Abstract: Using pyrene as the sole carbon and energy source, and by the method of plate sublimation, a strain SE12 was isolated from a contaminated soil near Woniushan Coking Plant in Xuzhou, China. According to the morphological, biochemical, and 16S rDNA analyses, this strain was identified as Mycobacterium sp., with 98% of homology to the rapid-growth nonpathogenic strain M. austroafricanum ATCC 33464. The optimum pH and temperature for the degradation of pyrene by SE12 were pH 9 and 30 ℃. When the soil samples were added with 100 and 200 mg·kg^-1 of pyrene and inoculated with 10⁷ CFU·g^-1of SE12, the degradation rates of pyrene reached to 97% and 99%, respectively after 28 days incubation at 30 ℃. By using primer-pairs nidAF/nidAR and nidBF/nidBR for amplification of ring-hydroxylating dioxygenase genes, it was shown that SE12 had the fragments of encoded large and small subunits of dioxygenase genes. Sequence analysis showed that these fragments were highly homologous to the known dioxygenase genes from pyrene-degrading Mycobacteria sp.

Key words: pyrene, microbial degradation, 16S rDNA identification, dioxygenase gene, Mycobacteria sp., natural reserve, camping site, environmental suitability, GIS technology, analytic hierarchy process (AHP).