Effects of Electrical Stimulation on Molecular Forms of Butyrylcholinesterase in Denervated Fast and Slow Latissimus Dorsi Muscles of Newly Hatched Chicken

The effects of denervation and direct electrical stimulation upon the activity and the molecular form distribution of butyrylcholinesterase (BuChE) were studied in fast-twitch posterior latissimus dorsi (PLD) and in slow-tonic anterior latissimus dorsi (ALD) muscles of newly hatched chicken. In PLD muscle, denervation performed at day 2 substantially reduced the rate of rapid decrease of BuChE specific activity which takes place during normal development, whereas in the case of ALD muscle little change was observed. Moreover, the asymmetric forms which were dramatically reduced in denervated PLD muscle were virtually absent in denervated ALD muscle at day 14. Denervated PLD and ALD muscles were stimulated from day 4 to day 14 of age. Two patterns of stimulation were applied, either 5-Hz frequency (slow rhythm) or 40-Hz frequency (fast rhythm). Both patterns of stimulation provided the same number of impulses per day (about 61,000). In PLD muscle, electrical stimulation almost totally prevented the postdenervation loss in asymmetric forms and led to a decrease in BuChE specific activity. In ALD muscle, electrical stimulation partially prevented the asymmetric form loss which occurs after denervation. This study emphasizes the role of evoked muscle activity in the regulation of BuChE asymmetric forms in the fast PLD muscle and the differential response of denervated slow and fast muscles to electrical stimulation.     

Characterization of rabbit lactate dehydrogenase-M and lactate dehydrogenase-H cDNAs. Control of lactate dehydrogenase expression in rabbit muscle

Two cDNA clones were isolated, one corresponding to the mRNA coding for lactate dehydrogenase-M (LDH-M), the other to the mRNA coding for lactate dehydrogenase-H (LDH-H). The cDNA inserts consist of the entire open reading frame for LDH-M and a partial sequence, from amino acid 117 to 332, for LDH-H. Using these two clones as probes we demonstrate that: (a) the abundance of mRNA is muscle-type dependent; (b) the ratio M/H subunit for protein and mRNA is well related in the muscles studied; and (c) the M + H mRNA level is not relative to the total LDH activity.     

Proton and carbon-13 nuclear magnetic resonance spectroscopy of diastereoisomeric 3- and 17 beta-tetrahydropyranyl ether derivatives of estrone and estradiol

Protection of 3- and 17 beta-hydroxyl groups of estrone and estradiol as tetrahydropyranyl ether derivatives led to mixtures of 2'(R)- and 2'(S)-diastereoisomers which were separated by crystallization (3-tetrahydropyranyl ethers), or by thin-layer chromatography (17-tetrahydropyranyl ethers), and characterized by 1H and 13C nuclear magnetic resonance (NMR). Assignments for NMR signals of estradiol 3,17 beta-ditetrahydropyranyl ether were facilitated by comparison with those of its 15 zeta, 16 zeta-dideuterio analog and by 2D 1H-13C heteroshift correlation experiments. Diastereoisomers of 3-tetrahydropyranyl ether derivatives could be identified through the 13C NMR doublet signals of the anomeric C-2' and the aromatic C-4 carbon atoms in CDCl3. Diastereoisomers of 17-tetrahydropyranyl ether derivatives were recognized from characteristic modifications of 1H NMR signals of H-2', H-6', H-1, H-17, and 18-CH3 protons as well as from the 13C NMR doublet signals corresponding to C-2', C-4', C-6', C-12, C-13, C-16, and C-17 carbon atoms. Low-temperature experiments showed a splitting of the C-2', C-6', and C-17 13C NMR signals of each of the two 17-tetrahydropyranyl ether isomers. The downfield signal (equatorial conformer) of the three resulting doublets was more intense for the 17-tetrahydropyranyl ether 2'(S)-isomer, whereas the upfield signal (axial conformer) was more intense for the 2'(R)-isomer.     

The Presence of (+)-S-Adenosyl-l-Methionine in the Rat Brain and Its Lack of Effect on Phenylethanolamine N-Methyltransferase Activity

Abstract: (+)-S-Adenosyl- l -methionine [(+)-SAM] was isolated from rat brain and was quantified by HPLC followed by UV spectrophotometric measurements and by ¹H-NMR. Its estimated ratio in brain is 3% of total SAM. Because of its commercial unavailability, (+)-SAM was also prepared from chemically synthesized SAM by separation of the two diastereoisomers on a preparative reverse-phase Nucleosil C8 column. The (+) diastereoisomer thus obtained was then assayed in vitro both as an inhibitor and a substrate of phenylethanolamine N -methyltransferase. Enzymatic activity was measured by HPLC analysis. It was shown that (+)-SAM has no effect on phenylethanolamine N -methyltransferase activity; therefore, it is unlikely that (+)-SAM plays any possible role in regulation of adrenaline synthesis in the brain.     

Chromosome behavior and cell lineage in triploid and mosaic salivary glands of species hybrids in Sciara

Summary A study of the salivary glands of triploid hybrids between females of Sciara ocellaris and males of Sciara reynoldsi throws light on several problems concerning chromosome behavior, species relationships and embryonic development. The specimens studied possess two sets of ocellaris chromosomes and one set of reynoldsi chromosomes. Three types of conditions are represented; 2X3A; 3X3A; and a mosaic possessing cells of both kinds.Heterozygosity of chromosome band pattern in the hybrids shows that the ocellaris homologs are not true sisters and that the sperm probably united with a diploid fusion nucleus composed of two polar bodies and not with the oötid nucleus. This indicates strongly that in a previously described diploid hybrid mosaic some cells developed parthenogenetically from such a fusion nucleus, while others were biparental in origin. The evidence supports the view that the initial influences or reactions of the foreign reynoldsi sperm differ from those of the ocellaris sperm immediately after entry into the egg, but that then and later the differences are relatively slight, although numerous. This agrees with our earlier evidence from the hybrids in indicating that the two parental species are separated genetically, as well as in chromosome band pattern, by many small differences.Species-specific characteristics of chromosome behavior are described which retain their specificity in the hybrids.The 2X3A cells lack a reynoldsi X. The double ocellaris X in such cells (including those in the mosaic) exhibits the peculiar features manifest by the single X in ordinary diploid XO males in the pure species (and in many other Diptera). It is pale and diffuse in structural appearance, and throughout its entire length is uniformly much greater in diameter than it is in the 3X3A cells. The possible significance of this behavior is discussed in relation to problems of sex determination (e. g., Bridges' ratio theory) and those concerning time of gene action. The structural resemblance to the puffs and bulbs found in salivary gland chromosomes is striking and raises the question as to how far morphological characteristics of chromosomes can be used as criteria of gene activity. The double X in the 2X cells of the mosaic, surrounded by 3X cells, exhibits the same peculiarities as those in a pure 2X3A male-type specimen, indicating that we are dealing with intracellular, not intercellular phenomena.Conditions in the mosaic gland support the evidence from the diploid hybrids (some described here for the first time) in indicating that the salivary gland is formed by differentiation of cells which happen to lie in the proper region, regardless of their ancestry. The triploid mosaic specimen (and also a diploid mosaic) is presumed to be a female in which the normal male-producing type of chromosome elimination occurred in one or more mitotic divisions during cleavage or later.     

A kinetic model of the branch-point between the methionine and threonine biosynthesis pathways in Arabidopsis thaliana.

This work proposes a model of the metabolic branch-point between the methionine and threonine biosynthesis pathways in Arabidopsis thaliana which involves kinetic competition for phosphohomoserine between the allosteric enzyme threonine synthase and the two-substrate enzyme cystathionine gamma-synthase. Threonine synthase is activated by S-adenosylmethionine and inhibited by AMP. Cystathionine gamma-synthase condenses phosphohomoserine to cysteine via a ping-pong mechanism. Reactions are irreversible and inhibited by inorganic phosphate. The modelling procedure included an examination of the kinetic links, the determination of the operating conditions in chloroplasts and the establishment of a computer model using the enzyme rate equations. To test the model, the branch-point was reconstituted with purified enzymes. The computer model showed a partial agreement with the in vitro results. The model was subsequently improved and was then found consistent with flux partition in vitro and in vivo. Under near physiological conditions, S-adenosylmethionine, but not AMP, modulates the partition of a steady-state flux of phosphohomoserine. The computer model indicates a high sensitivity of cystathionine flux to enzyme and S-adenosylmethionine concentrations. Cystathionine flux is sensitive to modulation of threonine flux whereas the reverse is not true. The cystathionine gamma-synthase kinetic mechanism favours a low sensitivity of the fluxes to cysteine. Though sensitivity to inorganic phosphate is low, its concentration conditions the dynamics of the system. Threonine synthase and cystathionine gamma-synthase display similar kinetic efficiencies in the metabolic context considered and are first-order for the phosphohomoserine substrate. Under these conditions outflows are coordinated.     

Cloning of a coconut endosperm cDNA encoding a 1-acyl-sn-glycerol-3-phosphate acyltransferase that accepts medium-chain-length substrates.

Immature coconut (Cocos nucifera) endosperm contains a 1-acyl-sn-glycerol-3-phosphate acyltransferase (LPAAT) activity that shows a preference for medium-chain-length fatty acyl-coenzyme A substrates (H.M. Davies, D.J. Hawkins, J.S. Nelsen [1995] Phytochemistry 39:989-996). Beginning with solubilized membrane preparations, we have used chromatographic separations to identify a polypeptide with an apparent molecular mass of 29 kD, whose presence in various column fractions correlates with the acyltransferase activity detected in those same fractions. Amino acid sequence data obtained from several peptides generated from this protein were used to isolate a full-length clone from a coconut endosperm cDNA library. Clone pCGN5503 contains a 1325-bp cDNA insert with an open reading frame encoding a 308-amino acid protein with a calculated molecular mass of 34.8 kD. Comparison of the deduced amino acid sequence of pCGN5503 to sequences in the data banks revealed significant homology to other putative LPAAT sequences. Expression of the coconut cDNA in Escherichia coli conferred upon those cells a novel LPAAT activity whose substrate activity profile matched that of the coconut enzyme.     

Rates of ingestion and their variability between individual calanoid copepods: direct observations

The goals of this study were to determine rates of ingestionand fecal pellet release, and their variability, for individualplanktonic copepods over extended periods of time (>20 min).Ingestions and rejections of individual cells of the diatomThalassiosira eccentrica by adult females of the calanoid Paracalanusaculeatus were directly quantified by observing individual copepodscontinuously at cell concentrations ranging from 0.1 toli mm³l^–1.Average ingestion rates increased with increasing food concentration,but were not significantly different between 0.3 and 1.0 mm³l^–1(9.8 and 32.7 µg Cl^–1) of T.eccentrica. Rates ofcell rejections were low and similar at 0.1 and 0.3, but weresignificantly higher at 1.0 mm³ l^–1. The coefficientsof variation for average ingestion rates of individual copepodshardly differed between food concentrations, ranging from 17to 22%, and were close to those for average fecal pellet releaseintervals which ranged from 15 to 21%. A comparison betweenindividuals at each food concentration found no significantdifferences at 1.0; at 0.1 and 0.3 mm³l^–1, respectively,ingestion rates of four out of five females did not differ significantlyfrom each other. Average intervals between fecal pellet releaseswere similar at 0.3 and 1.0 mm³l^–1 of T.eccentrica, butsignificantly longer at 0.1 mm³ l^–1. Fecal pellet releaseintervals between individuals were significantly different ateach food concentration; these significant differences wereattributed to rather narrow ranges of pellet release intervalsof each individual female. Potential sources/causes of variabilityin the sizes and rates of copepods in the ocean are evaluated. ³Present address: Great Lakes Environmental Research Laboratory,2205 Commonwealth Boulevard, Ann Arbor, Ml 48105, USA     

Maintenance of two genetic entities by habitat selection

Summary In the laboratory, the two species of copepodsLepeophtheirus thompsoni andLepeophtheirus europaensis, ectoparasites of flatfishes, can meet and mate on at least one host species. In the wild however, these two species are found isolated on their sympatric hosts. Habitat selection theoretically represents a powerful enough mechanism to explain the maintenance of genetic heterogeneity in the wide sense. In this paper, the host colonization process is studied for both parasite species. It is shown that each parasite can develop and reach adult age on each host species. However,L. thompsoni is highly selective; it almost totally refuses to colonize hosts other than its natural one.Lepeophtheirus europaensis, on the contrary, readily infests turbot and brill in single-host experiments, but strongly prefers the brill when it has a choice. It appears that these two genetic entities are sympatrically maintained due to strong habitat selection. Such a pattern could theoretically only occur in a soft-selection context (density dependence). This point is discussed with respect to the different patterns in host use found in the geographical distribution of these parasites.