Probing microscopic chaotic dynamics by observing macroscopic transport processes

We derive the Kramers equation, namely, the Fokker-Planck equation for an oscillator, from a completely deterministic picture. The oscillator is coupled to a “booster”, i.e., a deterministic system in a fully chaotic state, wherein diffusion is derived from the sensitive dependence of chaos on initial conditions and friction is a consequence of the linear response of the booster to the action exerted on it by the oscillator. To deal with the Hamiltonian nature of the system of interest and of its coupling to the booster, we extend the earlier theoretical derivation of macroscopic transport coefficients from deterministic dynamics. We show that the frequency of the oscillator can be tuned to the microscopic frequencies of the booster without affecting the canonical nature of the “macroscopic” statistics. The theoretical predictions are supported by numerical simulations.     

Pythagorean euclidean four point properties

Characterizations of real inner product spaces among a class of metric spaces have been obtained based on homogeneity of metric pythagorean orthogonality, a metrization of the concept of pythagorean orthogonality as defined in normed linear spaces. In the present paper a considerable weakening of this hypothesis is shown to characterize real inner product spaces among complete, convex, externally convex metric spaces, generalizing a result of Kapoor and Prasad [9], and providing a connection with the many characterizations of such spaces using euclidean four point properties.     

Characterization of supercommuting matrices

For a given n-by-n matrix A, we consider the set of matrices which commute with A and all of whose principal submatrices commute with the corresponding principal submatrices of A. The properties of this set are examined, with particular attention to its dimension.     

Fluorescence anisotropy decay study of self-association of bacterial luciferase intermediates

The fluorescence dynamics parameters of the fluorescent transient flavin-luciferase species from the typesVibrio fischeri andPhotobacterium leiognathi are presented. The fluorescence anisotropy decay is a single exponential function for both types. The correlation time is 70 ns for theP. leiognathi fluorescent transient intermediate (2°C, aqueous buffer, pH 7.0), consistent with the rotational correlation time of the luciferase macromolecule (77 kD) to which the flavin fluorophore is rigidly attached. In contrast, for theV. fischeri species the observed correlation time for the anisotropy decay function is 133 ns. This suggests that protein self-association occurs in theV. fischeri case and this is confirmed by filtration, where the fluorescent transient fromV. fischeri does not pass through a 100,000 molecular weight cutoff membrane, whereas theP. leiognathi species does. The filtration method also demonstrates self-association in the luciferase peroxyflavin and photoflavin fromV. fischeri. A monomer-dimer equilibrium also explains the previously reported high correlation times for theV. harveyi luciferase-flavin species. It is proposed that the self-association competes with the lumazine protein interaction in the bioluminescence reaction.     

Space tilings and local isomorphism

We prove for a large class of tilings that, given a finite tile set, if it is possible to tile Euclideann-space with isometric copies of this set, then there is a tiling with the ‘local isomorphism property’. Research supported in part by NSF Grant No. DMS-9001475.     

The thermolysis of dicarbonylcyclopentadienyliron dimer: The formation of biferrocene

The thermolysis of dicarbonylcyclopentadienyliron dimer in a sealed tube at 300°C has been reported to produce ferrocene, carbon monoxide, carbon dioxide, cyclopentadiene and elemental iron. We observe in addition to these products the production of biferrocene and elemental carbon. Thermolysis of carbonylcyclopentadienyliron tetramer (produced from the dimer by thermolysis in refluxing xylene) produces ferrocene, iron and carbon monoxidre; no biferrocene, carbon dioxide or elemental carbon are produced. A scheme is proposed to account for these products.     

Altered protein synthesis in rat kidney cells exposed to semiconductor materials

It is thought that the extensive industrial use of arsenic, gallium and indium, which have applications as the materials for III–V semiconductors, will increase human exposure to these compounds in the near future. We have undertaken the development of new biological indicators for assessing exposure to these elements. Element-specific alterations in protein synthesis patterns were expected to occur following exposure to arsenic compounds. We examined alterations in protein synthesis in primary cultures of rat kidney proximal tubule epithelial cells by sodium arsenite, gallium chloride and indium chloride, utilizing two-dimensional gel electrophoresis. After incubation with the chemicals for 20 h, newly synthesized proteins were labeled with [³⁵S]methionine. A protein with a molecular weight (M_r) of 30 000 was markedly induced on exposure to 10 μM arsenite or 300 μM gallium chloride, and synthesis of proteins with M_r values of 85 000, 71 000, 65 000, 51 000, 38 000 and 28 000 were also increased by exposure to arsenite and gallium chloride. No significant changes were observed upon exposure to indium. Some of these increased proteins could be heat-shock proteins.     

A convenient method for regioselective C-5 halogenation of 4(3H)-oxo-7H-pyrrolo[2,3-d]pyrimidines

N-7, O-Disilylation of 4(3H)-oxo-7H-pyrrolo[2,3-d]pyrimidines provides a convenient method for activation of these compounds toward regiospecific halogenation at C-5. The sequence is conveniently carried out without isolation of the silylated derivatives and desilylation is spontaneous upon addition of water to the reaction mixture.