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. 1999 Jun;120(2):371–382. doi: 10.1104/pp.120.2.371

Table II.

Purification of tobacco POXs from BY-2 cell-suspension culture medium: fast-protein liquid chromatography steps

Protein Anionic Exchanger Mono-Q
Cationic Exchanger Mono-S
Hydrophobic-Interaction Phenyl Superose
Gel-Filtration Superdex 75
Purification Factor
Elution peak Specific activity Elution peak Specific activity Elution peak Specific activity Molecular mass Specific activity
mM NaCl units μg−1 protein mM NaCl units μg−1 protein m (NH4)2SO4 units μg−1 protein kD units μg−1 protein
A1 60 59.1 0.57 165.3 45 180.6 258
A2 38 45.2
B1 16 1.7 0.80 5.6 33.5 7.1 10
B2 46 23.4 0.44 93.5 33 107.8 154
B3 68 74.1 0.59 122.0 33 137.2 196
P1 130 112.1 1.36 133.2 42 146.4 209
P2 143 168.0 1.09 198.8 40 213.7 305

NaCl concentrations corresponding to peaks of elution of each isoPOX are indicated, together with specific activities using o-dianisidine as a substrate, as described in Methods.