The cloning vector pBR322 is a common plasmid used in genetic engineering, particularly in E. coli.
pBR322 contains genes that provide resistance to two antibiotics:
The recognition site for the restriction enzyme BamHI is located within the tetracycline resistance gene (tet gene) of the pBR322 vector.
Inserting foreign DNA into a restriction site within a functional gene inactivates that gene.
Therefore, inserting foreign DNA at the BamHI site disrupts the tetracycline resistance gene, rendering it non-functional.
As a result of the inactivation of the tetracycline resistance gene, bacteria transformed with this recombinant plasmid will lose their resistance to Tetracycline. The ampicillin resistance gene is typically unaffected by insertion at the BamHI site, so resistance to ampicillin is usually retained.
| List I | List II |
| A. Genetically modified organism | I. Agrobacterium tumefaciens |
| B. Thermostable DNA polymerase | II. Bt cotton |
| C. Ti plasmid | III. Thermus aquaticus |
| D. pBR322 | IV. Escherichia coli |
| List I | List II |
| A. Genetically modified organism | I. Agrobacterium tumefaciens |
| B. Thermostable DNA polymerase | II. Bt cotton |
| C. Ti plasmid | III. Thermus aquaticus |
| D. pBR322 | IV. Escherichia coli |