Pharmakogenetik der oralen Antikoagulation mit Cumarinen

The recent identification of VKORC1 has made important contributions to our understanding of the vitamin K cycle. The VKORC1 enzyme was shown to be the molecular target of coumarin drugs. Mutations and polymorphisms in coding and noncoding regions of the VKORC1 gene have been shown to cause both a partial to total coumarin resistance and coumarin sensitivity. Availability of molecular diagnostics (VKORC1, CYP2C9) and drug monitoring by HCPLC (determination of coumarin, vitamin K, and vitamin K epoxide levels) is helpful for detecting hereditary and acquired factors influencing coumarin therapy. In the future, these tools may be instrumental in designing individualized oral anticoagulation therapy regimens.     

Purification of Neuronal Cell Surface Proteins and Generation of Epitope-Specific Monoclonal Antibodies Against Cell Adhesion Molecules

To establish a procedure for the purification of a broad spectrum of cell surface proteins, three separate methods based on different principles were compared with the aid of four marker proteins. Membrane preparation by sedimentation-flotation centrifugation, temperature-induced phase separation with Triton X-114, and lectin affinity chromatography were used separately as well as in combination. The two-step procedure of membrane preparation and lectin affinity chromatography provided by far the best enrichment of cell surface marker proteins. This result was further substantiated by screening greater than 6,600 hybridoma cultures that originated from mice that had been immunized with protein fractions obtained by different purification protocols. In addition, it was found that solubilized glycoproteins used as immunogens led to many more cell surface-specific monoclonal antibodies than glycoproteins immobilized on lectin-agarose beads. Three monoclonal antibodies that recognize distinct epitopes of cell adhesion molecules (CAMs) were isolated. Monoclonal antibody C4 bound to a detergent-labile epitope of G4 (neuron-glia CAM). Monoclonal antibody D1 recognized specifically nonreduced neural CAM (N-CAM) with intact disulfide bridges, and monoclonal antibody D3 recognized only the 180-kilodalton isoform of N-CAM. Because of these specificities, these monoclonal antibodies promise to be useful tools for the elucidation of the structural organization of adhesion molecules.     

Investigation by pyrolysis mass spectrometry,phage pattern and plasmid analysis of staphylococci that have reverted from ‘L’-phase to bacterial phase

No major differences have been found in series of Staphylococcus aureus strains which reverted from L-phase, either by pyrolysis mass spectrometry or by phage-typing or sensitivity testing. In L-phase they have been subcultured for a long time or transformed/reverted many times into/from L-phase. Plasmids were lost during transformations/reversions, but there was some difference between the tetracycline-connected plasmids on the one hand and the erythromycin-connected ones on the other.This investigation was supported by the Foundation for Fundamental Research on Matter (F.O.M.), subsidized by the Netherlands Organization for the Advancement of Pure Research (Z.W.O.).     

A new cell wall structure in a symbiotic and a free-living strain of the blue-green alga genus Chroococcidiopsis (Pleurocapsales)

Freeze etching studies in a symbiotic and a freeliving strain of Chroococcidiopsis revealed a specific layer in the outer cell wall not described so far from Cyanophyta. The layer showed a complex organisation: The main unit are ribbons, 2–3 nm thick, striated at right angle to the longitudinal axis. They are interwoven to a patchwork-like leaflet. The ribbons are virtually composed of globular particles associated in parallel rows. The cytoplasmic membrane and the cell walls of the symbiotic and the free-living strain were compared.Abbreviations cm cytoplasmic membrane - CW 1,2,3 cell wall layer 1,2,3 - EF exoplasmic fracture face - PF protoplasmic fracture face     

The role of ethylene in the control of cell division in cultured pea root tips: a mechanism to explain the excision effect

Summary A transitory cell division block, or excision effect, occurs in the meristem of roots after excision and transfer to culture medium. This block can be induced, in intact seedling roots, by exogenous treatment with ethylene gas. With continuous treatment, the block is longer and the recovery less than after a 4 hour pulse. In excised roots the excision effect can be eliminated by treatment with an inhibitor of ethylene synthesis (aminoethoxyvinylglycine) or action (silver thiosulfate). These experiments provide evidence to support the hypothesis that ethylene from the wounded end of an excised root is involved in a process resulting in a transitory block in cell cycle progression in the meristem. The implications of this hypothesis are discussed.     

Zur Ätiologie der Anreicherung von Aminosäuren und Amiden im Wurzelraum vonHelianthus Annuus L

Ohne ZusammenfassungMit 5 Textabbildungen     

Effects of low water potential on cortical cell length in growing regions of maize roots

Roots growing under low water potential commonly exhibit a marked decrease in growth rate and in diameter. Using median longitudinal sections of fixed maize (Zea mays L. cv WF9 × Mo 17) seedling roots, we investigated the cellular basis for these effects. Cortical cells in the shortened elongation zone of water stressed roots were longer than cortical cells in the comparable location of well-watered roots. Nearly twofold differences in cell length were seen in the region 2 to 4 millimeters behind the root apex. The shortened growth zone, however, leads to a final mean cortical cell length approximately 30% shorter in the stressed roots. These differences were present regardless of the age of the control roots. These data, and the slower growth rate seen in water-stressed roots, suggest that the water deficit causes a significant reduction in the rate of cell supply to the cortical cell files.