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. 2010 May 25;22(5):1633–1646. doi: 10.1105/tpc.110.075242

Figure 4.

Figure 4.

NRT1.8 Transports Nitrate.

(A) Representative inward currents elicited by 10 mM NO3 at pH 5.5 and a holding potential of −40 mV were recorded for control (top) and NRT1.8 cRNA injected oocytes (bottom).

(B) Quantification of the currents recorded; *P < 0.001, n = 11 for both injected and uninjected oocytes from four separate batches.

(C) High- and low-affinity nitrate uptake activity at pH 5.5. Oocytes were incubated for 3 h with 250 μM or 10 mM nitrate. The amount of nitrate removed from the medium (high-affinity activity) or retained in the oocytes (low-affinity activity) was analyzed by HPLC as described by Huang et al. (1999). *P <0.01, n = 5 samples for both high- and low-affinity uptake assays. Each sample consisted of four oocytes.

(D) NO3 concentration in xylem sap; *P < 0.01, n = 6 separate samples for both Ws and the nrt1.8-1 mutant; each sample pooled sap from approximately nine independent plants. Error bars denote sd in (B) to (D).