165,504 research outputs found

    Lifetime Measurement of the 8s Level in Francium

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    We measure the lifetime of the 8s level on a magneto-optically trapped sample of ^{210}Fr atoms with time-correlated single-photon counting. The 7P_{1/2} state serves as the resonant intermediate level for two-photon excitation of the 8s level completed with a 1300 nm laser. Analysis of the fluorescence decay through the the 7P_{3/2} level gives 53.30 +- 0.44 ns for the 8s level lifetime.Comment: 4 pages, 4 figure

    The Green--Schwarz Superstring in Extended Configuration Space and Infinitely Reducible First Class Constraints Problem

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    The Green--Schwarz superstring action is modified to include some set of additional (on-shell trivial) variables. A complete constraints system of the theory turns out to be reducible both in the original and in additional variable sectors. The initial 8s8s first class constraints and 8c8c second class ones are shown to be unified with 8c8c first and 8s8s second class constraints from the additional variables sector, resulting with SO(1,9)SO(1,9)-covariant and linearly independent constraint sets. Residual reducibility proves to fall on second class constraints only.Comment: 14 pages, LaTe

    Molecular studies on intraspecific diversity and phylogenetic position of Coniothyrium minitans

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    Simple sequence repeat (SSR)±PCR amplification using a microsatellite primer (GACA)% and ribosomal RNA gene sequencing were used to examine the intraspecific diversity in the mycoparasite Coniothyrium minitans based on 48 strains, representing eight colony types, from 17 countries world-wide. Coniothyrium cerealis, C. fuckelii and C. sporulosum were used for interspecific comparison. The SSR±PCR technique revealed a relatively low level of polymorphism within C. minitans but did allow some differentiation between strains. While there was no relationship between SSR±PCR profiles and colony type, there was some limited correlation between these profiles and country of origin. Sequences of the ITS 1 and ITS 2 regions and the 5±8S gene of rRNA genes were identical in all twenty-four strains of C. minitans examined irrespective of colony type and origin. These results indicate that C. minitans is genetically not very variable despite phenotypic differences. ITS and 5±8S rRNA gene sequence analyses showed that C. minitans had similarities of 94% with C. fuckelii and C. sporulosum (which were identical to each other) and only 64% with C. cerealis. Database searches failed to show any similarity with the ITS 1 sequence for C. minitans although the 5±8S rRNA gene and ITS 2 sequences revealed an 87% similarity with Aporospora terricola. The ITS sequence including the 5±8S rRNA gene sequence of Coniothyrium cerealis showed 91% similarity to Phaeosphaeria microscopica. Phylogenetic analyses using database information suggest that C. minitans, C. sporulosum, C. fuckelii and A. terricola cluster in one clade, grouping with Helminthosporium species and 'Leptosphaeria' bicolor. Coniothyrium cerealis grouped with Ampelomyces quisqualis and formed a major cluster with members of the Phaeosphaeriacae and Phaeosphaeria microscopica

    Precision study of 6p 2Pj - 8s 2S1/2 relative transition matrix elements in atomic Cs

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    A combined experimental and theoretical study of transition matrix elements of the 6p 2Pj - 8s 2S1/2 transition in atomic Cs is reported. Measurements of the polarization-dependent two-photon excitation spectrum associated with the transition were made in an approximately 200 cm-1 range on the low frequency side of the 6s 2S1/2 - 6p 2P3/2 resonance. The measurements depend parametrically on the relative transition matrix elements, but also are sensitive to far-off-resonance 6s 2S1/2 - np 2Pj - 8s 2S1/2 transitions. In the past, this dependence has yielded a generalized sum rule, the value of which is dependent on sums of relative two-photon transition matrix elements. In the present case, best available determinations from other experiments are combined with theoretical matrix elements to extract the ratio of transition matrix elements for the 6p 2Pj - 8s 2S1/2 (j = 1/2,3/2) transition. The resulting experimental value of 1.423(2) is in excellent agreement with the theoretical value, calculated using a relativistic all-order method, of 1.425(2)

    Breit Interaction and Parity Non-conservation in Many-Electron Atoms

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    We present accurate {\em ab initio} non-perturbative calculations of the Breit correction to the parity non-conserving (PNC) amplitudes of the 6s7s6s-7s and 6s5d3/26s-5d_{3/2} transitions in Cs, 7s8s7s-8s and 7s6d3/27s-6d_{3/2} transitions in Fr, 6s5d3/26s-5d_{3/2} transition in Ba+^+, 7s6d3/27s-6d_{3/2} transition in Ra+^+, and 6p1/26p3/26p_{1/2} - 6p_{3/2} transition in Tl. The results for the 6s7s6s-7s transition in Cs and 7s8s7s-8s transition in Fr are in good agreement with other calculations while calculations for other atoms/transitions are presented for the first time. We demonstrate that higher-orders many-body corrections to the Breit interaction are especially important for the sds-d PNC amplitudes. We confirm good agreement of the PNC measurements for cesium and thallium with the standard model .Comment: 9 pages, 1 figur

    \u3cem\u3eβ\u3c/em\u3e-Homopipitzolone

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    The structure of β-homopipitzolone (one of the two isomers of an intermediate product in the homocedrole synthesis) has been unequivocally established as 1 O-hydroxy-2,6,9-trimetbyltricyclo[6.3.1.01,6] dodeca-9-ene-5, II, 12-trione with relative IR,2R,6R,8S configuration

    A new class of fatty acid allene oxide formed by the DOX-P450 fusion proteins of human and plant pathogenic fungi, C. immitis and Z. tritic

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    Linoleate dioxygenase-cytochrome P450 (DOX-CYP) fusion enzymes are common in pathogenic fungi. The DOX domains form hydroperoxy metabolites of 18:2n-6, which can be transformed by the CYP domains to 1,2- or 1,4-diols, epoxy alcohols, or to allene oxides. We have characterized two novel allene oxide synthases (AOSs), namely, recombinant 8R-DOX-AOS of Coccidioides immitis (causing valley fever) and 8S-DOX-AOS of Zymoseptoria tritici (causing septoria tritici blotch of wheat). The 8R-DOX-AOS oxidized 18:2n-6 sequentially to 8R-hydroperoxy-9Z,12Z-octadecadienoic acid (8R-HPODE) and to an allene oxide, 8R(9)-epoxy-9,12Z-octadecadienoic acid, as judged from the accumulation of the α-ketol, 8S-hydroxy-9-oxo-12Z-octadecenoic acid. The 8S-DOX-AOS of Z. tritici transformed 18:2n-6 sequentially to 8S-HPODE and to an α-ketol, 8R-hydroxy-9-oxo-12Z-octadecenoic acid, likely formed by hydrolysis of 8S(9)-epoxy-9,12Z-octadecadienoic acid. The 8S-DOX-AOS oxidized [8R-2H]18:2n-6 to 8S-HPODE with retention of the 2H-label, suggesting suprafacial hydrogen abstraction and oxygenation in contrast to 8R-DOX-AOS. Both enzymes oxidized 18:1n-9 and 18:3n-3 to α-ketols, but the catalysis of the 8R- and 8S-AOS domains differed. 8R-DOX-AOS transformed 9R-HPODE to epoxy alcohols, but 8S-DOX-AOS converted 9S-HPODE to an α-ketol (9-hydroxy-10-oxo-12Z-octadecenoic acid) and epoxy alcohols in a ratio of ∼1:2. Whereas all fatty acid allene oxides described so far have a conjugated diene impinging on the epoxide, the allene oxides formed by 8-DOX-AOS are unconjugated

    A New Caspase-8 Isoform Caspase-8s Increased Sensitivity to Apoptosis in Jurkat Cells

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    Caspase-8 is a key initiator of death receptor-induced apoptosis. Here we report a novel short isoform of caspase-8 (caspase-8s), which encodes the first (Death Effector Domain) DED and part of the second DED, missing the C-terminal caspase domain. In vivo binding assays showed that transfected caspase-8s bound to (Fas-associated death domain protein) FADD, the adaptor protein in (death-induced signal complex) DISC. To investigate the potential effects of caspase-8s on cell apoptosis, Jurkat cells were stably transfected with caspase-8s. Overexpression of caspase-8s increased sensitivity to the apoptotic stimuli, Fas-agonistic antibody CH11. These results suggest that caspase-8s may act as a promoter of apoptosis through binding to FADD and is involved in the regulation of apoptosis. In addition, the results also indicate that the first DED was an important structure mediating combination between caspase-8 and FADD
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