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. 1976 Apr;126(1):377–383. doi: 10.1128/jb.126.1.377-383.1976

Chemical characterization of the regularly arranged surface layers of Clostridium thermosaccharolyticum and Clostridium thermohydrosulfuricum.

U B Sleytr, K J Thorne
PMCID: PMC233294  PMID: 816775

Abstract

Clostridum thermosaccharolyticum and Clostridium thermohydrosulfuricum possess as outermost cell wall layer a tetragonal or hexagonal ordered array of macromolecules. The subunits of the surface layer can be detached from isolated cell walls with urea (8M) or guanidine-HCl (4 to 5 M). Triton X-100, dithiothreitol, ethylenediaminetetracetate, and KCl (3 M) had no visible effect on the regular arrays. Sodium dodecyl sulfate-polyacrylamide electrophroesis showed that, in both organisms, the surface layer is composed of glycoprotein of molecular weight 140,000. The glycoprotein from both microorganisms has a predominantly acidic amino acid composition and an acidic isoelectric point after isoelectric focusing on polyacrylamide gels. The glycocomponent is composed of glucose, galactose, mannose, and rhamnose.

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Selected References

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  1. BITTER T., MUIR H. M. A modified uronic acid carbazole reaction. Anal Biochem. 1962 Oct;4:330–334. doi: 10.1016/0003-2697(62)90095-7. [DOI] [PubMed] [Google Scholar]
  2. Buckmire F. L., Murray R. G. Studies on the cell wall of Spirillum serpens. 1. Isolation and partial purification of the outermost cell wall layer. Can J Microbiol. 1970 Oct;16(10):1011–1022. doi: 10.1139/m70-171. [DOI] [PubMed] [Google Scholar]
  3. Buckmire F. L., Murray R. G. Studies on the cell wall of Spirillum serpens. II. Chemical characterization of the outer structured layer. Can J Microbiol. 1973 Jan;19(1):59–66. doi: 10.1139/m73-009. [DOI] [PubMed] [Google Scholar]
  4. Fairbanks G., Steck T. L., Wallach D. F. Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. Biochemistry. 1971 Jun 22;10(13):2606–2617. doi: 10.1021/bi00789a030. [DOI] [PubMed] [Google Scholar]
  5. Glaubert A. M., Sleytr U. B. Analysis of regular arrays of subunits on bacterial surfaces: evidence for a dynamic process of assembly. J Ultrastruct Res. 1975 Jan;50(1):103–116. doi: 10.1016/s0022-5320(75)90012-x. [DOI] [PubMed] [Google Scholar]
  6. Glauert A. M., Thornley M. J. Fine structure and radiation resistance in Acinetobacter: a comparison of a range of strains. J Cell Sci. 1971 Jan;8(1):19–41. doi: 10.1242/jcs.8.1.19. [DOI] [PubMed] [Google Scholar]
  7. Hollaus F., Sleytr U. On the taxonomy and fine structure of some hyperthermophilic saccharolytic Clostridia. Arch Mikrobiol. 1972;86(2):129–146. doi: 10.1007/BF00413368. [DOI] [PubMed] [Google Scholar]
  8. Howard L., Tipper D. J. A polypeptide bacteriophage receptor: modified cell wall protein subunits in bacteriophage-resistant mutants of Bacillus sphaericus strain P-1. J Bacteriol. 1973 Mar;113(3):1491–1504. doi: 10.1128/jb.113.3.1491-1504.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  10. Mescher M. F., Strominger J. L., Watson S. W. Protein and carbohydrate composition of the cell envelope of Halobacterium salinarium. J Bacteriol. 1974 Nov;120(2):945–954. doi: 10.1128/jb.120.2.945-954.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Nermut M. V., Murray R. G. Ultrastructure of the cell wall of Bacillus polymyxa. J Bacteriol. 1967 Jun;93(6):1949–1965. doi: 10.1128/jb.93.6.1949-1965.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Okuda S., Weinbaum G. An envelope-specific glycoprotein from Escherichia coli B. Biochemistry. 1968 Aug;7(8):2819–2825. doi: 10.1021/bi00848a018. [DOI] [PubMed] [Google Scholar]
  13. Sleytr U. B. Heterologous reattachment of regular arrays of glycoproteins on bacterial surfaces. Nature. 1975 Oct 2;257(5525):400–402. doi: 10.1038/257400a0. [DOI] [PubMed] [Google Scholar]
  14. Sleytr U., Adam H., Klaushofer H. Die Feinstruktur der Zellwandoberfläche von zwei thermophilen Clostridienarten, dargestellt mit Hilfe der Gefrierätztechnik. Mikroskopie. 1968 Aug;23(1):1–10. [PubMed] [Google Scholar]
  15. TREVELYAN W. E., PROCTER D. P., HARRISON J. S. Detection of sugars on paper chromatograms. Nature. 1950 Sep 9;166(4219):444–445. doi: 10.1038/166444b0. [DOI] [PubMed] [Google Scholar]
  16. Thorne K. J., Thornley M. J., Naisbitt P., Glauert A. M. The nature of the attachment of a regularly arranged surface protein to the outer membrane of an Acinetobacter sp. Biochim Biophys Acta. 1975 Apr 21;389(1):97–116. doi: 10.1016/0005-2736(75)90388-0. [DOI] [PubMed] [Google Scholar]
  17. Thornley M. J., Glauert A. M., Sleytr U. B. Structure and assembly of bacterial surface layers composed of regular arrays of subunits. Philos Trans R Soc Lond B Biol Sci. 1974 Jul 25;268(891):147–153. doi: 10.1098/rstb.1974.0022. [DOI] [PubMed] [Google Scholar]
  18. Thornley M. J., Thorne K. J., Glauert A. M. Detachment and chemical characterization of the regularly arranged subunits from the surface of an Acinetobacter. J Bacteriol. 1974 May;118(2):654–662. doi: 10.1128/jb.118.2.654-662.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Watson S. W., Remsen C. C. Macromolecular subunits in the walls of marine nitrifying bacteria. Science. 1969 Feb 14;163(3868):685–686. doi: 10.1126/science.163.3868.685. [DOI] [PubMed] [Google Scholar]
  20. Weber K., Osborn M. The reliability of molecular weight determinations by dodecyl sulfate-polyacrylamide gel electrophoresis. J Biol Chem. 1969 Aug 25;244(16):4406–4412. [PubMed] [Google Scholar]

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