A Dithiothreitol-Sensitive Tetrameric Protease from Spinach Thylakoids Has Polyphenol Oxidase Activity

Polyclonal antibody raised against a dithiothreitol-sensitive tetrameric protease (DSTP) from PSII membranes specifically inhibited the polyphenol oxidase (PPO) activity of spinach thylakoids. DSTP was copurified with PPO activity on an affinity column prepared with antibody against DSTP. These results suggest that DSTP and PPO are the same protein. During purification of DSTP, Tween 20 was essential for stabilization of the protein, which was degraded in the absence of the detergent. Gel-filtration chromatography of the purified DSTP revealed the presence of 230kDa (tetramer) and 60-kDa (monomer) species. The copper content of monomer species was determined to be 0.4 Cu atom per protein molecule, when the molecular weight of the protein was calculated to be 62,243, which is the value reported for spinach PPO [Hind et al. (1995) Biochemistry 34: 8157]. Purified DSTP caused the degradation as well as the dimerization of the extrinsic 23-kDa protein of PSII. The degradation of the protein was suppressed under anaerobic conditions induced by the presence of glucose oxidase and glucose together. This fact suggests that oxygen molecules are involved in the proteolytic reaction and that the proteolytic activity and PPO activity may be correlated with each other.