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. 1991 Jan;173(2):926–928. doi: 10.1128/jb.173.2.926-928.1991

Lipopolysaccharide structure required for in vitro trimerization of Escherichia coli OmpF porin.

K Sen 1, H Nikaido 1
PMCID: PMC207093  PMID: 1702785

Abstract

Deep rought mutants, which produce very defective lipopolysaccharides, are unable to export normal levels of porins into the outer membrane. In this study, we showed that lipopolysaccharides from such mutants were also unable to facilitate the trimerization, in vitro, of monomeric OmpF porin secreted by spheroplasts of Escherichia coli B/r. In contrast, lipopolysaccharides containing most or all of the core oligosaccharides were able to facilitate trimerization.

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Selected References

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  1. Ames G. F., Spudich E. N., Nikaido H. Protein composition of the outer membrane of Salmonella typhimurium: effect of lipopolysaccharide mutations. J Bacteriol. 1974 Feb;117(2):406–416. doi: 10.1128/jb.117.2.406-416.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Datta D. B., Arden B., Henning U. Major proteins of the Escherichia coli outer cell envelope membrane as bacteriophage receptors. J Bacteriol. 1977 Sep;131(3):821–829. doi: 10.1128/jb.131.3.821-829.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Funahara Y., Nikaido H. Asymmetric localization of lipopolysaccharides on the outer membrane of Salmonella typhimurium. J Bacteriol. 1980 Mar;141(3):1463–1465. doi: 10.1128/jb.141.3.1463-1465.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Galanos C., Lüderitz O., Westphal O. A new method for the extraction of R lipopolysaccharides. Eur J Biochem. 1969 Jun;9(2):245–249. doi: 10.1111/j.1432-1033.1969.tb00601.x. [DOI] [PubMed] [Google Scholar]
  5. Jap B. K. Molecular design of PhoE porin and its functional consequences. J Mol Biol. 1989 Jan 20;205(2):407–419. doi: 10.1016/0022-2836(89)90351-3. [DOI] [PubMed] [Google Scholar]
  6. Klebba P. E., Benson S. A., Bala S., Abdullah T., Reid J., Singh S. P., Nikaido H. Determinants of OmpF porin antigenicity and structure. J Biol Chem. 1990 Apr 25;265(12):6800–6810. [PubMed] [Google Scholar]
  7. Koplow J., Goldfine H. Alterations in the outer membrane of the cell envelope of heptose-deficient mutants of Escherichia coli. J Bacteriol. 1974 Feb;117(2):527–543. doi: 10.1128/jb.117.2.527-543.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Lindberg A. A., Hellerqvist C. G. Bacteriophage attachment sites, serological specificity, and chemical composition of the lipopolysaccharides of semirough and rough mutants of Salmonella typhimurium. J Bacteriol. 1971 Jan;105(1):57–64. doi: 10.1128/jb.105.1.57-64.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Mühlradt P. F. Biosynthesis of Salmonella lipopolysaccharide. Studies on the transfer of glucose, galactose, and phosphate to the core in a cell free system. Eur J Biochem. 1971 Jan 1;18(1):20–27. doi: 10.1111/j.1432-1033.1971.tb01209.x. [DOI] [PubMed] [Google Scholar]
  10. Mühlradt P. F., Golecki J. R. Asymmetrical distribution and artifactual reorientation of lipopolysaccharide in the outer membrane bilayer of Salmonella typhimurium. Eur J Biochem. 1975 Feb 21;51(2):343–352. doi: 10.1111/j.1432-1033.1975.tb03934.x. [DOI] [PubMed] [Google Scholar]
  11. Nikaido H., Vaara M. Molecular basis of bacterial outer membrane permeability. Microbiol Rev. 1985 Mar;49(1):1–32. doi: 10.1128/mr.49.1.1-32.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. OSBORN M. J. STUDIES ON THE GRAM-NEGATIVE CELL WALL. I. EVIDENCE FOR THE ROLE OF 2-KETO- 3-DEOXYOCTONATE IN THE LIPOPOLYSACCHARIDE OF SALMONELLA TYPHIMURIUM. Proc Natl Acad Sci U S A. 1963 Sep;50:499–506. doi: 10.1073/pnas.50.3.499. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Reid J., Fung H., Gehring K., Klebba P. E., Nikaido H. Targeting of porin to the outer membrane of Escherichia coli. Rate of trimer assembly and identification of a dimer intermediate. J Biol Chem. 1988 Jun 5;263(16):7753–7759. [PubMed] [Google Scholar]
  14. Schindler H., Rosenbusch J. P. Matrix protein in planar membranes: clusters of channels in a native environment and their functional reassembly. Proc Natl Acad Sci U S A. 1981 Apr;78(4):2302–2306. doi: 10.1073/pnas.78.4.2302. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Schlecht S., Schmidt G. Möglichkeiten zur Differenzierung von Salmonella-R-Formen mittels Antibiotica und antibakterieller Farbstoffe. Zentralbl Bakteriol Orig. 1970;212(2):505–511. [PubMed] [Google Scholar]
  16. Sen K., Nikaido H. In vitro trimerization of OmpF porin secreted by spheroplasts of Escherichia coli. Proc Natl Acad Sci U S A. 1990 Jan;87(2):743–747. doi: 10.1073/pnas.87.2.743. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Smit J., Kamio Y., Nikaido H. Outer membrane of Salmonella typhimurium: chemical analysis and freeze-fracture studies with lipopolysaccharide mutants. J Bacteriol. 1975 Nov;124(2):942–958. doi: 10.1128/jb.124.2.942-958.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Wilkinson R. G., Gemski P., Jr, Stocker B. A. Non-smooth mutants of Salmonella typhimurium: differentiation by phage sensitivity and genetic mapping. J Gen Microbiol. 1972 May;70(3):527–554. doi: 10.1099/00221287-70-3-527. [DOI] [PubMed] [Google Scholar]
  19. Yu F., Yamada H., Mizushima S. Role of lipopolysaccharide in the receptor function for bacteriophage TuIb in Escherichia coli. J Bacteriol. 1981 Nov;148(2):712–715. doi: 10.1128/jb.148.2.712-715.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]

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