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A
-type cyclodextrin glycosyltransferase that produces
-cyclodextrin as the main product has been crystallized and analyzed by X-ray diffraction. Phasing was successfully carried out using the molecular-replacement method.
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The expression, purification and crystallization of the collagen-binding region of the E. rhusiopathiae surface protein RspB is described. The crystals diffracted to 2.2 Å resolution using synchrotron radiation.



asHPAL, a member of the HpaI/HpcH subfamily of class II aldolases, was expressed, purified and crystallized in the absence and presence of 2-ketobutyrate as one of its substrates using the sitting-drop vapour-diffusion method. asHPAL crystals grown without and with 2-ketobutyrate diffracted to 1.60 and 1.55 Å resolution, respectively.


Variable-temperature X-ray crystal structure analyses of several N-benzylideneanilines revealed that a conformational change through a pedal motion takes place in the crystals.



Variable-temperature X-ray structure analysis of azobenzenes reveals that the torsional vibration of the N-Ph bonds is large enough to give rise to conformational interconversion in crystals.

Variable-temperature X-ray crystal structure analyses of N-benzylideneanilines revealed that the torsional vibration of the C-Ph and N-Ph bonds causes an apparent shortening of the C=N bond at room temperature.

Atomic ordering and lattice distortion in the zirconium-oxygen alloys with 28.2 and 29.2 at.% oxygen
The structure of the interstitially ordered lattice formed in zirconium-oxygen alloys has been studied with use of single-crystal data obtained by X-ray and neutron diffraction methods. The structure belongs to space group P312 and the lattice parameters a and c are related to a0 and c0 of the host hexagonal metal lattice by a =
3a0 and c = c0. The ordered arrangement of interstitial oxygen atoms is described as a regular stacking of layers parallel to the (00.1) plane with the sequence (AC)B(AC)B
which is of the same type as that of nitrogen atoms in
-Fe2N. The occupancy probability of oxygen atoms is high for interstitial sites of the A and B types while it is low for sites of the C type. The host metal lattice is distorted in such a way that spacings of successive (00.2) planes are not the same and a hexagonal network of atoms in these planes is periodically deformed.
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A new multipurpose X-ray small-angle scattering camera system consisting of a rotating-anode X-ray generator, a double-focusing collimator and a two-dimensional position-sensitive detector has been developed at the High-Intensity X-ray Laboratory of Kyoto University. The overall camera length is 6 m, and the sample-to-detector distance can be varied in 0.5 m increments up to 3 m to cover scattering angles ranging from 0.001 to 0.18 rad. The collimator consists of a pair of crossed-plane total-reflection mirrors of 40 cm in length. The mirrors, which are mechanically bent to form cylindrical surfaces, provide point collimation free of collimation error. General-purpose sample holders equipped with a programmable temperature controller are provided for both transmission and scattering measurements; the temperature is maintained within ± 0.1 K in the range of 223-573 K. A cryostat for measurements down to 20 K, a dynamic sample deformation apparatus, and a temperature-jump equipment are also available. The multi-wire delay-line position-sensitive proportional counter has an active area of 128 × 128 mm with a spatial resolution of 0.5 × 1.0 mm. The data acquisition is controlled by a real-time front-end processor through a CAMAC interface. The data are recorded in a dual-port histogramming memory of 32 bit × 1 Mwords, which enables direct access to the data from the main computer for real-time monitoring and analysis. The performance of the camera is demonstrated with some selected examples: diffraction patterns from carp lateral line nerve myelin and chicken-tendon collagen fibrils, a Guinier plot of the scattering from polystyrene in dilute solution, and time-resolved measurements of polypropylene during the annealing process.

The structure of the title compound was determined to confirm the position of the keto group in the molecule prepared enantioselectively by a bioconversion from myo-inositol. There are two independent molecules showing similar geometry.

The absolute configuration was determined for the title compound, which was prepared in a synthetic study on the natural products bryostatins. There are two independent molecules which show similar conformations, except for the orientation of the methoxy groups.

The absolute configuration was determined for the optically active title compound, which was prepared in a synthetic study on the natural products bryostatins.


A new interference technique to measure the transverse coherence of X-ray free-electron lasers is proposed and applied to the characterization of the coherence properties of ultra-intense focused X-ray pulses from the SPring-8 Ångstrom Compact free-electron LAser (SACLA).
