Nitrogen (N) and phosphorus (P) limitation affect the photosynthetic
apparatus of Dunaliella tertiolecta in markedly different ways.
When
grown at 0·25 d−1 (18 % of the resource-saturated
maximum rate, μmax=1·39 d−1) in chemostat
cultures, N- and P-limited cells were
chlorotic relative to nutrient-replete controls. The lutein-to-chlorophyll
a ratio increased under both N and P limitation, whereas the
neoxanthin-to-chlorophyll a ratio increased only under P limitation.
The ratio of accessory photoprotective pigments (α- and β-carotene)
to chlorophyll a increased under N-limited conditions. Despite differences
in accessory pigment complement, chlorophyll a-specific light
absorption coefficients of N- and P-limited cultures did not differ significantly,
and were greater than in nutrient-replete conditions. In
contrast, the initial slope of the photosynthesis–irradiance (PE)
response curve (αChl) declined under nutrient-limiting
conditions. There
were slight reductions in the maximum quantum efficiency of photosynthesis
(ϕm) in N- and P-limited cells. Reductions in ϕm
were
accompanied by reductions in the ratio of variable to maximum fluorescence
(Fv/Fm), and the ratio of the photosystem II
reaction centre
protein D1 to the large subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase
(Rubisco). Differences in light-saturated gross
photosynthesis rate, as measured by light/dark oxygen exchange, could
be accounted for by changes in the abundance of the
carboxylating enzyme Rubisco. Oxygen exchange and 14CO2
assimilation appeared to measure different processes in P-limited and N-
limited cultures. At light-saturation, 14C-bicarbonate assimilation
approximated gross photosynthesis (as measured by light/dark oxygen
exchange) in P-limited cultures. In contrast, 14C-bicarbonate
assimilation approximated net photosynthesis in N-limited cultures. When
all
culture conditions were compared, there was linear covariation of the rates
of reductant supply via light absorption and photochemical
charge separation with the rates of reductant demand for CO2
fixation and NO3− reduction.