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. 1978 Jul;89(3):439–451. doi: 10.1093/genetics/89.3.439

The Nature of Genetic Instability in Auxotrophs of SALMONELLA TYPHIMURIUM Requiring Cysteine or Methionine and Resistant to Inhibition by 1,2,4-Triazole

A J Kingsman 1, D A Smith 1
PMCID: PMC1213847  PMID: 352799

Abstract

We tested the hypothesis that unstable suppression of auxotrophy in triazole-resistant derivatives of Cym- mutants of Salmonella typhimurium is due to reversible insertion at the Cym - site of genetic material originating in the cysALKptsHI region. We have shown that the unstable phenotype was co-transducible with markers in the cysCDHIJ region. The suppression of the Cym phenotype was recA dependent and frequencies of segregation were affected by UV irradiation. Restored enzyme activity in suppressed strains was determined by wild-type enzyme, suggesting that the unstable regions are located in cys gene regulatory regions. These results support the hypothesis. In contradiction, we found no evidence for a deletion in the cysALKptsHI region.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Chelala C. A., Margolin P. Effects of deletions on cotransduction linkage in Salmonella typhimurium: evidence that bacterial chromosome deletions affect the formation of transducing DNA fragments. Mol Gen Genet. 1974;131(2):97–112. doi: 10.1007/BF00266146. [DOI] [PubMed] [Google Scholar]
  2. Cordaro J. C., Roseman S. Deletion mapping of the genes coding for HPr and enzyme I of the phosphoenolpyruvate: sugar phosphotransferase system in Salmonella typhimurium. J Bacteriol. 1972 Oct;112(1):17–29. doi: 10.1128/jb.112.1.17-29.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Fincham J. R., Sastry G. R. Controlling elements in maize. Annu Rev Genet. 1974;8:15–50. doi: 10.1146/annurev.ge.08.120174.000311. [DOI] [PubMed] [Google Scholar]
  4. Gottesman M. E., Yarmolinsky M. B. The integration and excision of the bacteriophage lambda genome. Cold Spring Harb Symp Quant Biol. 1968;33:735–747. doi: 10.1101/sqb.1968.033.01.084. [DOI] [PubMed] [Google Scholar]
  5. Holliday R. Biochemical measure of the time and frequency of radiation-induced allelic recombination in Ustilago. Nat New Biol. 1971 Aug 25;232(34):233–236. doi: 10.1038/newbio232233a0. [DOI] [PubMed] [Google Scholar]
  6. Kingsman A. J. The structure of the cysCDHIJ region in unstable cysteine or methionine requiring mutants of Salmonella typhimurium. Mol Gen Genet. 1977 Nov 18;156(3):327–332. doi: 10.1007/BF00267189. [DOI] [PubMed] [Google Scholar]
  7. MCCLINTOCK B. Controlling elements and the gene. Cold Spring Harb Symp Quant Biol. 1956;21:197–216. doi: 10.1101/sqb.1956.021.01.017. [DOI] [PubMed] [Google Scholar]
  8. Peterson P. A. Controlling elements and mutable loci in maize: their relationship to bacterial episomes. Genetica. 1970;41(1):33–56. doi: 10.1007/BF00958892. [DOI] [PubMed] [Google Scholar]
  9. Qureshi M. A., Smith D. A., Kingsman A. J. Mutants of Salmonella typhimurium responding to cysteine or methionine: their nature and possible role in the regulation of cysteine biosynthesis. J Gen Microbiol. 1975 Aug;89(2):353–370. doi: 10.1099/00221287-89-2-353. [DOI] [PubMed] [Google Scholar]
  10. ROMAN H., JACOB F. A comparison of spontaneous and ultraviolet-induced allelic recombination with reference to the recombination of outside markers. Cold Spring Harb Symp Quant Biol. 1958;23:155–160. doi: 10.1101/sqb.1958.023.01.019. [DOI] [PubMed] [Google Scholar]

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