Fig. S1. Addition of 1 mM IPTG is sufficient to restore the biofilm phenotype of the complemented strains. Wildtype SA113 and 10833 and the eap

and nptase deletion mutant strains containing either empty vector selleck compound library (pCL15) or vector with the complementary gene, were grown in polystyrene plates in TSB containing 5% human serum and 0mM, 0.1mM, or 1mM IPTG. The biofilm phenotype was partially restored in 0.1mM IPTG but 1mM IPTG was required for full complementation of the phenotype. Safranin-stained biofilms were solubilized in 30% acetic acid and the OD470nm was determined. Fig. S2. Nptase activity is restored in the complemented strains. Wildtype SA113 and 10833 and the eap and nptase deletion mutant strains containing either empty vector (pCL15) or vector with the complementary Bafetinib nmr gene, were

grown overnight in TSB containing 1mM IPTG. Surface proteins were extracted by sonication and phosphatase activity was measured using para-nitrophenyl phosphate. Phosphatase activity is shown as OD405nm. 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 article. “
“A Gram-negative, non-spore-forming, catalase- and oxidase-positive, strictly aerobic, short rod-shaped bacterium with a single, polar flagellum, designated strain WH169T, was isolated from seawater of the Yellow Sea in China. Buds and prosthecae were formed when the organism was grown at 20 °C for 12 days on marine 2216E

agar. The organism grew optimally at 37 °C, in pH 7.0–8.0, and in the presence of 4.0–6.0% w/v NaCl. Growth did not occur in a medium without Na+ or sea salts. Strain WH169T contained ubiquinone-8 as the predominant respiratory lipoquinone and C16:1ω7c and/or C16:1ω6c (35.9%), C16:0 (25.3%) and C18:1ω7c (9.7%) as the major fatty acids. The polar lipids consisted of phosphatidylethanolamine, phosphatidylglycerol and an unidentified phospholipid. Orotic acid The DNA G+C content of strain WH169T was 49.4 mol%. 16S rRNA gene sequence analysis showed that strain WH169T showed 95.1% sequence similarity to both type strains of the only two species in the genus Aestuariibacter. On the basis of the polyphasic taxonomic evidence presented in this study, it was concluded that strain WH169T should be classified as a novel species of Aestuariibacter, for which the name Aestuariibacter aggregatus sp. nov. is proposed, with the type strain WH169T (=CGMCC 1.8995T=LMG 25283T). The genus Aestuariibacter, which belongs to the family Alteromonadaceae, was proposed by Yi et al. (2004) for strictly aerobic, chemoheterotrophic, salt-requiring, mesophilic, neutrophilic and non-spore-forming rods, which were motile by means of single polar flagella. There are only two species with validly published names in the genus Aestuariibacter, i.e. Aestuariibacter salexigens and Aestuariibacter halophilus (Yi et al., 2004).