Genetic differentiation in Chilean hake Merluccius gayi gayi (Pisces: Merlucciidae)

The genetic structure of Chilean hake Merluccius gayi gayi, was analyzed using starch gel protein electrophoresis. Samples were collected from four localities along the coast off Chile. A total of 1500 specimens sampled from Coquimbo, San Antonio, Talcahuano and Puerto Montt were used in the study. Genetic information was obtained for six allozyme loci Pgi-1, Pgi-2, Pgm, Idh-1, Idh-2 and Aat. The results of the analysis showed no significant allelic differences among samples from various localities, with an average F_ST value of 0.007 for all loci and samples. A heterogeneity test for all loci and specimens from the four localities showed only two significant values. Thus, Chilean hake populations along the coast of Chile appear to be genetically homogeneous.     

Gillnet selectivity for Chilean hake (Merluccius gayi gayi Guichenot, 1848) in the bay of Valparaíso

To determine the selectivity of gillnets in the Chilean artisanal fishery for the Chilean hake Merluccius gayi gayi, an experimental net was used with three mesh sizes (5.2, 6.8 and 7.6 cm). A total of 2279 specimens of Chilean hake were caught (24–56 cm total length, TL), mainly via gilling and snagging. The catch proportion below the size of sexual maturity SSM_50% (37 cm TL) for each mesh size tested was estimated. Models were fitted separately according to the sex to compensate for differences in size compositions, with the males fitted to a binormal model and females fitted to the normal location model. Analysing both sexes combined, the model with the lowest deviance was lognormal, with estimated modal lengths of 30.9, 40.2 and 43.9 cm TL for meshes of 5.2, 6.8 and 7.6 cm, respectively. The estimated selectivity factor (SF) indicates that the modal size matches the SSM_50% with a mesh size of 6.2 cm, while the length of retention of 50% (l₅₀) coincides with the SSM_50% with a mesh size of 7.6 cm.     

Population structure in Chilean hake Merluccius gayi as revealed by mitochondrial DNA sequences

Genetic variation and divergence among samples of Chilean hake Merluccius gayi, from three localities off the coast of Chile and one locality off the coast of northern Peru, were assessed using sequences from the control region of mitochondrial DNA. Homogeneity tests revealed occurrence of at least three distinct genetic stocks of M. gayi within the region sampled. Factors potentially contributing to genetic divergence among M. gayi probably include hydrodynamics and behaviour.     

Larval anisakids and other helminths in the hake, Merluccius gayi (Guichenot) from Chile

One hundred and twenty hake Merluccius gayi caught off central Chile were examined for helminth parasites. Sixty hake were kept in ice from the catch of a trawler were examined upon arrival at port, while the other 60 hake were dissected on board immediately after collection. Ninety one per cent of hake were infected with one or more species of the following helminths: trypanorhynch plerocerci of Grillotia dollfusi Carvajal, 1971; adult worms of the genus Clestobothrium; larval nematodes of the genera Anisakis and Phocanema; 86% of the total were infected with Anisakis sp. and 42.5% with Phocanema sp. Infection with larval nematodes increased with length of the fish and there was a greater incidence of infection among the females. There was a greater frequency of occurrence of the parasites in the viscera than in the musculature.     

Populations and assemblages of parasites in hake, Merluccius gayi, from the southeastern Pacific Ocean: stock implications

To assess fish stocks, the populations and community assemblages of metazoan parasites were compared in 1172 Chilean hake Merluccius gayi landed at two major ports, and caught during 1991–1992 in three major fishing areas off central Chile. At least two ecological stocks are suggested, based on consistent differences in parasitism between body length classes for Grillotia dollfusi, Hysterothylacium sp., Clestobothrium crassiceps and Aporocotyle wilhelmi . More use should be made of the information on whole parasite assemblages including, for example, patterns of co-occurrence of parasite species. Univariate analyses on selected taxa in samples from different areas may show no differences because of the same prevalence or abundance for each parasite taxon, but opposite numerical arrangements of co-occurring taxa in community assemblages would remain undetected.     

On the control of arginine metabolism in chicken kidney and liver.

Arginases have been found to be located on the external side of the inner mitochondrial membrane of chicken kidney and liver. Transamidinase has been detected within the liver mitochondrial matrix space. Arginases and transamidinase act upon two different intracellular arginine pools. Penetration of arginine into the matrix space occurs only in respring mitochondria and in the presence of anions such as acetate and phosphate; D-arginine, L-ornithine, D-'ornithine and L-lysine penetrate with the same modalities. L-Histidine penetrates only kidney mitochondria. Because of transamidinase compartmentation, the rate of creatine synthesis is influenced by the rate of penetration of arginine into the mitochondria.     

A study of the migration of larval Anisakis simplex (Nematoda: Ascaridida) in the Chilean hake, Merluccius gayi (Guichenot)

Hake were collected during four trips to investigate a possible migration from viscera to somatic musculature of larval Anisakis simplex. On each trip 150 hake were examined and separated in five groups of 30 hake. One group consisted of fish gutted immediately after capture; two other groups were gutted 15 h after capture, one of which had been left at environmental temperature, and the other put in ice; the remaining two groups (exposed to the same treatment) were gutted 30 h after capture. All fish flesh was digested (HCl-pepsin digest); all nematodes found in the digest and in the viscera were counted. There was no increase of larval nematodes in flesh at 15 and 30 h. Temperature did not affect the migration of larvae. A regression test did not show significant differences between groups. Finally, there was no correlation between number of larvae in viscera and in musculature.     

Trypsin catalyzed hydrolysis of new chromogenic arginine substrates

Trypsin catalyzed hydrolysis of seven new chromogenic arginine substrates, N alpha-benzyloxycarbonyl-L-arginine-3-nitro-5X-anilide (X = H, CF3, SO2CH3, F, Cl, Br and I) were studied. These substrates are suitable for studying electronic effects on trypsin activity. The Km and kcat values for the hydrolysis of each substrate were determined and found to differ significantly for the various substrates. The Hammett plot of the catalytic rate constants gave a straight line with a negative rho value (-0.82) thus indicating that electron withdrawing substituents retard the trypsin catalyzed hydrolysis of the new anilide substrates.     

Studies on the enzymatic hydrolysis of amino acid carbamates

Several commercially available enzymes were tested for their ability to hydrolyze amino acid carbamates. No activity was found with pig liver esterase, the hydantoinase from Pseudomonas fluorescens DSM 84, or the urease from jack beans. A stereoselective cleavage of the carbamyl group yielding L-amino acids was observed by acylase and acetylcholinesterases from bovine and human erythrocytes. Racemic mixtures of N-(methoxycarbonyl)-DL-alanine, N-(ethoxycarbonyl)-DL-alanine, and the corresponding valine carbamates are hydrolyzed to L-alanine and L-valine, respectively, by acylases leaving the D-amino acid carbamates unchanged. The lysine carbamates were not hydrolyzed by acylases. In contrast only the methoxycarbonyl amino acids were split by acetylcholinesterases, which, however, also cleave alpha, epsilon-(N-methoxycarbonyl)-DL-lysine stereoselectively at the alpha position, yielding epsilon-N-methoxycarbonyl-L-lysine. The optimum pH for enzymatic activity of hog kidney acylase was 7.5 and a Km value of 8.2 mM for N-(methoxycarbonyl)-DL-alanine was determined. For the acetylcholinesterases the reaction rate reaches an optimum between pH 7.5 and 8. The Km value was 68 mM for N-(methoxycarbonyl)-DL-alanine.     

The effect of arginine on hydrolysis of fibrinogen by plasmin and mini-plasmin]

The rate of plasmin or Val442-plasmin catalyzed hydrolysis of fibrinogen decreases several times as affected by arginine in high concentrations. The enzyme is shown to be not inhibited by arginine. The observed effect is supposed to depend on saturation of the protein-proteins interaction sites located between 442 and 790 amino acid residues.