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11.
J Cell Biol ; 35(2): 347-56, 1967 Nov.
Article in English | MEDLINE | ID: mdl-4964313

ABSTRACT

Cells grown in suspension culture were incubated with EDTA-disodium salt and shown to have more easily deformable surfaces and raised electrophoretic mobility than controls, following this treatment. The reversibility of these observations by the addition of calcium ions, and other parallel experiments, support the conclusion that, in these cells, calcium is bound to anionic sites at the cell periphery, some of which are located at the cellular electrokinetic surface. These cells should, therefore, exhibit demonstrable calcium-sensitive aggregation, if current theories on the role of calcium in the physiological situation are correct. The fact that no calcium-sensitive aggregation was observed suggests that calcium does not form "bridges" between the adjacent anionic sites on different cells, and does not act directly by its effects on the diffuse electrical double-layer in this situation. An alternative hypothesis is advanced for the role played by calcium in cell adhesion and separation processes.


Subject(s)
Calcium/pharmacology , Cell Biology/drug effects , Edetic Acid/pharmacology , Culture Media , Culture Techniques , Electrophoresis , Humans , Mathematics , Models, Structural , Osteosarcoma
12.
J Bacteriol ; 94(4): 855-9, 1967 Oct.
Article in English | MEDLINE | ID: mdl-4860917

ABSTRACT

The effects of chloramphenicol and p-fluorophenylalanine (p-FPA) on growth, proportion of motile cells, average rate of motility, and the chemotactic response of a methionine auxotroph of Escherichia coli K-12 were studied. Kinetic studies revealed that the inhibition of chemotaxis by p-FPA can be explained by the effect on growth, proportion of motile cells, and average rate of motility rather than a selective inhibition of chemotaxis per se. The effect of chloramphenicol on chemotaxis could not be explained in terms of these characteristics. It is concluded that low concentrations of chloramphenicol, unlike p-FPA, selectively inhibit chemotaxis.


Subject(s)
Cell Biology/drug effects , Chloramphenicol/pharmacology , Escherichia coli/drug effects , Phenylalanine/pharmacology , Chemotaxis/drug effects , Culture Media , Escherichia coli/growth & development , Fluorine/pharmacology , Galactose/metabolism , Kinetics , Methionine/metabolism , Movement/drug effects
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