Optimization of a glycoengineered Pichia pastoris cultivation process for commercial antibody production

被引:45
|
作者
Ye, Jianxin [1 ]
Ly, Jeffrey [1 ]
Watts, Kathryn [1 ]
Hsu, Amy [1 ]
Walker, Andre [1 ]
McLaughlin, Kathleen [1 ]
Berdichevsky, Marina [1 ]
Prinz, Bianka [2 ]
Kersey, D. Sean [2 ]
d'Anjou, Marc [2 ]
Pollard, David [1 ]
Potgieter, Thomas [1 ]
机构
[1] Merck & Co Inc, Bioproc Res & Dev, Rahway, NJ 07065 USA
[2] GlycoFi Inc, Lebanon, NH 03766 USA
关键词
Pichia pastoris; fermentation; glycosylation; antibody production; N-LINKED GLYCOSYLATION; HIGH-LEVEL EXPRESSION; MONOCLONAL-ANTIBODIES; RECOMBINANT PROTEINS; FED-BATCH; YEAST; METHANOL; GLYCOPROTEINS; FERMENTATIONS; THERAPEUTICS;
D O I
10.1002/btpr.695
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Glycoengineering enabled the production of proteins with human N-linked glycans by Pichia pastoris. This study used a glycoengineered P. pastoris strain which is capable of producing humanized glycoprotein with terminal galactose for monoclonal antibody production. A design of experiments approach was used to optimize the process parameters. Followed by further optimization of the specific methanol feed rate, induction duration, and the initial induction biomass, the resulting process yielded up to 1.6 g/L of monoclonal antibody. This process was also scaled-up to 1,200-L scale, and the process profiles, productivity, and product quality were comparable with 30-L scale. The successful scale-up demonstrated that this glycoengineered P. pastoris fermentation process is a robust and commercially viable process. (C) 2011 American Institute of Chemical Engineers Biotechnol. Prog., 2011
引用
收藏
页码:1744 / 1750
页数:7
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