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Appl. Environ. Microbiol., Jan 1996, 55-60, Vol 62, No. 1
H Berges, E Joseph-Liauzun and O Fayet
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.
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
Laboratoire de Microbiologie et Genetique Moleculaire, Centre National de la Recherche Scientifique, Toulouse, France.
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