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Literature DB >> 4322346

D-Mannitol utilization in Salmonella typhimurium.

Abstract

A biochemical and genetic analysis of d-mannitol metabolism in Salmonella typhimurium indicates that d-mannitol is phosphorylated by the phosphoenolpyruvate-dependent phosphotransferase system. d-Mannitol-1-phosphate is converted to d-fructose-6-phosphate by mannitol-1-phosphate dehydrogenase. Two classes of mannitol mutants are described. Both map at about 115 min on the Salmonella chromosome. Mutants missing mannitol-1-phosphate dehydrogenase activity are mannitol sensitive; i.e., either growth is inhibited or the cells are lysed in the presence of mannitol. In a strain missing adenyl cyclase activity, the mannitol genes require exogenous cyclic adenosine-3',5'-monophosphate for expression.

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Year: 1971 PMID： 4322346 PMCID： PMC248346 DOI： 10.1128/jb.105.1.232-240.1971

Source DB: PubMed Journal: J Bacteriol ISSN： 0021-9193 Impact factor: 3.490

36 in total

7. The accumulation of glucose 6-phosphate from glucose and its effect in an Escherichia coli mutant lacking phosphoglucose isomerase and glucose 6-phosphate dehydrogenase.

Authors: D G Fraenkel
Journal: J Biol Chem Date: 1968-12-25 Impact factor: 5.157

8. Two classes of pleiotropic mutants of Aerobacter aerogenes lacking components of a phosphoenolpyruvate-dependent phosphotransferase system.

Authors: S Tanaka; E C Lin
Journal: Proc Natl Acad Sci U S A Date: 1967-04 Impact factor: 11.205

9. Replacement of a phosphoenolpyruvate-dependent phosphotransferase by a nicotinamide adenine dinucleotide-linked dehydrogenase for the utilization of mannitol.

Authors: S Tanaka; S A Lerner; E C Lin
Journal: J Bacteriol Date: 1967-02 Impact factor: 3.490

4. Transport of antibiotics and metabolite analogs by systems under cyclic AMP control: positive selection of Salmonella typhimurium cya and crp mutants.

Authors: M D Alper; B N Ames
Journal: J Bacteriol Date: 1978-01 Impact factor: 3.490

D-Mannitol utilization in Salmonella typhimurium.

1. Cyclic AMP as an antagonist of catabolite repression in Escherichia coli.

2. Phosphorus assay in column chromatography.

3. Acetylornithinase of Escherichia coli: partial purification and some properties.

4. Hexitol metabolism in Escherichia coli.

5. D-Mannitol 1-phosphate dehydrogenase and D-sorbitol 6-phosphate dehydrogenase in Aerobacter aerogenes.

6. Cyclic AMP receptor protein of E. coli: its role in the synthesis of inducible enzymes.

7. The accumulation of glucose 6-phosphate from glucose and its effect in an Escherichia coli mutant lacking phosphoglucose isomerase and glucose 6-phosphate dehydrogenase.

8. Two classes of pleiotropic mutants of Aerobacter aerogenes lacking components of a phosphoenolpyruvate-dependent phosphotransferase system.

9. Replacement of a phosphoenolpyruvate-dependent phosphotransferase by a nicotinamide adenine dinucleotide-linked dehydrogenase for the utilization of mannitol.

10. Genetic analysis of carbohydrate transport-deficient mutants of Salmonella typhimurium.

1. Molecular cloning and characterization of mannitol-1-phosphate dehydrogenase from Vibrio cholerae.

2. The role of cAMP in flagellation of Salmonella typhimurium.

3. Cyclic 3', 5'-adenosine monophosphate phosphodiesterase mutants of Salmonella typhimurium.

4. Transport of antibiotics and metabolite analogs by systems under cyclic AMP control: positive selection of Salmonella typhimurium cya and crp mutants.

5. Regulation of genes coding for enzyme constituents of the bacterial phosphotransferase system.

Review 6. Linkage map of Salmonella typhimurium, edition IV.

7. Mutations affecting the dissimilation of mannitol by Escherichia coli K-12.

8. Mutants with altered glucose repression of amidase enzymes in Aspergillus nidulans.

9. The mannitol repressor (MtlR) of Escherichia coli.

10. Mannitol sensitivity.