Abstract
Using UV laser microsurgery, the cell walls of root hairs from Medicago sativa (alfalfa) were perforated under plasmolysing conditions, giving direct access to the plasma membrane without enzyme treatment. The opening in the cell wall of a few μm in diameter results in immediate movement of the protoplasm and partial or complete extrusion of the cell contents. The movement of the protoplasm is retarded by increases in calcium concentration. The calcium-dependency of the movement of the protoplasm allows us to obtain preferentially the extrusion of protoplasm, or to gain access to a small area of plasma membrane in situ. The complete protoplasm can be expelled, to form a protoplast. Fluorescein diacetate staining indicated esterase activity and membrane integrity of the protoplasts. Microscopic examination revealed organelle movement and the presence of a nucleus. The plasma membrane was free from cell wall fragments, as shown by Tinopal staining. Conditions for obtaining plasmolysis without disturbing the physiology of the root hairs too much were achieved by slow, stepwise and reversible plasmolysis. Cytoplasmic streaming in root hairs was maintained during plasmolysis and laser microperforation. This laser technique should be suitable for the performance of electrophysiological studies using the patch-clamp technique on plasma membrane from
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Citation Formats
Kurkdjian, A., Leitz, G., Manigault, P., Harim, A., and Greulich, K. O.
Non-enzymatic access to the plasma membrane of Medicago root hairs by laser microsurgery.
FAO: N. p.,
1993.
Web.
Kurkdjian, A., Leitz, G., Manigault, P., Harim, A., & Greulich, K. O.
Non-enzymatic access to the plasma membrane of Medicago root hairs by laser microsurgery.
FAO.
Kurkdjian, A., Leitz, G., Manigault, P., Harim, A., and Greulich, K. O.
1993.
"Non-enzymatic access to the plasma membrane of Medicago root hairs by laser microsurgery."
FAO.
@misc{etde_22370763,
title = {Non-enzymatic access to the plasma membrane of Medicago root hairs by laser microsurgery}
author = {Kurkdjian, A., Leitz, G., Manigault, P., Harim, A., and Greulich, K. O.}
abstractNote = {Using UV laser microsurgery, the cell walls of root hairs from Medicago sativa (alfalfa) were perforated under plasmolysing conditions, giving direct access to the plasma membrane without enzyme treatment. The opening in the cell wall of a few μm in diameter results in immediate movement of the protoplasm and partial or complete extrusion of the cell contents. The movement of the protoplasm is retarded by increases in calcium concentration. The calcium-dependency of the movement of the protoplasm allows us to obtain preferentially the extrusion of protoplasm, or to gain access to a small area of plasma membrane in situ. The complete protoplasm can be expelled, to form a protoplast. Fluorescein diacetate staining indicated esterase activity and membrane integrity of the protoplasts. Microscopic examination revealed organelle movement and the presence of a nucleus. The plasma membrane was free from cell wall fragments, as shown by Tinopal staining. Conditions for obtaining plasmolysis without disturbing the physiology of the root hairs too much were achieved by slow, stepwise and reversible plasmolysis. Cytoplasmic streaming in root hairs was maintained during plasmolysis and laser microperforation. This laser technique should be suitable for the performance of electrophysiological studies using the patch-clamp technique on plasma membrane from non-enzyme-treated cells. (author)}
journal = []
issue = {1}
volume = {105}
journal type = {AC}
place = {FAO}
year = {1993}
month = {Jul}
}
title = {Non-enzymatic access to the plasma membrane of Medicago root hairs by laser microsurgery}
author = {Kurkdjian, A., Leitz, G., Manigault, P., Harim, A., and Greulich, K. O.}
abstractNote = {Using UV laser microsurgery, the cell walls of root hairs from Medicago sativa (alfalfa) were perforated under plasmolysing conditions, giving direct access to the plasma membrane without enzyme treatment. The opening in the cell wall of a few μm in diameter results in immediate movement of the protoplasm and partial or complete extrusion of the cell contents. The movement of the protoplasm is retarded by increases in calcium concentration. The calcium-dependency of the movement of the protoplasm allows us to obtain preferentially the extrusion of protoplasm, or to gain access to a small area of plasma membrane in situ. The complete protoplasm can be expelled, to form a protoplast. Fluorescein diacetate staining indicated esterase activity and membrane integrity of the protoplasts. Microscopic examination revealed organelle movement and the presence of a nucleus. The plasma membrane was free from cell wall fragments, as shown by Tinopal staining. Conditions for obtaining plasmolysis without disturbing the physiology of the root hairs too much were achieved by slow, stepwise and reversible plasmolysis. Cytoplasmic streaming in root hairs was maintained during plasmolysis and laser microperforation. This laser technique should be suitable for the performance of electrophysiological studies using the patch-clamp technique on plasma membrane from non-enzyme-treated cells. (author)}
journal = []
issue = {1}
volume = {105}
journal type = {AC}
place = {FAO}
year = {1993}
month = {Jul}
}