N. Bughio et al., Real-time [C-11]methionine translocation in barley in relation to mugineicacid phytosiderophore biosynthesis, PLANTA, 213(5), 2001, pp. 708-715
[C-11]Methionine was supplied through barley roots and the C-11 signal was
followed for 90 min using a real-time imaging system (PETIS), with subseque
nt development of autoradiographic images of the whole plant. In all cases,
[C-11]methionine was first translocated to the 'discrimination center', th
e basal part of the shoot, and this part was most strongly labeled. Methion
ine absorbed by the roots of the plants was subsequently translocated to ot
her parts of the plant. In Fe-deficient barley plants, a drastic reduction
in [C-11]methionine translocation from the roots to the shoot was observed,
while a greater amount of C-11 was found in the leaves of Fe-sufficient or
methionine-pretreated Fe-deficient plants. Treatment of Fe-deficient plant
s with aminooxyacetic acid, an inhibitor of nicotianamine aminotransferase,
increased the translocation of [C-11]methionine to the shoot. The retentio
n of exogenously supplied [C-11]methionine in the roots of Fe-deficient bar
ley indicates that the methionine is used in the biosynthesis of mugineic a
cid phytosiderophores in barley roots. This and the absence of methionine m
ovement from shoots to the roots suggest that the mugineic acid precursor m
ethionine originates in the roots of plants.