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1.
J Proteomics ; 294: 105061, 2024 03 15.
Artículo en Inglés | MEDLINE | ID: mdl-38154550

RESUMEN

Paenibacillus sonchi SBR5T is a Gram-positive, endospore-forming facultative aerobic diazotrophic bacterium that can fix nitrogen via an alternative Fe-only nitrogenase (AnfHDGK). In several bacteria, this alternative system is expressed under molybdenum (Mo)-limiting conditions when the conventional Mo-dependent nitrogenase (NifHDK) production is impaired. The regulatory mechanisms, metabolic processes, and cellular functions of N2 fixation by alternative and/or conventional systems are poorly understood in the Paenibacillus genus. We conducted a comparative proteomic profiling study of P. sonchi SBR5T grown under N2-fixing conditions with and without Mo supply through an LC-MS/MS and label-free quantification analysis to address this gap. Protein abundances revealed overrepresented processes related to anaerobiosis growth adaption, Fe-S cluster biosynthesis, ammonia assimilation, electron transfer, and sporulation under N2-fixing conditions compared to non-fixing control. Under Mo limitation, the Fe-only nitrogenase components were overrepresented together with the Mo-transporter system, while the dinitrogenase component (NifDK) of Mo­nitrogenase was underrepresented. The dinitrogenase reductase component (NifH) and accessory proteins encoded by the nif operon had no significant differential expression, suggesting post-transcriptional regulation of nif gene products in this strain. Overall, this was the first comprehensive proteomic analysis of a diazotrophic strain from the Paenibacillaceae family, and it provided insights related to alternative N2-fixation by Fe-only nitrogenase. SIGNIFICANCE: In this work, we try to understand how the alternative nitrogen fixation system, presented by some diazotrophic bacteria, works. For this, we used the SBR5 lineage of P. sonchi, which presents the alternative system in which the nitrogenase cofactor is composed only of iron. In addition, we tried to unravel the proteome of this strain in different situations of nitrogen fixation, since, for Gram-positive bacteria, these systems are little known. The results achieved, through LC-MS/MS and label-free quantitative analysis, showed an overrepresentation of proteins related to different processes involved with growth under stressful conditions in situations of nitrogen deficiency, in addition to suggesting that some encoded proteins by the nif operon may be regulated at post-transcriptional levels. Our findings represent important steps toward the elucidation of nitrogen fixation systems in Gram-positive diazotrophic bacteria.


Asunto(s)
Fijación del Nitrógeno , Paenibacillus , Proteoma/metabolismo , Proteómica , Cromatografía Liquida , Espectrometría de Masas en Tándem , Nitrogenasa/metabolismo , Paenibacillus/genética , Paenibacillus/metabolismo , Molibdeno/metabolismo , Hierro/metabolismo , Nitrógeno/metabolismo
2.
J Comp Pathol ; 198: 80-88, 2022 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-36209706

RESUMEN

Molybdate (MoO4) and tetrathiomolybdate (MoS4) supplementation of rats via drinking water had opposite effects on the establishment of Nippostrongylus brasiliensis larvae but both induced hypercupraemia, temporarily inhibited activities of superoxide dismutase in liver and duodenum after infection and enlarged the femoral head. Effects of MoO4 and MoS4 on activities of caeruloplasmin oxidase (CpO) in plasma, erythrocyte superoxide dismutase (ESOD) and tissue copper (Cu) and molybdenum (Mo) were compared to test the hypothesis that species lacking a rumen can thiolate MoO4. Three groups of 18 immature Wistar rats were given Mo (70 mg/L as MoO4) or MoS4 (5 mg/L) via drinking water or remained untreated; all received a commercial, cubed diet and 12 from each group were infected with larvae of N. brasiliensis. Rats were killed 7-9 days later and liver, kidney, spleen, heart, muscle (quadriceps), brain and bone (femur) removed for Cu and Mo analysis. Plasma Cu was greatly increased by MoO4 and MoS4, without changing CpO activity, but the effect was more variable with MoO4 and accompanied by a smaller decrease in ESOD. Tissue Cu and Mo were increased by MoS4 in all tissues examined except brain and bone, correlating with plasma Cu and with each other; relationships were strongest in spleen, followed by kidney. MoO4 also increased soft tissue Cu and Mo but increases were generally smaller than those induced by MoS4 and correlations between the two elements and with plasma Cu generally weaker. Since hypercupraemia and correlated increases in liver and kidney Cu and Mo are characteristic of systemic thiomolybdate (TM) exposure, we conclude that MoO4 was partially thiolated to give a different TM profile from that produced by MoS4. The pathophysiological significance of systemic exposure to di- and tri-TM merits investigation in non-ruminants as agents of chelation therapy and in ruminants as agents of short-lived TM toxicity on Mo-rich pastures.


Asunto(s)
Agua Potable , Molibdeno , Animales , Ceruloplasmina/metabolismo , Cobre/metabolismo , Suplementos Dietéticos , Hígado/química , Molibdeno/análisis , Molibdeno/metabolismo , Molibdeno/farmacología , Nippostrongylus/metabolismo , Ratas , Ratas Wistar , Superóxido Dismutasa
3.
Int J Mol Sci ; 23(14)2022 Jul 19.
Artículo en Inglés | MEDLINE | ID: mdl-35887282

RESUMEN

Alzheimer's disease (AD) and other forms of dementia was ranked 3rd in both the Americas and Europe in 2019 in a World Health Organization (WHO) publication listing the leading causes of death and disability worldwide. Copper (Cu) imbalance has been reported in AD and increasing evidence suggests metal imbalance, including molybdenum (Mo), as a potential link with AD occurrence.We conducted an extensive literature review of the last 60 years of research on AD and its relationship with Cu, sulfur (S), and Mo at out of range levels.Weanalyzed the interactions among metallic elements' metabolisms;Cu and Mo are biological antagonists, Mo is a sulfite oxidase and xanthine oxidase co-factor, and their low activities impair S metabolism and reduce uric acid, respectively. We found significant evidence in the literature of a new potential mechanism linking Cu imbalance to Mo and S abnormalities in AD etiology: under certain circumstances, the accumulation of Cu not bound to ceruloplasmin might affect the transport of Mo outside the blood vessels, causing a mild Mo deficiency that might lowerthe activity of Mo and S enzymes essential for neuronal activity. The current review provides an updated discussion of the plausible mechanisms combining Cu, S, and Mo alterations in AD.


Asunto(s)
Enfermedad de Alzheimer , Molibdeno , Enfermedad de Alzheimer/etiología , Cobre/metabolismo , Dieta , Humanos , Molibdeno/metabolismo , Azufre
4.
J Food Sci ; 85(5): 1605-1612, 2020 May.
Artículo en Inglés | MEDLINE | ID: mdl-32249421

RESUMEN

Lettuce is one of the most popular vegetables, and the market niche of the baby leaf variety is expanding. The manner in which nitrogen (N) is supplied and the available concentration of the micronutrient molybdenum (Mo) affect N metabolism, with reflects on the nutritional quality of that vegetable. Here, two Mo concentrations (0.06 and 0.12 mg/L) and four proportions (%) of nitrate (NO3 - )/ammonium (NH4 + )(100/0, 75/25, 50/50, and 25/75) were supplied to hydroponic baby leaf lettuce floating type to evaluate their effects on plant growth and leaf mineral and NO3 - compositions. Shoot dry mass did not differ among the different treatments, although fresh mass was lower in treatments with larger proportions of NH4 + . Higher leaf concentrations of NO3 - were observed in plants treated with 100% N-NO3 - , but they were still below tolerable limits for human health. The enzyme nitrate reductase was not found to be sensitive to the nitrogen sources or to Mo concentrations. N proportions and Mo concentrations differently affected macro- (C, N, P, K, Ca, Mg, and S) and micronutrients (Cu, Fe, Mn, Mo, and Zn) leaf concentrations. Although treatment with 100% N-NO3 - favored higher mineral concentrations in lettuce leaves, the addition of 25% N-NH4 + allowed fresh mass production with the lowest NO3 - concentrations. As such, and considering the healthy reduction of NO3 - consumption by humans and the maintenance of plant productivity, the 75/25 NO3 - /NH4 + proportion is recommended for the hydroponic cultivation of baby leaf var. Mimosa lettuce. PRACTICAL APPLICATION: We demonstrate a direct link between the constitution of nutrient solution with nitrate accumulation by hydroponic lettuce and indicate the best source of N as well as the concentration of Mn to healthy reduction of NO3 - consumption by humans and the maintenance of plant productivity.


Asunto(s)
Lactuca/metabolismo , Molibdeno/metabolismo , Nitratos/análisis , Hojas de la Planta/química , Compuestos de Amonio/análisis , Compuestos de Amonio/metabolismo , Humanos , Hidroponía , Lactuca/química , Lactuca/crecimiento & desarrollo , Molibdeno/análisis , Nitratos/metabolismo , Nitrógeno/análisis , Nitrógeno/metabolismo , Valor Nutritivo , Hojas de la Planta/crecimiento & desarrollo , Hojas de la Planta/metabolismo , Verduras/química , Verduras/crecimiento & desarrollo , Verduras/metabolismo
5.
J Food Sci ; 84(10): 2840-2846, 2019 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-31517998

RESUMEN

Cu, Fe, Mn, Mo, Selenium (Se), and Zn bioavailability from selenate- and selenite-enriched lettuce plants was studied by in vitro gastrointestinal digestion followed by an assay with Caco-2 cells. The plants were cultivated in the absence and presence of two concentrations (25 and 40 µmol/L of Se). After 28 days of cultivation, the plants were harvested, dried, and evaluated regarding the total concentration, bioaccessibility, and bioavailability of the analytes. The results showed that biofortification with selenate leads to higher Se absorption by the plant than biofortification with selenite. For the other nutrients, Mo showed high accumulation in the plants of selenate assays, and the presence of any Se species led to a reduction of the plant uptake of Cu and Fe. The accumulation of Zn and Mn was not strongly influenced by the presence of any Se species. The bioaccessibility values were approximately 71%, 10%, 52%, 84%, 71%, and 86% for Cu, Fe, Mn, Mo, Se, and Zn, respectively, and the contribution of the biofortified lettuce to the ingestion of these minerals is very small (except for Se and Mo). Due to the low concentrations of elements from digested plants, it was not possible to estimate the bioavailability for some elements, and for Mo and Zn, the values are below 6.9% and 3.4% of the total concentration, respectively. For Se, the bioavailability was greater for selenite-enriched than selenate-enriched plants (22% and 6.0%, respectively), because selenite is biotransformed by the plant to organic forms that are better assimilated by the cells.


Asunto(s)
Cobre/análisis , Hierro/análisis , Lactuca/química , Manganeso/análisis , Molibdeno/análisis , Selenio/análisis , Zinc/análisis , Biofortificación , Disponibilidad Biológica , Células CACO-2 , Cobre/metabolismo , Humanos , Hierro/metabolismo , Lactuca/metabolismo , Manganeso/metabolismo , Molibdeno/metabolismo , Ácido Selénico/análisis , Ácido Selénico/metabolismo , Ácido Selenioso/análisis , Ácido Selenioso/metabolismo , Selenio/metabolismo , Zinc/metabolismo
6.
World J Microbiol Biotechnol ; 32(12): 205, 2016 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-27804104

RESUMEN

Postbloom fruit drop (PFD) caused by Colletotrichum acutatum affects flowers and causes early fruit drop in all commercial varieties of citrus. Biological control with the isolate ACB-69 of Bacillus subtilis has been considered as a potential method for controlling this disease. This study aimed to develop and optimize a B. subtilis based-formulation with a potential for large-scale applications and evaluate its effect on C. acutatum in vitro and in vivo. Bacillus subtilis based-formulations were developed using different carrier materials, and their ability to control PFD was evaluated. The results of the assays led to the selection of the B. subtilis based-formulation with talc + urea (0.02 %) and talc + ammonium molybdate (1 mM), which inhibited mycelial growth and germination of C. acutatum. Studies with detached citrus flowers showed that the formulations were effective in controlling the pathogen. In field conditions, talc + urea (0.02 %) provided 73 % asymptomatic citrus flowers and 56 % of the average number of effective fruit (ANEF), equating with fungicide treatment. On the contrary, non-treated trees had 8.8 % of asymptomatic citrus flowers and 0.83 % ANEF. The results suggest that B. subtilis based-formulations with talc as the carrier supplemented with a nitrogen source had a high potential for PFD control.


Asunto(s)
Bacillus subtilis/fisiología , Citrus/crecimiento & desarrollo , Colletotrichum/efectos de los fármacos , Fungicidas Industriales/farmacología , Enfermedades de las Plantas/prevención & control , Citrus/microbiología , Colletotrichum/patogenicidad , Flores/crecimiento & desarrollo , Flores/microbiología , Fungicidas Industriales/metabolismo , Pruebas de Sensibilidad Microbiana , Viabilidad Microbiana/efectos de los fármacos , Molibdeno/metabolismo , Molibdeno/farmacología , Talco/metabolismo , Talco/farmacología , Urea/metabolismo , Urea/farmacología
7.
Arch Biochem Biophys ; 539(1): 20-30, 2013 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-24035743

RESUMEN

The periplasmic-binding proteins in ATP-binding cassette systems (ABC Transporters) are responsible for the capture and delivery of ligands to their specific transporters, triggering a series of ATP-driven conformational changes that leads to the transport of the ligand. Structurally consisting of two lobes, the proteins change conformation after interaction with the ligand. The structure of the molybdate-binding protein (ModA) from Xanthomonas citri, bound to molybdate, was previously solved by our group and an interdomain interaction, mediated by a salt bridge between K127 and D59, apparently supports the binding properties and keeps the domains closed. To determinate the importance of this interaction, we built two ModA mutants, K127S and D59A, and analysed their functional and structural properties. Based on a set of spectroscopic experiments, crystallisation trials, structure determination and molecular dynamics (MD) simulations, we showed that the salt bridge is essential to maintain the structure and binding properties. Additionally, the MD simulations revealed that this mutant adopted a more compact structure that packed down the ligand-binding pocket. From the closed bound to open structure, the positioning of the helices forming the dipole and the salt bridge are essential to induce an intermediate state.


Asunto(s)
Proteínas Bacterianas/química , Proteínas Bacterianas/metabolismo , Xanthomonas , Secuencia de Aminoácidos , Proteínas Bacterianas/genética , Sitios de Unión , Permeabilidad de la Membrana Celular , Disulfuros/química , Interacciones Hidrofóbicas e Hidrofílicas , Ligandos , Simulación de Dinámica Molecular , Datos de Secuencia Molecular , Molibdeno/metabolismo , Mutación , Unión Proteica , Estabilidad Proteica , Estructura Secundaria de Proteína , Estructura Terciaria de Proteína , Transporte de Proteínas , Temperatura
8.
Biometals ; 24(5): 891-902, 2011 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-21432624

RESUMEN

The purification and biochemical characterization of the respiratory membrane-bound nitrate reductase from Sinorhizobium meliloti 2011 (Sm NR) is reported together with the optimal conditions for cell growth and enzyme production. The best biomass yield was obtained under aerobic conditions in a fed-batch system using Luria-Bertani medium with glucose as carbon source. The highest level of Sm NR production was achieved using microaerobic conditions with the medium supplemented with both nitrate and nitrite. Sm NR is a mononuclear Mo-protein belonging to the DMSO reductase family isolated as a heterodimeric enzyme containing two subunits of 118 and 45 kDa. Protein characterization by mass spectrometry showed homology with respiratory nitrate reductases. UV-Vis spectra of as-isolated and dithionite reduced Sm NR showed characteristic absorption bands of iron-sulfur and heme centers. Kinetic studies indicate that Sm NR follows a Michaelis-Menten mechanism (K (m) = 97 ± 11 µM, V = 9.4 ± 0.5 µM min(-1), and k (cat) = 12.1 ± 0.6 s(-1)) and is inhibited by azide, chlorate, and cyanide with mixed inhibition patterns. Physiological and kinetic studies indicate that molybdenum is essential for NR activity and that replacement of this metal for tungsten inhibits the enzyme. Although no narGHI gene cluster has been annotated in the genome of rhizobia, the biochemical characterization indicates that Sm NR is a Mo-containing NR enzyme with molecular organization similar to NarGHI.


Asunto(s)
Membrana Celular/metabolismo , Nitrato Reductasas/metabolismo , Nitratos/metabolismo , Sinorhizobium meliloti/metabolismo , Azidas/farmacología , Cloratos/farmacología , Cianuros/farmacología , Cinética , Molibdeno/metabolismo , Nitrato Reductasas/antagonistas & inhibidores , Oxidación-Reducción , Sinorhizobium meliloti/enzimología , Relación Estructura-Actividad
9.
Biometals ; 24(4): 687-707, 2011 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-21301930

RESUMEN

Sulfur is an essential element for microorganisms and it can be obtained from varied compounds, sulfate being the preferred source. The first step for sulfate assimilation, sulfate uptake, has been studied in several bacterial species. This article reviews the properties of different bacterial (and archaeal) transporters for sulfate, molybdate, and related oxyanions. Sulfate uptake is carried out by sulfate permeases that belong to the SulT (CysPTWA), SulP, CysP/(PiT), and CysZ families. The oxyanions molybdate, tungstate, selenate and chromate are structurally related to sulfate. Molybdate is transported mainly by the high-affinity ModABC system and tungstate by the TupABC and WtpABC systems. CysPTWA, ModABC, TupABC, and WtpABC are homologous ATP-binding cassette (ABC)-type transporters with similar organization and properties. Uptake of selenate and chromate oxyanions occurs mainly through sulfate permeases.


Asunto(s)
Molibdeno/metabolismo , Sulfatos/metabolismo , Proteínas de Transporte de Anión/metabolismo , Aniones/metabolismo , Bacterias/metabolismo , Transporte Biológico , Cromatos/metabolismo , Ácido Selénico , Compuestos de Selenio/metabolismo , Compuestos de Tungsteno/metabolismo
10.
Lett Appl Microbiol ; 46(3): 344-9, 2008 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-18266641

RESUMEN

AIMS: The aim of this study was to develop an approach based on a reverse transcriptase (RT)-PCR/denaturing gradient gel electrophoresis (DGGE) for the detection of the functional genes nifH and anfH in Paenibacillus durus. METHODS AND RESULTS: Two sets of primers were employed to study the expression of the nitrogen fixation genes in a pure-culture system of P. durus grown in media with increasing concentrations of ammonium (NH(4)(+)), tungsten (W) or molybdenum (Mo). The results obtained indicate that the expression of nitrogenase genes from P. durus can take place in the presence of relatively high levels of fixed nitrogen. It was also observed that the addition of 20 micromol l(-1) molybdenum and 2 mmol l(-1) tungstate did not interfere in the mRNA levels of nifH and anfH genes. CONCLUSIONS: Our results demonstrate the presence and transcription of nifH and anfH in P. durus under a variety of growth conditions. A specific set of primers was designed for the detection of the alternative system for nitrogen fixation in P. durus. SIGNIFICANCE AND IMPACT OF THE STUDY: The RT-PCR/DGGE system enables the rapid gathering of incremental data about the regulation of conventional and alternative nitrogenase genes in P. durus strains.


Asunto(s)
Proteínas Bacterianas/metabolismo , Electroforesis en Gel de Poliacrilamida/métodos , Regulación Bacteriana de la Expresión Génica , Bacterias Grampositivas Formadoras de Endosporas/crecimiento & desarrollo , Fijación del Nitrógeno , Oxidorreductasas/metabolismo , Compuestos de Amonio Cuaternario/metabolismo , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa/métodos , Proteínas Bacterianas/genética , Medios de Cultivo , Bacterias Grampositivas Formadoras de Endosporas/clasificación , Bacterias Grampositivas Formadoras de Endosporas/genética , Bacterias Grampositivas Formadoras de Endosporas/metabolismo , Molibdeno/metabolismo , Oxidorreductasas/genética , Tungsteno/metabolismo
11.
Biochim Biophys Acta ; 1784(2): 393-9, 2008 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-18088604

RESUMEN

In Xanthomonas axonopodis pv. citri (Xac or X. citri), the modA gene codes for a periplasmic protein (ModA) that is capable of binding molybdate and tungstate as part of the ABC-type transporter required for the uptake of micronutrients. In this study, we report the crystallographic structure of the Xac ModA protein with bound molybdate. The Xac ModA structure is similar to orthologs with known three-dimensional structures and consists of two nearly symmetrical domains separated by a hinge region where the oxyanion-binding site lies. Phylogenetic analysis of different ModA orthologs based on sequence alignments revealed three groups of molybdate-binding proteins: bacterial phytopathogens, enterobacteria and soil bacteria. Even though the ModA orthologs are segregated into different groups, the ligand-binding hydrogen bonds are mostly conserved, except for Archaeglobus fulgidus ModA. A detailed discussion of hydrophobic interactions in the active site is presented and two new residues, Ala38 and Ser151, are shown to be part of the ligand-binding pocket.


Asunto(s)
Molibdeno/química , Molibdeno/metabolismo , Proteínas de Unión Periplasmáticas/química , Proteínas de Unión Periplasmáticas/metabolismo , Xanthomonas axonopodis/química , Xanthomonas axonopodis/metabolismo , Secuencia de Aminoácidos , Sitios de Unión , Secuencia Conservada , Cristalografía por Rayos X , Ligandos , Datos de Secuencia Molecular , Proteínas de Unión Periplasmáticas/genética , Filogenia , Enfermedades de las Plantas/microbiología , Unión Proteica , Estructura Terciaria de Proteína , Alineación de Secuencia , Homología Estructural de Proteína , Xanthomonas axonopodis/genética , Xanthomonas axonopodis/patogenicidad
12.
Protein Expr Purif ; 50(2): 215-22, 2006 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-16879982

RESUMEN

The modABC operon of phytopathogen Xanthomonas axonopodis pv. citri (X. citri) encodes a putative ABC transporter involved in the uptake of the molybdate and tungstate anions. Sequence analyses showed high similarity values of ModA orthologs found in X. campestris pv. campestris (X. campestris) and Escherichia coli. The X. citri modA gene was cloned in pET28a and the recombinant protein, expressed in the E. coli BL21 (DE3) strain, purified by immobilized metal affinity chromatography. The purified protein remained soluble and specifically bound molybdate and tungstate with K(d) 0.29+/-0.12 microM and 0.58+/-0.14 microM, respectively. Additionally binding of molybdate drastically enhanced the thermal stability of the recombinant ModA as compared to the apoprotein. This is the first characterization of a ModA ortholog expressed by a phytopathogen and represents an important tool for functional, biochemical and structural analyses of molybdate transport in Xanthomonas species.


Asunto(s)
Transportadoras de Casetes de Unión a ATP/aislamiento & purificación , Proteínas Bacterianas/aislamiento & purificación , Molibdeno/metabolismo , Proteínas de Unión Periplasmáticas/aislamiento & purificación , Xanthomonas/genética , Transportadoras de Casetes de Unión a ATP/genética , Transportadoras de Casetes de Unión a ATP/metabolismo , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Clonación Molecular , Operón , Proteínas de Unión Periplasmáticas/genética , Proteínas de Unión Periplasmáticas/metabolismo , Pliegue de Proteína , Proteínas Recombinantes/aislamiento & purificación , Proteínas Recombinantes/metabolismo , Termodinámica , Compuestos de Tungsteno/metabolismo , Xanthomonas/metabolismo
13.
Artículo en Inglés | MEDLINE | ID: mdl-16511325

RESUMEN

Xanthomonas axonopodis pv. citri ModA protein is the ABC periplasmic binding component responsible for the capture of molybdate. The protein was crystallized with sodium molybdate using the hanging-drop vapour-diffusion method in the presence of PEG or sulfate. X-ray diffraction data were collected to a maximum resolution of 1.7 A using synchrotron radiation. The crystal belongs to the orthorhombic space group C222(1), with unit-cell parameters a = 68.15, b = 172.14, c = 112.04 A. The crystal structure was solved by molecular-replacement methods and structure refinement is in progress.


Asunto(s)
Transportadoras de Casetes de Unión a ATP/química , Molibdeno/metabolismo , Proteínas de Unión Periplasmáticas/química , Xanthomonas/química , Cristalización/métodos , Cristalografía por Rayos X , Escherichia coli/metabolismo , Proteínas Recombinantes/química
14.
Curr Opin Chem Biol ; 10(2): 109-14, 2006 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-16480912

RESUMEN

Mononuclear 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.


Asunto(s)
Molibdeno/metabolismo , Tungsteno/metabolismo , Xantina Oxidasa/metabolismo , Sitios de Unión , Transporte de Electrón , Modelos Moleculares , Conformación Proteica , Xantina Oxidasa/antagonistas & inhibidores , Xantina Oxidasa/química
15.
FEMS Microbiol Lett ; 224(2): 255-9, 2003 Jul 29.
Artículo en Inglés | MEDLINE | ID: mdl-12892890

RESUMEN

Herbaspirillum seropedicae strains mutated in the nifX or orf1 genes showed 90% or 50% reduction in nitrogenase activity under low levels of iron or molybdenum respectively. Mutations in nifX or orf1 genes did not affect nif gene expression since a nifH::lacZ fusion was fully active in both mutants. nifX and the contiguous gene orf1 are essential for maximum nitrogen fixation under iron limitation and are probably involved in synthesis of nitrogenase iron or iron-molybdenum clusters.


Asunto(s)
Proteínas Bacterianas/metabolismo , Betaproteobacteria/enzimología , Genes Bacterianos , Hierro/metabolismo , Fijación del Nitrógeno/fisiología , Nitrogenasa/metabolismo , Proteínas Bacterianas/genética , Betaproteobacteria/genética , Betaproteobacteria/crecimiento & desarrollo , Operón Lac , Molibdeno/metabolismo , Fijación del Nitrógeno/genética , Plásmidos
16.
Acta physiol. pharmacol. ther. latinoam ; 49(3): 170-6, 1999. tab, graf
Artículo en Español | LILACS | ID: lil-246056

RESUMEN

Con el objetivo de diferenciar los efectos producidos por la deficiencia primaria cobre y los provocados por el excesso de molibdeno se evaluó un modelo experimental en ratas. Sesenta ratas de destete (30 machos y 30 hembras) recibieron una dieta compuesta por 70 por ciento de leche entera en polvo (1 ppm Cu) y 30 por ciento de harina de maíz (0.8 - 1.5 ppm Cu). Los animales se dividieron en tres grupos conforme a la suplementación mineral recibida: deficiencia primaria de cobre (40 ppm Fe), molibdenosis (40 ppm Fe + 40 ppm Cu + 500 ppm Mo) y controles (40 ppm Fe + 40 ppm Cu). Se pesaron cada 14 días. Al cabo de 70 días de tratamiento se obtuvieron muestras de sangre para determinación de hematocrito y actividad sérica de ceruloplasmina y se sacrificaron para medir concentraciones hepáticas de Cu y Mo. El grupo deficiente en Cu tuvo valores significativamente inferiores en la actividad de ceruloplasmina. Las concentraciones hepáticas de Cu y Mo fueron superiores significativamente en los animales con molibdenosis. Se concluye que con niveles de Cu por encima de los requerimientos mínimos, la alimentación con alto contenido de Mo, no afecta la actividad sérica de ceruloplasmina. Esto sumado a la concentración hepática de Mo lograda, permitirá identificar efectos "per se" de la molibdenosis.


Asunto(s)
Animales , Ratas , Masculino , Femenino , Ceruloplasmina/metabolismo , Cobre/deficiencia , Molibdeno/administración & dosificación , Cobre/análisis , Hematócrito , Molibdeno/análisis , Molibdeno/metabolismo , Ratas Wistar , Aumento de Peso
17.
Acta physiol. pharmacol. ther. latinoam ; 49(3): 170-6, 1999. tab, gra
Artículo en Español | BINACIS | ID: bin-14757

RESUMEN

Con el objetivo de diferenciar los efectos producidos por la deficiencia primaria cobre y los provocados por el excesso de molibdeno se evaluó un modelo experimental en ratas. Sesenta ratas de destete (30 machos y 30 hembras) recibieron una dieta compuesta por 70 por ciento de leche entera en polvo (1 ppm Cu) y 30 por ciento de harina de maíz (0.8 - 1.5 ppm Cu). Los animales se dividieron en tres grupos conforme a la suplementación mineral recibida: deficiencia primaria de cobre (40 ppm Fe), molibdenosis (40 ppm Fe + 40 ppm Cu + 500 ppm Mo) y controles (40 ppm Fe + 40 ppm Cu). Se pesaron cada 14 días. Al cabo de 70 días de tratamiento se obtuvieron muestras de sangre para determinación de hematocrito y actividad sérica de ceruloplasmina y se sacrificaron para medir concentraciones hepáticas de Cu y Mo. El grupo deficiente en Cu tuvo valores significativamente inferiores en la actividad de ceruloplasmina. Las concentraciones hepáticas de Cu y Mo fueron superiores significativamente en los animales con molibdenosis. Se concluye que con niveles de Cu por encima de los requerimientos mínimos, la alimentación con alto contenido de Mo, no afecta la actividad sérica de ceruloplasmina. Esto sumado a la concentración hepática de Mo lograda, permitirá identificar efectos "per se" de la molibdenosis. (AU)


Asunto(s)
Animales , Ratas , Masculino , Femenino , RESEARCH SUPPORT, NON-U.S. GOVT , Molibdeno/administración & dosificación , Cobre/deficiencia , Ceruloplasmina/metabolismo , Cobre/análisis , Molibdeno/análisis , Molibdeno/metabolismo , Hematócrito , Ratas Wistar , Aumento de Peso
18.
J Pediatr ; 123(4): 595-8, 1993 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-8410516

RESUMEN

We describe a new case of molybdenum cofactor deficiency, an underrecognized inborn error of metabolism that results in neonatal seizures and neurologic abnormalities. Characteristic biochemical defects in affected individuals include hypouricemia, elevated urine sulfate (detectable by dipstick), and elevated S-sulfocysteine (detectable by anion exchange chromatography). This disorder should be considered in the differential diagnosis of neonatal seizures.


Asunto(s)
Coenzimas/deficiencia , Errores Innatos del Metabolismo/diagnóstico , Metaloproteínas/metabolismo , Molibdeno/metabolismo , Pteridinas/metabolismo , Convulsiones/etiología , Femenino , Genes Recesivos , Humanos , Recién Nacido , Errores Innatos del Metabolismo/genética , Cofactores de Molibdeno
19.
J Gen Microbiol ; 139(8): 1869-75, 1993 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-8409926

RESUMEN

Molybdenum uptake was examined in Escherichia coli K12 using the radionuclide 99Mo. The molybdenum uptake system was characterized in an unusual chlD strain, which appeared to be normal in uptake of the MoO4(2-) ion but altered in subsequent molybdenum processing. As a consequence, molybdenum could be chased from cells in the chlD strain, while it was irreversibly assimilated in the wild-type strain. Molybdenum uptake showed a biphasic kinetic curve, with a very rapid binding followed by a slow uptake phase. The uptake appeared to involve an active transport system. Molybdenum, probably in the form of molybdate, accumulated by a factor of about 30 in the cells. An energy source was necessary and uptake was inhibited by arsenate, but not by CCCP (carbonyl cyanide m-chlorophenylhydrazone). The uptake system saturated with a Km of 2.5-2.7 x 10(-8) M. Uptake seemed to depend on a periplasmic binding protein, since cold shock treatment and arsenate abolished uptake. A molybdate binding protein activity was detected in the periplasmic fluid with a KD of 9 nM. Sulphate inhibited uptake and the uptake activity was pH dependent, with an apparent pK of 6.7. These results imply that molybdate transport belongs to the family of energy-dependent periplasmic binding protein systems. An explanation for the peculiar behaviour of the chlD strain used in this work is proposed.


Asunto(s)
Escherichia coli/metabolismo , Molibdeno/metabolismo , Arseniatos/farmacología , Transporte Biológico Activo , Carbonil Cianuro m-Clorofenil Hidrazona/farmacología , Frío , Medios de Cultivo , Concentración de Iones de Hidrógeno , Cinética
20.
La Plata; Federación Bioquímica de la Provincia de Buenos Aires; 1985. 119 p. ilus, Tab. (67018).
Monografía en Español | BINACIS | ID: bin-67018

RESUMEN

Origen y especificidad de iones metálicos en sistemas biológicos.- Bio-Inorgánica: Metodología y herramientas de trabajo, Captación y transformacián de elementos-traza por parte de los seres vivos.- Aspectos fundamentales de la Química Bio-inorgánica en elementos individuales: Hierro, Oxígeno, Nitrógeno, Cobre, Cinc, Molibdeno, Cobalto, Metales de transición, Alcalinos, Alcalino-térreos y No Metálicos, Mineralizació biológica.- Relaciones con otras ramas de la Ciencia y Técnica: Contaminación del medio ambiente, Toxicología, Medicina, Farmacología Inorgánica, Agricultura, Ganadería, Metalurgia y Procesos Industriales diversos


Asunto(s)
Humanos , Química Bioinorgánica/educación , Análisis Espectral/métodos , Hierro/metabolismo , Hierro/química , Oxígeno/metabolismo , Oxígeno/química , Nitrógeno/metabolismo , Nitrógeno/química , Cobre/metabolismo , Cobre/química , Zinc/metabolismo , Zinc/química , Molibdeno/metabolismo , Molibdeno/química , Cobalto/metabolismo , Cobalto/química , /metabolismo , /química , Metales Alcalinotérreos/metabolismo , Metales Alcalinotérreos/química , Contaminantes Ambientales/efectos adversos , Contaminantes Ambientales/toxicidad
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