Two Escherichia coli strains, widely used for the production of various recombinant proteins, were compared for their pre-induction growth and acetate accumulation patterns. The strains studied were €, coliBL21 (ADES), transformed with a plasmid encoding Pseudomonas exotoxin A, and an €. coli K12 de
Influence of acetate on the growth of recombinant Escherichia coli JM103 and product formation
✍ Scribed by H. H. Lischke; L. Brandes; Xiaoan Wu; K. Schügerl
- Publisher
- Springer
- Year
- 1993
- Tongue
- English
- Weight
- 218 KB
- Volume
- 9
- Category
- Article
- ISSN
- 1615-7605
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✦ Synopsis
The influence of the acetate addeed to the M9 minimal medium and to the Luria-Bertani medium without and with glucose supplement on the growth of recombinant Escherichia coli J 103 with three different types of multicopy plasmids and on the production of the fusion protein SpA :: EcoRI were investigated in shake flasks without and with induction of the gene expression by a temperature shift from 30 ~ to 42 ~ At the beginning of the induction of gene expression concentrated LB-medium was added to the shake flask. Without this supplement of M9 medium no gene expression occurred.
List of symbols
LB
Luria Bertani cultivation medium (
Table 2) M9 cultivation medium (Table 1) P enzym activity [u ml 1] TCC total cell count [106 cells ml 1] # specific growth rate [h-1]
📜 SIMILAR VOLUMES
EcoRI fusion protein was produced by Escherichia coli JM103 carrying the multicopy expression plasmid pMTC48, the multicopy repressor plasmid pRK248, and the multicopy protection plasmid pEcoR4 in a 60-L working volume airlift tower loop reactor on M9 minimal medium with glucose. Cell mass concentra