TABLE 2.
Name | Genusa | Class | Coverage –identityb | nodD1c | nodAc | fixNdc | nifHc | GFPc | Nodulationd |
TER22 | Brevundimonas sp. | Alphaproteobacteria | 100–99.88% | + | + | + | + | + | + |
TER23 | Pseudomonas sp. | Gammaproteobacteria | 100–100% | + | + | + | + | + | − |
TER31 | Stenotrophomonas sp. | Gammaproteobacteria | 100–94.16% | + | + | + | + | + | + |
TER33 | Bacillus sp. | Firmicutes-Bacilli | 100–99.88 | + | + | + | + | + | − |
TER38 | Achromobacter sp. | Betaproteobacteria | 100–99.25% | + | + | + | + | + | + |
TER39 | Ochrobactrum sp. | Alphaproteobacteria | 100–100% | + | + | + | + | + | − |
TER40 | Mesorhizobium sp. | Alphaproteobacteria | 99–98.75% | + | + | + | + | + | − |
TER49 | Phyllobacterium sp. | Alphaproteobacteria | 100–98.64% | + | + | + | + | + | + |
TER55 | Achromobacter sp. | Betaproteobacteria | 99–98.61% | + | + | + | + | + | − |
aGenera were identified by sequencing PCR products obtained with 16S primers, using DNA of each strain as template. bThe coverage and identity were determined by BLASTn of the internal fragments of the 16s RNA. cPresence of R. etli CFNX182-1 pSym sequence was determined by the obtention of PCR products of the different genes, using DNA of each strain as template. dNodulation ability was determined by inoculating bean seedlings with cultures of each purified strain, and determining the presence of nodules at 20 dpi.