Recombinant Protein Expression in High Cell Density Fed-Batch Cultures of Escherichia Coli
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[1] S. Schultz,et al. Cation Transport in Escherichia coli , 1965, The Journal of general physiology.
[2] J. Shiloach,et al. High‐yield growth of E. coli at different temperatures in a bench scale fermentor , 1975 .
[3] T. Wood,et al. Effect of chemically‐induced, cloned‐gene expression on protein synthesis in E. Coli , 1991, Biotechnology and bioengineering.
[4] J. Bailey,et al. Effects of recombinant plasmid content on growth properties and cloned gene product formation in Escherichia coli , 1985, Biotechnology and bioengineering.
[5] J. Mandelstam,et al. The intracellular turnover of protein and nucleic acids and its role in biochemical differentiation. , 1960, Bacteriological reviews.
[6] K Konstantinov,et al. A balanced DO‐stat and its application to the control of acetic acid excretion by recombinant Escherichia coli , 1990, Biotechnology and bioengineering.
[7] Tsuneo Yamane,et al. Fed-batch techniques in microbial processes , 1984 .
[8] J. Shiloach,et al. Maximal exponential growth rate and yield of E. coli obtainable in a bench‐scale fermentor , 1974, Biotechnology and bioengineering.
[9] K. Fujimori,et al. Mass production of human epidermal growth factor using fed‐batch cultures of recombinant Escherichia coli , 1991, Biotechnology and bioengineering.
[10] H. Chang,et al. High cell density culture of a recombinant Escherichia coli producing penicillin acylase in a membrane cell recycle fermentor , 1990, Biotechnology and bioengineering.
[11] Armin Fiechter,et al. Mass culture of Escherichia coli: Medium development for low and high density cultivation of Escherichia coli B/r in minimal and complex media , 1985 .
[12] N. Nishimura,et al. Cultivation of Escherichia coli Harbouring Hybrid Plasmids , 1987 .
[13] K. Taylor,et al. Optimization of Escherichia coli growth by controlled addition of glucose , 1989, Biotechnology and bioengineering.
[14] I. Olafsson,et al. High-level expression of active human cystatin C in Escherichia coli. , 1989, Gene.
[15] H G Crabtree,et al. Observations on the carbohydrate metabolism of tumours. , 1929, The Biochemical journal.
[16] G W Luli,et al. Comparison of growth, acetate production, and acetate inhibition of Escherichia coli strains in batch and fed-batch fermentations , 1990, Applied and environmental microbiology.
[17] D. Martens,et al. Calorimetric control of fed‐batch fermentations , 1990, Biotechnology and bioengineering.
[18] Persistence of pBR322-related plasmids in Escherichia coli grown in chemostat cultures , 1984 .
[19] H. Doelle,et al. Regulation of glucose metabolism in bacterial systems , 1982 .
[20] H. Blanch,et al. Recombinant trypsin production in high cell density fed‐batch cultures in Escherichia coli , 1993, Biotechnology and bioengineering.
[21] Steven M. Schlasner,et al. An automatic, on-line glucose analyzer for feed-back control of fed-batch growth of Escherichia coli , 1987 .
[22] Shoichi Shimizu,et al. HIGH DENSITY CULTIVATION OF BIOMASS IN FED-BATCH SYSTEM WITH DO-STAT , 1979 .
[23] Norio Shimizu,et al. Fed-batch cultures of recombinant Escherichia coli with inhibitory substance concentration monitoring , 1988 .
[24] W. Holms,et al. Control of carbon flux to acetate excretion during growth of Escherichia coli in batch and continuous cultures. , 1989, Journal of general microbiology.
[25] T. Ritch,et al. Production of human alpha consensus interferon in recombinant Escherichia coli , 1986 .
[26] R. Siegel,et al. Kinetic study of instability of recombinant plasmid pPLc23trpAl in E. coli using two‐stage continuous culture system , 1985, Biotechnology and bioengineering.
[27] Satoru Mizutani,et al. On-line control of glucose concentration using an automatic glucose analyzer , 1987 .
[28] C. Curless,et al. Effect of Preinduction Specific Growth Rate on Recombinant Alpha Consensus Interferon Synthesis in Escherichia coli , 1990, Biotechnology progress.
[29] P. Denéfle,et al. High-cell density fermentation studies of recombinant Escherichia coli strains expressing human interleukin-1β , 1988 .
[30] J. Bailey,et al. A parametric study of cloned fusion protein expression in Escherichia coli. , 1988, Biotechnology and bioengineering.
[31] S. Bauer,et al. Pilot scale exponential growth of Escherichia coli W to high cell concentration with temperature variation , 1976, Biotechnology and bioengineering.
[32] S. Shimizu,et al. Effect of amino acid supplement on cell yield and gene product in Escherichia coli harboring plasmid , 1986, Biotechnology and bioengineering.
[33] Armin Fiechter,et al. Acetate formation in continuous culture of Escherichia coli K12 D1 on defined and complex media , 1984 .
[34] S. Carlsen,et al. Production of recombinant human growth hormone in Escherichia coli: Expression of different precursors and physiological effects of glucose, acetate, and salts , 1990, Biotechnology and bioengineering.
[35] C. Curless,et al. Design and evaluation of a two‐stage, cyclic, recombinant fermentation process , 1991, Biotechnology and bioengineering.
[36] D. Tempest. The Place of Continuous Culture in Microbiological Research , 1969 .
[37] A. Kahru,et al. Glucose-limited fed-batch cultivation of Escherichia coli with computer-controlled fixed growth rate. , 1990, Biotechnology and bioengineering.
[38] A. E. Humphrey,et al. Estimation of Fermentation Biomass Concentration by Measuring Culture Fluorescence , 1978, Applied and environmental microbiology.
[39] E. Ziv,et al. Dense growth of aerobic bacteria in a bench‐scale fermentor , 1976, Biotechnology and bioengineering.
[40] T. Holme,et al. Removal of inhibitors of bacterial growth by dialysis culture. , 1977, Journal of general microbiology.
[41] Charles L. Cooney,et al. Computer control of bakers' yeast production , 1979 .
[42] M. Klein,et al. Control of misincorporation of de novo synthesized norleucine into recombinant interleukin-2 in E. coli. , 1988, Biochemical and biophysical research communications.
[43] B G Thompson,et al. Control of ammonium concentration in Escherichia coli fermentations , 1985, Biotechnology and bioengineering.