165,504 research outputs found
Lifetime Measurement of the 8s Level in Francium
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
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 first class constraints and second
class ones are shown to be unified with first and second class
constraints from the additional variables sector, resulting with
-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
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
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
We present accurate {\em ab initio} non-perturbative calculations of the
Breit correction to the parity non-conserving (PNC) amplitudes of the
and transitions in Cs, and transitions in
Fr, transition in Ba, transition in Ra, and
transition in Tl. The results for the transition
in Cs and 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 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
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
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
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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