Abstract

Survival of Escherichia coli , quick-frozen under conditions similar to those employed for freeze-etching, is close to 100%. For determination of cell shrinkage, the diameters of freeze-etched E. coli cells (average, 0.99 μm) were compared with those of preparations after negative staining and after ultrathin sectioning. Negatively stained cells measured from 0.65 to 1.0 μm in diameter, and ultrathin sections showed average cell diameters of 0.70 μm. Freeze-etched replicas of logarithmically growing, as well as stationary, E. coli B cells revealed a smooth, finely pitted cell surface in contrast to cell surfaces seen with other preparative methods. The frozen cell wall may cleave in two planes, exposing (i) a smooth fracture face within the lipid layer and (ii) in rare instances an ill-defined particulate layer. Most frequently, however, cleavage of the envelope occurred between wall and protoplasmic membrane; large areas of the membrane were then exposed and showed a surface studded with predominantly spherical particles, an appearance which did not significantly change when the cells were fixed in formaldehyde and osmium tetroxide before freeze-etching. The distribution of these particles differed between logarithmically growing cells and stationary cells.

Keywords

ProtoplasmOsmium tetroxideBiophysicsStainingCell membraneMembraneEscherichia coliBiologyCell wallCellNegative stainCleavage (geology)CytoplasmElectron microscopeBiochemistry

MeSH Terms

Cell MembraneCell WallCytoplasmEscherichia coliFreeze EtchingFreezingHistological TechniquesMicroscopyElectronStaining and Labeling

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Publication Info

Year
1970
Type
article
Volume
101
Issue
1
Pages
304-313
Citations
103
Access
Closed

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Cite This

M. E. Bayer, Charles C. Remsen (1970). Structure of <i>Escherichia coli</i> After Freeze-Etching. Journal of Bacteriology , 101 (1) , 304-313. https://doi.org/10.1128/jb.101.1.304-313.1970

Identifiers

DOI
10.1128/jb.101.1.304-313.1970
PMID
4189229
PMCID
PMC250482

Data Quality

Data completeness: 86%