Four clusters were discernible at 50% similarity level using HaeIII (Figure 1). Cluster 1 consisted of bacterial DNA from nodules of Omondaw (grown in South Africa and Ghana), IT82D-889 and Bechuana white (grown in South Africa), and check details Glenda (grown in Ghana). Cluster 2, on the other hand, was made up of i) IGS types from nodules of all the 9 genotypes grown in South Africa, ii) IGS types from nodules of ITH98-46, IT82D-889, Glenda, Mamlaka, Brown eye, Bechuana white and Apagbaala grown in Botswana, and iii) IGS types from nodules of Glenda, Bechuana white and IT82D-889 grown in Ghana. In contrast, cluster 3 consisted of IGS types coming

from root nodules of only Glenda and Fahari grown in South Africa. Like cluster 2, cluster 4 was made of IGS types SCH 900776 from nodules of cowpea genotypes grown in all the 3 countries. Figure 1 UPGMA dendrogram derived from PCR-RFLP of bradyrhizobial DNA in cowpea nodules collected from South Africa, Botswana and Ghana, generated by HaeIII digestion of amplified rDNA products. Scale indicates % buy Gefitinib similarity. Strain IGS type symbiotic efficiency Relating symbiotic functioning (measured here as specific nodule nitrogenase activity) to the IGS types found inside root nodules revealed significant differences in the N2-fixing efficiency of these IGS types (Figure 2). For example, IGS types V and VIII fixed very low N in IT82D-889 and Bechuana white relative to IGS type III in Apagbaala at Wa in Ghana (see

Figure 2). It was also interesting to note that sole nodule occupancy by IGS type VIII in Omondaw resulted in significantly very high N yield relative to its poor performance as a sole occupant of nodules in ITH98-46 at Wa in Ghana (Figure 2A). Similar differences in symbiotic functioning were obtained for combinations of resident IGS types SPTLC1 found in root nodules of the 9 cowpea genotypes at Taung in South Africa (Figure 2B). Figure 2 Specific nodule activity for the 9 genotypes

grown at A) Wa in Ghana, B) Taung in South Africa. Bars with dissimilar letters indicate significant differences at p ≤ 0.05. Numerals on the top of each bar represent the different IGS types (strains) that were found in the cowpea nodules from the particular genotype. 16S-23S rDNA IGS sequencing Out of 18 IGS types samples submitted for gene sequencing (see Table 5), only 13 (i.e. samples with sequence numbers 104, 27, 36, 103, 115, 68, 5, 201, 22, 117, 153, 146 and 107) were successfully sequenced. As a result, the 13 16S-23S rDNA IGS sequences for Bradyrhizobium (i.e. sequence 104, 27, 36, 103, 115, 68, 5, 201, 22, 117, 153, 146 and 107) were deposited in the GenBank database under accession numbers [GenBank: FJ983128 to FJ983140] for sequence alignments with those of existing Bradyrhizobium species in the GenBank. The results from the Genbank database showed that IGS sequences 104, 27, 36, 115, 68 and 103 clustered with Bradyrhizobium yuanmingense and Bradyrhizobium sp.