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Development of bacteriophage resistant starter cultures - genetic engineering vs. classical methods

机译:噬菌体抗性启动培养的发展 - 基因工程与古典方法

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Infections with bacteriophages are still a major problem during dairy fermentations. A possible way to solve this problem is the introduction of phage insensitive starter cultures. However, due to strict legislative regulations and lack of consumer acceptance in Europe the improvement of phage resistance by genetic engineering is problematic. Here we describe three different possibilities to generate phage insensitive mutants with different degrees of using genetic tools: 1. Genetic engineering resulting in a GMO: inactivation of pip gene. 2. Spontaneous mutant selection resulting in nonGMO variants: screening for spontaneous phage resistant mutants towards c2-type phages. 3. Combination of genetic engineering tools with a classical method resulting in a new variant: introduction of a marker plasmid by electroporation, conjugative transfer of phage resistance plasmids and successive curing of the marker plasmid.
机译:乳酸发酵过程中患有噬菌体的感染仍然是一个主要问题。解决这个问题的可能方法是引入噬菌体不敏感的起始培养物。然而,由于欧洲严格的立法法规和缺乏消费者接受,基因工程的噬菌体抗性的提高是有问题的。在这里,我们描述了三种不同的可能性,以产生具有不同遗传工具的不同程度的噬菌体不敏感突变体:1。遗传工程导致GMO:灭活pIP基因。 2.自发突变体选择产生的Nongmo变体:筛选自发性噬菌体抗突变体朝C2型噬菌体的抗突变体。 3.遗传工程工具与经典方法的组合导致新变种:通过电穿孔,噬菌体抗性质粒的共轭转移和标记质粒的连续固化引入标志物质粒。

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