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Molecular cloning and DNA sequence analysis of a diphtheria tox iron-dependent regulatory element (dtxR) from Corynebacterium diphtheriae.
254
Citations
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References
1990
Year
EngineeringGeneticsBacteriologyMolecular BiologyMolecular GeneticsGenomicsTranscriptional RegulationProtein ExpressionDiphtheria ToxinStructural GeneGene StructureTranscription FactorsDna Sequence AnalysisVirulence FactorTox ExpressionMolecular CloningMolecular MicrobiologyCorynebacterium DiphtheriaeGene ExpressionFunctional GenomicsSynthetic BiologyMicrobiologySystems BiologyMedicineMicrobial Genetics
Although the structural gene for diphtheria toxin, tox, is carried by a family of closely related corynebacteriophages, the regulation of tox expression is controlled, to a large extent, by its bacterial host Corynebacterium diphtheriae. Optimal yields of tox gene products are obtained only when iron becomes the growth-rate-limiting substrate. Previous studies suggest that regulation of tox expression is mediated through an iron-binding aporepressor. To facilitate molecular cloning of the tox regulatory element from genomic libraries of C. diphtheriae, we constructed a tox promoter/operator (toxPO)-lacZ transcriptional fusion in Escherichia coli strain DH5 alpha. We report the molecular cloning and nucleic acid sequence of a diphtheria tox iron-dependent regulatory element, dtxR, and demonstrate that expression of beta-galactosidase from the toxPO-lacZ fusion is regulated by dtxR-encoded protein in an iron-sensitive manner. In addition, we show that expression of the toxPO-lacZ fusion is not affected by the E. coli iron-regulatory protein Fur and that the dtxR protein does not inhibit expression of fur-regulated outer-membrane proteins.
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