Cellular Distribution of Extractives in Redwood and Incense Cedar - Part II. Microscopic Observation of the Location of Cell Wall and Cell Cavity Extractives

Holzforschung ◽  
1980 ◽  
Vol 34 (2) ◽  
pp. 41-47 ◽  
Author(s):  
Mon-Lin Kuo ◽  
Donald G. Arganbright
eLife ◽  
2019 ◽  
Vol 8 ◽  
Author(s):  
Felix Wong ◽  
Ethan C Garner ◽  
Ariel Amir

MreB is an actin homolog that is essential for coordinating the cell wall synthesis required for the rod shape of many bacteria. Previously we have shown that filaments of MreB bind to the curved membranes of bacteria and translocate in directions determined by principal membrane curvatures to create and reinforce the rod shape (Hussain et al., 2018). Here, in order to understand how MreB filament dynamics affects their cellular distribution, we model how MreB filaments bind and translocate on membranes with different geometries. We find that it is both energetically favorable and robust for filaments to bind and orient along directions of largest membrane curvature. Furthermore, significant localization to different membrane regions results from processive MreB motion in various geometries. These results demonstrate that the in vivo localization of MreB observed in many different experiments, including those examining negative Gaussian curvature, can arise from translocation dynamics alone.


1927 ◽  
Vol 11 (2) ◽  
pp. 193-205 ◽  
Author(s):  
W. J. V. Osterhout ◽  
E. B. Damon ◽  
A. G. Jacques

The protoplasm of Valonia macrophysa forms a delicate layer, only a few microns in thickness, which contains numerous chloroplasts and nuclei. The outer surface is in contact with the cell wall, the inner with the vacuolar sap. As far as microscopic observation goes, these two surfaces seem alike; but measurements of potential difference indicate that they are decidedly different. We find that the chain sap | protoplasm | sap gives about 14.5 millivolts, the inner surface being positive to the outer. In order to explain this we may assume that the protoplasm consists of layers, the outer surface, X, differing from the inner surface, Y, and from the body of the protoplasm, W. We should then have the unsymmetrical chain sap | X | W | Y | sap which could produce an electromotive force. If the two surfaces of such a very thin layer of protoplasm can be different, it is of fundamental significance for the theory of the nature of living matter.


1970 ◽  
Vol 7 (3) ◽  
pp. 755-785
Author(s):  
D. C. BARKER ◽  
KAREEN J. I. THORNE

Spheroplasts of L. casei were prepared by the simultaneous action of trypsin and lysozyme in the presence of EDTA and 20% sucrose. Electron microscopy of thin sections of cells during the formation of spheroplasts showed that the spheroplasts emerged from the cell wall through a weak point at one end of the cell. Electron microscopy of negatively stained preparations showed that the structure of spheroplast membranes obtained by disruption in hypotonic medium varied according to the nature of the hypotonic medium used. Disruption in water gave small, delicate membrane fragments; disruption in 0.1 M tris-Cl gave large pieces with tubulo-vesicular attachments. The effects of Mg2+ and EDTA were also investigated. Bactoprenol, the C55 isoprenoid alcohol concerned in cell wall biosynthesis, was located by growing L. casei in [14C]mevalonic acid. Over 90% of the cellular bactoprenol was found in the spheroplast membrane when this was obtained with 0.1 M tris-Cl, but only 42% when the spheroplasts were burst in water. It is suggested that the missing bactoprenol may be solubilized with the membranes of mesosomal orgin, and that bactoprenol is therefore a component of both plasma and mesosomal membranes.


1971 ◽  
Vol 49 (8) ◽  
pp. 1487-1496 ◽  
Author(s):  
Albert R. Gordon ◽  
Norman A. Alldridge

Four soluble and two cell wall bound peroxidases account for most of the peroxidase activity in sections of tomato stem tissues. These peroxidases differ in heat sensitivity when incubated in acidic media. Two of the six peroxidases are inactivated at higher temperatures in tissue sections than in tissue extracts treated in the same way. Under defined conditions of heating, all but one of the tomato peroxidases can be inactivated in tissue sections and extracts. A cytochemical peroxidase method is described and used to determine the cellular distribution of this heat-stable peroxidase in developing stem tissues. Changes in the activity and cellular distribution of this peroxidase occur in tissues of the stem during development.


1997 ◽  
Vol 161 ◽  
pp. 491-504 ◽  
Author(s):  
Frances Westall

AbstractThe oldest cell-like structures on Earth are preserved in silicified lagoonal, shallow sea or hydrothermal sediments, such as some Archean formations in Western Australia and South Africa. Previous studies concentrated on the search for organic fossils in Archean rocks. Observations of silicified bacteria (as silica minerals) are scarce for both the Precambrian and the Phanerozoic, but reports of mineral bacteria finds, in general, are increasing. The problems associated with the identification of authentic fossil bacteria and, if possible, closer identification of bacteria type can, in part, be overcome by experimental fossilisation studies. These have shown that not all bacteria fossilise in the same way and, indeed, some seem to be very resistent to fossilisation. This paper deals with a transmission electron microscope investigation of the silicification of four species of bacteria commonly found in the environment. The Gram positiveBacillus laterosporusand its spore produced a robust, durable crust upon silicification, whereas the Gram negativePseudomonas fluorescens, Ps. vesicularis, andPs. acidovoranspresented delicately preserved walls. The greater amount of peptidoglycan, containing abundant metal cation binding sites, in the cell wall of the Gram positive bacterium, probably accounts for the difference in the mode of fossilisation. The Gram positive bacteria are, therefore, probably most likely to be preserved in the terrestrial and extraterrestrial rock record.


Author(s):  
D. James Morré ◽  
Charles E. Bracker ◽  
William J. VanDerWoude

Calcium ions in the concentration range 5-100 mM inhibit auxin-induced cell elongation and wall extensibility of plant stems. Inhibition of wall extensibility requires that the tissue be living; growth inhibition cannot be explained on the basis of cross-linking of carboxyl groups of cell wall uronides by calcium ions. In this study, ultrastructural evidence was sought for an interaction of calcium ions with some component other than the wall at the cell surface of soybean (Glycine max (L.) Merr.) hypocotyls.


Author(s):  
L. V. Leak

Electron microscopic observations of freeze-fracture replicas of Anabaena cells obtained by the procedures described by Bullivant and Ames (J. Cell Biol., 1966) indicate that the frozen cells are fractured in many different planes. This fracturing or cleaving along various planes allows one to gain a three dimensional relation of the cellular components as a result of such a manipulation. When replicas that are obtained by the freeze-fracture method are observed in the electron microscope, cross fractures of the cell wall and membranes that comprise the photosynthetic lamellae are apparent as demonstrated in Figures 1 & 2.A large portion of the Anabaena cell is composed of undulating layers of cytoplasm that are bounded by unit membranes that comprise the photosynthetic membranes. The adjoining layers of cytoplasm are closely apposed to each other to form the photosynthetic lamellae. Occassionally the adjacent layers of cytoplasm are separated by an interspace that may vary in widths of up to several 100 mu to form intralamellar vesicles.


Sign in / Sign up

Export Citation Format

Share Document