The redox state of the plastoquinone pool is a result of a balance between electron transfer in and electron transfer out of the pool. It is estimated by the parameter (1 − qL). The pool is more reduced in acetate-grown iron-limited cells, which could be attributed to a failure of PSI to draw electrons out of the pool or activation of a mechanism (such as chlororespiration) to increase electron flow into the pool (Fig. 6). The fact that the pool remained reduced in these cells even in the dark suggests this website the activation of a mechanism for acetate-dependent reduction

of the plastoquinone pool in iron-limited cells. Table 4 Maximum quantum efficiency of PSII in SN-38 mouse phototrophic versus photoheterotrophic cells in response to Selleckchem Akt inhibitor iron nutrition Fe (μM) F v /F m Acetate CO2 0.1 0.54 ± 0.07* 0.72 ± 0.01 0.2 0.67 ± 0.01 0.70 ± 0.02 1 0.73 ± 0.02 0.72 ± 0.01 3 0.73 ± 0.01 0.72 ± 0.01 20 0.74 ± 0.01 0.72 ± 0.01 200 0.74 ± 0.01 0.72 ± 0.00 Standard deviation based on biological triplicates * Statistically significant difference relative to 20 μM Fe (one-way ANOVA, P < 0.05) Fig. 4 Non-photochemical quenching of photoheterotrophic versus phototrophic cells in response to iron nutrition.

Cells were grown in the presence (A) and absence (B) of acetate in various concentrations of iron. Cells were dark acclimated for 15 min and probed with an actinic light intensity of 217 μmol photons m−2 s−1. Various concentrations of iron represented by gray triangles (0.1-μM Fe), gray squares (0.2-μM Fe), dark gray triangles (1-μM Fe), dark gray squares (3-μM Fe), black triangles (20-μM Fe), and black squares (200-μM Fe). Standard deviation based on biological triplicates Fig. 5 Abundance of the xanthophyll cycle pigments in photoheterotrophic versus phototrophic cells in response to iron nutrition. Cells were grown in the presence (A) and absence (B) of acetate in various concentrations of iron, and the abundance of xanthophyll cycle pigments was determined by HPLC. Etomidate Average of biological triplicate

samples shown Fig. 6 Estimation of the redox state of the plastoquinone pool of photoheterotrophic versus phototrophic cells in response to iron nutrition. Cells were grown in the presence (A) and absence (B) of acetate in various concentrations of iron. Cells were dark acclimated for 15 min and probed with an actinic light intensity of 217 μmol photons m−2 s−1 Various concentrations of iron represented by gray triangles (0.1-μM Fe), gray squares (0.2-μM Fe), dark gray triangles (1-μM Fe), dark gray squares (3-μM Fe), black triangles (20-μM Fe), and black squares (200-μM Fe). Standard deviation based on biological triplicates Abundance of Fe-containing components in energy transducing membranes The abundance of photosynthetic and respiratory proteins was determined by immunoblot analysis (Fig. 7).