PMID:8168498
Citation |
Missiakas, D, Georgopoulos, C and Raina, S (1994) The Escherichia coli dsbC (xprA) gene encodes a periplasmic protein involved in disulfide bond formation. EMBO J. 13:2013-20 |
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Abstract |
We have identified and functionally characterized a new Escherichia coli gene, dsbC, whose product is involved in disulfide bond formation in the periplasmic space. It corresponds to a previously sequenced open reading frame mapping upstream of recJ with no previously assigned function. Null mutations in dsbC were obtained using a screen for dithiothreitol (DTT)-sensitive mutants and were shown to result in the accumulation of reduced forms of a variety of disulfide bond-containing periplasmic proteins. This defect could be rescued by the addition of either oxidized DTT or cystine or by multicopy expression of dsbA, a known periplasmic disulfide oxidase. The DsbC protein is synthesized as a precursor form of 25.5 kDa which is processed to a 23.3 kDa mature species located in the periplasmic space. The DsbC protein was overexpressed, purified to homogeneity and shown to catalyse the reduction of insulin in a DTT-dependent manner at levels comparable with those of purified DsbA. The replacement of either cysteine residue of the predicted active site, F-(X4)-C-G-Y-C, completely inactivates DsbC protein function. We have further shown that in vivo overexpression of DsbC can functionally substitute for a loss of DsbA function. Taken together, all of our results demonstrate that DsbC acts in vivo as a disulfide oxidase. |
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Keywords |
Amino Acid Sequence; Base Sequence; Chromosome Mapping; Cloning, Molecular; DNA Mutational Analysis; Disulfides/metabolism; Escherichia coli/enzymology; Escherichia coli/genetics; Genes, Bacterial/genetics; Isomerases/genetics; Isomerases/metabolism; Membrane Proteins/genetics; Molecular Sequence Data; Mutagenesis, Site-Directed; Protein Disulfide Reductase (Glutathione)/genetics; Protein Disulfide Reductase (Glutathione)/metabolism; Protein Disulfide-Isomerases; Sequence Analysis, DNA; Sequence Homology, Amino Acid |
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Main Points of the Paper
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Materials and Methods Used
Please list the materials and methods used in this paper (strains, plasmids, antibodies, etc).
Phenotype Annotations
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Phenotype of | Taxon Information | Genotype Information (if known) | Condition Information | OMP ID | OMP Term Name | ECO ID | ECO Term Name | Notes | Status |
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a mutation or genetic difference within a strain |
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Sensitivity to DTT |
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a mutation or genetic difference within a strain |
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Reduced alkaline phosphatase activity |
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a mutation or genetic difference within a strain |
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Hypersensitivity to benzylpenicillin |
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a mutation or genetic difference within a strain |
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Inability to grow on minimal medium |
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a mutation or genetic difference within a strain |
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Inability to grow on minimal medium |
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a mutation or genetic difference within a strain |
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Defective Disulfude Bond formation. See figure 2 for experimental results. |
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a mutation or genetic difference within a strain |
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Defective Disulfude Bond formation. See figure 2 for experimental results. |
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a mutation or genetic difference within a strain |
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Defective Disulfude Bond formation. See figure 2 for experimental results. |
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a mutation or genetic difference within a strain |
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The strain possess primarily reduced dsbA protein. |
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Notes
References
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