AEM
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Berges, H.
Right arrow Articles by Fayet, O.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Berges, H.
Right arrow Articles by Fayet, O.
Agricola
Right arrow Articles by Berges, H.
Right arrow Articles by Fayet, O.

 Previous Article  |  Next Article 

Appl. Environ. Microbiol., Jan 1996, 55-60, Vol 62, No. 1
Copyright © 1996, American Society for Microbiology

Combined effects of the signal sequence and the major chaperone proteins on the export of human cytokines in Escherichia coli

H Berges, E Joseph-Liauzun and O Fayet
Laboratoire de Microbiologie et Genetique Moleculaire, Centre National de la Recherche Scientifique, Toulouse, France.

We have studied the export of two human proteins in the course of their production in Escherichia coli. The coding sequences of the granulocyte- macrophage colony-stimulating factor and of interleukin 13 were fused to those of two synthetic signal sequences to direct the human proteins to the bacterial periplasm. We found that the total amount of protein varies with the signal peptide-cytokine combination, as does the fraction of it that is soluble in a periplasmic extract. The possibility that the major chaperone proteins such as SecB and the GroEL-GroES and DnaK-DnaJ pairs are limiting factors for the export was tested by overexpressing one or the other of these chaperones concomitantly with the heterologous protein. The GroEL-GroES chaperone pair had no effect on protein production. Overproduction of SecB or DnaK plus DnaJ resulted in a marked increase of the quantity of human proteins in the periplasmic fraction, but this increase depends on the signal peptide-heterologous protein-chaperone association involved.


This article has been cited by other articles:




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. Microbiol. Mol. Biol. Rev. Eukaryot. Cell All ASM Journals

Copyright © 1996 by the American Society for Microbiology. All rights reserved.