Drosophila melanogaster aldehyde dehydrogenase

Summary Subcellular fractionation by differential centrifugation confirms the presence of aldehyde dehydrogenase inD. melanogaster. It is found principally in the heavy mitochondrial fraction.     

Drosophila melanogaster aldehyde dehydrogenase

Subcellular fractionation by differential centrifugation confirms the presence of aldehyde dehydrogenase in D. melanogaster. It is found principally in the heavy mitochondrial fraction.     

Toxicity of ouabain on Drosophila melanogaster

Summary Ouabain, also called g-strophantin, is an inhibitor of the Na⁺/K⁺-activated plasma membrane ATPase. Treatment of Drosophila melanogaster with 3–6 mM of this substance leads to a markedly reduced survival of the flies.     

Ethanol metabolism in Drosophila melanogaster.

A quantitative study of the transformation of ethanol into acetaldehyde shows that, in Drosophila melanogaster, the mitochondrial ethanol oxidizing system is not very active but that the part played by catalase appears more important than expected. For a strain without alcoholdehydrogenase, ethanol is highly toxic. The presence of acetaldehyde in the culture medium is toxic for all the strains studied. But, since even a strain without any aldehydeoxidase lives normally, the metabolic production of acetaldehyde does not seem dangerous.     

Enzymes of Sphingolipid metabolism in Drosophila melanogaster

Sphingolipids are important structural components of membranes that delimit the boundaries of cellular compartments, cells and organisms. They play an equally important role as second messengers, and transduce signals across or within the compartments they define to initiate physiological changes during development, differentiation and a host of other cellular events. For well over a century Drosophila melanogaster has served as a useful model organism to understand some of the fundamental tenets of development, differentiation and signaling in eukaryotic organisms. Directed approaches to study sphingolipid biology in Drosophila have been initiated only recently. Nevertheless, earlier phenotypic studies conducted on genes of unknown biochemical function have recently been recognized as mutants of enzymes of sphingolipid metabolism. Genome sequencing and annotation have aided the identification of homologs of recently discovered genes. Here we present an overview of studies on enzymes of the de novo sphingolipid biosynthetic pathway, known mutants and their phenotypic characterization in Drosophila.Received 14 June 2004; received after revision 15 August 2004; accepted 21 August 2004     

High resolution of heterochromatin of Drosophila melanogaster by distamycin A

A DNA-binding AT-specific antibiotic, distamycin A, was used as inhibitor of the condensation process of the heterochromatic regions in Drosophila melanogaster embryonic cells. By this treatment the structural organization of heterochromatin at interphase is preserved until metaphase. The different patterns observed are interpreted as chronological steps in the condensation process.     

Morphology of the carnation-light synthetic lethal focus in Drosophila melanogaster

A histological study of the carnation-light lethal focus revealed morphological abnormalities in brain tissue. The ratio of core width to total brain width and brain texture consistently differed between lethal (car-lt) and their non-lethal sibs.