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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Langmuir 4 (1988), S. 26-31 
    ISSN: 1520-5827
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Langmuir 5 (1989), S. 140-144 
    ISSN: 1520-5827
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Current genetics 12 (1987), S. 577-582 
    ISSN: 1432-0983
    Keywords: Saccharomyces cerevisiae ; Cell cycle ; Cyclic AMP ; G0 protein
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary When the cyr1-1 cells of Saccharomyces cerevisiae, which require cyclic AMP (cAMP) for growth, were starved for cAMP, cell division was arrested at the G1 state of the mitotic cell cycle and the cells entered the resting state (G0) also observed in wild-type cells transferred to sulfur-free medium. The level of cAMP in wild-type cells decreased rapidly when the cells were starved for sulfur and subsequently increased following its addition. The cyr1-1 cells starved for cAMP preferentially synthesized nine G0 proteins. The synthesis of these G0 proteins in the sulfur-starved cells was repressed by the addition of cAMP. The RAS2 val19 or bcy1 cells, which produced an elevated level of cAMP or cAMP-independent protein kinase, did not synthesize the G0 proteins under the sulfur-starved condition. The results suggest that cAMP plays a role in the transition between the proliferating state and G0 state.
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  • 4
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 333 (1988), S. 188-190 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] BALB/c mice were immunized with PIP2 prepared from bovine spinal cords13, and a clone of hybridoma cells producing an antibody of immunoglobulin G2b class was isolated. The immunoglobulin G preparation, designated antibody kt3g, had virtually no affinity for phosphatidylcholine, ...
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  • 5
    ISSN: 1432-072X
    Keywords: Neurospora crassa ; Morphological mutant ; Cyclic adenosine 3′,5′-monophosphate ; Protein kinase ; Cyclic AMP-binding protein
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A cpk mutant of Neurospora crassa with morphological alteration was obtained spontaneously during the cross between the wild-type and a glycerol utilizing cr-l strain. The growth rate of cpk was intermediate between the wild-type and cr-1 mutant strains. The cpk conidia contained a reduced level of carotenoid pigments as compared to the wild-type conidia. The cpk mutant had no detectable amount of cyclic adenosine 3′,5′-monophosphate (cAMP)-binding protein at all stages of growth tested. On a DEAE-Sephacel column chromatogram, protein kinase activity of the wild type was eluted at two peaks; the first peak was cAMP-dependent, and the second one was not. In contrast, the cpk strain had two peaks of cAMP-independent enzymes. It is suggested that cAMP-dependent protein kinase may be altered in the cpk mutant into a cAMP-independent type by an alteration of the regulatory subunit of this enzyme.
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  • 6
    ISSN: 1573-4889
    Keywords: Chromium carbides ; Cr23C6 ; Cr3C2 ; Cr7C3 ; sulfidation kinetics ; sulfide scales
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The sulfidation behavior of chromium carbide, Cr23C6, was investigated in H2S-H2 gas mixtures over a sulfur partial pressure range of 103.5−10−6 Pa at 1073 K using thermogravimetry, optical and scanning electron microscopy, X-ray diffraction analysis, and electron-probe microanalysis. The kinetics were rapid for short time periods and followed a linear rate law at low sulfur pressures, whereas sulfidation tends to obey a parabolic rate law at high pressures. Sulfidation rates decreased with increasing carbon content in the carbide. Surface morphologies could be divided into three groups: (I) at high sulfur pressures, petal-like. crystals (Cr2S3); (II) at intermediate pressures, a twinlike structure (Cr3S4); (III) and at low pressures, a flat surface with numerous hexagonal pits (Cr1−xS). The scale consisted of two distinct layers: an external scale with a single or multilayer structure and an inner scale with a mixture of Cr1−xS, Cr3C2, and Cr7C3. These higher carbides, Cr3C2 and Cr7C3, may be formed by the sulfidation-carburization of Cr23C6. Pt-marker experiments indicated that the external scale grew by chromium diffusion and that sulfur migration played an important role in the growth of the inner scale.
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  • 7
    ISSN: 1573-4889
    Keywords: Chromium ; sulfidation kinetics ; chromium sulfides ; multilayer structure ; H2S-H2 gas mixtures
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The sulfidation behavior of chromium was investigated over a temperature range of 973–1173 K in H2S-H2 gas mixtures of 104–10−6 Pa sulfur partial pressures using thermogravimetry, X-ray diffractometry, optical and scanning electron microscopy, and electron-probe microanalysis. Sulfidation kinetics are rapid for short periods and obey a linear rate law at low sulfur pressures, whereas at high sulfur pressures sulfidation tends to be parabolic. The surface morphologies can be divided into four types: at high sulfur pressures a petal-like crystal of Cr2S3(rho. and tri.) (type 1), at intermediate sulfur pressures a twinlike structure of Cr3S4 (type 2), at low sulfur pressures a flat surface with numerous hexagonal pits of Cr1−xS (type 3), and a fine twinlike structure of ordered Cr1−xS (type 4). At 973 K, the sulfur pressure ranges are type 1 at $$p_{S_2 } $$ 〉 10−4, type 2 at $$p_{S_2 } = 10^{ - 5} $$ , and type 3 at $$p_{S_2 }〈 10^{ - 6} Pa$$ . The critical sulfur pressure where type 2 was formed, 10−5 Pa at 973 K, shifts toward higherressures at higher temperatures and becomes 10−3 Pa at 1073 K and 10−1 Pa at 1173K. Type 4 is observed at 1173K and 10−6 Pa sulfur pressure. Thesulfide scale is composed of two distinct layers: an external layer, which is dense with a fine columnar structure, and an inner layer, which is porous with a layered structure of sulfides and voids. The external scale is composed offour layers at high sulfur pressures: at the scale-gas interface Cr2S3(rho.), next Cr2S3(tri.), third Cr3S4, and innermost Cr1−xS. With decreasing sulfur pressures,the number of layers in the external scale was reduced. Pt markers were positioned between the external and inner scales.
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  • 8
    ISSN: 1573-4889
    Keywords: Fe-Cr-S system ; spinel-monoclinic transition ; Cr3S4 ; FeCr2S4 ; Cr1−xS
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Phase relations and stability fields in the Fe-Cr-S system were investigated at 1073 and 1173 K in the sulfur pressure range 100–10−5 Pa. The sulfides, produced by the sulfidation-annealing process of Fe-Cr alloys followed by rapid quenching, were characterized using X-ray diffraction powder analysis at room temperature. The Cr3S4 in the Cr-S system extends beyond the FeCr2S4 stoichiometry in the Fe-Cr-S ternary system at intermediate sulfur pressures. The spinel-monoclinic transition of the FeCr2S4 was observed at sulfur pressures of 10−3–10−3.5Pa at 1073 K and at 100–10−0.5 Pa at 1173 K. The free energy change for formation of the spinel, FeCr2S4, from a monoclinic (Cr, Fe)3S4−y, hexagonal (Fe, Cr)1−xS, and sulfur vapor is given by the relation ΔG = −1523 + 1.09 T (kJ/mol). The phase-transition mechanism of FeCr2S4 is discussed on the basis of an enhancement of the cation coordination numbers from 4-6-6 for the spinel to 6-6-6 for the monoclinic, when the sulfur partial pressure decreases.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 27 (1987), S. 267-282 
    ISSN: 1573-4889
    Keywords: Co-Mn alloys ; high-temperature oxidation ; multilayer structures ; cation concentration profiles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The oxidation behavior of Co alloys containing up to 23.0 % Mn was investigated at temperatures of 1273–1473 K in an oxygen pressure range of 10–105 Pa using thermogravimetry, electron-probe microanalysis, and optical microscopy. Oxidation followed a parabolic rate law, except in the early reaction stage. For the growth of the (Co, Mn)O scale, parabolic rate constants increased with increasing manganese content, whereas with further additions of manganese the rate constants decreased due to an intermediate layer of (Co, Mn)3O4. This critical manganese content increased with increasing temperature. The scale structures were classified into three groups: group I, a single-layer scale; group II, an inner-outer double layer; and group III, an inner-intermediate-outer triple layer. The inner layer consisted of (Co, Mn)O; the outer layer was a mixture of (Co, Mn)O and (Co, Mn)3O4; the intermediate layer was composed of (Co, Mn)3O4. Cation concentration profiles were measured across the external scales with single- or multilayer structures. Diffusional analysis indicated that manganese moved 1.25 times faster than did cobalt in the (Co, Mn)O scale. Activation energies for oxidation are 118–126 kJ/moles for groups I and II, and for the alloys in group III they are 290–367 kJ/moles. Parabolic rate constants and scale structures are discussed on the basis of the Co-Mn-O phase diagram.
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  • 10
    ISSN: 1617-4623
    Keywords: Cyclic AMP ; Yeast adenylate cyclase ; Yeast RAS sequences ; Cell cycle control
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Various truncated CYR1 genes of Saccharomyces cerevisiae were fused to efficient promoters and expressed in Escherichia coli and S. cerevisiae cells with or without the RAS genes. The catalytic domain of adenylate cyclase encoded by the 3′-terminal 1.3 kb region of the open reading frame of the CYR1 gene produced cyclic AMP, irrespective of the presence of RAS genes. The product of the 3′-terminal 2.1 kb region of CYR1 showed guanine nucleotidedependent adenylate cyclase activity and produced a large amount of cAMP in the presence of the RAS gene. Thus, the domain encoded by the 0.8 kb region adjacent to the catalytic domain is associated with the regulatory function of the RAS products. The cyr1 RAS1 RAS2 cells carrying the 3′-terminal 1.3 kb region of CYR1 were unable to respond to environmental signals such as sulfur starvation and temperature shift, but the cyr1 cells carrying the 2.1 kb region and at least one RAS gene were able to respond to these signals. The environmental signals may be transferred to the adenylate cyclase system through the RAS products.
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