Protein production using recombinant yeast in an immobilized-cell-film airlift bioreactor

被引:0
|
作者
Zhang, ZG [1 ]
Scharer, J [1 ]
MooYoung, M [1 ]
机构
[1] UNIV WATERLOO, DEPT CHEM ENGN, WATERLOO, ON N2L 3G1, CANADA
关键词
immobilization; plasmid stability; recombinant yeast; glucoamylase; bioreactor;
D O I
10.1002/(SICI)1097-0290(19970720)55:2<241::AID-BIT1>3.0.CO;2-I
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
A recombinant Saccharomyces cerevisiae C468/pGAC9 (ATCC 20690), which expresses Aspergillus awamori glucoamylase gene under the control of the yeast enolase I (ENO1) promoter and secretes glucoamylase into the extracellular medium, was used as a model system to investigate the effect of cell immobilization on bioreactor culture performance. Free suspension cultures in stirred-tank and airlift bioreactors confirmed inherent genetic instability of the recombinant yeast. An immobilized-cell-film airlift bioreactor was developed by employing cotton cloth sheets to immobilize the yeast cells by attachment. Enhanced enzyme productivity and production stability in the immobilized-cell system were observed. Experimental data indicated that the immobilized cells maintained a higher proportion of plasmid-bearing cells for longer periods under continuous operation. The higher plasmid maintenance with immobilized cells is possibly due to reduced specific growth rate and increased plasmid copy number. Double-selection pressure was used to select and maintain the recombinant yeast. The selected strain showed better production performance than the original strain. (C) 1997 John Wiley & Sons, Inc.
引用
收藏
页码:241 / 251
页数:11
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