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  • Schizosaccharomyces pombe  (3)
  • nuclear magnetic resonance (NMR) imaging  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Current genetics 10 (1985), S. 297-311 
    ISSN: 1432-0983
    Keywords: Mitosis ; Meiosis ; Schizosaccharomyces pombe
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary We have investigated the genetic and physiological control of meiosis in fission yeast. Nutritionally depleted h +/h − diploid cells become irreversibly commited to meiosis immediately prior to the initiation of premeiotic S phase. Premeiotic DNA synthesis requires matP +, matM +, mei2 + and mei3 + but not the mitotic cell cycle control gene, cdc2 +, ran1 + is an essential gene, loss of which provokes sexual conjugation, premeiotic DNA synthesis, pseudo-meiosis and the sporulation of haploid cells. Our experiments suggest that sexual differentiation is achieved physiologically by the inhibition of ran1 + activity in a two-step process. In the first step, partial inhibition of ran1 + in starved haploid cells, leads to cell cycle arrest in G1 followed by sexual conjugation. In the second step, a pathway requiring the matP +, matM + and mei3 + genes of the newly-formed zygote, further inhibits ran1 + and thereby commits the cell to meiosis. mei2 + is required for meiotic commitment after full inhibition of ran1 +. ran1 + is normally essential for vegetative cell reproduction but is inessential in cells which have abnormally high levels of cAMP-dependent protein kinase. We propose that the ran1 + gene encodes a highly controlled protein kinase which shares key substrates with cAMP-dependent protein kinase.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Current genetics 14 (1988), S. 235-240 
    ISSN: 1432-0983
    Keywords: Cell Cycle ; Phosphoprotein ; Schizosaccharomyces pombe
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The 34 kilodalton protein product (p34) of the cdc2 + cell cycle control gene of Schizosaccharomyces pombe was expressed in bacteria. Monoclonal antibodies raised against this protein are capable of immunoprecipitating p34dc2 from yeast lysates. Immunoprecipitates of [35S]methionine- and [32P]orthophosphate-labeled p34cdc2 were analyzed by two-dimensional gel electrophoresis. The cdc2 + gene product is homogeneous in size but resolves into seven species of differing charge. At least four of these species are phosphorylated. Phosphoamino acid analysis reveals that phosphorylation occurs mainly on threonine residues. The pattern of p34 phosphorylation is unaltered at the nonpermissive temperature in strains carrying temperature sensitive alleles of wee1-50 and ran1-114 or in a strain over-producing the ran1 + gene product.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Current genetics 23 (1993), S. 547-548 
    ISSN: 1432-0983
    Keywords: Autonomously replicating sequence ; Recombinant DNA ; Nested deletions ; Mutagenesis ; Schizosaccharomyces pombe
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Plasmids pSP1 and pSP2 are two new Schizosaccharomyces pombe ars1 multicopy vectors with the Saccharomyces cerevisiae LEU2 and URA3 genes as selectable markers. They are derivatives of S. cerevisiae integrative plasmids. These plasmids allow classical molecular genetic techniques, such as mutagenesis, nested deletions and sequencing, to be performed directly.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-904X
    Keywords: nuclear magnetic resonance (NMR) imaging ; hydroxypropyl cellulose matrix ; water penetration rate ; slow-release formulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract An NMR imaging method was developed to estimate the rate of water movement in slow-release capsule matrices of pseudoephedrine HC1 and hydroxypropyl cellulose (HPC). Test capsules were first placed in a USP method 2 (paddles, 50 rpm) dissolution apparatus. Each plug was removed from the dissolution medium at predetermined times, blotted dry, and placed within the magnetic field of a General Electric 400-MHz wide-bore NMR spectrometer equipped with a microimaging accessory. Images were recorded along the transverse plane of each plug. The water penetration rate was determined by comparison of the cut and weighed contour plots of the images acquired. After 1 hr, the plugs tamped to 200 N exhibited water penetration to the center, while only 45% of the drug was released. The percentage dry matrix was fitted to the lost equation to obtain a diffusion coefficient of 4.15 × 10−6 cm2/sec. NMR imaging is set forth as an important and practicable technique to investigate drug formulations. In the HPC matrix system of this study, the NMR imaging results convincingly revealed the rate of hydration front penetration not to be a rate-limiting step in the drug release process.
    Type of Medium: Electronic Resource
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