Extracts from R. grahamii CCGE502 and mutants were prepared from 5-ml cultures grown in PY medium. Briefly, cultures were extracted twice with equal volumes of ethyl acetate, bacteria were removed by centrifugation

and supernatants evaporated to dryness. Residues from 5-ml cultures were dissolved in 50–100 μl of ethyl acetate. Eckhardt gel analysis This was performed as described [39], with liquid early-exponential-phase cultures in horizontal gels with sodium dodecyl sulfate in agarose. Gap closure Gap filling was done over the contigs of the sequence assembly AEYE01000000 [40]. Ten contigs corresponding to symbiotic plasmid pRgrCCGE502a and sixteen corresponding to megaplasmid pRgrCCGE502b were selected. A new assembly click here was done with Phrap assembler using the 454 pyrosequencing mate-paired reads and edited with Consed (23.0) program [41]. A total of 1920 contigs were obtained and compared with the scaffolds corresponding to pRgrCCGE502a MK-0457 supplier and pRgrCCGE502b of the original assembly. Contigs that overlapped with the pRgrCCGE502a and pRgrCCGE502b scaffolds were Apoptosis inhibitor selected and analyzed at their ends to obtain the sequence that protruded into the gap region. Those protruding sequences were edited manually to fill the scaffold gaps. The complete pRgrCCGE502a and pRgrCCGE02b sequences were aligned with Illumina reads using Consed to verify the coverage of the new molecules.

In some cases these processes located small contigs (corresponding to IS or repetitive sequences) to close a gap. A final annotation of the new version AEYE02000000 was performed by the NCBI Prokaryotic Genomes Automatic Annotation Pipeline (PGAAP). The replicons gave an estimated genome size of 7,156 kbp. Sequence comparisons Average nucleotide identity (ANI) between sequences and sequence conservation was calculated with JSpecies software [22]. Phylogenetic inference Multiple sequence alignments were performed

with CLUSTAL_X version 1.83 [42] and manually checked with BioEdit [43]. Best-fit models of sequence evolution were selected for each gene with ProtTest 2.4, using the Akaike information criterion [44]. Maximum-likelihood phylogenies Quisqualic acid were constructed with PhyML 3 using subtree pruning and regrafting moves to improve tree topology [45]. Support for tree nodes was evaluated by the Shimodaira–Hasegawa-like approximate likelihood-ratio test implemented in PhyML. Results The genome of R. grahamii CCGE502 consists of three circular replicons, one chromosome and two ERs: one megaplasmid and a symbiotic plasmid. The first draft sequence [40] consisted of ten contigs for the symbiotic plasmid pRgrCCGE502a and sixteen corresponding to the megaplasmid pRgrCCGE502b. The version described in this paper is version AEYE02000000. Chromosome The ca. 5,400-kbp chromosome of R. grahamii CCGE502 is the largest reported to date in Rhizobium. A genomic island of ca.