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. 1999 Apr;119(4):1483–1496. doi: 10.1104/pp.119.4.1483

Table I.

In vitro inactivation of soybean root GS by different MCO systems

Addition Remaining GS Activity
% of control with EDTA
Control (buffer only) 100.0
1 mm FeCl3 99.63  ± 0.62
1 mm EDTA 99.98  ± 0.17
1 mm FeCl3/1 mm EDTA 101.89  ± 0.28
5 mm DTT 120.34  ± 4.14
10 mm GSH 125.53  ± 4.00
20 mm ascorbate 122.01  ± 3.15
5 mm DTT/0.125 mm FeCl3 10.10  ± 0.39
5 mm DTT/0.125 mm FeCl3/1 mm EDTA 100.59  ± 0.19
10 mm GSH/0.5 mm FeCl3 24.54  ± 0.12
10 mm GSH/0.5 mm FeCl3/1 mm EDTA 98.90  ± 0.02
20 mm ascorbate/0.5 mm FeCl3 52.22  ± 0.62
20 mm ascorbate/1 mm FeCl3 36.45  ± 0.51
20 mm ascorbate/0.5 mm FeCl3/1 mm EDTA 106.98  ± 0.69

A 4-d-old root extract (desalted ammoniun sulfate fraction) was incubated in 50 mm imidazol (pH 7.4) with FeCl3 (0.25–1 mm) and either DTT, GSH, or ascorbate in the presence or absence of 1 mm EDTA for 2 h at 4°C, and samples were assayed for transferase activity. Values are the averages ± se of at least three independent experiments and were calculated as the percentages of the remaining activity compared with the control with no addition (n ≥ 3).