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Appl. Environ. Microbiol., 05 1997, 1808-1813, Vol 63, No. 5
E Lammertyn, L Van Mellaert, S Schacht, C Dillen, E Sablon, A Van Broekhoven and J Anne
In order to evaluate the expression and secretion signals of the highly
secreted subtilisin inhibitor of Streptomyces venezuelae CBS762.70 (VSI)
for the production of heterologous proteins by Streptomyces lividans, mouse
tumor necrosis factor alpha (mTNF) was chosen as a model protein. The mTNF
cDNA was fused to the vsi signal sequence. The analysis of secretion by
sodium dodecyl sulfate-polyacrylamide gel electrophoresis and biological
activity measurements revealed an efficient translocation of mTNF. Up to
300 mg of secreted biologically active mTNF per liter could be obtained in
shaken-flask cultures. By analyzing the effects of mutations in the N
region of the VSI signal peptide on secretion, we found that decreasing the
+3 charge of the wild-type protein to +2 resulted in a 3- to 10-fold
increase in secretion.
Copyright © 1997, American Society for Microbiology
Evaluation of a novel subtilisin inhibitor gene and mutant derivatives for the expression and secretion of mouse tumor necrosis factor alpha by Streptomyces lividans
Laboratory of Bacteriology, Rega Institute, Katholieke Universiteit Leuven, Belgium.
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