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1.
J Dev Orig Health Dis ; 12(2): 203-219, 2021 04.
Artigo em Inglês | MEDLINE | ID: mdl-33349289

RESUMO

Cardiovascular diseases (CVD) are important consequences of adverse perinatal conditions such as fetal hypoxia and maternal malnutrition. Cardiac magnetic resonance imaging (CMR) can produce a wealth of physiological information related to the development of the heart. This review outlines the current state of CMR technologies and describes the physiological biomarkers that can be measured. These phenotypes include impaired ventricular and atrial function, maladaptive ventricular remodeling, and the proliferation of myocardial steatosis and fibrosis. The discussion outlines the applications of CMR to understanding the developmental pathways leading to impaired cardiac function. The use of CMR, both in animal models of developmental programming and in human studies, is described. Specific examples are given in a baboon model of intrauterine growth restriction (IUGR). CMR offers great potential as a tool for understanding the sequence of dysfunctional adaptations of developmental origin that can affect the human cardiovascular system.


Assuntos
Envelhecimento , Retardo do Crescimento Fetal/fisiopatologia , Coração/embriologia , Coração/fisiopatologia , Imageamento por Ressonância Magnética/métodos , Animais , Feminino , Humanos , Gravidez
2.
Biochim Biophys Acta ; 1810(5): 526-31, 2011 May.
Artigo em Inglês | MEDLINE | ID: mdl-21371529

RESUMO

BACKGROUND: In vitro studies on hyperbaric oxygen (HBO) therapy suggest that HBO may cause DNA damage, but this has not been evaluated using endothelial cells. METHODS: Human umbilical cord endothelial cells (HUVECs) were exposed either to H(2)O(2) or to HBO for 90 min, with or without subsequent H(2)O(2) exposure. Measurements included the comet assay for DNA damage, and reduced and oxidised glutathione levels. RESULTS: HUVECs showed sensitivity to H(2)O(2) (EC(50) of 0.2mM for DNA migration). A single 90 min HBO treatment at 2.2 ATA caused a statistically significant (ANOVA, P<0.05) increase of DNA migration in HUVECs to 6.8 ± 0.3% (mean ± SEM, n=8), which returned to normal levels (4.9 ± 0.1%, n=6) after 24h. Further exposure to 0.2mM H(2)O(2) after HBO treatment significantly increased the DNA migration in HBO-treated cells immediately post-treatment; but 24h later the cells showed 22% less DNA damage and higher glutathione than controls. CONCLUSION: A single HBO exposure causes limited DNA damage to HUVECs, which repairs quickly. HBO treatment protects against H(2)O(2)-induced DNA damage and involves cellular glutathione. SIGNIFICANCE: Endothelial cells are unlikely to be compromised during HBO therapy.


Assuntos
Dano ao DNA , Células Endoteliais/efeitos dos fármacos , Peróxido de Hidrogênio/farmacologia , Oxigênio/farmacologia , Células Cultivadas , Ensaio Cometa , DNA/genética , DNA/metabolismo , Relação Dose-Resposta a Droga , Células Endoteliais/citologia , Células Endoteliais/metabolismo , Glutationa/metabolismo , Dissulfeto de Glutationa/metabolismo , Humanos , Oxidantes/farmacologia , Fatores de Tempo
3.
J Fish Biol ; 77(4): 947-62, 2010 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-20840622

RESUMO

Bonefish Albula vulpes (n = 7) exercised to exhaustion and air exposed for 1 min as part of a catch-and-release angling event were found to excrete both ammonia and urea, but cortisol and lactate were below detectable levels. Urea made up a greater proportion of total nitrogen excretion from these fish at all time points following an angling event. When captive juvenile lemon sharks Negaprion brevirostris (n = 12) were exposed to a 30 s pulse of these chemicals [ammonia (500 mM), cortisol (20 µg l(-1) ), lactate (6 mM) or urea (3 mM)], they showed a significant reduction in the frequency of resting behaviours when exposed to ammonia and urea than when exposed to control water. It appears that products excreted by A. vulpes, particularly ammonia and urea, may provide an olfactory cue for the post-release predation of A. vulpes by N. brevirostris during catch-and-release angling events.


Assuntos
Sinais (Psicologia) , Peixes/fisiologia , Comportamento Predatório , Tubarões/fisiologia , Amônia/química , Animais , Estresse Fisiológico , Ureia/química
4.
Biochim Biophys Acta ; 1787(7): 828-34, 2009 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-19298791

RESUMO

Hyperbaric oxygen therapy (HBO) is suggested to promote angiogenesis during wound healing, but the mechanisms involved are not understood. This study used a novel isolated blood vessel preparation to explore the effects of air, normobaric oxygen or hyperbaric oxygen (2.2 ATA for 90 min) on the angiogenesis factor, vascular endothelial growth factor (VEGF), nitrite and nitrate (NO(x)), lactate dehydrogenase (LDH) and lactate release from the tissue in normal Krebs Ringer, and the Ringer supplemented with either l-arginine, or 15 mM lactate to mimic a wound environment, or both (l-arginine+lactate). The in vitro blood vessel preparation remained viable during all experiments. There were no effects of HBO treatment on any of the parameters measured in normal Krebs Ringer, but some treatment-dependent effects were observed in supplemented Krebs Ringer. In the lactate supplemented Krebs Ringer, medium LDH levels increased in response to either normobaric oxygen (NBO) or HBO, compared to air alone. There were also small, but statistically significant increases in total glutathione due to HBO treatment, compared to NBO or air in the lactate supplemented medium, and in the combined supplement. There were no effects of HBO on NO(x), changes in external medium lactate levels, or tissue VEGF in any of the Krebs Ringers tested. However, post treatment increases in VEGF were observed in the lactate supplemented medium, and for lactate release into the medium for the combined supplement. We conclude that HBO does not cause NO or VEGF production from the blood vessel in normal Krebs Ringer, but the data from supplemented medium show that the response of the tissue is subtly affected by the chemical environment around the blood vessel, and the tissue is more responsive to HBO when wound conditions are mimicked.


Assuntos
Arginina/metabolismo , Oxigenoterapia Hiperbárica , L-Lactato Desidrogenase/metabolismo , Óxido Nítrico/metabolismo , Fator A de Crescimento do Endotélio Vascular/metabolismo , Animais , Aorta/metabolismo , Glutationa/análise , Masculino , Nitratos/análise , Nitritos/análise , Técnicas de Cultura de Órgãos , Oxigênio/metabolismo , Distribuição Aleatória , Ratos , Ratos Sprague-Dawley , Fatores de Tempo , Fator A de Crescimento do Endotélio Vascular/análise
5.
Undersea Hyperb Med ; 32(5): 327-40, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-16457082

RESUMO

Repeated hyperbaric oxygen (HBO2) treatments at 2.2 ATA for 90 minutes each are used to treat chronically ill patients with problem wounds, but there are concerns about the cytotoxicity of oxygen to blood cells and platelet function during prolonged HBO2 therapy. We recruited 31 consenting patients scheduled for multiple HBO2 treatments to evaluate oxidative metabolism in platelets, platelet aggregation, and hematology (mean age +/- standard error, 61 +/- 2.6 years, 20 males, 11 females). Venous blood was collected before and after the 1st and 20th HBO2 treatments. No effect of HBO2 was observed on red cell counts, hematocrit, hemoglobin, mean red cell volume (MCV), platelet counts, basal levels of lactate production by platelets, ferric reducing ability of plasma (FRAP), or plasma protein. The capacity for oxidative metabolism (lactate ratio) in platelets was not affected by HBO2, except in smokers where it increased by the 20th HBO2 treatment. Mean lymphocyte count was increased by 38% after the 20th treatment. There was also a 23% increase in platelet protein content, and a 24% increase in arachidonic acid-dependent platelet activation. Collagen-dependent platelet aggregation was unaffected. Blood glucose showed HBO2-dependent variability, but remained in the normal range. Plasma lactate levels decreased significantly from 3.2 to 2.5 mmol/l by the end of the study. Overall, we found no evidence that 20 HBO2 sessions caused adverse effects on platelet aggregation or oxidative metabolism in platelets, red or white cell counts, or total antioxidant status of the plasma.


Assuntos
Plaquetas/metabolismo , Oxigenoterapia Hiperbárica/efeitos adversos , Ácido Láctico/sangue , Agregação Plaquetária/fisiologia , Cicatrização/fisiologia , Acetaminofen/farmacologia , Idoso , Idoso de 80 Anos ou mais , Analgésicos não Narcóticos , Análise de Variância , Glicemia/análise , Plaquetas/efeitos dos fármacos , Contagem de Eritrócitos , Índices de Eritrócitos , Feminino , Hematócrito , Humanos , Oxigenoterapia Hiperbárica/métodos , Ácido Láctico/metabolismo , Masculino , Pessoa de Meia-Idade , Estresse Oxidativo , Fosforilação , Agregação Plaquetária/efeitos dos fármacos , Estatísticas não Paramétricas
6.
Biochem J ; 331 ( Pt 2): 459-64, 1998 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-9531485

RESUMO

Cytochrome bo forms complexes with chloride, bromide and iodide in which haem o remains high-spin and in which the '630 nm' charge-transfer band is red-shifted by 7-8 nm. The chloride and bromide complexes each have a characteristic set of integer-spin EPR signals arising from spin coupling between haem o and CuB. The rate and extent of chloride binding decreases as the pH increases from 5.5 to 8.5. At pH 5.5 the dissociation constant for chloride is 2 mM and the first-order rate constant for dissociation is 2 x 10(-4) s-1. The order of rate of binding, and of affinity, at pH 5.5 is chloride (1) > bromide (0.3) >iodide (0.1). It is suggested that the halides bind in the binuclear site but, unlike fluoride, they are not direct ligands of the iron of haem o. In addition, both the stability of the halide complexes and the rate of halide binding seem to be increased by the co-binding of a proton.


Assuntos
Brometos/metabolismo , Cloretos/metabolismo , Grupo dos Citocromos b , Citocromos/metabolismo , Proteínas de Escherichia coli , Escherichia coli/enzimologia , Iodetos/metabolismo , Sítios de Ligação , Brometos/farmacologia , Cloretos/farmacologia , Citocromos/química , Espectroscopia de Ressonância de Spin Eletrônica , Heme/química , Concentração de Íons de Hidrogênio , Iodetos/farmacologia , Cinética , Cianeto de Potássio/metabolismo , Espectrofotometria Infravermelho
7.
FEBS Lett ; 412(1): 43-7, 1997 Jul 21.
Artigo em Inglês | MEDLINE | ID: mdl-9257686

RESUMO

The spectroscopic and ligand-binding properties of a copper-deficient cytochrome bo3, a member of the haem-copper superfamily of terminal oxidases, are reported and contrasted with those of the native enzyme. The enzyme lacks the copper atom (CuB) which is normally an integral part of the catalytic site. The consequences of loss of the CuB are the loss of antiferromagnetic coupling to the high-spin haem and an inability to form any of the integer-spin derivatives of the enzyme. Low-spin compounds of the normally high-spin haem are still formed with appropriate ligands, although these are modified.


Assuntos
Cobre/análise , Grupo dos Citocromos b , Citocromos/química , Espectroscopia de Ressonância de Spin Eletrônica , Proteínas de Escherichia coli , Escherichia coli/química , Azidas/metabolismo , Sítios de Ligação , Catálise , Cianetos/metabolismo , Citocromos/metabolismo , Fluoretos/farmacologia , Formiatos/farmacologia , Oxirredução , Relação Estrutura-Atividade , Sulfetos/farmacologia
8.
Biochem J ; 324 ( Pt 3): 743-52, 1997 Jun 15.
Artigo em Inglês | MEDLINE | ID: mdl-9210397

RESUMO

The binding of four anionic ligands, cyanide, fluoride, azide and formate, to cytochrome bo purified from Escherichia coli cells grown with a copper supplement (+Cu cyt.bo) is described. Membrane-bound cytochrome bo that lacks the copper component, CuB, of its active site can be prepared from cells grown under conditions where the availability of copper is limited by the presence of a CuI chelator, 2,2'-bicinchinonic acid. The ligand-binding properties of this copper-less enzyme (-Cu cyt.bo) are compared with those of +Cu cyt. bo. As judged from near-UV/visible spectroscopic changes, cyanide forms a low-spin complex with +Cu cyt.bo, whereas azide, fluoride and formate form high-spin complexes. The pH-dependences of binding suggest that for all four of these anionic ligands, both the rates of binding and the binding affinities are primarily dependent on the concentration of their protonated forms. -Cu cyt.bo, which shows less than 15% of the duroquinol oxidase activity of +Cu cyt.bo, binds cyanide, azide and fluoride, but with greatly decreased affinity (<1/30, 1/2000 and 1/2500 respectively at pH5.5 compared with +Cu cyt.bo). The complex of azide with -Cu cyt.bo still seems to be high-spin and azide binding to -Cu cyt.bo is still pH-dependent, although less so than azide binding to +Cu cyt.bo.


Assuntos
Cobre/metabolismo , Grupo dos Citocromos b , Citocromos/metabolismo , Proteínas de Escherichia coli , Escherichia coli/enzimologia , Azidas/metabolismo , Cianetos/metabolismo , Citocromos/química , Fluoretos/metabolismo , Formiatos/metabolismo , Cinética , Ligantes , Ligação Proteica
12.
Biochemistry ; 34(23): 7576-85, 1995 Jun 13.
Artigo em Inglês | MEDLINE | ID: mdl-7779803

RESUMO

Cyanide binds to fully reduced cytochrome bo and induces a blue shift of the Soret absorption band of the high-spin heme o and a change in the visible region spectrum consistent with the expected conversion to a low-spin state. The dissociation constant, determined by titration of the extent of the binding spectrum, is 7.0 +/- 0.6 mM at pH 7.0. In contrast, cyanide does not bind significantly in this concentration range to the reduced form of cytochrome bd. The reduced cyanide compound of cytochrome bo can be laser photolyzed. Typically, less than 20% photolysis was attained with conditions that give essentially full photolysis of the carbon monoxide compound. The subsequent monophasic kinetics of recombination of cyanide at varying cyanide concentrations were used to determine kon, koff, and dissociation constant values at pH 7.0 of 572 +/- 43 M-1 s-1, 4.2 +/- 0.7 s-1, and 7.3 +/- 1.3 mM, respectively. The dissociation constant changes very little in the pH range 6-8, indicating that a proton is bound together with the cyanide anion, as predicted by our recent proposal of a requirement for electroneutrality in the binuclear center [Mitchell, R., & Rich, P. R. (1994) Biochim. Biophys. Acta 1186, 19-26]. Competition studies confirm that cyanide and carbon monoxide cannot bind simultaneously, so that their binding sites must overlap. A small fraction of the reduced unliganded enzyme appears to have a distinct photolysis spectrum in the absence of added ligands, and this is transformed into a typical ferrous cyanide compound only at very high cyanide concentrations. Cyanide binding and photolysis were also examined in a number of mutant forms of cytochrome bo, and in a wild-type form which was partially depleted in CuB. Dramatic changes in rate constants and binding constants were found in several cases. Data from several mutants were compared with analogous data on the binding and photolysis of carbon monoxide, and the effects of mutation were quite different with the two ligands. A model is developed to explain the observed effects of point mutations on the recombination kinetics of both carbon monoxide and cyanide. Overall, the results indicate that the CuB site is required for binding of cyanide, but not carbon monoxide, to the reduced enzyme, possibly by providing the site for binding of the associated proton.


Assuntos
Monóxido de Carbono/metabolismo , Cianetos/metabolismo , Grupo dos Citocromos b , Citocromos/metabolismo , Proteínas de Escherichia coli , Proteínas de Bactérias/metabolismo , Ligação Competitiva , Escherichia coli , Mutagênese Sítio-Dirigida , Oxirredução , Fotólise , Ligação Proteica , Relação Estrutura-Atividade
13.
Biochemistry ; 34(20): 6838-46, 1995 May 23.
Artigo em Inglês | MEDLINE | ID: mdl-7756314

RESUMO

The fully oxidized fast form of cytochrome bo from Escherichia coli is shown to convert spontaneously to a slow form when stored at -20 degrees C in 50 mM potassium borate, pH 8.5, containing 0.5 mM potassium EDTA. Evidence for the conversion, and that the form produced is analogous to the slow form of bovine heart cytochrome c oxidase, comes from (a) decreases in the extents of fast (k = 1-2 x 10(3) M-1 s-1) H2O2 binding and fast (k = 20-30 M-1 s-1) cyanide binding; (b) changes in the optical spectrum that are like those induced by formate, i.e., a blue shift in the Soret absorption band, loss of absorbance in the alpha and beta bands, and a red shift in the "630 nm" charge-transfer band; (c) changes in the EPR spectrum that are like those induced by formate, i.e., disappearance of signals at g = 8.6 and g = 3.71, and appearance of signals at g approximately 13, g = 3.14, and g = 2.58; and (d) appearance of a slow phase of reduction of heme o by dithionite. The mutant enzyme E286Q also converts to a slow form under the same conditions, as shown by (a) a decrease in the extent of fast H2O2 binding; (b) changes in the optical spectrum like those seen with wild-type enzyme; and (c) changes in the EPR spectrum that are like those induced by formate, i.e., disappearance of signals at g = 7.3 and g = 3.6 and appearance of signals at g approximately 13, g = 3.18, and g = 2.59.(ABSTRACT TRUNCATED AT 250 WORDS)


Assuntos
Grupo dos Citocromos b , Citocromos/química , Proteínas de Escherichia coli , Escherichia coli/química , Boratos , Citocromos/genética , Citocromos/metabolismo , Ditionita/química , Espectroscopia de Ressonância de Spin Eletrônica , Peróxido de Hidrogênio/metabolismo , Concentração de Íons de Hidrogênio , Cinética , Mutação , Oxirredução , Espectrofotometria , Relação Estrutura-Atividade , Ubiquinona/análogos & derivados , Ubiquinona/metabolismo
14.
Diabetologia ; 38(1): 14-23, 1995 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-7744224

RESUMO

The enzyme L-glutamic acid decarboxylase is a major autoantigen of the beta cell. Autoantibodies against this enzyme are observed before the onset of insulin-dependent diabetes mellitus (IDDM) in man and may be of predictive value. There is evidence that this enzyme is involved in the development of autoimmune diabetes in animals. In order to facilitate the investigation of the role of L-glutamine acid decarboxylase in IDDM, we expressed the 65 kDa isoform of human islet L-glutamic acid decarboxylase in insect cells using a baculovirus-based vector. The material was expressed at high levels (up to 50 mg/l of cells). Partially purified metabolically labelled L-glutamic acid decarboxylase bound to immunoglobulins in the sera from 20 of 49 subjects with newly-diagnosed IDDM. The enzyme was isolated in high yields (up to 26 mg/l cell culture) with fully maintained enzymatic activity by either ion-exchange chromatography or immunoaffinity chromatography. Purified L-glutamic acid decarboxylase inhibited the binding of radioactive L-glutamic acid decarboxylase, prepared by in vitro translation of mRNA, to immunoglobulins in the sera of subjects with IDDM. Recombinant human islet L-glutamic acid decarboxylase, isolated from Sf9 cells, is a suitable material for the large scale investigation of the utility of this enzyme in the prediction and prevention of autoimmune diabetes.


Assuntos
Glutamato Descarboxilase/isolamento & purificação , Ilhotas Pancreáticas/enzimologia , Adolescente , Adulto , Animais , Autoanticorpos/imunologia , Baculoviridae/genética , Sequência de Bases , Criança , Pré-Escolar , Cromatografia por Troca Iônica , Primers do DNA/química , Diabetes Mellitus Tipo 1/imunologia , Regulação Enzimológica da Expressão Gênica , Glutamato Descarboxilase/genética , Glutamato Descarboxilase/imunologia , Humanos , Lactente , Recém-Nascido , Pessoa de Meia-Idade , Dados de Sequência Molecular , Proteínas Recombinantes/imunologia , Proteínas Recombinantes/isolamento & purificação , Spodoptera
15.
Eur J Biochem ; 226(2): 731-7, 1994 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-8001590

RESUMO

The reaction of hydrogen peroxide (H2O2) with pulsed cytochrome bo leads to characteristic spectral changes in the enzyme. The difference spectrum shows minima at 401, 494 and 628 nm, and maxima at 420, approximately 468, 526 and 556 nm. delta epsilon 420-epsilon 401 is in the range 73-86 mM-1.cm-1 and delta epsilon 556-epsilon 628 is 7.7-9.6 mM-1.cm-1 (taking delta epsilon 560-epsilon 580 for the reduced minus oxidised spectrum to be 20.5 mM-1.cm-1). The stoichiometry of the reaction, determined by titration of the spectral changes, is 1:1. The second order rate constant for the reaction, which is 1.0-1.5 x 10(3) M-1.s-1 at 20 degrees C, is independent of pH over the range 6.5-8.0. The product of the reaction decays with a first-order rate constant in the range 1-4 x 10(-4) s-1, so the Kd value is apparently in the range 0.05-0.40 microM. The spectral changes observed immediately after quinol-induced turnover, or during steady-state turnover induced by hydrazine or by carbon monoxide, are qualitatively the same as those induced by H2O2 though of lower amplitude. H2O2 addition perturbs the hydrazine-induced or CO-induced steady states by increasing the amplitude of the spectral changes, but there is no qualitative change. From this observation, and the 1:1 stoichiometry of the reaction, we conclude that the intermediate induced by H2O2, which we term F., requires donation of only two electrons to the enzyme from an external source.


Assuntos
Grupo dos Citocromos b , Citocromos/química , Citocromos/metabolismo , Proteínas de Escherichia coli , Escherichia coli/enzimologia , Peróxido de Hidrogênio/metabolismo , Monóxido de Carbono/farmacologia , Hidrazinas/farmacologia , Concentração de Íons de Hidrogênio , Cinética , Oxigênio/farmacologia , Espectrofotometria
16.
Biochem J ; 302 ( Pt 3): 821-6, 1994 Sep 15.
Artigo em Inglês | MEDLINE | ID: mdl-7945208

RESUMO

A form of fully oxidized bovine heart cytochrome c oxidase that is induced by CO2/HCO3- is described. The ligand-binding properties of this form are similar to those of Cl(-)-ligated oxidase [Moody, Cooper and Rich (1991) Biochim. Biophys. Acta 1059, 189-207]. Both bind cyanide at a rate (0.2 M-1.s-1 at pH 6.5) intermediate between the rate of binding to the fast and slow forms of the enzyme, and binding of formate to both is almost undetectable. They are also similar in showing poor reactivity with H2O2, or with CO in the presence of O2, which, with fast oxidase, induce the formation of the 'ferryl' and 'peroxy' states respectively. However, there is a clear difference in the near-u.v./visible absorption spectra of the two forms; that induced by CO2/HCO3- has a Soret maximum at 427 nm whereas Cl(-)-ligated oxidase has a Soret maximum similar to that of fast oxidase at about 424 nm. It appears that both CO2/HCO3- and Cl- are members of a class of ligands that lowers the reactivity of the binuclear centre but does not impede intramolecular electron transfer from haem a to the binuclear centre, unlike the putative endogenous ligand responsible for slow oxidase.


Assuntos
Dióxido de Carbono/metabolismo , Cloretos/metabolismo , Complexo IV da Cadeia de Transporte de Elétrons/metabolismo , Animais , Bicarbonatos/metabolismo , Bicarbonatos/farmacologia , Sítios de Ligação , Dióxido de Carbono/farmacologia , Bovinos , Cloretos/farmacologia , Cianetos/metabolismo , Formiatos/metabolismo , Peróxido de Hidrogênio/farmacologia , Cinética , Miocárdio/enzimologia , Oxirredução , Espectrofotometria Ultravioleta
18.
Biochim Biophys Acta ; 1183(3): 521-32, 1994 Jan 04.
Artigo em Inglês | MEDLINE | ID: mdl-8286401

RESUMO

The carbon monoxide compounds of the fully reduced and mixed valence forms of cytochrome bo from Escherichia coli were laser photolysed under anaerobic conditions at room temperature. The carbon monoxide recombined with characteristic rate constants of 50 s-1 or 35 s-1 in the fully reduced and mixed valence forms, respectively. Rates of CO recombination with the fully reduced enzyme were examined in a variety of mutant forms of cytochrome bo, produced by site-directed mutagenesis. A method was developed to deconvolute cytochromes bo and bd, leading to some reassessment of histidine ligands to the metals. Significant changes in the rate constant of recombination of carbon monoxide occurred in many of these mutants and these results could be rationalised generally in terms of our current working model of the folding structure of subunit I. In the mixed valence form of the enzyme the transient photolysis spectra in the visible region are consistent with a rapid electron redistribution from the binuclear centre to the low-spin haem. This electron transfer is biphasic, with rate constants of around 10(5) and 8000 s-1. The process was also examined in the His-333-Leu mutant, in which a putative histidine ligand to CuB is replaced by leucine, and which results in the loss of the CuB. It appeared that rapid haem-haem electron transfer could still occur. The observation that CuB is apparently not required for rapid haem-haem electron transfer is consistent with the recently proposed model in which the two haems are positioned on opposite sides of transmembrane helix X in subunit I of the oxidase.


Assuntos
Monóxido de Carbono/química , Grupo dos Citocromos b , Citocromos/química , Proteínas de Escherichia coli , Escherichia coli/enzimologia , Sequência de Aminoácidos , Dados de Sequência Molecular , Mutação , Oxirredução , Fotólise
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