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The flagellar membrane of Ochromonas danica. Lipid composition.

The lipids of the whole flagella and the flagella membrane of the phytoflagellate Ochromonas danica were isolated and compared with those of the whole cell. The polar lipids were separated by two-dimensional thin layer chromatography. One-dimensional thin layer chromatography was used for the separation of the nonpolar lipids. In all respects the lipids of the whole flagella were identical with those of the flagellar membrane. These methods established the presence in flagellar membrane of the polychlorosulfolipids of O. danica as more than 90 molar per cent of the total polar lipids. These sulfolipids had been previously characterized as 1,14-docosanediol-1, 14-disulfate and 1,15-tetracosanediol-1,15-disulfate, containing zero to six chloro groups substituting for hydrogen on the chain. Seven unknown polar lipids were found. Both phosphorus analysis on each lipid and the molybdenum spray reagent for phospholipids on the chromatogram showed that there is no phospholipid present in O. danica flagellar membrane. Positive reactions to the diphenylamine spray reagent suggest that up to four of the unknown polar lipids are glycolipids. Of these, three reacted positively with ninhydrin. All of the unknown lipids reacted with the acidified 2,4-dinitrophenylhydrazine spray reagent suggesting the presence of aldehyde, ketone, glycoside, or plasmalogen. One unknown substance appeared near the origin of thin layer chromatograms. It showed a positive reaction with Dragendorff reagent, suggesting the presence of a quaternary amine group. This substance is presumed to be nonlipid, since it is not synthesized from [1-14C]acetate under the growth conditions used, as revealed by autoradiograms of thin layer chromatograms. It contained 35% hexose or hexosamine. It is devoid of phosphorus (0.7%) and is less than 4% protein (or phenolic groups or peptide), as judged by the Lowry assay using bovine serum albumin as a standard. Analysis of the nonpolar lipids of the flagellar membrane showed that free fatty acids constitute about 12 molar per cent of the total lipids. These fatty acids could be true components of the membrane or artifacts of the extraction procedure although every precaution was taken to prevent artifactual production of free fatty acids. The sterols constitute nearly 10 molar per cent of total lipids. Sterol esters were absent from the membrane. There are two additional major unknown nonpolar lipids present. The implications of such a high proportion of chlorosulfolipids as a polar lipid component in the membrane are important because of the unique structures of these lipids, which have ionic groups at or near both ends of the aliphatic chain.

Animals↗

Differences in heart phospholipids in two inbred rat strains differing in sensitivity to the development of heart lesions.

The content of phospholipids and their fatty acid composition were followed in the hearts of two inbred strains of rats: IR, resistant against the development of isoprenaline-induced myocardial lesions and IS, sensitive to their development. In the hearts of rats of the resistant strain, a lower content of phosphatidylcholine and its plasmalogen fraction was found compared to IS rats. The total amount of phospholipids was only insignificantly lower in IR rats. Greater differences were found in individual fatty acids. The most important finding concerned lower arachidonic acid and higher linoleic acid content in heart phospholipids of IR rats. These differences were exactly opposite to changes reported in the literature in animals known to have a higher resistance against myocardial damage due to various interventions. Our results do not support the hypothesis claiming the importance of changes in phospholipids and their FA composition for the resistance of the heart against the development of necrotic lesions.

Animals↗

Analysis of isoprenoid biosynthesis in peroxisomal-deficient Pex2 CHO cell lines.

ZR-78 and ZR-82 cells are two peroxisomal-deficient Chinese hamster ovary (CHO) cell mutants. These cells lack normal peroxisomes and show reduced levels of plasmalogen synthesis and other peroxisomal functions attributed to the deficiency of peroxisomal matrix enzymes. As we have recently identified two HMG-CoA reductase proteins in CHO cells, a 97 kDa reductase localized in the ER and a 90 kDa reductase protein localized in peroxisomes, this enabled us to study the two reductase proteins for the first time in peroxisomal-deficient CHO cells. In this study we report the results of a detailed analysis of the isoprenoid biosynthetic pathway in the peroxisomal-deficient CHO cell lines ZR-78 and ZR-82. We demonstrate that total HMG-CoA reductase activity is significantly reduced in the peroxisomal-deficient cells as compared to the wild type cells. Analysis of the two reductase proteins in permeabilized cells indicated that in the ZR-78 and ZR-82 cells the 90 kDa peroxisomal reductase protein was mainly localized to the cytosol. We further show that the rates of both sterol (cholesterol) and non-sterol (dolichols) biosynthesis were significantly lower in the peroxisomal-deficient cells, when either [3H] acetate or [3H] mevalonate was used as substrate. In contrast, the rate of dolichol biosynthesis in the peroxisomal-deficient cells was similar to that of the wild type cells when incubated with [3H] farnesol. In addition, we demonstrate that the peroxisomal-deficient cells exhibited increased rates of lanosterol biosynthesis as compared to wild type cells. The results of this study provide further evidence for the essential requirement of peroxisomes for cholesterol biosynthesis as well as for dolichol production.

Acetates↗

[Brain lipid composition of the rat with experimental morphine dependence].

The brain phospholipid content was studied in rats with morphine physical dependence. It was found that level of total lipids, total phospholipids and cholesterol was diminished. The significant decrease of absolute amounts of phosphotidyl serine, phosphotidyl inositol, sphingomyelin and phosphatidyl choline was shown. At the same time the percent relation of individual phospholipids did not change. As the exclusion, the quantity of phosphatidyl ethanolamine plasmalogen lowered in rats with morphine dependence. The percent content of fatty acids 16:0, 18:1 omega 9, 20:1 omega 11, 20:4 omega 6 and 22:5 omega 3 was found to be reduced. At the same time the percent amount of i18:0 and 20:0 was shown to increase. As a result the unsaturation index dramatically diminished. It was also shown that under morphine physical dependence the acyl residues of phosphatidyl choline and phosphatidyl ethanolamine changed. It was concluded that lipids play significant role in the development of morphine physical dependence.

Animals↗

Rapid separation and identification of phosphatidylethanolamine molecular species.

A novel high performance liquid chromatography method is presented for the separation and identification of intact molecular species of phosphatidylethanolamine (PE). After isocratic separation, detection of species can be achieved by measurement of UV absorbance as well as by the quantitative method of light scattering detection. A mathematical relationship exists between i) the relative retention time of a PE molecular species and ii) the number of carbon atoms and double bonds in the aliphatic groups of the species. This relationship can aid in the identification of the species. Furthermore, the absence of non-volatile components in the solvent allows the use of electrospray mass spectrometry to identify the eluting components and to establish the position of the individual radyl groups at the glycerol backbone. Using this method, samples of bovine heart PE (rich in plasmalogens) and rat liver PE (rich in diacyl species) have been analyzed.

Animals↗