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Expression patterns in Escherichia coli of two small archaeal proteins with a natural content of about 30% rare codons were analyzed. The proteins, a histone-like protein from Sulfolobus shibatae (Ssh10), and a glutaredoxin-like protein from Methanobacterium thermoautotrophicum (mtGrx), were produced with expression plasmids encoding wild-type genes, codon-optimized synthetic, and GST-fusion genes. These constructs were expressed in BL21 (DE3), its LysS derivative, and modified strains carrying copies for rare codon tRNAs or deletions in the RNAseE gene. Both Ssh10 and mtGrx expression levels were constitutively high in BL21(DE3) and its derivatives, with the exception of the LysS phenotype, which prevented high level expression of the Ssh10 wild-type gene. Surprisingly, a codon-optimized mtGrx gene construct displayed undetectable levels of protein production. The translational block observed with the synthetic mtGrx gene could be circumvented by using a synthetic mtGrx-glutathione S-transferase (GST) fusion construct or by in vitro translation. Taken together, the results underscore the importance of mRNA levels and RNA stability, but not necessarily tRNA abundance for efficient heterologous protein production in E. coli.

Original publication

DOI

10.1016/j.bbrc.2003.11.091

Type

Journal article

Journal

Biochemical and biophysical research communications

Publication Date

01/2004

Volume

313

Pages

89 - 96

Addresses

Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm SE-171 77, Sweden.

Keywords

Escherichia coli, Sulfolobus, Methanobacterium, Archaeal Proteins, Recombinant Fusion Proteins, RNA, Messenger, Codon, RNA, Transfer, Circular Dichroism, Spectrometry, Mass, Electrospray Ionization, Protein Biosynthesis, Gene Expression Regulation, Bacterial, Protein Structure, Secondary, RNA Stability, Genes, Archaeal, Artificial Gene Fusion