PMID:4353875
| Citation |
Lambden, PR and Drabble, WT (1973) The gua operon of Escherichia coli K-12: evidence for polarity from guaB to guaA. J. Bacteriol. 115:992-1002 |
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| Abstract |
Guanine auxotrophs of Escherichia coli K-12 were isolated after mutagenesis with N-methyl-N'-nitro-N-nitrosoguanidine, ethyl methane sulfonate, or the acridine mustard ICR 372. guaA (xanthosine 5'-monophosphate [XMP] aminase-less) mutants were distinguished from guaB (inosine 5'-monophosphate [IMP] dehydrogenase-less) mutants by their growth response to xanthine and by enzyme assay. Mutations were classified as base substitutions or frameshift on the basis of mutagen-induced reversion patterns. All guaA strains, including three frameshift mutants, produced derepressed levels of IMP dehydrogenase when cultured with a growth-limiting concentration of guanine. The guaB strains were of two types: (i) those producing derepressed levels of XMP aminase, and (ii) those producing basal levels of XMP aminase when grown under conditions of guanine starvation. In the guaB strains of the second type, the expression of the adjacent guaA gene is reduced. It is proposed that this pleiotropic effect of some guaB mutations is a result of polarity. The orientation of polarity suggests the gene order "operator"-guaB-guaA. Gel diffusion studies with IMP dehydrogenase antiserum showed that strains carrying polar guaB mutations do not produce cross-reacting material (CRM). The remaining guaB mutants were either CRM(+) or CRM(-). Mapping the mutations by three-factor crosses showed that polar and nonpolar guaB sites are clustered in a small genetic region cotransducible with guaA. The relative positions of the guaB mutational sites established that the polar mutations lie within the structural gene for IMP dehydrogenase. |
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| Keywords |
Alkanesulfonates; Antigens, Bacterial; Cell-Free System; Chromosome Mapping; Crosses, Genetic; Escherichia coli/classification; Escherichia coli/enzymology; Escherichia coli/immunology; Escherichia coli/metabolism; Guanine/metabolism; Immunodiffusion; Ketone Oxidoreductases/biosynthesis; Ligases/biosynthesis; Mustard Compounds; Mutagens; Mutation; Nitrosoguanidines; Operon; Transduction, Genetic; Xanthines/metabolism |
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