Scanning near-field optical/atomic force microscopy for fluorescence imaging and spectroscopy of biomaterials in air and liquid: Observation of recombinantEscherichia coli with gene coding to green fluorescent protein

We have developed a system of scanning near-field optical/atomic force microscopy (SNOM/AFM) for fluorescence imaging and spectroscopy of biomaterials in air and liquid. SNOM/AFM uses a bent optical fiber simultaneously as a dynamic force AFM cantilever and a SNOM probe. Optical resolution of SNOM images shows about 50 nm in an illumination mode for a standard sample of a patterned chromium layer of 20 nm thickness on a quartz glass plate. The SNOM/AFM system contains a photon counting system and polychrometer/ICCD (intensified charge coupled device) system for observation of the fluorescence image and spectrograph of micro areas, respectively. The gene coding to green fluorescence protein (GFP) was cloned in recombinantEscherichia coli (E. coli). Topography, fluorescence image and spectrograph of recombinantE. coli by SNOM/AFM showed a difference in fluorescence in individualE. coli. Fluorescence activity of GFP can thus be used as a convenient indicator of transformation. SNOM/AFM is also applicable to observe immobilizedE. coli on a glass plate in water with a liquid chamber and may allow the viewing of observation of floating organisms.     

Positron annihilation in dextro and laevo amino acid

High-precision positron lifetime spectra in tryptophan do not confirm the pronounced asymmetries in the interaction of positrons from radioactive sources with the d and l forms that were reported earlier and quoted as a cause for the the evolution of living matter with laevo amino acids.     

Selective determination of pentoses,hexoses and 6-deoxyhexoses by dual-wavelength spectrophotometry with the cysteine—phenol—sulfuric acid system

A convenient method is described for the selective determination of pentoses, hexoses and 6-deoxyhexoses by dual-wavelength spectrophotometry with the l-cysteine—phenol—sulfuric acid system. Excellent linearity was observed for 25–250 nmol of pentoses, and for 25–500 nmol of hexoses and 6-deoxyhexoses. These aldoses in those sample ranges could be determined selectively with high accuracy and precision by the k -factor mode. The appropriate, wavelength of λ₂ was 462, 499 and 398 nm for pentoses, hexoses and 6-deoxyhexoses, respectively, whereas that of λ₁ was commonly 424 nm.     

Cation-controlled assembly of Na+-linked lacunary alpha-Keggin tungstosilicates

Two novel salts of lacunary tungstosilicates with guanidinium and alkali metal cations, (CH6N3)7Na[SiW11O39].(CH3)2CO.8H2O (1) and (CH6N3)K6Na[SiW11O39].11.5H2O (2), have been synthesized and their crystal structures have been determined by synchrotron X-ray diffraction. In both crystals, the Na+ cations link the lacunary Keggin-type tungstosilicate anions into linear structures. The neighboring [SiW11O39]8- anions are related by two-fold screw and translational operations in compounds 1 and 2, respectively. Second harmonic generation was observed for compound 1.     

Domain-wall resistance in ferromagnetic (Ga,Mn)As

A series of microstructures designed to pin domain walls (DWs) in (Ga,Mn)As with perpendicular magnetic anisotropy has been employed to determine extrinsic and intrinsic contributions to DW resistance. The former is explained quantitatively as resulting from a polarity change in the Hall electric field at DW. The latter is 1 order of magnitude greater than a term brought about by anisotropic magnetoresistance and is shown to be consistent with disorder-induced mistracking of the carrier spins subject to spatially varying magnetization.     

Velocity of domain-wall motion induced by electrical current in the ferromagnetic semiconductor (Ga,Mn)As

Current-induced domain-wall motion with velocity spanning over 5 orders of magnitude up to 22 m/s has been observed by the magneto-optical Kerr effect in (Ga,Mn)As with perpendicular magnetic anisotropy. The data are employed to verify theories of spin transfer by the Slonczewski-like mechanism as well as by the torque resulting from spin-flip transitions in the domain-wall region. Evidence for domain-wall creep at low currents is found.     

Determination of selenium in sediment by isotope-dilution inductively coupled plasma mass spectrometry with an octapole reaction cell

A method is described for determination of selenium in sediment by isotope-dilution inductively coupled plasma mass spectrometry with an octapole reaction cell (ID–ICP–ORCMS). Sediment samples were digested with HNO₃, HClO₄, and HF, and the digestion included an elaborate evaporation process to remove bromine from the digested solution. Simple strong cation-exchange disk filtration was used to remove rare earth elements (REE) from the digested solution, because REE²⁺ seriously interfere with Se isotopes (i.e. ¹⁵⁶Gd²⁺ with ⁷⁸Se⁺, ¹⁶⁰Gd²⁺ with ⁸⁰Se⁺). Addition of acetic acid to the filtrate was examined to improve the sensitivity of ICP–ORCMS measurement of Se⁺ by means of a carbon-enhancement effect. The interfering for selenium isotopes were almost eliminated by use of H₂ as reaction gas. Interference from BrH⁺ formed in the reaction cell was negligible because the Br was removed in the evaporation process. Approximately 99.5% of REE were removed by cation-exchange disk filtration yet more than 99% of Se remained in the filtrate solution. The intensity for Se⁺ was enhanced approximately fourfold by addition of 5% (v/v) of acetic acid whereas that for was barely enhanced. Measured ⁸⁰Se/⁷⁸Se ratios in unspiked digested solutions of the sample were in good agreement with that for an Se standard solution. The analytical results for Se in the certified reference materials MESS-3 and PACS-1 were in good agreement with their certified values, with small uncertainties.