In this study, a high-temperature-tolerant strain of the king oyster mushroom (Pleurotus eryngii) was generated by chemical mutagenesis. Cultivation of P. eryngii generally involves incubating the mycelia at 25°C and then moving the spawns for further incubation at 18°C for fruitification. However, in tropical countries, the temperature is a major concern in the production of oyster mushroom where the average temperature is 32°C. In the current study, the mycelia were treated with ethyl methane sulphonate (EMS) or methyl methane sulphonate (MMS) for chemical-induced mutation. Seven mutants (EMS 1, 2, 6, 26, 35, 36, and 38) from EMS mutagenesis exhibited higher growth rates than the wild-type strain at 32°C. However, mutant strains from MMS mutagenesis showed a low growth rate when compared with wild-type. On sawdust substrate, the spawn running conditions for these strains were performed at 32°C, and fruitification occurred at 18°C. The yield and biological efficiency of EMS 36 and 38 mutants were higher than those of the wild-type strain. The activities of cellulase and xylanase of EMS 36 and 38 mutants showed that both these mutants had higher activities than the wild-type strain which may influence mushroom production. Therefore, these EMS 36 and 38 mutants can be cultivated in tropical countries, which could provide a high yield and reduce the cost during spawn running step.
CHEMICALLY INDUCED MUTAGENESIS IN THE KING OYSTER MUSHROOM Pleurotus eryngii TO GENERATE HIGH-TEMPERATURE TOLERANT STRAIN
