J Bacteriol. 1974 January; 117(1): 302-311
Copyright © 1974 American Society for Microbiology. All Rights Reserved.
Ultrastructural and Chemical Alteration of the Cell Envelope of Pseudomonas aeruginosa, Associated with Resistance to Ethylenediaminetetraacetate Resulting from Growth in a Mg2+-Deficient Medium
H. E. Gilleland Jr.1,
J. D. Stinnett and
R. G. Eagon
Department of Microbiology, University of Georgia, Athens, Georgia 30602
ABSTRACT
Cells of Pseudomonas aeruginosa became resistant to the lytic effect of ethylenediametetraacetate (EDTA) when grown in a Mg2+-deficient medium. To correlate ultrastructural changes in the cell wall associated with the shift to EDTA-resistance, a freeze-etch study was performed. Upon fracturing, the outer cell wall membrane split down the hydrophobic center to reveal the outer (concave) and inner (convex) layers. The concave cell wall layer of EDTA-sensitive cells grown in Mg2+-sufficient medium contained spherical units resting on an underlying smooth support layer. Upon EDTA treatment, approximately one-half of these spherical units were extracted. Cells grown in Mg2+-deficient medium were resistant to EDTA. The concave cell wall layer of EDTA-resistant cells had increased numbers of highly compacted spherical units, giving this layer a disorganized appearance. The highly compacted appearance of this layer was unaltered by EDTA treatment. Thus, growth in Mg2+-deficient medium resulted in cells which were resistant to EDTA and which possessed an ultrastructurally altered outer layer of the outer cell wall membrane. Cell envelopes from EDTA-resistant cells were found to possess 18% less phosphorus, 16.4% more total carbohydrate, and 13.3% more 2-keto-3-deoxyoctonate than cell envelopes from EDTA-sensitive cells. There were also qualitative, but not quantitative, differences in the protein content of cell envelopes from EDTA-resistant and EDTA-sensitive cells.
FOOTNOTES
1 Present address: Department of Bacteriology and Immunology, University of Western Ontario, London 72, Ontario, Canada.
J Bacteriol. 1974 January; 117(1): 302-311
Copyright © 1974 American Society for Microbiology. All Rights Reserved.
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Copyright © 1974 by the American Society for Microbiology. All rights reserved.