An engineered Escherichia coli having a high intracellular level of ATP and enhanced recombinant protein production

2011 ◽  
Vol 94 (4) ◽  
pp. 1079-1086 ◽  
Author(s):  
Hye-Jung Kim ◽  
Yeong Deok Kwon ◽  
Sang Yup Lee ◽  
Pil Kim
Author(s):  
Gilson Campani ◽  
Maurício Possedente dos Santos ◽  
Gabriel Gonçalves da Silva ◽  
Antônio Carlos Luperni Horta ◽  
Alberto Colli Badino ◽  
...  

2016 ◽  
Vol 74 (5) ◽  
pp. 891-908 ◽  
Author(s):  
Susan Schlegel ◽  
Pierre Genevaux ◽  
Jan-Willem de Gier

2019 ◽  
Vol 116 (6) ◽  
pp. 1259-1268 ◽  
Author(s):  
Martin Lemmerer ◽  
Juergen Mairhofer ◽  
Alexander Lepak ◽  
Karin Longus ◽  
Rainer Hahn ◽  
...  

2007 ◽  
Vol 9 (2) ◽  
pp. 133-141 ◽  
Author(s):  
Shamik S. Sharma ◽  
Frederick R. Blattner ◽  
Sarah W. Harcum

2020 ◽  
Vol 3 (1) ◽  
Author(s):  
Patrick J. Shilling ◽  
Kiavash Mirzadeh ◽  
Alister J. Cumming ◽  
Magnus Widesheim ◽  
Zoe Köck ◽  
...  

AbstractThe pET series of expression plasmids are widely used for recombinant protein production in Escherichia coli. The genetic modules controlling transcription and translation in these plasmids were first described in the 1980s and have not changed since. Herein we report design flaws in these genetic modules. We present improved designs and demonstrate that, when incorporated into pET28a, they support increases in protein production. The improved designs are applicable to most of the 103 vectors in the pET series and can be easily implemented.


Sign in / Sign up

Export Citation Format

Share Document