Anaerobic amino acid metabolism in the locust nervous system

• 1.1. Changes in the concentration of amino acids and other metabolites have been followed in the isolated locust nervous system under anaerobic conditions.
• 2.2. The results (accumulation of alanine, pyruvate, lactate, succinate and α-glycerophosphate, decline in asparate, glutamine and glycogen) are qualitatively similar to those found in many other invertebrate and vertebrate tissues, although the pathways in the insect tissue show some differences.
• 3.3. The locust nervous tissue does not show that very large accumulation of α-glycerophosphate shown by whole insects, and which is due to the influence of the flight muscle.
• 4.4. It can be concluded that the locust nervous system has only a limited capacity for anaerobic metabolism, and cannot support normal nervous activity for more than a few minutes in the absence of O₂.

     

Digestive protease,lipase and amylase activities in stage i larvae of the american lobster,Homarus americanus

• 1.1. Digestive protease, lipase, and amylase of Stage I larvae of the American lobster Homarus americanus are characterized.
• 2.2. A sensitive method for detection of crustacean lipase was developed using an latroscan which combines thin-layer chromatography and flame ionization detection to quantify free fatty acids generated by lipase digestion.
• 3.3. pH optima of the three enzymes occurred at or near the pH of gastric fluid.
• 4.4. A time course study demonstrated slight increases in protease and amylase activities during the first larval stage, regardless of whether the lobsters were fed or not, whereas lipase activity was constant.

     

Thermal properties for digestive enzymes of a sub-antarctic beetle,hydromedion sparsutum (coleoptera,perimylopidae) compared to those in two thermophilic insects

• 1.1. Proteolytic, lipolytic, amylolytic and cellulolytic activities were studied in adults of the phytophagous beetle, Hydromedion sparsutum, indigenous to the sub-Antarctic island of South Georgia.
• 2.2. Gastric enzyme activities were measured at experimental temperatures of 5–40°C and results were compared with those obtained from two thermophilic insects, Gryllus bimaculatus and Tenebrio molitor.
• 3.3. Protease and lipase activities in Hydromedion were 10–15 times lower than in Gryllus and Tenebrio.
• 4.4. In the temperature range of 5–15°C, α-amylase activity from Hydromedion was only slightly lower than that from Gryllus.
• 5.5. Hydromedion gut homogenates exhibited a distinct cellulolytic activity, even at a low temperature of 5°C.
• 6.6. Cellulolytic activity in the digestive tract of Hydromedion was confirmed by the evolution of ¹⁴CO₂ after consumption of labelled cellulose.
• 7.7. The thermal properties of digestive enzymes agree well with the role of Hydromedion as primary decomposer in its ecosystem.

     

The activities of lipases and carnitine palmitoyl-transferase in muscles from vertebrates and invertebrates

1. The activities of tri-, di- and mono-glyceride lipase and carnitine palmitoyltransferase were measured in homogenates of a variety of muscles. These activities were used to estimate the rate of utilization of glycerides and fatty acids by muscle. In muscles whose estimated rates of fat utilization can be compared with rates calculated for the intact muscle from such information as O₂ uptake, there is reasonable agreement between the estimated and calculated rates. 2. In all muscles investigated the maximum rates of hydrolysis of glycerides increase in the order triglyceride, diglyceride, monoglyceride. The activity of diglyceride lipase is highest in the flight muscles of insects such as the locust, waterbug and some moths and is lowest in the flight muscles of flies, bees and the wasp. These results are consistent with the utilization of diglyceride as a fuel for some insect flight muscles. 3. In many muscles from both vertebrates and invertebrates the activity of glycerol kinase is similar to that of lipase. It is concluded that in these muscles the metabolic role of glycerol kinase is the removal of glycerol produced during lipolysis. However, in some insect flight muscles the activity of glycerol kinase is much greater than that of lipase, which suggests a different role for glycerol kinase in these muscles.     

Characterization of Colorado potato beetle lipophorin: A hydrocarbon-rich diacylgycerol-poor lipophorin

• 1.1. The lipid composition of lipophorin from the Colorado potato beetle, Leptinotarsa decemlineata Say, was analyzed.
• 2.2. This insect lipophorin contains 44% lipid and is characterized by large amounts of hydrocarbons and small amounts of diacylglycerol.
• 3.3. This is the first observation of a diacylglycerol-poor insect lipophorin in haemolymph.
• 4.4. Since the main energy source for flight in the Colorado potato beetle is proline, the low diacylglycerol content in lipophorin must be related to its peculiar flight metabolism.
• 5.5. This lipophorin, however, can still take up appreciable amounts of diacylglycerol from the locust fat body. Hydrocarbon uptake by this lipophorin was also demonstrated.
• 6.6. The main function of this lipophorin therefore seems to be transport of hydrocarbons from oenocytes to the cuticle.

     

Protease,amylase and lipase activities in the midgut and hindgut of the cricket,Gryllus rubens and mole cricket,Scapteriscus acletus

• 1.1. Midgut is the major source of protease, amylase and lipase in a cricket, Gryllus rubens and in a mole cricket, Scapteriscus actetus.
• 2.2. Hindgut makes a significant contribution, and possibly even the major contribution, to digestion in both crickets, with enzyme activities from 20% (amylase and lipase) to 30% (protease) of midgut level, and a pH favorable to action of all three.
• 3.3. Ingested food helps regulate digestive enzyme levels, and crickets starved for 5 days had only 50–60% of normal levels of enzyme activity.

     

Comparative morphological,anatomical and biochemical studies of the urticating apparatus and urticating hairs of some lepidoptera: Thaumetopoea pityocampa Schiff., Th. processionea L. (Lepidoptera,Thaumetopoeidae) and Hylesia metabus Cramer (Lepidoptera,Saturniidae)

• 1.1. Morphological similarities and differences for the urticating apparatus of three Lepidoptera were studied using a scanning electron microscope.
• 2.2. Complementary anatomical studies of the urticant apparatus were undertaken to explain the morphological results.
• 3.3. Biochemical identity of a thaumetopoein-like protein (an urticating protein) was demonstrated for Thaumatopoea urticating hairs but not for Hylesia moth spicules.
• 4.4. Urticating mechanisms appear to be different across species of Lepidoptera.

     

Changes in the activities of lysosomal enzymes in the fat body and midgut of two lepidopteran insects (Mamestra brassicae and Pieris brassicae) during metamorphosis

• 1.1. The activities of three lysosomal enzymes (acid phosphatase, β-galactosidase, catepsin D) was observed during metamorphosis in the fat body and midgut cells of two insects (Mamestra brassicae and Pieris brassicae).
• 2.2. The activities increased slightly during the feeding period and showed a sharp rise at the beginning of the wandering period.
• 3.3. Subsequently, a decrease was observed during the pre-pupal stage and pupation.
• 4.4. The activities increased again 2 days after the larval-pupal moult.
• 5.5. We suggest that an inhibitory mechanism works in the studied cells before pupation to protect the stored proteins from the degradation until the beginning of differentiation of imaginai cells in the pupal stage.

     

A comparison of tissue lipoprotein lipase activities determined in either fresh or defatted tissue preparations

• 1.1. Lipoprotein lipase activities were determined in either fresh aqueous homogenates or homogenates of acetone-diethyl ether dried powders of adipose tissue, heart, skeletal muscle and lung tissue taken from both fed and 24 hr starved rats.
• 2.2. The total tissue enzyme activities detectable in powder preparations were considerably higher than those of fresh preparations in all the tissue except lung.
• 3.3. The identity of the enzyme activity was more clearly demonstrable with homogenates of solvent-dried powders.
• 4.4. The use of both types of preparation in an experiment where rats were injected with either saline or colchicine further demonstrated the advantages of the acetone-diethyl ether-dried tissue preparation in total tissue lipoprotein lipase activity determinations.

     

Purification and some properties of isocitrate dehydrogenase of a blowfly Aldrichina grahami

• 1.1. NADH-dependent isocitrate dehydrogenase has been purified 110-fold from the crude extract of the flight muscle mitochondria of Aldrichina grahami.
• 2.2. The purification procedure involved Triton X-100 treatment of isolated mitochondria, column chromatography on DEAE-cellulose, Affi-gel blue, and P-cellulose.
• 3.3. The purified enzyme was homogeneous by criteria of the polyacrylamide gel electrophoresis.
• 4.4. The enzyme of the blowfly contains more acidic amino acids and less hydrophobic amino acids than that of pig heart.
• 5.5. The molecular weight was determined to be 330,000 daltons. The subunit construction differs from ghat of mammalian isocitrate dehydrogenase.

     

Purification of two lipases with high phospholipase A1 activity from guinea-pig pancreas

• 1.1. Two cationic lipases (Ia and Ib) were purified from homogenates of fresh guinea-pig pancreas by ion-exchange chromatography on DEAE-Sepharose and CM-Sepharose (twice for the latter) followed by gel filtration on Sephadex G-100.
• 2.2. Both enzymes were homogeneous upon polyacrylamide gel electrophoresis. Their molecular weights are 37000 and 42000 for lipases Ia and Ib, respectively, as determined by gel filtration on Sephadex G-100. Very close values for isoelectric points were found in the pH range 9.3–9.4.
• 3.3. The cationic lipases are characterized by a high phospholipase A activity (500 IU/mg protein using a potentiometric assay with egg yolk lecithin as substrate), resulting in an unusual phospholipase/lipase activity ratio of 1.
• 4.4. Using doubly labelled phosphatidylcholine, a specificity, A₁, was described for the two enzymes, which are unaffected by N-ethylmaleimide, diisopropylfluorophosphate and p-bromophenacylbromide. The enzymes are insensitive to EDTA and slightly inhibited by CaCl₂and MgCl₂, whereas sodium deoxycholate is required for maximal activity.

     

The occurrence of relaxing granules in the muscle of the locust,Locust migratoria

• 1.1. A granular or vesicular fraction was isolated from the muscles of the locust, Locust migratoria, and allowed to react with isolated myofibrils in order to examine whether or not this fraction could act as a relaxing factor as in the case of mammalian muscle.
• 2.2. The granules obtained from the muscle of this insect were very effective in inhibiting myofibrillar ATPase, whether the myofibrils were prepared from the same muscles or from the rabbit muscles.
• 3.3. Superprecipitation of a puridied actomyosin preparation was greatly retarded by the addition of these granules.
• 4.4. Evidence was put forward that the granules are acting, in the presence of ATP, by removing calcium from myofibrils because of their strong calcium-binding capacity.
• 5.5. These observations seem to suggest that the insect granules are also capable of acting as relaxing factor and that all muscles, whether in the vertebrates or in the invertebrates, can be considered as identical systems in so far as the chemical mechanism of contraction-relaxation is concerned.

     

Purification and partial characterization of an AMP deaminase from the marine invertebrate Palaemon serratus

• 1.1. AMP deaminase from Palaemon serratus tail muscle was partially purified by chromatography on cellulose phosphate.
• 2.2. Muscle homogenates expressed very low enzyme activities and the presence of ATP was necessary to detect AMP deaminase. The specific activity and substrate affinity of the purified enzyme were also very low.
• 3.3. The purified prawn muscle AMP deaminase was contaminated by contractile proteins, one of the major contaminants being actin.
• 4.4. The enzyme displayed a very high affinity for actomyosin which was only partially abolished by pyrophosphate.

     

Metabolic capacity,fibre type area and capillarization of rat plantaris muscle. Effects of age,overload and training and relationship with fatigue resistance

• 1.1. The influences of age (5, 13 and 25-month-old rats), overload as obtained by denervation of synergists, and training on the metabolic capacity, relative muscle cross-sectional area occupied by each fibre type, capillarization and fatigue resistance of the rat m. plantaris were investigated.
• 2.2. Creatine kinase, phosphorylase and citrate synthase activities were lower in muscles of 25 than in those of 13-month-old rats (P < 0.001).
• 3.3. Overload resulted in an increased relative area of type I and II a fibres at all ages (P = 0.001).
• 4.4. Capillary density decreased with overload and increasing age (P < 0.001).
• 5.5. Fatigue resistance was higher in muscles of 13 than in those of 5-month-old rats (P < 0.05), and increased with overload (P < 0.05) at all ages.
• 6.6. Fatigue resistance of the whole muscle was not closely related to its oxidative capacity in contrast to what is generally found for single fibres or motor units.

     

Purification and characterization of lipoprotein lipase from the white adipose,skeletal muscle,cardiac muscle,mammary gland and lung tissues of the rat

• 1.1. Lipoprotein lipase (LPL) was isolated from five rat tissues: white adipose, skeletal muscle, cardiac muscle, mammary gland and lung.
• 2.2. Specific activity of the preparations varied from 75 U/mg for skeletal muscle and 720 U/mg for adipose.
• 3.3. The preparations were further analysed using SDS-PAGE and a single component identified. The mol. wt of 61,000 Da of this component was consistent for all five of the tissue sources.
• 4.4. Significant differences in the values of the isoelectric points of the enzyme species were revealed. The values varied from 7.23 (SEM 0.022) for cardiac and lung to 7.51 (SEM 0.037) for mammary.
• 5.5. Two-dimensional electrophoresis, using isoelectric focusing in the first dimension and SDS-PAGE in the second revealed differences in the patterns of stained material derived from the five tissue sources.

     

Comparative study on AMP deaminase in gill,muscle and blood of fish

• 1.1. High AMP deaminase activities were determined in the gill of one selachian, Scyliorhinus caniculus, and five teleosts, Anguilla anguilla, Cyprinus carpio, Salmo gairdneri, Perca fluviatilis and Esox lucius.
• 2.2. The highest activity was generally found in skeletal white muscle, except in A. anguilla and S. caniculus.
• 3.3. In s. caniculus a very high AMP deaminase activity was found in the blood where it was shown to be tightly regulated by inorganic phosphate.
• 4.4. Seasonal variations were observed for AMP deaminase activity in gill and white muscle, but also for blood Hb and protein concentration in the three tissues examined.

     

Locust vitellogenin receptor: an acidic glycoprotein with N- and O-linked oligosaccharides

• 1.1. The locust vitellogenin (VTG) receptor which is embedded in oocyte plasma membranes is a glycoprotein.
• 2.2. With various lectins oligosaccharide units have been identified, among them neuraminic acid linked to Gal or GalNAc, mannose chains, Gal linked to GalNAc or GlcNAc and fucose linked to GlcNAc.
• 3.3. With specific enzymes it could be shown that mannose and most other oligosaccharides are O-linked while others like fucose are N-linked.
• 4.4. Enzymatic removal of all O-linked carbohydrates resulted in a drop of the molecular mass of the receptor protein from 200,000 to 110,000.
• 5.5. A total of N- and O-linked oligosaccharides of 54% was calculated.
• 6.6. The isoelectric point of the receptor was found to be at pH 3.4 increasing slightly after removal of neuraminic acid.
• 7.7. Removal of neuraminic acids destroyed the binding ability for VTG.

     

Glycolytic and hexosemonophosphate enzyme activities in the lantern muscles of the sea urchins,Arbacia lixula (Linn.), Echinometra lucunter (Linn.) and Lytechinus variegatus (Lamarck)

• 1.1. Activities of nine glycolytic and related enzymes were measured in lantern muscle extracts of the echinoids Arbacia lixula, Echinometra lucunter and Lytechinus variegatus.
• 2.2. The specific activities of these enzymes were comparatively low, being often the highest in L. variegatus and the lowest in A. lixula. The major differences referred to HK, PGK and G-6-PDH activities.
• 3.3. Noticeable differences in LDH activities were recorded in comparison with other invertebrate muscles. The implications of these results are discussed.

     

Programmed loss of flight ability in the early adult life of the blowfly Phormia terrae novae as a possible mechanism of intraspecific niche building with respect to the duration of life

• 1.1. The age related flight performance of males and females of the blowfly Phormia terrae novae was studied and the influence of artificially fed glucose determined.
• 2.2. Maximum flight ability—measured as flight distance, duration and initial velocity—was achieved during the first week after emergence, thereafter the flight performance drops precipitously between the 12th and 17th day of adult life.
• 3.3. Males and females, fed and unfed individuals, show no difference in their time course of flight ability.
• 4.4. The possible causes of the programmed loss of flight performance were discussed with regard to histological and enzyme activity changes observed at the same and other species.
• 5.5. The biological significance of this physiological age effect was revealed.

     

Some tethered flight characteristics of a rose chafer beetle,Pachynoda sinuata (Coleoptera: Scarabaeidae)

• 1.1. The relationships between wingspan, body mass and wing-beat frequency for the beetle. Pachynoda sinuata, have been established.
• 2.2. Thrust and lift generated during tethered flight have been measured using a simple technique and the beetles' responses to the unnatural constraints are discussed.
• 3.3. The biophysical correlates of P. sinuata tethered flight are compared with similar relationships obtained from flying animals and machines.