Abstract
The translational motility of Pseudomonas fluorescens was weakly inhibited by oligomycin, Dicumarol, 2,4-dinitrophenol, 2n-heptyl-4-hydroxyquinoline N-oxide, and potassium cyanide. Atabrine and antimycin A together with potassium cyanide immediately immobilized this bacterium, but antimycin A alone was without effect. Gramicidin D also immobilized P. fluorescens, but its action was inhibited by K(+) and NH(4) (+) ions. In like manner, the effect of p-chloromercuribenzoate could be counteracted with cysteine, thereby suggesting the involvement of -SH groups in flagellar motility processes. It appears that the energy required for motility of P. fluorescens is generated by oxidative phosphorylation mediated by the cytochrome system.
MeSH Terms
Adenosine Triphosphate/metabolism
Antimycin A/pharmacology
Azides/pharmacology
Chloromercuribenzoates/pharmacology
Cyanides/pharmacology
Dicumarol/pharmacology
Dinitrophenols/pharmacology
Movement/drug effects
Oligomycins/pharmacology
Oxidative Phosphorylation
Oxygen Consumption/drug effects
Phenols/pharmacology
Pseudomonas/drug effects,metabolism
Quinacrine/pharmacology
Quinolines/pharmacology
Tyrothricin/pharmacology
Chemicals
Azides
Chloromercuribenzoates
Cyanides
Dinitrophenols
Oligomycins
Phenols
Quinolines
Tyrothricin
Antimycin A
Dicumarol
Adenosine Triphosphate
Quinacrine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Faust M A
Doetsch R N
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