It is difficult to control concentrations of methanol/dissolved oxygen at high levels simultaneously in heterologous proteins productions by Pichia pastoris during induction phase. Two strains, a methanol utilization slow (Mut(s)) type and a plus (Mut(+)) type were used with methanol/sorbitol co-feeding strategy to induce porcine interferon-a and human serum albumin-human granulocyte colony stimulating factor respectively, under the conditions of "methanol sufficient-oxygen limited (MS-OL)" and "methanol limited-oxygen sufficient (ML-OS)". For the Mut(s)/Mut(+) strains, the target proteins titers under "MS-OL" were 6-fold/19.2% of those under "ML-OS". The key genes in methanol metabolism of the Mut(s) strain were up-regulated under "MS-OL", but they were not differently expressed in the Mut(+) strain. Methanol utilization rate (r(MeOH)) of the Mut(s) strain reduced when decreasing methanol concentration, but r(MeOH) of the Mut(+) strain unchanged unless methanol concentration decreased to a low-limit of 0.6 g/L. Finally, kinetic models were designed to describe the methanol/sorbitol co-feeding process.