Abstract

Random amplified polymorphic of DNA-polymerase chain reaction (RAPD-PCR) analysis of the DNA extracted from seven Streptomyces strains of western region, KSA was the aim of this study. Partial sequence of 16S rRNA gene of Streptomycespolychromogenes was also attempted. Results showed that a total number of 240 amplified fragments were amplified using ten RAPD-PCR primers (OPA11, OPB10, OPB15, OPC03, OPC07, OPC18, OPD05, OPE05, OPO14 and OPO17). A total number of 97, 73, 88, 79, 100, 108 and 82 fragments were amplified from the DNA extracts of S. polychromogenes, Streptomyces chattanoogensis, Streptomyces lucensis, Streptomyces antibioticus, Streptomyces violans, Streptomyces griseorubiginosus and Streptomyces violaceus, respectively. An obvious variation in the amplified fragments was recorded using the ten RAPD-PCR primers (31, 27, 17, 19, 23, 29, 24, 26, 23 and 21 fragments for the primers, respectively). The highest similarity (66.7%) was found between S. lucensis and S. chattanoogensis; lowest similarity (35%) was recorded between the gray S. chattanoogensis and the red  S. violaceus. The 16S rRNA gene was isolated via PCR from the DNA of S. polychromogenes (1) and sequenced. Fragments of 1003 and 837 nts were amplified using the forward and reverse primers, respectively. On matching, a final sequence of about 1452 nts (GenBank: JQ962978.1) was obtained and compared with five universal Streptomyces strains and four bacterial clones. The percent identities between the isolate of this study and the compared bacterial strains was lowest (79.1%) compared to HQ844464.1 and highest (98.3%) compared to EU520331.1. Based on the phenotypic and genotypic (16S rRNA gene) features, the strain could be classified as a new strain of S. polychromogenes.

Key words: Identification, Streptomyces, RAPD-PCR, 16S rRNA gene, KSA.