A wild type strain of Bradyrhizobium spp. that associates with Neonoto
nia wightii (a tropical forage legume) was analysed with molecular bio
logy techniques. A genomic bank of the total DNA from this bacteria wa
s constructed by using the high copy number pUC 119 plasmid, as the cl
oning vector, established in Escherichia coli HB101 by transformation.
The total DNA of Bradyrhizobium was cloned as a collection of San 3AI
fragments. Tile hybrid plasmids of tile bank contain 10-20kb, rhizobi
a DNA fragments inserted into die Inc z region. Assuming that tile mol
ecular weight of tile Bradyrhizobium genome is about 4,200kb, and tile
average size of tile inserts is 15kb, there is more than 95% probabil
ity that a nan sequence will be represented in each 10(3) transformant
s, according to tile Clarke and Carbon (Cel 9: 91-99, 1976) mathematic
al expression. Although various chemical and physical methods were use
d, symbiotic plasmids were not detected ill this strain of rhizobia.