, 2004). PratA consists of nine consecutive tetratricopeptide repeat (TPR) units, a motif that is known to mediate protein–protein interactions. Thereby, it could form a bridge connecting multiple proteins and serve as a scaffold factor for correct assembly of PSII

Ruxolitinib solubility dmso (Schottkowski et al., 2009a). PratA directly interacts with the C-terminus of the D1 reaction center protein of PSII, and its inactivation affects the C-terminal processing of D1, an early step of PSII biogenesis. This D1 maturation occurs in almost all photosynthetic organisms, and it is required for the subsequent docking of the subunits of the oxygen-evolving complex to the lumenal side of PSII. Most intriguingly, PratA was shown to be a soluble protein

located in the periplasm, which forms part of a ∼200 kDa complex of an as yet unknown composition and function (Fulda et al., 2000; Klinkert et al., 2004; Schottkowski et al., 2009a). However, a minor fraction (10–20%) of PratA was found to associate with membranes in a D1-dependent manner. Cellular fractionation experiments using two consecutive sucrose gradients revealed that the membrane-bound PratA is apparently not associated with either the PM or TMs, but co-sediments with an intermediate membrane subfraction, which was therefore named PratA-defined membrane (PDM) subfraction (Schottkowski et al., 2009a). Albeit the different density of PDMs as compared with that of PMs, it cannot be ruled out that PDMs might be identical to previously described specialized PM subregions, in which PSII subunits tend to accumulate (Srivastava et al., 2006). Membrane fractions resembling PDMs with regard www.selleckchem.com/products/AG-014699.html to their density have already been observed in earlier

studies, where they have been postulated to be linked to so-called thylakoid centers (Hinterstoisser et al., 1993). Based on electron microscopic analyses, thylakoid centers were initially described in some cyanobacteria as tubular structures found at the inner face of the Cediranib (AZD2171) PM, at points where thylakoids extend projections into the cytoplasm (Kunkel, 1982). Recently, this idea was revisited based on a more detailed cryo-electron tomography analysis in Synechocystis 6803 (van de Meene et al., 2006). Interestingly, PratA inactivation and, thus, defective PSII assembly leads to a significant accumulation of the pD1 precursor protein in PDM fractions (Schottkowski et al., 2009a). This suggests that PratA function is required for efficient membrane flow from PDMs to TMs, underlining the role of PDMs for PSII reaction-center assembly. Interestingly, related ‘biogenesis regions/centers’ have recently been observed in the eukaryotic green alga Chlamydomonas reinhardtii, where they are formed by membranes surrounding the pyrenoid structure of the chloroplast (Uniacke & Zerges, 2007). This might indicate an evolutionary conservation of the molecular principles that underlie TM biogenesis.