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The Journal of Biophysical and Biochemical Cytology logoLink to The Journal of Biophysical and Biochemical Cytology
. 1960 Jul 1;7(4):697–716. doi: 10.1083/jcb.7.4.697

On Flagellar Structure in Certain Flagellates

I R Gibbons 1, A V Grimstone 1
PMCID: PMC2224891  PMID: 13827900

Abstract

This paper describes the structure of the flagella, basal bodies, and some of the associated fibre systems in three genera of complex flagellates, Trichonympha, Pseudotrichonympha, and Holomastigotoides. Three groups of longitudinal fibres occur in a flagellum: two central and nine outer fibres such as have been repeatedly described in other material, and an additional set of nine smaller secondary fibres not previously identified as such. Each central fibre shows a helical substructure; the pair of them are enveloped in a common sheath. Each outer fibre is a doublet with one subfibre bearing projections—called arms—that extend toward the adjacent outer fibre. The basal body is formed by a cylinder of nine triplet outer fibres. Two subfibres of each triplet continue into the flagellum and constitute the doublets. The third subfibre terminates at the transition of basal body to flagellum, possibly giving rise to the nine radial transitional fibres that seem to attach the end of the basal body to the surface of the organism. The central and secondary flagellar fibres are not present in the lumen of the basal body, but other complex structures occur there. The form of these intraluminal structures differs from genus to genus. The flagellar unit is highly asymmetrical. All the flagella examined have possessed the same one of the two possible enantiomorphic forms. At least two systems of fibres are associated with the basal bodies of all three genera.

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Selected References

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  1. AFZELIUS B. Electron microscopy of the sperm tail; results obtained with a new fixative. J Biophys Biochem Cytol. 1959 Mar 25;5(2):269–278. doi: 10.1083/jcb.5.2.269. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. ANDERSON E., BEAMS H. W. The cytology of Tritrichomonas as revealed by the electon microscope. J Morphol. 1959 Mar;104:205–235. doi: 10.1002/jmor.1051040203. [DOI] [PubMed] [Google Scholar]
  3. BERNHARD W., DE HARVEN E. Etude au microscope électronique de l'ultrastructure du centriole chez les vertébrés. Z Zellforsch Mikrosk Anat. 1956;45(3):378–398. [PubMed] [Google Scholar]
  4. BESSIS M., BRETON-GORIUS J., THIERY J. P. Centriole, corps de Golgi et aster des leucocytes; étude au microscope électronique. Rev Hematol. 1958 Jul-Sep;13(3):363–386. [PubMed] [Google Scholar]
  5. BURNASHEVA S. A. K kharakteristike sokratitel'nogo belka semennykh kletok spermozina. Biokhimiia. 1958 Jul-Aug;23(4):558–563. [PubMed] [Google Scholar]
  6. CHILD F. M. The characterization of the cilia of Tetrahymena pyriformis. Exp Cell Res. 1959 Oct;18:258–267. doi: 10.1016/0014-4827(59)90005-9. [DOI] [PubMed] [Google Scholar]
  7. GIBBS S. P., LEWIN R. A., PHILPOTT D. E. The fine structure of the flagellar apparatus of Chlamydomonas moewusii. Exp Cell Res. 1958 Dec;15(3):619–622. doi: 10.1016/0014-4827(58)90112-5. [DOI] [PubMed] [Google Scholar]
  8. GLAUERT A. M., GLAUERT R. H. Araldite as an embedding medium for electron microscopy. J Biophys Biochem Cytol. 1958 Mar 25;4(2):191–194. doi: 10.1083/jcb.4.2.191. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. GRIMSTONE A. V. Cytoplasmic membranes and the nuclear membrane in the flagellate Trichonympha. J Biophys Biochem Cytol. 1959 Dec;6:369–378. doi: 10.1083/jcb.6.3.369. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. HOFFMANN-BERLING H. Geisselmodelle und Adenosintriphosphat (ATP). Biochim Biophys Acta. 1955 Jan;16(1):146–154. doi: 10.1016/0006-3002(55)90192-x. [DOI] [PubMed] [Google Scholar]
  11. HUXLEY H. E. The double array of filaments in cross-striated muscle. J Biophys Biochem Cytol. 1957 Sep 25;3(5):631–648. doi: 10.1083/jcb.3.5.631. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. PEACHEY L. D. Thin sections. I. A study of section thickness and physical distortion produced during microtomy. J Biophys Biochem Cytol. 1958 May 25;4(3):233–242. doi: 10.1083/jcb.4.3.233. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. RANDALL J. T., JACKSON S. F. Fine structure and function in Stentor polymorphous. J Biophys Biochem Cytol. 1958 Nov 25;4(6):807–830. doi: 10.1083/jcb.4.6.807. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. RHODIN J., DALHAMN T. Electron microscopy of the tracheal ciliated mucosa in rat. Z Zellforsch Mikrosk Anat. 1956;44(4):345–412. doi: 10.1007/BF00345847. [DOI] [PubMed] [Google Scholar]
  15. ROTH L. E. A filamentous component of protozoan fibrillar systems. J Ultrastruct Res. 1958 Apr;1(3):223–234. doi: 10.1016/s0022-5320(58)80002-7. [DOI] [PubMed] [Google Scholar]
  16. ROTH L. E. Aspects of ciliary fine structure in Euplotes patella. J Biophys Biochem Cytol. 1956 Jul 25;2(4 Suppl):235–240. doi: 10.1083/jcb.2.4.235. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. SATIR P. G., PEACHEY L. D. Thin sections. II. A simple method for reducing compression artifacts. J Biophys Biochem Cytol. 1958 May 25;4(3):345–348. doi: 10.1083/jcb.4.3.345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. SEDAR A. W., PORTER K. R. The fine structure of cortical components of Paramecium multimicronucleatum. J Biophys Biochem Cytol. 1955 Nov 25;1(6):583–604. doi: 10.1083/jcb.1.6.583. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. TOKUYASU K., YAMADA E. The fine structure of the retina studied with the electron microscope. IV. Morphogenesis of outer segments of retinal rods. J Biophys Biochem Cytol. 1959 Oct;6:225–230. doi: 10.1083/jcb.6.2.225. [DOI] [PMC free article] [PubMed] [Google Scholar]

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