181 research outputs found

    Strongly magnetized classical plasma models

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    Discrete particle processes in the presence of a strong external magnetic field were investigated. These processes include equations of state and other equilibrium thermodynamic relations, thermal relaxation phenomena, transport properties, and microscopic statistical fluctuations in such quantities as the electric field and the charge density. Results from the equilibrium statistical mechanics of two-dimensional plasmas are discussed, along with nonequilibrium statistical mechanics of the electrostatic guiding-center plasma (a two-dimensional plasma model)

    A numerical code for the solution of the Kompaneets equation in cosmological context

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    Context: The cosmic microwave background (CMB) spectrum probes physical processes and astrophysical phenomena occurring at various epochs of the Universe evolution. Current and future CMB absolute temperature experiments are aimed to the discovery of the very small distortions such those associated to the cosmological reionization process or that could be generated by different kinds of earlier processes. The interpretation of future data calls for a continuous improvement in the theoretical modeling of CMB spectrum. Aims: In this work we describe the fundamental approach and, in particular, the update to recent NAG versions of a numerical code, KYPRIX, specifically written for the solution of the Kompaneets equation in cosmological context, first implemented in the years 1989-1991, aimed at the very accurate computation of the CMB spectral distortions under quite general assumptions. Methods: We describe the structure and the main subdivisions of the code and discuss the most relevant aspects of its technical implementation. Results: We present some of fundamental tests we carried out to verify the accuracy, reliability, and performance of the code. Conclusions: All the tests done demonstrates the reliability and versatility of the new code version and its very good accuracy and applicability to the scientific analysis of current CMB spectrum data and of much more precise measurements that will be available in the future. The recipes and tests described in this work can be also useful to implement accurate numerical codes for other scientific purposes using the same or similar numerical libraries or to verify the validity of different codes aimed at the same or similar problems.Comment: 14 pages, 6 figures. Accepted for publication on Astronomy and Astrophysics on July 23, 2009. Abstract shorter than in the version in publicatio

    Metabolite Profiling Uncovers Plasmid-Induced Cobalt Limitation under Methylotrophic Growth Conditions

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    BACKGROUND:The introduction and maintenance of plasmids in cells is often associated with a reduction of growth rate. The reason for this growth reduction is unclear in many cases. METHODOLOGY/PRINCIPAL FINDINGS:We observed a surprisingly large reduction in growth rate of about 50% of Methylobacterium extorquens AM1 during methylotrophic growth in the presence of a plasmid, pCM80 expressing the tetA gene, relative to the wild-type. A less pronounced growth delay during growth under non-methylotrophic growth conditions was observed; this suggested an inhibition of one-carbon metabolism rather than a general growth inhibition or metabolic burden. Metabolome analyses revealed an increase in pool sizes of ethylmalonyl-CoA and methylmalonyl-CoA of more than 6- and 35-fold, respectively, relative to wild type, suggesting a strongly reduced conversion of these central intermediates, which are essential for glyoxylate regeneration in this model methylotroph. Similar results were found for M. extorquens AM1 pCM160 which confers kanamycin resistance. These intermediates of the ethylmalonyl-CoA pathway have in common their conversion by coenzyme B(12)-dependent mutases, which have cobalt as a central ligand. The one-carbon metabolism-related growth delay was restored by providing higher cobalt concentrations, by heterologous expression of isocitrate lyase as an alternative path for glyoxylate regeneration, or by identification and overproduction of proteins involved in cobalt import. CONCLUSIONS/SIGNIFICANCE:This study demonstrates that the introduction of the plasmids leads to an apparent inhibition of the cobalt-dependent enzymes of the ethylmalonyl-CoA pathway. Possible explanations are presented and point to a limited cobalt concentration in the cell as a consequence of the antibiotic stress

    Methylobacterium Genome Sequences: A Reference Blueprint to Investigate Microbial Metabolism of C1 Compounds from Natural and Industrial Sources

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    Methylotrophy describes the ability of organisms to grow on reduced organic compounds without carbon-carbon bonds. The genomes of two pink-pigmented facultative methylotrophic bacteria of the Alpha-proteobacterial genus Methylobacterium, the reference species Methylobacterium extorquens strain AM1 and the dichloromethane-degrading strain DM4, were compared. Methodology/Principal Findings The 6.88 Mb genome of strain AM1 comprises a 5.51 Mb chromosome, a 1.26 Mb megaplasmid and three plasmids, while the 6.12 Mb genome of strain DM4 features a 5.94 Mb chromosome and two plasmids. The chromosomes are highly syntenic and share a large majority of genes, while plasmids are mostly strain-specific, with the exception of a 130 kb region of the strain AM1 megaplasmid which is syntenic to a chromosomal region of strain DM4. Both genomes contain large sets of insertion elements, many of them strain-specific, suggesting an important potential for genomic plasticity. Most of the genomic determinants associated with methylotrophy are nearly identical, with two exceptions that illustrate the metabolic and genomic versatility of Methylobacterium. A 126 kb dichloromethane utilization (dcm) gene cluster is essential for the ability of strain DM4 to use DCM as the sole carbon and energy source for growth and is unique to strain DM4. The methylamine utilization (mau) gene cluster is only found in strain AM1, indicating that strain DM4 employs an alternative system for growth with methylamine. The dcm and mau clusters represent two of the chromosomal genomic islands (AM1: 28; DM4: 17) that were defined. The mau cluster is flanked by mobile elements, but the dcm cluster disrupts a gene annotated as chelatase and for which we propose the name “island integration determinant” (iid).Conclusion/Significance These two genome sequences provide a platform for intra- and interspecies genomic comparisons in the genus Methylobacterium, and for investigations of the adaptive mechanisms which allow bacterial lineages to acquire methylotrophic lifestyles.Organismic and Evolutionary Biolog
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