scholarly journals Freeze-fracture planes of methanogen membranes correlate with the content of tetraether lipids.

1993 ◽  
Vol 175 (4) ◽  
pp. 1191-1197 ◽  
Author(s):  
T J Beveridge ◽  
C G Choquet ◽  
G B Patel ◽  
G D Sprott
1985 ◽  
Vol 115 (1) ◽  
pp. 103-127 ◽  
Author(s):  
Michael J. Kell ◽  
Louis J. DeFelice ◽  
W. Goolsby

1972 ◽  
Vol 10 (2) ◽  
pp. 555-561
Author(s):  
F. V. HEREWARD ◽  
D. H. NORTHCOTE

In freeze-etch replicas the position of the plane of fracture along membranes is controversial; in an attempt to clarify the situation we have examined drops of yeast suspension frozen at -160 °C, fractured and then freeze-substituted with a solution of osmium tetroxide in acetone. The drops were embedded in Araldite and sections were cut perpendicular to the plane of fracture to show where the cleavage had occurred. At the tonoplast the membrane split and the plane of fracture ran between the 2 darkly staining lines. At the plasmalemma the cleavage plane was not clearly localized. The inner half of the membrane remained with the protoplast and darkly staining material could be seen on the wall. However, in some places the dark line at the surface of the protoplast could be resolved into 2 lines. The cleavage plane appeared to change at the invaginations of the plasmalemma, where on fracture the whole membrane sometimes remained attached to the wall.


1973 ◽  
Vol 57 (1) ◽  
pp. 66-76 ◽  
Author(s):  
Camillo Peracchia

Low resistance junctions between axons of crayfish ganglia are studied by freeze-fracture and negative staining. In freeze-fracture, fracture planes that go through a junctional membrane expose two faces, both internal, called face A and face B. Face A belongs to the internal membrane leaflet and faces the gap. Face B belongs to the external membrane leaflet and faces the axoplasm. Face A displays pits, 60–100 Å in diameter, arranged in a hexagonal array with a unit cell of ∼200 Å. An ∼25 Å bump is frequently seen at the center of each pit. Some pits are occupied by a globule ∼125 Å in diameter, which displays a central depression ∼25 Å in size. Face B contains globules also arranged in a fairly regular hexagonal pattern. The center-to-center distance between adjacent globules is most frequently ∼200 Å; however, occasionally certain globules are seen separated by a distance as short as ∼125 Å. The top surface of the globules occasionally displays a starlike profile and seems to contain a central depression ∼25 Å in diameter. In negatively stained preparations of membranes from the nerve cord, two types of membranes are seen containing a fairly regular pattern. In one, globules ∼95 Å in diameter form a hexagonal close packing with a unit cell of ∼95 Å. In the other, globules of the same size are organized in a larger hexagonal array with a unit cell of ∼155 Å (swollen arrangement). Some of the globules forming the swollen arrangement are seen containing six subunits. The six subunits form a hexagon which is skewed with respect to the main rows of hexagons in such a way that the subunits lie on rows which make an angle of ∼37° with the main rows.


1982 ◽  
Vol 19 (1) ◽  
pp. 111-114 ◽  
Author(s):  
Pierre Delage ◽  
Daniel Tessier ◽  
Martine Marcel-Audiguier

The cryoscan is an apparatus equipping the JEOL scanning electron microscopes, and allowing the observation of freeze-fracture planes of samples whose temperature is maintained below −100 °C. The application of this method to a sensitive clay from Quebec shows an aggregated structure, the aggregates being separated by 1 μm size voids.


Author(s):  
P.L. Moore

Previous freeze fracture results on the intact giant, amoeba Chaos carolinensis indicated the presence of a fibrillar arrangement of filaments within the cytoplasm. A complete interpretation of the three dimensional ultrastructure of these structures, and their possible role in amoeboid movement was not possible, since comparable results could not be obtained with conventional fixation of intact amoebae. Progress in interpreting the freeze fracture images of amoebae required a more thorough understanding of the different types of filaments present in amoebae, and of the ways in which they could be organized while remaining functional.The recent development of a calcium sensitive, demembranated, amoeboid model of Chaos carolinensis has made it possible to achieve a better understanding of such functional arrangements of amoeboid filaments. In these models the motility of demembranated cytoplasm can be controlled in vitro, and the chemical conditions necessary for contractility, and cytoplasmic streaming can be investigated. It is clear from these studies that “fibrils” exist in amoeboid models, and that they are capable of contracting along their length under conditions similar to those which cause contraction in vertebrate muscles.


Author(s):  
A. Tonosaki ◽  
M. Yamasaki ◽  
H. Washioka ◽  
J. Mizoguchi

A vertebrate disk membrane is composed of 40 % lipids and 60 % proteins. Its fracture faces have been classed into the plasmic (PF) and exoplasmic faces (EF), complementary with each other, like those of most other types of cell membranes. The hypothesis assuming the PF particles as representing membrane-associated proteins has been challenged by serious questions if they in fact emerge from the crystalline formation or decoration effects during freezing and shadowing processes. This problem seems to be yet unanswered, despite the remarkable case of the purple membrane of Halobacterium, partly because most observations have been made on the replicas from a single face of specimen, and partly because, in the case of photoreceptor membranes, the conformation of a rhodopsin and its relatives remains yet uncertain. The former defect seems to be partially fulfilled with complementary replica methods.


Author(s):  
H. Gross ◽  
H. Moor

Fracturing under ultrahigh vacuum (UHV, p ≤ 10-9 Torr) produces membrane fracture faces devoid of contamination. Such clean surfaces are a prerequisite foe studies of interactions between condensing molecules is possible and surface forces are unequally distributed, the condensate will accumulate at places with high binding forces; crystallites will arise which may be useful a probes for surface sites with specific physico-chemical properties. Specific “decoration” with crystallites can be achieved nby exposing membrane fracture faces to water vopour. A device was developed which enables the production of pure water vapour and the controlled variation of its partial pressure in an UHV freeze-fracture apparatus (Fig.1a). Under vaccum (≤ 10-3 Torr), small container filled with copper-sulfate-pentahydrate is heated with a heating coil, with the temperature controlled by means of a thermocouple. The water of hydration thereby released enters a storage vessel.


Author(s):  
Russell L. Steere ◽  
Eric F. Erbe

It has been assumed by many involved in freeze-etch or freeze-fracture studies that it would be useless to etch specimens which were cryoprotected by more than 15% glycerol. We presumed that the amount of cryoprotective material exposed at the surface would serve as a contaminating layer and prevent the visualization of fine details. Recent unexpected freeze-etch results indicated that it would be useful to compare complementary replicas in which one-half of the frozen-fractured specimen would be shadowed and replicated immediately after fracturing whereas the complement would be etched at -98°C for 1 to 10 minutes before being shadowed and replicated.Standard complementary replica holders (Steere, 1973) with hinges removed were used for this study. Specimens consisting of unfixed virus-infected plant tissue infiltrated with 0.05 M phosphate buffer or distilled water were used without cryoprotectant. Some were permitted to settle through gradients to the desired concentrations of different cryoprotectants.


Author(s):  
Ulrich Dierkes

Calcium is supposed to play an important role in the control of protoplasmic streaming in slime mold plasmodia. The motive force for protoplasmic streaming is generated by the interaction of actin and myosin. This contraction is supposed to be controlled by intracellular Ca-fluxes similar to the triggering system in skeleton muscle. The histochemical localisation of calcium however is problematic because of the possible diffusion artifacts especially in aquous media.To evaluate this problem calcium localisation was studied in small pieces of shock frozen (liquid propane at -189°C) plasmodial strands of Physarum polycephalum, which were further processed with 3 different methods: 1) freeze substitution in ethanol at -75°C, staining in 100% ethanol with 1% uranyl acetate, and embedding in styrene-methacrylate. For comparison the staining procedure was omitted in some preparations. 2)Freeze drying at about -95°C, followed by immersion with 100% ethanol containing 1% uranyl acetate, and embedding. 3) Freeze fracture, carbon coating and SEM investigation at temperatures below -100° C.


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