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PMID: 5971649 Published · ppublish English Journal Article

Basal bodies of bacterial flagella in Proteus mirabilis. I. Electron microscopy of sectioned material.

The Journal of cell biology ·Vol. 31 ·No. 3 ·1966-12-00 ·Pages 585-601

Van Iterson W, Hoeniger JF, Van Zanten EN

Abstract

Years ago (16, 18, 19), in a study of shadowed preparations of Proteus vulgaris that had been autolyzed in the cold, the observation was made that the flagella arose from basal bodies. However, recently (3, 7, 24, 33) doubt has been cast on the conclusion that the flagella of bacteria emerge from sizable basal bodies. This problem has, therefore, been reinvestigated with actively developing cultures of Proteus mirabilis, the cell walls of which had been expanded slightly by exposure to penicillin. Two techniques were applied: ultramicrotomy, and negative staining of whole mount preparations. This paper deals with the thin sections of bacteria after the usual fixation technique had been altered slightly: the cells were embedded in agar prior to their fixation and further processing. The flagella then remained attached to the cells and were seen to extend between the cell wall and the plasma membrane. Occasionally, the flagella appeared to be anchored in the cell by means of a hook-shaped ending. In sections of cells rich in cytoplasm, the basal bodies are particularly difficult to visualize due to their small size (25 to 45 mmicro) and the lack of properties that would enable one to distinguish them from the ribonucleoprotein structures; in addition, their boundary appears to be delicate. However, when the cytoplasm is sparse in the cells, either naturally or as a result of osmotic shocking in distilled water, the flagella can be observed to emerge from rounded structures approximately 25 to 45 mmicro wide. Contrary to a previous suggestion (21), the flagella do not terminate in the peripheral sites of reduced tellurite, i.e. the chondrioids. The observations in this part of the study agree with those described in the following paper (15) dealing with negatively stained preparations.

MeSH Terms
Cell Membrane Cell Wall Cytoplasm Flagella Microscopy, Electron Proteus/cytology
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Van Iterson W
Hoeniger J F
Van Zanten E N
References (23)
23 references, click to expand
  1. ELECTRON MICROSCOPE STUDIES OF BACTERIAL FLAGELLA.
    J Mol Biol. 1965 Feb;11:293-313 PMID: 14290347
  2. Electron microscopy of flagellation in species of Spirillum.
    J Bacteriol. 1961 Feb;81:195-203 PMID: 13785467
  3. Structure of the proximal ends of bacterial flagella.
    J Mol Biol. 1965 Nov;14(1):297-9 PMID: 5327655
  4. Bacterial flagella and motility.
    Ergeb Mikrobiol Immunitatsforsch Exp Ther. 1957;30:37-95 PMID: 13473784
  5. STRUCTURE OF BACTERIAL FLAGELLA.
    Nature. 1964 May 9;202:538-40 PMID: 14195046
  6. Basal structure and attachment of flagella in cells of Proteus vulgaris.
    J Bacteriol. 1965 Nov;90(5):1337-54 PMID: 5848332
  7. Basal bodies of bacterial flagella in Proteus mirabilis. II. Electron microscopy of negatively stained material.
    J Cell Biol. 1966 Dec;31(3):603-18 PMID: 4165908
  8. Fine structure and morphogenesis in Protozoa.
    Biol Rev Camb Philos Soc. 1961 Feb;36:97-150 PMID: 13708746
  9. THE ULTRASTRUCTURE OF FLAGELLAR FIBRILS.
    J Cell Biol. 1963 Aug;18:313-26 PMID: 14079491
  10. THE FINE STRUCTURE AND MODE OF ATTACHMENT OF THE SHEATHED FLAGELLUM OF VIBRIO METCHNIKOVII.
    J Cell Biol. 1963 Aug;18:327-36 PMID: 14079492
  11. The use of lead citrate at high pH as an electron-opaque stain in electron microscopy.
    J Cell Biol. 1963 Apr;17:208-12 PMID: 13986422
  12. Some observations upon the development and mode of attachment of the flagella in Vibrio and Spirillum species.
    Exp Cell Res. 1956 Feb;10(1):234-7 PMID: 13294134
  13. The fine structure of the ribonucleoprotein in bacterial cytoplasm.
    J Cell Biol. 1966 Mar;28(3):563-70 PMID: 4163863
  14. Electron-microscopic study on the flagella of Vibrio comma.
    J Bacteriol. 1957 Jan;73(1):89-90 PMID: 13405866
  15. The isolation of protoplasts from Bacillus megaterium by controlled treatment with lysozyme.
    J Bacteriol. 1953 Dec;66(6):688-95 PMID: 13117795
  16. Electron microscope observations on the structure of fimbriae, with particular reference to Klebsiella strains, by the use of the negative staining technique.
    J Gen Microbiol. 1962 Apr;28:51-6 PMID: 13921046
  17. Some observations on the flagella and blepharoplasts of Spirillum and Vibrio spp.
    J Gen Microbiol. 1954 Apr;10(2):325-7 PMID: 13152344
  18. [Electron microscopic study of the ultrastructure of centrioles in vertebra].
    Z Zellforsch Mikrosk Anat. 1956;45(3):378-98 PMID: 13402087
  19. A "microtubule" in a bacterium.
    J Cell Biol. 1967 Jan;32(1):1-10 PMID: 10976198
  20. Structural components of flagella from Salmonella typhimurium.
    J Mol Biol. 1962 Apr;4:227-38 PMID: 14455344
  21. Evidence for the presence of DNA at basal body sites in Tetrahymena pyriformis.
    Proc R Soc Lond B Biol Sci. 1965 Jul 27;162(989):473-91 PMID: 4378460
  22. A CYTOCHEMICAL LOCALIZATION OF REDUCTIVE SITES IN A GRAM-NEGATIVE BACTERIUM. TELLURITE REDUCTION IN PROTEUS VULGARIS.
    J Cell Biol. 1964 Mar;20:377-87 PMID: 14128043
  23. Fine structure and function in Stentor polymorphous.
    J Biophys Biochem Cytol. 1958 Nov 25;4(6):807-30 PMID: 13610947
Article Info
Journal
The Journal of cell biology
Abbr.
J Cell Biol
ISSN
0021-9525
Published
1966-12-00
Pages
585-601
Language
English
Region
United States
NLM ID
0375356
PMCID
PMC2107067
Subset
IM
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