Hayashi Nobuyuki, Arai Ritsuko, Tada Setsuzo, Taguchi Hiroshi, Ogawa Yutaka
Research Laboratories for Brewing, Kirin Brewery Co Ltd, 1-17-1 Namamugi, Yokohama, Japan.
Food Microbiol. 2007 Oct-Dec;24(7-8):778-85. doi: 10.1016/j.fm.2007.01.007. Epub 2007 Feb 4.
Primer sets for a loop-mediated isothermal amplification (LAMP) method were developed to specifically identify each of the four Brettanomyces/Dekkera species, Dekkera anomala, Dekkera bruxellensis, Dekkera custersiana and Brettanomyces naardenensis. Each primer set was designed with target sequences in the ITS region of the four species and could specifically amplify the target DNA of isolates from beer, wine and soft drinks. Furthermore, the primer sets differentiated strains of the target species from strains belonging to other species, even within the genus Brettanomyces/Dekkera. Moreover, the LAMP method with these primer sets could detect about 1 x 10(1) cfu/ml of Brettanomyces/Dekkera yeasts from suspensions in distilled water, wine and beer. This LAMP method with primer sets for the identification of Brettanomyces/Dekkera yeasts is advantageous in terms of specificity, sensitivity and ease of operation compared with standard PCR methods.
开发了用于环介导等温扩增(LAMP)方法的引物组,以特异性鉴定四种酒香酵母/德克酵母属物种,即异常德克酵母、布鲁塞尔德克酵母、库斯特德克酵母和纳登酒香酵母。每个引物组都针对这四个物种的ITS区域中的靶序列进行设计,并且能够特异性扩增来自啤酒、葡萄酒和软饮料中的分离株的靶DNA。此外,这些引物组能够将靶物种的菌株与属于其他物种的菌株区分开来,即使在酒香酵母/德克酵母属内也是如此。而且,使用这些引物组的LAMP方法能够从蒸馏水、葡萄酒和啤酒中的悬浮液中检测到约1×10¹ cfu/ml的酒香酵母/德克酵母属酵母。与标准PCR方法相比,这种用于鉴定酒香酵母/德克酵母属酵母的带有引物组的LAMP方法在特异性、灵敏度和操作简便性方面具有优势。