A superoxide dismutase (SOD) gene of Thermoascus aurantiacus var. levisporus, a thermophilic fungus, was cloned, sequenced, and expressed in Pichia pastoris and its gene product was characterized. The coding sequence predicted a 231 residues protein with a unique 35 amino acids extension at the N-terminus indicating a mitochondrial-targeting sequence. The content of Mn was 2.46 ${mu}g$/mg of protein and Fe was not detected in the purified enzyme. The enzyme was found to be inhibited by $NaN_3$, but not by KCN or $H_2O_2$. These results suggested that the SOD in Thermoascus aurantiacus var. levisporus was the manganese superoxide dismutase type. In comparison with other MnSODs, all manganese-binding sites were also conserved in the sequence (H88, H136, D222, H226). The molecular mass of a single band of the enzyme was estimated to be 21.7 kDa. The protein was expressed in tetramer form with molecular weight of 68.0 kDa. The activity of purified protein was 2,324 U/mg. The optimum temperature of the enzyme was $55^{circ}C$ and it exhibited maximal activity at pH 7.5. The enzyme was thermostable at 50 and $60^{circ}C$ and the half-life at $80^{circ}C$ was approximately 40 min.