Fj. Turano et al., THE EFFECT OF METHIONINE, ETHYLENE AND POLYAMINE CATABOLIC INTERMEDIATES ON POLYAMINE ACCUMULATION IN DETACHED SOYBEAN LEAVES, Physiologia Plantarum, 101(3), 1997, pp. 510-518
In the present study we determined the effects of methionine, intermed
iates of polyamine catabolic pathways and inhibitors of either ethylen
e biosynthetic or polyamine catabolic pathways on polyamine accumulati
on in soybean leaves. Inhibitors to SAM decarboxylase and spermidine s
ynthase, methylglyloxal-bis-(guanylhydrazone) and cyclohexylamine, res
pectively, suggest that methionine may provide aminopropyl groups for
the synthesis of polyamine via S-adenosylmethionine (SAM). Results fro
m experiments that utilized a combination of compounds which altered e
ither ethylene or polyamine biosynthesis, namely, aminoethoxyvinyl gly
cine, CoSO4, 2,5-norbornadiene, and CuSO4, suggest the two pathways co
mpete for a common precursor. However, exogenous addition of ethylene
(via ethephon treatments) had little or no effect on polyamine biosynt
hesis. Likewise, polyamine treatments had little or no effect on ethyl
ene biosynthesis. These data suggest that there are few or no inhibito
ry effects from the end products of one pathway on the synthesis of th
e other. Data from leaves treated with metabolic intermediates in the
catabolic pathway of polyamines and inhibitors of enzymes in the catab
olic pathway, i.e. aminoguanidine, hydroxyethyldrazine and gabaculine,
suggest that the observed increases in polyamine titers were not due
to decreased catabolism of the polyamines. One catabolic intermediate,
gamma-aminobutyric acid (GABA), elevated putrescine, spermidine and s
permine by 12-, 1.4-, and 2-fold, respectively. Ethylene levels decrea
sed (25%) in GABA-treated leaves. This small decrease in ethylene coul
d not account for such large increase in putrescine titers. Further an
alysis demonstrated that the GABA-mediated polyamine accumulation was
inhibited by difluoromethylarginine, an inhibitor of arginine decarbox
ylase, but not by difluoromethylornithine, an inhibitor of ornithine d
ecarboxylase. These data suggest that GABA directly or indirectly affe
cts the biosynthesis of polyamines via arginine decarboxylase.