We will obtain rhizobial inoculants from commercial sources. Pure cultures of rhizobial bacteria will be isolated from these inoculants using mannitol-yeast extract-Congo red agar. ACC deaminase activity of each bacterial isolate will then be determined by measuring the production of alpha-ketobutyrate using a spectrophotometer. Subsequently, greenhouse experiments will be conducted to evaluate if rhizobial isolates with different ACC deaminase activities lead to differences in soybean root nodulation by measuring nodule number and weight. Presence of ACC-deaminase-encoding gene in rhizobia, root nodules and rhizosphere soil will be determined by PCR amplification using primers and thermal cycling conditions available in the literature.