Evaluation of Pollen Viability by Enzymatically Induced Fluorescence; Intracellular Hydrolysis of Fluorescein Diacetate
- 1 January 1970
- journal article
- research article
- Published by Taylor & Francis in Stain Technology
- Vol. 45 (3) , 115-120
- https://doi.org/10.3109/10520297009085351
Abstract
Viable pollen grains immersed in a solution of fluorescein diacetate, made up in a concentration of about 10−6 M in sucrose of suitable tonicity (usually about 0.5 M), rapidly accumulate free fluorescein, which can be detected by its fluorescence. This fluorochromatic reaction (FCR) probably depends upon the entry of the nonpolar substrate into the vegetative cell where it is hydrolyzed by esterase to give the polar product, fluorescein, which is retained by the cell membrane. The test is primarily one for the integrity of the plasmalemma of the vegetative cell. Since this integrity is likely to be closely correlated with viability, the FCR provides an effective method for assessing pollen quality.This publication has 4 references indexed in Scilit:
- Pollen-wall proteins: localization and enzymic activityJournal of Cell Science, 1970
- Cytochemical Localization of Enzymes in the Wall of the Pollen GrainNature, 1969
- Membrane properties of living mammalian cells as studied by enzymatic hydrolysis of fluorogenic esters.Proceedings of the National Academy of Sciences, 1966
- The Cytochemical Reduction of Nitro Blue Tetrazolium as an Index of Pollen ViabilityAmerican Journal of Botany, 1964