Li Guiying Y, Fu Man, Qin Mei, Xue Liming M
Key Laboratory of Development and High-Value Utilization of Beibugulf Seafood Resources for Guangxi Colleges, School of Food Engineering, Qinzhou University, Qinzhou, China.
Institute of Chemical Toxicity, Shanghai Municipal Center of Disease Control and Prevention, Shanghai, China.
J Mol Microbiol Biotechnol. 2017;27(6):363-370. doi: 10.1159/000486395. Epub 2018 Feb 6.
Human cathepsin S production by recombinant Pichia pastoris using cod skin as the co-nitrogen source was investigated in this study. The addition of carbon sources of glycerol in the fed-batch phase and of methanol in the induction stage was also investigated. A new approach to the highly expression of human cathepsin S was developed using 90 g/L of cod skin (wet weight). After 24 h of the initial fermentation, 4% glycerol (v/v, glycerol/culture) was added once to enhance the cell density (OD600) in the cultivation. Then, adding and maintaining methanol at 0.5% (v/v, methanol/cultivation) after about 48 h of fermentation achieved a high expression of human cathepsin S in a 5-L bioreactor. The results demonstrate that the maximum activity of human cathepsin S in the fermentation supernatant reached 7,152 U/L after 96 h of methanol induction. The methylotrophic yeast P. pastoris grown in the medium containing cod skin (90 g/L) as the co-nitrogen source provided a 21% higher cell density (OD600) and 18.3% higher human cathepsin S yield than P. pastoris grown in BMGY medium. For the first time, human cathepsin S was successfully expressed by P. pastoris with cod skin as the co-nitrogen source. The glycerol fed-batch controlling strategy and method of maintaining methanol at a constant concentration of 0.5% (v/v, methanol/cultivation) in the induction stage was efficient for P. pastoris growth and the expression of human cathepsin S.
J Mol Microbiol Biotechnol. 2017
Bioresour Technol. 2008-11
J Biosci Bioeng. 2005-3