It is proposed that inhibition of extensin peroxidase activity leads to a l
ess rigid cell wall and thus promotes cell expansion and plant growth. A lo
w-molecular-weight inhibitor derived from the cell walls of suspension-cult
ured tomato cells was found to completely inhibit extensin peroxidase-media
ted extensin cross-linking in vitro at a concentration of 260 mu g/ml. The
inhibitor had no effect upon,guaiacol oxidation catalyzed by extensin perox
idase or horseradish peroxidase. We have demonstrated that the light-irradi
ated inhibition of plant growth may be partially offset by inhibition of en
dogenous extensin peroxidase activity. Overall plant growth was enhanced by
up to 15% in the presence of inhibitor relative to control plants. Inhibit
or-treated and illuminated tomato hypocotyls grew up to 15% taller than unt
reated controls. The inhibitor had no effect upon etiolated plants over a 1
5-d period, suggesting that only low levels of peroxidase-mediated cross-li
nking can be found in the eel walls of etiolated plants. SDS-PAGE/Western b
lots of ionically bound protein from both etiolated and illuminated hypocot
yls identified a doublet at 57/58.5 kDa which is immunoreactive with antibo
dies raised to tomato extensin peroxidase. Levels of the 58.5-kDa protein,
determined by SDS-PAGE, were at least threefold higher in illuminated tomat
o hypocotyls than in etiolated hypocotyls. Three fold higher levels of exte
nsin peroxidase, elevated in-vitro extensin cross-linking activity and 15%
higher levels of cross-linked, non-extractable extensin were observed in il
luminated tomato hypocotyls compared with etiolated tomato hypocotyls. This
suggests that white-light inhibition of tomato hypocotyl growth appears to
be mediated, at least partially, by deposition of cell wall extensin, a pr
ocess regulated by M-r-58,500 extensin peroxidase. Our results indicate tha
t the contribution of peroxidase-mediated extensin deposition to plant cell
wall architecture may have an important role in plant growth.