Pollen-Wall Proteins: Electron-Microscopic Localization of Acid Phosphatase in the Intine of Crocus Vernus

1971 ◽  
Vol 8 (3) ◽  
pp. 727-733
Author(s):  
R. B. KNOX ◽  
J. HESLOP-HARRISON

Acid phosphatase has been localized in the wall of the pollen grain of Crocus vernus Wulf at the electron-microscope level by a method using 2-naphthyl thiol phosphate as substrate in a simultaneous coupling reaction with fast blue BBN at pH 5.0, the product being given electron opacity by osmication. Activity was found to be concentrated mainly in the intine, and to be associated with ribbon-like or filamentous inclusions believed to be proteinaceous on the basis of other criteria. Some activity was also detectable in the interstices of the exine. The observations confirm the general interpretation of the distribution of wall-held enzyme based upon light-microscopic cytochemistry, and provide the resolution necessary to establish unambiguously that they are associated with protein layers inserted during intine growth.

1973 ◽  
Vol 21 (12) ◽  
pp. 1047-1052 ◽  
Author(s):  
J. F. ARONSON ◽  
A. P. FISHMAN ◽  
G. G. PIETRA

We have demonstrated that soluble hemin derivatives have electron microscope-detectable peroxidase activity. Hemin was coupled to several different size classes of dextran, to sucrose and to glucuronic acid. The peroxidase activity of the attached hemin was detected with the electron microscope using the method described by Graham and Karnovsky for horseradish peroxidase. These observations indicate that hemin may be used as a prosthetic group to label macromolecules for electron microscopic localization and raise the prospect of creating groups of inexpensive tracer substances of varying size, charge and specificity for histologic and ultrastructural studies.


1974 ◽  
Vol 22 (11) ◽  
pp. 1039-1047 ◽  
Author(s):  
RICHARD A. COLEMAN ◽  
LEE H. PRATT

The use of polyethylene glycol as a preembedding medium for immunocytochemistry at the electron microscope level has been adapted to the localization of phytochrome in etiolated oat (Avena sativa L., cv. Garry) seedlings. Phytochrome was indirectly labeled in 3-µm sections with rabbit antiperoxidase-peroxidase complex using sheep antirabbit serum and a specific rabbit antiphytochrome serum. Following localization the 3-µm sections were reembedded for ultrathin sectioning. In the absence of information regarding the subcellular distribution of phytochrome, it was necessary to develop a control which would demonstrate that all organelles and areas of the tissue being localized were penetrated by all reagents. Such a control is described. In those cells which contained phytochrome it was found to be generally distributed throughout the cytoplasm and to be associated with both amyloplasts and mitochondria. No activity was observed in nuclei.


Pathology ◽  
1976 ◽  
Vol 8 (1) ◽  
pp. 73-80 ◽  
Author(s):  
I.P. McCausland ◽  
R.N. Seelye ◽  
J.B. Gavin ◽  
P.B. Herdson

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