Add time:07/12/2019         Source:sciencedirect.com

The polar flagella of Vibrio alginolyticus are driven by sodium motive force and those motors are specifically and strongly inhibited by phenamil, an amiloride analog that is thought to interact with a sodium channel of the flagellar motor. To study the sodium ion coupling site, we isolated motility mutants resistant to phenamil and named the phenotype Mpar for motility resistant to phenamil. The motility of the wild-type (Mpas) was inhibited by 50 μM phenamil, whereas Mpar strains were still motile in the presence of 200 μM phenamil. The Ki value for phenamil in the Mpar strain was estimated to be five times larger than that in the Mpas strain. However, the sensitivities to amiloride or benzamil, another amiloride analog, were not distinctly changed in the Mpar strain. The rotation rate of the wild-type Na+-driven motor fluctuates greatly in the presence of phenamil, which can be explained in terms of a relatively slow dissociation rate of phenamil from the motor. We therefore studied the stability of the rotation of the Mpar and Mpas motors by phenamil. The speed fluctuations of the Mpar motors were distinctly reduced relative to the Mpas motors. The steadier rotation of the Mpar motors can be explained by an increase in the phenamil dissociation rate from a sodium channel of the motor, which suggests that a phenamil-specific binding site of the motor is mutated in the Mpar strain.

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