A model for L-lactate binding to Cancer magister hemocyanin

L-Lactate raises the oxygen affinity of Cancer magister hemocyanin. The L-lactate analogs, D-lactate, glycolate and 2-methyl-lactate cause smaller increases in an oxygen binding affinity. Other analogs have no detectable effect. These data suggest that L-lactate binds to the hemocyanin at all four positions around the chiral carbon. The carboxyl and hydroxyl groups are required for activity. The protein can only partially distinguish between the methyl group and hydrogen atom.     

Automatic measurement of the oxygen affinity of Cancer magister hemocyanin.

1. The P50 of Cancer Magister hemocyanin in hemolymph was 40.0 mm at 25 degrees C, nmax = 3.9; at 14 degrees C, 15.0 mm and 3.4; and at 10 degrees C. 10.2 mm and 3.3. 2. In the absence of Ca2+ and Mg2+, the P50 at 25 degrees C was in the range of 150 to 250 mm, depending upon pH. 3. Our results show that temperature variation and pH variation may be important factors in the physiological regulation of oxygen delivery in this species. 4. The automatic recording device of Imai et al. (1970) previously used for the study of hemoglobins, was found to be eminently suitable for the study of O2 affinities of hemocyanins.     

cDNA cloning of a developmentally regulated hemocyanin subunit in the crustacean Cancer magister and phylogenetic analysis of the hemocyanin gene family

The complete cDNA sequence and protein reading frame of a developmentally regulated hemocyanin subunit in the Dungeness crab (Cancer magister) is presented. The protein sequence is aligned with 18 potentially homologous hemocyanin-type proteins displaying apparent sequence similarities. Functional domains are identified, and a comparison of predicted hydrophilicities, surface probabilities, and regional backbone flexibilities provides evidence for a remarkable degree of structural conservation among the proteins surveyed. Parsimony analysis of the protein sequence alignment identifies four monophyletic groups on the arthropodan branch of the hemocyanin gene tree: crustacean hemocyanins, insect hexamerins, chelicerate hemocyanins, and arthropodan prophenoloxidases. They form a monophyletic group relative to molluscan hemocyanins and nonarthropodan tyrosinases. Arthropodan prophenoloxidases, although functionally similar to tyrosinases, appear to belong to the arthropodan hexamer- type hemolymph proteins as opposed to molluscan hemocyanins and tyrosinases.      

The binuclear cupric cluster of Cancer magister methemocyanin

Cancer magister hemocyanin oxidized by H₂O₂ (Felsenfeld, G.F. and Printz, M.P. (1959) J. Am. Chem. Soc. 81, 6259–6264) contained 80–95% cupric copper, small amounts of EPR-detectable Cu(II), and native hemocyanin. The small amounts of EPR-detectable Cu(II) showed a signal characteristic of mononuclear Cu(II) in the region of g = 2 between 233°K and 10°K, with normal Curie behavior, and no Δm = 2 signal. Magnetic susceptibility measurements show the methemocyanin to be diamagnetic over the temperature range 1.5–77°K. It had an optical absorption maximum at 680 nm, ϵ = 60 ± 7 M_Cu⁻¹ · cm⁻¹ at 25°C, and at 327 nm (ϵ = 3 · 10² M_Cu⁻¹ · cm⁻¹), 360 nm, 420 nm, and 680 nm at 77°K. CD bands were observed at 340, 400–450, and 650 nm (very broad). Methemocyanin was not reduced to O₂-binding cuprous hemocyanin by dithionite, hydroxylamine, ascorbate, ferrocyanide, H₂O₂, or superoxide. Based upon the normal Curie behavior of the small EPR-detectable signal, the absence of paramagnetism, and some similarities of optical spectra between methemocyanin and oxyhemocyanin, we conclude that the diagmagnetic Cu(II) of this methemocyanin occurs in spin-coupled binuclear Cu(II) clusters having a configuration related to the binuclear Cu(II) cluster in oxyhemocyanin; but that inability of methemocyanin to undergo reductive reactivation, and the low molecular extinction coefficients of the optical absorption bands indicate that some chemical or steric alteration, perhaps peroxidatic in nature, takes place during its formation.     

Peptidergic modulation of cardiovascular dynamics in the Dungeness crab,Cancer magister

Decapod crustacean pericardial organs contain extensive neurohormonal reserves which can be released directly into the haemolymph to act as physiological modulators. The present paper concerns the in vivo effects of two pericardial peptides, proctolin and crustacean cardioactive peptide, on cardiovascular dynamics in the crab Cancer magister. Infusion of proctolin into the pericardial sinus caused a slight decrease in heart rate concurrent with a large increase in cardiac stroke volume. It decreased haemolymph flow anteriorly through the paired anterolateral arteries and increased flow posteriorly and ventrally through the posterior aorta and sternal artery, respectively. The threshold for responses occurred at circulating concentrations of 10^-9 mol·l^-1, and haemolymph flows remained elevated for up to 30 min after peptide infusion. The effects of crustacean cardioactive peptide were less dramatic. Heart rate was not affected but a significant increase in stroke volume was observed. Crustacean cardioactive peptide increased haemolymph flow through the anterolateral arteries and increased scaphognathite rate. The threshold for crustacean cardioactive peptide activity was higher than for proctolin (10^-7 mol·l^-1 and 10^-6 mol·l^-1) but the responses to crustacean cardioactive peptide were of longer duration. The effects of proctolin on regional haemeolymph distribution in Cancer magister closely resemble the cardiovascular responses of this species when exposed to hypoxic conditions. These peptides may be implicated as cardiovascular regulators during environmental perturbations.     

Kinetic properties of catecholoxidase activity of tarantula hemocyanin

Phenoloxidases occur in almost all organisms, being essentially involved in various processes such as the immune response, wound healing, pigmentation and sclerotization in arthropods. Many hemocyanins are also capable of phenoloxidase activity after activation. Notably, in chelicerates, a phenoloxidase has not been identified in the hemolymph, and thus hemocyanin is assumed to be the physiological phenoloxidase in these animals. Although phenoloxidase activity has been shown for hemocyanin from several chelicerate species, a characterization of the enzymatic properties is still lacking. In this article, the enzymatic properties of activated hemocyanin from the tarantula Eurypelma californicum are reported, which was activated by SDS at concentrations above the critical micellar concentration. The activated state of Eurypelma hemocyanin is stable for several hours. Dopamine is a preferred substrate of activated hemocyanin. For dopamine, a K(M) value of 1.45 +/- 0.16 mm and strong substrate inhibition at high substrate concentrations were observed. Typical inhibitors of catecholoxidase, such as l-mimosine, kojic acid, tyramine, phenylthiourea and azide, also inhibit the phenoloxidase activity of activated hemocyanin. This indicates that the activated hemocyanin behaves as a normal phenoloxidase.     

Structural states of the binuclear copper cluster of Cancer magister methemocyanin.

The binuclear cupric copper cluster of $\text{Cancer}\text{magister}$ methemocyanin prepared from hemocyanin and hydrogen peroxide is diamagnetic (1). Upon treatment with azide, it is transformed into magnetic dipolar coupled (paramagnetic) Cu(II) pairs and then into magnetically isolated Cu(II) complexes. This progressive uncoupling of the binuclear cupric pairs in methemocyanin is interpreted in terms of a relaxation of superexchange through one or more bridging ligands.     

Influence of hypoxia on bacteremia in the Dungeness crab, Cancer magister

We examined the possibility that decreased environmental oxygen can elevate the levels of indigenous bacteria in the hemolymph of Cancer magister. Crabs were exposed to air-saturated and hypoxic (50% air-saturation) water for 3 days and levels of culturable bacteria in hemolymph were measured every 24 h as the total number of colony-forming units (CFU) per milliliter of hemolymph. Bacteremia increased after 24 h of exposure to hypoxia and persisted for 72 h, whereas crabs exposed to normoxia had no measurable change in number of culturable bacteria. The predominant persistent bacteria in the hemolymph was isolated and identified by DNA sequence-based methods as Psychrobacter cibarus. Crabs were injected with P. cibarus or with buffered saline as a control after 3 h of hypoxia. Levels of culturable bacteria were significantly higher in hypoxic crabs than in normoxic ones (about 2500 versus 1000 CFU ml(-1) 80 min post-injection, respectively), and circulating levels of oxygen were significantly reduced in infected animals compared to uninfected ones after 48 h in hypoxia and after 72 h in air-saturated water post-injection. These data demonstrate that P. cibarius is present in Dungeness crabs, that environmental hypoxia can dramatically elevate levels of persistent bacteria, and that hypoxia in the presence of hemolymph bacteria may ultimately reduce immune and respiratory ability.     

Responses of bender apodeme tension receptors in the Dungeness crab,Cancer magister

Receptors monitoring tension are located on the apodemes of the bender (productor propoditis) muscle of walking legs and chelipeds of the Dungeness crab, Cancer magister. The bipolar neurons form a nerve, the bender apodeme sensory nerve (BASN), which joins the CP1 chordotonal organ nerve proximally, BASN units exhibit spontaneous activity at rest, and fire bursts of action potentials to rapid passive reduction of the carpopodite-propodite joint. Isometric contraction of the bender muscle results in BASN output that is directly related to force. Afferent activity ceases upon quick release of isometric tension, when tension drops to zero, and the unloaded muscle contracts isotonically.     

Gastric processing in the Dungeness crab, Cancer magister, during hypoxia

The gastric physiology of the Dungeness crab, Cancer magister, was investigated over a range of oxygen tensions. Postprandial crabs reacted differently to hypoxia compared with unfed animals. The bradycardic response in postprandial animals was reduced, suggesting a summation of responses with feeding. A similar pattern was observed for ventilation rate. In unfed animals ventilation rate increased slightly as oxygen levels declined, but dropped significantly in oxygen tensions below 3.2 kPa, whereas in postprandial crabs it increased significantly in the lower oxygen regimes. Gastric processing of the meal was followed using a fluoroscope. Pyloric contraction rates were maintained during mild hypoxia, but decreased in 5.3 kPa oxygen tension and below. This led to an increase in clearance times of digesta from the foregut, midgut and hindgut regions. The slowing of gastric processing in the lower oxygen tensions suggested that the animals were unable to maintain their internal oxygen concentration. A significant reduction in efficiency of assimilation only occurred in the lowest oxygen regime tested (1.6 kPa). The range of hypoxia where gastric processing was affected corresponded closely to the levels of oxygen that modulate the foraging behaviour of C. magister. By using both physiological and behavioural mechanisms C. magister can maintain digestive processes, even in severely oxygen depleted environments.     

Isolation and characterization of polymorphic microsatellite loci from the Dungeness crab Cancer magister

The Dungeness crab, Cancer magister, is the focus of one of the most intensely harvested fisheries in North America. Given its economic importance, there is considerable interest in assessing the degree and spatial pattern of genetic structure in C. magister. To that end, we developed a series of 17 hypervariable microsatellite loci. Six of these 17 loci could be amplified in a single multiplex PCR reaction. Using dye‐labelled primers all six loci can be coamplified and scored simultaneously on an automated sequencer. The ability to multiplex multiple loci greatly increases the ease and speed of genotyping for this species.     

Endogenous rhythms of haemolymph flow and cardiac performance in the crab Cancer magister

Heart rate and arterial haemolymph flow rates were measured in freshly trapped Dungeness crabs, Cancer magister, using a pulsed-Doppler flowmeter. In the laboratory, freshly collected subtidal crabs exhibited endogenous rhythms in both cardiac function and haemolymph flow through one or more arterial systems, of both tidal and diurnal periodicity. The strongest tidal rhythms were recorded in the sternal and paired anterolateral arteries. These endogenous rhythms of selective tissue perfusion are related to an underlying locomotor activity, but may also be involved with hormonal transport or feeding. Changes in both heart rate and stroke volume were responsible for the increases in haemolymph flow rates. These rhythms were not entrained by aerial exposure, since confinement of arhythmic crabs in intertidal cages did not re-entrain an endogenous tidal rhythm. Endogenous locomotory rhythms are known to be controlled by neurohormones released in cycles from the sinus gland on the eyestalk. These hormones may also control the endogenous cardiovascular rhythms, since these were abolished after eyestalk ablation in freshly collected Cancer magister. These results suggest that hormones synthesized and released by the X-organ/sinus gland complex may, together with pericardial hormones, play a role in modulation of crustacean cardiovascular function.