Exposure of nodulated leguminous plants to prolonged periods of continuous
darkness has been used as a convenient tool to investigate host plant contr
ol on nitrogen fixing systems in legume root nodules. Foliar dark treatment
of plants results in a rapid decline in N-2-fixation in terms of acetylene
reduction activity (ARA) and predisposes the nodules to metabolic and stru
ctural senescence. After 2 d of darkness, a significant decrease is seen in
nitrogenase (N-2-ase) proteins of common bean nodules. The effect of dark
treatments on nodule respiration varies with plant species. A variable decr
ease in nodule carbohydrates is observed in different plant species under d
ark treatments, but no direct correlation between N-2-ase activity and gros
s levels of carbohydrates present in the nodules has been detected. Usually
nodule leghemoglobin (Lb) shows a decrease of variable intensity depending
on plant species. The mRNA of Lb, sucrose synthase and glutamine synthetas
e shows a significant decline within 24 h of complete darkness. Dark-induce
d acceleration of proteolytic activity and decreased plant growth are refle
cted in decreased nodule proteins and accumulation of free amino acids foll
owing a drop in ARA. Antioxidants such as ascorbic acid and glutathione, al
ong with the enzymes of their oxidation-reduction cycle, show a considerabl
e decrease in their content and activity in nodules from dark-treated plant
s. Among H2O2 scavengers, nodule catalase activity decreases in most of the
plants studied, but peroxidase activity shows an increase. Dark-induced ad
verse effects on N-2-fixation are completely or partially reversible on shi
fting the plants back to a normal light/dark regime. Significant changes in
nodule ultrastructure are induced by dark treatment. Attempts have been ma
de to explain the mechanisms underlying dark-induced changes in nodule func
tioning.