Skip to main content
Genetics logoLink to Genetics
. 1991 Apr;127(4):657–670. doi: 10.1093/genetics/127.4.657

A Genetic Characterization of the Nadc Gene of Salmonella Typhimurium

K T Hughes 1, J R Roth 1, B M Olivera 1
PMCID: PMC1204394  PMID: 2029967

Abstract

The nadC gene of Salmonella encodes the pyridine biosynthetic enzyme PRPP-quinolinate phosphoribosyltransferase. Using a combination of genetic techniques, a deletion map for the Salmonella nadC gene has been generated which includes over 100 point mutants and 18 deletion intervals. The nadC alleles obtained by hydroxylamine mutagenesis include those suppressed by either amber, ochre, or UGA nonsense suppressors as well as alleles suppressed by the missense suppressor, sumA. Deletions were obtained by three separate protocols including spontaneous selection for loss of the nearby aroP gene, recombination between aroP::MudA and nadC::MudA insertion alleles, and selection for spontaneous loss of tetracycline resistance in a nearby guaC::Tn10dTc insertion mutant allele. The nadC mutants comprise one complementation group and the nadC(+) allele is dominant to simple, nadC auxotrophic mutant alleles. Intragenic complementation of two nadC alleles, nadC493 and nadC494, mapping to deletion intervals 17 and 18, respectively, suggests that nadC encodes a multimeric enzyme. Both nadC and the nearby aroP locus are transcribed counterclockwise on the standard genetic map of Salmonella, in opposite orientation to the direction of chromosome replication.

Full Text

The Full Text of this article is available as a PDF (1.2 MB).

Selected References

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

  1. AMES G. F. UPTAKE OF AMINO ACIDS BY SALMONELLA TYPHIMURIUM. Arch Biochem Biophys. 1964 Jan;104:1–18. doi: 10.1016/s0003-9861(64)80028-x. [DOI] [PubMed] [Google Scholar]
  2. Ames G. F., Roth J. R. Histidine and aromatic permeases of Salmonella typhimurim. J Bacteriol. 1968 Nov;96(5):1742–1749. doi: 10.1128/jb.96.5.1742-1749.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Andreoli A. J., Okita T. W., Bloom R., Grover T. A. The pyridine nucleotide cycle: presence of a nicotinamide mononucleotide-specific glycohydrolase in Escherichia coli. Biochem Biophys Res Commun. 1972 Oct 6;49(1):264–269. doi: 10.1016/0006-291x(72)90039-3. [DOI] [PubMed] [Google Scholar]
  4. Bochner B. R., Huang H. C., Schieven G. L., Ames B. N. Positive selection for loss of tetracycline resistance. J Bacteriol. 1980 Aug;143(2):926–933. doi: 10.1128/jb.143.2.926-933.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bruyn R. P., Stoof J. C. The quinolinic acid hypothesis in Huntington's chorea. J Neurol Sci. 1990 Jan;95(1):29–38. doi: 10.1016/0022-510x(90)90114-3. [DOI] [PubMed] [Google Scholar]
  6. Casadaban M. J., Cohen S. N. Lactose genes fused to exogenous promoters in one step using a Mu-lac bacteriophage: in vivo probe for transcriptional control sequences. Proc Natl Acad Sci U S A. 1979 Sep;76(9):4530–4533. doi: 10.1073/pnas.76.9.4530. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Castilho B. A., Olfson P., Casadaban M. J. Plasmid insertion mutagenesis and lac gene fusion with mini-mu bacteriophage transposons. J Bacteriol. 1984 May;158(2):488–495. doi: 10.1128/jb.158.2.488-495.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Chan R. K., Botstein D., Watanabe T., Ogata Y. Specialized transduction of tetracycline resistance by phage P22 in Salmonella typhimurium. II. Properties of a high-frequency-transducing lysate. Virology. 1972 Dec;50(3):883–898. doi: 10.1016/0042-6822(72)90442-4. [DOI] [PubMed] [Google Scholar]
  9. Cookson B. T., Olivera B. M., Roth J. R. Genetic characterization and regulation of the nadB locus of Salmonella typhimurium. J Bacteriol. 1987 Sep;169(9):4285–4293. doi: 10.1128/jb.169.9.4285-4293.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Foster J. W., Holley-Guthrie E. A., Warren F. Regulation of NAD metabolism in Salmonella typhimurium: genetic analysis and cloning of the nadR repressor locus. Mol Gen Genet. 1987 Jun;208(1-2):279–287. doi: 10.1007/BF00330454. [DOI] [PubMed] [Google Scholar]
  11. Foster J. W., Moat A. G. Nicotinamide adenine dinucleotide biosynthesis and pyridine nucleotide cycle metabolism in microbial systems. Microbiol Rev. 1980 Mar;44(1):83–105. doi: 10.1128/mr.44.1.83-105.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Gholson R. K., Tritz G. J., Matney T. S., Andreoli A. J. Mode of nicotinamide adenine dinucleotide utilization by Escherichia coli. J Bacteriol. 1969 Sep;99(3):895–896. doi: 10.1128/jb.99.3.895-896.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Holley E. A., Foster J. W. Bacteriophage P22 as a vector for Mu mutagenesis in Salmonella typhimurium: isolation of nad-lac and pnc-lac gene fusions. J Bacteriol. 1982 Nov;152(2):959–962. doi: 10.1128/jb.152.2.959-962.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Holley E. A., Spector M. P., Foster J. W. Regulation of NAD biosynthesis in Salmonella typhimurium: expression of nad-lac gene fusions and identification of a nad regulatory locus. J Gen Microbiol. 1985 Oct;131(10):2759–2770. doi: 10.1099/00221287-131-10-2759. [DOI] [PubMed] [Google Scholar]
  15. Hong J. S., Ames B. N. Localized mutagenesis of any specific small region of the bacterial chromosome. Proc Natl Acad Sci U S A. 1971 Dec;68(12):3158–3162. doi: 10.1073/pnas.68.12.3158. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Hughes K. T., Olivera B. M., Roth J. R. Rec dependence of mu transposition from P22-transduced fragments. J Bacteriol. 1987 Jan;169(1):403–409. doi: 10.1128/jb.169.1.403-409.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. IMSANDE J., HANDLER P. Biosynthesis of diphosphopyridine nucleotide. III. Nicotinic acid mononucleotide pyrophos-phorylase. J Biol Chem. 1961 Feb;236:525–530. [PubMed] [Google Scholar]
  18. Johnston H. M., Roth J. R. Genetic analysis of the histidine operon control region of Salmonella typhimurium. J Mol Biol. 1981 Feb 5;145(4):713–734. doi: 10.1016/0022-2836(81)90311-9. [DOI] [PubMed] [Google Scholar]
  19. Langley D., Guest J. R. Biochemical and genetic characterics of deletion and other mutant strains of Salmonella typhimurium LT2 lacking alpha-keto acid dehydrogenase complex activities,. J Gen Microbiol. 1974 Jun;82(2):319–335. doi: 10.1099/00221287-82-2-319. [DOI] [PubMed] [Google Scholar]
  20. Langley D., Guest J. R. Biochemical genetics of the alpha-keto acid dehydrogenase complexes of Escherichia coli K12: isolation and biochemical properties of deletion mutants. J Gen Microbiol. 1977 Apr;99(2):263–276. doi: 10.1099/00221287-99-2-263. [DOI] [PubMed] [Google Scholar]
  21. MAGASANIK B., KARIBIAN D. Purine nucleotide cycles and their metabolic role. J Biol Chem. 1960 Sep;235:2672–2681. [PubMed] [Google Scholar]
  22. Maloy S. R., Nunn W. D. Selection for loss of tetracycline resistance by Escherichia coli. J Bacteriol. 1981 Feb;145(2):1110–1111. doi: 10.1128/jb.145.2.1110-1111.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Packman P. M., Jakoby W. B. Crystalline quinolinate phosphoribosyltransferase. II. Properties of the enzyme. J Biol Chem. 1967 May 10;242(9):2075–2079. [PubMed] [Google Scholar]
  24. Sanderson K. E., Roth J. R. Linkage map of Salmonella typhimurium, Edition VI. Microbiol Rev. 1983 Sep;47(3):410–453. doi: 10.1128/mr.47.3.410-453.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Sanderson K. E., Roth J. R. Linkage map of Salmonella typhimurium, edition VII. Microbiol Rev. 1988 Dec;52(4):485–532. doi: 10.1128/mr.52.4.485-532.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Saxton R. E., Rocha V., Rosser R. J., Andreoli A. J., Shimoyama M., Kosaka A., Chandler J. L., Gholson R. K. A comparative study of the regulation of nicotinamide-adenine dinucleotide biosynthesis. Biochim Biophys Acta. 1968 Feb 1;156(1):77–84. doi: 10.1016/0304-4165(68)90106-2. [DOI] [PubMed] [Google Scholar]
  27. Way J. C., Davis M. A., Morisato D., Roberts D. E., Kleckner N. New Tn10 derivatives for transposon mutagenesis and for construction of lacZ operon fusions by transposition. Gene. 1984 Dec;32(3):369–379. doi: 10.1016/0378-1119(84)90012-x. [DOI] [PubMed] [Google Scholar]
  28. Zhu N., Olivera B. M., Roth J. R. Activity of the nicotinamide mononucleotide transport system is regulated in Salmonella typhimurium. J Bacteriol. 1991 Feb;173(3):1311–1320. doi: 10.1128/jb.173.3.1311-1320.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Zhu N., Olivera B. M., Roth J. R. Genetic characterization of the pnuC gene, which encodes a component of the nicotinamide mononucleotide transport system in Salmonella typhimurium. J Bacteriol. 1989 Aug;171(8):4402–4409. doi: 10.1128/jb.171.8.4402-4409.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Zhu N., Olivera B. M., Roth J. R. Identification of a repressor gene involved in the regulation of NAD de novo biosynthesis in Salmonella typhimurium. J Bacteriol. 1988 Jan;170(1):117–125. doi: 10.1128/jb.170.1.117-125.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Zhu N., Roth J. R. The nadI region of Salmonella typhimurium encodes a bifunctional regulatory protein. J Bacteriol. 1991 Feb;173(3):1302–1310. doi: 10.1128/jb.173.3.1302-1310.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Genetics are provided here courtesy of Oxford University Press

RESOURCES