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1.
  • 1.1. Labelling of free fatty acids, diacylglycerols, triacylglycerols, phosphatidylethanolamine, phosphatidylcholine and their lysoderivatives was followed during the development of Ceratitis capitata after feeding larvae with mixtures of either (3H)glycerol and (14C)palmitate or (3H)glycerol and (14C)linoleate. Both, specific activity and dpm/individual were plotted vs the time of development.
  • 2.2. Palmitate and linoleate moieties of the diacylglycerol fraction had two exponential components with a similar initial rapid decay component. The turnover times corresponding to the slow decay components were different for both acids in the free form and acylating diacylglycerols.
  • 3.3. Triacylglycerols exhibited a monophasic behaviour with different half-life values for either palmitate or linoleate.
  • 4.4. Palmitate and linoleate show different turnover in the phosphoglycerides phosphatidylethanolamine and phosphatidylcholine. Palmitate exhibited a monophasic decay curve whereas linoleate exhibited a biphasic decay for both phospholipid classes.
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2.
  • 1.1. Three common species of North Atlantic krill, Meganyctiphanes norvegica (M. Sars), Thysanoessa inermis (Krøyer) and T. raschii (M. Sars), have been stored at 0°C post mortem, and the lipolytic activity followed by measuring changes in the lipid composition during storage.
  • 2.2. Both phosphoglycerides and triacylglycerols were subjected to extensive hydrolysis with the formation of free fatty acids in all krill species examined, whereas wax esters, constituting a considerable proportion of the lipids in the Thysanoessa species, were not hydrolysed at all.
  • 3.3. In M. norvegica the triacylglycerols and phosphoglycerides were hydrolysed at similar rates, whereas in T. inermis and T. raschii the phosphoglycerides were hydrolysed most rapidly.
  • 4.4. For all krill species examined, the rate of production of free fatty acids was nearly constant during the initial phase of storage, and subsequently declined on prolonged storage.
  • 5.5. At the end of the storage period of 16–24 days, the free fatty acids constituted about 35% of the total lipid in M. norvegica, and about 50% in the Thysanoessa species.
  • 6.6. The rate of production of free fatty acids was about the same in all the three species of krill and seemed to be independent of the total lipid content.
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3.
  • 1.1. Metabolism of tritiated water and 22sodium was studied in six beef cows under Mediterranean summer conditions in order to find whether the turnover of these tracers can be used to evaluate pasture intake.
  • 2.2. The diet of the cows included ad libitum access to two components which were given separately in different troughs: one was poultry litter and the other was wheat straw, to simulate the dry pasture.
  • 3.3. Voluntary daily dry matter intake (111 g/kg0.75) was unexpectedly high considering the low digestibility of the feed.
  • 4.4. The assumptions of constant ratios of water intake to water turnover and of dry matter intake to water intake were confirmed. Consequently, dry matter intake was determined accurately from water turnover measurements.
  • 5.5. Sodium intake was practically equal to sodium turnover and most of the sodium secreted in feces was of endogenous origin.
  • 6.6. Pasture intake can be predicted from sodium turnover once the concentration in feed and water consumed is known.
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4.
  • 1.1. A pulse-chase autoradiographic study of incorporation of 3H-leucine into body-wall, digestive and reproductive tissue of virgin adult Panagrellus redivivus demonstrates both tissue and sex-specific patterns of protein biosynthesis and turnover.
  • 2.2. Female body wall has a higher rate of protein synthesis and turnover than male body wall.
  • 3.3. Uptake of leucine into macromolecule in the digestive tissue is more rapid in males than females, as is the rate of turnover.
  • 4.4. The ovary is more rapidly labelled than the testis, with a much more rapid turnover rate.
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5.
  • 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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6.
  • 1.1. Cholesterol metabolism has been characterized in three species of New World primates, the cotton-top tamarin, the saddle-back tamarin, and the squirrel monkey.
  • 2.2. When fed a diet containing cholesterol, the three species exhibited differing responses of plasma cholesterol levels.
  • 3.3. Dietary cholesterol absorption was determined and plasma cholesterol die-away kinetics were analyzed in terms of a two-pool model.
  • 4.4. The results of the analyses of cholesterol turnover are consistent with the observed species-specific differences in plasma cholesterol values and cholesterol absorption.
  • 5.5. Cholesterol metabolism differs between the two tamarin species, as well as between the tamarins and the squirrel monkey.
  • 6.6. Implications of species-specific differences between tamarin species are discussed in terms of the use of tamarin species as animal models for comparative studies of cholesterol metabolism and the etiology of cancer and cardiovascular disease.
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7.
  • 1.1. The effect of brefeldin A (BFA) on generation of transport vesicles, synthesis of phospho-glycerides, sphingosine and ceramides, and utilization of the sphingolipid precursors in the formation of sphingomyelin and glycosphingolipids in Golgi was investigated.
  • 2.2. In the presence of 5–10 gmg/ml BFA, the incorporation of [3H]palmitate into glycerides, phosphoglycerides and sphingolipids decreased 45–60%, and the production of endoplasmic reticulum transport vesicles was reduced 30–50%.
  • 3.3. In Golgi membranes, the presence of 5–10 gmg/ml BFA in the mixture, assembled to generate Golgi vesicles, evoked inhibitory effect on the synthesis of sphingomyelin, glycosphingolipids and phosphatidylcholine. On average, the synthesis of the sphingolipids and phosphatidylcholine and production of Golgi transport vesicles declined to 30–40%.
  • 4.4. Addition of 5–10 gmg/ml BFA to the assay mixture prepared to measure the activity of cytidylyltransferase, phosphocholine diacylglyceroltransferase, and serine palmitoyltransferase, caused up to 50% inhibition of the enzymes involved in the synthesis of phosphatidylcholine and up to 70% inhibition of the enzyme generating 3-ketosphinganine.
  • 5.5. The results suggest that BFA inhibits the synthesis of phosphoglycerides and sphingolipids. This, at first, is displayed in reduced production of endoplasmic reticulum and Golgi transport vesicles, while the depletion of sphingolipids abrogates the identity of Golgi membranes.
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8.
  • 1.1. The composition of HDL, the major lipoprotein fraction from chick serum, drastically changed after 2 weeks of coconut oil feeding. Total cholesterol and triacylglycerols significantly increased following dietary 10 or 20% coconut oil supplementation.
  • 2.2. Changes in LDL composition were less profound, cholesterol being the only component that increased by coconut oil supplementation (10 or 20%).
  • 3.3. IDL proteins were the only components that increased following the same dietary treatment (20%).
  • 4.4. VLDL cholesterol and proteins also increased after 1–2 weeks of 20% coconut oil supplementation to the diet.
  • 5.5. Of total lipoproteins, the cholesterol content strongly increased after dietary treatment, while triacylglycerols did not change significantly.
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9.
  • 1.1. Malleefowl Leipoa ocellata have a lower than predicted metabolic rate, a finding common to many arid adapted avian species.
  • 2.2. Evaporative water loss was as expected by allometric analysis. However, in the wild this species probably reduces its evaporative water loss because their water turnover rate is extremely low.
  • 3.3. Malleefowl coped with temperatures up to 40°C well, but above this temperature they become highly agitated.
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10.
  • 1.1. Metabolic rates were highest during periods of maximum reproduction.
  • 2.2. The exponent of the metabolic rate-weight equation varied seasonally, rates of metabolism of small animals exhibited greater annual fluctuations than those of large animals.
  • 3.3. Absolute and weight-specific Q10s (determined at 5–10°C above field temperatures) for smaller clams were greatest in the winter; absolute values of Q10 were highest for larger individuals in the summer.
  • 4.4. Small clams had Q10 < 1.0 in the summer; Q10-values for larger clams were near 1.0 at this time.
  • 5.5. 38.9% of the total energy assimilated by the population annually was allocated to metabolism, which is near the low end of the range of values reported for freshwater molluscs, suggesting that this species can partition a large amount of energy to growth and reproduction.
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11.
  • 1.1. The specific activity of Na-K ATPase was determined from the microsomal preparation of gills dissected from adult Macrobrachium rosenbergii.
  • 2.2. Maximal ATPase activity was achieved at a substrate concentration of 0.5 mM ATP.
  • 3.3. Optimal enzyme activity was obtained at pH of 7.5.
  • 4.4. The Arrhenius plot of Na-K ATPase activity revealed a marked discontinuity at 30°C. “Mg” ATPase activity did not exhibit a marked discontinuity.
  • 5.5. The Ea for Na-K ATPase and “Mg” ATPase was 14.6 kCal/mole and 9.31 kCal/mole respectively. Q10 values for Na-K ATPase was 2.34 and for “Mg” ATPase 1.65.
  • 6.6. ATPase activity and gill homogenate protein concentration exhibited a linear relationship up to 130 μg protein/ml.
  • 7.7. Na-K ATPase activity was inhibited by 10−3 M ouabain. It was equally inhibited by the removal of K+ from the reaction medium.
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12.
  • 1.1. The major form of acetylcholinesterase (AChE) from Lygus hesperus demonstrated a greater affinity to selected substrates than unresolved AChE.
  • 2.2. The turnover numbers of the native AChE were 7000 min−1 for acetylthiocoline, 4800 for acetyl-(β-methyl) thiocholine, 3000 for propionylthiocholine, and 390 for S-butyrylthiocholine.
  • 3.3. Each molecule of the major form had two active sites and each subunit had one active site.
  • 4.4. Paraoxon or dichlorvos had a higher affinity to the major AChE form than to the unresolved AChE, resulting in a higher potency for the inhibition.
  • 5.5. Some references of comparison are also made with AChE from other animal species.
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13.
  • 1.1. In the rat chronic metabolic acidosis increases the net synthesis of 17 renal cortex proteins by amounts ranging from 1.5 to 4.5-fold.
  • 2.2. These proteins have molecular weights between 13,000 and 42,000 and isoelectric points between approximately 5.5 and 7.0.
  • 3.3. No new proteins not also present in normal animals are detected in renal cortex samples from acidotic animals.
  • 4.4. Three proteins undergo substantial reductions in their net synthetic rates in chronic metabolic acidosis.
  • 5.5. On the basis of their physical properties and similar alterations in net synthetic rate in acidosis some of these proteins appear to be closely related and may be coordinately expressed in the rat kidney.
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14.
  • 1.1. Results of investigations on direct calorimetry and simultaneous measurements of oxygen consumption and carbon dioxide and ammonia production of fish are summarized.
  • 2.2. By means of indirect calorimetric formulae, the heat production and the protein, carbohydrate and fat oxidation are calculated from the oxygen consumption and carbon dioxide and ammonia production.
  • 3.3. The lowest heat production values are obtained by long-term monitoring of groups of fish during darkness and under fasting conditions.
  • 4.4. It is concluded that the heat production of standard metabolism at 20°C is 700J/hr/MW (MW = metabolic weight, kg0.85).
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15.
  • 1.1. The percentage distribution of T. cruzi phospholipids remained constant during the latent, logarithmic and stationary phases of growth.
  • 2.2. Short term incubations with 32Pi revealed a higher turnover of phosphatidylinostitol when cells were in lag phase, whereas in exponential or stationary phases its specific radioactivity was equal to phosphatidylethanolamine.
  • 3.3. When 32Pi was present in the culture medium all throughout the three phases, phosphatidylethanolamine and phosphatidylinositol displayed equally high phosphate moiety turnover.
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16.
  • 1.1. NAD(P)H dehydrogenase from rabbit liver was purified to electrophoretic homogeneity using a procedure also found applicable for the rat liver enzyme.
  • 2.2. Rabbit and rat liver enzymes showed different behaviour in isoelectric focusing and different Km values and turnover numbers.
  • 3.3. Both enzymes were inhibited to similar extents by warfarin.
  • 4.4. The rabbit enzyme is composed of two subunits of mol. wt 27,000 and contained 1 FAD group per subunit.
  • 5.5. Some absorption and circular dichroism properties of the rat enzyme are shown.
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17.
  • 1.1. The effects of niacin deficiency on the relative turnover rates of proteins in various tissues of Japanese quail were investigated.
  • 2.2. The level of liver NAD was not affected by niacin deficiency whereas the level of pectoral muscle NAD was markedly reduced.
  • 3.3. In all dietary treatments the liver had the highest turnover rates of proteins, heart and brain had intermediate rates, and pectoral muscle had the lowest rates.
  • 4.4. Relative turnover rates of proteins in all tissues (particularly pectoral muscle) of the niacin deficient group were significantly higher than those of pair-fed control group, although there were no significant differences in turnover rate between pair-fed control and control groups.
  • 5.5. The high turnover rate of proteins in niacin deficiency was primarily attributed to enhanced degradation rate of proteins rather than enhanced synthesis rate of proteins.
  • 6.6. Optical density scanning (or densitometric) of water-soluble pectoral muscle proteins separated by isoelectric focusing revealed several additional minor protein bands between major protein bands in the niacin deficient group which were more pronounced in the acidic region of the gel.
  • 7.7. These results suggest that proteins with a low pI value in pectoral muscle of the niacin deficient animal are highly sensitive to protein degradation.
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18.
  • 1.1. Fingerlings of intergenious hybrid Russian sturgeon (Acipenser guldenstadti) × beluga (Huso huso) weighing 22 g reared in water with salinity 18 ppt were fed nine diets differing in protein and fat content.
  • 2.2. The increase of dietary protein content (from 45 to 52%) improved the fingerlings growth rate, food and protein conversion efficiencies. No effect of further protein content increase to 60% was observed.
  • 3.3. The increase of dietary fat content from 10 to 20% positively influenced all growth results.
  • 4.4. The muscular lipid content increased following the increase in dietary fat due to accumulation of triacylglycerols.
  • 5.5. Distinctive leucopenia in neutrophils and leucophilia in lymphocytes following dietary protein and fat content increase were observed.
  • 6.6. It was concluded that within the analysed range of values the increase of dietary protein and lipid content improved the physiological status of sturgeon hybrid fingerlings.
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19.
  • 1.1. In late winter, oxygen consumption of honey bee (Apis mellifera L.) clusters showed marked 24-hr periodicity, even when held under constant temperature conditions.
  • 2.2. Minimal rates of metabolism (as low as 3.4 w kg −1) were usually reached at night (ca. 0500 hr), and maximum rates (as high as 33.5 w kg−1) in midday (ca. 1400 hr).
  • 3.3. Colonies with brood showed less excursion in daily metabolic rate, by maintaining higher night-time levels.
  • 4.4. There is a pronounced decrease in metabolic rate for the intact cluster of 9480–23,394 bees from the rates reported for individuals or small groups of bees.
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20.
  • 1.1. Kinetic constant values of the reaction catalyzed by bass liver glucose 6-phosphate dehydrogenase show to be modified between 10 and 40°C.
  • 2.2. The Arrhenius plot between 10 and 50°C shows two slopes with different activation energies.
  • 3.3. These results suggest a regulation of this enzyme by environmental temperature.
  • 4.4. Kinetics of ATP inhibition were examined between pH 6.2 and 7.8: patterns and Ki values obtained are affected by the pH variation.
  • 5.5. NADH is an effective inhibitor of bass glucose 6-phosphate dehydrogenase but this enzyme does not show NAD-linked activity.
  • 6.6. Kinetics of pyridoxal 5′-phosphate inhibition have indicated the presence of a lysine in the catalytic site for NADP+.
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