Type I CM-type II DM transitions of lyotropic liquid crystals

1981 ◽  
Vol 103 (7) ◽  
pp. 1641-1647 ◽  
Author(s):  
Bruce J. Forrest ◽  
Leonard W. Reeves
Keyword(s):  
Liquid Crystals ◽  
Lyotropic Liquid Crystals ◽  
Type I ◽  
Type Ii

Liquid crystal/glass interface effects on the orientation of lyotropic liquid crystals in magnetic fields

1978 ◽  
Vol 56 (16) ◽  
pp. 2178-2183 ◽  
Author(s):  
Fred Y. Fujiwara ◽  
Leonard W. Reeves
Keyword(s):  
Magnetic Field ◽  
Liquid Crystal ◽  
Liquid Crystals ◽  
Cylindrical Tube ◽  
Lyotropic Liquid Crystals ◽  
Crystal Glass ◽  
Type I ◽  
Type Ii ◽  
Glass Interface ◽  
Interface Effects

Lyotropic mesophases of both positive (type I) and negative (type II) diamagnetic anisotropy have been prepared. The deuterium magnetic resonance signal from D2O in the sample bas been studied during the process of orientation in a magnetic field. A type II mesophase oriented by a magnetic field in a cylindrical tube perpendicular to the lines of force does not achieve a uniform distribution of directors in a plane perpendicular to the field. The re orientation of a type I mesophase after an initial displacement of the director at an angle to the field has been studied. Previous equations derived for thermotropic liquid crystals are applicable but the velocity of re-orientation was found to be an inverse function of the radius, for nmr tubes of less than 4 mm in diameter, indicating that liquid crystal/glass interface effects are important.

Micellar super-structure in magnetically aligned lyotropic liquid crystals studied by light scattering

1979 ◽  
Vol 57 (9) ◽  
pp. 1108-1110 ◽  
Author(s):  
Paulo C. Isolani ◽  
Leonard W. Reeves ◽  
J. Atílio Vanin
Keyword(s):  
Liquid Crystals ◽  
Light Scattering ◽  
Laser Light ◽  
Angular Separation ◽  
Average Diameter ◽  
Laser Light Scattering ◽  
Lyotropic Liquid Crystals ◽  
Type Ii ◽  
X Ray ◽  
Magnetically Aligned

Depolarized components of laser light scattering patterns have been investigated for type II lyotropic liquid crystals. These patterns are characterized by intensity maxima and minima with constant angular separation. By using the Bragg equation, a set of distances typical for lamellar arrays can be derived. Two possible models are proposed to explain the results: the first is that the distances are related to the average diameter of lyomesomorphic micelles not accessible to low angle X-ray studies and the second model is a repeating hyperstructure of micellar microdomains.

Heat-Etching with a Bullivant Type II Simple Freeze-Cleave Device

1970 ◽  
Vol 28 ◽  
pp. 106-107 ◽  
Author(s):  
Ronald S. Weinstein ◽  
N. Scott McNutt
Keyword(s):  
New Zealand ◽  
General Hospital ◽  
Massachusetts General Hospital ◽  
Type I ◽  
Type Ii ◽  
Collaborative Effort ◽  
Temperature And Pressure ◽  
The University

The Type I simple cold block device was described by Bullivant and Ames in 1966 and represented the product of the first successful effort to simplify the equipment required to do sophisticated freeze-cleave techniques. Bullivant, Weinstein and Someda described the Type II device which is a modification of the Type I device and was developed as a collaborative effort at the Massachusetts General Hospital and the University of Auckland, New Zealand. The modifications reduced specimen contamination and provided controlled specimen warming for heat-etching of fracture faces. We have now tested the Mass. General Hospital version of the Type II device (called the “Type II-MGH device”) on a wide variety of biological specimens and have established temperature and pressure curves for routine heat-etching with the device.

Labelling of non-A, non-B hepatitis infected chimpanzee hepatocytes with nuclease-gold conjugates

1984 ◽  
Vol 42 ◽  
pp. 250-251
Author(s):  
G. D. Gagne ◽  
M. F. Miller ◽  
D. A. Peterson
Keyword(s):  
Endoplasmic Reticulum ◽  
Experimental Infection ◽  
Uranyl Acetate ◽  
Type I ◽  
Cellular Injury ◽  
Type Ii ◽  
Tubular Structures ◽  
Type Iii ◽  
Type Iv ◽  
Infected Chimpanzee

Experimental infection of chimpanzees with non-A, non-B hepatitis (NANB) or with delta agent hepatitis results in the appearance of characteristic cytoplasmic alterations in the hepatocytes. These alterations include spongelike inclusions (Type I), attached convoluted membranes (Type II), tubular structures (Type III), and microtubular aggregates (Type IV) (Fig. 1). Type I, II and III structures are, by association, believed to be derived from endoplasmic reticulum and may be morphogenetically related. Type IV structures are generally observed free in the cytoplasm but sometimes in the vicinity of type III structures. It is not known whether these structures are somehow involved in the replication and/or assembly of the putative NANB virus or whether they are simply nonspecific responses to cellular injury. When treated with uranyl acetate, type I, II and III structures stain intensely as if they might contain nucleic acids. If these structures do correspond to intermediates in the replication of a virus, one might expect them to contain DNA or RNA and the present study was undertaken to explore this possibility.

Comparative surface and ultrastructural views of methylotrophic bacteria by TEM, STEM, SE, and freeze-etch electron microscopy.

1987 ◽  
Vol 45 ◽  
pp. 792-793
Author(s):  
T.A. Fassel ◽  
M.J. Schaller ◽  
M.E. Lidstrom ◽  
C.C. Remsen
Keyword(s):  
Cytoplasmic Membrane ◽  
Structural Features ◽  
Methylotrophic Bacteria ◽  
Type I ◽  
Type Ii ◽  
Membrane Complex ◽  
Oxidation Of Methane ◽  
Methane Oxidizing Bacteria ◽  
Wall Structures ◽  
Methylomonas Albus

Methylotrophic bacteria play an Important role in the environment in the oxidation of methane and methanol. Extensive intracytoplasmic membranes (ICM) have been associated with the oxidation processes in methylotrophs and chemolithotrophic bacteria. Classification on the basis of ICM arrangement distinguishes 2 types of methylotrophs. Bundles or vesicular stacks of ICM located away from the cytoplasmic membrane and extending into the cytoplasm are present in Type I methylotrophs. In Type II methylotrophs, the ICM form pairs of peripheral membranes located parallel to the cytoplasmic membrane. Complex cell wall structures of tightly packed cup-shaped subunits have been described in strains of marine and freshwater phototrophic sulfur bacteria and several strains of methane oxidizing bacteria. We examined the ultrastructure of the methylotrophs with particular view of the ICM and surface structural features, between representatives of the Type I Methylomonas albus (BG8), and Type II Methylosinus trichosporium (OB-36).

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