Fedbatch design for periplasmic product retention in Escherichia coli

被引:32
作者
Backlund, Emma [1 ]
Reeks, Dominic [2 ]
Markland, Katrin [1 ]
Weir, Neil [2 ]
Bowering, Leigh [2 ]
Larsson, Gen [1 ]
机构
[1] Royal Inst Technol, Sch Biotechnol, SE-10691 Stockholm, Sweden
[2] UCB Celltech, Slough SL1 3WE, Berks, England
关键词
fedbatch; outer membrane proteins; feed rate; recombinant proteins; E; coli; periplasmic retention;
D O I
10.1016/j.jbiotec.2008.05.002
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 feed profile of glucose during fedbatch cultivation could be used to influence the retention of the periplasmic product ZZ-cutinase. An increased feed rate led to a higher production rate but also to an increased specific leakage, which reduced the periplasmic retention. Three growth rates: 0.3, 0.2 and 0.1 h(-1) where studied and resulted in 20, 9 and 6%, respectively, of the total ZZ-cutinase accumulating in the medium. It was also shown that leakage during fedbatch production of a Fab fragment was also influenced by the feed Fate in a similar manner to ZZ-cutinase. If intracellular product accumulation is desired the advantage of a high productivity, resulting from a high substrate feed rate, is diminished because of a reduced product retention. Biochemical analysis revealed that the growth rate, resulting from a glucose limited feed, influenced the outer membrane Protein compositions with respect to OmpF and LamB, whilst OmpA was largely unaffected. As the feed Fate increased the amount of total Outer membrane protein decreased. When ZZ-cutinase was produced there were further reductions in outer membrane Protein accumulation, by 82, 100 and 22% for OmpF, LamB and OmpA, respectively, and the total reduction was almost 60% with a high product formation Fate. We suggest that the reduced titre of the outer membrane proteins, OmpF and LamB, may have contributed to a reduced ability for the cell to retain recombinant protein secreted to the periplasm. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:358 / 365
页数:8
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