scholarly journals Cultivation and Serial Transfer of the Slime Mould, Dictyostelium discoideum in Liquid Nutrient Medium

1961 ◽  
Vol 25 (3) ◽  
pp. 375-378 ◽  
Author(s):  
M. SUSSMAN
Keyword(s):  
Dictyostelium Discoideum ◽  
Nutrient Medium ◽  
Serial Transfer ◽  
Slime Mould ◽  
Liquid Nutrient Medium

Stationary phase and the cell cycle of Dictyostelium discoideum in liquid nutrient medium

1976 ◽  
Vol 20 (3) ◽  
pp. 513-523 ◽  
Author(s):  
D.R. Soll ◽  
J. Yarger ◽  
M. Mirick
Keyword(s):  
Cell Cycle ◽  
Stationary Phase ◽  
Dictyostelium Discoideum ◽  
Nutrient Medium ◽  
Nuclear Dna ◽  
Cell Concentration ◽  
Phase Cell ◽  
Cell Multiplication ◽  
Mean Cell Volume ◽  
Liquid Nutrient Medium

Cells of the axenic strain of the cellular slime mould Dictyostelium discoideum, AX-3, multiply in the liquid nutrient medium HL-5 with a doubling time of 12 h. When the cell concentration reaches approximately 1 X10(7) per ml the rate of cell multiplication begins decreasing and after 20–30 h reaches zero, at a stationary phase cell concentration of 2 to 2–5 X 10(7) cells per ml. The intercept of the extrapolated log phase and stationary phase plots has arbitrarily been considered the onset of the stationary phase. We have found that after cells have been in stationary phase for 24–32 h, mean cell volume increases by 25%, average dry weight by 37%, and average protein content by 24%. These values are close to the expected values for a cell population which is blocked at a point late in the cell cycle. Stationary phase cells also contain 25% more nuclear DNA than log phase cells, indicating that the population of cells at stationary phase is blocked after the DNA replication phase. Finally, when stationary phase cells are washed free of stationary phase medium and reinoculated into fresh medium, they reinitiate cell division synchronously. In the light of the demonstrated relationship between stationary phase and the cell cycle, a possible role for the growth inhibitor produced at stationary phase is considered.

Comparative Investigation on Formation and Accumulation of Rare Phenylpropanoids in Plants and in vitro Cultures of Pimpinella major

1990 ◽  
Vol 45 (6) ◽  
pp. 602-606 ◽  
Author(s):  
B. Merkel ◽  
J. Reichling
Keyword(s):  
Callus Culture ◽  
Nutrient Medium ◽  
Callus Cultures ◽  
Comparative Investigation ◽  
In Vitro Cultures ◽  
Liquid Nutrient Medium ◽  
Whole Plants ◽  
Plant Seedlings

Abstract Unorganized callus and leaf/root-differentiating callus cultures of Pimpinella major have been established in liquid nutrient medium. Their capacity to accumulate rare phenylpropanoids such as epoxy-pseudoisoeugenol tiglate, epoxy-anol tiglate and anol tiglate was compared with that of seedlings and whole plants. The unorganized callus cultures were not able to accumulate any phenylpropanoids. In comparison, the leaf/root-differentiating callus culture promoted the accumulation of epoxy-pseudoisoeugenol tiglate (up to 90 mg/100 g fr.wt.) but not that of anol-derivatives. The accumulated amount of EPT in PMD-SH was comparable with that in plant seedlings.

Electrical properties of the slime mould grex

Development ◽  
1970 ◽  
Vol 23 (2) ◽  
pp. 311-322
Author(s):  
D. R. Garrod ◽  
J. F. Palmer ◽  
L. Wolpert
Keyword(s):  
Electrical Properties ◽  
Dictyostelium Discoideum ◽  
Fruiting Body ◽  
Fruiting Bodies ◽  
Electrophysiological Investigation ◽  
Slime Mould ◽  
Cellular Pattern ◽  
Electric Potentials

An electrophysiological investigation of the migrating grex of the slime mould, Dictyostelium discoideum, has been carried out with two aims in view. It was hoped to obtain information which would be relevant to, first, the formation and regulation of cellular pattern in the grex, and secondly, the problem of grex movement. During migration the grex develops a simple, linear cellular pattern. The cells at the front become the so-called ‘prestalk’ cells which will form the stalk of the fruiting body while those at the back become ‘prespore’ cells and form spores at culmination (Raper, 1940; Bonner, 1944; Bonner & Slifkin, 1949). Moreover, this cellular pattern is capable of polarized regulation. Raper (1940) has shown that portions isolated from the front or back of the grex are capable of forming normally proportioned fruiting bodies. A number of workers have suggested that bio-electric potentials may be involved in regulation of linear cellular pattern.

Cell movement within aggregates of the slime mould Dictyostelium discoideum revealed by surface markers

Development ◽  
1965 ◽  
Vol 13 (1) ◽  
pp. 97-117
Author(s):  
B. M. Shaffer
Keyword(s):  
Dictyostelium Discoideum ◽  
Cell Movement ◽  
Surface Markers ◽  
Slime Mould ◽  
Culture Plate ◽  
Multicellular Organisms

Earlier workers examined the behaviour of foreign particles placed as markers on aggregates of D. discoideum that were migrating over the surface of the culture plate (Bonner, 1959; Francis, 1959, 1962). Comparable observations, made on aggregates in other conditions and at other stages, have now provided further information about the movement of individual cells within the aggregates. Before reporting them, the course of development must be described in some detail. During aggregation on an ordinary culture plate, D. discoideum amoebae crawl towards centres, in which they pack themselves together, forming rounded aggregates of no fixed shape. Papillae develop on the side of the aggregates away from the agar, and by extension, roughly perpendicular to the substratum, transform them into cylindrical multicellular organisms with tapered tips (Text-fig. 1, A—E). Such an organism, which contains from a dozen to a few hundred thousand cells, has been named a grex (Shaffer, 1962) because ‘aggregation’ is derived from the Latin aggregare, to form a grex.

scholarly journals Growth of myxamoebae of the cellular slime mould Dictyostelium discoideum in axenic culture

1970 ◽  
Vol 119 (2) ◽  
pp. 171-174 ◽  
Author(s):  
D. J. Watts ◽  
J. M. Ashworth
Keyword(s):  
Cell Differentiation ◽  
Dictyostelium Discoideum ◽  
Axenic Culture ◽  
Axenic Medium ◽  
Cellular Slime Mould ◽  
Slime Mould ◽  
Solid Media ◽  
Cellular Slime

1. A simple axenic medium suitable for the growth of the myxamoebae of a strain of the cellular slime mould Dictyostelium discoideum is described. 2. Procedures suitable for the growth of this strain in liquid and on solid media are described. 3. Conditions suitable for initiating the cell differentiation of myxamoebae grown axenically are described.

Control of cellular differentiation by temperature in the cellular slime mould Dictyostelium discoideum

1984 ◽  
Vol 69 (1) ◽  
pp. 159-165
Author(s):  
M. Maeda
Keyword(s):  
Low Temperature ◽  
Dictyostelium Discoideum ◽  
Cellular Differentiation ◽  
Cellular Slime Mould ◽  
Slime Mould ◽  
Cellular Slime

The effects of low temperature on morphogenesis and cellular differentiation of Dictyostelium discoideum were examined. During incubation at 5 degrees C, the vegetative and preaggregation cells never developed, but cell masses at the aggregation or slug stage developed to form hemispherical, or dumbbell-shaped multicellular structures. By staining with FITC-antispore IgG, the structures formed after 10 days of incubation of tipped aggregates at 5 degrees C were found to be composed of 90% spores, 5% prespore cells and 5% non-stained cells. Since only 20% of the total cells constituting the tipped aggregate had been prespore cells at the beginning of incubation, this showed that spore differentiation proceeded even at low temperature, while stalk differentiation was completely inhibited. Similar results were obtained when the cells were incubated at 3 degrees C. However, at 0 degree C, morphogenesis and cellular differentiation did not occur, although most of the prespore cells at the late culmination stage differentiated incompletely into spores. Possible reasons for the high proportion of spores being induced by low temperature are discussed.

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