Lipase production with free and immobilized cells of cold-adapted yeast Rhodotorula glutinis HL25

This study was undertaken to produce the lipase by free and immobilized cells of cold-adapted yeast Rhodotorula glutinis HL25 using waste frying oils as substrate. The optimization of culture parameters was performed using traditional one-factor-at-a-time protocol. The temperature 20°C and initial pH 6.0 were optimal for lipase production by both free and immobilized cells. An inoculum size of 40mL/L for free cells and beads number of 150g/L for immobilized cells were optimal for lipase production. Optimal waste frying oil concentration and incubation time were 30mL/L and 84h for free cells but 40mL/L and 72h for immobilized cells, respectively. The maximum increases for free and immobilized cells were achieved at the Triton X-100 concentrations of 5 and 7.5mL/L, respectively. The maximum lipase activities were determined as 54.4 and 75.2U/L for free and immobilized cells, respectively. Immobilized cells could be used in five successive reaction cycles without any loss in the maximum activity. Immobilized cells could retained about 70% of their maximum activity by the end of the cycle 10. This is the first attempt on lipase production potential of a cold-adapted strain of the yeast R. glutinis. Furthermore, lipase production using immobilized cells of cold-adapted yeasts was investigated for the first time.