Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1990 Sep;172(9):5312–5325. doi: 10.1128/jb.172.9.5312-5325.1990

Genetic analysis of lipopolysaccharide core biosynthesis by Escherichia coli K-12: insertion mutagenesis of the rfa locus.

E A Austin 1, J F Graves 1, L A Hite 1, C T Parker 1, C A Schnaitman 1
PMCID: PMC213195  PMID: 2168379

Abstract

Tn10 insertions were selected on the basis of resistance to the lipopolysaccharide (LPS)-specific bacteriophage U3. The majority of these were located in a 2-kilobase region within the rfa locus, a gene cluster of about 18 kb that contains genes for LPS core biosynthesis. The rfa::Tn10 insertions all exhibited a deep rough phenotype that included hypersensitivity to hydrophobic antibiotics, a reduction in major outer membrane proteins, and production of truncated LPS. These mutations were complemented by a Clarke-Carbon plasmid known to complement rfa mutations of Salmonella typhimurium, and analysis of the insert from this plasmid showed that it contained genes for at least six polypeptides which appear to be arranged in the form of a complex operon. Defects in two of these genes were specifically implicated as the cause of the deep rough phenotype. One of these appeared to be rfaG, which encodes a function required for attachment of the first glucose residue to the heptose region of the core. The other gene did not appear to be directly involved in determination of the sugar composition of the core. We speculate that the product of this gene is involved in the attachment of phosphate or phosphorylethanolamine to the core and that it is the lack of one of these substituents which results in the deep rough phenotype.

Full text

PDF

Images in this article

Selected References

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

  1. Aronson B. D., Ravnikar P. D., Somerville R. L. Nucleotide sequence of the 2-amino-3-ketobutyrate coenzyme A ligase (kbl) gene of E. coli. Nucleic Acids Res. 1988 Apr 25;16(8):3586–3586. doi: 10.1093/nar/16.8.3586. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Beher M. G., Schnaitman C. A. Regulation of the OmpA outer membrane protein of Escherichia coli. J Bacteriol. 1981 Sep;147(3):972–985. doi: 10.1128/jb.147.3.972-985.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Beutin L., Manning P. A., Achtman M., Willetts N. sfrA and sfrB products of Escherichia coli K-12 are transcriptional control factors. J Bacteriol. 1981 Feb;145(2):840–844. doi: 10.1128/jb.145.2.840-844.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Blasband A. J., Marcotte W. R., Jr, Schnaitman C. A. Structure of the lc and nmpC outer membrane porin protein genes of lambdoid bacteriophage. J Biol Chem. 1986 Sep 25;261(27):12723–12732. [PubMed] [Google Scholar]
  5. Catron K. M., Schnaitman C. A. Export of protein in Escherichia coli: a novel mutation in ompC affects expression of other major outer membrane proteins. J Bacteriol. 1987 Sep;169(9):4327–4334. doi: 10.1128/jb.169.9.4327-4334.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Ciampi M. S., Schmid M. B., Roth J. R. Transposon Tn10 provides a promoter for transcription of adjacent sequences. Proc Natl Acad Sci U S A. 1982 Aug;79(16):5016–5020. doi: 10.1073/pnas.79.16.5016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Click E. M., McDonald G. A., Schnaitman C. A. Translational control of exported proteins that results from OmpC porin overexpression. J Bacteriol. 1988 May;170(5):2005–2011. doi: 10.1128/jb.170.5.2005-2011.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Coleman W. G., Jr The rfaD gene codes for ADP-L-glycero-D-mannoheptose-6-epimerase. An enzyme required for lipopolysaccharide core biosynthesis. J Biol Chem. 1983 Feb 10;258(3):1985–1990. [PubMed] [Google Scholar]
  9. Creeger E. S., Chen J. F., Rothfield L. I. Cloning of genes for bacterial glycosyltransferases. II. Selection of a hybrid plasmid carrying the rfah gene. J Biol Chem. 1979 Feb 10;254(3):811–815. [PubMed] [Google Scholar]
  10. Creeger E. S., Schulte T., Rothfield L. I. Regulation of membrane glycosyltransferases by the sfrB and rfaH genes of Escherichia coli and Salmonella typhimurium. J Biol Chem. 1984 Mar 10;259(5):3064–3069. [PubMed] [Google Scholar]
  11. Crowell D. N., Reznikoff W. S., Raetz C. R. Nucleotide sequence of the Escherichia coli gene for lipid A disaccharide synthase. J Bacteriol. 1987 Dec;169(12):5727–5734. doi: 10.1128/jb.169.12.5727-5734.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. 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]
  13. Hasin M., Kennedy E. P. Role of phosphatidylethanolamine in the biosynthesis of pyrophosphoethanolamine residues in the lipopolysaccharide of Escherichia coli. J Biol Chem. 1982 Nov 10;257(21):12475–12477. [PubMed] [Google Scholar]
  14. Henikoff S. Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing. Gene. 1984 Jun;28(3):351–359. doi: 10.1016/0378-1119(84)90153-7. [DOI] [PubMed] [Google Scholar]
  15. Hitchcock P. J., Brown T. M. Morphological heterogeneity among Salmonella lipopolysaccharide chemotypes in silver-stained polyacrylamide gels. J Bacteriol. 1983 Apr;154(1):269–277. doi: 10.1128/jb.154.1.269-277.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Kadam S. K., Rehemtulla A., Sanderson K. E. Cloning of rfaG, B, I, and J genes for glycosyltransferase enzymes for synthesis of the lipopolysaccharide core of Salmonella typhimurium. J Bacteriol. 1985 Jan;161(1):277–284. doi: 10.1128/jb.161.1.277-284.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Kohara Y., Akiyama K., Isono K. The physical map of the whole E. coli chromosome: application of a new strategy for rapid analysis and sorting of a large genomic library. Cell. 1987 Jul 31;50(3):495–508. doi: 10.1016/0092-8674(87)90503-4. [DOI] [PubMed] [Google Scholar]
  18. Kozulić B., Ries B., Mildner P. N-acetylation of amino sugar methyl glycosides for gas-liquid chromatographic analysis. Anal Biochem. 1979 Apr 1;94(1):36–39. doi: 10.1016/0003-2697(79)90786-3. [DOI] [PubMed] [Google Scholar]
  19. Kumamoto C. A., Beckwith J. Evidence for specificity at an early step in protein export in Escherichia coli. J Bacteriol. 1985 Jul;163(1):267–274. doi: 10.1128/jb.163.1.267-274.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Kuo T. T., Stocker B. A. Mapping of rfa Genes in Salmonella typhimurium by ES18 and P22 Transduction and by Conjugation. J Bacteriol. 1972 Oct;112(1):48–57. doi: 10.1128/jb.112.1.48-57.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Lee J. S., An G., Friesen J. D., Isono K. Cloning and the nucleotide sequence of the genes for Escherichia coli ribosomal proteins L28 (rpmB) and L33 (rpmG). Mol Gen Genet. 1981;184(2):218–223. doi: 10.1007/BF00272908. [DOI] [PubMed] [Google Scholar]
  22. Morona R., Manning P. A., Reeves P. Identification and characterization of the TolC protein, an outer membrane protein from Escherichia coli. J Bacteriol. 1983 Feb;153(2):693–699. doi: 10.1128/jb.153.2.693-699.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Mühlradt P. Biosynthesis of Salmonella lipopolysaccharide. The in vitro transfer of phosphate to the heptose moiety of the core. Eur J Biochem. 1969 Dec;11(2):241–248. doi: 10.1111/j.1432-1033.1969.tb00766.x. [DOI] [PubMed] [Google Scholar]
  24. Mühlradt P., Risse H. J., Lüderitz O., Westphal O. Biochemical studies on lipopolysaccharides of Salmonella R mutants 5. Evidence for a phosphorylating enzyme in lipopolysaccharide biosynthesis. Eur J Biochem. 1968 Apr 3;4(2):139–145. doi: 10.1111/j.1432-1033.1968.tb00184.x. [DOI] [PubMed] [Google Scholar]
  25. Nikaido H., Nakae T. The outer membrane of Gram-negative bacteria. Adv Microb Physiol. 1979;20:163–250. doi: 10.1016/s0065-2911(08)60208-8. [DOI] [PubMed] [Google Scholar]
  26. 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]
  27. Schnaitman C. A., McDonald G. A. Regulation of outer membrane protein synthesis in Escherichia coli K-12: deletion of ompC affects expression of the OmpF protein. J Bacteriol. 1984 Aug;159(2):555–563. doi: 10.1128/jb.159.2.555-563.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Silverman J. A., Benson S. A. Bacteriophage K20 requires both the OmpF porin and lipopolysaccharide for receptor function. J Bacteriol. 1987 Oct;169(10):4830–4833. doi: 10.1128/jb.169.10.4830-4833.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. 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]

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

RESOURCES