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1.
  • 1.1. Lipid changes occur in the developing tadpole of A. dacnicolor. The phosphatidylcholine content of liver and tail decrease during metamorphosis.
  • 2.2. In liver, the fatty acids of phosphatidylcholine and phosphatidylethanolamine become more unsaturated.
  • 3.3. In skin, phosphatidylcholine becomes more unsaturated and phosphatidylethanolamine becomes more saturated.
  • 4.4. In tail, phosphatidylcholine becomes more saturated and phosphatidylethanolamine shows no change.
  • 5.5. Triglycerides become more unsaturated in skin but become more saturated in tail.
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2.
  • 1.1. Preparative Isoelectric focusing (PIEF) was used to isolate hydroxylasic and dehydrogenasic activities, at different pI.
  • 2.2. The fraction at pI 4.7 and 4.9 displays a pure dehydrogenase activity (substrate l-DOPA).
  • 3.3. This fraction did not react with tyrosine, either in the spot-test or in absorption spectra (200–620 nm), and did not exhibit any oxygen consumption.
  • 4.4. The fraction at pI 4.1 and 4.3 reacted with both l-DOPA and tyrosine as substrate, showing dehydrogenase and hydroxylase activity.
  • 5.5. The latter activity was confirmed by the oxygen consumption test, showing that molecular oxygen is used to ortho-hydroxylate tyrosine.
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3.
  • 1.1. The unidirectional transepithelial fluxes of L-phenylalanine, β-methyl-D-glucoside and sodium ions across emusculated sheets of tench mid-intestine were determined in flux chambers.
  • 2.2. No net sodium flux was detectable, but phenylalanine was preferentially transferred from the mucosal to the serosal fluid.
  • 3.3. There was also a net movement of β-methyl-glucoside towards the serosal medium, but it was much smaller than that of phenylalanine.
  • 4.4. This transport was accompanied by an accumulation of each substrate from the mucosal medium into the tissue to a similar level and against a concentration gradient.
  • 5.5. The poor transfer of the monosaccharide into the serosal medium could therefore be attributed to a low permeability of the baso-lateral membrane of the enterocyte for this substance.
  • 6.6. The influx of L-phenylalanine and of β-methyl-d-glucoside into the epithelial cells of tench midintestine was examined by incubating slices of emusculated intestine in radioactively-labelled solutions of the substrate for 2 min.
  • 7.7. The steady-state uptake was assessed after similar incubations lasting 45 min.
  • 8.8. Phenylalanine influx obeys the Michaelis-Menten equation with a Km of 2.9 mM and is dependent on the presence of sodium ions in the incubation medium.
  • 9.9. β-Methyl-glucoside influx reveals the same characteristics with a Km of 2.0 mM but a considerably lower Vmax; in addition, it is inhibited by galactose.
  • 10.10. The influx of both substrates is reduced by harmaline, which also inhibits the uptake of radioactive sodium by this preparation.
  • 11.11. The steady-state uptake of β-methyl-glucoside is also inhibited by ouabain and by 2.4-dinitrophenol.
  • 12.12. These results suggest that the mechanisms for sodium-dependent influx of monosaccharides and neutral amino-acids in the tench intestine are similar to those found in mammalian tissues.
  • 13.13. The principal difference appears to involve the release of monosaccharides across the baso-lateral membrane of the enterocyte.
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4.
  • 1.1. This study examined the effect of the monoamines dopamine and octopamine, as well as tyrosine on the oxygen affinity and cooperativity of oxygen binding by the hemocyanin of the marine gastropod Busycon canaliculatum. The effect of temperature on hemocyanin oxygen affinity was also examined.
  • 2.2. Freezing Busycon hemocyanin did not affect the binding of oxygen.
  • 3.3. Dopamine, octopamine and tyrosine had no significant effect on the oxygen affinity or cooperativity of oxygen binding by the hemocyanin of B. canaliculatum.
  • 4.4. It was concluded that Busycon hemocyanin either has no binding sites for the two monoamines or for tyrosine, or that binding of the molecules has no functional significance.
  • 5.5. Both temperature sensitivity and affinity of hemocyanin-oxygen binding were similar to values previously reported for hemocyanin of Busycon from other localities.
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5.
  • 1.1. Electrophysiological responses to NaCl, sucrose, and a complex mixture containing NaCl, glucose, fructose, phenylalanine and valine were obtained from large, medium, and small hair sensilla on the proboscis of the fleshfly Sarcophaga bullata.
  • 2.2. Responses from up to three cells in each sensillum were analysed and compared across the three types of sensilla.
  • 3.3. We found qualitative differences in the patterns of responses from the different hair types.
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6.
  • 1.1. A lipoxygenase activity was purified from Thermoactinomyces vulgaris and some of its properties were characterized.
  • 2.2. The enzyme showed a temperature activity range of 40–55°C with still significant activity over 60°C.
  • 3.3. The pH of activity on linoleic acid had a broad range with an optimum at pH 6.0 and a weaker one at pH 11.0.
  • 4.4. On arachidonic acid the pattern was narrow bell-shaped with an optimum at pH 6.5.
  • 5.5. The purified lipoxygenase from Th. vulgaris showed an apparent Km of 1 mM and Vmax of 0.84 μmol diene/min/mg protein.
  • 6.6. It was inhibited by the oxidation products, 9-HPOD and 13-HPOD.
  • 7.7. A 160,000 Da molecular weight of the enzyme was determined by molecular filtration. Methionine, tyrosine, tryptophan and cysteine are apparently involved in its activity.
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7.
  • 1.1. DEAE-cellulose chromatography of mycelial alkaline phosphatase (orthophosphoric monoester phosphohydrolase, EC 3.1.3.1) from Basidiobolus haptosporosus, produced three iso-enzymes “A”, “B” and “C”.
  • 2.2. Fraction “A” was further characterized and showed maximum activity at pH 10 in 0.1 M sodium carbonate-bicarbonate buffer.
  • 3.3. The enzyme was stimulated by Mg2+, Co2+ and Mn2+ and inactivated by Zn2+, Cu2+, EDTA, citrate and tartrate.
  • 4.4. Phosphate ions inhibited it competitively, phenylalanine uncompetitively and urea noncompetitively.
  • 5.5. It was heat stable for 60 min at 37°C but labile above 55°C.
  • 6.6. Its Km with p-nitrophenylphosphate was 0.5 mM; its estimated molecular weight was 160,000.
  • 7.7. The results are compared with the properties of alkaline phosphatases from the rainbow lizard and man and discussed in terms of a triadic association between the fungus, the lizard and man.
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8.
  • 1.1. Free amino acids were analysed in the haemolymph of Galleria mellonella larvae by HPLC chromatography with o-phthaldialdehyde (OPA)-l-thio-β-d-glucose as derivatization agent.
  • 2.2. Fourteen primary amino acids were detected among which glutamine, alanine, γ-aminobutyric acid (GABA) and glycine predominated and constituted 67.7% of the amino acids found.
  • 3.3. The concentration of GABA increased significantly with the age of larvae entering the wandering phase and reached a maximum during metamorphosis.
  • 4.4. Analysis of cold-acclimated larvae revealed a net increase of free primary amino acids from 96 to 151.8 μmol/ml during consecutive acclimation to 0°C within 20 days and to 205.4μmol/ml during cold shock injury at 0°C (3 hr).
  • 5.5. The bulk of this increase was accounted for by alanine, glycine, phenylalanine and lysine.
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9.
  • 1.1. Human placental alkaline phosphatase was inactivated with tetranitromethane in a biphasic process.
  • 2.2. Spectral and amino acid analysis demonstrated that the inactivation was due to the conversion of tyrosine residues to 3-nitrotyrosine.
  • 3.3. The inactivation process showed saturation kinetics.
  • 4.4. Protection of the enzyme against tetranitromethane inactivation was afforded by inorganic phosphate.
  • 5.5. The binding affinity between the modified enzyme and inorganic phosphate was decreased.
  • 6.6. Our results suggest the involvement of tyrosyl residues in the locus of phosphoryl site of the phosphorylated enzyme forms.
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10.
  • 1.1. Unlike common fishes and as its Latin name implies, the upside-down catfish, Synodontis nigriventris, possesses dark ventral skin. Microscopic observation reveals that melanophores are present on both the ventral and the dorsal skin but differ in size and density of distribution.
  • 2.2. The darkness of both sides of the fish changes in accordance with that of the background.
  • 3.3. At night, the fish are very active and the body becomes pale. The change in color is more noticeable in the dorsal than the ventral skin.
  • 4.4. When melatonin was added to the bathing water, the fish became pale and swam restlessly even when they were exposed to the black background.
  • 5.5. It was found that the catfish preferred the black background to the white one.
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11.
  • 1.1. Specific Dynamic Action (SDA) effects of diet were investigated in the supralittoral isopod, Ligia pallasii, using defined chemical diets.
  • 2.2. “Apparent SDA”, or the total rise in metabolic rate following a meal, was resolved in animals eating a nutritionally complete chemical diet into three components: 8% mechanical costs of moving food through the gut, 40% “excitement costs” due to investigator disturbance and presence of food, and 52% SDA.
  • 3.3. Excitement costs in animals exposed to food but which chose not to eat showed non-significant variation between diets containing different levels of chemical nutrients, but were significantly less on a diet containing only cellulose and agar.
  • 4.4. SDA increased with increasing concentration of amino acids in the diet.
  • 5.5. Substitution of whole-protein casein for free amino acids in the diet had no significant SDA effect, while substitution of free amino acids in the ratio found in casein more than doubled the SDA effect.
  • 6.6. Deletion of alanine from the diet caused no significant effect on SDA, while deletion of phenylalanine caused a highly significant elevation in SDA.
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12.
  • 1.1. Teratocytes (dissociated trophamnion cells liberated from eggs of certain hymenopteran endoparasites into host hemolymph upon hatch) from Lygus hesperus parasitized by Peristenus stygicus or Leiophron uniformis were analyzed and compared.
  • 2.2. Fatty acid profiles were similar in the 2 types of teratocytes except for myristic acid (C14:0) which was found in higher concentrations in P. stygicus and linolenic acid (C18:3) which was found in higher concentrations in L. uniformis.
  • 3.3. Of 22 amino acids found in both species, there were 12 that differed significantly between the 2 species (aspartic acid, threonine, α-aminoadipic acid, alanine, valine, isoleucine, leucine, tyrosine, phenylalanine, lysine, histidine, and arginine). Most of these were essential amino acids, and in every case, concentrations were higher in P. stygicus than in L. uniformis associated teratocytes.
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13.
  • 1.1. A choriolytic enzyme was isolated from the hatching medium of the pike, Esox lucius.
  • 2.2. The enzyme is defined as hatching enzyme.
  • 3.3. The molecular weight of the enzyme is 24,000.
  • 4.4. The enzyme is a glycoprotein containing 2% carbohydrate.
  • 5.5. Its isoelectric point is 6.5.
  • 6.6. The pH optimum is around pH 8.
  • 7.7. The enzyme molecule contains two disulfide bonds but no free cysteine.
  • 8.8. Inhibitor studies and metal analysis show that the enzyme is a zinc-metalloprotease.
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14.
  • 1.1. Signal transduction in response to platelet-derived growth factor (PDGF)-BB and bradykinin (BK) have been examined by measuring inositol polyphosphate formation in NIH3T3 fibrobalst and v-Ki-ras -transformed NIH3T3 fibroblast (DT).
  • 2.2. The PDGF-induced inositol polyphosphate formation in NIH3T3 was greater than that in DT cells, in which autophosphorylation of PDGF receptor and tyrosine phosphorylation of phospholipase C (PLC)-γ 1 were suppressed when examined by immunoblotting with anti-phosphotyrosine antibody.
  • 3.3. On the other hand, BK-stimulation produced a much higher level of inositol polyphosphate in DT cells which have a greater number of BK receptors.
  • 4.4. These results indicate that in Ki-ras transformed cells the decrease (caused by PDGF) and the increase (caused by BK) in phosphoinositide hydrolysis are due to the defective autophosphorylation of PDGF receptors leading to a reduction in PLC-γ 1 tyrosine phosphorylation and the overexpression of BK receptors, respectively.
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15.
This paper comments on: Low, B. S., Alexander, R. D., and Noonan, K.M. Human hips, breast, and buttocks: Is fat deceptive? Ethology and Sociobiology 8: 249-247, 1987. In it I argue that:
  • 1.1. Sexual selection has probably not been the most important selection pressure on
  • 2.female human body shape.
  • 3.2. Male humans in different cultures find different aspects of the female body attractive
  • 4.and therefore are unlikely to have exerted consistent directional sexual selection on
  • 5.the female body.
  • 6.3. Breast size is not correlated with lactation success.
  • 7.4. Visible hip width is not correlated with parturition success.
  • 8.5. Women would lower their fitness if they tried to deceive men about their internal
  • 9.pelvic dimensions.
  • 10.6. There are many alternative hypothesis to explain the existence of fat onwomen's
  • 11.breast, hips, and buttocks.
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16.
  • 1.1. Alkaline phosphatase (orthophosphoric monoester phosphohydrolase EC 3.1.3.1.) was extracted from the small intestines of the rainbow lizard Agama agama, partially purified by DEAE-cellulose and Sephadex G-200 column chromatography and characterized.
  • 2.2. The enzyme had an optimum pH at 9.5 in sodium carbonate/bicarbonate buffer: a Km of 1.6 mM with p-nitrophenyl phosphate; a molecular weight of 132,000; was inhibited by Zn2+, EDTA, urea and phenylalanine; stimulated by Co2+, Mn2+ and Mg2+, but Ca2+ had little or no effect on the activity of the enzyme.
  • 3.3. The inhibition by urea was non-competitive, that by phenylalanine was uncompetitive. The enzyme was heat-labile.
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17.
  • 1.1. Two species of hydrothermal vent bivalve molluscs have high glycine content periostraca but that of Calyptogena magnifica is rich in methionine and tyrosine while that of Bathymodiolus thermophilus has the highest glycine content recorded for any natural polypeptide.
  • 2.2. The amino acid compositions are compared with other periostracal proteins, as found in species adapted to “normal” environments, in terms of hydrophobic character, polar content and conformational potential.
  • 3.3. The significance of the composition and possible physico-chemical characteristics of the hydrothermal species periostraca for adaptation to and protection against the unusual environmental conditions are discussed.
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18.
  • 1.1. The number of tyrosine and tryptophan residue-equivalents on the surfaces of the α-amylase and of two of its protein inhibitors has been determined.
  • 2.2. The solvent-exposed tyrosine and tryptophan residue-equivalents in the dimeric inhibitor are respectively four and two times as much as those ones of the monomeric inhibitor.
  • 3.3. On the basis of the homology among their polypeptide chains, it is suggested that the outer tryptophan residues in either inhibitors are located at the positions 4 and 51 of the primary structure.
  • 4.4. On the interaction of the monomeric inhibitor with the amylase, two tryptophan residue-equivalents became no more accessible to the solvent.
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19.
  • 1.1. Procarboxypeptidase (W-PCPA) was purified from the pancreas of the sei whale Balaenoptera bolealis.
  • 2.2. W-PCPA was obtained as a homogeneous protein in polyacylamide gel disc electrophoresis.
  • 3.3. W-PCPA has a molecular weight of 75,000.
  • 4.4. Amino acid composition of W-PCPA was compared with that of bovine procarboxypeptidase as A S5 (PCPA-S5).
  • 5.5. W-PCPA may be two subunits, and the aggregate form may resemble PCPA-S5.
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20.
  • 1.1. A circannual study of tyrosine aminotransferase and other metabolic enzymes in frog liver is reported. The subcellular distribution of all enzymatic activities under investigation was also studied.
  • 2.2. Results show significant oscillations of all enzymatic activities throughout the year; in particular tyrosine aminotransferase has a marked summer maximum.
  • 3.3. The subcellular distribution of tyrosine aminotransferase shows significant variations: the soluble activity of the enzyme presents a bimodal circannual distribution, which has its counterpart in an increased activity of heavier fractions.
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