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Evidence for an Altered Operator Specificity: Catabolite Repression Control of the Leucine Operon in Salmonella Typhimurium

Overview
Journal J Bacteriol
Specialty Microbiology
Date 1968 Jun 1
PMID 4876135
Citations 12
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Abstract

A mutation, GD-1, in the leucine operon imposed unusual growth characteristics upon a leucine auxotrophic strain bearing the leucine operator mutation, leu-500. The strain with the GD-1 mutation was able to grow on a minimal salts medium when citrate was the sole carbon source, but required leucine when glucose was present. Tests with a large number of carbohydrates suggest that in the strain bearing the GD-1 mutation the leucine biosynthetic enzymes are under catabolite repressor control. Recombination studies indicate that the GD-1 mutation is a secondary alteration of the leucine operator at or very close to the site of the leu-500 mutation. Mutations at the supX locus (previously termed su leu 500 and located on the chromosome between the cysteine B and tryptophan gene clusters) result in elimination of the catabolite repression effect. The data are interpreted as an indication that the GD-1 and leu-500 mutations alter the leucine operator with respect to its specificity of response to repressors.

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References
1.
Epps H, GALE E . The influence of the presence of glucose during growth on the enzymic activities of Escherichia coli: comparison of the effect with that produced by fermentation acids. Biochem J. 1942; 36(7-9):619-23. PMC: 1266845. DOI: 10.1042/bj0360619. View

2.
Margolin P, Mukai F . A model for mRNA transcription suggested by some characteristics of 2-aminopurine mutagenesis in Salmonella. Proc Natl Acad Sci U S A. 1966; 55(2):282-9. PMC: 224137. DOI: 10.1073/pnas.55.2.282. View

3.
MAGASANIK B, Neidhardt F . Inhibitory effect of glucose on enzyme formation. Nature. 1956; 178(4537):801-2. DOI: 10.1038/178801b0. View

4.
Gross S, BURNS R, Umbarger H . THE BIOSYNTHESIS OF LEUCINE. II. THE ENZYMIC ISOMERIZATION OF BETA-CARBOXY-BETA-HYDROXYISOCAPROATE AND ALPHA-HYDROXY-BETA-CARBOXYISOCAPROATE. Biochemistry. 1963; 2:1046-52. DOI: 10.1021/bi00905a023. View

5.
RAMALEY R, BERNLOHR R . APPARENT INDUCTION OF ORNITHINE TRANSCARBAMYLASE AND ARGINASE BY ARGININE IN BACILLUS LICHENIFORMIS. J Mol Biol. 1965; 11:842-4. DOI: 10.1016/s0022-2836(65)80041-9. View