Beech nuts (Fagus sylvatica L.) were germinated and grown in soil inoc
ulated with the ectomycorrhizal fungus Laccaria laccata or Paxillus in
volutus for 18-20 wk. The success of mycorrhizal infection was monitor
ed by measuring the ergosterol contents of the mycorrhizas. Ergosterol
levels ranged from 122 +/- 23 mu g g(-1) d. wt (Laccaria mycorrhizas)
to 94 +/- 36 mu g g(-1) d. wt (Paxillus mycorrhizas), indicating that
ectomycorrhizal symbiosis was established. In root incubation chamber
s, rates of sulphate uptake and the xylem loading of sulphate of excis
ed mycorrhizas were investigated. Both types of mycorrhizas showed sat
uration kinetics in external sulphate concentrations from 2.5-1000 mu
mol l(-1). Linearization of these kinetics revealed two phases with lo
w apparent K-m (Laccaria mycorrhizas: 15 +/- 3 mu mol l(-1); Paxillus
mycorrhizas: 13 +/- 3 mu mol l(-1)) and V-max (Laccaria mycorrhizas: 1
9 +/- 3 nmol h(-1) g(-1) f. wt; Paxillus mycorrhizas: 25 +/- 4 nmol h(
-1) g(-1) f. wt) at low external sulphate concentrations and significa
ntly higher kinetic constants at higher sulphate supplies. Relative xy
lem loading, i.e. the portion of sulphate loaded, into the xylem that
was taken up, remained constant over the entire concentration range in
vestigated (c. 4-7 % of the sulphate taken up). If trees were supplied
for 72 h with different N and sulphur concentrations, both uptake of
sulphate and relative xylem loading were unaffected by sulphur availab
ility, but modulated by N supply. Nitrogen depletion diminished the ra
tes of sulphate uptake in Laccaria and Paxillus mycorrhizas. In respon
se to higher N availability combined with sulphur depletion, sulphate
uptake of Laccaria mycorrhizas, but not of Paxillus mycorrhizas, incre
ased. Organic compounds considered to be possible signals for the regu
lation of sulphate uptake were fed to excised mycorrhizas. L-Cysteine
but not L-methionine and glutathione (gamma-Glu-Cys-Gly) inhibited sul
phate uptake of the two mycorrhizas and xylem loading of sulphate was
stimulated rather than inhibited by L-Cys in both types. In Paxillus m
ycorrhizas glutathione had a similar effect. O-Acetyl-L-serine (OAS),
a precursor of L-cysteine, stimulated sulphate uptake, but did not aff
ect xylem loading. Apparently, GAS, generated in N metabolism, and L-c
ysteine, a product of assimilatory sulphate reduction, act as antagoni
sts, together mediating regulation of sulphate uptake.