Molecular Rotations of Glucides in Relation to their Structures. V. The Internal Conformation ofC6–OBond in D-Galactopyranose in the Aqueous Solution and the Direction of the Optical Axis of Methylol Group

Shukichi Yamana

doi:10.1246/bcsj.31.558

Residue rotations of L-leucine in the Di-,Tri-,Tetra-, and Penta-peptides of L-leucine and Glycine containing one L-leucyl residue

Australian Journal of Chemistry ◽

10.1071/ch9671983 ◽

1967 ◽

Vol 20 (9) ◽

pp. 1983 ◽

Cited By ~ 2

Author(s):

AF Beechham

Keyword(s):

Aqueous Solution ◽

Molecular Rotations

The molecular rotations, in aqueous solution, at 589 mμ, are tabulated for two hexapeptides and all the di-, tri-, tetra-, and penta-peptides of L-leucine and glycine containing one L-leucyl residue. The molecular rotations of the corresponding N-benzyloxycarbonyl peptides are also listed. It is shown that the ?residue rotation? of L-leucine varies widely, not only between those compounds in which the site of the residue is N-terminal, C-terminal, or internal, but also within these categories. Syntheses of certain of the compounds are described.

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Structures Formed by Cryoprotective Agents Used in Freezc-Etching

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100066292 ◽

1971 ◽

Vol 29 ◽

pp. 448-449

Author(s):

G. G. Cocks ◽

C. E. Cluthe

Keyword(s):

Aqueous Solution ◽

Polyethylene Oxide ◽

Liquid Nitrogen Temperature ◽

Ice Crystals ◽

Etching Technique ◽

Structural Constituent ◽

Cryoprotective Agents ◽

Quick Freezing ◽

Freeze Etching ◽

Fractured Surface

The freeze etching technique is potentially useful for examining dilute solutions or suspensions of macromolecular materials. Quick freezing of aqueous solutions in Freon or propane at or near liquid nitrogen temperature produces relatively large ice crystals and these crystals may damage the structures to be examined. Cryoprotective agents may reduce damage to the specimem, hut their use often results in the formation of a different set of specimem artifacts.In a study of the structure of polyethylene oxide gels glycerol and sucrose were used as cryoprotective agents. The experiments reported here show some of the structures which can appear when these cryoprotective agents are used.Figure 1 shows a fractured surface of a frozen 25% aqueous solution of sucrose. The branches of dendritic ice crystals surrounded hy ice-sucrose eutectic can be seen. When this fractured surface is etched the ice in the dendrites sublimes giving the type of structure shown in Figure 2. The ice-sucrose eutectic etches much more slowly. It is the smooth continuous structural constituent surrounding the branches of the dendrites.

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Analysis of 3-d molecular distribution with the digital imaging microscope

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100102286 ◽

1988 ◽

Vol 46 ◽

pp. 40-41

Author(s):

W.A. Carrington ◽

F.S. Fay ◽

K.E. Fogarty ◽

L. Lifshitz

Keyword(s):

Image Restoration ◽

Digital Imaging ◽

Fluorescent Dyes ◽

Optical Axis ◽

Computer Hardware ◽

Computer Algorithms ◽

Low Contrast ◽

Specific Proteins ◽

Effective Use ◽

Single Living Cells

Advances in digital imaging microscopy and in the synthesis of fluorescent dyes allow the determination of 3D distribution of specific proteins, ions, GNA or DNA in single living cells. Effective use of this technology requires a combination of optical and computer hardware and software for image restoration, feature extraction and computer graphics.The digital imaging microscope consists of a conventional epifluorescence microscope with computer controlled focus, excitation and emission wavelength and duration of excitation. Images are recorded with a cooled (-80°C) CCD. 3D images are obtained as a series of optical sections at .25 - .5 μm intervals.A conventional microscope has substantial blurring along its optical axis. Out of focus contributions to a single optical section cause low contrast and flare; details are poorly resolved along the optical axis. We have developed new computer algorithms for reversing these distortions. These image restoration techniques and scanning confocal microscopes yield significantly better images; the results from the two are comparable.

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Field Distribution of Strongly Excited Magnetic Lenses

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100114323 ◽

1975 ◽

Vol 33 ◽

pp. 140-141

Author(s):

M. Strojnik

Keyword(s):

Flux Density ◽

Field Distribution ◽

Optical Axis ◽

Operating Point ◽

Pole Piece ◽

Partial Saturation ◽

Axial Flux ◽

The Stability

Magnetic lenses operating in partial saturation offer two advantages in HVEM: they exhibit small cs and cc and their power depends little on the excitation IN. Curve H, Fig. 1, shows that the maximal axial flux density Bz max of one of the lenses investigated changes between points (3) and (4) by 5% as the excitation varies by 40%. Consequently, the designer can relax the requirements concerning the stability of the lens current supplies. Saturated lenses, however, can only be used if (i) unwanted fields along the optical axis can be controlled, (ii) 'wobbling' of the optical axis due to inhomogeneous saturation around the pole piece faces is prevented, (iii) ample ampere-turns can be squeezed into the space available, and (iv) the lens operating point covers a sufficient range of accelerating voltages.

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Preparation and characterisation of vanadium pentoxide supported rhodium catalyst

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s042482010010679x ◽

1988 ◽

Vol 46 ◽

pp. 946-947

Author(s):

A. Legrouri

Keyword(s):

Aqueous Solution ◽

Thermal Decomposition ◽

Physicochemical Properties ◽

Surface Area ◽

Vanadium Pentoxide ◽

High Purity ◽

Gas Adsorption ◽

Rhodium Catalyst ◽

Optical Methods ◽

Reducible Oxides

The industrial importance of metal catalysts supported on reducible oxides has stimulated considerable interest during the last few years. This presentation reports on the study of the physicochemical properties of metallic rhodium supported on vanadium pentoxide (Rh/V2O5). Electron optical methods, in conjunction with other techniques, were used to characterise the catalyst before its use in the hydrogenolysis of butane; a reaction for which Rh metal is known to be among the most active catalysts.V2O5 powder was prepared by thermal decomposition of high purity ammonium metavanadate in air at 400 °C for 2 hours. Previous studies of the microstructure of this compound, by HREM, SEM and gas adsorption, showed it to be non— porous with a very low surface area of 6m2/g3. The metal loading of the catalyst used was lwt%Rh on V2Q5. It was prepared by wet impregnating the support with an aqueous solution of RhCI3.3H2O.

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TEM observation of iron oxide pillars in montmorillonite

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100177544 ◽

1990 ◽

Vol 48 (4) ◽

pp. 882-883

Author(s):

H. Mori ◽

Y. Murata ◽

H. Yoneyama ◽

H. Fujita

Keyword(s):

Aqueous Solution ◽

Iron Oxide ◽

Fine Particles ◽

Aqueous Suspension ◽

Volume Ratio ◽

Exchange Capacity ◽

Nano Composites ◽

Pillared Montmorillonite ◽

Topographic Features ◽

Transmission Electron

Recently, a new sort of nano-composites has been prepared by incorporating such fine particles as metal oxide microcrystallites and organic polymers into the interlayer space of montmorillonite. Owing to their extremely large specific surface area, the nano-composites are finding wide application[1∼3]. However, the topographic features of the microstructures have not been elucidated as yet In the present work, the microstructures of iron oxide-pillared montmorillonite have been investigated by high-resolution transmission electron microscopy.Iron oxide-pillared montmorillonite was prepared through the procedure essentially the same as that reported by Yamanaka et al. Firstly, 0.125 M aqueous solution of trinuclear acetato-hydroxo iron(III) nitrate, [Fe3(OCOCH3)7 OH.2H2O]NO3, was prepared and then the solution was mixed with an aqueous suspension of 1 wt% clay by continuously stirring at 308 K. The final volume ratio of the latter aqueous solution to the former was 0.4. The clay used was sodium montmorillonite (Kunimine Industrial Co.), having a cation exchange capacity of 100 mequiv/100g. The montmorillonite in the mixed suspension was then centrifuged, followed by washing with deionized water. The washed samples were spread on glass plates, air dried, and then annealed at 673 K for 72 ks in air. The resultant film products were approximately 20 μm in thickness and brown in color.

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The microstructure of functionalized poLyacrylonitrile beads for bioseparations

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100178604 ◽

1990 ◽

Vol 48 (4) ◽

pp. 1094-1095

Author(s):

Eduardo A. Kamenetzky ◽

David A. Ley

Keyword(s):

Aqueous Solution ◽

Affinity Chromatography ◽

Pore Size Distribution ◽

Pore Size ◽

Surface Coverage ◽

Vacuum Impregnation ◽

Thin Sections ◽

Selective Staining ◽

Low Viscosity ◽

Diamond Knife

The microstructure of polyacrylonitrile (PAN) beads for affinity chromatography bioseparations was studied by TEM of stained ultramicrotomed thin-sections. Microstructural aspects such as overall pore size distribution, the distribution of pores within the beads, and surface coverage of functionalized beads affect performance properties. Stereological methods are used to quantify the internal structure of these chromatographic supports. Details of the process for making the PAN beads are given elsewhere. TEM specimens were obtained by vacuum impregnation with a low-viscosity epoxy and sectioning with a diamond knife. The beads can be observed unstained. However, different surface functionalities can be made evident by selective staining. Amide surface coverage was studied by staining in vapor of a 0.5.% RuO4 aqueous solution for 1 h. RuO4 does not stain PAN but stains, amongst many others, polymers containing an amide moiety.

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