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1.
Biochemical and Immunological Study of Cell Envelope Proteins in Sulfate-Reducing Bacteria 总被引:1,自引:1,他引:0
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The envelope proteins of 5 strains of the genus Desulfotomaculum and 12 strains of the genus Desulfovibrio were studied by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblotting. The Desulfovibrio strains exhibited a typical gram-negative cell envelope, whereas the cell envelope of Desulfotomaculum strains appeared to be gram-positive. A close relationship between strains of Desulfotomaculum nigrificans was observed. A comparison between different species of Desulfotomaculum revealed some degree of similarity between Desulfotomaculum nigrificans and Desulfotomaculum ruminis, whereas Desulfotomaculum orientis seemed unique. The strains of Desulfovibrio salexigens were quite different from the strains of the other species of Desulfovibrio. In two of the strains of Desulfovibrio desulfuricans, a species-specific antigen was observed. The strains of Desulfovibrio vulgaris, Desulfovibrio africanus, and Desulfovibrio gigas and one strain of Desulfovibrio desulfuricans exhibited a similar outer membrane protein profile and also showed very similar antigenic reactions. 相似文献
2.
Catarina M. Paquete Patrícia M. Pereira Teresa Catarino David. L. Turner Ricardo O. Louro 《BBA》2007,1767(2):178-188
Type I cytochrome c3 is a key protein in the bioenergetic metabolism of Desulfovibrio spp., mediating electron transfer between periplasmic hydrogenase and multihaem cytochromes associated with membrane bound complexes, such as type II cytochrome c3. This work presents the NMR assignment of the haem substituents in type I cytochrome c3 isolated from Desulfovibrio africanus and the thermodynamic and kinetic characterisation of type I and type II cytochromes c3 belonging to the same organism. It is shown that the redox properties of the two proteins allow electrons to be transferred between them in the physiologically relevant direction with the release of energised protons close to the membrane where they can be used by the ATP synthase. 相似文献
3.
Patrícia M. Paes de Sousa Sofia R. Pauleta M. Lurdes Simões Gonçalves Graham W. Pettigrew Isabel Moura José J. G. Moura Margarida M. Correia dos Santos 《Journal of biological inorganic chemistry》2011,16(2):209-215
In this work it is demonstrated that the characterization of c-type haem containing proteins by electrochemical techniques needs to be cautiously performed when using pyrolytic graphite
electrodes. An altered form of the cytochromes, which has a redox potential 300 mV lower than that of the native state and
displays peroxidatic activity, can be induced by interaction with the pyrolytic graphite electrode. Proper control experiments
need to be performed, as altered conformations of the enzymes containing c-type haems can show activity towards the enzyme substrate. The work was focused on the study of the activation mechanism
and catalytic activity of cytochrome c peroxidase from Paracoccus
pantotrophus. The results could only be interpreted with the assignment of the observed non-turnover and catalytic signals to a non-native
conformation state of the electron-transferring haem. The same phenomenon was detected for Met–His monohaem cytochromes (mitochondrial
cytochrome c and Desulfovibrio
vulgaris cytochrome c-553), as well as for the bis-His multihaem cytochrome c
3 from Desulfovibrio
gigas, showing that this effect is independent of the axial coordination of the c-type haem protein. Thus, the interpretation of electrochemical signals of c-type (multi)haem proteins at pyrolytic graphite electrodes must be carefully performed, to avoid misassignment of the signals
and incorrect interpretation of catalytic intermediates. 相似文献
4.
Immunological Cross-Reactivities of Adenosine-5′-Phosphosulfate Reductases from Sulfate-Reducing and Sulfide-Oxidizing Bacteria
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Crude extracts from 14 species of sulfate-reducing bacteria comprising the genera Desulfovibrio, Desulfotomaculum, Desulfobulbus, and Desulfosarcina and from three species of sulfide-oxidizing bacteria were tested in an enzyme-linked immunosorbent assay with polyclonal antisera to adenosine 5′-phosphosulfate reductase from Desulfovibrio desulfuricans G100A. The results showed that extracts from Desulfovibrio species were all highly cross-reactive, whereas extracts from the other sulfate-reducing genera showed significantly less cross-reaction. An exception was Desulfotomaculum orientis, which responded more like Desulfovibrio species than the other Desulfotomaculum strains tested. Extracts from colorless or photosynthetic sulfur bacteria were either unreactive or exhibited very low levels of reactivity with the antibodies to the enzyme from sulfate reducers. These results were confirmed by using partially purified enzymes from sulfate reducers and the most cross-reactive sulfide oxidizer, Thiobacillus denitrificans. Two types of monoclonal antibodies to adenosine 5′-phosphosulfate reductase were also isolated. One type reacted more variably with the enzymes of the sulfate reducers and poorly with the Thiobacillus enzyme, whereas the second reacted strongly with Desulfovibrio, Desulfotomaculum orientis, and Thiobacillus enzymes. 相似文献
5.
《FEBS letters》1986,206(1):157-161
Desulfovibrio desulfuricans grown in a lactate-sulfate medium produces, in addition to soluble cytochromes, c-type cytochromes which appear to be integral membrane proteins. Two cytochromes can be separated, an abundant 15 kDa cytochrome and a 22 kDa cytochrome. Both have optical spectra characteristics of c-type cytochromes. The 15 kDa cytochrome shows two n = 1 components in potentiometric redox titrations with midpoint potentials at −130 and −270 mV in the membrane; both were slightly lower in detergent-solubilized preparations. We suggest a designation of cytochrome ccm for this species. Its properties suggest a function as a transmembrane electron carrier between hydrogen and sulfate. 相似文献
6.
The cytochromes of the filamentous bacteriaStreptomyces clavuligerus andSaccharopolyspora erythraea have been studied by low-temperature (77K) difference spectra and room-temperature potentiometric titrations. Difference spectra of membranes fromSa. erythraea indicate the presence of twoc- and twob-type cytochromes. A furtherb-type cytochrome is revealed by potentiometric titration. The soluble and membrane-bound forms of a green pigment, believed to be involved in electron transport to oxygen, are each shown to have complex absorption spectra which, in the case of the soluble form, may be potentiometrically resolved into several components. Threeb-type and threec-type cytochromes are shown to be present in the membranes ofSt. clavuligerus. 相似文献
7.
P. Bertrand M. Bruschi M. Denis J.P. Gayda F. Manca 《Biochemical and biophysical research communications》1982,106(3):756-760
Cytochrome c553 is a monohaemic c type cytochrome isolated from the sulfate reducing bacteria ,. Its midpoint potential value, determined by optical, EPR and polarographic studies is significantly lower than the midpoint potentials reported for other monohaemic cytochromes c (+ 10 mV instead of + 290 mV). In an attempt to study correlations between amino acid sequence, haem iron coordination and haem exposure in cytochromes c, cytochrome c553 is compared with mitochondrial and bacterial c type cytochromes. 相似文献
8.
Enzymatic reduction of chromate: comparative studies using sulfate-reducing bacteria 总被引:1,自引:0,他引:1
Michel C Brugna M Aubert C Bernadac A Bruschi M 《Applied microbiology and biotechnology》2001,55(1):95-100
Various sulfate-reducing bacteria of the genera Desulfovibrio and Desulfomicrobium were tested and compared for enzymatic reduction of chromate. Our study demonstrated that the ability to reduce chromate
is widespread among sulfate-reducing bacteria. Among them, Desulfomicrobium norvegicum reduced Cr(VI) with the highest reaction rate. This strain grew in the presence of up to 500 μM chromate, but Cr(VI) reduction
in the absence of sulfate was not associated with growth. The presence of chromate induced morphological changes and leakage
of periplasmic proteins into the medium. The ability of isolated polyheme cytochromes c from sulfate- and sulfur-reducing bacteria to reduce chromate was also analyzed. Tetraheme cytochrome c
3(M
r. 13,000) from Desulfomicrobium norvegicum showed twice as much activity as either tetraheme cytochrome c
3 from Desulfovibrio vulgaris strain Hildenborough or triheme cytochrome c
7 from Desulfuromonas acetoxidans. Results with cytochromes c
3 and other c-type cytochromes altered by site-directed mutagenesis indicated that negative redox potential hemes are crucial for metal
reductase activity. The present study also demonstrated that the (Fe) hydrogenase from sulfate-reducing bacteria could reduce
chromate.
Received: 14 April 2000 / Received revision: 6 July 2000 / Accepted: 9 July 2000 相似文献
9.
Lígia M. Saraiva Carlos A. Salgueiro Jean LeGall Walter M. A. M. van Dongen António V. Xavier 《Journal of biological inorganic chemistry》1996,1(6):542-550
Reduction of the haems in tetrahaem cytochromes c
3 is a cooperative process, i.e., reduction of each of the haems depends on the redox states of the other haems. Furthermore,
electron transfer is coupled to proton transfer (redox-Bohr effect). Two of its haems and a strictly conserved nearby phenylalanine
residue, F20, in Desulfovibrio vulgaris (Hildenborough) cytochrome c
3 form a structural motif that is present in all cytochromes c
3 and also in cytochrome c oxidase. A putative role for this phenylalanine residue in the cooperativity of haem reduction was investigated. Therefore,
this phenylalanine was replaced, with genetic techniques, by isoleucine and tyrosine in D. vulgaris (Hildenborough) cytochrome c
3. Cyclic voltammetry studies revealed a small increase (30 mV) in one of the macroscopic redox potentials in the mutated cytochromes.
EPR showed that the main alterations occurred in the vicinity of haem I, the haem closest to residue 20 and one of the haems
responsible for positive cooperativities in electron transfer of D. vulgaris cytochrome c
3. NMR studies of F20I cytochrome c
3 demonstrated that the haem core architecture is maintained and that the more affected haem proton groups are those near the
mutation site. NMR redox titrations of this mutated protein gave evidence for only small changes in the relative redox potentials
of the haems. However, electron/electron and proton/electron cooperativity are maintained, indicating that this aromatic residue
has no essential role in these processes. Furthermore, chemical modification of the N-terminal amino group of cytochrome c
3 backbone, which is also very close to haem I, had no effect on the network of cooperativities.
Received: 25 June 1996 / Accepted: 26 August 1996 相似文献
10.
Thomas C. Strekas 《BBA》1984,765(2):133-137
Resonance Raman spectroscopy has been used to obtain complete spectra of each individual cytochrome type — a, b and c — in the reduced state within membrane vesicle preparations from two species of obligately alkalophilic bacteria: Bacillus alcalophilus and Bacillus firmus RAB. The vibrational spectra, in the range 250–1700 cm?1, were obtained with tunable dye laser excitation in the wavelength range 550–600 nm tuned to resonance with the appropriate reduced alpha band maximum for the cytochrome type of interest. The spectra reveal details which serve to characterize the specific type of cytochrome as well as to confirm the similarity of the heme prosthetic group to previously well-characterized cytochromes of the the a- b- or c-type. Preliminary evidence in support of heterogeneity of b-type, and possibly a-type cytochromes, or of heme-heme interaction within the membrane is presented. 相似文献
11.
A sulfate-reducing bacterium, strain HDv, was isolated from the anoxic soil of a ricefield using lactate as electron donor. Cells were gram-negative, motile, nonsporulating curved rods, with single polar flagella. Substrates were incompletely oxidized to acetate and included glycerol, 1,2-and 1,3-propanediol. Sulfate, sulfite, thiosulfate, elemental sulfur, fumarate, maleate, and malate were utilized as electron acceptors. Pyruvate, fumarate, maleate, malate and dihydroxyacetone were fermented. Desulfoviridin and c-type cytochromes were present. The DNA base composition was 66.6 ± 0.3 mol% G+C. The isolate was identified as a Desulfovibrio sp.; its metabolic properties were somewhat different from those of previously described Desulfovibrio species. Comparative biochemical study of 1,2-propanediol dissimilation by the new isolate and Desulfovibrio alcoholovorans showed that NAD-dependent dehydrogenases play a key role in the catabolism of this substrate. The hypothetical pathways of 1,2-propanediol degradation by Desulfovibrio spp. are presented. 相似文献
12.
An indirect enzyme-linked immunoadsorption assay (ELISA) was developed for cytochrome c3 using antisera to the cytochromes fromDesulfovibrio africanus Benghazi, Desulfovibrio vulgaris Hildenborough andDesulfovibrio salexigens British Guiana. The ELISA system was used to test for cross-reactions between these antisera and the heterologous antigens. In contrast to previous experiments using the Ouchterlony technique, all of the cytochromes c3 tested exhibited some degree of cross-reaction. Considerable variation was seen in cross-reactions for cytochromes c3 from differing strains ofD. desulfuricans. This observation raises questions about the taxonomic relatedness of these strains. No cross-reaction was seen with eukaryotic cytochrome c or withD. vulgaris cytochrome c553. The data demonstrate that cytochrome c3 is capable of undergoing nonprecipitating cross-reactions, and thus may not be as immunologically unique as was once thought.Abbreviations ELISA
Enzyme-linked immunoadsorption assay 相似文献
13.
Optical and Potentiometric Study of the b- and c-Type Cytochromes in Mushroom Agaricus bisporus Lge Mitochondria
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Differential spectrometry revealed two species for the b-type, as well as for the c-type, cytochromes in mitochondria from Agaricus bisporus Lge. The two b-type components are denoted according to their peak position in the α region at room temperature, i.e. b560 and b566. The b556 component present in all the studied higher plant mitochondria was not detected in the system. At 293 K, the c-type cytochromes exhibit a common α band with a maximum at 550 nanometers. This band is split at 77 K, with peak positions at 547 nanometers (cytochrome c) and 552 nanometers (cytochrome c1). 相似文献
14.
Brochothrix thermosphacta, grown in batch culture in a yeast-dextrose broth, at temperatures from 30 °C to 10 °C, contained diverse membrane-bound respiratory cytochromes. Under conditions of moderate aeration, cytochromes of the a-, b- and d-type were detected at all growth temperatures, but the proportions changed as a function of temperature, with the spectra of cells grown at 10 or 15 °C being dominated by a-type cytochrome(s). Cytochrome a
3 was detected by its reactions with CO and cyanide in cells from all growth conditions. An additional cytochrome a, which was not cyanide-reactive, was also detected, suggesting the presence of an aa
3 oxidase complex. Cytochrome d was cyanide- and CO-reactive, but not detectable in photodissociation spectra, presumably because of the very rapid recombination of CO at the sub-zero temperatures used. Decreasing the oxygen transfer rates to batch cultures resulted in enhanced expression of cytochrome d and changed the proportion of the aa
3-type oxidase that could be attributed to ligand-binding cytochrome a
3; at the lowest oxygen transfer rates, no cytochrome a was detected, suggesting the presence of a cytochrome ba
3 terminal oxidase complex. Intact cells showed no evidence of a c-type cytochrome and no haem C was detected in membrane preparations. After growth at 10°C, the cytochrome composition of B. campestris was essentially identical to that of B. thermosphacta. The multiplicity of putative terminal oxidases in B. thermosphacta is discussed. 相似文献
15.
Rhizobium phaseoli cytochrome c-deficient mutant induces empty nodules on Phaseolus vulgaris L. 总被引:2,自引:0,他引:2
A Rhizobium phaseoli cytochrome mutant, unable to oxidize N,N,N′,N′ -tetramethyl-p-phenylend(amine (TMPD), was isolated after Mu-dl (Kan lac) mutagenesis of the wild-type strain CE-3. Mutant strain CFN4202 had sixfold less haem-c but similar levels of b type, o and aa3 cytochromes than the wild-type strain. CFN402 strain also showed reduced NADH- and TMPD-oxidase activity than the wild-type strain. Succinate-oxidase activities were very similar. Western blot experiments, using antiserum against bovine c1 and c cytochromes, revealed that both proteins were present in CFN4202 membranes, suggesting a defect of haem binding to cytochrome c. Nodules formed by this strain in Phaseolus vulgaris did not contain bacteroids. These data suggest that the cytochrome c-aa3 chain or some other respiratory chain, containing c-type cytochromes in R. phaseoli, is essential for bacterial division during the early steps of the symbiotic interaction with the legume-host. 相似文献
16.
An apo form of cytochrome C550 can be detected by immunoblotting cell-free extracts of a mutant of Paracoccus denitrificans that is deficient in c-type cytochromes. This apoprotein is found predominantly in the periplasm, the location of the holocytochrome in the wild-type organism, indicating that translocation of the polypeptide occurs in the absence of haem attachment. The polypeptide molecular weight, as judged by sodium dodecyl sulphate/polyacrylamide gel electrophoresis, is indistinguishable from that of the holoprotein and the chemically prepared apoprotein; this suggests that the N-terminal signal sequence is removed in the mutant as in the wild-type organism. In the presence of levulinic acid, an inhibitor of haem biosynthesis, apocytochrome c550 and aponitrite reductase (cytochrome cd1) accumulated in the periplasm of wild-type cells. Synthesis of these apoproteins was blocked by chloramphenicol. Thus in P. denitrificans the synthesis of these polypeptides is neither autoregulated nor regulated by the availability of haem. That the apoproteins appear in the periplasm argues against the possibility of polypeptide/haem co-transport from cytoplasm to periplasm. These observations are related to, and contrasted with, the biosynthesis of c-type cytochromes in eukaryotic cells. 相似文献
17.
Enzyme activities conceivably involved in the activation of sulfate were studied with Desulfotomaculum ruminis, D. acetoxidans, D. nigrificans, D. orientis, and Desulfovibrio vulgaris. Cell lysates of these species revealed activities of at least 8 nkat/mg protein (i.e., 480 nmol per min and mg protein) of ATP sulfurylase, acetate kinase, phosphotransacetylase and adenylate kinase. ADP sulfurylase was not detected. Pyrophosphatase activity was high (73 to 97 nkat/mg protein) in Desulfotomaculum orientis and Desulfovibrio vulgaris. In these strains pyrophosphatase was activated by addition of a reductant (dithionite). In Desulfotomaculum ruminis, D. acetoxidans, and D. nigrificans, only low pyrophosphatase activity (2.5 to 6.3 nkat/mg protein) was measured, which was not reductant-activated. Some hints indicated a membrane association of the pyrophosphatase in D. ruminis, and possibly also in D. acetoxidans and D. nigrificans. Activities of a pyrophosphate-dependent acetate kinase (PPi:acetate kinase), a PPi:AMP kinase or a polyphosphate:AMP kinase were not detected or negligible. The results are not in favour of the assumption that pyrophosphate formed by ATP sulfurylase during sulfate activation might be utilized to form acetyl phosphate in Desulfotomaculum species. Contrary results of other authors were shown to be artefacts caused by chemical hydrolysis of acetyl phosphate in the molybdate-sulfuric acid reagent used for phosphate determination.Abbreviations Pi
orthophosphate
- PPi
pyrophosphate
- APS
adenosine phosphosulfate
- AP5A, P1
P5-di(adenosine-5-)pentaphosphate
- CTAB
cetyltrimethylammonium bromide
- MOPS
3-(N-morpholino)propanesulfonic acid
- HEPES
N(-2-hydroxyethyl)piperazine-N-2-ethanesulfonic acid 相似文献
18.
Effects of amino acids on the kinetic properties of three noninterconvertible rat pyruvate kinases 总被引:1,自引:0,他引:1
1. Resonance Raman spectra excited by laser photons in resonance with the α and β electronic transitions of the reduced forms of cytochrome b5 and c were recorded and used as model systems to distinguish the “b”- and “c”-type Cytochromes of succinate-cytochrome c reductase. 2. The scattering intensity of a particular cytochrome depends on the proximity of the laser excitation to the electronic transition which is involved in the resonance enhancement; thus, exciting at different wavelengths provides a method of selectively investigating one hemoprotein in a mixture of several. 3. The spectra of the reduced succinate-cytochrome c reductase excited at 514.5-nm laser light were due to both c- and b-type Cytochromes in agreement with the position of their respective electronic absorption bands. Spectra excited at 568.2 nm were due mostly to b-type cytochromes because of the proximity of the excitation wavelength to the position of their α absorption bands. 4. The identification of the individual cytochromes is aided by the set of characteristic vibrational bands recorded at each excitation wavelength. 5. A possible explanation of the differences in number of bands and frequency of normal modes, involving the strong interaction between the vinyl side groups and porphyrin ring, is suggested. 6. Comparison of spectra of purified cytochrome b5 with the b cytochromes of the reductase preparations shows vibrational bands of protoheme in different hemeproteins which are sensitive to the particular protein environment. 相似文献
19.
The cytochromes of the bacteriumStreptomyces erythreus have been investigated. Membrane-bounda-, b-, andc-type cytochromes were found together with a green pigment, which was found in both a soluble and membrane-bound form. Cells containing the green pigment exhibited cyanide-insensitive oxygen uptake. The CO-binding pigments included cytochromea
3, ab-type cytochrome, cytochrome P450, and the green pigment. Photodissociation spectra at various low temperatures, in the presence or absence of oxygen, revealed cytochromeaa
3 to be the predominant cytochrome terminal oxidase. The green pigment was capable of electron transport; the relationship of the pigment to the remainder of the electron transport chain remains to be ascertained. 相似文献
20.
Efforts have been made to solubilize cytochrome components from particulate fractions of etiolated mung bean seedlings. Low temperature spectrophotometry reveals that the cytochrome composition of mitochondria isolated from whole seedlings is the same as that reported by Bonner for mung bean hypocotyls. On the basis of the identity in position of the α-bands in low temperature difference spectra for mitochondria, for a partially purified haemoprotein from mitochondria, and for purified cytochrome b-555, it is suggested that cytochrome b-555 is an intrinsic component of mung bean mitochondria. Difference spectra show that both the mitochondrial and microsomal fractions contain at least 2 b-type cytochromes. Cytochrome b-555 is almost certainly present in the microsomes, since the low temperature difference spectrum for the cytochrome is identical with the spectrum for this particulate fraction.
By freezing and thawing mung bean mitochondria in 4% cholate and centrifuging, cytochrome oxidase activity can be concentrated in the supernatant fraction, although it is not completely solubilized. The oxidase is inhibited by high concentrations of cytochrome c. A particle-bound cytochrome c can be obtained from mitochondria by digestion with snake venom. However, the autoxidizability of the preparation indicates that the cytochrome has been solubilized in a modified form. A CO-binding pigment can be obtained from mung bean microsomes by digestion with snake venom.
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