Previous Article | Next Article ![]()
J. Bacteriol., 06 1996, 3008-3014, Vol 178, No. 11
RN Grishanin, SI Bibikov, IM Altschuler, AD Kaulen, SB Kazimirchuk, JP Armitage and VP Skulachev
It has been shown previously that the proton-pumping activity of
bacteriorhodopsin from Halobacterium salinarium can transmit an attractant
signal to the bacterial flagella upon an increase in light intensity over a
wide range of wavelengths. Here, we studied the effect of blue light on
phototactic responses by the mutant strain Pho8l-B4, which lacks both
sensory rhodopsins but has the ability to synthesize bacteriorhodopsin.
Under conditions in which bacteriorhodopsin was largely accumulated as the
M412 bacteriorhodopsin photocycle intermediate, halobacterial cells
responded to blue light as a repellent. This response was pronounced when
the membrane electric potential level was high in the presence of arginine,
active oxygen consumption, or high-background long-wavelength light
intensity but was inhibited by an uncoupler of oxidative phosphorylation
(carbonyl cyanide 3-chlorophenylhydrazone) and was inverted in a background
of low long-wavelength light intensity. The response to changes in the
intensity of blue light under high background light was asymmetric, since
removal of blue light did not produce an expected suppression of reversals.
Addition of ammonium acetate, which is known to reduce the pH gradient
changes across the membrane, did not inhibit the repellent effect of blue
light, while the discharge of the membrane electric potential by
tetraphenylphosphonium ions inhibited this sensory reaction. We conclude
that the primary signal from bacteriorhodopsin to the sensory pathway
involves changes in membrane potential.
Copyright © 1996, American Society for Microbiology
delta psi-mediated signalling in the bacteriorhodopsin-dependent photoresponse
A.N. Belozersky Institute of Physico-Chemical Biology, Moscow State University, Russia.
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»