We thank Paul Muir (Queensland Department of Primary Industries and JCU) for isolation of strain 47666-1, and Greg Smith, Matthew Salmon and Grant Milton (AIMS) for initial sampling and plating of diseased P. ornatus larvae. We thank Linda Blackall for critically reading the manuscript. Fig. S1. Phylogenetic analysis selleck screening library based on the (a) MP and (b) ML methods, using concatenated sequences

of rpoA (884 bp), pyrH (421 bp), topA (587 bp), ftsZ (443 bp) and mreB (507 bp) loci (total length, 2842 bp) from Vibrio owensii strains and other species of the Harveyi clade. Table S1. Fatty acid composition of Vibrio owensii sp. nov. and related species as reported by Gómez-Gil et al. (2003). Data are expressed as percentages of total fatty acids. Percentages <1 % are not shown. All strains were grown on TSA supplemented with 1.5% NaCl at 28°C for 24h. Table S2. DNA–DNA hybridization values among Vibrio owensii sp. nov. and type strains of related species. Table S3. List of strains and sequence accession numbers included in the MLSA. Please note: Wiley-Blackwell is not responsible for the content or functionality of any supporting materials supplied by the authors. Any queries (other than missing material) should be directed to the corresponding author for the Sirolimus manufacturer article. “
“We studied growth temperature as a factor controlling the expression of genes involved in capsular polymers of

Escherichia coli K92. These genes are shown to be regulated by growth temperature. Expression levels of genes belonging to the kps cluster, responsible for polysialic acid (PA) biosynthesis, were significantly increased at 37 °C compared with at 19 °C, being up to 500-fold increased for neuE and neuS genes. Similarly, the genes for the nan operon, responsible for PA catabolism, also reached higher expression levels at 37 °C, although with slightly lower values (39–141-fold). In contrast, genes of Protein Tyrosine Kinase inhibitor the cps operon, which are implicated in colanic acid (CA) metabolism, were upregulated when the bacteria were grown at 19 °C, albeit to

a much lesser extent (around twofold). This different regulation of genes involved in the biosynthesis of polysialic and CAs correlates with the reported maximal production temperatures for the two polymers. The results suggest that the metabolism of PA is predominantly regulated by changes in gene expression, while CA production may be regulated mainly by post-transcriptional processes such as phosphorylation–dephosphorylation reactions. Exopolysaccharides are important constituents of the surface of the bacterial cell envelope. Many bacteria produce extracellular polysaccharides, which can remain attached to the cell in a capsular form or alternatively be released as a slime. Capsules are high-molecular-mass structures, many of them composed of polysaccharides (CPSs) that are firmly attached to the surface of the cell (Whitfield, 2006).