Cloned diphtheria toxin fragment A is expressed from the tox promoter and exported to the periplasm by the SecA apparatus of Escherichia coli K12.
The diphtheria toxin fragment A-related polypeptide encoded by the recombinant plasmid pDT201 (Leong, D., Coleman, K. D., and Murphy, J. R. (1983) Science 220, 515-517) and expressed in Escherichia coli K12 was found to have an electrophoretic mobility in sodium dodecyl sulfate-polyacrylamide gels corresponding to 28,500 daltons. Immunoprecipitation experiments revealed that the mature form of the fragment A-related polypeptide was exported to the periplasmic compartment of E. coli K12 harboring plasmid pDT201. The polypeptide was sensitive to trypsin "nicking." Following treatment an Mr = 24,000 fragment was released which co-electrophoresed with fragment A of diphtheria toxin. The precursor form (Mr = 31,000) of the fragment A-related polypeptide was found to accumulate in the cytoplasmic fraction of the temperature-sensitive secretion-defective strain of E. coli K12 under nonpermissive conditions. We further demonstrate that a 263-base pair HaeIII fragment of pDT201 which carries the putative diphtheria tox promoter has promoter activity in E. coli K12.[1]References
- Cloned diphtheria toxin fragment A is expressed from the tox promoter and exported to the periplasm by the SecA apparatus of Escherichia coli K12. Leong, D., Coleman, K.D., Murphy, J.R. J. Biol. Chem. (1983) [Pubmed]
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