Azospirillum amazonense revealed genomic organization patterns of the nitro
gen fixation genes similar to those of the distantly related species A. bra
silense. Our work suggests that A. brasilense nifHDK, nifENX, fixABC operon
s and nifA and glnB genes may be structurally homologous to the counterpart
genes of A. amazonense. This is the first analysis revealing homology betw
een A. brasilense nif genes and the A. amazonense genome. Sequence analysis
of PCR amplification products revealed similarities between the amino acid
sequences of the highly conserved nifD and glnB genes of A. amazonense and
related genes of A. brasilense and other bacteria. However, the A. amazone
nse non-coding regions (the upstream activator sequence region and the regi
on between the nifH and nifD genes) differed from related regions of A. bra
silense even in nitrogenase structural genes which are highly conserved amo
ng diazotrophic bacteria. The feasibility of the 16S ribosomal RNA gene-bas
ed PCR system for specific detection of A. amazonense was shown. Our result
s indicate that the PCR primers for 16S rDNA defined in this article are hi
ghly specific to A. amazonense and can distinguish this species from A. bra
silense.