Localization of a 64‐kDa phosphoprotein in the lumen between the outer and inner envelopes of pea chloroplasts

Abstract

The identification and localization of a marker protein for the intermembrane space between the outer and inner chloroplast envelopes is described. This 64‐kDa protein is very rapidly labeled by [γ‐³²P]ATP at very low (30 nM) ATP concentrations and the phosphoryl group exhibits a high turnover rate. It was possible to establish the presence of the 64‐kDa protein in this plastid compartment by using different chloroplast envelope separation and isolation techniques. In addition comparison of labeling kinetics by intact and hypotonically lysed pea chloroplasts support the localization of the 64‐kDa protein in the intermembrane space. The 64‐kDa protein was present and could be labeled in mixed envelope membranes isolated from hypotonically lysed plastids. Mixed envelope membranes incorporated high amounts of ³²P from [γ‐³²P]ATP into the 64‐kDa protein, whereas separated outer and inner envelope membranes did not show significant phosphorylation of this protein. Water/Triton X‐114 phase partitioning demonstrated that the 64‐kDa protein is a hydrophilic polypeptide. These findings suggest that the 64‐kDa protein is a soluble protein trapped in the space between the inner and outer envelope membranes. After sonication of mixed envelope membranes, the 64‐kDa protein was no longer present in the membrane fraction, but could be found in the supernatant after a 110000 ×g centrifugation.