Recombinant Candida rugosa LIP2 expression in Pichia pastoris under the control of the AOX1 promoter

被引:28
|
作者
Ferrer, Pau [1 ]
Alarcon, Manuel [1 ]
Ramon, Ramon [1 ]
Dolors Benaiges, Maria [1 ]
Valero, Francisco [1 ]
机构
[1] Univ Autonoma Barcelona, Dept Engn Quim, ETSE, E-08193 Barcelona, Spain
关键词
Lip2; Candida rugosa; Pichia pastoris; AOX1; promoter; Enzyme; On-line fed-batch; Stirred tanks; Protein engineering; CANDIDA-RUGOSA LIPASE; HETEROLOGOUS PROTEIN-PRODUCTION; MULTIPLE MUTAGENESIS; PSEUDOMONAS-CEPACIA; ORGANIC MEDIA; LIP1; GENE; PURIFICATION; OVEREXPRESSION; AGGREGATION; ISOENZYMES;
D O I
10.1016/j.bej.2009.05.018
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
The LIP2 isoenzyme gene from Candida rugosa has been completely synthesised and functionally expressed under the AOX1 promoter control in Pichia pastoris. The on-line monitoring and control of methanol, the key inducer carbon source in fed-batch cultures, has enhanced the yield product/biomass 7.8-fold and the productivity 12.8-fold compared to the best batch cultivation with the Pichia system and, 10-fold compared to the fed-batch cultivation process using the native C. rugosa strain. Nevertheless, the high ionic strength of culture broth favoured aggregation of Lip2, leading to total loss of lipolytic activity. After cultivation, a diaultrafiltration process was implemented to diminish ionic strength, allowing for the recovery of lipolytic activity in the diaultrafiltrate. The developed bioprocess resulted into a reproducible product in terms of quality and productivity. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:271 / 277
页数:7
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