Cloning and expression of plasmid genes encoding resistances to chromate and cobalt in Alcaligenes eutrophus
- 1 September 1989
- journal article
- research article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 171 (9) , 5065-5070
- https://doi.org/10.1128/jb.171.9.5065-5070.1989
Abstract
Resistances to chromate and cobalt were cloned on a 30-kilobase-pair (kb) DNA region from the large Alcaligenes eutrophus plasmid pMOL28 into the broad-host-range mobilizable cosmid vector pVK102. A restriction nuclease map of the 30-kb region was generated. The resistances expressed from the hybrid plasmids after transfer back into A. eutrophus were inducible and conferred the same degree of resistance as the parent plasmid pMOL28. Resistances were expressed in metal-sensitive Alcaligenes strains and related bacteria but not in Escherichia coli. Resistance to chromate was further localized on a 2.6-kb EcoRI fragment, and resistance to cobalt was localized on an adjoining 8.5-kb PstI-EcoRI fragment. When the 2.6-kb EcoRI fragment was expressed in E. coli under the control of a bacteriophage T7 promoter, three polypeptides with molecular masses of 31,500, 21,000, and 14,500 daltons were visible on autoradiograms. The 31,500- and 21,000-dalton polypeptides were membrane bound; the 14,500-dalton polypeptide was soluble. ImagesThis publication has 26 references indexed in Scilit:
- Plasmid-determined resistance to chromate inPseudomonas aeruginosaFEMS Microbiology Letters, 1988
- Plasmid pMOL28-encoded resistance to nickel is due to specific effluxFEMS Microbiology Letters, 1988
- Plasmid pMOL28-mediated inducible nickel resistance inAlcaligenes eutrophusstrain CH34FEMS Microbiology Letters, 1987
- The Basics of Molecular BiologyPublished by Elsevier ,1986
- A bacteriophage T7 RNA polymerase/promoter system for controlled exclusive expression of specific genes.Proceedings of the National Academy of Sciences, 1985
- Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectorsGene, 1985
- A Broad Host Range Mobilization System for In Vivo Genetic Engineering: Transposon Mutagenesis in Gram Negative BacteriaBio/Technology, 1983
- Vector Plasmids for in-Vivo and in-Vitro Manipulations of Gram-Negative BacteriaPublished by Springer Nature ,1983
- Wide host range cloning vectors: A cosmid clone bank of an Agrobacterium Ti plasmidPlasmid, 1982
- Broad host range DNA cloning system for gram-negative bacteria: construction of a gene bank of Rhizobium meliloti.Proceedings of the National Academy of Sciences, 1980