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. 1998 Nov;118(3):835–841. doi: 10.1104/pp.118.3.835

Table III.

Carbohydrate required for 15NH4+ assimilation by maize roots

Day Photoperiod 15NH4+ Assimilation Carbohydrate
Requirementa Change in shoot Change in root Transport to rootb
μmol N plant−1 μmol C plant−1
7–8 Dark 39  ± 4 117  ± 13 −319  ± 7 −57  ± 10 60  ± 15
8 Light 102  ± 18 310  ± 53 +556  ± 35 +61  ± 7 371  ± 55
8–9 Dark 91  ± 11 275  ± 34 −550  ± 12 −103  ± 6 172  ± 37
9 Light 110  ± 24 333  ± 74 +590  ± 67 +42  ± 11 375  ± 64
9–10 Dark 120  ± 28 365  ± 84 −501  ± 24 −38  ± 13 327  ± 97
10 Light 288  ± 30 872  ± 91 +1193  ± 147 +118  ± 21 990  ± 108

The diurnal assimilation of 15NH4+ was measured during a 3-d exposure of maize seedlings to highly labeled 15NH4+. The minimal transport of C from shoot to root required to support 15NH4+ assimilation was calculated from the theoretical C requirement for 15NH4+ assimilation and the changes in tissue carbohydrate. Each value is the mean of four replicates ± se.

a

Calculation of the total C requirement for 15NH4+ assimilation is based on the assumption that assimilation of entering 15NH4+ occurs in the root, and that the initial product of NH4+ assimilation is Gln, which requires 0.505 mol of Glc equivalents mol−1 NH4+ to provide the necessary reductant, ATP, and C skeletons (Schubert, 1982). 

b

Minimal C transport to the root required to support 15NH4+ assimilation is equal to the total C required for 15NH4+ assimilation plus the change in root C content.