Using (NO3-)-N-13 -efflux analysis, the induction of nitrate uptake by
externally supplied nitrate was monitored in roots of intact Picea gl
auca (Moench) Voss. seedlings over a 5-d period. In agreement with our
earlier studies, efflux analysis revealed three compartments, which h
ave been identified as surface adsorption, apparent free space, and cy
toplasm. While induction of nitrate uptake was pronounced, NO3- fluxes
in induced plants were decidedly lower and the induction response was
slower than in other species. Influx rose from 0.1 mu mol . g(-1). h(
-1) (measured at 100 mu M [NO3-](o)) in uninduced plants to a maximum
of 0.5 mu mol . g(-1). h(-1) after 3d of exposure to 100 mu M [NO3-]o
and declined to 0.3-0.4 mu mol . g(-1). h(-1) at the end of the 5-d pe
riod. Efflux remained relatively constant around 0.02-0.04 mu mol . g(
-1). h(-1), but its percentage with respect to influx declined from in
itially high values (around 30%) to steady-state values of 4-7%. Cytop
lasmic [NO3-] ranged from the low micromolar in uninduced plants to a
maximum of 2 mM in plants fully induced at 100 mu M [NO3-](o). In-vivo
root nitrate reductase activity (NRA) was measured over the same time
period, and was found to follow a similar pattern of induction as inf
lux. The maximum response in NRA slightly preceded that of influx. It
increased from 25 nmol . g(-1). h(-1) without prior exposure to NO3- t
o peak values around 150 nmol . g(-1). h(-1) after 2 d of exposure to
100 mu M [NO3-](o). Subsequently, NRA declined by about 50%. The dynam
ics of flux partitioning to reduction, to the vacuole, the xylem, and
to efflux during the induction process are discussed.