All phytometallophores are derived from methionine through S-adenosylm
ethionine (SAM) via nicotianamine. Ethylene is synthesized from methio
nine via SAM and 1-aminocyclopropane-1-carboxylic acid (ACC). This clo
se similarity in biochemical pathways suggests that root-ethylene may
play a role in regulating Fe(III)-phytometallophore homeostasis in cer
eal (Strategy II species) roots as well as in the regulation of Fe(III
)-chelate reductase activity in Strategy I species. Barley (Hordeum vu
lgare L.) seedlings were grown in chelate-buffered nutrient solutions
with increasing levels of Fe (i.e., 5, 25 or 100 mu M Fe) as Fe(III)-H
EDTA. Seedlings at each level of Fe were treated with either an inhibi
tor or a promoter of ethylene action. Treatment with the promoter, ACC
(1 mu M), had no significant effect on phytometallophore root efflux
or Fe uptake by 19-d-old barley seedlings at all Fe levels. However, t
reatment with the inhibitor, aminooxyacetic acid (AOA, 10 mu M) repres
sed the ability of cereal roots to absorb sufficient Fe to meet metabo
lic needs, but surprisingly enhanced phytometallophore root efflux rat
es at all Fe(III)-HEDTA levels. These results support a possible role
of root-ethylene in Fe(III) uptake in cereals, but the mechanism remai
ns unclear.