Literature DB >> 8415720

Bacteriorhodopsin is involved in halobacterial photoreception.

S I Bibikov1, R N Grishanin, A D Kaulen, W Marwan, D Oesterhelt, V P Skulachev.   

Abstract

The bacterio-opsin gene was introduced into a "blind" Halobacterium salinarium mutant that (i) lacked all the four retinal proteins [bacteriorhodopsin (BR), halorhodopsin, and sensory rhodopsins (SRs) I and II] and the transducer protein for SRI and (ii) showed neither attractant response to long wavelength light nor repellent response to short wavelength light. The resulting transformed cells acquired the capability to sense light stimuli. The cells accumulated in a light spot, demonstrating the BR-mediated orientation in spatial light gradients. As in wild-type cells, a decrease in the intensity of long wavelength light caused a repellent response by inducing reversals of swimming direction, but, in contrast to wild-type cells, a decrease in the intensity of short wavelength light also repelled the cells. An increase in light intensity evoked an attractant response (i.e., a transient suppression of spontaneous reversals). Signal processing times and adaptation kinetics were similar to the SRI-mediated reactions. However, compared to SR-mediated photoresponses, higher light intensities were necessary to induce the BR-mediated responses. The light sensitivity of the transformant was increased by adding 1 mM cyanide and decreased by the addition of arginine, agents that respectively reduce and increase the light-independent generation of the electrochemical potential difference of H+ ions (delta mu H+). A decrease in irradiance to an intensity that was still high enough to saturate BR-initiated delta mu H+ changes failed to induce the repellent effect, but the addition of a protonophorous uncoupler sensitized the cell to these light stimuli. The BR D96N mutant (Asp-96 is replaced by Asn) with decreased proton pump activity showed strongly reduced BR-mediated responses. Azide, which increases this mutant's H+ pump efficiency, increased the photosensitivity of the mutant cells. Moreover, azide diminished (i) the membrane potential decreasing and (ii) repellent effects of blue light added to the orange background illumination in this mutant. We conclude that the BR-mediated photoreception is due to the light-dependent generation of delta mu H+. Our data are consistent with the assumption that the H. salinarium cell monitors the membrane energization level with a "protometer" system measuring total delta mu H+ changes or its electric potential difference component.

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Year:  1993        PMID: 8415720      PMCID: PMC47585          DOI: 10.1073/pnas.90.20.9446

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  32 in total

1.  Transformation of a bop-hop-sop-I-sop-II-Halobacterium halobium mutant to bop+: effects of bacteriorhodopsin photoactivation on cellular proton fluxes and swimming behavior.

Authors:  B Yan; S W Cline; W F Doolittle; J L Spudich
Journal:  Photochem Photobiol       Date:  1992-10       Impact factor: 3.421

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Journal:  Eur J Biochem       Date:  1973-08-17

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Authors:  W Marwan; P Hegemann; D Oesterhelt
Journal:  J Mol Biol       Date:  1988-02-20       Impact factor: 5.469

4.  Identification of a third rhodopsin-like pigment in phototactic Halobacterium halobium.

Authors:  R A Bogomolni; J L Spudich
Journal:  Proc Natl Acad Sci U S A       Date:  1982-10       Impact factor: 11.205

5.  Halorhodopsin is a light-driven chloride pump.

Authors:  B Schobert; J K Lanyi
Journal:  J Biol Chem       Date:  1982-09-10       Impact factor: 5.157

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Journal:  J Theor Biol       Date:  1980-01-21       Impact factor: 2.691

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Authors:  E N Spudich; C A Hasselbacher; J L Spudich
Journal:  J Bacteriol       Date:  1988-09       Impact factor: 3.490

8.  Negative phototaxis from blue light and the role of third rhodopsinlike pigment in halobacterium cutirubrum.

Authors:  T Takahashi; M Watanabe; N Kamo; Y Kobatake
Journal:  Biophys J       Date:  1985-08       Impact factor: 4.033

9.  Replacement of aspartic acid-96 by asparagine in bacteriorhodopsin slows both the decay of the M intermediate and the associated proton movement.

Authors:  M Holz; L A Drachev; T Mogi; H Otto; A D Kaulen; M P Heyn; V P Skulachev; H G Khorana
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

10.  A defective proton pump, point-mutated bacteriorhodopsin Asp96----Asn is fully reactivated by azide.

Authors:  J Tittor; C Soell; D Oesterhelt; H J Butt; E Bamberg
Journal:  EMBO J       Date:  1989-11       Impact factor: 11.598

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  9 in total

Review 1.  Bioenergetics of the Archaea.

Authors:  G Schäfer; M Engelhard; V Müller
Journal:  Microbiol Mol Biol Rev       Date:  1999-09       Impact factor: 11.056

2.  The M intermediate of Pharaonis phoborhodopsin is photoactive.

Authors:  S P Balashov; M Sumi; N Kamo
Journal:  Biophys J       Date:  2000-06       Impact factor: 4.033

Review 3.  Light and the evolution of vision.

Authors:  D L Williams
Journal:  Eye (Lond)       Date:  2015-11-06       Impact factor: 3.775

4.  delta psi-mediated signalling in the bacteriorhodopsin-dependent photoresponse.

Authors:  R N Grishanin; S I Bibikov; I M Altschuler; A D Kaulen; S B Kazimirchuk; J P Armitage; V P Skulachev
Journal:  J Bacteriol       Date:  1996-06       Impact factor: 3.490

5.  The primary structures of the Archaeon Halobacterium salinarium blue light receptor sensory rhodopsin II and its transducer, a methyl-accepting protein.

Authors:  W Zhang; A Brooun; M M Mueller; M Alam
Journal:  Proc Natl Acad Sci U S A       Date:  1996-08-06       Impact factor: 11.205

6.  Removal of transducer HtrI allows electrogenic proton translocation by sensory rhodopsin I.

Authors:  R A Bogomolni; W Stoeckenius; I Szundi; E Perozo; K D Olson; J L Spudich
Journal:  Proc Natl Acad Sci U S A       Date:  1994-10-11       Impact factor: 11.205

7.  Behavioral responses of Escherichia coli to changes in redox potential.

Authors:  V A Bespalov; I B Zhulin; B L Taylor
Journal:  Proc Natl Acad Sci U S A       Date:  1996-09-17       Impact factor: 11.205

8.  Signal transduction in the archaeon Halobacterium salinarium is processed through three subfamilies of 13 soluble and membrane-bound transducer proteins.

Authors:  W Zhang; A Brooun; J McCandless; P Banda; M Alam
Journal:  Proc Natl Acad Sci U S A       Date:  1996-05-14       Impact factor: 11.205

9.  Chemotaxis and phototaxis require a CheA histidine kinase in the archaeon Halobacterium salinarium.

Authors:  J Rudolph; D Oesterhelt
Journal:  EMBO J       Date:  1995-02-15       Impact factor: 11.598

  9 in total

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