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1.
  • 1.1. Neonatal mice received subcutaneous injections of buffer, thiourea (TU) or propylthiouracil (PTU).
  • 2.2. The PTU-treated mice were sacrificed on postnatal day 14 (P14) and the TU-treated mice on P28.
  • 3.3. Brain weights of the TU- and PTU-treated mice were not significantly different from the controls.
  • 4.4. Acid but not alkaline phosphatase activity in the braistem decreased after TU and PTU treatment.
  • 5.5. Myelination as indicated by intensity of luxol fast blue staining was weaker in drug-treated animals.
  • 6.6. The level of myelin marker enzyme, 2′,3′-cyclic nucleotide 3′-phosphohydrolase, was lower in the brainstem of PTU-treated animals.
  • 7.7. The results suggest a correlation between acid phosphatase but not alkaline phosphatase activity with myelination in the developing mouse brain.
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2.
  • 1.1. From the muscle of 20 species of fresh-water fishes, l-histidine, carnosine, anserine, and balenine were analysed by high-performance liquid chromatography.
  • 2.2. All cyprinoidei fishes contained significant amount of l-histidine and trace of dipeptides.
  • 3.3. High concentration of anserine was found in salmonoidei fishes, irrespective of salmonidae and osmeridae.
  • 4.4. Two species of anguilloidei contained large amount of carnosine, small of l-histidine, and determinable of anserine and balenine.
  • 5.5. Only trace amounts of these compounds were found in percoidei fishes.
  • 6.6. The levels of these compounds represented no large difference among species belonging to sub-order group as well as family.
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3.
  • 1.1. Eggs of wild cod, and of farmed cod fed (a) a diet supplemented with astaxanthin and (b) a diet supplemented with both astaxanthin and canthaxanthin, were analysed with respect to carotenoids.
  • 2.2. The total carotenoid contents in eggs were 0.7 ppm for wild cod and 0.5 ppm for farmed cod.
  • 3.3. Cod, having white flesh, deposit ketocarotenoids in the eggs, preferably astaxanthin.
  • 4.4. Canthaxanthin can replace astaxanthin in the eggs, but astaxanthin appears to be deposited preferentially when both carotenoids are present in the diet.
  • 5.5. The isomer distribution of (3S, 3′S):(3R, 3′S, meso):(3R, 3′R) astaxanthin in the eggs reflected the isomer composition of the diet.
  • 6.6. Echinenone, 4′-hydroxyechinenone, adonixanthin and zeaxanthin encountered in cod eggs may represent reductive metabolites of canthaxanthin and astaxanthin.
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4.
  • 1.1. Total lipid content, and lipid class and fatty acid compositions in the muscle were analyzed for marine and landlocked forms of sockeye salmon.
  • 2.2. Little difference was found for the total lipid content in the muscle between both forms.
  • 3.3. Triglycerides were higher in the marine form than those in the landlocked one, but phospholipids showed an opposite tendency.
  • 4.4. In the fatty acid composition of total lipid, percentages of 20:1 and 22: 6n-3 were higher in the marine form, while 18:2, 18:3n-3, 18:4n-3 and 20:4n-3 were more abundant in the landlocked one. Fairly high levels of 22:1 were present only in the marine form.
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5.
  • 1.1. The fatty acid composition of normal hairless mouse skin and actinically induced skin tumors were compared.
  • 2.2. There were no gross differences in the qualitative pattern of fatty acids between the two tissues. The C18:1 fatty acids were the most prevalent in both tissues.
  • 3.3. The percentage fatty acid per total lipid content was almost two-fold greater in tumorous tissue than in normal skin.
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6.
  • 1.1. Protein phosphorylation in intact chicken latissimus dorsi muscle, slow anterior (ALD) and fast posterior (PLD), was compared.
  • 2.2. A major difference in [32P]phosphate incorporation was found between the ALD and PLD in a 25,000-dalton heat soluble protein.
  • 3.3. The 25,000-dalton protein was purified from both the ALD and PLD.
  • 4.4. The two proteins had similar amino acid composition and both contained approximately 1 mole phosphate per mole of protein.
  • 5.5. The difference in their content of radioactive phosphate was determined to be due to faster turnover in the ALD.
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7.
  • 1.1. The myelin protein profiles in the CNS and PNS of three species of amphibians were analyzed by biochemical and immunohistochemical methods.
  • 2.2. The CNS myelin of the African clawed frog (Xenopus) and the Mexican salamander (axolotl) contained, in addition to proteolipid protein, a unique protein zero (P0)-like protein, whereas the adult bullfrog did not.
  • 3.3. A strong expression of the P0-like protein in the bullfrog CNS myelin was found transiently at ontogenetically early phases including at the time of metamorphosis.
  • 4.4. The CNS P0-like protein and the PNS P0 protein showed a difference in reactivity with lectins and anti-L2/HNK-1 antibodies, suggesting that the two proteins differ in some aspects of their carbohydrate structures.
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8.
  • 1.1. The haploid amount of DNA was determined for 31 species of elasmobranchs and 8 other non-teleost fishes.
  • 2.2. The elasmobranchs have a modal DNA amount of about 4 pg, compared to 1 pg for the teleosts.
  • 3.3. The DNA content of the other non-teleosts ranges from 1.2 at the low end to 142 pg for lungfishes that have been assayed.
  • 4.4. Several characteristics that are common to DNA distributions in many different groups of organisms, such as a skewed distribution and the positive correlation between specialization and a low amount of DNA, are apparent here. The lungfishes appear to be an exception to the latter characteristic.
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9.
  • 1.1. The metabolic fate of 1-14C-acetate administered to the marine bivalve mollusc Mytilus edulis was investigated.
  • 2.2. The active incorporation of the label in 20:2 non-methylene-interrupted dienoic (NMID) fatty acids was found.
  • 3.3. Acetate incorporation patterns and specific radioactivity of mussel acids suggest that 22:2Δ7,13 and 22:2/gD7,15 arose by C2 elongation of 20:2Δ5,11 and 20:2Δ5,13 respectively.
  • 4.4. The proposed pathway of NMID fatty acid biosynthesis in molluscs is discussed.
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10.
  • 1. We have examined the oxygen-affinity of the fresh, whole blood from representatives of 40 genera of Amazonian fishes.
  • 2. When all the air-breathing fishes and all the water-breathing fishes were considered, no differentiation in oxygen affinity could be distinguished, although in two cases of closely related species, i.e.Osteoglossum, a water breather, vsArapaima, an air breather, andHoplias, a water breather, vsHoplerythrinus, an air breather; the air breathers have bloods with lower oxygen affinity than do the water breathers.
  • 3. Significant differences in the oxygen affinity were found when fishes were considered by habitat: the oxygen affinities were in general correlated with available environmental oxygen and relative oxygen demand of the fishes.
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11.
  • 1. We have measured the temperature dependence of the oxygen equilibria of blood and hemoglobin solutions from four neotropical and three temperate zone fishes.
  • 2. Significant differences exist in the heats of oxygenation of the bloods but not the hemoglobin solutions from different species.
  • 3. The differences in thermal sensitivity of the oxygenation of the bloods appear to depend on differences in intracellular pH, organic phosphates and other ligand-linked variables and not the intrinsic enthalpies of the oxygenation of the hemoglobins themselves.
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12.
  • 1.1. The composition of bile pigments in the blood and bile of 39 species were studied.
  • 2.2. Conjugated bilirubin (trace to 4.62 mg/100 ml) was detected in the serum of most fish, while biliverdin (trace to 2.0 mg/100ml) was detected only in Anguilla Japonica, Thalassoma lunare and Clinocottus analis.
  • 3.3. Analysis showed tht there are two types of bile pigments excretion pattern in these fishes. The first pattern excretes bilirubin (most conjugate) predominantly, the other excretes mostly biliverdin with some bilirubin. However, during starvation, the excretion of conjugate bilirubin gradually shifted to unconjugated biliverdin. The rate of shifting varies with species.
  • 4.4. Introduction of bilirubin into Anguilla japonica produced an initial excretion of mono-conjugates, followed by di-conjugates. Introduction of biliverdin caused an increased in the excretion of unconjugated biliverdin, but no significant increase of bilirubin in the bile was detected.
  • 5.5. A binary excretion pathway of bile pigments in fish is proposed. The evolutionary characteristics of heme catabolism in terrestrial animals with respect to this pathway is discussed.
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13.
  • 1.1. A manganese containing superoxide dismutase from bovine heart mitochondria was isolated and characterized.
  • 2.2. It has a molecular weight of about 86,000 and is composed of 4 noncovalently bound subunits of equal size.
  • 3.It appears to contain 2 mole manganese per mole enzyme.
  • 4.The carbohydrate content is very low.
  • 5.The specific activity and amino acid composition are similar to those of other mitoehondrial superoxide dismutases.
  • 6.The enzyme forms complexes with ampholytes and can therefore not be analysed by isoelectric focusing.
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14.
  • 1.1. Females, copepodid stages V and IV of Calanus finmarchicus were collected in Fram Strait area of the Arctic and in the northern North Sea to compare their lipid composition.
  • 2.2. For the comparison only copepods were considered which contained more than 8% of 18:4 fatty acid and high amounts of wax esters to exclude seasonal and spatial variabilities and different reproductive status of females.
  • 3.3. Animals are heavier in the Fram Strait area than in the North Sea with similar lipid proportion of dry weight and wax ester proportion of total lipid.
  • 4.4. Only some statistical significant differences exist between the fatty acid and alcohol compositions. The levels of 16:0 acid and alcohol and of 22:1 alcohol are higher and of 20:1 acid and alcohol are lower in the North Sea than in the Arctic.
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15.
  • 1.1. Main serum α1-protein (α1P) of rainbow trout was purified and its biochemical and physico-pathological properties were studied.
  • 2.2. α1P was suggested to be a primitive protein having both properties of albumin and AFP in serum proteins of mammals according to the following results.
  • 3.3. Molecular weight (75,000), two kinds of molecules (pI 4.55 and 5.05) and amino acid composition.
  • 4.4. Dye- or ConA binding activity.
  • 5.5. Estrogen binding activity and inhibitory effect on lymphoblastoid-forming activity.
  • 6.6. Possible osmotic regulator.
  • 7.7. Significant elevation of blood α1P level in the course of hepatoma induction.
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16.
  • 1.1. An esterase which hydrolyzes 4-nitrophenyl(phenyl)phosphonic acid (4-NPPP) was purified from M. senile (sea anemone).
  • 2.2. The enzyme showed no 5′-nucleotide phosphodiesterase activity with 5′-(4-nitrophenyl) TMP or phosphomonoesterase activity with 4-nitrophenylphosphate.
  • 3.3. Addition of excess Zn2+ restored activity after inactivation by EDTA.
  • 4.4. Thiol reagents and phenylmenthanesulfonylfluoride did not inactivate, whereas, dithiothreitol inactivated.
  • 5.5. Aminoethylphosphonic acid (AEP) was a competitive inhibitor of 4-NPPP indicating possible activity with phosphonomonoesters of AEP.
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17.
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18.
  • 1.1. Homogenous human skeletal muscle AMP-deaminase was obtained by chromatography on phosphocellulose.
  • 2.2. Native enzyme molecular weight was 290,000, while a value of 71,000 was found for the subunit molecular weight.
  • 3.3. No distinct differences were found in amino-acid composition of human skeletal muscle AMP-deaminase as compared with other vertebrate enzymes.
  • 4.4. Human muscle AMP-deaminase contains about 2g-atom of zinc per 280,000; considerable amounts of calcium and magnesium were also found.
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19.
  • 1.1. The fatty acid composition of the triglyceride fraction of mink milk sampled during mid-lactation (day 28 post partum) from two nursing mink was compared to that of plasma samples and to the fatty acid composition of the feed rations used.
  • 2.2. Chemical analysis of the triglyceride composition of mink milk demonstrated only minute concentrations of fatty acids with a chain length below C14.
  • 3.3. The saturated C16:0- and C18:0-unit fatty acids in mink milk made up for 24–40% of the total amount of fatty acids extracted, the remainder being represented by mono and polyunsaturated long-chain (C16-C24) fatty acids.
  • 4.4. Preliminary in vitro experiments proved the incorporation of14C-labelled glucose, acetate or palmitate into triacylglycerols in cultures of mink mammary tissue to be linear for at least 2 hr.
  • 5.5. The in vitro capacity for de novo fatty acid synthesis in mink mammary tissue using 14C-labelled glucose or acetate was low, i.e. ranging from 0.096–0.109 nmol/g (fresh tissue)/min, and amounted to only about 5% of that obtained in the case of [14C]palmitic acid incubation.
  • 6.6. Following 14C-labeIled acetic or palmitic acid incubation of mink mammary tissue neither desaturation nor chain elongation was observed.
  • 7.7. In response to long-term feeding on rations with two different sources of animal fat (F = fish oil or L = lard) the influence of compositional changes in dietary neutral lipids on the fatty acid composition of the lipids of mink milk is discussed.
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20.
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Highlights
  • •Knockout of arginine methyltransferase Hmt1p in S. cerevisiae was investigated.
  • •RNA-seq and SILAC MS/MS found downregulation of phosphate-associated processes.
  • •Phosphate homeostasis and extracellular levels of acid phosphatases were perturbed.
  • •Pho4p was an in vitro Hmt1p substrate, but this was not confirmed in vivo.
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