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  • Springer  (2)
  • 1970-1974  (2)
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  • Springer  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 77 (1973), S. 165-180 
    ISSN: 1615-6102
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Protoplasts were enzymatically isolated from “Paul's scarlet” rose suspension culture cells. They were cultured in medium similar to that used to culture the cells from which they were isolated with the addition of sucrose as an osmotic stabiliser. They were studied by light and electron microscopy and their changes in size and number per culture were recorded. Expansion was greater when the protoplasts were cultured in medium plus 12% sucrose than with 24% sucrose. Budding was observed. In medium plus 12% sucrose about 45% of the protoplasts divided but in medium plus 24% sucrose far fewer divided. Cytokinesis was abnormal: the phragmoplast disappeared soon after cytokinesis began and the cell plate became a groove and then a fibril-lined or filled tongue which progressed across the vacuole, unconnected by strands to other parts of the protoplast. The wall regenerated after several days culture in medium plus 12% sucrose fluoresced with calcofluor. The wall regenerated in medium with 24% sucrose fluoresced usually only after several weeks culture. Cytokinesis hastened formation of a wall fluorescing with calcofluor. In the electron microscope the wall was seen to contain fibrils and non-fibrillar material. The latter was the minor component in medium plus 12% sucrose but was usually the major component in medium plus 24% sucrose. The growth in plasmolysing and nonplasmolysing medium of the cells from which protoplasts are isolated was also studied. It appears that loss of the wall alters the potential of protoplasts to expand and possibly also to regenerate a wall and to divide. Wall regeneration is initially linked with expansion and cytokinesis. Osmotic pressure of the external medium is also an important factor.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1615-6102
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Unusual bodies are of general occurrence in cultured protoplasts isolated from tomato “Ailsa Craig” fruit locule tissue. They are also common in the equivalent cultured plasmolysed tissue, but do not occur when the culture medium is non-plasmolysing. Similar bodies are of universal occurrence in cultured protoplast spontaneous fusion bodies from tobacco “Xanthi” leaves, but are not found when the cultured protoplasts are not initially fused. Bodies also occur in cultured protoplasts isolated from leaves of rye “Dominant”. They do not occur in cultured protoplasts from rose “Paul's Scarlet” cells. These bodies have been studied by light and electron microscopy. Schiff and periodic acid—Schiff—phosphotungstic acid stains indicate the presence in them of cellulose, and this is also suggested by their fluorescence with calcofluor and their appearance in the electron microscope. Some of them fluoresce with aniline-blue. Some material within the bodies stains with phosphotungstic acid-chromic acid, suggesting that some of the contents of the bodies is plasmalemma-like. The bounding membrane is only partly stained with phosphotungstic acid-chromic acid. There is a general parallel between the composition of the wall regenerated by the protoplasts and the composition of these bodies, and between the timing and extent of their development and that of the regenerated wall. On the basis of these observations, these bodies are named “wall-bodies” and regarded as composed of similar materials to those making up the regenerated wall. The observations, especially of wall-body production by tobacco fusion bodies, strongly suggest a plasmalemma origin for the membranes of the vesicles in which these bodies arise.
    Type of Medium: Electronic Resource
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