 26S rRNA genes of all five currently known Dekkera/Brettanomyces species (Dekkera bruxellensis, D. anomala, Brettanomyces custersianus, B. nanus and B. naardenensis), several regions with high nucleotide sequence variability yet distinct from the D1/D2 domains were identified. FISH species-specific probes targeting the 26S rRNA gene's most variable regions were designed. Accessibility of probe targets for hybridization was facilitated by the construction of partially complementary 'side'-labeled probes, based on secondary structure models of the rRNA sequences. The specificity and routine applicability of the FISH-based method for yeast identification were tested by analyzing different wine isolates. Investigation of the prevalence of Dekkera/Brettanomyces yeasts in the German viticultural regions Wonnegau, Nierstein and Bingen (Rhinehesse, Rhineland-Palatinate) resulted in the isolation of 37 D. bruxellensis strains from 291 wine samples.
对定殖于不同饮料中的所有德克酵母/酒香酵母属物种的完整26S rRNA基因进行测序,结果表明有可能设计出特异性引物和探针,以支持诊断性PCR方法和荧光原位杂交技术(FISH)。通过分析目前已知的所有五个德克酵母/酒香酵母属物种(布鲁塞尔德克酵母、异常德克酵母、库斯特酒香酵母、矮小酒香酵母和纳ardenensis酒香酵母)的完整26S rRNA基因,确定了几个核苷酸序列变异性高但不同于D1/D2结构域的区域。设计了针对26S rRNA基因最可变区域的FISH物种特异性探针。基于rRNA序列的二级结构模型构建部分互补的“侧翼”标记探针,促进了杂交探针靶标的可及性。通过分析不同的葡萄酒分离株,测试了基于FISH的酵母鉴定方法的特异性和常规适用性。对德国葡萄酒产区翁内高、尼尔施泰因和宾根(莱茵黑森,莱茵兰-普法尔茨州)的德克酵母/酒香酵母属酵母的流行情况进行调查,结果从291个葡萄酒样品中分离出37株布鲁塞尔德克酵母菌株。