The outer membranes of many gram-negative bacteria contain a major heat-modifiable protein which shows serological cross-reactivity with the OmpA protein of E. coli K-12. Using the cloned gene for the E. coli K-12 protein as a DNA-DNA hybridization probe, the authors were able to identify the corresponding genes from S. dysenteriae, E. aerogenes, and S. marcescens. These were cloned in a phage λ vector, and their expression in E. coli K-12 was studied. All 3 OmpA proteins were fully produced and correctly exported to the outer membrane. In several cases, complete or partial restoration of known functions of the E. coli K-12 protein was observed.
CITATION STYLE
Cole, S. T., Sonntag, I., & Henning, U. (1982). Cloning and expression in Escherichia coli K-12 of the genes for major outer membrane protein OmpA from Shigella dysenteriae, Enterobacter aerogenes, and Serratia marcescens. Journal of Bacteriology, 149(1), 145–150. https://doi.org/10.1128/jb.149.1.145-150.1982
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