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委内瑞拉链霉菌ISP5230中邻氨基苯甲酸合酶基因的定位:克隆基因整合后的遗传图谱

Location of the genes for anthranilate synthase in Streptomyces venezuelae ISP5230: genetic mapping after integration of the cloned genes.

作者信息

Paradkar A S, Stuttard C, Vining L C

机构信息

Department of Biology, Dalhousie University, Halifax, NS, Canada.

出版信息

J Gen Microbiol. 1993 Apr;139(4):687-94. doi: 10.1099/00221287-139-4-687.

Abstract

The anthranilate synthase (trpEG) genes in Streptomyces venezuelae ISP5230 were located by allowing a segregationally unstable plasmid carrying cloned S. venezuelae trpEG DNA and a thiostrepton resistance (tsr) marker to integrate into the chromosome. The integrated tsr was mapped by conjugation and transduction to a location close to tyr-2, between arg-6 and trpA13. A genomic DNA fragment containing trpC from S. venezuelae ISP5230 was cloned by complementation of a trpC mutation in Streptomyces lividans. Evidence from restriction enzyme analysis of the cloned DNA fragments, from Southern hybridization using the cloned trp DNA as probes, and from cotransduction frequencies, placed trpEG at a distance of 12-45 kb from the trpCBA cluster. The overall arrangement of tryptophan biosynthesis genes in the S. venezuelae chromosome differs from that in other bacteria examined so far.

摘要

委内瑞拉链霉菌ISP5230中的邻氨基苯甲酸合酶(trpEG)基因是通过让携带克隆的委内瑞拉链霉菌trpEG DNA和硫链丝菌素抗性(tsr)标记的分离不稳定质粒整合到染色体中来定位的。整合的tsr通过接合和转导定位到靠近tyr-2的位置,在arg-6和trpA13之间。通过互补淡紫链霉菌中的trpC突变,克隆了包含委内瑞拉链霉菌ISP5230的trpC的基因组DNA片段。来自克隆DNA片段的限制性酶切分析、使用克隆的trp DNA作为探针的Southern杂交以及共转导频率的证据表明,trpEG与trpCBA簇的距离为12 - 45 kb。委内瑞拉链霉菌染色体中色氨酸生物合成基因的总体排列与迄今为止检查的其他细菌不同。

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