Studies on lactate dehydrogenase activity in the shrimp Palaemon serratus

The influence of seasonal variations in the temperature of the environment on the kinetic parameters of LDH have been followed in the shrimp Palaemon serratus. The results obtained show that this system compensates partially the effects of the temperature on its activity. The complex pattern of the monthly variations of Km values along the year can be resolved into a 2 plateaux system corresponding to the extreme temperature of the environment.     

Lactate content and lactate dehydrogenase activity inPalaemon serratus abdominal muscle during temperature changes

Summary Lactate concentration was measured in the abdominal muscle of the shrimpPalaemon serratus. Rapid and seasonal temperature changes result in an increase of the lactate content of approximately 3–4 fold.Lactate dehydrogenase from the abdominal muscle exhibits a temperature dependent pyruvate inhibition with pyruvate as substrate.The kinetic parameters of lactate dehydrogenase fromPalaemon serratus are found to vary during rapid temperature changes: V_max increases with temperature from 0.06 mol min^–1 (mg protein)^–1 at 10°C to 0.28 mol min^–1 (mg protein)^–1 at 30°C with lactate as substrate, and from 5.5 mol min^–1 (mg protein)^–1 at 10°C to 26.2 mol min^–1 (mg protein)^–1 at 30°C, with pyruvate (Table 1). The Hill coefficientn _H, decreases with temperature from 2.2 to 1.2 when the pyruvate reduction is examined, but remains near 1.2 when the activity is measured with lactate as substrate (Table 1). The S_0.5 values for lactate show a tendency to increase below 30 °C (18.9 mM l^–1 at 20 °C) whereas the S_0.5 for pyruvate is found to increase greatly with temperature (0.004 mM l^–1 at 10 °C and 0.06 mM l^–1 at 20 °C).Long term temperature changes involve variations of lactate dehydrogenase activity leading to inverse thermal compensation (Table 2).Activation energy (about 56 kJ both with pyruvate and lactate) does not vary during the year, suggesting that temperature adaptation does not induce important catalytic changes (Table 3).Abbreviation LDH lactate dehydrogenase     

Effect of thermal acclimation on subunit cooperativity in Palaemon serratus glutamate dehydrogenase

Glutamate dehydrogenase (GDH) from the abdominal muscle of the shrimp Palaemon serratus displays a complex cooperatively pattern with respect to the cofactor (NAD) and substrate (glutamate) concentrations: at low concentrations negative cooperativitiy is predominant whereas positive cooperativity prevails at high concentrations. GDH is sensitive to thermal variations of the environment and to conditions of thermal acclimation. The maximum cooperativity indexes (positive and negative) are obtained at 13° for NAD irrespective of the acclimation temperature (13 or 18°). In contrast, for glutamate, positive cooperativity is only observed at temperatures near the acclimation temperature. At 13° for animals adapted at 18° and at 27° for animals adapted at 13° a complete loss of subunit cooperativity and a Michaelian kinetic pattern are observed.     

Short term cadmium intoxication of the shrimp Palaemon serratus: Effect on adenylate metabolism

• 1.1. Shrimps were exposed for 96 hr to various concentrations of cadmium under laboratory conditions. The LC₅₀ was around 4 ppm Cd in water, which corresponded to 0.180 μg/g wet weight of cadmium in tail muscles.
• 2.2. The effect of various concentrations of cadmium on adenylates was analyzed in tail muscles: At subletal cadmium concentrations, no variation of ATP, ADP and of the adenylate sum occurred, while the AMP concentration began to decrease from 0.06 ppm.

At the LC₅₀, the ATP, ADP and AMP concentrations dropped acutely, the ATP/ADP ratio increased acutely.The apparent equilibrium constant of the adenylate kinase reaction increased significantly from 2 ppm Cd, indicating an impairment in energetic metabolism.Cadmium intoxication did not influence the value of the adenylate energy charge.     

The hearing abilities of the prawn Palaemon serratus

The mechanism of sound reception and the hearing abilities of the prawn (Palaemon serratus) have been studied using a combination of anatomical, electron microscopic and electrophysiological approaches, revealing that P. serratus is responsive to sounds ranging in frequency from 100 to 3000 Hz. It is the first time that the Auditory Brainstem Response (ABR) recording technique has been used on invertebrates, and the acquisition of hearing ability data from the present study adds valuable information to the inclusion of an entire sub-phylum of animals when assessing the potential impact of anthropogenic underwater sounds on marine organisms. Auditory evoked potentials were acquired from P. serratus, using two subcutaneous electrodes positioned in the carapace close to the supraesophageal ganglion and the statocyst (a small gravistatic organ located below the eyestalk on the peduncle of the bilateral antennules). The morphology of the statocyst receptors and the otic nerve pathways to the brain have also been studied, and reveal that P. serratus possesses an array of sensory hairs projecting from the floor of the statocyst into a mass of sand granules embedded in a gelatinous substance. It is the purpose of this work to show that the statocyst is responsive to sounds propagated through water from an air mounted transducer. The fundamental measure of the hearing ability of any organism possessing the appropriate receptor mechanism is its audiogram, which presents the lowest level of sound that the species can hear as a function of frequency. The statocyst of P. serratus is shown here to be sensitive to the motion of water particles displaced by low-frequency sounds ranging from 100 Hz up to 3000 Hz, with a hearing acuity similar to that of a generalist fish. Also, recorded neural waveforms were found to be similar in both amplitude and shape to those acquired from fish and higher vertebrates, when stimulated with low-frequency sound, and complete ablation of the electrophysiological response was achieved by removal of the statocyst.     

Effect of acclimatization temperatures on incorporation of amino acids into proteins of abdominal muscle from the shrimp Palaemon serratus

The effect of thermal acclimatization on the incorporation of [³H]-l-leucine into muscular acid-soluble amino acids, soluble proteins and into the lactate dehydrogenase was studied in the shrimp Palaemon serratus As far as protein synthesis is concerned, a period of time of 10 to 15 days is required for the achievement of the process. During acclimatization to 10° or 20° three periods can be distinguished. During the first 3–4 days the temperature increment exert a direct decreasing or increasing effect on the protein synthesis. The system then tends to reach a new equilibrium respectively below or above the initial level: the synthesis mechanisms were able to partially compensate the effect of thermal variations. The synthesis of LDH follows the general pattern of incorporation of the labelled precursor into the macromolecules     

Circadian variations of haemolymph lipoprotein of Palaemon serratus

The electrophoretic behaviour of haemolymph lipoprotein was determined throughout a 24 h light-dark cycle. All of the 14 lipoprotein bands did not always appear at the same time, and their level did not remain constant, showing mainly tri- and tetracircadian variations. Values are not the same in males and females. Despite the fact that the lipoprotein variation was not closely synchronized with circadian periodicity, some lipoproteins were responsible for light-dark transition.     

Ultrastructure of the microsporidian Inodosporus octospora (Thelohaniidae), a parasite of the shrimp Palaemon serratus (Crustacea, Decapoda)

A parasite of the muscle of the shrimp Palaemon serratus has been examined by light and electron microscopy. Development occurs among myofibrils and induces ultrastructural alterations of the muscle fibers causing white discoloration. This microsporidian is characterized by uninucleate, later diplokaryotic and di-diplokaryotic meronts. The mother cell develops by rosette-like budding into 8 uninucleate sporoblasts, each containing 3 tape-like filaments attached to the wall that is enclosed in a persistent sporophorous vacuole. Each sporoblast gives rise to a uninucleate spore that possesses 3 elongated tape-like filaments attached to the spore wall, like spore tails. The morphological characters of the spores, redescribed in the present study, suggested that the spores belonged to Inodosporous octospora. The possibility that in the future members of Inodosporus sp. may be considered a new parasite group is discussed.     

Changes in basic nuclear proteins during sperm maturation in Palaemon serratus (Crustacea natantia)

The spermatozoa from the shrimp Palaemon serratus have been studied with respect to their morphological and biochemical characters.At the ultrastructural level the acrosomal vesicle of the nail-shaped spermatozoon displays a periodically striated bundle. This appearance seems to be characteristic for the Palaemonidae.The biochemical parameters of the chromatin, extracted from the spermatozoa, have been compared with those obtained from the testes and the hepatopancreas. The basic proteins of testes and sperm have been characterized by polyacrylamide gel electrophoresis. Protamines appear to be absent in the sperm of P. serratus. On the contrary, histones with a somatic character remain present. Moreover, supplementary histone fractions have been identified. These proteins have been further studied after purification on Biogel P-100. Their amino acid composition shows similarities to that of the H_2A and H_2B histone and has a molecular weight of 15,500±300.     

Variations of D (-)-beta-hydroxybutyrate dehydrogenase activity of rat liver mitochondria during post-natal development

1. D(-)-beta-hydroxybutyrate dehydrogenase specific activity of rat liver mitochondria changes during ontogenesis: at birth, the activity is low, then increases to a maximum at 12 days, decreases until 50 days to keep constant thereafter. At the same time, mitochondrial protein amount increases regularly while succinatecytochrome c reductase specific activity slightly increases after birth to keep constant afterwards. 2. The observed changes in activity of D(-)-beta-hydroxybutyrate dehydrogenase are not related to possible interactions between the enzyme and phospholids since addition of lecithin to mitochondria does not change the activity. 3. Electrophoresis of mitochondrial proteins isolated from rats at different development stages demonstrates the presence of a protein band characterized by the same electrophoretic mobility as beta-hydroxybutyrate dehydrogenase and by significative changes of its proportion during maturation: the relative amount of this protein increases from the new-born to the 10-12 days old rat, to decrease afterwards. 4. These findings may signify that the increased activity of the enzyme with a maximum at 10-12 days followed by a decrease is related to the rate of the enzymes biosynthesis.     

Blood lactate dehydrogenase activity in newborn children

Arterial and venous blood samples from babies' umbilical cord vessels before lung breath beginning were used to measure arterial-venous difference between lactate dehydrogenase activity, pH and oxygen blood saturation (sO2). Enzyme activity was 735.4 +/- 90.8 U/L in venous blood and 672.0 +/- 108.1 U/L in arterial one, pH 7.21 +/- 0.06 and 7.32 +/- 0.06, sO2 32.9 +/- 12.7 and 56.5 +/- 18.3%, respectively. Reverse correlation between enzyme activity, pH and sO2 was found.     

Analysis of total lactate dehydrogenase isoenzyme activity in mouse ova during clevage]

The total activity of lactate dehydrogenase isoenzymes was detected in the intact ova of mice during the clevage and, in particular, blastomeres at the 2-cell stage. Routine histochemical technique was employed in addition to microspectrometry. During the clevage, the ova differ in their enzyme activity. At the 2-cell stage there are ova with similar reaction in both the blastomeres as well as those with different enzyme activity in each blastomere.     

A study of lactate dehydrogenase levels and turnover rates during postnatal development in the rat

Specific radioimmunoassays for lactate dehydrogenase A and B subunits have been employed to quantify cellular contents of these proteins more precisely than hitherto possible and to monitor changes during postnatal development. Liver, skeletal muscle, heart muscle and kidney cortex all demonstrated alterations in cellular levels of lactate dehydrogenase subunits over the first 56 days of life, the particular pattern being specific to each tissue. Studies on the turnover of lactate dehydrogenase in vivo and in vitro indicated that the developmental changes in total lactate dehydrogenase content in liver and kidney were regulated at some point(s) during both the biosynthesis and the degradation of the proteins.