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首页> 外文期刊>Journal of the Institute of Brewing >Beer enemy number one: genetic diversity, physiology and biofilm formation of Lactobacillus brevis
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Beer enemy number one: genetic diversity, physiology and biofilm formation of Lactobacillus brevis

机译:啤酒的第一敌人:短乳杆菌的遗传多样性,生理学和生物膜形成

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Lactobacillus brevis is the most significant beer spoilage bacteria worldwide. It is found as a contaminant at all stages of brewing, including during primary and secondary fermentation, storage, filtration and the packaging process. In production with flash pasteurisation and subsequent hygienic filling, avoiding and tracing secondary contaminations is the key to a microbiologically stable product. However, L. brevis strains vary in their spoilage potential and can grow in many different beer types. This study presents a physiological test scheme for growth potential and biofilm formation in various media. It was determined that a large number of L. brevis strains can form biofilms as a first coloniser. The identification of the species alone is therefore not enough to be sure of the spoilage risk, which shows the need for a more in depth differentiation. DNA fingerprint techniques are crucial to differentiate isolates of this species at strain level. The rep-PCR fingerprint system (GTG)(5) was used to differentiate a selected collection of 20 isolates, which were characterised in growth and biofilm formation in various media. The data showed a high variation within the selected isolates. As second step, generated fingerprint clusters of L. brevis were traced back to contamination sources in a German brewery, revealing a high number of isolates with potentially varying growth, spoilage and biofilm potential. L. brevis being the demonstrator species, the PCR system used is a powerful and compatible tracing and troubleshooting tool for all kinds of spoilage bacteria in the brewing industry. (C) 2019 The Institute of Brewing & Distilling
机译:短乳杆菌是全世界最重要的啤酒变质细菌。在酿造的所有阶段(包括初次和二次发酵,储存,过滤和包装过程中)均会发现污染物。在采用快速巴氏杀菌和随后的卫生灌装的生产中,避免和追溯二次污染是微生物稳定产品的关键。但是,短乳杆菌菌株的腐败潜力不同,并且可以在许多不同类型的啤酒中生长。这项研究提出了一种生理测试方案,用于各种培养基中的生长潜力和生物膜形成。已确定大量的L. brevis菌株可以形成生物膜作为第一定居者。因此,仅对物种进行识别还不足以确保存在变质风险,这表明需要更深入的区分。 DNA指纹技术对于在菌株水平上区分该物种的分离株至关重要。 rep-PCR指纹系统(GTG)(5)用于区分20种分离株的选定集合,这些分离株的特征在于在各种培养基中的生长和生物膜形成。数据显示所选菌株中有很大差异。第二步,将产生的短乳杆菌指纹群追溯到德国啤酒厂的污染源,发现大量分离株具有潜在的生长,变质和生物膜潜力。短乳杆菌是示范物种,所用的PCR系统是一种功能强大且兼容的跟踪和故障排除工具,适用于酿造行业中的各种腐败细菌。 (C)2019酿造与蒸馏研究所

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