Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1977 Nov 15;168(2):195–204. doi: 10.1042/bj1680195

Transport of adenine, hypoxanthine and uracil into Escherichia coli.

K Burton
PMCID: PMC1183752  PMID: 413544

Abstract

Uptake of adenine, hypoxanthine and uracil by an uncA strain of Escherichia coli is inhibited by uncouplers or when phosphate in the medium is replaced by less than 1 mM-arsenate, indicating a need for both a protonmotive force and phosphorylated metabolites. The rate of uptake of adenine or hypoxanthine was not markedly affected by a genetic deficiency of purine nucleoside phosphorylase. In two mutants with undetected adenine phosphoribosyltransferase, the rate of adenine uptake was about 30% of that in their parent strain, and evidence was obtained to confirm that adenine had then been utilized via purine nucleoside phosphorylase. In a strain deficient in both enzymes adenine uptake was about 1% of that shown by wild-type strains. Uptake of hypoxanthine was similarly limited in a strain lacking purine nucleoside phosphorylase, hypoxanthine phosphoribosyltransferase and guanine phosphoribosyltransferase. Deficiency of uracil phosphoribosyltransferase severely limits uracil uptake, but the defect can be circumvented by addition of inosine, which presumably provides ribose 1-phosphate for reversal of uridine phosphorylase. The results indicate that there are porter systems for adenine, hypoxanthine and uracil dependent on a protonmotive force and facilitated by intracellular metabolism of the free bases.

Full text

PDF
195

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. Bachmann B. J. Pedigrees of some mutant strains of Escherichia coli K-12. Bacteriol Rev. 1972 Dec;36(4):525–557. doi: 10.1128/br.36.4.525-557.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bagnara A. S., Finch L. R. The effects of bases and nucleosides on the intracellular contents of nucleotides and 5-phosphoribosyl 1-pyrophosphate in Escherichia coli. Eur J Biochem. 1974 Feb 1;41(3):421–430. doi: 10.1111/j.1432-1033.1974.tb03283.x. [DOI] [PubMed] [Google Scholar]
  4. Beacham I. R., Pritchard R. H. The role of nucleoside phosphorylases in the degradation of deoxyribonucleosides by thymine-requiring mutants of E. coli. Mol Gen Genet. 1971;110(4):289–298. doi: 10.1007/BF00438271. [DOI] [PubMed] [Google Scholar]
  5. Beck C. F., Ingraham J. L. Location on the chromosome of Salmonella typhimurium of genes governing pyrimidine metabolism. Mol Gen Genet. 1971;111(4):303–316. doi: 10.1007/BF00569782. [DOI] [PubMed] [Google Scholar]
  6. Berger E. A., Heppel L. A. Different mechanisms of energy coupling for the shock-sensitive and shock-resistant amino acid permeases of Escherichia coli. J Biol Chem. 1974 Dec 25;249(24):7747–7755. [PubMed] [Google Scholar]
  7. Burton K. Analysis of RNA turnover in bacteria using histidine as a radioactivity trap for (2-H)adenine nucleotides. J Mol Biol. 1976 Apr 5;102(2):333–348. doi: 10.1016/s0022-2836(76)80058-7. [DOI] [PubMed] [Google Scholar]
  8. Collins S. H., Jarvis A. W., Lindsay R. J., Hamilton W. A. Proton movements coupled to lactate and alanine transport in Escherichia coli: isolation of mutants with altered stoichiometry in alanine transport. J Bacteriol. 1976 Jun;126(3):1232–1244. doi: 10.1128/jb.126.3.1232-1244.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Glover S. W. Functional analysis of host-specificity mutants in Escherichia coli. Genet Res. 1970 Apr;15(2):237–250. doi: 10.1017/s0016672300001567. [DOI] [PubMed] [Google Scholar]
  10. Hochstadt-Ozer J., Stadtman E. R. The regulation of purine utilization in bacteria. I. Purification of adenine phosphoribosyltransferase from Escherichia coli K12 and control of activity by nucleotides. J Biol Chem. 1971 Sep 10;246(17):5294–5303. [PubMed] [Google Scholar]
  11. Hochstadt-Ozer J., Stadtman E. R. The regulation of purine utilization in bacteria. II. Adenine phosphoribosyltransferase in isolated membrane preparations and its role in transport of adenine across the membrane. J Biol Chem. 1971 Sep 10;246(17):5304–5311. [PubMed] [Google Scholar]
  12. Hochstadt-Ozer J., Stadtman E. R. The regulation of purine utilization in bacteria. III. The involvement of purine phosphoribosyltransferases in the uptake of adenine and other nucleic acid precursors by intact resting cells. J Biol Chem. 1971 Sep 10;246(17):5312–5320. [PubMed] [Google Scholar]
  13. Hochstadt J. The role of the membrane in the utilization of nucleic acid precursors. CRC Crit Rev Biochem. 1974 Mar;2(2):259–310. doi: 10.3109/10409237409105449. [DOI] [PubMed] [Google Scholar]
  14. Jochimsen B., Nygaard P., Vestergaard T. Location on the chromosome of Escherichia coli of genes governing purine metabolism. Adenosine deaminase (add), guanosine kinase (gsk) and hypoxanthine phosphoribosyltransferase (hpt). Mol Gen Genet. 1975 Dec 30;143(1):85–91. doi: 10.1007/BF00269424. [DOI] [PubMed] [Google Scholar]
  15. KALLE G. P., GOTS J. S. Mechanism of resistance to 2,6-diaminopurine in Salmonella typhimurium. Biochim Biophys Acta. 1961 Jul 22;51:130–137. doi: 10.1016/0006-3002(61)91023-x. [DOI] [PubMed] [Google Scholar]
  16. KOCH A. L., VALLEE G. The properties of adenosine deaminase and adenosine nucleoside phosphorylase in extracts of Escherichia coli. J Biol Chem. 1959 May;234(5):1213–1218. [PubMed] [Google Scholar]
  17. Kaback H. R., Reeves J. P., Short S. A., Lombardi F. J. Mechanisms of active transport in isolated bacterial membrane vesicles. 18. The mechanism of action of carbonylcyanide m-chlorophenylhydrazone. Arch Biochem Biophys. 1974 Jan;160(1):215–222. doi: 10.1016/s0003-9861(74)80028-7. [DOI] [PubMed] [Google Scholar]
  18. Kocharian Sh M., Livshits V. A., Sukhodolets V. V. Geneticheskoe izuchenie mutantov Escherichia coli K-12, ustoichivykh k 2,6-diaminopurinu. Genetika. 1975;11(11):79–89. [PubMed] [Google Scholar]
  19. Lieberman M. A., Hong J. S. Energization of osmotic shock-sensitive transport systems in Escherichia coli requires more than ATP. Arch Biochem Biophys. 1976 Jan;172(1):312–315. doi: 10.1016/0003-9861(76)90080-1. [DOI] [PubMed] [Google Scholar]
  20. Molloy A., Finch L. R. Uridine-5'-monophosphate pyrophosphorylase activity from Escherichia coli. FEBS Lett. 1969 Nov 12;5(3):211–213. doi: 10.1016/0014-5793(69)80334-0. [DOI] [PubMed] [Google Scholar]
  21. Munch-Petersen A., Mygind B. Nucleoside transport systems in Escherichia coli K12: specificity and regulation. J Cell Physiol. 1976 Dec;89(4):551–559. doi: 10.1002/jcp.1040890410. [DOI] [PubMed] [Google Scholar]
  22. Piérard A., Glansdorff N., Yashphe J. Mutations affecting uridine monophosphate pyrophosphorylase or the argR gene in Escherichia coli. Effects on carbamoyl phosphate and pyrimidine biosynthesis and on uracil uptake. Mol Gen Genet. 1972;118(3):235–245. doi: 10.1007/BF00333460. [DOI] [PubMed] [Google Scholar]
  23. Robertson B. C., Hoffee P. A. Purification and properties of purine nucleoside phosphorylase from Salmonella typhimurium. J Biol Chem. 1973 Mar 25;248(6):2040–2043. [PubMed] [Google Scholar]
  24. Roy-Burman S., Visser D. W. Transport of purines and deoxyadenosine in Escherichia coli. J Biol Chem. 1975 Dec 25;250(24):9270–9275. [PubMed] [Google Scholar]
  25. Schairer H. U., Haddock B. A. -Galactoside accumulation in a Mg 2+ -,Ca 2+ -activated ATPase deficient mutant of E.coli. Biochem Biophys Res Commun. 1972 Aug 7;48(3):544–551. doi: 10.1016/0006-291x(72)90382-8. [DOI] [PubMed] [Google Scholar]
  26. Taketo A., Kuno S. Internal localization of nucleoside-catabolic enzymes in Escherichia coli. J Biochem. 1972 Dec;72(6):1557–1563. doi: 10.1093/oxfordjournals.jbchem.a130047. [DOI] [PubMed] [Google Scholar]
  27. Thomas G. A., Varney N. F., Burton K. Nucleic acid synthesis and nucleotide pools in purine-deficient Escherichia coli. Biochem J. 1970 Nov;120(1):117–124. doi: 10.1042/bj1200117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Winkler H. H., Wilson T. H. The role of energy coupling in the transport of beta-galactosides by Escherichia coli. J Biol Chem. 1966 May 25;241(10):2200–2211. [PubMed] [Google Scholar]
  29. von Dippe P. J., Leung K., Roy-Burman S., Visser D. W. Deoxycytidine transport in the presence of a cytidine deaminase inhibitor and the transport of uracil in Escherichia coli B. J Biol Chem. 1975 May 25;250(10):3666–3671. [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES