Pyruvate and citrate metabolism in the muscle tissue of Ascaris lumbricoides.

Aconitase and NAD linked isocitrate dehydrogenase were present in Ascaris lumbricoides muscle at only very low activities, whilst there were significant levels of citrate synthase, NADP linked isocitrate dehydrogenase, 2-oxoglutarate dehydrogenase and succinic thiokinase. Pyruvate dehydrogenase was present in A. lumbricoides muscle at levels comparable with mammalian tissues and results suggest that it is modulated via a phosphotransferase/phosphatase system. The tricarboxylic acid cycle intermediates, citrate, isocitrate and 2-oxoglutarate were all detected in freeze clamped muscle, but their steady state levels were considerably lower than those found in mammalian tissues.     

Nucleoside triphosphate metabolism in the muscle tissue of Ascaris lumbricoides (Nematoda)

Barrett J. 1973. Nucleoside triphosphate metabolism in muscle tissue of Ascaris lumbricoides (Nematoda). International Journal for Parasitology3: 393–400. Nucleosidediphosphate kinase and adenylate kinase were found to be extremely active in Ascaris muscle. Apart from adenylate kinase, no other nucleosidemonophosphate kinases could be detected. There was no measurable AMP deaminase activity or arginine or creatine phosphokinase activity in Ascaris muscle. Analysis of perchlorate extracts of freeze clamped Ascaris muscle revealed no arginine or creatine phosphate and negligible amounts of acid labile phosphate. Adenosine tri-, di- and monophosphates were the major nucleotides, constituting 93 per cent of the total, with only small amounts of inosine and guanosine di- and triphosphates being detected. The significance of these results in the energy metabolism of Ascaris muscle is discussed.     

Molecular aspects of chromatin elimination in Ascaris lumbricoides

DNA from spermatids, 4-cell stages, and larvae of Ascaris lumbricoides was isolated, and the genome size before and after chromatin elimination was determined by isotope dilution. According to these determinations, 27% of the DNA is lost during the process of chromatin elimination. This value is based on the assumption that larval nuclei are diploid. The genomes were then characterized by CsCl equilibrium density gradient centrifugation and renaturation kinetics. The eliminated DNA does not differ from the retained DNA in base composition. About 26% of the DNA of 4-cell stage embryos sediments as a light satellite and was shown to be mitochondrial DNA by electron microscopy. Renaturation kinetics revealed that 10% of the retained somatic DNA is repetitious with an average family size of 5500 to 7000 copies, whereas 90% of the retained DNA is presumably composed of unique sequences. By contrast, germ-line DNA contains 23% fast renaturing DNA with a family size of 7000 to 10,000 copies. Thus, eliminated DNA consists of repetitious and unique sequences in a ratio of about 1:1.