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1.
  • 1. The haemoglobin of the South American lungfishLepidosiren paradoxa has a single component.
  • 2. The equilibria of this respiratory protein with oxygen have been investigated both in the blood and with the purified haemoglobin. There is a substantial, normal, alkaline Bohr effect and marked sensitivity to organic phosphates in the haemoglobin solutions.
  • 3. Studies on the pH dependence of the kinetics of oxygen dissociation can be interpreted in terms of a normal Bohr effect.
  • 4. The kinetics of combination of carbon monoxide have an unusual pH dependence.
  • 5. These findings are discussed in terms of the two-state model of Monodet al. (1965)
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2.
  • 1.1. Blood parameters determining oxygen capacity and oxygen affinity were measured in brown trout at different times of the year.
  • 2.2. Haematological data indicate a slight decrease in blood oxygen capacity during the warm seasons. 3. Oxygen affinity increases significantly during summer and decreases in winter.
  • 3.4. The changes in P50 exhibited a positive correlation with the amount of anodic haemoglobin components, and a negative correlation with the amount of cathodic haemoglobin components.
  • 4.5. The changes observed in the [ATP]/[Hb] molar ratio were not correlated with oxygen affinity and gave values near one.
  • 5.6. We conclude that the oxygen affinity increase could be a physiological adaptation to oxygen transport during the wanner period. A possible mechanism is discussed.
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3.
  • 1. The four main hemoglobin components of the hemolysate ofPterygoplichthys pardalis have been isolated and characterized.
  • 2. The functional properties investigated for the isolated components comprise the effect of pH and ATP on (i) the O2 equilibrium, (ii) the O2 dissociation kinetics, (iii) the CO combination kinetics.
  • 3. Component I, corresponding to approx 50% of the total hemoglobin, is characterized by functional properties which are distinctly different from those of Components II, III and IV, which are alike
  • 4. Thus it is shown, once more, that multiple components in an hemolysate fall into categories of hemoglobins characterized by distinct and complementary functional properties
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4.
  • 1. The equilibria and kinetics of oxygen binding by blood and hemoglobin from adult and fetal caecilians,Typhlonectes compressicauda, have been measured.
  • 2. The oxygen affinity of fetal blood is higher than that of adult blood.
  • 3. Electrophoresis of adult and fetal hemoglobins suggests that they may be identical: a major and minor component occurs in each.
  • 4. Adult and fetal hemoglobins have identical oxygen equilibria. Stripped hemoglobins have a high oxygen affinity and no Bohr effect between pH 6.5 and 10.0. An “acid”, reversed Bohr effect is present below pH 6.5. The addition of 1 mM ATP reduces the oxygen affinity markedly and produces a moderate, normal Bohr effect.
  • 5. The major nucleoside triphosphate in fetal and adult erythrocytes is adenosine triphosphate: about 10% of the nucleoside triphosphates is guanosine triphosphate. Adult erythrocytes contain 3 times as much ATP as do the fetal erythrocytes.
  • 6. The fetal to maternal shift in the oxygen equilibrium is mediated entirely by the difference in ATP content of the maternal and fetal red blood cells.
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5.
  • 1. The two hemoglobins, Hb I and II, of the obligate air-breathing catfish,Hoplosternum littorale have been isolated.
  • 2. The unfractionated stripped hemoglobin has a high oxygen affinity, a normal alkaline Bohr effect, and a Root effect.
  • 3. Both the Bohr and Root effects are enhanced by 1 mM ATP.
  • 4. Stripped Hb I has a relatively high oxygen affinity, a reversed Bohr effect between pH 6.0 and 8.0 (Δlog P502DpH> 0), but no Root effect. Addition of 1 mM ATP to Hb I causes a marked reduction in the oxygen affinity, a change to a normal alkaline Bohr effect (Δlog P50ΔpH< 0), but no Root effect.
  • 5. Stripped Hb II has a lower oxygen affinity at low pH and a higher oxygen affinity at high pH than does Hb I. Hb II shows a large alkaline Bohr effect which is only slightly increased by 1 mM ATP and a Root effect at low pH which is enhanced by 1 mM ATP.
  • 6. The observed rates of O2 dissociation and of CO combination with Hbs I and II show differences which parallel those observed in the oxygen equilibrium measurements.
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6.
  • 1.1. To define the respiratory function of haemoglobin in male Daphnia magna, the swimming activity, the depression of oxygen uptake by treatment with carbon monoxide and in vivo oxygenation of Hb at various oxygen pressures were investigated.
  • 2.2. The P50, values for the purified Hbs from male and female red animals were 2.0 and 2.7 torr in 0.1 M phosphate buffer (pH 7.2) at 20°C, respectively.
  • 3.3. The isoelectric focusing patterns of the purified Hbs from male and female red animals showed only small differences in Hb components of high PI values.
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7.
  • 1.1. We studied the haemoglobin content, erythrocyte indices, erythrocyte enzymes and haemoglobin electrophoresis patterns of the metallic skink Niveoscineus metallicus and compared them to the small amount of published data on other small lizards.
  • 2.2. Haemoglobin was much lower than that recorded for the salamander.
  • 3.3. Erythrocyte enzymes (glucose phosphate isomerase and glucose 6 phosphate dehydrogenase) were lower in the skink than in the salamander. Glyceraldehyde phosphate dehydrogenase, phosphoglycerate kinase and pyruvate kinase were much higher in the skink than in the salamander.
  • 4.4. A single, slow, haemoglobin component was identified by electrophoresis.
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8.
  • 1.1. Babesia hylomysci has an aminopeptidase and an acid endoprotease
  • 2.2. The amino-peptidase has properties very similar to the aminopeptidase in Plasmodium yoelii nigeriensis and P. chabaudi.
  • 3.3. The acid endoprotease is specific towards haemoglobin and practically has no action on bovine serum albumin.
  • 4.4. In mouse normal red blood cells we find an acid protease having physico-chemical properties similar to the enzyme present in B. hylomysci extracts.
  • 5.5. The similarity of electrophoretic velocity between acid protease in B. hylomysci and non-infected red blood cells leads us to think that the acid protease of parasitic extracts comes from the host-cell.
  • 6.6. The proteolytic system of Babesia and Plasmodium are similar.
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9.
  • 1.1. This study examined the effect of the monoamines dopamine and octopamine, as well as tyrosine on the oxygen affinity and cooperativity of oxygen binding by the hemocyanin of the marine gastropod Busycon canaliculatum. The effect of temperature on hemocyanin oxygen affinity was also examined.
  • 2.2. Freezing Busycon hemocyanin did not affect the binding of oxygen.
  • 3.3. Dopamine, octopamine and tyrosine had no significant effect on the oxygen affinity or cooperativity of oxygen binding by the hemocyanin of B. canaliculatum.
  • 4.4. It was concluded that Busycon hemocyanin either has no binding sites for the two monoamines or for tyrosine, or that binding of the molecules has no functional significance.
  • 5.5. Both temperature sensitivity and affinity of hemocyanin-oxygen binding were similar to values previously reported for hemocyanin of Busycon from other localities.
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10.
  • 1.1. The hemoglobins of Leporinus friderici were separated by liquid chromatography on DEAE-Sepharose in order to isolate the two major electrophoretic components.
  • 2.2. The chromatographic fraction I (electrophoretically slow anodic) showed no Bohr effect and no nucleoside triphosphate modulation.
  • 3.3. The chromatographic fraction III (electrophoretically fast anodic) showed a normal Bohr effect and addition of nucleoside triphosphate decreased oxygen affinity but did not alter the Bohr effect.
  • 4.4. The whole hemolysate showed a normal Bohr effect and phosphate modulation altered both Bohr effect and oxygen affinity.
  • 5.5. No or little difference between the effect of adenosine or guanosine triphosphates on hemoglobin function was observed.
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11.
  • 1.1. A variety of haematological parameters were determined in adult Dasyurus viverrinus.
  • 2.2. Haemoglobin and red cell counts were high with a very low mean cell volume.
  • 3.3. Basophils are absent but the eosinophils contain small numbers of basophilic granules which may indicate a dual role for this cell.
  • 4.4. “Ring Form” leucocytes are present.
  • 5.5. Three types of red cell picture could be identified, some animals showing large numbers of spherocytes, spicule cells, and inclusion bodies.
  • 6.6. These cells resemble those found in some inherited human haemolytic anaemias but there was no evidence of haemolysis in the animals.
  • 7.7. An alkali resistant haemoglobin component is present.
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12.
  • 1.1. The lipid components of three animals, the rock crab Nectocarcinus integrifons, the rock flathead Platycephalus laevigatus and the southern garfish Hyporhamphus melanochir, feeding in the seagrass beds at Corner Inlet, Victoria, Australia have been examined in detail in order to provide further information on seagrass community structure.
  • 2.2. Biological marker compounds detected within animal gut content material were used to recognize dietary sources and then utilized by community members.
  • 3.3. Both H. melanochir and N. integrifons have been shown to ingest and to varying degrees incorporate seagrass lipid material, thus further confirming the importance of seagrass carbon in the Corner Inlet environment.
  • 4.4. The southern sea garfish H. melanochir is observed to remove C18 PUFAs (polyunsaturated fatty acids) from ingested seagrass material.
  • 5.5. Seagrass sterols are altered during incorporation into the lipids of this fish.
  • 6.6. Lipid-rich digestive juices play a role in the digestive processes of all three animals.
  • 7.7. Components tentatively identified as (NMI) (non-methylene interrupted) fatty acids have been detected in the lipids of the garfish H. melanochir and the crab N. integrifons.
  • 8.8. The fecal material of all three animals represent possible sources of these lipids (NMI acids) in Corner Inlet sediments.
  • 9.9. Based on lipid compositional data, N. integrifons feeds on Posidonia australis detritus and associated epiphyte material.
  • 10.10. The removal of both plant and epibiota cellular lipids along the digestive tract of the crab was observed, although structural components such as long chain mono- and α,ω-dicarboxylic acids, which have been previously recognized as seagrass marker lipids are not directly absorbed.
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13.
  • 1.1. The Hcy of a mediterranean opisthobranch gastropod, Aplysia limacina, has been characterized. Amino acid composition, sedimentation coefficients, the reaction with oxygen and the ultrastructure have been studied.
  • 2.2. This Hcy is very similar to other gastropod Hey, as are amino acid composition and general structure.
  • 3.3. Differences are observed both in the ability to form supramolecular aggregates and in the size and shape of the subunits observed by electron microscopy.
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14.
  • 1.1. The oxygen consumption of the marine teleost, Lichia amia was investigated under controlled laboratory conditions.
  • 2.2. The routine oxygen consumption showed a strong circadian rhythm with the fish being mainly active during the light period.
  • 3.3. The specific mass exponent (dimension: μg O2/g/hr) is temperature independent and ranges from 0.27–0.29.
  • 4.4. Starving the fish results in a mean decrease in active, routine and standard oxygen consumption of 21%, 24% and 20%, respectively.
  • 5.5. Feecling led to an increase in the oxygen consumption of the teleosts, with the mean metabolic rate over the 24 hr that followed, being 58% and 50% higher for fish that had been starved for 162hr and 40 hr, respectively.
  • 6.6. Apparent SDA showed some variation and ranged from 6.0 to 35.5%.
  • 7.7. The results obtained are generally in agreement with those recorded for other teleosts.
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15.
  • 1.1. The rate of oxygen consumption has been monitored continuously in M. edulis during acute exposure to high sublethal concentrations of formaldehyde, phenol and benzene and subsequent recovery periods of 96 hr.
  • 2.2. The results are discussed in relation to changes in the electrochemical potential difference of sodium, the content of ATP and the tissue concentration of strombine.
  • 3.3. After exposure to benzene and phenol, an increase in the rate of oxygen consumption that could not be explained by oxygen debt from the exposure period was observed.
  • 4.4. Depression of the rate of oxygen consumption after exposure to formaldehyde may be explained by a reduced ability to extract oxygen from the water.
  • 5.5. The pattern of oxygen consumption and behavioural responses, as well as the combined changes in the biochemical markers, were distinctly different in the three cases.
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16.
  • 1.1. The oxygen consumption of red and green Carcinus in normoxic and hypoxic sea water was determined, using an oxygen electrode in a sealed respirometer.
  • 2.2. The red crabs had significantly higher “excited” oxygen uptake rates and a lower ability to compensate for hypoxia than the green crabs.
  • 3.3. Red Carcinus display an emersion response to declining oxygen at lower oxygen tensions than the green crabs.
  • 4.4. Mortality of red crabs exposed to prolonged anoxia was much greater.
  • 5.5. The relationship of these findings to the zonation of the two colour forms on the shore is discussed.
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17.
  • 1.1. Adult male Atremia salina L. were acclimated to five different oxygen concentrations and their respiration in response to environmental oxygen concentrations was determined.
  • 2.2. Anemia is a respiratory regulator over a wide range of partial O2 pressures. A critical oxygen tension exists and decreases with acclimation to lower pO2.
  • 3.3. Hypoxic conditions induce the production of hemoglobin III.
  • 4.4. Lactic acid is produced during anaerobiosis.
  • 5.5. Production of Hb III and lactic acid, being inversely proportional to the acclimation level, has to be considered as a long term or short term adaptation to hypoxic conditions.
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18.
  • 1.Loricariichthys sp., an air-breathing fish from the Amazon River has one major hemoglobin component.
  • 2. Quantitative studies on the kinetics of O2 dissociation and CO combination to the protein were performed by stopped-flow experiments at different pH values and a constant ATP concentration of 1.25 mM.
  • 3. The oxygen dissociation shows a simple first order behavior and a strong pH dependence.
  • 4. The CO combination kinetics, on the other hand, were homogeneous and fast at higher pH values and slow and clearly autocatalytic at pH values below 7.0.
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19.
  • 1.1. The entire oxygen dissociation curve (ODC) and the effects of temperature, pH and 2,3-diphosphoglycerate (DPG) on this curve, have been compared in four mammalians: man, dog, horse and cattle.
  • 2.2. If the oxyphoric capacities are similar between these species (around 1.39ml O2/gHb), their P50, measured in standard conditions, i.e. at pH 7.4;.pCO2 40mmHg and T 37°C, varies between 23.8 (± 0.8) mmHg for the horse, 25.0 (± 1.4) mmHg for cattle, 26.6 (± 1.2) for man and 28.8 (± 2.6) mmHg for the dog.
  • 3.3. The higher dispersion of the dog's P50 is due to difference between breeds; in seven breeds investigated, the P50 ranges from 25.8 (spaniel) to 35.8 (hound).
  • 4.4. We noted no sex difference in the four species.
  • 5.5. The DPG level is confirmed to be low in cattle (< 1 μmol/gHb) as compared to man (13.5 ± 2.1 gmmol/gHb), horse (16.9 ± 1.1 gmmol/gHb) and dog (19.4 ± 2.8 μmol/gHb).
  • 6.6. The oxygen exchange fraction defined as the difference in vol% between a pO2 of 80 and 35 mmHg is, respectively, 3.6 (± 0.6) vol% for cattle, 4.0 (0.4) vol% for the horse, 5.5 (± 0.5) vol% for man and 6.6 (± 1.7) vol% for the dog.
  • 7.7. The position and shape of the ODC, as well as T, DPG and pH effects, indicate that the haemoglobin of man and dog seem better adapted to O2 delivery as compared to the horse and cattle.
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20.
  • 1.1. The binding of O2 to goldfish haemoglobin showed a strong pH dependence P50=5.5 mmHg; n = 2.4 at pH 8.0 and P50 = 170 mmHg; n = 1.0 at pH 5.5 such that the protein is only 50% saturated in a solution of air equilibrated buffer at pH 5.5.
  • 2.2. The binding of CO is cooperative at high pH (n = 2.8; L = 1000; KR = 0.1 μM; KT = 4 μM) and non-cooperative (n = 1) at pH 5.5.
  • 3.3. The rate of O2 dissociation is extremely fast and pH dependent; being 30 sec−1 at pH 8.0 and 400 sec−1 at pH 6.0 at 1°C. At 23°C the rate of this process is too fast to obtain accurate data using stopped-flow techniques.
  • 4.4. Partial photolysis of the oxyhaemoglobin species leads to homogeneous recombination kinetics at pH 8.0 with an associated rate constant of 4.7 × 107 M−1 sec−1. At pH < 7.5 the recombination process occurs in two steps. One rate is equal to that observed at pH 8.0. The slower process is favoured at low pH.
  • 5.5. Photolysis of the CO haemoglobin complex indicates that, at high pH, combination of CO with deoxyhaemoglobin is cooperative, whilst recombination with Hb(CO)3 is non-cooperative and occurs at a rate of 1.2 × 106 M−1 sec−1.
  • 6.6. At neutral pH recombination of CO with partially linganded haemoglobin occurs in a two-step process. The proportion contributed by each of these two steps in pH dependent.
  • 7.7. The functioning of this Root effect haemoglobin is discussed in terms of the two state-model of cooperativity in which the αβ chain heterogeneity is minimal
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