Carbon nutrition was determined in mineral base RM2 supplemented with an organic carbon source and 0.03% yeast extract. Growth was monitored by measuring the OD660 nm using an Amersham-Pharmacia Novaspec Plus spectrophotometer, and the final reading was taken after 2 weeks of incubation. Whole-cell SP600125 mouse fatty acids were analyzed by gas–liquid chromatography of their methyl ester derivatives as described previously (Suzuki & Hiraishi, 2007). Quinones were extracted with a chloroform–methanol mixture and analyzed by HPLC as described (Fujii & Hiraishi, 2009). Genomic DNA was extracted and purified according to the method of Marmur (1961). The guanine plus cytosine (G+C) ratio of genomic DNA was determined using the

HPLC method with external nucleotide standards as described by Mesbah et al. (1989). 16S rRNA Ribociclib ic50 gene fragments were PCR amplified, purified, and sequenced directly using an automated DNA sequencer as described previously (Hisada et al., 2007). Sequence data were compiled using the genetyx program (Software Developing Co., Tokyo, Japan) and compared with those retrieved from the database. Multiple alignment of sequence data, calculation of the corrected evolutionary distance (Kimura, 1980), and construction of a neighbor-joining (NJ) phylogenetic tree (Saito & Nei, 1987) were performed

using the arb program package (Ludwig et al., 2004). The topology of the NJ tree was evaluated by bootstrapping with 1000 replicates (Felsenstein, 1985). Tree construction was also carried out by the maximum likelihood (ML) method using the treefinder (Jobb, 2008) program package. The 16S rRNA gene sequences of strains AP8T and AP9 determined (1461 bases) were identical to each other, and were most closely related to that of the type strain of A. capsulatum (96% similarity). An NJ phylogenetic tree based on the sequences showed that the isolates represent a distinct lineage within subdivision 1 of the phylum Acidobacteria with A. capsulatum as their nearest phylogenetic neighbor (Fig. 1). The topology of the ML tree constructed was RVX-208 similar to that of the NJ tree (data not shown). The cells of the two isolates stained Gram-negative and were nonmotile, asporogenous

cocci and coccobacilli measuring 0.5–0.8 μm in diameter (Supporting Information, Fig. S1). Cells occurred singly or occasionally in pairs and reproduced by binary fission. Similar to A. capsulatum, cells of the isolates were capsulated. Colonies grown on GYSG medium for 7 days of incubation were circular (1.0–2.0 mm in diameter), smooth, translucent, mucous, and pale pink. The isolates were strictly aerobic and chemoorganotrophic bacteria that had a respiratory type of metabolism with oxygen as the terminal electron acceptor. Neither anaerobic respiratory growth with nitrate nor anaerobic fermentation with sugars or pyruvate occurred. No chemolithotrophic growth with sulfide, elemental sulfur, thiosulfate, or Fe2+ as electron donors was found.