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  • 1
    ISSN: 1615-6102
    Keywords: Endoplasmic reticulum ; Marker enzymes ; Mitochondria ; Soybean (Glycine max)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary This communication confirms the validity of two marker enzymes, NADH-cytochrome c reductase and succinate dehydrogenase (as succinate-INT reductase). for quantitation of the content of endoplasmic reticulum and mitochondria of plant cell fractions. Membrane fractions enriched to varying degrees in rough endoplasmic reticulum and mitochondria as well as reference fractions containing smooth membranes and dictyosomes were prepared from homogenates of etiolated soybean (Glycine max L.) hypocotyls. The NADPH-cytochrome c reductase activities of the fractions correlated with the content of rough endoplasmic reticulum as determined by morphometry; succinate-INT reductase activity correlated with the content of mitochondria. The absolute specific activity for pure endoplasmic reticulum was calculated from the regression analysis to be 17.8 Μmoles cytochrome c reduced hr−1 mg−1 protein and for mitochondria was determined to be 37.1 Μmoles INT reduced hr−1 mg−1 protein. These values permit estimation of endoplasmic reticulum and mitochondrial contamination of soybean fractions in the absence of pure reference fractions.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1615-6102
    Keywords: Fungi ; Gilbertella persicaria ; Membranes ; Mitochondria ; Organelle isolation ; Plasma membrane ; Ultrastructure ; Vacuoles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Methods are described for isolating and identifying subcellular membranes from walled hyphae ofGilbertella persicaria. Differences in thickness and symmetry of membranes and in contents of vesicles were used to distinguish different types of membranes. Mitochondria, vacuoles, plasma membrane, and vesicles with attached ribosomes from homogenized germlings equilibrated at the 1.2/1.4 M interface in discontinuous sucrose gradients. Accelerated flotation in centrifuged Ficol-sucrose gradients resulted in the additional separation of the mixed membranes into three fractions: one contained predominantly intact mitochondria, another was composed of vacuoles and vesicles coated with ribosomes, and a third was enriched in plasma membranes. Based upon morphometric analysis, these fractions contained 92% mitochondria, 53% vacuoles, and 89% plasma membranes, respectively. The source of vesicles coated with ribosomes was investigated since rapidly growing hyphae ofG. persicaria contained little rough endoplasmic reticulum as compared with other classes of membranes. Reconstruction from electron micrographs of mitochondrial fragmentation and vesiculation suggested that most of the ribosome-coated vesicles originated from disrupted mitochondria rather than from rough endoplasmic reticulum. The study demonstrates the utility of ultrastructural markers to identify membranesin vitro independent of, or as an adjunct to, cytochemical and biochemical markers.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1615-6102
    Keywords: Antitumor sulfonylurea ; NADH oxidase ; Plasma membranes ; Growth ; Golgi apparatus ; Mitochondria ; HeLa cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Growth of K-562 cells in culture is inhibited by the antitumor sulfonylureaLY181984 (N-(4-methylphenylsulfonyl)-N′-(4-chlorophenyl)urea) with an ED50 of about 30 μM. LY181984 was shown previously to inhibit NADH oxidation by plasma membranes from HeLa cells and other sources and to influence mitochondrial oxidative phosphorylation. With K-562 cells, NADH oxidation by plasma membranes was transiently stimulated and then inhibited by LY181984. NADH oxidation by whole cells was transiently stimulated and then inhibited by 0.1 to 100 μM LY181984 as well. Both the stimulations and inhibitions of activity were time-dependent. NADH oxidation by lower phase membranes depleted of plasma membranes by aqueous two-phase partition also was inhibited by micromolar and submicromolar concentrations of LY181984. Inhibition did not correlate with mitochondrial presence but rather with membranes that appeared to be fragments of the Golgi apparatus. The oxidation of NADH by whole cells and of plasma membranes that was inhibited by LY181984 was distinguished from mitochondrial NADH oxidation by resistance to inhibition by cyanide and by proceeding under oxygen-depleted conditions or an argon atmosphere. In contrast to the active antitumor agent LY181984, the inactive but chemically-related analog, LY181985 (N-(4-methylphenyl-sulfonyl)-N′-(4-phenylurea), inhibited neither growth nor NADH oxidation with K-562 cells or cell fractions.
    Type of Medium: Electronic Resource
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