Literature DB >> 14066417

FINE STRUCTURE OF LISTERIA MONOCYTOGENES.

M R EDWARDS, R W STEVENS.   

Abstract

Edwards, Mercedes R. (New York State Department of Health, Albany) and Roy W. Stevens. Fine structure of Listeria monocytogenes. J. Bacteriol. 86:414-428. 1963.-Cells of Listeria monocytogenes, at different stages of growth, were fixed with osmium tetroxide and treated with uranyl acetate. The material was dehydrated in alcohol, embedded in prepolymerized methacrylate, and studied in thin sections. In most of the micrographs, the plasmalemma (or plasma membrane) showed a pattern of three dense lines, each ca. 25 A thick, alternating with two light zones, each ca. 30 A thick. The outer light zone was regularly bridged by strands of dense material, and the inner one was not. The dense line at the edge of the cytoplasm was not always discernible because of its similarity in density with the ground cytoplasm, although it could be easily demonstrated in lysed cells and in protoplasts. The latter were found to be limited by a pair of dense lines, each ca. 25 A thick, bounding a light core ca. 30 A thick. This structure corresponds to a "unit" membrane, but it represents only a part of the plasmalemma of the intact cell; it was therefore interpreted as being more complex than a single unit membrane. Intracytoplasmic membranes of various configurations were clearly shown to be extensions of the plasmalemma. They may branch repeatedly and anastomose to form a complicated honeycomb-like organelle or organelles of different appearances, sometimes lamellate. The lamellar bodies are envisioned as resulting from spiraled ingrowths. The various kinds of ingrowths of the plasmalemma were designated "plasmalemmosomes" to indicate their origin; however, some of these organelles in Listeria were similar to those described in different bacteria by other authors. Plasmalemmosomes have been found in both aerobically and anaerobically grown cells. Another outstanding feature in many micrographs was the nucleoid, which contains dense fibrils measuring 25 to 50 A in diameter. These fibrils frequently appeared to be coiled and were of the order of magnitude ascribed to deoxyribonucleic acid molecules.

Entities:  

Keywords:  EXPERIMENTAL LAB STUDY; LISTERIA MONOCYTOGENES; MICROSCOPY, ELECTRON

Mesh:

Substances:

Year:  1963        PMID: 14066417      PMCID: PMC278451          DOI: 10.1128/jb.86.3.414-428.1963

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  34 in total

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3.  An electron microscope study of the disposition and fine structure of Mycobacterium lepraemurium in mouse spleen.

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4.  Mitochondria-like structures in ultrathin sections of Mycobacterium avium.

Authors:  C SHINOHARA; K FUKUSHI; J SUZUKI
Journal:  J Bacteriol       Date:  1957-09       Impact factor: 3.490

5.  Structure in the bacterial cell-wall during cell division.

Authors:  I M DAWSON; H STERN
Journal:  Biochim Biophys Acta       Date:  1954-01

6.  Electron microscopy of ultra-thin sections of bacteria I. Cellular division in Bacillus cereus.

Authors:  G B CHAPMAN; J HILLIER
Journal:  J Bacteriol       Date:  1953-09       Impact factor: 3.490

7.  Cytology of bacteria. I. The bacterial cell.

Authors:  S MUDD
Journal:  Annu Rev Microbiol       Date:  1954       Impact factor: 15.500

8.  Evidence suggesting that the granules of mycobacteria are mitochondria.

Authors:  S MUDD; L C WINTERSCHEID; E D DeLAMATER; H J HENDERSON
Journal:  J Bacteriol       Date:  1951-10       Impact factor: 3.490

9.  Electron microscope study of DNA-containing plasms. II. Vegetative and mature phage DNA as compared with normal bacterial nucleoids in different physiological states.

Authors:  E KELLENBERGER; A RYTER; J SECHAUD
Journal:  J Biophys Biochem Cytol       Date:  1958-11-25

10.  Staining of tissue sections for electron microscopy with heavy metals. II. Application of solutions containing lead and barium.

Authors:  M L WATSON
Journal:  J Biophys Biochem Cytol       Date:  1958-11-25
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  34 in total

1.  ELECTRON MICROSCOPIC FEATURES OF GRAM-NEGATIVE AND GRAM-POSITIVE BACTERIA EMBEDDED IN PHOSPHOTUNGSTATE.

Authors:  L O ZWILLENBERG
Journal:  Antonie Van Leeuwenhoek       Date:  1964       Impact factor: 2.271

2.  TIME-LAPSE PHOTOMICROGRAPHY OF CELL GROWTH AND DIVISION IN ESCHERICHIA COLI.

Authors:  H HOFFMAN; M E FRANK
Journal:  J Bacteriol       Date:  1965-01       Impact factor: 3.490

3.  ELECTRON MICROSCOPY OF THE ENDOPHYTE OF ALNUS GLUTINOSA.

Authors:  J H BECKING; W E DE BOER; A L HOUWINK
Journal:  Antonie Van Leeuwenhoek       Date:  1964       Impact factor: 2.271

4.  FORMATION AND STRUCTURE OF MESOSOMES IN MYXOCOCCUS XANTHUS.

Authors:  H VOELZ
Journal:  Arch Mikrobiol       Date:  1965-05-28

5.  The membraneous type of lomasome (membranosome) in the hyphae of Aspergillus nidulans.

Authors:  S H Weisberg; G Turian
Journal:  Protoplasma       Date:  1974       Impact factor: 3.356

6.  Effect of lysozyme treatment on cell wall ultrastructure in Sarcina flava.

Authors:  M I Hunter; D D Muir; D Thirkell
Journal:  J Bacteriol       Date:  1973-10       Impact factor: 3.490

7.  Fractionation and characterization of the plasma and mesosome membrane of Listeria monocytogenes.

Authors:  B K Ghosh; R G Murray
Journal:  J Bacteriol       Date:  1969-01       Impact factor: 3.490

Review 8.  Bacterial growth and the cell envelope.

Authors:  H J Rogers
Journal:  Bacteriol Rev       Date:  1970-06

9.  Trichophyton rubrum invasion of human hair apparatus in tinea capitis and tinea barbae: light- and electron microscopic study.

Authors:  C Okuda; M Ito; Y Sato
Journal:  Arch Dermatol Res       Date:  1991       Impact factor: 3.017

10.  Two-enzyme systems for glycolipid and polyglycerolphosphate lipoteichoic acid synthesis in Listeria monocytogenes.

Authors:  Alexander J Webb; Maria Karatsa-Dodgson; Angelika Gründling
Journal:  Mol Microbiol       Date:  2009-08-04       Impact factor: 3.501

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