A M Dawson

Bio: A M Dawson is an academic researcher. The author has an hindex of 1, co-authored 1 publications receiving 16 citations.

Molecular Sieving by the Bacillus megaterium Cell Wall and Protoplast

Abstract: Passive permeabilities of the cell wall and protoplast of Bacillus megaterium strain KM were characterized by use of 50 hydrophilic probing molecules (tritiated water, sugars, dextrans, glycols, and polyglycols) which varied widely in size. Weight per cent uptake values (R(w)) were measured at diffusional equilibrium under conditions that negated the influences of adsorption or active transport. Plots of R(w) for intact cells as a function of number-average molecular weight ( M(n)) or Einstein-Stokes hydrodynamic radius ( r(ES)) of the solutes showed three phases: a protoplast uptake phase with a polydisperse exclusion threshold of M(n) = 0.6 x 10(3) to 1.1 x 10(3), r(ES) = 0.6 to 1.1 nm; a cell wall uptake phase with a polydisperse exclusion threshold of M(n) = 0.7 x 10(5) to 1.2 x 10(5), r(ES) congruent with 8.3 nm; and a total exclusion phase. Isolated cell walls showed only the latter two phases. However, it became evident that the cell wall selectively passed only the smallest molecules in a heterodisperse polymer sample. When the molecular-weight distributions of polyglycol samples ( M(n) = 1,000, 1,450, and 3,350) were determined by analytical gel chromatography before and after uptake by intact cells or isolated cell walls, a quasi-monodisperse exclusion threshold was obtained corresponding to M(n) = 1,200, r(ES) = 1.1 nm. The permeability of isolated protoplasts was assessed by the relative ability of solutes to effect osmotic stabilization. An indefinite exclusion threshold, evident even with monodisperse sugars, was attributed to lengthwise orientation of the penetrating rod-shaped molecules. Altogether, the best estimate of the limiting equivalent porosity of the protoplast was 0.4 to 0.6 nm in radius and of the cell wall, 1.1 nm.

Ultimate Computing: Biomolecular Consciousness and NanoTechnology

Abstract: Toward Ultimate Computing. Brain/Mind/Computer. Origin and Evolution of Life. From Brain to Cytoskeleton. Cytoskeleton/Cytocomputer. Protein Conformational Dynamics. Anesthesia: Another Side of Consciousness. Models of Cytoskeletal Computing. Viruses/Ambiguous Life Forms. NanoTechnology. The Future of Consciousness. Bibliography. Appendices. Index.

The cationic composition of incubated cerebral cortex slices.

Abstract: — 1. A new type of cutting table is described. It makes use of the elastic properties of a nylon thread, 0·08 mm thick, in which longitudinal vibrations greatly increase its ability to cut through soft tissue. Two slices of cerebral cortex may thus be obtained within 3–4 min after the death of an animal. 2. The extent of the swelling of a brain slice, as well as the ionic shift, is directly related to the amount of oxygen in the incubating fluid. Under the best conditions of oxygen supply, the swelling of a first slice was close to 12·2 ± 4·3 per cent after 5 hr of incubation. The corresponding values for the Na+ and K+ contents were respectively 119·3 ± 6·9 and 70·9 ± 5·0 μequiv./g of final fresh weight (P2). 3. Incubation in complete anoxia leads to a considerable shift in the cation content of the slice, which acquires a composition close to that of the incubating fluid. This suggests that a large part of the cell population is still metabolically active when oxygen is present. 4. The inulin space represents 47·1 ± 5·8 per cent of the initial fresh weight. It is independent of the amount of fluid taken up by the slice as well as of anoxia. 5. The cation content of the non-inulin space, calculated by assuming that the inulin space has the same composition as the incubation medium, was 77·7 μequiv./ml and 160·3 μequiv./ml for Na+ and K+ respectively. 6. The meaning of the inulin space, as well as the physico-chemical state of the cations in the slice, are discussed.

The effect of sodium concentration on the content and distribution of sodium in the frog skin.

Abstract: 1. The content and distribution of sodium in the epithelium of the frog skin (Leptodactylus ocellatus L.) have been studied.2. The inulin space, the (22)Na exchange, and the amounts of water and sodium were measured in samples of connective tissue. The results indicate that the necessary assumptions generally made to calculate the sodium and water contents of the epithelial cells as the difference between the total content in the tissue and the amounts contained in the inulin space are not valid in the frog skin.3. The mean concentration of sodium in the epithelium has been obtained from direct measurements of sodium and water in samples of epithelium. To measure the water content of the epithelium a new technique has been developed. When the skin is bathed with Ringer solution containing 115 mM-Na on both sides, the mean concentration of sodium in the epithelium is 79 mM. When the concentration of sodium in the Ringer is 1 mM the mean concentration in the epithelium is 25 mM. When the skin is bathed with Ringer with 1 mM-Na on the outside and 115 mM-Na on the inside-a situation which resembles the natural condition in the skin-the mean concentration of sodium in the epithelium is 52 mM.4. The compartmentalization of Na was studied by comparing the sodium content and the degree of exchange with (22)Na in the bathing solutions. In these experiments the skins were exposed to Ringer solutions with different concentrations of sodium, and (22)Na on one or both sides.5. The results indicate that the epithelium has a compartment of sodium which is not exchangeable in 40-80 min and whose size is not appreciably changed by a threefold change in the Na content in the epithelium and a hundredfold change in the concentration of the bathing solution.6. Sodium exchangeable in 40-80 min seems to be contained in two different compartments: (a) a large one that contains fixed sodium is mainly connected to the inside, and does not appear to participate directly in sodium transport across the frog skin; (b) a small one, that is bounded on the inside by a Na-impermeable barrier, and that seems to comprise the sodium involved in active transport. When the skin is bathed with Ringer solutions with 115 mM-Na on the inside and 1 mM-Na on the outside, the transporting compartment contains some 13% of the total sodium in the epithelium.7. The results are interpreted on the basis of a model recently proposed by Cereijido & Rotunno (1968). The major feature of this model is that the sodium transporting compartment is confined to the plasma membrane of the epithelial cells.

Maintenance of low sodium and high potassium levels in resting muscle cells.

Abstract: 1. Previous work has shown that a frog sartorius muscle consists of parallel cells running all the way from one end of the muscle to the other and that amputation of one end of the muscle is not followed by regeneration of a new cell membrane. If now only the cut end of the amputated muscle is exposed to a Ringer solution in which the solutes 42K and 22Na act as radioactive labels and the rest of the cell is suspended in air, we have what is described as an effectively membraneless open-ended cell or EMOC preparation. In this case the only remaining anatomically intact plasma membrane and pumps are made nonfunctional by the removal of 'sources' for inward pumps and 'sinks' for outward pumps. 2. The healthy region of a frog sartorius muscle EMOC preparation continues to accumulate labelled K+ to a level higher than that in the Ringer solution and to exclude labelled Na+ to a level below that in the Ringer solution, much as a normal uncut muscle does in its normal environment. The differences were reduced by inclusion of ouabain in the medium. 3. The diffusion coefficient of Na+ in the normal muscle cytoplasm at 25 degrees C was measured using two methods. The average diffusion coefficient measured was 2.07 X 10(-6) cm2/sec, roughly 1/6 that of the diffusion coefficient of Na+ in a 0.1 N-NaCl solution. 4. The data obtained are discussed in terms of the association-induction hypothesis. In this theory asymmetrical solute distribution, basically an expression of a non-energy consuming metastable equilibrium state, is the result of specific combinations of two opposing mechanisms: adsorption which raises the level of the intracellular solute; and exclusion from cell water which tends to lower it.