5 g/L NeuNAc (blue line). CAT A-1155463 mouse medium alone as a source of carbon is in grey line. All strains were grown for 38 hours at 37°C in 200 μl of medium in a 96 well microplate with reading intervals of 10 min. For the fermentation assay (panel D) bacteria were incubated for 24 and 48 h with serial dilutions of either ManNAc (left columns) or NeuNAc (right columns) as sole carbon sources in microtiter plates containing phenol red as a pH indicator. www.selleckchem.com/products/AZD1152-HQPA.html Sugar fermentation is evidenced by a yellow colour change due to acidification of the

culture medium. Carbohydrate concentrations (% w/v) are shown on the right. Neuraminidase locus induction in S. pneumoniae The putative regulator of the nanAB locus SPG1583 contains a classical N-terminal helix-turn-helix motif and a SIS domain, found in many phosphosugar binding proteins including transcriptional regulators binding to the phosphorylated end-products of the pathways [26]. Given the Sapanisertib mw probable catabolic pathway of sialic acid (Figure 1B), ManNAc-6-phosphate appears to be the most probably compound having a regulatory role on the expression of pneumococcal neuraminidase operon and thus possibly in sialic acid metabolism [23]. Therefore we analysed the growth curves and the expression levels of some key genes associated with the transporter systems in the neuraminidase

locus. First we compared the growth in the presence of ManNAc as a carbon source of a un-encapsulated G54 derivative FP65 and two isogenic mutants devoid of the whole nanAB locus and of the transcriptional regulator SPG1583 respectively (Figure 3A). The growth curves showed

absence of growth in the presence of ManNAc for both mutants, indicating that the nanAB locus is essential for efficient growth of ManNAc and that the phosphosugar binding regulator SPG1583 gene appears to acts as a transcriptional activator. Then Tacrolimus (FK506) we focused our attention on growth of the wild type strain in the presence or absence of ManNAc, preferred by us for the indication assays over NeuNAc, as this amino sugar does not acidify the medium. In these experiments bacteria initially grew on residual yeast-extract derived dextran of non-supplemented CAT medium (40 min) and continued to grow thereafter with a lower generation time of 140 min on ManNAc only (Figure 3B). For gene expression profiling bacteria were sampled in early exponential growth (OD590 = 0.02), when growth was still due to the residual yeast extract-derived sugar (Figure 3B, black arrows). For bacteria grown on yeast extract derived sugar in presence of ManNAc, gene expression data showed a significant induction of the satABC SPG1589-91 and SPG1592 PTS transporters, and a non-significant induction of nanA (Figure 3C). We performed a second experiment that compared the influence of ManNAc at OD590 = 0.02 and 0.05 on gene expression (Figure 3B, open arrows).