Growing E-coli to high cell density -: A historical perspective on method development

被引:322
作者
Shiloach, J
Fass, R
机构
[1] NIDDK, Biotechnol Unit, NIH, Bethesda, MD 20892 USA
[2] IIBR, Dept Biotechnol, IL-74100 Ness Ziona, Israel
关键词
E; coli; growth strategies; acetate excretion; high density;
D O I
10.1016/j.biotechadv.2005.04.004
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
E. coli is the major bacterial platform for expressing simple heterologous proteins. Growing E coli to high densities has been the subject of numerous studies since the early 1970s, exploring the limits of bacterial culture density in order to achieve maximum productivity. Research strategies were focused on improving the cultivation techniques, manipulating the bacteria's physiology or both. As a result, batch, fed batch and dialysis fermentation techniques had been developed. These growth strategies, together with optimization of media composition and the application of molecular biology methods, made it possible to grow E. coli to cell densities of up to 190 g/l (dry weight), while avoiding media precipitation and preventing acetate accumulation. Additional research on the effects of heterologous protein biosynthesis on signal transduction, proteolysis and post transcription events in E. coli may improve its productivity. Published by Elsevier Inc.
引用
收藏
页码:345 / 357
页数:13
相关论文
共 71 条
[1]   MODIFICATION OF CENTRAL METABOLIC PATHWAY IN ESCHERICHIA-COLI TO REDUCE ACETATE ACCUMULATION BY HETEROLOGOUS EXPRESSION OF THE BACILLUS-SUBTILIS ACETOLACTATE SYNTHASE GENE [J].
ARISTIDOU, AA ;
SAN, KY ;
BENNETT, GN .
BIOTECHNOLOGY AND BIOENGINEERING, 1994, 44 (08) :944-951
[2]  
BAUER KA, 1990, APPL ENVIRON MICROB, V56, P1256
[3]   MAXIMAL EXPONENTIAL-GROWTH RATE AND YIELD OF ESCHERICHIA-COLI OBTAINABLE IN A BENCH-SCALE FERMENTOR [J].
BAUER, S ;
SHILOACH, J .
BIOTECHNOLOGY AND BIOENGINEERING, 1974, 16 (07) :933-941
[4]   DENSE GROWTH OF AEROBIC BACTERIA IN A BENCH-SCALE FERMENTOR [J].
BAUER, S ;
ZIV, E .
BIOTECHNOLOGY AND BIOENGINEERING, 1976, 18 (01) :81-94
[5]   PLASMID-ENCODED PROTEIN - THE PRINCIPAL FACTOR IN THE METABOLIC BURDEN ASSOCIATED WITH RECOMBINANT BACTERIA [J].
BENTLEY, WE ;
MIRJALILI, N ;
ANDERSEN, DC ;
DAVIS, RH ;
KOMPALA, DS .
BIOTECHNOLOGY AND BIOENGINEERING, 1990, 35 (07) :668-681
[6]  
Bermejo LL, 1998, APPL ENVIRON MICROB, V64, P1079
[7]  
CHEN R, 1993, BIOTECHNOL BIOENG, V142, P215
[8]   EFFECT OF MODIFIED GLUCOSE-UPTAKE USING GENETIC-ENGINEERING TECHNIQUES ON HIGH-LEVEL RECOMBINANT PROTEIN-PRODUCTION IN ESCHERICHIA-COLI DENSE CULTURES [J].
CHOU, CH ;
BENNETT, GN ;
SAN, KY .
BIOTECHNOLOGY AND BIOENGINEERING, 1994, 44 (08) :952-960
[9]   Effects of mutations in acetate metabolism on high-cell-density growth of Escherichia coli [J].
Contiero, J ;
Beatty, C ;
Kumari, S ;
DeSanti, CL ;
Strohl, WR ;
Wolfe, A .
JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY, 2000, 24 (06) :421-430
[10]   Phosphate glass as a phosphate source in high cell density Escherichia coli fermentations [J].
Curless, C ;
Baclaski, J ;
Sachdev, R .
BIOTECHNOLOGY PROGRESS, 1996, 12 (01) :22-25