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1.
Biochim Biophys Acta ; 1757(5-6): 369-79, 2006.
Article in English | MEDLINE | ID: mdl-16829225

ABSTRACT

Femtosecond absorption difference spectroscopy was applied to study the time and spectral evolution of low-temperature (90 K) absorbance changes in isolated reaction centers (RCs) of the HM182L mutant of Rhodobacter (Rb.) sphaeroides. In this mutant, the composition of the B-branch RC cofactors is modified with respect to that of wild-type RCs by replacing the photochemically inactive BB accessory bacteriochlorophyll (BChl) by a photoreducible bacteriopheophytin molecule (referred to as PhiB). We have examined vibrational coherence within the first 400 fs after excitation of the primary electron donor P with 20-fs pulses at 870 nm by studying the kinetics of absorbance changes at 785 nm (PhiB absorption band), 940 nm (P*-stimulated emission), and 1020 nm (BA- absorption band). The results of the femtosecond measurements are compared with those recently reported for native Rb. sphaeroides R-26 RCs containing an intact BB BChl. At delay times longer than approximately 50 fs (maximum at 120 fs), the mutant RCs exhibit a pronounced BChl radical anion (BA-) absorption band at 1020 nm, which is similar to that observed for Rb. sphaeroides R-26 RCs and represents the formation of the intermediate charge-separated state P+ BA-. Femtosecond oscillations are revealed in the kinetics of the absorption development at 1020 nm and of decay of the P*-stimulated emission at 940 nm, with the oscillatory components of both kinetics displaying a generally synchronous behavior. These data are interpreted in terms of coupling of wave packet-like nuclear motions on the potential energy surface of the P* excited state to the primary electron-transfer reaction P*-->P+ BA- in the A-branch of the RC cofactors. At very early delay times (up to 80 fs), the mutant RCs exhibit a weak absorption decrease around 785 nm that is not observed for Rb. sphaeroides R-26 RCs and can be assigned to a transient bleaching of the Qy ground-state absorption band of the PhiB molecule. In the range of 740-795 nm, encompassing the Qy optical transitions of bacteriopheophytins HA, HB, and PhiB, the absorption difference spectra collected for mutant RCs at 30-50 fs resemble the difference spectrum of the P+ PhiB- charge-separated state previously detected for this mutant in the picosecond time domain (E. Katilius, Z. Katiliene, S. Lin, A.K.W. Taguchi, N.W. Woodbury, J. Phys. Chem., B 106 (2002) 1471-1475). The dynamics of bleaching at 785 nm has a non-monotonous character, showing a single peak with a maximum at 40 fs. Based on these observations, the 785-nm bleaching is speculated to reflect reduction of 1% of PhiB in the B-branch within about 40 fs, which is earlier by approximately 80 fs than the reduction process in the A-branch, both being possibly linked to nuclear wave packet motion in the P* state.


Subject(s)
Bacterial Chromatophores/physiology , Bacteriochlorophylls/physiology , Pheophytins/physiology , Photosynthetic Reaction Center Complex Proteins/physiology , Pigments, Biological/metabolism , Rhodobacter sphaeroides/physiology , Bacterial Chromatophores/genetics , Bacteriochlorophylls/genetics , Electron Transport , Kinetics , Mutagenesis, Site-Directed , Pheophytins/genetics , Photosynthetic Reaction Center Complex Proteins/genetics , Pigments, Biological/genetics , Rhodobacter sphaeroides/genetics , Spectrum Analysis
2.
Biochemistry ; 44(12): 4755-64, 2005 Mar 29.
Article in English | MEDLINE | ID: mdl-15779902

ABSTRACT

The purple phototrophic bacterium, Thermochromatium tepidum, contains a gene for a chimeric photoactive yellow protein/bacteriophytochrome/diguanylate cyclase (Ppd). We produced the Tc. tepidum PYP domain (Tt PYP) in Escherichia coli, and found that it has a wavelength maximum at 358 nm due to a Leu46 substitution of the color-tuning Glu46 found in the prototypic Halorhodospira halophila PYP (Hh PYP). However, the 358 nm dark-adapted state is in a pH-dependent equilibrium with a yellow species absorbing at 465 nm (pK(a) = 10.2). Following illumination at 358 nm, photocycle kinetics are characterized at pH 7.0 by a small bleach and red shift to what appears to be a long-lived cis intermediate (comparable to the I(2) intermediate in Hh PYP). The recovery to the dark-adapted state has a lifetime of approximately 4 min, which is approximately 1500 times slower than that for Hh PYP. However, when the Tt PYP is illuminated at pH values above 7.5, the light-induced difference spectrum indicates a pH-dependent equilibrium between the I(2) intermediate and a red-shifted 440 nm intermediate. This equilibrium could be responsible for the sigmoidal pH dependence of the recovery of the dark-adapted state (pK(a) = 8.8). In addition, the light-induced difference spectrum shows that, at pH values above 9.3, there is an apparent bleach near 490 nm superimposed on the 358 and 440 nm changes, which we ascribe to the equilibrium between the protonated and ionized dark-adapted forms. The L46E mutant of Tt PYP has a wavelength maximum at 446 nm, resembling wild-type Hh PYP. The kinetics of recovery of L46E following illumination with white light are slow (lifetime of 15 min at pH 7), but are comparable to those of wild-type Tt PYP. We conclude that Tt PYP is unique among the PYPs studied to date in that it has a photocycle initiated from a dark-adapted state with a protonated chromophore at physiological pH. However, it is kinetically most similar to Rhodocista centenaria PYP (Ppr) despite the very different absorption spectra due to the lack of E46.


Subject(s)
Bacterial Chromatophores , Bacterial Proteins/chemistry , Chromatiaceae/chemistry , Photoreceptors, Microbial/chemistry , Adaptation, Physiological , Bacterial Chromatophores/chemistry , Bacterial Chromatophores/genetics , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Chromatiaceae/enzymology , Chromatiaceae/genetics , Cloning, Molecular , Darkness , Escherichia coli Proteins , Glutamic Acid/genetics , Halorhodospira halophila/chemistry , Hydrogen-Ion Concentration , Kinetics , Leucine/genetics , Phosphorus-Oxygen Lyases/chemistry , Phosphorus-Oxygen Lyases/genetics , Photochemistry , Photoreceptors, Microbial/genetics , Photoreceptors, Microbial/metabolism , Protein Structure, Tertiary/genetics , Spectrometry, Mass, Electrospray Ionization , Spectrophotometry, Ultraviolet
3.
Biochemistry ; 40(2): 429-39, 2001 Jan 16.
Article in English | MEDLINE | ID: mdl-11148037

ABSTRACT

The influence of metal ion (Cd(2+), Zn(2+), Ni(2+)) binding on the electrogenic phases of proton transfer connected with reduction of quinone Q(B) in chromatophores from Rhodobacter sphaeroides was studied by time-resolved electric potential changes. In the presence of metals, the electrogenic transients associated with proton transfer on first and second flash at pH 8 were found to be slower by factors of 3-6. This is essentially the same effect of metal binding that was observed on optical transients in isolated reaction centers (RC), where the metal ion was shown to inhibit proton transfer [Paddock, M. L., Graige, M. S., Feher, G., and Okamura, M. Y. (1999) Proc. Natl. Acad. Sci. U.S.A. 96, 6183-6188]. The effect of metal binding on the kinetics in chromatophores is, therefore, similarly attributed to inhibition of proton uptake, which becomes rate-limiting. A striking observation was an increase in the amplitude of the electrogenic proton-uptake phase after the first flash with bound metal ion. We attribute this to a loss of internal proton rearrangement, requiring that the protons that stabilize Q(B)(-) come from solution. In mutant RCs, in which His-H126 and His-H128 are replaced with Ala, the apparent binding of Cd(2+) and Ni(2+) was decreased, showing that the binding site of these metal ions is the same as found in RC crystals [Axelrod, H. L., Abresch, E. C., Paddock, M. L., Okamura, M. Y., and Feher, G. (2000) Proc. Natl. Acad. Sci. U.S.A. 97, 1542-1547]. Therefore, the unique proton entry point near His-H126, His-H128, and Asp-M17 that was identified in isolated RCs is also the entry point in chromatophores.


Subject(s)
Bacterial Chromatophores/chemistry , Metals, Heavy/chemistry , Photosynthetic Reaction Center Complex Proteins/chemistry , Protons , Quinones/chemistry , Rhodobacter sphaeroides/chemistry , Alanine/genetics , Bacterial Chromatophores/genetics , Binding Sites/genetics , Cadmium/chemistry , Histidine/genetics , Mutagenesis, Site-Directed , Nickel/chemistry , Oxidation-Reduction , Photochemistry/instrumentation , Photochemistry/methods , Photolysis , Photosynthetic Reaction Center Complex Proteins/genetics , Rhodobacter sphaeroides/genetics , Zinc/chemistry
4.
J Mol Biol ; 297(1): 49-65, 2000 Mar 17.
Article in English | MEDLINE | ID: mdl-10704306

ABSTRACT

In many bacteria the ccoGHIS cluster, located immediately downstream of the structural genes (ccoNOQP) of cytochrome cbb(3) oxidase, is required for the biogenesis of this enzyme. Genetic analysis of ccoGHIS in Rhodobacter capsulatus demonstrated that ccoG, ccoH, ccoI and ccoS are expressed independently of each other, and do not form a simple operon. Absence of CcoG, which has putative (4Fe-4S) cluster binding motifs, does not significantly affect cytochrome cbb(3) oxidase activity. However, CcoH and CcoI are required for normal steady-state amounts of the enzyme. CcoI is highly homologous to ATP-dependent metal ion transporters, and appears to be involved in the acquisition of copper for cytochrome cbb(3) oxidase, since a CcoI-minus phenotype could be mimicked by copper ion starvation of a wild-type strain. Remarkably, the small protein CcoS, with a putative single transmembrane span, is essential for the incorporation of the redox-active prosthetic groups (heme b, heme b(3 )and Cu) into the cytochrome cbb(3) oxidase. Thus, the ccoGHIS products are involved in several steps during the maturation of the cytochrome cbb(3) oxidase.


Subject(s)
Electron Transport Complex IV/metabolism , Genes, Bacterial/physiology , Rhodobacter capsulatus/enzymology , Rhodobacter capsulatus/genetics , Bacterial Chromatophores/enzymology , Bacterial Chromatophores/genetics , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Copper/metabolism , Electron Transport Complex IV/chemistry , Electron Transport Complex IV/genetics , Enzyme Stability , Gene Expression/genetics , Gene Expression Regulation, Bacterial/genetics , Gene Expression Regulation, Enzymologic/genetics , Genes, Bacterial/genetics , Genes, Reporter/genetics , Genetic Complementation Test , Heme/metabolism , Iron-Sulfur Proteins/genetics , Iron-Sulfur Proteins/metabolism , Models, Biological , Mutation/genetics , Operon/genetics , Oxidation-Reduction , Phenotype , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , Rhodobacter capsulatus/cytology , Sequence Homology, Amino Acid , Transcription Factors/genetics , Transcription Factors/metabolism , Transcription, Genetic/genetics
5.
Biochemistry ; 39(5): 1100-13, 2000 Feb 08.
Article in English | MEDLINE | ID: mdl-10653656

ABSTRACT

Photoactive yellow protein (PYP) undergoes a light-driven cycle of color and protonation states that is part of a mechanism of bacterial phototaxis. This article concerns functionally important protonation states of PYP and the interactions that stabilize them, and changes in the protonation state during the photocycle. In particular, the chromophore pK(a) is known to be shifted down so that the chromophore is negatively charged in the ground state (dark state) even though it is buried in the protein, while nearby Glu46 has an unusually high pK(a). The photocycle involves changes of one or both of these protonation states. Calculations of pK(a) values and protonation states using a semi-macroscopic electrostatic model are presented for the wild-type and three mutants, in both the ground state and the bleached (I(2)) intermediate state. Calculations allowing multiple H-bonding arrangements around the chromophore also have been carried out. In addition, ground-state pK(a) values of the chromophore have been measured by UV-visible spectroscopy for the wild-type and the same three mutants. Because of the unusual protonation states and strong electrostatic interactions, PYP represents a severe test of the ability of theoretical models to yield correct calculations of electrostatic interactions in proteins. Good agreement between experiment and theory can be obtained for the ground state provided the protein interior is assumed to have a relatively low dielectric constant, but only partial agreement between theory and experiment is obtained for the bleached state. We also present a reinterpretation of previously published data on the pH-dependence of the recovery of the ground state from the bleached state. The new analysis implies a pK(a) value of 6.37 for Glu46 in the bleached state, which is consistent with other available experimental data, including data that only became available after this analysis. The new analysis suggests that signal transduction is modulated by the titration properties of the bleached state, which are in turn determined by electrostatic interactions. Overall, the results of this study provide a quantitative picture of the interactions responsible for the unusual protonation states of the chromophore and Glu46, and of protonation changes upon bleaching.


Subject(s)
Bacterial Proteins/chemistry , Photochemistry/methods , Photoreceptors, Microbial , Protons , Amino Acid Substitution/genetics , Bacterial Chromatophores/chemistry , Bacterial Chromatophores/genetics , Bacterial Proteins/genetics , Binding Sites/genetics , Halorhodospira halophila/chemistry , Halorhodospira halophila/genetics , Hydrogen Bonding , Hydrogen-Ion Concentration , Kinetics , Mathematical Computing , Models, Molecular , Mutagenesis, Site-Directed , Photolysis , Protein Folding , Static Electricity , Titrimetry/methods
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