PMID:2687246

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Citation

Vogler, AP, Trentmann, S and Lengeler, JW (1989) Alternative route for biosynthesis of amino sugars in Escherichia coli K-12 mutants by means of a catabolic isomerase. J. Bacteriol. 171:6586-92

Abstract

By inserting a lambda placMu bacteriophage into gene glmS encoding glucosamine 6-phosphate synthetase (GlmS), the key enzyme of amino sugar biosynthesis, a nonreverting mutant of Escherichia coli K-12 that was strictly dependent on exogenous N-acetyl-D-glucosamine or D-glucosamine was generated. Analysis of suppressor mutations rendering the mutant independent of amino sugar supply revealed that the catabolic enzyme D-glucosamine-6-phosphate isomerase (deaminase), encoded by gene nagB of the nag operon, was able to fulfill anabolic functions in amino sugar biosynthesis. The suppressor mutants invariably expressed the isomerase constitutively as a result of mutations in nagR, the locus for the repressor of the nag regulon. Suppression was also possible by transformation of glmS mutants with high-copy-number plasmids expressing the gene nagB. Efficient suppression of the glmS lesion, however, required mutations in a second locus, termed glmX, which has been localized to 26.8 min on the standard E. coli K-12 map. Its possible function in nitrogen or cell wall metabolism is discussed.

Links

PubMed PMC210551

Keywords

Aldose-Ketose Isomerases; Carbohydrate Epimerases/genetics; Carbohydrate Epimerases/metabolism; Escherichia coli/enzymology; Escherichia coli/genetics; Genes, Bacterial; Genetic Markers/analysis; Genotype; Glutamine-Fructose-6-Phosphate Transaminase (Isomerizing)/genetics; Hexosamines/biosynthesis; Mutation; Operon; Phenotype; Plasmids; Restriction Mapping; Suppression, Genetic; Transduction, Genetic

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