Distribution of ATPases in wheat root membranes separated by phase partition [Triticum aestivum, plasmalemma membrane LIAC]

The distribution of divalent cation stimulated ATPase activity in relation to the distribution of other enzyme activities was studied for membrane fractions from wheat roots (Triticum aestivum L. cv. Svenno). A homogenate from dark grown plants was fractionated by differential centrifugation at 1000g, 10,000g, 30,000g and 60,000g (1, 10, 30 and 60 KP fractions), followed by partition in an aqueous polymer two-phase system, using polyethylene glycol 4000/dextran T500 concentrations of 5.7/5.7, 5.9/5.9, 6.1/6.1, 6.3/6.3 and 6.5/6.5% (w/w). The 30 KP fraction was also separated by counter-current distribution in a 6.3/6.3% two-phase system. Protein and activities of Ca('2+), Mg('2+), and Mn('2+) stimulated ATPases, cytochrome oxidase, light induced absorbance change (LIAC) related to cyt b reductions, inosine diphosphatase and NADH dependent antimycin A insensitive cytochrome c reductase were measured. The partition of ATPase activities stimulated by Ca('2+), Mg('2+) or Mn('2+) was similar at all polymer concentrations tested, indicating a low cation specificity of the dominating ATPases. The distribution of ATPases agreed with different marker enzymes in different centrifuge fractions. Divalent cation stimulated ATPases were evidently related to several of the organelles. In the different fractions the distribution of ATPase activity should then follow that of the marker enzyme of the dominant organelle. From studies with different polymer concentrations the 6.3/6.3 -system was selected for further separation of the membranes in the 30 KP fraction by counter-current distribution. By this method one fraction was obtained, which probably consisted of plasmalemma and was free from mitochondrial material. Indications for plasmalemma in this fraction were (a) similar partition as protoplasts and (b) high LIAC activity