In our previous

study, the S10-GERMS method was demonstrated to be a useful tool for bacterial classification at species, subspecies, and strain levels of genera Bacillus and Pseudomonas strains based on phylogenetic analysis (Hotta et al., 2010b, 2011). In this study, our research focused on the identification of diverse APEOn-degrading bacteria, the Sphingomonadaceae, in the environment using the S10-GERMS method. First, the ribosomal subunit protein masses were calculated by S10 and spc operon sequencing of the Sphingomonadaceae. To construct the database, their masses were corrected by the observed Selumetinib mass analyzed by MALDI-TOF MS. Finally, ribosomal subunit proteins as biomarkers coded in S10 and spc operons were selected based on the corrected database. The selected biomarkers enabled rapid bacterial identification and phylogenetic classification

of the Sphingomonadaceae selleckchem by constructing a ribosomal protein database. The Sphingomonadaceae strains listed in Table 1 were used in this study. A number of isolated APEOn-degrading bacteria were identified as diverse species of the Sphingomonadaceae in our laboratory. The NBRC and JCM strains were purchased from the National Institute of Technology and Evaluation (NITE)-Biological Resource Center (NBRC, Kisarazu, Japan) and the RIKEN BRC (JCM, Wako, Japan) through the National Bio-Resource Project of MEXT, Japan, respectively. Each bacterial strain was grown aerobically in the medium and at the temperature recommended by suppliers. Sphingopyxis macrogoltabidus Sphingopyxis terraea t-Octylphenol polyethoxylates (OPEOn), which have the commercial name Triton X-100 (TX-100), were purchased from Wako (Kyoto, Japan) and Aldrich Chemical Co., respectively. The liquid basal salt medium with 0.1% (w/v) TX-100 as the sole carbon source, named TX-A medium, Flavopiridol (Alvocidib) was used for APEOn-degrading bacteria. TX-A medium was described in our previous study (Hotta et al., 2010a). Chromosomal DNA was extracted from the bacteria

as described previously (Hotta et al., 2010b). The quantity and quality of the extracted DNA were estimated by measuring the UV absorption spectrum (BioSpce-mini; Shimadzu, Kyoto, Japan). PCR amplification of S10 and spc operons was performed using KOD containing dNTP at a concentration of 200 μM, each of the primers at a concentration of 4 μM, 100 ng template DNA, and 2.5 U KOD polymerase (Toyobo, Tokyo, Japan) in a total volume of 50 μL. PCR amplification conditions of S10 and spc operons were as follows: (1) 2 min at 98 °C, (2) 30 cycles of 10 s at 98 °C, 30 s at 50–55 °C, and 6.5 min at 68 °C. PCR and sequencing primers used in this study were designed on the basis of consensus nucleotide sequences of S10 and spc operons from seven genome-sequenced strains of the Sphingomonadaceae with the clustal x program for the alignment of nucleotide sequences (Table 2). The sequencing reaction was carried out using a bigdye ver. 3.