U. Kutschera, CESSATION OF CELL ELONGATION IN RYE COLEOPTILES IS ACCOMPANIED BY A LOSS OF CELL-WALL PLASTICITY, Journal of Experimental Botany, 47(302), 1996, pp. 1387-1394
The mechanism by which endogenous cessation of coleoptile elongation a
fter emergence of the primary leaf is brought about was investigated i
n rye seedlings (Secale cereale L.) that were either grown in darkness
or irradiated with continuous white light. In 3-d-old etiolated (grow
ing) coleoptiles a turgor pressure of 0.59 MPa was measured, In 6-d-ol
d coleoptiles, which had ceased to elongate, cell turgor was 0.51 MPa
and thus only 13% lower than in the rapidly growing organ, Hence, the
driving force for growth (turgor) is largely maintained. Cell-wall pla
sticity (E(pl)) and elasticity (E(el)) were determined with a constant
-load extensiometer both in vivo (turgid coleoptile segments) and in v
itro (frozen-thawed samples). Cessation of coleoptile elongation was c
orrelated with a 95% reduction in E(pl), whereas E(el) was only slight
ly affected, Extension kinetics were measured with living and frozen-t
hawed segments cut from growing and non-growing coleoptiles. The corre
sponding stress-strain (load-extension) curves indicate that the cell
wall of the growing coleoptile behaves like an elastic-plastic materia
l whereas that of the non-growing organ shows the behaviour of an elas
tic solid, These data demonstate that E(pl) represents a true plastic
(irreversible) deformation of the cell wall. It is concluded that cess
ation of coleoptile growth after emergence of the primary leaf is attr
ibutable to a loss of cell-wall plasticity, Hence, a mechanical stiffe
ning of the cell wall and not a loss of turgor pressure may be respons
ible for the deceleration of cell elongation in the rye coleoptile.