F. Grolig et al., Interaction between gravitropism and phototropism in sporangiophores of Phycomyces blakesleeanus, PLANT PHYSL, 123(2), 2000, pp. 765-776
The interaction between gravitropism and phototropism was analyzed for spor
angiophores of Phycomyces blakesleeanus: Fluence rate-response curves for p
hototropism were generated under three different conditions: (a) for statio
nary sporangiophores, which reached photogravitropic equilibrium; (b) for s
porangiophores, which were clinostated head-over during phototropic stimula
tion; and (c) for sporangiophores, which were subjected to centrifugal acce
lerations of 2.3g to 8.4g. For blue light (454 nm), clinostating caused an
increase of the slope of the fluence rate-response curves and an increase o
f the maximal bending angles at saturating fluence rates. The absolute thre
shold remained, however, practically unaffected. In contrast to the results
obtained with blue light, no increase of the slope of the fluence rate-res
ponse curves was obtained with near-ultraviolet light at 369 nm. Bilateral
irradiation with near-ultraviolet or blue light enhanced gravitropism, wher
eas symmetric gravitropic stimulation caused a partial suppression of photo
tropism. Gravitropism and phototropism appear to be tightly linked by a ton
ic feedback loop that allows the respective transduction chains a mutual in
fluence over each other. The use of tropism mutants allowed conclusions to
be drawn about the tonic feedback loop with the gravitropic and phototropic
transduction chains. The results from clinostating mutants that lack octah
edral crystals (implicated as statoliths) showed that these crystals are no
t involved in the tonic feedback loop. At elevated centrifugal acceleration
s, the fluence-rate-response curves for photogravitropic equilibrium were d
isplaced to higher fluence rates and the slope decreased. The results indic
ate that light transduction possesses a logarithmic transducer, whereas gra
vi-transduction uses a linear one.