[Determination of pharmacokinetic variables in veterinary medicine using a computer program].
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Biomedical subjects
Publications and source records attributed to B Kuhn.
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The effectiveness of tetracycline therapy on Listeria-infection in compromised host was evaluated in three different murine models. In normal adult mice infected with a tetracycline susceptible strain of Listeria monocytogenes, treatment with this antibiotic caused a reduced rate of multiplication of bacteria. That is, a low bacterial count was found in the spleen. When the macrophage system which in Listeria-infection represents a major defense mechanism was blocked through dextran sulfate 500, treatment with tetracycline was still very effective. In this case, bacterial multiplication has ceased. However, an elimination of the organisms could only be achieved after the macrophage system recovered from its temporary blockade. Secondly, nude athymic mice which are unable to develop cell mediated immunity were used to establish chronic infection with Listeria. Treatment with tetracycline in this instance only reduced bacterial counts moderately. Thirdly, five days old baby mice which are extremely susceptible to Listeria could at least partially be protected with tetracycline therapy against fatal infection.
In a mixture of Escherichia coli DNA polymerase III holoenzyme, single-strand-binding protein, artificially forked lambda bacteriophage DNA with primer annealed to the leading side of the fork, dNTPs and ATP, DNA synthesis is enhanced by helicase II, less so by helicases, I, III or rep protein of E. coli or T4 phage helicase. The effect of helicase II depends on ATP, it is enhanced by helicase III, and it is not observed using DNA polymerase I or T4 DNA polymerase. In the absence of dNTPs helicase II is less active than helicase I or T4 helicase in unwinding the forked DNA. We believe that helicase II both shifts the forks and stimulates DNA polymerase III. The results support the conclusion derived from previous studies that helicase II is part of the DNA-synthesizing system of E. coli.
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In summary, we postulate that DNA unwinding and ATP dephosphorylation are coupled in different ways, depending on whether the fibrous ATPase or one of the globular ATPases provides the catalytic agent. Unanswered is the question of whether there is stoichiometry of ATP utilization during the unwinding of a duplex, and unsolved is the role of the individual enzyme in the cell.
In a population sample from southwestern Germany the frequency of UMPK1 was estimated to be 0.949. The segregation of the children's phenotypes is in agreement with the formal model: 2 common alleles UMPK1 and UMPK2 at an autosomal locus. Data on linkage relations are referred.