Mo-Cu metal cluster formation and binding in an orange protein isolated from Desulfovibrio gigas,
Carepo, M. S., Pauleta S. R., Wedd A. G., Moura J. J. G., and Moura I.
, J Biol Inorg Chem, Volume 19, p.605-614, (2014)
Modeling protein complexes with BiGGER,
Krippahl, L., Moura J. J., and Palma P. N.
, Proteins, Jul 1, Volume 52, Number 1, p.19-23, (2003)
AbstractThis article describes the method and results of our participation in the Critical Assessment of PRediction of Interactions (CAPRI) experiment, using the protein docking program BiGGER (Bimolecular complex Generation with Global Evaluation and Ranking) (Palma et al., Proteins 2000;39:372-384). Of five target complexes (CAPRI targets 2, 4, 5, 6, and 7), only one was successfully predicted (target 6), but BiGGER generated reasonable models for targets 4, 5, and 7, which could have been identified if additional biochemical information had been available.
Modelling metallothionein induction in the liver of Sparus aurata exposed to metal-contaminated sediments,
Costa, P. M., Repolho T., Caeiro S., Diniz M. E., Moura I., and Costa M. H.
, Ecotoxicology and Environmental Safety, Sep, Volume 71, Number 1, p.117-124, (2008)
AbstractMetallothionein (MT) in the liver of gilthead seabreams (Sparus aurata L., 1758) exposed to Sado estuary (Portugal) sediments was quantified to assess the MT induction potential as a biomarker of sediment-based contamination by copper (Cu), cadmium (U), lead (Pb) and arsenic (As). Sediments were collected from two control sites and four sites with different levels of contamination. Sediment Cu, Cd, Pb, As, total organic matter (TOM) and fine fraction (FF) levels were determined. Generalized linear models (GLM) allowed integration of sediment parameters with liver Cu, Cd, Pb, As and MT concentrations. Although sediment metal levels were lower than expected, we relate NIT with liver Cd and also with interactions between liver and sediment Cu and between liver Cu and TOM. We suggest integrating biomarkers and environmental parameters using statistical models such as GLM as a more sensitive and reliable technique for sediment risk assessment than traditional isolated biomarker approaches. (C) 2007 Elsevier Inc. All rights reserved.
Modelling the electron-transfer complex between aldehyde oxidoreductase and flavodoxin,
Krippahl, Ludwig, Palma Nuno P., Moura Isabel, and Moura Jose J. G.
, European Journal of Inorganic Chemistry, Oct 2, Number 19, p.3835-3840, (2006)
AbstractThree-dimensional protein structures of the xanthine oxidase family show different solutions for the problem of transferring electrons between the flavin adenine dinucleotide (FAD) group and the molybdenum cofactor. In xanthine oxidase all the cofactors he within domains of the same protein chain, whereas in CO dehydrogenase the Fe-S centres, FAD and Mo cofactors are enclosed in separate chains and the enzyme exists as a stable complex of all three. In aldehyde oxidore-ductase, only Fe-S and Mo co-factors are present in a single protein chain. Flavodoxin is docked to aldehyde oxidoreductase to mimic the flavin component on the intramolecular electron transfer chain of aanthine oxidase and CO dehydrogenase and, remarkably, the main features of the electron-transfer pathway are observed.
Moessbauer study of D. gigas ferredoxin II and spin-coupling model for Fe3S4 cluster with valence delocalization,
Papaefthymiou, V., Girerd J. J., Moura I., Moura J. J. G., and Muenck E.
, Journal of the American Chemical Society, 1987/07/01, Volume 109, Number 15, p.4703-4710, (1987)
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Molecular aspects of denitrification/nitrate dissimilation,
Moura, I., Cabrito I., Almeida G., Cunha C., Romao M. J., and Moura J. J. G.
, Journal of Inorganic Biochemistry, Jul 15, Volume 96, Number 1, p.195-195, (2003)
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Molecular cloning and sequence analysis of the gene of the molybdenum-containing aldehyde oxido-reductase of Desulfovibrio gigas. The deduced amino acid sequence shows similarity to xanthine dehydrogenase,
Thoenes, U., Flores O. L., Neves A., Devreese B., Van Beeumen J. J., Huber R., Romao M. J., Legall J., Moura J. J., and Rodrigues-Pousada C.
, Eur J Biochem, Mar 15, Volume 220, Number 3, p.901-10, (1994)
AbstractIn this report, we describe the isolation of a 4020-bp genomic PstI fragment of Desulfovibrio gigas harboring the aldehyde oxido-reductase gene. The aldehyde oxido-reductase gene spans 2718 bp of genomic DNA and codes for a protein with 906 residues. The protein sequence shows an average 52% (+/- 1.5%) similarity to xanthine dehydrogenase from different organisms. The codon usage of the aldehyde oxidoreductase is almost identical to a calculated codon usage of the Desulfovibrio bacteria.
Molybdenum and tungsten enzymes: the xanthine oxidase family,
Brondino, C. D., Romao M. J., Moura I., and Moura J. J.
, Curr Opin Chem Biol, Apr, Volume 10, Number 2, p.109-14, (2006)
AbstractMononuclear molybdenum and tungsten are found in the active site of a diverse group of enzymes that, in general, catalyze oxygen atom transfer reactions. Enzymes of the xanthine oxidase family are the best-characterized mononuclear Mo-containing enzymes. Several 3D structures of diverse members of this family are known. Recently, the structures of substrate-bound and arsenite-inhibited forms of two members of this family have also been reported. In addition, spectroscopic studies have been utilized to elucidate fine details that complement the structural information. Altogether, these studies have provided an important amount of information on the characteristics of the active site and the electron transfer pathways.
Molybdenum EXAFS of the Desulfovibrio gigas Mo(2Fe-2S) protein--structural similarity to "desulfo" xanthine dehydrogenase,
Cramer, S. P., Moura J. J., Xavier A. V., and Legall J.
, J Inorg Biochem, Apr, Volume 20, Number 4, p.275-80, (1984)
AbstractThe molybdenum EXAFS of the Mo(2Fe-2S) protein from Desulfovibrio gigas has been examined using fluorescence detection and synchrotron radiation. In the oxidized form the molybdenum environment is found to contain two terminal oxo groups and two long (2.47 A) Mo-S bonds. Evidence was also found for an oxygen or nitrogen donor ligand at 1.90 A. Addition of dithionite to the oxidized enzyme results in loss of a terminal oxo group, perhaps due to protonation. In addition, a 0.1 A contraction in the Mo-S bond lengths is observed. The behavior of both oxidized and dithionite-treated forms is similar to that observed previously with "desulfo" xanthine oxidase.
Molybdenum induces the expression of a protein containing a new heterometallic Mo-Fe cluster in Desulfovibrio alaskensis,
Rivas, M. G., Carepo M. S., Mota C. S., Korbas M., Durand M. C., Lopes A. T., Brondino C. D., Pereira A. S., George G. N., Dolla A., Moura J. J., and Moura I.
, Biochemistry, Feb 10, Volume 48, Number 5, p.873-82, (2009)
AbstractThe characterization of a novel Mo-Fe protein (MorP) associated with a system that responds to Mo in Desulfovibrio alaskensis is reported. Biochemical characterization shows that MorP is a periplasmic homomultimer of high molecular weight (260 +/- 13 kDa) consisting of 16-18 monomers of 15321.1 +/- 0.5 Da. The UV/visible absorption spectrum of the as-isolated protein shows absorption peaks around 280, 320, and 570 nm with extinction coefficients of 18700, 12800, and 5000 M(-1) cm(-1), respectively. Metal content, EXAFS data and DFT calculations support the presence of a Mo-2S-[2Fe-2S]-2S-Mo cluster never reported before. Analysis of the available genomes from Desulfovibrio species shows that the MorP encoding gene is located downstream of a sensor and a regulator gene. This type of gene arrangement, called two component system, is used by the cell to regulate diverse physiological processes in response to changes in environmental conditions. Increase of both gene expression and protein production was observed when cells were cultured in the presence of 45 microM molybdenum. Involvement of this system in Mo tolerance of sulfate reducing bacteria is proposed.
The molybdenum iron-sulphur protein from Desulfovibrio gigas as a form of aldehyde oxidase,
Turner, N., Barata B., Bray R. C., Deistung J., Legall J., and Moura J. J.
, Biochem J, May 1, Volume 243, Number 3, p.755-61, (1987)
AbstractThe molybdenum iron-sulphur protein originally isolated from Desulfovibrio gigas by Moura, Xavier, Bruschi, Le Gall, Hall & Cammack [(1976) Biochem. Biophys. Res. Commun. 72, 782-789] has been further investigated by e.p.r. spectroscopy of molybdenum(V). The signal obtained on extended reduction of the protein with sodium dithionite has been shown, by studies at 9 and 35 HGz in 1H2O and 2H2O and computer simulations, to have parameters corresponding to those of the Slow signal from the inactive desulpho form of various molybdenum-containing hydroxylases. Another signal obtained on brief reduction of the protein with small amounts of dithionite was shown by e.p.r. difference techniques to be a Rapid type 2 signal, like that from the active form of such enzymes. In confirmation that the protein is a molybdenum-containing hydroxylase, activity measurements revealed that it had aldehyde:2,6-dichlorophenol-indophenol oxidoreductase activity. No such activity towards xanthine or purine was observed. Salicylaldehyde was a particularly good substrate, and treatment of the protein with it also gave rise to the Rapid signal. Molybdenum cofactor liberated from the protein was active in the nit-1 Neurospora crassa nitrate reductase assay. It is concluded that the protein is a form of an aldehyde oxidase or dehydrogenase. From the intensity of the e.p.r. signals and from enzyme activity measurements, 10-30% of the protein in the sample examined appeared to be in the functional form. The evolutionary significance of the protein, which may represent a primitive form of the enzyme rather than a degradation product, is discussed briefly.
A molybdenum-containing (2Fe, 2S) protein from desulphovibrio gigas, a sulphate reducer,
Moura, J. J. G., Xavier A. V., Bruschi M., Legall J., and Cabral J. M. P.
, Journal of the Less Common Metals, Volume 54, Number 2, p.555-562, (1977)
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A molybdenum-containing iron-sulphur protein from Desulphovibrio gigas,
Moura, J. J., Xavier A. V., Bruschi M., Legall J., Hall D. O., and Cammack R.
, Biochem Biophys Res Commun, Oct 4, Volume 72, Number 3, p.782-9, (1976)
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Mossbauer And Electron-Paramagnetic-Res Studies Of Desulforedoxin From Desulfovibrio-Gigas,
Moura, I., Huynh B. H., Hausinger R. P., Legall J., Xavier A. V., and Munck E.
, Journal of Biological Chemistry, 1980, Volume 255, Number 6, p.2493-2498, (1980)
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Mössbauer and EPR evidence for nickel and 3Fe cluster in the hydrogenases of D. desulfuricans and D. gigas,
Huynh, B. H., Legall J., Dervartanian D. V., Peck Jr H. D., Krüger H. J., Moura I., Moura J. J. G., and Xavier A. V.
, Inorganica Chimica Acta, Volume 79, p.136, (1983)
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Mossbauer and EPR studies on nitrite reductase from Thiobacillus denitrificans,
Huynh, B. H., Lui M. C., Moura J. J., Moura I., Ljungdahl P. O., Munck E., Payne W. J., Peck, H. D. Jr., Dervartanian D. V., and Legall J.
, J Biol Chem, Aug 25, Volume 257, Number 16, p.9576-81, (1982)
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Mossbauer characterization of Paracoccus denitrificans cytochrome c peroxidase. Further evidence for redox and calcium binding-induced heme-heme interaction,
Prazeres, S., Moura J. J., Moura I., Gilmour R., Goodhew C. F., Pettigrew G. W., Ravi N., and Huynh B. H.
, J Biol Chem, Oct 13, Volume 270, Number 41, p.24264-9, (1995)
AbstractMossbauer and electron paramagnetic resonance (EPR) spectroscopies were used to characterize the diheme cytochrome c peroxidase from Paracoccus denitrificans (L.M.D. 52.44). The spectra of the oxidized enzyme show two distinct spectral components characteristic of low spin ferric hemes (S = 1/2), revealing different heme environments for the two heme groups. The Paracoccus peroxidase can be non-physiologically reduced by ascorbate. Mossbauer investigation of the ascorbate-reduced peroxidase shows that only one heme (the high potential heme) is reduced and that the reduced heme is diamagnetic (S = 0). The other heme (the low potential heme) remains oxidized, indicating that the enzyme is in a mixed valence, half-reduced state. The EPR spectrum of the half-reduced peroxidase, however, shows two low spin ferric species with gmax = 2.89 (species I) and gmax = 2.78 (species II). This EPR observation, together with the Mossbauer result, suggests that both species are arising from the low potential heme. More interestingly, the spectroscopic properties of these two species are distinct from that of the low potential heme in the oxidized enzyme, providing evidence for heme-heme interaction induced by the reduction of the high potential heme. Addition of calcium ions to the half-reduced enzyme converts species II to species I. Since calcium has been found to promote peroxidase activity, species I may represent the active form of the peroxidatic heme.
Mossbauer characterization of the iron-sulfur clusters in Desulfovibrio vulgaris hydrogenase,
Pereira, A. S., Tavares P., Moura I., Moura J. J., and Huynh B. H.
, J Am Chem Soc, Mar 28, Volume 123, Number 12, p.2771-82, (2001)
AbstractThe periplasmic hydrogenase of Desulfovibrio vulgaris (Hildenbourough) is an all Fe-containing hydrogenase. It contains two ferredoxin type [4Fe-4S] clusters, termed the F clusters, and a catalytic H cluster. Recent X-ray crystallographic studies on two Fe hydrogenases revealed that the H cluster is composed of two sub-clusters, a [4Fe-4S] cluster ([4Fe-4S](H)) and a binuclear Fe cluster ([2Fe](H)), bridged by a cysteine sulfur. The aerobically purified D. vulgaris hydrogenase is stable in air. It is inactive and requires reductive activation. Upon reduction, the enzyme becomes sensitive to O(2), indicating that the reductive activation process is irreversible. Previous EPR investigations showed that upon reoxidation (under argon) the H cluster exhibits a rhombic EPR signal that is not seen in the as-purified enzyme, suggesting a conformational change in association with the reductive activation. For the purpose of gaining more information on the electronic properties of this unique H cluster and to understand further the reductive activation process, variable-temperature and variable-field Mossbauer spectroscopy has been used to characterize the Fe-S clusters in D. vulgaris hydrogenase poised at different redox states generated during a reductive titration, and in the CO-reacted enzyme. The data were successfully decomposed into spectral components corresponding to the F and H clusters, and characteristic parameters describing the electronic and magnetic properties of the F and H clusters were obtained. Consistent with the X-ray crystallographic results, the spectra of the H cluster can be understood as originating from an exchange coupled [4Fe-4S]-[2Fe] system. In particular, detailed analysis of the data reveals that the reductive activation begins with reduction of the [4Fe-4S](H) cluster from the 2+ to the 1+ state, followed by transfer of the reducing equivalent from the [4Fe-4S](H) subcluster to the binuclear [2Fe](H) subcluster. The results also reveal that binding of exogenous CO to the H cluster affects significantly the exchange coupling between the [4Fe-4S](H) and the [2Fe](H) subclusters. Implication of such a CO binding effect is discussed.