Effect of specific production rate of recombinant protein on multimerization of plasmid vector and gene expression level

被引:10
作者
Saraswat, V [1 ]
Kim, DY [1 ]
Lee, J [1 ]
Park, YH [1 ]
机构
[1] Korea Res Inst Biosci & Biotechnol, Biochem Proc Engn RU, Taejon 305600, South Korea
关键词
recombinant human interleukin-2; specific production rate; plasmid multimerization; Escherichia coli;
D O I
10.1016/S0378-1097(99)00436-X
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In fed-batch cultures of recombinant Escherichia coli BL21 (DE3)[pT7-G3IL2] at high cell concentration, the post-induction specific growth rate was carefully regulated by controlled medium feed to maximize the synthesis level of recombinant fusion interleukin-7, G3.IL-2. A maximum concentration of G3.IL-2 (11.25 g l(-1)) was achieved in the induced recombinant culture growing at the rate of 0.056 h(-1). A steep decrease in the expression level of G3.IL-2 was observed at the post-induction specific growth rates higher than its optimal value (0.056 h(-1)). In the induced recombinant cultures, plasmid multimerization was observed and highly dependent on specific growth and production rate: a higher post-induction specific growth rate and an increased specific production rate tended to significantly promote it much further. Moreover, plasmid stability was found to decrease rapidly in a faster growing culture. (C) 1999 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:367 / 373
页数:7
相关论文
共 32 条
[1]   RECOMBINATION BETWEEN BACTERIAL PLASMIDS LEADING TO FORMATION OF PLASMID MULTIMERS [J].
BEDBROOK, JR ;
AUSUBEL, FM .
CELL, 1976, 9 (04) :707-716
[2]  
CARRIER MJ, 1983, TRENDS BIOTECHNOL, V8, P706
[3]   EFFECT OF PREINDUCTION SPECIFIC GROWTH-RATE ON RECOMBINANT ALPHA-CONSENSUS INTERFERON SYNTHESIS IN ESCHERICHIA-COLI [J].
CURLESS, C ;
POPE, J ;
TSAI, L .
BIOTECHNOLOGY PROGRESS, 1990, 6 (02) :149-152
[4]   EFFECT OF PREINDUCTION SPECIFIC GROWTH-RATE ON SECRETION OF GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR BY ESCHERICHIA-COLI [J].
CURLESS, CE ;
POPE, J ;
LOREDO, L ;
TSAI, LB .
BIOTECHNOLOGY PROGRESS, 1994, 10 (05) :467-471
[5]   SUSTAINING PROTEIN-SYNTHESIS IN THE ABSENCE OF RAPID CELL-DIVISION - AN INVESTIGATION OF PLASMID-ENCODED PROTEIN EXPRESSION IN ESCHERICHIA-COLI DURING VERY SLOW GROWTH [J].
FLICKINGER, MC ;
ROUSE, MP .
BIOTECHNOLOGY PROGRESS, 1993, 9 (06) :555-572
[6]   OPTIMIZING THE PRODUCTION OF RECOMBINANT PROTEINS IN MICROORGANISMS [J].
GEORGIOU, G .
AICHE JOURNAL, 1988, 34 (08) :1233-1248
[7]   MAINTENANCE OF MULTICOPY PLASMID CLO DF13 IN ESCHERICHIA-COLI-CELLS - EVIDENCE FOR SITE-SPECIFIC RECOMBINATION AT PARB [J].
HAKKAART, MJJ ;
VANDENELZEN, PJM ;
VELTKAMP, E ;
NIJKAMP, HJJ .
CELL, 1984, 36 (01) :203-209
[8]   SOS and Mayday:: multiple inducible mutagenic pathways in Escherichia coli [J].
Humayun, MZ .
MOLECULAR MICROBIOLOGY, 1998, 30 (05) :905-910
[9]   PRODUCTION OF RECOMBINANT HUMAN GROWTH-HORMONE IN ESCHERICHIA-COLI - EXPRESSION OF DIFFERENT PRECURSORS AND PHYSIOLOGICAL-EFFECTS OF GLUCOSE, ACETATE, AND SALTS [J].
JENSEN, EB ;
CARLSEN, S .
BIOTECHNOLOGY AND BIOENGINEERING, 1990, 36 (01) :1-11
[10]  
Kang F, 1993, Chin J Biotechnol, V9, P273