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1. Alkaline phosphatases were purified from human placenta, bovine milk, shrimp and clam with a final spec. act. of 67,000, 32,000, 22,000 and 15,000 U/mg of protein respectively. 2. The alkaline phosphatase from Meretrix lusoria is unique with its thermostability at 65 degrees C for 30 min; whereas the remaining enzymes studied, including the human placental alkaline phosphatase, are inactivated and have negligible activities. 3. The alkaline phosphatase from Penaeus monodon can be differentiated by its pH optimum at 9.0; the remaining enzymes studied have their optimal pH at 10.0. 4. The alkaline phosphatases from shrimp and clam are proposed to be applied as "reporters" in the study of mammalian cells.
1. A heat-stable alkaline phosphatase was purified from Penaeus japonicus, with a final specific activity of 21,280 U/mg of protein. 2. In polyacrylamide-gel electrophoresis under non-denaturing conditions, the purified shrimp alkaline phosphatase was found to have an identical molecular size and surface charge as the human placental enzyme. 3. By using SDS-PAGE, the monomers of shrimp alkaline phosphatase were discovered to have a Mr 55,000 but those of human placental enzyme with a Mr 70,000. Deglycosylation decreases the Mr values of the subunits to 33,000 for shrimp alkaline phosphatase. 4. The purified alkaline phosphatase from shrimp was recovered with both the attachment sites for sialic acids and phosphatidylinositol. 5. The shrimp alkaline phosphatase has an isoelectric point (pI) of 7.6 and the human placental enzyme has a pI of 4.8.
1. alpha-L-Fucosidase was purified ca 10,889-fold to homogeneity from Penaeus monodon, with a final spec. act. of 31,250 U/mg of protein. 2. By using SDS-polyacrylamide gel electrophoresis, the monomers of shrimp alpha-L-fucosidase were discovered to have mol. wts of 63,000 and those of human placental enzyme, 46,000 and 20,000. Since the active shrimp alpha-L-fucosidase was found to have a mol. wt of 233,000 by Superose 12 FPLC, it was concluded that the purified shrimp enzyme was tetrameric. 3. In contrast to the discovery of thermolability with human placental alpha-L-fucosidase, the shrimp enzyme was found to be stable to heating at 65 degrees C for 10 min. 4. The shrimp alpha-L-fucosidase has an isoelectric point (pI) of 8.5, but the human placental enzyme has a pI of 4.0. The shrimp enzyme was sialyated. 5. The shrimp alpha-L-fucosidase has a pH optimum at 5.5 and its Km was 22.2 microM with 4-methyl-umbelliferyl-alpha-L-fucopyranoside as substrate. The human enzyme has a broad pH optimum between 5.0 and 6.5.
DNA topoisomerase I was partially purified from the hepatopancreas of the shrimp Penaeus japonicus. The specific activity of the final preparation was 7,000,000 units/mg of protein with SV40 viral DNA as substrate. SDD-polyacrylamide gel electrophoresis of the final preparation yielded two major bands of proteins with M(r) 70,000 and M(r) 67,000, as well as less intense bands of proteins with M, 64,000 and M(r) 56,000. Incubation of the partially purified enzyme fraction with rabbit antiserum against human DNA topoisomerase I, allowed all these proteins except that of M(r) 56,000, to be positively reacted. Treatment of the partially purified DNA topoisomerase I with tyrosine kinase p43v-abl resulted in phosphorylation of only the two major subunits. Phosphorylation by tyrosine kinase p43v-abl or dephosphorylation by phosphotyrosyl protein phosphatase resulted in a decrease of the enzymatic activity. The treatment with shrimp alkaline phosphatase abolished the enzymatic activity of the purified DNA topoisomerase I in a dose-dependent manner. Thus, the DNA topoisomerase I was apparently isolated from the hepatopancreas of the shrimp P. japonicus in a phosphorylated form, and this phosphorylation was essential for expression of enzymatic activity in vitro. The activity of DNA topoisomerase I is inhibited by ZnCl2, CuCl2 and Pb(NH3)3 at millimolar concentrations, but less inhibition was observed with CaCl2.
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1. The sialidase purified from the hepatopancreas of Penaeus japonicus is able to bind the acidic beta-galactosidase in vitro. No protective protein, Mr 32,000, was detected in either purified enzyme preparation. 2. The specific activity of the isolated sialidase is 55.0 mU/mg of protein. After polyacrylamide gel electrophoresis under denaturing conditions, the purified shrimp enzyme was found to consist of monomers of Mr 32,000. 3. The sialidase from shrimp has an isoelectric point (pI) of 4.6 +/- 0.1. 4. The shrimp enzyme has the pH optimum at 5.0 and its Km was 5.5 microM with 2'-(4-methylumbelliferyl)-alpha-D-N-acetylneuraminic acid as substrate. The enzyme activity was inhibited by either Hg2+ or Cu2+ ions.
1. The effects of temperature on the anesthetic potencies of halothane, enflurane and ethanol have been studied in the water flea Daphnia magna. 2. In the absence of anaesthetics, decreasing temperature resulted in decreased activity by the daphnids. 3. Potencies in the gas phase decreased with increasing temperature for all of the anaesthetics, while aqueous potency decreased for halothane and enflurane but increased for ethanol. 4. Enthalpy calculations suggest that the observed potency changes for the inhalational anaesthetics cannot be accounted for in terms of changing solubility in lipid bilayers but most likely reflect more specific interactions with animal target sites.
The present study was designed to evaluate the effect of amount of dietary protein levels on blood indicators of protein metabolism and immune condition (blood protein, hemocyanin, osmotic pressure, and hemocytes concentrations), and reproductive capacity of pre-adult Litopenaeus setiferus males (F0). Assessments were made of the relationship between amount of dietary protein, immune condition, and reproductive condition of the shrimp during the maturation process. Three different diets, with different amounts of protein (DP; 35, 45, and 55%), were evaluated over 55 days and compared with shrimp that were from a baseline group before treatments were administrated. Osmotic pressure, hemocyanin, blood protein, and hemocytes were greater in shrimp from control ponds than those obtained of shrimp fed 35 and 45% DP and similar to that obtained in shrimp fed 55% DP, demonstrating that food in the control pond had a nutritional value to that obtained by feeding amounts of dietary protein beyond 45%. Osmotic pressure, hemocyanin (Hc), blood protein (BP), and hemocytes were influenced by amount of DP with the physiology and immune system of shrimp being influenced by diet. At the same time, a maximum reproductive condition (measured as a proportion of normal cells of the total sperm cells) of shrimp males was observed in shrimp fed 45% DPL with lesser normal cells being present in shrimp fed 35 and 55% DPL. These results indicate that an immune reaction can occur in response to dietary protein with excess DP affecting several physiological functions included the sperm synthesis and sperm quality. Influence on hemocytes concentration in shrimp fed protein in excess could activate an attack on sperm cells in the vas deferens provoking lose of sperm quality in such conditions. Results indicate an optimal DP of 45 for maintaining the broodstock bank of L. setiferus.
Inorganic lead has been measured in high concentrations in certain streams in Brazil. This study has evaluated the osmoregulatory effects of lead on the native freshwater red crab Dilocarcinus pagei. In order to probe its osmoregulatory and tissue volume regulatory capabilities and how it would be affected by lead, the crab has been submitted to individual and combined salt and chemical stresses (Pb2+). Male crabs were exposed for 10 days to either: (1) control (freshwater, FW), (2) brackish water of salinity 15 (BW), (3) inorganic lead in freshwater (FWPb), and (4) inorganic lead in brackish water (BWPb), 2.7 mgPb/L. In vivo, whole crabs lost weight transiently when exposed to Pb2+, both in FW and in BW. Haemolymph osmolality and ion concentrations increased and remained elevated upon exposure of crabs to BW, with or without Pb2+, showing a trend to hyper-conformation. In vitro, muscle weight decreased in isosmotic conditions upon exposure to Pb2+. Na+, Cl-, and ninhydrin positive substances (NPS) were increased in muscle exposed to hyperosmotic saline, well above what would be expected from simple efflux of water, suggesting a partial regulatory volume increase (RVI) capacity. This partial RVI involves the Na+, K+, 2Cl- -cotransporter and the Na+/H+ exchanger on Na+ and Cl- uptake, as judged from further decreases in muscle weight in the presence of the respective inhibitors. A breakdown of proteins into NPS seems to follow the uptake of inorganic ions. Pb2+ has affected water and ion movements in D. pagei both in the whole animal and in the isolated tissue. This study has highlighted the relevance of evaluating tissue volume regulation in aquatic animals confronted with metal polluted waters.
A 291-kDa lectin (LsL) was purified from the hemolymph of the white shrimp Litopenaeus setiferus by affinity chromatography on glutaraldehyde-fixed stroma from rabbit erythrocytes. LsL is a heterotetramer of two 80-kDa and two 52-kDa subunits, with no covalently-liked carbohydrate, and mainly composed by aspartic and glutamic acids, glycine and alanine, with relatively lower methionine and cysteine contents. Edman degradation indicated that the NH2-terminal of the 80-kDa subunit is composed DASNAQKQHDVNFLL, whereas the NH2-terminal of the 52-kDa subunit is blocked. The peptide mass fingerprint of LsL was predicted from tryptic peptides from each subunit by MALDI-TOF, and revealed that each subunit showed 23 and 22%, respectively, homology with the hemocyanin precursor from Litopenaeus vannamei. Circular dichroism analysis revealed beta sheet and alpha helix contents of 52.7 and 6.1%, respectively. LsL agglutinate at higher titers guinea pig, murine, and rabbit erythrocytes its activity is divalent cation-dependent. N-acetylated sugars, such as GlcNAc, GalNAc, and NeuAc, were the most effective inhibitors of the LsL hemagglutinating activity. Sialylated O-glycosylated proteins, such as bovine submaxillary gland mucin, human IgA, and fetuin, showed stronger inhibitory activity than sialylated N-glycosylated proteins, such as human orosomucoid, IgG, transferrin, and lactoferrin. Desialylation of erythrocytes or inhibitory glycoproteins abolished their capacity to bind LsL, confirming the relevance of sialic acid in LsL-ligand interactions.
Glial fibrillary acidic protein (GFAP) is the main intermediate filament protein used as a marker for the identification of astrocytes in the central nervous system of vertebrates. Analogous filaments have been observed in the glial cells of many mollusks and annelids but not in crustaceans. The present study was carried out to identify by light microscopy immunohistochemistry, immunoelectronmicroscopy and immunoblotting, GFAP-like positive structures in the visual system of the crab Ucides cordatus as additional information to help detect and classify glial cells in crustaceans. Conventional electron microscopy, light microscopy of semithin sections and fluorescence light microscopy were also employed to characterize cells and tissues morphology. Our results indicated the presence of GFAP-like positive cell processes and cell bodies in the retina and adjoining optic lobe. The labeling pattern on the reactive profiles was continuous and very well defined, differing considerably from what has been previously reported in the central nervous system of some mollusks, where a diffuse spotted fluorescence pattern of labeling was observed. We suggest that this glial filament protein may be conserved in the evolution of the invertebrate nervous systems and that it may be used as a label for some types of glial cells in the crab.
This study investigated the effects of circadian and seasonal fluctuations on the intermediate metabolism of the freshwater crustacean Aegla platensis. Individuals were collected each month, at 6:00 h, 12:00 h and 18:00 h, between August 1999 and June 2002 in the Municipality of Taquara, Rio Grande do Sul, Brazil (29 degrees 30'0.2''S and 50 degrees 46'50''W). Anomuran crabs were separated by sex, and samples of haemolymph, hepatopancreas, abdominal muscle, and gills were collected for quantification of glucose, proteins, lipids, triglycerides, and glycogen. No variations were observed in the analyzed metabolic parameters for the different tissues during the different times of day, either for males or females. However, the storage and use of the energetic substrates analyzed did fluctuate seasonally. These results suggest an increase in energy demand, possibly for the production of gametes during summer, incubation and egg laying during autumn and winter, and parental care during spring and summer, respectively. A similar pattern has been observed for other crustaceans.
We investigated the effect of hyposmotic stress upon osmotic capacity (OC), heart rate (HR) and heart rate variability (HRV) of an Atlantic population of the sandhopper Talitrus saltator. Strictly consecutive monitoring of cardiac activity and measurement of OC was achieved by employing a non-invasive infrared technique to monitor heart activity and direct cardiac puncture to collect the haemolymph. Body mass (range 60-160 mg) had no effect on mean HR nor the mean HRV in adult individuals of both sexes. Both OC and HR, but not HRV, were influenced by the interaction between osmotic stress and exposure time. In addition, OC and HR were coupled within a moderate range of osmotic stress, beyond which this association breaks down, and bradycardia and a positive correlation between HR and HRV occur. A possible rise in metabolic cost, indicated by HR increase, was described for hyper-osmotic regulation. This is the first assessment of the relationship OC and HR in a non-decapod crustacean, and the results indicate that, in sandhoppers, the disruptions of cardiac activity may lead to impairment in maintaining an efficient haemolymph osmotic regulation.
Clip domain containing serine peptidases (CSPs) include one or more N-terminal clip domain(s) and a C-terminal serine peptidase domain that shares traits with both chymotrypsin and trypsin. CSPs are found in arthropods and are involved in embryonic patterning, immune responses and blood clotting. Among crustaceans only one CSP, which activates prophenoloxidase in crayfish, have previously been reported. We here present LsCSP1, the first CSP found in copepods. LsCSP1 is expressed in the subcuticular tissue and the transcription appears to be upregulated during development. In conjunction with previous studies of CSPs, this study suggests that LsCSP1 may play a role in the immune responses of L. salmonis. Phylogenetic and structural analyses indicate that the CSPs and catalytically inactive CSP homologs (CSPHs) constitute a monophyletic lineage.