Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1996 Mar;178(5):1363–1373. doi: 10.1128/jb.178.5.1363-1373.1996

Identification of TonB homologs in the family Enterobacteriaceae and evidence for conservation of TonB-dependent energy transduction complexes.

R A Larsen 1, P S Myers 1, J T Skare 1, C L Seachord 1, R P Darveau 1, K Postle 1
PMCID: PMC177811  PMID: 8631714

Abstract

The transport of Fe(III)-siderophore complexes and vitamin B12 across the outer membrane of Escherichia coli requires the TonB-dependent energy transduction system. A set of murine monoclonal antibodies (MAbs) was generated against an E. coli TrpC-TonB fusion protein to facilitate structure and function studies. In the present study, the epitopes recognized by these MAbs were mapped, and their distribution in gram-negative organisms was examined. Cross-species reactivity patterns obtained against TonB homologs of known sequence were used to refine epitope mapping, with some epitopes ultimately confirmed by inhibition experiments using synthetic polypeptides. Epitopes recognized by this set of MAbs were conserved in TonB homologs for 9 of 12 species in the family Enterobacteriaceae (including E. coli), including previously unidentified TonB homologs in Shigella, Citrobacter, Proteus, and Kluyvera species. These homologs were also detected by a polyclonal alpha-TrpC-TonB serum that additionally recognized the known Yersinia enterocolitica TonB homolog and a putative TonB homolog in Edwardsiella tarda. These antibody preparations failed to detect the known TonB homologs of either Pseudomonas putida or Haemophilus influenzae but did identify potential TonB homologs in several other nonenteric gram-negative species. In vivo chemical cross-linking experiments demonstrated that in addition to TonB, auxiliary components of the TonB-dependent energy transduction system are broadly conserved in members of the family Enterobacteriaceae, suggesting that the TonB system represents a common system for high-affinity active transport across the gram-negative outer membrane.

Full Text

The Full Text of this article is available as a PDF (768.1 KB).

Selected References

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

  1. Ahmad S., Weisburg W. G., Jensen R. A. Evolution of aromatic amino acid biosynthesis and application to the fine-tuned phylogenetic positioning of enteric bacteria. J Bacteriol. 1990 Feb;172(2):1051–1061. doi: 10.1128/jb.172.2.1051-1061.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ahmer B. M., Thomas M. G., Larsen R. A., Postle K. Characterization of the exbBD operon of Escherichia coli and the role of ExbB and ExbD in TonB function and stability. J Bacteriol. 1995 Aug;177(16):4742–4747. doi: 10.1128/jb.177.16.4742-4747.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bassford P. J., Jr, Bradbeer C., Kadner R. J., Schnaitman C. A. Transport of vitamin B12 in tonB mutants of Escherichia coli. J Bacteriol. 1976 Oct;128(1):242–247. doi: 10.1128/jb.128.1.242-247.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bell P. E., Nau C. D., Brown J. T., Konisky J., Kadner R. J. Genetic suppression demonstrates interaction of TonB protein with outer membrane transport proteins in Escherichia coli. J Bacteriol. 1990 Jul;172(7):3826–3829. doi: 10.1128/jb.172.7.3826-3829.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bitter W., Tommassen J., Weisbeek P. J. Identification and characterization of the exbB, exbD and tonB genes of Pseudomonas putida WCS358: their involvement in ferric-pseudobactin transport. Mol Microbiol. 1993 Jan;7(1):117–130. doi: 10.1111/j.1365-2958.1993.tb01103.x. [DOI] [PubMed] [Google Scholar]
  6. Bradbeer C. The proton motive force drives the outer membrane transport of cobalamin in Escherichia coli. J Bacteriol. 1993 May;175(10):3146–3150. doi: 10.1128/jb.175.10.3146-3150.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Bruske A. K., Anton M., Heller K. J. Cloning and sequencing of the Klebsiella pneumoniae tonB gene and characterization of Escherichia coli-K. pneumoniae TonB hybrid proteins. Gene. 1993 Sep 6;131(1):9–16. doi: 10.1016/0378-1119(93)90663-n. [DOI] [PubMed] [Google Scholar]
  8. Bruske A. K., Heller K. J. Molecular characterization of the Enterobacter aerogenes tonB gene: identification of a novel type of tonB box suppressor mutant. J Bacteriol. 1993 Oct;175(19):6158–6168. doi: 10.1128/jb.175.19.6158-6168.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Byrd T. F., Horwitz M. A. Chloroquine inhibits the intracellular multiplication of Legionella pneumophila by limiting the availability of iron. A potential new mechanism for the therapeutic effect of chloroquine against intracellular pathogens. J Clin Invest. 1991 Jul;88(1):351–357. doi: 10.1172/JCI115301. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Cornelissen C. N., Biswas G. D., Tsai J., Paruchuri D. K., Thompson S. A., Sparling P. F. Gonococcal transferrin-binding protein 1 is required for transferrin utilization and is homologous to TonB-dependent outer membrane receptors. J Bacteriol. 1992 Sep;174(18):5788–5797. doi: 10.1128/jb.174.18.5788-5797.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Eick-Helmerich K., Braun V. Import of biopolymers into Escherichia coli: nucleotide sequences of the exbB and exbD genes are homologous to those of the tolQ and tolR genes, respectively. J Bacteriol. 1989 Sep;171(9):5117–5126. doi: 10.1128/jb.171.9.5117-5126.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Elkins C., Chen C. J., Thomas C. E. Characterization of the hgbA locus encoding a hemoglobin receptor from Haemophilus ducreyi. Infect Immun. 1995 Jun;63(6):2194–2200. doi: 10.1128/iai.63.6.2194-2200.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Fortier A. H., Leiby D. A., Narayanan R. B., Asafoadjei E., Crawford R. M., Nacy C. A., Meltzer M. S. Growth of Francisella tularensis LVS in macrophages: the acidic intracellular compartment provides essential iron required for growth. Infect Immun. 1995 Apr;63(4):1478–1483. doi: 10.1128/iai.63.4.1478-1483.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Frost G. E., Rosenberg H. Relationship between the tonB locus and iron transport in Escherichia coli. J Bacteriol. 1975 Nov;124(2):704–712. doi: 10.1128/jb.124.2.704-712.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Gaisser S., Braun V. The tonB gene of Serratia marcescens: sequence, activity and partial complementation of Escherichia coli tonB mutants. Mol Microbiol. 1991 Nov;5(11):2777–2787. doi: 10.1111/j.1365-2958.1991.tb01986.x. [DOI] [PubMed] [Google Scholar]
  16. Goldberg M. B., Boyko S. A., Butterton J. R., Stoebner J. A., Payne S. M., Calderwood S. B. Characterization of a Vibrio cholerae virulence factor homologous to the family of TonB-dependent proteins. Mol Microbiol. 1992 Aug;6(16):2407–2418. doi: 10.1111/j.1365-2958.1992.tb01415.x. [DOI] [PubMed] [Google Scholar]
  17. Guterman S. K., Dann L. Excretion of enterochelin by exbA and exbB mutants of Escherichia coli. J Bacteriol. 1973 Jun;114(3):1225–1230. doi: 10.1128/jb.114.3.1225-1230.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Hancock R. W., Braun V. Nature of the energy requirement for the irreversible adsorption of bacteriophages T1 and phi80 to Escherichia coli. J Bacteriol. 1976 Feb;125(2):409–415. doi: 10.1128/jb.125.2.409-415.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Hannavy K., Barr G. C., Dorman C. J., Adamson J., Mazengera L. R., Gallagher M. P., Evans J. S., Levine B. A., Trayer I. P., Higgins C. F. TonB protein of Salmonella typhimurium. A model for signal transduction between membranes. J Mol Biol. 1990 Dec 20;216(4):897–910. doi: 10.1016/S0022-2836(99)80009-6. [DOI] [PubMed] [Google Scholar]
  20. Hantke K., Braun V. Membrane receptor dependent iron transport in Escherichia coli. FEBS Lett. 1975 Jan 1;49(3):301–305. doi: 10.1016/0014-5793(75)80771-x. [DOI] [PubMed] [Google Scholar]
  21. Heller K. J., Kadner R. J., Günther K. Suppression of the btuB451 mutation by mutations in the tonB gene suggests a direct interaction between TonB and TonB-dependent receptor proteins in the outer membrane of Escherichia coli. Gene. 1988 Apr 15;64(1):147–153. doi: 10.1016/0378-1119(88)90488-x. [DOI] [PubMed] [Google Scholar]
  22. Hill C. W., Harnish B. W. Inversions between ribosomal RNA genes of Escherichia coli. Proc Natl Acad Sci U S A. 1981 Nov;78(11):7069–7072. doi: 10.1073/pnas.78.11.7069. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Jarosik G. P., Hansen E. J. Cloning and sequencing of the Haemophilus influenzae exbB and exbD genes. Gene. 1995 Jan 11;152(1):89–92. doi: 10.1016/0378-1119(94)00675-i. [DOI] [PubMed] [Google Scholar]
  24. Jarosik G. P., Sanders J. D., Cope L. D., Muller-Eberhard U., Hansen E. J. A functional tonB gene is required for both utilization of heme and virulence expression by Haemophilus influenzae type b. Infect Immun. 1994 Jun;62(6):2470–2477. doi: 10.1128/iai.62.6.2470-2477.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Jaskula J. C., Letain T. E., Roof S. K., Skare J. T., Postle K. Role of the TonB amino terminus in energy transduction between membranes. J Bacteriol. 1994 Apr;176(8):2326–2338. doi: 10.1128/jb.176.8.2326-2338.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Kampfenkel K., Braun V. Membrane topologies of the TolQ and TolR proteins of Escherichia coli: inactivation of TolQ by a missense mutation in the proposed first transmembrane segment. J Bacteriol. 1993 Jul;175(14):4485–4491. doi: 10.1128/jb.175.14.4485-4491.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Klebba P. E., Rutz J. M., Liu J., Murphy C. K. Mechanisms of TonB-catalyzed iron transport through the enteric bacterial cell envelope. J Bioenerg Biomembr. 1993 Dec;25(6):603–611. doi: 10.1007/BF00770247. [DOI] [PubMed] [Google Scholar]
  28. Koebnik R., Bäumler A. J., Heesemann J., Braun V., Hantke K. The TonB protein of Yersinia enterocolitica and its interactions with TonB-box proteins. Mol Gen Genet. 1993 Feb;237(1-2):152–160. doi: 10.1007/BF00282796. [DOI] [PubMed] [Google Scholar]
  29. Kyte J., Doolittle R. F. A simple method for displaying the hydropathic character of a protein. J Mol Biol. 1982 May 5;157(1):105–132. doi: 10.1016/0022-2836(82)90515-0. [DOI] [PubMed] [Google Scholar]
  30. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  31. Larsen R. A., Thomas M. G., Wood G. E., Postle K. Partial suppression of an Escherichia coli TonB transmembrane domain mutation (delta V17) by a missense mutation in ExbB. Mol Microbiol. 1994 Aug;13(4):627–640. doi: 10.1111/j.1365-2958.1994.tb00457.x. [DOI] [PubMed] [Google Scholar]
  32. Larsen R. A., Wood G. E., Postle K. The conserved proline-rich motif is not essential for energy transduction by Escherichia coli TonB protein. Mol Microbiol. 1993 Dec;10(5):943–953. doi: 10.1111/j.1365-2958.1993.tb00966.x. [DOI] [PubMed] [Google Scholar]
  33. Lundrigan M. D., Kadner R. J. Nucleotide sequence of the gene for the ferrienterochelin receptor FepA in Escherichia coli. Homology among outer membrane receptors that interact with TonB. J Biol Chem. 1986 Aug 15;261(23):10797–10801. [PubMed] [Google Scholar]
  34. Park Y. M., Stauffer G. V. DNA sequence of the metC gene and its flanking regions from Salmonella typhimurium LT2 and homology with the corresponding sequence of Escherichia coli. Mol Gen Genet. 1989 Mar;216(1):164–169. doi: 10.1007/BF00332246. [DOI] [PubMed] [Google Scholar]
  35. Pettersson A., van der Ley P., Poolman J. T., Tommassen J. Molecular characterization of the 98-kilodalton iron-regulated outer membrane protein of Neisseria meningitidis. Infect Immun. 1993 Nov;61(11):4724–4733. doi: 10.1128/iai.61.11.4724-4733.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Postle K. Aerobic regulation of the Escherichia coli tonB gene by changes in iron availability and the fur locus. J Bacteriol. 1990 May;172(5):2287–2293. doi: 10.1128/jb.172.5.2287-2293.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Postle K., Good R. F. DNA sequence of the Escherichia coli tonB gene. Proc Natl Acad Sci U S A. 1983 Sep;80(17):5235–5239. doi: 10.1073/pnas.80.17.5235. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Postle K., Reznikoff W. S. Identification of the Escherichia coli tonB gene product in minicells containing tonB hybrid plasmids. J Mol Biol. 1979 Jul 5;131(3):619–636. doi: 10.1016/0022-2836(79)90011-1. [DOI] [PubMed] [Google Scholar]
  39. Postle K., Skare J. T. Escherichia coli TonB protein is exported from the cytoplasm without proteolytic cleavage of its amino terminus. J Biol Chem. 1988 Aug 5;263(22):11000–11007. [PubMed] [Google Scholar]
  40. Postle K. TonB protein and energy transduction between membranes. J Bioenerg Biomembr. 1993 Dec;25(6):591–601. doi: 10.1007/BF00770246. [DOI] [PubMed] [Google Scholar]
  41. Reynolds P. R., Mottur G. P., Bradbeer C. Transport of vitamin B12 in Escherichia coli. Some observations on the roles of the gene products of BtuC and TonB. J Biol Chem. 1980 May 10;255(9):4313–4319. [PubMed] [Google Scholar]
  42. Roof S. K., Allard J. D., Bertrand K. P., Postle K. Analysis of Escherichia coli TonB membrane topology by use of PhoA fusions. J Bacteriol. 1991 Sep;173(17):5554–5557. doi: 10.1128/jb.173.17.5554-5557.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Rutz J. M., Abdullah T., Singh S. P., Kalve V. I., Klebba P. E. Evolution of the ferric enterobactin receptor in gram-negative bacteria. J Bacteriol. 1991 Oct;173(19):5964–5974. doi: 10.1128/jb.173.19.5964-5974.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Schramm E., Mende J., Braun V., Kamp R. M. Nucleotide sequence of the colicin B activity gene cba: consensus pentapeptide among TonB-dependent colicins and receptors. J Bacteriol. 1987 Jul;169(7):3350–3357. doi: 10.1128/jb.169.7.3350-3357.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Schöffler H., Braun V. Transport across the outer membrane of Escherichia coli K12 via the FhuA receptor is regulated by the TonB protein of the cytoplasmic membrane. Mol Gen Genet. 1989 Jun;217(2-3):378–383. doi: 10.1007/BF02464907. [DOI] [PubMed] [Google Scholar]
  46. Skare J. T., Ahmer B. M., Seachord C. L., Darveau R. P., Postle K. Energy transduction between membranes. TonB, a cytoplasmic membrane protein, can be chemically cross-linked in vivo to the outer membrane receptor FepA. J Biol Chem. 1993 Aug 5;268(22):16302–16308. [PubMed] [Google Scholar]
  47. Skare J. T., Postle K. Evidence for a TonB-dependent energy transduction complex in Escherichia coli. Mol Microbiol. 1991 Dec;5(12):2883–2890. doi: 10.1111/j.1365-2958.1991.tb01848.x. [DOI] [PubMed] [Google Scholar]
  48. Skare J. T., Roof S. K., Postle K. A mutation in the amino terminus of a hybrid TrpC-TonB protein relieves overproduction lethality and results in cytoplasmic accumulation. J Bacteriol. 1989 Aug;171(8):4442–4447. doi: 10.1128/jb.171.8.4442-4447.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES