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).