Beech nuts (Fagus sylvatica L.) were germinated and grown
in soil inoculated with the ectomycorrhizal fungus
Laccaria laccata or Paxillus involutus for 18–20
wk. The success of mycorrhizal infection was monitored by
measuring the ergosterol contents of the mycorrhizas. Ergosterol levels
ranged from 122±23 μg g−1 d. wt (Laccaria
mycorrhizas) to
94±36 μg g−1 d. wt (Paxillus mycorrhizas),
indicating that ectomycorrhizal symbiosis was
established. In root incubation chambers, rates of sulphate uptake and
the xylem loading of sulphate of excised
mycorrhizas were investigated. Both types of mycorrhizas showed saturation
kinetics in external sulphate
concentrations from 2·5–1000 μmol l−1.
Linearization of these kinetics revealed two phases with low apparent Km
(Laccaria mycorrhizas: 15±3 μmol l−1;
Paxillus mycorrhizas: 13±3 μmol l−1)
and
Vmax (Laccaria mycorrhizas:
19±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 significantly higher kinetic constants at higher sulphate supplies.
Relative xylem loading, i.e. the portion of
sulphate loaded into the xylem that was taken up, remained constant over
the entire concentration range
investigated (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 availability, but
modulated by N supply. Nitrogen depletion diminished the rates of sulphate
uptake in Laccaria and Paxillus
mycorrhizas. In response to higher N availability combined with sulphur
depletion, sulphate uptake of Laccaria
mycorrhizas, but not of Paxillus mycorrhizas, increased. Organic
compounds considered to be possible signals for
the regulation of sulphate uptake were fed to excised mycorrhizas. l-Cysteine
but not l-methionine and
glutathione (γ-Glu-Cys-Gly) inhibited sulphate uptake of the two
mycorrhizas and xylem loading of sulphate was
stimulated rather than inhibited by l-Cys in both types. In Paxillus
mycorrhizas glutathione had a similar effect.
O-Acetyl-l-serine (OAS), a precursor of l-cysteine,
stimulated sulphate uptake, but did not affect xylem loading.
Apparently, OAS, generated in N metabolism, and l-cysteine, a
product of assimilatory sulphate reduction, act
as antagonists, together mediating regulation of sulphate uptake.