High-level production of membrane proteins in E. coli BL21(DE3) by omitting the inducer IPTG-Reference-Cited by-同舟云学术

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High-level production of membrane proteins in E. coli BL21(DE3) by omitting the inducer IPTG

Published:2015-09-16 Issue:1 Volume:14 Page:
ISSN:1475-2859
Container-title:Microbial Cell Factories
language:en
Short-container-title:Microb Cell Fact

Author:

Zhang Zhe,Kuipers Grietje,Niemiec Łukasz,Baumgarten Thomas,Slotboom Dirk Jan,de Gier Jan-Willem,Hjelm Anna

Funder

European Molecular Biology Organization (DE)

Marie Curie Initial Training Network grant

Swedish Research Council (VR-NT)

Stiftelsen för Strategisk Forskning (SE)

Publisher

Springer Science and Business Media LLC

Subject

Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

Link

http://link.springer.com/content/pdf/10.1186/s12934-015-0328-z

Reference29 articles.

1. Makino T, Skretas G, Georgiou G. Strain engineering for improved expression of recombinant proteins in bacteria. Microb Cell Fact. 2011;10:32.

2. Schlegel S, Klepsch M, Gialama D, Wickstrom D, Slotboom DJ, de Gier JW. Revolutionizing membrane protein overexpression in bacteria. Microb Biotechnol. 2010;3(4):403–11.

3. Studier FW. Stable expression clones and auto-induction for protein production in E. coli. Methods Mol Biol. 2014;1091:17–32.

4. Studier FW, Moffatt BA. Use of bacteriophage T7 RNA polymerase to direct selective high-level expression of cloned genes. J Mol Biol. 1986;189(1):113–30.

5. Chamberlin M, McGrath J, Waskell L. New RNA polymerase from Escherichia coli infected with bacteriophage T7. Nature. 1970;228(5268):227–31.

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