Cloning and expression in Escherichia coli of genes encoding a multiprotein complex involved in secretion of proteins from Staphylococcus aureus

Author:

Adler L A1,Arvidson S1

Affiliation:

1. Department of Bacteriology, Karolinska Institutet, Stockholm, Sweden.

Abstract

The genes encoding the multiprotein membrane-bound ribosomal protein (MBRP) complex (mrp genes), associated with membrane-bound ribosomes in Staphylococcus aureus, were cloned in Escherichia coli. All four components (molecular sizes 71, 60, 46, and 41 kilodaltons) of the MBRP complex were expressed from an 8.5-kilobase DNA fragment as judged by Western blot (immunoblot) analysis. The order of the individual genes within the cloned DNA fragment was determined by deletion mutagenesis and subcloning of various restriction fragments. Three RNAs, transcribed from the same DNA strand, were identified within the MBRP-coding region: one large RNA of approximately 5.9 kilobases, presumably coding for all four MBRP components, and two minor RNAs, coding for MBRP-71 and MBRP-60. The two minor RNAs seemed to be transcribed from promoters within the large transcription unit. Attempts to make insertional inactivations of the mrp genes with an internal 600-base-pair DNA fragment of the MBRP-coding region as a target were unsuccessful, presumably because such insertions are lethal.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference30 articles.

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2. Immunological crossreaction between proteins supposed to be involved in protein secretion in Staphylococcus aureus and Bacillus subtilis;Adler L.;FEMS Microbiol. Lett.,1984

3. Correlation between the rate of exoprotein synthesis and the amount of the multiprotein complex on membrane bound ribosomes (MBRP-complex) in Staphylococcus aureus;Adler L.;J. Gen. Microbiol.,1987

4. Analysis of gene control signals by DNA fusion and cloning in Escherichia coli;Casadaban M.;J. Mol. Biol.,1980

5. Secretory S-complex of Bacillus subtilis forms a large, organized structure when released from ribosomes;Caulfield M. P.;Proc. Natl. Acad. Sci. USA,1985

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