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Limiting factors in Escherichia coli fed‐batch production of recombinant proteins
Author(s) -
Sandén Anna Maria,
Prytz Ingela,
Tubulekas Ioannis,
Förberg Cecilia,
Le Ha,
Hektor Andrea,
Neubauer Peter,
Pragai Zoltan,
Harwood Colin,
Ward Alan,
Picon Antonia,
de Mattos Joost Teixeira,
Postma Pieter,
Farewell Anne,
Nyström Thomas,
Reeh Solvejg,
Pedersen Steen,
Larsson Gen
Publication year - 2002
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.10457
Subject(s) - protein biosynthesis , growth rate , biochemistry , ribosome , acetic acid , recombinant dna , escherichia coli , lac operon , biology , chemistry , guanosine , rna , gene , geometry , mathematics
Fed‐batch production of recombinant β‐galactosidase in E. coli was studied with respect to the specific growth rate at induction. The cultivations were designed to induce protein production by IPTG at a glucose feed rate corresponding to high (μ = 0.5 h −1 ) or low (μ = 0.1 h −1 ) specific growth rate. Protein production rate was approximately 100% higher at the higher specific growth rate, resulting in the accumulation of β‐galactosidase up to 30% of the total cell protein. Transcription analysis showed that β‐galactosidase‐specific messenger RNA was immediately formed after induction (<5 min), but the amount was the same in both cases and was thus not the initial limiting factor. The content of ribosomes, as represented by rRNA, rapidly decreased with specific growth rate from a relative level of 100%, at the high specific growth rate, to 20% at the low specific growth rate. At high specific growth rate, ribosomes were additionally degraded upon induction due to the high production level. Translation therefore seemed to be the initial limiting factor of the protein synthesis capacity. The alarmone guanosine tetraphosphate increased at both high and low feed level inductions, indicating an induction‐forced starvation of charged tRNA and/or glucose. The altered physiological status was also detected by the formation of acetic acid. However, the higher production rate resulted in high‐level accumulation of acetic acid, which was absent at low feed rate production. Acetic acid production is thus coupled to the high product formation rate and is proposed to be due either to a precursor drain of Krebs cycle intermediates and a time lag before induction of the glyoxalate shunt, or to single amino acid overflow, since the model product is relatively poor in glycin and alanin. In conclusion, it is proposed that production at high specific growth rate becomes precursor‐limited, while production at low specific growth rate is carbon‐ and/or energy‐limited. © 2002 Wiley Periodicals, Inc. Biotechnol Bioeng 81: 158–166, 2003.