Magnetic dipole transitions and proton-neutron degrees of freedom in nuclear deformation

The M1 transitions between low-lying collective states are discussed from the viewpoint of the Proton-Neutron Interacting Boson Model, with particular emphasis on the mixed-symmetry states. Mixed-symmetry 2⁺ states are studied for⁵⁶Fe and⁵⁴Cr in terms of realistic and large-scale shell-model calculations, including M1 properties. The Doorway-state character of the mixed-symmetry 2⁺ state is proposed with examples in these nuclei. The possible candidate of the mixed-symmetry 2⁺ state in¹³⁴Ba is analyzed based on recent experiment by Molnaret al. on M1 transitions. The M1 transitions from the quasi-γ to quasi-g bands in γ-unstable or O(6) nuclei are discussed next, by taking Ba isotopes as an example. It is suggested that such M1 transitions are enhanced compared to axially symmetric nuclei as an indication of softness towards proton-neutron incoherent motion in γ-unstable nuclei,i.e., mixture of mixed-symmetry states. A new mirror-type symmetry is introduced for γ-unstable nuclei, and the M1 selection rule due to this symmetry is presented, making 4 ₂ ⁺ →4 ₁ ⁺ transition allowed but 3 ₁ ⁺ →2 ₁ ⁺ forbidden, for instance.     

RECONSTITUTION OF SQUID RHODOPSIN IN RHABDOMAL MEMBRANES

Abstract— Squid opsin which is capable of combining with 11- cis or 9- cis retinal to reconstitute photo-pigment has been prepared by irradiation of rhabdomal membranes with orange light (> 530 nm) in the presence of 0.2 M hydroxylamine. When the irradiation is carried out either at concentrations of hydroxylamine higher than 0.2 M or with light of wavelength shorter than 530 nm, rhodopsin in the membranes is bleached quickly, but the ability of the resultant opsin to form rhodopsin is greatly reduced.
The optimum pH for rhodopsin regeneration in rhabdomal membranes was found to be between 6.5 and 8.5. The rate of regeneration of rhodopsin increases with raising temperature, and at about 20°C it is almost the same as that of isorhodopsin. Even after solubilization in digitonin solution, opsin still preserves the ability to reform rhodopsin.
All- trans retinal can be incorporated into retinochrome-bearing membranes, in which it is isomerized into 11- cis isomer by the photoisomerase activity of retinochrome. Rhabdomal membranes retaining active opsin can take up 11- cis retinal from retinochrome membranes so as to synthesize rhodopsin.     

Facile oxidation of aldehydes and α-keto acids as catalyzed by flavin and thiazolium ion

Oxidation of aldehydes and α-keto acids to carboxylic acids ocurrs readily in the presence of a flavin, thiazolium ion, and cationic micelles, the reaction involving trapping by the flavin of the intermediate formed from the substrate-thiazolium adducts through deprotonation or decarboxylation.     

Spin-dependent nuclear weak processes and nucleosynthesis in stars

Spin dependent nuclear weak processes and nucleosynthesis in stars are investigated based on recent advances in shell model studies of stable and unstable exotic nuclei. Three topics on (1) neutrino-nucleus reactions in supernova explosions and nucleosynthesis of light elements as well as Mn, (2) electron capture reaction rates on Ni and Co isotopes at high densities and temperatures in the core-collapse process, and (3) new β-decay half-lives of N=126 isotones obtained by including both the Gamow-Teller and the first-forbidden transitions, and the effects on the element abundance in the r-process at the third peak region (A∼195), are studied with the use of new shell model Hamiltonians.     

Midpoint cell method for hybrid (MPI+OpenMP) parallelization of molecular dynamics simulations

We have developed a new hybrid (MPI+OpenMP) parallelization scheme for molecular dynamics (MD) simulations by combining a cell‐wise version of the midpoint method with pair‐wise Verlet lists. In this scheme, which we call the midpoint cell method, simulation space is divided into subdomains, each of which is assigned to a MPI processor. Each subdomain is further divided into small cells. The interaction between two particles existing in different cells is computed in the subdomain containing the midpoint cell of the two cells where the particles reside. In each MPI processor, cell pairs are distributed over OpenMP threads for shared memory parallelization. The midpoint cell method keeps the advantages of the original midpoint method, while filtering out unnecessary calculations of midpoint checking for all the particle pairs by single midpoint cell determination prior to MD simulations. Distributing cell pairs over OpenMP threads allows for more efficient shared memory parallelization compared with distributing atom indices over threads. Furthermore, cell grouping of particle data makes better memory access, reducing the number of cache misses. The parallel performance of the midpoint cell method on the K computer showed scalability up to 512 and 32,768 cores for systems of 20,000 and 1 million atoms, respectively. One MD time step for long‐range interactions could be calculated within 4.5 ms even for a 1 million atoms system with particle‐mesh Ewald electrostatics. © 2014 Wiley Periodicals, Inc.     

Different coordination modes of 2-(diphenylphosphino)azobenzenes in complexation with hard and soft metals

Control of coordination modes of a ligand in metal complexes is significant because the coordination modes influence catalytic properties of transition metal catalysts. Reactions of 2-diphenylphosphinoazobenzenes, which are in equilibrium with the inner phosphonium salts, with ZnCl(2), W(CO)(5)(THF), and PtCl(2)(cod) gave three different coordination types of metal complexes with distinctive UV-vis absorptions. All the complexes were characterized by X-ray crystallographic analyses. In the zinc and tungsten complexes, the source molecule functions as an amide ligand and a phosphine ligand, respectively. In the platinum complex, the phosphorus molecule works as a tridentate ligand with formation of a carbon-platinum bond.     

Nucleophilic Cyclopropanation Reaction with Bis(iodozincio)methane by 1,4‐Addition to α,β‐Unsaturated Carbonyl Compounds

Treatment of α,β‐unsaturated ketones with an electrophilic site at the γ‐position in the presence of trimethylsilyl cyanide with bis(iodozincio)methane afforded the (Z)‐silyl enol ether of the β‐cyclopropyl substituted ketone in good yields. The reaction proceeds by 1,4‐addition to form an enolate, and its sequential intramolecular nucleophilic attack to an adjacent electrophilic site. The reaction of γ‐ethoxycarbonyl‐α,β‐unsaturated ketone and bis(iodozincio)methane in the presence of trimethylsilyl cyanide afforded 1‐ethoxy‐1‐trimethylsiloxycyclopropane derivatives, which can be regarded as the homoenolate equivalent. Additionally, reaction of the obtained homoenolate equivalents with imines give 1‐(E)‐alkenyl‐2‐(1‐aminoalkyl)alkanols diastereoselectively.     

Ultrasound activates ataxia telangiectasia mutated- and rad3-related (ATR)-checkpoint kinase 1 (Chk1) pathway in human leukemia Jurkat cells

Low-intensity ultrasound (US) has been shown to induce death of cancer cells; however, the underlying mechanism remains unclarified. Here, we provide novel evidence that the inhibition of checkpoint kinase 1 (Chk1) by a selective inhibitor or small interfering RNA (siRNA) enhances US-induced apoptosis in Jurkat cells. Jurkat cells showed insignificant lysis immediately after US at any applied intensity, whereas approximately 70% of the cells were γH2AX-positive 30min after US at 0.4W/cm(2). Regarding DNA damage response (DDR), Chk1, known as a target of ataxia telangiectasia mutated (ATM) and rad3-related (ATR), was phosphorylated in cells after US exposure. An ATM inhibitor showed nearly no effect on Chk1 phosphorylation, whereas chemicals showing the ATR inhibitory effect markedly abrogated the phosphorylation, indicating that Chk1 phosphorylation is preferentially more dependent on ATR than on ATM in cells exposed to US. The pharmacological inhibition of Chk1 promoted caspase-3 cleavage and increased the percentage of cells in SubG1 after US exposure. siRNA targeting Chk1 abrogated approximately 55% of Chk1 expression and also promoted apoptosis, suggesting that Chk1 plays anti-apoptotic roles in response to US. These findings revealed, for the first time, that US activates Chk1 dependently on ATR and the activated Chk1 is involved in apoptosis of cells exposed to US. Moreover, we propose that Chk1 may be a promising target in US-aided therapy.