Comparative Studies of the Indoleamine Dioxygenase-like Myoglobin from the Abalone Sulculus diversicolor

The abalone Sulculus diversicolor contains abundant myoglobin in its buccal mass. The myoglobin is homodimeric and the molecular mass of the constituent polypeptide chain is 41,000 Da. The amino acid sequence and gene structure are highly homologous with those of a vertebrate tryptophan-degrading enzyme, indoleamine dioxygenase (IDO). Thus Sulculus myoglobin evolved from an IDO gene, and represents a typical case of functional convergence. The oxygen equilibrium properties of Sulculus myoglobin were examined and compared with those of myoglobins from other sources. It binds oxygen reversibly, and the P₅₀ was determined to be 3.8 mmHg at 20°C and pH 7.4, showing that the oxygen affinity of Sulculus myoglobin is significantly lower than those of usual 16 kDa myoglobins. It also displays no cooperativity (n_max: 1.02–1.06) and no alkaline Bohr effect between pH 7.0 and 7.9. The cDNA-derived amino acid sequences of vertebrate IDOs, molluscan IDO-like myoglobins and a homolog in the yeast Saccharomyces were aligned, and several amino acid residues were proposed as candidates for key residues to control the function of IDO or myoglobin.     

Quantitative aspects of oxygen and carbon dioxide exchange through the lungs in Ocypode ceratophthalmus (Crustacea: Decapoda) during rest and exercise in water and air

Ghost crabs Ocypode ceratophthalmus were exercised in air and water to measure CO₂ and O₂ exchange rates using the method of instantaneous measurements of oxygen consumption rate (MO₂) where applicable. Average heart rate increased from 100 to nearly 400 pulses per minute after five minutes of exercise on a treadmill at a run rate of 0.133 m s^?1. It took less than a minute for oxygen taken up through the lung epithelium from the air inside the branchial cavity to reach the maximal oxygen consumption rate of 26.1 mmol O₂ kg^?1 h^?1. Resting MO₂ was 4.06 mmol O₂ kg^?1 h^?1 in air, but decreased to 3.37 mmol O₂ kg^?1 h^?1 in seawater. Radioactive CO₂ from injected l-lactate is released linearly by the lung. The percent accumulated 14-CO₂ in exhaled air, plotted against time, intersects zero time on the x -axis, indicating rapid gas exchange at the lung surface. The P ₅₀ values for native haemocyanin of 4.89 mm Hg before exercise, and 8.99 mm Hg after exercise, are typical of a high-affinity haemocyanin usually associated with terrestrial crabs. The current notion that Ocypode ceratophthalmus drown when submerged in seawater was not substantiated by our experiments. MO₂ in seawater increased from 3.37 mmol O₂ kg^?1 h^?1 for resting crabs to 5.72 mmol O₂ kg^?1 h^?1 during exercise. When submerged by wave-seawater in the natural environment and during exercise in respirometer-seawater O. ceratophthalmus do not swim but, having a specific density of 1.044, float nearly weightless with a minimum of body movements.     

Observations on the haematology and oxygen transport of the New Zealand fur seal,Arctocephalus forsteri

Abstract

Red cell count, haemoglobin concentration, haematocrit, mean cell volume, and mean cell haemoglobin concentration were recorded for the fur seal Arctocephalus forsteri (Lesson). The data did not indicate haematological adaptations for deep diving nor for extended periods of submergence. Two distinct haemoglobin types were isolated from the red cells by electrophoresis. The oxygen affinity of the blood was low as measured by half-saturation values (p50) of 42.3 mm Hg at pH 7.1 and 26.2 mm Hg at pH 7.4 and 37°c. The low oxygen affinity was mediated by erythrocytic 2,3-diphosphoglycerate, and on this basis a high turnover of oxygen to the tissues is postulated. The role of the blood in oxygen transport appears to be suited for feeding near the surface rather than by deep diving.     

Amino Acid Sequence, Spectral, Oxygen-Binding, and Autoxidation Properties of Indoleamine Dioxygenase-Like Myoglobin from the Gastropod Mollusc Turbo cornutus

Myoglobin was isolated from the radular muscle of the archaeogastropod mollusc Turbo cornutus (Turbinidae). This myoglobin is a monomer carrying one protoheme group; the molecular mass was estimated by SDS–PAGE to be about 40 kDa, 2.5 times larger than that of usual myoglobin. The cDNA-derived amino acid sequence of 375 residues was determined, of which 327 residues were identified directly by chemical sequencing of internal peptides. The amino acid sequence of Turbo myoglobin showed no significant homology with any other usual 16-kDa globins, but showed 36% identity with the myoglobin from Sulculus diversicolor (Haliotiidae) and 27% identity with human indoleamine 2,3-dioxygenase, a tryptophan-degrading enzyme containing heme. Thus, the Turbo myoglobin can be counted among the myoglobins which evolved from the same ancestor as that of indoleamine 2,3-dioxygenase. The absorbance ratio of to CT maximum (/CT) of Turbo metmyoglobin was 17.8, indicating that this myoglobin probably possesses a histidine residue near the sixth coordination position of heme iron. The Turbo myoglobin binds oxygen reversibly. Its oxygen equilibrium properties are similar to those of Sulculus myoglobin, giving P ₅₀ = 3.5 mm Hg at pH 7.4 and 20°C. The pH dependence of autoxidation of Turbo oxymyoglobin was quite different from that of mammalian myoglobin, suggesting a unique protein folding around the heme cavity of Turbo myoglobin. A kinetic analysis of autoxidation indicates that the amino acid residue with pK _a = 5.4 is involved in the reaction. The autoxidation reaction was enhanced markedly at pH 7.6, but not at pH 5.5 and 6.3 in the presence of tryptophan. We suggest that a noncatalytic binding site for tryptophan, in which several dissociation groups with pK _a 7.6 are involved, remains in Turbo myoglobin as a relic of molecular evolution.     

Respiratory characteristics of the blood pigments of three worms from an intertidal mudflat

Abstract

Three worms living in an intertidal mudflat near Auckland have respiratory pigments with different oxygen-binding properties. The burrowing sipunculid Xenosiphon mundanus has hemerythrin contained within coelomic cells. Oxygen is co-operatively bound to the hemerythrin (Hill's coefficient, n, = 1.8), resulting in a sigmoidal oxygen-binding curve of high oxygen affinity (halfsaturation tension, P₅₀, = 7.0 mm Hg at pH 7.5 and 20°C). Oxygen release is regulated by pH, and the Bohr effect is quantified by Ф = Δ log P₅₀ / ΔpH = - 0.30. The errant polychaete Glycera sp. has hemoglobin-charged coelomocytes with low oxygen affinity (P₅₀ = 13.5 mm Hg at pH 7.3 and 20°C)? and the oxygen-binding curve is essentially hyperbolic and insensitive to pH. The burrowing polychaete Abarenicola affinis has a vascular (circulating) erythrocruorin which binds and releases much oxygen for small changes in PO₂ (Hill's n = 3.8) and is insensitive to pH (Ф = -0.09). The physiological properties of these pigments cannot be related to the availability of oxygen in the near-environment, or to the habits of the animals, but appear to be dictated by the level of body organisation, particularly with regard to the gas exchange surfaces.     

Amino Acid Sequence, Spectral, Oxygen-Binding, and Autoxidation Properties of Indoleamine Dioxygenase-Like Myoglobin from the Gastropod Mollusc Turbo cornutus

Myoglobin was isolated from the radular muscle of the archaeogastropod mollusc Turbo cornutus (Turbinidae). This myoglobin is a monomer carrying one protoheme group; the molecular mass was estimated by SDS–PAGE to be about 40 kDa, 2.5 times larger than that of usual myoglobin. The cDNA-derived amino acid sequence of 375 residues was determined, of which 327 residues were identified directly by chemical sequencing of internal peptides. The amino acid sequence of Turbo myoglobin showed no significant homology with any other usual 16-kDa globins, but showed 36% identity with the myoglobin from Sulculus diversicolor (Haliotiidae) and 27% identity with human indoleamine 2,3-dioxygenase, a tryptophan-degrading enzyme containing heme. Thus, the Turbo myoglobin can be counted among the myoglobins which evolved from the same ancestor as that of indoleamine 2,3-dioxygenase. The absorbance ratio of γ to CT maximum (γ/CT) of Turbo metmyoglobin was 17.8, indicating that this myoglobin probably possesses a histidine residue near the sixth coordination position of heme iron. The Turbo myoglobin binds oxygen reversibly. Its oxygen equilibrium properties are similar to those of Sulculus myoglobin, giving P ₅₀ = 3.5 mm Hg at pH 7.4 and 20°C. The pH dependence of autoxidation of Turbo oxymyoglobin was quite different from that of mammalian myoglobin, suggesting a unique protein folding around the heme cavity of Turbo myoglobin. A kinetic analysis of autoxidation indicates that the amino acid residue with pK _a = 5.4 is involved in the reaction. The autoxidation reaction was enhanced markedly at pH 7.6, but not at pH 5.5 and 6.3 in the presence of tryptophan. We suggest that a noncatalytic binding site for tryptophan, in which several dissociation groups with pK _a ≥ 7.6 are involved, remains in Turbo myoglobin as a relic of molecular evolution.     

Effects of thiosulphate on haemocyanin oxygen affinity in the isopod Saduria entomon (L.) and the brown shrimp Crangon crangon (L.)

The sulphide-tolerant brackish water isopod Saduria entomon has haemocyanin with a high affinity for oxygen. Sulphide is oxidized in the hepatopancreas to thiosulphate. Oxygen needed for this oxidation is transported bound to haemocyanin. Thiosulphate was found to improve haemocyanin oxygen affinity in S. entomon. The modulating effect was time and concentration dependent. The effect was greater at higher pH, i.e. the Bohr effect was greater (−1.82) compared to that seen without thiosulphate (−1.36). S. entomon exposed to simultaneous severe hypoxia and sulphide had a low haemolymph pH and the partial pressure of oxygen required to reach 50% saturation was even lower than that measured in vitro. This is ascribed to the combined effects of thiosulphate and lactate as well as unknown co-factors. Thiosulphate had no effect at all in the sulphide and hypoxia non-tolerant natantian Crangon crangon. It is suggested that thiosulphate can be important as a haemocyanin modulator for crustaceans digging in sulphide-rich sediments or constantly exposed to sulphide. Accepted: 11 August 1999     

The influence of dissolved oxygen concentration on phosphofructokinase and the glucose metabolism ofEscherichia coli K-12

The glucose metabolism and the response of phosphofructokinase activity to oxygen were investigated using glucose-limited chemostat cultures ofE. coli K-12. With a dilution rate of 0.2 hr^–1 and a glucose input concentration of 0.83 g/litre, 10 steady states were obtained ranging from 320 to 0 mm HgO₂. Dissolved oxygen reached zero level at a pO₂ of 25.8 mm Hg. The specific phosphofructokinase activity was constant above 28 mm Hg O₂ and increased linearly at lower pO₂ levels until it reached highest activity at 0 mm Hg O₂. Cell dry weight also started to decrease linearly from 28 to 5.9 mm Hg O₂, and fell sharply thereafter. Acid production rate did not start before pO₂ reached 25.6 mm Hg, increased progressively with an additional sharp increase below 5.9 mm Hg O₂. The main endproducts formed were acetic acid and ethanol with lactic acid appearing below 5.9 mm Hg O₂. The results suggest an effect of oxygen on phosphofructokinase synthesis rather than an ATP inhibition of the enzyme.This work was supported by a grant from the Australian Research Grant Commission.     

Aerial and Aquatic Respiration in the River Crab Potamonautes Warreni Calman with Notes on Gill Structure

Summary

The oxygen consumption rate (?O₂) for Potamonauteus warreni Calman (= Potamon warreni (Calman) kept in 25 °C water was 34,4 μmol 1^?1 O₂ kg^?1 and after 72 hours in 98% R.H. air the rate was 31,9 μmol 1^?1 O₂ kg^?1 min^?1. The ?O₂ values for each of the two groups are not significantly different (P > 0,05). The partial oxygen tension of pre-branchial (v = venous) haemolymph (P_vCO₂) is 15,3 mm Hg in water and 13,0 mm Hg in air); partial carbon dioxide tension of pre-branchial (v) haemolymph (P_vCO₂) is 13,2 mm Hg in water and 13,0 mm Hg in air); the total carbon dioxide concentration in pre-branchial (v) haemolymph (C_vCO₂) tot. is 12,3 mmol 1^?1 in air and 13,9 mmol 1^?1 in water) are not significantly different for the two groups (P > 0,05). The haemolymph pH and the lactate concentration for crabs in water was found to be 7,51 and 0,38 mmol 1^?1 respectively. No significant differences were found in pre-branchial haemolymph oxygen tension, carbon dioxide tension, total carbon dioxide content, haemolymph pH, lactate level, chloride concentration, P₅₀ and haemocyanin-oxygen cooperativity in control crabs kept in water, and experimental crabs held in air for 72 hours. The chloride concentration, (327,0 mmol 1^?1) for crabs kept in water does not differ from that of crabs held in air for 72 hours but is at least 15% higher than the sodium concentration (255 mmol 1^?1) for crabs kept in water. The gill surface area is 520 mm² g^?1 wet body mass; on average 9,2 gill platelets (lamellae) can be found on a gill length of one millimetre. Each lamella is spaced 60–70 μm apart, each with a thickness of 30–40 μm. It is concluded that P. warreni may be described as a truly amphibious fresh-water crab.     

Metabolic and ventilatory responses to hypoxia in two altitudinal populations of the toad, Bufo bankorensis

Effects of hypoxia on resting oxygen consumption ( ), lung ventilation, and heart rate at different ambient P_O2 were compared between lowland and high altitude populations of the toad, Bufo bankorensis. Resting decreased significantly in mild hypoxia (P_O2=120 mm Hg) at 10°C and in moderate hypoxia (P_O2=80 mm Hg) at 25°C in both altitudinal populations; however, resting did not differ significantly between the two populations. Numbers of lung ventilation periods (VP) and total inspired volume (V_L) did not change with P_O2 at 10°C, but did increase at moderate and severe hypoxia (40 mm Hg), respectively, at 25°C. Resting heart rates did not change during hypoxia and did not differ between altitude populations. The results suggest (1) the effect of P_O2 change on should be considered in future studies involving transfer of anurans to a different altitude; and (2) the metabolic and ventilatory physiology in B. bankorensis does not compensate for the low temperature and P_O2 at high altitude.     

The dual nature of haemocyanin in the establishment and persistence of the squid–vibrio symbiosis

We identified and sequenced from the squid Euprymna scolopes two isoforms of haemocyanin that share the common structural/physiological characteristics of haemocyanin from a closely related cephalopod, Sepia officinalis, including a pronounced Bohr effect. We examined the potential roles for haemocyanin in the animal''s symbiosis with the luminous bacterium Vibrio fischeri. Our data demonstrate that, as in other cephalopods, the haemocyanin is primarily synthesized in the gills. It transits through the general circulation into other tissues and is exported into crypt spaces that support the bacterial partner, which requires oxygen for its bioluminescence. We showed that the gradient of pH between the circulating haemolymph and the matrix of the crypt spaces in adult squid favours offloading of oxygen from the haemocyanin to the symbionts. Haemocyanin is also localized to the apical surfaces and associated mucus of a juvenile-specific epithelium on which the symbionts gather, and where their specificity is determined during the recruitment into the association. The haemocyanin has an antimicrobial activity, which may be involved in this enrichment of V. fischeri during symbiont initiation. Taken together, these data provide evidence that the haemocyanin plays a role in shaping two stages of the squid–vibrio partnership.     

Vampire blood: respiratory physiology of the vampire squid (Cephalopoda: Vampyromorpha) in relation to the oxygen minimum layer

The functional properties of the haemocyanin ofVampyroteuthis infernalis (Cephalopoda: Vampyromorpha), measured at 5 °C, are reported and discussed in relation to hypoxia. The oxygen affinity of this haemocyanin (P₅₀=0.47−0.55 kPa) is higher than any previously measured for a cephalopod. The high cooperativity (n₅₀=2.20−2.23) and Bohr coefficient (−0.22) suggest a true transport function for this haemocyanin. This high-affinity haemocyanin, in conjunction with moderate gill diffusion capacity, provides a sufficient oxygen gradient from the environment to the blood to support the low routine oxygen consumption rate of V. infernalis     

Enzymatic elucidation of haemocyanin from Kuruma shrimp Marsupenaeus japonicus and its molecular recognition mechanism towards pathogens

Haemocyanin is an important non-specific immune protein present in the hemolymph of invertebrates, which have the ability to recognize the microbial pathogens and trigger the innate immune system. In this study, we isolated and purified the haemocyanin using gel filtration chromatography and investigated its microbial recognition mechanism against the invading pathogens. Kuruma shrimp Marsupenaeus japonicus haemocyanin showed the single band with a molecular weight of 76?kDa on SDS-PAGE and its molecular mass was analysed through the MALDI. Pathogen recognition mechanism of M. japonicus haemocyanin was detected through bacterial agglutination, agglutination inhibition and prophenoloxidase activity. M. japonicus haemocyanin agglutinate all human blood RBC types and showed the bacterial agglutination against all tested Gram positive Staphylococcus aureus, Enterococcus faecalis and Bacillus subtilis and Gram negative Pseudomonas aeruginosa, Proteus vulgaris and Vibrio parahaemolyticus at the concentrations ranging from 30 to 50?μg/ml. Agglutination was inhibited by 50–200?mM of N-acetylneuraminic acid, a-D-glucose, D-galactose and D-xylose. Our results suggest that, 76?kDa subunit of M. japonicus haemocyanin recognize the pathogenic surface proteins which are present on the outer membrane of the bacteria and mediates the bacterial agglutination through haemocytes. This bacterial agglutination was visualized through Confocal Laser Scanning Microscopy (CLSM). This present study would be helpful to explore the importance of haemocyanin in innate immune response of M. japonicus and its eliciting pathogen recognition mechanism leads to the development of innate immunity in crustaceans.     

Influence of variations in pericellular oxygen tension on individual cell growth,muscle-characteristic proteins,and lactate dehydrogenase isoenzyme pattern in cultures of beating rat heart cells

Summary Primary cell cultures from neonatal rat ventricles were continuously exposed for 7 days in a modified roller apparatus to defined pericellular oxygen tension varying from 0.6 to 600 mm Hg. 5-Fluorodeoxyuridine was added to the medium to prevent over-growth of muscle cells by nonmuscle cells. A pericellular pO₂ of 600 mm Hg was lethal. The range of about 15 to 150 mm Hg was favorable, as indicated by increases in total and muscle-characteristic proteins. Between the 2nd and 8th day of cultivation at a pO₂ of 38 mm Hg, myosin content per cell increased 3.2-fold and creatine kinase activity 2.5-fold. At 0.6 mm Hg, myosin content increased only 1.3-fold and there was no increase in creatine kinase activity. The rate of myosin synthesis was diminished at this low pO₂. ATP level and beating rate at 0.6 mm Hg did not differ from values at 38 mm Hg. The isoenzyme pattern of lactate dehydrogenase remained unchanged during cultivation at 38 mm Hg, whereas at 0.6 mm Hg it shifted towards an M-type pattern. These experiments suggest that neonatal rat heart cells maintained in vitro can adapt themselves to low oxygen tensions.     

Binding of organic phosphates by human hemoglobin at alkaline pH-values

The hemoglobin-oxygen equilibrium binding curve was found to be sensitive to the addition of inositol hexaphosphate at pH 9.1. A solution of hemoglobin A in 0.050 $\text{M}$ sodium borate was half-saturated with oxygen at a partial pressure of 0.55mm Hg. Hemoglobin A in 0.050 $\text{M}$ sodium borate, 0.001 $\text{M}$ inositol hexaphosphate, pH 9.1 was half-saturated with oxygen at a partial pressure of 0.95mm Hg. The Hill plot was linear with a slope of 2.0 in the absence of phosphates. In the presence of inositol hexaphosphate the slope of the Hill plot increased from 1.0 to 2.36. The dependence of fractional saturation of hemoglobin with oxygen on concentration of inositol hexaphosphate was determined at partial pressures of oxygen of 0.46 and 1.07mm Hg.     

Respiratory rate,haemolymph oxygen tension and haemocyanin level in the shrimp Palaemon adspersus: Rathke

The marine shrimp Palaemon adspersus Rathke, frequenting Zostera meadows, shows an oxygen consumption rate (MO₂) that is independent of water oxygen tension (P_wO₂) as PO₂ decreases to a critical point (P_cr) near 70 mm Hg. This respiratory independence is associated with maintenance of a relatively constant “arterial” (post-branchial) haemolymph tension (P_aO₂) at 70–80 mm Hg. At lower P_wO₂ values, both MO₂ and P_aO₂ fall, reflecting, in contrast to the above independence, a direct dependence of MO₂ on internal PO₂.Haemolymph copper measurements demonstrate relatively high haemocyanin concentrations and oxygen-carrying capacities, but MO₂ levels reflect an insignificant rôle for the pigment as an oxygen store.The data are discussed as regards adaptations for aerobic metabolism.     

The physiological ecology of haemocyanin in some selected crabs. I. The characteristics of haemocyamn in a tropical population of the blue crab Callinectes sapidus Rathbun

The haemocyanin in Callinectes sapidus Rathbun, a fully aquatic crab has been investigated in a population inhabiting a salt pond in a tropical mangrove swamp. Compared with the results of an earlier study on the haemocyanin perhaps on a subtropical population (Redfield, Coolidge & Hurd, 1926), the P₅₀ found here at 0 mm Hg CO₂ is remarkably low. It is suggested that this is in adaptation to low environmental oxygen concentrations resulting from, 1) high mean water temperature and salinity, and 2) the tendency of the animals to burrow into the sediment. High sensitivity to temperature and a relatively strong Bohr shift are demonstrated, and the possible physiological-ecological pressures involved are discussed. The responses to pH and temperature (Hill's n) of the shapes of the equilibrium curves have also been investigated; the significance of these responses is still obscure. A possibly significant difference in Bohr shifts is noted with P_CO2-dependent variation in pH, and with a naturally occurring variation among individual serum pH values.     

The influence of hypoxia on the blood regulation of the brackish water shrimp Palaemonetes varians Leach

During periods of hypoxia in hypotonic media, Palaemonetes varians Leach showed an unimpaired regulation of blood chloride until some minutes before death. Heart rate showed no clear dependence on the water oxygen tension (P_wO₂) and postbranchial haemolymph oxygen tensions slowly decreased during progressive hypopoxia from a normoxic level of ≈ 30 mm Hg until the animals turned opaque some minutes before they died. Blood pH increased in hypoxia, from 7.6 in normoxia to > 8 in P_wO₂ 10 mm Hg. Taken together, these data have been taken to indicate that the oxygen consumption rate at the critical point (MO₂ P_cr) of this species is very low (P_wO₂ = < 10 mm Hg) compared with other brackish water natantians studied. The ecological significance of this to the species is considered.     

Temperaturadaptation der Sauerstoffaffinität des Blutes von Rana esculenta L.

Zusammenfassung Die Sauerstoffaffinität des Blutes (ausgedrückt im Sauerstoffhalbsättigungsdruck P ₅₀) von an 5° C adaptierten Fröschen (Rana esculenta L.) ist bei gleicher Umgebungstemperatur geringer als bei an 20° C adaptierten Fröschen. P ₅₀ bei pH 7,4 und 20° C Umgebungstemperatur betrug 42,4 mm Hg bei den kälte- und 39,1 mm Hg bei den wäremadaptierten Fröschen (Abb. 1). Die Sauerstoffkapazität der kälteangepaßten Frösche von 12,33 ml O₂/100 ml Blut ist höher als die der wärmeangepaßten von 10,43 ml O₂/100 ml Blut (Tabelle 1). Die Bedeutung und die Ursache der Sauerstoffkapazitäts- und Sauerstoffaffinitätsadaptation im Hinblick auf die Stoffwechseladaptation werden diskutiert.

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Temperature adaptation of the oxygen affinity of the blood in Rana esculenta L.

Summary The oxygen affinity of blood (expressed by the oxygen half saturation pressure P ₅₀) in frogs (Rana esculenta L.), adapted to 5° C is less as in frogs, adapted to 20° C at equal experimental temperature. P ₅₀ in cold-adapted frogs related to pH 7.4 and 20° C is 42.4 mm Hg and in heat-adapted frogs 39.1 mm Hg (Fig. 1). The oxygen capacity of the cold-adapted frogs is with 12.33 ml O₂/100 ml blood higher than of the heat-adapted frogs with 10.43 ml O₂/100 ml blood (Table 1). The importance and the origin of the adaptation of the oxygen affinity and capacity in view to the adaptation of the metabolic rate are discussed.