Magnesium-Chelatase from Developing Pea Leaves

Mg-chelatase catalyzes the ATP-dependent insertion of Mg(2+) into protoporphyrin-IX to form Mg-protoporphyrin-IX. This is the first step unique to chlorophyll synthesis, and it lies at the branch point for porphyrin utilization; the other branch leads to heme. Using the stromal fraction of pea (Pisum sativum L. cv Spring) chloroplasts, we have prepared Mg-chelatase in a highly active (1000 pmol 30 min(−1) mg(−1)) and stable form. The reaction had a lag in the time course, which was overcome by preincubation with ATP. The concentration curves for ATP and Mg(2+) were sigmoidal, with apparent K(m) values for Mg(2+) and ATP of 14.3 and 0.35 mm, respectively. The K(m) for deuteroporphyrin was 8 nm. This K(m) is 300 times lower than the published porphyrin K(m) for ferrochelatase. The soluble extract was separated into three fractions by chromatography on blue agarose, followed by size-selective centrifugal ultrafiltration of the column flow-through. All three fractions were required for activity, clearly demonstrating that the plant Mg-chelatase requires at least three protein components. Additionally, only two of the components were required for activation; both were contained in the flow-through from the blue-agarose column.