LOCATION OF THE GENES FOR ANTHRANILATE SYNTHASE IN STREPTOMYCES-VENEZUELAE ISP5230 - GENETIC-MAPPING AFTER INTEGRATION OF THE CLONED GENES

被引:9
作者
PARADKAR, AS
STUTTARD, C
VINING, LC
机构
[1] DALHOUSIE UNIV,DEPT BIOL,HALIFAX B3H 4J1,NS,CANADA
[2] DALHOUSIE UNIV,DEPT MICROBIOL & IMMUNOL,HALIFAX B3H 4J1,NS,CANADA
来源
JOURNAL OF GENERAL MICROBIOLOGY | 1993年 / 139卷
关键词
D O I
10.1099/00221287-139-4-687
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
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页码:687 / 694
页数:8
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