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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Current genetics 11 (1986), S. 119-125 
    ISSN: 1432-0983
    Keywords: Cell cycle ; cdc2 ; Flow cytometry ; Schizosaccharomyces
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The cell cycle of Schizosaccharomyces pombe in continuous culture is controlled at two steps, one which limits the transition from G1 to S phase and the other which determines the timing of cell division. We have investigated, by means of flow-cytofluorometry, the cell cycle characteristics of nutritionally starved cells in stationary phase. Cells were shown to become arrested in either G1 or G2, in ratios which depended on the composition of the growth medium. G1 and G2 stationary phase cells share certain properties. (1) They become relatively resistant to heat shock. (2) They can reenter the cell cycle after subculture into fresh medium. (3) The G1 and G2 arrested populations have equal long-term viability in stationary phase. (4) Both populations require the activity of the cdc2 + gene for reentry into the cell cycle. We suggest that cell cycle arrest in stationary phase is regulated by the activity of the same G1 and G2 controls which limit the rate of cell cycle progression in continuous culture. The data demonstrate that in fission yeast the transition from G1 to S phase does not mark a point of commitment to the completion of the cell cycle.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1617-4623
    Keywords: Yeast ; Cell cycle ; Extragenic suppressors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary A DNA fragment called suc1 has been found to rescue cells mutated in the cell cycle control gene cdc2 of the fission yeast Schizosaccharomyces pombe. The suppressing activity of suc1 is observed when it is present on a multicopy number plasmid. The gene does not hybridise to cdc2 and maps elsewhere in the genome. Its effect is cdc2 allele specific suggesting that it interacts directly with the cdc2 gene function.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This study represents the first systematic attempt to characterize the possible sources of artifacts that can interfere with the measurement of circular intensity differential scattering (CIDS) as a function of the scattering angle. A theoretical analysis of the effect of imperfect incident circular polarizations in the measurement of baselines from nonchiral scatterers and in the signals from chiral samples is derived. From this analysis the requirements of the tolerance on the quality of the incident circular polarizations to unequivocally measure the CIDS effect are established. The protocol for alignment of the CIDS instrument and the characterization of the incident polarizations utilized in these studies are described in detail. CIDS measurements on suspensions of helical sperm cells are presented. The experimental results are modeled computationally with the use of the current CIDS theory. Good agreement between the data and the computations is obtained. The results clearly indicate the ability of CIDS to provide information on the long-range chiral organization of samples in solution.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 1069-1084 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The previous paper in this series described several catalytic systems which can be used for simultaneous ethylene dimerization to 1-butene and copolymerization of the in situ-formed olefin with ethylene to form branched polyethylene. Such catalytic systems allow the synthesis of linear low-density polyethylene from a single monomer source. This article presents a more detailed description of one of the dual-functional catalyst systems studied, a mixed homogeneous-heterogeneous Ziegler-Natta catalyst, Al(C2H2)3-Ti(Oi-C3H7)4-TiCl4/MgCl2/polyethylene, at 90°C. Discussed are kinetics of ethylene dimerization with the soluble component, Al(C2H5)3-Ti(Oi-C3H7)4, and the effects of aluminum alkoxides on the system. Addition of the ethylene dimerization catalyst to the solid component, Al(C2H5)3-TiCl4/MgCl2/polyethylene, results in a partial decrease in polymerization activity. Some of the decrease can be attributed to the presence of 1-butene in the reaction medium. Measurement of the reactivity ratio kEE/kEB for two catalytic systems, the solid component and the title dual-functional catalyst, demonstrated that the presence of the dimerization component results in a twofold increase in the reactivity ratio, from 20 to ca. 40.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 147-155 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Various organoaluminum compounds strongly affect reactivity of a sulfonated nickel ylide complex in its reactions with ethylene. The complex, if used alone, is an active single-component catalyst for ethylene oligomerization to linear 1-alkenes. Al(C2H5)3 and tetraethylaluminoxane completely deactivate the catalyst by reducing it to Ni(O). Alkylaluminum halides, such as Al(C2H5)2Cl and Al(C2H5)Cl2, convert the nickel complex into a very active catalyst for ethylene dimerization to mixtures of butenes. Aluminum alkoxides, e.g., Al(C2H5)2OC2H5, AlC2H5(OC2H5)2, and Al(OC2H5)3, significantly increase oligomerization activity by a factor of 20-100. The distribution of 1-alkenes (in the C4—C40 + range) produced with the sulfonated nickel ylide-aluminum alkoxide catalyst follows the Flory molecular weight distribution law. The ratio of the chain termination to chain propagation rate constants is ca. 0.3 and is not temperature-sensitive in the 50-120°C range. Kinetic analysis of the ethylene oligomerization reaction with the binary catalytic system showed that the number of active centers is proportional to the nickel complex concentration. The effective activation energy of ethylene oligomerization with the catalyst is ca. 27 kJ/mol. The oligomerization catalysts loose their activity in time. The activity decay follows the first-order kinetic law. The rate of the decay increases with increasing temperature and is caused mainly by the intrinsic instability of active species.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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