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1.
  • 1.1. Seven natural populations of Dacus dorsalis were analyzed for a dimeric esterase by means of horizontal starch-gel electrophoresis.
  • 2.2. The electrophoretic phenotypes were governed by nine codominant Est-D alleles.
  • 3.3. The commonest allele in all seven population samples was Est-D100 which encoded an electrophoretic band with intermediate mobility.
  • 4.4. The distribution of EST-D phenotypes were in accordance with Hardy-Weinberg expectations.
  • 5.5. There was no geographic variation in the distribution of Est-D alleles.
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2.
  • 1.1. Ovaries of Therobia domestica, dissected from inseminated females and incubated with tritiated amino acids, synthesize labeled proteins, the major fraction of which is indistinguishable from the major vitellogenin secreted by the fat body, when considering the electrophoretic mobility, the polypeptide composition and the immunoreactivity.
  • 2.2. Peptide mapping, using two different proteases, shows a striking structural similarity between the proteins of both origins and reveals interrelationships between their subunits.
  • 3.3. The ovary synthesizes the 210–212 kD precursors of the major vitellogenin, as does the fat body, and processes them intensively into smaller subunits (176–182, 57 and 46 kD). The follicle cells are tentatively nominated for both roles.
  • 4.4. The quantitative contribution of the two ovaries to the vitellogenin pool was found to be much higher than that of the fat body.
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3.
  • 1.1. Molecular polymorphism of tropomyosin from various muscle sources of the scallop, Patinopecten yessoensis, was investigated by electrophoretic and immunochemical methods.
  • 2.2. Treatment of the muscle sources with trichloroacetic acid (TCA) prior to tropomyosin preparation was found useful to prevent proteolytic degradation of this protein.
  • 3.3. Electrophoretic and immunochemical analysis revealed that at least six kinds of tropomyosin isoforms may exist in scallop muscle tissues.
  • 4.4. The tropomyosin isoforms showed tissue-specific distribution in amounts and molecular species among the various muscle sources.
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4.
  • 1.1. Myosin light chains and parvalbumins have been compared in several trunk and head muscles from small and large size barbels (Barbus barbus) living in river or reared in hatchery.
  • 2.2. These proteins isolated from white, red and ventricle fibres exhibit identical electrophoretic characteristics in the four batches.
  • 3.3. The slow fibre content and the parvalbumin distribution are generally similar in river and hatchery barbels of the same size but differ between small and large barbels within a population.
  • 4.4. Alterations of the mode of fertilization and breeding conditions do not modify the differentiation of myosin and parvalbumins in barbels.
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5.
  • 1.1. A method for purifying undischarged nematocysts from Hydra and other cnidarians is described.
  • 2.2. Isolated cysts (relative densities 1.22–1.24) evaginate their tubular content even after previous dehydration.
  • 3.3. The cyst wall is permeable to dyes of mol. wts up to 600,000.
  • 4.4. Approximately two-thirds of the cyst's dry wt are soluble proteins. Eighty per cent of them are of low mol. wt and highly anionic, presumably serving as binding sites for Ca2+ and Mg2+.
  • 5.5. The other 20% includes 30 different proteins amongst them toxins and enzymes (phospholipase and little proteases but no collagenase, chitinase or hyaluronidase).
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6.
  • 1.1. The utility of biochemical genetic methods of bird identification was investigated for some common species which create a hazard for commercial aviation in Ireland.
  • 2.2. Sixteen enzyme loci were assayed in eight species, using starch gel electrophoresis; three larids, three corvids and two columbids.
  • 3.3. Genera were distinguishable using all but two loci.
  • 4.4. Differences within genera were small, but all species except for the gulls Larus argentatus and L. marinus, could be identified using one or more loci.
  • 5.5. Arising from the success of the method using fresh specimens, a protocol for the electrophoretic identification of traumatized remains of strikes is suggested.
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7.
  • 1.1. The total histone complement of early plutei were compared with that of intermediate and late larvae of the sea urchin Tetrapygus niger.
  • 2.2. Electrophoretic comparison indicates that there are quantitative and qualitative shifts of the five classes throughout late larval development.
  • 3.3. The strong similarity in the amino acid composition of total histones isolated from early, intermediate and late plutei indicates that the observed electrophoretic heterogeneity is due to post-translational modifications.
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8.
  • 1.1. In lobster hepatopancreas, extracellular protreases cause the inactivation of glycogen phosphorylase.
  • 2.2. The proteolysis of glycogen phosphorylase purified from rabbit muscle by these proteases has been shown by SDS-polyacrylamide gel electrophoresis.
  • 3.3. A cell isolation technique has allowed us to remove proteases of extracellular digestion and to measure glycogen phosphorylase activity in lobster hepatopancreas.
  • 4.4. The glycogen phosphorylase activity seems to be mainly associated with R cells while it could not be detected in B cells.
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9.
  • 1.1. Ontogenic changes of both proteases and carbohydrases of Penaeus monodon from different larva stages to adult were investigated.
  • 2.2. Total protease activity was low during nauplius and zoea but peaked up in mysis. This was due to the activity increase of both trypsin and chymotrypsin.
  • 3.3. The change of isozyme pattern of these two enzymes from different life stages of the shrimp was further determined by functional staining on an electrophoregram.
  • 4.4. Activity of α-amylase increased after the post-larva stage, while that of chitinase and maltase showed a peak in zoea then gradually decreased to adult.
  • 5.5. The ratio of α-amylase activity to protease coincided with the dietary change of the shrimp in different life stage.
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10.
H. Hirata  S Yamasaki 《Hydrobiologia》1987,147(1):283-288
The effect of feeding on the respiration rate of Brachionus plicatilis was studied. Oxygen consumption was determined under two feeding regimes, duplicate feeding and constant feeding. Oxygen consumption rate increased during feeding. The oxygen consumption profile is discussed in relation to the following processes:
  1. filtration, mastication, and locomotion during feeding
  2. specific dynamic action (SDA)
  3. egg formation and routine metabolism.
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11.
  • 1.1. The acute toxicity of endosulfan was determined for the freshwater rotifer Brachionus calyciflorus.
  • 2.2. The mean 24 hr lc50 value for endosulfan was 5.15 ppm with a coefficient of variation of 14.7%.
  • 3.3. Rotifers were exposed at two sublethal concentrations (1.5–2.0 ppm) of endosulfan for bioaccumulation experiments, for an exposure time of 24, 48, 72 and 96 hr. The rotifers were fed with Nannochloris oculata (5 × 105cell/ml).
  • 4.4. The highest accumulation of endosulfan was found 24 hr after the start of the exposure to 1.5 ppm of the toxicant. A steady-state concentration in rotifer was reached between 24–48 hr, followed by a gradual decrease until 96 hr.
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12.
  • 1.1. Soluble eye lens proteins of three species of Italian freshwater ictalurids were analyzed: Ictalurus sp., I. nebulosus marmoratus and I. punctatus.
  • 2.2. The electrophoretic and isoelectric focusing patterns were compared.
  • 3.3. Both techniques revealed species-specific patterns. I. sp. and I. nebulosus marmoratus exhibited very similar patterns, I. punctatus a quite distinct one.
  • 4.4. Some hypotheses warranting further investigation of the subject were proposed.
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13.
  • 1.1. The in vitro digestion of soya protein by pancreatic proteases of the trout was measured following various conditions of stomach digestion.
  • 2.2. Peptic hydrolysis results in an increase of small peptides.
  • 3.3. Acid treatment and peptic proteolysis do not affect the degradation of insoluble proteins or the formation of free amino acids during intestinal digestion, but they do lead to a significant shift from soluble polypeptides to di- and oligopeptides.
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14.
  • 1.1. Basic nuclear proteins from spermatozoa of the three mollusc species belonging to the class Bivalvia have been analyzed using one- and two-dimensional electrophoresis.
  • 2.2. Four nuclear basic proteins have been purified and their amino acid compositions determined.
  • 3.3. In these spermatozoa histone-type proteins coexist with protamine-like proteins.
  • 4.4. The protamine-like proteins that have been studied show different electrophoretic behavior but in general are similar, with a high content of lysine, arginine, alanine and serine.
  • 5.5. Interspecific variability has been found for the H1-like histone.
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15.
  • 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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16.
  • 1.1. Biliverdin reductase from the liver of eel, Anguilla japonica was characterized and purified with a novel enzymatic staining method on polyacrylamide electrophoretic gel.
  • 2.2. This enzyme could use both NADPH and NADH as coenzyme. The Km of NADPH was 5.2 μM, while that of NADH was 5.50 μM.
  • 3.3. The optimum reaction pH for using HADPH as coenzyme was 5.3. That for NADH was 6.1. The optimum reaction temperature is 37°C.
  • 4.4. When NADPH was used as coenzyme, the Km of biliverdin was 0.6 μM. When NADH was used as coenzyme, the Km of biliverdin was 7.0 μM.
  • 5.5. The activity of the enzyme was inhibited by the concentration of biliverdin. Also, the potency of the enzyme was much less than that of the analogous enzyme isolated from mammals.
  • 6.6. This is a fairly stable enzyme with a mol. wt around 67,000. Its estimated pI was pH 3.5–4.0.
  • 7.7. This is the first time biliverdin reductase has been isolated and characterized from a vertebrate other than mammals. The property of it is quite different from that of mammals.
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17.
  • 1.1. The proximate composition, total and free amino acids, and proteases of Artemia nauplii were determined during early development.
  • 2.2. Moisture increased from 71.0% to 80.8%, crude protein decreased from 13.2% to 8.8%, crude fat and ash varied slightly.
  • 3.3. The total amino acids decreased. Free amino acids changed in three patterns.
  • 4.4. Trypsin, chymotrypsin, carboxypeptidase A, B and cathepsin B and C increased in activity. The activity of trypsin was lower, while cathepsin B and C were the highest.
  • 5.5. The protease activities were maximal at pH 7.5 and 8.0, and at 45°C on casein.
  • 6.6. The optimal pH for carboxypeptidase A was 4.0, for carboxypeptidase B was 4.5, for trypsin and chymotrypsin were 7.0–7.5. The protease(s) active at pH 9.0–9.5 were to be determined.
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18.
  • 1.1. Coelomic fluid of the earthworm, Lumbricus terrestris, contains lipid agglutinins that are primarily glycolipids. They are present in fluid from both immunized (induced) and unimmunized (naturally occurring) worms.
  • 2.2. Lumbricus agglutinins partially purified by Folch extraction followed by silicic acid chromatography, were present in all fractions but in highest concentration in acetone and methanol fractions.
  • 3.3. Immunodetection revealed agglutinin activity in acetone and methanol fractions, but not in the chloroform fraction.
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19.
  • 1.1. Digestive proteases from the midgut gland of male Atlantic blue crabs, Callinectes sapidus, were investigated. Tentative identities of proteolytic enzymes were determined with synthetic substrates and inhibitors.
  • 2.2. Trypsin, chymotrypsin, carboxypeptidase A and B and leucine aminopeptidase activities were found and quantified.
  • 3.3. Activity against Succinyl-(Ala)3-nitroanalide was also found. This as yet unidentified enzyme has a mol. wt of about 26,000 and has elastolytic activity.
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20.
  • 1.1. Hemoglobin, hematological parameters, intraerythrocytic phosphates and whole blood Bohr effect of Pterygoplichthys multiradiatus, from the Amazon river, were studied in three different conditions: in their natural environment, acclimated to normoxia and acclimated hypoxia conditions.
  • 2.2. Nine anodal hemoglobin fractions were detected on starch gel electrophoresis. No qualitative differences in the Hb electrophoretic patterns were detected in the three studied groups.
  • 3.3. Hematocrit, hemoglobin concentration, MCV, MCHC and MCH were different among studied conditions.
  • 4.4. GTP was almost absent in the blood of animals in natural conditions and acclimated to hypoxia, but was present at a concentration similar to ATP in normoxic acclimated animals.
  • 5.5. There is a tendency for higher Hb-O2 affinity for hypoxic acclimated/acclimatized animals.
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