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Identity, beer spoiling and biofilm forming potential of yeasts from beer bottling plant associated biofilms

机译:啤酒瓶装厂相关生物膜中酵母的身份,啤酒变质和生物膜形成潜力

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Wild yeasts were isolated from process surfaces of two breweries. In total, 41 strains were obtained and differentiated by cultivation on CuSO4 or crystal violet containing selective media, by fatty acid profiling and by a restriction analysis of the region spanning the internal transcribed spacers (ITS1 and ITS2) and the 5.8S rRNA gene. The restriction analysis showed the highest differentiating capacity and resulted in eleven groups. These groups were identified by the API ID 32 C kit or by sequencing the D1/D2 region of the 26S rRNA gene. Most of the wild yeasts were identified as Saccharomyces cerevisiae (46% of all isolates) and Candida pelliculosa (anamorph: Pichia anomala) (24%). No obvious differences were detected between the two breweries. While all of the S. cerevisiae isolates were able to grow in beer, only six out of 10 C. pelliculosa strains were able to tolerate this substrate. However, most of the C. pelliculosa strains showed biofilm formation in a microplate assay, but none of the S. cerevisiae isolates. Therefore, it is assumed that the former species is involved in attachment and primary biofilm formation on beer bottling plants, while S. cerevisiae is a late colonizer of a preformed biofilm but increased the beer spoiling potential of the biofilm.
机译:从两个啤酒厂的加工表面分离出野生酵母。通过在含CuSO 4 或结晶紫的选择性培养基上进行培养,通过脂肪酸谱分析以及对内部转录间隔区(ITS1和ITS2)的区域进行限制性分析,总共获得了41个菌株并进行了分化。 5.8S rRNA基因。限制性酶切分析显示最高的分化能力,并导致11组。这些组通过API ID 32 C试剂盒或通过对26S rRNA基因的D1 / D2区进行测序来鉴定。大多数野生酵母被鉴定为酿酒酵母(占所有分离菌的46%)和糙皮假丝酵母(变种:奇异毕赤酵母)(占24%)。两家啤酒厂之间未发现明显差异。尽管所有酿酒酵母分离株都能在啤酒中生长,但10株C. pelliculosa菌株中只有6株能够耐受这种底物。但是,大多数C. pelliculosa菌株在微孔板检测中均显示出生物膜形成,但没有酿酒酵母分离株。因此,假定前者参与了啤酒装瓶厂的附着和主要生物膜的形成,而酿酒酵母是预先形成的生物膜的晚期定殖者,但增加了生物膜的啤酒变质潜力。

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