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1.
  • 1.1. The effects of sublethal concentrations of organic and inorganic pollutants on intracellular energy-rich phosphates in blue mussels, Mytilus edulis, were investigated by in vivo 31P-NMR.
  • 2.2. Formaldehyde (30 and 10mg/l), phenol, pyridine, mercury and cadmium gave marked reductions in phosphoarginine and, in some cases, the ATP amounts. The reduction in high-energy phosphate was accompanied by an increase in inorganic phosphate in all groups.
  • 3.3. A “phosphorus index”, the product of the ratios between phosphoarginine and inorganic phosphate, and ATP and inorganic phosphate, is suggested, which might serve as an early warning (“alarm”) parameter in environmental monitoring.
  • 4.4. Diversity in the responses to different pollutants make phosphorus compounds in M. edulis also an interesting element in a finger print parameter system designed to distinguish between pollutants in the marine environment.
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2.
  • 1.1. The muscle tension and the state of high-energy phosphate metabolism during contraction of the sartorius muscle in frogs (Rana catesbeiana) starved for 1–5 months was studied by in vivo31P-NMR spectrometry.
  • 2.2. Muscle tension began to decrease after 2-month starvation compared with the control group and decreased to about one-third of the control value after a 5-month starvation.
  • 3.3. Muscle contraction induced by electrical stimulation or the use of anaerobic perfusion fluid did not decrease the concentration of creatine phosphate (PCr) or β-ATP, and only negligibly changed the PCr/Pi ratio from starvation.
  • 4.4. These results suggest a decrease in creatine kinase activity in the muscle of starved frogs.
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3.
  • 1.1.|The high-energy phosphorylation metabolism in crayfish, Procambarus clarkii eggs during brooding and juvenile crayfish after hatching was studied by in vivo31P nuclear magnetic resonance (31P NMR) spectroscopy.
  • 2.2.|Inorganic phosphoric acid (Pi) and adenosine-5′-triphosphate ATP(γ-,α-,β-) were detected in the dark brownish red eggs after oviposition.
  • 3.3.|In orange unhatched eggs, only sugar phosphate (SP), Pi and resolved phosphometabolite from ATP were observed.
  • 4.4.|Peaks of SP, Pi, arginine phosphate (Arg-P), and ATP (γ,α,β) appeared in larvae of crayfish after hatching (nauplius, zoea and juvenile crayfish).
  • 5.5.|The high-energy phosphorylation metabolism changed to an anaerobic condition along with a decrease in the concentration of dissolved oxygen in fresh water.
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4.
  • 1.1. To evaluate changes in high-energy phosphate metabolism in the water scorpion (Ranatra chinensis) under restraint and cold water-warm water stresses, in vivo [31P]NMR spectra were obtained.
  • 2.2. Under restraint stress, arginine phosphate (Arg-P) decreased by 10% after 1 hr and remained at that level thereafter, while β-ATP showed negligible changes over 6 hr.
  • 3.3. As the water temperature gradually increased or decreased, the relative concentration of Arg-P decreased due to enzyme regulation.
  • 4.4. Repeated cold water-warm water stress, which consisted of repeated 15 min exposures to cold water (5°C) followed by 15 min exposures to warm water (30°C) caused distinct decreases in Arg-P and β-ATP concentration. These decreases were dependent on the frequency of exposure.
  • 5.5. Phosphomonoesters (PME) increased not only with restraint stress but also with cold water-warm water stress.
  • 6.6. The effect of cold water-warm water stress on high-energy phosphate metabolism was greater than that of restraint stress.
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5.
  • 1.1. An alkaline p-nitrophenylphosphate phosphatase has been purified 440-fold from extracts of Hatobacterium halobium.
  • 2.2. The enzyme has an apparent molecular weight of 24,000.
  • 3.3. A Km value for p-nitrophenylphosphate of 1.12mM has been found under optimal conditions.
  • 4.4. The enzyme is selectively activated and stabilized by Mn2+.
  • 5.5. It requires high salt concentrations for stability and maximum activity.
  • 6.6. It displays an unusual restricted substrate specificity of 25 phosphate esters tested, only phosphotyrosine and casein were hydrolysed besides p-nitrophenylphosphate.
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6.
  • 1.1. A thermostable orthophosphoric monoester phosphohydrolase (EC 3.1.3.1) from Thermus sp strain Rt41A has been purified 400-fold to give a specific activity of 25 U/mg at 60°C in IM diethanolamine (pH 11.1).
  • 2.2. The enzyme has a Mr of 160,000 and is trimeric.
  • 3.3. The half-life of the enzyme is 5 min at 85°C.
  • 4.4. The enzyme has a wide specificity for a number of phosphate monoesters.
  • 5.5. The Hm of the enzyme is pH dependent, so the pH optimum of the enzyme is affected by the substrate concentration.
  • 6.6. The enzyme is inhibited 50% by 20 mM Ca2+ or Mg2+.
  • 7.7. The Ki for phosphate, EDTA-di sodium salt and arsenate (in 1 M diethanolamine, pH 11.1) is approx 1.2, 1.6 and 4mM respectively.
  • 8.8. Urea (200 mM) is not inhibitory.
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7.
  • 1.The thermal coadaptation hypothesis predicts that (1) ectotherms experiencing a narrow range of body temperatures in the wild will evolve to perform well over a narrow range of body temperatures and that (2) the optimal temperature for performance will be equal to the preferred body temperature of the species.
  • 2.We tested the predictions of the thermal coadaptation hypothesis with black rat snakes (Elaphe obsoleta) and northern water snakes (Nerodia sipedon) because black rat snakes experience lower and more variable body temperatures than northern water snakes at our study site.
  • 3.We measured swimming speed, tongue-flicking speed, and striking speed in black rat snakes, and swimming speed and tongue-flicking speed in northern water snakes.
  • 4.Adult water snakes generally had narrower performance breadths and higher optimum performance temperatures than adult black rat snakes.
  • 5.Performance breadths were the same for swimming, tongue flicking, and striking within adult black rat snakes, but performance optima for these behaviours differed significantly. Performance breadths differed and performance optima were the same for swimming and tongue flicking within adult northern water snakes.
  • 6.The relative swimming performance of neonates of the two species was similar in breadth to that of adults, but the thermal optimum for neonate black rat snakes was higher than that of adults.
  • 7.Overall, our results provided support for the thermal coadaptation hypothesis.
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8.
  • 1.1. Inorganic phosphate (Pi) was absorbed rapidly by suspension-cultured cells of Catharanthus roseus which had previously been cultured in Pi-free Murashige Skoog medium.
  • 2.2. The intracellular levels of ATP, ADP and 5-phosphoribosyl-l-pyrophosphate (PRPP) increased markedly during the 24 hr which followed the addition of Pi (1.25mM).
  • 3.3. Availability of PRPP in vivo, estimated by the measurement of nucleotide synthesis from [8-14C]adenine, was also increased by addition of Pi.
  • 4.4. Only a 20% increase in the maximum catalytic activity of PRPP synthetase was observed in extracts of cells, prepared 24 hr after addition of Pi.
  • 5.5. In contrast to results for mammalian PRPP synthetase, the activity of PRPP synthetase, partially purified from Catharanthus roseus, was inhibited by concentration of Pi greater than 5mM.
  • 6.6. The mechanisms involved in the increased availability of PRPP and the synthesis of adenine nucleotides in the plant cells cultured in Pi-containing medium are discussed.
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9.
  • 1.1. To define the respiratory function of haemoglobin in male Daphnia magna, the swimming activity, the depression of oxygen uptake by treatment with carbon monoxide and in vivo oxygenation of Hb at various oxygen pressures were investigated.
  • 2.2. The P50, values for the purified Hbs from male and female red animals were 2.0 and 2.7 torr in 0.1 M phosphate buffer (pH 7.2) at 20°C, respectively.
  • 3.3. The isoelectric focusing patterns of the purified Hbs from male and female red animals showed only small differences in Hb components of high PI values.
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10.
  • 1.1. Effects of hypoxia were investigated in red abalones (Haliotis rufescens) using a flow-through exposure system and in vivo31P NMR spectroscopy.
  • 2.2. Following seawater acclimation, abalones were exposed to air for 1 hr, then seawater for 2.5 hr to check recovery; parallel controls were performed without air exposure.
  • 3.3. In foot muscle, hypoxia produced a decrease in phosphoarginine concentration and intracellular pH, an increase in inorganic monophosphate concentration, and no change in that of ATP; upon resubmergence, all effects generally recovered.
  • 4.4. The changes induced by hypoxia during normal tidal changes are consistent with the blockage of mitochondrial oxidative phosphorylation.
  • 5.5. Use of in vivo NMR allows measurement of the biochemical effects of natural stress factors in live, intact aquatic organisms in the laboratory.
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11.
  • 1.1. Carp red cells were treated with drugs that affect the cell membranes. The water content of the cells and the accumulation of cAMP in the cells were measured in normoxia and in hypoxia using non-stimulated and adrenergically stimulated cells.
  • 2.2. WGA, DIDS + CCCP and A23187 increased the water content of nonstimulated normoxic cells.
  • 3.3. In hypoxia ouabain and DIDS + CCCP increased the water content but cytochalasin B, NPM, DIDS, CCCP and A23187 + CA2+ abolished the hypoxia-induced swelling.
  • 4.4. Any membrane perturbation induced some cAMP formation, Sophora and Anquilla lectins being most potent.
  • 5.5. Also in adrenergically stimulated cells, membrane perturbation generally increased cAMP formation.
  • 6.6. However, cAMP accumulation diminished in cells treated with cytochalasin B, CCCP and DIDS + CCCP.
  • 7.7. The adrenergic swelling of carp red cells was reduced in normoxia by DIDS. NPM and CCCP increased the adrenergic swelling in normoxia to hypoxic level.
  • 8.8. In hypoxia WGA and Anquilla lectin decreased the swelling.
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12.
  • 1.1. Co-isolating proteins (Mr 170,000–220,000) from sodium channel preparations made from the electric organ of the electric eel (Electrophorus electricus) were detected on Western blots using monoclonal a antibodies.
  • 2.2. Similar protein patterns were seen on immunoblots containing immunoprecipitated protein from eel muscle and brain tissues but not heart.
  • 3.3. These co-isolating proteins could be separated from the mature TTX-sensitive channel protein (Mr 280,000) using a lentil lectin-Sepharose column.
  • 4.4. The 180 kDa proteins do not appear to be channel-related and can be detected as contaminants in electroplax sodium channel preparations using the monoclonal antibodies described here.
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13.
  • 1.1. DNase-I-like activity occurs in the carp (Cyprinus carpio) liver cytosol (supernatant 105,000g).
  • 2.2. The enzyme resembles DNase I from bovine pancreas in respect to the molecular mass (~31 kDa), pH (7.4) and ion requirements (Mg2+, Ca2+) and the ability to degrade native as well as denatured DNA.
  • 3.3. As judged by comparison of DNase zymograms obtained after native- and SDS-PAGE, the enzyme occurs in the three molecular forms of similar molecular weight and different charges.
  • 4.4. All these forms are inhibited by rabbit skeletal muscle actin as well as by endogenous actin isolated from the carp liver cytosol.
  • 5.5. DNase from the carp liver cytosol does not interact with the antibodies directed against DNase I from bovine pancreas and against DNase I from the rat and bovine parotid glands.
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14.
  • 1.1. We studied the haemoglobin content, erythrocyte indices, erythrocyte enzymes and haemoglobin electrophoresis patterns of the metallic skink Niveoscineus metallicus and compared them to the small amount of published data on other small lizards.
  • 2.2. Haemoglobin was much lower than that recorded for the salamander.
  • 3.3. Erythrocyte enzymes (glucose phosphate isomerase and glucose 6 phosphate dehydrogenase) were lower in the skink than in the salamander. Glyceraldehyde phosphate dehydrogenase, phosphoglycerate kinase and pyruvate kinase were much higher in the skink than in the salamander.
  • 4.4. A single, slow, haemoglobin component was identified by electrophoresis.
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15.
  • 1.1. Neurospora cells were grown at 28°C for 14hr and subjected to heat shock (HS) at 48°C for 45 min. Protein synthesis profiles, monitored by labelling with [35S]methionine and one and two-dimensional electrophoresis, revealed nine heat shock proteins (HSPs).
  • 2.2. Crossed-immunoelectrophoresis revealed five polypeptides in the shocked cell extracts that were not detectable in normal cells.
  • 3.3. Synthesis of HSPs occurred rapidly during the shock treatment and ceased upon transfer to normal conditions. One of the HSPs—~43 K in size—may be a developmentally-regulated protein.
  • 4.4. Metal ions—cadmium, zinc, manganese, copper—did not elicit a stress response when used alone but appeared to modulate the heat shock response.
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16.
  • 1.1. Relative to rabbit erythrocytes, chicken red blood cells exhibit a much greater capacity to utilize [3H]adenine for nucleotide synthesis in vitro, even at 5°C and in the absence of added inorganic phosphate.
  • 2.2. This difference is largely due to a higher concentration of phosphoribosylpyrophosphate and greater activity of adenine phosphoribosyltransferase in the avian cells. lli]3. The capacity of avian erythrocytes for utilization of guanine and hypoxanthine is several fold less than that of adenine.
  • 3.4. The data are consistent with lower activity for hypoxanthine/guanine phosphoribosyltransferase than for adenine phosphoribosyltransferase in intact chicken erythrocytes.
  • 4.5. The results indicate that reutilization of adenine by chicken erythrocytes may be physiologically significant.
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17.
  • 1.1. African sharptooth catfish individuals, heterozygous for glucose phosphate isomerase (GPI-2), were selected as broodstock by using horizontal starch-gel electrophoresis.
  • 2.2. Ova of one heterozygous female were inseminated with cryopreserved and fresh milt from a corresponding male.
  • 3.3. Significant deviations from expected Hardy-Weinberg proportions occured for offspring obtained by using cryopreserved milt.
  • 4.4. Differences in genotypic variation seems to relate to different cryodiluents and the fertility thereof.
  • 5.5. Selection of breeding stock for aquacultural practices based on the above information is discussed.
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18.
  • 1.1. Eyestalk unablated and unilaterally ablated Penaeus monodon juveniles had survival rates after 5 months of 75–72.5 and 67.5–60%, respectively.
  • 2.2. Unilaterally ablated shrimps had significantly higher (P < 0.05) growth rate than unablated shrimps.
  • 3.3. Eyestalk-ablatement resulted in a decrease in the haemolymph sodium concentration and an increase in the potassium and calcium concentration of shrimps.
  • 4.4. The osmolarity of haemolymph and total protein concentration of unablated shrimps were demonstrated to be higher than those of unilaterally ablated shrimps.
  • 5.5. The eyestalk-ablated shrimps possess higher total ATPase and Na+,K+-ATPase activities in the gill than those of unablated shrimps.
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19.
  • 1.1. Berenil, administered to rats in vivo, promoted a decrease in liver SAMDC activity, but an increase in ODC and SAT activity.
  • 2.2. Its effect on ODC was completely prevented by cycloheximide, that on SAT only partially.
  • 3.3. Berenil had no effect on ODC activity in adrenalectomized rats. Adrenergic antagonists counteracted the effect of Berenil on ODC activity.
  • 4.4. Polyamine content was increased. The maximum modification was observed for putrescine and N1-acetylspermidine.
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20.
  • 1.1. Crude extract of the whole digestive tract from the brown shrimp (P. californiensis) was investigated for digestive amylase activity.
  • 2.2. Considerable amylase activity was found at pH 6.5–8.0, with optimum pH at around 7.5.
  • 3.3. Optimum temperature was found between 30–40°C, similar to amylases from other crustaceans.
  • 4.4. Amylase activity was highly halotolerant, having 50% maximum activity at 3 M NaCl.
  • 5.5. Maximum amylase activity was found at 0.01 M NaCl.
  • 6.6. Amylase activity was partially inhibited by the divalent ions Hg2+, Zn2+, Cu2+ and Cr2+.
  • 7.7. Mg2+ and Ca2+ ions seemed to enhance amylase activity.
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