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J Bacteriol, April 1998, p. 2033-2042, Vol. 180, No. 8
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Suppressor Mutation Analysis of the Sensory
Rhodopsin I-Transducer Complex: Insights into the
Color-Sensing Mechanism
Kwang-Hwan
Jung and
John L.
Spudich*
Department of Microbiology and Molecular
Genetics, University of Texas
Houston Medical School, Houston,
Texas 77030
Received 5 November 1997/Accepted 10 February 1998
The molecular complex containing the phototaxis receptor sensory
rhodopsin I (SRI) and transducer protein HtrI (halobacterial transducer
for SRI) mediates color-sensitive phototaxis responses in the archaeon
Halobacterium salinarum. One-photon excitation of the
complex by orange light elicits attractant responses, while two-photon
excitation (orange followed by near-UV light) elicits repellent
responses in swimming cells. Several mutations in SRI and HtrI cause an
unusual mutant phenotype, called orange-light-inverted signaling, in
which the cell produces a repellent response to normally attractant
light. We applied a selection procedure for intragenic and extragenic
suppressors of orange-light-inverted mutants and identified 15 distinct
second-site mutations that restore the attractant response. Two of the
3 suppressor mutations in SRI are positioned at the cytoplasmic ends of
helices F and G, and 12 suppressor mutations in HtrI cluster at the
cytoplasmic end of the second HtrI transmembrane helix (TM2). Nearly
all suppressors invert the normally repellent response to two-photon
stimulation to an attractant response when they are expressed with
their suppressible mutant alleles or in an otherwise wild-type strain.
The results lead to a model for control of flagellar reversal by the
SRI-HtrI complex. The model invokes an equilibrium between the A
(reversal-inhibiting) and R (reversal-stimulating) conformers of the
signaling complex. Attractant light and repellent light shift the
equilibrium toward the A and R conformers, respectively, and mutations
are proposed to cause intrinsic shifts in the equilibrium in the dark
form of the complex. Differences in the strength of the two-photon signal inversion and in the allele specificity of suppression are
correlated, and this correlation can be explained in terms of different
values of the equilibrium constant (Keq) for
the conformational transition in different mutants and
mutant-suppressor pairs.
*
Corresponding author. Mailing address: Department of
Microbiology and Molecular Genetics, University of Texas
Houston
Medical School, Houston, TX 77030. Phone: (713) 500-5458. Fax: (713)
500-5499. E-mail: spudich{at}utmmg.med.uth.tmc.edu.
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