A technique to treat a single plant cell with chemicals was devised us
ing gel beads and epidermal cells of barley coleoptile. Acridine orang
e (a fluorescent dye) and cytochalasin A (an inhibitor of cytoplasmic
streaming) were separately infiltrated into gel beads that were then i
ndividually transferred onto a single cell of the coleoptile using a m
icromanipulator. Coleoptile cells on which a gel bead infiltrated with
acridine orange had been placed gave a characteristic greenish fluore
scence when observed with a fluorescence microscope 24 h after the ons
et of incubation. These results indicate that acridine orange diffused
from the gel bead and permeated into the coleoptile cell. When coleop
tile cells were treated with gel beads infiltrated with cytochalasin A
, cytoplasmic streaming ceased in more than 90% of the cells by 6 h af
ter the onset of treatment. These results demonstrate that cytochalasi
n A diffused from the gel bead and permeated into the symplast of the
target cells. The technique could be applied to test physiological eff
ects of fungal products on a single plant cell.