ABSTRACT
Electrostatic coupling leading to conformational changes in proteins is challenging to demonstrate directly, it requires that both the local, discrete electronic details and dynamic information relevant to the functional descriptions are probed. Here, as a novel study to address this challenge, the roles of an aromatic residue in influencing the functional conformational changes of a membrane receptor in its natural membrane environment are reported. Previously intractable discrete electronic details have been obtained using 2D solid-state NMR of specifically labelled receptor, reinforced with molecular dynamic simulations, mutational analysis and functional assays, supported by and compared with rigid-atom crystal structural models. Hydrogen bonding and hydrophobic interactions are identified as the mechanistic origin for direct electromechanical coupling to the dynamics of conformational changes within the receptor.
Subject(s)
Bacteriorhodopsins/chemistry , Protons , Amino Acid Substitution , Bacteriorhodopsins/genetics , Bacteriorhodopsins/metabolism , Halobacterium/chemistry , Isomerism , Molecular Dynamics Simulation , Protein Conformation , Tyrosine/chemistry , Tyrosine/geneticsABSTRACT
Archaerhodopsin-2 (aR2), the sole protein found in the claret membrane of Halorubrum sp. Aus-2, functions as a light-driven proton pump. In this study, structural analysis of aR2 was performed using a novel three-dimensional crystal prepared by the successive fusion of claret membranes. The crystal is made up of stacked membranes, in each of which aR2 trimers are arranged on a hexagonal lattice. This lattice structure resembles that found in the purple membrane of H. salinarum, except that lipid molecules trapped within the trimeric structure are not distributed with perfect threefold symmetry. Nonetheless, diffraction data at 1.8â Å resolution provide accurate structural information about functionally important residues. It is shown that two glutamates in the proton-release channel form a paired structure that is maintained by a low-barrier hydrogen bond. Although the structure of the proton-release pathway is highly conserved among proton-pumping archaeal rhodopsins, aR2 possesses the following peculiar structural features: (i) the motional freedom of the tryptophan residue that makes contact with the C13 methyl group of retinal is restricted, affecting the formation/decay kinetics of the L state, and (ii) the N-terminal polypeptide folds into an Ω-loop, which may play a role in organizing the higher-order structure.
Subject(s)
Halobacterium/chemistry , Rhodopsins, Microbial/chemistry , Crystallization , Crystallography, X-Ray , Glutamic Acid/chemistry , Hydrogen Bonding , Kinetics , Models, Molecular , Protein Conformation , Proton Pumps/chemistry , Rhodopsins, Microbial/metabolismABSTRACT
RNase H1 from Halobacterium sp. NRC-1 (Halo-RNase H1) is characterized by the abundance of acidic residues on the surface, including bi/quad-aspartate site residues. Halo-RNase H1 exists in partially folded (I) and native (N) states in low-salt and high-salt conditions respectively. Its folding is also induced by divalent metal ions. To understand this unique folding mechanism of Halo-RNase H1, the active site mutant (2A-RNase H1), the bi/quad-aspartate site mutant (6A-RNase H1), and the mutant at both sites (8A-RNase H1) were constructed. The far-UV CD spectra of these mutants suggest that 2A-RNase H1 mainly exists in the I state, 6A-RNase H1 exists both in the I and N states, and 8A-RNase H1 mainly exists in the N state in a low salt-condition. These results suggest that folding of Halo-RNase H1 is induced by binding of divalent metal ions to the bi/quad-aspartate site. To examine whether metal-induced folding is unique to Halo-RNase H1, RNase H2 from the same organism (Halo-RNase H2) was overproduced and purified. Halo-RNase H2 exists in the I and N states in low-salt and high-salt conditions respectively, as does Halo-RNase H1. However, this protein exists in the I state even in the presence of divalent metal ions. Halo-RNase H2 exhibits junction ribonuclease activity only in a high-salt condition. A tertiary model of this protein suggests that this protein does not have a quad-aspartate site. We propose that folding of Halo-RNase H1 is induced by binding of divalent metal ion to the quad-aspartate site in a low-salt condition.
Subject(s)
Archaeal Proteins/chemistry , Halobacterium/chemistry , Magnesium/chemistry , Manganese/chemistry , Ribonuclease H/chemistry , Amino Acid Sequence , Archaeal Proteins/genetics , Aspartic Acid/chemistry , Catalytic Domain , Cations, Divalent , Crystallography, X-Ray , Escherichia coli/genetics , Escherichia coli/metabolism , Gene Expression , Halobacterium/enzymology , Models, Molecular , Molecular Sequence Data , Mutation , Protein Binding , Protein Folding , Protein Structure, Secondary , Protein Structure, Tertiary , Recombinant Proteins/chemistry , Recombinant Proteins/genetics , Ribonuclease H/genetics , Sequence Alignment , Sodium Chloride/chemistryABSTRACT
Light is harvested by natural photosynthetic systems to generate electrochemical gradients that power various reactions. Implementing nature's lessons in photosynthesis holds great promise for technological advances. With a focus on designs and concepts, recent progress in generating electrochemical gradients by light, mimicking the two general types of photosynthetic centers in nature that make use of either light-induced charge separation or photo-isomerization are summarized here. Light induced electrochemical gradients pave new ways for photoelectric conversion. While extensive research in this direction has focused on light-induced charge separation, recent work has shown that energy conversion based on photo-isomerization is very promising. Photoswitchable compounds have been found in nature, such as the retinal molecule in bacteriorhodopsin. These compounds may form an attractive molecular basis for future progress in this field.
Subject(s)
Bacteriorhodopsins/chemistry , Electrochemical Techniques , Light , Halobacterium/chemistry , Halobacterium/metabolism , Ion Transport , Isomerism , PhotosynthesisABSTRACT
Monomeric bacteriorhodopsin (bR) reconstituted into POPC/POPG-containing nanodiscs was investigated by combined small-angle neutron and X-ray scattering. A novel hybrid approach to small-angle scattering data analysis was developed. In combination, these provided direct structural insight into membrane-protein localization in the nanodisc and into the protein-lipid interactions. It was found that bR is laterally decentred in the plane of the disc and is slightly tilted in the phospholipid bilayer. The thickness of the bilayer is reduced in response to the incorporation of bR. The observed tilt of bR is in good accordance with previously performed theoretical predictions and computer simulations based on the bR crystal structure. The result is a significant and essential step on the way to developing a general small-angle scattering-based method for determining the low-resolution structures of membrane proteins in physiologically relevant environments.
Subject(s)
Archaeal Proteins/chemistry , Bacteriorhodopsins/chemistry , Halobacterium/chemistry , Phosphatidylcholines/chemistry , Phosphatidylglycerols/chemistry , Archaeal Proteins/biosynthesis , Archaeal Proteins/isolation & purification , Bacteriorhodopsins/biosynthesis , Bacteriorhodopsins/isolation & purification , Halobacterium/metabolism , Lipid Bilayers/chemistry , Membranes, Artificial , Models, Molecular , Neutron Diffraction , Protein Conformation , Scattering, Small Angle , X-Ray DiffractionABSTRACT
BACKGROUND: Bioactive molecules have received increasing attention due to their nutraceutical attributes and anticancer, antioxidant, antiproliferative and apoptosis-inducing properties. This study aimed to investigate the biological properties of carotenoids extracted from Archaea. METHODS: Halophilic Archaea strains were isolated from the brine of a local crystallizer pond (TS7) of a solar saltern at Sfax, Tunisia. The most carotenoid-producing strain (M8) was investigated on heptoma cell line (HepG2), and its viability was assessed by the MTT-test. The cells were incubated with different sub-lethal extract rates, with carotenoid concentrations ranging from 0.2 to 1.5 µM. Antioxidant activity was evaluated through exposing the cells to sub-lethal extract concentrations for 24 hours and then to oxidative stress induced by 60 µM arachidonic acid and 50 µM H2O2. RESULTS: Compared to non-treated cells, bacterial carotenoid extracts inhibited HepG2 cell viability (50%). A time and dose effect was observed, with cell viability undergoing a significant (P < 0.05) decrease with extract concentration. After exposure to oxidative stress, control cells underwent a significant (P < 0.05) decrease in viability as compared to the non-treated cells. CONCLUSIONS: The bacterial extracts under investigation were noted to exhibit the strongest free radical scavenging activity with high carotenoid concentrations. The carotenoid extract also showed significant antiproliferative activity against HepG2 human cancer cell lines.
Subject(s)
Antioxidants/pharmacology , Carotenoids/pharmacology , Halobacterium/chemistry , Seawater/microbiology , Antioxidants/chemistry , Antioxidants/isolation & purification , Carotenoids/chemistry , Carotenoids/isolation & purification , Cell Shape/drug effects , Cell Survival/drug effects , Halobacterium/classification , Halobacterium/isolation & purification , Hep G2 Cells , Humans , Oxidative Stress/drug effects , TunisiaABSTRACT
The highly conserved 29-mer RNA motif corresponding to the peptidyl transferase central circle region of the domain V of Halobacterium halobium 23S rRNA has been characterised by multidimensional NMR spectroscopy. The NMR structure has a good all atom average RMSD of 1.28 Å and a stable A-form helical conformation. The NMR structure differs from the X-ray crystal structure of an analogous motif, contained within the Escherichia coli ribosome, as none of the bases are flipped out and a number of non-canonical base pairs are formed in the solution structure. Thus in the observed NMR structure, the predicted A7 to U30 base pair is not seen and a non-canonical U6 to U30 base pair was formed in its place. Similarly the predicted A9 to U26 base pair was also not observed and another non-canonical A9 to A27 base pair was formed. It was also seen from the conformational analysis that the steps near the bulges had the greatest deviation from the canonical Watson-Crick base pair step parameters. Despite these differences, the 29-mer structure provides a working model of the RNA within the ribosome in a more natural solution state than that observed in the intact ribosome crystal structures, particularly around the A27 residue. The NMR structure determination of the 29-mer RNA motif provides a solid foundation for determining the NMR structure of the RNA-amicetin complex in the next step. To extend the above study, a fully (13)C and (15)N isotopically labelled 37-mer RNA version of the Halobacterium halobium RNA sample has been characterised using ultra high field 1 GHz spectroscopy. The results have been used to demonstrate the advantages conferred by the use of a 1 GHz spectrometer frequency over 800 MHz in terms of superior sensitivity and greater spectral dispersion achieved in the spectrum of the RNA.
Subject(s)
Halobacterium/chemistry , RNA, Ribosomal, 23S/chemistry , Crystallography, X-Ray , Models, Molecular , Nuclear Magnetic Resonance, Biomolecular , Nucleic Acid ConformationABSTRACT
We recently published procedures describing the isolation of absolute infrared spectra for the intermediates of the bacteriorhodopsin (BR) photocycle and from these, obtaining transitional difference spectra between consecutive intermediates. In that work, we concentrated mainly on proton-binding centers and the route of proton transport across the membrane. In the current study, we used isolated spectra for the amide I, amide II, and amide III envelopes to obtain quantitative information on the extent of conformational change accompanying each transition in the photocycle. Our main finding was that most of the conformational changes occur in the conversion of the M(F) intermediate to N. In our earlier publication, a new proton acceptor, absorbing at 1650 cm(-1) was identified, which appeared to accept a proton from Asp96COOH during the transformation of BR to L. Below, we present evidence that supports this interpretation and propose a possible role for this new component.
Subject(s)
Bacteriorhodopsins/chemistry , Protons , Bacteriorhodopsins/isolation & purification , Halobacterium/chemistry , Protein Conformation , Spectroscopy, Fourier Transform InfraredABSTRACT
In this study, the carotenoids produced by the extremophile microorganisms Halococcus morrhuae, Halobacterium salinarium and Thermus filiformis were separated and identified by high-performance liquid chromatography connected to a diode array detector and a tandem mass spectrometer. The in vitro scavenging capacity of the carotenoid extracts against radical and non-radical species was evaluated. In halophilic microorganisms, the following carotenoids were identified: bacterioruberin, bisanhydrobacterioruberin, trisanhydrobacterioruberin and their derivatives. In the thermophilic bacterium, the carotenoids all-trans-zeaxanthin, zeaxanthin monoglucoside, thermozeaxanthins and thermobiszeaxanthins were identified. The antioxidant capacities of the carotenoid extracts of H. morrhuae (trolox equivalent antioxidant capacity = 5.07 and IC(50) = 0.85 µg mL(-1)) and H. salinarium (trolox equivalent antioxidant capacity = 5.28 and IC(50) = 0.84 µg mL(-1)) were similar and higher than those of the bacterium T. filiformis (trolox equivalent antioxidant capacity = 2.87 and IC(50) = 2.41 µg mL(-1)). This difference is related to the presence of acyclic carotenoids with both large numbers of conjugated double bounds and of hydroxyl groups in the major carotenoid of the halophilic microorganisms.
Subject(s)
Antioxidants/isolation & purification , Carotenoids/isolation & purification , Halobacterium/chemistry , Halococcus/chemistry , Thermus/chemistry , Antioxidants/analysis , Carotenoids/analysis , Chromatography, High Pressure Liquid , Tandem Mass SpectrometryABSTRACT
BACKGROUND: Incidence of food-borne infections from Listeria monocytogenes, a parasite that has adapted intracellular residence to avoid antibody onslaught, has increased dramatically in the past few years. The apparent lack of an effective vaccine that is capable of evoking the desired cytotoxic T cell response to obliterate this intracellular pathogen has encouraged the investigation of alternate prophylactic strategies. It should also be noted that Archaebacteria (Archae) lipid-based adjuvants enhance the efficacy of subunit vaccines. In the present study, the adjuvant properties of archaeosomes (liposomes prepared from total polar lipids of archaebacteria, Halobacterium salinarum) combined with immunogenic culture supernatant antigens of L. monocytogenes have been exploited in designing a vaccine candidate against experimental listeriosis in murine model. METHODS: Archaeosome-entrapped secretory protein antigens (SAgs) of L. monocytogenes were evaluated for their immunological responses and tendency to deplete bacterial burden in BALB/c mice challenged with sublethal listerial infection. Various immunological studies involving cytokine profiling, lymphocyte proliferation assay, detection of various surface markers (by flowcytometric analysis), and antibody isotypes (by enzyme-linked immunosorbent assay) were used for establishing the vaccine potential of archaeosome-entrapped secretory proteins. RESULTS: Immunization schedule involving archaeosome-encapsulated SAgs resulted in upregulation of Th1 cytokine production along with boosted memory in BALB/c mice. It also showed protective effect by reducing listerial burden in various vital organs (liver and spleen) of the infected mice. However, the soluble form of the antigens (SAgs) and their physical mixture with sham (empty) archaeosomes, besides showing feeble Th1 response, were unable to protect the animals against virulent listerial infection. CONCLUSION: On the basis of the evidence provided by the current data, it is inferred that archaeosome-entrapped SAgs formulation not only enhances cytotoxic T cell response but also helps in the clearance of pathogens and thereby increases the survival of the immunized animals.
Subject(s)
Antigens, Bacterial/immunology , Bacterial Vaccines/administration & dosage , Bacterial Vaccines/immunology , Listeria monocytogenes/immunology , Listeriosis/prevention & control , Analysis of Variance , Animals , Antigens, Bacterial/chemistry , Antigens, CD/immunology , Bacterial Vaccines/chemistry , Blotting, Western , Cell Proliferation , Cytokines/metabolism , Electrophoresis, Polyacrylamide Gel , Female , Flow Cytometry , Halobacterium/chemistry , Immunologic Memory , Liposomes/administration & dosage , Liposomes/chemistry , Liposomes/immunology , Listeria monocytogenes/chemistry , Listeriosis/immunology , Mice , Mice, Inbred BALB C , Th1 Cells/immunology , Th1 Cells/metabolismABSTRACT
In the present work spectral shifts of adsorption maxima for the number of mutants of bacteriorhodopsin have been calculated using QM/MM hybrid methodology. Along with this calculation an analysis of possible mechanisms of spectral modulation has been performed. Also we have carried out a comparative analysis of modern quantum chemical methods in respect of the level of optical spectra predictability they allow. We have shown that modern hybrid quantum chemical methods reach an acceptable level of preciseness when applied in the calculation of spectral shifts even if the absolute values of adsorption maxima predicted by these methods are underestimated. The number of rules has been found linking the value of spectral shift with the structural rearrangement in the apoprotein. The methods we were using as well as those rules we have found out both may be useful for development of nanoelectronical devices based on mutant species of bacteriorhodopsin (memory elements, optical triggers etc.).
Subject(s)
Bacteriorhodopsins/chemistry , Halobacterium/chemistry , Models, Chemical , Molecular Dynamics Simulation , Mutation , Bacteriorhodopsins/genetics , Halobacterium/genetics , Spectrum Analysis/methodsABSTRACT
We demonstrate the extension of the principle of difference Fourier transform infrared (FTIR) spectroscopy to difference 2D-IR spectroscopy. To this end, we measure difference 2D-IR spectra of the protein bacteriorhodopsin in its early J- and K-intermediates. By comparing with the static 2D-IR spectrum of the protonated Schiff base of all-trans retinal, we demonstrate that the 2D-IR spectrum of the all-trans retinal chromophore in bacteriorhodopsin can be measured with the background from the remainder of the protein completely suppressed. We discuss several models to interpret the detailed line shape of the difference 2D-IR spectrum.
Subject(s)
Bacteriorhodopsins/analysis , Spectroscopy, Fourier Transform Infrared/methods , Halobacterium/chemistry , Models, Molecular , Retinaldehyde/chemistry , Schiff Bases/chemistryABSTRACT
Liquid chromatography coupled to mass spectrometry (LC-MS) has become a major tool for the study of biological processes. High-throughput LC-MS experiments are frequently conducted in modern laboratories, generating an enormous amount of data per day. A manual inspection is therefore no longer a feasible task. Consequently, there is a need for computational tools that can rapidly provide information about mass, elution time, and abundance of the compounds in a LC-MS sample. We present an algorithm for the detection and quantification of peptides in LC-MS data. Our approach is flexible and independent of the MS technology in use. It is based on a combination of the sweep line paradigm with a novel wavelet function tailored to detect isotopic patterns of peptides. We propose a simple voting schema to use the redundant information in consecutive scans for an accurate determination of monoisotopic masses and charge states. By explicitly modeling the instrument inaccuracy, we are also able to cope with data sets of different quality and resolution. We evaluate our technique on data from different instruments and show that we can rapidly estimate mass, centroid of retention time, and abundance of peptides in a sound algorithmic framework. Finally, we compare the performance of our method to several other techniques on three data sets of varying complexity.
Subject(s)
Algorithms , Chromatography, Liquid/methods , Mass Spectrometry/methods , Peptides/analysis , Animals , Halobacterium/chemistry , Humans , Myoglobin/chemistry , Regression Analysis , SoftwareABSTRACT
Photoactive yellow proteins (PYP) are bacterial photoreceptors with a Per-Arnt-Sim (PAS) domain fold. We report the identification of six new PYPs, thus nearly doubling the size of this protein family. This extends the taxonomic diversity of PYP-containing bacteria from photosynthetic to nonphotosynthetic bacteria, from aquatic to soil-dwelling organisms, and from Proteobacteria to Salinibacter ruber from the phylum Bacteriodetes. The new PYPs greatly increase the sequence diversity of the PYP family, reducing the most prevalent pair-wise identity from 45% to 25%. Sequence alignments and analysis indicate that all 14 PYPs share a common structure with 13 highly conserved residues that form the chromophore binding pocket. Nevertheless, the functional properties of the PYPs vary greatly--the absorbance maximum extends from 432 to 465 nm, the pK(a) of the chromophore varies from pH 2.8 to 10.2, and the lifetime of the presumed PYP signaling state ranges from 1 ms to 1 h. Thus, the PYP family offers an excellent opportunity to investigate how functional properties are tuned over a wide range, while maintaining the same overall protein structural fold. We discuss the implications of these results for structure-function relationships in the PYP family.
Subject(s)
Bacterial Proteins/chemistry , Bacterial Proteins/genetics , Photoreceptors, Microbial/chemistry , Photoreceptors, Microbial/genetics , Amino Acid Sequence , Bacterial Proteins/metabolism , Genetic Variation , Halobacterium/chemistry , Halobacterium/classification , Light , Models, Molecular , Molecular Sequence Data , Photoreceptors, Microbial/metabolism , Phylogeny , Protein Conformation , Rhodobacter/classificationABSTRACT
The structural changes of bacteriorhodopsin during its photochemical cycle, as revealed by crystal structures of trapped intermediates, have provided insights to the proton translocation mechanism. Because accumulation of the last photointermediate, O, appears to be hindered by lattice forces in the crystals, the only information about the structure of this state is from suggested analogies with the determined structures of the non-illuminated D85S mutant and wild-type bacteriorhodopsin at low pH. We used electron paramagnetic resonance spectroscopy of site-directed spin labels at the extracellular protein surface in membranes to test these models. Spin-spin dipolar interactions in the authentic O state compared to the non-illuminated state revealed that the distance between helices C and F increases by ca 4 Angstroms, there is no distance change between helices D and F, and the distance between helix D and helix B of the adjacent monomer increases. Further, the mobility changes of single labels indicate that helices E and F move outward from the proton channel at the center of the protein, and helix D tilts inward. The overall pattern of movements suggests that the model at acid pH is a better representation of the O state than D85S. However, the mobility analysis of spin-labels on the B-C interhelical loop indicates that the antiparallel beta-sheet maintains its ordered secondary structure in O, instead of the predicted disorder in the two structural models. During decay of the O state, the last step of the photocycle, a proton is transferred from Asp85 to proton release complex in the extracellular proton channel. The structural changes in O suggest the need of large conformational changes to drive the Arg82 side-chain back to its initial orientation towards Asp85, and to rearrange the numerous water molecules in this region in order to conduct the proton away from Asp85.
Subject(s)
Bacteriorhodopsins/chemistry , Halobacterium/chemistry , Light , Amino Acids , Deuterium Oxide , Electron Spin Resonance Spectroscopy , Models, Molecular , Mutant Proteins/chemistry , Protein Structure, Secondary , Spectrophotometry , Spin Labels , TemperatureABSTRACT
Development of bacteriorhodopsin (bR) analogues employing chromophore substitution technique for the purpose of characterizing the binding site of bR and generating bR analogues with novel opto-electronic properties for applications as photoactive element in nanotechnical devices are described. Additionally, the photophysical and photochemical properties of variously substituted diarylpolyenes as models of photobiologically relevant linear polyenes are discussed. The role of charge separated dipolar excited states in the photoprocesses of linear polyenes is highlighted.
Subject(s)
Bacteriorhodopsins/chemistry , Bacteriorhodopsins/radiation effects , Halobacterium/chemistry , Photochemistry , Polyenes/chemistry , Bacteriorhodopsins/physiology , Binding Sites , Models, Biological , Models, Chemical , Nanotechnology , Polyenes/metabolism , StereoisomerismABSTRACT
A novel halophilic archaeon, NG4(T), was isolated from Jilantai salt lake in Inner Mongolia, China. The taxonomy of strain NG4(T) was studied by polyphasic methods. Strain NG4(T) grew at pH 5.5-8.5 and at a temperature of 22-55 degrees C. It was chemo-organotrophic, aerobic and required concentrations of 2.7-5.2 M NaCl and 0.05-0.3 M Mg(2+) for growth. Cells were Gram-negative, slender rods. Colonies on agar plates containing 25 % (w/v) total salts were red, elevated and round. According to 16S rRNA gene sequence similarity, strain NG4(T) was phylogenetically related to Halobacterium salinarum DSM 3754(T) (98.2 %) and Halobacterium noricense A1(T) (97.3 %). The DNA G+C content was 64.2 mol%. DNA-DNA relatedness values with Hbt. salinarum DSM 3754(T) and Hbt. noricense A1(T) were 47 and 35 %, respectively. The polar lipids of strain NG4(T) consisted of phosphatidylglycerol, methylated phosphatidylglycerol phosphate, phosphatidylglycerol sulfate, triglycosyl diether, sulfated triglycosyl diether and sulfated tetraglycosyl diether. It was concluded that strain NG4(T) represents a novel species of the genus Halobacterium, for which the name Halobacterium jilantaiense sp. nov. is proposed. The type strain is NG4(T) (=CGMCC 1.5337(T)=JCM 13558(T)).
Subject(s)
Fresh Water/microbiology , Halobacterium/classification , Sodium Chloride , Bacterial Typing Techniques , Base Composition , China , DNA, Archaeal/analysis , DNA, Ribosomal/analysis , Fresh Water/chemistry , Genes, rRNA , Halobacterium/chemistry , Halobacterium/genetics , Halobacterium/isolation & purification , Molecular Sequence Data , Nucleic Acid Hybridization , Phenotype , Phylogeny , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , Species SpecificityABSTRACT
Nine halophilic archaea viz., Halobacterium salinarum, Halobacterium sp.1, Halobacterium sp.2, Halobaculum sp., Halococcus saccharolyticus, Halorubrum saccharovorum, Haloterrigena turkmenica, Halogeometricum sp. and Natrialba sp. isolated from marine salterns around Bhavnagar coast were screened for siderophore production. Five isolates viz., Halococcus saccharolyticus, Halorubrum saccharovorum, Haloterrigena turkmenica, Halogeometricum sp. and Natrialba sp. produced siderophores as evidenced by positive reaction in FeCl3 test, CAS assay and CAS agar plate test. Determination of chemical nature of siderophores by chemical assays and bioassays identified them as carboxylates. Quantification of siderophores indicated Halorubrum saccharovorum to be the maximum siderophore producer (2.62 RE mg/ml) and Halococcus saccharolyticus to be the least (1.33 RE mg/ml). The present study is the first report on siderophore production in Indian haloarchaeal strains. Mechanism of iron assimilation in four non-siderophore isolates still needs to be investigated further.
Subject(s)
Halobacterium/chemistry , Siderophores/chemistry , Siderophores/metabolism , Halobacterium/metabolismABSTRACT
Archaerhodopsin-1 and -2 (aR-1 and aR-2) are light-driven proton pumps found in Halorubrum sp. aus-1 and -2, which share 55-58% sequence identity with bacteriorhodopsin (bR), a proton pump found in Halobacterium salinarum. In this study, aR-1 and aR-2 were crystallized into 3D crystals belonging to P4(3)2(1)2 (a = b = 128.1 A, c = 117.6 A) and C222(1) (a = 122.9 A, b = 139.5 A, c = 108.1 A), respectively. In both the crystals, the asymmetric unit contains two protein molecules with slightly different conformations. Each subunit is composed of seven helical segments as seen in bR but, unlike bR, aR-1 as well as aR-2 has a unique omega loop near the N terminus. It is found that the proton pathway in the extracellular half (i.e. the proton release channel) is more opened in aR-2 than in aR-1 or bR. This structural difference accounts for a large variation in the pKa of the acid purple-to-blue transition among the three proton pumps. All the aromatic residues surrounding the retinal polyene chain are conserved among the three proton pumps, confirming a previous argument that these residues are required for the stereo-specificity of the retinal isomerization. In the cytoplasmic half, the region surrounded by helices B, C and G is highly conserved, while the structural conservation is very low for residues extruded from helices E and F. Structural conservation of the hydrophobic residues located on the proton uptake pathway suggests that their precise arrangement is necessary to prevent a backward flow of proton in the presence of a large pH gradient and membrane potential. An empty cavity is commonly seen in the vicinity of Leu93 contacting the retinal C13 methyl. Existence of such a cavity is required to allow a large rotation of the side-chain of Leu93 at the early stage of the photocycle, which has been shown to accompany water translocation across the Schiff base.
Subject(s)
Bacteriorhodopsins/chemistry , Bacteriorhodopsins/metabolism , Proton Pumps/chemistry , Proton Pumps/metabolism , Amino Acid Sequence , Bacteriorhodopsins/genetics , Crystallography, X-Ray , Cytoplasm/chemistry , Cytoplasm/metabolism , Halobacterium/chemistry , Halobacterium/genetics , Halobacterium/metabolism , Models, Molecular , Molecular Sequence Data , Protein Structure, Quaternary , Protein Structure, Tertiary , Protein Subunits/chemistry , Protein Subunits/genetics , Protein Subunits/metabolism , Proton Pumps/genetics , Sequence Alignment , Structural Homology, ProteinABSTRACT
To better understand the extremely halophilic archaeon Halobacterium species NRC-1, we analyzed its soluble proteome by two-dimensional liquid chromatography coupled to electrospray ionization tandem mass spectrometry. A total of 888 unique proteins were identified with a ProteinProphet probability (P) between 0.9 and 1.0. To evaluate the biochemical activities of the organism, the proteomic data were subjected to a biological network analysis using our BMSorter software. This allowed us to examine the proteins expressed in different biomodules and study the interactions between pertinent biomodules. Interestingly an integrated analysis of the enzymes in the amino acid metabolism and citrate cycle networks suggested that up to eight amino acids may be converted to oxaloacetate, fumarate, or oxoglutarate in the citrate cycle for energy production. In addition, glutamate and aspartate may be interconverted from other amino acids or synthesized from citrate cycle intermediates to meet the high demand for the acidic amino acids that are required to build the highly acidic proteome of the organism. Thus this study demonstrated that proteome analysis can provide useful information and help systems analyses of organisms.