Circular plasmid DNA which is used as a vector, can be cleaved at one site with the help of enzyme to give a linear DNA molecule. A foreign DNA segment can now be inserted, by joining the ends of broken circular DNA to the two ends of foreign DNA, thus regenerating a bigger circular DNA molecule that can now be separated by gel electrophoresis on the basis of its size Bacteriophages provide another source of cloning vectors. Since, usually, a phage has a linear DNA molecule, a single break will generate two fragments, which are later joined together with foreign DNA to generate a chimeric phage particle