Literature DB >> 4165908

Basal bodies of bacterial flagella in Proteus mirabilis. II. Electron microscopy of negatively stained material.

J F Hoeniger, W Van Iterson, E N Van Zanten.   

Abstract

This paper investigates further the question of whether the flagella of Proteus mirabilis emerge from basal bodies. The bacteria were grown to the stage of swarmer differentiation, treated lightly with penicillin, and then shocked osmotically. As a result of this treatment, much of the cytoplasmic content and also part of the plasma membrane were removed from the cells. When such fragmented organisms were stained negatively with potassium phosphotungstate, the flagella were found to be anchored-often by means of a hook-in rounded structures approximately 50 mmicro wide, thus confirming Part I of our study. In these rounded structures a more brilliant dot was occasionally observed, which we interpret as being part of the basal granule. A prerequisite for the demonstration of the basal granules within the cells was, however, the removal of both the cytoplasm and the plasma membrane from their vicinity. In some experiments, the chondrioids were "stained" positively by the incorporation into them of the reduced product of potassium tellurite. The chondrioids were here observed to be more or less circular areas from which rodlike structures extended. The chondrioids adhered so firmly to the plasma membrane that they were carried away with it during its displacement by osmotic shocking, while the basal bodies were left behind. This observation disproves our previous suggestion that the flagella might terminate in the chondrioids. The basal bodies often occur in pairs, which suggest that they could be self-reproducing particles.

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Year:  1966        PMID: 4165908      PMCID: PMC2107066          DOI: 10.1083/jcb.31.3.603

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  21 in total

1.  RECONSTITUTION OF BACTERIAL FLAGELLA IN VITRO.

Authors:  S ASAKURA; G EGUCHI; T IINO
Journal:  J Mol Biol       Date:  1964-10       Impact factor: 5.469

2.  [COMPOSITION OF THE CELL WALL SUPPORTING MEMBRANE OF NORMAL CELLS AND PENICILLIN SPHEROPLASTS OF PROTEUS MIRABILIS].

Authors:  H H MARTIN
Journal:  Zentralbl Bakteriol Orig       Date:  1963-12

3.  THE LOCATION OF THE MUCOPEPTIDE IN SECTIONS OF THE CELL WALL OF ESCHERICHIA COLI AND OTHER GRAM-NEGATIVE BACTERIA.

Authors:  R G MURRAY; P STEED; H E ELSON
Journal:  Can J Microbiol       Date:  1965-06       Impact factor: 2.419

4.  Electron microscope observations on the structure of fimbriae, with particular reference to Klebsiella strains, by the use of the negative staining technique.

Authors:  M J THORNLEY; R W HORNE
Journal:  J Gen Microbiol       Date:  1962-04

5.  Structural components of flagella from Salmonella typhimurium.

Authors:  D KERRIDGE; R W HORNE; A M GLAUERT
Journal:  J Mol Biol       Date:  1962-04       Impact factor: 5.469

6.  The occurrence of cell wall constituents in stable Proteus L forms.

Authors:  T H MORRISON; C WEIBULL
Journal:  Acta Pathol Microbiol Scand       Date:  1962

7.  Evidence for the presence of DNA at basal body sites in Tetrahymena pyriformis.

Authors:  J Randall; C Disbrey
Journal:  Proc R Soc Lond B Biol Sci       Date:  1965-07-27

Review 8.  Symposium on the fine structure and replication of bacteria and their parts. II. Bacterial cytoplasm.

Authors:  W van Iterson
Journal:  Bacteriol Rev       Date:  1965-09

9.  A CYTOCHEMICAL LOCALIZATION OF REDUCTIVE SITES IN A GRAM-NEGATIVE BACTERIUM. TELLURITE REDUCTION IN PROTEUS VULGARIS.

Authors:  W LEENE
Journal:  J Cell Biol       Date:  1964-03       Impact factor: 10.539

10.  THE DEVELOPMENT OF BASAL BODIES AND FLAGELLA IN ALLOMYCES ARBUSCULUS.

Authors:  F L RENAUD; H SWIFT
Journal:  J Cell Biol       Date:  1964-11       Impact factor: 10.539

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  21 in total

1.  New structural features of the flagellar base in Salmonella typhimurium revealed by rapid-freeze electron microscopy.

Authors:  S Khan; I H Khan; T S Reese
Journal:  J Bacteriol       Date:  1991-05       Impact factor: 3.490

2.  Novel bacterium infecting an African snail.

Authors:  R M Cole; C S Richards; T J Popkin
Journal:  J Bacteriol       Date:  1977-12       Impact factor: 3.490

3.  Ultrastructure of Treponema pallidum Nichols following lysis by physical and chemical methods. II. Axial filaments.

Authors:  S Jackson; S H Black
Journal:  Arch Mikrobiol       Date:  1971

Review 4.  Genetics and chemistry of bacterial flagella.

Authors:  T Iino
Journal:  Bacteriol Rev       Date:  1969-12

Review 5.  The structure of flagella and the genetic control of flagellation in Eubacteriales. A review.

Authors:  T M Joys
Journal:  Antonie Van Leeuwenhoek       Date:  1968       Impact factor: 2.271

6.  [Intracellular cilia in human epidermal cells].

Authors:  I Anton-Lamprecht
Journal:  Arch Dermatol Forsch       Date:  1972

7.  Relationship between cell wall, cytoplasmic membrane, and bacterial motility.

Authors:  Z Vaituzis; R N Doetsch
Journal:  J Bacteriol       Date:  1969-10       Impact factor: 3.490

8.  Fine structure of Ectothiorhodospira mobilis strain 8113 thylakoids: chemical fixation and freeze-etching studies.

Authors:  S C Holt; H G Trüper; B J Takács
Journal:  Arch Mikrobiol       Date:  1968

9.  Attachment of flagellar basal bodies to the cell envelope: specific attachment to the outer, lipopolysaccharide membrane and the cyoplasmic membrane.

Authors:  M L DePamphilis; J Adler
Journal:  J Bacteriol       Date:  1971-01       Impact factor: 3.490

10.  Differentiation within the bacterial flagellum and isolation of the proximal hook.

Authors:  D Abram; J R Mitchen; H Koffler; A E Vatter
Journal:  J Bacteriol       Date:  1970-01       Impact factor: 3.490

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