Polycations as outer membrane-disorganizing agents

The outer membrane-disorganizing effect of a short (10-min) treatment with polycationic agents was studied with smooth Salmonella typhimurium used as a test organism. The polycationic agents were the protamine salmine, a lysine polymer with 20 lysine residues (lysine20), and the deacylated polymyxin B derivative polymyxin B nonapeptide. Two different types of outer membrane-disorganizing were found. Protamine and lysine20 released 20 to 30% of the lipopolysaccharide from the outer membrane and sensitized the bacteria to the anionic detergent sodium dodecyl sulfate but did not (under these conditions) make the bacteria permeable to the hydrophobic probes fusidic acid and actinomycin D. In contrast, polymyxin B nonapeptide did not release lipopolysaccharide or sensitize the bacteria to sodium dodecyl sulfate but made the outer membrane permeable to the hydrophobic probes. None of the agents was bactericidal under the conditions used or caused any leakage of periplasmic beta-lactamase. Polymyxin B was used as a reference and showed characteristic outer membrane-disorganizing action. In thin-section electron microscopy, polymyxin B nonapeptide caused the appearance of long, narrow, finger-like projections on the outer membrane. Protamine and lysine20 caused a distinctly wrinkled appearance of the outer membrane but no projections.

[1]  Jeffrey H. Miller Experiments in molecular genetics , 1972 .

[2]  H. Odeberg,et al.  Purification and characterization of a potent bactericidal and membrane active protein from the granules of human polymorphonuclear leukocytes. , 1978, The Journal of biological chemistry.

[3]  T. Nakae,et al.  The outer membrane of Gram-negative bacteria. , 1979, Advances in microbial physiology.

[4]  Georg Keleti,et al.  Handbook of micromethods for the biological sciences , 1975 .

[5]  M. Teuber,et al.  Action of Polymyxin B on Bacterial Membranes: Morphological Changes in the Cytoplasm and in the Outer Membrane of Salmonella typhimurium and Escherichia coli B , 1975, Antimicrobial Agents and Chemotherapy.

[6]  M. Sargent Rapid fixed-time assay for penicillinase , 1968, Journal of bacteriology.

[7]  D. Storm,et al.  Polymyxin and related peptide antibiotics. , 1977, Annual review of biochemistry.

[8]  K. Sanderson,et al.  Comparison of the cell envelope structure of a lipopolysaccharide-defective (heptose-deficient) strain and a smooth strain of Salmonella typhimurium , 1975, Journal of bacteriology.

[9]  M. Vaara,et al.  Polycations sensitize enteric bacteria to antibiotics , 1983, Antimicrobial Agents and Chemotherapy.

[10]  K. Sanderson,et al.  F + , Hfr, and F' strains of Salmonella typhimurium and Salmonella abony. , 1972, Bacteriological reviews.

[11]  H. Neu,et al.  The release of enzymes from Escherichia coli by osmotic shock and during the formation of spheroplasts. , 1965, The Journal of biological chemistry.

[12]  D. Klumpp,et al.  The effects of protamine and histone on enterobacterial lipopolysaccharides and hemolysis. , 1958, Canadian journal of microbiology.

[13]  P. Gemski,et al.  Non-smooth mutants of Salmonella typhimurium: differentiation by phage sensitivity and genetic mapping. , 1972, Journal of general microbiology.

[14]  D. Storm,et al.  Disruption of the Escherichia coli outer membrane permeability barrier by immobilized polymyxin B. , 1977, The Journal of antibiotics.

[15]  L. Leive THE BARRIER FUNCTION OF THE GRAM‐NEGATIVE ENVELOPE , 1974, Annals of the New York Academy of Sciences.

[16]  N. Nanninga,et al.  Effect of polymyxin on the outer membrane of Salmonella typhimurium: freeze-fracture studies , 1976, Journal of bacteriology.

[17]  H. Neu,et al.  Release of Surface Enzymes in Enterobacteriaceae by Osmotic Shock , 1967, Journal of bacteriology.

[18]  M. Vaara Polymyxin B nonapeptide complexes with lipopolysaccharide , 1983 .

[19]  O. H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.

[20]  H. Nikaido,et al.  Outer membrane of Salmonella typhimurium. Transmembrane diffusion of some hydrophobic substances. , 1976, Biochimica et biophysica acta.

[21]  R. Langdon [24] Glucose 6-phosphate dehydrogenase from erythrocytes , 1966 .

[22]  M. Vaara Increased outer membrane resistance to ethylenediaminetetraacetate and cations in novel lipid A mutants , 1981, Journal of bacteriology.

[23]  J. Spitznagel,et al.  Bactericidal activity of fractionated granule contents from human polymorphonuclear leukocytes: antagonism of granule cationic proteins by lipopolysaccharide , 1979, Infection and immunity.

[24]  D. Storm,et al.  Disruption of Escherichia coli outer membranes by EM 49. A new membrane active peptide. , 1976, Biochemistry.

[25]  M. Schindler,et al.  Interaction of divalent cations and polymyxin B with lipopolysaccharide. , 1979, Biochemistry.

[26]  L. Leive,et al.  Controlling EDTA treatment to produce permeable Escherichia coli with normal metabolic processes. , 1967, Biochemical and Biophysical Research Communications - BBRC.

[27]  K. Iida,et al.  Electron microscopic studies on mode of action of polymyxin , 1969, Journal of bacteriology.

[28]  P. Mäkelä,et al.  Lipopolysaccharide heterogeneity in Salmonella typhimurium analyzed by sodium dodecyl sulfate polyacrylamide gel electrophoresis. , 1980, European journal of biochemistry.