All further steps were carried out on ice. Glass beads were removed by centrifugation for 6 min (14,000 rpm, 4°C, Hermle Z513K centrifuge). Membranes were

separated from cytoplasmic proteins by ultracentrifugation (Beckman centrifuge, TLA 100.4 rotor) for JNK-IN-8 in vivo 2 h at 60,000 rpm and 4°C. Pellets were resuspended in half of the volume of the supernatant, and fractions stored at −80°C. For SDS polyacrylamide gel electrophoresis, 3 μl per fraction were used. Western blotting was performed as described previously [54] and CpoA was visualized using a 1:10,000 dilution of rabbit antiserum raised against a purified CpoA-derivative as described [7]. Microarray-based transcriptome analysis Extraction of total RNA from exponentially growing S. pneumoniae cultures (40 NU), reverse transcription of RNA into labeled cDNA, prehybridization, hybridization, slide washing, scanning, and analysis of the data were performed as described previously [55]. For each strain, data sets from at least four hybridizations were used for normalization and statistical analysis. Only data which showed P values below 10-4 in a paired t test, and relative changes in the transcript amount of greater than threefold were considered further. The oligonucleotide microarray covering

genes and intergenic regions of S. pneumoniae R6/TIGR4 has been described [21]. Accession number S. pneumoniae R6/TIGR4 oligonucleotide microarray: ArrayDesign check details R6/TIGR4 Wortmannin in vivo ArrayExpres accession number A-MEXP-1846. Availability of supporting data The data sets supporting the results of this article are included within the article and its additional files. Acknowledgements This work was supported by the EU (Intafar LSHM-CT-2004-512138), the

DFG (Ha 1011/11-1), and the Stiftung Rheinland-Pfalz für Innovation (15202–38 62). We thank Martin Rieger for his assistance in analyzing microarray data, and Reinhold Brückner for helpful discussions. Electronic supplementary material Additional file 1: Figure S1: Phospholipids in S. pneumoniae R6. Lipids were extracted and separated by two dimensional TLC. 1.D and 2.D: first and second dimension (first dimension: CHCl3/MeOH/H20 = 65:25:4; second dimension: CHCl3/AcOH/MeOH/H20 = 80:14:10:3). Phospholipids were visualized by spraying Reverse transcriptase with Molybdenum Blue spray reagent. PG: phosphatidylgylcerol; CL: cardiolipin. Standards: PG, 0.3 μMol; CL, 0.17 μmol. Figure S2. Membrane association of CpoA. Membrane (m) and cytoplasmic proteins (s) were separated by SDS-PAGE followed by immunostaining with anti-CpoA antiserum (see Methods for detail). Closed arrows indicate the position of CpoA in the membrane fractions of S. pneumoniae R6 and P104, the open arrow shows the absence of CpoA in R6ΔcpoA. M: marker proteins. (PDF 175 KB) Additional file 2: Table S1: Primers. Table S2.