Genomic DNA of the strains was isolated and the PCR
amplified 16S rRNA was cloned into E. coli and sequenced.
By using six primers (three forward and three reverse), 1 461
bp of the 16S rRNA was sequenced. The 16S rRNA sequence
was aligned with the known 16S rRNA sequences of other
bacteria. It was found from 16S rRNA sequence that the
strains C11 and C12 were Streptomyces species.