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A collection of strains containing genetically linked alternating antibiotic resistance elements for genetic mapping of Escherichia coli.

机译:包含遗传关联的交替抗生素抗性元件的菌株的集合,用于大肠杆菌的遗传作图。

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We present a collection of 182 isogenic strains containing genetically linked antibiotic resistance elements located at approximately 1-min intervals around the Escherichia coli chromosome. At most positions both Tn10 (Tetr) and TN10kan (Kanr) elements are available, so that the collection contains a linked set of alternating antibiotic resistance markers. The map position of each insertion has been aligned to the E. coli genetic map as well as to the Kohara ordered clone bank. These strains are designed to be used in a rapid two-step mapping system in E. coli. In the first step, the mutation is localized to a 5- to 15-min region of the chromosome by Hfr mapping with a set of Hfr strains containing either Tn10 or Tn10kan elements located 20 min from their respective origins of transfer. In the second step, the mutation is localized to a 1-min region by P1 transduction, with a collection of isogenic insertion strains as donors. We discuss the uses of this collection of strains to map and eventually to clone a variety of mutations in E. coli.
机译:我们提出了182个同基因菌株的集合,这些菌株包含在大肠杆菌染色体周围大约1分钟间隔处的遗传连锁抗生素抗性元件。在大多数位置,都可以使用Tn10(Tetr)和TN10kan(Kanr)元素,因此该集合包含一系列交替的抗生素抗性标记。每个插入的图谱位置已与大肠杆菌遗传图谱以及Kohara订购的克隆库对齐。这些菌株被设计用于大肠杆菌中的快速两步定位系统。在第一步中,通过使用一组含有距各自转移起点20分钟的Tn10或Tn10kan元素的Hfr菌株进行Hfr定位,将突变定位于染色体的5至15分钟区域。在第二步中,通过P1转导将突变定位于1分钟区域,并以等基因插入菌株作为供体。我们讨论了该菌株集合的用途,以作图并最终在大肠杆菌中克隆各种突变。

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