Molecular analysis of the UV protection and mutation genes carried by the I incompatibility group plasmid TP110
Open Access
- 30 September 1986
- journal article
- research article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 168 (1) , 251-256
- https://doi.org/10.1128/jb.168.1.251-256.1986
Abstract
The imp genes, responsible for the UV protection and mutation effects of the I incompatibility group plasmid TP110, have been cloned into vector plasmids, and their products have been analyzed. The genetic information required for expression of these properties was carried in a continuous DNA sequence of approximately 1.7 kilobases, encoding the production of two proteins with molecular weights of 11,000 and 51,000. The genetic arrangement of this system therefore appears similar but not identical to the functionally related umuDC and mucAB operons. A third protein with a molecular weight of 40,000 was produced from sequences downstream from imp and could be overproduced by high-level transcription through the imp genes. This protein was not required for the protection and mutation properties.This publication has 28 references indexed in Scilit:
- Expression of eight unrelated Muc+ plasmids in eleven DNA repair-deficient E. coli strainsMutation Research/DNA Repair Reports, 1983
- Cloning and characterization of the umu operon responsible for inducible mutagenesis in Escherichia coliGene, 1983
- Proteins required for ultraviolet light and chemical mutagenesisJournal of Molecular Biology, 1983
- Identification of plasmid (pKM101)-coded proteins involved in mutagenesis and UV resistanceNature, 1982
- DNA-damage inducible genes on the I group plasmid TP 110Biochimie, 1982
- A restriction map of the Incl1 plasmid TP110Plasmid, 1982
- Specific-purpose plasmid cloning vectors I. Low copy number, temperature-sensitive, mobilization-defective pSC101-derived containment vectorsGene, 1981
- Plasmid vectors for high-efficiency expression controlled by the promoter of coliphage lambdaGene, 1981
- Construction and characterization of new cloning vehicles III. Derivatives of plasmid pBR322 carrying unique Eco RI sites for selection of Eco RI generated recombinant DNA moleculesGene, 1978
- A simple method for the preparation of large quantities of pure plasmid DNABiochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis, 1975